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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2015 · IF 2.587

Simultaneous Oxidation of p-Chlorophenol and Reduction of Cr(VI) on Fluorinated Anatase TiO2 Nanosheets with Dominant {001} Facets under Visible Irradiation

Zhiqiao He,Lixian Jiang,Da Wang,Jianping Qiu,Jianmeng Chen,Shuang Song

A series of fluorinated anatase TiO2 nanosheets with dominant {001} facets were synthesized to oxidize p-chlorophenol (PCP) and reduce Cr(VI) simultaneously under visible light. The {001}/{101} surface facets ratio of TiO2 was controlled by varying the initial HF concentration, and fluorine-free samples were obtained by alkaline-washing. A synergistic effect among TiO2, Cr(VI), and PCP was observed, which is ascribed to effective trapping of photogenerated electrons and holes by Cr(VI) and PCP, respectively. A maximum synergistic effect was obtained at a molar ratio of [PCP] to [Cr(VI)] of one. Using X-ray diffraction, X-ray photoelectron spectroscopy, electron paramagnetic resonance spectroscopy, field-emission scanning electron microscopy, transmission electron microscopy, and Brunauer–Emmett–Teller analyses, the optimum ratio of exposed {001} to {101} facets for TiO2 was determined to be 80:20 because of selective transfer and charge balance of photogenerated carriers. Surface fluorination facilitates the formation of oxygen vacancies and unsaturated Ti atoms, which is useful for visible light activity induction, extending the lifetime of photogenerated electron-hole pairs, and enhancing the rate of PCP oxidation and Cr(VI) reduction.

研究领域: 环境科学 · 材料科学
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Analytical Methods · 2022 ·Vol. 14 ·期 17 ·1721-1729 · IF 3.532

A gel fluorescence sensor based on CDs@SiO2/FeS2@MIPs for the visual detection of p-chlorophenol

Di Deng,Xiaoyu Fang,Ding Duan,Kang Li

There is a critical need for the rapid detection of p-chlorophenol produced by pesticide abuse and industrial wastewater discharge, which has been an urgent problem in the realm of environmental protection. Here, a green and environmentally friendly method was developed to prepare stable and low toxicity quantum dots. First, blue-green fluorescent FeS2 quantum dots (B-FeS2 QDs) were prepared with FeCl3·6H2O (an iron source) and L-cysteine (a capping agent) by the solvothermal method. By combining B-FeS2 QDs with orange carbon dots (O-CDs), a CDs@SiO2/FeS2@MIPs visual fluorescence sensor for the selective detection of p-chlorophenol was constructed. Under optimum conditions, this sensor exhibited a detection limit of 1.265 μM with a linear range of 5.00–50.00 μM and was successfully applied to detect p-chlorophenol in real samples. Moreover, this sensor was successfully applied to visual semi-quantitative detection of p-chlorophenol. This work demonstrated that these sensors, based on FeS2 QDs and CDs, had potentials for in situ and visual detection of environmental contaminants.

CAS / MDL: 97-90-5 25852-47-5
研究领域: 环境科学 · 分析化学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Enhanced biocatalytic laccase production using agricultural waste in solid-state fermentation by Aspergillus oryzae for p-chlorophenol degradation

Palanisamy Vasudhevan,Dharman Kalaimurugan,Sivarasan Ganesan,Naveed Akbar,Saurav Dixit,Shengyan Pu

Agricultural residues are one of the most cost-effective and readily accessible carbon resources for producing commercially significant enzymes. Several enzymes have been used in different industries like pharmaceuticals, foods, textiles, and dyes that can be generated by various species of microbes found in waste from agriculture. The current research investigated laccase production by Aspergillus oryzae utilizing agricultural wastes. Physical and chemical properties, including pH, temperature, sucrose, yeast extract, and copper sulfate levels, were optimized. The utilization of the response surface methodology along with the centralized composite design method, which assesses multiple media parameters and utilizes a two-level experimental approach, aids in determining the variable and its significance in increasing production quality. The centralized composite design enhancement showed that the optimal conditions for highest laccase activity (623.16 U/mL) were pH 7.0, temperature 25 °C, corn cobs as substrate, sucrose (2.0 %), yeast extract (1.0 %), and copper sulfate (0.1 mM) level. The laccase enzyme was optimized using various pH, temperature, metal ions, and inhibitors combinations. The extracted laccase enzyme maximum activity was attained at pH 6.0 and 40 °C. The inclusion of divalent ions can enhance laccase activity, while the use of various inhibitors decreases laccase activity. Under various pH circumstances, the Aspergillus oryzae laccase enzyme can successfully degrade p-chlorophenol. The present study describes statistically validated optimal methodologies for enhancing laccase synthesis, leading to a laccase production technique that is simultaneously highly efficient and economically profitable, with possible use of p-chlorophenol degradation.

