CATALYSIS COMMUNICATIONS
·
2016
·
IF 3.389
Xiaomin Xiang,Bin Zhang,Guoqiang Ding,Jinglei Cui,Hongyan Zheng,Yulei Zhu
The oxidation of furfural in H 2 O 2 and H 2 O 2 –Mg(OH) 2 system were systematically investigated and a rational explanation for the reaction mechanism was proposed. 2-formyloxyfuran, from selective oxidation of HC O group in furfural, was a crucial intermediate. The addition of Mg(OH) 2 suppressed the oxidation of furan ring of furfural and enhanced selectivities of 2(5H)-furanone (44.8%) and succinic acid (38.0%). FT-IR, Gaussian calculation and experimental results indicated that the process of furfural oxidation with H 2 O 2 is homogeneous, and the synergy between dissolved Mg 2 + cations and OH − ions facilitates the HOO − attacking the carbon atom of HC O other than the C C bound of furan ring.
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高影响因子
JOURNAL OF MATERIALS RESEARCH
·
2013
·Vol. 28
·期 12
·1582-1588
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IF 1.713
Wenyan Wang,Zhanwei Ma,Runjuan Liang,Tinghua Wu,Ying Wu
SnZn(OH)6 (ZHS) with different morphologies were synthesized by a facile self-templated method at room temperature. It was found that the morphology of ZHS could be controlled by varying the concentration of OH−. The crystalline structure and morphology of the particles were characterized by x-ray diffraction, UV-vis diffuse reflectance spectroscopy, scanning electron microscopy images, and N2 adsorption. The results indicated that the particles had almost uniform monoclinic geometry and uniform size. The photocatalytic activity of ZHS with different morphologies was tested through degradation of Rhodamine B (RhB). Therein, the hollow ZHS showed the highest light catalytic performance due to its large BET surface area, wide band gap, and high crystallinity.
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高影响因子
Heritage Science
·
2013
·Vol. 1
·期 1
·1-10
·
IF 0
Zhao Jing,Luo Hongjie,Wang Liqin,Li Weidong,Zhou Tie,Rong Bo
The use of organic–inorganic hybrid compounds containing tetraethoxysilane (TEOS) and hydroxyl-terminated polydimethylsiloxane (PDMS-OH) is one of the most promising approaches for using alkoxysilane-based formulations to improve the effectiveness of the consolidation of traditional silicate artifacts, such as ancient stone. Based on analysis of existing damaged potteries influenced by the crystallization of NaCl salt, the hybrid we prepared in this study provided a crack-free and homogeneous gel on the premise of appropriate PDMS-OH content. The consolidants were applied to samples prepared following procedures that simulate old pottery and the effect of the protective products was evaluated by characterizing the surface morphology, the determination of the consolidant uptake, color changes, water vapour permeability and several wet-dry cycles with salt. The best formulation found for the hybrid in the present work was made up of 10% PDMS-OH with TEOS, which showed a significant increase in compressive strength, with a value of 3.50 MPa at 3 mm depth of consolidation, similar to the sample treated with Primal SF(the commercial protective agents used for comparison purposes), which had 3.20 MPa in compressive strength at 2 mm depth of consolidation. Except for small color changes and excellent water vapor permeability, there was still no significant change, and the destructive effects from NaCl crystallization for the hydrophobic surface of the sample treated with hybrid material was different to what happened for the hydrophilic case in the original. Thus, this study has revealed, for the first time, the addition of an appropriate amount of PDMS-OH to TEOS helps to improve the mechanical properties, hydrophobic behavior and salt resistance of damaged pottery effloresced by the NaCl crystals; in addition small color changes and excellent water vapor permeability should also be taken into consideration.
