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Sirisoma Wanigatunga

age ~74

from Yorktown, VA

Also known as:
  • Shanthi Wanigatunga
  • Wanigatunga Sirisoma
  • Shanthi Paranawithana
  • Sirisoma U
Phone and address:
205 Chadwick Ct, Yorktown, VA 23693
757 766-2288

Sirisoma Wanigatunga Phones & Addresses

  • 205 Chadwick Ct, Yorktown, VA 23693 • 757 766-2288
  • 22 Belles Cove Dr, Poquoson, VA 23662 • 757 772-5944
  • 3012 Sandpiper Cir, Clearwater, FL 33762 • 727 540-9603
  • Largo, FL
  • Bridgewater, NJ
  • Redington Shores, FL
  • Gainesville, FL
  • 3012 Sandpiper Pl, Clearwater, FL 33762 • 727 540-9603

Work

  • Position:
    Construction and Extraction Occupations

Education

  • Degree:
    Associate degree or higher

Us Patents

  • Photopolymerization Of Episulfides Using Metal Complexes And Its Use For Making Ophthalmic Lenses

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  • US Patent:
    6592801, Jul 15, 2003
  • Filed:
    Apr 30, 2001
  • Appl. No.:
    09/846669
  • Inventors:
    Sirisoma Wanigatunga - Largo FL
    Yassin Yusef Turshani - Largo FL
    Peiqi Jiang - Palm Harbor FL
  • Assignee:
    Essilor International Compagnie Generale dOptique - Charenton cedex
  • International Classification:
    C08G 7508
  • US Classification:
    264496, 522 25, 522 28, 522 29, 522168, 522169
  • Abstract:
    A process for polymerizing episulfide monomers comprising the steps of: (c) mixing to an episulfide monomer or a mixture of episulfide monomers an effective amount of at least one photopolymerization catalyst selected from the group consisting of (cyclopentadienyl) ruthenium and osmium complexes and an effective amount of at least a co-catalyst selected from phosphonium salts, phosphines and amines; and (d) irradiating the mixture of (a) with an ultra-violet radiation to polymerize the mixture.
  • Cationic Photopolymerization Of Diepisulfides And Application To The Manufacture Of Optical Lenses

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  • US Patent:
    6635195, Oct 21, 2003
  • Filed:
    Feb 4, 2000
  • Appl. No.:
    09/499070
  • Inventors:
    Sirisoma Wanigatunga - Largo FL
    Yassin Turshani - Largo FL
  • Assignee:
    Essilor International Compagnie Generale dOptique - Charenton cedex
  • International Classification:
    B29D 1100
  • US Classification:
    264 11, 522 25, 522 27, 522168, 528377, 528378, 528380, 264494, 264496
  • Abstract:
    A process for polymerizing/curing a photopolymerizable monomer composition comprising at least one diepisulfide monomer which comprises the steps of: a) mixing to the monomer composition an effective amount of a cationic photopolymerization initiator, and b) irradiating the mixture of a) with an ultraviolet radiation to at least partially cationically photopolymerize the monomer composition.
  • Anionic And Lewis Base Photopolymerization Process And Its Use For Making Optical Articles

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  • US Patent:
    6911485, Jun 28, 2005
  • Filed:
    Apr 19, 2002
  • Appl. No.:
    10/126572
  • Inventors:
    Charles R. Kutal - Athens GA, US
    Sirisoma Wanigatunga - Largo FL, US
    Gabriel Keita - Oldsmar FL, US
    Yassin Turshani - Largo FL, US
  • Assignee:
    The University of Georgia Research Foundation, Inc. - Athens GA
    Essilor International Campagnie Generale D'Optique - Charenton Cedex
  • International Classification:
    C08F002/48
    C08F004/52
    C08F004/78
    G03C001/735
    G03F007/029
  • US Classification:
    522 49, 522 57, 522 62, 522 65, 522 66, 522174, 522180, 522173, 522182
  • Abstract:
    The invention relates to a process for polymerising a monomer, polymerizing and/or crosslinking a oligomer, or crosslinking a polymer or copolymer, said monomer, oligomer, polymer and copolymer being selected among precursor monomers, urethane, thiourethane and episulfide oligomers, and urethane, thiourethane and episulfide polymers and copolymers, which comprises:.
  • Thiophosphine Compounds And Methods Of Making Polymerizable Compositions Containing Them And Their Use For Making Ophthalmic Lenses

