Abstract: Process for the production of PCTFE homopolymer and/or copolymer resins by the use of an aqueous suspension system incorporating a redox initiator system which comprises t-butyl hydroperoxide and sodium metabisulfite to initiate the polymerization or copolymerization process. The process parameters may be controlled to provide a PCTFE homopolymer or copolymer resin having a desired target range of molecular weights. The process provides stable PCTFE polymer suspensions which exhibit a low tendency to coagulate and further exhibit good wettability of the homopolymer and copolymer particles, notably in the absence of soaps.

Abstract: This invention relates to fiber surface treating agnets containing a pyromellitate nucleus which have fungicidal, anti-microbial and anti-static properties, and blends of such agents with other types of surface modifiers.

Abstract: The present invention is directed to a copolymer of a fluoromonomer having the formula R.sub.1 R.sub.2 C.dbd.CR.sub.3 F wherein R.sub.1, R.sub.2 and R.sub.3 are selected from H and F, and R.sub.3 may be Cl when R.sub.1 and R.sub.2 are F; and a vinyl monomer having the formula H.sub.2 C.dbd.CHR.sub.x, wherein R.sub.x is a radical having the formula --O.sub.2 CR.sub.y, wherein R.sub.y is a radical selected from CH.sub.3 and C.sub.2 H.sub.5.The resulting copolymer comprises fluorinated units having the formula (R.sub.1 R.sub.2 C--CR.sub.3 F) wherein R.sub.1, R.sub.2 and R.sub.3 are selected from H and F, and R.sub.3 may be Cl when R.sub.1 and R.sub.2 are F, and corresponding amounts of vinyl units having the formula (H.sub.2 C--CHR.sub.x), wherein R.sub.x is selected from --CH.sub.3 and C.sub.2 H.sub.5. In an alternate and preferred embodiment the copolymer is hydrolyzed so that R.sub.x becomes --OH.

Abstract: A process of preparing a copolymer of vinyl monomer such as vinyl acetate, vinyl propionate and vinyl trifluoroacetate, and of fluorinated monomers such as tetrafluoroethylene and trifluoroethylene, said copolymer having an alternating or substantially alternating distribution of vinyl recurring monomeric units and fluorinated recurring monomeric units in the copolymer backbone which comprises copolymerizing said monomers in an aqueous reaction medium comprising water and a water miscible organic co-solvent in an amount less than the amount sufficient to form a distinct organic co-solvent phase.

Abstract: A process of preparing a copolymer of vinyl monomer selected from the group consisting of vinyl acetate, vinyl propionate and vinyl trifluoroacetate, and of fluorinated monomer selected from the group consisting of tetrafluoroethylene and trifluoroethylene, said copolymer having an alternating or substantially alternating distribution of vinyl recurring monomeric units and fluorinated recurring monomeric units in the copolymer backbone which comprises copolymerizing said monomers in an aqueous reaction medium comprising water and a water miscible organic co-solvent in an amount less than the amount sufficient to form a distinct organic co-solvent phase.

Abstract: A process of preparing a copolymer of a vinyl monomer such as vinyl acetate, vinyl propionate and vinyl trifluoroacetate, and of fluorinated monomer such as tetrafluoroethylene and trifluoroethylene, said copolymer having an alternating or substantially alternating distributing of vinyl recurring monomeric units and fluorinated recurring monomeric units in the copolymers backbone which comprises copolymerizing said monomers in a reaction medium of a chlorocarbon, a fluorocarbon a chlorofluorocarbon or a mixture thereof.

Abstract: A process of preparing a copolymer of vinyl monomer selected from the group consisting of vinyl acetate, vinyl propionate and vinyl trifluoroacetate, and of fluorinated monomer selected from the group consisting of tetrafluoroethylene and trifluoroethylene, said copolymer having an alternating or substantially alternating distribution of vinyl recurring monomeric units and fluorinated recurring monomeric units in the copolymer backbone which comprises copolymerizing said monomers in an aqueous reaction medium comprising water and a water miscible organic co-solvent in an amount less than the amount sufficient to form a distinct organic co-solvent phase.

Abstract: The present invention is directed to a copolymer of a fluoromonomer having the formula R.sub.1 R.sub.2 C=CR.sub.3 F wherein R.sub.1, R.sub.2 and R.sub.3 are selected from H and F, and R.sub.3 may be Cl when R.sub.1 and R.sub.2 are F; and a vinyl monomer having the formula H.sub.2 C=CHR.sub.x, wherein R.sub.x is a radical having the formula --O.sub.2 CR.sub.y, wherein R.sub.y is a radical selected from CH.sub.3 and C.sub.2 H.sub.5.The resulting copolymer comprises fluorinated units having the formula (R.sub.1 R.sub.2 C-CR.sub.3 F) wherein R.sub.1, R.sub.2 and R.sub.3 are selected from H and F, and R.sub.3 may be Cl when R.sub.1 and R.sub.2 are F, and corresponding amounts of vinyl units having the formula (H.sub.2 C-CHR.sub.x), wherein R.sub.x is selected from --CH.sub.3 and C.sub.2 H.sub.5. In an alternate and preferred embodiment the copolymer is hydrolyzed so that R.sub.x becomes --OH.

