CHEMICAL ENGINEERING JOURNAL
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2016
·
IF 5.31
Wen-Long Wang,Qian-Yuan Wu,Zhi-Ming Li,Yun Lu,Ye Du,Ting Wang,Nan Huang,Hong-Ying Hu
Carbamazepine (CBZ) is a ubiquitous micropollutant in wastewater and reclaimed water. In this study, we evaluated CBZ degradation by light-emitting diode (LED)-driven UV/chlorine oxidation. Under LED irradiation of 280 nm (LED280) and 310 nm (LED310), UV/chlorine could efficiently degrade CBZ. Compared with LED UV/H 2 O 2 treatment, LED UV/chlorine oxidation achieved a CBZ degradation rate that was one order of magnitude higher. The CBZ degradation followed pseudo-first-order kinetics, and the rate constants ( k obs,CBZ ) for LED280 UV/chlorine and LED310 UV/chlorine increased from 0.072 to 0.91 min −1 and 0.044 to 0.65 min −1 , respectively, when chlorine dosage increased from 0.07 to 0.14 mM. Under neutral conditions, the generated OH and Cl accounted for over 80% of the CBZ degraded by LED UV/chlorine. The maximum k obs,CBZ for LED UV/chlorine was observed at pH 8.5; k obs,CBZ decreased when solution pH increased to 9.5 or decreased to 5.5. This is because the main UV-absorbing chlorine species in the LED280 and LED310 systems is OCl − , which is different from those in low-pressure mercury lamp/chlorine systems. The acute toxicity for CBZ solution treated by LED UV/chlorine increased at lower fluence (<752 mJ/cm 2 ) and decreased at higher fluence (>1233 mJ/cm 2 ). However, the cytotoxicity to Chinese hamster ovary cells and adsorbable organic halide content of CBZ solution both increased after chlorination and LED UV/chlorine. The lowest electrical cost for the degradation of CBZ by LED UV/chlorine occurred under neutral conditions with a chlorine dosage of 0.4–0.7 mM (28.4–49.7 mg/L).
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Journal of Materials Chemistry A
·
2025
·
IF 9.5
Hui Wang,Xuefeng Zhang,Xiangfeng Wu,Yewei Kang,Yirui Huang,Zhaoye Zhao,Ziyan Li,Tingting Zhou,Junchuan Wang,Wei Zhu,Chengsi Pan
Bimetallic iron-based metal organic frameworks (MFe-MOFs) exhibit promising photocatalytic properties but face challenges typical of pristine MOFs, including low photoresponsive activity, inadequate band gap regulation, and weak photoconductivity. Here, we designed porphyrin-based COFs (TpPAM-COFs) to serve as a shell grown on NH2-Fe-MIL-101 nanoparticles (NPs) using an in situ solvothermal approach. Subsequently, a ligand-anchoring full-range metallization process was applied to introduce hetero metal ions throughout the core–shell composites, establishing a type-II scheme heterojunction (Fe/Cu-M@PC-Cu) via covalent bonding between NH2-Fe/Cu-MIL-101 and Cu-TpPAM-COFs. The Cu-TpPAM-COF shell, with broad light absorption range, enhanced the generation of photogenerated electrons, facilitating the reduction of Cu2+ and Fe3+ within the Fe/Cu-M@PC-Cu heterojunction and promoting the regeneration of Cu+ and Fe2+ Fenton active sites. Moreover, rapid electron transfer between Fe3+ and Cu+ centers amplified the Fe3+/Fe2+ redox cycle, accelerating the catalytic decomposition of H2O2 and increasing ·OH radical production. Additionally, the optimized bandgap structure of Cu-TpPAM-COFs enhanced the oxidation capacity, as evidenced by the Fe/Cu-M@PC-Cu composite achieving exceptional photo-Fenton catalytic efficiency with 92.7% tetracycline hydrochloride (TCH) degradation in 35 minutes, surpassing that of most reported similar catalysts. Furthermore, the composite showed excellent stability, with only an 11.9% loss in photo-Fenton degradation efficiency after 8 cycles, highlighting its great potential for addressing challenging environmental pollutants.
