Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From reactant having at least one -n=c=x group as well as...
Reexamination Certificate
2011-08-23
2011-08-23
Puttlitz, Karl J (Department: 1621)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
From reactant having at least one -n=c=x group as well as...
Reexamination Certificate
active
08003748
ABSTRACT:
Polythiourethane polymer compositions, methods of making the polythiourethane polymer compositions, and methods of using the polythiourethane polymer compositions are provided. The polythiourethane can be produced by contacting a thiol ester composition and an isocyanate to produce a mixture and then heating the mixture to produce the polythiourethane polymer. In some embodiments, the thiol ester compositions include thiol esters, hydroxy thiol esters, and cross-linked thiol esters.
REFERENCES:
patent: 2411954 (1946-12-01), Burke
patent: 2476891 (1949-07-01), Mortenson
patent: 3028417 (1962-04-01), Elsenmann
patent: 3041284 (1962-06-01), Calhoun et al.
patent: 3114734 (1963-12-01), Gobran et al.
patent: 3211674 (1965-10-01), Sandridge
patent: 3278496 (1966-10-01), LeFave et al.
patent: 3352810 (1967-11-01), McLay
patent: 3446780 (1969-05-01), Bertozzi
patent: 3465057 (1969-09-01), Cameron et al.
patent: 3686326 (1972-08-01), Oswald et al.
patent: 3707552 (1972-12-01), Dobinson et al.
patent: 3742006 (1973-06-01), Doss
patent: 3746685 (1973-07-01), Dobinson et at.
patent: 3832328 (1974-08-01), Eggensperger
patent: 3853959 (1974-12-01), Dobinson et al.
patent: 3884951 (1975-05-01), Oswald
patent: 3914288 (1975-10-01), Garnish et al.
patent: 3916067 (1975-10-01), Jones et al.
patent: 3926822 (1975-12-01), Habiby
patent: 3953347 (1976-04-01), Habiby
patent: 3981901 (1976-09-01), Guthrie et al.
patent: 3986966 (1976-10-01), Wakim
patent: 3991089 (1976-11-01), Schwab et al.
patent: 4045472 (1977-08-01), Guthrie et al.
patent: 4119640 (1978-10-01), Hodakowski et al.
patent: 4218332 (1980-08-01), Schwab et al.
patent: 4231956 (1980-11-01), Sullivan et al.
patent: 4254185 (1981-03-01), Buter
patent: 4340707 (1982-07-01), Quels et al.
patent: 4504651 (1985-03-01), Yamaguchi et al.
patent: 4521320 (1985-06-01), Spivack et al.
patent: 4566878 (1986-01-01), Karol et al.
patent: 4594193 (1986-06-01), Regen
patent: 4626562 (1986-12-01), Motomura et al.
patent: 4636242 (1987-01-01), Timmons
patent: 4788083 (1988-11-01), Dammann et al.
patent: 5126425 (1992-06-01), Sasagawa et al.
patent: 5154950 (1992-10-01), Rosthauser et al.
patent: 5405426 (1995-04-01), Timmons et al.
patent: 5411776 (1995-05-01), Schmidt et al.
patent: 5422422 (1995-06-01), Bader et al.
patent: 5454851 (1995-10-01), Zlotnikov et al.
patent: 5538531 (1996-07-01), Hudson et al.
patent: 5925726 (1999-07-01), Seppala et al.
patent: 5932681 (1999-08-01), Herold et al.
patent: 6039781 (2000-03-01), Goertz et al.
patent: 6221994 (2001-04-01), Galbiati et al.
patent: 6231633 (2001-05-01), Hirano et al.
patent: 6358296 (2002-03-01), Markusch et al.
patent: 6583302 (2003-06-01), Erhan et al.
patent: 7153917 (2006-12-01), Rink et al.
patent: 7169737 (2007-01-01), Hidaka et al.
patent: 7557236 (2009-07-01), Brown et al.
patent: 7585932 (2009-09-01), Byers et al.
patent: 7713326 (2010-05-01), Carstens et al.
patent: 7781484 (2010-08-01), Byers et al.
patent: 2003/0204030 (2003-10-01), Higuchi et al.
patent: 2005/0096222 (2005-05-01), Hidaka et al.
patent: 2005/0176902 (2005-08-01), Rink et al.
patent: 2005/0197390 (2005-09-01), Byers et al.
patent: 2005/0197391 (2005-09-01), Refvik et al.
patent: 2006/0000252 (2006-01-01), Carstens et al.
patent: 2006/0009365 (2006-01-01), Erhan et al.
patent: 2006/0036110 (2006-02-01), Brown et al.
patent: 2006/0111520 (2006-05-01), Byers et al.
patent: 2007/0055033 (2007-03-01), Byers et al.
patent: 2007/0088146 (2007-04-01), Nakamura et al.
patent: 2007/0112100 (2007-05-01), Byers et al.
patent: 2008/0214774 (2008-09-01), Brown et al.
patent: 2009/0124762 (2009-05-01), Brown et al.
patent: 2009/0124784 (2009-05-01), Brown et al.