研究领域: 环境科学 · 生物技术
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2018 ·Vol. 165 ·期 11 ·H717 · IF 3.662

Enhancement of the Activity and Stability of PbO2 Electrodes by Modifying with Polydimethylsiloxane

Zhiqiao He,Jiajie Zhou,Xinwen Huang,Shihan Zhang,Shuang Song

The β-PbO2 of a Ti/Sn-SbOx/PbO2 electrode was modified with polydimethylsiloxane (PDMS) (Ti/Sn-SbOx/PbO2-PDMS) through a facile electrodeposition method. The results from scanning electron microscopy, energy-dispersive spectrometry and X-ray diffraction demonstrated that the PDMS was irreversibly adsorbed on the β-PbO2 of Ti/Sn-SbOx/PbO2-PDMS, leading to a decrease in the crystal size, surface cracks and preferential growth trend of β-PbO2. Compared with its PDMS-unmodified counterparts, the Ti/Sn-SbOx/PbO2-PDMS electrode exhibited relatively higher activity, selectivity and stability in the anodic oxidation of p-chlorophenol. Moreover, the Ti/Sn-SbOx/PbO2-PDMS electrode was more stable than the Ti/Sn-SbOx/PbO2 electrode, as evidenced by the accelerated life test. Based on the quantitative measurements of contact angle, hydroxyl radicals (HO•) and the initial surface concentration of various p-substituted phenols, including p-cresol, p-methoxyphenol, phenol, and p-chlorophenol, and with the help of electrochemical characterization of linear sweep voltammetry, it could be concluded that the improved electrochemical activity and stability of Ti/Sn-SbOx/PbO2-PDMS originated from the enhanced hydrophobicity of the electrode surface. Different from a traditional Ti/Sn-SbOx/PbO2 electrode with adsorbed HO• as the dominant active species, the Ti/Sn-SbOx/PbO2-PDMS with a hydrophobic surface favors the generation of more free HO•.

CAS / MDL: 98-54-4 70131-67-8
研究领域: 材料科学 · 环境科学 · 电化学
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CHEMOSPHERE · 2022 · IF 8.943

Effect of activator/precursor mass ratio on sulfur-doped porous carbon for catalytic oxidation of aqueous organics with persulfate

Yaoping Guo,Keng Xuan,Chenxi Pu,Yifan Li,Yaxiong Huang,Yadan Guo,Meiyu Jia,Jiale Li,Hao Ruan

Sulfur-doped porous carbon has emerged as promising metal-free catalysts toward persulfate (PS) for catalytic oxidation of aqueous organics. Wherein, thermal pyrolysis with activator activation is very common for the preparation of activated carbon. However, the relationship between the mass ratio of activator/precursor and catalytic efficiency has been rarely reported. Herein, a series of sulfur-doped porous carbons (S-AC) were synthesized by one-step chemical activation of (Poly(phenylene sulphide) (PPS)) with K 2 CO 3 as activator at K 2 CO 3 /PPS mass ratio ranging from 0 to 3. The effects of K 2 CO 3 /PPS mass ratio on its physicochemical properties and its catalytic performance for p-chlorophenol (PCP) degradation with PS were comprehensively investigated. Experiment results show that sulfur doping enhanced its catalytic activity and the sample synthesized with K 2 CO 3 /PPS mass ratio of 2 (S-AC-2) exhibited the best adsorption and catalytic performance toward PS for PCP removal. More importantly, S-AC-2 with PS could efficiently degrade various aqueous toxic organics other than PCP, and S-AC-2 showed superior catalytic activity to many recently reported advanced materials. In addition, the effects of several operate parameters, including reaction temperature, PS concentration, pH, humic acid , and inorganic ions on PCP oxidation were evaluated. By combining with the results of quenching experiments and EPR, the PS activation mechanism over S-AC-2 was revealed. Moreover, the reusability and regenerability of S-AC-2 was also studied. It indicates that S-AC-2 showed inferior reusability, but the catalytic activity of which could be fully recovered through thermal treatment at 600 °C for 2 h in N 2 .

