01 - Chemical and biological materials for industrial, scientific and agricultural use
05 - Pharmaceutical, veterinary and sanitary products
31 - Agricultural products; live animals
Goods & Services
Chemicals used in industry, science and photography, as well
as in agriculture, horticulture and forestry; amino acids
for use in industry; peptides for industrial purposes;
proteins for use in industry; chemical substances, chemical
materials and chemical preparations; filtering materials
[chemical, mineral, vegetable and other unprocessed
materials]; chemical preparations and materials for film,
photography and printing; salts for industrial purposes;
starches for use in manufacturing and industry; detergents
for use in manufacture and industry; putties, paste fillers
and glue for use in industry; synthetic resins, unprocessed;
unprocessed plastics; unprocessed and synthetic resins;
growing media, fertilizers and chemicals for use in
agriculture, horticulture and forestry; fire extinguishing
compositions; tempering and soldering preparations; chemical
substances for preserving foodstuffs; tanning substances;
adhesives for use in industry; chemical and organic
compositions for use in the manufacture of food and
beverages. Pharmaceutical and veterinary preparations, medical and
veterinary preparations; medicated additives for animal
foods; additives with medicinal effect for animal feed;
chemical preparations for medical purposes; chemical
preparations for pharmaceutical purposes; chemical
preparations for veterinary purposes; medicated animal feed;
fodder additives for medical purposes; amino acids for
medical purposes; amino acids for veterinary purposes;
esters, fats and oils for medical and veterinary purposes;
salts, especially potassium and sodium salts for medicinal
purposes; steroids; biological preparations for medical
purposes; biological preparations for veterinary purposes;
ferments for pharmaceutical purposes; yeast for dietetic
purposes; yeast for pharmaceutical purposes; starch for
dietetic or pharmaceutical purposes; enzymes for medical
purposes; enzymes for veterinary purposes; enzyme
preparations for medical purposes; enzyme preparations for
veterinary purposes; bacterial preparations for medical
purposes; bacterial preparations for veterinary purposes;
bacteriological preparations for medical use;
bacteriological preparations for veterinary use; cultures of
microorganisms for medical or veterinary use; nutritive
substances for microorganisms; bouillons for bacteriological
cultures; probiotic supplements; probiotic bacterial
formulations for veterinary use; probiotic bacterial
formulations for medical use; probiotic preparations for
dietetic purposes; antioxidants; sanitary preparations for
medical purposes; foodstuffs and dietetic substances for
medical or veterinary purposes; dietetic foods adapted for
medical use; nutritional supplements; albuminous
preparations for medical purposes; candy medicated;
medicinal drinks; dietetic beverages adapted for medical
purposes; dietetic substances for medical purposes; medical
preparations for slimming purposes; food for babies; dietary
supplements for humans; dietary supplements for animals;
dietary supplements and dietetic preparations; sugars, candy
and glucose for medicinal purposes; glucose for medical
purposes; albuminous foodstuffs for medical purposes;
protein dietary supplements; dietary fibre; mineral dietary
supplements; preparations of trace elements for human and
animal use; vitamin preparations; plasters; materials for
dressings; medical dressings, teeth filling material; dental
impression materials; dental preparations; disinfectants;
preparations for destroying vermin; pest control
preparations; fungicides; herbicides; dietary supplements,
not for medical purposes; food supplements in the form of
amino acids, peptides and proteins for animal feed, fish
feed and aquaculture; feed supplements, not for medical
purposes. Agricultural, horticultural, forestry and aquaculture
products; live animals; foodstuffs and fodder for animals;
bedding and litter for animals; animal foodstuffs; formula
animal feed; animal feed; foodstuffs for animals in the form
of foodstuffs for fish and aquaculture; bait, not
artificial; yeast for animal consumption; foodstuffs for
animals containing botanical extracts.
2.
Method to prepare metal oxide or silica for electronics application using recycled spherical metal oxide or silica
A method to process a raw metal oxide or silica, comprising the following steps: 1) Processing the raw metal oxide or silica using jet milling, and 2) Recovering the processed metal oxide or silica obtained from Step 1); wherein the raw metal oxide or silica is preferably a recycled spherical metal oxide or silica and has a primary particle size of less than 550 nm and larger than 80 nm; and the processed metal oxide or silica has a D95 of less than 5 μm.
01 - Chemical and biological materials for industrial, scientific and agricultural use
05 - Pharmaceutical, veterinary and sanitary products
31 - Agricultural products; live animals
Goods & Services
Chemicals used in industry, science and photography, as well
as in agriculture, horticulture and forestry; amino acids
for use in industry; peptides for industrial purposes;
proteins for use in industry; chemical substances, chemical
materials and chemical preparations; filtering materials
[chemical, mineral, vegetable and other unprocessed
materials]; chemical preparations and materials for film,
photography and printing; salts for industrial purposes;
starches for use in manufacturing and industry; detergents
for use in manufacture and industry; putties, paste fillers
and glue for use in industry; synthetic resins, unprocessed;
unprocessed plastics; unprocessed and synthetic resins;
growing media, fertilizers and chemicals for use in
agriculture, horticulture and forestry; fire extinguishing
compositions; tempering and soldering preparations; chemical
substances for preserving foodstuffs; tanning substances;
adhesives for use in industry; chemical and organic
compositions for use in the manufacture of food and
beverages. Pharmaceutical and veterinary preparations, medical and
veterinary preparations; medicated additives for animal
foods; additives with medicinal effect for animal feed;
chemical preparations for medical purposes; chemical
preparations for pharmaceutical purposes; chemical
preparations for veterinary purposes; medicated animal feed;
fodder additives for medical purposes; amino acids for
medical purposes; amino acids for veterinary purposes;
esters, fats and oils for medical and veterinary purposes;
salts, especially potassium and sodium salts for medicinal
purposes; steroids; biological preparations for medical
purposes; biological preparations for veterinary purposes;
ferments for pharmaceutical purposes; yeast for dietetic
purposes; yeast for pharmaceutical purposes; starch for
dietetic or pharmaceutical purposes; enzymes for medical
purposes; enzymes for veterinary purposes; enzyme
preparations for medical purposes; enzyme preparations for
veterinary purposes; bacterial preparations for medical
purposes; bacterial preparations for veterinary purposes;
bacteriological preparations for medical use;
bacteriological preparations for veterinary use; cultures of
microorganisms for medical or veterinary use; nutritive
substances for microorganisms; bouillons for bacteriological
cultures; probiotic supplements; probiotic bacterial
formulations for veterinary use; probiotic bacterial
formulations for medical use; probiotic preparations for
dietetic purposes; antioxidants; sanitary preparations for
medical purposes; foodstuffs and dietetic substances for
medical or veterinary purposes; dietetic foods adapted for
medical use; nutritional supplements; albuminous
preparations for medical purposes; candy medicated;
medicinal drinks; dietetic beverages adapted for medical
purposes; dietetic substances for medical purposes; medical
preparations for slimming purposes; food for babies; dietary
supplements for humans; dietary supplements for animals;
dietary supplements and dietetic preparations; sugars, candy
and glucose for medicinal purposes; glucose for medical
purposes; albuminous foodstuffs for medical purposes;
protein dietary supplements; dietary fibre; mineral dietary
supplements; preparations of trace elements for human and
animal use; vitamin preparations; plasters; materials for
dressings; medical dressings, teeth filling material; dental
impression materials; dental preparations; disinfectants;
preparations for destroying vermin; pest control
preparations; fungicides; herbicides; dietary supplements,
not for medical purposes; food supplements in the form of
amino acids, peptides and proteins for animal feed, fish
feed and aquaculture; feed supplements, not for medical
purposes. Agricultural, horticultural, forestry and aquaculture
products; live animals; foodstuffs and fodder for animals;
bedding and litter for animals; animal foodstuffs; formula
animal feed; animal feed; foodstuffs for animals in the form
of foodstuffs for fish and aquaculture; bait, not
artificial; yeast for animal consumption; foodstuffs for
animals containing botanical extracts.
01 - Chemical and biological materials for industrial, scientific and agricultural use
05 - Pharmaceutical, veterinary and sanitary products
Goods & Services
Chemicals used in industry, science and photography, as well
as in agriculture, horticulture and forestry; chemicals for
use in the pharmaceutical industry; chemical excipients and
chemical intermediates for use in the manufacture of
pharmaceutical products; amino acids for industrial
purposes; peptides for industrial purposes; proteins for use
in industry, proteins for the food industry, proteins for
use in manufacture; saccharide preparations, other than for
medical use; galactose for industrial purposes; mannose;
antioxidants for use in the manufacture of pharmaceuticals;
lipids for use in industry; chemical preparations for use in
the food industry, chemical preparations for the manufacture
of food supplements; chemical excipients and chemical
intermediate products for use in the manufacture of
foodstuffs, in particular food supplements; chemical
additives for use in the manufacture of probiotic products;
chemical additives for use in the manufacture of
pharmaceuticals, foodstuffs and pharmaceutical products;
probiotic bacterial formulations [other than for medical
use]; bacteria for use in food manufacture; bacterial
preparations for the food industry; probiotic bacteria for
the food industry; bacterial cultures for addition to food
products; probiotic bacterial cultures for the food
industry; milk ferments [bacteria preparations] used in
making foodstuffs; bacteria [other than for medical or
veterinary purposes]; bacteriological cultures [other than
for medical and veterinary use]; bacterial products [other
than for medical and veterinary use]; bacterial
preparations, other than for medical and veterinary use;
diagnostic kits comprising specimen receptors and reagents
for testing for selected bacteria; catalysts, in particular
biochemical catalysts; chemical substances for preserving
foodstuffs. Pharmaceutical and veterinary preparations; medical and
veterinary preparations; chemical preparations for medical,
pharmaceutical and veterinary purposes; antioxidants;
adjuvants for medical purposes; amino acids for medical and
veterinary purposes; amino acid preparations for medical,
veterinary and pharmaceutical purposes; synthetic peptides
for pharmaceutical purposes; esters, fats and oils for
medical and veterinary uses; salts, in particular potassium
and sodium salts for medicinal purposes; steroids;
biological preparations for medical and veterinary purposes;
ferments for pharmaceutical purposes; yeast or starch for
dietary and pharmaceutical purposes; enzymes and enzyme
preparations for medical and veterinary purposes; bacterial
and bacteriological preparations for medical or veterinary
purposes; bacterial poisons; cultures of microorganisms for
medical or veterinary use; nutritive substances for
microorganisms; bouillons for bacteriological cultures;
biological tissue cultures for medical and veterinary
purposes; tissue-regenerative pharmaceutical preparations;
probiotic supplements; probiotic bacterial formulations for
veterinary use; probiotic bacterial formulations for medical
use; probiotic preparations for dietary purposes; probiotic
preparations for medical use to help maintain a natural
flora in the digestive system; probiotic preparations for
dietary purposes; probiotic preparations for medicinal
purposes to maintain a natural flora in the digestive
system; dietetic foods and products for medical and
veterinary purposes; dietetic foods adapted for medical
purposes; albuminous preparations for medical purposes;
candy, medicated; medicinal drinks; dietetic beverages
adapted for medical purposes; dietetic substances for
medical purposes; medical preparations for slimming
purposes; food for babies; dietary supplements for human
beings; dietary supplements for animals; dietary supplements
and dietetic preparations; cachets for pharmaceutical
purposes; sugar, in particular rock candy and dextrose for
medical purposes; glucose for medical purposes; albuminous
foodstuffs for medical purposes; protein dietary
supplements; dietary fibre; mineral dietary supplements;
preparations of trace elements for human and animal use;
vitamin preparations.
