A colloidal dispersion is provide which is particularly suitable for use in a cleaning system or a personal care product. The colloidal dispersion has a Brookfield Yield Value of at least 50 dyn/cm2 and the cleaning system comprises a structurant and a sulfate-free surfactant.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for use in the manufacture of a wide variety of goods such as paint, ink, paper, textiles, chemicals, and agricultural, metalworking, and personal care formulations
A01N 25/30 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
Provided is an improved herbicide formulation and an improved method of treating a crop. The herbicide formulation comprises a herbicide and a volatility reduction adjuvant comprising a salt of a volatile acid and a salt of a nonvolatile acid.
A01N 25/22 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
A01N 25/02 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
A01N 37/10 - Aromatic or araliphatic carboxylic acids, or thio-analogues thereofDerivatives thereof
A01N 43/38 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
A01N 57/20 - Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
5.
HPPD AND PPO AGROCHEMICAL FORMULATIONS CONTAINING DRIFT REDUCTION TECHNOLOGIES
An improved agrochemical formulation, and method for treating crops, is provided herein. The agrochemical formulation at least one herbicide selected from the group consisting of a 4-hydroxyphenylpyruvate dioxygenase herbicide and a protoporphyrinogen oxidase inhibiting herbicide; and an organic drift control agent.
A01N 25/24 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients to enhance the sticking of the active ingredients
A01N 25/24 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients to enhance the sticking of the active ingredients
A01N 25/30 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
7.
IMPROVED HPPD AND PPO AGROCHEMICAL FORMULATIONS CONTAINING DRIFT REDUCTION TECHNOLOGIES
An improved agrochemical formulation, and method for treating crops, is provided herein. The agrochemical formulation at least one herbicide selected from the group consisting of a 4-hydroxyphenylpyruvate dioxygenase herbicide and a protoporphyrinogen oxidase inhibiting herbicide; and an organic drift control agent.
A01N 25/30 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
A01N 25/24 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients to enhance the sticking of the active ingredients
A colloidal dispersion is provide which is particularly suitable for use in a cleaning system or a personal care product. The colloidal dispersion has a Brookfield Yield Value of at least 50 dyn/cm2 and the cleaning system comprises a structurant and a sulfate-free surfactant.
Provided is an improved herbicide formulation and an improved method of treating a crop. The herbicide formulation comprises a herbicide and a volatility reduction adjuvant comprising a salt of a volatile acid and a salt of a nonvolatile acid.
A01N 25/22 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
A01N 25/02 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
A01N 43/38 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
A01N 37/10 - Aromatic or araliphatic carboxylic acids, or thio-analogues thereofDerivatives thereof
A01N 57/20 - Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
12.
SYNERGISTIC COMBINATIONS FOR REDUCING VOLATILITY OF AUXIN HERBICIDES
Provided is an improved herbicide formulation and an improved method of treating a crop. The herbicide formulation comprises a herbicide and a volatility reduction adjuvant comprising a salt of a volatile acid and a salt of a nonvolatile acid.
A01N 43/34 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
A01N 43/04 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atom with one hetero atom
A01N 43/40 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
A01N 43/00 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
13.
Composition and Method for Improving the Water Transport Characteristics of Hydrophobic Soils
Provided is a method and mixture for treating a hydrophobic surface. The mixture comprises a wetting agent comprising;
Provided is a method and mixture for treating a hydrophobic surface. The mixture comprises a wetting agent comprising;
a compound of Formula I:
Provided is a method and mixture for treating a hydrophobic surface. The mixture comprises a wetting agent comprising;
a compound of Formula I:
Provided is a method and mixture for treating a hydrophobic surface. The mixture comprises a wetting agent comprising;
a compound of Formula I:
wherein:
R and R′ are independently selected from the group consisting of H, C1-24 alkyl, aryl, C1-24 alkylaryl, aryl(C1-24)alkyl, —C(═O)—R1, C(═O)—NHR1, and C(═O)—O—R1 wherein R1 is selected from the group consisting of C1-24 alkyl, aryl, C1-24 alkylaryl, C1-24 arylalkyl; A is an organic moiety derived from the group consisting of alkylene oxides having 4-12 carbon atoms and aryl epoxides having 8-12 carbon atoms; x=1-300; y=0-200; z=0-200; and
with the proviso that R and R′ cannot be H or ether functionality at the same time; and a compound of Formula II:
Provided is a method and mixture for treating a hydrophobic surface. The mixture comprises a wetting agent comprising;
a compound of Formula I:
wherein:
R and R′ are independently selected from the group consisting of H, C1-24 alkyl, aryl, C1-24 alkylaryl, aryl(C1-24)alkyl, —C(═O)—R1, C(═O)—NHR1, and C(═O)—O—R1 wherein R1 is selected from the group consisting of C1-24 alkyl, aryl, C1-24 alkylaryl, C1-24 arylalkyl; A is an organic moiety derived from the group consisting of alkylene oxides having 4-12 carbon atoms and aryl epoxides having 8-12 carbon atoms; x=1-300; y=0-200; z=0-200; and
with the proviso that R and R′ cannot be H or ether functionality at the same time; and a compound of Formula II:
[R2O—(CH2CH2O)x—(CH2CH(CH3)O)y]z—P(O)(OM)3-z Formula II
Provided is a method and mixture for treating a hydrophobic surface. The mixture comprises a wetting agent comprising;
a compound of Formula I:
wherein:
R and R′ are independently selected from the group consisting of H, C1-24 alkyl, aryl, C1-24 alkylaryl, aryl(C1-24)alkyl, —C(═O)—R1, C(═O)—NHR1, and C(═O)—O—R1 wherein R1 is selected from the group consisting of C1-24 alkyl, aryl, C1-24 alkylaryl, C1-24 arylalkyl; A is an organic moiety derived from the group consisting of alkylene oxides having 4-12 carbon atoms and aryl epoxides having 8-12 carbon atoms; x=1-300; y=0-200; z=0-200; and
with the proviso that R and R′ cannot be H or ether functionality at the same time; and a compound of Formula II:
[R2O—(CH2CH2O)x—(CH2CH(CH3)O)y]z—P(O)(OM)3-z Formula II
where R2 is C1-C24 alkyl, aryl, alkaryl; x=0-20; y=0-20; z=1 or 2 and M is H, Na, K, Ca, Mg or Li.
A mixture for treating a hydrophobic surface and a method for treating hydrophobic surfaces is provided. The mixture comprises:
a wetting agent comprising;
a compound of Formula I:
A mixture for treating a hydrophobic surface and a method for treating hydrophobic surfaces is provided. The mixture comprises:
a wetting agent comprising;
a compound of Formula I:
R1((CH2CH2O)nR2)x Formula I
wherein:
R1 is a core group derived from a linear, cyclic or branched polyol with 1-55 carbons or a linear, cyclic or branched polyamine with 1-22 carbons wherein hydrogens on the alcohol group or hydrogens on the amine group are replaced with (CH2CH2O)n or R1 is defined by —R6(—C(═O)O—)m;
R2 is a hydrophobic group preferably selected from the group consisting of R3, the elements necessary to form an ester, specifically —COR4, or the elements necessary to form a urethane, specifically —CONHR5;
R3-R5 are each independently an alkyl of 6-22 carbons, wherein the alkyl is a linear, cyclic or branched and preferably linear;
n, on average is 4-100;
x is 2-20;
R6 represents a bond or a linear, cyclic or branched alkyl with 6-22 carbons; and
m is 2-20.
