← Back to Patent Explorer
US4086212A Expired / Lapsed US ⏱️ 0.0 years remaining

Poly(ethylene/alkylene) terephthalates which crystallize rapidly

Assignee: Bayer AG
•
Filing: 1976-02-17
•
Granted: 1978-04-25
•
Expires: 1996-02-17
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract Terephthalic copolyesters, the diol component of which mainly consists of ethylene glycol units, crystallize more rapidly than pure polyethylene terephthalate and can be moulded in a way comparable to polybutylene terephthalate.

Inventors

  • 👤 Peter Bier
  • 👤 Rudolf Binsack
  • 👤 Hugo Vernaleken

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 23:17
CPC Classifications
C; C08; C08G; C08G63/00; C08G63/02; C08G63/12; C08G63/16; C08G63/18; C08G63/181; C08G63/183; C08G63/78

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 152 words
A process for the production of thermoplastic terephthalic acid copolyesters which crystallize more rapidly than polyethylene terephthalate homopolymer comprising (1) esterifying or transesterifying an acid component consisting of (a) at least 90 mol % of terephthalic acid and dimethyl terephthalic acid ester, and (b) up to 10 mol % of other aliphatic and aromatic dicarboxylic acids and acid esters with (2) 1.05 to 2.04 equivalents of a diol component consisting of (a) 90 to 99.5 mol % of ethylene glycol, and (b) 10 to 0.5 mol % of 2,2-diethylpropane-1,3-diol at (3) a temperature of between 150° and 250° C in the presence of esterification or transesterification catalysts, and (4) polycondensing the initial reaction products at a temperature between 200 and 300° under reduced pressure in the presence of an esterification catalyst, wherein the 2,2-diethylpropane-1,3-diol is added to the reaction mixture after substantially all of the acid component has been reacted to di(2-hydroxyethyl)ester.
Claim 2
Dependent Claim 152 words
A process for the production of thermoplastic terephthalic acid copolyesters which crystallize more rapidly than polyethylene terephthalate homopolymer comprising (1) esterifying or transesterifying an acid component consisting of (a) at least 90 mol % of terephthalic acid and dimethyl terephthalic acid ester, and (b) up to 10 mol % of other aliphatic and aromatic dicarboxylic acids and acid esters with (2) 1.05 to 2.04 equivalents of a diol component consisting of (a) 90 to 99.5 mol % of ethylene glycol, and (b) 10 to 0.5 mol % of 2,2-diethylpropane-1,3-diol at (3) a temperature of between 150° and 250° C in the presence of esterification or transesterification catalysts, and (4) polycondensing the initial reaction products at a temperature between 200 and 300° under reduced pressure in the presence of an esterification catalyst, wherein the 2,2-diethylpropane-1,3-diol is added to the reaction mixture after substantially all of the acid component has been reacted to di(2-hydroxyethyl)ester.
Claim 3
Dependent Claim 8 words
The product of the process of claim 1.
Claim 4
Dependent Claim 34 words
The process of claim 1 wherein the 2,2-diethylpropane-1,3-diol is added to the reaction mixture after formation of a polyethylene terephthalate prepolymer with a degree of polymerization greater than 4 but before the polycondensation step.
Claim 5
Dependent Claim 82 words
A highly crystalline unbranched linear thermoplastic terephthalic acid copolyester which crystallizes more rapidly than polyethylene terephthalate homopolymer which consists of (1) an acid component consisting of (a) at least 90 mol % of terephthalic acid and dimethyl terephthalic acid ester and (b) up to 10 mol % of other aliphatic and aromatic dicarboxylic acids and acid esters, and (2) a diol component consisting of (a) 90 to 99.5 mol % of ethylene glycol, and (b) 10 to 0.5 mol % of 1,4-butane-diol.
Claim 6
Dependent Claim 82 words
A highly crystalline unbranched linear thermoplastic terephthalic acid copolyester which crystallizes more rapidly than polyethylene terephthalate homopolymer which consists of (1) an acid component consisting of (a) at least 90 mol % of terephthalic acid and dimethyl terephthalic acid ester and (b) up to 10 mol % of other aliphatic and aromatic dicarboxylic acids and acid esters, and (2) a diol component consisting of (a) 90 to 99.5 mol % of ethylene glycol, and (b) 10 to 0.5 mol % of 1,4-butane-diol.

References Cited (Backward Citations)

GB985936A Cited
GB1118538A Cited
US3714126A Cited
US3592876A Cited
GB1268442A Cited
US3498952A Cited
US3678128A Cited
US3789031A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-04-24 1981-10-24 1982-04-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-04-24 1985-10-24 1986-04-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-04-24 1989-10-24 1990-04-25 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag