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The oxidative behaviors of target pollutants in single-atom catalysts-activated peroxymonosulfate (SACs/PMS) system has mostly been studied from the loaded metal and coordination structure of SACs. However, the origin of the altered degradation behavior caused by the specific properties of pollutants has been neglected. Herein, Cu atoms coordinated with four N atoms embedded in biochar (Cu SA30 @C) was prepared to establish the relationship between the selective degradation behavior of sulfonamide antibiotics in Cu SA30 @C/PMS system and their own properties. Four representative sulfonamide pollutants (SAs) were selected and their redox potentials were determined by measuring half-wave potentials (φ 1/2 ). Results showed that a good correlation (R 2 =0.916) between the φ 1/2 values of different SAs and their corresponding degradation rate constants (k obs ) in Cu SA30 @C/PMS system was established. Additionally, the φ 1/2 values of SAs correlate well with the energy gap between SAs and the Cu SA30 @C/PMS complexes, further proving that the redox potential of SAs played a crucial role for electron-transfer oxidation in Cu SA30 @C/PMS system. This work contributes to the understanding of the selective degradation activity of sulfonamide antibiotics in Fenton-like systems from the perspective of pollutants properties, and provides new ideas for the efficient treatment of sulfonamide antibiotic wastewater., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Cerium-based adsorbents have been gradually used for the adsorption removal of highly toxic Cr(VI) from wastewater due to their low toxicity and wide working pH. However, the intrinsic properties of adsorbents contribute significantly to their adsorption performance, and the relationship between them needs to be clarified. Herein, series of nano-cerium based adsorbents (Ce@Cs) with different surface defects and Ce(III) content were prepared to explore their effects on the Cr(VI) adsorption capacity. Results showed that the optimal Ce@C performed well over a wide pH range of 2.0-12.0, and the calculated Cr(VI) adsorption capacity reached 302.43 mg/g at 45 ℃. Ce(III) and surface defects in cerium-based adsorbents exhibited an important influence on the Cr(VI) adsorption performance of Ce@Cs, and their contents showed a good positive correlation with the Cr adsorption capacity (R 2 =0.988 and 0.827). A series of evidences confirmed that the generated Ce(III) and oxygen vacancies could provide more sufficient coordination number to promote Cr(VI) complexation with Ce@Cs and lower the impedance of Ce@Cs to improve the reduction of Cr(VI) to low-toxic Cr(III). This work provides new insights into the Cr(VI) adsorption using cerium-based adsorbents, which helps to improve their potential in the purification of Cr(VI)-containing wastewater., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

GEX1 (gamete expressed 1) proteins are critical membrane proteins conserved among flowering plants that are involved in the nuclear fusion and embryonic development. Herein, we identified the 32 GEX1 proteins from representative land plants. In cotton, GEX1 genes expressed in various tissues across all stages of the life cycle, especially in pollen. Subcellular localization indicated the position of GhGEX1 protein was localized in the endoplasmic reticulum. Experimental research has demonstrated that GhGEX1 has the potential to improve the partial abortion phenotype in Arabidopsis. CRISPR/Cas9-mediated knockout of GhGEX1 exhibited the seed abortion. Paraffin section of the ovule revealed that the polar nuclear fusion of ghgex1 plants remains at a standstill when the wild type has developed into a normal embryo. Comparative transcriptome analysis showed that the DEGs of reproductive-related processes and membrane-related processes were repressed in the pollen of knockout lines. The predicted protein interactions showed that GhGEX1 probably functioned through interactions with proteins related to reproduction and membrane. From all these investigations, it was possible to conclude that the GEX1 proteins are evolutionarily conserved in flowering plants and elucidated the pivotal roles during fertilization and early embryonic development in cotton., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

