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Optimization of reed-specific degrading bacteria by response surfaces for remediation of crude oil-polluted soil in Xinjiang,China 被引量:2
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作者 YaMing DONG chaocheng zhao +1 位作者 Yun CAI DongFeng zhao 《Journal of Arid Land》 SCIE CSCD 2013年第3期408-414,共7页
This paper discussed the optimization of conditions for remediation of crude oil-polluted soil based on pot experiment by applying reed-specific degrading bacteria, and using response surfaces methodology. We took the... This paper discussed the optimization of conditions for remediation of crude oil-polluted soil based on pot experiment by applying reed-specific degrading bacteria, and using response surfaces methodology. We took the initial crude oil concentration, the amount of inoculation, the ratio of nitrogen and phosphorus, and the use of surfactant (Tween-80) as independent variables (factors), and the degrading ratio of crude oil as the dependent variable (response) after a 90-day experiment. The experiment explored the impacts of each independent variable and their interactions on the bioremediation of crude oil-polluted soil using the Box-Behnken design. Working with a simulated forecasting model the study obtained optimization va reed+specific degrading bacteria, a nitrogen to phosphorus ues for the treatment parameters of 200 g/kg of the ratio of about 6.0. and 0.2% surfactant. Under experimental conditions, for crude oil concentrations of 10, 30 and 50 g/kg, the optimal effects of the treatments achieved 71.87%, 66.61% and 54.52% degradation of the crude oil, respectively. The results can provide a basis for the technical development of plant-microorganism combined bioremediation of crude oil-polluted soil. 展开更多
关键词 crude oil pollution plant-microorganism response surfaces soil remediation
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增强π共轭结构的电子密度和面内电荷输运促进g-C_(3)N_(4)的光催化析氢 被引量:1
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作者 张洋 曹宁 +4 位作者 刘晓明 贺凤婷 郑彬 赵朝成 王永强 《Science China Materials》 SCIE EI CAS CSCD 2023年第6期2274-2282,共9页
石墨相氮化碳(g-C_(3)N_(4))已成为一种新兴的无金属光催化剂并引起了研究人员的关注.然而,通过传统热缩聚得到的纯g-C_(3)N_(4)(PCN)的庚烷环链聚合度低,含有大量的电荷重组中心,阻碍了平面内的电荷传输,导致光催化性能不理想.本文采... 石墨相氮化碳(g-C_(3)N_(4))已成为一种新兴的无金属光催化剂并引起了研究人员的关注.然而,通过传统热缩聚得到的纯g-C_(3)N_(4)(PCN)的庚烷环链聚合度低,含有大量的电荷重组中心,阻碍了平面内的电荷传输,导致光催化性能不理想.本文采用一水合草酸铵热处理PCN制备了高分散的多孔g-C_(3)N_(4)纳米片(CN-A),并在不引入杂原子的情况下,成功地提高了其平面内庚烷环链的完整度.电子顺磁共振和^(13)C核磁共振分析表明,π共轭结构的电子密度和离域效应显著提高.所制备的样品表现出优异的稳定性和光催化活性,在无助催化剂Pt和有助催化剂Pt下的氢气还原速率分别是PCN的11.2倍和5.3倍. 展开更多
关键词 电子顺磁共振 电子密度 石墨相氮化碳 离域效应 完整度 电荷输运 电荷传输 氢气还原
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Enhanced activity of ZnS(111) by N/Cu co-doping:Accelerated degradation of organic pollutants under visible light
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作者 Guofei Jiang Benjie Zhu +3 位作者 Junzhi Sun Fang Liu Yongqiang Wang chaocheng zhao 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2023年第3期244-257,共14页
