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JOURNAL OF MEMBRANE SCIENCE · 2023 · IF 9.5

Constructing robust and anti-fouling superwettable membrane with layer-by-layer assembly of Fe(OH)3 colloid

Zewen Xu,Zhongyi Ren,Haojiang Zhu,Hao Guo,Xinliang Liu,Ming Wang,Yingfei Hou

Layer-by-layer (LBL) assembly method, with the advantages of simple operation and strong universality, has attracted much attention recently. However, the weak molecule-to-molecule and molecule-to-ion interactions have limited its development. During this work, the molecule-to-solid interaction was adopted and a robust LBL coating was achieved by alternately depositing positively charged Fe(OH) 3 colloids and negatively charged sodium alginate molecules. The molecule-to-solid interaction could continuously regenerate under corrosive conditions due to water insolubility and the chemical stability of solids. When the electrostatic interaction was broken, the abundant chemically stable solids acted as anchors to immobilize the soluble molecules and maintain the stability of the LBL coating. The prepared superwettable membranes exhibited superior oil-in-water emulsion separation efficiency, anti-fouling properties, and chemical stability. Meanwhile, the separation performance survived one week's harsh environments of strong acid and alkali.

CAS / MDL: 9005-38-3
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JOURNAL OF HAZARDOUS MATERIALS · 2023 · IF 13.6

Oxygen-doped carbon nanotubes with dual active cites to enhance •OH formation through three electron oxygen reduction

Jiayu Zhang,Shan Qiu,Fengxia Deng

The electro-Fenton (EF) process generates H 2 O 2 through the 2e- oxygen reduction reaction (ORR), which is subsequently activated to •OH by iron-based catalysts. To alleviate the potential risk of external Fe-based catalysts, along with metal dissolution in acidic or neutral environments, in this study we employed oxygen-doped carbon nanotubes (OCNT) as a bifunctional, metal-free cathode to establish a metal-free EF process for organic pollutant degradation. The results demonstrate that the metal-free electrode has excellent H 2 O 2 accumulation (12 mg L −1 cm −1 ) and degrades sulfathiazole (STZ) with 97.05 % efficiency in 180 min with an explanation kinetic of 0.0189 min −1 . For the first time, this enhancement came from the dual active site centers in OCNT: Ⅰ) -COOH and defects active sites were responsible for H 2 O 2 production, Ⅱ) then -C O triggered H 2 O 2 into •OH, avoiding the introduction of metal-based catalysts. These findings suggest that the EF system with in situ oxygen-doped cathodes have great potential for treating antibiotic wastewater.

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JOURNAL OF MOLECULAR STRUCTURE · 2022 · IF 3.841

HPLC, fluorescence spectroscopy, UV spectroscopy and DFT calculations on the mechanism of scavenging •OH radicals by Hypericin

Wan-ping Chen,Run-quan Wang,Yue-rong Zhang,Kai Song,Yuan Tian,Jia-xian Li,Guo-ying Wang,Gao-feng Shi

In this article, the scavenging ability of hypericin on hydroxyl radicals was evaluated by UV spectra, HPLC and fluorescence spectra. The reaction mechanism of the scavenging of free radicals by hypericin was also investigated. The Gaussian calculations obtained for the spatial structure and electrostatic potential of hypericin revealed that the active site for the reaction of hypericin with hydroxyl radicals is on the phenolic hydroxyl group of hypericin. The dissociation energy, spin density and frontline orbitals of the dehydrogenated hypericin radicals yielded that hypericin 7-OH and 7′ -OH are most likely to react with hydroxyl radicals. the transition state structure, enthalpy change and Gibbs free energy change and energy change of the reaction between hypericin and hydroxyl radicals,and the results of the above calculations indicate that hypericin 7-OH and 7′ -OH have the highest activity, can be directly involved in the scavenging process of radicals, followed by 5-OH and 5′ -OH, and finally 4-OH (4′ - OH).In-depth study of the antioxidant mechanism of hypericin molecules can help to design and synthesize new antioxidants in a more rational way.

