Patent application number | Description | Published |
20110277844 | POLYMERS DERIVED FROM N-VINYL FORMAMIDE, VINYL AMIDES OR ACRYLAMIDES, AND REACTION SOLVENT, AND THE USES THEREOF - Polymers are provided that are derived from at least (A) N-vinyl formamide, (B) one vinyl amide moiety or one acrylamide moiety, and (C) a reaction solvent. The polymers are random, block, or alternating polymers. A particular useful poly-mer comprises about 20% N-vinyl formamide, about 50% N-vinyl-ε-caprolactam, about 30% N-vinyl-2-pyrrolidone, being synthesized in ethylene glycol. In preferred embodiments, polymers of the invention exhibit a cloud point temperature of 66° C. or more, inhibit the formation of gas hydrates, and/or inhibit corrosion. Especially preferred uses of the polymers are in oilfield operations as gas hydrate inhibitors and/or corrosion inhibitors. | 11-17-2011 |
20110293540 | BRANCHED POLYMERS, COMPOSITIONS, AND USES THEREOF - Provided herein are branched polymers synthesized from: at least one (A1) reactive monomer having a vinyl functional group, or (A2) a hybrid reactive monomer having (a) at least one vinyl functional group and (b) at least one reactive non-vinyl functional group; and at least one: (B1) branching agent having at least two N-vinyl formamide functional groups or (B2) a hybrid branching agent having (a) at least one N-vinyl formamide functional group, and (b) at least one vinyl functional group. The polymers exhibit branching behavior, which in some embodiments lends to lower viscosity, enhanced processability, and/or improved sprayability compared to a corresponding polymer of equal molecular weight synthesized without the second reactive moiety. Formulations with the invention's polymers also are presented. | 12-01-2011 |
20120041040 | FUNCTIONALIZED 4- AND 5-VINYL SUBSTITUTED REGIOISOMERS OF 1, 2, 3-TRIAZOLES VIA 1, 3-DIPOLAR CYCLOADDITION AND POLYMERS THEREOF - The present invention provides novel functionalized mixtures 4- and 5-vinyl substituted regioisomers of 1,2,3-triazoles via 1,3-dipolar cycloaddition. Functionalized alkyne moieties with a terminal alcoholic functionality are reacted with functionalized organic moieties with a terminal leaving group and an azide to provide an alcoholic functionalized mixture of 4- and 5-substituted regioisomers of 1,2,3-triazole moieties. The mixture may be converted to a wide variety of useful functionalized mixtures of 4- and 5-vinyl substituted regioisomers of 1,2,3-triazole moieties, which in turn can be converted to a wide variety of useful polymers The novel alcoholic functionalized mixtures of 4- and 5-substituted regioisomers can be separated by chromatography to provide the purified 4- and 5-alcoholic functionalized substituted 1,2,3-triazole moieties. The novel compounds of the invention can be employed in a wide variety of compositions (Formulae (I), (II)); wherein R | 02-16-2012 |
20120041137 | THERMOSETTING RING-OPENING METATHESIS POLYMERIZATION MATERIALS WITH THERMALLY DEGRADABLE LINKAGES - The present invention provides a new class of thermosetting ring-opening metathesis polymerization materials based on norbornene and oxanorbornene dicarboximide moieties containing at least one acetal ester group linkage. The acetal ester group is degradable when subjected to heat or acidic aqueous hydrolysis. The polymerization materials can be used in reworkable thermosetting compositions. R1-Rs, X, and n are defined herein. | 02-16-2012 |
20120077717 | Polymers Having N-Vinyl Amide And Hydroxyl Moieties, Their Compositions And The Uses Thereof - The invention relates to polymers derived at least from one: (A) one N-vinyl amide unit, and (B) one hydroxyl-containing acrylate unit, and to polymers derived at least from: (A) N-vinyl-2-caprolactam, and (B) one non-acrylate unit having: (i) at least one hydroxyl group, and/or (ii) at least one functional group convertible to a hydroxyl group wherein at least one group is converted to hydroxyl functionality in the final polymer product. Such polymers may exhibit degradability, e.g., in seawater or soil environments. In preferred embodiments, these polymers and compositions thereof are used in oilfield applications, such as an inhibitor of gas hydrates and/or a kinetic inhibitor of gas hydrates. The polymer can assume alternating, block, and/or random configurations of the repeating units, with at least one ester group. The chemical structure subscripts m, and n may be any integer equal to or greater than 1. | 03-29-2012 |
