US2547113A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Production of poly-ester-amides
Assignee: Celanese Corp
•
Filing: 1947-12-02
•
Granted: 1951-04-03
•
Expires: 1967-12-02
Abstract
No abstract record available.
Inventors
- 👤 Drewitt James Gordon Napier
- 👤 Harding Gordon Frank
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 15:50
CPC Classifications
C; C08; C08G; C08G69/00; C08G69/44
Claims Analysis
Total Claims: 2
Claim 1
Independent Claim
184 words
PROCESS FOR THE PRODUCTION OF POLY-ESTERAMIDES BY CONDENSATION OF MORE THAN TWO BIFUNCTIONAL REAGENTS FREE FROM REACTIVE GROUPS OTHER THAN THE TWO FUNCTIONAL GROUPS, INCLUDING 5 TO 50 MOLAR PERCENT OF A SINGLE HIGH-MELTING CONSTITUENT SELECTED FROM THE CLASS CONSISTING OF AROMATIC PRIMARY DIAMINES WHOSE DIACETYL DERIVATIVES DO NOT MELT BELOW 230* C. AND DICARBOXYLIC ACIDS WHOSE DIMETHYL ESTERS DO NOT MELT BELOW 110* C. AND THE AMIDE-FORMING DERIVATIVES OF SUCH ACIDS, THE FUNCTIONAL GROUPS OF SAID REAGENTS BEING MUTUALLY COMPLEMENTARY AND COMPRISING MEMBERS SELECTED FROM EACH OF THE FOLLOWING CLASSES, NAMELY (A) AMINO GROUPS CARRYING HYDROGEN ATOMS, (B) HYDROXY GROUPS AND THEIR ESTER-FORMING DERIVATIVES, AND (C) CARBOXY GROUPS AND THEIR ESTER- AND AMIDE-FORMING DERIVATIVES, COMPRISING FIRST CONDENSING THE REAGENTS OTHER THAN SAID HIGH-MELTING CONSTITUTENT UNTIL THE REACTION MIXTURE FORMED BY MIXING THE LIQUID CONDENSATE WITH THE HIGH-MELTING CONSITITUENT REMAINS HOMOGENEOUS THROUGHOUT SUBSEQUENT CONDENSATION, ADDING THE HIGH-MELTING CONSTITUENT AND COMPLETING THE CONDENSATION, THE CONDENSATION BEING CARRIED OUT SO THAT THE AMINO GROUPS AND THE HYDROXY-GROUPS AND THEIR ESTER-FORMING DERIVATIVES REACT WITH SUBSTANTIALLY EQUIVALENT PROPORTIONS OF THE CARBOXY GROUPS AND THEIR ESTER- AND AMIDE-FORMING DERIVATIVES.
Claim 2
Dependent Claim
184 words
PROCESS FOR THE PRODUCTION OF POLY-ESTERAMIDES BY CONDENSATION OF MORE THAN TWO BIFUNCTIONAL REAGENTS FREE FROM REACTIVE GROUPS OTHER THAN THE TWO FUNCTIONAL GROUPS, INCLUDING 5 TO 50 MOLAR PERCENT OF A SINGLE HIGH-MELTING CONSTITUENT SELECTED FROM THE CLASS CONSISTING OF AROMATIC PRIMARY DIAMINES WHOSE DIACETYL DERIVATIVES DO NOT MELT BELOW 230* C. AND DICARBOXYLIC ACIDS WHOSE DIMETHYL ESTERS DO NOT MELT BELOW 110* C. AND THE AMIDE-FORMING DERIVATIVES OF SUCH ACIDS, THE FUNCTIONAL GROUPS OF SAID REAGENTS BEING MUTUALLY COMPLEMENTARY AND COMPRISING MEMBERS SELECTED FROM EACH OF THE FOLLOWING CLASSES, NAMELY (A) AMINO GROUPS CARRYING HYDROGEN ATOMS, (B) HYDROXY GROUPS AND THEIR ESTER-FORMING DERIVATIVES, AND (C) CARBOXY GROUPS AND THEIR ESTER- AND AMIDE-FORMING DERIVATIVES, COMPRISING FIRST CONDENSING THE REAGENTS OTHER THAN SAID HIGH-MELTING CONSTITUTENT UNTIL THE REACTION MIXTURE FORMED BY MIXING THE LIQUID CONDENSATE WITH THE HIGH-MELTING CONSITITUENT REMAINS HOMOGENEOUS THROUGHOUT SUBSEQUENT CONDENSATION, ADDING THE HIGH-MELTING CONSTITUENT AND COMPLETING THE CONDENSATION, THE CONDENSATION BEING CARRIED OUT SO THAT THE AMINO GROUPS AND THE HYDROXY-GROUPS AND THEIR ESTER-FORMING DERIVATIVES REACT WITH SUBSTANTIALLY EQUIVALENT PROPORTIONS OF THE CARBOXY GROUPS AND THEIR ESTER- AND AMIDE-FORMING DERIVATIVES.
References Cited (Backward Citations)
US2224037A
Cited
US2333639A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1954-04-02 | 1954-10-02 | 1955-04-03 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1958-04-02 | 1958-10-02 | 1959-04-03 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1962-04-02 | 1962-10-02 | 1963-04-03 | $7700.00 | Window Closed / Lapsed |