Organic acid carbohydrate binders and materials made therewith

Patent metadata

Field	Value
Publication number	US-2017190801-A1
Application number	US-201715463273-A
Country	US
Kind code	A1
Filing date	Mar 20, 2017
Priority date	Sep 17, 2010
Publication date	Jul 6, 2017
Grant date	—

Abstract

A binder comprising a polymeric binder comprising the products of a carbohydrate reactant and organic acid is disclosed. The binder is useful for consolidating loosely assembled matter, such as fibers. Fibrous products comprising fibers in contact with a carbohydrate reactant and an organic acid are also disclosed. The binder composition may be cured to yield a fibrous product comprising fibers bound by a cross-linked polymer. Further disclosed are methods for binding fibers with the carbohydrate based binder using an organic acid.

First claim

1 . A binder comprising a polymeric product of a carbohydrate reactant, an amine base, and an organic acid, wherein
the organic acid is R-Q(═O) m (—OH) n , Q is phosphorus (P), m is 1, and n is 2 or Q is sulfur (S), m is 2, and n is 1, and R is alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heteroalkyl, heteroalkenyl, cycloheteroalkyl, cycloheteroalkenyl, aryl, or arylalkyl, each of which is optionally substituted.

2 . The binder of claim 1 , in which the organic acid is characterized by at least one of the following embodiments:
a) wherein R is alkyl, cycloalkyl, heteroalkyl, cycloheteroalkyl, alkenyl, cycloalkenyl, or aryl each of which is optionally substituted; b) wherein R is selected from the group consisting of phenyl, benzyl, a tolyl, a xylyl, and a naphthalenyl, each of which is optionally substituted; c) wherein R is 4-methylphenyl; d) wherein R is selected from the group consisting of 2-aminophenyl, 3-aminophenyl, 2-methylphenyl, 3-methylphenyl, 2,3-dimethylphenyl, and 2,4-dimethylphenyl; e) wherein R is an alkyl selected from the group consisting of C 1 -C 24 each of which is optionally substituted; f) wherein R is an alkyl selected from the group consisting of C 1 -C 8 , each of which is optionally substituted; g) wherein R is selected from the group consisting of methyl, ethyl, 2-amino-ethyl, piperidinyl, and trifluoromethyl; and h) wherein R is selected from the group consisting of 2-sulfophenyl, 3-sulfophenyl, sulfomethyl, 2-phosphonophenyl, 3-phosphonophenyl, and phosphonomethyl.

3 - 9 . (canceled)

10 . The binder of claim 1 , in which the carbohydrate reactant is characterized by at least one of the following embodiments:
a) wherein the carbohydrate reactant is a monosaccharide or a disaccharide; b) wherein the carbohydrate reactant is a disaccharide selected from the group consisting of sucrose, lactose, lactulose, maltose, trehalose, and cellobiose; c) wherein the carbohydrate reactant is a monosaccharide in its aldose or ketose form; d) wherein the carbohydrate reactant is a reducing sugar; e) wherein the carbohydrate reactant is selected from the group consisting of dextrose, xylose, fructose, dihydroxyacetone, and mixtures thereof; f) wherein the carbohydrate reactant is a polysaccharide; g) wherein the carbohydrate reactant is polysaccharide with a degree of polymerization between 3 and 10; h) wherein the carbohydrate reactant is polysaccharide with a degree of polymerization between 3 and 5; and i) wherein the carbohydrate reactant is a starch, cellulose, hydrolysates thereof, or molasses.

11 - 18 . (canceled)

19 . The binder of claim 1 , in which a mole ratio of the carbohydrate reactant to the organic acid is characterized by at least one of the following embodiments:
a) wherein a mole ratio of the carbohydrate reactant to the organic acid is in the range of about 2:1 to about 30:1; and b) wherein a mole ratio of the carbohydrate reactant to the organic acid is in the range of about 3:1 to about 10:1.

20 . (canceled)

21 . The binder of claim 1 , wherein an aqueous extract of the polymeric product has a pH in the range of about 5 to about 10.

