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Nanomaterials · 2022 ·Vol. 12 ·期 21 ·3844 · IF 5.719

Aggregation, Sedimentation and Dissolution of Cu(OH)2-Nanorods-Based Nanopesticide in Soil Solutions

Zhenlan Xu,Qing Tang,Aimei Hong,Lingxiangyu Li

Along with the development of nanotechnology, nanomaterials have been gradually applied to agriculture in recent years, such as Cu(OH)2-nanorods-based nanopesticide, an antibacterial agrochemical with a high efficacy. Nevertheless, knowledge about physical stability of Cu(OH)2nanopesticide in soil solutions is currently scarce, restricting comprehensive understanding of the fate and risk of Cu(OH)2nanopesticide in the soil environment. Herein we investigated aggregation, sedimentation and dissolution of Cu(OH)2nanopesticide in soil solutions extracted from three different soil samples, wherein commercial Cu(OH)2nanopesticide formulation (NPF), as well as its active ingredient (AI) and laboratory-prepared Cu(OH)2nanorods (NR) with similar morphology as AI, were used as model Cu(OH)2nanopesticides. We found that NPF compared to AI showed less extents of aggregation in ultrapure water due to the presence of dispersing agent in NPF. Yet, moderated aggregation and sedimentation were observed for Cu(OH)2nanopesticide irrespective of NPF, AI or NR when soil solutions were used instead of ultrapure water. The sedimentation rate constants of AI and NPF were 0.023 min−1and 0.010 min−1in the ultrapure water, whereas the rate constants of 0.003–0.021 min−1and 0.002–0.007 min−1were observed for AI and NPF in soil solutions, respectively. Besides aggregation and sedimentation, dissolution of Cu(OH)2nanopesticide in soil solutions was highly dependent on soil type, wherein pH and organic matter played important roles in dissolution. Although the final concentrations of dissolved copper (1.08–1.37 mg/L) were comparable among different soil solutions incubating 48 mg/L of AI, NPF or NR for 96 h, a gradual increase followed by an equilibrium was only observed in the soil solution from acidic soil (pH 5.16) with the low content of organic matter (1.20 g/kg). This work would shed light on the fate of Cu(OH)2nanopesticide in the soil environment, which is necessary for risk assessment of the nanomaterials-based agrochemical.Keywords:soil solutions;aggregation;sedimentation;Cu(OH)2nanopesticide;dissolution

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Natural Product Communications · 2020 · IF 0.468

The Role of C-8 OH on the Antioxidant Activity of Norwogonin and Isowogonin

Qiushan Zhang,Jin Shao,Tong Zhao,Lei He,Huiping Ma,Linlin Jing

In the present study, the antioxidant property of 4 flavones (moslosooflavone, wogonin, isowogonin, and norwogonin) was evaluated using 6 different assays: 1,1-diphenyl-2-picrylhydrazyl (DPPH·), superoxide (O2 •−), and nitric oxide (NO) radical scavenging assays, ferrous iron chelation, reducing power, and total antioxidant capacity. The 4 flavones exhibited antioxidant activities with decreasing order as norwogonin > isowogonin >> wogonin> moslosooflavone. The present results demonstrated that norwogonin and isowogonin exhibited excellent antioxidant activity, which was mainly based on the presence of C-8 hydroxyl group.

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AICHE JOURNAL · 2023 · IF 3.7

Ionization-engineered two-dimensional confined channels in GO membranes for highly efficient OH− separation

Yong Li,Rui Jia,Ruonan Tan,Ziqiang Hong,Jingjing Gu,Peng Cui,Suixin Zhang,Hongwei Shao,Jin Ran,Cen-Feng Fu

OH − sieving membranes provide a valuable means for treating alkaline effluents but their development presents several challenges. In this study, the concept of ionization engineering is applied to two-dimensional (2D) laminated membranes to facilitate OH − separation. This concept is demonstrated through the stacking of the self-designed sulfonated graphene oxide (SGO) nanosheets to fabricate 2D membranes. The SGO membranes enhance synergistically the OH − dialysis coefficients and separation factors when treating simulated NaOH/Na 2 WO 4 alkaline wastewater, compared with the performance of 2D GO membranes and commonly adopted polymeric cation exchange membranes. Furthermore, the separation factor achieved by the SGO membranes is considerably higher than that of most of the existing alkali recovery membranes. Results of molecular dynamics simulations indicate that the high efficiency of OH − separation in the 2D SGO confined channels is attributable to dehydration effects and intensified electrostatic repulsion. Overall, this research provides an alternative strategy for achieving rapid OH − sieving through the ionization of 2D confined channels.

