Semiconductor substrate treatment liquid, treatment method, and method for manufacturing semiconductor-substrate product using these
US-2016254139-A1 · Sep 1, 2016 · US
US10370620B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10370620-B2 |
| Application number | US-201615757469-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 5, 2016 |
| Priority date | Sep 8, 2015 |
| Publication date | Aug 6, 2019 |
| Grant date | Aug 6, 2019 |
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.
Provided herein is a method for producing polyaspartic acid under reflux cooling. Further provided herein are compositions including polyaspartic acid obtainable through the method. Also provided herein is a use of polyaspartic acids obtainable through the method in dishwashing agents, detergents, and cleaning agents.
Opening claim text (preview).
The invention claimed is: 1. A method for producing polyaspartic acid, the method comprising: (a) contacting a mixture of: (i) aspartic acid, and (ii) 1 to 25 mol % of an acidic catalyst; in a reactor; (b) heating the mixture according to (a) under reflux cooling without distillative removal of water at a reaction temperature of 100 to 220° C. up to a degree of conversion of the aspartic acid of at least 1%; (c) polycondensing the reaction mixture according to (b) with simultaneous distillative removal of water at 170 to 250° C. to produce polycondensates; and (d) hydrolyzing the polycondensates according to (c) with addition of a base. 2. The method according to claim 1 , wherein contacting the mixture according to (a) comprises adding 3 to 15 mol % of the acidic catalyst. 3. The method according to claim 1 , wherein the acidic catalyst is methanesulfonic acid. 4. The method according to claim 1 , wherein the polycondensing (c) is carried out at 200 to 250° C. 5. The method according to claim 1 , wherein the base is selected from the group consisting of aqueous sodium hydroxide solution, aqueous potassium hydroxide solution, calcium hydroxide, barium hydroxide, sodium carbonate, potassium carbonate, ammonia, and ammonium hydroxide. 6. The method according to claim 1 , wherein the degree of conversion of the aspartic acid during the heating (b) is at least 5%. 7. The method according to claim 1 , wherein the temperature of the heating (b) is 160 to 180° C. 8. The method according to claim 1 , wherein the contacting (a) further comprises adding water to the mixture. 9. The method according to claim 1 further comprising: (e) acidifying salts of polyaspartic acid obtained by the hydrolyzing (d). 10. The method according to claim 9 , wherein the acidifying (e) is carried out with a mineral acid or an acidic ion exchanger.
Polyamides or polyimides · CPC title
Polysuccinimides · CPC title
Preparatory processes · CPC title
Alpha-amino-carboxylic acids {(polysuccinimides C08G73/1092)} · CPC title
Amino carboxylic acids · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.