A mixture for treating a hydrophobic surface and a method for treating hydrophobic surfaces is provided. The mixture comprises: a wetting agent comprising; a compound of Formula I: wherein: R1 is a core group derived from a linear, cyclic or branched polyol with 1-55 carbons or a linear, cyclic or branched polyamine with 1-22 carbons wherein hydrogens on the alcohol group or hydrogens on the amine group are replaced with (Ch2CH2O)n or R1 is defined by -R6(-C(=O)O-)m; R2 is a hydrophobic group preferably selected from the group consisting of R3, the elements necessary to form an ester, specifically -COR4, or the elements necessary to form a urethane, specifically -CONHR5; R3-R5 are each independently an alkyl of 6-22 carbons, wherein the alkyl is a linear, cyclic or branched and preferably linear; n, on average is 4-100; x is 2-20; R6 represents a bond or a linear, cyclic or branched alkyl with 6-22 carbons; and m is 2-20.
C05G 3/70 - Mixtures of one or more fertilisers with additives not having a specifically fertilising activity for affecting wettability, e.g. drying agents
C08G 65/00 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
A mixture for treating a hydrophobic surface and a method for treating hydrophobic surfaces is provided. The mixture comprises: a wetting agent comprising; a compound of Formula I: wherein: R1222O)n or R1is defined by -R6mm; R2 is a hydrophobic group preferably selected from the group consisting of R3, the elements necessary to form an ester, specifically -COR4, or the elements necessary to form a urethane, specifically -CONHR5; R3-R5are each independently an alkyl of 6-22 carbons, wherein the alkyl is a linear, cyclic or branched and preferably linear; n, on average is 4-100; x is 2-20; R6 represents a bond or a linear, cyclic or branched alkyl with 6-22 carbons; and m is 2-20.
C05G 3/70 - Mixtures of one or more fertilisers with additives not having a specifically fertilising activity for affecting wettability, e.g. drying agents
C08G 65/00 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
17.
COMPOSITION AND METHOD FOR IMPROVING THE WATER TRANSPORT CHARACTERISTICS OF HYDROPHOBIC SOILS
Provided is a method and mixture for treating a hydrophobic surface. The mixturecomprises a wetting agent comprising;a compound of Formula 1:wherein:R and R' are independently selected from the group consisting of H, C1-24 alkyl, aryl, C1-24 alkylaryl, aryl(C1-24)alkyl, -C(=0)-R1, C(=0)-NHR1, and C(=0)-0-R1 wherein Rlis selected from the group consisting of C1-24 alkyl, aryl, 01-24 alkylaryl, C1-24 arylalkyl; A is an organic moiety derived from the group consisting of alkylene oxides having 4-12 carbon atoms and aryl epoxides having 8-12 carbon atoms; x=1-300; y=0-200; z=0-200; andwith the proviso that R and R' cannot be H or ether functionality at the same time; and a compound of Formula 11:where R2 is 01-024 alkyl, aryl, alkaryl; x = 0-20; y = 0-20; z = 1 or 2 and M is H, Na, K, Ca, Mg or Li.
Provided herein is a compound which is particularly suitable for use as a cannabinoid, as an emulsifier for a cannabinoid, in a formulation comprising the compound and in a method of treatment using the compound. The compound is defined by the General Formula wherein: R1-R10 are independently selected from H or an alkyl of 1-10 carbons; alkenyl of up to 10 carbons; or groups on adjacent carbons may be taken together to form an alkene; R11 and R12 are independently H or -(CH2CHR16O)x-R17 with the proviso that at least one of R11 or R12 represents -(CH2CHR16O)xR17-; R11 and R10 may be taken together to represent -C(R19)2-; R13-R15 independently represent H or an alkyl of 1-8 carbons; each R16 independently represents H or an alkyl of 1-3 carbons; each R17 independently represents H, an alkyl or substituted alkyl of 1-22 carbons, aryl or substituted aryl or the ester of an acid; each R19 independently represents H or an alkyl of 1-5 carbons; and each x is independently an integer of 1-100.
A61K 31/045 - Hydroxy compounds, e.g. alcoholsSalts thereof, e.g. alcoholates
A61K 31/352 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. cannabinols, methantheline
Provided herein is a compound which is particularly suitable for use as a cannabinoid, as an emulsifier for a cannabinoid, in a formulation comprising the compound and in a method of treatment using the compound. The compound is defined by the General Formula:
Provided herein is a compound which is particularly suitable for use as a cannabinoid, as an emulsifier for a cannabinoid, in a formulation comprising the compound and in a method of treatment using the compound. The compound is defined by the General Formula:
Provided herein is a compound which is particularly suitable for use as a cannabinoid, as an emulsifier for a cannabinoid, in a formulation comprising the compound and in a method of treatment using the compound. The compound is defined by the General Formula:
wherein:
R1-R10 are independently selected from H or an alkyl of 1-10 carbons; alkenyl of up to 10 carbons; or groups on adjacent carbons may be taken together to form an alkene;
R11 and R12 are independently H or —(CH2CHR16O)x—R17 with the proviso that at least one of R11 or R12 represents —(CH2CHR16O)xR17—; R11 and R10 may be taken together to represent —C(R19)2—;
R13-R15 independently represent H or an alkyl of 1-8 carbons;
each R16 independently represents H or an alkyl of 1-3 carbons;
each R17 independently represents H, an alkyl or substituted alkyl of 1-22 carbons, aryl or substituted aryl or the ester of an acid;
each R19 independently represents H or an alkyl of 1-5 carbons; and
each x is independently an integer of 1-100.
C07C 43/285 - Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings having unsaturation outside the six-membered aromatic rings
A61K 47/08 - Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen
Provided herein is a compound which is particularly suitable for use as a cannabinoid, as an emulsifier for a cannabinoid, in a formulation comprising the compound and in a method of treatment using the compound. The compound is defined by the General Formula wherein: R1-R10are independently selected from H or an alkyl of 1-10 carbons; alkenyl of up to 10 carbons; or groups on adjacent carbons may be taken together to form an alkene; R11and R1222CHR16xx-R17with the proviso that at least one of R11or R1222CHR16xxR17-; R11and R10may be taken together to represent -C(R1922-; R13-R15independently represent H or an alkyl of 1-8 carbons; each R16independently represents H or an alkyl of 1-3 carbons; each R17independently represents H, an alkyl or substituted alkyl of 1-22 carbons, aryl or substituted aryl or the ester of an acid; each R19 independently represents H or an alkyl of 1-5 carbons; and each x is independently an integer of 1-100.
