Search Results (64)

This study aimed to evaluate the antibacterial activity of several technical lignins against major environmental bacteria that cause mastitis in dairy cattle. The efficacy of four types of technical lignins against environmental mastitis pathogens was evaluated using MIC and MBC assays. The best candidate, sodium lignosulfonate (NaL-O), was further tested using sawdust bedding substrates. Substrates were prepared in different cleanliness conditions: sawdust only, sawdust plus urine, sawdust plus feces, or sawdust plus a combination of both. The antimicrobial activity of NaL-O against the mixture of environmental mastitis-causing pathogens was determined on days 0, 2, and 6 of incubation. In addition, the components of bedding substrates were analyzed to help understand the dynamics of pathogen loads. In the MIC and MBC assays, NaL-O showed the best antimicrobial performance against all pathogens except Escherichia coli. When testing in the bedding substrates, the addition of NaL-O decreased the concentration of Staphylococcus chromogenes, Streptococcus uberis, and Pseudomonas aeruginosa across all bedding cleanliness levels at d 0, 2, and 6 of incubation. As the incubation time increased, the antimicrobial effect decreased. NaL-O also lowered the counts of E. coli and Klebsiella pneumoniae across all incubation times, but to a lesser extent. The presence of feces significantly reduced the antibacterial effects of NaL-O for these two bacteria. Among the technical lignins tested, NaL-O showed the broadest antibacterial activity against the mastitis pathogens tested. This study suggests that NaL-O has promising potential as a bedding conditioner to control environmental pathogens on dairies due to its low cost, ready availability, and compatibility with sustainable livestock practices. Combined with bedding cleanliness, bedding conditioner application may play a crucial role in reducing the growth of EM pathogens and subsequent mastitis incidence. Full article

It is a great challenge to obtain an ideal hydrogel for the clinical treatment of intrauterine adhesion (IUA) disease. Here, a novel injectable chitosan–lignin/poloxamer hydrogel loaded with platelet-rich plasma (CL-PF127@PRP) was prepared by self-assembly at room temperature. Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), rheological analysis, and injectable writing were used to characterize the structure of the hydrogel. The results confirmed that the amino group of chitosan and the sulfonic group of sodium lignosulfonate were ionic-crosslinked by electrostatic attraction, which stabilized the three-dimensional structure of the PF127 hydrogel loaded with PRP, and PRP made the porous structure gradually become tight. Moreover, the CL-PF127@PRP hydrogel displayed good injectability and a solid state. The soaking experiment showed that the CL-PF127@PRP hydrogel had suitable degradation at pH = 7 and a good PRP release rate (PRP release 70% at 96 h). Cell experiments in vitro demonstrated that the CL-PF127@PRP hydrogel possessed good biocompatibility, an anti-inflammatory function, and pro-angiogenic activity. Furthermore, an animal experiment of skin wound and IUA confirmed that the skin wound closure rate of the CL-PF127@PRP hydrogel was over 50% on the seventh day. PRP improved the thickness of the endometrium and uterus receptivity, suggesting that the CL-PF127@PRP hydrogel offers great promise for the clinical treatment of IUA. Full article

Technical lignins are globally available and a sustainable feedstock. The unique properties of technical lignins suggest that these materials should have several industrial applications. The main proposal of this study is to evaluate the relationship between the structure and properties of two technical lignins. Morphological, chemical, physical, and thermal properties of sodium lignosulfonate (LGNa) and magnesium lignosulfonate (LGMg) were investigated. The results showed that a higher formation of intramolecular hydrogen bonds may occur in lignins with a higher content of phenolic hydroxyl groups, such as LGMg. As a result, an increase in the energy of hydrogen bonds in the lignosulfonate structure was observed, without significant change in the hydrogen bond distances. In addition, higher content of phenolic hydroxyl groups might also reduce lignosulfonates thermal stability. The combustion index value was three times higher for LGMg than for LGNa. The characterization study also revealed that phenolic hydroxyl groups influence the main properties of technical lignins and can be a determining factor when these lignosulfonates are used in industrial applications. Full article