20120142846 | 4- AND 5 SUBSTITUTED 1,2,3-TRIAZOLE MOIETIES WITH AT LEAST ONE REMOTE POLYMERIZABLE MOIETY AND POLYMERS THEREOF - The present invention provides novel 4- and 5-substituted 1,2,3-triazole moieties, with at least one remote polymerizable moiety. The novel mixtures of 4- and 5-substituted regioisomers of 1,2,3-triazole moieties can be separated by chromatography to provide the purified 4- and 5-substituted 1,2,3-triazole moieties. The novel mixtures of 4- and 5-substituted regioisomers of 1,2,3-triazole moieties, and the purified 4- and 5-substituted 1,2,3-triazole moieties, with at least one remote polymerizable moiety, can be converted to a wide variety of useful polymers. The novel compounds of the invention can be employed in a wide variety of compositions. E, Q, Z, X, a, and R | 06-07-2012 |
20120148514 | N-ALKYL LACTAM ETHERS, AND COMPOSITIONS AND USES THEREOF - Described is a class of symmetrical and asymmetrical N-alkyl lactam ethers. One preferred ether is bis-N-ethyl pyrrolidone ether. Preferred compositions and uses of the ethers are in performance chemicals, personal care, and pharmaceutical fields, where they function a variety of roles, including as a solvent, solubilizer, freezing point depressor, diluent, extracting agent, cleaning agent, degreaser, absorbent and/or dispersion agent. | 06-14-2012 |
20120149578 | Manipulation of Cloud Point for Two-Phase, Aqueous Polymeric Systems - Two-phase, aqueous polymeric systems comprised of lactamic monomers containing additives suitable for adjusting the cloud point temperature of the polymeric compositions are described. Of particular utility is the use of these additives to adjust the cloud point in aqueous solutions comprised of salts. | 06-14-2012 |
20120149861 | LACTAM-BASED COMPOUNDS WITH A URETHANE OR UREA FUNCTIONAL GROUP, AND USES THEREOF - Compounds comprising a lactam moiety, and a urethane or urea functional group are presented. By a preferred synthesis route, they are prepared using at least one polymerizable compound comprising an isocyanate moiety and reacting it with at least one hydroxyalkyl lactam compound or one aminoalkyl lactam compound. In preferred embodiments the lactam moiety is a pyrrolidone or caprolactam ring, and the polymerizable compound is a functionalized aryl isocyanate. The compounds and homopolymers and non-homopolymers thereof find useful application in a wide variety of arts, including: adhesive, agricultural, biocides, cleaning, coating, electronics, encapsulation, membrane, microelectronics, oilfield, performance chemical, personal care, sealant, and sensor applications. | 06-14-2012 |
20120157352 | DEGRADABLE POLYMER COMPOSITIONS AND USES THEREOF - The invention relates to novel polymers derived from: (A) at least one N-vinyl amide-based unit and/or at least one acrylamide-based unit, and (B) at least one unit comprising: (i) at least one hydroxyl group, and/or (ii) at least one functional group convertible to a hydroxyl group wherein at least one group is converted to hydroxyl functionality in the final polymer product, wherein the polymer comprises at least one ester group. The polymers and compositions are used in oilfield applications, such as an inhibitor of gas hydrates and/or a kinetic inhibitor of gas hydrates. The polymer can assume alternating, block, and/or random configurations of the repeating units, with at least one ester group. | 06-21-2012 |
20120312191 | REACTIVE MONOMER FOR A COATING AND/OR REACTIVE COATING - Disclosed herein are coating solutions comprising a reactive monomer, process and compositions for preparing the same that are suitable for a coating and/or reactive coating. More particularly, the present invention relates to monomers of functionalized 4- or 5-vinyl substituted regioisomers of 1,2,3-triazoles comprising a polymerizable functionality and their use in coatings. Also disclosed are applications and compositions comprising coating solutions of a reactive monomer and its application in printing processes and inks. | 12-13-2012 |
