Abstract: A method of making a polybenzimidazole (PBI) includes the steps of: reacting, in a solution, an organic compound having at least 2 amino groups with an organic aldehyde adduct, the reactants comprise at least 8% by weight of the solution. A solvent of the solution may be selected from the group of: N,N-dimethylacetamide (DMAc), N,N-dimethylformamide (DMF), dimethylsulfoxide (DMSO), N-methyl-2-pyrrolidone (NMP), tetramethylene sulfone, and combinations thereof. The organic aldehyde adduct may be an organic aldehyde bisulfite adduct. The organic aldehyde portion of the organic aldehyde adduct being aliphatic, alicyclic, aromatic, heterocyclic, or heteroaromatic aldehyde or mixtures thereof. The polybenzimidazole may have an intrinsic viscosity of at least 0.40 dl/g.

Abstract: Methods for making and using amino-aldehyde resins. The method for making an amino-aldehyde resin can include mixing an intermediate amino-aldehyde reaction product having a total aldehyde compound to total amino compound molar ratio ranging from about 1.4:1 to about 3:1 with a first aldehyde compound and a first amino compound to produce an amino-aldehyde resin having a total aldehyde compound to total amino compound molar ratio ranging from about 0.5:1 to about 1.2:1. The concentration of the first aldehyde compound mixed with the intermediate reaction product can be about 1.9 wt % or more based on a combined solids weight of the aldehyde compounds and the amino compounds in the amino-aldehyde resin.

Abstract: Provided is a novel polyazomethine which is soluble in relatively versatile organic solvents including hydrophobic solvents such as toluene, alcohol solvents such as methanol and ethanol, glycol solvents such as propylene glycol monomethyl ether, and ester solvents such as methyl lactate, while securing carrier mobility sufficient for a semiconductor material. The polyazomethine is a repeating unit that contains a divalent aromatic ring-containing conjugated group wherein an azomethine group and a divalent aromatic group which may have a substituent are alternately bonded and conjugated and a divalent hydrocarbon group which may have a group that is not conjugated with the azomethine group and has an oxygen atom, a sulfur atom or a cycloalkylene group, with the aromatic ring-containing conjugated group and the hydrocarbon group being bonded with each other via the azomethine group.

Abstract: An electronic device, such as a thin film transistor, is disclosed having a dielectric layer formed from a composition comprising a compound having at least one phenol group and at least one group containing comprising silicon. The resulting dielectric layer has good electrical properties.

Abstract: An ordered structured organic film comprising a plurality of segments and a plurality of linkers arranged as a covalent organic framework, wherein the structured organic film may be a multi-segment thick structured organic film.

Abstract: A method for the production of a functionalized polytriazole polymer, particularly a poly(1,2,4-triazole)-polymer, includes the steps of (a) mixing a hydrazine salt, particularly hydrazine sulfate, with at least an aromatic and/or heteroaromatic dicarboxylic acid and/or at least a dicarboxylic acid derivate in polyphosphoric acid and if necessary further components for obtaining a solution; (b) heating the solution in a protective gas atmosphere for obtaining polyhydrazides and adding aromatic and/or heteroaromatic primary amines to the solution; and (c) precipitating a polymer. If necessary, neutralization in a basic solution may be carried out.

Abstract: A process of synthesizing hyperbranched polytriazoles, linear and hyperbranched poly(aroyltriazoles) by Huisgen 1,3-dipolar cycloaddition. The polytriazoles were prepared by A2+B3 method to avoid self-polymerization during monomer preparation and storage. The polymers are light emissive and can be crosslinked to generate well-resolution photopatterns upon UV irradiation. White light emission patterns were observed with fluorescence microscopy. The high molecular weight poly(aroyltriazoles) (up to 26000 Da) are prepared in high yields (up to 92.0%) and with high regioselectivity (the ratio of 1,4- and 1,5-disubstituted 1,2,3-triazole is equal or larger than 9:1). The polycyclomerization is not moisture or oxygen sensitive and therefore, no special precautions are necessary before and during the reaction. All the polymers are processible, easily film-forming, and curable into thermosets by heat or irradiation. The hyperbranched polymers can act as fluorescent adhesive materials with large tensile strength.

