2012
DOI: 10.1016/j.polymer.2012.10.010
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Novel polyelectrolyte gels as absorbent polymers for nonpolar organic solvents based on polymerizable ionic liquids

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Cited by 29 publications
(23 citation statements)
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“…All the organic solvent absorption measurements were similar to our earlier reports . A quantity of about 0.10 g of dried sliced gel was placed in four different organic solvents (carbon tetrachloride, toluene, chloroform, and dichloromethane) at room temperature.…”
Section: Methodssupporting
confidence: 73%
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“…All the organic solvent absorption measurements were similar to our earlier reports . A quantity of about 0.10 g of dried sliced gel was placed in four different organic solvents (carbon tetrachloride, toluene, chloroform, and dichloromethane) at room temperature.…”
Section: Methodssupporting
confidence: 73%
“…This modification of MWCNTs, not only causes the polymerization becomes more easily on the surface, but also inserts the hydrophobic dissociable ionic groups into polymeric network that can improve the swelling capacity of ILMPGs in organic solvents. It should be noted that the effect of incorporation of the monomers with lipophilic ionic groups into polymeric gels on the organic solvent absorbency was investigated . In spite of the great achievements made in these studies, there are some limitations in these polyelectrolyte gels, in particular the formation of a polyelectrolyte gel with less effective network volume due to the presence of long alkyl chains in 1‐vinyl‐3‐alkylimidazolium tetrafluoroborate units.…”
Section: Resultsmentioning
confidence: 99%
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“…▪ Organic vegetable sorbents (peat moss (Cojocaru et al, 2011;Klavins and Porshnov, 2012), straw (Li et al, 2013a(Li et al, , 2013b, kenaf (Choi and Cloud, 1992) and wood fibers (Likon et al, 2013), etc). ▪ Organic synthetic sorbents (polypropylene (Wei et al, 2003), polyurethane foam (Yang et al, 2005), polyesters (Tanaka et al, 2012), styrene-alkyl acrylate polymers (Jang and Kim, 2000a, b;Ji et al, 2011), hydrophobic aerogels (Hrubesh et al, 2001;Korhonen et al, 2011), polyelectrolyte gels (Ono et al, 2012(Ono et al, , 2008Pourjavadi et al, 2012), polyorthocarbonates Sonmez and Wudl, 2005;Yati et al, 2013), cryogels based on rubber (Dogu and Okay, 2008;Karakutuk and Okay, 2010) and low molecular weight organogelators (Basak et al, 2012;Bhattacharya and Krishnan-Ghosh, 2001;Jadhav et al, 2010;Liu et al, 2013) etc).…”
Section: Introductionmentioning
confidence: 99%
“…The availability of functional monomers and cross-linkers with variable properties makes the cross-linked organic polymers applicable to different kinds of compounds [12,13]. In addition, both polar and nonpolar compounds can be extracted by polymers [14,15]. Cross-linked organic polymers have been applied in sample pretreatment methods such as miniaturized solid-phase extraction [14], solid-phase microextraction (SPME) [7] and stir-bar sorptive extraction (SBSE) [13].…”
Section: Introductionmentioning
confidence: 99%