A composition comprising a post‐consumer recycled polypropylene polyolefin; a virgin polypropylene polyolefin; and a non‐, partially, or fully hydrogenated resin is described, in addition to a biaxially oriented film produced from the composition, and methods for preparing and using the film.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemical products; synthetic resins; chemical and mineral products and substances and those of animal or plant origin, predominantly intended for industrial use; Resins in general.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Synthetic resins for industrial use; synthetic resins; plastics in the form of powders, liquids, pastes, flakes, granulates and pellets, all for industrial use; all included in Class 1.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
chemicals used in industry; adhesives for use in industry; dispersions, in particular colloidal dispersions of macromolecules; aqueous dispersions; dispersions of polymers; dispersions of co-polymers; plastics dispersions; binder dispersions; binder dispersions of polymers; binder dispersions of co-polymers; emulsions, in particular aqueous emulsions; emulsions of polymers; emulsion of co-polymers; latex, particularly in the form of aqueous dispersions and concentrated dispersions; unprocessed artificial resins; adhesives used in industry; adhesives for labels; chemical additives for adhesives; adhesives for use in bonding labels to substrates
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals used in industry; adhesives for use in industry; dispersions, in particular colloidal dispersions of macromolecules; aqueous dispersions; dispersions of polymers; dispersions of co-polymers; plastics dispersions; binder dispersions; binder dispersions of polymers; binder dispersions of co-polymers; emulsions, in particular aqueous emulsions; emulsions of polymers; emulsion of co-polymers; latex (as included in this class), particularly in the form of aqueous dispersions and concentrated dispersions; unprocessed artificial resins; adhesives used in industry; adhesives for labels; chemical additives for adhesives; adhesives for use in bonding labels to substrates.
8.
HEAT RESISTANT PROPYLENE-ETHYLENE COPOLYMERS AND ADHESIVES CONTAINING THE PROPYLENE-ETHYLENE COPOLYMERS
A family of propylene-ethylene copolymers have been discovered can be readily utilized in high heat resistance applications and form adhesives with improved mechanical strength and heat resistance. More particularly, the propylene-ethylene copolymers have a particular propylene content, triad tacticity, Ring and Ball softening point, and crystallinity that provide copolymers that exhibit desirable high heat resistance, tensile strength, and elongation. Furthermore, the propylene-ethylene copolymers may be used to produce adhesives that exhibit excellent heat resistance characteristics and superior cohesive strength.
01 - Chemical and biological materials for industrial, scientific and agricultural use
02 - Paints, varnishes, lacquers
Goods & Services
Unprocessed artificial and synthetic resins; synthetic resin compositions [unprocessed] for industrial purposes; synthetic resins for industrial use; synthetic resin for the manufacture of varnishes; Synthetic resins, adhesives, resinates and other applications using non-crystallisable, high-melting resins; varnish resins [synthetic]; core oils; rosins; rosin resins, rosin based artificial resins (unprocessed) and rosin derivatives. Colophony; raw natural resins; unprocessed natural resins; natural resins; resins for use in varnishes; resin acid salts and for other purposes in which high melting point non-crystallizing resins are used; raw natural resins for use in the manufacture of varnishes; gum resin.
01 - Chemical and biological materials for industrial, scientific and agricultural use
02 - Paints, varnishes, lacquers
Goods & Services
Industrial chemicals; raw chemicals; unprocessed artificial and synthetic resins; synthetic resin compositions [unprocessed] for industrial purposes; synthetic resins for industrial use inn liquid, semi-solid or solid form or in the form of flakes; rosins; rosin resins, rosin based artificial resins (unprocessed) and rosin derivatives. Colophony; raw natural resins; unprocessed natural resins.
A process to produce a polyolefin composition is provided comprising: 1) extruding at least one recycled polyolefin in the presence of at least one radical initiator (E) to produce an extruded visbroken recycled polyolefin; and 2) melt blending (A) about 60 to about 96 wt % of the extruded recycled polyolefin; (B) about 2 to about 20 wt % of at least one random alpha-olefinic copolymer; and (C) optionally, about 2 to about 20 wt % of at least one tackifier; (D) optionally, at least one additional polymer; wherein the polyolefin composition has a weight ratio of random alpha-olefinic copolymer to tackifier of between about 0.2 to about 5.0; and wherein the extruded, visbroken polyolefin composition has a melt flow rate increase of about 5 to about 1500% compared to the recycled polyolefin.
01 - Chemical and biological materials for industrial, scientific and agricultural use
02 - Paints, varnishes, lacquers
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Rosin salts and rosin derivatives; Chemicals for use in industry, science, photography, as well as in agriculture, horticulture and forestry; unprocessed artificial resins, unprocessed plastics; fertilizers for the land; compositions for extinguishing fire; preparations for tempering and welding of metals; chemicals intended for preserving food; tanning substances; adhesives (glues) for use in industry; Salts of rosin and derivatives of rosin for use as emulsifying agents, detergent additives, dispersants, foaming and flotation agents, viscosity control agents, and industrial sizing compounds; RESIN SOAP (RESIN THAT HAS BEEN SAPONIFIED WITH AN ALKALI); artificial resins; synthetic resins; resins in raw state; unprocessed synthetic resins. Colophony salts and derivatives; Colophony; raw natural resins. Resins in extruded form; Raw and semi-worked rubber, gutta-percha, gum, asbestos, mica and substitutes for all these materials; Extruded plastics [semi-finished products]; sealing and insulating materials; flexible pipes, not of metal; ARTIFICIAL RESINS AND SYNTHETIC RESINS (SEMI-FINISHED PRODUCTS); semi-processed synthetic resins; semi-processed artificial resins; Semi-worked polymer resins.