Abstract: An electronic device, such as a thin film transistor, is disclosed having a dielectric layer formed from a composition comprising a compound having at least one phenol group and at least one group containing comprising silicon. The resulting dielectric layer has good electrical properties.

Abstract: Water-resistant, protein-based adhesive dispersion compositions and methods for preparing them are provided. The adhesive dispersions are prepared by copolymerizing a denatured vegetable protein, such as soy flour, that has been functionalized with methylol groups with one or more reactive comonomers, and preparing an acidic dispersion of the adhesive. The adhesive dispersions exhibit superior water resistance, and can be used to bond wood substrates, such as panels or laminate, or in the preparation of composite materials.

Abstract: The present invention relates to an aromatic polycarbonate resin which comprises repetitive units originating in residual groups of a 2,2-bis(4-hydroxyphenyl)adamantane compound and a 1,3-bis(4-hydroxyphenyl)adamantane compound having a substituent on an aromatic ring and which is excellent in a transparency, a heat resistance and a mechanical strength and has a good moldability and a production process for the aromatic polycarbonate resin described above in which the adamantane compounds described above are reacted with a carbonic ester-forming compound. Further, it relates to an aromatic polycarbonate resin which is excellent in an optical characteristic and an optical part prepared by molding the same.

Abstract: The invention relates to a process for making a modified thermoplastic polyester by reacting a thermoplastic polyester with a nitrogen-containing compound, wherein the thermoplastic polyester is first contacted in the solid state with an inert gas atmosphere containing at least one amino-compound of formula H2N—R—(X)n, wherein n is an integer?0, R=a linear, branched or cyclo-aliphatic or aromatic residue comprising 1–24 C-atoms and optionally containing hetero atoms, X?—NH2 or another functional group reactive with the polyester, at a temperature T(a) between room temperature and the melting point Tm of the polyester, during at least 1 s; and then heated to a temperature T(b) between T(a) and Tm, during up to 10 hours; and thereafter solid state polymerized at a temperature T(c) between (Tm?50) and Tm, during up to 100 hours, where T(a)<T(b)<T(c).

Abstract: The present invention relates to an electrodepositable coating composition having a resinous phase dispersed in an aqueous medium. The resinous phase includes (a) an ungelled, active hydrogen-containing, ionic salt group-containing resin; and (b) a curing agent reactive with the active hydrogens of the resin (a). The resinous phase has a covalently bonded halogen content based on total weight of resin solids present in the resinous phase such that when the composition is electrodeposited and cured, the cured film passes flame resistance testing in accordance with IPC-TM-650, and has a dielectric constant of less than or equal to 3.50. The invention also is directed to a method for forming a dielectric coating on an electroconductive substrate using the electrodepositable coating composition, as well as to a substrate coated with the electrodepositable composition.

Abstract: A polymeric composition and process for making the same suitable for injection molding processes and procedures containing an olefinic polymer component selected from at least one a group which includes polyalkylenes, copolymers of polyalkylenes and a thermoplastic polyamide. The polyamide and olefinic polymeric components are present in random orientable locations in the initial polymeric composition. When injection molded against a temperature gradient, the resulting workpiece composed of the composition has distinctive regions of elevated polyamide concentration proximate the outwardly oriented surface and distinctive regions of elevated olefinic polymeric concentration proximate to interior regions of the workpiece.

Abstract: New water-soluble polycondensation products are obtained by reaction of polyfunctional amines with cyanamide, its derivatives or polymers in the presence of sulfamic acid. They are excellent fixing agents which improve fastness properties of dyeings with substantive dyestuffs on cellulose fiber materials, paper, board and non-wovens.

