2014
DOI: 10.1016/j.biortech.2014.10.014
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Production of modified bentonite via adsorbing lignocelluloses from spent liquor of NSSC process

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Cited by 14 publications
(7 citation statements)
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“…26,28 Lignin is negatively charged, mainly because of the presence of carboxylate and in some cases sulfonate groups. 26,29 It is proposed that the charge interaction was the primary bonding mechanism between lignin (as an anionic polymer) and cationic polymers, such as polydiallyldimethylammonium chloride 30,31 and poly(ethylenimine). 32 On the basis of the chemical structures of lignin and HPU, two mechanisms of interaction between HPU and lignin are suggested.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…26,28 Lignin is negatively charged, mainly because of the presence of carboxylate and in some cases sulfonate groups. 26,29 It is proposed that the charge interaction was the primary bonding mechanism between lignin (as an anionic polymer) and cationic polymers, such as polydiallyldimethylammonium chloride 30,31 and poly(ethylenimine). 32 On the basis of the chemical structures of lignin and HPU, two mechanisms of interaction between HPU and lignin are suggested.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…Considering the impact of lignin on mechanical and physical properties of lignin-HPU hydrogels, it is important to elucidate the source of interaction between lignin and HPU macromolecules. Lignin has a complex chemical structure that contains carboxylate, sulfonate and hydroxyl groups, which depends on the initial pulping process and the origin of lignin. , Lignin is negatively charged, mainly because of the presence of carboxylate and in some cases sulfonate groups. , It is proposed that the charge interaction was the primary bonding mechanism between lignin (as an anionic polymer) and cationic polymers, such as polydiallyldimethylammonium chloride , and poly­(ethylenimine) . On the basis of the chemical structures of lignin and HPU, two mechanisms of interaction between HPU and lignin are suggested.…”
Section: Results and Discussionmentioning
confidence: 99%
“…The hemicellulose (sugar) content of the SL was determined following 3,5‐dinitrosalicylic acid (DNS) method, as explained previously . However, the DNS reagent can only indicate monomeric sugars . In this regard, all samples were hydrolyzed in a 4 wt% sulfuric acid solution in a Haak‐S45 oil bath at 121°C for 1 h so that all oligomeric sugars were broken to monomeric sugars .…”
Section: Methodsmentioning
confidence: 99%
“…Previous studies reported that the extraction of lignocelluloses from SLs would significantly reduce the chemical oxygen demand (COD) and turbidity of lignocellulosic wastewater effluents . The application of lignocelluloses extracted from SL as an energy source, fillers, flocculants, composites and resins were reported in the past.…”
Section: Introductionmentioning
confidence: 99%
“…The temperature of these experiments was fixed at 30 °C, as an earlier study showed that the adsorption of lignin on activated carbon was the maximum at 30 °C . The stirring rate was chosen based on previous studies on SL and prehydrolysis liquor. ,, However, more studies on the effect of stirring rate should be considered in order to investigate if the adsorption/coagulation process of lignocelluloses on fly ash were possible under different conditions. The treated SLs were centrifuged at 1000 rpm for 10 min using a Survall ST16 centrifuge.…”
Section: Materials and Methodsmentioning
confidence: 99%