01 - Chemical and biological materials for industrial, scientific and agricultural use
02 - Paints, varnishes, lacquers
Goods & Services
Synthetic resins; Artificial resins; Hydrocarbon resins; Petroleum hydrocarbon resins; Petroleum hydrocarbon resins not included in other classes; Crude petroleum-based hydrocarbon resins in the form of powders, granules and emulsions; Petroleum hydrocarbonated resins; Resins derived from petroleum hydrocarbons; Resins from petroleum hydrocarbons; Resins for industrial use; Light-coloured synthetic resins composed chiefly of hydrocarbon polymers of deeply cracked petroleum. Raw natural resins.
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Synthetic resins; Synthetic resins (semi-finished products); Unprocessed synthetic resins; Synthetic resin in the raw state; Raw synthetic resins for use in the coating, adhesives, sealants and ink industries; Resins for industrial use; Artificial resins. Synthetic resins (semi-finished products); semi-processed synthetic resins; Artificial resins (semi-finished products); Semi-processed synthetic polymer resins.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Artificial resins for industrial purposes, in particular for the plastics industry, unprocessed plastics; Synthetic resins; Artificial resins; Industrial resins for the plastics industry; Unprocessed artificial resins for use in industry, namely for the plastics industry; Industrial resins for use in the plastic industry.
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
C08F 20/16 - Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
C08F 20/26 - Esters containing oxygen in addition to the carboxy oxygen
C08F 30/08 - Homopolymers or 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
A polyolefin composition is provided comprising: (A) about 60 to about 96 wt % of at least one recycled polyolefin; B) about 2 to about 20 wt % of at least one random alpha-olefinic copolymer; C) at least one tackifier; D) about 1 to about 60 wt % of at least one additional polymer; and wherein the polyolefin composition has a weight ratio of random alpha-olefinic copolymer to tackifier of between about 0.2 to about 5.0; and wherein the polyolefin composition has a melt flow rate increase of about 5 to about 400% compared to the same polyolefin, composition without the random alpha-olefinic copolymer, the tackifier, and the additional polymer. Processes for making and articles produced from the polyolefin compositions are also provided.
Propylene-ethylene copolymers are provided that exhibit superior tensile strength and mechanical properties due to their specific propylene and ethylene content, triad tacticity, viscosity, and crystallinity. Moreover, we have discovered that certain processing conditions, such as polymerization temperature and external donor to catalyst ratios, can facilitate the production of the high tensile strength propylene-ethylene copolymers described herein. Furthermore, the high tensile strength propylene-ethylene copolymers may be used to produce a variety of hot melt adhesives, such as those for hygiene applications, woodworking applications, lamination applications, and packaging applications, which exhibit unique and superior mechanical properties.
Propylene-ethylene copolymers are provided that exhibit superior tensile strength and mechanical properties due to their specific propylene and ethylene content, triad tacticity, viscosity, and crystallinity. Moreover, we have discovered that certain processing conditions, such as polymerization temperature and external donor to catalyst ratios, can facilitate the production of the high tensile strength propylene-ethylene copolymers described herein. Furthermore, the high tensile strength propylene-ethylene copolymers may be used to produce a variety of hot melt adhesives, such as those for hygiene applications, woodworking applications, lamination applications, and packaging applications, which exhibit unique and superior mechanical properties.
Propylene-ethylene copolymers are provided that exhibit superior tensile strength and mechanical properties due to their specific propylene and ethylene content, triad tacticity, viscosity, and crystallinity. Moreover, we have discovered that certain processing conditions, such as polymerization temperature and external donor to catalyst ratios, can facilitate the production of the high tensile strength propylene-ethylene copolymers described herein. Furthermore, the high tensile strength propylene-ethylene copolymers may be used to produce a variety of hot melt adhesives, such as those for hygiene applications, woodworking applications, lamination applications, and packaging applications, which exhibit unique and superior mechanical properties.
Propylene-ethylene copolymers are provided that exhibit superior tensile strength and mechanical properties due to their specific propylene and ethylene content, triad tacticity, viscosity, and crystallinity. Moreover, we have discovered that certain processing conditions, such as polymerization temperature and external donor to catalyst ratios, can facilitate the production of the high tensile strength propylene-ethylene copolymers described herein. Furthermore, the high tensile strength propylene-ethylene copolymers may be used to produce a variety of hot melt adhesives, such as those for hygiene applications, woodworking applications, lamination applications, and packaging applications, which exhibit unique and superior mechanical properties.
Propylene-ethylene copolymers are provided that exhibit superior tensile strength and mechanical properties due to their specific propylene and ethylene content, triad tacticity, viscosity, and crystallinity. Moreover, we have discovered that certain processing conditions, such as polymerization temperature and external donor to catalyst ratios, can facilitate the production of the high tensile strength propylene-ethylene copolymers described herein. Furthermore, the high tensile strength propylene-ethylene copolymers may be used to produce a variety of hot melt adhesives, such as those for hygiene applications, woodworking applications, lamination applications, and packaging applications, which exhibit unique and superior mechanical properties.
