Abstract: A halogenated copolycarbonate, which contains reduced levels of phenolic end groups and end groups which result from side reactions of process chemicals with the copolycarbonate chain, has improved resistance to the degradation-inducing effects of such end groups and has improved washability.

Abstract: A curable coating composition which comprisesa) a condensation polymer in which the backbone contains activated unsaturated groupings.b) a compound containing at least three blocked primary amino groupsc) a cyclic ketone of formula ##STR1## in which R.sup.1 to R.sup.6 are any non-interfering groups.

Abstract: A process for producing an aromatic polycarbonate in a water-in-oil emulsified form, having an improved heat stability during molding at a high temperature, is described. In the process according to the present invention, a tertiary amine is added to the water-to-oil emulsion after the average diameter of liquid droplets of the water phase is reduced to not more than 10.mu.m. The polycarbonate obtained by the process of the present invention is improved in heat stability and can provide a molded article with less coloration.

Abstract: This invention relates to thermoplastic, aromatic polycarbonates in which mesogenic compounds corresponding to the following formula ##STR1## are incorporated as chain terminating agents, to their preparation by the known processes for the preparation of polycarbonates, and to their use for the production of moulded articles for optical purposes.

Abstract: A process for producing a branched polycarbonate by an interfacial polycondensation method comprising condensing a first reaction mixture comprising an inert organic solvent, an alkaline aqueous solution of divalent phenol, a branching agent, and phosgene, the branching agent having a partition coefficient of at least 1, wherein the partition coefficient is defined as the ratio of the concentration in inert organic solvent/concentration in water, to form a second mixture containing a polycarbonate oligomer or a polycarbonate and unreacted branching agent, separating the second mixture into an organic solvent layer and an aqueous layer which contains the unreacted branching agent, extracting the unreacted branching agent from the aqueous layer with inert organic solvent and recycling the inert organic solvent which contains the unreacted branching agent extracted from the aqueous layer to the first reaction mixture.

Abstract: Polycarbonate prepolymers are produced by adding phosgene, one or more dihydric phenols, a halogenated organic solvent, and an aqueous caustic solution together with mixing in motionless mixers to form fine dispersions of partially phosgenated phenols, allowing for interfacial reactions to occur in residence time sections and repeating the steps after the addition of caustic to form high molecular weight prepolymers. These prepolymers are then polymerized with amines to form high molecular weight polycarbonates.

Abstract: An aromatic polycarbonate containing at least one terminal group represented by the formula ##STR1## wherein R and R' are the same or different and are alkyl, aryl or halogen; a and b are the same or different and are zero or an integer of one to four; W is O, S, SO, SO.sub.2, CH.sub.2, CHR or CR.sub.2 wherein R is identified above;X=O, ##STR2## arylO, or ##STR3## Preferably a and b are the same or different and are zero or one, more preferably each is zero. W is CH.sub.2, CHR or CR.sub.2.

Abstract: A process for preparing polycarbonates according to the invention by melt polycondensation of aromatic dihydroxy compounds and carbonic acid diesters, is characterized by using an aromatic dihydroxy compound and a carbonic acid diester, wherein the combined content of hydrolyzable chlorine in those monomers falls within the particular range. Another process for preparing polycarbonates according to the invention by melt polycondensation of aromatic dihydroxy compounds and carbonic acid diesters, is characterized by using a catalyst comprising (a) a nitrogen containing basic compound and (b) aromatic hihydroxy compound of an alkali metal or alkaline earth metal compound, or (a) and (b) and (c) boric acid or boric ester.

Abstract: A polycarbonate is produced by melt-polycondensing (A) a dihydric phenol with a co-monomer selected from the group consisting of (B) bisphenol carbonate, (C) bis(2,4,6-trichlorophenyl) carbonate (D) bis(2,4,-dichlorophenyl) carbonate and (E) bis(2-cyanophenyl) carbonate in the presence of a catalyst selected from among electron-donating amine compounds and salts thereof. The process of the invention saves the use of phosgene which is poisonous and prevents the resulting polycarbonate from incorporation thereinto of chlorine ions.

Abstract: A polycarbonate resin comprising either a structural unit derived from a spiro ring-containing dihydric phenol, or such a structural unit and a structural unit derived from a dihydric phenol, and a process for producing the same. The polycarbonate resin has excellent flowability and moldability, and also improved optical properties (low refractive index, large Abbe number, etc.), and can be advantageously used in various fields, e.g., as a material for molded articles for optical use and other precision molded articles.

