Abstract: Disclosed are polymers of average molecular weight ranging from 400 to 20,000 comprising thiosubstituted groups per molecule and resulting from the reaction, in the presence of an addition catalyst, of at least one compound with a thiol function, having 1 to 60 carbon atoms per molecule, with an unsaturated polyester resulting from the condensation of an aliphatic epoxide with an unsaturated aliphatic dicarboxylic compound comprising at least one ethylenic unsaturation in the alpha position of one of the carboxyl groups. Also disclosed are middle distillate compositions having a distillation range from 150.degree. to 450.degree. C. and comprising a minor proportion, preferably from 0.001 to 2% by weight, of at least one of the polymers defined hereinabove.

Abstract: A curing composition for curing a polysulphide polymer, which composition comprises as the curing agent sodium birnessite, Na.sub.4 Mn.sub.14 O.sub.27.9H.sub.2 O.A process for the preparation of sodium birnessite comprises the steps of adding excess in the range of from 25% to 225% of a solution of sodium hydroxide to a solution of manganese (II) chloride or manganese (II) sulphate to form a slurry of manganese (II) hydroxide and passing air free of carbon dioxide therethrough for at least 3 hours or oxygen for 1.5 hours, these steps being carried out at ambient temperature.

Abstract: The invention relates to water-dilutable binders for cationic electrocoating finishes. For the preparation of the binders, a di-epoxide compound, together with at least one mono-epoxide compound if desired, is converted by a polyaddition, carried out at 100.degree. to 195.degree. C. and initiated by a monofunctionally reacting initiator carrying either an alcoholic OH group, a phenolic OH group or an SH group, to form an epoxy resin which then subsequently is modified with(A) primary and/or secondary amines or their salts and/or the salt of a tertiary amine, a sulfide/acid mixture or a phosphine/acid mixture and with, if desired,(B) a polyfunctional alcohol, a polycarboxylic acid, a polysulfide or a polyphenol.

Abstract: A process for preparing polyarylene thioethers wherein thiophenols of formula ##STR1## are electrolytically polymerized in the presence of a Lewis acid and/or a proton acid.

Abstract: A polyether having molecular weight from 1,000 to 50,000, end-blocked with hydrolyzable silyl groups and represented by the general formula (P): ##STR1## where R.sup.1, R.sup.2, R.sup.6 and R.sup.7 individually represent a divalent hydrocarbon group, R.sup.4 represents a monovalent hydrocarbon group, R.sup.8 represents an alkyl group with 1 to 6 carbon atoms, X represents an aromatic or heterocyclic ring, a represents a number from 1 to 3, m represents a number from 10 to 500, n represents a number of 1 or greater is produced and utilized in room temperature curing compositions containing inorganic filler and curing catalyst. There is also disclosed a method for producing the above polyether by reacting polyoxyalkylene end-blocked with epoxy groups, dimercapto compound and organo silicon compound.

Abstract: A process for preparing a substantially straight-chain polyarylene thioether by polymerizing a diphenyldisulfide of the formula ##STR1## in the presence of a lewis acid catalyst at temperatures of between -20.degree. C. and 50.degree. C.

Abstract: Polythiols prepared by the reaction of hydrogen sulfide or organic dithiols with polyglycidyl substituted amines have been found to be outstanding curing agents for epoxy resins. Epoxy resins cured with these polythiols are characterized by not only improved gel times, but also improved cure rates, better heat resistance and greater resistance to absorption of water.A useful polythiol is the reaction product of N,N,N',N'-tetraglycidyl-m-xylylenediamine with hydrogen sulfide.

Abstract: Acetylene terminated aspartimides are prepared using two methods. In the first, an amino-substituted aromatic acetylene is reacted with an aromatic bismaleimide in a solvent of glacial acetic acid and/or m-c=resol. In the second method, an aromatic diamine is reacted with an ethynyl containing maleimide, such as N-(3-ethynylphenyl) maleimide, in a solvent of glacial acetic acid and/or m-cresol. In addition, acetylene terminated aspartimides are blended with various acetylene terminated oligomers and polymers to yield composite materials exhibiting improved mechanical properties.