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Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Zhenjun Xiao,Junlong Zhang,Yijie Lin,Kaixuan Zheng,Zili Lin,Mengyang Niu,Wanlin Lin,Yuchun Hong,Zhongyang Li,Ping Chen,Qingbin Song,Wenying Lv,Guoguang Liu
Developing new technologies to address emerging contaminants are urgently needed. To this end, a novel advanced oxidation system (US/CaSO 3 /PDS) utilizing ultrasound to activate persulfate (PDS) and calcium sulfite (CaSO 3 ) for the effective degradation of emerging contaminants was constructed in this study. The pseudo first-order kinetics constant of Phoxim (PHO) can reach 4.3 × 10 −2 min −1 in US/CaSO 3 /PDS system, revealing the prospects for the treatment of pollutants in water. Electron paramagnetic resonance spectra demonstrated that persulfate anion radicals, hydroperoxyl radicals, hydroxyl radicals, and singlet oxygen were produced in the system. Further, quenching experiments and reactive species probes were used to verify the chemical reaction mechanism of this novel system, and the experimental results highlight the key role of 1 O 2 in the degradation of pollutants thanks to the participation of oxygen. In addition, 11 main products in the PHO degradation process were identified by liquid chromatography-high-resolution precise mass spectrometry, and the possible degradation path of PHO in US/CaSO 3 /PDS system was proposed. US/CaSO 3 /PDS system had high pollutant removal efficiency against a variety of emerging pollutants and was applicable in real water matrix. This study provides a new scheme for the development of advanced oxidation technology based on PDS activation for the removal of refractory emerging pollutants in water.
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ChemCatChem
·
2017
·Vol. 10
·期 5
·1019-1026
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IF 4.803
Qinhong Wei,Qingxiang Ma,Pingping Zuo,Huailin Fan,Shijie Qu,Wenzhong Shen
Graphical Hollow hydrogenation : A hollow CeO 2 spheres supported metallic Pd catalyst was prepared by employing a glucose hydrothermal method and impregnation method. The Pd/CeO 2 hollow sphere catalyst, which consisted of a hollow cavity and outer shell, presented a higher catalytic hydrogenation performance of styrene and nitrobenzene to produce ethylbenzene and aniline, better than that of the general CeO 2 -supported Pd catalyst. A hollow structured CeO 2 spheres supported metallic Pd catalyst (Pd/CeO 2 -H) was designed and prepared by a glucose hydrothermal method and impregnation method. The CeO 2 -H consisted of an inner hollow cavity and an outer shell on which a large number of mesopores were formed. The Pd/CeO 2 -H hollow sphere catalyst, which presented abundant surface oxygen vacancies, was investigated for catalytic hydrogenations of styrene and nitrobenzene to produce ethylbenzene and aniline. Activity tests indicated that the mesoporous Pd/CeO 2 -H hollow sphere catalyst exhibited striking catalytic activity, which was attributed to the spatial core–shell structure that provided more active sites and facilitated reactant diffusion as well as surface defects (oxygen vacancies), which were capable of transferring electrons to metallic Pd. All of these advances are beneficial to give a higher catalytic hydrogenation performance.
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APPLIED SURFACE SCIENCE
·
2017
·
IF 3.387
Zhiwang Yang,Xueqing Xu,Xixi Liang,Cheng Lei,Lihong Gao,Ruoxue Hao,Dedai Lu,Ziqiang Lei
This study investigates the photocatalytic reduction of nitroaromatic compounds upon visible light over novel Ce-doped UiO-66/graphene nanocomposites. Ce doped UiO-66 nanostructures and the corresponding graphene hybridized nanocomposites were facilely synthesized by means of one step solvothermal reaction. It has been demonstrated that produced nanocomposites could be used as highly efficient and chemical stable photocatalysts for the reduction of nitroaromatic compounds under visible irradiation and ambient conditions. Compared with the bare UiO-66, Ce-UiO-66/GR distinctly enhanced photocatalytic activity. Ce as “ mediator ” introduced into the MOFs materials can greatly improve the electron transfer across the interface between grephene and the UiO-66 and further improve the visible light driven photoactivity. This is an effective strategy for the development of high photocatalytic activity MOFs based materials.
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TALANTA
·
2025
·
IF 6.1
Zitao Shen,Zhuo Wang,Pengfei Ye,Lihong Guo,Sheng Peng,Yuefan Liu,Yongsheng Cui,Juan Zheng,Gangfeng Ouyang
Macrocyclic polymer materials exhibit excellent selectivity and adsorption performance in pollutant adsorption due to unique host-guest recognition. Herein, three kinds of calixarene polymers (C4P, C6P and C8P) were synthesized through Sonogashira reaction, and were characterized through 1 H NMR, FT-IR, SEM, and TEM. The water contact angle experiments revealed that three kinds of calixarene polymers were highly hydrophobic, and they all exhibited high enrichment efficiency for weak polar chloro-substituted benzene compounds (chlorobenzene, o -chlorotoluene, p-dichlorobenzene and o-dichlorobenzene) and BTEX (benzene, toluene, ethylbenzene and xylenes). Surprisingly, three types of calixarene polymers also showed satisfactory enrichment performance for polar nitrobenzene compounds (NBCs). Among them, C8P showed the most outstanding enrichment factors for NBCs (825-1913), which was about 2–7 times better than those of the commercial fibers. Using C8P as coating fiber, a sensitive analytical method was further developed based on solid phase microextraction (SPME), coupled with gas chromatography-mass spectrometry (GC-MS). The established analytical method demonstrated low detection limits (0.06–5.08 ng L −1 ), a wide linear range (0.5–1000 ng L −1 ), and good repeatability. The established method was further applied to the quantification of NBCs in environmental water samples, verifying its feasibility.
