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
2011-06-21
2011-06-21
Choi, Ling-Siu (Department: 1761)
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...
C528S044000, C528S059000, C552S301000, C564S269000, C564S271000, C564S277000
Reexamination Certificate
active
07964695
ABSTRACT:
This invention provides chain extender compositions. These compositions comprise(i) an aromatic primary diamine, and(ii) a component selected from the group consisting of:(a) an aliphatic secondary diamine;(b) an aliphatic primary diamine;(c) an aliphatic secondary diamine and an aliphatic primary diamine;(d) a diimine; and(e) a combination of any two or more of (a) through (d).When (ii) is (a), (a) has amino hydrocarbyl groups which are secondary or tertiary hydrocarbyl groups; when (ii) is (d), and (d) is an aromatic diimine, each imino hydrocarbylidene group has at least two carbon atoms. Processes for producing polyurethanes, polyureas, and polyurea-urethanes are also provided.
REFERENCES:
patent: 2380420 (1945-07-01), Emerson
patent: 2582128 (1952-01-01), Hurwitz et al.
patent: 2953579 (1960-09-01), Williams et al.
patent: 2965605 (1960-12-01), Reynolds et al.
patent: 3209030 (1965-09-01), Bicek
patent: 3275567 (1966-09-01), Keith et al.
patent: 3336386 (1967-08-01), Dovell et al.
patent: 3350450 (1967-10-01), Dovell et al.
patent: 3414616 (1968-12-01), Summers
patent: 3519603 (1970-07-01), Lohse et al.
patent: 3538161 (1970-11-01), Dovell
patent: 3609121 (1971-09-01), Lohse et al.
patent: 3625710 (1971-12-01), Rizzi
patent: 3658937 (1972-04-01), Terni et al.
patent: 3761425 (1973-09-01), Baessler et al.
patent: 3937730 (1976-02-01), Vogel et al.
patent: 3943158 (1976-03-01), Dietrich et al.
patent: 3952056 (1976-04-01), Vogel et al.
patent: 3994975 (1976-11-01), Oude Alink et al.
patent: 4045486 (1977-08-01), Krall et al.
patent: 4140718 (1979-02-01), Symon
patent: 4161492 (1979-07-01), Weissel
patent: 4317916 (1982-03-01), Degischer et al.
patent: 4373107 (1983-02-01), Tahara et al.
patent: 4520186 (1985-05-01), Hess et al.
patent: 4521624 (1985-06-01), Jackisch
patent: 4528363 (1985-07-01), Tominaga
patent: 4631298 (1986-12-01), Presswood
patent: 4663201 (1987-05-01), House et al.
patent: 4714512 (1987-12-01), House et al.
patent: 4760183 (1988-07-01), Papenfuhs et al.
patent: 4789691 (1988-12-01), Matzke et al.
patent: 4798862 (1989-01-01), Gillis, Jr.
patent: 4806616 (1989-02-01), Baumann et al.
patent: 4900868 (1990-02-01), Merten et al.
patent: 4925974 (1990-05-01), Gras
patent: 5001267 (1991-03-01), Speranza et al.
patent: 5002806 (1991-03-01), Chung
patent: 5008453 (1991-04-01), Nalepa et al.
patent: 5041668 (1991-08-01), Nalepa et al.
patent: 5059672 (1991-10-01), Engebretson
patent: 5145825 (1992-09-01), Deeba et al.
patent: 5312886 (1994-05-01), House et al.
patent: 5430188 (1995-07-01), Bader et al.
patent: 5470890 (1995-11-01), House et al.
patent: 5498585 (1996-03-01), Bartels et al.
patent: 5591807 (1997-01-01), Cai et al.
patent: 5616799 (1997-04-01), Planker et al.
patent: 5646235 (1997-07-01), Zimmerman et al.
patent: 5744642 (1998-04-01), Lantzsch et al.
patent: 5847067 (1998-12-01), Gras
patent: 5859164 (1999-01-01), Gras et al.
patent: 5874619 (1999-02-01), Wiggins et al.
patent: 6013755 (2000-01-01), Primeaux, II et al.
patent: 6103799 (2000-08-01), Lassila et al.
patent: 6156863 (2000-12-01), Wenning
patent: 6218480 (2001-04-01), Rappoport
patent: 6399736 (2002-06-01), Primeaux, II et al.
patent: 6403752 (2002-06-01), House et al.
patent: 6429338 (2002-08-01), Burdeniuc et al.
patent: 6444721 (2002-09-01), Schwalm et al.
patent: 6803445 (2004-10-01), Ishikawa et al.
patent: 7767858 (2010-08-01), Wiggins et al.
patent: 2002/0028901 (2002-03-01), Gunatillake et al.
patent: 2003/0004265 (2003-01-01), Gupta et al.
patent: 2004/0015016 (2004-01-01), Su et al.
patent: 2004/0019238 (2004-01-01), Su et al.
patent: 2004/0054150 (2004-03-01), Murray
patent: 2004/0167311 (2004-08-01), Slagel et al.
patent: 2004/0180778 (2004-09-01), Small
patent: 2007/0066786 (2007-03-01), Hanson, Jr.
patent: 2007/0073030 (2007-03-01), Wiggins et al.
patent: 2008/0194788 (2008-08-01), Lee et al.
