IP Library Granted Patent US 8,492,565
Granted Patent B2
US 8,492,565 · App. 13/617,457 · Granted Jul 23, 2013

Biphenyltetracarboxylic acid dianhydride and process for producing the same, and polyimide formed from the same and process for producing the same

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Quick Facts
Patent No.
US 8,492,565
App. No.
13/617,457
Granted
Jul 23, 2013
Kind
B2
Abstract

To provide a process for producing BPDA whereby high productivity is attained while high purity is maintained. A process for producing biphenyltetracarboxylic acid dianhydride, which comprises heating biphenyltetracarboxylic acid to produce biphenyltetracarboxylic acid dianhydride, characterized in that the heating is carried out at a pressure of from 1×10 2 Pa to 1.1×10 5 Pa to a maximum temperature in a range of from 210° C. to 250° C. in such a manner that the temperature rising rate is higher than 50° C./hr for a period of at least ¼ of the time for the temperature rise from 60° C. to 210° C., and the temperature is maintained to be from 150° C. to 250° C. for from 0.5 to 10 hours.

Claims (8)

1. A process for producing biphenyltetracarboxylic acid dianhydride, which comprises heating biphenyltetracarboxylic acid to produce biphenyltetracarboxylic acid dianhydride, characterized in that the heating is carried out by means of a heating device which houses a hollow rotary shaft provided with a plurality of hollow rotary heating members and which is designed to feed a heated heating medium to hollow portions of the rotary heating members via a hollow portion of the rotary shaft, and also to a heating jacket provided as the case requires, thereby to supply an amount of heat required for the reaction by heat transfer from each surface of such a rotary shaft, rotary heating members, and, if required, a heating jacket, wherein each of the hollow rotary heating members has a wedge shape as viewed from the side and a fan shape as viewed from the front and is secured at the neck portion of the fan shape to the hollow rotary shaft, and yet, from one end of the heating device, a biphenyltetracarboxylic acid powder as a starting material is continuously supplied, and the powder is heated as it is contacted with the hollow rotary heating members which are rotating and is subjected to a dehydration reaction while it is transferred in an axial direction in the heating device, and biphenyltetracarboxylic acid dianhydride as a product is continuously discharged from the other end of the heating device.

2. The process for producing biphenyltetracarboxylic acid dianhydride according to claim 1 , wherein in the heating device, at least two such hollow rotary shafts are provided in a horizontal direction in parallel to one another; on each rotary shaft, rotary heating members disposed at two positions symmetrical about a point, as viewed from the front, are provided alternately in the axial direction in a predetermined number at equal distances; and the groups of rotary heating members provided on the adjacent rotary shafts take such spatial disposition that they are mutually free from contact with each other during rotation of both rotary shafts.

3. The process for producing biphenyltetracarboxylic acid dianhydride according to claim 2 , wherein the heating device is provided with a heating jacket.

4. The process for producing biphenyltetracarboxylic acid dianhydride according to claim 1 , wherein the heating is carried out at a pressure of from 1×10 2 Pa to 1.1×10 5 Pa at from 150° C. to 250° C.

5. The process for producing biphenyltetracarboxylic acid dianhydride according to claim 1 , wherein the heating is carried out at a maximum temperature in a range of from 210° C. to 250° C.

6. Biphenyltetracarboxylic acid dianhydride obtained by the process for producing biphenyltetracarboxylic acid dianhydride according to any one of claims 1 - 5 .

7. The biphenyltetracarboxylic acid dianhydride according to claim 6 , wherein a total content of biphenyltricarboxylic acid and its anhydride, and biphenytetracarboxylic acid monoanhydride is not more than 0.3 mass %.

8. A polyamide obtained by reacting the biphenyltetracarboxylic acid dianhydride as defined in claim 6 and an aromatic diamine.

Assignments (3)
NUNC PRO TUNC ASSIGNMENT Recorded Aug 3, 2023
From: MITSUBISHI CHEMICAL CORPORATION
To: SHINRYO CORPORATION
Reel/Frame 064477/0154 →
CHANGE OF NAME Recorded Sep 5, 2017
From: MITSUBISHI RAYON CO., LTD.
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 043750/0834 →
MERGER Recorded Sep 4, 2017
From: MITSUBISHI CHEMICAL CORPORATION
To: MITSUBISHI RAYON CO., LTD.
Reel/Frame 043750/0207 →