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PubMed
高影响因子
Frontiers in Chemistry
·
2025
·
IF 4.2
Jinwei Li,Yifei Wei,Qiang Liu,Huanhuan Guan,Chengchun Jiang,Xiaohui Sun
In this study, CuO-CoOx/SBA-15 catalysts were successfully synthesized via ultrasonic impregnation, and their performance in degrading nitrobenzene within a Fenton-like system was investigated. The catalyst materials were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma mass spectrometry (ICP-MS), scanning electron microscopy (SEM), transmission electron microscope(TEM) and energy-dispersive X-ray spectroscopy (EDS). The CuO-CoOx/SBA-15 catalysts featured well-distributed CuO-CoOx nanoparticles within the mesoporous SBA-15 support. Compared to CuO/SBA-15 and Co3O4/SBA-15 catalysts with similar microstructures, the CuO-CoOx/SBA-15 catalysts exhibited Cu-Co dual active centers and a higher abundance of redox-active sites. During catalytic degradation, H2O2 was continuously activated on the catalyst surface through efficient Cu+/Cu2+ and Co2+/Co3+ redox cycles. The experimental conditions (initial pH, catalyst dosage, and H2O2 dosage) were optimized, resulting in 99% nitrobenzene removal over a wide pH range (3.0–9.0). The primary mechanisms for the oxidation and subsequent removal of nitrobenzene in the CuO-CoOx/SBA-15-H2O2 system were identified as reactions with hydroxyl radicals (·OH).
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2025
·
IF 21.1
Linhao Wang,Jia Wei,Jiangkai Huo,Wei Ji,Xiaohui Zhang,Yanan Li,Jiamei Li,Nan Cui,Wenhao Yan,Yuxin Zhao,Jun Li,Ju Wang
Herein, an electron-optimized core-shell CoFe alloy-carbon composite (CoFeC) was developed from prepared CoFe Prussian blue analogues (CoFe PBAs) through pyrolysis and applied for peracetic acid (PAA) activation. Characterization analysis and theoretical calculations indicated that the Co sites as the primary active centers, with the presence of C and Fe in CoFeC significantly narrowed the difference between the d-band center ( Ɛ d ) and the Fermi level ( E F ), thereby reducing PAA adsorption energy on Co sites and enhancing electron transfer. The identification of reactive species confirmed that acetylperoxy radicals (CH 3 C(O)OO·) and singlet oxygen ( 1 O 2 ) were the dominant species driving the reaction. The CoFeC/PAA system demonstrated exceptional pollutant degradation efficiency, achieving nearly 100% removal within 30 min, along with strong interference resistance and high durability in continuous-flow reactors. This work provided novel insights into the activation of PAA by bimetallic carbon catalysts and offered guidance for the development of efficient and sustainable water treatment technologies.
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JOURNAL OF SOILS AND SEDIMENTS
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2025
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IF 3
Xie Xin,Liu Wei,Wang Mingxin,Pan Xinxing,Xue Jinjuan,Yao Meng
Purpose This study provides a novel resource utilization strategy for the carbonized soil derived from lubricant-contaminated soil. Materials and methods In this study, the lubricant-contaminated soil was treated by pyrolysis and ball milling with manganese carbonate to obtain Mn-loaded carbonized soil (Mn@BCS), which was then reused to activate peroxymonosulfate (PMS) oxidation for degradation of aniline (AN) in wastewater. Results and discussion When the dosage of Mn@BCS and PMS was both 1 g/L, 100 mg/L of AN was almost completely removed within 6 h. Three reactive oxygen species (ROS), including \({\text{SO}}_{4}^{\bullet -}\) , •OH and \({}^{1}{\text{O}}_{2}\) , were detected and verified. The probe-based kinetics models were established with atrazine, nitrobenzene and metronidazole as probes to quantify the generation of ROS. The exposure of the \({\text{SO}}_{4}^{\bullet -}\) , \(\bullet \text{OH}\) and \({}^{1}{\text{O}}_{2}\) at 6 h was 5.32 × 10 –11 , 5.40 × 10 –12 , 2.52 × 10 –10 M s, which contributed 33.62%, 2.02% and 2.98% to AN degradation, respectively. The main active sites include Mn–O, oxygen containing groups and graphitized carbon. The Mn–O and oxygen containing groups can activate PMS to produce \({\text{SO}}_{4}^{\bullet -}\) and \({}^{1}{\text{O}}_{2}\) , respectively. The graphitized carbon promotes AN degradation by generation of \({\text{SO}}_{4}^{\bullet -}\) and accelerating direct electron transfer. Conclusions Ball milling with manganese carbonate significantly improves the activation performance of carbonized soil for PMS oxidation, and thus promote the resource utilization of post-remediation soil.