20130004667 | COMPOSITIONS COMPRISING A REACTIVE MONOMER AND WITH A UREA OR URETHANE FUNCTIONAL GROUP - Disclosed herein are compositions comprising a reactive monomer, and, in particular, coating and/or reactive coating compositions. More particularly, compositions containing monomers comprising a lactam moiety, a urethane or urea functional group, and a polymerizable moiety are disclosed. | 01-03-2013 |
20130025495 | COMPOSITIONS COMPRISING A REACTIVE MONOMER AND USES THEREOF - Disclosed herein are compositions such as ink or coating compositions that include at least one reactive monomer that includes a maleimide of the general formula (I) A- is or includes an aryl, an alkylaryl, or an arylalkyl. The reactive monomer may be or include 4-butylphenyl maleimide. The composition may also include a reactive co-solvent that may include at least one of a (meth)acryl monomer or prepolymer, a (meth)acryl ester of an epoxy type monomer or prepolymer, and a urethane type monomer or prepolymer. | 01-31-2013 |
20130078879 | REACTIVE MONOMER FOR A COATING AND/OR REACTIVE COATING - Disclosed herein are coating solutions comprising a reactive monomer, process and compositions for preparing the same that are suitable for a coating and/or reactive coating. More particularly, the present invention relates to monomers comprising a multifunctional N-vinylformamide crosslinking moiety and their use in coatings. Also disclosed are applications and compositions comprising coating solutions of a reactive monomer and its application in printing processes and inks. | 03-28-2013 |
20130085230 | REACTIVE SOLUTION OF POLYMERIZABLE POLYMER COMPRISING POLYMERIZABLE REACTIVE FUNCTIONALITIES, PROCESS AND COMPOSITIONS THEREOF - Disclosed herein a process for the preparation of reactive solution of polymerizable polymers comprising polymerizable reactive functionality and wherein one approach discloses a polymerizable polymer comprising a (i) N-vinyl amide monomer; (ii) dual functional monomer; and (iii) polymerizable monomelic solvent. An additional approach reveals about polymerizable polymer comprising (i) a base polymer made from N-vinyl amide monomer and a co-monomer with the proviso for grafting; (ii) graft functional monomer; and (iii) a polymerizable monomelic solvent to enable a medium for polymerization. Also, discloses about the compositions comprising reactive solution of polymerizable polymer and its various possible applications. | 04-04-2013 |
20130085248 | POLYMERS PREPARED FROM MIXTURES OF MULTIFUNCTIONAL N-VINYLFORMAMIDE AND HYBRID REACTIVE N-VINYLFORMAMIDE CROSSLINKING MONOMER MOIETIES AND USES THEREOF - The present invention provides polymers resulting from polymerization of at least one reactive vinyl monomer moiety and a multifunctional N-vinylformamide crosslinking moiety; polymers resulting from polymerization of at least one reactive vinyl monomer moiety and a hybrid N-vinylformamide crosslinking moiety having at least one N-vinylformamide functionality and at least one other reactive vinyl functionality; polymers resulting from polymerization of at least one hybrid reactive N-vinylformamide monomer moiety having one N-vinylformamide functionality and at least one other reactive non-vinyl functionality and a multifunctional N-vinylformamide crosslinking moiety; and polymers resulting from polymerization of at least one hybrid reactive N-vinylformamide monomer moiety having one N-vinylformamide functionality and at least one other reactive non-vinyl functionality and a hybrid N-vinylformamide crosslinking moiety having at least one N-vinylformamide functionality and at least one other reactive vinyl functionality. The invention further provides a wide variety of compositions comprising the novel crosslinked polymers. | 04-04-2013 |
20130090443 | POLYMERIZABLE CARBAMATE AND THIOCARBAMATE COMPOUNDS, POLYMERS DERIVED FROM THEM, AND COMPOSITIONS THEREOF - Carbamate and thiocarbamate compounds are described that comprise a polymerizable moiety and one or more free hydroxyl and/or thiol groups. Polymers may be obtained by polymerizing these carbamate and/or thiocarbamate compounds. The carbamate and thiocarbamate compounds, as well as the polymers they produce may be formulated into adhesive, agricultural, biocide, cleaning, coating, encapsulation, membrane, oilfield, performance chemical, and personal care compositions. | 04-11-2013 |
