참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Terephthaloyl chloride | HCID 7488 | — |
| 반응물 | P-Phenylenediamine | HCID 7814 | — |
| 반응물 | 4-Aminobenzoic acid hydrazide | HCID 21450 | — |
| 반응물 | Benzoyl chloride, 4-amino- | HCID 177720 | — |
| 반응물 | 4-(Hydrazinocarbonyl)benzoic acid | HCID 279437 | — |
| 생성물 | Terephthalohydrazide | HCID 67294 | — |
반응 단계
Terephthalic acid hydrazide, p-aminobenzoic acid hydrazide, p-phenylenediamine, p-aminobenzoyl chloride and terephthaloyl chloride are properly combined, and a 5 wt% solution of polyamide resin comprising 33 mol% of terephthalhydrazide, 33 mol% of p-benzamide, and 33 mol% of p-phenyleneterephthalamide is obtained by low temperature (about 10° to 35° C.) solution polymerization process. The solvent used for the solution polymerization is preferably dimethylacetamide and calcium chloride is contained in the polymerization solution as a neutralization product. This solution is cast on a metallic belt and dried until the polymer concentration becomes about 30 wt% by heating at about 100° C. for 5 minutes. The film is then dipped for about 2 minutes in water at normal temperatures (about 10° to 35° C.) to remove the solvent and calcium chloride. After further washing with water and drying at 230° C., the resulting film is rolled up. Orientation is conducted by stretching the dried film in the longitudinal direction in a 50° C. dimethylacetamide aqueous solution through the difference in rotating speeds of associated nip rolls, and subsequently stretching it in a lateral direction by guiding it to a tenter and expanding the rail distance. The draw ratio is generally kept from about 1.1 to 2.0 times in both longitudinal and lateral directions. Thus, a 3 μm thick aromatic polyamide film is obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04308311 |
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| 출처 데이터셋 | uspto-grants-1981_12 |
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| ORD ID | ord-58a6422fa5a4409583e0e1c213ba6bfc |
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| 출처 메모 | uspto-grants-1981_12 |
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