Abstract: This invention relates to novel compositions for imparting stain resistance to fibers, which composition comprises a phenolic or naphtholic resin.

Abstract: This invention relates to fiber surface treating agents containing a pyromellitate nucleus which have fungicidal, anti-microbial and anti-static properties, and blends of such agents with other types of surface modifiers.

Abstract: A novel process is disclosed for producing fluorinated pyromellitate surfactants. The process comprises two primary steps. The first step involves reacting pyromellitic dianhydride with fluorinated alcohol at a mole ratio of about two moles of fluorinated alcohol per mole of pyromellitic dianhydride, thereby producing a pyromellitate having two fluorinated esters moieties and two carboxylic acid moieties. Thereafter, the fluorinated pyromellitate with carboxylic acid moieties is reacted with an oxirane compound in the presence of trimellitic anhydride to produce fluorinated pyromellitate mixtures having a reduced percentage of fluorine.

Abstract: A novel process is disclosed for producing fluorinated pyromellitate surfactants. The process comprises two primary steps. The first step involves reacting pyromellitic dianhydride with fluorinated alcohol at a mole ratio of about two moles of fluorinated alcohol per mole of pyromellitic dianhydride, thereby producing a pyromellitate having two fluorinated esters moieties and two carboxylic acid moieties. Thereafter, the fluorinated pyromellitate with carboxylic acid moieties is reacted with an oxirane compound in the presence of trimellitic anhydride to produce fluorinated pyromellitate mixtures having a reduced percentage of fluorine.

Abstract: Novel polycarboxy benzene dianhydrides useful as surfactants are disclosed. The novel compounds of this invention are pyromellitate tetraesters wherein two ester moieties characteristically contain fluorinated alkyl groups or saturated hydrocarbon alkyl groups and wherein two ester moieties contain alkylene moieties having a terminal halogen.

Abstract: This invention relates to novel fluorinated compounds derived from 3,3',4,4'-benzophenone tetracarboxylic dianhydride that are useful as surface modifiers for various fibers. The novel compounds contain two fluorinated ester derived from fluorinated alcohols and two esters derived from oxirane compounds.

Abstract: A reaction between pyromellitic dianhydride (PMDA) and less than two moles of fluoroalcohol produces an intermediate with ester, free acid and anhydride groups. Reaction with an oxirane compound such as epichlorohydrin reacts at the acid sites to produce pendant hydroxyls which react with anhydride on adjacent molecules to produce oligomers. Products with fluoroalcohol:PMDA ratios of, for example, about 1:0.6 to about 1:0.85 produce treated fibers with improved retention of oil repellancy, especially when annealed at 100.degree.-130.degree. C.

Abstract: Pyromellitate diester-diacid chlorides are disclosed that are useful as intermediates in the synthesis of a variety of soil and water repelling compounds. The pyromellitates of this invention characteristically contain two ester moieties wherein said ester moieties contain a fluorinated or saturated hydrocarbon alkyl moiety. The pyromellitates additionally contain two acid chloride moieties which are capable of reacting with various compounds to produce various products useful as surfactants.

Abstract: Pyromellitate tetraesters are disclosed that are useful as water repellents. The pyromellitates of this invention characteristically contain two ester moieties wherein said ester moieties contain a fluorinated or saturated hydrocarbon alkyl group. Additionally, pyromellitates of this invention contain two ester moieties which contain siloxyl groups.

Abstract: A reaction between pyromellitic dianhydride (PMDA) and less than two moles of fluoroalcohol produces an intermediate with ester, free acid and anhydride groups. Reaction with an oxirane compound such as epichlorohydrin reacts at the acid sites to produce pendant hydroxyls which react with anhydride on adjacent molecules to produce oligomers. Products with fluoroalcohol:PMDA ratios of, for example, about 1:0.6 to about 1:0.85 produce treated fibers with improved retention of oil repellancy, especially when annealed at 100.degree.-130.degree. C.

Abstract: Oligomers containing pyromellitic rings, divalent linking groups, pendant fluoroalkoxy or hydrocarbon alkoxy groups and pendant polar groups of various kinds impart soil repellency to fibers that persists after repeated laundering. An exemplary material is prepared by the reaction of pyromellitic difluoroester/diacid chloride with 1,4-butanediol (the linking group) and 3-chloro-1,2-propanediol (the pendant polar group).

Abstract: A process for the production of oligomeric mixtures useful as surfactants is disclosed. The initial step of the process comprises reacting pyromellitic dianhydride with a fluoroalcohol using a mole ratio of about one mole pyromellitic dianhydride per two moles of fluoroalcohol to produce an intermediate which contains two fluorinated ester moieties and two free acid moieties. Thereafter, the intermediate diester-diacid is reacted with an excess of an oxirane compound such as epichlorohydrin, epibromohydrin or propylene oxide wherein said oxirane compound reacts with the free acid moieties to produce ester moieties containing a primary or secondary alcohol moiety. In the final step of the process, additional pyromellitic dianhydride is added to the reaction mixture so that the alcohol moieties may react with anhydride moieties to produce ester linking groups (between pyromellitate nuclei) and additional free acid moieties capable of reacting with the oxirane compound.