Patent application number | Description | Published |
20080207804 | Stabilization of polymers with styrenated-p-cresols - Disclosed herein is a process for the preparation of a mixture of styrenated p-cresol species that is liquid at room temperature and has a viscosity of less than 40,000 cps at 25° C., wherein said process affords 2,6-distyrenated p-cresol assaying at 70% minimum by GC area percent, comprising reacting styrene with p-cresol at a molar ratio of 1.85 to 2.1:1, respectively, in the presence of an acid catalyst at elevated temperature, wherein said mixture comprises monostyrenated-p-cresol, distyrenated-p-cresol, and tristyrenated-p-cresol and exhibits an acid number of less than 0.1 mg KOH/gram. | 08-28-2008 |
20080221242 | Stabilizer blend for improved chlorine resistance - A method for increasing the stability of a thermoplastic resin in the presence of water is disclosed wherein said method comprises adding to said resin a stabilizing amount of a blend consisting of: (1) an aromatic amine stabilizer; (2) a sterically hindered phenol; (3) optionally, one or more co-stabilizers; and (4) optionally, one or more additives selected from the group consisting of UV absorbers, light stabilizers, metal deactivators, peroxide scavengers, polyamide stabilizers, basic co-stabilizers, nucleating agents, fillers, reinforcing agents, aminoxy propanoate derivatives, plasticizers, epoxidized vegetable oils, lubricants, emulsifiers, pigments, optical brighteners, flame-proofing agents, anti-static agents, and blowing agents. | 09-11-2008 |
20090005478 | LIQUID STYRENATED PHENOLIC COMPOSITIONS AND PROCESSES FOR FORMING SAME - Disclosed herein are highly stable styrenated phenolic compositions that are liquids at room temperature, and polymer articles and lubricant compositions containing such styrenated phenolic compositions. Also disclosed are processes for forming such styrenated phenolic compositions, which processes afford distyrenated phenolics assaying at 70% minimum by total GC area, comprising reacting styrene with one or more phenolics, e.g., at least one of phenol, p-cresol and/or o-cresol, in the presence of an acid catalyst, preferably a sulfonic acid catalyst, at elevated temperature, wherein the resulting product mixture comprises one or more monostyrenated phenolics, one or more distyrenated phenolics, and one or more tristyrenated phenolics. | 01-01-2009 |
20090326112 | LIQUID AMYLARYL PHOSPHITE COMPOSITIONS - A phosphite composition comprising at least two of a tris(diamylaryl) phosphite, a tris(monoamylaryl) phosphite, a bis(diamylaryl)monoamylaryl phosphite, and a bis(monoamylaryl)diamylaryl phosphite. The inventive phosphite composition is a liquid at ambient conditions. | 12-31-2009 |
20100004363 | LIQUID PHOSPHITE BLENDS AS STABILIZERS - A composition is disclosed that comprises a blend of at least two different phosphites of the structure | 01-07-2010 |
20100016196 | PHOSPHITE STABILIZER FOR LUBRICATING BASE STOCKS AND THERMOPLASTIC POLYMERS - A substituted phosphite suitable for lubricating base stocks and thermoplastic polymers represented by the structure: | 01-21-2010 |
20100025636 | LIQUID PHOSPHITE COMPOSITIONS HAVING DIFFERENT ALKYL GROUPS - A composition comprising at least two different alkylaryl phosphites, wherein some alkyl groups have a different number of carbon atoms than other alkyl groups and wherein the composition is a liquid at ambient conditions. | 02-04-2010 |
20100048782 | Liquid phosphite blends as stabilizers - A composition is disclosed that comprises a blend of at least two different phosphites of the structure | 02-25-2010 |
20100069542 | LIQUID AMYLARYL PHOSPHITE COMPOSITIONS AND ALKYLATE COMPOSITIONS FOR MANUFACTURING SAME - Alkylate compositions comprising a monoamylphenol in an amount ranging from 25 weight percent to 99 weight percent and a diamylphenol in an amount ranging from 1 weight percent to 60 weight percent, the weight percentages being based on the total weight of all components in the alkylate composition. The invention is also to processes for making such alkylate compositions and to processes for forming stable liquid amylaryl phosphite compositions from such alkylate compositions. | 03-18-2010 |