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ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
·
2014
·
IF 1.251
Fengting Chen,Jiachang Zhao,Jingli Xu,Yuandong Wu
The hetero-bimetallic polyanionic compound BiCu 2 (TeO 3 )(SO 4 )(OH) 3 was synthesized using hydrothermal techniques. Single-crystal X-ray diffraction analysis revealed that title compound crystallizes in the monoclinic space group P 2 1 / n (No. 14) with lattice parameters a = 9.5513(15), b = 6.3022(10), c = 13.955(2) Å, β = 102.845(3)°, and Z = 4. The structure of title compound is a three-dimensional tunnel framework consisting of edge-sharing two-dimensional [Cu 3 O 10 ] 14– layers linked by BiO 8 bicapped trigonal prisms, TeO 3 2– trigonal pyramids and SO 4 2– tetrahedra. Along [010], each Cu(1)O 6 octahedron shares two edges with adjacent Cu(1)O 6 units to form infinite one-dimensional zigzag chains, which are connected by double inverted Cu(2)O 6 octahedral units via edge sharing (O9 ··· O8). The suitability of crystal for optical applications was investigated by UV/Vis/NIR spectroscopy. Raman and FTIR spectra were used to confirm the presence of various functional groups such as TeO 3 2– , SO 4 2– , OH – in the crystals.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Xin Li,Jielin Wang,Jieyuan Li,Chunling Zhang,Ruimin Chen,Shujie Shen,Yanjuan Sun,Lili Zhang,Fan Dong
As one of the most important bulk chemicals, nitric acid is primarily produced by the Ostwald process with extensive energy consumption and carbon emission. Therefore, it is necessary to develop alternative green routes for nitric acid synthesis. Photocatalytic nitrate synthesis via complete ammonia oxidation is a promising strategy for efficiently producing nitrate under ambient conditions. However, the reaction route of ammonia oxidation is complex with diverse product distribution since it is a multi-electron involved reaction. It is a great challenge to directionally regulate the selectivity for the targeted conversion of ammonia into nitrate with a high conversion ratio. Herein, the CuO x clusters are constructed on the TiO 2 substrate as the active sites to facilitate ammonia-to-nitrate photosynthesis via the enhanced activation of H 2 O molecules. It is revealed that a new reaction pathway is established, in which the •OH-driven direct ammonia oxidation contributes to the promoted nitrate synthesis rate at 116.8 ± 3.5 μmol·q·h −1 . Moreover, the competitive conversion ratio for ammonia (91.1 ± 1.2 %) and selectivity for nitrate (91.7 ± 0.8 %) are reached, manifesting the significance of effective nitrate production with low energy consumption and carbon emission. A new opportunity is provided in this work for the artificial nitrogen cycle and N-involving resource utilization.
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高影响因子
JOURNAL OF SOLID STATE ELECTROCHEMISTRY
·
2024
·
IF 2.6
Li Gang,Ren Haifang,Geng Chunping,Wu Xiang
Electrical energy storage devices (EES) play an important role in the development of portable electronic devices, power grids, and electric vehicles. Supercapacitors (SCs) become the focus of the EES field due to their high power density and high energy density. ZnCo 2 O 4 ternary metal oxides show considerable potential as electrodes for SCs. In this work, Ni(OH) 2 and PPy materials are combined on the surface of ZnCo 2 O 4 samples. The synthesized products possess a specific capacitance of 1256 C/g at 1 A/g and an energy density of 69 Wh/kg at 1350 W/kg. Moreover, the assembled device retains 81% of its capacity after being fully charged and discharged 10,000 times.