The present invention provides for the use of a composition comprising at least one epoxy-functional silicone-epoxide copolymer (A) as sealant for sealing against hydrogen; a sealing element producible by curing said composition; an apparatus for producing and/or conducting and/or storing and/or converting and/or controlling hydrogen that has at least two joining partners separated from one another by said sealing element; a method of producing said apparatus; and a method of operating said apparatus.
Bacillaene producing bacteria and compositions containing bacillaene producing bacteria can be used as probiotic feed ingredients. Bacillaene or derivatives thereof can be used for treating bacterial diseases.
The present invention relates to a monomer composition comprising 5 wt.% to 15 wt.% of a phosphorus-containing monomer and a process for preparing a polymer dispersion from said monomer composition.
C08F 220/18 - Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
C08F 230/02 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing phosphorus
C09D 143/02 - Homopolymers or copolymers of monomers containing phosphorus
The invention relates to a flame-retardant composition, a polymeric composition, a lacquer or varnish or coating comprising the same, a system for producing the flame-retardant system and the use of the flame-retardant composition as well as a method of preparing the same.
C08F 230/02 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing phosphorus
A process for preparing polyether-siloxane block copolymers by hydrosilylation of alpha,omega-modified hydrosiloxanes with alpha,omega-modified di(meth)allyl polyethers in the presence of a hydrosilylation catalyst, wherein the reaction is performed in a solvent mixture comprising aromatic solvents and alkoxylated alcohol, is described.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Industrial chemicals; chromatography chemicals; releasing
agents [chemical]; chemicals for use in the refining of
hydrocarbons; chemical substances for removing impurities
from gases; chemical cleaning agents for use in industrial
manufacturing processes; chemical gas purifying agents;
oil-purifying chemicals; industrial chemical materials and
preparations, and organic chemicals for the industry;
chemical products for the production of catalysts; salts for
industrial purposes; catalysts; biochemical and chemical
catalysts; catalysts for the refining of hydrocarbons;
chemical catalysts for use in synthesis and olefin
purification; cracking catalysts for use in the petroleum
industry; catalysts for cracking hydrocarbons; catalyst
carriers; catalyst supports made of inorganic oxides;
catalysts to limit hydrocarbon emissions; catalysts for use
in industrial processes; chemical adsorbents; chemical
adsorbents for the removal of catalyst poisons; oxides;
oxides of metal; modified metal oxides for industrial
purposes; bauxite; aluminum oxides [aluminum oxide];
aluminium oxides [aluminum oxide] for the adsorption of
catalyst poisons; modified aluminum oxides for the
adsorption of catalyst poisons; china clay; chemical
adsorbents for removing contaminants from fuel; technical
ceramics and composite materials for heat transfer or heat
management applications, namely ceramic materials in the
form of granules for industrial purposes, ceramic matrix
composites [cmc] for use in production processes, heat
transfer fluids for use in heating systems; chemical
adsorbents for the removal of catalyst poisons from
hydrocarbons; chemical adsorbents for the removal of
catalyst poisons from a hydrocarbon stream; chemical
adsorbents for the removal of catalyst poisons from a heavy
oil stream; chemical adsorbents for the removal of catalyst
poisons from refinery process streams; catalysts for the
production of plastics, rubber and polymers; catalysts for
the petroleum processing industry; petroleum dispersants;
catalysts for use in the production of rubber; catalysts for
oxidation treatment; catalysts for use in the production of
plastics; chemical adsorbents; active chemical ingredients;
oxidising preparations; metal oxide powder for industrial
purposes; non-metal oxides for use in manufacture; synthetic
materials for absorbing oil; chemical cleaning additives for
gasoline; chemical additives for oils; chemical additives
for gasoline.
11.
COMPOSITION AND METHOD FOR A PROTECTIVE LAYER OF A METAL ELECTRODE OF A SECONDARY BATTERY
A composition is provided as a coating layer of an electrode of a secondary battery, especially a lithium battery. The composition includes an organic binder and a metal compound selected from the group consisting of a surface modified magnesium oxide, surface modified lithium doped magnesium oxide, surface modified magnesium phosphate and mixtures thereof.
A material composition to prepare a polymer electrolyte precursor composition capable to form a solid polymer electrolyte, which has: A) a comb-branched polymer with pendant functional groups; B)surface-modified silica particles; and C) a polymerizable solvent or a crosslinker; wherein the silica particles are capable to be dispersed in the polymerizable solvent or a non-polymerizable volatile organic solvent and form a colloidal silica dispersion can be made. The material composition can be used in preparation of a solid polymer electrolyte in a lithium ion battery to improve performance, a polymer electrolyte precursor composition, a preparation method of a solid polymer electrolyte, a method to prepare a lithium ion battery, a solid polymer electrolyte, an electrochemical device and a device.
The present invention relates to a method for producing pressed products made of a crosslinkable material based on an elastomer-containing powder or granulate, in particular a recycled material such as scrap tyres. The method also relates to the pressed products obtained therefrom and to the furtlier processing thereof. The pressed products are very well suited for further processing to form crosslinked elastomer compounds and moulded bodies formed therefrom, and for the substitution of raw rubber or compositions containing raw rubber.
A monomer composition is made, particularly to prepare a polymer electrolyte precursor composition capable of forming a solid polymer electrolyte. The monomer composition includes A) an alkylene oxide-based monomer and B) a siloxane monomer. A copolymer electrolyte precursor composition is made for preparation of a solid polymer electrolyte. A polymerization method prepares solid copolymer electrolyte. A copolymer, a solid copolymer electrolyte, and a solid-state lithium secondary battery are made. A method to prepare a solid-state lithium secondary battery is developed, and another method improves electrolyte mechanical property, ionic conductivity, and/or cycling performance in a lithium secondary battery by preparing a solid polymer electrolyte the monomer. An electrochemical device and a device are also provided.
H01M 10/0565 - Polymeric materials, e.g. gel-type or solid-type
C08F 220/28 - Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
C08F 230/08 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
Provided is a waterborne epoxy curing agent comprising a reaction product of a) at least one amine having at least one moiety in the formula of -QNH—, wherein Q is a divalent hydrocarbon group, and wherein the amine has at least one tertiary amino group and at least one primary amino group per molecule; and b) at least one polyether polyol modified epoxide having one or more epoxide groups. Also provided is preparation methods thereof.
The present invention relates to a composition for production of a polyurethane foam, containing a polyalkylene oxide-modified aryl sulfonate as additive, and to the use of the aryl sulfonate in the production of a polyurethane foam.
C08G 18/18 - Catalysts containing secondary or tertiary amines or salts thereof
C08G 18/24 - Catalysts containing metal compounds of tin
C08G 18/28 - Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
The invention is concerned with laminates composed of LiSICon material, and production and use thereof. The object of the invention was to specify a membrane for separation of lithium out of contaminated lithium-containing waters, which is comparatively inexpensive and permits good permeance for lithium in electrodialysis operation. This object is achieved by coating a substrate with a LiSICon by way of aerosol-based cold deposition. In this way, a laminate that is of excellent suitability as membrane for electrodialytic lithium deposition owing to its particular material combination is obtained.
C23C 14/22 - Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
B01D 67/00 - Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
C23C 24/04 - Impact or kinetic deposition of particles
B05D 1/02 - Processes for applying liquids or other fluent materials performed by spraying
B05D 3/04 - Pretreatment of surfaces to which liquids or other fluent materials are to be appliedAfter-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to gases
C04B 35/447 - Shaped ceramic products characterised by their compositionCeramic compositionsProcessing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxides based on phosphates
C04B 38/00 - Porous mortars, concrete, artificial stone or ceramic warePreparation thereof
C04B 41/00 - After-treatment of mortars, concrete, artificial stone or ceramicsTreatment of natural stone
20.
PHOTOSTABILIZED COMPOSITIONS AND A METHOD FOR STABILIZING PHOTOSENSITIVE COMPONENTS
Photostabilized compositions may include a water-soluble tyrosine-containing compound with a molecular weight of below 1 kDa and at least one photosensitive component. A method for stabilizing one or more photosensitive components may include the addition of a tyrosine-containing dipeptide with the one or more photosensitive components. The water-soluble tyrosine-comprising compound may be present at a concentration of at least 0.5 mM. The composition may be a culture medium.
C08J 11/14 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with steam or water
C08J 11/16 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with inorganic material
22.
IMPROVED METHOD FOR DEPOLYMERISING POLYETHYLENE TEREPHTHALATE
The invention relates to a method for depolymerising polyethylene terephthalate ("PET"), in which PET is reacted with electrolytically prepared alkali metal glycolate, in particular sodium or potassium glycolate, to form a mixture M1 comprising bis(2-hydroxyethyl) terephthalate ("BHET"). The method according to the invention is characterised in that BHET accounts for a particularly high proportion of the breakdown products in the mixture M1. As a result, the method according to the invention provides a high yield of BHET, which can be used directly for renewed PET production. The present invention also relates to a method for recycling PET, in which the BHET obtained in the method for depolymerising PET is polymerised again to PET, optionally after further purification from M1.
