资源类型

期刊论文 220

年份

2023 31

2022 28

2021 30

2020 19

2019 14

2018 11

2017 8

2016 6

2015 10

2014 5

2013 6

2012 6

2011 5

2010 8

2009 6

2008 6

2007 7

2005 2

2004 1

2003 2

展开 ︾

关键词

氢能 5

燃料电池 5

制氢 4

可再生能源 3

力常数 2

新能源 2

无氢渗碳 2

氢燃料电池 2

硫化氢 2

过氧化氢 2

键能 2

键长 2

2035 1

N3C空位 1

n-Si 1

产业规模化 1

产业链 1

产氢活性 1

亲/疏水界面修饰 1

展开 ︾

检索范围：

排序： 展示方式：

Efficient production of hydrogen peroxide in microbial reverse-electrodialysis cells coupled with thermolytic

《环境科学与工程前沿（英文）》 2023年 第17卷 第9期 doi: 10.1007/s11783-023-1708-y

摘要：

● Appreciable H2O2 production rate was achieved in MRCs utilizing NH4HCO3 solutions.

关键词： Microbial reverse-electrodialysis cell     Hydrogen peroxide production     Ammonium bicarbonate     Electrolysis cell     Optimization    

HTML PDF 收藏

Reactive extraction for preparation of hydrogen peroxide under pressure

CHENG Yongxi, LI Hongtao, WANG Li, LÜ Shuxiang

《化学科学与工程前沿（英文）》 2008年 第2卷 第3期   页码 335-340 doi: 10.1007/s11705-008-0042-z

摘要： The preparation of hydrogen peroxide from anthrahydroquinone by reactive extraction was investigated. The integration process of oxidation of anthrahydroquinone by air and extraction of hydrogen peroxide from the organic phase with water was carried out in a sieve plate column under pressure. The conversion of anthrahydroquinone increased with increasing pressure resulting in an increase of hydrogen peroxide concentration in the aqueous phase. However, no change in extraction efficiency of hydrogen peroxide was observed. A mathematical model for gas-liquid-liquid reactive extraction was established. In the model, the effects of pressure and gas superficial velocity on reaction were considered. With increasing gas superficial velocity, the conversion of anthrahydroquinone increased, and the fraction of hydrogen peroxide extracted reached a plateau with a maximum of 72.94%. However, both the conversion of anthrahydroquinone and the fraction of hydrogen peroxide extracted decreased with increasing organic phase superficial velocity.
HTML PDF 收藏

Toward better understanding vacuum ultraviolet–iodide induced photolysis via hydrogen peroxide formation

《环境科学与工程前沿（英文）》 2022年 第16卷 第5期 doi: 10.1007/s11783-021-1489-0

摘要：

• UV/VUV/I– induces substantial H2O2 and IO3– formation, but UV/I– does not.

关键词： Vacuum ultraviolet     Hydrogen peroxide     Iodate     Hydroxyl radical     Redox transition    

HTML PDF 收藏

Evaluation of the technoeconomic feasibility of electrochemical hydrogen peroxide production for decentralized

Yang Li, Yixin Zhang, Guangshen Xia, Juhong Zhan, Gang Yu, Yujue Wang

《环境科学与工程前沿（英文）》 2021年 第15卷 第1期 doi: 10.1007/s11783-020-1293-2

摘要： Abstract • Gas diffusion electrode (GDE) is a suitable setup for practical water treatment. • Electrochemical H2O2 production is an economically competitive technology. • High current efficiency of H2O2 production was obtained with GDE at 5–400 mA/cm2. • GDE maintained high stability for H2O2 production for ~1000 h. • Electro-generation of H2O2 enhances ibuprofen removal in an E-peroxone process. This study evaluated the feasibility of electrochemical hydrogen peroxide (H2O2) production with gas diffusion electrode (GDE) for decentralized water treatment. Carbon black-polytetrafluoroethylene GDEs were prepared and tested in a continuous flow electrochemical cell for H2O2 production from oxygen reduction. Results showed that because of the effective oxygen transfer in GDEs, the electrode maintained high apparent current efficiencies (ACEs,>80%) for H2O2 production over a wide current density range of 5–400 mA/cm2, and H2O2 production rates as high as ~202 mg/h/cm2 could be obtained. Long-term stability test showed that the GDE maintained high ACEs (>85%) and low energy consumption (<10 kWh/kg H2O2) for H2O2 production for 42 d (~1000 h). However, the ACEs then decreased to ~70% in the following 4 days because water flooding of GDE pores considerably impeded oxygen transport at the late stage of the trial. Based on an electrode lifetime of 46 days, the overall cost for H2O2 production was estimated to be ~0.88 $/kg H2O2, including an electricity cost of 0.61 $/kg and an electrode capital cost of 0.27 $/kg. With a 9 cm2 GDE and 40 mA/cm2 current density, ~2–4 mg/L of H2O2 could be produced on site for the electro-peroxone treatment of a 1.2 m3/d groundwater flow, which considerably enhanced ibuprofen abatement compared with ozonation alone (~43%–59% vs. 7%). These findings suggest that electrochemical H2O2 production with GDEs holds great promise for the development of compact treatment technologies for decentralized water treatment at a household and community level.