CAS / MDL: 5144-89-8
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2023 · IF 5.2

Environmentally friendly tea saponin foam detergents costabilized by GO-OH/SiO2 nanoparticles for removing radioactive surface contaminants

Datong Liu,Sijie Lei,Yang Hu,Zhanguo Li,Hailing Xi,Xiaoyan Lin

Currently, bare silica nanoparticles with low surface activity and weak stabilizing foam ability have restricted applicability in treating surface radioactive pollutants. To address potential issues with SiO 2 as a foam stabilizer , a highly efficient foam stabilizer was fabricated by compounding silica with hydroxylated graphene oxide (GO-OH), which was prepared by hydrothermal modification of graphene oxide (GO). Then, an environmentally friendly foam detergent with high stability and high decontamination efficiency was developed using the natural surfactant tea saponin (TAS) as a foaming agent and a composite of silica and GO-OH (GO-OH/SiO 2 ) as a foam stabilizer, which is named tea saponin foam detergent. For different types of surfactants, the structural and morphological characteristics of GO-OH, such as hydrophilic and surface oxygen groups, as well as the synergistic influence of GO-OH with SiO 2 on foamability, foam stability, and detergency of the foam detergent, were studied. As a consequence, the TAS foam detergent has good stability with a drain half-life of 68 min. By hydrothermal modification of GO, the contact angle of water on GO-OH in air dropped to 63.2°, which was lower than that (73.0°) on GO. Furthermore, the hydrophilicity of GO-OH increased, and more oxygen-containing groups on GO-OH enhanced its absorption and enrichment of the radionuclide uranium and improved the decontamination rate of the TAS foam detergent. Moreover, when GO-OH was combined with SiO 2 , the dispersion and stability of SiO 2 in the foam detergent improved, and the foam stability of the detergent subsequently further improved. Adding 2 wt% SiO 2 and 0.1 wt% GO-OH to the detergent enhanced the foam drainage half-life of the detergent from 40 min to 68 min and improved the stability of the detergent by 70%. In addition, the synergistic action of GO-OH/SiO 2 with TAS surfactant increased the liquid film thickness of the foam and the airflow resistance to support the weight-bearing capacity of the foam skeleton. As a result, it slowed the rate of foam disproportionation , reduced the bubble size, increased the bubble number, and finally improved the foam stability of the detergent. For simulated radioactive uranium pollutants on the surfaces of glass, stainless steel , and tiles, the foam detergent with the synergistic action of GO-OH/SiO 2 and TAS surfactant had decontamination rates of 91.7%, 91.16% and 91.76%, respectively, which were 14.96%, 15.67% and 19.39% higher than that of TAS foam detergent without GO-OH/SiO 2 . The synergistic enhancement of GO-OH and SiO 2 on foam stability and its adsorption and combination action with uranyl ions would be the main reasons to improve the detergency of the TAS foam detergent. Therefore, TAS foam detergent stabilized synergistically by GO-OH/SiO 2 with high stability and efficient decontamination will be widely applied in nuclear emergencies and decommissioning decontamination of nuclear facilities.

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Analytical Methods · 2017 ·Vol. 9 ·期 19 ·2812-2820 · IF 1.9

Au nanoparticles anchored on Ni(OH)2 nanowires with multiple cavities for selective electrochemical detection of dopamine