C08J 11/22 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds
C08J 11/24 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds containing hydroxyl groups
C08L 67/02 - Polyesters derived from dicarboxylic acids and dihydroxy compounds
23.
IMPROVED METHOD FOR THE DEPOLYMERIZATION OF POLYETHYLENE TEREPHTHALATE
The present invention relates to a method for the depolymerization of polyethylene terephthalate (PET), in which method PET is reacted with sodium glycolate or potassium glycolate which has been obtained via reactive distillation, to form a mixture M1 comprising bis(2-hydroxyethyl) terephthalate (BHET). The method according to the invention is characterized in that BHET forms a particularly high proportion of the cleavage products in the mixture M1. As a result, the method according to the invention provides a high yield of BHET, which can be used directly to produce PET again. The present invention therefore also relates to a method for recycling PET, in which method the BHET that is obtained in the method for the depolymerization of PET and, if necessary, has been further purified from M1, is repolymerized to form PET.
B01J 23/16 - Catalysts comprising metals or metal oxides or hydroxides, not provided for in group of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
C08J 11/18 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material
C08J 11/22 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds
The present invention relates to a composition Z which comprises at least one quaternary ammonium compound. The compositions Z can be used as active substances for cleaning and active-substance compositions, especially softener compositions. The compositions Z have good softening properties and are at the same time characterized by an improved rewetting power.
C11D 3/00 - Other compounding ingredients of detergent compositions covered in group
C07C 219/06 - Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having the hydroxy groups esterified by carboxylic acids having the esterifying carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms of an acyclic saturated carbon skeleton
The present invention relates to a composition (Z) which comprises at least one quaternary ammonium compound. The compositions (Z) can be used as active substances for cleaning and active-substance compositions, especially softener compositions. The compositions (Z) have good softening properties and are at the same time characterized by an improved rewetting power.
C11D 3/00 - Other compounding ingredients of detergent compositions covered in group
C07C 217/42 - Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having etherified hydroxy groups and at least two amino groups bound to the carbon skeleton
The present invention relates to a pH responsive polymer composition for enteric coating of a hard shell capsule for delivering a pharmaceutical dosage form, especially microbiota, in the ileum and colon. The pH responsive polymer composition comprises at least one anionic poly(meth)acrylate copolymer, at least one glidant, at least one plasticizer, and 1 to < 6 wt. % of at least one non-ionic emulsifier based on total wt. % of the pH responsive polymer composition.
A61K 9/00 - Medicinal preparations characterised by special physical form
A61K 9/48 - Preparations in capsules, e.g. of gelatin, of chocolate
A61K 47/32 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers
A61K 47/14 - Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
A61P 1/00 - Drugs for disorders of the alimentary tract or the digestive system
A61P 1/04 - Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
A61P 31/00 - Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
The present disclosure relates to precipitated silicas characterized by a primary particle size mean of greater than 80 nm, a BET surface area of 10-40 m2/g, a total mercury intruded volume of 0.75-2.00 cc/g and an oil absorption of 60-120 cc/100 g. The inventive silica is produced by a process comprises
The present disclosure relates to precipitated silicas characterized by a primary particle size mean of greater than 80 nm, a BET surface area of 10-40 m2/g, a total mercury intruded volume of 0.75-2.00 cc/g and an oil absorption of 60-120 cc/100 g. The inventive silica is produced by a process comprises
(a) continuously feeding an acid and an alkali metal silicate or alkaline earth metal into a liquid medium at a silicate addition rate V1 and a temperature 70-96° C. with stirring to form the silica particles,
The present disclosure relates to precipitated silicas characterized by a primary particle size mean of greater than 80 nm, a BET surface area of 10-40 m2/g, a total mercury intruded volume of 0.75-2.00 cc/g and an oil absorption of 60-120 cc/100 g. The inventive silica is produced by a process comprises
(a) continuously feeding an acid and an alkali metal silicate or alkaline earth metal into a liquid medium at a silicate addition rate V1 and a temperature 70-96° C. with stirring to form the silica particles,
(b) stopping the feed of alkali metal silicate or alkaline earth metal silicate and acid and then increasing the temperature to 90 to 100° C. with stirring,
The present disclosure relates to precipitated silicas characterized by a primary particle size mean of greater than 80 nm, a BET surface area of 10-40 m2/g, a total mercury intruded volume of 0.75-2.00 cc/g and an oil absorption of 60-120 cc/100 g. The inventive silica is produced by a process comprises
(a) continuously feeding an acid and an alkali metal silicate or alkaline earth metal into a liquid medium at a silicate addition rate V1 and a temperature 70-96° C. with stirring to form the silica particles,
(b) stopping the feed of alkali metal silicate or alkaline earth metal silicate and acid and then increasing the temperature to 90 to 100° C. with stirring,
(c) adding an alkali metal silicate or alkaline earth metal silicate and an acid with stirring, wherein the silicate addition rate is 1 to 40% of the silicate addition rate V1 and the pH value of 9.0 to 10.0 is kept constant during the addition of the alkali metal silicate or alkaline earth metal silicate, by adjusting the acid rate,
The present disclosure relates to precipitated silicas characterized by a primary particle size mean of greater than 80 nm, a BET surface area of 10-40 m2/g, a total mercury intruded volume of 0.75-2.00 cc/g and an oil absorption of 60-120 cc/100 g. The inventive silica is produced by a process comprises
(a) continuously feeding an acid and an alkali metal silicate or alkaline earth metal into a liquid medium at a silicate addition rate V1 and a temperature 70-96° C. with stirring to form the silica particles,
(b) stopping the feed of alkali metal silicate or alkaline earth metal silicate and acid and then increasing the temperature to 90 to 100° C. with stirring,
(c) adding an alkali metal silicate or alkaline earth metal silicate and an acid with stirring, wherein the silicate addition rate is 1 to 40% of the silicate addition rate V1 and the pH value of 9.0 to 10.0 is kept constant during the addition of the alkali metal silicate or alkaline earth metal silicate, by adjusting the acid rate,
(d) stopping the addition of alkali metal silicate or alkaline earth metal silicate and adding acid with stirring until the pH of 5.0 to 7.0 is reached.
The present disclosure relates to precipitated silicas characterized by a primary particle size mean of greater than 80 nm, a BET surface area of 10-40 m2/g, a total mercury intruded volume of 0.75-2.00 cc/g and an oil absorption of 60-120 cc/100 g. The inventive silica is produced by a process comprises
(a) continuously feeding an acid and an alkali metal silicate or alkaline earth metal into a liquid medium at a silicate addition rate V1 and a temperature 70-96° C. with stirring to form the silica particles,
(b) stopping the feed of alkali metal silicate or alkaline earth metal silicate and acid and then increasing the temperature to 90 to 100° C. with stirring,
(c) adding an alkali metal silicate or alkaline earth metal silicate and an acid with stirring, wherein the silicate addition rate is 1 to 40% of the silicate addition rate V1 and the pH value of 9.0 to 10.0 is kept constant during the addition of the alkali metal silicate or alkaline earth metal silicate, by adjusting the acid rate,
(d) stopping the addition of alkali metal silicate or alkaline earth metal silicate and adding acid with stirring until the pH of 5.0 to 7.0 is reached.
The inventive precipitated silica is used in cosmetics, anti-caking free/flow, food, carrier applications, dentifrice and mouthwash.
C01B 33/193 - Preparation of finely divided silica neither in sol nor in gel formAfter-treatment thereof by acidic treatment of silicates of aqueous solutions of silicates
09 - Scientific and electric apparatus and instruments
42 - Scientific, technological and industrial services, research and design
44 - Medical, veterinary, hygienic and cosmetic services; agriculture, horticulture and forestry services
Goods & Services
Herunterladbare und aufgezeichnete Daten; Datenbanken; Software; Anwendungssoftware; Software für die Daten- und Dateiverwaltung sowie für Datenbanken; Modelle für wissenschaftliche Laborversuche; Medien- und Veröffentlichungssoftware; Künstliche Intelligenz-Software und maschinelle Lernsoftware; Software zur Überwachung, Analyse, Steuerung und Ausführung von Vorgängen in der physischen Welt; System- und Systemunterstützungssoftware sowie Firmware; Software für virtuelle und erweiterte Realität; Informationstechnologische, audiovisuelle, multimediale und fotografische Geräte; Datenspeichergeräte und -medien; Computer und Computerhardware; Magnete, Magnetisierungs- und Entmagnetisierungsvorrichtungen; Wissenschaftliche Geräte und Laborgeräte für physikalische Reaktionen mittels Elektrizität; Mess-, Erkennungs-, Überwachungs- und Kontrollgeräte; Prüf- und Qualitätskontrollgeräte; Messgeräte und -apparate; Sensoren, Detektoren sowie Überwachungsinstrumente und -apparate; Apparate für wissenschaftliche Forschung und Labor, Unterrichtsapparate und Simulatoren. IT-Dienstleistungen; Entwicklung, Programmierung und Implementierung von Software; Entwurf von Modellen; Entwurf mathematischer Modelle; Entwurf und Entwicklung von Prüf- und Analyseverfahren; Entwicklung und Prüfung chemischer Herstellungsverfahren; Entwicklung von Computerhardware; Hosting-Dienste; IT-Beratungs-, -Auskunfts- und -Informationsdienstleistungen; Wissenschaftliche und technologische Dienstleistungen; Wissenschaftliche Forschung und Analysen; wissenschaftliche Forschung bezüglich Kosmetika; wissenschaftliche Forschungsberatung auf dem Gebietder Kosmetik; industrielle Analyse und Forschung im Bereich Chemie und Kosmetik; Kosmetikforschung; Medizinische und pharmazeutische Forschungsdienstleistungen; Dienstleistungen von Ingenieuren; Ingenieurtechnologische Analysen; Naturwissenschaftliche Dienstleistungen; Dienstleistungen eines Chemikers; wissenschaftliche Analysen; biologische Analysen; Dienstleistungen im Bereich chemische Forschung und Analyse; chemische Forschung und Analyse; technologische Analysedienstleistungen; computergestützte wissenschaftliche Analyse; computergestützte industrielle Analysedienstleistungen; industrielle Analyse- und Forschungsdienstleistungen; chemische Beratung; Erteilung wissenschaftlicher Auskünfte; Erteilung von Auskünften bezüglich Informationstechnologie; Erteilung von Auskünften zum Thema wissenschaftliche Forschung auf dem Gebiet der Chemie und Kosmetik; Erteilung von wissenschaftlichen Auskünften zum Thema kosmetische Inhaltsstoffe; Bereitstellung wissenschaftlicher Informationen betreffend chemische Erzeugnisse und Kosmetika; Bereitstellung wissenschaftlicher Informationen im Bereich kosmetischer Inhaltsstoffe; Bereitstellung wissenschaftlicher Forschungsinformationen und Forschungsergebnisse über eine online durchsuchbare Datenbank; Bereitstellung wissenschaftlicher Forschungsinformationen und Forschungsergebnisse über eine interaktive Website; Bereitstellung von Online-Informationen zur industriellen Analyse und Forschung; Prüfung, Authentifizierung und Qualitätskontrolle; Durchführung wissenschaftlicher Untersuchungen; Durchführung chemischer Analysen für die Materialprüfung; Durchführung chemischer Analysen; Analyse- und Testdienstleistungen für die chemische und kosmetische Industrie; Prüfung von Kosmetika; Tests von Kosmetika; Materialprüfung und -analyse; Durchführung von Materialanalysen; Prüfung von chemischen Erzeugnissen und Kosmetika; Analysedienstleistungen bezüglich der Prüfung von chemischen Erzeugnissen und Kosmetika; chemische Analysedienstleistungen zur Verwendung bei Bewertungen; Prüfung kosmetischer Inhaltsstoffe; Prüfung, Analyse und Bewertung von Waren und Dienstleistungen Dritter für Zertifizierungszwecke; chemische Analysen; Bakteriologische Analysen; biochemische Analysen; analytische Labordienstleistungen; Designdienstleistungen; Design von computersimulierten Modellen; Computerdienstleistungen für Datenanalysen; Design und Entwicklung von Computerhardware und -software. Gesundheitspflege für den Menschen; Hygiene- und Schönheitspflege für den Menschen.