Propylene-ethylene copolymers are provided that exhibit superior tensile strength and mechanical properties due to their specific propylene and ethylene content, triad tacticity, viscosity, and crystallinity. Moreover, we have discovered that certain processing conditions, such as polymerization temperature and external donor to catalyst ratios, can facilitate the production of the high tensile strength propylene-ethylene copolymers described herein. Furthermore, the high tensile strength propylene-ethylene copolymers may be used to produce a variety of hot melt adhesives, such as those for hygiene applications, woodworking applications, lamination applications, and packaging applications, which exhibit unique and superior mechanical properties.
Propylene-ethylene copolymers are provided that exhibit superior tensile strength and mechanical properties due to their specific propylene and ethylene content, triad tacticity, viscosity, and crystallinity. Moreover, we have discovered that certain processing conditions, such as polymerization temperature and external donor to catalyst ratios, can facilitate the production of the high tensile strength propylene-ethylene copolymers described herein. Furthermore, the high tensile strength propylene-ethylene copolymers may be used to produce a variety of hot melt adhesives, such as those for hygiene applications, woodworking applications, lamination applications, and packaging applications, which exhibit unique and superior mechanical properties.
Propylene-ethylene copolymers are provided that exhibit superior tensile strength and mechanical properties due to their specific propylene and ethylene content, triad tacticity, viscosity, and crystallinity. Moreover, we have discovered that certain processing conditions, such as polymerization temperature and external donor to catalyst ratios, can facilitate the production of the high tensile strength propylene-ethylene copolymers described herein. Furthermore, the high tensile strength propylene-ethylene copolymers may be used to produce a variety of hot melt adhesives, such as those for hygiene applications, woodworking applications, lamination applications, and packaging applications, which exhibit unique and superior mechanical properties.
A process for producing a polyolefin composition is provided comprising melt blending: A) about 60 to about 96 wt % of at least one recycled polyolefin; B) about 2 to about 20 wt % of at least one random alpha-olefinic copolymer; and C) about 2 to about 20 wt % of at least one tackifier; and D) optionally, at least one additional polymer; wherein the polyolefin composition has a weight ratio of random alpha-olefinic copolymer to tackifier of between about 0.2 to about 5.0; and wherein the polyolefin composition has a melt flow rate increase of about 5 to about 400% compared to the same polyolefin composition without the random alpha-olefinic copolymer, the tackifier, and the optional additional polymer.
A polyolefin composition is provided comprising: A) about 60 to about 96 wt % of at least one recycled polyolefin; B) about 2 to about 20 wt % of at least one random alpha-olefinic copolymer; and C) about 2 to about 20 wt % of at least one tackifier; wherein the polyolefin composition has a weight ratio of random alpha-olefinic copolymer to tackifier of between about 0.2 to about 5.0; and wherein the polyolefin composition has a melt flow rate increase of about 5 to about 400% compared to the same polyolefin composition without the random alpha-olefinic copolymer and the tackifier. Processes for making and articles produced from the polyolefin compositions are also provided.
A family of propylene-ethylene copolymers have been discovered can be readily utilized in high heat resistance applications and form adhesives with improved mechanical strength and heat resistance. More particularly, the propylene-ethylene copolymers have a particular propylene content, triad tacticity, Ring and Ball softening point, and crystallinity that provide copolymers that exhibit desirable high heat resistance, tensile strength, and elongation. Furthermore, the propylene-ethylene copolymers may be used to produce adhesives that exhibit excellent heat resistance characteristics and superior cohesive strength.
Disclosed are curable adhesive compositions comprising hydroxyl functional polymers and silane functionalized resins. Such adhesive compositions are capable of providing unexpected properties for various uses and end products. The adhesive may be used for woodworking, automotive, textile, appliances, electronics, bookbinding, and packaging. Suitable substrates can be metal, polymer film, plastics, wood, glass, ceramic, paper, and concrete.
C09J 7/30 - Adhesives in the form of films or foils characterised by the adhesive composition
C08F 212/14 - Monomers containing only one unsaturated aliphatic radical containing one ring substituted by hetero atoms or groups containing hetero atoms
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
C08G 63/91 - Polymers modified by chemical after-treatment
Disclosed are curable adhesive compositions comprising hydroxyl functional polymers and silane functionalized resins. Such adhesive compositions are capable of providing unexpected properties for various uses and end products. The adhesive may be used for woodworking, automotive, textile, appliances, electronics, bookbinding, and packaging. Suitable substrates can be metal, polymer film, plastics, wood, glass, ceramic, paper, and concrete.
C09J 167/00 - Adhesives based on polyesters obtained by reactions forming a carboxylic ester link in the main chainAdhesives based on derivatives of such polymers
C09J 167/02 - Polyesters derived from dicarboxylic acids and dihydroxy compounds
C09J 201/10 - Adhesives based on unspecified macromolecular compounds characterised by the presence of specified groups containing hydrolysable silane groups
C09J 133/10 - Homopolymers or copolymers of methacrylic acid esters
C08F 8/00 - Chemical modification by after-treatment
Disclosed are silane functionalized rosins having multiple functionalities. Such silane functionalized rosins are curable and thus capable of providing unexpected properties for various uses and end products. Also disclosed are synthetic routes to prepare silane functionalized rosins, which are formulated with hydroxyl functional polymers to provide curable adhesive compositions. The adhesives may be used for woodworking, automotive, textile, appliances, electronics, bookbinding, and packaging. Suitable substrates can be metal, polymer film, plastics, wood, glass, ceramic, paper, and concrete.