This study introduces a novel water-insoluble dispersant for coal water slurry (CWS), namely, a poly(sodium styrene sulfonate)-grafted SiO₂ nanoparticle (SiO₂-g-PSSNa). SiO₂-g-PSSNa was synthesized by combining the surface acylation reaction with surface-initiated atom transfer radical polymerization (SI-ATRP). Fourier transform infrared spectrometry (FTIR), X-ray photoelectron spectroscopy (XPS), energy dispersive spectrometer (EDS), nuclear magnetic resonance spectroscopy (NMR) and thermogravimetric analysis (TGA) verified that SiO₂-g-PSSNa with the desired structure was successfully obtained. Afterwards, the performance of SiO₂-g-PSSNa as a dispersant in CWS preparation was evaluated. The results indicated that the optimal dosage of SiO₂-g-PSSNa was 0.3%. Compared to the famous commercial products, PSSNa and lignosulfonate (LS), SiO₂-g-PSSNa exhibits improved viscosity reduction performance. When SiO₂-g-PSSNa was used as the dispersant, the maximum coal loading of CWS was 64.2%, which was higher than LS (63.4%) and PSSNa (63.9%). All CWSs obtained in this study were pseudoplastic fluids and more consistent with the Herschel–Bulkley rheological model. The turbiscan stability index (TSI) of CWS prepared with SiO₂-g-PSSNa was 0.05, which was significantly lower than CWSs obtained from PSSNa (0.30) and LS (0.36). Therefore, SiO₂-g-PSSNa also exhibits excellent stability performance. This result was confirmed by rod penetration tests. The underlying mechanism was also clarified by various measurements, such as contact angle, zeta potential, EDS and low-field nuclear magnetic resonance spectra (low-field NMR). The results reveal that SiO₂-g-PSSNa can adsorbed onto the coal surface. SiO₂-g-PSSNa possesses a special branched structure, which bears a higher charge density as compared to linear ones with approximate chemical composition. As a result, coal particles adsorbed with SiO₂-g-PSSNa exhibit more electronegativity. With the enhancement of the electrostatic repulsive between coal particles, the apparent viscosity was lowered and the static stability was improved. This study demonstrated that solubility in water is not an essential factor in engineering the dispersant. Densely charged groups are probably more important. Full article

The thermal washing of oily sludge using sodium persulfate (SD) assisted by sodium lignosulfonate surfactant has been demonstrated to be an effective method for oily sludge remediation. To further explore the underlying mechanisms of this process, a systematic study was conducted by simulating oily sludge systems consisting of saturated hydrocarbons (SaH), aromatics hydrocarbons (ArH), resins (Res), and asphaltenes (Asp). The effects of reaction conditions, such as pH, sodium lignosulfonate alkyl (LSA) concentration, SD concentration, and washing temperature, were analyzed. Furthermore, the oxidative kinetic mechanism during the reaction process was investigated. The results demonstrated that neither petroleum hydrocarbons nor SD underwent significant chemical transformations when exposed to LSA, while SD exhibited a marked oxidative degradation effect on all four types of hydrocarbons. Oxidation kinetics indicated that sodium hydroxide played a catalytic role, with SD being the main oxidant and particularly efficient in degrading Asp and Res. Meanwhile, LSA contributed to the removal of hydrocarbons by reducing the surface tension of the solution, enhancing solubilization. This study not only elucidates the central role of SD in the thermal washing process but also provides a solid theoretical foundation for the practical application of this technology in oily sludge treatment. Full article

Transition metal oxide magnetite (Fe₃O₄) is recognized as a potential anode material for lithium-ion batteries owing to its high theoretical specific capacity, modest voltage output, and eco-friendly character. It is a challenging task to engineer high-performance composite materials by effectively dispersing Fe₃O₄ crystals with limited sizes in a well-designed supporting framework following sustainable approaches. In this work, the naturally abundant plant products sodium lignosulfonate (Lig) and sodium cellulose (CMC) were selected to coprecipitate with Fe³⁺ ions under mild hydrothermal conditions. The Fe-Lig/CMC intermediate sediment with an optimized microstructure can be directly converted to the Lig/CMC-derived carbon matrix-supported Fe₃O₄ nanocomposite sample (Fe₃O₄@LigC/CC). Compared with the controlled Fe₃O₄@LigC material, the Fe₃O₄@LigC/CC nanocomposite provides superior electrochemical performance in the anode, which has inspiring specific capacities of 820.6 mAh g⁻¹ after 100 cycles under a current rate of 100 mA·g⁻¹ and 750.5 mAh g⁻¹ after 250 cycles, as well as more exciting rate capabilities. The biomimetic sample design and synthesis protocol closely follow the criteria of green chemistry and can be further developed in wider scenarios. Full article