A61K 31/045 - Hydroxy compounds, e.g. alcoholsSalts thereof, e.g. alcoholates
A61K 31/352 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. cannabinols, methantheline
An improved broad-spectrum sunscreen formulation is provided. The sunscreen formulation comprises at least one organic sunscreen filter, at least one of which avobenzone, and an alkyl benzoate comprising 25-55 mole% C12-14 alkyl benzoate and 45-75 mole% C12-C15 alkyl benzoate.
An improved broad-spectrum sunscreen formulation is provided. The sunscreen formulation comprises at least one organic sunscreen filter, at least one of which avobenzone, and an alkyl benzoate comprising 25-55 mole % C12-14 alkyl benzoate and 45-75 mole % C12-C15 alkyl benzoate.
The present invention is related to a plant biostimulant adjuvant and a method of treating a crop with a plant biostimulant adjuvant. The plant biostimulant adjuvant comprises a plant biostimulant comprising at least one of an amino acid or a peptide derived from a plant source. The plant biostimulant adjuvant also comprises an alkyl amine alkoxylate defined by the formula (I) wherein: R1is an alkyl of 6 to 22 carbons; each R2and R333. n and m are each at least one and taken together n+m is 5 to 25; and water.
A01N 25/02 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
A01N 25/30 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
Provided is a sulfate-free surfactant system comprises a liquid comprising an organic phase and a solvent wherein the organic phase comprises glyceride and surfactant and the liquid comprises: 4 - 40 wt% glyceride wherein the glyceride is the condensation reaction product of at least 1.10 moles of a mixture of acids to no more than 2.1 moles of mixture of acids per mole of glycerin; wherein mixture of acids comprises: at least 0.275 to no more than 0.990 moles of a first acid comprising a branched acid with 16-20 aliphatic carbons; at least 0.250 to no more than 0.810 moles of a second acid comprising an alkyl acid with 9-11 carbons; and at least 0.250 to no more than 0.810 moles of a third acid comprising an alkyl acid with 7-9 carbons wherein the third acid has a lower molecular weight than the second acid; and 6 - 45 wt% surfactant.
Provided is a sulfate-free surfactant system which is particularly suitable for use in personal hygiene products. The sulfate-free surfactant system comprises a liquid comprising an organic phase and a solvent wherein the organic phase comprises glyceride and surfactant and the liquid comprises:
4-40 wt % glyceride wherein the glyceride is the condensation reaction product of at least 1.10 moles of a mixture of acids to no more than 2.1 moles of mixture of acids per mole of glycerin;
wherein mixture of acids comprises:
at least 0.275 to no more than 0.990 moles of a first acid comprising a branched acid with 16-20 aliphatic carbons;
at least 0.250 to no more than 0.810 moles of a second acid comprising an alkyl acid with 9-11 carbons; and
at least 0.250 to no more than 0.810 moles of a third acid comprising an alkyl acid with 7-9 carbons wherein the third acid has a lower molecular weight than the second acid; and
6-45 wt % surfactant; and
2.
Provided is a sulfate-free surfactant system comprises a liquid comprising an organic phase and a solvent wherein the organic phase comprises glyceride and surfactant and the liquid comprises: 4 - 40 wt% glyceride wherein the glyceride is the condensation reaction product of at least 1.10 moles of a mixture of acids to no more than 2.1 moles of mixture of acids per mole of glycerin; wherein mixture of acids comprises: at least 0.275 to no more than 0.990 moles of a first acid comprising a branched acid with 16-20 aliphatic carbons; at least 0.250 to no more than 0.810 moles of a second acid comprising an alkyl acid with 9-11 carbons; and at least 0.250 to no more than 0.810 moles of a third acid comprising an alkyl acid with 7-9 carbons wherein the third acid has a lower molecular weight than the second acid; and 6 - 45 wt% surfactant.
01 - Chemical and biological materials for industrial, scientific and agricultural use
02 - Paints, varnishes, lacquers
Goods & Services
Chemical coatings used in the manufacture of radiation curable resins, inks, paints, and packaging Ink for printers and for multifunction electronic devices for use in copying, printing, scanning, video capture or transmitting documents and images
01 - Chemical and biological materials for industrial, scientific and agricultural use
05 - Pharmaceutical, veterinary and sanitary products
44 - Medical, veterinary, hygienic and cosmetic services; agriculture, horticulture and forestry services
Goods & Services
Combination of surfactants with a biologically based plant health activator that provide plant health benefits for use in agriculture; adjuvants that improve pesticide performance along with providing plant health benefits for use in agricultural sprays and adjuvants; water conditioning agents, namely, chemical agricultural conditioners; chemical additives, namely, drift reduction additives, volatility reduction additives, deposition aid additives, defoamers, wetters, spreaders and stickers in the nature of agricultural chemicals for agricultural use Agricultural chemicals, namely, pesticides, herbicides, and fungicides Aerial and surface spreading of fertilizers and other agricultural chemicals
01 - Chemical and biological materials for industrial, scientific and agricultural use
05 - Pharmaceutical, veterinary and sanitary products
44 - Medical, veterinary, hygienic and cosmetic services; agriculture, horticulture and forestry services
Goods & Services
Combination of surfactants with a biologically based plant health activator that provide plant health benefits for use in agriculture; adjuvants that improve pesticide performance along with providing plant health benefits for use in agricultural sprays and adjuvants; water conditioning agents, namely, chemical agricultural conditioners; chemical additives, namely, drift reduction additives, volatility reduction additives, deposition aid additives, defoamers, wetters, spreaders and stickers in the nature of agricultural chemicals for agricultural use Agricultural chemicals, namely, pesticides, herbicides, and fungicides Aerial and surface spreading of fertilizers and other agricultural chemicals
31.
Process for recovering precious metals from clay-containing ores
A solution for leaching metals from clay containing ore and a method of leaching ore is described. The solution comprises a cyanide; a wetting agent; and a clay stabilizing polymer.
Novel natural oil derived ink vehicles are provided by a two step process that does not require the addition of gelants or the irreversible heat bodying or polymerization of the oil. The gelled natural oil may be used as the vehicle/carrier in the ink formulation or alternatively used as a carrier or dispersant for additives in ink formulations. The gelled ink vehicles disclosed have many advantages over ink vehicles disclosed in the prior art.
A solution for leaching metals from clay containing ore and a method of leaching ore is described. The solution comprises a cyanide; a wetting agent; and a clay stabilizing polymer.
An improved metal working composition is provided. The composition comprises an additive defined by Formula I: [R1-(CO)yO(CH2CHR2O)z]nPO4-nX3-n Formula I wherein: R1 is a saturated or unsaturated, branched or linear, alkyl or aryl hydrocarbon group comprising at least 10 to no more than 24 carbons; each R2 is independently selected from H and alkyl of 1-5 carbons; X is a cation or hydrogen; y is 0 or 1; z is an integer of 1 to 20; and n is 1 or 2.