Catalytic oxidation is considered to be the most efficient technology for eliminating benzene from waste gas. The challenge is the reduction of the catalytic reaction temperature for the deep oxidation of benzene. Here, highly efficient Ru x CeO 2 catalysts were utilized to turn the number of surface oxygen vacancies and Ce-O-Ru bonds via a one-step hydrothermal method, resulting in a preferable low-temperature reducibility for the total oxidation of benzene. The T 50 of the Ru 0.2 CeO 2 catalyst for benzene oxidation was 135 °C, which was better than that of pristine CeO 2 (239 °C) and 0.2Ru/CeO 2 (190 °C). The superior performance of Ru 0.2 CeO 2 was attributed to its large surface area (approximately 114.23 m 2 ·g -1 ), abundant surface oxygen vacancies, and Ce-O-Ru bonds. The incorporation of Ru into the CeO 2 lattice could effectively facilitate the destruction of the CeO bond and the facile release of lattice oxygen, inducing the generation of surface oxygen vacancies. Meanwhile, the bridging action of Ce-O-Ru bonds accelerated electron transfer and lattice oxygen transportation, which had a synergistic effect with surface oxygen vacancies to reduce the reaction temperature. The Ru 0.2 CeO 2 catalyst also exhibited high catalytic stability, water tolerance, and impact resistance in terms of benzene abatement. Using in situ infrared spectroscopy, it was demonstrated that the Ru 0.2 CeO 2 catalyst can effectively enhance the accumulation of maleate species, which are key intermediates for benzene ring opening, thereby enhancing the deep oxidation of benzene., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

In this work, a bimetallic Ni/La nanoparticle-laded biosorbent was fabricated from pomegranate fibers by solvothermal synthesis method. The material exhibited a high-efficient phosphate removal capability. The results of the characterization analysis showed that the surface of pomegranate fibers was rough and evenly coated with Ni and La after modification, and the specific surface area of Ni-La@Peel increased to 50.20 m 2 /g, providing a large number of adsorption sites for phosphate removal. The maximum phosphate removal rate of adsorbent was higher than 97% in a wide pH range (3.7-10.8). The maximum adsorption capacities of Ni-La@Peel were 226.55 mg-P/g and 220.31 mg-P/g under alkaline and acidic conditions, respectively, as calculated using the Langmuir model. Meanwhile, all the results were consistent with the Langmuir isothermal (R 2  = 0.99) and kinetic pseudo-second order models (R 2  = 0.99), indicating that the phosphate removal mechanism of Ni-La@Peel was mainly related to homogeneous chemisorption. Experimental results showed that in the presence of other anions, such as chloride, sulfate, nitrate, bromide and fluoride, the adsorption capacity of phosphate was only reduced by about 10% compared to the blank sample individually. In addition, the phosphate removal efficiency of Ni-La@Peel remained 82.05% at 7th adsorption-desorption cycle. These findings show that Ni-La@Peel is a promising material for purification of phosphate-containing wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Herein, we attempted to apply an alumina-based bimetallic (Mn-Ce) catalyst as an O 3 activator and explored the feasibility of the treatment of hypersaline organic wastewater. Compared with independent O 3 (35.00 ± 4.20%), mineralization of ciprofloxacin (CIP) under the Mn-CeO x @γ-Al 2 O 3 /O 3 (MCAO) process was elevated to 76.04 ± 2.30%. The synergetic corporation among multivalence redox pairs of Mn (III)/Mn (IV), Ce (III)/Ce (IV) promoted the protonation of the surface hydroxyl group (S-OH 2 + ), and subsequently the dominant reactive oxygen species in the MCAO process, OH and O 2 - , were generated rapidly. However, the mineralization of CIP decreased in MCAO/SO 4 2- system due to the formation of SO 4 - , which reacted with CIP more slowly (8.4 × 10 8  M -1  s -1 ) than OH (4.1 × 10 9  M -1  s -1 ). In MCAO/SO 4 2- /Cl - mixture saline conditions, mineralization of CIP was improved at low Cl - concentration (0.5 wt%) due to the generation of Cl, while inhibited with excessive Cl - (≥1.5 wt%) owing to the formation of residual chlorides (Cl 2 , Cl 2 - and ClO - ). Meanwhile, the MCAO process possessed promising capability to remediate hypersaline wastewater containing dyes, phenol and pesticides, as well as actual salinity-rich wastewater. Based on the above, the present study would provide new insights into hypersaline organic wastewater treatment by the MCAO process., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Modified biomass-based adsorption technique has attracted much attention in heavy metal ions removal, but selective adsorption behavior and mechanism of heavy metal ions adsorption onto biosorbent still need to be further clarified. Herein, a carboxylated biogas residue (BR-COOH) was prepared to remove the Cu 2+ and Zn 2+ from single/binary heavy metal ions solution and explore selective adsorption mechanism. The results exhibited that the adsorption capacities of BR-COOH for Cu 2+ was higher than that for Zn 2+ obviously, whether in the single or binary heavy metal ions solution. Meanwhile, the introduced carboxy groups were identified as the main sites for metal ions adsorption. Density functional theory (DFT) calculation results exhibited that the adsorption energy of Cu 2+ (-0.51 eV) onto BR-COOH was lower than that of Zn 2+ (-0.47 eV), indicating that the Cu 2+ adsorbed on BR-COOH was more stable than Zn 2+ . Moreover, the metal ions adsorption capacity of BR-COOH was positively correlated with their electronegativity, which was