The clean and efficient utilization of coal is a promising way to achieve carbon neutrality. Coking coal is a scarce resource and an important raw material in the steel industry. However, the presence of pyrite sulfur affects its clean utilization. Nonetheless, this pyrite could be removed using depressants during flotation. Commonly used organic depressants (sodium lignosulfonate (SL), calcium lignosulfonate (CL), and pyrogallol (PY)) and inorganic depressants (calcium oxide (CaO) and calcium hypochlorite (Ca(ClO)₂)) were chosen in this study. Their inhibition mechanism was discussed using FTIR, XPS, and molecular dynamics (MD) methods. The desulfurization ability of organic depressants was shown to be better than inorganic ones. Among the organic depressants, PY proved to be advantageous in terms of low dosage. Physical adsorption was identified as the main interaction form of SL, CL, and PY onto the surface of pyrite, as evidenced from FTIR and XPS analyses. Similarly, MD simulation results showed that hydrogen bonds played a proactive role in the interactions between PY and pyrite. The diffusion coefficient of water molecules on the pyrite surface was also observed to decrease when organic depressants were present, indicating an increase in the hydrophilicity of pyrite. This research is of great significance to utilize sulfur-containing coal and minerals. Full article

Soybean meal (SM) adhesive is widely acknowledged as a viable substitute for traditional formaldehyde-based adhesives, given its ability to be easily modified, the utilization of renewable sources, and its eco-friendly characteristics. However, the application of SM adhesive in manufacturing has been impeded due to its restricted bonding capacity and inadequate water resistance. Researchers in the wood industry have recognized the significance of creating an SM-based adhesive, which possesses remarkable adhesive strength and resistance to water. This study endeavors to tackle the issue of inadequate water resistance in SM adhesives. Sodium lignosulfonate (L) was oxidized using hydrogen peroxide (HP) to oxidized lignin (OL) with a quinone structure. OL was then used as a modifier, being blended with SM to prepare SM-based biomass (OLS) adhesives with good water resistance, which was found practically through its utilization in the production of plywood. The influence of the HP dosage and OL addition on plywood properties was examined. The changes in the lignin structure before and after oxidation were confirmed using gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). The curing behavior and thermal stability of OLS adhesives were analyzed using dynamic mechanical analysis (DMA) and thermogravimetric (TG) analysis. The reaction mechanism was also investigated using FT-IR and XPS. The outcomes indicated a decrease in the molecular weight of L after oxidation using HP, and, at the same time, quinone and aldehyde functionalized structures were produced. As a result of the reaction between the quinone and aldehyde groups in OL with the amino groups in SM, a dense network structure formed, enhancing the water resistance of the adhesive significantly. The adhesive displayed exceptional resistance to water when the HP dosage was set at 10% of L and the OL addition was 10% based on the mass of SM. These specific conditions led to a notable enhancement in the wet bonding strength (63 °C, 3 h) of the plywood prepared using the adhesive, reaching 0.88 ± 0.14 MPa. This value represents a remarkable 125.6% increase when compared to the pure SM adhesive (0.39 ± 0.02 MPa). The findings from this study introduce a novel approach for developing adhesives that exhibit exceptional water resistance. Full article