C11C 3/00 - Fats, oils or fatty acids obtained by chemical modification of fats, oils or fatty acids, e.g. by ozonolysis
C11C 3/04 - Fats, oils or fatty acids obtained by chemical modification of fats, oils or fatty acids, e.g. by ozonolysis by esterification of fats or fatty oils
The invention provides a compound of the formula:
wherein Ar is selected from the group consisting of aryl, monosubstituted aryl and polysubstituted aryl, heteroaryl, monosubstituted heteroaryl and polysubstituted heteroaryl; Ar′ is selected from the group consisting of aryl, monosubstituted aryl and polysubstituted aryl, heteroaryl, monosubstituted heteroaryl and polysubstituted heteroaryl; R is an alkylene radical having 2-20 carbon atoms; and n=1-20. The compounds of the invention are used with polymer resins to enhance their gas barrier properties.
C07C 69/76 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring
C07C 69/92 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring of monocyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of a six-membered aromatic ring with etherified hydroxyl groups
38.
Additives to improve open-time and freeze-thaw characteristics of water-based paints and coatings
Waterborne coatings are described having an acceptable balance of properties both during the storage of coating, application and drying. The period in which irregularities in a freshly applied coating can be repaired without resulting in brush marks is referred to as the open time. Aqueous coatings generally employ dispersed high molecular weight polymers as binders. These binders often provide short open times when the coating is dried since the dispersed polymer particles tend to be immobilized quickly in the edge region of an applied coating. As a result, the viscosity of the coating increases rapidly, which leads to a limited window of workability. The instant invention provides additives that are not volatile but that will extend the time that the film is malleable after it is applied without interfering with other attributes, such as the resistance of the coating to freezing while in the can prior to application.
B01F 17/00 - Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
C08G 65/22 - Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
C09K 8/588 - Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific polymers
A01N 25/30 - Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of applicationSubstances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
40.
Chemical additives and use thereof in corn stillage processing
An improved process is provided for separating corn oil from stillage comprising forming stillage from the fermentation of corn; mixing the stillage with a chemical additive comprising alkoxylated modified corn oil prepared by the transesterification of corn oil with glycerine followed by alkoxylation; and separating the corn oil from the stillage.
C11C 3/04 - Fats, oils or fatty acids obtained by chemical modification of fats, oils or fatty acids, e.g. by ozonolysis by esterification of fats or fatty oils
Waterborne coatings are described having an acceptable balance of properties both during the storage of coating, application and drying. The period in which irregularities in a freshly applied coating can be repaired without resulting in brush marks is referred to as the open time. Aqueous coatings generally employ dispersed high molecular weight polymers as binders. These binders often provide short open times when the coating is dried since the dispersed polymer particles tend to be immobilized quickly in the edge region of an applied coating. As a result, the viscosity of the coating increases rapidly, which leads to a limited window of workability. The instant invention provides additives that are not volatile but that will extend the time that the film is malleable after it is applied without interfering with other attributes, such as the resistance of the coating to freezing while in the can prior to application.
C08G 65/02 - 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
C08G 65/22 - Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
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 65/326 - Polymers modified by chemical after-treatment with inorganic compounds containing sulfur
C08G 65/331 - Polymers modified by chemical after-treatment with organic compounds containing oxygen
An aqueous alkyd resin coating composition, comprising (a) at least one alkyd resin as a dispersed phase; (b) an emulsifier based on styrenated phenols that have been converted into reactive surfactants by first reaction with one or more equivalents of an allyl glycidyl ether to provide pendant allyl groups and then oxyalkylated and (c) water. The invention also provides a method for preparing these aqueous alkyd resin coating compositions from solvent borne alkyd compositions.
C08L 67/08 - Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
C08G 65/326 - Polymers modified by chemical after-treatment with inorganic compounds containing sulfur
C08G 65/327 - Polymers modified by chemical after-treatment with inorganic compounds containing phosphorus
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
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for use in the manufacture of a wide variety of goods such as paint, ink, paper, textiles, chemicals, and agricultural, metalworking, and personal care formulations
45.
IMPROVED PROCESS FOR RECOVERING PRECIOUS METALS FROM CLAY-CONTAINING ORES
A solution for leaching precious metals from clay containing ore and a method of leaching ore is described. The solution comprises a cyanide, a wetting agent, and a clay stabilizing polymer. In a first embodiment a solution for leaching precious metals from clay containing ore comprises cyanide, a wetting agent, and a clay stabilizing polymer with a pH of at least 8 to no more than 11.
The invention provides biobased lubricants comprising the reaction product of a natural oil, fatty acid or derivative having unsaturation sites with a suitable substrate such as maleic anhydride that is capable of undergoing an “ene” or Diels Alder reaction with the natural oil to form an adduct; followed by a controlled non-aqueous neutralization with a suitable inorganic base such as lithium hydroxide.
C10M 169/04 - Mixtures of base-materials and additives
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
C10M 105/26 - Carboxylic acids or their salts having more than one carboxyl group bound to an acyclic carbon atom or cycloaliphatic carbon atom
C10M 111/02 - 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 non-macromolecular organic compound
47.
POLYALKANOIC OR POLYALKENOIC ACID BASED HIGH PERORMANCE, WATER-DILUTABLE LUBRICITY ADDITIVE FOR MULTI-METAL METALWORKING APPLICATIONS
The invention provides lubricating composition comprising: (1) a reaction product selected from the group consisting of: (a) a polyalkanoic or polyalkenoic acid derived from hydroxyfatty acids and a block copolymer selected from the group consisting of polyoxyethylene-polyoxypropylene and a reverse block copolymer of polyoxypropylene-polyoxyethylene-polyoxypropylene; (b) the reaction product of (a) with a maleic acid or anhydride; and (c) the reaction product of (a) with maleated soybean oil; and (2) at least one base oil selected from the group consisting of alkyl benzene, normal paraffin, isoparaffin, mineral oil and a-olefin.
C08G 65/331 - Polymers modified by chemical after-treatment with organic compounds containing oxygen
C08G 65/332 - Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides or esters thereof
C08L 71/00 - Compositions of polyethers obtained by reactions forming an ether link in the main chainCompositions of derivatives of such polymers
C10M 115/04 - Lubricating compositions characterised by the thickener being a non-macromolecular organic compound other than a carboxylic acid or salt thereof containing oxygen
The invention provides lubricating composition comprising: (1) a reaction product selected from the group consisting of: (a) a polyalkanoic or polyalkenoic acid derived from hydroxyfatty acids and a block copolymer selected from the group consisting of polyoxyethylene-polyoxypropylene and a reverse block copolymer of polyoxypropylene-polyoxyethylene-polyoxypropylene; (b) the reaction product of (a) with a maleic acid or anhydride; and (c) the reaction product of (a) with maleated soybean oil; and (2) at least one base oil selected from the group consisting of alkyl benzene, normal paraffin, isoparaffin, mineral oil and α-olefin.