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高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2022
·Vol. 29
·期 51
·77344-77358
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IF 5.19
Ding Baoting,Wang Xiaomeng,Feng Kun,Fu Jingran,Liang Jianru,Zhou Lixiang
Acidic Cr(VI)-containing wastewater has received increasing attention in recent years. Schwertmannite is a suitable adsorbent for its acid resistance and good adsorption ability. However, it shows poor Cr(VI) adsorption performance under acidic conditions. Herein, inspired by the fast neutralization-mineralization process of acid mine drainage (AMD) triggered by alkaline rocks, a novel nano-scaled schwertmannite (Sch-2.7) with high Cr(VI) adsorption capacity was synthesized at constant pH of 2.7 via adding OH − . Compared with common schwertmannite (Sch), appropriate OH − effectively improved mineral yield (the precipitation efficiency of Fe: 96.75% vs. 29.93%), specific surface area (65.1 m 2 /g vs. 18.9 m 2 /g), surface group content, and further Cr(VI) adsorption ability of Sch-2.7. The maximum adsorption capacity was 54.17 (pH = 3), 61.59 (pH = 4), and 66.5 mg/g (pH = 5) for Sch-2.7, whereas only 20.35, 24.51, and 27.17 mg/g for Sch. On average, the former was 2.53 times higher than the latter. Temperature and coexisting ions had little influences on the sorption process of Sch-2.7. The mechanism analysis demonstrated that the Cr(VI) removal by Sch-2.7 was a more thermodynamic favorable process due to abundant reactive-active components on Sch-2.7 for adsorption reaction. This work provided new insight into performance optimization and application potential on Cr(VI) removal of schwertmannite.
研究领域:
环境科学
·
材料科学
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DOI
PubMed
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2018
·
IF 3.141
Ying Huo,Xuyu Wang,Zebao Rui,Xiaoqing Yang,Hongbing Ji
Insight into the relationship between catalytic trends and physicochemical properties of composite nanoparticles is essential for their rational design. Herein, a series of 3d-M (M = Mn, Fe, Co, Ni) metal hydroxide-promoted PtM(OH)x/Al2O3 catalysts are developed and well characterized for establishing the catalytic HCHO oxidation reactivity trend as a function of more fundamental properties, such as hydroxyl concentration and adsorption strength. The reactivity of PtM(OH)x/Al2O3 exhibits an increasing trend of Mn < Fe < Co < Ni, which is governed by their OH–M2+δ bond strength (Ni < Co < Fe < Mn) and surface hydroxyl concentration (Mn < Fe < Co < Ni). Both PtCo(OH)x/Al2O3 and PtNi(OH)x/Al2O3 exhibit a (>)95% HCHO conversion and (>)100 h performance stability at 30 °C with a low 0.2 wt % Pt loading amount. The identification of these catalytic trends provides foundations for composite active sites design for HCHO oxidation and other hydroxyl-involved reactions.
研究领域:
催化化学
·
材料科学
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高影响因子
Journal of Environmental Chemical Engineering
·
2026
·Vol. 14
·期 5
·124167
·
IF 7.5
Chen Chen,Zhenyu Wang,Yasen Li,Jiayao Gao,Xin Chen,Mingjie Jia,Die Shao,Yiming Wang,Xuejian Li,Fuqiang Yu,Guangwen Xu,Junli Xu,Hong-bin Sun
Transition-metal borides have long been developed as promising electrocatalysts for the hydrogen evolution reaction (HER); however, the identity of their true active phase remains controversial. Here, in conjunction with our previous studies, by systematically investigating a series of cobalt- and nickel-boride-derived catalysts through a combined computational and experimental screening, we reveal that HER activity universally originates from the synergistic interaction between metallic sites and hydroxide matrices, enabled by lattice expansion, interfacial electronic transfer, and dynamic surface evolution. As a representative high-performance example, Pt-modified Co(OH) 2 derived from cobalt boride exhibits ultralow overpotentials of 11 mV at 10 mA cm −2 and 95 mV at 500 mA cm −2 , together with long-term stability. Importantly, the same reconstruction principle applies to Ni-boride systems, confirming the generality of this approach. Beyond water electrolysis, we further demonstrate that these HER catalysts are highly effective in Al-H 2 O batteries, where hydrogen evolution is coupled with electrical energy harvest. An alkaline Al-H 2 O battery employing the reconstructed catalyst delivers a power density of 21.96 mW cm −2 . This work establishes that the activity of “boride-based” HER catalysts fundamentally arises from reconstructed metal-hydroxide active centers, providing a development paradigm of transition-metal electrocatalysts.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Guocui Cai,Helong Jiang,Fangyi Chu,Xiangcun Li,Xiaobin Jiang,Xiao Wu,Gaohong He,Yan Dai
