C08G63/6956

Process for Preparing Organic Solvent-Based Dispersions, Coating Compositions and Coated Metal Substrate Useful for Packaging Applications

The invention relates to a process for preparing an organic solvent-based dispersion comprising a melt-blended network of an epoxy-functional and/or amino-functional polymer having a polymer-O—Si—O-polymer linkage and a polyolefin (co)polymer having carboxylic acid and/or carboxylic acid anhydride groups, the process comprising the steps of a) forming the melt-blended network from a prepolymer, a silane-functional compound and the polyolefin (co)polymer in the absence of a solvent, b) mixing the melt-blended network with an organic solvent to make the organic solvent-based dispersion, and c) cooling the organic solvent-based dispersion. The invention further relates to a coating composition and to a coated metal substrate.

THERMOPLASTIC COMPOSITIONS, METHOD OF MANUFACTURE, AND ARTICLES THEREFROM
20170355832 · 2017-12-14 ·

A thermoplastic composition including a polycarbonatesiloxane-arylate; a phthalone compound; and optionally an additional component different from the polycarbonatesiloxane-arylate and the phthalone compound; wherein the phthalone compound has a formula: wherein Z.sub.1 represents the atoms necessary to complete a 9- to 13-membered single or fused aromatic ring structure, Z.sub.2 represents the atoms necessary to complete a pyridine or quinoline ring, each R.sub.1 and each R.sub.2 are independently halogen, an alkyl group, an aryl group, a heterocyclic group, an alkoxy group, an aryloxy group, an aromatic or aliphatic thioether group, an aromatic or aliphatic carboxylic acid ester group, or an aromatic or aliphatic amide group, a is an integer from 0 to 6, b is an integer from 0 to 4, n is 1 or 2, and X is present only if n=2 and is a single bond or a divalent organic radical bonded to the Z.sub.1 ring structure through an ether, ketone, or thio linkage.

##STR00001##

Aminosilane adhesion promoter for urethane system

A polyester polyol comprising at least one esterified unit of formula (I) ##STR00001##
wherein L is a difunctional aliphatic group having from two to six carbon atoms and R is a C.sub.1-C.sub.4 alkyl group.

Copolyester tape

Provided is a tape including a composition having a copolyester including polymeric units derived from ethylene glycol and terephthalic acid or a diester thereof and >0.50 and <5.00 wt % of polymeric units with regard to the total weight of the polyester derived from an oligomeric dihydroxy compound having a number average molecular weight of >500 g/mol and <5000 g/mol. Such tape has an improved tensile-impact strength and a reduced proneness to splitting during weaving.

BINDERS AND CURABLE RESINS FOR MINERAL WOOL

Embodiments of a curable formaldehyde-free resin, and a method for the manufacture of the curable formaldehyde-free resin are provided herein. The curable formaldehyde-free resin is provided in the form of an aqueous dispersion. The curable formalde-hyde-free resin comprises component a) a reducing sugar, component b) a polycarboxylic acid, component c) one or more polyols having a molecular weight of less than 1000 g/mol, and component d) epoxysilane. The total amount of component c) in the curable formaldehyde-free resin is between 0.5 and 10% wt. with respect to the sum of components a) and b). The amount of component d) is from 0.1% wt. to less than or equal to 2% wt. with respect to the sum of components a) and b). Further, a method for the manufacture of the curable formaldehyde-free resin according to one of the embodiments of the present disclosure is provided.

METHOD FOR PRODUCING SILANE-MODIFIED POLYMERS

A method for producing an alkoxysilane polymer via a carbamate, thiocarbonate or carbonate-terminated prepolymer (IIIa) or (IIIb) includes reaction of a polymer backbone of formula (I) terminated with at least two amino, mercapto or hydroxyl groups and with a chloroformate of formula (IIa) or a pyrocarbonate of formula (Ilb) (I) (IIa) (IIb) (IIIa) (IIIb), wherein R.sup.1 and R.sup.3 represent a linear or branched, saturated or unsaturated alkyl or alkenyl group with 1 to 10 carbon atoms or a mono- or polycyclic aliphatic or aromatic ring system with 5 to 18 carbon atoms in the ring system, which is optionally substituted by one or more groups R.sup.2, X is oxygen or sulphur, n is 0 for a linear or branched, saturated or unsaturated alkyl or alkenyl group and is 0.1 or 2 for a mono- or polycyclic aliphatic or aromatic ring system, and A represents a polymer backbone.