C10M 145/00 - Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
C11C 3/00 - Fats, oils or fatty acids obtained by chemical modification of fats, oils or fatty acids, e.g. by ozonolysis
C08G 65/332 - Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides or esters thereof
C10M 145/16 - 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 polycarboxylic
The invention provides lubricating composition comprising: (1) a reaction product selected from the group consisting of: (a) a polyalkanoic or polyalkenoic acid derived from hydroxyfatty acids and a block copolymer selected from the group consisting of polyoxyethylene-polyoxypropylene and a reverse block copolymer of polyoxypropylene-polyoxyethylene-polyoxypropylene; (b) the reaction product of (a) with a maleic acid or anhydride; and (c) the reaction product of (a) with maleated soybean oil; and (2) at least one base oil selected from the group consisting of alkyl benzene, normal paraffin, isoparaffin, mineral oil and α-olefin.
C11C 3/00 - Fats, oils or fatty acids obtained by chemical modification of fats, oils or fatty acids, e.g. by ozonolysis
C08G 65/331 - Polymers modified by chemical after-treatment with organic compounds containing oxygen
C08G 65/332 - Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides or esters thereof
C08L 71/00 - Compositions of polyethers obtained by reactions forming an ether link in the main chainCompositions of derivatives of such polymers
C10M 115/04 - Lubricating compositions characterised by the thickener being a non-macromolecular organic compound other than a carboxylic acid or salt thereof containing oxygen
50.
Additives to resin compositions for improved impact strength and flexibility
The invention provides a composition comprising: (a) about 0% to 99% by weight of at least one resin wherein the resin is selected from the group consisting of epoxy, latex, polyurethane, polyurea, polyspartic, or alkyd resins; (b) about 1%-99% by weight of tristyrenated phenol or distyrenated phenol; and (c) optionally about 2% to 98% by weight of an additional solvent.
The invention provides a composition comprising: (a) about 0% to 99% by weight of at least one resin wherein the resin is selected from the group consisting of epoxy, latex, polyurethane, polyurea, polyspartic, or alkyd resins; (b) about 1% - 99% by weight of tristyrenated phenol or distyrenated phenol; and (c) optionally about 2% to 98% by weight of an additional solvent.
C08L 101/06 - Compositions of unspecified macromolecular compounds characterised by the presence of specified groups containing oxygen atoms
C08L 63/00 - Compositions of epoxy resinsCompositions of derivatives of epoxy resins
C08L 95/00 - Compositions of bituminous materials, e.g. asphalt, tar or pitch
C08L 33/00 - Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereofCompositions of derivatives of such polymers
The invention provides a composition comprising: (a) about 0% to 99% by weight of at least one resin wherein the resin is selected from the group consisting of epoxy, latex, polyurethane, polyurea, polyspartic, or alkyd resins; (b) about 1% - 99% by weight of tristyrenated phenol or distyrenated phenol; and (c) optionally about 2% to 98% by weight of an additional solvent.
C08L 33/00 - Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereofCompositions of derivatives of such polymers
C08L 63/00 - Compositions of epoxy resinsCompositions of derivatives of epoxy resins
C08L 95/00 - Compositions of bituminous materials, e.g. asphalt, tar or pitch
C08L 101/06 - Compositions of unspecified macromolecular compounds characterised by the presence of specified groups containing oxygen atoms
C09D 1/08 - Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances cement with organic additives
The present invention relates to novel dispersants based on reaction products of two and one moles respectively of the branched ester alcohol or alkokylated ester alcohol with maleic anhydride that has been subjected to a further sulfonation reaction. The compounds are useful as dispersing and wetting agents. The invention further relates to the use of the dispersants of the invention to produce stable aqueous dispersions of high performance thermoplastic polymers.
The present invention relates to novel dispersants based on reaction products of two and one moles respectively of the branched ester alcohol or alkokylated ester alcohol with maleic anhydride that has been subjected to a further sulfonation reaction. The compounds are useful as dispersing and wetting agents. The invention further relates to the use of the dispersants of the invention to produce stable aqueous dispersions of high performance thermoplastic polymers.
C08J 3/03 - Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
An aqueous alkyd resin coating composition, comprising (a) at least one alkyd resin as a dispersed phase; (b) an emulsifier based on styrenated phenols that have been converted into reactive surfactants by first reaction with one or more equivalents of an allyl glycidyl ether to provide pendant allyl groups and then oxyalkylated and (c) water. The invention also provides a method for preparing these aqueous alkyd resin coating compositions from solvent borne alkyd compositions.
An aqueous alkyd resin coating composition, comprising (a) at least one alkyd resin as a dispersed phase; (b) an emulsifier based on styrenated phenols that have been converted into reactive surfactants by first reaction with one or more equivalents of an allyl glycidyl ether to provide pendant allyl groups and then oxyalkylated and (c) water. The invention also provides a method for preparing these aqueous alkyd resin coating compositions from solvent borne alkyd compositions.
C08J 3/07 - Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media from polymer solutions
An aqueous alkyd resin coating composition, comprising (a) at least one alkyd resin as a dispersed phase; (b) an emulsifier based on styrenated phenols that have been converted into reactive surfactants by first reaction with one or more equivalents of an allyl glycidyl ether to provide pendant allyl groups and then oxyalkylated and (c) water. The invention also provides a method for preparing these aqueous alkyd resin coating compositions from solvent borne alkyd compositions.
The invention provides a novel bio-based dispersant comprising the reaction product of a natural triglyceridic oil, fatty acid oil or fatty acid oil derivative wherein said natural triglyceridic oil, fatty acid oil, or fatty acid oil derivative containing greater than about 80 percent of unsaturated or conjugated unsaturated fatty acids with a substrate capable of undergoing an ene or Diels Alder reaction to form an adduct that is further esterified and/or neutralized with an alkanolamine or alkoxylated alkanolamine.
C07C 209/68 - Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
C07C 213/06 - Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton from hydroxy amines by reactions involving the etherification or esterification of hydroxy groups
C07C 219/12 - 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 at least one of the hydroxy groups esterified by a carboxylic acid having the esterifying carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
C07C 51/347 - Preparation of carboxylic acids or their salts, halides, or anhydrides by reactions not involving formation of carboxyl groups
C07C 51/353 - Preparation of carboxylic acids or their salts, halides, or anhydrides by reactions not involving formation of carboxyl groups by isomerisationPreparation of carboxylic acids or their salts, halides, or anhydrides by reactions not involving formation of carboxyl groups by change of size of the carbon skeleton
C07C 51/41 - Preparation of salts of carboxylic acids by conversion of the acids or their salts into salts with the same carboxylic acid part
C08J 3/03 - Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
C08J 3/09 - Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
C08L 23/02 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondCompositions of derivatives of such polymers not modified by chemical after-treatment
C08L 61/00 - Compositions of condensation polymers of aldehydes or ketonesCompositions of derivatives of such polymers
2—OXnR). Freeze thaw resistance and improved stability is obtained in epoxy mixtures used in dispersion form. Improved pot life and cure time is obtained using either the epoxy mixture, the hardener mixture or a combination of the two in epoxy hardener formulations.