Abstract: Polycyclic polycarbonate (or thiol analog) oligomers are prepared from a mixture of at least one bishaloformate with at least one tetraphenol, or thio analogs thereof. Such mixture may also contain at least one dihydroxy or dimercapto compound. The oligomers are formed by the reaction of such mixtures with alkali metal hydroxides and various amines. The polycyclic oligomer mixtures may be converted to crosslinked polycarbonates or their thiol analogs.

Abstract: Halogen-free polyarylene sulfides which are insoluble in organic solvents and infusible, essentially consisting of structural elements of the formula I ##STR1## these elements being present in the molecule more than five times and in which R is one of the following radicals ##STR2## in which R.sub.1 and R.sub.2 independently of one another are each --H, C.sub.1 -C.sub.20 -alkyl, aryl having not more than 12 C atoms, aralkyl having not more than 20 C atoms, alkaryl having not more than 20 C atoms, --CN, --OCOR.sub.3, --OH or --SR.sub.4, in which R.sub.3 and R.sub.4 independently of one another are each a C.sub.1 -C.sub.20 alkyl or aryl having not more than 12 C atoms, X is NH, NR.sub.5, S or O, in which R.sub.5 is a C.sub.1 -C.sub.20 alkyl or an aryl having not more than 12 C atoms, can be used after doping with oxidizing agents, for example iodine, bromine, SbF.sub.5, AsF.sub.5, PF.sub.5 or SbCl.sub.5, as electroconductive polymers.

Abstract: Novel processes are provided for synthesizing 2,2-bis(4-fluorophenyl)hexafluoropropane and the use of this synthesized monomer in polymerization reactions to form poly(arylethers) or poly(arylthioethers). Synthesis of 2,2-bis(4-fluorophenyl)hexafluoropropane involves converting the commonly available compound Bisphenol AF to an amino-substituted form, followed by treatment with borofluoric acid and a nitrite, and then an aromatic solvent to obtain the monomer. The monomer can be mixed with either a dihydroxy diphenyl hexafluoropropane or a dimercapto diphenyl hexafluorpropane to cause a nucleophilic substitution reaction, thereby yielding the desired poly(arylether) or poly(arylthioether).

Abstract: Polymeric metal complexes were prepared by coordination reactions of 2,5-diamino-1,4-benzenedithiol (DADT) with divalent metal halides (cobalt chloride, iron chloride, copper chloride and nickel chloride) in an aqueous alkaline solution at reflux temperatures. A black precipitate which conducted electricity was formed. Resistivity of the material increased upon exposure to air but decreased when oxygen was removed from the material.

Abstract: Dense star polymers on immobilized cores are very useful as ion-exchange resins and chelation resins. For example, an aminated form of chloromethylated styrene/divinyl benzene copolymer can be employed as an immobilized core compound and reacted successively with methyl acrylate via a Michael addition reaction and then with ethylenediamine to form a first generation dense star polymer or dendrimer. These reactions can then be repeated to form second and third generation dendrimers.

Abstract: Non-fluorinated epoxy resins of a known type are cross-linked by means of polyfunctional fluoroalkanes containing groups which are reactive with the epoxy groups and/or with the hydroxy groups present in the starting resin. The cross-linked products so obtained, having a fluorine content not higher than 15% by weight, and preferably ranging from 1% to 5%, exhibit a complex of properties which are typical of the corresponding fluorinated resins having a much higher fluorine content; in particular, oil- and water-repellency, resistance to hydrolysis and to solvents, and minimum absorption of water.

Abstract: A polyether having molecular weight from 1,000 to 50,000, end-blocked with hydrolyzable silyl groups and represented by the general formula (P): ##STR1## where R.sup.1, R.sup.2, R.sup.6 and R.sup.7 individually represent a divalent hydrocarbon group, R.sup.4 represents a monovalent hydrocarbon group, R.sup.8 represents an alkyl group with 1 to 6 carbon atoms, X represents an aromatic or heterocyclic ring, a represents a number from 1 to 3, m represents a number from 10 to 500, n represents a number of 1 or greater is produced and utilized in room temperature curing compositions containing inorganic filler and curing catalyst. There is also disclosed a method for producing the above polyether by reacting polyoxyalkylene end-blocked with epoxy groups, dimercapto compound and organo silicon compound.