Abstract: Oligomeric carbonate dihydroxyaromatic-based chainstoppers are disclosed. One example of this type of chainstopper is a bisphenol A bischloroformate oligomer monocapped with phenol. These chainstoppers may be prepared by phosgenating a dihydroxyaromatic compound to terminate one or both of the terminal oxygen atoms with chlorocarbonyl groups, followed by reaction of the chlorocarbonyl-terminated material with a phenolic-type compound in the presence of an amine catalyst. The chainstoppers of the present invention are very useful in accurately controlling the molecular weight of polycarbonates formed by various processes, while also preventing the formation of undesirable by-products, such as diarylcarbonates.

Abstract: A process for producing a weather-resistant polycarbonate resin by solution polymerization, of at least one dihydric phenol and phosgene in which a compound represented by formula (I): ##STR1## wherein R.sup.1, R.sup.2, and R.sup.3, each represents a hydrogen atom, a halogen atom, a nitro group, an alkyl group having from 1 to 20 carbon atoms, an alkoxy group having from 1 to 20 carbon atoms, or an aryl group having from 6 to 20 carbon atoms; m represents 1 or 2; and n represents an integer of from 1 to 10, is used as a terminator. The polycarbonate resin produced exhibits high weather resistance without suffering from volatilization.

Abstract: Homo- and copolycarbonates of spirobiindane bisphenols are prepared by first reacting phosgene with a substantially pure spirobiindane bisphenol in the presence of aqueous base in a heterogeneous medium at a pH in the range of about 9-11, and subsequently adding an interfacial polycarbonate formation catalyst and, optionally, a dihydroxyaromatic compound and a chain termination agent and continuing phosgene passage at a pH of at least about 10. By this method, there may be prepared homo- and copolycarbonates of 6,6'-dihydroxy-3,3,3',3'-tetramethyl-1,1-spiro(bis)indane having high molecular weight. Said homopolycarbonates and copolycarbonates with bisphenol A may be used for manufacture of optical disks having low birefrigence.

Abstract: Polycarbonate and polyarylate resins are chain-terminated with a group selected from those of the formula: ##STR1## wherein each R independently represents one of hydrogen or lower alkyl. The resins are reactive polycarbonates, poly(ester carbonates) and polyarylates, useful as intermediates in the preparation of block and graft copolymers, with other polymers having functional, reactive groups.

Abstract: A polycarbonate composition, and process for making same, wherein the monocarbonate and dicarbonate content is eliminated or limited to negligibly low levels by withholding introduction of chain terminator to the reaction mixture until the reaction of dihydroxy and carbonic acid derivative starting materials has run substantially to completion.

Abstract: A process for producing a polycarbonate resin having excellent heat stability from a dihydric phenol compound represented by the formula (1) shown below by an interfacial polymerization method wherein fatty acid represented by the formula (2), (3), (4) or (5) shown below is used as a terminator and as a polymerization catalyst, a quaternary ammonium salt is used, and after 5 to 40 minutes from the addition and emulsification of the polymerization catalyst, tertiary amine is added to cause polymerization. ##STR1## wherein all the symbols are the same as defined before.

Abstract: An aromatic polycarbonate containing at least one terminal group represented by the formula ##STR1## wherein R and R' are the same or different and are alkyl, aryl or halogen; a and b are the same or different and are zero or an integer of one to four; W is 0, S, SO, SO.sub.2, CH.sub.2, CHR or CR.sub.2 wherein R is identified above: ##STR2## Preferably a and b are the same or different and are zero or one, more preferably each is zero. W is CH.sub.2, CHR or CR.sub.2.

Abstract: Cyclic polycarbonate oligomers are converted to linear polycarbonates by the catalytic action of an aryl tetrahydropyranyl ether. The polymerization reaction is slow, and therefore particularly useful in such operations as resin transfer molding.

Abstract: Cyclic polycarbonate oligomers are converted to linear polycarbonates by the catalytic action of a zwitterionic compound containing positively charged nitrogen and negatively charged oxygen. The polymerization reaction is slow, and therefore particularly useful in such operations as resin transfer molding.

Abstract: Branched, thermoplastic polycarbonates, suitable for being processed according to the blow-molding technique, are prepared by copolymerization with hydroxy-naphthoic acids or their derivatives.

Abstract: A process for producing polycarbonate is disclosed, comprising reacting a halogenated bisphenol-containing organic dihydroxy compound and a carbonate-forming derivative in a liquid medium in the presence of pentahalogenophenol as a molecular weight modifier. This polycarbonate is superior in flame retardance, impact resistance and fluidity, and further in transparency.