Waterborne coatings are described having an acceptable balance of properties both during the storage of coating, application and drying. The period in which irregularities in a freshly applied coating can be repaired without resulting in brush marks is referred to as the open time. Aqueous coatings generally employ dispersed high molecular weight polymers as binders. These binders often provide short open times when the coating is dried since the dispersed polymer particles tend to be immobilized quickly in the edge region of an applied coating. As a result, the viscosity of the coating increases rapidly, which leads to a limited window of workability. The instant invention provides additives that are not volatile but that will extend the time that the film is malleable after after it is applied without interfering with other attributes, such as the resistance of the coating to freezing while in the can prior to application.
The present invention relates to novel non-aqueous gels of natural oils and their derivatives and provides a novel process for the gelation of natural oils and their derivatives that does not require the addition of gellants or the irreversible heat bodying of the oil. The gels and method of the present invention are applicable to a wide range of natural oils, and the method is easily tailored to provide thermoreversible gels of any desired viscosity. The natural oil based gels of the present invention and the method of their preparation have many advantages over the prior art. The natural oil based gels provided have exemplary properties and find use in a variety of applications.
Liquid hydrocarbons are gelled by the introduction of a phosphate ester and a crosslinking agent for use in oil recovery. Generally a proppant, delayed gel breaker and other modifiers are added to the gelled hydrocarbon to improve the oil recovery process. The phosphate ester used in this method and composition for oil recovery has low volatility and good stability during hydrocarbon distillation resulting in improved distillation efficiency in a refinery.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for use in the manufacture of a wide variety of
goods such as paint, ink, paper, textiles, chemicals, and
agricultural, metalworking, and personal care formulations.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
(1) Chemicals for use in the manufacture of goods, namely paint, ink, paper, textiles, chemicals, namely industrial and agricultural chemicals, agricultural formulations, metalworking formulations, namely, metalworking fluids and personal care formulations, namely, cosmetics, skin care preparations, lotions, cleaners and creams, sunscreens and hair care formulations, namely, hair care preparations, creams, cleaners and lotions.
65.
Bis(aryloxyalkyl) esters of aromatic polycarboxylic acids and method of preparation
The invention provides a compound of the formula:
wherein Ar is selected from the group consisting of aryl, monosubstituted aryl and polysubstituted aryl, heteroaryl, monosubstituted heteroaryl and polysubstituted heteroaryl; Ar′ is selected from the group consisting of aryl, monosubstituted aryl and polysubstituted aryl, heteroaryl, monosubstituted heteroaryl and polysubstituted heteroaryl; R is an alkylene radical having 2-20 carbon atoms; and n=1-20. The compounds of the invention are used with polymer resins to enhance their gas barrier properties.
C07C 67/08 - Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
C07C 69/76 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring
C08K 5/12 - EstersEther-esters of cyclic polycarboxylic acids
C07C 67/29 - Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by introduction of oxygen-containing functional groups
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
POLYETHOXYLATED ALCOHOLS AND PHENOLS FOR USE AS WETTING AGENTS, DETERGENTS AND PENETRANTS; POLYETHOXYLATED ALCOHOLS AND PHENOLS FOR USE IN THE MANUFACTURE OF WETTING AGENTS, DETERGENTS AND PENETRANTS; NONE OF THE AFORESAID GOODS USED FOR OR IN MOTOR FUELS
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
CHEMICALS, NAMELY, ALCOHOL PHOSPHATES AND POLYETHOXYLATED ALCOHOL ETHER PHOSPHATES, NAMELY, ALIPHATIC ALCOHOL PHOSPHATES, AROMATIC ALCOHOL PHOSPHATES, POLYETHOXYLATED ALIPHATIC PHOSPHATES, AND POLYETHOXYLATED AROMATIC ALCOHOL PHOSPHATES, ALL IN ACID FORM OR NEUTRALIZED AS POTASSIUM OR ALKYLAMMONIUM SALTS, FOR USE AS DETERGENTS, ANTISTATIC AGENTS, LUBRICANTS, AND SURFACTANTS; CHEMICALS, NAMELY, ALCOHOL PHOSPHATES AND POLYETHOXYLATED ALCOHOL ETHER PHOSPHATES, NAMELY, ALIPHATIC ALCOHOL PHOSPHATES, AROMATIC ALCOHOL PHOSPHATES, POLYETHOXYLATED ALIPHATIC PHOSPHATES, AND POLYETHOXYLATED AROMATIC ALCOHOL PHOSPHATES, ALL IN ACID FORM OR NEUTRALIZED AS POTASSIUM OR ALKYLAMMONIUM SALTS, FOR USE IN THE MANUFACTURE OF DETERGENTS, ANTISTATIC AGENTS, LUBRICANTS, AND SURFACTANTS
68.
METHOD FOR IMPROVING THE EFFECTIVENESS OF TITANIUM DIOXIDE-CONTAINING COATINGS
The invention provides a method for forming a Ti02-latex composite particle dispersion comprising combining an aqueous Ti()2 dispersion with a latex manufactured with a phosphate-containing ethylenically unsaturated reactive surfactant. The dispersions have improved opacity or hiding.
Waterborne coatings are described having an acceptable balance of properties both during the storage of coating, application and drying. The period in which irregularities in a freshly applied coating can be repaired without resulting in brush marks is referred to as the open time. Aqueous coatings generally employ dispersed high molecular weight polymers as binders. These binders often provide short open times when the coating is dried since the dispersed polymer particles tend to be immobilized quickly in the edge region of an applied coating. As a result, the viscosity of the coating increases rapidly, which leads to a limited window of workability. The instant invention provides additives that are not volatile but that will extend the time that the film is malleable after it is applied without interfering with other attributes, such as the resistance of the coating to freezing while in the can prior to application.
C09D 171/00 - Coating compositions based on polyethers obtained by reactions forming an ether link in the main chainCoating compositions based on derivatives of such polymers
C09D 171/10 - Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
C08G 65/02 - 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
C08G 65/22 - Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
C08G 65/38 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
C08G 65/40 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols and other compounds
C07C 43/11 - Polyethers containing —O—(C—C—O—)n units with 2 ≤ n ≤ 10
C07C 15/24 - Polycyclic condensed hydrocarbons containing two rings
70.
WATER BORNE EPOXY RESIN DISPERSIONS AND EPOXY HARDENER COMPOSITIONS
An epoxy or hardener mixture comprising (a) optionally water, (b) at least one hardener or epoxy resin, and (c) from 0.1 to 20 weight percent, based on epoxy resin of at least one distyryl phenol, tristyryl phenol or cumylphenol based additive surfactant with phosphate or sulfonate end groups having the structure R - OXn - W wherein R designates a polystyrylphenol or cumylphenol, preferentially chosen from among distyrylphenol, tristyrylphenol or cumylphenol, and mixtures thereof, and wherein OX designates ethylene oxide and/or propylene oxide. The number of groups "n" varies from 0 to 200, and W designates H, sulfate (-SO3 -) or phosphate (-PO3H or -P02-OXnR). Freeze thaw resistance and improved stability is obtained in epoxy mixtures used in dispersion form. Improved pot life and cure time is obtained using either the epoxy mixture, the hardener mixture or a combination of the two in epoxy hardener formulations.