20130123147 | POLYMERS HAVING ACID AND AMIDE MOIETIES, AND USES THEREOF - Polymers are described that are polymerized from at least one reactive vinyl monomer having acid functionality or a salt thereof, and at least one reactive vinyl monomer having amide functionality. These polymers have a molecular weight from about 500 Da to about 15,000 Da; and may additionally comprise one or more solvent adducts. These polymers may be included in compositions that find use in oilfield applications, such as for inhibition and/or prevention of gas hydrates and/or corrosion. | 05-16-2013 |
20130150481 | COMPOSITIONS COMPRISING A REACTIVE MONOMER AND USES THEREOF - Disclosed herein are compositions that include at least one reactive monomer that includes a lactam functional group and an ester functional group represented by formula (1): and a reactive co-solvent having a carbon-carbon double bond. The reactive monomer is one that is capable of reacting with the co-solvent to form a polymer. The compositions may be an ink composition including curable ink compositions. | 06-13-2013 |
20130150520 | MODIFICATION OF POLYMERS CONTAINING AN ANHYDRIDE AND USES THEREOF - The present invention provides polymers resulting from modification of polymeric moieties containing an anhydride with modifying reactant moieties. The invention further provides a wide variety of compositions comprising the and modified polymeric moieties containing an anhydride. The letters b, d, e, and z are described herein. | 06-13-2013 |
20130198968 | FUNCTIONAL ADDITIVES FOR CLEANSING COMPOSITIONS - Functional additives for cleansing compositions exhibiting enhanced anti soil-re-deposition and/or dye transfer inhibitory properties comprising polymers in the form of homopolymers, copolymers or terpolymers synthesized from at least one hydrophobic monomer. Examples of hydrophobic monomers include N-vinyl caprolactam, vinyl acetate, vinyl esters, acrylated glycols, methacrylamide, C1 to C12 alkyl- and C1 to C12 dialkylacrylamide, C1 to C12 alkyl- and C1 to C12 dialkylmethacrylamide, C1 to C12 alkyl aery late, C1 to C12 alkyl methacrylate, 4-butyl phenyl maleimide, octyl acrylamide. | 08-08-2013 |
20130261275 | NON-HOMOPOLYMERS EXHIBITING GAS HYDRATE INHIBITION, SALT TOLERANCE AND HIGH CLOUD POINT - Polymers are provided that offer gas hydrate inhibition, salt tolerance, and high cloud point. The polymers are polymerized from at least (A) 50 mole percent or more of a monomer selected from the group consisting of: N-vinyl-2-caprolactam, one of its analogues, and combinations thereof, (B) an alkenyl sulfonic acid monomer, salt thereof, or combinations thereof, and (C) an TV-vinyl amide, a (meth)acrylamide or one of its analogues, or combinations thereof. In one embodiment, the (A) monomer is N-vinyl-2-caprolactam, the (B) monomer is 2-acrylamido-2-methylpropane sulfonic acid or salt thereof, and the (C) monomer is N-vinyl-2-pyrrolidone, acrylamide, methacrylamide, or combinations thereof. | 10-03-2013 |
20130289284 | RENEWABLE MODIFIED NATURAL COMPOUNDS - Provided are modified natural compounds that are produced, at least in part, from (A) at least one epoxidized and/or maleated natural fatty acid, or epoxidized and/or maleated natural oil, and (B) at least one lactam having at least one hydroxyl functional group, wherein the lactam may be in a blend with one or more optional alcohol(s). Among other properties, the modified natural compounds may exhibit dispersibility or solubility characteristics in water and/or alcohols. The invention further provides a wide variety of compositions comprising the modified natural compounds. | 10-31-2013 |
20130324443 | SALT-TOLERANT, THERMALLY-STABLE RHEOLOGY MODIFIERS - A salt-tolerant, thermally-stable rheology modifier and, in particular, a rheology modifier for applications in oil-field well-bore fluids. In accordance with one aspect, the rheology modifier comprises a terpolymer of acrylamide, 2-acrylamido-2-methyl-propanesulfonic acid (AMPS) and a long-chain alkyl acrylate wherein the terpolymer is prepared by dispersion polymerization. | 12-05-2013 |
20130324687 | COMPOUNDS, MONOMERS, AND POLYMERS CONTAINING A CARBONATE LINKAGE - The invention provides compounds and monomers having a carbonate linkage. The monomers can be used to form homopolymers or can be coupled with other monomers to provide a wide variety of non-homopolymers. The invention further provides a wide variety of compositions comprising the compounds, monomers, and polymers. In the exemplary structures below, Q, A, R, and n are as described herein. | 12-05-2013 |