Disclosed are silane functionalized rosins having multiple functionalities. Such silane functionalized rosins are curable and thus capable of providing unexpected properties for various uses and end products. Also disclosed are synthetic routes to prepare silane functionalized rosins, which are formulated with hydroxyl functional polymers to provide curable adhesive compositions. The adhesives may be used for woodworking, automotive, textile, appliances, electronics, bookbinding, and packaging. Suitable substrates can be metal, polymer film, plastics, wood, glass, ceramic, paper, and concrete.
A rubber composition includes: a rubber component; a filler in an amount of 40 to 125 parts by mass per 100 parts by mass of the rubber component; and a hydrogenated resin in an amount of 5 to 50 parts by mass per 100 parts by mass of the rubber component, the resin having a softening point of higher than 110° C. and a weight average molecular weight, as determined in terms of polystyrene, of 200 to 1200 g/mol. The rubber composition can be used to produce a tire having an excellent wet grip performance and a low rolling resistance, and a vulcanized rubber having excellent handling properties.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Polymers and polymeric additives; polymers and polymeric
additives for use in the manufacture of coatings or
adhesives or in connection with paper laminating; synthetic
resins; masterbatches for use in the manufacture of polymer
compositions.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
(1) Polymers in the nature of unprocessed polypropylene resins, unprocessed polyester resins, unprocessed polyamide resins, polymer beads and unprocessed polymer resins and polymeric additives in the nature of stabilizers for flame retardants and plasticizers, all for use in the manufacture of plastics, cosmetics, personal care products, coatings, adhesives, and lubricants; polymers and polymeric additives in the nature of stabilizers for flame retardants and plasticizers for use in the manufacture of coatings and adhesives, and in connection with paper laminating; unprocessed synthetic resins; synthetic resin adhesives for industrial purposes; synthetic resin adhesives for laminating purposes, namely contact adhesives for use with laminates; industrial adhesives for use in coating and sealing, namely unprocessed synthetic coating resin and unprocessed synthetic sealing resin; polymeric additives in the form of masterbatches.
42.
RECYCLED POLYOLEFIN COMPOSITIONS COMPRISING RANDOM ALPHA-OLEFINIC COPOLYMERS AND ADDITIONAL POLYMERS
A polyolefin composition is provided comprising: (A) about 60 to about 96 wt % of at least one recycled polyolefin; (B) about 2 to about 20 wt % of at least one random alpha-olefinic copolymer; (C) optionally, at least one tackifier; (D) about 1 to about 60 wt % of at least one additional polymer; and wherein the polyolefin composition has a melt flow rate increase of about 3 to about 400% compared to the same polyolefin composition without said random alpha-olefinic copolymer, said optional tackifier, and said additional polymer. Processes for making and articles produced from the polyolefin compositions are also provided.
B29C 48/00 - Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired formApparatus therefor
B29C 48/40 - Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws, e.g. twin screw extruders
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Polymers and copolymers for use in connection with
laminating, adhesives, sealants, wire and cable
applications, adhesives for industrial purposes; hot melt
adhesives for use on tapes and labels; chemicals and
chemical compositions, namely, amorphous polyolefins for use
in the chemicals and plastics industry.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Polymers and copolymers for use in connection with
laminating, adhesives, sealants, wire and cable
applications, adhesives for industrial purposes; hot melt
adhesives for use on tapes and labels; chemicals and
chemical compositions, namely, amorphous polyolefins for use
in the chemicals and plastics industry.
Modified thermoplastic hydrocarbon thermoplastic resins are provided, as well as methods of their manufacture and uses thereof in rubber compositions. The modified thermoplastic resins are modified by decreasing the relative quantity of the dimer, trimer, tetramer, and pentamer oligomers as compared to the corresponding unmodified thermoplastic resin polymers, resulting in a product that exhibits a greater shift in the glass transition temperature of the elastomer(s) used in tire formulations. This translates to better viscoelastic predictors of tire tread performance, such as wet grip and rolling resistance. The modified thermoplastic resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the modified thermoplastic resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, snow performance, and wet braking performance.
C09J 7/25 - PlasticsMetallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
B60C 1/00 - Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
C08F 10/14 - Monomers containing five or more carbon atoms
C08F 32/00 - Homopolymers or copolymers of cyclic compounds having no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system
C08G 61/08 - Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
C08J 11/02 - Recovery or working-up of waste materials of solvents, plasticisers or unreacted monomers
C09J 123/26 - Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondAdhesives based on derivatives of such polymers modified by chemical after-treatment
C09J 131/04 - Homopolymers or copolymers of vinyl acetate
C09J 153/02 - Vinyl aromatic monomers and conjugated dienes
C09J 191/00 - Adhesives based on oils, fats or waxesAdhesives based on derivatives thereof
G01N 25/48 - Investigating or analysing materials by the use of thermal means by investigating the development of heat, i.e. calorimetry, e.g. by measuring specific heat, by measuring thermal conductivity on solution, sorption, or a chemical reaction not involving combustion or catalytic oxidation
G01N 5/04 - Analysing materials by weighing, e.g. weighing small particles separated from a gas or liquid by removing a component, e.g. by evaporation, and weighing the remainder
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Polymers and polymeric additives for use in the manufacture of plastics, cosmetics, personal care products, coatings, adhesives, and lubricants; polymers and polymeric additives for use in the manufacture of coatings and adhesives, and in connection with paper laminating; unprocessed synthetic resins; adhesives for industrial purposes; synthetic resin adhesives for laminating purposes; industrial adhesives for use in coating and sealing; polymeric additives in the form of masterbatches
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals and chemical compositions, namely, amorphous polyolefins for use in the chemicals and plastics industry; Polymers and polymeric additives for use in the manufacture of industrial products, consumer and household products, sealants, and automotive fluids; Adhesives for industrial purposes; Synthetic resin adhesives for laminating purposes; Industrial adhesives for use in coating and sealing
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals and chemical compositions, namely, amorphous polyolefins for use in the chemicals and plastics industry; Polymers and polymeric additives for use in the manufacture of industrial products, consumer and household products, sealants, and automotive fluids; Adhesives for industrial purposes; Synthetic resin adhesives for laminating purposes; Industrial adhesives for use in coating and sealing
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Artificial and synthetic resins; artificial and synthetic resins for industrial use; Chemical agents for binding and reducing free formaldehyde in synthetic resins, plastics, glues and adhesives (as far as included in class 1); plastics, glues and adhesives treated with a chemical agent that binds and reduces free formaldehyde, in the raw state, in the form of powders, pastes, granules or liquids for industrial purposes, resin esters as synthetic resins in the raw state.