The present invention relates to novel non-aqueous gels of natural oils and their derivatives and provides a novel process for the gelation of natural oils and their derivatives that does not require the addition of gellants or the irreversible heat bodying of the oil. The gels and method of the present invention are applicable to a wide range of natural oils, and the method is easily tailored to provide thermoreversible gels of any desired viscosity. The natural oil based gels of the present invention and the method of their preparation have many advantages over the prior art. The natural oil based gels provided have exemplary properties and find use in a variety of applications.
C07C 209/68 - Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
C07C 213/06 - Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton from hydroxy amines by reactions involving the etherification or esterification of hydroxy groups
C07C 219/08 - 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 at least one of the hydroxy groups esterified by a carboxylic acid having the esterifying carboxyl group bound to an acyclic carbon atom of an acyclic unsaturated carbon skeleton
C07C 219/12 - 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 at least one of the hydroxy groups esterified by a carboxylic acid having the esterifying carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
C07C 51/347 - Preparation of carboxylic acids or their salts, halides, or anhydrides by reactions not involving formation of carboxyl groups
C07C 51/353 - Preparation of carboxylic acids or their salts, halides, or anhydrides by reactions not involving formation of carboxyl groups by isomerisationPreparation of carboxylic acids or their salts, halides, or anhydrides by reactions not involving formation of carboxyl groups by change of size of the carbon skeleton
C07C 51/41 - Preparation of salts of carboxylic acids by conversion of the acids or their salts into salts with the same carboxylic acid part
Novel natural oil derived ink vehicles are provided by a two step process that does not require the addition of gelants or the irreversible heat bodying or polymerization of the oil. The gelled natural oil may be used as the vehicle/carrier in the ink formulation or alternatively used as a carrier or dispersant for additves in ink formulations. The gelled ink vehicles disclosed have many advantages over ink vehicles disclosed in the prior art.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for use in the manufacture of a wide variety of goods such as paint, ink, paper, textiles, chemicals, and agricultural, metalworking, and personal care formulations
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for use in the manufacture of a wide variety of goods such as paint, ink, paper, textiles, chemicals, and agricultural, metalworking, and personal care formulations
75.
NEW REACTIVE SURFACTANTS FOR FREEZE-THAW STABLE EMULSION POLYMERS AND COATINGS THEREOF
The invention provides aqueous coating composition having freeze thaw stability, comprising: (a) at least one latex polymer derived from at least one monomer and at least one reactive surfactant of the formula R1O- (CH2CHR2O)x-(CH2CH2O)y-(CH2CHR3O)z-R4 where R1 is either alkyl, aryl, alkylaryl, or aralkylaryl of 8 - 30 carbon atoms, R2 is - CH2OCH2CH=CH2 (AGE); R3 is either H, CH3, or CH2CH3; R4 is H or -SO3M or -PO3M where M is H or K, Na, NH4, NR4, alkanolamine, or other cationic species and x = 2 - 100; y = 4 - 200 and z = 0 - 50.
C08L 71/10 - Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
C09D 171/00 - Coating compositions based on polyethers obtained by reactions forming an ether link in the main chainCoating compositions based on derivatives of such polymers
C09D 171/10 - Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
C08G 65/02 - 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
C08G 65/22 - Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
C08G 65/334 - Polymers modified by chemical after-treatment with organic compounds containing sulfur
C08G 65/38 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
C08G 65/40 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols and other compounds
C07C 43/11 - Polyethers containing —O—(C—C—O—)n units with 2 ≤ n ≤ 10
76.
NEW REACTIVE SURFACTANTS FOR FREEZE-THAW STABLE EMULSION POLYMERS AND COATINGS THEREOF
The invention provides aqueous coating composition having freeze thaw stability, comprising: (a) at least one latex polymer derived from at least one monomer and at least one reactive surfactant of the formula R1O- (CH2CHR2O)x-(CH2CH2O)y-(CH2CHR3O)z-R4 where R1 is either alkyl, aryl, alkylaryl, or aralkylaryl of 8 - 30 carbon atoms, R2 is - CH2OCH2CH=CH2 (AGE); R3 is either H, CH3, or CH2CH3; R4 is H or -SO3M or -PO3M where M is H or K, Na, NH4, NR4, alkanolamine, or other cationic species and x = 2 - 100; y = 4 - 200 and z = 0 - 50.
C09D 151/08 - Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bondsCoating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
77.
NEW REACTIVE SURFACTANTS FOR EMULSION POLYMERIZATION, PIGMENT DISPERSION, AND UV COATINGS
The present invention provides reactive surfactants of the formula R1O- (CH2CHR20)x-(CH2CH20)y-(CH2CHR30)z-R4 where R1 is either alkyl, aryl, alkylaryl, or aralkylaryl of 8 - 30 carbon atoms, R2 is - CH2OCH2CH=CH2 (AGE); R3 is either H, CH3, or CH2CH3; R4 is H or -S03M or -P03M where M is H or K, Na, NH4, NR4, alkanolamine, or other cationic species and x = 2 - 100; y = 4 - 200 and z = 0 - 50.
C07C 43/11 - Polyethers containing —O—(C—C—O—)n units with 2 ≤ n ≤ 10
C08G 65/02 - 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
C08G 65/22 - Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
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 65/334 - Polymers modified by chemical after-treatment with organic compounds containing sulfur
C08G 65/40 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols and other compounds
C09D 171/00 - Coating compositions based on polyethers obtained by reactions forming an ether link in the main chainCoating compositions based on derivatives of such polymers
The present invention provides reactive surfactants of the formula R1O- (CH2CHR20)x-(CH2CH20)y-(CH2CHR30)z-R4 where R1 is either alkyl, aryl, alkylaryl, or aralkylaryl of 8 - 30 carbon atoms, R2 is - CH2OCH2CH=CH2 (AGE); R3 is either H, CH3, or CH2CH3; R4 is H or -S03M or -P03M where M is H or K, Na, NH4, NR4, alkanolamine, or other cationic species and x = 2 - 100; y = 4 - 200 and z = 0 - 50.
C08G 65/02 - 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
C08G 65/22 - Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
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 65/334 - Polymers modified by chemical after-treatment with organic compounds containing sulfur
C08G 65/40 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols and other compounds
C07C 43/11 - Polyethers containing —O—(C—C—O—)n units with 2 ≤ n ≤ 10
C09D 171/00 - Coating compositions based on polyethers obtained by reactions forming an ether link in the main chainCoating compositions based on derivatives of such polymers
C07C 43/23 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
C07C 309/10 - Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing oxygen atoms bound to the carbon skeleton containing etherified hydroxy groups bound to the carbon skeleton with the oxygen atom of at least one of the etherified hydroxy groups further bound to an acyclic carbon atom
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
The present invention relates to the use of Styrenated Phenol Ethoxylates as surfactants in emulsion polymerization. The present invention further relates to the use of both anionic and nonionic Styrenated Phenol Ethoxylates in emulsion polymerization. Latexes with small average particle and narrow particle size distributions are obtained. Prepared latexes also have low coagulum levels and exhibit excellent mechanical and chemical stability.