关键词： Advanced oxidation process     Electro-peroxone     Gas diffusion electrode     Hydrogen peroxide     Oxygen reduction    

HTML PDF 收藏

Hydrogen peroxide is correlated with browning in peach fruit stored at low temperature

Zhansheng DING, Shiping TIAN, Xianghong MENG, Yong XU,

《化学科学与工程前沿（英文）》 2009年 第3卷 第4期   页码 363-374 doi: 10.1007/s11705-009-0246-x

摘要： The objective of this present research is to study the biological basis of browning in peach fruit during storage at low temperatures. After being immersed in 0 or 2mmol·L salicylic acid (SA) aqueous solution for 10min, peach fruit (Prunus persica L. cv. Hongtao) were stored at 10°C, 5°C or 0°C with or without shelf life at 25°C. During storage, the progress of browning, lipid per-oxidation, phenol content, activities of polyphenol oxidase (PPO, E.C. 1.14.18.1) and guaiacol peroxidase (POD, EC 1.11.1.7), redox state of ascorbate and glutathione, as well as the content, location and metabolism of hydrogen peroxide (HO) in the fruit were examined. The results indicated that a decrease in HO content was correlated with browning, whereas phenol content and activities of PPO and POD were not correlated with the change in HO content. Moreover, HO content was influenced by different responses of antioxidants at different storage conditions. It was concluded that the main effect of HO on browning was to regulate its appearance and development as a signal molecule, and lower HO content was beneficial to browning.

关键词： beneficial     per-oxidation     appearance     decrease     hydrogen peroxide    

HTML PDF 收藏

Degradation of 4-aminophenol by hydrogen peroxide oxidation using enzyme from Serratia marcescens as

SUN Min, YOU Yahua, DENG Shengsong, GAO Wenxia, YAO Risheng

《环境科学与工程前沿（英文）》 2007年 第1卷 第1期   页码 95-98 doi: 10.1007/s11783-007-0018-0

摘要： AB 90027 as catalyst. The effecting factors during degradation and the degrading mechanism were studied. Also, the location of the enzyme in the cell, which could catalyze the degradation of 4-aminophenol, was analyzed. The results showed that to degrade 50 mL of 4-aminophenol whose concentration was 500 mg/L, the optimal conditions were: volume of HO = 3 mL, temperature = 40 60?C and pH = 9 10. In the degradation process, 4-aminophenol was first converted to benzoquinone and NH, then organic acids including maleic acid, fumaleic acid, and oxalic acid were formed, and then finally CO and HO were generated as final products. The enzyme that could catalyze the degradation of 4-aminophenol was mainly extracellular enzyme.

关键词： degradation process     temperature     effecting     degradation     volume    

HTML PDF 收藏

Kinetics of microwave-enhanced oxidation of phenol by hydrogen peroxide

Deming ZHAO, Jie CHENG, Michael R. HOFFMANN

《环境科学与工程前沿（英文）》 2011年 第5卷 第1期   页码 57-64 doi: 10.1007/s11783-010-0251-9

摘要： Aqueous solutions of phenol were oxidized by hydrogen peroxide assisted by microwave (MW) irradiation. A simple kinetic model for the overall degradation of phenol in the presence of excess H O is proposed in which the degradation rate of phenol is expressed as a linear function of the concentrations of phenol and H O . A detailed parametric study showed that the degradation rate of phenol increased with increasing [H O ] until saturation was observed. Phenol degradation followed apparent zero-order kinetics under MW radiation or H O oxidation. However, after 90 min of irradiation, the observed kinetics shifted to pseudo first order. The overall reaction rates were significantly enhanced in the combined MW/H O system, mainly because microwave could accelerate H O to generate hydroxyl radical ( OH) and other reactive oxygen intermediates. The observed synergetic effects of the MW/H O process resulted in an increased in the net reaction rate by a factor of 5.75. When hydrogen peroxide is present in a large stoichiometric excess, the time required to achieve complete mineralization is reduced significantly.