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
C08F 8/42 - Introducing metal atoms or metal-containing groups
C08C 19/25 - Incorporating silicon atoms into the molecule
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 30/08 - Homopolymers or 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
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
C08F 8/00 - Chemical modification by after-treatment
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 30/08 - Homopolymers or 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
Modified thermoplastic hydrocarbon thermoplastic resins are provided, as well as methods of their manufacture and uses thereof in rubber compositions. The modified thermoplastic resins are modified by decreasing the relative quantity of the dimer, trimer, tetramer, and pentamer oligomers as compared to the corresponding unmodified thermoplastic resin polymers, resulting in a product that exhibits a greater shift in the glass transition temperature of the elastomer(s) used in tire formulations. This translates to better viscoelastic predictors of tire tread performance, such as wet grip and rolling resistance. The modified thermoplastic resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the modified thermoplastic resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, snow performance, and wet braking performance.
G01N 30/88 - Integrated analysis systems specially adapted therefor, not covered by a single one of groups
G01N 25/48 - Investigating or analysing materials by the use of thermal means by investigating the development of heat, i.e. calorimetry, e.g. by measuring specific heat, by measuring thermal conductivity on solution, sorption, or a chemical reaction not involving combustion or catalytic oxidation
B60C 1/00 - Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
C08J 11/02 - Recovery or working-up of waste materials of solvents, plasticisers or unreacted monomers
C08F 32/00 - Homopolymers or copolymers of cyclic compounds having no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system
C09J 191/00 - Adhesives based on oils, fats or waxesAdhesives based on derivatives thereof
C08F 10/14 - Monomers containing five or more carbon atoms
C08G 61/08 - Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
C09J 7/25 - PlasticsMetallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
C09J 123/26 - Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondAdhesives based on derivatives of such polymers modified by chemical after-treatment
C09J 131/04 - Homopolymers or copolymers of vinyl acetate
C09J 153/02 - Vinyl aromatic monomers and conjugated dienes
G01N 5/04 - Analysing materials by weighing, e.g. weighing small particles separated from a gas or liquid by removing a component, e.g. by evaporation, and weighing the remainder
Modified thermoplastic hydrocarbon thermoplastic resins are provided, as well as methods of their manufacture and uses thereof in rubber compositions. The modified thermoplastic resins are modified by decreasing the relative quantity of the dimer, trimer, tetramer, and pentamer oligomers as compared to the corresponding unmodified thermoplastic resin polymers, resulting in a product that exhibits a greater shift in the glass transition temperature of the elastomer(s) used in tire formulations. This translates to better viscoelastic predictors of tire tread performance, such as wet grip and rolling resistance. The modified thermoplastic resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the modified thermoplastic resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, snow performance, and wet braking performance.
G01N 30/88 - Integrated analysis systems specially adapted therefor, not covered by a single one of groups
G01N 25/48 - Investigating or analysing materials by the use of thermal means by investigating the development of heat, i.e. calorimetry, e.g. by measuring specific heat, by measuring thermal conductivity on solution, sorption, or a chemical reaction not involving combustion or catalytic oxidation
B60C 1/00 - Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
C08J 11/02 - Recovery or working-up of waste materials of solvents, plasticisers or unreacted monomers
C08F 32/00 - Homopolymers or copolymers of cyclic compounds having no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system
C09J 191/00 - Adhesives based on oils, fats or waxesAdhesives based on derivatives thereof
C08F 10/14 - Monomers containing five or more carbon atoms
C08G 61/08 - Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
C09J 7/25 - PlasticsMetallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
C09J 123/26 - Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondAdhesives based on derivatives of such polymers modified by chemical after-treatment
C09J 131/04 - Homopolymers or copolymers of vinyl acetate
C09J 153/02 - Vinyl aromatic monomers and conjugated dienes
G01N 5/04 - Analysing materials by weighing, e.g. weighing small particles separated from a gas or liquid by removing a component, e.g. by evaporation, and weighing the remainder
54.