patent: 1218190 (1987-02-01), None
patent: 1352202 (2002-06-01), None
patent: 1939949 (2007-04-01), None
patent: 1163315 (1964-02-01), None
patent: 2940738 (1981-04-01), None
patent: 264014 (1989-01-01), None
patent: 3728141 (1989-03-01), None
patent: 19701835 (1998-07-01), None
patent: 102005046641 (2007-04-01), None
patent: 0014985 (1980-09-01), None
patent: 0288067 (1988-10-01), None
patent: 0309980 (1989-04-01), None
patent: 0420426 (1991-04-01), None
patent: 0469751 (1992-02-01), None
patent: 0688802 (1995-12-01), None
patent: 0779278 (1997-06-01), None
patent: 1067116 (2001-01-01), None
patent: 1229020 (2002-08-01), None
patent: 0802209 (2003-04-01), None
patent: 1070759 (1967-06-01), None
patent: 1320863 (1973-06-01), None
patent: 1478446 (1977-06-01), None
patent: 63052146 (1988-03-01), None
patent: 5274914 (1993-10-01), None
patent: 09100260 (1997-04-01), None
patent: WO-92/18575 (1992-10-01), None
patent: WO-97/01529 (1997-01-01), None
patent: WO-00/26181 (2000-05-01), None
patent: WO-02/102869 (2002-12-01), None
patent: WO 02/102869 (2002-12-01), None
patent: WO-03/018531 (2003-03-01), None
patent: WO-2004/073634 (2004-09-01), None
patent: WO-2004/092632 (2004-10-01), None
patent: WO-2005/033119 (2005-04-01), None
patent: WO-2006/028728 (2006-03-01), None
patent: WO-2006/104528 (2006-10-01), None
patent: 2007050542 (2007-05-01), None
John T. Lai, Ketoform reaction. Synthesis of hindered imines from 2,6-dialkylanilines and ketones, Tetrahedron Letters 43 (2002) 1965-1967, 2002 Elsevier Science Ltd.
Pamphlate © 2001 Albemarle Corporation , Ethacure and Albemarle are trademarks of Albemarle Corporation http://www.albemarle.com/TDS/Curatives/SC7008F—ETHACURE—100LC.pdf.
Adams et al., “Restricted Rotation in Aryl Amines. XIV. Isopropyl Derivatives of Dibenzenesulfonamidomesitylene”, J. Am. Chem. Soc., 1950, pp. 5077-5079, vol. 72.
Barmetter, “Acid-Catalyzed [3.3]-Sigmatropic Rearrangethents of N-Propargylanilines”, Helvetica Chimica Acta, 1990, pp. 1515-1573, vol. 73, Verlag Helvetica Chimica Acta, Basel, CH.
Billaud et al., “Quantitative Analysis of Epoxy Resin Cure Reaction: A Study by Near-Infrared Spectroscopy”, Applied Spectroscopy, 2002, pp. 1413-1421, vol. 56(11).
Borges-Lopes et al., “Synthesis and Characterization of New Methyl-Substituted Azomethine-Siloxane Liquid Crystal Macrocycles Influence of the Methyl-Substitution on the Cycle Formation”, Polymer Bulletin, 1995, pp. 523-530, vol. 34, Springer, Heidelberg, Berlin, DE.
Campbell et al., “The Preparation of Unsymmetrical Secondary Aliphatic Amines”,.J. Am. Chem. Soc., 1944, pp. 82-84, vol. 66.
Childs et al., “Assembly of a Nanoscale Chiral Ball Through Supramolecular Aggregation of Bowl-Shaped Triangular Helicates”, Angewandte Chemie, 2002, pp. 4244-4247, vol. 41, VCH Verlagsgesellschaft, Weinheim, DE.
Childs et al., “Using Noncovalent Intra-strand and Inter-strand Interactions to Prescribe Helix Formation within a Metallo-supramolecular System”, Chem. Eur. J., 2004, pp. 4291-4300, vol. 10(17).
Deschenaux et al., “Structural Isomerism in Polycondensates. IV. Synthesis and Characterization of Liquid Crystalline Poly(azomethines) and Low Molecular Weight Model Compounds”, Helvetica Chimica Acta, 1986, pp. 1349-1355, vol. 69(6).
Distefano, “Reinvestigation of the Formaldehyde-Aniline Condensation. Part 4. Ultraviolet Photoelectron and Electron Transmission Spectra of N-Methyleneaniline and its Symmetric Dimethyl Ring-substituted Homologues and Semiempirical Theoretical Evaluations”, J. Chem. Soc. Perkin Trans II, 1985, pp. 1623-1627.
Dovell & Greenfield, “Platinum Metal Sulfides as Heterogeneous Hydrogenation Catalysts”, J. Am. Chem. Soc., 1965, pp. 2767-2768, vol. 87.
Dvolaitzky et al., “Stable N,N′-di-tert-butyl-meta-phenylenebisnitroxides-Unexpected Ground-State Singlets”, Angewandte Chemie Int. Ed. Engl., 1992, pp. 180-181, vol. 31(2).
Emerson et al., “The Reductive Alkylation of Hindred Aromatic Primary Amines”, J. Am. Chem. Soc., 1941, pp. 972-974, vol. 63.
Hine et al., “Polar Effects on the Formation of Imines
Brandt Vernon O.
Lee John Y.
Orgad Judit
Sabahi Mahmood
Wiggins Paul L.
Ahvazi Bijan
Albemarle Corporation
Choi Ling-Siu
Jubinsky James A.
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