To develop more green, practical and efficient biochar amendments for acidic soils, chitosan-modified biochar (CRB) and alginate-modified biochar (ARB) were prepared, and their effects on promoting soil pH buffering capacity (pHBC) and immobilizing cadmium (Cd) in the paddy soils were investigated through indoor incubation experiments. The results of Fourier transform infrared spectroscopy and Boehm titration indicated that the introduction of chitosan and sodium alginate effectively amplified the functional groups of the biochar, and improved acid buffering capacity of the biochar. Since there was a plateau region between pH 4.5 and 5.5 in acid-base titration curve of the CRB, adding this biochar to acidic paddy soils apparently improved the pHBC and enhanced the acidification resistance of the paddy soils. The addition of ARB enhanced the reduction reactions during submerging and weakened the oxidation reactions during draining, thus retarded the decline of paddy soil pH during drainage. Furthermore, the pH of the paddy soils with ARB addition was higher at the end of draining, which reduced the activity of soil Cd. Considering the environmental sustainability of chitosan and sodium alginate and convenience of preparation method, biochars modified with these two materials provided alternatives for acidic paddy soil amelioration and heavy metal immobilization. However, the additional experiments should be conducted under field conditions to confirm practical application effects in the future.

Di-(2-ethylhexyl) phthalate (DEHP) has been classified as a priority pollutant which increased the healthy risk to human and animals dramatically. Hence, a novel biochemical system combined by DEHP-resistant bacterial flora (B) and a green oxidant of persulfate (PS) activated by Nano-Fe₃O₄ was applied to degrade DEHP in contaminated soil. In this study, the resistant bacterial flora was screened from activated sludge and immobilized by sodium alginate (SAB). Nano-Fe₃O₄ was coated on biochar (BC@Fe₃O₄) to prevent agglomerating in soil. X-ray diffraction (XRD) and scanning electron microscope (SEM) were utilized to characterize BC@Fe₃O₄. Results demonstrated that the treatment of biochemical system (SAB + BC@Fe₃O₄ + PS) presented the maximum degradation rate about 92.56% within 24 days of incubation and improved soil microecology. The 16S rDNA sequences analysis of soil microorganisms showed a significantly different abundance and a similar diversity among different treatments. Kyoto Encyclopedia of Genes and Genomes (KEGG) functional genes difference analysis showed that some metabolic pathways, such as metabolism of cofactors and vitamins, energy metabolism, cell growth and death, replication and repair, were associated with the biodegradation of DEHP. Besides, DEHP was converted to MEHP and PA by biodegradation, while DEHP was converted to DBP and PA by persulfate and BC@Fe₃O₄, and then ultimately degraded to CO₂ and H₂O.

Understanding of the interaction of graphene with natural polysaccharides (e.g., alginate) is crucial to elucidate its environmental fate. We investigated the impact of alginate on the agglomeration and stability of ¹⁴C-labeled few-layer graphene (FLG) in varying concentrations of monovalent (NaCl) and divalent (CaCl₂) electrolytes. Enhanced agglomeration occurred at high CaCl₂ concentrations (≥5 mM) due to the alginate gel networks formation in the presence of Ca²⁺. FLG enmeshed within extended alginate gel networks was observed under transmission electron microscope and atomic force microscope. However, background Na⁺ competition for binding sites with Ca²⁺ at the alginate surfaces shielded the gelation of alginate. FLG was readily dispersed by alginate under environmentally relevant ionic strength conditions (i.e., <200 mM Na⁺ and <5 mM Ca²⁺). In comparison with the bare FLG, the slow sedimentation of the alginate-stabilized FLG (158 μg/L) caused continuous exposure of this nanomaterial to freshwater snails, which ingested 1.9 times more FLG through filter-feeding within 72 h. Moreover, surface modification of FLG by alginate significantly increased the whole-body and intestinal levels of FLG, but reduced the internalization of FLG to the intestinal epithelial cells. These findings indicate that alginate will act as a stabilizing agent controlling the transport of FLG in aqueous systems. This study also provides the first evidence that interaction of graphene with natural polysaccharides affected the uptake of FLG in the snails, which may alter the fate of FLG in aquatic environments.

