2012
DOI: 10.1016/j.polymer.2012.06.043
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Controlled synthesis of sulfonated block copolymers having thermoresponsive property by RAFT polymerization of vinyl sulfonate esters

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Cited by 20 publications
(16 citation statements)
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References 55 publications
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“…Controlled radical polymerizations of sulfur-containing vinyl monomers, such as pyridyl disulfide ethyl methacrylate [17][18][19][20], disulfide-based di(meth)acrylates [21][22][23][24], and vinyl monomers with protected thiol groups [25][26][27][28], have been employed in the production of a variety of functional polymers with well-defined structures and highly ordered architectures. Recently, we have also explored the controlled synthesis of sulfurcontaining polymers by reversible addition-fragmentation chain transfer (RAFT) polymerization of S-vinyl sulfonate esters [29,30] and S-vinyl sulfides [31][32][33], which belong to the family of S-vinyl monomers. Indeed, the RAFT polymerization of phenyl vinyl sulfide (PVS) and its derivatives has been successfully used to synthesize well-defined homopolymers and block copolymers with pendant thioether groups [31].…”
Section: Introductionmentioning
confidence: 99%
“…Controlled radical polymerizations of sulfur-containing vinyl monomers, such as pyridyl disulfide ethyl methacrylate [17][18][19][20], disulfide-based di(meth)acrylates [21][22][23][24], and vinyl monomers with protected thiol groups [25][26][27][28], have been employed in the production of a variety of functional polymers with well-defined structures and highly ordered architectures. Recently, we have also explored the controlled synthesis of sulfurcontaining polymers by reversible addition-fragmentation chain transfer (RAFT) polymerization of S-vinyl sulfonate esters [29,30] and S-vinyl sulfides [31][32][33], which belong to the family of S-vinyl monomers. Indeed, the RAFT polymerization of phenyl vinyl sulfide (PVS) and its derivatives has been successfully used to synthesize well-defined homopolymers and block copolymers with pendant thioether groups [31].…”
Section: Introductionmentioning
confidence: 99%
“…As the temperature increases, the thermosensitive blocks tend to self-aggregate, exhibiting enhanced viscosity, which gives them greater stability to the effect of temperature and salinity of the medium [166]. These polymers are characterized by having AM units in the backbone and contain side-hydrophobic groups, including N-allyl benzamide, vinyl naphthalene, divinyl sulfone, oleic imidazoline, and perfluorinated chains along the polymer chain; these units have been shown to be hydrophobic [167][168][169]. The main thermoviscosifying polymers for oilfield application are N-alkyl-substituted AM copolymers, grafted polyethers, and cellulose derivatives [170].…”
Section: Hydrophobically Associating and Thermoviscosifying Polymersmentioning
confidence: 99%
“…These polymers are characterized by having AM units in the backbone and contain side‐hydrophobic groups, including N ‐allyl benzamide, vinyl naphthalene, divinyl sulfone, oleic imidazoline, and perfluorinated chains along the polymer chain; these units have been shown to be hydrophobic 167–169. The main thermoviscosifying polymers for oilfield application are N ‐alkyl‐substituted AM copolymers, grafted polyethers, and cellulose derivatives 170.…”
Section: Syntheticx Polymersmentioning
confidence: 99%
“…This is imperative because a predominantly weak associative effect would not necessarily guarantee the needed rheological impact in terms of recovery efficiency even if polymer injectivity is not affected. (Pu and Xu, 2009) Gudong HPAM 68.0 3022 (Zhijian et al, 1998) Bohai Bay HPAM 65.0 6070 (Mogollon and Lokhandwala, 2013) Xing Long Tai HPAM 56.6 3112 (Zhang et al, 1999) Bohai oil field HAPAM 65.0 32423 (Han et al, 2006) Henan oil field HPAM 75.0 5060 (Chen et al, 1998) Shengli HPAM 70.0 10000 (Gao, 2014) USA Cambridge Minnelusa PAM 55.6 Not specified (Vargo et al, 2000) Tambaredjo HPAM 36.0 Not Specified (Mogollon and Lokhandwala, 2013) Tanner PAM 80.0 66800 (P) a (Pitts et al, 2006) West Khiel HPAM 57.0 46,480 (P) a (Meyers et al, 1992) Canada Pelican HPAM 23.0 6800 (Mogollon and Lokhandwala, 2013) David pool PAM 31.0 6660 (I) b (Pitts et al, 2004 (Algi and Okay, 2014;Fang et al, 2016) 2-vinylnaphtahlene (Zeng et al, 2002) Methacrylic Acid (Fernyhough et al, 2009;Bang et al, 2017) N-vinylpyrrolidinone (Taghizadeh and Foroutan, 2004;Willersinn and Schmidt, 2017) 4-vinylbenzenesulfonate (Kang et al, 2015) 2-Acrylamido-2-methyl-1-propanesulfonic acid (Çavuş, 2010;Kundakci et al, 2011) Methyl methacrylate (Cilurzo et al, 2014;Khromiak et al, 2018) Poly(propylene glycol) methacrylate (Shemper et al, 2002) Sodium vinylsulfonate (Mori et al, 2010;Mori et al, 2012) Carboxymethyl cellulose (Han et al, 2010;Han et al, 2013) N-phenylacrylamide (Zhou and Lai, 2004) N-tert-Octylacrylamide (Zhu et al, 2012) N-dodecylacrylamide…”
Section: Conclusion and Recommendationsmentioning
confidence: 99%