CAS / MDL: 5329-14-6
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Synthesis of Co(OH)F@Al nanobelt array on various substrates for pyro-MEMS

Yuxiang Li,Xi Chen,Lei Zhang,Ruishan Han,Iftikhar Hussain,Xiaoxia Ma,Kaili Zhang

Metastable intermolecular composites (MICs) composed by solid fuel and oxidizer can undergo violent redox reaction with release of huge amount of energy. Integration of MIC with microelectromechanical-system (MEMS) is of particular interest to meet the demand of miniaturization in modern pyrotechnic devices. Meanwhile, fluorine-containing oxidizers are favored in MIC owing to their potential to fluorinate the oxide passivation layer in common elemental fuels. Herein, Co(OH)F was employed for the first time as a novel fluorine-containing oxidizer in Al-based MIC. Vertically aligned Co(OH)F@Al nanobelt arrays (NAs) with tunable morphology were successfully fabricated on a variety of substrates (Si, glass, Ni, Cu, Ti) via a facile hydrothermal synthesis followed by electron beam evaporation. The whole fabrication process is highly compatible with modern MEMS technology. The thermal behavior of pure Co(OH)F and Co(OH)F@Al composites was comprehensively investigated by TG-DSC and a series of ex-situ and in-situ characterization. It was found that, Co(OH)F@Al composites achieved main exothermal reaction before melting of Al regardless of morphology and equivalence ratio. This feature is attributed to the etching of Al 2 O 3 shell by HF released from Co(OH)F which is termed as pre-ignition reaction. To elucidate the effect of micro-structure on the actual specific heat release, we proposed a phenomenological model which can be a reference for future micro-structure design of MIC.

CAS / MDL: 12125-01-8 10026-22-9
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International Journal of Electrochemical Science · 2023 · IF 1.5

In Situ Growth of Co(OH)2/NiS on Cobalt Foam for Supercapacitor Application

Zhe Li,Chun-yong Zhang,Hao-yu Wang,Lin Zhu,Hai-tao Liu,Li Shu,Ying-pin Weng

Herein, a simple hydrothermal method was used to synthesize cobalt hydroxide/nickel sulfide and cobalt foam (Co(OH) 2 /NiS@CF) composite electrode. By simply heating cobalt foam in the aqueous solution containing cobalt nitrate, nickel nitrate, and thiourea, Co(OH) 2 /NiS nano stereoscopic website was synthesized on Cobalt foam. X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and electrochemical tests were used to characterize these composite electrodes. When the molar ratio of Co(NO 3 ) 2 ·6H 2 O to Thiourea of 4:5, Co(OH) 2 /NiS@CF exhibits excellent performance under these tests. The specific capacitance was 1260 F/g at 1.0 A/g. The composite electrode had 92.3% capacitance retention after 2000 charge-discharge cycles at 1.0 A/g.

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Small · 2023 ·Vol. 19 ·期 20 ·2207569 · IF 13.3

Significantly Stabilizing Hydrogen Evolution Reaction Induced by Nb-Doping Pt/Co(OH)2 Nanosheets

Yakun Tian,Ming Wen,Aijian Huang,Qingsheng Wu,Zhiguo Wang,Quanjing Zhu,Tao Zhou,Yongqing Fu

High stability and efficiency of electrocatalysts are crucial for hydrogen evolution reaction (HER) toward water splitting in an alkaline media. Herein, a novel nano-Pt/Nb-doped Co(OH) 2 (Pt/Nb  Co(OH) 2 ) nanosheet is designed and synthesized using water-bath treatment and solvothermal reduction approaches. With nano-Pt uniformly anchored onto Nb  Co(OH) 2 nanosheet, the synthesized Pt/Nb  Co(OH) 2 shows outstanding electrocatalytic performances for alkaline HER, achieving a high stability for at least 33 h, a high mass activity of 0.65 mA µg −1 Pt, and a good catalytic activity with a low overpotential of 112 mV at 10 mA cm −2 . Both experimental and theoretical results prove that Nb-doping significantly optimizes the hydrogen adsorption free energy to accelerate the Heyrovsky step for HER, and boosts the adsorption of H 2 O, which further enhances the water activation. This study provides a new design methodology for the Nb-doped electrocatalysts in an alkaline HER field by facile and green way.

