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Sulfonation degree is an important structural parameter of lignosulfonates which affect their water solubility, surface activity, and dispersing performance. Presently, the methods for determining sulfonation degree include elemental analysis and potentiometric titration; they have some shortcomings such as complex purification process, high equipment requirements, and time-consuming. Hence, a simple and rapid method to determine the sulfonation degree of lignosulfonates was proposed based on the electrostatic interaction between cationic surfactant (hexadecyl trimethyl ammonium bromide (CTAB)) and anionic lignosulfonates. CTAB was added and co-precipitated with lignosulfonates and then the ultraviolet absorbance of the supernatant was determined. The sulfonation degree of lignosulfonates was calculated according to the titration curve of the supernatant absorbance to the amount of CTAB. This method is applicable to lignosulfonates recovered from acid pulping as well as sulfonation products of alkali lignin. Because of the easy operation process and no purification process for lignosulfonates, this method was simple and rapid when compared to existing methods for sulfonation degree determination of lignosulfonates. [ABSTRACT FROM AUTHOR]

Sodium lignosulfonate (NaLS) was dissolved in saline solutions, and the dissolving process was examined by a combination of static and dynamic light scattering. When NaLS was dissolved in 1.2 mol l-1 NaCl solution for 24 h and filtered through a 0.45 μm syringe filter, only a fast relaxation mode was observed, which was attributed to the co-diffusion of NaLS molecular ions and counterions. When the concentration of NaCl was below 1.2 mol l-1 or the dissolving time was <24 h, an additional slow relaxation mode (SRM) appeared due to hindered motions of electrostatically interacting chains. Without filtering or filtering followed by rising temperature to 38°C, SRM appeared due to aggregation, which occurred at a position similar to that caused by electrostatic interaction. For poly(sodium styrenesulfonate) (NaPSS) and modified bamboo lignin derivate with open polyelectrolyte structures, 0.1 mol l-1 NaCl was enough to inhibit the electrostatic interaction. For NaLS with a closed polyelectrolyte structure, the SRM could not be removed until the concentration of NaCl reached 1.2 mol l-1. Above observations give insights for the first time into the relationship between the SRM caused by electrostatically interacting chains and the diffusion mode due to NaLS aggregation, and the influence of the closed polyelectrolyte structure on the SRM. [ABSTRACT FROM AUTHOR]

Highlights: [•] A modified lignosulfonate GCL4-1 improves stability of DMM suspension significantly. [•] GCL4-1 fraction with Mw of 10,000–30,000 has strongest dispersive ability. [•] Dispersive ability of GCL4-1 is contributed to sulfonated degree and adsorbed amount. [•] GCL4-1 fraction with largest Mw has strongest adsorption, but may cause flocculation. [ABSTRACT FROM AUTHOR]

Abstract: As a plasticizer and retarder, calcium lignosulfonate (CL) frequently leads to quick set of Portland cement containing anhydrite. For exploring the cause of this problem, the hydration characteristics of the tricalcium aluminate–anhydrite system in the saturated calcium hydroxide solution with and without CL were researched from two aspects: the compositions of liquid phases and the formations of hydration products. Results show that the CL can promote the formation of ettringite, which induces a significant decrease in sulfate ion concentration at the initial time of hydration. The size of ettringite crystals becomes large in the presence of CL, which seems to be related to a decrease in calcium sulfate saturation ratio. It can be deduced that the quick set in the presence of CL is mainly caused by the accelerated reaction between the tricalcium aluminate and the anhydrite at the initial time of hydration. [Copyright &y& Elsevier]

Abstract: Different lignosulfonate (LS) samples were prepared via a three-step method and were characterized by FT-IR, UV, GPC and functional groups measurement. FT-IR and UV spectra confirmed the prepared samples had typical characteristics of lignin materials. GPC and functional groups measurement results indicated the samples had different molecular mass (M w), but same quantities of sulfonic groups (S). The influence of M w of LS on the resulting surface charges of dimethomorph particles via adsorption was further investigated. The results indicated that the adsorption isotherms of LS on dimethomorph surfaces belonged to L-type and the adsorption capacity (q m) increased with increasing M w. However, the non-linear correlation between zeta potentials with the products of S and adsorption amount (SA) indicated SA did not positively improve the surface charges expectedly. Based on the analysis, an adsorption confirmation was proposed allowing prediction of the relation between M w and surface charge efficiency of LS for solid particles. [Copyright &y& Elsevier]