Adhesive composition comprising amorphous propylene-ethylene copolymer and polyolefins
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
C08L 23/10 - Homopolymers or copolymers of propene
C09J 123/10 - Homopolymers or copolymers of propene
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
C08K 11/00 - Use of ingredients of unknown constitution, e.g. undefined reaction products
C08F 4/646 - Catalysts comprising at least two different metals, in metallic form or as compounds thereof, in addition to the component covered by group
C08F 4/654 - Pretreating with metals or metal-containing compounds with magnesium or compounds thereof
A tackifier composition comprising at least one thermoplastic hydrocarbon resin and an antioxidant composition is provided; wherein a portion of the volatile organic compounds in the thermoplastic hydrocarbon resin has been removed; wherein the antioxidant composition comprises at least one primary antioxidant and at least one secondary antioxidant; and wherein the levels of individual volatile organic compound monitored in the tackifier composition are less than about 0.5 ppm as measured by GC/MS headspace analysis. Processes for producing the tackifier composition are also provided as well as adhesives comprising the tackifier compositions.
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
C09J 123/26 - Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondAdhesives based on derivatives of such polymers modified by chemical after-treatment
A61L 15/20 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
A61L 15/22 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
C09J 153/02 - Vinyl aromatic monomers and conjugated dienes
C09J 153/00 - Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsAdhesives based on derivatives of such polymers
C08L 23/26 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondCompositions of derivatives of such polymers modified by chemical after-treatment
C08K 5/105 - EstersEther-esters of monocarboxylic acids with phenols
C08K 5/12 - EstersEther-esters of cyclic polycarboxylic acids
A tackifier composition comprising at least one thermoplastic hydrocarbon resin and an antioxidant composition is provided; wherein a portion of the volatile organic compounds in the thermoplastic hydrocarbon resin has been removed; wherein the antioxidant composition comprises at least one primary antioxidant and at least one secondary antioxidant; and wherein the levels of individual volatile organic compound monitored in the tackifier composition are less than about 0.5 ppm as measured by GC/MS headspace analysis. Processes for producing the tackifier composition are also provided as well as adhesives comprising the tackifier compositions.
C09J 123/26 - Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondAdhesives based on derivatives of such polymers modified by chemical after-treatment
A61L 15/20 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
A61L 15/22 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
C09J 153/02 - Vinyl aromatic monomers and conjugated dienes
C09J 153/00 - Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsAdhesives based on derivatives of such polymers
C08L 23/26 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondCompositions of derivatives of such polymers modified by chemical after-treatment
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
C08K 5/105 - EstersEther-esters of monocarboxylic acids with phenols
C08K 5/12 - EstersEther-esters of cyclic polycarboxylic acids
A tackifier composition comprising at least one thermoplastic hydrocarbon resin and an antioxidant composition is provided; wherein a portion of the volatile organic compounds in the thermoplastic hydrocarbon resin has been removed; wherein the antioxidant composition comprises at least one primary antioxidant and at least one secondary antioxidant; and wherein the levels of individual volatile organic compound monitored in the tackifier composition are less than about 0.5 ppm as measured by GC/MS headspace analysis. Processes for producing the tackifier composition are also provided as well as adhesives comprising the tackifier compositions.
C09J 153/00 - Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsAdhesives based on derivatives of such polymers
A tackifier composition comprising at least one thermoplastic hydrocarbon resin and an antioxidant composition is provided; wherein a portion of the volatile organic compounds in the thermoplastic hydrocarbon resin has been removed; wherein the antioxidant composition comprises at least one primary antioxidant and at least one secondary antioxidant; and wherein the levels of individual volatile organic compound monitored in the tackifier composition are less than about 0.5 ppm as measured by GC/MS headspace analysis. Processes for producing the tackifier composition are also provided as well as adhesives comprising the tackifier compositions.
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
C09J 123/26 - Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondAdhesives based on derivatives of such polymers modified by chemical after-treatment
A61L 15/20 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
A61L 15/22 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
C09J 153/02 - Vinyl aromatic monomers and conjugated dienes
C09J 153/00 - Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsAdhesives based on derivatives of such polymers
C08L 23/26 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondCompositions of derivatives of such polymers modified by chemical after-treatment
C08K 5/105 - EstersEther-esters of monocarboxylic acids with phenols
C08K 5/12 - EstersEther-esters of cyclic polycarboxylic acids
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
C09J 125/10 - Copolymers of styrene with conjugated dienes
C09J 131/04 - Homopolymers or copolymers of vinyl acetate
C09J 133/10 - Homopolymers or copolymers of methacrylic acid esters
Modified thermoplastic hydrocarbon thermoplastic resins are provided, as well as methods of their manufacture and uses thereof in rubber compositions. The modified thermoplastic resins are modified by decreasing the relative quantity of the dimer, trimer, tetramer, and pentamer oligomers as compared to the corresponding unmodified thermoplastic resin polymers, resulting in a product that exhibits a greater shift in the glass transition temperature of the elastomer(s) used in tire formulations. This translates to better viscoelastic predictors of tire tread performance, such as wet grip and rolling resistance. The modified thermoplastic resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the modified thermoplastic resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, snow performance, and wet braking performance.
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
C08L 23/10 - Homopolymers or copolymers of propene
C09J 123/10 - Homopolymers or copolymers of propene
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
C08F 4/646 - Catalysts comprising at least two different metals, in metallic form or as compounds thereof, in addition to the component covered by group
C08F 4/654 - Pretreating with metals or metal-containing compounds with magnesium or compounds thereof
C09J 153/02 - Vinyl aromatic monomers and conjugated dienes
62.