due to that the metal ions with stronger electronegativity was more easily interacted with the negatively charged oxygen in carboxyl groups. The same results were also verified in the control experiment conducted with two other biosorbents. Therefore, the work provided a new and in-depth insight into selective adsorption of metal ions onto carboxylated biosorbent., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Members of DOMAIN OF UNKNOWN FUNCTION 679 membrane protein (DMP) gene family, a type of plant-specific membrane proteins, have been proposed to function in various physiological processes such as reproductive development and senescence in plants. Here, a total of 174 DMP genes were identified and analyzed in 16 plant species (including 58 DMPs in four cotton species). Phylogenetic analysis showed that these DMPs could be clustered into five subfamilies (I-V). 137 duplicated cotton gene pairs were identified and most duplicate events were formed by whole-genome duplication (WGD)/segmental duplications. Expression analysis revealed that most of cotton DMPs were mainly expressed in the reproductive organs (the sepal, petal, pistil and anther) and the fiber of secondary cell wall stage. GhDMPs promoter regions containing the different cis-elements also showed different responses to abiotic stress. In addition, gene interaction networks showed that DMPs, as an endomembrane system, were involved in plant senescence process and flower reproductive development. We speculated GhDMP8-A/-D, GbDMP8-A/-D could be used as some candidate gene for inducing cotton haploid. This genome-wide study provides a systematic analysis of the cotton DMP gene family, and further insights towards understanding the potential functions of candidate genes., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Herein, we attempted to apply an exhausted magnetic biochar with adsorbed Cu 2+ (Cu-Fe@BRC) directly as a PMS activator and explored the feasibility of this attempt. Density functional theory (DFT) and electrochemical analysis illuminated the adsorbed Cu 2+ in Cu-Fe@BRC improved PMS activation and NOR degradation efficiency by elevating the adsorption capacity of PMS and performance of electron transfer. About 91.47% of norfloxacin (NOR) was rapidly degraded in Cu-Fe@BRC/PMS system with low Fe and Cu leaching. An in-depth mechanistic study was conducted with radical scavenging, radical capturing and solvent exchange, which demonstrated that the adsorbed Cu 2+ could facilitate the formation of both different radicals and non-radical. Importantly, Cu-Fe@BRC can maintain a long-term stable operation and excellent catalytic performance in surface water treatment. The potential toxicity of by-product generated in the NOR degradation process was also predicated, and results suggested that most identified by-products were less toxic than NOR itself. Notably, the preparation cost of exhausted adsorbent-based catalysts could be negligible, so the expenditure of the corresponding oxidation process is reduced accordingly. Based on above, this work provides not only a low-cost exhausted biochar-based catalyst for water purification but also the insight into the PMS activation by adsorbed transition metal ions., (Copyright © 2021 Elsevier B.V. All rights reserved.)

The agricultural wastes disposal and polluted water purification are always the key issues of environmental restoration. In this work, a magnetic biogas residue-based biochar (mBR-C) by direct pyrolysis and sonochemical method was prepared from biogas residue (BR). Response design methodology based on Box-Behnken design was used for the preparation parameters optimization. The characterization results identified that mBR-C had well-developed pore structure and surface area, which was beneficial to diffuse and capture heavy metal ions. Traces of toxic heavy metal in mBR-C was leached (˂0.04 mg/L) through TCLP method, indicating the environmental safety of the magnetic biochar. Meanwhile, the mBR-C exhibited excellent solid-liquid separation efficiency because of its strong magnetism. The series of adsorption experiments indicated that mBR-C could capture Cu 2+ and Pb 2+ rapidly, and the maximum adsorption capacity for Cu 2+ and Pb 2+ was 75.76 and 181.82 mg/g, respectively, which was higher than some other biochars previously reported. mBR-C was further applied in the synthetic wastewater treatment, which could effectively purify at least 600 mL (150 BV) to meet emission standards. After several column adsorption-desorption cycles, the adsorption capacity could still reach 85%, implying that mBR-C has good reusability and stability. Overall, the mBR-C can be used as an eco-friendly, desirable, economic and recyclable biosorbent in heavy metal polluted water treatment, providing a new idea for a combination of biogas residue recycle and wastewater treatment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