关键词： microwave (MW) irradiation     hydrogen peroxide     phenol     synergetic effects     kinetic model    

HTML PDF 收藏

Deep desulfurization of diesel fuels by catalytic oxidation

YU Guoxian, CHEN Hui, LU Shanxiang, ZHU Zhongnan

《化学科学与工程前沿（英文）》 2007年 第1卷 第2期   页码 162-166 doi: 10.1007/s11705-007-0030-8

摘要： Reaction feed was prepared by dissolving dibenzothiophene (DBT), which was selected as a model organosulfur compound in diesel fuels, in -octane. The oxidant was a 30 wt-% aqueous solution of hydrogen peroxide. Catalytic performance of the activated carbons with saturation adsorption of DBT was investigated in the presence of formic acid. In addition, the effects of activated carbon dosage, formic acid concentration, initial concentration of hydrogen peroxide, initial concentration of DBT and reaction temperature on the oxidation of DBT were investigated. Experimental results indicated that performic acid and the hydroxyl radicals produced are coupled to oxidize DBT with a conversion ratio of 100%. Catalytic performance of the combination of activated carbon and formic acid is higher than that of only formic acid. The concentration of formic acid, activated carbon dosage, initial concentration of hydrogen peroxide and reaction temperature affect the oxidative removal of DBT. The higher the initial concentration of DBT in the -octane solution, the more difficult the deep desulfurization by oxidation is.

关键词： organosulfur compound     performic     presence     activated     hydrogen peroxide    

HTML PDF 收藏

Hydroxyl radical-involved cancer therapy via Fenton reactions

《化学科学与工程前沿（英文）》 2022年 第16卷 第3期   页码 345-363 doi: 10.1007/s11705-021-2077-3

摘要： The tumor microenvironment features over-expressed hydrogen peroxide (H2O2). Thus, versatile therapeutic strategies based on H2O2 as a reaction substrate to generate hydroxyl radical (•OH) have been used as a prospective therapeutic method to boost anticancer efficiency. However, the limited Fenton catalysts and insufficient endogenous H2O2 content in tumor sites greatly hinder •OH production, failing to achieve the desired therapeutic effect. Therefore, supplying Fenton catalysts and elevating H2O2 levels into cancer cells are effective strategies to improve •OH generation. These therapeutic strategies are systematically discussed in this review. Furthermore, the challenges and future developments of hydroxyl radical-involved cancer therapy are discussed to improve therapeutic efficacy.

关键词： hydroxyl radical     Fenton catalyst     hydrogen peroxide     cancer therapy    

HTML PDF 收藏

过氧化氢作为环境胁迫指标在植被管理中的应用 Article

Takashi Asaeda, Senavirathna Mudalige Don Hiranya Jayasanka, Li-Ping Xia, Abner Barnuevo

《工程（英文）》 2018年 第4卷 第5期   页码 610-616 doi: 10.1016/j.eng.2018.09.001

摘要：

适应性植被管理非常耗时，其需要长时间的野外监测以获取可靠的数据。目前适应性植被管理手段虽已被广泛应用，但在进行栖息地状况评估时，仍然依赖于长时间的野外观测。目前的植被相关研究中，活性氧类（ROS）已经被视为一种环境胁迫指标。在这些ROS中，过氧化氢（H2O2）相对稳定，并且可以被准确、方便地量化。植物中H2O2含量可以被用作岸生和水生植被管理过程的胁迫指标，同时可以用来评估栖息地中单一植物物种的生长状况。本研究证明了植被管理中应用H2O2作为定量化环境胁迫指标的可行性。在实验室和野外（日本的真嗣湖、沙巴河、伊诺河和海河）条件下，分别开展了不同胁迫程度下大型水生植物和岸生植物生成H2O2情况的研究，结果表明H2O2可以作为环境管理中的胁迫指标。