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  • US Patent:
    7129321, Oct 31, 2006
  • Filed:
    Mar 24, 2004
  • Appl. No.:
    10/807742
  • Inventors:
    Sirisoma Wanigatunga - Clearwater FL, US
    Aref Jallouli - Largo FL, US
    Martin Rickwood - Clarks Green PA, US
    Yassin Yusef Turshani - Largo FL, US
  • Assignee:
    Essilor International Compagnie Generale d'Optique - Charenton Cedex
  • International Classification:
    C08G 79/02
  • US Classification:
    528398, 528373, 528389, 528487
  • Abstract:
    Thiophosphine compounds (also named phosphine sulfide compounds) and their use for making polymerizable compositions which after polymerization give optically transparent articles, such as ophthalmic lenses, having improved mechanical and optical properties and in particular having an improved UV cut.
  • Anionic And Lewis Base Photopolymerization Process And Its Use For Making Optical Articles

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  • US Patent:
    7253213, Aug 7, 2007
  • Filed:
    Apr 26, 2005
  • Appl. No.:
    11/114753
  • Inventors:
    Charles R. Kutal - Athens GA, US
    Sirisoma Wanigatunga - Largo FL, US
    Gabriel Keita - Oldsmar FL, US
    Yassin Turshani - Largo FL, US
  • International Classification:
    C07F 11/00
    C07F 15/00
    C08J 3/28
  • US Classification:
    522 57, 522 60, 522 63, 522 65, 522 66, 556 58, 556 59, 556138, 556140
  • Abstract:
    The invention relates to a process for polymerising a monomer, polymerizing and/or crosslinking an oligomer, or crosslinking a polymer or copolymer, said monomer, oligomer, polymer and copolymer being selected among precursor monomers, urethane, thiourethane and episulfide oligomers, and urethane, thiourethane and episulfide polymers and copolymers, which comprises:.
  • Process For Making Thiophosphine Compounds

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  • US Patent:
    7378556, May 27, 2008
  • Filed:
    Oct 20, 2006
  • Appl. No.:
    11/551439
  • Inventors:
    Sirisoma Wanigatunga - Largo FL, US
    Aref Jallouli - Largo FL, US
    Martin Rickwood - Clarks Summit PA, US
    Yassin Yusef Turshani - Largo FL, US
  • Assignee:
    Essilor International Compagnie Generale d'Optique - Charenton Cedex
  • International Classification:
    C07F 9/02
  • US Classification:
    568 14, 568 15
  • Abstract:
    Disclosed is a process for making a thiophosphine compound of formula (I):.
  • Thiophosphine Compounds

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  • US Patent:
    7446228, Nov 4, 2008
  • Filed:
    Oct 20, 2006
  • Appl. No.:
    11/551409
  • Inventors:
    Sirisoma Wanigatunga - Largo FL, US
    Aref Jallouli - Largo FL, US
    Martin Rickwood - Clarks Summit PA, US
    Yassin Yusef Turshani - Largo FL, US
  • Assignee:
    Essilor International Compagnie Generale d'Optique - Charenton Cedex
  • International Classification:
    C07F 9/02
  • US Classification:
    568 14, 568 15
  • Abstract:
    Disclosed is a thiosphosphine compound of formula:.
  • Spirotetrathiocarbamates And Spirooxothiocarbamates

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  • US Patent:
    7732507, Jun 8, 2010
  • Filed:
    Dec 19, 2003
  • Appl. No.:
    10/540176
  • Inventors:
    Aref Jallouli - Largo FL, US
    Martin Rickwood - Clarks Green PA, US
    Kimberly Morgan - Moosic PA, US
    Sirisoma Wanigatunga - Largo FL, US
  • Assignee:
    Essilor International Compagnie Generale d'Optique - Charenton-le-Pont
  • International Classification:
    G02B 1/04
  • US Classification:
    523106, 549 29, 549 30, 549 31, 549 32, 549 35, 549331, 549333, 549334
  • Abstract:
    Spirotetrathiocarbamates (STOCs) or oxa substituted compounds (SOTOCs) of Formula I: Formula (I) or bisSTOC or bisSOTOC compounds of Formula II: Formula (II) wherein X, X, X, X, X, X, X, and X, are independently O or S; and preferably at least two and up to all four of X, X, Xand X, and at least two and up to all four of X, X, X, and Xare sulfur; Z is —CRwherein m=1 to 4; —C(R)SC(R)—, C(R)SSC(R)—, or —C(R)OC(R); n is from 0 to 4; M is selected from CHCl, CHSC(O)R, CHSC(S)R, CHS(CHCHS)qH wherein q is 0, 1 or 2; —CR═CH, —CHOC(O)CR═CH, CHN═C═S, CHN═C═O, CHNRH, CHOH, CHSCHCHCR═CH, phenyl, C(R)phenyl, furan, thiophene, halogen, C-Ccycloalkyl, C-Cheretocyclics, thiol, H, (III) or (IV) wherein A is S, O or phenyl; x is 0 or 1; Ris C-Calkyl; and Ris H or C-Calkyl have excellent optical properties. Methods for preparing these compositions and optical lenses prepared from the compounds are also provided.

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  • Duration:
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