Slaughter wastewater is an important and wide range of environmental issues, and even threaten human health through meat production. A high efficiency and stability microsphere-immobilized Bacillus velezensis strain was designed to remove organic matter and inhibit the growth of harmful bacteria in process of slaughter wastewater. Bacillus velezensis was immobilized on the surface of sodium alginate (SA)/Polyvinyl alcohol (PVA)/Nano Zinc Oxide (Nano-ZnO) microsphere with the adhesion to bio-carrier through direct physical adsorption. Results indicated that SA/PVA/ZnO and SA/ZnO microspheres could inhibit E.coli growth with adding 0.15 g/L nano-ZnO and not affect Bacillus velezensis strain, and the removal the chemical oxygen demand (COD) rates of SA/PVA/ZnO microsphere immobilized cells are 16.99%, followed by SA/ZnO (13.69%) and free bacteria (7.61%) from 50% concentration slaughter wastewater within 24 h at 37 °C, pH 7.0, and 120 rpm, a significant difference was found between the microsphere and control group. Moreover, when the processing time reaches 36 h, COD degradation of SA/PVA/ZnO microsphere is obviously higher than other groups (SA/PVA/ZnO:SA/ZnO:control vs 18.535 : 15.446: 10.812). Similar results were obtained from 30% concentration slaughter wastewater. Moreover, protein degradation assay was detected, and there are no significant difference (SA/PVA/ZnO:SA/ZnO:control vs 35.4 : 34.4: 36.0). The design of this strategy could greatly enhance the degradation efficiency, inhibit the growth of other bacteria and no effect on the activity of protease in slaughter wastewater. These findings suggested that the nano-ZnO hydrogel immobilization Bacillus velezensis system wastewater treatment is a valuable alternative method for the remediation of pollutants from slaughter wastewater with a novel and eco-friendly with low-cost investment as an advantage.

In this study, an electrokinetic technique for remediation of Pb²⁺, Zn²⁺ and Cu²⁺ contaminated soil was explored using sodium alginate (SA) and chitosan (CTS) as promising biodegradable complexing agents. The highest Cu²⁺ (95.69%) and Zn²⁺ (95.05%) removal rates were obtained at a 2 wt% SA dosage, which demonstrated that SA significantly improved the Cu²⁺ and Zn²⁺ removal efficiency during electrokinetic process. The abundant functional groups of SA allowed metal ions desorption from soil via ion-exchange, complexation, and electrolysis. Pb²⁺ ions were difficult to remove from soil by SA due to the higher gelation affinity with Pb²⁺ than Cu²⁺ and Zn²⁺, despite the Pb²⁺ exchangeable fraction partially transforming to the reducible and oxidizable fractions. CTS could complex metal ions and migrate into the catholyte under the electric field to form crosslinked CTS gelations. Consequently, this study proved the suitability of biodegradable complexing agents for treating soil contaminated with heavy metals using electrokinetic remediation.

Magnetic carbon were synthesized from sugarcane bagasse using hydrothermal carbonization followed by thermal activation was converted to solid state as beads (hydrogels SACFe) using sodium alginate and applied as adsorbent in removal sulfamethoxazole in batch and column mode. From adsorption parameter analysis it was confirmed that 0.6 g L⁻¹ SACFe was effective in removing 50 mg L⁻¹ of SMX at pH 6.2. Sorption of SMX on SACFe beads followed Elovich kinetics and Freundlich isotherm. It was further confirmed that sorption occurred on heterogeneous surface of SACFe beads with chemisorption as rate limiting step. Maximum adsorption capacity was obtained as 58.439 mg g⁻¹ pH studies revealed that charged assisted hydrogen bonding, EDA interactions are some of the mechanism that favoured removal of SMX. From column studies it was found that bead height of 2 cm and flow rate of 1.5 mL min⁻¹ found to be best in removing pollutant. Thomas model fitted better the experimental data stating that improved interaction between adsorbent and adsorbate act as major driving force tool in obtaining maximum sorption capacity. Breakthrough curve was completely affected by varied flow rate and bed height. Column adsorption was effective in reducing COD and BOD levels of sewage which are affected by toxic pollutants and miscellaneous compounds. Feasibility analysis showed that SACFe beads could be employed for real-time applications as it is cost, energy effective and easy recovery.

High removal efficiency and excellent recyclability are the fundamental qualities that an outstanding adsorbent used for organic dye removal should possess. In this study, two recyclable gels (sodium alginate/Ca/fiber: SCFA hydrogels; cellulose nanofiber/chitosan: CNFCS aerogels) were successfully fabricated using the facile method. Additionally, the as-prepared adsorbents were investigated using a series of characterizations. The adsorption behavior and anti-interference performance of the synthesized gels were compared by choosing methylene blue (MB) as the model pollutant. The kinetic behavior of the gels towards MB was consistent with the pseudo first-order model, and the SCFA hydrogels reached adsorption equilibrium faster than the CNFCS aerogels. The maximum adsorption capacity of MB on the SCFA hydrogels and CNFCS aerogels was 1335.0 and 164.5 mg g⁻¹ (pH = 7.0, dosage: 0.5 g/L; initial concentration from 15 to 180 mg L⁻¹), respectively. More specifically, we found that the co-existing anions had different effects on MB adsorption over the gels used for MB removal. Furthermore, for the SCFA hydrogels, co-existing natural organic matter (NOM) at low concentrations enhanced MB adsorption, and then stabilized as the concentration of NOM increased. However, this increasing trend was not observed for MB adsorption on CNFCS aerogels; these gels exhibited a slight decrease at first, and then showed no change. Nevertheless, both the gels exhibited superior regeneration and recycling abilities.