Abstract: A process for the catalytic self-condensation of halothiophenol to form a poly(arylene sulfide) is disclosed. The reaction mixture includes an alcohol solvent, the halothiophenol, an alkaline reagent and a catalyst comprising a Group VIII metal. The polymerization process can be carried out at pressures as low as 1 atmosphere and temperatures of 200.degree. C. or less.

Abstract: A process is disclosed for preparing an advanced epoxy resin by reacting a relatively low molecular weight polyepoxide with a phenol, thiophenol, carboxylic acid or carboxylic acid anhydride in the presence of a catalytic amount of an alkyl substituted phosphonium salt such as tributyl phosphonium bromide. The process can be carried out under reaction conditions, such as the presence of water, which are deleterious to certain epoxy advancement catalysts.

Abstract: A highly modified polyphenylene sulfide (hereinafter refer to as "PPS") which contains covalently bonded chlorine in a far less amount than conventional PPS's and is substantially free from ionically bonded chlorine and sodium, is produced by heat-treating a conventional PPS with at least one of organic, sulfur-containing compounds in a solvent capable of dissolving the PPS. Such a PPS is very useful as a coating or encapsulating material for electrical and electronic components, etc.

Abstract: A process for the production of oligourethanes containing terminal mercapto groups in which the adduct of propylene oxide with trimethylol propane and/or glycerol and/or trimethylol ethane as alkylene oxide adduct containing OH-groups is reacted with isomeric tolylene diisocyanates in excess, based on hydroxyl groups, and the isocyanate groups are further reacted with mercaptoethanol. The adduct of propylene oxide with the trifunctional alcohol is intended to have a calculated molecular weight of from about 1800 to about 6000 and preferably of from about 2000 to about 5000, the reaction products being used for the production of sealing compounds hardening by oxidation or as an additive for crosslinkable epoxy resin systems.

Abstract: Non-fluorinated epoxy resins of known type are crosslinked by means of polyfunctional perfluoropolyethers containing groups which are reactive with the epoxy groups and/or with the hydroxy groups present in the starting resin. The so-obtained crosslinked products, with a fluorine content not higher than 20% by weight, preferably comprised within the range of from 5% to 15%, are endowed with a set of properties typical of the corresponding fluorinated resins with a much higher fluorine content, in particular, water- and oil-repellence, resistance to hydrolysis and to solvents, minimum water absorption.

Abstract: Composition comprising an epoxy resin, an adduct of a tetra-substituted titanate and a di-substituted hydrogen phosphite, a neutral ester of a phosphorous acid, and a curing agent for the epoxy resin.The composition is particularly useful as an adhesive for bonding structures made of sheet molding compound to like structures, to steel, and to other substrates commonly used in the automotive area.

Abstract: The invention relates to a water-dilutable binder for cationic electrocoating finishes. For the preparation of the binders(A) a di-epoxide compound with an epoxide equivalent weight below 2,000 is reacted with(B) a phenol- or thiol-containing compound which reacts monofunctionally with epoxide groups, and with(C) primary and/or secondary amines or their salts and/or the salt of a tertiary amine, a sulfide/acid mixture or phosphine/acid mixture or a mixture of these compounds, as well as, if desired, with(D) a polyfunctional alcohol, a polycarboxylic acid, a polysulfide or a polyphenol.The components A and B are used in a molar ratio of from 10:1 to 1:1, preferably from 4:1 to 1.5:1 and the reaction of the component A with the component B is carried out at 100.degree. to 190.degree. C., if desired in the presence of a catalyst.

Abstract: The process for preparing hydroxy alkyl amide thio ethers by the reaction of a bicyclic amide acetal with a thiol is described.

Abstract: Bridged dense star polymers having terminal group densities greater than conventional extended star polymers exhibit greater and more uniform reactivity than their corresponding conventional star polymers. For example, a third generation, hydroxy-terminated polyether dense star polymer can be prepared from pentaerythrityltetrabromide and 4-hydroxymethyl-2,6,7-trioxabicyclo[2.2.2]-octane which has a molecular volume less than 80 percent of the volume of a conventional extended star polymer made from similar materials. This dense star polymer can then be bridged by reacting it with a suitable difunctional reactant such as toluene diisocyanate. Such polymers of dense star polymers are useful as demulsifiers for oil/water emulsions, wet strength agents in the manufacture of paper, proton scavengers, calibration standards for electron microscopy, and agents for modifying viscosity in aqueous formulations such as paints.

