Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Processes of preparing a desired or intentional composition...
Reexamination Certificate
2005-12-20
2005-12-20
Harlan, Robert D. (Department: 1713)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Processes of preparing a desired or intentional composition...
C524S038000, C524S039000, C524S040000, C524S041000, C524S042000, C524S043000, C524S050000
Reexamination Certificate
active
06977275
ABSTRACT:
The invention relates to methods of making carbohydrate and polyol esters suitable for use as plasticizers for polymer compositions. The invention also relates to plasticized polymer compositions comprising such carbohydrate and polyol esters. The invention also relates to articles prepared from such plasticized polymer compositions. The invention further relates to methods of using these compositions.
REFERENCES:
patent: 1683347 (1928-09-01), Gray et al.
patent: 1698049 (1929-01-01), Clarke et al.
patent: 1880560 (1932-10-01), Webber et al.
patent: 1880808 (1932-10-01), Clarke et al.
patent: 1984147 (1934-12-01), Malm
patent: 2129052 (1938-09-01), Fordyce
patent: 2687970 (1954-08-01), Brander et al.
patent: 2857378 (1958-10-01), Hales et al.
patent: 3518249 (1970-06-01), Hiatt et al.
patent: 3617201 (1971-11-01), Beral et al.
patent: 3781381 (1973-12-01), Koleske et al.
patent: 4195112 (1980-03-01), Sheard et al.
patent: 4474846 (1984-10-01), Doerer et al.
patent: 4568581 (1986-02-01), Peoples, Jr.
patent: 4675393 (1987-06-01), Coxon
patent: 4731122 (1988-03-01), Cortese et al.
patent: 5205863 (1993-04-01), Elion
patent: 5292783 (1994-03-01), Buchanan et al.
patent: 5294703 (1994-03-01), Hyatt et al.
patent: 5480922 (1996-01-01), Mulhaupt et al.
patent: 5502178 (1996-03-01), Gupta
patent: 5589566 (1996-12-01), White et al.
patent: 5766752 (1998-06-01), Cox et al.
patent: 5830872 (1998-11-01), Baldwin et al.
patent: 5883025 (1999-03-01), Karstens et al.
patent: 5922451 (1999-07-01), Cox et al.
patent: 6123172 (2000-09-01), Byrd et al.
patent: 6184272 (2001-02-01), Foelster et al.
patent: 6506824 (2003-01-01), Bastioli et al.
patent: 1 261 312 (1968-02-01), None
patent: 1261312 (1968-02-01), None
patent: 42 08 946 (1993-09-01), None
patent: 43 08 427 (1994-09-01), None
patent: 295 01 100 (1996-07-01), None
patent: 0 254 376 (1988-01-01), None
patent: 0 540 279 (1993-05-01), None
patent: 0707037 (1996-04-01), None
patent: 1 585 200 (1981-02-01), None
patent: 49-1333 14 (1974-04-01), None
patent: 54071141 (1979-06-01), None
patent: 60-21618 (1994-01-01), None
patent: 06-278785 (1994-10-01), None
patent: 9263603 (1997-10-01), None
patent: 9316092 (1997-12-01), None
patent: 10-237084 (1998-09-01), None
patent: 00- 351871 (2000-12-01), None
patent: 2001-247717 (2001-09-01), None
patent: 534477 (1976-11-01), None
patent: (11) 1420592 (1988-08-01), None
patent: WO 96/01832 (1996-01-01), None
patent: WO 00/12616 (2000-03-01), None
patent: WO 01/98404 (2001-12-01), None
patent: WO 02/18400 (2002-03-01), None
Akoh and Swanson, “Optimized Synthesis of Sucrose Polyesters: Comparison of Physical Properties of Sucrose Polyesters, Raffinose Polyesters and Salad Oils”, J. Food Sci. 55:236 (1990).
Ballini et al., “Zeolite HSZ-360 as a New Reusable Catalyst for the Direct Acetylation of Alchols and Phenols Under Solventless Conditions,”Tetra. Lett.39:6049-6052 (1998).
Chatterjee and Nuhn, “Stereoselective α-glycosidation using FeCl3as a Lewis acid catalyst,”Chem Commun.16:1729-1730 (1998).
Conchie et al., “Methyl and Phenyl Glycosides of the Common Sugars,” Carbohydr. Chem. 12:157 (1957).
Connors and Wachowiak, “N-Methylimidazole as a Catalyst in Hydroxy Compounds Esterification,” Herba Polonica, 44:33-38 (1998).
Curini et al., “Heterogeneous Catalysis in Acetylation of Alochols and Pheonols Promoted by Zirconium Sulfophenyl Phosphonate,” Synthetic Communications, 30:1319-1329 (2000).
Dasgupta et al., “Acetylation of Carbhoydrates Using Ferric Chloride in Acetic Anhydride,” Carbohydrate Research 80:346-349 (1980).
Debenham et al., “Two New Orthogonal Amine-Protecting Groups That Can Be Cleaved Under Mild or Neutral Conditions,” J. Am. Chem. Soc. 117:3302-3303 (1995).