20140023601 | PERFORMANCE BOOSTING UV-ABSORBING COMPOUNDS - UV-absorbing compounds are disclosed that are derived from at least: (a) a UV absorber having at least one hydroxyl group, primary amine group, or secondary amine group, (b) a coupling agent having anhydride functionality, and (c) a graft host comprising an unsaturated fatty acid. These compounds absorb, scatter, deflect, or scatter ultraviolet radiation in a variety of personal care and performance chemical applications. | 01-23-2014 |
20140045698 | N-ALKYL LACTAM ETHERS, AND COMPOSITIONS AND USES THEREOF - Described is a class of symmetrical and asymmetrical N-alkyl lactam ethers. One preferred ether is bis-N-ethyl pyrrolidone ether. Preferred compositions and uses of the ethers are in performance chemicals, personal care, and pharmaceutical fields, where they function a variety of roles, including as a solvent, solubilizer, freezing point depressor, diluent, extracting agent, cleaning agent, degreaser, absorbent and/or dispersion agent. | 02-13-2014 |
20140128550 | 4- AND 5-SUBSTITUTED 1,2,3-TRIAZOLE, AND REGIOISOMER MIXTURES THEREOF, MODIFIED POLYMERS - Provided are novel 4- and 5-substituted 1,2,3-triazoles, and regioisomer mixtures thereof, modified polymers, wherein the substituted 1,2,3-triazoles are modified by reaction with a modifying polymer (maleic anhydride based polymer). Depending upon the ratio of the substituted 1,2,3-triazole to the maleic anhydride based polymer employed, the resulting modified polymers can provide maleic anhydride based polymers that are partially or fully reacted with the substituted 1,2,3-triazoles. The resulting modified polymers may be partially or fully opened to provide amic acids, carboxylic acids, carboxylic acidic salts, imides, or esters. The novel 4- or 5-substituted 1,2,3-triazoles, and regioisomer mixtures thereof, modified polymers can be converted to a wide variety of useful polymers and may be employed in a wide variety of compositions. An example of a modified polymer may be represented by the structure: formule: (1) wherein m, n, and q are defined herein. | 05-08-2014 |
20140303313 | SOLUBLE BRANCHED POLYMERS - Branched polymers are prepared from at least (A) at least one monomer having an electron donor moiety, (B) at least one monomer having an electron acceptor moiety, and (C) at least one multifunctional branching agent comprising a urea moiety and at least two N-vinyl groups. The branched polymers are least 20% (by weight) soluble in a solvent for which the corresponding polymer of equal molecular weight made without said multifunctional branching agent is at least 20% (by weight) soluble. Due in part to the wide range of chemistries and solubility and rheological properties, the branched polymers find application in personal care, pharmaceutical/nutritional, and performance chemicals compositions. | 10-09-2014 |
20150044161 | MULTIFUNCTIONAL POLYMERS - Described herein are multifunctional polymers comprising a first repeating unit having at least one pseudo-cationic moiety, a second repeating unit having at least a hydrophobic moiety, and a third repeating unit, where the weight-average molecular weight is less than about 10,000 Da. In one embodiment the polymers exhibit antimicrobial activity. Also provided are compositions formulated with the multifunctional polymers, and a method of providing antimicrobial activity. | 02-12-2015 |
20150051352 | MULTI-FUNCTIONAL GRAFTED POLYMERS - Provided are multifunctional polymers comprising at least one anhydride repeating unit with at least one pseudo-cationic moiety graft and at least one hydrophobic graft. The grafting functionalizations can occur before, during, or after polymerizing the monomer(s). The anhydride employed may be partially or fully opened to provide amic acids, carboxylic acids, carboxylic acidic salts, imides, esters, and mixtures thereof. The polymers also may comprise other repeating units, including, but not limited to, alpha-olefins. In one embodiment the polymers exhibit antimicrobial activity, and can be employed in a wide variety of compositions, including those where antimicrobial activity is useful. A method of providing microbial activity also is provided. | 02-19-2015 |