Abstract: A process for preparing thermoset polymers at an improved rate by copolymerizing a bisoxazoline with a compound having both thiol and carboxylic acid groups in the presence of a catalytic amount of an alkali metal or an alkaline earth metal cationic complex of formula MX.sub.n wherein M represents lithium, potassium, sodium, magnesium, calcium or zinc, X represents BF.sub.4, BPh.sub.4, ClO.sub.4, PF.sub.6, SbF.sub.6 or AsF.sub.6 is described.

Abstract: A process for preparing thermoset polymers at an improved rate by copolymerizing a bisoxazoline with a polythiol compound in the presence of a catalytic amount of an alkali metal or an alkaline earth metal cationic complex of formula MX.sub.n wherein M represents lithium, potassium, sodium, magnesium, calcium or zinc, X represents BF.sub.4, BPh.sub.4, ClO.sub.4, PF.sub.6, SbF.sub.6 or AsF.sub.6 is described.

Abstract: According to the invention, a relatively low molecular weight epoxy resin is reacted with a hydroxyl group-containing compound in the presence of a bis(trihydrocarbyl phosphine)iminium salt catalyst to produce a high molecular weight fusion reaction product. The process is particularly useful in reacting an epoxy resin having a molecular weight of less than about 500 with bisphenol-A in the presence of a bis(phosphine)iminium halide to produce a fusion reaction product having a molecular weight within the range of about 500 to 7000. The catalyst is relatively water-insensitive, and the reaction can therefore be carried out in the presence of water.

Abstract: A method for producing mercaptan terminated liquid polymers with increased chemical reactivity and reduced odor is disclosed which involves heating the polymeric liquid material under conditions which avoid oxidation and depolymerization of the material while removing at least 50 weight percent of low molecular weight mercaptan compounds to produce a stripped polymer material having an increased cure rate and reduced obnoxious mercaptan odor.

Abstract: [2,2,2-Trifluoro-1-(trifluoromethyl)]ethylidene-bisbenzenethiols are new compounds useful as precursors in the manufacture of polysulfide polymers and copolymers.

Abstract: Polymer compositions exhibiting liquid-crystalline phases contain chemically bonded mesogenic groups of the formula Ia and/or Ib: ##STR1## in which Q.sup.1 is H, alkyl or alkoxy having 1-5 C atoms, F, Cl, Br or CN,X.sup.1 to X.sup.5 each, independently of one another, are H or an alkyl group having up to 15 C atoms, in which it is also possible for one or two non-adjacent CH.sub.2 groups to be replaced by a group from the group comprising --O--, --S--, --O--CO--O--, O--CO--NH--, --CO--, --CO--O--, --CO--S--, --S--CO--, --SO-- and --SO.sub.2 --.Process for the preparation of polymer compositions of this type comprises the polymerization or grafting of suitable monomers.Polymer compositions of this type are used as substrates in electronics for the fiber and foil techniques.

Abstract: Oligomers of polyarylene polyethethers (PAPE) having a mol wt Mn in the range from 1000 to about 10,000 are converted to difunctionalized oligomers so as, in the first instance, to provide a reactive double bond (for example, a vinylbenzyl group) at each end of the PAPE; and, in the second instance, to provide a triple bond (benzylethynyl group) at each end of the PAPE. The PAPE most preferably has a repeating unit which is the residuum of two dihydric phenols or thiophenols ("DHP") linked through a C=O, --S--S--, or --SO.sub.2 -group, or a Si or C atom, and or ether O, or thioether S atoms. The preferred repeating unit is formed by reaction of a DHP such as bisphenol A (BPA) with a halogenated DHP such as dichlorophenyl sulfone (DCPS) so as to provide an alternating configuration. The repeating unit may also include a linking residue of a reactive solvent which residue provides chain extension in the backbone.