Abstract: A composition for the detackification and clarification of acid and alkaline paint and lacquer waste waters and paint spray booth wastes, comprising:an inorganic-organic and/or organic adduct alloy polymer composition having the formula:A.multidot.B.sup.+ .multidot.D.sup.+wherein: A=[(SiO.sub.2 /Me.sup.I.sub.2 O).sub.u Me.sup.II.sub.m Me.sub.m.sup.III(OH).sbsp.p.sup.(SO.sbsp.4.sup.).sbsp.y.sup.(Aci) (2m+3n)-p-2y].sub.rwhere r=1 to 98% bw; u=0 to 10% bw; ##STR1## where: x=0 to 98% bw; Z is a divalent substituted or unsubstituted aliphatic, cycloaliphatic, heterocyclic or aromatic radicalD.sup.+ =(PQAM).sub.wwherew=2 to 98% b.w. of polyquaternized polymer (PQAM)Me.sub.m.sup.II is selected from the divalent cationic group comprising: Mg, Zn, Ca, and Fe.sup.2+m=0 to 5Me.sub.n.sup.III is a tri-or more valent metal selected from the group comprising: Fe, Al, and Al--Zn complexes;n=1 to 20Aci is selected from the monovalent anionic group comprising Cl.sup.-, Br.sup.-, I.sup.-, NO.sub.3 --, H.sub.2 PO.sub.4 --, CH.

Abstract: A method of forming a urea formaldehyde resin includes the step of heating solid paraformaldehyde to a temperature of 60 to 120.degree. C. Urea is added to the heated paraformaldehyde to form a urea mixture, which is dry mixed and heated until a temperature of 80 to 110.degree. C. has been reached. After this, a methanolic quanine base is added to the urea mixture to form a quanine-urea-formaldehyde mixture, which is heated until the quanine-urea-formaldehyde mixture is liquefied and cooled to 65.degree. C. Then, the quanine-urea-formaldehyde mixture is heated until it boils, at which point it is condensed for a period of 30 to 100 minutes. After this, additional urea is added to the liquified urea mixture to form a urea enriched mixture. The urea enriched mixture is condensed for 90 to 180 minutes. After condensation, the urea enriched mixture is buffered with lactic acid to form a buffered mixture. This buffered mixture is cooled.

Abstract: There is described a process for the preparation of basic poIycondensates, which comprises(a) reacting an amine of formula ##STR1## wherein R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are each independently of one another hydrogen or alkyl which is unsubstituted or substituted by amino, hydroxy, cyano or C.sub.1 -C.sub.4 alkoxy, and A is alkylene which may be substituted or interrupted by one or more than one hetero atom, with an ammonium salt in the presence of an anhydrous solvent, and(b) reacting the protonised product obtained according to (a) with a cyanamide at elevated temperature.The polycondensates or salts thereof prepared according to this process are particularly suitable aftertreatment agents for enhancing the wetfastness properties of dyed or printed textile material.

Abstract: To prepare nitrogen-containing aromatic polymers, for example polyamides, polyimides and polybenzimidazoles, polyvalent aromatic carboxylic acids and aromatic diamines and/or aminocarboxylic acids or reactive derivatives thereof are reacted in a high-boiling inert solvent with the addition of a heat-stable dispersing auxiliary, and volatile by-products formed in this reaction are distilled off. When the reaction has ended, the batch is cooled and the polymer formed is filtered off.

Abstract: A composition for the detackification and clarification of acid and alkaline paint and lacquer waste waters and paint spray booth wastes, comprising:an inorganic-organic and/or organic adduct alloy polymer composition having the formula:A.multidot.B.sup.+ .multidot.D.sup.+wherein:A=[(SiO.sub.2 /Me.sup.I.sub.2 O).sub.u Me.sup.II.sub.m Me.sub.m.sup.III(OH) p.sup.(SO 4.sup.) y.sup.(Aci) (2m+3n)-p-2y].sub.4wherer=1 to 98% bw;u=0 to 10% bw; ##STR1## where: x=0 to 98% bw; Z is a divalent substituted or unsubstituted aliphatic, cycloaliphatic, heterocyclic or aromatic radicalD.sup.+ (PQAM).sub.wwherew=2 to 98% b.w. of polyquaternized polymer (PQAM)Me.sub.m.sup.II is selected from the divalent cationic group comprising: Mg, Zn, Ca, and Fe.sup.2+m=0 to 5Me.sub.n.sup.III is a tri-or more valent metal selected from the group comprising: Fe, Al, and Al-Zn complexes;n=1 to 20Aci is selected from the monovalent anionic group comprising Cl.sup.-, Br.sup.-, I.sup.-, NO.sub.3 --, H.sub.2 PO.sub.4 --, CH.sub.3 COO.sup.-, OH.

