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Zastosowanie 1,3-arylowych pochodnych 1,3-propanodionu i ich chelatów w technologii polimerów

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Warianty tytułu
EN
The applications of 1.3-aryl derivatives of 1,3-propanedione and their chelates in the polymer technology
Języki publikacji
PL
Abstrakty
PL
Przedstawiono zastosowanie l,3-ary Iowych pochodnych l ,3propanodionu, ich soli i chelatów z metalami w technologii polimerów. Związki te są stosowane gfównie jako specjalistyczne dodatki do tworzyw polimerowych i po-wiok. Szerzej omówiono zastosowanie tych związków jako kostabilizatorów w procesach termicznej.obróbki halogenowanych polimerów.
EN
The applications of 1,3-diaryl derivatives of 1,3-propandione, their salts and chelates with metals in polymer technology were presented. These compounds are used mainly as additives to poiymers and coatings. Their activity as costabilizers in thermal processes of halogenated polymers are discused widely.
Czasopismo
Rocznik
Strony
275--279
Opis fizyczny
Bibliogr. 53 poz.
Twórcy
  • Wydział Chemiczny Politechniki Śląskiej, Gliwice
Bibliografia
  • 1. Drewes R., Friedrich H-H, Mehner H-L, Braun B., Wecht W.: Process for the preparation of linear 1,3-diketones, Ciba-Geigy Corporation, US 5344992 (l994).
  • 2. Drewes R., Friedrich H-H., Mehner H-L., Braun B., Wecht W.: Process for the production of linear 1,3-diketones, Ciba-Geigy AG, EP 0454623 A l (1991).
  • 3. Wallet J. C., Gaydou E. M.: Synth. Commun., 1996, 26 (22), 4097.
  • 4. FuquaS. A., Silverstein R.M.: J. Org. Chem., 1964, 29, 395.
  • 5. Frater G., Huber U.: Process for the purification of 1,3-diketones, Roche Vitamins Inc., US 6844470 B2 (2005).
  • 6. Meixner H., ReutherW, Hahn E., Koenigstein V: Process for the preparation of 1,3-diketones and their use as stabilizers for plastics, Basf Aktiengesellschaft, EP 0697390 Al (1996).
  • 7. Chassaing S., Gay M., Mur G.: Beta-diketones, processes for making beta-diketones and use of beta -diketones as stabilizers for PVC, Rhone-Poulenc Chimie, US 5808165 (1998).
  • 8. Chisolm D., Weiss R., Rozov L.: Process for the preparation of aromatic beta-diketones, Witco Corporation, US 5015777 (1991).
  • 9. Hasegawa E., Ishiyama K., Horaguchi T., Shimazu T., J. Org. Chem., 19991, 56, 1631.
  • 10. Bender J.L., Shen Q-D., Fraser C.L.: Tetrahedron, 2004, 60 (34), 7277.
  • 11. Magnani A., McElvain S.M.: Org. Synth., 2002, 3, 251.
  • 12. Fisch M., Krainer E., Bacaloglu R.: Process for bose-promoted condensation reactions and base reagent therefor, Crompton Corporation, WO 02/055466 (2002).
  • 13. Zorich R.S., Thurmond J.R., Roberts D.A.; Use of water and acidic water to purify liquid MOCVD precursors, Air Products and Chemicals, Inc., US 6534666 B l (2003).
  • 14. Thompson N.J., Goodby J.W, Toyne K.J.: Mol. Cryst. Liq. Cryst. Sci.Technol. Sect. A, 1992,213, 187.
  • 15. Melby L.R., Rose N.J., Abramson E., Caris J.C.: J. Am. Chem. Soc., 1964, 86,5117.
  • 16. Campo J.A., Cano M., Heras J.V., Lagunas M.C., Perles J., Pinilla E., Torres M.R.: Hevl. Chim. Acta, 2001, 84, 2316.
  • 17. Ma B., Gao S., Wang Z., Liao C., Yan C., Xu G.: J. Chem. Crystallography, 1999, 29 (7), 793.
  • 18. Reedy J.D.: Preparation of metal complexes of 1,3-diketones, Union Carbide Corporation, US 3946057 (1976).
  • 19. Ohmori T., Miyahara R., Kakoki H., Namba T.: Skin preparations for external use, Shiseido Company, Ltd., US 6607736 B2 (2003).
  • 20. Wuest H-H., Janssen B.: Aromatic keto compounds, the preparation thereof, and drugs and cosmetics containing these, Basf Aktiengesellschaft, CA2007935 (l989).
  • 21. Kurihara K., Ata M., Miyashita M., Kishii N., Kamei T.: Magnetic recording medium, Sony Corporation, US 5998009 (1999).
  • 22. Juengling S., Schade Ch., Gausepohl H., Warzelhan V., Moors R., Schaech H., Queisser J., Luinstra G.: Polymerization of diene in solvent containing vinyl-aromatic monomer to give rubber for production of e.g. impact polystyrene involves using group 4,5 or 6 transition metal chelate catalyst and Lewis acid cocatalyst, BASF AG, DE 19923579 A l (2000).
  • 23. Williams D.F., Schmitt W.H.: Chemistry and Technology of the Cosmetics and Toiletries Industry, Second Edition, Chapman & Hall, London, 1992.
