2009
DOI: 10.1016/j.carbpol.2009.04.004
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Synthesis, characterization, and applied properties of carboxymethyl cellulose and polyacrylamide graft copolymer

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Cited by 147 publications
(40 citation statements)
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“…It is obvious that introduction of MS exhibited great influence on the thermal behaviors of the superabsorbents. The weight loss about 6.4 wt% below 251ºC for CMC-g-PNaA (corresponding to an endothermic step at 248ºC) and about 4.9 wt% below 254.7ºC for CMC-g-PNaA/ MS (corresponding to an endothermic step at 253ºC) can be ascribed to the removal of water absorbed, the dehydration of saccharide rings in the chain of CMC [36]. The successive weight loss about 20.4 wt% (251~432ºC) for CMC-g-PNaA and about 17.3 wt% (255~436ºC) for CMC-gPNaA/MS can be attributed to the breaking of C-O-C bonds in CMC chains (corresponding to the endothermic peaks at 399ºC for CMC-g-PNaA and 401ºC for CMC-g-PNaA/MS) and the elimination of water molecule derived from the two neighboring carboxylic groups of the grafted PNaA chains due to the formation of anhydride (corresponding to the endothermic peak at 424ºC for CMC-g-PNaA and 425ºC for CMC-g-PNaA/MS) [37].…”
Section: Results and Discussion 31 Ftir Spectra Analysismentioning
confidence: 99%
“…It is obvious that introduction of MS exhibited great influence on the thermal behaviors of the superabsorbents. The weight loss about 6.4 wt% below 251ºC for CMC-g-PNaA (corresponding to an endothermic step at 248ºC) and about 4.9 wt% below 254.7ºC for CMC-g-PNaA/ MS (corresponding to an endothermic step at 253ºC) can be ascribed to the removal of water absorbed, the dehydration of saccharide rings in the chain of CMC [36]. The successive weight loss about 20.4 wt% (251~432ºC) for CMC-g-PNaA and about 17.3 wt% (255~436ºC) for CMC-gPNaA/MS can be attributed to the breaking of C-O-C bonds in CMC chains (corresponding to the endothermic peaks at 399ºC for CMC-g-PNaA and 401ºC for CMC-g-PNaA/MS) and the elimination of water molecule derived from the two neighboring carboxylic groups of the grafted PNaA chains due to the formation of anhydride (corresponding to the endothermic peak at 424ºC for CMC-g-PNaA and 425ºC for CMC-g-PNaA/MS) [37].…”
Section: Results and Discussion 31 Ftir Spectra Analysismentioning
confidence: 99%
“…Considerable research has been devoted to the development of copolymers in which CMC is reacted with acrylic monomers and various crosslinking agents to form SAPs (Kuwabara and Kubota 1996;Pourjavadi and Mahdavinia 2005;Pourjavadi and Ghasemzadeh 2006;Abd El-Mohdy 2007;Ibrahim et al 2007;Pourjavadi et al 2007aPourjavadi et al -b, 2008Pourjavadi et al , 2009Pourjavadi et al , 2010Suo et al 2007;Ali et al 2008;Chen et al 2008;Yang et al 2009;El-Din et al 2010;Feng et al 2010a;Lin et al 2010;Bao et al 2011;Eldin et al 2011;Huang et al 2011;Liu et al 2011;Shu et al 2011;Varaprasad et al 2011;Wang et al 2011c). Water absorbency values generally in the range of 40 to 1400 g/g have been reported in such studies, with the highest value reported by Pourjavadi et al (2008).…”
Section: Copolymers Of Cmc By Reaction With Monomersmentioning
confidence: 99%
“…A number of authors have reported progress in development of somewhat "salt-tolerant" hydrogels (Kulicke and Nottelmann 1989;Yang et al 2009;Wu et al 2012). Yang et al (2009) attributed the observed salt-tolerance to graft polymerization between CMC and polyacrylamide.…”
Section: Effects Of Salinitymentioning
confidence: 99%
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“…Carboxymethylation is followed by an etherification using chloroacetic acid or its sodium salt. The aim is to convert hydroxyl groups in carboxymethyl groups [1,2]. CMC has many desirable applications such as coating, formation of emulsions and suspensions, and water retention.…”
Section: Introductionmentioning
confidence: 99%