Cerium added corn-based biochar as particle electrode for electrochemical oxidation industrial wastewater.

Three-dimensional (3D) electrochemical oxidation has become a popular advanced oxidation technology for wastewater treatment due to its various benefits. In this study, cerium (Ce) loaded biochar (Ce/BC) was used as a particle electrode to conduct the degradation of industrial wastewater released by the chemical industry. SEM, EDS, XRD, FTIR, XPS, and BET were used to characterize the properties of Ce/BC. The effects of some variables, including Ce loading (0-5%), pH (5-9), Ce/BC dosage (12.5-50.0 g/L), and working voltage (12-20 V), were evaluated with regard to COD elimination. The kinetics of COD oxidation and the energy consumption were carefully investigated. Tert-butanol significantly reduced the removal efficiency of COD, indicating that hydroxyl radicals generated during the process rather than direct electro-oxidation were the main mechanism for COD degradation. The treatment of industrial wastewater might benefit from the use of Ce/BC as particle electrode.

A review of additives use in straw composting.

Straw composting is not only a process of decomposition and re-synthesis of organic matter, but also a process of harmless treatment, avoiding air pollution caused by straw burning. Many factors, including raw materials, humidity, C/N, and microbial structure, may determine the composting process and the quality of final product. In recent years, many researches have focused on composting quality improvement by adding one or more exogenous substances, including inorganic additives, organic additives, and microbial agents. Although a few review publications have compiled the research on the use of additives in composting, none of them has specifically addressed the composting of crop straw. Additives used in straw composting can increase degradation of recalcitrant substances and provide ideal living surroundings for microorganism, and thus reduce nitrogen loss and promote humus formation, etc. This review's objective is to critically evaluate the impact of various additives on straw composting process, and analyze how these additives enhance final quality of composting. Furthermore, a vision for future perspectives is provided. This paper can serve as a reference for straw composting process optimization and composting end-product improvement.

Self-regeneration hybrid hydrogel for bisphenol a adsorption in water.

Hybrid hydrogel was synthesized by immobilizing TiO2 in polyethylene glycol diacrylate (TiO2@PEGDA) as an efficient adsorbent with photocatalysis property for bisphenol A (BPA) elimination. TiO2@PEGDA exhibited spherical and rough structure with limited crystallinity and abundant functional groups. The contact angle increased to 61.96° (TiO2@PEGDA) from 46.73° (pristine PEGDA), indicating that hydrogel hydrophilicity decreased due to the presence of TiO2. The swelling capacity of TiO2@PEGDA (9.0%) was decreased compared with pristine PEGDA (15.6%). Adsorption results demonstrated that the maximum adsorption capacity of TiO2@PEGDA (101.4 mg/g) for BPA was slightly higher than that of pristine PEGDA (97.68 mg/g). The adsorption capacity was independent with pH below 8 and decreased obviously when the value of pH was higher than 8. The adsorption behavior was fitted well with the pseudo-second-order kinetic and the Langmuir isotherm model. Both ΔG0 and ΔH0 were negative, indicating that BPA adsorbed on TiO2@PEGDA was an exothermic and spontaneous process. Regeneration study was performed by photocatalysis, and the adsorption capacity was 85.6% compared with the initial capacity after four-cycle use, indicating that TiO2@PEGDA could be recycled without significant adsorption capacity loss. Consequently, TiO2@PEGDA can serve as an eco-friendly and promising material for efficiently adsorbing BPA with self-clean property.

Processing and modification of hydrogel and its application in emerging contaminant adsorption and in catalyst immobilization: a review.

Due to the wonderful property of hydrogels, they can provide a platform for a wide range of applications. Recently, there is a growing research interest in the development of potential hydrogel adsorbents in wastewater treatment due to their adsorption ability toward aqueous pollutants. It is important to prepare such a hydrogel that possesses appropriate robustness, adsorption capacity, and adsorption efficiency to meet the need of water treatment. In order to improve the property of hydrogels, much effort has been made by researchers to modify hydrogels, among which incorporating inorganic components into the polymeric networks is the most common method, which can reduce the product cost and simplify the preparation procedure. Not only can hydrogel be applied as adsorbent, but it also can be used as matrix for catalyst immobilization. In this review, the key advancement on the preparation and modification of hydrogels is discussed, with special emphasis on the introduction of inorganic materials into polymeric networks and consequential changes in the properties of mechanical strength, swelling, and adsorption. Besides, hydrogels used as adsorbents for removal of dyes and inorganic pollutants have been widely explored, but their use for adsorbing emerging contaminants from aqueous solution has not received much attention. Thus, this review is mainly focused on hydrogels' application in removing emerging contaminants by adsorption. Furthermore, hydrogels can be also applied in immobilizing catalysts, such as enzyme and photocatalyst, to remove pollutants completely and avoid secondary pollution, so their progress as catalyst matrix is overviewed.

Immobilization of laccase on magnetically separable biochar for highly efficient removal of bisphenol A in water.