Abstract: A method is disclosed for deactivating a hydrocarbyl phosphonium salt catalyst of an epoxy resin fusion reaction. The method involves contacting the hydrocarbyl phosphonium salt catalyst with a sulfonic acid, such as p-toluenesulfonic acid or methane sulfonic acid. The method is particularly suited for deactivation of moisture-resistant phosphonium salts such as methylene bis(triphenyl phosphonium halide)s.

Abstract: Anhydrous adhesives and sealants based on mercapto terminated polymers and/or oligomers and manganese (IV) oxide as the hardener are thermosetting if they contain only alkaline or neutral fillers and additives. The mixtures can be used for application with heating.

Abstract: Stable liquid adduct compositons are prepared by an addition reaction between epoxy-terminated polymers and mercaptan-terminated polymers. One of the polymers is in stoichiometric excess so that the composition has free epoxy or mercaptan functional groups. The liquid polymer composition can be stored for long periods before curing with a curing agent reactive with the free functional groups.

Abstract: Novel dimercapto thiadiazoles and cyanodithioimidocarbonate polymers and oil soluble lubricating additives thereof.

Abstract: The process for preparing hydroxy alkyl amide thio ethers by the reaction of a bicyclic amide acetal with a thiol is described.

Abstract: Polyorganosiloxane polymers which include at least one group of the formula: ##STR1## where R.sup.1 is an organo group; R.sup.2 is alkylene or alkenylene; G is a n+1 valent hydrocarbon, oxyhydrocarbon or poly(oxyhydrocarbon) radical in which some or all of the hydrogen atoms may optionally be substituted by halogen atoms; R.sup.3 is H or an organic functional group, particularly polymerizable groups, polymerization accelerating groups or polymerization initiating groups; n is an integer of 2 or more provided that when n is 2 and one of R.sup.3 is H, the other R.sup.3 group is also H; and a is 0, 1 or 2.Additional polyorganosiloxane polymers include at least one group of the formula: ##STR2## where R.sup.4 R.sup.5 are H or a mono valent hydrocarbon group.

Abstract: Poly(benzodithiolenes) containing transition metals having desirable chemical, physical, electrical and magnetic properties are prepared by reacting an aromatic tetrathiol with a transition metal salt.

Abstract: A liquid polymer composition curable to a solid elastomer having good thermal stability which contains a mercaptan terminated disulfide polymer of the formula HS(RSS).sub.m R'SH wherein R is --C.sub.2 H.sub.4 --O--CH.sub.2 O--C.sub.2 H.sub.4 --; R' is a member selected from the group consisting of alkyl of from 2 to 12 carbon atoms; alkyl thioether of from 4 to 20 carbon atoms; alkyl ether of from 4 to 20 carbon atoms and one oxygen atom; alkyl ether of from 4 to 20 carbon atoms and from 2 to 4 oxygen atoms each of which is separated from the other by at least 2 carbon atoms, alicyclic of from 6 to 12 carbon atoms and aromatic lower alkyl; and the value of m is such that mercaptan terminated disulfide polymer has a molecular weight of between 1,000 to about 4,000. The method includes cleaving a polymer having disulfide linkages with an organic dimercaptan in the presence of an organic amine.

Abstract: Dense star polymers having terminal group densities greater than conventional extended star polymers exhibit greater and more uniform reactivity than their corresponding conventional star polymers. For example, a third generation, hydroxy-terminated polyether dense star polymer can be prepared from pentaerythrityltetrabromide and 4-hydroxymethyl-2,6,7-trioxabicyclo[2.2.2]-octane which has a molecular volume less than 80 percent of the volume of a conventional extended star polymer made from similar materials. Such dense star polymers are useful as demulsifiers for oil/water emulsions, wet strength agents in the manufacture of paper, proton scavengers, calibration standards for electron microscopy, and agents for modifying viscosity in aqueous formulations such as paints.

Abstract: Tractable doped electroactive polymers, comprising recurring units of a fused nitrogen-containing unsaturated heterocyclic ring system, are fabricated from the virgin polymer by contacting the polymer with donor or acceptor conductivity modifier atoms or groups of atoms.

