Method for modifying polysaccharide material by sequenced homogeneous chemical functionalisation
US-2023331873-A1 · Oct 19, 2023 · US
US10030078B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10030078-B2 |
| Application number | US-201615046500-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 18, 2016 |
| Priority date | Feb 24, 2015 |
| Publication date | Jul 24, 2018 |
| Grant date | Jul 24, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Processes for making reduced molecular weight ethersuccinylated polysaccharides, for example ethersuccinylated starches are provided.
Opening claim text (preview).
What is claimed is: 1. A process for reducing the molecular weight of an ethersuccinylated polysaccharide derived from an unmodified polysaccharide comprising native corn starch wherein the process comprises the step of reacting an ethersuccinylated polysaccharide with an acid to achieve a pH of the reaction mixture of from about 2 to about 6; and the step of reacting the unmodified polysaccharide with an α, β-unsaturated dicarboxylic acid or salt thereof to produce an ethersuccinylated polysaccharide comprising an ethersuccinate moiety having the formula: wherein R 1 , R 2 and R 3 are independently selected from H, branched or linear C 1 -C 4 alkyl and mixtures thereof; R 4 is (CH 2 ) y ; M is independently selected from H, cations and mixtures thereof; x is greater than 0 but less than or equal to 1; y is 0 or 1; under conditions such that at least a partially protonated reduced molecular weight ethersuccinylated polysaccharide is obtained. 2. The process according to claim 1 wherein the pH of the reaction mixture is from about 2.5 to about 6. 3. The process according to claim 1 wherein the acid comprises an acid that is capable of forming a water-soluble salt within the reaction mixture. 4. The process according to claim 3 wherein the water-soluble salt comprises a cation selected from the group consisting of: calcium, sodium, ammonium, and mixtures thereof. 5. The process according to claim 1 wherein the acid is selected from the group consisting of: hydrochloric acid, acetic acid, maleic acid, carbonic acid, nitric acid, and mixtures thereof. 6. The process according to claim 1 wherein the reaction occurs at a temperature of from about 30° C. to about 170° C. 7. The process according to claim 1 wherein the at least partially protonated reduced molecular weight ethersuccinylated polysaccharide exhibits a weight average molecular weight of less than 12,000,000 g/mol as measured according to the Molecular Weight Test Method. 8. The process according to claim 1 wherein the at least partially protonated reduced molecular weight ethersuccinylated polysaccharide exhibits a polydispersity of less than 6 as measured according to the Molecular Weight Test Method. 9. The process according to claim 1 wherein the α, β-unsaturated dicarboxylic acid or salts thereof comprises an alkene dicarboxylic acid or salt thereof. 10. The process according to claim 9 wherein the alkene dicarboxylic acid is selected from the group consisting of: maleic acid, itaconic acid, citraconic acid and mixtures thereof. 11. The process according to claim 1 wherein the step of reacting the unmodified polysaccharide with an α, β-unsaturated dicarboxylic acid or salt thereof occurs in the presence of an alkaline earth metal salt. 12. The process according to claim 11 wherein the alkaline earth metal salt comprises Ca(OH) 2 . 13. The process according to claim 11 wherein the ratio of the mmoles of excess alkaline earth metal salt per gram of unmodified polysaccharide is 0.3 mmol/g or greater. 14. The process according to claim 13 wherein the ratio is from about 0.3 to about 0.7 mmol/g. 15. The process according to claim 1 wherein the unmodified polysaccharide is selected from the group consisting of: starch, chitosan, cellulose, and mixtures thereof. 16. The process according to claim 1 wherein the ethersuccinylated polysaccharide comprises ethersuccinylated starch. 17. The process according to claim 1 wherein the reduced molecular weight ethersuccinylated polysaccharide comprises reduced molecular weight ethersuccinylated starch.
Recycling of unreacted starting or intermediate materials · CPC title
Ether-esters · CPC title
Chitin, i.e. 2-acetamido-2-deoxy-(beta-1,4)-D-glucan or N-acetyl-beta-1,4-D-glucosamine; Chitosan, i.e. deacetylated product of chitin or (beta-1,4)-D-glucosamine; Derivatives thereof · CPC title
Preparation of cellulose ether-esters · CPC title
Alkyl or cycloalkyl ethers · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.