Yanyi Fu,Qinglin Sheng,Jianbin Zheng

Au nanoparticles supported on nickel hydroxide nanowires with multiple cavities (Au/m-Ni(OH)2) were synthesized and used for the enhanced electrochemical sensing of dopamine (DA). m-Ni(OH)2 nanowires were first fabricated based on an anion exchange strategy and then chosen as supports for Au nanoparticles without an additional stabilizer and surfactant. The morphology and composition of the nanocomposites were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD) and energy-dispersive X-ray spectroscopy (EDS). TEM observations revealed that Au nanoparticles were uniformly embedded in the cavities of m-Ni(OH)2 nanowires, with a high dispersion and a narrow size of 2 nm. Electrochemical investigations indicated that the as-prepared sensor exhibited fascinating performance towards the oxidation of DA. The linear range for DA detection was 0.45 μM to 1.78 mM with a low detection limit of 0.09 μM (S/N = 3). Additionally, the DA sensor possessed an excellent selectivity in the presence of potentially interfering substances such as ascorbic acid (AA), uric acid (UA) and glucose (Glu). Therefore, it is expected that Au/m-Ni(OH)2 nanocomposites could be used as electroactive materials for developing DA sensors.

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2021 · IF 5.816

Morphological and compositional modification of β-Ni(OH)2 nanoplates by ferrihydrite for enhanced oxygen evolution reaction

Chi Zhang,Zhuohong Xie,Yi Liang,Dingding Meng,Zheng Wang,Xin He,Weiye Qiu,Mei Chen,Ping Liang,Zhonghua Zhang

Ni(OH) 2 has been long studied as an effective oxygen evolution electrocatalyst . Nevertheless, its catalytic activity can still be further enhanced by microstructural modification and Fe-doping. In this study, with the assistance of adsorbent ferrihydrite (FH), we obtain Fe-doped β-Ni(OH) 2 nanoplates with Fe 2 O 3 nanoparticles decorated on the surface via a facile hydrothermal process. The Fe-doping, decorated Fe 2 O 3 nanoparticles , and special microstructure endow β-Ni(OH) 2 nanoplates with an improved oxygen evolution activity in alkaline solutions. For the sample with optimal FH amount, the overpotential to motivate a current density of 10 mA cm −2 is 280 mV, with a low Tafel slope of ~64.17 mV dec −1 . During the 10 h i-t test at 1.50 V vs. RHE , the current density has an attenuation of only 23.7%. The study opens a facile avenue to modify Ni(OH) 2 -based OER catalyst from perspectives of both microstructures and compositions .

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ELECTROCHIMICA ACTA · 2021 · IF 6.901

Controlled preparation of Ni(OH)2/NiS nanosheet heterostructure as hybrid supercapacitor electrodes for high electrochemical performance

Kun Song,Wenting Li,Rui Yang,Yongjie Zheng,Xiaoshuang Chen,Xin Wang,Guoli Chen,Weichao Lv

As a battery-type electrode material , Ni(OH) 2 has been widely concerned for its ultra-high theoretical specific capacity, however, its poor conductivity and lack of effective active sites hinder its application. It is a great challenge to develop Ni(OH) 2 based supercapacitors . It is critical to improve the electrical conductivity and effective active sites to make full use of the energy storage of Ni(OH) 2 -based materials. Therefore, Ni(OH) 2 /NiS composites are designed and prepared by controllable low temperature chemical deposition and ion exchange method. Ni(OH) 2 nanosheets with various morphology are controllably prepared by low temperature chemical deposition, and then Ni(OH) 2 /NiS composites are controllably prepared on Ni(OH) 2 substrate by ion exchange. Due to the doping of NiS into Ni(OH) 2 nanosheets, the conductive network structure is formed, which makes the composite exhibit excellent electrochemical properties, such as high specific capacity, large specific surface area and good electrical conductivity. The as-fabricated Ni(OH) 2 /NiS indicates an outstanding specific capacity of 240.5 mAh g −1 at 1 A g −1 . This paper detailed studies the practical application of hybrid supercapacitors , which may inspire future researchers to design Ni(OH) 2 -based materials with desired applications.