Don et al., “Rheed Studies of CulnSe2Epitaxial Films,”Eighteenth IEEE Photovoltaic Specialists Conference—1985,Riviera Hotel, Las Vegas, Nevada, 10/21-25/85.
Erwig and Koenigs, “Note on Pentaacetyladextrose,”Berichte d. D. Chem. Gesellschaft22:1464-1467.
Grujić and Michel, “Exponential Stability and Trajectory Bounds of Neural Networks under Structural Variations,”IEEE Transactions on Circuits and Systems,vol. 38, No. 10, Oct. 1991.
Hofmann et al., “Bleaching Activators as Acylating Agents Kinetics of the Acetylation of Piperidine by Some Bleaching Activators,” J. Parkt. Chem. 332:176-180 (1990).
Holfe et al., “4-Dialkylaminopyridines as Highly Active Acylation Catalysts,” Angrew. Chem. Int. Ed. Engl. 17:569 (1978).
Holla, “Enzymatische Schutzgruppenchemie An Glaucalen,” J. Carbohydr. Chem. 9:113 (1990).
Li et al., “Synthesis of Xylitol C5-9 Fatty Acid Esters and Their Applications,” Huaxue Shijie (Chemistry World) 36:632-633 (1995).
JP 42008607, 1968, Dainippon Ink Rikagaku Kenkyusho, Abstract.
Ikeda et al., “Lipase-Catalyzed Acylation of Sugars Solubilized in Hydrophobic Solvents by Complexation,” Biotechnol. Bioeng. 42:788-791 (1993).
Iqbal et al., “Cobalt(II) Chloride Catalyzed Acylation of Alcohols with Acetic Anhydride: Scope and Mechanism” J. Org. Chem. 57:2001-2007 (1992).
Kartha and Field, “Iodine : A versatile Reagent in Carbohydrate Chemistry IV. Per-O-Acetylation, Regioselective Acylation and Acetolysis,”Tetrahedron,53(34):11753-11766 (1997).
Konen et al., “Esterification of Unsaturated Fatty Acids,” Oil and Soap 22:57-60 (1945).
Kopf et al., “Structure of 1,2,3,4,5,6-Hexa-O-acetyl-oglucitol (Sorbitol Hexaacetate),”Acta Cryst.C47:2425-2428 (1991).
Kopf et al., “The crystal and molecular structures of the hexitol hexa-acetates,”Carbohydr. Res.229:17-32 (1992).
Kou and Xu, “Enzymatic Synthesis of Saccharide Fatty Acid Esters,”Ann. N.Y. Acad. Sci.864:352-358 (1998).
Kumareswaran et al., “Nafion-H Catalyzed Acetylation of Alcohols,” Synlett 11:1652-1654 (2000).
Lay et al., “Regioselective Acylation of Disaccharides by Enzymatic Transesterification,”Carbohydr. Res.291:197-204 (1996).
Li and Li, “Montmorillonite clay catalysis. Part 10. K-10 and KSF-catalysed acylation of alcohols, phenols, thiols and amines: scope and limitation,”J. Chem. Soc. Perkin Trans1:1913-1917 (1998).
Li et al., “Montmorillonite K-10 and KSF as remarkable acetylation catalysts,”Chem: Commun.1389-1390 (1997).
Liebermann et al., “Concerning the Formulas of Rhamnetin and Xanthorhamnin,” Ber. 11:1618 (1878).
McBrierty et al., “Hydration and plasticization effects in cellulose acetate: Molecular motion and relaxation,”Faraday Discuss.103:225-268 (1996).
Obaje et al., “Solvent-Free Interesterification Process for the Synthesis of Acetylated Glucose Fatty Esters,”Sci. Int.11(2):165-168 (1999).
Procopiou et al., “A extremely fast and efficient acylation teaction of alcohols with acid anhydrides in the presence of trimethylsilyl trifluotomethanesulfonate as catalyst,”Chem. Commun.2625-2626 (1996).
Schmidt and Michel, “Direct O-Glycosyl Trichloroactimidate Formation. Nucleopholicity of the Anomeric Oxygen Atom,”Tetra. Lett.25(8):821-824 (1984).
Schmidt, “News Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs-Knoor Method?”Angrew. Chem. Int. Ed. Engl.25:212-235 (1986).
Sharma and Chattopadhyay, “Lipase Catalyzed Acetylation of Carbohydrates,” Biotechnol. Lett. 15:1145-1146 (1993).
Shuiin'sh et al., “High-Molecular Catalysts in Organic Synthesis,”Chemistry Series2:221-228 (1990).
Swain and Brown, “Concerted Displacement Reactions,”Polyfunctional Catalysis74:2538-2543 (May 20, 1952).
Takada et al., “discotic Columnar Liquid Crystals in Oligosaccharide Derivatives III. Anomeric Effects on the Thermo-Mesomorphic Properties of Cellobiose Octa-Alkanoates,” Liq Cryst. 19:411-448 (1995).
Tsuzuki et al.
Buchanan Charles M.
Buchanan Norma L.
Edgar Kevin J.
Lambert Juanelle L.
Eastman Chemical Company
Harlan Robert D.
Needle & Rosenberg PC
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