20100076125 | LIQUID PHOSPHITE COMPOSITION DERIVED FROM CRESOLS - A composition at least two different phosphites, one of which is derived from an alkylated cresol, wherein the composition is a liquid at ambient conditions. The other phosphites may be derived from alkylated cresol, alkylated phenol or other alkylated hydroxyaryl compounds. The cresol may be mono-alkylated or di-alkylated with a C | 03-25-2010 |
20100076131 | LIQUID BUTYLARYL PHOSPHITE COMPOSITIONS AND ALKYLATE COMPOSITIONS FOR MANUFACTURING SAME - Alkylate compositions comprising a monobutylphenol in an amount ranging from 50 weight percent to 99 weight percent and a dibutylphenol in an amount ranging from 1 weight percent to 50 weight percent, the weight percentages being based on the total weight of all components in the alkylate composition. The invention is also to processes for making such alkylate compositions and to processes for forming stable liquid butylaryl phosphite compositions from such alkylate compositions. | 03-25-2010 |
20100190900 | LIQUID BUTYLARYL PHOSPHITE COMPOSITIONS - A phosphite composition comprising at least two of a tris(dibutylaryl) phosphite, a tris(monobutylaryl) phosphite, a bis(dibutylaryl)monobutylaryl phosphite, and a bis(monobutylaryl)dibutylaryl phosphite. The inventive phosphite composition is a liquid at ambient conditions. | 07-29-2010 |
20100197837 | POLYMERS WITH LOW GEL CONTENT AND ENHANCED GAS-FADING - A polymer stabilizing composition comprising a sterically hindered phenol and a phosphite that provides low gel content and enhanced resistance to gas-fading. The stabilizer composition is particular useful for stabilizing polyethylene homopolymers and copolymers, such as linear low density polyethylenes produced from metallocene catalyst. The sterically hindered phenol is selected from the group consisting of 1,3,5-tris-(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate, 1,3,5-tris-(3,5-dicyclohexyl-4-hydroxybenzyl)isocyanurate, 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate, 1,3,5-tris(4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-Triazine-2,4,6-(1H,3H,5H)-trione, and 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene. The phosphite preferably is a liquid phosphite composition comprising two or more alkylated aryl phosphites. | 08-05-2010 |
20110028616 | Liquid phosphite compositions having different alkyl groups - A composition comprising a mixture of at least two different alkylaryl phosphites, wherein some alkyl groups have a different number of carbon atoms than other alkyl groups and wherein the mixture is a liquid at ambient conditions. | 02-03-2011 |
20110028618 | Solid alkylaryl phosphite compositions and methods for manufacturing same - The invention is directed to various alkylaryl phosphite compositions that ideally are suitable for use as secondary antioxidants in polymers. In one aspect, the phosphite composition comprises a tris(monoalkylaryl)phosphite in an amount from 51 to 95 weight percent; and at least one of: a bis(monoalkylaryl)dialkylaryl phosphite; a bis(dialkylaryl)monoalkylaryl phosphite; and a tris(dialkylaryl)phosphite. The inventive phosphite composition is a solid at ambient conditions. The invention also relates to alkylate compositions and processes for forming such alkylate compositions and such phosphite compositions. | 02-03-2011 |
20120035305 | Polymers with Low Gel Content and Enhanced Gas-Fading - A polymer stabilizing composition comprising a sterically hindered phenol and a phosphite that provides low gel content and enhanced resistance to gas-fading. The stabilizer composition is particular useful for stabilizing polyethylene homopolymers and copolymers, such as linear low density polyethylenes produced from metallocene catalyst. The sterically hindered phenol is, for example, selected from the group consisting of 1,3,5-tris-(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate, 1,3,5-tris-(3,5-dicyclohexyl-4-hydroxybenzyl)isocyanurate, 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate, 1,3,5-tris(4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-Triazine-2,4,6-(1H,3H,5H)-trione, and 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene. | 02-09-2012 |