关键词： 大型植物     河岸边区域     环境梯度     胁迫指标     活性氧类     过氧化氢    

HTML PDF 收藏

Degradation of trace nitrobenzene in water by microwave-enhanced H

Honghu ZENG, Lanjing LU, Meina LIANG, Jie LIU, Yanghong LI

《环境科学与工程前沿（英文）》 2012年 第6卷 第4期   页码 477-483 doi: 10.1007/s11783-012-0395-x

摘要： To evaluate possible use of microwave-enhanced H O -based (MW/H O ) process to degrade trace nitrobenzene (NB) in water, a series of batch experiments were conducted. The results showed that 2450MHz microwave irradiation significantly enhanced oxidative decomposition of nitrobenzene (NB) in a H O system. About 90% NB was degraded by the MW/ H O process in 30 min. Moreover, the MW/ H O process could enhanced the oxidative degradation of NB even at relatively low temperature (50°C). When the initial concentration of NB was 300μg/L, the optimum ratio of H O to NB and MW power were 70 and 300 W respectively. The presence of humic acid significantly increased H O dosage. The ultraviolet absorbance at 254 nm (UV ) indicated degradation of NB was stepwise and some intermediates were produced. The gas chromatography-mass spectrometric (GC-MS) analysis showed that main intermediates were nitrophenolic and carbonyl compounds.

关键词： microwave     hydrogen peroxide     nitrobenzene     humic acid    

HTML PDF 收藏

Simultaneous removal of total oxidizable carbon, phosphate and various metallic ions from HO solution with amino-functionalized zirconia as adsorbents

《化学科学与工程前沿（英文）》 2023年 第17卷 第4期   页码 470-482 doi: 10.1007/s11705-022-2231-6

摘要： Amino-functionalized zirconia was synthesized by the co-condensation method using zirconium butanol and 3-aminopropyltriethoxy silane for the simultaneous removal of various impurities from aqueous 30% H2O2 solution. The results of Fourier transform infrared (FTIR) and Zeta potential showed that the content of N in amino-functionalized zirconia increased with the added amount of 3-aminopropyltriethoxy silane. Accordingly, the removal efficiency of total oxidizable carbon, phosphate and metallic ions from the H2O2 solution increased. The adsorbent with an N content of 1.62% exhibited superior adsorption performance. The removal efficiency of 82.7% for total oxidizable carbon, 34.2% for phosphate, 87.1% for Fe3+, 83.2% for Al3+, 55.1% for Ca2+ and 66.6% for Mg2+, with a total adsorption capacity of 119.6 mg·g–1, could be achieved. The studies conducted using simulated solutions showed that the adsorption process of phosphate on amino-functionalized zirconia is endothermic and spontaneous, and the behaviors could be well described by the pseudo-second-order model and Langmuir model with a maximum adsorption capacity of 186.7 mg·g–1. The characterizations of the spent adsorbents by Zeta potential, FTIR and X-ray photoelectron spectroscopy revealed that the adsorption mechanism of phosphate is predominantly electrostatic attraction by the protonated functional groups and complementary ligand exchange with zirconium hydroxyl groups.

关键词： adsorption     zirconia     total oxidizable carbon     phosphate     metallic ions     hydrogen peroxide    

HTML PDF 收藏

Advances in the slurry reactor technology of the anthraquinone process for H

Hongbo Li, Bo Zheng, Zhiyong Pan, Baoning Zong, Minghua Qiao

《化学科学与工程前沿（英文）》 2018年 第12卷 第1期   页码 124-131 doi: 10.1007/s11705-017-1676-5

摘要： This paper overviews the development of the anthraquinone auto-oxidation (AO) process for the production of hydrogen peroxide in China and abroad. The characteristics and differences between the fixed-bed and fluidized-bed reactors for the AO process are presented. The detailed comparison indicates that the production of hydrogen peroxide with the fluidized-bed reactor has many advantages, such as lower operation cost and catalyst consumption, less anthraquinone degradation, higher catalyst utilization efficiency, and higher hydrogenation efficiency. The key characters of the production technology of hydrogen peroxide based on the fluidized-bed reactor developed by the Research Institute of Petroleum Processing, Sinopec are also disclosed. It is apparent that substituting the fluidized-bed reactor for the fixed-bed reactor is a major direction of breakthrough for the production technology of hydrogen peroxide in China.

关键词： anthraquinone process     fixed-bed reactor     slurry-bed reactor     hydrogen peroxide    

HTML PDF 收藏

Study on tribological and electrochemistry properties of metal materials in H2O2 solutions

Chengqing YUAN, Li YU, Jian LI, Xinping YAN

《机械工程前沿（英文）》 2012年 第7卷 第1期   页码 93-98 doi: 10.1007/s11465-012-0313-8

摘要：

Hydrogen peroxide (H2O2) is a kind of ideal green propellant. It is crucial to study the wear behavior and failure modes of the metal materials under the strong oxidizing environment of H2O2. This study aims to investigate the wear of rubbing pairs of 2Cr13 stainless steel against 1045 metal in H2O2 solutions, which has a great effect on wear, the decomposition and damage mechanism of materials. The comparison analysis of the friction coefficients, wear mass loss, worn surface topographies and current densities was conducted under different concentrations of H2O2 solutions. There were significant differences in the tribological and electrochemistry properties of the rubbing pairs in different H2O2 solutions.