研究领域: 环境科学 · 材料科学
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DIAMOND AND RELATED MATERIALS · 2024 · IF 4.3

Robust advantage of MXene/g-C3N4 loaded on Fe2WO6/BiIO4 nano-platform for chemo-peroxidase colorimetric detection of uranyl ions, antifungal properties, photocatalytic degradation of p-chlorophenol, and eco-toxicity studies

Baadal Jushi Janani,Safaa Mohammed Ibrahim,Asad Syed,Morug Salih Mahdi,Abdallah M. Elgorban,Haider Radhi Saud,Manjula Subramaniam,Ling Shing Wong,Ramadan Fallah Amer

In this study, we have designed a nanocomposites based on MXene/g-C 3 N 4 (MX/CN) loaded on Fe 2 WO 6 /BiIO 4 (FWO/BIO) for different applications. The nanocomposites were identified by using the structural and morphological studies including XRD , FESEM, EDS , DLS , TGA , BET, UV–vis, XPS techniques. The average sizes of BIO, FWO/BIO, and MX/CN/FWO/BIO were 44, 46, and 58 nm, respectively. The synthesized MX/CN/FWO/BIO nanocomposites was utilized for the peroxidase colorimetric identification of uranyl ions (UO 2 2+ ) with the excellent selectivity and sensitivity properties (LOD: 3.21 nM). The antifungal efficiency of the as-fabricated nanomaterials was investigated and the inhibition zone at high concentration 2.5 mg/mL of MX/CN/FWO/BIO nanocomposites were 19.74, 17.91, 24.25, and 21.32 mm against Aspergillus spp., Penicillum spp., Candida spp. and Fusarium spp., respectively. The MX/CN/FWO/BIO nanocomposites was utilized in photocatalysis process for decomposition of p-chlorophenol under visible light lamp. The findings showed that the MX/CN/FWO/BIO nanocomposites can be degrade p-chlorophenol (100.0 %) under visible light irradiation (80 min). The photocatalytic response was decreased about 2 % after 5th cycle times, and showed the best stability of the MX/CN/FWO/BIO nanocomposites. The quenching test shows the mechanism of p-chlorophenol degradation was conducted by •O 2 − , and •OH species. Additionally, the ecological structure activity relationships ECOSAR software was utilized to evaluate the toxicity of the p-chlorophenol and the intermediates produced. This work can lead for manufacturing innovation in near future.

研究领域: 材料科学 · 环境科学 · 生物医学工程 · 化学
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JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL · 2015 · IF 3.615

Theoretical and experimental investigation into photoelectrocatalytic oxidation and reduction property of ZnFeTi mixed metal oxides

Shengjie Xia,Mengmeng Shao,Xiaobo Zhou,Guoxiang Pan,Zheming Ni

In this paper, we synthesized ZnFeTi layered double hydroxides (LDHs) by hydrothermal synthetic method at high temperature. The LDHs was further calcined by microwave to make ZnFeTi mixed metal oxides (MMO) with special particle size. In addition, the band gap of ZnFeTi-LDHs and MMO were calculated by DFT for the first time, which was in good agreement with the experimental result from UV–vis. MMO was finally dye sensitized and used as thin film electrode to test the photoelectrocatalytic performance for both p -chlorophenol oxidation degradation and CO 2 reduction under visible light. The results showed that without the applied voltage, the p -chlorophenol degradation and CO 2 reduction rates were not high; after the electric filed was introduced into the reaction, not only the degradation efficiency of p -chlorophenol was increased to 99.1% within 210   min, but also the reactivity of CO 2 reduction reaction was enhanced a lot. Furthermore, from the results of HPLC and UV–vis, we could conclude that p -chlorophenol was finally decomposed into small inorganic molecules going through 4-chloropyrocatechol and hydrochinone under the co-effect of hydroxide radicals and the photoelectrons. This result could be proved by frontier electron densities on atoms of p -chlorophenol calculated by DFT.

CAS / MDL: 106-48-9
研究领域: 材料科学 · 环境科学 · 化学工程
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CATALYSIS COMMUNICATIONS · 2023 · IF 3.7

Synergistic pollutant degradation by Ag3PO4/Fe3O4/graphene oxide visible light–persulfate coupled system: Mechanism elucidation and performance optimization

Hua Jin,Lin Zhu,Xinyuan Xu,Xiaoyang Yu,Xiaoshu Qu,Zhigang Liu,Yanyan Yang,Yan Gao,Qingling Wei

Herein, we investigated the synergistic degradation of p -chlorophenol by a Ag 3 PO 4 /Fe 3 O 4 /graphene oxide visible light – peroxydisulfate coupled system, probed the effects of catalyst and peroxydisulfate dosage, pH, operating mode, and coexisting substances, identified decomposition intermediates, and proposed plausible degradation pathways. The advantages of the coupled system, namely reduced agent dosage and efficient and thorough degradation, justified the involvement of a precious metal (Ag), while mechanistic investigations suggested the importance of the peroxydisulfate peroxo bond and electron transfer between multivalent metal catalyst components for degradation performance enhancement. Thus, this work facilitates the development of high-efficiency and low-cost combinations of advanced oxidation processes.

研究领域: 环境科学 · 材料科学
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