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SCIENCE OF THE TOTAL ENVIRONMENT · 2021 · IF 7.963

Regenerable magnetic aminated lignin/Fe3O4/La(OH)3 adsorbents for the effective removal of phosphate and glyphosate

Changsong Li,Yijing Li,Qiang Li,Junling Duan,Juying Hou,Qin Hou,Shiyun Ai,Houshen Li,Yuechao Yang

Phosphates and organophosphorus cause environmental pollution , and excessive phosphate leads to water eutrophication . Glyphosate , an organophosphorus herbicide, harms the environment and human health. In this study, regenerable magnetic AL/Fe 3 O 4 /La(OH) 3 adsorbents were developed by modifying Fe 3 O 4 and La(OH) 3 on aminated lignin (AL) for phosphate and glyphosate removal. The adsorption capacity for phosphate and glyphosate reached 60.36 mg g −1 and 83.87 mg g −1 when the initial concentrations were 150 mg L −1 and 250 mg L −1 , respectively. The thermodynamic data showed that adsorption is a spontaneous and endothermic process. Adsorption can be applied at pH values ranging from 3 to 11 and is more suitable under acidic conditions. Fe 3 O 4 and La(OH) 3 both enhanced the adsorption capacities of phosphate and glyphosate. Phosphate and glyphosate compete slightly when coexisting in the adsorption process at low concentrations. Due to the magnetic properties of Fe 3 O 4 , the adsorbents can be separated rapidly and effectively with an external magnetic field. 89% adsorption capacity remained after four adsorption-desorption recycles. Thus, AL/Fe 3 O 4 /La(OH) 3 shows potential for phosphate and glyphosate removal as an effective and reusable adsorbent.

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APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING · 2021 ·Vol. 127 ·期 2 ·1-11 · IF 2.584

A new core–shell Z-scheme heterojunction structured La(OH)3@In2S3 composite with superior photocatalytic performance

Hu Shuting,He Junfeng,Chen Fuming,Liu Bin,zhai Wangjian,He Qinyu

Constructing Z-scheme heterojunction photocatalyst with strong redox ability to make for enhanced photocatalytic performance and efficient charge separation is extremely attractive but still underdeveloped. Herein, a Z-scheme heterojunction structured La(OH) 3 @In 2 S 3 composite (labeled by “LIS”) with photocatalytic for the methylene orange (MO) degradation under simulated light irradiation has been developed. The as-prepared LIS, together with commercial La(OH) 3 and pure In 2 S 3 fabricated with the identical processing method and starting materials as those of LIS, was characterized by X-ray diffraction, UV–vis diffuse reflectance spectra, scanning electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, photoluminescence spectra and electrochemical impedance spectroscopy. The results show the heterojunction of La(OH) 3 /In 2 S 3 has prolonged the lifetime of the photo-generated carriers. The photocatalytic activity test shows that over only a small amount (0.02 g in 100 ml MO) of LIS, the photodegradation rate of 95% toward MO can be obtained in 90 min, which is about 3.4 times higher than that over pure In 2 S 3 . The active species trapping experiments indicate that there were four active species playing roles in photodegradation as the following order: e –  = ∙OH < h +  < ∙O 2 – . A mechanism of Z-scheme heterojunction was proposed and well explained the enhanced photocatalytic performance. This work provides a new cost-effective photocatalyst with high photocatalytic properties.

CAS / MDL: 207398-97-8 547-58-0
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DALTON TRANSACTIONS · 2020 ·Vol. 50 ·期 1 ·391-397 · IF 4.174

(Ni,Co)Se@Ni(OH)2 heterojunction nanosheets as an efficient electrocatalyst for the hydrogen evolution reaction

Yunmei Du,Huimin Zhao,Wensi Wang,Yu Yang,Minghui Wang,Shaoxiang Li,Yanru Liu,Lei Wang