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CHINESE JOURNAL OF CATALYSIS · 2023 · IF 16.5

Boosting 5-hydroxymethylfurfural electrooxidation in neutral electrolytes via TEMPO-enhanced dehydrogenation and OH adsorption

Hongfang Wang,Leitao Xu,Jingcheng Wu,Peng Zhou,Shasha Tao,Yuxuan Lu,Xianwen Wu,Shuangyin Wang,Yuqin Zou

5-Hydroxymethylfurfural (HMF) electrooxidation in neutral conditions is a promising strategy to suppress the formation of humins and corrosive effects on electrochemical devices. However, scarce studies have been reported in neutral media due to the deficiency in electrophilic oxygen (eg OH – ) required for the activation of HMF. Herein, 2,2,6,6-tetramethyl-piperidine-1-oxyl (TEMPO)/Co 3 O 4 was utilized to co-catalyze HMF in neutral media, successfully achieving 2,5-furandicarboxylic acid (FDCA) with yield > 99%. It was found that TEMPO could promote HMF dehydrogenation to 2,5-diformylfuran (DFF) and simultaneously activated water via hydrogen-bonding interactions. As a result, the formation of OH* in neutral electrolytes was favored, which was absorbed by electrogenerated active Co species to facilitate subsequent conversion of formyl-group-involved intermediates to FDCA. This work provides a current understanding of the catalytic mechanism for HMFOR in neutral media and guides the design of highly efficient electrocatalysts for biomass upgrading.

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Nanoscale · 2019 ·Vol. 11 ·期 19 ·9444-9456 · IF 6.97

Enhancing the photocatalytic activity of ZnSn(OH)6 achieved by gradual sulfur doping tactics

Xinyi Lian,Zhou Chen,Xiang Yu,Tingting Fan,Yunyun Dong,Hesheng Zhai,Weiping Fang,Xiaodong Yi

To solve the intrinsic deficiency inherited from the large band gap of ZnSn(OH)6 (ZSH), a gradual sulfur doping strategy is first proposed here to expand the optical absorption range, improve the separation efficiency of photogenerated electron–hole pairs, and thus enhance the photocatalytic activity. It is demonstrated that the distribution of sulfur in the flower-like ZSH (the sulfur doped sample is denoted as S-ZSH) tends to be largest on the outer most surface and becomes smaller towards the interior. The S-ZSH therefore has a gradual bandgap structure that is beneficial for transferring photogenerated charge carriers from the interior to the surface, which will greatly enhance the utilization of photoelectrons. As a result, the visible light photocurrent density of S-ZSH and the photocatalytic degradation rate of rhodamine (RhB) are about 5 and 10 times higher than with pristine ZSH, respectively.

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RESEARCH ON CHEMICAL INTERMEDIATES · 2018 ·Vol. 44 ·期 5 ·3613-3627 · IF 1.674

CO2 capture and sequestration by sodium humate and Ca(OH)2 from carbide slag

Sun Zhiguo,Feng Run,Zhang Li,Xie Hongyong

A new method of carbon capture and sequestration (CCS) by sodium humate (HA–Na) and Ca(OH) 2 from carbide slag (CS) solution was proposed. The effects of various operating parameters, such as the additive amount of HA–Na, pH, temperature, gas flow rate, CO 2 inlet concentration, and stirring rate on both the Ca ion concentration and Ca conversion rate were investigated in a lab-scale bubbling reactor. The synergistic mechanism of HA–Na and Ca(OH) 2 from CS on CCS is also put forward and demonstrated. The experimental results indicate that HA–Na may improve significantly the CCS capability of CS since the Ca conversion rate of CS is increased 10% by HA–Na additive. The pH is a key factor for the CO 2 absorption process and HA–Na may lower the rate of pH decrease of Ca(OH) 2 solution. The increasing temperature, stirring rate, and CO 2 inlet concentration are favorable to CO 2 capture, as well as low gas flow rate. Ca(OH) 2 from CS mixed with HA–Na solution shows good performance in CO 2 uptake, and the Ca conversion rate reaches 99% with 100 mL of Ca(OH) 2 (1.5 g/L) solution mixed with 0.1 g HA–Na at 40 °C, a gas flow rate of 0.1 L/min, and an inlet CO 2 concentration of 100% at ambient pressure. Moreover, calcite CaCO 3 is is identified as the main product of CO 2 capture by X-ray diffraction and scanning electron microscopy analysis.