20150265522 | POLYMER-BOUND UV ABSORBERS IN PERSONAL CARE COMPOSITIONS - Personal care compositions comprising a polymer-bound UV absorber are described that provide enhanced properties, including customizable UV spectrum protection, broad-spectrum UV spectrum protection, water resistance, and labile UV stabilization. The polymer comprises anhydride functionality, such as maleic anhydride or a derivative thereof, and the UV absorber contains at least one hydroxyl, primary amine, or secondary amine group. | 09-24-2015 |
20150315307 | MODIFICATION OF POLYMERS CONTAINING AN ANHYDRIDE AND USES THEREOF - The present invention provides polymers resulting from modification of polymeric moieties containing an anhydride with modifying reactant moieties. The invention further provides a wide variety of compositions comprising the and modified polymeric moieties containing an anhydride. The letters b, d, e, and z are described herein. | 11-05-2015 |
20150344461 | HEMI-AMINAL ETHERS AND THIOETHERS OF N-ALKENYL CYCLIC COMPOUNDS - Described herein are hemi-aminal ethers and thioethers of N-alkenyl cyclic compounds that may be produced through a reaction comprising: (A) at least one first reactant represented by a structure (I), wherein X is a functionalized or unfunctionalized C | 12-03-2015 |
20150344767 | SHALE SWELLING INHIBITORS - The present invention provides amidic polymers, which exhibit shale swelling inhibitor activity having improved biodegradability. The amidic polymers of the invention may be employed in a wide variety of compositions, particularly in subterranean drilling operations. Non-limiting generic structures of the amidic polymers are set out below: formula (1) wherein R | 12-03-2015 |
20150353663 | POLYMERS POLYMERIZED FROM AT LEAST FOUR MONOMERS, AND COMPOSITIONS AND USES THEREOF - Described herein is a class of non-homopolymers polymerized from at least: (A) 10-22 mole percent of at least one N-vinyl lactam, (B) 30-35 mole percent of at least one monomer selected from the group consisting of acrylic acid, methacrylic acid, and combinations thereof, (C) 40-52 mole percent of at least one (meth)acrylate of a straight- or branched-chain alkyl alcohol, and (D) 5-20 mole percent of at least one (meth)acrylate of a saturated or unsaturated cyclic alcohol having 6 to 20 carbon atoms. In one embodiment, the non-homopolymers exhibit solubility in the lower molecular weight alcohols. The non-homopolymers may be used in personal care or performance chemicals compositions. In one embodiment, the polymers are used in various personal care formulations, such as used for skin, sun, hair, and preservatives. | 12-10-2015 |
20150353666 | POLYMERS POLYMERIZED FROM AT LEAST FOUR MONOMERS, AND COMPOSITIONS AND USES THEREOF - Family of non-homopolymers synthesized from N-vinyl lactam, (meth)acrylic acid, hydrophobic (meth)acrylic ester of a straightchain or branched-chain alkyl alcohol and monomer selected from the group consisting of functionalized and unfunctionalized: dialkyl maleates, dialkyl fumarates, and combinations thereof. The non-homopolymers may exhibit solubility in one or more lower molecular weight alcohols and/or a glass transition temperature greater than 80° C. | 12-10-2015 |
20160083356 | FUNCTIONALIZED 4- AND 5-VINYL SUBSTITUTED REGIOISOMERS OF 1, 2, 3-TRIAZOLES VIA 1, 3- DIPOLAR CYCLOADDITION AND POLYMERS THEREOF - The present invention provides novel functionalized mixtures 4- and 5-vinyl substituted regioisomers of 1,2,3-triazoles via 1,3-dipolar cycloaddition. Functionalized alkyne moieties with a terminal alcoholic functionality are reacted with functionalized organic moieties with a terminal leaving group and an azide to provide an alcoholic functionalized mixture of 4- and 5-substituted regioisomers of 1,2,3-triazole moieties. The mixture may be converted to a wide variety of useful functionalized mixtures of 4- and 5-vinyl substituted regioisomers of 1,2,3-triazole moieties, which in turn can be converted to a wide variety of useful polymers The novel alcoholic functionalized mixtures of 4- and 5-substituted regioisomers can be separated by chromatography to provide the purified 4- and 5-alcoholic functionalized substituted 1,2,3-triazole moieties. The novel compounds of the invention can be employed in a wide variety of compositions (Formulae (I), (II)); wherein R | 03-24-2016 |