The charge densities (CD) and molecular weights (MW) of the flocculants are closely related to their application performances, but seldom researches focus on the effects of flocculant CD and MW on decolorization efficiencies. Herein, a series of flocculants with various CD and MW levels, named as PBF 1 - 9 , were designed and synthesized from papermaking sludge. The physicochemical characteristics of the PBF 1 - 9 were measured by fourier transform infrared spectroscopy (FTIR), gel permeation chromatography (GPC), X-ray photoelectron spectroscopy (XPS) and particle charge density analyzer (PCD). The efficiencies of PBF 1 - 9 were studied in the reactive blue (RB) dye removals by flocculation under different process conditions. The operation costs of the flocculants were evaluated at their optimal dosages. Also, the pH-independences and ion-tolerances of the aforementioned flocculants were studied in terms of the molecular levels. The experimental results exhibited that the flocculants CD or MW values were relevant to their flocculation behaviors and operation costs. CD values played a dominant role in color removal efficiencies and the costs, whereas MW values were critical to the floc structure. The pH or ion-independences of the flocculants were significantly dependent on the CD and MW values. However, some conclusions, conflicted with prior studies, were observed in this work. For instance, flocculant with the highest CD and MW levels was not the most effective one in enduring pH variation and the coexisting ions. The floc properties, including floc size, resistance and recovery ability, were relatively insensitive to flocculant intrinsic CD and MW levels when the flocculants were used at their optimal dosages. Furthermore, the possible relevance between CD or MW levels and the flocculation mechanisms have been proposed in this work. Exploring the effects of flocculants CD and MW levels could precisely control the flocculant characteristics to achieve satisfactory decontamination efficiencies with low costs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Effective managements of organic solid waste and surface water eutrophication can reuse/reduce solid waste resources, and ensure surface water safety. Herein, an easily-recoverable amine-functionalized biosorbent was developed from biogas residue (BR-N) for nitrate and phosphate removals from surface water. Physicochemical characteristics revealed that BR-N has a cross-staggered structure with abundant quaternary-amine groups to enhance the diffusion and electrostatic attraction of nitrate/phosphate. In batch studies, nitrate/phosphate could be effectively removed by the BR-N within a wide pH range of 5.0-9.0, and the maximum adsorption capacities of BR-N were 64.12 mg/g for nitrate and 34.40 mg P/g for phosphate. After continuous 8 cycles of adsorption-desorption, BR-N still exhibited >82% adsorption capacity for nitrate/phosphate removals, implying the high chemical stability and reusability for water treatment. Whereafter, BR-N has real application prospect in water treatment, which could effectively treat ˜380, ˜260 and ˜760 bed volumes (BV) of three actual eutrophic surface water to satisfy the surface water standard of China (GB3838-2002). The cost of BR-N was 2.89 $/kg evaluated by energy-economy assessment, indicating the low-cost production of biogas residue-based adsorbent for treating eutrophic surface water. Overall, this study provides a new idea for high-value utilization of organic solid waste and purification of eutrophic water., (Copyright © 2019 Elsevier B.V. All rights reserved.)

To understand the mechanism responsible for the α-amylase inhibitory activity of tea polysaccharides, the interaction between α-amylase and an acidic branched tea polysaccharide (TPSA) was investigated using fluorescence spectroscopy and resonance light scattering analysis. TPSA, exhibiting inhibitory activity towards α-amylase (the maximum inhibition percentage of 65%), was isolated from green tea (Camellia sinensis) and characterized by nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, and gas chromatography. Synchronous fluorescence spectroscopy revealed that the binding interaction between the tryptophan residues of α-amylase and TPSA was predominant. Based on the fluorescence quenching effect of tryptophan residues induced by TPSA, the binding constants between α-amylase and TPSA were determined to be 18.6×10 6 , 8.0×10 6 and 4.6×10 6 L·mol -1 at 20, 30 and 37°C, respectively. The calculated Gibbs free-energy changes were negative, indicating that the bonding interaction was a spontaneous process. The enthalpy and the entropy changes were -62.13 KJ·mol -1 and -0.0728 KJ·mol -1 ·K -1 , suggesting that hydrogen bonding interactions might play a major role in the binding process. The formation of an α-amylase/TPSA complex was evidenced by fluorescence quenching and resonance light scattering analysis, and this complex could be the main contributor to the α-amylase inhibitory activity of TPSA., (Copyright © 2016 Elsevier B.V. All rights reserved.)