Claims
- 1. A process for the preparation of a 4,4'-diisocyanato dicyclohexylmethane containing at least 90% by weight of the trans,trans-isomer comprising:
- (a) melting a mixture of 4,4'-diisocyanato dicyclohexylmethane isomers containing at least 30% by weight of the trans,trans-isomer,
- (b) cooling the melted mixture to a temperature of from about 0.degree. to about 25.degree. C. to form:
- (1) a liquid phase which contains from about 12 to about 25% by weight of the trans,trans-isomer, and
- (2) a solid phase which contains from about 70 to about 85% by weight of the trans,trans-isomer,
- (c) removing said liquid phase,
- (d) heating said solid phase to a temperature of from about 60.degree. to about 83.degree. C. and removing that portion of said solid phase which has melted, with the melted material containing from about 35 to about 65% by weight, of the trans,trans-isomer, and
- (e) recovering that portion of said solid phase which has not melted by heating the said remaining portion to a temperature of at least about 90.degree. C. with the resultant product containing at least about 90% by weight of the trans,trans-isomer.
- 2. The process of claim 1, wherein the mixture of step (a) contains from 45 to 55% by weight of the trans,trans-isomer.
- 3. The process of claim 1, wherein the melted mixture removed in step (d) contains from 45 to 55% by weight of the trans,trans-isomer.
- 4. The process of claim 1, wherein the product recovered in step (e) contains at least 94% by weight of the trans,trans-isomer.
- 5. The process of claim 1, wherein the melted material of step (d) is returned to step (a).
- 6. A process for the preparation of a 4,4'-diisocyanato dicyclohexylmethane containing at least 90% by weight of the trans,trans-isomer comprising:
- (a) melting a mixture of 4,4'-diisocyanato dicyclohexylmethane isomers containing at least 30% by weight of the trans,trans-isomer,
- (b) cooling the melted mixture to a temperature of from about 40.degree. to about 45.degree. C. for a period of time sufficient to allow crystallization to occur, and then subsequently cooling to a temperature of from about 0.degree. to about 25.degree. C. to form:
- (1) a liquid phase which contains from about 12 to about 25% by weight of the trans,trans-isomer, and
- (2) a solid phase which contains from about 70 to about 85% by weight of the trans,trans-isomer,
- (c) removing said liquid phase,
- (d1) heating said solid phase to a temperature of from about 65.degree. to about 70.degree. C.,
- (d2) removing that portion of said solid phase which has melted, and
- (e) recovering that portion of said solid phase which has not melted during step (d2) by heating the said remaining portion to a temperature of about 100.degree. C. with the resultant product containing at least about 90% by weight of the trans,trans-isomer.
- 7. The process of claim 6, wherein the mixture of step (a) contains from 45 to 55% by weight of the trans,trans-isomer.
- 8. The process of claim 6, wherein the product recovered in step (e) contains at least 94% by weight of the trans,trans-isomer.
- 9. The process of claim 6, wherein the liquid phase of step (c) and the melted product removed during step (d2) are combined to make a liquid product.
CROSS REFERENCE TO RELATED APPLICATION
This application is a continuation of U.S. application Ser. No. 07/654,862 filed on Feb. 13, 1991, which is a continuation-in-part of U.S. application Ser. No. 07/513,698, filed on Apr. 24, 1990, both applications, now abandoned.
US Referenced Citations (7)
Foreign Referenced Citations (3)
Number |
Date |
Country |
961049 |
Jan 1975 |
CAX |
971184 |
Jul 1975 |
CAX |
1220715 |
Jan 1971 |
GBX |
Non-Patent Literature Citations (2)
Entry |
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Wong et al., Advances In Urethane Science and Tech., vol. 19, (1984), pp. 77-101. |
Continuations (1)
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Date |
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Parent |
654862 |
Feb 1991 |
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Continuation in Parts (1)
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513698 |
Apr 1990 |
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