2015
DOI: 10.1080/01932691.2015.1022658
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Sulfobutylated Lignosulfonate with Ultrahigh Sulfonation Degree and Its Dispersion Property in Low-Rank Coal-Water Slurry

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Cited by 18 publications
(7 citation statements)
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“…An example would be the oxypropylation of sodium lignosulfonate, as it has been conducted to increase reactivity with methane diisocyanate for lignin-polyurethane synthesis [154]. When considering the dispersant application of lignosulfonates, sulfobutylation (alkyl sulfonic acid grafting) has been conducted [155]. The lignosulfonates accordingly showed a high degree of sulfonation with 3.86 mmol/g and improved viscosity reduction of low-rank coal-water slurries.…”
Section: Relationship Between the Chemical Make-up And The Physicochemical Behaviormentioning
confidence: 99%
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“…An example would be the oxypropylation of sodium lignosulfonate, as it has been conducted to increase reactivity with methane diisocyanate for lignin-polyurethane synthesis [154]. When considering the dispersant application of lignosulfonates, sulfobutylation (alkyl sulfonic acid grafting) has been conducted [155]. The lignosulfonates accordingly showed a high degree of sulfonation with 3.86 mmol/g and improved viscosity reduction of low-rank coal-water slurries.…”
Section: Relationship Between the Chemical Make-up And The Physicochemical Behaviormentioning
confidence: 99%
“…The lignosulfonates accordingly showed a high degree of sulfonation with 3.86 mmol/g and improved viscosity reduction of low-rank coal-water slurries. The underlying implication is that by placing the sulfonate groups on alkyl chains, these would not only be more accessible, but also possessed a higher degree of freedom, which could play out as a more effective anchoring effect and hence improve dispersion ability [155].…”
Section: Relationship Between the Chemical Make-up And The Physicochemical Behaviormentioning
confidence: 99%
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“…Specific experimental steps are as follows: 10 g of TA was dissolved in a 250 mL three-necked flask equipped with 100 mL of water, adjusted to pH 12 with aqueous sodium hydroxide solution, and heated to 80 °C to fully dissolve, and then to a three-necked flask was added dropwise 1,6-dibromohexane for a 1 h drop finish at 80 °C reaction for 5 h. Then, hydrochloric acid was used to adjust the pH to 3–4, and 1.2 mL of hydrogen peroxide was added at 80 °C for 0.5 h. Next, different proportions of IA and AMPS aqueous solution and initiator were added to the three-necked flask. After 3 h of reaction, the mixture was cooled to room temperature , and excess 1,6-dibromohexane , was removed using hexane. , Finally, the filtrate was dialyzed in 3500 dialysis bags for 3 days and then oven-dried to obtain TIA-1. Adding 15 and 20 g of TA in the same way can give TIA-2 and TIA-3, respectively.…”
Section: Experimental Sectionmentioning
confidence: 99%
“…However, in water, lignosulfonates are dissolved as an aggregate of curled‐up molecules, resulting in low reactivity. To expand the application field of lignosulfonates, their reactivity can be improved by chemical modification in green solvents for different application fields [24] . Moreover, the free phenolic hydroxyl group is easily ionized, so that the para and ortho positions of the phenolic hydroxyl group are activated, and then it can be oxidized, degraded, or dealkylated with nucleophiles such as formaldehyde.…”
Section: Introductionmentioning
confidence: 99%