Here, the conventionally disordered Co(OH)F filaments are rearranged to form highly-ordered flower-like Co(OH)F architectures in a conductive membrane substrate. The important findings contribute to designing delicate nanostructures and improving the catalytic activity of advanced materials for energy applications. The hierarchically porous CNT@NC membrane with CNT as the core and N -doped carbon as the crosslinking shell is scalably designed firstly for strengthening the transport of Li + and electrons in the electrode, providing an ultrahigh porosity for growing flower-like Co(OH)F on both surfaces and interior of the membrane, as well as offering electrons for the redox reactions through the roots of the Co(OH)F flowers. Furthermore, the ordered Co(OH)F bundles with divergent and open-ended structures provide the catalyst with the broad reaction interface and active sites for polysulfides (LiPSs) anchoring and catalytic conversion at a low energy barrier, significantly facilitating the diffusion of ions and electrolyte in the catalyst, and thus effectively alleviating the shuttle effect. Owing to the synergistic effect between the conductive membrane substrate and the grown Co(OH)F catalyst, the Co(OH)F-CNT@NC cathode generates a high reversible capacity and excellent long-term cycling performance (622 mAh·g −1 at 1C after 600 cycles). Conclusively, the proposed facile strategy provides insights regarding the design of novel cathode materials for high-areal-capacity Li–S batteries.
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高影响因子
ACS Catalysis
·
2020
·
IF 12.35
Yang Chen,Yingxin Feng,Lin Li,Jingyue Liu,Xiaoli Pan,Wei Liu,Fenfei Wei,Yitao Cui,Botao Qiao,Xiucheng Sun,Xiaoyu Li,Jian Lin,Sen Lin,Xiaodong Wang,Tao Zhang
Exclusive Pt species supported on inert substrates have not achieved satisfactory performance for cryogenic CO oxidation because of the constraint of the competitive Langmuir–Hinshelwood process in which the strongly adsorbed CO inhibits the activation of O2. Here, we develop a catalyst of Pt nanoparticles on Al2O3 that exhibits extremely high activity with 100% CO conversion at −20 °C and orders of magnitude higher specific rate than current commercial catalysts. Detailed catalyst characterizations reveal the presence of metallic Pt sites and positively charged ones associated with the OH species in Pt/Al2O3. Both experimental data and theoretical calculations suggest that CO adsorbed on Pt(OH) kink sites reacts with OH species covering Pt0 terrace sites to release CO2. Afterward, O2 is facilely activated on terrace sites to regenerate OH. The presence of OH species and the synergy between Pt kink and terrace sites on the Pt species lead to an ultralow reaction barrier for CO oxidation.
研究领域:
催化化学
·
材料科学
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高影响因子
APPLIED CATALYSIS A-GENERAL
·
2024
·
IF 4.7
Li Zou,Jiale Xie,Shuxiang Wang,Yixing Yu,Jing Huang,Liuliu Wang,Pingping Yang,Wenyan Tao
Low charge separation efficiency ( η sep ) of TiO 2 impedes its applications of photoelectrochemical (PEC) water splitting. A positive potential pretreatment approach has been developed to construct a surface polarization with −OH groups at a potential of 1.48 V RHE . When the pretreatment time of 6 h is used, the η sep and photocurrent density ( J ph ) reach up to 54% (vs. 24%, TiO 2 ) and 0.92 mA cm −2 (vs. 0.32 mA cm −2 , TiO 2 ) under AM 1.5 G illumination, respectively. The photovoltage can be increased from 0.17 V to 0.52 V. When the pretreatment time is extended to 22 h, a higher J ph of 1.57 mA cm −2 and η sep of 87% can be obtained. Furthermore, the positive potential pretreated TiO 2 possesses excellent PEC stability. The PEC improvements can be attributed to the surface polarization with the −OH groups and favorable surface states of Ti-OH, but not to the formation of Ti 3+ or oxygen vacancies.
研究领域:
材料科学
·
能源科学
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高影响因子
危险品化学品经营许可证（带存储）