Process to modify polymeric materials and resulting...

Details Process to modify polymeric materials and resulting... Process to modify polymeric materials and resulting...

2002-08-02

2009-12-15

Mc Ginty, Douglas (Department: 1796)

Synthetic resins or natural rubbers -- part of the class 520 ser

Synthetic resins

Treating polymer containing material or treating a solid...

C528S480000, C528S503000, C525S326200, C525S326100, C525S242000, C525S491000

Reexamination Certificate

active

07632916

ABSTRACT:
Disclosed is a method for modifying a polymer by carrying out a thermally-induced reaction in a mixing apparatus having a high shear environment and devolatilization capabilities. Also disclosed are the resulting materials.

REFERENCES:
patent: 2803615 (1957-08-01), Ahlbrecht et al.
patent: 2915554 (1959-12-01), Ahlbrecht et al.
patent: 3036997 (1962-05-01), Campbell
patent: 3687422 (1972-08-01), List
patent: 3689035 (1972-09-01), List
patent: 3778393 (1973-12-01), Greber et al.
patent: 3787351 (1974-01-01), Olson
patent: 3880407 (1975-04-01), List
patent: 4039024 (1977-08-01), List
patent: 4086151 (1978-04-01), Stevens et al.
patent: 4172859 (1979-10-01), Epstein
patent: 4346193 (1982-08-01), Warfel
patent: 4415615 (1983-11-01), Esmay et al.
patent: 4458064 (1984-07-01), Chatterjee
patent: 4500687 (1985-02-01), Wolfe
patent: 4533482 (1985-08-01), Bollinger
patent: 4572819 (1986-02-01), Priddy et al.
patent: 4820778 (1989-04-01), Ohtani et al.
patent: 4948832 (1990-08-01), Ostermayer et al.
patent: 4985486 (1991-01-01), Westeppe et al.
patent: 5002676 (1991-03-01), Willis et al.
patent: 5112918 (1992-05-01), Boocock et al.
patent: 5122571 (1992-06-01), Westeppe et al.
patent: 5144069 (1992-09-01), Stern et al.
patent: 5218053 (1993-06-01), DuBois
patent: 5225496 (1993-07-01), Yamamoto et al.
patent: 5227460 (1993-07-01), Mahabadi et al.
patent: 5256489 (1993-10-01), Maringer et al.
patent: 5288840 (1994-02-01), Morishita et al.
patent: 5336717 (1994-08-01), Rolando et al.
patent: 5338802 (1994-08-01), DuBois et al.
patent: RE34791 (1994-11-01), Kazmierzak et al.
patent: 5374688 (1994-12-01), Besecke et al.
patent: 5478886 (1995-12-01), Kim
patent: 5480922 (1996-01-01), Mulhaupt et al.
patent: 5571655 (1996-11-01), Mahabadi et al.
patent: 5587423 (1996-12-01), Brandstetter et al.
patent: 5644007 (1997-07-01), Davidson et al.
patent: 5804625 (1998-09-01), Temperante et al.
patent: 5907017 (1999-05-01), Ober et al.
patent: 5917011 (1999-06-01), Duda et al.
patent: 6013735 (2000-01-01), Mishra et al.
patent: 6121479 (2000-09-01), Müllner et al.
patent: 6150498 (2000-11-01), Abel et al.
patent: 6160054 (2000-12-01), Schwindeman et al.
patent: 6184338 (2001-02-01), Schwindeman et al.
patent: 6197891 (2001-03-01), Schwindeman et al.
patent: 6221991 (2001-04-01), Letchford et al.
patent: 6268532 (2001-07-01), DesMarteau et al.
patent: 6277491 (2001-08-01), Sakoda et al.
patent: 6316112 (2001-11-01), DuBois et al.
patent: 6319881 (2001-11-01), Coolbaugh et al.
patent: 6350820 (2002-02-01), Hahnfeld et al.
patent: 6379791 (2002-04-01), Cernohous et al.
patent: 6444762 (2002-09-01), Fischer et al.
patent: 6448353 (2002-09-01), Nelson et al.
patent: 6521710 (2003-02-01), Roth et al.
patent: 6586541 (2003-07-01), Citron
patent: 6613870 (2003-09-01), Harder et al.
patent: 6649719 (2003-11-01), Moore et al.
patent: 6716935 (2004-04-01), Nelson et al.
patent: 6737026 (2004-05-01), Bergh
patent: 6749814 (2004-06-01), Bergh
patent: 6753373 (2004-06-01), Winowiecki
patent: 6852781 (2005-02-01), Savu et al.
patent: 6890493 (2005-05-01), Bergh
patent: 6902934 (2005-06-01), Bergh
patent: 7157283 (2007-01-01), Nelson et al.
patent: 2001/0027234 (2001-10-01), Binder et al.
patent: 2002/0007083 (2002-01-01), DesMarteau et al.
patent: 2002/0010267 (2002-01-01), Klaerner et al.
patent: 2002/0128336 (2002-09-01), Kolb et al.
patent: 2002/0170976 (2002-11-01), Bergh
patent: 2003/0035917 (2003-02-01), Hyman
patent: 2003/0236369 (2003-12-01), Komoriya et al.
patent: 2004/0023398 (2004-02-01), Nelson et al.
patent: 2004/0265188 (2004-12-01), Marx et al.
patent: 196 52 312 (1998-06-01), None
patent: 19715035 (1998-10-01), None
patent: 199 10 810 (2000-09-01), None
