US5290747A
Expired / Lapsed
US
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Nylon 6 catalyst system
Assignee: Industrial Technology Research Institute
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Filing: 1992-09-18
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Granted: 1994-03-01
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Expires: 2012-09-18
Abstract
Abstract A catalyst composition for the polymerization of Nylon 6 from caprolactam comprising a primary catalyst which comprises an alkali metal hypophosphite or an alkaliearth metal hypophosphite, and an organic phosphite cocatalyst. The catalyst composition of this invention is most useful when used in conjunction with the reactive extrusion technology which requires a very fast polymerization rate to take full advantage of this evolving technology.
Inventors
- 👤 Wu-Bin Yuo
- 👤 Jeng-Yue Wu
- 👤 Mao-Song Lee
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 11:04
CPC Classifications
B; B01; B01J; B01J31/00; B01J31/02; B01J31/0234; B01J31/0255; B01J31/0257; B01J31/0259; C; C08; C08G; C08G69/00; C08G69/02; C08G69/08; C08G69/14; C08G69/16; C08G69/18; C08G69/20
Claims Analysis
Total Claims: 12
Claim 1
Independent Claim
133 words
A catalyst composition for the preparation of Nylon 6 from caprolactam, said catalyst composition comprising: (a) a primary catalyst selected from the group consisting of alkali metal hypophosphites and alkali earth metal hypophosphites; (b) an organic phosphite cocatalyst selected from either compound I or compound II wherein compound I is represented by the following structure: ##STR3## wherein R 1 , R 2 , and R 3 are selected, independently, from the group consisting of aliphatic and aromatic radicals, and compound II is represented by the following structure: ##STR4## wherein n is an integer from 1 to 10, and R 4 , and R 5 are selected, independently, from the group consisting of aliphatic and aromatic radicals; (c) the ratio between said organic phosphite cocatalyst and said primary catalyst is between 0.002 and 500.
Claim 2
Dependent Claim
133 words
A catalyst composition for the preparation of Nylon 6 from caprolactam, said catalyst composition comprising: (a) a primary catalyst selected from the group consisting of alkali metal hypophosphites and alkali earth metal hypophosphites; (b) an organic phosphite cocatalyst selected from either compound I or compound II wherein compound I is represented by the following structure: ##STR3## wherein R 1 , R 2 , and R 3 are selected, independently, from the group consisting of aliphatic and aromatic radicals, and compound II is represented by the following structure: ##STR4## wherein n is an integer from 1 to 10, and R 4 , and R 5 are selected, independently, from the group consisting of aliphatic and aromatic radicals; (c) the ratio between said organic phosphite cocatalyst and said primary catalyst is between 0.002 and 500.
Claim 3
Dependent Claim
14 words
The catalyst composition of claim 1 wherein said alkali metal hypophosphite is sodium hypophosphite.
Claim 4
Dependent Claim
40 words
The catalyst composition of claim 1 wherein said organic phosphite cocatalyst is represented by the following formula: ##STR5## wherein R 1 , R 2 , and R 3 are, independently, selected from the group consisting of aliphatic or aromatic radicals.
Claim 5
Dependent Claim
15 words
The catalyst composition of claim 3 wherein said aliphatic radicals contain 1 to 24 carbons.
Claim 6
Dependent Claim
15 words
The catalyst composition of claim 3 wherein said aliphatic radicals contain 4 to 18 carbons.
Claim 7
Dependent Claim
85 words
The catalyst composition of claim 3 wherein said organic phosphite cocatalyst is selected from the group consisting of diisodecyl pentaerythritol phosphite, triisodecyl phosphite, triisooctyl phosphite, trilauryl phosphite, tristearyl phosphite, trimethyl phosphite, triethyl phosphite, trinonylphenyl phosphite, tris-(2,4-di-tert-butyl-phenyl) phosphite, tris-(2,4-dimethylphenyl) phosphite, tributyl phosphite, trioctyl phosphite, triisooctyl phosphite, isooctyl diphenyl phosphite, diisooctyl phenyl phosphite, didecyl phenyl phosphite, decyl diphenyl phosphite, didodecyl phenyl phosphite, dodecyl diphenyl phosphite, dodecyl dioctyl phosphite, decyl dioctyl phosphite, di-(2,4-di-tert-butylphenyl) dodecyl phosphite, di-(2,4-di-tert-butylphenyl) octal phosphite, 2,4-di-tert-butyl-phenyl diisooctyl phosphite, dinonylphenyl decyl phosphite and diisodecyl nonylphenyl phosphite.
Claim 8
Dependent Claim
44 words
The catalyst composition of claim 1 wherein said organic phosphite cocatalyst is represented by the following structure: ##STR6## wherein n is an integer from 1 to 10, and R 4 and R 5 are, independently, selected from the group consisting aliphatic and aromatic radicals.
Claim 9
Dependent Claim
15 words
The catalyst composition of claim 7 wherein n is an integer from 1 to 4.
Claim 10
Dependent Claim
15 words
The catalyst composition of claim 7 wherein said aliphatic radicals contain 1 to 24 carbons.
Claim 11
Dependent Claim
15 words
The catalyst composition of claim 7 wherein said aliphatic radicals contain 1 to 18 carbons.
Claim 12
Dependent Claim
104 words
The catalyst composition of claim 7 wherein said organic phosphite cocatalyst is selected from the group consisting of cyclic neopentanetetrayl dioctadecyl ester, phosphorous acid cyclic neopentanetetrayl dioctyl ester, phosphorous acid cylic neopentanetetrayl didecyl ester, phosphorous acid cyclic neopentanetetrayl dihexyl ester, phosphorous acid cyclic neopentanetetrayl bis (2,4-di-tert-butylphenyl) ester, phosphorous acid cyclic neopentanetetrayl bis-(2,4,6-tri-tert-butylphenyl) ester, phosphorous cyclic neopentanetetrayl bis-(2-tert-butylphenyl) ester, phosphorous acid cyclic neopentanetetrayl bis-(2,6-di-tert-butylphenyl) ester, phosphorous acid cyclic neopentanetetrayl octyl 2,6-di-tert-butylphenyl ester, phosphorous acid cyclic neopentanetetrayl decyl 2,6-di-tert-butylphenyl ester, phosphorous cyclic neopentanetetrayl distearyl ester, phosphorous acid cyclic neopentanetetrayl diphenyl ester, phosphorous acid cyclic neopentanetetrayl phenol 2,4-di-tert-butylphenyl ester, and phosphorous acid cyclic neopentanetetrayl phenol decyl ester.
References Cited (Backward Citations)
US4229606A
Cited
DE3633033A1
Cited
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