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ELECTROCHIMICA ACTA · 2018 · IF 5.116

Surface engineering of hierarchical Ni(OH)2 nanosheet@nanowire configuration toward superior urea electrolysis

Zhihao Yue,Siyu Yao,Yuanzhen Li,Wenxin Zhu,Wentao Zhang,Rong Wang,Jing Wang,Lunjie Huang,Dongyang Zhao,Jianlong Wang

In order to resolve the pollution and waste caused by urea-rich wastewater, designing superior and stable earth-abundant catalysts for urea oxidation reaction (UOR) have always been attractive and urgent but still challenging. Herein, we report on a facile surface-engineering strategy of building hierarchical nickel hydroxide nanosheet@nanowire array on Ni foam (Ni(OH) 2 NS@NW/Ni foam) as anode material toward superior urea electrolysis. This Ni(OH) 2 based-catalyst with peculiar nanosheet@nanowire configuration just requires a small potential of 0.34 V ( vs. SCE) to drive 10 mA cm −2 in 1.0 M KOH with 0.33 M urea, which outperforms the one with pure nanosheet array architecture and even the commercial Pt/C catalyst. Further, a two-electrode electrolysis system is built here with the cathode of cobalt phosphide nanowire array on Ni foam (Co 2 P NW/Ni foam) and anode of Ni(OH) 2 NS@NW/Ni foam for overall urea electrolysis, which needs a low voltage of 1.58 V to drive 5 mA cm −2 in 1.0 M KOH with 0.33 M urea. Note that, the current density presented in this work is based on the real surface area of Ni foam but not the geometric area, unless otherwise specified.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

Degradation of Levofloxacin by heterogeneous activation of oxone using Co(OH)2/graphene composites

Yunqing Pi,Peng Zhao,Lingjia Ma,Yangdan Cao,Huiqing Gao,Shuying Dong,Jianhui Sun

The Co(OH) 2 /reduced graphene oxide hybrids (Co(OH) 2 /rGO) was prepared and used as catalyst to enhanced heterogeneous activation of Oxone for the decomposition of Levofloxacin (LVF). The Co(OH) 2 /rGO composites with different Co(OH) 2 loading have been successfully synthesized, where the sample contain 20% Co(OH) 2 exhibited superior activation, attributing to the synergistic effect between Co(OH) 2 and rGO. Meanwhile, the effects of some important reaction parameters on the decomposition of LVF by Co(OH) 2 /rGO/Oxone process were investigated. The results indicated that the decomposition rate of LVF(>94.5%) was increased with the increasing of Oxone concentration, and 20% Co(OH) 2 /rGO dosage neutral pH. Moreover, the Co(OH) 2 /rGO catalyst showed high activity and stability during the repeated experiments.

CAS / MDL: 7782-42-5
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BIORESOURCE TECHNOLOGY · 2018 · IF 5.807

La(OH)3-modified magnetic pineapple biochar as novel adsorbents for efficient phosphate removal

Taiwan Liao,Ting Li,Xiangde Su,Xiang Yu,Huiyu Song,Yi Zhu,Yuanming Zhang

A series of La(OH) 3 -modified magnetic pineapple biochar (La x -MC) with different contents of La(OH) 3 were prepared and used as phosphate adsorbents for the first time. With the increase of La(OH) 3 content, the adsorption capacity for phosphate increased while the magnetic property decreased. La10-MC exhibited excellent magnetic property for easy recovery and high adsorption capacity up to 101.16 mg P/g, which was 27 times that of pineapple biochar and much higher than most phosphate adsorbents. Adsorption isotherm and adsorption kinetics were better fitted by Langmuir model and pseudo second-order model, respectively. The removal efficiency >96.04% in coexisting ions indicated its high selectivity to phosphate. Little decrease in removal efficiency after three adsorption-desorption cycles suggested its excellent stability and cyclic utilization. Leaching study demonstrated the negligible risk of La 3+ and Fe 3+ leakage during adsorption process. Mechanism study revealed that the adsorption mechanism involved precipitation, electrostatic interaction, ligand exchange and inner-sphere complexation.

CAS / MDL: 7778-77-0
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