Abstract: Segmented block copolycarbonates from diphenols and tetrahalogenated diphenols are prepared by phosgenation, under interfacial reaction conditions, initially at a higher pH during which diphenol polycarbonate oligomers are formed, and thereafter at a lower pH during which tetrahalogenated diphenol bischloroformates are formed, followed by copolymerization utilizing an activated pyridine catalyst. Alternatively, diphenol polycarbonate oligomers and tetrahalogenated diphenol chloroformates may be coupled, utilizing an activated pyridine catalyst, to prepare segmented block copolycarbonates.

Abstract: Thermotropic, fully aromatic polyesters and polyester carbonates are produced by esterification of optionally substituted p-hydroxybenzoic acids and aromatic dicarboxylic acids with diaryl carbonate at temperatures in the range from 100.degree. to 220.degree. C. and subsequent transesterification of the aryl ester obtained with diphenols and, optinally, more diaryl carbonate, accompanied by polycondensation, at temperatures in the range from 250.degree. to 330.degree. C., the esterification, the transesterification and the polycondensation being carried out in the presence of heterocyclic compounds containing 1 to 3 nitrogen atoms.

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: Thermoplastic, branched, high-molecular weight polycarbonates endowed with properties of flame-resistance (self-extinguishing polycarbonates) are characterized by the presence in their polymeric chain of units deriving from a di-hydroxy-aromatic compound having the formula: ##STR1## wherein: R is a single bond; or is a substituted or non-substituted, linear or branched alkyl group containing from 1 to 5 carbon atoms; or is a group selected from O, S, SO.sub.2, CO;X and Y are equal to, or different from, each other and stay for H or CH.sub.3 ;m and n are integers, equal to or different from each other, ranging from 1 to 4;and of units deriving from a mono-halogenated tetraphenyl compound having the formula: ##STR2## wherein: R, R.sub.2, R.sub.4, R.sub.6 stay for OH;R.sub.1, R.sub.3, R.sub.5, R.sub.7, either equal to, or different, from one another, stay for OH, H, or a linear or branched alkyl group of from 1 to 5 carbon atoms.

Abstract: High molecular weight polycarbonates are prepared by reacting a sterically hindered, substituted aromatic bischloroformate with an alkali metal hydroxide in the presence of a substituted pyridine.

Abstract: A composition comprising an aromatic carbonate polymer end-capped with a group of the structure ##STR1## wherein --+NR.sub.1 R.sub.2 R.sub.3 is meta or para to the O and R.sub.1, R.sub.2 and R.sub.3 are the same or different and are alkyl of one to three carbon atoms; R is alkyl of one to six carbon atoms, perfluoroalkyl of one to eight carbon atoms, inclusive, phenyl or phenyl substituted with one to three substituents. These substituents can be any of the ordinary substituents which are essentially inert to reaction conditions, such as alkyl, cycloalkyl, alkoxy, phenyl, halo, trifluoromethyl and the like. The alkyl or alkyl group of the alkoxy is generally from one to six carbon atoms, inclusive, branched or normal. Generally, electronegative groups such as fluoro, chloro, bromo and trifluoromethyl are preferred.

Abstract: Polycarbonate prepolymers are produced by adding phosgene, one or more dihydric phenols, a halogenated organic solvent, and an aqueous caustic solution together with mixing in motionless mixers to form fine dispersions of partially phosgenated phenols, allowing for interfacial reactions to occur in residence time sections and repeating the steps after the addition of caustic to form high molecular weight prepolymers. These prepolymers are then polymerized with amines to form high molecular weight polycarbonates.

Abstract: High molecular weight polyhalobisphenol polycarbonates are produced by adding phosgene to a polyhalobisphenol in the alkali metal phenate form whereby the chloroformates of the bisphenol are formed and then adding an activated pyridine such as 4-aminopyridines or 2-substituted pyridines to generate a high molecular weight polycarbonate having an inherent viscosity in the range from about 0.4 to about 0.9.

Abstract: A reusable electrophotographic imaging element having a photoconductive surface layer in which the binder resin comprises a block copolyester or copolycarbonate having a fluorinated polyether block. The layer has low surface adhesion and affords improved transfer of toner images to receiver sheets.

Abstract: Polycyclic polycarbonate oligomers are prepared by the reaction of a bishaloformate and a tetrahydroxyaromatic compound (and optionally also a dihydroxy compound) in the presence of an olefinic tertiary amine and an aqueous slurry of an aldaline earth metal base. The proportion of water in the reaction mixture is up to about 15% by volume of the organic phase. The bishaloformate and hydroxy compounds, and most often also the amine, are preferably added gradually to the other materials.

