Claims
- 1. A process for the preparation of polyimides or their polypeptide hydrolysates which are at least 80% biodegradable, by thermal polycondensation of at least one amino acid, optionally followed by hydrolysis, the process comprising carrying out the thermal polycondensation step in the presence of at least one "acid catalyst" selected from the group consisting of
- a) sulfuric, nitric, phosphorus, sulfurous, hydrofluoric, silicic and sulphonic acids, organic sulphonic acids, containing less than 50 carbon atoms, amino acids bearing a non-carboxyl strong acid function, organic phosphonic acids, organic carboxylic acids having a pK.sub.a lower than or equal to 5;
- b) precursors of these acids;
- c) salts of the acids of step a)with an amino acid which is similar to or different from that or those used;
- d) salts of the acids of step a) with a polyimide derived from the polycondensation of at least one amino acid which is similar to or different from that or those used;
- e) hydrochloric acid and its precursors
- f) hydrochloric acid salts of an amino acid which is similar to or different from that or those used, when the amino acid to be polycondensed is other than glutamic acid;
- g) hydrochloric acid salts of a polyimide derived from the polycondensation of at least one amino acid which is similar to or different from that or those used;
- h) acid salts of sulfuric, phosphoric or phosphorous acids or their precursors;
- i) phosphoric acid precursors other than phosphoric anhydride or polyphosphoric acids; and
- j) Lewis acids;
- according to an "acid catalyst"/amino acid molar ratio of at least 0.001; said thermal polycondensation operation being carried out in bulk, with a reaction medium remaining in the pulverulent or friable form throughout the whole of the polycondensation operation, in which reaction medium the "acid catalyst" is distributed homogeneously.
- 2. A process according to claim 1, wherein the "acid catalyst" is
- a) methanesulphonic, benzenesulphonic, trifluoromethanesulphonic, dodecylbenzenesulphonic, para-toulenesulphonic or cysteic acid;
- b) anhydrous or hydrated sulfuric acid, oleum, acid sulfates of potassium, lithium, sodium or quaternary ammonium, SO.sub.3 ;
- c) ammonium sulfate;
- d) neutral alkali metal sulfate/sulfuric acid or neutral alkali metal or alkaline-earth metal sulfate/phosphoric or pyrophosphoric acid mixtures, according to an acid/neutral salt molar ratio of the order of 0.5/1 to 10/1;
- e) hydrogen phosphate of potassium, sodium, lithium or quaternary ammonium;
- f) HCl, PCl.sub.3, PCl.sub.5, POCl.sub.3, cyanuric chloride;
- g) SiCl.sub.4, CH.sub.3 SiCl.sub.3 ;
- h) salicylic acid, chloroacetic acids, and the like;
- i) phosphomethylglycine, ethylphosphonic acid;
- j) aspartic acid hydrochloride, salts of aspartic acid with sulfuric, methanesulphonic and para-toulenesulphonic acids;
- k) polyanhydroaspartic acid hydrochloride; and
- l) AlCl.sub.3, BF.sub.3, ZnCl.sub.2.
- 3. A process according to claim 1, wherein the amino acid used is aspartic acid or glutamic acid taken alone or mixed together or with another amino acid.
- 4. A process according to claim 1, wherein the thermal polycondensation operation is carried out at a temperature of the order of 100.degree. to 250.degree. C.
- 5. A process according to claim 1, wherein the thermal polycondensation operation is carried out in bulk or in a solvent medium.
- 6. A process according to claim 1, wherein an acid salt of an amino acid salt is used as sole constituent of the reaction in place of an amino acid/"acid catalyst" mixture.