Aiming at the problems of complex environment and serious dust pollution in large open-pit coal yards, a dust suppression gel with a dual network structure was prepared by modifying the soluble starch and sodium alginate with iron ions. The changes of functional groups, thermal stability, and morphology structure before and after the reaction were analyzed by FTIR, TG-DSC, and SEM, and the formation mechanism of the dual network was revealed by XPS. Furthermore, the water absorption and water retention experiments proved that the dual network structure is more conducive to water retention than the single-layer network. According to molecular dynamics simulations and contact angle experiments, gel and adsorbed water molecules can approach coal dust molecules on their own to contact, wet, and combine with coal dust. The adhesion test proved that the dust suppression gel with iron ions had better adhesion to dust. The anti-freezing test shows that the dust suppression gel has good anti-freezing performance. The antifreeze test shows that the dust suppression gel still has excellent freeze–thaw resistance at the test temperature of -20℃. The mechanical property test shows that the dust suppressant gel can prevent the product from being damaged by external force. The acid and alkali resistance experiments showed that the acid and alkali resistance of the gel was improved under the condition of iron ion modification, and the flying of coal powder was effectively prevented. This research provides a new theoretical idea for coal dust control in complex environment.

In this study, L-methionine and nano-Fe₃O₄ were encapsulated and cured on sodium alginate by the ionic cross-linking method to form magnetic composite gel spheres (SML) as an adsorbent for the removal of Zn(II) from water. The influence of adsorbent dosages, pH, reaction time, and initial ion concentration on the ability of the gel spheres to adsorb Zn(II) was investigated, and the adsorption mechanism was identified. The experimental results showed that under the optimum conditions (pH = 5, t = 60 min, dosage of SML is 0.7 g·L⁻¹), the maximum amount of Zn(II) adsorbed by the adsorbent gel spheres reached 86.84 mgˑg⁻¹. The reaction process of this adsorbent fits well with the Langmuir and pseudo-second-order kinetic models and is a heat absorption reaction. The adsorbent would preferentially adsorb Pb(II), and the adsorption efficiency of Zn(II) decreased when the concentration of interfering ions increased in the coexistence system. Further mechanistic research showed that this magnetic composite adsorbent is a mesoporous material with superior adsorption performance, and the amino and carboxyl groups on it react with Zn(II) via ligand chelation; the ion exchange effect of Ca(II) also plays a role. The adsorption amount of Zn(II) was maintained at a higher level after 5 cycles, and the loss of Fe was approximately 0.2%. In summary, SML, which is environmentally friendly, efficient, and recyclable, is an ideal adsorbent for Zn(II) removal.

This study focuses on the preparation of sodium alginate–coated iron-carbon granules (FeCGs) and their capacity to remove ibuprofen (IBU) by combining Fenton and ultrasound technologies. The preferred preparation conditions are as follows: 2% (w/v) sodium alginate, 10% (w/v) iron fillings and biochar, and used CaCl₂ as the cross-linking agent. 74.72% of IBU was removed by ultrasound/FeCG under 10 g/L FeCG and 250 W ultrasound power. Fenton/FeCG could remove 92.41% of IBU under 10 g/L FeCG and 2 mM H₂O₂. Under the above experimental conditions, ultrasound/FeCG has higher reaction speed (9.44 × 10⁻³ min⁻¹) than Fenton/FeCG (4.95 × 10⁻³ min⁻¹). However, Fenton/FeCG could remove more TOC than ultrasound/FeCG. During the reaction using the Fenton/FeCG system, 11 degradation intermediates were detected, but only 7 intermediates were produced by the ultrasound/FeCG system. A common single-chain product C₅H₁₀O₃ formed by IBU degradation was detected in the reaction products during Fenton/FeCG reaction, which benzene ring structure was destroyed; however, the minimum molecular weight of the product detected using the ultrasound/FeCG system was that of C₈H₁₀O; the benzene ring structure of IBU is not destroyed. This study provides guidance in the preparation of sodium alginate–coated FeCGs, evaluating the applicability of Fenton/FeCG and ultrasound/FeCG, which was meaningful for organic pollution wastewater treatment.