Two pretreatment methods to overcome recalcitrance of lignocelluloses, sulfite pretreatment (SPORL) and dilute acid (DA), were conducted to pretreat softwood masson pine and hardwood eucalyptus for enzymatic hydrolysis. In the presence of corresponding pre-hydrolysates, adding moderate cetyltrimethylammonium bromide (CTAB) could enhance the enzymatic hydrolysis of the SPORL-pretreated substrates, but had no enhancement for the DA-pretreated substrates. The results showed that sodium lignosulfonate (SL) in pre-hydrolysates and CTAB together had a strong enhancement on the enzymatic hydrolysis of lignocelluloses. The compound of commercial lignosulfonate SXSL and CTAB (SXSL-CTAB) could enhance the substrate enzymatic digestibility (SED) of SPORL-pretreated masson pine from 27.1% to 71.0%, and that of DA-pretreated eucalyptus from 37.6% to 67.9%. The mechanism that CTAB increased the adsorption of SL on lignin to form more effective steric hindrance and reduced the non-productive adsorption of cellulase on lignin by neutralizing the negative charge of SL was proposed. [ABSTRACT FROM AUTHOR]

Effect of the molecular structure of lignosulfonate-based polyoxyethylene ether (LS-PEG) on the enzymatic hydrolysis of Avicel and corn stover was investigated. With the increase of PEG contents and M w of LS-PEG, glucose yield of corn stover increased from 16.7% to 51.9%. When LS-PEG was compounded with cationic surfactant cetyltrimethylammonium bromide (CTAB), the enhancement of glucose yield of corn stover was further increased from 45.3% to 62.8%. Sulfonic group of LS-PEG preferentially interacted with quaternary ammonium group of CTAB by the electrostatic attraction to form a similar non-ionic surfactant CTAB-LS-PEG. CTAB-LS-PEG showed electrically neutral and more hydrophobic, and blocked more nonproductive adsorption of cellulase on the lignin. Therefore, CTAB-LS-PEG enhanced enzymatic hydrolysis efficiency of lignocelluloses more significantly. The understanding developed in this study can help to develop potential approaches and strategies for effective application of lignosulfonate to improve bioconversion of lignocellulosic biomass. [ABSTRACT FROM AUTHOR]

Sodium lignosulfonate (SXSL) and long-chain fatty alcohols (LFAs) could enhance the enzymatic hydrolysis of xylan, and the compound of SXSL and LFAs have synergies on the enzymatic hydrolysis. SXSL shows a strong enhancement in buffer pH range from 4.0 to 6.0. The enhancement increased with the SXSL dosage and the xylanase loading. The cellulose and lignin in corncob substrate could not only adsorb xylanase nonproductively, but also seriously reduce the accessibility of xylanase on xylan to impede the enzymatic hydrolysis of xylan. Cellulase could break the plant cell wall structure of corncob and make additives work better. The xylose yield of corncob at 72 h increased from 59.4% to 73.7% by adding the compound of 5 g/L SXSL and 0.01% (v/v) n -decanol, which was higher than that without cellulase and additives by 30.7%. Meanwhile, the glucose yield at 72 h of corncob increased from 45.8% to 62.3%. [ABSTRACT FROM AUTHOR]

Abstract: Lignosulfonate is an anionic surfactant from pulp processing industries. Alcohols are often used as cosurfactants in the application of surfactant. The improvement of straight-chain alcohols with different alkyl chain lengths as cosurfactant on the physicochemical properties of calcium lignosulfonate (CL) aqueous solution has been investigated. The results indicate that small amounts of straight-chain alcohols with longer alkyl chains are helpful in improving the surface activity of CL, especially when the number of carbon atoms in alcohols is 10 or larger. The adsorption amount of CL solutions with additives of longer chain alcohols on TiO2 particles increases greatly, and the zeta potential of TiO2 particles adsorbing CL rises significantly. It can be concluded that there is a cooperative effect of the longer chain alcohols on lignosulfonate to form a tighter adsorption layer at the interface. The steric hindrance increases with the increasing amount of adsorption, and the static repulsive force increases with the increasing zeta potential. Therefore, the effect of CL on the stability of the TiO2 suspension is enhanced dramatically by addition of longer chain alcohols. This understanding can lead to further development in expanding the functionalities of the lignosulfonate through manipulation of the adsorption capacity of CL on solid particles and enhance the dispersive ability of CL on solid suspensions by adding longer straight-chain alcohols. [Copyright &y& Elsevier]