Aromatic polyamide-type films

• US 3,966,686 A
• Filed: 12/24/1974
• Issued: 06/29/1976
• Est. Priority Date: 12/28/1973
• Status: Expired due to Term

• Current Assignee: Toray Industries Incorporated
• Original Assignee: Toray Industries Incorporated
• Inventors: Itoga, Masaaki, Hayakawa, Takeshi, Asakura, Toshiyuki, Tanimura, Masamitu
• Primary Examiner(s): Phynes, Lucille M.
• Application Number:
  US05/536,256
• Time in Patent Office: 553 Days
• Field of Search: 260/78 A, 260/857 PA, 260/47 ET, 264/184, 264/212
• US Class Current: 528/331
• CPC Class Codes: C08G 69/46 Post-polymerisation treatment
• CPC Class Codes: G11B 5/73937 Substrates having an organic polymer comprising a ring structure
• CPC Class Codes: Y10S 428/90 Magnetic feature
• CPC Class Codes: Y10T 428/31739 Nylon type

Abstract

Aromatic polyamide-hydrazide films, consisting of p-benzamide p-phenylene terephthalamide and/or terephthaloyl hydrazide recurring units, as major chain constituents, are removed from inorganic residue by an aqueous mixture which dissolves or swells the films, and are heated up to their crystallization temperatures in tension, giving rise to high tensile strength and modulus, good hygroscopic dimensional stability and excellent electrical insulation properties.

Claims

1. An aromatic polyamide-type film, substantially consisting of a member of the group consisting of at least one of p-benzamide, p-phenylene terephthalamide and terephthaloyl hydrazide recurring units as essential chain constituents, which constituents comprise at least about 70 mol % of the entire film, and which have an inherent viscosity of more than 1.0 at 25°

C, a density of more than 1.41 g/cm³ at 25°

C and 0% relative humidity and a planar orientation coefficient of larger than 0.65, obtained by the X-ray pole figure method, said film being substantially free of organic solvent and inorganic ionic compounds, and having been prepared by heating to the polymer crystallization temperatures while preventing free shrinkage in the machine direction and in the transverse direction.

2. Aromatic polyamide-type films of claim 1, which have a density of more than 1.44 g/cm³ at 25°

C and 0% relative humidity.

3. Aromatic polyamide-type films of claim 1, which have a planar orientation coefficient larger than 0.75, obtained by the X-ray pole figure method.

4. Aromatic polyamide-type films of claim 1, which have an ionic inorganic residue of less than 500 ppm, consisting of sulfuric acid, alkali metal halides, alkali metal nitrates, alkali earth metal halides and/or alkali earth metal nitrates.

5. Aromatic polyamide-type films of claim 1, consisting of p-benzamide (A), p-phenylene terephthalamide (PT), and terephthaloyl hydrazide (HT) recurring units whole molar ratio is defined by the area upon and within the area defined by lines connecting the points P, Q, R and S in FIG. 1, where

P:

ht/a/pt = 75/0/25 mol %

Q;

ht/a/pt = 75/25/0

r;

ht/a/pt = 50/50/0

s;

ht/a/pt = 0/0/100

6. aromatic polyamide-type films of claim 1, which have a tensile strength of more than 30 kg/mm², a tensile modulus of greater than 600 kg/mm² both in the machine and transverse direction, a water absorption of less than 3.0% by weight at 25°

C and 75% relative humidity and a hygroscopic linear expansion coefficient of less than 2.0 ×

10^-5 mm/mm/% relative humidity at least in one direction.

7. The method of manufacturing aromatic polyamide-type films, consisting of at least one member selected from the group consisting of p-benzamide, p-phenylene terephthalamide and terephthaloyl hydrazide recurring units as essential chain constituents, which constituents comprise at least about 70 mol % of the entire film, comprising the removal of organic solvents and inorganic compounds from the polymer films, and heating to their crystallization temperatures, while preventing free shrinkage in the machine and in the transverse direction, so that the treated films have a density of more than 1.41 g/cm³ at 25°

C and 0% relative humidity, an inherent viscosity of more than 1.0 at 25°

C and a planar orientation coefficient of more than 0.65, obtained by the X-ray pole figure method.

8. The method of manufacturing aromatic polyamide-type films of claim 7, comprising the removal of organic solvents and inorganic compounds from the polymer films and heating to their crystallization temperatures, while preventing free shrinkage, so that the treated films have a density of more than 1.44 g/cm³ at 25°

C and 0% relative humidity, an inherent viscosity of more than 1.0 at 25°

C and a planar orientation coefficient of more than 0.75, obtained by the X-ray pole figure method.

9. The method of manufacturing aromatic polyamide-type films of claim 7, consisting of p-benzamide (A), p-phenylene terephthalamide (PT) and terephthaloyl hydrazide (HT) recurring units, whose molar ratio is defined by the area on and within the area defined by lines connecting the points P, Q, R and S in FIG. 1, where

P:

ht/a/pt = 75/0/25 mol %

Q;

ht/a/pt = 75/25/0

r;

ht/a/pt = 50/50/0

s;

ht/a/pt = 0/0/100

10. the method of manufacturing aromatic polyamide-type films of claim 7, comprising the heating of films, removed of inorganic compounds, within the range enclosed by the following equations:

space="preserve" listing-type="equation">1/T = 1.3 ×

10.sup.-.sup.3

space="preserve" listing-type="equation">1/t = 1.75 ×

10.sup.-.sup.3 ##EQU3## where T and t are absolute temperature (°

K) and time period (min).

11. The method of manufacturing aromatic polyamide-type films of claim 7, comprising the evaporation of an organic solvent from the cast film until the attainment of self-supporting of the film, wherein the solvent content is more than 50% based on the weight of net polymer, and the removal of inorganic compounds from the polymer films by extracting at 40°

to 80°

C with an aqueous mixture containing an organic solvent by 10 to 70%, based on the total weight of the mixture, which can dissolve or swell the said films.