- 7. A process according to claim 1 further characterized in that the "acid catalyst" is distributed homogeneously in the reaction medium by a step selected from the group consisting of
- a) forming a paste of a mixture of amino acid and of solid or liquid "acid catalyst" with water or other volatile liquid diluent by evaporation under vacuum or at atmospheric pressure and then grinding the mass obtained;
- b) dissolving the amino acid and solid or liquid "acid catalyst" in water or other dissolver of the amino acid and of the catalyst and then atomizing the solution;
- c) atomizing a suspension of amino acid in a solution of solid or liquid "acid catalyst" in water or other dissolver of the catalyst;
- d) evaporating a solution of solid or liquid "acid catalyst" in water or other dissolver of the catalyst on a fluidized bed of amino acid; and
- e) cogrinding or micronizing a mixture of amino acid and solid "acid catalyst".
- 8. A process according to claim 1 wherein the "acid catalyst"/amino acid molar ration is of the order of 0.001 to 0.15, when the "acid catalyst" consists of an acid salt or of an acid salt precursor, and of the order of 0.001 to 0.05, when the "acid catalyst" is other than an acid salt or an acid salt precursor.
- 9. A process according to claim 1, wherein the polyimide obtained by thermal condensation is hydrolyzed to a polypeptidic salt by addition of a basic agent, the said salt optionally being subsequently neutralized to a polypeptidic acid by addition of an inorganic or organic acid.
- 10. An aqueous detergent solution containing a detergent composition comprising a polyimide which has a charge density COO.sup.- ranging from 0 to 5.times.10.sup.-4 mol/g of polymer and which is capable of acquiring in the aqueous solution a charge density COO.sup.- at least equal to 10.sup.-3 mol/g of polymer or a polypeptide hydrolysate of the said polyimide, said polyimide or its polypeptide hydrolysate being obtained according to the process which forms the subject of claim 1.
- 11. An aqueous detergent solution according to claim 10, wherein the polyimide or its polypeptide hydrolysate represents of the order of 0.2 to 80%, of the weight of the said detergent solution.
- 12. A detergent composition containing the polyimides or their polypeptide hydrolysate obtained according to the process of claim 1.
- 13. A process according to claim 1, wherein said organic sulphonic acids contain less than 25 carbons.
- 14. A process according to claim 1, wherein said organic carboxylic acid of step a) has a pK.sub.a lower than or equal to 3.
- 15. A process according to claim 1, wherein the "acid catalyst"/amino acid molar ratio is of the order of 0.005 to 10.
- 16. A process according to claim 1, wherein the "acid catalyst"/amino acid molar ration is of the order of 0.01 to 5.
- 17. A process according to claim 2, wherein the acid neutral salt molar ratio is of the order of 1/1 to 3/1.
- 18. A process according to claim 8, wherein said "acid catalyst"/amino acid molar ration is of the order of 0.005 to 0.15 when the "acid catalyst" consists of an acid salt or of an acid salt precursor.
- 19. A process according to claim 8, wherein said "acid catalyst"/amino acid molar ratio is of the order of 0.005 to 0.05 when the "acid catalyst" is other than an acid salt or an acid salt precursor.
- 20. An aqueous detergent solution according to claim 11 wherein the polyimide or its polypeptide hydrolysate represents of the order of 2 to 50%.
Priority Claims (2)
Number |
Date |
Country |
Kind |
93 14042 |
Nov 1993 |
FRX |
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93 14043 |
Nov 1993 |
FRX |
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Parent Case Info
This application is a continuation of application Ser. No. 08/342,943 filed Nov. 21, 1994, which application is now abandoned.
US Referenced Citations (5)
Foreign Referenced Citations (7)
Number |
Date |
Country |
2059475 |
Jul 1970 |
FRX |
0130935A1 |
Apr 1984 |
FRX |
WO8703891 |
Jul 1987 |
FRX |
0454126A1 |
Apr 1991 |
FRX |
0511037A1 |
Mar 1992 |
FRX |
2461350 |
Dec 1971 |
DEX |
2246786 |
Feb 1992 |
GBX |
Non-Patent Literature Citations (3)
Entry |
Journal of Medicinal Chemistry (Neri et al.), vol. 18, No. 8, pp. 893-897, Aug. 1973. |
French Preliminary Search Report #FR9314043. |
French Preliminary Search Report #FR9314042. |
Continuations (1)
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Number |
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Parent |
342943 |
Nov 1994 |
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