Ab Initio Batch Emulsion Thiol-Ene Photopolymerization

被引:17
|
作者
Cuong Minh Quoc Le [1 ,2 ]
Schmutz, Marc [3 ]
Chemtob, Abraham [1 ,2 ]
机构
[1] Univ Haute Alsace, CNRS, IS2M, UMR7361, F-68100 Mulhouse, France
[2] Univ Strasbourg, F-67034 Strasbourg 2, France
[3] Univ Strasbourg, Inst Charles Sadron, CNRS, UPR 22, F-67034 Strasbourg 2, France
关键词
PARTICLE NUCLEATION LOCI; CONDENSATION POLYMERIZATION; CLICK CHEMISTRY; STABILIZATION; POLYURETHANE; POLYADDITION; MECHANISMS; CHALLENGES; KINETICS; LATEXES;
D O I
10.1021/acs.macromol.0c00265
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Very few step polymer latexes have been produced by aqueous emulsion polymerization and never with a clear picture of the operating mechanism. Therefore, finding new means to expand this widely used process industrially beyond chain radical polymerization is highly desirable. Herein, we report the successful photo-initiated thiolene radical polyaddition of an emulsion based on two bifunctional monomers diallyl phthalate and 2,2-(ethylenedioxy)diethanedithiol. After 20 min of irradiation (lambda(max) = 385 nm, 3.7 mW cm(-2)), polymerization resulted in a conversion above 99%, a coagulum-free poly(thioether) latex with a solid content of 10 wt %, a number-average molecular weight of 14 kDa, and an average particle diameter of 60 nm. Reaction kinetics, particle size distribution, and molecular weight progress have been studied in detail. To clarify the mechanism dictating particle formation, the number of particles per unit volume of water has been determined depending on reaction time and surfactant and initiator concentration. The nucleation mode is found to depart significantly from conventional chain radical emulsion polymerization. Polymer particle formation mainly proceeds through the precipitation of oligo-radicals (homogeneous nucleation) even when the concentration of the surfactant exceeds its critical micelle concentration. The end of nucleation (interval I) occurs until a monomer conversion of about 95%. The dispersion's solid content can reach as high as 40%, and the molecular weights remain reasonable (>4 kDa) even if the functional groups are stoichiometrically imbalanced. In contrast to conventional thermally induced polymerization, temporal control is demonstrated through sequential "on"/"off' cycles, and tuning of molecular weights is achieved by precise energetic dosage of radiation. This new step photopolymerization in emulsion thus opens an avenue for the synthesis of linear polysulfide latexes without high energy homogenization and at low irradiance.
引用
收藏
页码:2369 / 2379
页数:11
相关论文
共 50 条
  • [1] Mechanism and modeling of a thiol-ene photopolymerization
    Cramer, NB
    Davies, T
    O'Brien, AK
    Bowman, CN
    [J]. MACROMOLECULES, 2003, 36 (12) : 4631 - 4636
  • [2] Photopolymerization of pigmented thiol-ene systems
    Roper, TM
    Kwee, T
    Lee, TY
    Guymon, CA
    Hoyle, CE
    [J]. POLYMER, 2004, 45 (09) : 2921 - 2929
  • [3] Photopolymerization of thiol-ene/graphene nanocomposites
    Hoff, Ethan F. T.
    Sparks, Bradley J.
    Hayes, LaTonya
    Patton, Derek L.
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2013, 245
  • [4] Nanocomposite based on thiol-ene photopolymerization
    Wei, Huanyu
    Goswami, Shailesh K.
    Mathias, Lon J.
    Hoyle, Charles E.
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 233
  • [5] UNUSUAL ADDITION BY THE THIOL-ENE PHOTOPOLYMERIZATION
    KLEMM, E
    BEIL, U
    [J]. POLYMER BULLETIN, 1992, 28 (06) : 653 - 656
  • [6] Engineering the wettability of surfaces with thiol-ene photopolymerization
    Xiong, Li
    Patton, Derek
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 254
  • [7] Thiol-ene photopolymerization of functionalized resorcinarene cavitand thiols
    Johnston, Stephen Andrew
    Allmon, Storm-Marie
    Ramjee, Balasubramanian
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 255
  • [8] Photopolymerization of Thiol-Ene Systems Based on Oligomeric Thiols
    Clark, Tolecia
    Kwisnek, Luke
    Hoyle, Charles E.
    Nazarenko, Serge
    [J]. JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2009, 47 (01) : 14 - 24
  • [9] Accessing functional materials via thiol-ene photopolymerization
    Patton, Derek
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 256
  • [10] Rate mechanisms of a novel thiol-ene photopolymerization reaction
    Reddy, SK
    Cramer, NB
    O'Brien, AK
    Cross, T
    Raj, R
    Bowman, CN
    [J]. MACROMOLECULAR SYMPOSIA, 2004, 206 : 361 - 374