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NEW JOURNAL OF CHEMISTRY
·
2018
·Vol. 42
·期 4
·2718-2725
·
IF 3.201
Fan Yang,Yan Cao,Zhuo Chen,Xing He,Liqiang Hou,Yongfeng Li
Boron and nitrogen co-doped graphene-like carbon (BNG) is a metal-free catalyst that has been synthesized by combining ball-milling with thermal treatment. Firstly, the edge-selectively-functionalized graphene nanoplatelets (EFGnPs) were prepared by ball milling of the pristine graphite, which can facilitate boron incorporation. BNG catalysts with a high content of boron and nitrogen can then be obtained by pyrolysis of a mixture of EFGnPs and boric acid. We found that the reduction of nitroarenes can be catalyzed using a low BNG loading and a small amount of N2H4 in ethanol to form aminoarenes in high yields. The type of boron species in the BNG catalyst has an important effect on the reduction reaction. Furthermore, the catalyst containing the most B/N shows the highest catalytic activity during the reduction of nitroarenes, indicating that the doped B/N within the BNG is a key active site in impelling this reaction. Moreover, the BNG catalyst can be used six times, and no dehalogenation phenomenon occurs during the reduction process for halogen-substituted nitroarenes in contrast to the case when conventional metal catalysts are used.
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BIOMACROMOLECULES
·
2025
·
IF 5.4
Mingyu Ding,Qianyu Jiang,Pengchao Wu,Pengliang Sui,Zichao Sun,Xiaoling Yang,Haibao Jin,Shaoliang Lin
Ultrathin organic nanofibers (UTONFs) have favorable potential as emerging nanomaterials due to their large aspect ratio, lightweight nature, and mechanical flexibility. Achieving dual stimuli-responsive UTONFs is necessary to satisfy the on-demand requirements of smart and miniature devices but remains challenging. Herein, amphiphilic alternating peptoids (AAPs) modified with azobenzene and histamine groups were successfully synthesized using the solid-phase submonomer synthesis technique. Following subsequent solution self-assembly, photo/CO2 dual-responsive ultrathin peptoid nanofibers (UTPNFs) with a diameter of ∼1.8 nm and a length of up to several micrometers were generated based on the pendant hydrophobic conjugate stacking mechanism. The photoisomerization of azobenzene was accountable for the reversible transformation from UTPNFs to spherical micelles (∼60 nm) under recyclable light irradiation. Owing to the protonation and the resulting electrostatic repulsion interaction, both UTPNFs and spherical micelles displayed a reversible variation in shape and physicochemical properties, including the size, diameter, zeta potential, and pH. Our work offers prospective guidance on the construction of dual-responsive ultrathin organic nanofibers with controllable shape transformation and performance transition.
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ACS Applied Nano Materials
·
2024
·
IF 5.3
Hui Lin,Yandong Liu,Chenglong Hu,Xuefan Deng,Long Zhang,Shaoyun Chen,Haibo Zhang
In catalytic reactions, the diverse binding sites of nanometals located in nanomaterials considerably influence the activity of nanocatalysts. In this study, the special nanostructure and charge distribution of halloysite nanotubes (HNTs) incorporating a weak reducing agent closo-dodecaborate (closo-[B12H12]2–) were leveraged to immobilize Au nanoparticles (NPs) on the inner and outer surfaces of HNTs. The introduction of closo-[B12H12]2– into HNTs was achieved via vacuum extraction and acid immersion. Subsequently, nanocatalysts loaded with Au NPs on the diverse surfaces of the HNTs were obtained from a direct reaction with a KAuCl4 solution. The Au NPs loaded on the inner surface of the HNTs were found to have highly dispersed and exhibited excellent catalytic activity in the reduction of nitroaromatics. At room temperature, the Au NPs loaded on the inner surface of the HNTs with a mass fraction of 0.02% showed a high turnover frequency value of 47.28 min–1 in a model reaction of the catalytic reduction of 4-nitrophenol to 4-aminophenol and exhibited excellent stability in cycling tests. Therefore, this study provides a new approach for synthesizing nanocomposites for various practical applications.
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