Abstract: A carrier web of a sheet-like fiber material consisting of a glass fiber mat and a mat of synthetic fibers, which and are needled together and are end-consolidated with a polymer-free low-formaldehyde melamine-formaldehyde precondensate, and a process for its preparation are described.The carrier web is preferably end-consolidated with a melamine-formaldehyde precondensate which is partly etherified and/or sulfamate-modified.

Abstract: A continuous preparation method of an amino resin particulate having a maximum particle size of 40 .mu.m or less and an average particle size of from 5 to 15 .mu.m is described. The method comprises the steps of reacting amino compounds with aldehydes in the presence of an acid catalyst in an aqueous solution to form a solid product and classifying said solid product in the form of a slurry with a combination of at least two grinders and at least two classifiers.

Abstract: Modified poly(alkylene carbonate) polyahls comprising the residue of at least one polyahl, at least one modifier, poly(alkyleneoxy) units, poly(alkylene carbonate) units, and a plurality of active hydrogen end groups are disclosed. The modifed polyahls have an average molecular weight higher than any known polyahls containing at least the same weight percent modifier and the same poly(alkyleneoxy) and poly(alkylene carbonate) residues. Also disclosed are isocyanate-functional prepolymer compositions of these modified poly(alkylene carbonate) polyahls, which contain the residue of at least one modified poly(alkylene carbonate) polyahl of this invention and excess organic polyisocyanate units. Urethane/urea polymers formed by the reactions of the isocyanate-functional prepolymers with polyahls are also disclosed.

Abstract: Cationic fixing agents based on the reaction products of(a) a monofunctional or polyfunctional amine having one or more primary and/or secondary and/or tertiary amino groups and(b) cyanamide, dicyandiamide, guanidine or bisguanidinegive improved results when the reaction takes place in the presence of a catalyst (K) selected from metals, metal salts and heterocyclic nitrogen-containing organic bases, particularly zinc chloride.

Abstract: A solid urea-formaldehyde resin is provided, having a degree of condensation of 25% to 45%.A process for making the resin is also described and includes several steps. Urea and formaldehyde is first reacted with a molar ratio of U:F of 1:2.5 or more then concentrated. Further urea is added to reduce the ratio to the range 1:1.1 to 1:2 and further concentration is achieved without precipitation of solid resin by the use of a stabilization agent.

Abstract: The wet fastness properties of direct or reactive dyeings on cellulosic substrates are improved by aftertreatment with a precondensate of(A) the product of reacting a mono- or polyfunctional primary or secondary amine with cyanamide, dicyandiamide (DCDA), guanidine or biguanidine; or ammonia with cyanamide or DCDA; whereby up to 50 mole % of the cyanamide, DCDA, guanidine or biguanide may be replaced with a dicarboxylic acid or a mono- or di-ester thereof, said product (A) containing reactive hydrogen atoms bound to nitrogen, and either(B) an epihalohydrin or a precursor thereof, or(C) formaldehyde or a formaldehyde precursor, or(D) a dihydroxyalkyleneurea or a methyl ether thereof,followed by formaldehyde or a formaldehyde precursor optionally together with(E) an N-methylol derivative of a urea, melamine, guanamine, triazinone, urone, carbamate or acid amideand, if (A) is used with (C) or (D), or if (E) is present, together with(F) a catalyst for the cross-linking of N-methylol compounds of the type (E) abov

Abstract: The fastness properties of basic dyeings on cellulosic substrates are improved by treating the substrate with a fixing agent comprising a precondensate or mixture of(A) the reaction product of an amine with cyanamide, dicyandiamide, guanidine or biguanidine, or,(B) a quaternary polyalkylene polyamine with(C) formaldehyde and/or,(D) an N-methylol compound optionally together with(E) a catalyst, e.g. MgCl.sub.2.The fixing agents are normally applied as an aftertreatment, with a subsequent heat-curing step.