To broaden the applications of wood, it is necessary to prepare flame-retardant coatings that can protect wood substrates during combustion. In this study, a bio-based, intumescent, flame-retardant phytic acid–melamine polyelectrolyte (PM) was prepared using phosphorus-rich biomass phytic acid and nitrogen-rich melamine as raw materials through an ion crosslinking reaction. Subsequently, a series of bio-based, flame-retardant wood coatings were prepared by optimizing the structure of urea–formaldehyde resin with the addition of melamine, sodium lignosulfonate, and PM as a flame-retardant curing agent. Woods coated with PM-containing coatings displayed significantly improved flame-retardant performances in comparison to uncoated woods. For PM-cured woods, the measured values of total heat release and total smoke production were 91.51% and 57.80% lower, respectively, compared with those of uncoated wood. Furthermore, the fire growth index decreased by 97.32%, indicating a lower fire hazard. This increase in flame retardancy and smoke suppression performance is due to the dense expanded carbon layer formed during the combustion of the coating, which isolates oxygen and heat. In addition, the mechanical properties of the flame-retardant coatings cured with PM are similar to those cured with a commercial curing agent, NH₄Cl. In addition, the prepared flame-retardant coating can also stain the wood. This study proves the excellent flame-retarding and curing effect of ammonium phytate in urea–formaldehyde resin coatings and provides a new approach for the application of bio-based flame retardants in wood coatings. Full article

Improving the thermal storage stability of nanosuspension concentrate (SC) prepared from low-melting-point pesticide is a recognized problem. In this work, using pyraclostrobin as the raw material, 25 wt% of pyraclostrobin nano-SC was prepared through a water-based grinding method, and the optimal grinding conditions were obtained as follows: a grinding time of 23 h, D-3911 as dispersant and a dispersant dosage of 12 wt%. The pyraclostrobin nano-SC D₉₀ size prepared based on this best formula was 216 nm. Adding glycerin could improve the stability of nano-SC at room temperature, but its thermal storage stability was still poor. For this problem, sodium lignosulfonate and cetyltrimethylammonium bromide (NaLS/CTAB) colloidal spheres were prepared through electrostatic and hydrophobic self-assembly and characterized. The delamination and precipitation of nano-SC can be significantly improved by adding an appropriate amount of colloidal spheres, and the nano-SC D₉₀ size decreased from 2726 to 1023 nm after 7 days of thermal storage. Farmland experiments indicated the control efficiency of pyraclostrobin nano-SC against flowering cabbage downy mildew disease was about 30% higher than that of SC. Especially after adding the wetting agent, the effect of nano-SC could be comparable to that of commercial Kairun (currently the best pyraclostrobin formulation in the world). Full article

Synthetic dyes are prone to water pollution during use, jeopardizing biodiversity and human health. This study aimed to investigate the adsorption and photocatalytic assist potential of sodium lignosulfonate (LS) in in situ reduced silver nanoparticles (AgNPs) and chitosan (CS)-loaded silver nanoparticles (CS-LS/AgNPs) as adsorbents for Rhodamine B (RhB). The AgNPs were synthesized by doping LS on the surface of chitosan for modification. Fourier transform infrared (FT-IR) spectrometry, energy-dispersive spectroscopy (EDS), scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) were used to confirm the synthesis of nanomaterials. The adsorption and photocatalytic removal experiments of RhB were carried out under optimal conditions (initial dye concentration of 20 mg/L, adsorbent dosage of 0.02 g, time of 60 min, and UV power of 250 W), and the kinetics of dye degradation was also investigated, which showed that the removal rate of RhB by AgNPs photocatalysis can reach 55%. The results indicated that LS was highly effective as a reducing agent for the large-scale production of metal nanoparticles and can be used for dye decolorization. This work provides a new catalyst for the effective removal of dye from wastewater, and can achieve high-value applications of chitosan and lignin. Full article

The aminated sodium lignosulfonate (AELS) was prepared through a Mannich reaction and characterized via FT-IR, TG, SEM and XPS in this study. Subsequently, the adsorption capacity of AELS for methyl blue (MB) was evaluated under various conditions such as pH, adsorbent dosage, contact time, initial concentration and temperature. The adsorption kinetics, isotherms and thermodynamics of AELS for methyl blue were investigated and analyzed. The results were found to closely adhere to the pseudo-second-order kinetic model and Langmuir isotherm model, suggesting a single-molecular-layer adsorption process. Notably, the maximum adsorption capacity of AELS for methyl blue (153.42 mg g⁻¹) was achieved under the specified conditions (T = 298 K, M_AELS = 0.01 g, pH = 6, V_MB = 25 mL, C₀ = 300 mg L⁻¹). The adsorption process was determined to be spontaneous and endothermic. Following five adsorption cycles, the adsorption capacity exhibited a minimal reduction from 118.99 mg g⁻¹ to 114.33 mg g⁻¹, indicating good stability. This study contributes to the advancement of utilizing natural resources effectively and sustainably. Full article