31.
GRAPHENE SUPRAPARTICLES, PROCESS FOR PRODUCTION THEREOF AND USE THEREOF
The present invention relates to a process for producing graphene supraparticles by dispersing graphene material having a particles size diameter d50 of 0.5 microns to 100microns in a solvent, preferably adding an additive to the dispersion, and at least partly removing the solvent from the dispersion thus obtained by spray drying to give graphene supraparticles
The present invention relates to a process for producing functionalized graphene supraparticles by dispersing the particles in a solvent, adding an additive to the dispersion, and at least partly removing the solvent from the dispersion thus obtained to give functionalized graphene supraparticles.
The present invention relates to a process for producing supraparticles composed of dry-coated graphene particles by dry-coating graphene material, dispersing the particles obtained in a solvent, adding an additive to the dispersion, and at least partly removing the solvent from the dispersion thus obtained by spray drying to give supraparticles composed of dry-coated graphene particles
The present invention relates to a process for producing functionalized supraparticles composed of dry-coated graphene particles by dry-coating graphene material, dispersing the particles obtained in a solvent, adding an additive to the dispersion, and at least partly removing the solvent from the dispersion thus obtained to give functionalized supraparticles composed of dry-coated graphene particles.
Polyether-modified siloxanes can be used as a dust binder for seed. Methods of reducing the evolution of dust from seed can be used with the polyether-modified siloxanes, and a treated seed is obtainable by these methods. Seed-dressing compositions or seed-dressing liquors contain the polyether-modified siloxanes.
The invention relates: 1) to a method for preparing polyetheramide aminophosphonic acids or polyetheramide aminophosphonate salts or aqueous solutions thereof, the method comprising the following steps: a) reacting at least one salicylic acid ester as a starting compound of an alkoxylation reaction in the presence of at least one double metal cyanide (DMC) catalyst with at least one epoxide to form at least one polyether; b) reacting the at least one polyether from step a) with at least one polyamine which bears at least two amino groups, selected from the group consisting of primary and secondary amino groups, to form at least one polyetheramide amine; c) reacting the at least one polyetheramide amine from step b) with at least one aldehyde and phosphonic acid to form at least one polyetheramide aminophosphonic acid; and optionally d) dissolving the at least one polyetheramide aminophosphonic acid from step c) in water; and optionally e) fully or partially neutralising the at least one polyetheramide aminophosphonic acid from step c) or the aqueous solution thereof from step d) using at least one base to form at least one polyetheramide aminophosphonate salt or the aqueous solution thereof; characterised in that (i) the at least one salicylic acid ester is selected from compounds of formula (1), where R is a hydrocarbon group having at least three carbon atoms; and (ii) at least propylene oxide is used as the epoxide, and, prior to optional reaction with further epoxides, the at least one salicylic acid ester is firstly reacted with propylene oxide; 2) to products which can be prepared according to this method; 3) to the use of these products as dispersant; 4) and to a hydraulically curing composition which these products contain.
C08G 65/26 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
An in vitro method for predicting the biological age of a subject includes: (a) bisulfite treatment of genomic DNA extracted from a biological sample obtained from the subject; (b) amplifying the bisulfite treated genomic DNA from step (a) with specific primers that target at least two Low Methylated Region (LMR) in the genomic DNA from (a) to obtain at least one PCR product; (c) measuring the methylation level of CpG sites in the PCR product of step (b); and (d) determining the biological age of the subject with a statistical prediction algorithm, wherein the statistical prediction algorithm is applied to the measured methylation level to determine the epigenetic age of the subject; wherein the subject is from the Galliformes family; and wherein at least three LMRs are amplified in step (b); and with a proviso that the CpG sites associated with single nucleotide polymorphisms are not considered.
C12Q 1/6881 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for tissue or cell typing, e.g. human leukocyte antigen [HLA] probes
C12Q 1/6806 - Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay
The present disclosure relates to an amine composition comprising a) an alkylated diamine b) a tertiary amine; and c) a polyoxyalkyleneamnne. Also disclosed are an epoxy system prepared from the amine composition and an epoxy resin and use thereof.
A spray polyurethane foam composition comprising the contact product of at least one polyisocyanate, at least one active hydrogen-containing compound, at least one blowing agent, and a catalyst composition.
C08G 18/72 - Polyisocyanates or polyisothiocyanates
C08J 9/12 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
C08J 9/14 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
40.
COMPOSITIONS OF EPOXY CURING AGENT INCORPORATING NAPHTHOL AND NAPHTHOL DERIVATIVES
The present invention relates to epoxy curing agent compositions comprising naphthol and naphthol derivatives in combination with at least one polyamine having three or more active amine hydrogens, and use of these curing agents as hardener for epoxy resins. These curing agent compositions may be used to cure, harden and/or crosslink an epoxy resin.
C07C 49/747 - Unsaturated compounds containing a keto group being part of a ring containing hydroxy groups containing six-membered aromatic rings
C07C 215/50 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups with amino groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
C07D 241/04 - Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
C09D 163/00 - Coating compositions based on epoxy resinsCoating compositions based on derivatives of epoxy resins
41.
TUNING OF FORMULATIONS BASED ON ANION-CONDUCTIVE POLYMERS (IONOMERS) FOR PRODUCING ELECTROCHEMICALLY ACTIVE LAYERS
The invention relates to the production of an electrochemically active layered body, to an electrochemically active layered body especially obtained by the production process, and to an electrochemical cell containing at least one such layered body. The invention additionally relates to a dispersion for producing the layered body. The problem addressed by the invention is that of making alternative ionomers useful for the production of electrochemically active layered bodies. The invention is based on the concept of processing an ionomer in a dispersion and using this dispersion to produce catalytically active layered bodies for electrochemical cells.
C25B 1/04 - Hydrogen or oxygen by electrolysis of water
C25B 11/077 - Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalysts material consisting of a single catalytic element or catalytic compound the compound being a non-noble metal oxide
42.
METHOD FOR THE FERMENTATIVE PRODUCTION OF L-LYSINE USING C. GLUTAMICUM STRAINS EXPRESSING HETEROLOGOUS NICOTINAMIDE NUCLEOTIDE TRANSHYDROGENASE PNTAB
Certain C. glutamicum strains overexpress genes coding for enzymes having the function of aspartate-semialdehyde dehydrogenase, aspartate aminotransferase, dihydrodipicolinate synthase, dihydrodipicolinate reductase, diaminopimelate decarboxylase, aspartatokinase and diaminopimelate dehydrogenase. The C. glutamicum strains also express NAD(P)(+) transhydrogenase subunit alpha PntA and NAD(P)(+) transhydrogenase subunit beta PntB of Corynebacterium urealyticum. A method is developed for the fermentative production of L-lysine using such C. glutamicum strains.
C12N 15/77 - Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora for CorynebacteriumVectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora for Brevibacterium
The invention relates to peroxide compatible heat treated precipitated silicas and preparation process thereof. The invention also relates to the use of peroxide compatible silicas in oral care formulations, in particular to improve whitening performance of toothpaste by controlling the timing of decomposition of peroxides in the toothpaste formulation.
A method synthesizes at least one 3-halopropyltrihalosilane compound. The method includes I) at least one unsaturated compound selected from the group consisting of allyl halide and methallyl halide; and II) at least one H-silane selected from the group consisting of trihalosilane, methyldihalosilane and dimethylhalosilane. The reaction of the at least one unsaturated compound and the at least one H-silane is carried out in the presence of: III) a Karstedt catalyst and IV) at least one cocatalyst according to formula (A). In formula (A), R1 is an aryl group; each R2 is independently an alkyl group; and n is 0 or 1. A catalyst composition suitable for mediating a hydrosilylation reaction. A reactive composition is produced from the reaction products.
A method for the physical reutilization of siliconized papers includes at least a first step (a), treating at least one siliconized paper by contacting it with at least one alcohol and at least one alkali metal alkoxide with introduction of heat, and without removing from the reaction mixture any water that occurs, and then, a second step (b), removing the at least one desiliconized paper resulting from the first step (a) from the optionally previously neutralized reaction mixture.
