Abstract:
The invention relates to multilayer materials for producing packaging comprising at least two films and also a layer which is printed with a packaging printing ink, said packaging printing ink comprising a certain hyperbranched polyester containing functional groups. The invention further relates to a packaging printing ink which comprises a certain hyperbranched polyester containing functional groups, and to the use of said printing ink for producing multilayer materials.
Abstract:
Dispersion-stable polymeric acid functional polyols and dispersions of such materials, a method for improving the long term storage dispersibility and hydrolytic resistance of an acid functional polyol and a method for making a water-borne polyurethane, as well as personal care and industrial lubricants, using such improved acid functional polymeric polyols are provided. The polymeric acid functional polyols are reaction products of reaction mixtures including a base polyol having at least one of a terminal secondary and/or tertiary hydroxyl group and an aromatic anhydride.
Abstract:
A hyperbranched polyester polyol macromolecule, having a plurality of both embedded and exterior hydroxyl groups thereon, may be synthesized in a polymerization reaction having several steps. The hyperbranched polyol includes a central nucleus, a first chain extension, an intermediate substituent and a second chain extension. The central nucleus is a hydrocarbon structure with a plurality of oxygen atoms. The first chain extender is attached to the central nucleus and includes a carboxylic ester group and a plurality of hydroxyl groups. The intermediate substituent is attached to the first chain extender, and is a polyfunctional carboxylic acid or anhydride thereof. The preferred intermediate substituent is a cyclic compound. The second chain extension is attached to the intermediate substituent. The preferred second chain extension includes a glycidyl ester or epoxy. Methods of making a hyperbranched polyester polyol are also disclosed. Coating compositions in which the hyperbranched polyol is reacted with an aminoplast or with an isocyanate are also encompassed by the invention.
Abstract:
A polyester resin for a toner, wherein a maximum molecular weight is in a range of 1.times.10.sup.3 to 8.times.10.sup.3, Mw/Mn is in a range of 20 to 200, a proportion of component having a molecular weight of 1.times.10.sup.5 or less is comprised at a range of 80 weight % or greater, and at least one component selected from the group consisting of polycarboxylic acid having more than 3 carboxyl groups and polyalcohol having more than 3 hydroxyl groups.
Abstract:
The invention relates to a powder paint, comprising a polyepoxy compound, a polyester resin and customary additives, the polyester resin having an acid number ranging from 15 through 70 and a hydroxyl number of 10 or below and being substantially based on units of dicarboxylic acids, glycols and monomers of functionality three or higher, wherein the dicarboxylic acids are comprised of at least 15 mole % of isophthalic acid and at least 5 mole % of 1,4-cyclohexane dicarboxylic acid and wherein the glycols are comprised of at least 50 mole % of branched aliphatic glycols with 5-11 carbon atoms, which may optionally comprise an ester group, and at most 50 mole % of aliphatic glycol with 2-6 carbon atoms, and wherein the monomers have a functionality three or higher in an amount of at most 8 mole % of dicarboxylic acids plus glycols.
Abstract:
The invention relates to multilayer materials for producing packaging comprising at least two films and also a layer which is printed with a packaging printing ink, said packaging printing ink comprising a certain hyperbranched polyester containing functional groups. The invention further relates to a packaging printing ink which comprises a certain hyperbranched polyester containing functional groups, and to the use of said printing ink for producing multilayer materials.
Abstract:
A film that is formed from a biodegradable polymer blend of different aliphatic-aromatic copolyesters is provided. More specifically, the blend contains a first copolyester formed from a terephthalic acid monomer. The use of a terephthalic acid monomer results in a polymer chain containing 1,4-(para-)terephthalate units linked in a generally linear configuration (e.g., ˜180°). The blend also contains a second aliphatic-aromatic copolyester formed from a phthalic acid and/or isophthalic acid monomer.
Abstract:
A film that is formed from a biodegradable polymer blend of different aliphatic-aromatic copolyesters is provided. More specifically, the blend contains a first copolyester formed from a terephthalic acid monomer. The use of a terephthalic acid monomer results in a polymer chain containing 1,4-(para-) terephthalate units linked in a generally linear configuration (e.g., ˜180°). The blend also contains a second aliphatic-aromatic copolyester formed from a phthalic acid and/or isophthalic acid monomer. The use of such a monomer results in a polymer chain containing 1,2-(ortho-) and/or 1,3-(meta-) linked units. The inclusion of 1,2-(ortho-) and/or 1,3-(meta-) linked units into the polymer backbone of the second copolyester introduces an angle or “kink” (e.g., ˜120° kink for a 1,3-linkage) into the otherwise linear polymer chain. The “kinks” in the second copolyester backbone reduce its melting point and degree of crystallinity, which have an influence on its physical properties (e.g., toughness, tensile strength, and crystallization rate). Thus, the physical properties of the second copolyester may differ substantially from those of the first copolyester. In this regard, the “kinked” second copolyester can provide flexibility for forming films with a wide range of properties that is superior to that which may be achieved using either of copolyesters alone.
Abstract:
Crosslinked polycondensation products of: (a) polyols selected from the group consisting of: (1) polyols with three or more hydroxyl groups, (2) acetal forms of (1), and (3) mixtures thereof, and (b) polyacids selected from the group consisting of: (1) polyacids with two or more carboxylic groups, (2) anhydrides of (1), (3) esters of (1), and (4) mixtures thereof are disclosed. The resulting polyesters have a molar ratio of polyol to polyacid from about 1:3 to about 3:1 and are highly-crosslinked. Preferred monomers are sustainable monomers such as glycerol, citric acid, fumaric acid, and sebacic acid. Two-step heating processes for preparing the high molecular weight polyesters are also provided.
Abstract:
The present invention provides novel one-step processes for preparing highly branched macromolecule polymers that have highly controlled molecular architectures. The process comprise the reaction of a branching monomer such as a substituted phenyl compound having the formula: ##STR1## wherein R.sub.1, R.sub.2, and R.sub.3 are defined herein, with a second monomer (a core monomer) such as a dihydric phenol for a sufficient period of time and at a sufficient temperature to directly produce the highly branched polymer, characterized by having a single core, in a single processing step.