Polyester yarn for industrial sewing thread and preparing method thereof

A type of polyester yarn for an industrial sewing thread and preparing method thereof are provided. The preparing method is composed of a viscosity enhancing by a solid state polycondensation and a melt spinning for a modified polyester, and the modified polyester is a product of esterification and polycondensation of evenly mixed terephthalic acid, ethylene glycol, tert-butyl branched dicarboxylic acid, trimethylsilyl branched diol and a doped Sb.sub.2O.sub.3 powder, wherein the tert-butyl branched dicarboxylic acid is selected from the group consisting of 5-tert-butyl-1,3-benzoic acid, 2-tert-butyl-1,6-hexanedioic acid, 3-tert-butyl-1,6-hexanedioic acid and 2,5-di-tert-butyl-1,6-hexanedioic acid. Moreover, the modified polyester is dispersed with a doped ZrO.sub.2 powder. An obtained fiber has an intrinsic viscosity drop of 23-28% when stored at 25° C. and R.H. 65% for 60 months.

POLYESTER YARN FOR INDUSTRIAL SEWING THREAD AND PREPARING METHOD THEREOF

A type of polyester yarn for an industrial sewing thread and preparing method thereof are provided. The preparing method is composed of a viscosity enhancing by a solid state polycondensation and a melt spinning for a modified polyester, and the modified polyester is a product of esterification and polycondensation of evenly mixed terephthalic acid, ethylene glycol, tert-butyl branched dicarboxylic acid, trimethylsilyl branched diol and a doped Sb.sub.2O.sub.3 powder, wherein the tert-butyl branched dicarboxylic acid is selected from the group consisting of 5-tert-butyl-1,3-benzoic acid, 2-tert-butyl-1,6-hexanedioic acid, 3-tert-butyl-1,6-hexanedioic acid and 2,5-di-tert-butyl-1,6-hexanedioic acid. Moreover, the modified polyester is dispersed with a doped ZrO.sub.2 powder. An obtained fiber has an intrinsic viscosity drop of 23-28% when stored at 25° C. and R.H. 65% for 60 months.

Easy-to-dye porous modified polyester fiber and preparing method thereof

A type of easy-to-dye porous modified polyester fibers and preparing method thereof are disclosed. The preparing method is using the modified polyester melt through a porous spinneret with FDY process; wherein the modified polyester is a product of an esterification and successive polycondensation reactions of an evenly mixed terephthalic acid, ethylene glycol, main chain silicated diol, 2,2,3,4,5,5-hexamethyl-3,4-hexanediol, and metal oxide doped Sb.sub.2O.sub.3 powder; wherein the main chain silicated diol is selected from the group consisting of dimethylsiloxane diol, dimethyldiphenyldisiloxane glycol and tetramethyldisiloxane diol. The structural formula of 2,2,3,4,5,5-hexamethyl-3,4-hexanediol is as follows: ##STR00001## The dye uptake and the K/S value of the prepared easy-to-dye porous modified polyester fiber are high. This invention features a method with ease of application and a product with good dyeing performance and good quality.

EASY-TO-DYE POROUS MODIFIED POLYESTER FIBER AND PREPARING METHOD THEREOF

A type of easy-to-dye porous modified polyester fibers and preparing method thereof are disclosed. The preparing method is using the modified polyester melt through a porous spinneret with FDY process; wherein the modified polyester is a product of an esterification and successive polycondensation reactions of an evenly mixed terephthalic acid, ethylene glycol, main chain silicated diol, 2,2,3,4,5,5-hexamethyl-3,4-hexanediol, and metal oxide doped Sb.sub.2O.sub.3 powder; wherein the main chain silicated diol is selected from the group consisting of dimethylsiloxane diol, dimethyldiphenyldisiloxane glycol and tetramethyldisiloxane diol. The structural formula of 2,2,3,4,5,5-hexamethyl-3,4-hexanediol is as follows:

##STR00001##

The dye uptake and the K/S value of the prepared easy-to-dye porous modified polyester fiber are high. This invention features a method with ease of application and a product with good dyeing performance and good quality.