The present invention relates to a method of preparing a bioactive glass containing sponge based on collagen-like protein comprising or consisting of the steps: i) providing an aqueous solution comprising at least one collagen-like protein, at least one bioactive glass and optionally at least one additive; ii) performing a lyophilization step to obtain a sponge; iii) thereafter performing a dehydrothermal treatment to the sponge obtained in step ii); and iv) optionally sterilizing the sponge obtained after step iii). Furthermore, the present invention pertains to a sponge obtained by the method according to the present invention. Moreover, the present invention refers to particles obtained by shredding, milling or fragmentation of the sponge according to the present invention. Finally, the present invention refers to the use of the sponge according to the present invention or the particles according to the present invention for bone regeneration, cartilage repair, skin repair or as dental membrane.
A61L 27/46 - Composite materials, i.e. layered or containing one material dispersed in a matrix of the same or different material having a macromolecular matrix with phosphorus-containing inorganic fillers
The present invention relates to a composition for producing phenolic foam, comprising at least one phenolic resin, at least one blowing agent, at least one catalyst and at least one foam stabilizer according to formula 1. The invention also relates to a method for producing phenolic foam, to phenolic foam produced according to the method, and to the use of the phenolic foam.
C08G 65/26 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
C08G 65/336 - Polymers modified by chemical after-treatment with organic compounds containing silicon
C08J 9/00 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof
C08J 9/14 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
C08L 61/04 - Condensation polymers of aldehydes or ketones with phenols only
01 - Chemical and biological materials for industrial, scientific and agricultural use
05 - Pharmaceutical, veterinary and sanitary products
Goods & Services
Chemicals used in industry, science and photography, as well
as in agriculture, horticulture and forestry; chemicals for
use in the pharmaceutical industry; amino acids, peptides
and proteins for use industry purposes; protein [raw
material]; proteins for use in science; proteins for the
food industry; proteins for use in the manufacture of food
supplements; proteins for use in manufacture; protein for
use in the manufacture of foodstuffs; proteins for use in
the manufacture of beverages; proteins for use in
recombinant DNA technology [other than for medical use];
protein for use in the manufacture of cosmetics; proteins
for recognizing antibodies [other than for medical use];
proteins for binding antibodies [other than for medical
use]; chemical substances, chemical materials and chemical
preparations; chemical compositions and materials for use in
science; filtering materials [chemical, mineral, vegetable
and other unprocessed materials]; chemical preparations and
materials for film, photography and printing; salts for
industrial purposes; starches for use in manufacturing and
industry; detergents for use in manufacture and industry;
putties, and fillers and pastes for use in industry;
synthetic resins, unprocessed; unprocessed plastics; protein
plastics; unprocessed artificial and synthetic resins;
growing media, fertilizers and chemicals for use in
agriculture, horticulture and forestry; chemical substances
for preserving foodstuffs; adhesives for use in industry;
chemical and organic compositions for use in the manufacture
of food and beverages. Pharmaceutical and veterinary preparations; medical and
veterinary preparations; chemical preparations for medical,
pharmaceutical and veterinary purposes; amino acids for
medical and veterinary purposes; esters, fats and oils for
medical and veterinary uses; salts, in particular potassium
and sodium salts for medicinal purposes; steroids;
biological preparations for medical and veterinary purposes;
ferments for pharmaceutical purposes; yeast or starch for
dietary and pharmaceutical purposes; enzymes and enzyme
preparations for medical and veterinary purposes; bacterial
and bacteriological preparations for medical or veterinary
purposes; bacteriological preparations for pharmaceutical
use; biological tissue cultures for medical purposes;
biological tissue cultures for veterinary purposes; cultures
of microorganisms for medical or veterinary use; cultures
for veterinary use; cultures for medical use; culture media
for veterinary use; nutritive substances for microorganisms;
bouillons for bacteriological cultures; cell growth media
for growing cells for medical use; probiotic supplements;
probiotic bacterial formulations for veterinary use;
probiotic bacterial formulations for medical use; probiotic
preparations for dietary purposes; antioxidants; dietary
supplements and dietetic preparations; cachets for
pharmaceutical purposes; dietetic foods adapted for medical
purposes; dietetic preparations adapted for medical use;
dietetic food adapted for veterinary use; dietetic
substances adapted for veterinary use; nutritional
supplements; albuminous preparations for medical purposes;
candy, medicated; medicinal drinks; dietetic beverages
adapted for medical purposes; dietetic substances for
medical purposes; medical preparations for slimming
purposes; food for babies; dietary supplements for human
beings; dietary supplements for animals; sugar, in
particular rock candy and dextrose for medical purposes;
glucose for medical purposes; albuminous foodstuffs for
medical purposes; protein dietary supplements; dietary
fibre; mineral dietary supplements; preparations of trace
elements for human and animal use; vitamin preparations;
food supplements, not for medical use; food supplement made
from amino acids, peptides and proteins.
49.
TRANSITION METAL OXIDE PARTICLES ENCAPSULATED IN NANOSTRUCTURED LITHIUM TITANATE OR LITHIUM ALUMINATE, AND THE USE THEREOF IN LITHIUM ION BATTERIES
A process for producing a coated transition metal oxide involves subjecting a transition metal oxide and a pyrogenically produced lithium titanate and/or pyrogenically produced lithium aluminate to dry mixing. A coated transition metal oxide is obtainable by this process; and cathode for a lithium ion battery and a lithium ion battery containing such coated particles is useful.
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodesLithium-ion batteries
50.
HIGH-TEMPERATURE SPIRAL-WOUND MODULE MADE OF METAL COMPONENTS
The invention relates to a spiral-wound module (0) comprising a permeate tube (1), a spiral-wound coil (6), two ATDs (2f, 2r) and an outer tube (3) which extends coaxially with respect to the permeate tube (1), encloses the spiral-wound coil (6) and is joined to both ATDs (2f, 2r). It addresses the problem of specifying a spiral-wound module (0) which can be used at high operating temperatures, preferably above 150°C, and has a simple, robust and inexpensive design. This problem is solved in that the ATDs (2f, 2r) are fitted onto the permeate tube (1) and each lie against the respective end face of the spiral-wound coil (6), at least one of the two ATDs (2r) has a sleeve-like extension which is enclosed at its circumference by the outer tube (3) in such a way that a force-fit and/or form-fit connection (8) between the outer tube (3) and the ATD (2r) is realised via the extension (7) of the latter.
The present invention relates to an electrochemical cell (0) comprising an anode (1), a cathode (2) and an anion-conducting membrane (3) located between the anode (1) and the cathode (2). The invention also relates to the use of the cell (0) in a method for preparing hydrogen (H2) and oxygen (O2) by electrochemically splitting water (H2O). Moreover, the invention relates to an electrolyser (6, 8) comprising a multiplicity of the cells (0), and to a method for producing the electrolyser (6, 8). The aim of the invention is to provide an electrochemical cell (0) by means of which anion-exchange-membrane-based water splitting can be carried out on an industrial scale. The aim is also for the cell to be inexpensive in terms of production and to allow for the energy-efficient preparation of hydrogen and oxygen. The aim is achieved in that at least part of the anode is in the form of a first textile fabric comprising catalytically active textile line structures, and in that the first textile fabric directly contacts the membrane.
C25B 11/056 - Electrodes formed of electrocatalysts on a substrate or carrier characterised by the substrate or carrier material consisting of textile or non-woven fabric
C25B 1/04 - Hydrogen or oxygen by electrolysis of water
The present invention discloses a waterborne curing agent composition for epoxy coatings, a coating formulation comprising said curing agent composition and a coating comprising the cured coating formulation. The curing agent composition comprises an adduct of a polyaminoamide and an epoxide; a polyoxyalkyleneamine; a cycloaliphatic amine; and water.
C09D 163/00 - Coating compositions based on epoxy resinsCoating compositions based on derivatives of epoxy resins
C08G 59/18 - Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
A new method for recycling polyurethane, in particular polyurethane foam via solvolysis can be performed. The new method includes a very efficient pre-treatment method of the polyurethane, wherein it is converted into a polyurethane dispersion. The method also includes providing the polyurethane, preparing a dispersion, and solvolyzing the dispersion. The polyurethane has an average particle size of 0.1 to 12 mm.
C08J 11/16 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with inorganic material
The present invention relates to a method to prepare a composition for feeding a ruminant. The composition contains i) a non-protein nitrogen compound, and ii) a coating surrounding the non-protein nitrogen compound, wherein said coating includes one or more layers of a mixture of a saturated fat and a fatty acid, having from 60 wt. %+/−10% to 85 wt. %+/−10% of the saturated fat, e.g. hydrogenated fat, and from 15 wt. %+/−10% to 40 wt. %+/−10% of the fatty acid, each based on the total weight of the coating. A method for improving nitrogen utilization in a ruminant is also provided.
The invention relates to branched monoesters of formula (I), as well as to a dielectric fluid composition, intended for use as a cooling fluid for electrical equipment systems, comprising at least one of these branched monoesters of formula (I). The invention is also directed to a method of cooling electrical equipment systems by using the dielectric fluid compositions according to the invention.
C07C 69/24 - Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with monohydroxylic compounds
H01B 3/20 - Insulators or insulating bodies characterised by the insulating materialsSelection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils
56.
ETHYLENE VINYL ACETATE-BASED DISPERSIONS SUITABLE AS POUR POINT DEPRESSANTS WITH IMPROVED PERFORMANCE AND STABILITY
The invention relates to new ethylene vinyl acetate-based polymer dispersions with increased stability compared to state-of-the-art and to a preparation process thereof. The invention also relates to a method for inhibiting wax deposition and reducing the pour point, viscosity and yield stress of crude oils by treating the crude oils with these stable ethylene vinyl acetate-based polymer dispersions.
The present invention relates to processes for producing copper phyllosilicate shaped bodies, comprising the steps of:
providing a plastically deformable material comprising at least one SiO2 source, at least one Cu source and aqueous ammonia solution,
shaping the plastically deformable material so as to obtain blanks having a longitudinal expansion of at least 0.1 mm in all directions in space,
thermally treating the blanks so as to obtain shaped bodies comprising copper phyllosilicate.
The present invention relates to processes for producing copper phyllosilicate shaped bodies, comprising the steps of:
providing a plastically deformable material comprising at least one SiO2 source, at least one Cu source and aqueous ammonia solution,
shaping the plastically deformable material so as to obtain blanks having a longitudinal expansion of at least 0.1 mm in all directions in space,
thermally treating the blanks so as to obtain shaped bodies comprising copper phyllosilicate.