Adhesive composition comprising amorphous propylene-ethylene copolymer and propylene polymer
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
C08L 23/10 - Homopolymers or copolymers of propene
C09J 123/10 - Homopolymers or copolymers of propene
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
C08K 11/00 - Use of ingredients of unknown constitution, e.g. undefined reaction products
C08F 4/646 - Catalysts comprising at least two different metals, in metallic form or as compounds thereof, in addition to the component covered by group
C08F 4/654 - Pretreating with metals or metal-containing compounds with magnesium or compounds thereof
The invention provides (meth)acrylic oligomers prepared from C1-C20 alkyl and C5-C20 cycloalkyl (meth)acrylates, wherein said oligomers have a Mn of about 300 g/mole to about 3,000 g/mole; a Mw of about 700 g/mole to about 6,000 g/mole; a Mz of about 900 g/mole to about 10,000 g/mole. The oligomers may have a Yellowness Index, according to ASTM E313 of less than 2. The oligomers of the invention are useful as tackifiers in adhesive compositions, but also are believed to be useful also in general polymer modification as plasticizers, leveling agents, viscosity reducers (i.e., rheology modifiers), and for increasing solids content in solvent-borne applications of all types with little detrimental impact on viscosity. The invention also provides adhesive compositions and laminate articles coated on at least one side with the adhesive compositions of the invention.
C07C 67/465 - Preparation of carboxylic acid esters by oligomerisation
C09J 133/06 - Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
C09J 123/10 - Homopolymers or copolymers of propene
C08L 23/10 - Homopolymers or copolymers of propene
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
C08F 12/00 - Homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
C08F 30/08 - Homopolymers or 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
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
C08F 8/30 - Introducing nitrogen atoms or nitrogen-containing groups
C08F 8/32 - Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
C08F 8/42 - Introducing metal atoms or metal-containing groups
C08F 8/46 - Reaction with unsaturated dicarboxylic acids or anhydrides thereof, e.g. maleinisation
C08F 30/08 - Homopolymers or 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
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
C08F 30/08 - Homopolymers or 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
Modified thermoplastic hydrocarbon thermoplastic resins are provided, as well as methods of their manufacture and uses thereof in rubber compositions. The modified thermoplastic resins are modified by decreasing the relative quantity of the dimer, trimer, tetramer, and pentamer oligomers as compared to the corresponding unmodified thermoplastic resin polymers, resulting in a product that exhibits a greater shift in the glass transition temperature of the elastomer(s) used in tire formulations. This translates to better viscoelastic predictors of tire tread performance, such as wet grip and rolling resistance. The modified thermoplastic resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the modified thermoplastic resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, snow performance, and wet braking performance.
G01N 30/88 - Integrated analysis systems specially adapted therefor, not covered by a single one of groups
G01N 25/48 - Investigating or analysing materials by the use of thermal means by investigating the development of heat, i.e. calorimetry, e.g. by measuring specific heat, by measuring thermal conductivity on solution, sorption, or a chemical reaction not involving combustion or catalytic oxidation
B60C 1/00 - Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
C08J 11/02 - Recovery or working-up of waste materials of solvents, plasticisers or unreacted monomers
C08F 32/00 - Homopolymers or copolymers of cyclic compounds having no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system
C09J 191/00 - Adhesives based on oils, fats or waxesAdhesives based on derivatives thereof
C08F 10/14 - Monomers containing five or more carbon atoms
C08G 61/08 - Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
C09J 7/25 - PlasticsMetallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
C09J 123/26 - Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondAdhesives based on derivatives of such polymers modified by chemical after-treatment
C09J 131/04 - Homopolymers or copolymers of vinyl acetate
C09J 153/02 - Vinyl aromatic monomers and conjugated dienes
G01N 5/04 - Analysing materials by weighing, e.g. weighing small particles separated from a gas or liquid by removing a component, e.g. by evaporation, and weighing the remainder
69.
Adhesive composition comprising amorphous propylene-ethylene copolymer and polyolefins
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
C08L 23/10 - Homopolymers or copolymers of propene
C09J 123/10 - Homopolymers or copolymers of propene
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
C08F 4/646 - Catalysts comprising at least two different metals, in metallic form or as compounds thereof, in addition to the component covered by group
C08F 4/654 - Pretreating with metals or metal-containing compounds with magnesium or compounds thereof
70.
Tires comprising polyindane resins and uses thereof
The present invention is generally related to various types of compositions that comprise a polyindane resin. In particular, the polyindane resins may be utilized in various polymer-based and elastomer-based formulations in order to enhance several properties and characteristics of those formulations. More specifically, elastomeric compositions are provided that comprise at least one polyindane resin, which may be used to replace or enhance the functionality of existing hydrocarbon resins used in elastomeric formulations. The elastomeric compositions may be used to produce various tire components.
C08L 45/00 - Compositions of homopolymers or copolymers of compounds having no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic or in a heterocyclic ring systemCompositions of derivatives of such polymers
C08L 9/00 - Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
The present invention is generally related to various types of compositions that comprise a polyindane resin. In particular, the polyindane resins may be utilized in various polymer-based and elastomer-based formulations in order to enhance several properties and characteristics of those formulations. More specifically, adhesive formulations are provided that comprise at least one polyindane resin, which may be used to replace or enhance the functionality of existing hydrocarbon resins typically used in adhesive formulations. Compositions comprising at least one thermoplastic elastomer and at least one polyindane resin are also provided.