Abstract: Bischloroformate oligomer compositions are prepared by passing phosgene into a heterogeneous aqueous-organic mixture containing at least one dihydroxyaromatic compound, with simultaneous introduction of a base at a rate to maintain a specific pH range and to produce a specific volume ratio of aqueous to organic phase. By this method, it is possible to employ a minimum amount of phosgene. The reaction may be conducted batchwise or continuously. The bischloroformate composition may be employed for the preparation of cyclic polycarbonate oligomers or linear polycarbonate, and linear polycarbonate formation may be integrated with bischloroformate composition formation in a batch or continuous process.

Abstract: A method for preparing thermoplastic carbonate polymers terminated with hydroxy groups is disclosed, in which a dihydric phenol is reacted with a carbonyl halide in the presence of a monotetrahydropyranyl ether salt. The hydroxy-terminated polymer is then obtained by cleaving the tetrahydropyranyl group with oxalic acid or a hydrogen halide acid.

Abstract: Coating compositions which are capable of curing at room temperature comprise (i) a condensation polymer in which the polymer backbone contains at least one grouping of the formula --CO--C(R).dbd.C(R)--CO--, where R is hydrogen, a halogen or an alkyl or aryl group, and (ii) a compound carrying at least three primary amine or thiol groups. The compositions are of particular interest as undercoats in the automobile refinish trade.

Abstract: A catalyzed interfacial polycondensation aromatic polycarbonate process comprising mixing a water soluble metal salt of a dihydric phenol with an aqueous solution of a strong base and a polymerization catalyst in an inert organic solvent; heating the mixture; concurrently adding a carbonyl halide, additional strong base and additional water soluble metal salt of a dihydric phenol to the heated mixture to form the cyclic oligomeric polycarbonate; and recovering the cyclic oligomeric polycarbonate. The preferred process utilizes the di-sodium salt of bisphenol-A, triethylamine polymerization catalyst and methylene chloride solvent with phosgene to form the cyclic oligomeric polycarbonates. The cyclic oligomeric polycarbonate products are accumulated in the organic phase of the reaction mixture and recovered therefrom by conventional techniques.

Abstract: Compositions comprising polyester or polycarbonate having reacted therein a total of from about 1.0 to about 5,000 parts by weight per million parts by weight of polyester of at least one UV absorbing compound of the formula ##STR1## wherein R is alkyl or the like, X is carbonyl or sulfonyl, R.sup.1 is hydrogen or a substituent, and Y and Z are hydrogen or substituents such as cyano or alkoxycarbonyl, with the provision that at least one of R, R.sup.1, Y, and Z is, or forms part of, or contains one or more reactive groups capable of undergoing a condensation reaction under polyester forming conditions, such that the UV absorbing compound is reacted into the polymer. The compound has a maximum light absorbance within the range of from about 320 nm to about 380 nm, which is nonextractable from the polyester and stable under the polyester processing conditions, for imparting UV screening properties to the polymer.

Abstract: Cyclic polycarbonate oligomers are polymerized to linear polycarbonates by contact with a polycarbonate formation catalyst which has been modified by contacting the same with at least one diaryl carbonate, preferably diphenyl carbonate. Said modification decreases the polymerization rate or introduces an induction period into the polymerization reaction.

Abstract: A transparent optical article is disclosed, which is produced by molding a branched polycarbonate resin having a viscosity average molecular weight of from 13,000 to 20,000 as prepared from at least one dihydric phenol compound in the presence of a polyfunctional organic compound having at least two phenolic hydroxyl groups as a branching agent in an amount of from 0.02 to 3 mol % based on the total amount of the dihydric phenol compound. The transparent molded optical article includes digital audio discs, video discs, memory discs and lenses used in the optical reading system. The optical article is greatly reduced in double refraction and has a high mechanical strength.

Abstract: Polycarbonates exhibiting improved heat resistances comprised of the reaction products of (i) a carbonate precursor and (ii) at least one dihydric phenol represented by the general formula ##STR1## wherein: R and R.sup.1 are independently selected from alkyl radicals;A is selected from divalent hydrocarbon radicals, ##STR2## and n is either zero or one.

Abstract: The present invention is directed to a process for the preparation of a segmented, aliphatic-aromatic polyether-copolycarbonate containing structural units conforming to ##STR1## wherein --D-- is a diphenolate radical and units conforming to ##STR2## wherein --O--Polyether--O-- is an aliphatic polyether-diolate radical, by the phase boundary process in which aliphatic polyether diol and a mixture of dihydroxy compounds are reacted with a carbonic acid halide which is employed in molar excess in relation to the dihydroxy compounds and in which the aqueous phase is kept at a pH value of at least 13 and where the polycondensation reaction is carried out in a reactor by addition of an amine catalyst.The invention is further directed to the polyether polycarbonate which is obtained by the process and to the preparation of membranes from said polyether copolycarbonate.