patent: 300174 (1992-05-01), None
patent: 0 308 664 (1988-08-01), None
patent: 0 716 057 (1996-06-01), None
patent: 0716057 (1996-06-01), None
patent: 1 194 553 (1959-11-01), None
patent: 1194553 (1959-11-01), None
patent: 908986 (1962-10-01), None
patent: 1 292 214 (1972-10-01), None
patent: 1 312 821 (1973-04-01), None
patent: 1 312 822 (1973-04-01), None
patent: 1 484 062 (1977-08-01), None
patent: 1484062 (1977-08-01), None
patent: 2188327 (1987-09-01), None
patent: 60123506 (1985-07-01), None
patent: 1 090169 (1989-04-01), None
patent: 1090167 (1989-06-01), None
patent: 1090168 (1989-06-01), None
patent: 1090170 (1989-06-01), None
patent: 2003-252956 (2003-09-01), None
patent: WO 86/06371 (1986-11-01), None
patent: WO2002053672 (2002-07-01), None
patent: WO2003006569 (2003-01-01), None
patent: WO 03/082958 (2003-10-01), None
patent: WO 2005/080325 (2005-01-01), None
patent: WO 2005/014564 (2005-02-01), None
patent: WO2005/123862 (2005-12-01), None
patent: WO2005022217 (2007-02-01), None
patent: WO2007021960 (2007-02-01), None
patent: WO2007035215 (2007-03-01), None
patent: WO2008/106637 (2008-09-01), None
Kanemura, Y, et al. “Dithiols as Improvers for Polyurethanes,” Chemical Abstracts, American Chemical Society, vol. 11, No. 22, Nov. 27, 1989 (XP000251903).
Search Report from International Patent Application No. PCT/US2006/031393, dated Jan. 1, 2007.
Search Report from Internatinal Patent Application No. PCT/US2006/031901 dated Nov. 11, 2006.
Search Report for International Patent Application No. PCT/US2005/005110 dated Jan. 24, 2006.
Elchueva, A.D., et al., “Influence of the Type of Oligoisocyanate on the Properties of Thiourethane Compounds,” Russian J of Applied Chem, vol. 74 (2001) pp. 1040-1043.
Fitt, Peter S., et al., “Dithiols. Part XIX. Further Studies on the Deacetylation of Acetylated Dithiols,” J of the Chem Society No. 5 (1957) pp. 2240-2249.
Derkach, N. Ya, et al., “Mercapto Derivatives of Alkylmalonic Esters,” Chemical Abstracts, vol. 54, No. 22, (1960), Abstract No. 24386a.
Blackman L.C.F., et al. “Promoters for the Dropwise Condensation of Steam. Part II . . . ,” J of the Chem Society, No. 1 (1957) pp. 165-169.
Mazaev, V.E., et al., “Preparation Reflux Mercaptoethanol Appropriate Acid,” Derwent Publications, Week 197442, Abstract No. SU410010 (1974).
Demchuk, Dmitry V., et al. “Synthesis of 12- and 13-Membered Sulfur-Containing Lactones by Homolytic Macrocyclization . . . ,” Synthesis, (1995) pp. 307-311.
Sudmeier, James L., et al. “Fast Kinetics by Stopped-Flow Chlorine-35 Nuclear Magnetic Resonance . . . ” Inorganic Chem vol. 10 No. 4 (1971) pp. 860-863.
Tanaka, Kiyoshi, et al., “Oxidation of Thiol by 5-Arylidene, 1,3-Dimethylbarbituric Acid and Its Application . . . ,” Tetrahedron Letters, vol. 28, No. 36 (1987) pp. 4173-4176.
Troyansky, Emmanuil I., et al. “Stereoselective Free Radical Cycloaddition-Macrocyclization in Facile Synthesis . . . ,” Tetrahedron, vol. 51, No. 42 (1995) pp. 11431-11444.
Chavdarian, Charles G., et al. “Synthesis, Redox Characteristics, and in Vitro Norepinephrine Uptake . . . ” J of Medicinal Chem, vol. 22, No. 11 (1979) pp. 1317-1322.
Sjoberg, Bertil, “Uber Thioglycerine und einige verwandte Schwefelverbindungen,” Berichte der Deutschen Chemischen Gesellschaft, vol. 75, No. 1 (1942) pp. 13-29.
Mayadunne, Roshan T.A., et al. “Multiarm organic compounds for use as reversible chain-transfer agents . . . ,” Tetrahedron Letters, vol. 43, No. 38 (2002) pp. 6811-6814.
Miyake, Y., et al., “Enantioselective conversion of meso-cyclic disulfides to chiral cyclic sulfides . . . ” J of the Chem Society, Perkin Trans 1, No. 10 (2000) pp. 1595-1599.
Bhattacharya, S., et al., “Synthesis of Macrocyclic Diacy/Dialkyl Glycerols Containing Disulfide Tether and Studies . . . ” J Org Chem vol. 63, No. 25 (1998) pp. 9232-9242.
Apitzsch, et al. “Uber Sulfide aus alfa,alfa1-Disulfhydryl-thio-gamma-pyron-beta, beta1- . . . ,” Berichte der Deutschen Chemischen Gesellschaft, vol. 42 (1909) pp. 2940-2943.
Teplenicheva, Y.L., et al., “Ethyl 2-(alpha-hydroxyhexafluoroisopropyl)acrylate as a potential . . . ” Russian Chemical Bulletin, vol. 46, No. 4 (1997) pp. 755-758.
Gala, D., et al., “A Practical Conversion
Brown Chad W.
Byers Jim D.
Hankinson Michael S.
Matson Michael S.
Refvik Mitchell D.
Chevron Phillips Chemical Company LP
Merchant & Gould P.C.
Puttlitz Karl J
LandOfFree
Polythiourethane compositions and processes for making and... does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Polythiourethane compositions and processes for making and..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Polythiourethane compositions and processes for making and... will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-2762284