Integrated process for the preparation of compounds useful as fuel components
US-2015376523-A1 · Dec 31, 2015 · US
US9969704B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9969704-B2 |
| Application number | US-201415302368-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 19, 2014 |
| Priority date | Apr 10, 2014 |
| Publication date | May 15, 2018 |
| Grant date | May 15, 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.
A process for preparing materials derived from sugar alcohols such that the dehydration products exhibit better accountability and improved color to water-clear or near water-white appearance is described. In particular, the process involves employing a reducing Brnsted acid (e.g., phosphonic acid) for the catalysis of sugar alcohols to their corresponding dehydrated-cyclized products.
Opening claim text (preview).
We claim: 1. A method for preparing isosorbide from sorbitol, comprising: dehydrating sorbitol with a phosphonic acid catalyst at elevated temperatures to produce a product mixture including isosorbide and sorbitans, then recovering isosorbide from the product mixture. 2. The method according to claim 1 , wherein isosorbide is recovered from the product mixture by at least a means selected from the group consisting of chromatography, crystallization, and distillation. 3. The method according to claim 1 , wherein said phosphonic acid is present at a catalyst load of about 1 mol. % to about 20 mol. % relative to a concentration of sorbitol. 4. The method according to claim 3 , wherein said phosphonic acid is at a catalyst load of about 2 mol. % to about 15 mol. % relative to a concentration of sorbitol. 5. The method according to claim 1 , wherein said reaction temperature is in a range from about 100° C. up to about 160° C. 6. The method according to claim 1 , wherein is produced as the primary product and 1,4-sorbitan is the next most favored product. 7. The method according to claim 1 , wherein said the reaction time is up to about 3 hours. 8. The method according to claim 1 , wherein said reaction is at an operating pressure of about 5 torr to about 100 torr. 9. The method according to claim 1 , wherein said reaction is at an operating pressure of about 10 torr to about 30 torr.
Catalysts of the Raney type · CPC title
Food compositions, function of food ingredients or processes for food or foodstuffs · CPC title
Tetrahydroxylic alcohols, e.g. pentaerythritol · CPC title
Ortho-condensed systems · CPC title
Hexahydroxylic alcohols · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.