22 . The binder of claim 1 , in which the amine base is characterized by at least one of the following embodiments:
a) wherein the amine base is selected from the group consisting of ammonia, a primary amine, and a secondary amine; and b) wherein the amine base is NHR 1 R 2 , wherein R 1 and R 2 are each independently selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, cycloalkenyl, and heterocyclyl, each of which can be optionally substituted.

23 . (canceled)

24 . The binder of claim 1 , in which the biobased carbon content is characterized by at least one of the following embodiments:
a) wherein the binder has a biobased carbon content of between 50% and 98% according to ASTM-D 6866-10; and b) wherein the binder has a biobased carbon content of between 60% and 95% according to ASTM-D 6866-10.

25 . (canceled)

26 . The binder of claim 1 , in which the binder is characterized by at least one of the following embodiments:
a) wherein the polymeric product is selected from the group consisting of phenol-free, formaldehyde-free, carboxylic acid-free, sulfate-free, phosphate-free, and combinations thereof; b) wherein the carbohydrate reactant and the organic acid are non-volatile; c) wherein the polymeric product strongly absorbs light at 420 nm; d) wherein an aqueous extract of the polymeric product is essentially colorless; e) wherein a wet laid mat made therewith has a weathered tensile strength of at least about 250 lbs/in 2 ; and f) wherein the binder resists a solvent challenge from water.

27 - 31 . (canceled)

32 . A method of making a collection of matter bound with a polymeric binder comprising:
preparing a solution containing reactants for producing the polymeric binder and a solvent, wherein the reactants include a carbohydrate reactant, an amine base reactant, and an organic acid reactant; disposing the solution onto the collection of matter; volatilizing the solvent to form an uncured product, and subjecting the uncured product to conditions that cause the carbohydrate reactant to react with amine base to polymerize to form the polymeric binder.

33 . The method of claim 32 wherein
the carbohydrate reactant is a monosaccharide, a disaccharide, a polysaccharide, or a reaction product thereof;
the amine base is selected from the group consisting of ammonia, a primary amine, and a secondary amine;
the organic acid is R-Q(═O) m (—OH) n ,
Q is phosphorus (P), m is 1, and n is 2 or Q is sulfur (S), m is 2, and n is 1, and
R is alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heteroalkyl, heteroalkenyl, cycloheteroalkyl, cycloheteroalkenyl, aryl, or arylalkyl, each of which is optionally substituted.

34 . The method of claim 32 , in which the collection of matter is characterized by at least one of the following embodiments:
a) wherein the collection of matter comprises fibers selected from the group consisting of mineral fibers, aramid fibers, ceramic fibers, metal fibers, carbon fibers, polyimide fibers, polyester fibers, rayon fibers, and cellulosic fibers; b) wherein the collection of matter is glass fibers; c) wherein the collection of matter is glass fibers and wherein the glass fibers are present in the range from about 70% to about 99% by weight; d) wherein the collection of matter comprises cellulosic fibers; and e) wherein the collection of matter comprises cellulosic fibers and wherein the cellulosic fibers are selected from the group consisting of wood shavings, sawdust, wood pulp, and ground wood.

35 - 38 . (canceled)

39 . The method of claim 32 , further comprising packaging the uncured product in a packaging material suitable for storage.

40 . The method of claim 32 , wherein the uncured product comprises about 70% to about 90% carbohydrate reactant, about 1% to about 5% amine base reactant, and about 5% to about 25% organic acid reactant.

41 . The method of claim 32 , in which preparing a solution containing reactants is characterized by at least one of the following embodiments:
a) wherein preparing the solution includes adding the carbohydrate reactant, the amine base reactant, and the organic acid reactant to an aqueous solution; and b) wherein preparing the solution includes adjusting the pH of the solution to within the range of about 8 to about 12.

42 . (cancele

Assignees

• Knauf Insulation Inc
• Knauf Insulation Sprl

Inventors

• Mueller Gert R

Classifications

• C08J5/24

  Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs · CPC title

• C08K7/04

  inorganic · CPC title

• C08B37/0009 Primary

  alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof · CPC title

• C08J2305/00

  Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2301/00 or C08J2303/00 · CPC title

• C08J5/249

  characterised by the additives used in the prepolymer mixture · CPC title