The present invention further relates to the shaped bodies obtainable by the processes according to the invention.
The present invention relates to processes for producing copper phyllosilicate shaped bodies, comprising the steps of:
providing a plastically deformable material comprising at least one SiO2 source, at least one Cu source and aqueous ammonia solution,
shaping the plastically deformable material so as to obtain blanks having a longitudinal expansion of at least 0.1 mm in all directions in space,
thermally treating the blanks so as to obtain shaped bodies comprising copper phyllosilicate.
The present invention further relates to the shaped bodies obtainable by the processes according to the invention.
These shaped bodies are used, as precursor of copper/silica catalysts, in numerous chemical transformations, for example for the hydrogenation of aldehydes and ketones to alcohols or in the dehydrogenation of alcohols.
The invention relates to a peroxo-polyoxometalate comprising a repeating unit selected from A, A' or B, wherein the units A, A', B consist of formula (I), wherein M is a metal ion selected from a group of Zr, Hf, Rf, Ce, Th, Nb, Ta, Re and any transition metal ion with a coordination number ≥ 8, wherein X is selected from the group of O or OH, wherein the repeating units A, A' and B can be fused directly to each other via a common metal atom 25 M or linked via an oxo, hydroxo or hydroperoxo group connecting two metal atoms M of two repeating units A, A', B, wherein the peroxo-polyoxometalate comprises m repeating units A, n repeating units B and o repeating units A', wherein n, m and o are an integer number selected from 0 to 20, wherein m, n and o cannot simultaneously be equal to 0, 30 wherein M is coordinated to polyoxometalate (POM), wherein the coordination number of each M is at least 8, wherein the peroxo-polyoxometalate comprises a ligand based on a mono-, di-, tri- lacunary Keggin or Wells-Dawson ions or wheels and its derivatives, wherein the peroxo-polyoxometalate has a linear, cyclic or spherical structure.
C07C 29/48 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups
C07C 45/29 - Preparation of compounds having C=O groups bound only to carbon or hydrogen atomsPreparation of chelates of such compounds by oxidation of hydroxy groups
C07C 51/285 - Preparation of carboxylic acids or their salts, halides, or anhydrides by oxidation with peroxy-compounds
C07C 51/31 - Preparation of carboxylic acids or their salts, halides, or anhydrides by oxidation of cyclic compounds with ring-splitting
59.
MIXED COMPOSITIONS COMPRISING 1,3-PROPANEDIOL ESTERS FOR COSMETIC FORMULATIONS IN PARTICULAR
The present invention relates to mixed compositions of 1,3-propanediol esters which have thickening and/or antimicrobial properties in cosmetic formulations in particular, and to the preparation and use thereof.
A61Q 17/00 - Barrier preparationsPreparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
The present invention discloses a method for separating gases from a crude gas stream a gas to be separated, a main remaining gas and optionally one or more further gas components, wherein in an apparatus comprising a feed stream separation stage, a first permeate separation stage and a second permeate separation stage, each stage being a membrane separation stage with gas separation membranes, a) a feed stream is fed into the feed stream separation stage, where it is separated to a first permeate stream and a first retentate stream, which is removed from the membrane system as second product or further processed or discarded, a) a feed stream is fed into the feed stream separation stage (1), where it is separated to a first permeate stream and a first retentate stream and the first retentate stream is removed from the membrane system as second product or further processed or discarded, b) the first permeate stream is compressed with compression unit (6) such that after compression, said compressed first permeate stream is fed into the first permeate separation stage (2), where it is separated to a second permeate stream and a second retentate stream, the second retentate stream is recycled to the feed stream or to the raw gas stream or further processed in the multistage membrane apparatus or removed from the multistage membrane apparatus or combined with the first retentate stream or discarded, c) the second permeate stream is without compression with a compressor fed into the second permeate separation stage (4), where it is separated to a third permeate stream, the third permeate stream is removed from the multistage membrane apparatus as first product stream or further processed or removed from the multistage membrane apparatus and thereafter further processed, and a third retentate stream, and d) the third retentate stream is fed to the first permeate stream to obtain a combined gas stream that is fed the compression unit (6) or is fed directly into the compression unit (6). A multistage membrane apparatus is also provided.
B01D 53/22 - Separation of gases or vapoursRecovering vapours of volatile solvents from gasesChemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by diffusion
The present invention relates a to a solid dispersion for feeding a ruminant comprising or consisting of i) from 40 wt.-% to 60 wt.-% of a biologically active ingredient, based on the total weight of the solid dispersion, ii) from 60 wt.-% to 40 wt.-% of a carrier, wherein the carrier comprises a mixture comprising from 35 wt.-% to less than 60 wt.-% of a hydrogenated fat and from more than 0 to 5 wt.- % of cellulose, each based on the total weight of the solid dispersion.
The invention relates to a method for producing a carboxylic acid, which comprises following reaction steps: a) providing an alicyclic ketone, an alicyclic alcohol or a mixture of an alicyclic ketone and an alicyclic alcohol, b) reacting the alicyclic alcohol and/or the alicyclic ketone from step a) with a peroxide or peroxide providing reagent in the presence of a catalyst to an oxidation product, c) separating the oxidation product from the catalyst, wherein the catalyst comprises a peroxo-polyoxometalate, wherein the peroxo-polyoxometalate comprising a repeating unit selected from A, A' or B, wherein the units A, A' and B consist of formula (I), wherein M is a metal ion selected from a group of Zr, Hf, Rf, Ce, Th, Nb, Ta, Re and any transition metal ion with a coordination number > 8, wherein the repeating units A, A' and/or B can be fused directly to each other via a common metal atom M or linked via an oxo, hydroxo or hydroperoxo group connecting two metal atoms M of two repeating units A, A' and/or B, wherein the peroxo-polyoxometalate comprises m repeating units A, n repeating units B and o repeating units A', wherein n, m and o are integer numbers selected from 0 to 20, wherein m, n and o cannot simultaneously be equal to 0, wherein M is coordinated to polyoxometalate (POM), wherein the coordination number of each M is at least 8, wherein the peroxo-polyoxometalate comprises a ligand based on mono-, di-, tri- lacunary Keggin or Wells-Dawson ions or wheels and its derivatives, wherein the peroxo-polyoxometalate has a linear, cyclic or spherical structure.
B01J 27/188 - PhosphorusCompounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
B01J 35/70 - Catalysts, in general, characterised by their form or physical properties characterised by their crystalline properties, e.g. semi-crystalline
63.
REACTOR, PLANT AND PROCESS FOR SYNTHESIS OF PRODUCTS BY STRONGLY EXOTHERMIC REACTIONS
Reactor for performing a synthesis process for producing products from at least two reactants comprising a main body having a longitudinal axis, an inflow side and an outflow side; an interior; at least two reactant conduits, each connected at the inflow side to at least one distributor channel; at least one product conduit connected at the outflow side to the at least one collection channel; at least one distribution section comprising at least two distributor channels and at least one flow splitter; at least one mixing section in which via mixing channels at least two distributor channels are connected and at least two reactants are combinable; at least one reaction channel; at least one collection section comprising at least one collection channel; at least one inflow-side feed conduit for a heat transfer medium into the interior and at least one discharge conduit for the heat transfer medium out of the interior, wherein the heat transfer medium can flow around at least a partial length of the at least one reaction channel in the interior and/or at least one heat exchange channel in which the heat transfer medium can flow is provided, wherein this at least one subsection is arranged adjacent to the at least one reaction channel and wherein at least one heat exchange channel and at least one reaction channel are separated from one another by a common channel wall, wherein the at least one reaction channel is a multiple helix which comprises two or more helix channels, wherein at the inflow side each helix channel of a multiple helix is connected via the at least one mixing section to at least one distributor channel of each of the at least two reactants and wherein at the outflow side each helix channel of a multiple helix is connected to at least one collection channel.
The invention relates to a polyglycerol partial ester obtainable by esterification of a) a polyglycerol mixture, b) poly(hydroxycarboxylic) acid, c) at least one dicarboxylic acid having 6 to 12, preferably 9 to 10, carbon atoms, more preferably selected from azelaic acid and sebacic acid, and d) oleic acid.
C07C 69/675 - Esters of carboxylic acids having esterified carboxyl groups bound to acyclic carbon atoms and having any of the groups OH, O-metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
C10M 129/78 - Complex esters, i.e. compounds containing at least three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compound: monohydroxy compounds, polyhydroxy compounds, monocarboxylic acids, polycarboxylic acids, hydroxy carboxylic acids
C10M 169/04 - Mixtures of base-materials and additives
The invention relates to a polyglycerol partial ester obtainable by esterification of a) a polyglycerol mixture, b) at least one dicarboxylic acid having 24 to 44, preferably 30 to 40, particularly preferably 34 to 38, carbon atoms, and c) oleic acid, characterized in that oleic acid makes up for at least 50 wt.-%, preferably at least 60 wt.-%, more preferably at least 68 wt.-% of all monocarboxylic acids esterified into the polyglycerol partial ester.
C08G 63/48 - Polyesters chemically modified by esterification by unsaturated higher fatty oils or their acidsPolyesters chemically modified by esterification by resin acids
C10M 129/78 - Complex esters, i.e. compounds containing at least three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compound: monohydroxy compounds, polyhydroxy compounds, monocarboxylic acids, polycarboxylic acids, hydroxy carboxylic acids
C10M 169/04 - Mixtures of base-materials and additives
Salts of dipeptides can be used in cell cultures. A culture medium can be used for culturing cells, preferably plant cells, animal cells or mammalian cells and a method of manufacturing a cell culture product. The dipeptide salt has at least one basic amino acid and a chloride-counterion. The molar ratio of the basic amino acid to chloride-ion is between 0.8 and 1.2
C07K 5/068 - Dipeptides the side chain of the first amino acid containing more amino groups than carboxyl groups, or derivatives thereof, e.g. Lys, Arg
C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor
67.
USE OF POLYETHER SILOXANES AS PROCESSING AIDS FOR MELT GRANULATION
The invention relates to the use of polyether siloxanes with less than 20 silicon atoms as a parting agent or parting agent constituent in melt granulation, a process for producing melt granules using these polyether siloxanes, and melt granules which are obtained by the use or by the process according to the invention.