The invention provides a compound of the formula:
wherein Ar is selected from the group consisting of aryl, monosubstituted aryl and polysubstituted aryl, heteroaryl, monosubstituted heteroaryl and polysubstituted heteroaryl; Ar′ is selected from the group consisting of aryl, monosubstituted aryl and polysubstituted aryl, heteroaryl, monosubstituted heteroaryl and polysubstituted heteroaryl; R is an alkylene radical having 2-20 carbon atoms; and n=1-20. The compounds of the invention are used with polymer resins to enhance their gas barrier properties.
C08K 5/105 - EstersEther-esters of monocarboxylic acids with phenols
C07C 69/92 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring of monocyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of a six-membered aromatic ring with etherified hydroxyl groups
C07C 69/76 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring
C07C 67/08 - Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
C07C 67/29 - Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by introduction of oxygen-containing functional groups
82.
Dispersions containing alkoxylates of alicyclic and polycyclic compounds
The present invention provides a dispersant for aqueous and non-aqueous systems which can disperse insoluble fine powders in aqueous and non-aqueous liquids in a short period of time and give long-term dispersion stability to the resulting dispersions. The dispersant is a compound of the formula
22 alkyl or alkenyl.
C04B 28/14 - Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing calcium sulfate cements
B60C 1/00 - Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
C08J 3/22 - Compounding polymers with additives, e.g. colouring using masterbatch techniques
83.
Pet container and compositions having enhanced mechanical properties and gas barrier properties
A container comprising a polyester composition with enhanced mechanical properties is provided. The polyester composition comprises a polyester and a creep control agent. In particular embodiments, the polyester composition comprises a polyester, a creep control agent, and a gas barrier additive. In particular embodiments, the creep control agents are molecules or polymers comprising dianhydrides, bis-lactams, bis-oxazoles, and epoxides.
Liquid hydrocarbons are gelled by the introduction of a phosphate ester and a crosslinking agent for use in oil recovery. Generally a proppant, delayed gel breaker and other modifiers are added to the gelled hydrocarbon to improve the oil recovery process. The phosphate ester used in this method and composition for oil recovery has low volatility and good stability during hydrocarbon distillation resulting in improved distillation efficiency in a refinery.
C02F 5/10 - Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
The invention provides a composition comprising reaction products. from a reaction of a natural butter or natural oil such as shea butter with glycerirfin the presence of a basic catalyst and wherein the reaction products retain the unsaponifiable portion of -said natural butter or natural oil. The resulting reaction products are self-emulsfiable and are particularly useful in personal care, cosmetic, pharmaceutical, paper and textuile applications.
A61K 8/18 - Cosmetics or similar toiletry preparations characterised by the composition
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
86.
Styrenated phenol ethoxylates in emulsion polymerization
The present invention relates to the use of Styrenated Phenol Ethoxylates as surfactants in emulsion polymerization. The present invention further relates to the use of both anionic and nonionic Styrenated Phenol Ethoxylates in emulsion polymerization. Latexes with small average particle and narrow particle size distributions are obtained. Prepared latexes also have low coagulum levels and exhibit excellent mechanical and chemical stability.
This invention relates to novel compounds derived from the reaction of diamines or polyamines with alkylene oxides. The invention also relates to novel compounds derived from the reaction of amine terminated polyethers with epoxide functional compounds. The novel compounds of the invention are particularly useful as wetting and foam control agents. The disclosed compounds exhibit exceptional antifoaming and defoaming activity while simultaneously reducing the dynamic surface tension when incorporated at low levels in water- based systems.
The present invention relates to the use of Styrenated Phenol Ethoxylates as surfactants in emulsion polymerization. The present invention further relates to the use of both anionic and nonionic Styrenated Phenol Ethoxylates in emulsion polymerization. Latexes with small average particle and narrow particle size distributions are obtained. Prepared latexes also have low coagulum levels and exhibit excellent mechanical and chemical stability.
Embodiments of the present invention provide a composition useful as an additive to a. printing ink. In one embodiment a composition is used that includes a biologically derived base material formed from one or more saturated or unsaturated straight or branched, chain triglycerides or combinations thereof, wherein the triglycerides are partially to fully hydrogenated and have a viscosity between about (50) and about (200,000) centipoise at temperatures about (72) degrees Fahrenheit. In another embodiment, the composition further includes a finely divided additive selected from the group consisting of polytetrafluoroethylene or hydrogenated triglycerides in an intimate admixture with the base material. Other aspects relate to a method of making an ink additive and method for printing paper stock by letter press or lithography.
The invention provides compounds having the general structure: formula (I). wherein R and R' are independently selected from the group consisting of H, C1-24 alkyl, aryl, C1-24 alkylaryl, aryl(C1-24)alkyl, -C(=O)-Ri (esters), CC=O)-NHR, (urethanes), or C(=O)-O-R1 (carbonates) wherein R1 is selected from the group consisting of C1-24 alkyl, aryl, C1-24 alkylaryl, C1-24 arylalkyl; A is an organic moiety derived from the group consisting of alkylene oxides having 4-12 carbon atoms and aryl epoxides having 8-12 carbon atoms; JC= 1-300; y= 0-200; z=0-200; and with the proviso that R and R' can not be H or ether functionality at the same time. The compounds are useful for improving the water transport characteristics of hydrophobic surfaces.
The invention provides compounds having the general structure:
1-24 arylalkyl; A is an organic moiety derived from the group consisting of alkylene oxides having 4-12 carbon atoms and aryl epoxides having 8-12 carbon atoms; x=1-300; y=0-200; z=0-200; and with the proviso that R and R′ can not be H or ether functionality at the same time. The compounds are useful for improving the water transport characteristics of hydrophobic surfaces.
C09K 17/14 - Soil-conditioning materials or soil-stabilising materials containing organic compounds only
C08G 67/00 - Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing oxygen or oxygen and carbon, not provided for in groups
A01G 1/00 - Horticulture; Cultivation of vegetables (labels or name-plates G09F 3/00, G09F 7/00)
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 65/332 - Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides or esters thereof
Liquid hydrocarbons are gelled by the introduction of a phosphate ester and a crosslinking agent for use in oil recovery. Generally a proppant, delayed gel breaker and other modifiers are added to the gelled hydrocarbon to improve the oil recovery process. The phosphate ester used in this method and composition for oil recovery has low volatility and good stability during hydrocarbon distillation resulting in improved distillation efficiency in a refinery.
C02F 5/10 - Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
The present invention provides a dispersant for aqueous and non-aqueous systems which can disperse insoluble fine powders in non-aqueous liquids in a short period of time and give long-term dispersion stability to the resulting dispersions without allowing the formation of hard cake or precipitates. The dispersant is a compound of the formula
22 saturated or unsaturated group; x=1–100; y=1–3; z=1–100 and s=1–100. The dispersant of the invention is also particularly effective for dispersing additives into polymers such as polyesters, polyamides, polycarbonates, polyethylene and polypropylene.