Abstract: The present invention relates to a process for the preparation of polyether-polycarbonates, a process for stabilizing the polyether-polycarbonates thus prepared, a process for the production of membranes from the polyether-polycarbonates prepared according to the invention, stabilized membranes obtainable by the process according to the invention and the use of the polyether-polycarbonate membranes obtainable by the process according to the invention for dialysis, ultrafiltration and reverse osmosis.

Abstract: Described is a process for improving the color of thermoplastic polymers by contacting the monomer(s) before or during polymerization with an alkali or alkaline earth metal formate.

Abstract: This invention relates to an improved interfacial polycondensation aromatic polycarbonate process which does not require large quantities of strong base to provide a particulate product. The process is specific to interfacial polycondensation processes wherein the polycarbonate is formed in the aqueous phase by using a low organic to aqueous phase volume ratio. The quantity of strong base required to provide a particular product is reduced by adding the aromatic dihydroxy compound to the reaction mixture in small increments. This maintains a high mole ratio of strong base to aromatic dihydroxy compound during reaction.

Abstract: A composition comprising an end-capped aromatic carbonate polymer wherein the end-cap is of the structure ##STR1## wherein R is ##STR2## wherein R.sub.1 and R.sub.2 are the same or different and are alkyl of one to six carbon atoms, inclusive; cycloalkyl of four to seven carbon atoms, inclusive; phenyl; one to three alkyl substituted phenyl each alkyl having one to three carbon atoms, inclusive; and R.sub.1 and R.sub.2 taken together with the nitrogen to which they are attached form a ring of four to six carbon atoms; and wherein R.sub.3 is alkyl of one to ten carbon atoms, inclusive; or cycloalkyl of four to eight carbon atoms, inclusive.

Abstract: The present invention is directed to a continuous process for the preparation of copolycarbonates of sulfonyl diphenol (SDP) containing at least about 15, preferably about 15 to about 80 percent by weight of SDP and characterized in the particular system catalyzing the process reaction. The invention thus entails improvements and modifications to the known interfacial polycondensation process rendering it applicable to the preparation of copolycarbonates containing a high level of SDP comprising a combination of catalysts namely a phase transfer catalyst and a condensation catalyst.

Abstract: This invention relates to an improved interfacial polycondensation polycarbonate process wherein a dihydric phenol is reacted with a carbonyl halide in the presence of a quaternary-phosphonium amino halide catalyst.

Abstract: An interfacial process for the preparation of polycarbonates having improved optical properties is disclosed wherein dihydric phenols are reacted with phosgene in the presence of an aqueous alkali solution and an organic solvent. After the polycarbonate oligomers are formed, the reaction mixture is diluted with additional solvent (25 to 125 volume percent). A polymerization catalyst such as triethylamine is then added to generate high molecular polycarbonates and the resins are then recovered.

Abstract: Novel heat resistant polycarbonates are provided which are the polymerized reaction products of:(i) a carbonate precursor; and(ii) at least one dihydric phenol selected from dihydric phenols represented by the general formulae ##STR1## wherein: each R.sup.1 is independently selected from halogen radicals, monovalent hydrocarbon radicals, and monovalent hydrocarbonoxy radicals;each R.sup.2 is independently selected from halogen radicals, monovalent hydrocarbon radicals, and monovalent hydrocarbonoxy radicals;R.sup.4 and R.sup.5 are independently selected from monovalent hydrocarbon radicals;R.sup.3 is selected from hydrogen and monovalent hydrocarbon radicals, with the proviso that if R.sup.3 is a hydrogen radical than at least one of the monovalent hydrocarbon radicals represented by R.sup.4 and R.sup.5 contains at least two carbon atoms;R.sup.7 is selected from hydrogen and monovalent hydrocarbon radicals;R.sup.

Abstract: The present invention is directed to molding compositions comprising aromatic, thermoplastic polycarbonate resins at least some molecular chains thereof are characterized in that their terminal groups contain conjugated double bonds. The invention is further directed to a process for the preparation of said compositions.

Abstract: This invention relates to a catalyzed interfacial polycondensation aromatic polycarbonate process which comprises forming an agitated two-phase mixture comprising an organic solvent phase with catalyst and an aqueous phase containing an aromatic dihydroxy compound, a base and an ionic surfactant. A carbonyl halide is added to the mixture and reacted with the aromatic dihydroxy compound to form an aromatic polycarbonate. The aromatic polycarbonate is recovered from the aqueous phase.