关键词： hydrogen peroxide     wear     corrosion     wear mechanism    

HTML PDF 收藏

A comparison of the catalytic hydrogenation of 2-amylanthraquinone and 2-ethylanthraquinone over a Pd/Al

Enxian Yuan, Xiangwei Ren, Li Wang, Wentao Zhao

《化学科学与工程前沿（英文）》 2017年 第11卷 第2期   页码 177-184 doi: 10.1007/s11705-016-1604-0

摘要： The hydrogenation of 2-ethylanthraquinone (eAQ), 2- -amylanthraquinone (taAQ) and their mixtures with molar ratios of 1:1 and 1:2 to the corresponding hydroquinones (eAQH and taAQH ) were studied over a Pd/Al O catalyst in a semi-batch slurry reactor at 60 °C and at 0.3 MPa. Compared to eAQ, TaAQ exhibited a significantly slower hydrogenation rate (about half) but had a higher maximum yield of H O and a smaller amount of degradation products. This can be ascribed to the longer and branched side chain in taAQ, which limits its accessibility to the Pd surface and its diffusion through the pores of the catalyst. Density functional theory calculations showed that it is more difficult for taAQ to adsorb onto a Pd (111) surface than for eAQ. The hydrogenation of the eAQ/taAQ mixtures had the slowest rates, lowest H O yields and the highest amounts of degradation products.

关键词： hydrogenation     hydrogen peroxide     anthraquinone     Pd catalyst     AO process    

HTML PDF 收藏

标题 作者 时间 类型 操作

Efficient production of hydrogen peroxide in microbial reverse-electrodialysis cells coupled with thermolytic

期刊论文

Reactive extraction for preparation of hydrogen peroxide under pressure

CHENG Yongxi, LI Hongtao, WANG Li, LÜ Shuxiang

期刊论文

Toward better understanding vacuum ultraviolet–iodide induced photolysis via hydrogen peroxide formation

期刊论文

Evaluation of the technoeconomic feasibility of electrochemical hydrogen peroxide production for decentralized

Yang Li, Yixin Zhang, Guangshen Xia, Juhong Zhan, Gang Yu, Yujue Wang

期刊论文

Hydrogen peroxide is correlated with browning in peach fruit stored at low temperature

Zhansheng DING, Shiping TIAN, Xianghong MENG, Yong XU,

期刊论文

Degradation of 4-aminophenol by hydrogen peroxide oxidation using enzyme from Serratia marcescens as

SUN Min, YOU Yahua, DENG Shengsong, GAO Wenxia, YAO Risheng

期刊论文

Kinetics of microwave-enhanced oxidation of phenol by hydrogen peroxide

Deming ZHAO, Jie CHENG, Michael R. HOFFMANN

期刊论文

Deep desulfurization of diesel fuels by catalytic oxidation

YU Guoxian, CHEN Hui, LU Shanxiang, ZHU Zhongnan

期刊论文

Hydroxyl radical-involved cancer therapy via Fenton reactions

期刊论文

过氧化氢作为环境胁迫指标在植被管理中的应用

Takashi Asaeda, Senavirathna Mudalige Don Hiranya Jayasanka, Li-Ping Xia, Abner Barnuevo

期刊论文

Degradation of trace nitrobenzene in water by microwave-enhanced H

Honghu ZENG, Lanjing LU, Meina LIANG, Jie LIU, Yanghong LI

期刊论文

Simultaneous removal of total oxidizable carbon, phosphate and various metallic ions from HO solution with amino-functionalized zirconia as adsorbents

期刊论文

Advances in the slurry reactor technology of the anthraquinone process for H

Hongbo Li, Bo Zheng, Zhiyong Pan, Baoning Zong, Minghua Qiao

期刊论文

Study on tribological and electrochemistry properties of metal materials in H2O2 solutions

Chengqing YUAN, Li YU, Jian LI, Xinping YAN

期刊论文

A comparison of the catalytic hydrogenation of 2-amylanthraquinone and 2-ethylanthraquinone over a Pd/Al

Enxian Yuan, Xiangwei Ren, Li Wang, Wentao Zhao

期刊论文