C08L 53/00 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers
C08F 12/34 - Monomers containing two or more unsaturated aliphatic radicals
C09J 125/16 - Homopolymers or copolymers of alkyl-substituted styrenes
C09J 165/00 - Adhesives based on macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chainAdhesives based on derivatives of such polymers
wherein x in the above formula is the softening point of the low molecular weight copolymer, and wherein the low molecular weight copolymer has a molecular weight polydispersity index of about 3 to about 25, a crystallinity of about 18% to about 30% measured by X-Ray diffraction, and a Brookfield viscosity in the range of about 1000 to about 4000 cp at 190° C. measured by ASTM D 3236. Adhesive compositions comprising the low molecular weight copolymer are also provided.
C09J 123/10 - Homopolymers or copolymers of propene
C08L 23/10 - Homopolymers or copolymers of propene
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
C08L 53/02 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers of vinyl aromatic monomers and conjugated dienes
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
B29C 47/00 - Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor (extrusion blow-moulding B29C 49/04)
C08F 4/44 - MetalsMetal hydridesMetallo-organic compoundsUse thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths, or actinides
C08L 23/00 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondCompositions of derivatives of such polymers
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
B29C 47/00 - Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor (extrusion blow-moulding B29C 49/04)
C08F 4/44 - MetalsMetal hydridesMetallo-organic compoundsUse thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths, or actinides
C08L 23/00 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondCompositions of derivatives of such polymers
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
C08F 4/58 - MetalsMetal hydridesMetallo-organic compoundsUse thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths, or actinides together with silicon, germanium, tin, lead, antimony, bismuth, or compounds thereof
C08F 4/10 - Metallic compounds other than hydrides and other than metallo-organic compoundsBoron halide or aluminium halide complexes with organic compounds containing oxygen of alkaline earth metals, zinc, cadmium, mercury, copper, or silver
C08F 4/16 - Metallic compounds other than hydrides and other than metallo-organic compoundsBoron halide or aluminium halide complexes with organic compounds containing oxygen of silicon, germanium, tin, lead, titanium, zirconium or hafnium
Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Polymers and polymeric additives for use in the manufacture of adhesives for personal hygiene product applications, namely, disposable adult diapers, disposable baby diapers, and feminine hygiene pads.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Polymers and polymeric additives for use in the manufacture of adhesives for personal hygiene product applications, namely, disposable adult diapers, disposable baby diapers, and feminine hygiene pads
A low z-average molecular weight, high softening point polystyrene resin having a narrow molecular weight distribution, as well as methods of making and using the same, are provided. The use of an inert solvent and/or the order of addition of reactants during polymerization may contribute to the unique properties of the final homopolymeric resin. The polystyrene resin can be partially or fully hydrogenated and may have particular use as a tackifying agent in a variety of hot melt adhesive and rubber compositions.
C08L 53/00 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers
C09B 67/00 - Influencing the physical, e.g. the dyeing or printing, properties of dyestuffs without chemical reaction, e.g. by treating with solventsProcess features in the making of dyestuff preparationsDyestuff preparations of a special physical nature, e.g. tablets, films
C08L 31/04 - Homopolymers or copolymers of vinyl acetate
B01F 17/00 - Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
A low z-average molecular weight, high softening point polystyrene resin having a narrow molecular weight distribution, as well as methods of making and using the same, are provided. The use of an inert solvent and/or the order of addition of reactants during polymerization may contribute to the unique properties of the final homopolymeric resin. The polystyrene resin can be partially or fully hydrogenated and may have particular use as a tackifying agent in a variety of hot melt adhesive and rubber compositions.
This invention relates to a composition suitable for use in making moisture resistant gypsum products. In particular, this invention relates to resin dispersions and their use in combination with gypsum to form moisture resistant gypsum compositions which are settable by hydration. Further, the invention relates to moisture resistant products formed from such settable gypsum compositions, e.g. panels and boards, and a method for the manufacture of such moisture resistant gypsum products.
Disclosed are hot-melt adhesives prepared from polyesters containing 1,4-cyclohexane-dicarboxylic acid as a diacid component and a diol component containing at least two diols chosen from 1,4-cyclohexanedimethanol, triethylene glycol, and diethylene glycol. These adhesives set up rapidly within a well-defined temperature window. The hot-melt adhesives can be used in a variety of applications, but are especially suited as seaming adhesives for roll-applied labels. These adhesives have melting temperatures and crystallization properties that allow their application at temperatures cool enough to prevent curling and premature shrinkage of the shrink label during seaming, and yet produce strong label seams that can withstand the elevated temperatures of a shrink tunnel without sacrificing line speed. Also disclosed are labeled containers and a process for applying a roll-on, shrink label to a container using the hot-melt adhesives of the invention.
Disclosed are hot-melt adhesives prepared from aromatic-aliphatic polyesters containing terephthalic acid in combination with adipic acid, glutaric acid, or a mixture thereof, as diacid components and a diol component containing 1,4-butanediol, 1,6-hexanediol, or a combination thereof. These adhesives set up rapidly within a well-defined temperature window. The hot-melt adhesives can be used in a variety of applications, but are especially suited as seaming adhesives for roll-applied labels. These adhesives have melting temperatures and crystallization properties that allow their application at temperatures cool enough to prevent curling and premature shrinkage of the shrink label during seaming, and yet produce strong label seams that can withstand the elevated temperatures of a shrink tunnel without sacrificing line speed. Also disclosed are labeled containers and a process for applying a roll-on, shrink label to a container using the hot-melt adhesives of the invention.