  • 24. Hori K., Nakamura K., Takaishi N.: Process for preparing 2-carboxydibenzoylmethanes, Kao Corporation, US 4670585 (1987).
  • 25. Virnig M., Fisher G. T., Kordosky G. A.: Process for extraction of metals from aqueous ammoniacal solutions with beta-diketone extractants while maintaining a voltage potential to control entrainment of the aqueous layer into the organic layer, Henkel Corporation, US 6060029 (2000).
  • 26. Ares J.J., Outt P.E., Kakodkar S.V., Buss R.C., Geiger J.C.: J. Org. Chem., 1993,58,7903.
  • 27. Idznsnenko A.V., Dztadznkova N.V: Method for photometric determination of boron in steels, SU 1620936 A l (1991).
  • 28. Bender J.L., Corbin P.S., Fraser C.L., Metcalf D.H., Richardson F.S., Thomas E.L., Urbas A.M.: J. Am. Chem. Soc., 2002, 124, 8526.
  • 29. Wilkes Ch.E., Daniels Ch.A., Summers J.W.: PCV Handbook, Hanser, Munchen, 2005, 329-35.
  • 30. Benavides R., Edge M., Allen N. S., Mellor M., Harvey H., Schmets G.: Polym. Degr. Stab., 1996,53,319.
  • 31. Benavides R., Edge M., Allen N.S., Tellez M.M.: J. Appl. Polym. Sci., 1998, 68, l.
  • 32. Ito M., Numajiri Y., Kimura S., Sekiguchi T.: Anti-yellowing composition, Argus Chemical Corporation, US 4252698 (1981).
  • 33. Chochemore M., Gay M.: Hitzestabilisator fuer homopolymerisate und copolymerisate auf der basis von vinylchloridt Rhone-Poulenc Industries, DE 2600516 A l (1976).
  • 34. Minagawa M., Nakahara Y, Kitsukawa K.: Ortho-substituted phenyl phosphite additive composition, Argus Chemical Corporation, US 4282141 (1981).
  • 35. Gay M., Henrio F.: Composition based on calcium of magnesium acetylacetonate and free or chelated beta-diketones, preparation and use, Rhodia Chimie, US 6455621 B l (2002).
  • 36. Henrio R, Gay M., Mur G.: Composition for chlorine-containing polymer based on beta-diketone and acetylacetonate, Rhone-Poulenc Chimie, US 5714095 (l998).
  • 37. Gay M., Henrio F.: Coated calcium or magnesium acetylacetonate, and its use for stabilizing halogenated polymers, Rhodia Chimie, US 6482887 B l (2002).
  • 38. Layrisse J-L.: Stabiliser compasitions for halogenated polymers containing beta-diketone, hydrotalcite and dihydropyridine, and polymers stabilized therewith., Atochem Elf SA, EP 0362012 (1990).
  • 39. Herbst H., Hoffmann K., Pfaendner R.: Stabilized PVDC-containing PVC, Ciba Specialty Chemicals Corporation, US 5726234 (1998).
  • 40. Shkolnik S., Well E.D.: J. Appl. Polym. Sci.,l998, 69, 1691.
  • 41. Gerlowski L., Kastelic J., Lutz R G.: Blends of polyketone polymers with polyvinyl alcohol, Shell Oil Company, US 4866122 (1989).
  • 42. Schunk T.C., Schroeder K.M., Appell Ch.H., Linehan D.T.: Ultraviolet light filter element, Eastman Kodak Company, US 6872766 B2 (2005).
  • 43. Matsumura K., Yamaya M., Higuchi K.: Coating composition, coating method, and coated article, Shin-Etsu Chemical Co., Ltd., US 6676740 B2 (2004).
  • 44. Wilkey J.D., Diaz Z.: Removal of lithium from polymer cements, Shell Oil Company, US 5767207 (l998).
  • 45. Mase S., Otani N., Yoshida M.: Process for producing plastic lens, Nippon Sheet Glass Co., Ltd., US 5310577 (1994).
  • 46. Gorczynski J.L., Chen J., Fraser C.L: J. Am. Chem. Soc., 2005, 127, 14956.
  • 47. Gray S.D., Coffy T.J., Shamshoum E.S.: Mognesium-diketonate complex derived polyolefin catalysts, method ofmaking same, method of polymerizing with same, Fina technology, Inc., US 6790804 B2 (2004).
  • 49. Marlin L., Schwarz E.: Process for production of a polyurethane foam from a heat curable froth, Union Carbide Corporation, US 3772224 (1973).
  • 50. Oberth A.E., Smith D.G., Bruenner R.S.: Polyurethane propellant formulations and process, Aerojet - General Corporation, US 3291660 (l 966).
  • 51. Rodney F.J.: Polyurethane preparation, Aerojet - General Corporation, US 3231597 (l966).
  • 52. Page L.A.G., Ma S-H., Simms J.A.: Smear resistant pigmented ink jet inks containing beta-diketone or ureido dispersants, E. I. du Pont de Nemours and Company, US 6037390 (2000).
  • 53. Mcgibbon G., Robinson J.E.: Aqueous compositions, Tioxide Specialtes Limited, US 5286774 (1994).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BPP1-0074-0101
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