Method for producing bisphenol-A
View Patent ↗Provided is a process for producing a bisphenol A by continuously feeding phenol and acetone into a reactor unit having at least two reaction zones connected in series. In the process, an acidic cation-exchange resin partially neutralized with a sulfur-containing nitrogen compound in from 15 to 50% of the acid site thereof is used as the catalyst, and acetone having a methanol concentration of at most 3,000 ppm is separately fed into at least two reaction zones in the reactor unit. The life of the acidic cation-exchange resin catalyst used in the process is prolonged.
1. A process for producing a bisphenol A by continuously feeding phenol and acetone into a reactor unit having at least two reaction zones connected in series, which is characterized in that an acidic cation-exchange resin partially neutralized with a sulfur-containing nitrogen compound in from 15 to 50% of the acid site thereof is used as the catalyst, and acetone having a methanol concentration of from 1,000 to 3,000 ppm is separately fed into at least two reaction zones in the reactor unit.
2. The process for producing bisphenol A as claimed in claim 1 , wherein the ratio (by mol) of phenol/all acetone falls between 6 and 13.
3. The process for producing bisphenol A as claimed in claim 1 , wherein the sulfur-containing nitrogen compound is at least one selected from pyridinealkanethiols, pyridylalkanethioacetals, aminoalkanethiols and thiazolidines.
4. The process for producing bisphenol A as claimed in claim 1 , wherein the reaction temperature falls between 60 and 100° C.
5. The process for producing bisphenol A as claimed in claim 1 , wherein from 30 to 50% of all acetone to be fed into the reactor unit is fed into the first reaction zone.
6. The process for producing bisphenol A as claimed in claim 1 , wherein the liquid hourly space velocity (LHSV) in each reaction zone falls between 0.2 and 30 hr −1 .
7. The process for producing bisphenol A as claimed in claim 1 , wherein the acidic cation-exchange resin catalyst is a sulfonic acid cation-exchange resin.
8. The process for producing bisphenol A as claimed in claim 1 , wherein the acidic cation-exchange resin is selected from the group consisting of a sulfonated styrene-divinylbenzene copolymer, a sulfonated crosslinked styrene polymer, a phenol-formaldehyde-sulfonic acid resin, a benzene-formaldehyde-sulfonic acid resin, and mixtures thereof.
9. The process as claimed in claim 1 , wherein the acidic cation-exchange resin is partially neutralized with a sulfur-containing nitrogen compound in from 20 to 50% of the acid sites.
10. The process for producing bisphenol A as claimed in claim 1 , wherein the sulfur-containing nitrogen compound is 2,2-diniethylthia zolidine.
11. A process for producing bisphenol A, comprising:
continuously feeding phenol and acetone into a reactor unit having at least two reaction zones connected in series, and
reacting the acetone and the phenol in the presence of an acidic cation-exchange resin,
wherein the cation-exchange resin is partially neutralized with a sulfur-containing nitrogen compound present in from 15 to 50% of the acid sites of the cation-exchange resin, and acetone having a methanol concentration of from 1,000 to 3,000 ppm is separately fed into at least two reaction zones in the reactor unit.
12. The process as claimed in claim 11 , wherein the molar ratio of phenol:(all acetone) is from 6 to 13.
13. The process as claimed in claim 11 , wherein the sulfur-containing nitrogen compound is at least one selected from the group consisting of a pyridinealkanethiol, a pyridylalkane thioacetal, an aminoalkanethiol and a thiazolidine.
14. The process as claimed in claim 11 , wherein the reacting is carried out at a temperature of from 60 to 100° C.
15. The process as claimed in claim 11 , wherein from 30 to 50% f the total amount of acetone fed into the reactor unit is fed into a first reaction zone.
16. The process as claimed in claim 11 , wherein the liquid hourly space velocity in each reaction zone is from 0.2 to 30 hr −1 .
17. The process as claimed in claim 11 , wherein the acidic cation-exchange resin catalyst is a sulfonic acid cation-exchange resin.
18. The process as claimed in claim 11 , wherein the acidic cation-exchange resin is selected from the group consisting of a sulfonated styrene-divinylbenzene copolymer, a sulfonated crosslinked styrene polymer, a phenol-formaldehyde-sulfonic acid resin, a benzene-formaldehyde-sulfonic acid resin, and mixtures thereof.
19. The process as claimed in claim 11 , wherein the acid cation-exchange resin is partially neutralized with a sulfur-containing nitrogen compound in from 20 to 50% of the acid sites.
20. The process as claimed in claim 11 , wherein the sulfur-containing nitrogen compound is 2,2-dimethylthiazolidine.