The present invention discloses multistage membrane apparatus and a method for separating gases from a crude gas stream a gas to be separated, a main remaining gas and optionally one or more further gas components, wherein in the apparatus comprises a feed stream separation stage, a first permeate separation stage and a second permeate separation stage, each stage being a membrane separation stage with gas separation membranes.
B01D 71/64 - PolyimidesPolyamide-imidesPolyester-imidesPolyamide acids or similar polyimide precursors
B01D 53/22 - Separation of gases or vapoursRecovering vapours of volatile solvents from gasesChemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by diffusion
The invention relates to compositions comprising biosurfactant and manganese. It further relates to a method to stabilize the colour of a composition comprising biosurfactant and to the use of manganese to stabilize the colour of a composition comprising biosurfactant.
A process for producing a lithium titanium phosphate based solid electrolyte material is disclosed, the process comprising the steps of: (i) providing a solution comprising a Li source material, a Ti source material, a P source material and optionally a Si source material and/or a source material of a metal M, wherein M is selected from the group of Al, Ga, Ge, In, Sc, V, Cr, Mn, Co, Fe, Y, the lanthanides or a combination thereof; (ii) generating an aerosol from the solution; (iii) subjecting the generated aerosol to flame pyrolysis to form a particulate precursor material therefrom; and (iv) subjecting the particulate precursor material to field-assisted sintering to form the lithium titanium phosphate based solid electrolyte material. Furthermore, disclosed are a solid electrolyte material obtainable through said production process and articles comprising the same.
H01M 4/58 - Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFySelection of substances as active materials, active masses, active liquids of polyanionic structures, e.g. phosphates, silicates or borates
71.
HYDRAULIC LUBRICANT FORMULATIONS WITH HIGH FLASH POINT AND IMPROVED SHEAR STABILITY
Compositions have a high content of saturated or unsaturated isoparaffinic hydrocarbons with 12-24 carbon atoms and a polyalkyl (meth)acrylate. A method prepares said compositions to promote the raise of the flash point of hydraulic fluids where a good low temperature flow is important, e.g. compressor oils, shock absorber fluids, power steering fluids, and central hydraulic fluids.
C10M 111/04 - Lubricating compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups , each of these compounds being essential at least one of them being a macromolecular organic compound
C08F 220/18 - Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
C10M 107/28 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
C10M 177/00 - Special methods of preparation of lubricating compositionsChemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes
C10N 20/04 - Molecular weightMolecular weight distribution
The invention relates to silane-azodicarbonamide mixtures containing 5-95% by weight of azocarbonyl-functionalized silane of formula I based on the total amount of azocarbonyl-functionalized silane of formula I, silane of formula II and azodicarbonamide of formula III, (R1)3-a(R2)aSi—R3—NH—C(O)—N═N—R4 (I), 0-90% by weight of silane of formula II based on the total amount of azocarbonyl-functionalized silane of formula I, silane of formula II and azodicarbonamide compound of formula III, (R1)y(R2)3-y Si—R3—Sx—R3—Si(R1)y(R2)3-y (II) and 1-80% by weight of azodicarbonamide compound of formula III based on the total amount of azocarbonyl-functionalized silane of formula I, silane of formula II and azodicarbonamide compound of formula III, R5—NH—C(O)—N═N—C(O)—NH—R5 (III). The silane-azodicarbonamide mixture is produced by mixing 5-95% by weight of azocarbonyl-functionalized silane of formula I, 0-90% by weight of silane of formula II and 1-80% by weight of azodicarbonamide compound of formula III. The invention further relates to a rubber mixture containing at least one rubber, 5-95% by weight of azocarbonyl-functionalized silane of formula I, 0-90% by weight, silane of formula II and 1-80% by weight of azodicarbonamide compound of formula III.
The invention relates to precipitated silicas having the following physicochemical parameters: CTAB 50 m2/g-450 m2/g. BET/CTAB ratio <1.3, tailing factor 5%≥150 nm. The precipitated silicas are produced by reacting waterglass with H2SO4 using various ageing steps. The precipitated silicas can be used for production of rubber mixtures.
C01B 33/193 - Preparation of finely divided silica neither in sol nor in gel formAfter-treatment thereof by acidic treatment of silicates of aqueous solutions of silicates
The present invention relates to a culture medium, preferably a cell culture medium, comprising at least one dipeptide, the dipeptide comprising asparagine (Asn) and glutamine (Gln).
The present invention relates to a culture medium, preferably a cell culture medium, comprising at least one dipeptide, the dipeptide comprising asparagine (Asn) and glutamine (Gln).
The invention further relates to the use of a culture medium of the invention for culturing cells, preferably plant cells, animal cells or mammalian cells.
The present invention relates to a culture medium, preferably a cell culture medium, comprising at least one dipeptide, the dipeptide comprising asparagine (Asn) and glutamine (Gln).
The invention further relates to the use of a culture medium of the invention for culturing cells, preferably plant cells, animal cells or mammalian cells.
Another aspect of the invention relates to a method of manufacturing a cell culture product comprising the steps of (i) providing a cell capable of producing said cell culture product; (ii) contacting said cell with a culture medium according to the invention; and (iii) obtaining said cell culture product from said culture medium or from said cell.
The invention relates to additives for NCO-containing adhesive formulations, to NCO-containing adhesive formulations based on isocyanate prepolymers, to the use thereof in adhesive systems, and to a method for bonding and the use.
The present invention relates to a method of producing a composition of Gram-negative bacteria, the method comprising
(a) subjecting a wet mass of Gram-negative bacteria to spray drying; and
(b) contacting the spray-dried Gram-negative bacteria from step (a) to a compound,
wherein the compound has a general formula (I) of,
The present invention relates to a method of producing a composition of Gram-negative bacteria, the method comprising
(a) subjecting a wet mass of Gram-negative bacteria to spray drying; and
(b) contacting the spray-dried Gram-negative bacteria from step (a) to a compound,
wherein the compound has a general formula (I) of,
R1O—[(C2H3R2)—O]n—H Formula (I)
where
R1 is a monovalent aliphatic radical having 1 to 22, preferably 2 to 10, especially 3 to 4, carbon atoms;
R2 is in each case independently a hydrogen radical or a methyl radical; and
n is a number from 1 to 300, preferably from 5 to 100, especially from 10 to 30,
with the proviso that at least one R2 radical is a methyl radical.
The present invention refers to a patch, comprising a hydrogel base layer obtained by reacting at least one collagen-like protein and at least one cross-linker selected from 4-(4,6-dimethoxy-1,3,5- triazin-2-yl)-4-methyl-morpholinium chloride (DMTMM), glutaraldehyde, transglutaminase, diisocyanate, or a combination of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) and N- hydroxysuccinimide (NHS); optionally a further hydrogel layer obtained by reacting at least one collagen-like protein and at least one cross-linker comprising at least two groups each comprising a polyalkylene glycol moiety and a succinimidyl group; wherein the hydrogel base layer has a thickness of at most 8 mm and the patch has a thickness of at most 16 mm as well as a manufacturing method thereof. Furthermore, the present invention refers to the use of the patch according to the present invention for wound sealing, drug delivery, occlusive application, tissue regeneration, or forming a barrier membrane.
The invention relates to a computer-implemented method for producing a CAD model for an apparatus carrying a material system, wherein the material system comprises at least two material streams, and the apparatus is a heat exchanger or a reactor for synthesising at least one product from at least one starting material of at least one material stream, chosen from the following group: tube reactor, reactor with reaction and heat exchange channels or heat exchange chambers, continuous reactor, column with at least one intermediate tray, comprising the steps of: a) inputting system parameters into CAD software, wherein the system parameters comprise mass data, thermodynamic data and/or reaction data of the material system; b) creating the CAD model, comprising a three-dimensional and multiphysical simulation of the material system; c) outputting the CAD model to an output unit, evaluation unit and/or memory unit, and d) at least one definition step by means of a program module, which is upstream of the creation of the CAD model, wherein the definition step comprises the following: providing at least one digital spatial element, providing digital design elements, arranging the design elements in the spatial element, outputting a primary model as a further system parameter; e) generating the CAD model by means of the CAD software using the primary model as a further system parameter.
The present invention relates to amine catalyst compositions, and methods for making the compositions and using the catalyst composition as a gelling or blowing catalyst to make polyurethane foam.
A process for producing hydrogen peroxide with an oxidizing unit in an anthraquinone process can be performed. The process and oxidizing unit have a compressor for obtaining hot compressed oxygen containing gas. The hot compressed oxygen containing gas is utilized in a heat exchanger to increase the temperature of a compressed (cold) offgas obtained in an oxidizing step for the production hydrogen peroxide. Accordingly, the compressed and heated offgas can subjected to an expander without the formation of droplets or damaging the equipment. Moreover, the process and an oxidizing unit reduce the required amount of energy in the form of electrical power and steam, as well as the required amount of cooling medium in an anthraquinone process.
The invention relates to a method for producing an alkali metal alcoholate solution L1 in an electrolysis cell E which comprises at least one cathode chamber KK, at least one anode chamber KA, and at least one central chamber KM lying therebetween. The interior IKK of the cathode chamber KK is separated from the interior IKM of the central chamber KM by a separating wall W comprising at least one alkali-cation-conductive solid ceramic electrolyte (=“AFK”) F (e.g. NaSICON). F has the surface OF. A part OA/MK of the surface OF directly contacts the interior IKM, and a part OKK of the surface OF directly contacts the interior IKK. The surface OA/MK and/or the surface OKK comprises at least one part of a surface OFΔ. OFΔ is produced from a pre-treatment step in which F is produced from an AFK F′ comprising the surface OF′. For this purpose, AFK is removed from F′ by etching the surface OF′ using an etching agent Ä, and the AFK F with the surface OF comprising the surface OFΔ formed by the etching process is obtained. During the electrolysis process for producing the alkali metal alcoholates with F instead of F′, an improved conductivity is provided, whereby for a constant current density, a lower voltage can be used.