Abstract: Oligomers of polyarylene polyethers (PAPE) having a mol wt Mn in the range from 1000 to about 10,000 are converted to difunctionalized oligomers so as, in the first instance, to provide a reactive double bond (for example, a vinylbenzyl group) at each end of the PAPE; and, in the second instance, to provide a triple bond (benzylethynyl group) at each end of the PAPE. The PAPE most preferably has a repeating unit which is the residuum of two dihydric phenols or thiophenols ("DHP") linked through a C.dbd.O, --S--S--, or --SO.sub.2 -group, or a Si or C atom, and or ether O, or thioether S atoms. The preferred repeating unit is formed by reaction of a DHP such as bisphenol A (BPA) with a halogenated DHP such as dichlorophenyl sulfone (DCPS) so as to provide an alternating configuration. The repeating unit may also include a linking residue of a reactive solvent which residue provides chain extension in the backbone.

Abstract: Adhesives adapted especially for bonding optical elements and consisting of, as major components, a polyfunctional acrylate and a polythiol, a radical generating photoinitiator, a radical generating heatactivated-curing initiator and a stabilizer against premature onset of curing.

Abstract: A method for producing poly(arylene sulfide) of high molecular weight by subjecting to polymerization conditions a reaction mixture of alkaline metal hydroxide, halothiophenol and organic amide with a molar ratio of alkaline metal hydroxide to halothiophenol in a range of about 1.6 to about 3.2.

Abstract: A fatigue crack growth retardant material for application to aluminum and alloys thereof utilizes certain organic nitrogen compounds and an elastomeric polymer compatible herewith with respect to the curing properties thereof as well as the ultimate properties of the material and capable of stabilizing the nitrogen compound so as to inhibit the evaporation thereof to the atmosphere. The material inhibits corrosion of and retards crack growth in aluminum and alloys thereof when applied thereto. The material has particular utility when applied to the surfaces of structural parts of aircraft and is utilized as a protective coating as well as a sealant, dependent upon the amount of solvent added to the polymeric elastomer.

Abstract: An addition product obtained by reacting (a) a polyfunctional epoxy compound and (b) a compound having at least one functional group of OH group, SH group, COOH group and CONHNH.sub.2 group together with a tertiary amino group in the molecule, and an addition product obtained (a), (b) and (c) an organic compound having two or more active hydrogen atoms in the molecule (excluding a compound having an epoxy group or tertiary amino group) are good curing agents for epxoy resin. The curing agents are useful in formulating novel storable one-package, heat-curable epoxy resin-based compositions.

Abstract: A tractable and reversible electroactive polymer which comprises a charged polymer backbone of recurring units of a fused 5,6,5-membered aromatic heterocyclic ring system wherein the 5-membered rings contain at least one nitrogen and a second heteroatom selected from the group consisting of O, S, Se, Te and substituted N, and a sufficient concentration of a charge-compensating ionic dopants associated therewith.

Abstract: Tractable doped electroactive polymers, comprising recurring units of a fused nitrogen-containing unsaturated heterocyclic ring system, are fabricated from the virgin polymer by contacting the polymer with donor or acceptor conductivity modifier atoms or groups of atoms.

Abstract: A curable liquid polysulfide polymer composition having improved toughness and tear resistance, comprising a major portion of a liquid organic polysulfide polymer having a molecular weight of about 500 to about 10,000 atomic mass units; zinc oxide; and a source of copper ions, preferably cupric acetate. In the preferred composition the liquid organic polysulfide polymer is a mixture of two polymers having different molecular weights.

Abstract: A layered oxide containing vanadium together with phosphorus or arsenic and an organic group may be prepared which has a unique layered structure of the formula: VORAO.sub.3.nS or VOROAO.sub.3.nS where A is phosphorus or arsenic, S is a solvent molecule, R is an unsubstituted or alkyl-, alkoxy- or aryl-substituted alkyl or aryl group, and n is zero or a positive number. These layered compounds are characterized in that the vanadium is substantially in a 4+ oxidation state and is present in an amount such that the molar ratio of A:V ranges from 0.8 to 1.2 throughout the oxide. Also the R groups are covalently bound to an A atom in the vanadium oxide layer directly through either carbon or oxygen atoms.