Abstract: The wet fastness properties of direct or reactive dyeings on cellulosic substrates are improved by aftertreatment with a precondensate of(A) the product of reacting a mono- or polyfunctional primary or secondary amine with cyanamide, dicyandiamide (DCDA), guanidine or biguanidine; or ammonia with cyanamide or DCDA; whereby up to 50 mole % of the cyanamide, DCDA, guanidine or biguanidine may be replaced with a dicarboxylic acid or a mono- or di-ester thereof, said product (A) containing reactive hydrogen atoms bound to nitrogen,and either (B) an epihalohydrin or a precursor thereofor (C) formaldehyde or a formaldehyde precursoror (D) a dihydroxyalkyleneurea or a methyl ether thereof, followed by formaldehyde or a formaldehyde precursoroptionally together with (E) an N-methylol derivative of a urea, melamine, guanamine, triazinone, urone, carbamate or acid amideand, if (A) is used with (C) or (D), or if (E) is present, together with (F) a catalyst for the cross-linking of N-methylol compounds of the type (E) ab

Abstract: There are provided metal containing polymeric coordination compounds which are prepared by a process which comprises reacting metal salts with polydentate ligand molecules obtained by the condensation of aromatic dialdehydes with .beta.-hydroxy-.alpha.,.gamma.-diamines. The above are electrical semiconductors. Such polymers containing platinum have a biological activity.

Abstract: Disclosed are novel water-soluble, thermosettable resinous compositions derived by reacting a precondensate of dicyandiamide, formaldehyde, a salt of a water-soluble polyaminopolyamide and an ammonium salt with acrylamide and then condensing the reaction product with additional formaldehyde. The resinous compositions are cationic and have particular utility in the manufacture of paper sized with cellulose reactive sizing agents such as ketene dimer sizing agents.

Abstract: Disclosed are novel water-soluble, thermosettable resinous compositions derived by reacting a precondensate of dicyandiamide, formaldehyde, a salt of a water-soluble polyaminopolyamide and an ammonium salt with epihalohydrin, condensing the reaction product with additional formaldehyde and then post-modifying the condensate with additional epihalohydrin or a nitrogen-containing compound. The resinous compositions are cationic and have particular utility in the manufacture of paper sized with cellulose reactive sizing agents such as ketene dimer sizing agents.

Abstract: Disclosed are novel water-souble, thermosettable resinous compositions derived by reacting a precondensate of dicyandiamide, formaldehyde, a salt of a water-soluble polyaminopolyamide and an ammonium salt with epihalohydrin and then condensing the reaction product with additional formaldehyde. The resinous compositions are cationic and have particular utility in the manufacture of paper sized with cellulose reactive sizing agents such as ketene dimer sizing agents.

Abstract: A process for flameproofing wood is claimed, which comprises treating the wood with aqueous preparations which contain(a) at least one water-soluble ammonium salt of a non-volatile inorganic acid, e.g. ammonium sulfate or ammonium phosphate,(b) at least one water-soluble cationic reaction product of dicyandiamide, formaldehyde, optionally an ammonium salt and/or an alkylenepolyamine containing at most 18 carbon atoms, or the acid salt thereof.Components (a) and (b) are applied in succession or preferably simultaneously and the wood is subsequently dried. The flameproof finish obtained is resistant to rinsing. The wood provided with the flameproof finish is used in particular as mine timber.

Abstract: An improved process for the preparation of alkoxylated formaldehyde-amino compound resins. By using a sequential procedure, and an alkanol of up to 8 carbon atoms it is possible to remove both the water in the aqueous formaldehyde used and the water from the alkoxylation reaction azeotropically. The products of this invention afford resins of better quality, especially in terms of color and clarity, than the products derived from alcoholic formaldehyde solutions.

Abstract: The invention relates to a liquid coating composition based on an aminoplast and an ester thiol built up from a polyol and a mercaptocarboxylic acid having 2 to 7 carbon atoms. The invention also relates to a process for coating a substrate with such a composition, and to the substrate thus manufactured.

Abstract: A formaldehyde resin solution compatible fire retardant agent solution compatible with formaldehyde resin solutions is prepared consisting essentially of(a) 30 to 75 weight percent of a phosphoric acid containing condensation product of guanidine and formaldehyde in which the molar ratio A of phosphoric acid to guanidine is between 0.7:1 and 1.5:1 and the molar ratio B of formaldehyde to guanidine is between 1.0:1 and 4.0:1 and in which additionally the product of the two molar ratios A and B is from 1.0 to 6.0, and(b) 70 to 25 weight percent of a saturated, straight chain monohydric alcohol having 1 to 3 carbon atoms or a mixture of such an alcohol and up to 25 weight percent, based on the weight of component (b) of water.