A heterogeneous structure formed by coupling two or more phases can reinforce the activity of active sites and expedite electron transfer, which is conducive to boosting its electrocatalytic activity. Herein, we designed nickel foam supported (NiCo2)Se@Ni(OH)2 (NCS@NH) heterojunction nanosheets by a two-step method. First of all, the NiCo2S4@Ni(OH)2 (NiCo2S4@NH) nanosheets coated on nickel foam were acquired via a hydrothermal method. In the selenization treatment that followed, NiCo2S4@NH was converted into NCS@NH heterogeneous nanosheets in which the selenide nanoparticles decorated on the surface of the Ni(OH)2 nanosheets formed heterojunction interfaces, and the heterogeneous structure could accelerate electron transfer, thus improving the catalytic activity. The Ni(OH)2 nanosheets can adequately contact the electrolyte and promote the decomposition of water. Meanwhile, the thickness of the Ni(OH)2 nanosheets gradually decreases with the increase of Co doping (1.5–2.5 mmol), consequently affecting the HER properties. Notably, when the amount of Co salt added is 2 mmol, NCS@NH exhibited superior HER properties (with a voltage of 253 mV at 100 mA cm−2) and excellent stability for 24 h.

CAS / MDL: 62-55-5
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Materials Today Chemistry · 2024 · IF 6.7

One-step solvothermal formation of Cu - Doped Cu2WO4(OH)2 nanocatalysts for efficient photocatalytic amine oxidation coupling

Zhizhu Yue,Yonghe Yu,Tianjun Hu,Ying Wang,Lulu Cao,Yanxia Zhang,Yuhong Chang,Linjuan Pei,Jianfeng Jia

The development of economical multiphase photocatalysts is a significant challenge in achieving large-scale industrialization. Rational catalyst design can help in achieving efficient, energy-saving, and green catalytic reactions, making it more feasible to screen potential catalyst candidates. In this paper, we have successfully developed a high-efficiency photocatalyst Cu-doped Cu 2 WO 4 (OH) 2 (CWOH-y, where y represents the molar ratio of copper tungsten source), which can catalyze the aerobic coupling reaction of amines to produce corresponding imines under visible light irradiation. N-benzylidenebenzylamine is synthesized under visible light at 25 °C with an 89 % yield. Under natural light at around 35 °C (mean light intensity of 50 mW/cm 2 ), 94 % of the benzylamine is converted, and 97 % of the product is N-benzylidenebenzylamine. The catalyst exhibits high efficiency due to the synergistic effect of doped Cu, Cu 2 WO 4 (OH) 2 , and visible light. This combination generates a significant amount of superoxide free radicals and singlet oxygen when exposed to visible light. Furthermore, the catalyst demonstrates universality and stability with a wide range of amine derivatives. This study introduces a new environmentally friendly photocatalytic pathway for the synthesis of imines and emphasizes the potential applications of Cu 2 WO 4 (OH) 2 .

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Scientific Reports · 2020 ·Vol. 10 ·期 1 ·1-12 · IF 3.998

Synergistic Catalysis of Co(OH)2/CuO for the Degradation of Organic Pollutant Under Visible Light Irradiation

Akram Naeem,Guo Jia,Ma Wenlan,Guo Yuan,Hassan Afaq,Wang Jide

The exploration of advanced water treatment technologies e.g. heterogeneous photocatalysis is the most promising way to address organic pollution issues. Semiconductors based bimetallic photocatalysis with wide bandgap, have displayed splendid degradation performance in the UV light region, but their extension to the visible light/near infra-red region is still a matter of great concern. CuO, Co(OH) 2 , CoO and Co(OH) 2 /CuO nanocomposites were synthesized via simple co-precipitation method and further practiced for Rhodamine B (RhB) decomposition by introducing per-sulfate (PS) as a sacrificial agent. Results revealed that Co(OH) 2 /CuO catalyst had shown robust catalytic activity for RhB photodegradation (degradation time 8 min, k = 0.864 min −1 ) under light illumination, significantly less (12–60 times) than the other reported bimetallic catalysts. Catalyst also have verified excellent performance for a broader pH range (5–9) with excellent stability. Main reactive species responsible for the photocatalytic reaction were sulfate (SO 4 •− ) and superoxide (O 2 • ) radicals, duly verified by ESR and by using radical scavengers. With outstanding recycling abilities, this is probably the fewer successful attempt for RhB decolorization and can be highly favorable for effluent treatment by using the synergic effect of absorption and photodegradation.

CAS / MDL: 81-88-9
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