In this work, a synthesis and activation path, which enabled the preparation of spherical activated carbon from a lignin precursor, characterized by high adsorption capacity in the removal of phenolic compounds from water, was successfully developed. Two industrial by-products, i.e., Kraft lignin and sodium lignosulfonate, were used to form spherical nanometric lignin grains using pH and solvent shift methods. The obtained materials became precursors to form porous activated carbons via chemical activation (using K₂CO₃ or ZnCl₂ as activating agents) and carbonization (in the temperature range of 600–900 °C). The thermal stabilization step at 250 °C was necessary to ensure the sphericity of the grains during high-temperature heat treatment. The study investigated the influence of the type of chemical activator used, its quantity, and the method of introduction into the lignin precursor, along with the carbonization temperature, on various characteristics including morphology (examined by scanning electron microscopy), the degree of graphitization (evaluated by powder X-ray diffraction), the porosity (assessed using low-temperature N₂ adsorption), and the surface composition (analyzed with X-ray photoelectron spectroscopy) of the produced carbons. Finally, the carbon materials were tested as adsorbents for removing phenol from an aqueous solution. A conspicuous impact of microporosity and a degree of graphitization on the performance of the investigated adsorbents was found. Full article

Using sodium lignosulfonate as feedstock, ZnCl₂ and NaHCO₃ co-activated the hierarchical porous carbons (HPCs) were prepared by one-pot pyrolysis with different NaHCO₃ dosages (0–4 g) and carbonization temperatures (400–600 °C). Subsequently, phosphotungstate (HPW) was supported with the resulting biochar for the α-pinene hydration reaction to produce α-terpineol. The optimum preparation conditions were determined according to the yield of α-terpineol. The formation mechanism and physicochemical properties of HPCs were analyzed through TG, SEM, XPS, XRD, FT-IR, and N₂ adsorption–desorption isotherms. The results demonstrated that NaHCO₃ underwent a two-step reaction which liberated a substantial quantity of CO₂, thereby enhancing activated carbon’s macroporous and mesoporous structures. Simultaneously, NaHCO₃ mitigated strong acid gas (HCl) emissions during ZnCl₂ activation. Compared with AC450-4:8:0 prepared by ZnCl₂ activation alone, the total pore volume of AC450-4:8:2 prepared by co-activation is increased from 0.595 mL/g to 0.754 mL/g and the mesopore rate from 47.7% to 77.8%, which is conducive to reducing the steric hindrance of the hydration reaction and improving the selectivity. Hydration experiments show that the selectivity of α-terpineol is 55.7% under HPW/AC450-4:8:2 catalysis, higher than 31.0% for HPW and 47.4% for HPW/AC450-4:8:0. Full article

The electrolytic refining of crude tin is generally carried out in the fluorosilicic acid (H₂SiF₆) system with the assistance of bone glue and β-naphthol. However, the high saturated vapor pressure and low stability of H₂SiF₆ present environmental concerns and do not align with sustainable development goals. In this paper, the electrochemical behavior of tin on a glassy carbon (GC) electrode was studied in a relatively green and environmentally friendly methanesulfonic acid (MSA) system. Bone glue, sodium lignosulfonate, and β-naphthol were used as additives to make the deposit morphology smooth and to ensure grain refinement. The electrochemical reduction process of Sn²⁺ in an MSA system is a quasi-reversible process controlled by diffusion. The apparent activation energy $E_a$ = 14.189 kJ/mol for the ion diffusion of Sn²⁺ was further calculated. The results of chronoamperometry showed that the electrocrystallization of Sn²⁺ on the GC electrode gradually tended to three-dimensional instantaneous nucleation with the increase in applied potential. The morphology and phase of the deposits were analyzed using scanning electron microscopy (SEM) and X-ray diffraction (XRD). The results showed that the deposits were uniform and dense pure tin. This work elucidates the electrochemical behavior of tin in a methanesulfonic acid system. Full article