Asgpr-binding compounds for the degradation of extracellular proteins
US-2024424108-A1 · Dec 26, 2024 · US
US2024391943A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024391943-A1 |
| Application number | US-202418793921-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 4, 2024 |
| Priority date | May 7, 2010 |
| Publication date | Nov 28, 2024 |
| Grant date | — |
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A binder comprising a polymeric binder comprising the products of a carbohydrate reactant and nucleophile 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 a nucleophile 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 reactant and polyamine based binder.
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1 .- 49 . (canceled) 50 . 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 and a nucleophile wherein (a) the nucleophile is R 1 -Q-R 2 , (b) Q is alkyl, cycloalkyl, heteroalkyl, or cycloheteroalkyl, each of which is optionally substituted having a nucleophilic moiety and a stabilization moiety, (c) R 1 is selected from the group consisting of an amine, an azide, a cyanate, an isocyanate, a thiol, a disulfide, a thiocyanate, a halogen, a haloformyl, a carboxyl, a carboxylate, a hydroxyl, and an alkoxide, and (d) R 2 is selected from the group consisting of an amine, an amide, an imine, an imide, a nitro, a nitrate, a pyridine, a phosphate, a phosphono, a hydroxyl, a hydrogen, a sulphono, a sulpho, a sulfinyl, and a sulfhydryl; disposing the solution onto the collection of matter; volatilizing the solvent to form an uncured product, and curing the uncured product to form the polymeric binder. 51 . The method of claim 50 , wherein the collection of matter includes 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. 52 . The method of claim 50 , wherein the collection of matter is glass fibers. 53 . The method of claim 50 , wherein the glass fibers are present in the range from about 70% to about 99% by weight. 54 . The method of claim 50 , wherein the collection of matter comprises cellulosic fibers. 55 . The method of claim 54 , wherein the cellulosic fibers are substrate selected from the group consisting of wood shavings, sawdust, wood pulp, and ground wood. 56 . The method of claim 50 , further comprising packaging the uncured product in a packaging material suitable for storage. 57 . The method of claim 50 , wherein preparing the solution includes adding an amount of the carbohydrate reactant and an amount of the nucleophile so a weight ratio is in the range of about 2:1 to about 10:1. 58 . The method of claim 50 , wherein preparing the solution includes adding the carbohydrate reactant and the nucleophile to an aqueous solution. 59 . The method of claim 58 , wherein preparing the solution includes adjusting the pH of the solution to within the range of about 8 to about 12. 60 . The method of claim 50 , wherein the method has at least one of the following features: the carbohydrate reactant is a polysaccharide; the carbohydrate reactant is a monosaccharide or a disaccharide; the carbohydrate reactant is a monosaccharide in its aldose or ketose form; the carbohydrate reactant is selected from the group consisting of dextrose, xylose, fructose, dihydroxyacetone, and mixtures thereof. 61 . The method of claim 50 , wherein the method has at least one of the following features: Q is an alkyl selected from the group consisting of C 2 -C 24 ; Q is an alkyl selected from the group consisting of C 2 -C 8 ; Q is an alkyl selected from the group consisting of C 3 -C 7 ; Q is a C 6 alkyl; Q is selected from the group consisting of a cyclohexyl, cyclopentyl or cyclobutyl; Q is a benzyl. 62 . The method of claim 50 , wherein a mole ratio of the carbohydrate reactant to the nucleophile is in the range of about 1:1 to about 30:1. 63 . The method of claim 50 , wherein a mole ratio of the carbohydrate reactant to the nucleophile is in the range of about 2:1 to about 10:1. 64 . The method of claim 50 , wherein R 1 and R 2 form covalent bonds with the carbohydrate reactant to form the polymeric product. 65 . The method of claim 50 , wherein the polymeric product is phenol-free and formaldehyde-free. 66 . A composition comprising a collection of matter and a binder, the binder comprising polymeric products of a reaction between a carbohydrate reactant and a nucleophile, the polymeric products being substantially water insoluble.
applied as a solution using water as the only solvent, e.g. in the presence of acid or alkaline compounds · CPC title
Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 (with polynitriles C08G69/38) · CPC title
Non-macromolecular compounds · CPC title
Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 · CPC title
Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen (aminophenols C08G8/16) · CPC title
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