A method of producing a composition of Gram-negative bacteria includes
(a) subjecting a wet mass of Gram-negative bacteria to spray drying; and
(b) contacting the spray-dried Gram-negative bacteria from step (a) to a mixture including at least one hydrophobic, partially water-insoluble polyglycerol ester in combination with at least one emulsifier to form the composition of Gram-negative bacteria,
wherein the polyglycerol ester has a general formula (I) of,
A method of producing a composition of Gram-negative bacteria includes
(a) subjecting a wet mass of Gram-negative bacteria to spray drying; and
(b) contacting the spray-dried Gram-negative bacteria from step (a) to a mixture including at least one hydrophobic, partially water-insoluble polyglycerol ester in combination with at least one emulsifier to form the composition of Gram-negative bacteria,
wherein the polyglycerol ester has a general formula (I) of,
MaDbTc Formula (I)
wherein, M=[C3H5(OR)2O1/2],
D=[C3H5(OR)1O2/2],
T=[C3H5O3/2],
a=1 to 10;
b=0 to 10;
c=0 to 3;
wherein, the sum total of a+b+c is 1 to 20,
wherein the radicals R are independently selected from acyl radicals R′—C(=0)- and H, with the proviso that at least one radical R is not equal to H;
wherein the radicals R′ are independently selected from monovalent aliphatic, saturated or unsaturated hydrocarbon radicals with 3 to 39 carbon atoms.
DEUTSCHES KREBSFORSCHUNGSZENTRUM STIFTUNG DES ÖFFENTLICHEN RECHTS (Germany)
Inventor
Böhl, Florian
Lyko, Frank
Nagarajan, Sanjanaa
Roy, Suki
Lyko-Tönges, Sina
Venkatesh, Geetha
Pfefferle, Walter
Abstract
The present invention relates to a method of determining the supplier from which a test animal-derived product sample originates, the method comprising the steps of:
(a) determining a test methylation profile of one or more pre-selected methylation sites within the genomic material contained in the test animal-derived product sample; and
(b) comparing the test methylation profile determined in (a) with a panel of predetermined reference methylation profiles of the same biological taxon of the test animal from which the product sample derives, wherein each of the predetermined reference methylation profiles is from a different reference animal and/or different supplier,
wherein if the test methylation profile of (a) is significantly similar to one of the predetermined reference methylation profiles, the test animal-derived product sample is confirmed of originating from a first supplier from which a first reference animal with the predetermined reference profile is obtained.
The present invention discloses a secondary amine terminated block polyamide and preparation method and use thereof, in particular a block polyamide comprising terminal secondary amine groups, an epoxy curing composition comprising said block polyamide, an epoxy formulation comprising said epoxy curing composition or said block polyamide as epoxy curing agent, a cured product of said epoxy formulation, an article comprising said cured product, a process for preparing said block polyamide and use of said block polyamide as epoxy curing agents in coatings, adhesives, fiber reinforced composites, and mortars.
C08G 69/34 - Polyamides derived from amino carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids using polymerised unsaturated fatty acids
C08G 69/40 - Polyamides containing oxygen in the form of ether groups
C08G 69/48 - Polymers modified by chemical after-treatment
C08L 63/00 - Compositions of epoxy resinsCompositions of derivatives of epoxy resins
A shaped flexible hot-cure PU foam article, preferably mattress and/or cushion, may be obtained by reaction of at least one polyol component and at least one isocyanate component in the presence of at least one blowing agent and one or more catalysts that catalyze the isocyanate-polyol and/or isocyanate-water reactions and/or isocyanate trimerization, foam stabilizer, and further additives. The foam stabilizer may include at least one compound of formula (1)
A shaped flexible hot-cure PU foam article, preferably mattress and/or cushion, may be obtained by reaction of at least one polyol component and at least one isocyanate component in the presence of at least one blowing agent and one or more catalysts that catalyze the isocyanate-polyol and/or isocyanate-water reactions and/or isocyanate trimerization, foam stabilizer, and further additives. The foam stabilizer may include at least one compound of formula (1)
[R12R2SiO1/2]a[R13SiO1/2]b[R12SiO2/2]c[R1R2SiO2/2]d[R3SiO3/2]e[SiO4/2]fGg (1).
C08J 9/00 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof
A47C 7/18 - Seat parts having foamed material included in cushioning part
A47C 27/14 - Spring, stuffed or fluid mattresses specially adapted for chairs, beds or sofas with foamed material inlays
B65B 63/02 - Auxiliary devices, not otherwise provided for, for operating on articles or materials to be packaged for compressing or compacting articles or materials prior to wrapping or insertion in containers or receptacles
C08G 18/18 - Catalysts containing secondary or tertiary amines or salts thereof
C08G 18/24 - Catalysts containing metal compounds of tin
Composition for production of phenolic foam, comprising at least one phenolic resin, at least one blowing agent, at least one catalyst and at least one polyethersiloxane of formula 1: MaMb1DcDd1.
C08J 9/00 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof
C08J 9/14 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
An electrochemical cell (0) including an anode (1), a cathode (2) and an anion-conducting membrane (3) arranged between anode (1) and cathode (2). It also relates to the use of the electrochemical cell (0) in a process for producing hydrogen (H2) and oxygen (O2) by electrochemical splitting of water (H2O). The invention additionally relates to an electrolyser (6) having a multitude of cells (0) and to a process for producing the electrolyser (6). With the electrochemical cell (0) an AEM water electrolysis can be carried out on an industrial scale.
The invention relates to a method for producing an alkali metal alcoholate solution L1 in an electrolysis cell E which comprises at least one cathode chamber KK, at least one anode chamber KA, and at least one central chamber KM lying therebetween. The interior IKK of the cathode chamber KK is separated from the interior IKM of the central chamber KM by a separating wall W comprising at least one alkali-cation-conductive solid ceramic electrolyte (=“AFK”) F (e.g. NaSICON). F has the surface OF. A part OA/MK of the surface OF directly contacts the interior IKM, and a part OKK of the surface OF directly contacts the interior IKK. The surface OA/MK and/or the surface OKK comprises at least one part of a surface OFΔ. OFΔ is produced from a pre-treatment step in which F is produced from an AFK F′ comprising the surface OF′. For this purpose, AFK is removed from F′ by carrying out a compressed air blasting process on the surface OF′ using a solid blasting agent N, and the AFK F with the surface OF comprising the surface OFΔ formed by the compressed air blasting process is obtained. During the electrolysis process for producing the alkali metal alcoholates with F instead of F′, an improved conductivity is provided, whereby for a constant current density, a lower voltage can be used.
The invention relates to a method of treating a food product for increasing the weight of the food product, wherein the food product is selected from a group consisting of: an animal carcass, poultry, meat, seafood and parts thereof, said method comprising: introducing nano-bubbles (NB) into water or an aqueous solution to provide NB-comprising water and contacting the food product with NB-comprising water for a time sufficient to increase the weight of the food product.
The application relates to the identification and application of microorganisms which inhibit virus binding to viral target receptors by displaying decoy receptors on their surface, conferring competitive binding affinity to the viral particles.
The present invention relates to a polyurea coating composition comprising (A) a polyisocyanate: (B) a polyaspartic ester; and (C) a 2-substituted butanedioic acid ester prepared by reacting the fumaric ester in the polyaspartic acid ester solution with a cyanoacetate, a malononitrile or a 1,3-diketone in the presence of a base.
C07C 253/18 - Preparation of carboxylic acid nitriles by reaction of ammonia or amines with compounds containing carbon-to-carbon multiple bonds other than in six-membered aromatic rings
C07C 253/30 - Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
A hydrogel can be obtained by reacting at least one collagen-like protein and at least one cross-linker that has at least two groups each having a polyalkylene glycol moiety and a succinimidyl group. Furthermore, the hydrogel can be used as a stent, for wound sealing, drug delivery, healing promotion, cell culture, spheroid production, embryoid body formation, anti-adhesion barriers, coatings, sponges, and antibacterial dressings.
The present invention relates to a microbial cell for producing at least one lipid with general formula (II) from at least one carbon substrate, wherein R1and R2122 a glycosyltransferase (EC 2.4) comprising SEQ ID NO: 2, SEQ ID NO: 8, or SEQ ID NO: 12, or a variant thereof, wherein the variant comprises 60% sequence identity to SEQ ID NO: 2, 8 or 12.
Mixture compositions made of specifically chosen alkyl carboxylates can be used in a process for the preparation of ester compositions. These mixture compositions and ester compositions can be used in cosmetic applications.
Compositions and methods can be used to reduce the population of microorganisms present during the processing of grain and seeds. More specifically, microorganism levels are reduced in grain and seeds being malted by contacting the grain or seeds with a sanitizing solution that contains a peroxyacid and hydrogen peroxide. This is done shortly before steeping, the first step in malting procedures. Optionally, a sanitizing solution containing a peroxyacid and hydrogen peroxide may also be used at other points in the malting process.
A method treats a food product for increasing the weight of the food product. The food product is an animal carcass, poultry, meat, seafood or parts thereof. The method includes introducing nano-bubbles (NB) into water or an aqueous solution to provide NB-comprising water and contacting the food product with NB-comprising water for a time sufficient to increase the weight of the food product.
C07C 1/207 - Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as hetero atoms from carbonyl compounds
C07C 1/22 - Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as hetero atoms by reduction
2244; wherein the gas composition is an off-gas from at least one steam methane reformer and the off gas from the steam methane reformer is directly brought into contact with the genetically modified homoacetogenic bacterium; and the homoacetogenic bacterium is genetically modified to produce acetone from the gas composition.
The invention relates to a curable composition containing a polymer having at least two isocyanate-reactive groups that can react with isocyanate groups, wherein at least one of these isocyanate-reactive groups is a CH-acidic group, and a polyfunctional isocyanate having at least one isocyanate group and an alkaline earth metal organyl catalyst.
C08G 18/28 - Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
C09J 177/00 - Adhesives based on polyamides obtained by reactions forming a carboxylic amide link in the main chainAdhesives based on derivatives of such polymers
A process for producing a rigid PU or PIR foam can be performed by contacting at least one organic polyisocyanate having two or more isocyanate functions with an isocyanate-reactive mixture. The isocyanate-reactive mixture has at least one polyol, water and at least one emulsifier, wherein the emulsifier has at least one alkoxylated aromatic alcohol. The parent aromatic alcohol has at least 6 and at most 40 carbon atoms and also at least one OH function. At most ⅕ of the carbon atoms of the parent aromatic alcohol are not aromatic, and at least one aromatic unit in the parent aromatic alcohol must bear an OH function.
C08G 18/28 - Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