patent: 199 10 811 (2000-09-01), None
patent: 0 076 691 (1983-04-01), None
patent: 0 603 965 (1994-06-01), None
patent: 4-63802 (1992-02-01), None
patent: 04-063820 (1992-02-01), None
patent: 4-110315 (1992-04-01), None
patent: 8-193107 (1996-07-01), None
patent: 09-277464 (1997-10-01), None
patent: 10-130348 (1998-05-01), None
patent: 2002-161110 (2002-06-01), None
patent: WO 96/07522 (1996-03-01), None
patent: WO 96/07674 (1996-03-01), None
patent: WO 97/40929 (1997-11-01), None
patent: WO 00/42084 (2000-07-01), None
patent: WO 01/30873 (2001-05-01), None
patent: WO 01/91723 (2001-12-01), None
patent: WO 02/081079 (2002-10-01), None
US 6,492,477, 12/2002, Savu et al. (withdrawn)
Symposium: Allen, “Studies on the Synthesis of Novel Block Ionomers, ”Coulombic Interactions in Macromolecular Systems, ACS Symposium Series 302, American Chemical Society, Aug. 26-31, 1984, Chapter 6, pp. 79-92.
Book Excerpt: Greene et al.,Protective Groups in Organic Synthesis, Second Edition, John Wiley & Sons, Inc., (1991), p. 41.
Book Excerpt: Greene et al.,Protective Groups in Organic Synthesis, Second Edition, John Wiley & Sons, Inc., (1991), pp. 80-83.
Article Abstract: Kassis et al, “XPS Studies of Fluorinated Acrylate Polymers and Block Copolymers with Polystyrene,”Macromolecules, (1996), vol. 29, No. 9, pp. 3247-3254.
U.S. Appl. No. 09/500,155, filed Feb. 8, 2000, Continuous Process for the Production of Controlled Architecture Materials.
U.S. Appl. No. 09/824,330, filed Apr. 2, 2001, A Continuous Process for the Production of Combinatorial Libraries of Materials.
U.S. Appl. No. 10/211,219, filed Aug. 2, 2002, Continuous Process for the Production of Combinatorial Libraries of Modified Materials.
U.S. Appl. No. 10/211,096, filed Aug. 2, 2002, Fluorinated Polymers.
Article: Busse et al., “Synthesis of Amphiphilic Block Copolymers Based ontert-Butyl Methacrylate and 2-(N-Methylperfluorobutanesulfonamido)ethyl Methacrylate and Its Behavior in Water,”Macromolecules, vol. 25, (2002), pp. 178-184.
Literature Examples: Baker et al., “PS/PE Blend,”Polymer, vol. 28, (1987), p. 2057.
Literature Examples: Hobbs et al., “PE/PA 6,6 Blend,”Polym. Eng. Sci., vol. 23, (1983), p. 380.
Article: Guegan at al., “Anionic Synthesis, Modification, and Characterization of ABC Triblock Copolymers,”Macromolecules, vol. 29, No. 13, (1996), pp. 4605-4612.
Article: Barclay et al., “The ‘Living’ Free Radical Synthesis of Poly(4-hydroxystyrene): Physical Properties and Dissolution Behavior,”Macromolecules, vol. 31, No. 4, (1998), pp, 1024-1031.
Article: Yang et al., “Clustering of Poly(methacrylic acid) around Appended Binaphthyl Labels as Reflected by the Disruption of γ-Cyclodextrin Complexation and Racemization Kinetics,”Macromolecules, vol. 32, No. 8, (1999), pp. 2577-2584.
Article: Leyh et al., “Shear-Induced Order in Aqueous Micellar Solutions of Amphiphilic Poly(tert-butylstyrene)-b-poly(Na methacrylate) Diblock,”Macromolecules, vol. 31, No. 26, (1998), pp. 9258-9264.
Article: Creutz at al., “Effectiveness of Poly(vinylpyridine) Block Copolymers as Stabilizers of Aqueous Titanium Dioxide Dispersions of a High Solid Content,”Langmuir, vol. 15, No. 21, (1999), pp. 7145-7156.
Article: Wang et al., “Synthesis of AB(BA), ABA and BAB Block Copolymers oftert-Butyl Methacrylate (A) and Ethylene Oxide (B),”Journal of Polymer Science: Part A: Polymer Chemistry, vol. 30, (1992), pp. 2251-2261.
Article: Huang et al., “Hydrogel-Coated Glassy Nanospheres: A Novel Method for the Synthesis of Shell Cross-Linked Knedels,”J. Am. Chem. Soc., vol. 119, No. 48, (1997), pp. 11653-11659.
Article: Lewandowski et al., “Polar, Monodisperse, Reactive Beads from Functionalized Methacrylate Monomers by Staged Templated Suspension Polymerization,”Chem. Mater., vol. 10, No. 1, (1998), pp. 385-391.
Article: Lai, “Thermal Behavior of Random Copolymers of Methacrylic Acid andtert-Butyl Methacrylate,”Macromolecules, vol. 17, No. 5, (1984), pp. 1010-1012.
Article: Peters et al., “Termination of Living Anionic Polymerizations Using Chlorosilane Derivatives: A General Synthetic Methodology for the Synthesis of End-Functionalized Polymers,”J. Am. Chem. Soc., vol. 117, No. 12, (1995),

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