Laccase was stably immobilized on a cost effective and nanosized magnetic biochar (L-MBC) by adsorption, precipitation and crosslinking, and it was used for high performance BPA removal. A large amount of enzyme could be immobilized on the magnetic biochar with high activity (2.251 U per mg MBC), and the L-MBC could be magnetically separated from the aqueous solution in 20 seconds. The successful immobilization of laccase was also confirmed via FTIR, SEM, and EDS analyses. The L-MBC presented better storage and stability performances, pH tolerance and thermal stability than the free laccase. It was found that BPA with an initial concentration of 25 mg L-1 could be thoroughly removed within 75 min, where BPA removal was attributed to enzymatic degradation and adsorption. In addition, the BPA removal efficiency by the L-MBC could be maintained above 85% even after seven cycles of repeated use. Due to high stability and efficient recyclability, the L-MBC-based biocatalyst has the potential to be a reliable method for treating BPA in environmental water sources.

Hydrophobic-force-driven adsorption of bisphenol A from aqueous solution by polyethylene glycol diacrylate hydrogel microsphere.

Polyethylene glycol diacrylate (PEGDA) hydrogel microsphere was synthesized by UV-assisted reverse emulsion polymerization as an efficient adsorbent for water purification. Optical microscopy and TEM proved its spherical and hollow structure, while XRD pattern proved that it was amorphous with limited crystallinity. Abundant oxygen-containing functional groups such as hydroxyl were detected by FTIR. The hydrogels exhibited low swelling capacities ranging from 0.19 to 0.77 g/g in water and would decrease in salty solutions. The effects of operation parameters on the bisphenol A (BPA) adsorption were studied, including the polymer composition between PEGDA and polyethylene glycol methacrylate (PEGMA), initial concentration of BPA, pH, and operation temperature. The resulting hydrogel, especially for PDM2 (the ratio between PEGDA and PEGMA is 2), was able to effectively enrich BPA in water. The adsorption capacity was nearly stable below pH 8.0 and decreased when beyond 8.0. Thermodynamic parameters reflected that BPA adsorbed by hydrogel was a spontaneous (ΔG0 < 0) and exothermic (ΔH0 < 0) progress. The adsorption capacity increased with the increase of the concentration of NaCl, exhibiting salinity-enhanced adsorption capacity driven by hydrophobic force. Excellent results were also achieved by applying hydrogel for spiked real surface waters, which accounted for more than 91% compared to simulated solution. As-prepared hydrogel was expected to be good candidate for treatment of endocrine disruptors with lower solubility in water.

High efficiency biotransformation of bisphenol A in a fluidized bed reactor using stabilized laccase in porous silica.

We developed a high efficiency bisphenol A (BPA) treating system in a fluidized bed reactor (FBR) using stabilized laccase (Lac) in mesoporous silica (SER/Lac). The SER/Lac, prepared by cross linking of each enzymes inside the porous silica using glutaraldehyde, presented improved stability than the free Lac over various pH and temperatures with shaking. When the SER/Lac was used for BPA biotransformation in a batch reaction, higher efficiency was achieved than the free or adsorbed Lac (ADS/Lac). Also, the SER/Lac presented better reusability compared to ADS/Lac, and it could be reused for three times without decrease of biotransformation efficiency, and half of it was remained after ten times use. Due to great stability and robustness property, SER/Lac was successfully applied for high efficiency and continuous BPA treatment in FBR with better performance than the batch reaction.

Multi-Functional Laccase Immobilized Hydrogel Microparticles for Efficient Removal of Bisphenol A.

Hghly stable, reusable, and multi-functional biocatalytic microparticles with Laccase (Lac) enzyme (Lac/particles) were synthesized for bisphenol A (BPA) removal from aqueous solution. The Lac/particles were prepared by encapsulating Lac enzymes into poly ethylene glycol (PEG) hydrogel via the UV assisted emulsion polymerization method followed by cross linking with glutaraldehyde (GA). The obtained Lac/particles were spherical and micron sized (137⁻535 µm), presenting high enzyme entrapment efficiency of 100%, high activity recovery of 18.9%, and great stability at various pHs (3⁻7) than the free Lac. The Lac/particles could adsorb the BPA into the catalytic particles in a short time, promoting contact between BPA and enzyme, and further enzymatically degrade them without the shaking process and independent surrounding buffer solution. The Lac/particles could be reused for another round BPA adsorption and biotranformation by maintaining over 90% of BPA removal efficiency after seven times reuse. The synergistic effects of adsorption and biocatalytical reaction of Lac/particles have significant values in high efficient and cost-effective BPA removal.

Facile preparation of microscale hydrogel particles for high efficiency adsorption of bisphenol A from aqueous solution.

Hydrogel microparticles (HMPs) were synthesized via reverse emulsion/UV light polymerization and employed as adsorbents for removing bisphenol A (BPA) from aqueous solution. Results demonstrated the smooth surface of HMPs, with particle size ranging from 137 to 535 µm. Functional groups, including -OH, C-O, C=O, and C-H, are all involved in BPA adsorption confirmed by FTIR. Effect of solution pH, contact time, and initial BPA concentration on adsorption process was examined. The adsorption capacity was found pH independent below pH 8.0 and decreased when pH values greater than 8.0. The maximum adsorption capacity of the HMPs for BPA was 174.77 mg/g. The adsorption process achieved an equilibrium state within 30 min by the pseudo-second-order kinetic rather than the other kinetic models and was fitted well with the Freundlich linear isotherm model. Also, the obtained isotherms reflected the formation of S-type isotherm curve according to Giles's classification. The BPA loaded on the HMPs could be totally regenerated by methanol/dimethylsulfoxide and can be used for five cycles maintaining 100% of adsorption capacity. When the HMPs were applied for the treatment of spiked real surface water, excellent results were also achieved indicating the high efficiency and potential of the adsorbent.