High-efficiency photocatalysts are of great significance for the application of photocatalytic technology in water treatment.In this study,N/Cu co-doped ZnS nanosphere photocatalys(N/Cu-ZnS) is synthesized by a hydrot... High-efficiency photocatalysts are of great significance for the application of photocatalytic technology in water treatment.In this study,N/Cu co-doped ZnS nanosphere photocatalys(N/Cu-ZnS) is synthesized by a hydrothermal method for the first time.After doping,the tex ture of nanosphere becomes loose,the nanometer diameter is reduced,making the specific surface area of catalyst increased from 34.73 to 101.59 m^(2)/g.The characterization results show that more ZnS (111) crystal planes are exposed by N/Cu co-doping;the calculations of density functional theory show that N/Cu co-doping can increase the catalytic activity of the ZnS (111) crystal plane,enhance the adsorption capacity of (111) crystal plane to O_(2)and promote the generation of·O_(2)-.The energy levels of the introduced impurities can be hybridized with the energy levels of S and Zn at the top of valence band and the bottom o conduction band,which makes the band gap narrower,thus enhancing the absorption o visible light.Compared with pure ZnS,the degradation rates of 2,4-dichlorophenol (2,4-DCP and tetracycline (TC) by N/Cu-ZnS under visible light (>420 nm) are increased by 83.7 and51 times,respectively.In this research,a promising photocatalyst for photocatalytic degra dation of organic pollutants in wastewater is provided. 展开更多
关键词 Catalytic degradation of visible light N/Cu co-doping ZnS(111) 2 4-DICHLOROPHENOL TETRACYCLINE
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氮杂酞菁钴光电催化降解水环境中聚丙烯酰胺 被引量:1
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作者 王德军 李慧 +2 位作者 姜锡仁 赵朝成 赵玉慧 《复合材料学报》 EI CAS CSCD 北大核心 2021年第5期1576-1587,共12页
针对水环境中聚丙烯酰胺(HPAM)难以被快速去除的问题,以导电炭黑(CB)为载体,制备了负载型氮杂酞菁钴(NCoPc/CB)和甲基取代氮杂酞菁钴(MeNCoPc/CB)复合材料,并对其光电催化降解HPAM的性能进行了研究。搭建分体式光电协同催化体系,选取50 ... 针对水环境中聚丙烯酰胺(HPAM)难以被快速去除的问题,以导电炭黑(CB)为载体,制备了负载型氮杂酞菁钴(NCoPc/CB)和甲基取代氮杂酞菁钴(MeNCoPc/CB)复合材料,并对其光电催化降解HPAM的性能进行了研究。搭建分体式光电协同催化体系,选取50 mg/L HPAM水溶液为目标污染物,以Na2SO4为电解质,对NCoPc的理化性能及光电协同催化工艺降解高分子聚合物的性能进行了考察。结果证实,光电协同催化工艺对HPAM去除率不但优于单独光催化和单独电催化工艺,更优于两者的代数和,说明光电联合体系中产生了协同增强效应。其中,以MeNCoPc/CB复合材料效果最佳,污染物去除率达到76.07%,溶液黏度由8.33 mPa·s降至1.81 mPa·s。对协同工艺进行反应动力学分析,证实此过程符合准一级反应动力学,其反应速率常数分别是光催化的6.03倍和电催化的3.97倍。电子自旋共振技术(ESR)证实,反应体系内主要活性物质为·OH和O2-·。 展开更多
关键词 氮杂酞菁钴 光电催化 降解 聚丙烯酰胺 反应机制
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锰基催化剂催化燃烧VOCs 被引量:3
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作者 刘昕 王永强 +3 位作者 刘芳 赵朝成 刘华欣 时林 《化学进展》 SCIE CAS CSCD 北大核心 2019年第8期1159-1165,共7页
锰基催化剂作为一种催化活性高、稳定性强、价格低廉的非贵金属类材料,在催化燃烧VOCs领域显示出了广阔的应用前景。然而,该材料存在表面电子传递能力弱,比表面积低等缺点须通过掺杂改性等方式得到优化。本文分别对单一锰氧化物、贵金... 锰基催化剂作为一种催化活性高、稳定性强、价格低廉的非贵金属类材料,在催化燃烧VOCs领域显示出了广阔的应用前景。然而,该材料存在表面电子传递能力弱,比表面积低等缺点须通过掺杂改性等方式得到优化。本文分别对单一锰氧化物、贵金属掺杂、负载以及钙钛矿型的锰基催化剂近年来从制备方法、催化剂的化学组分、形貌结构等方面提高催化剂活性的最新研究进展进行综述,并对锰基催化剂整体化、工业化的发展提出展望。 展开更多
关键词 锰基催化剂 催化燃烧 VOCS 改性 钙钛矿
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Acidification and bubble template derived porous g-C_(3)N_(4) for efficient photodegradation and hydrogen evolution 被引量:2
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作者 Yixuan Wang Fengting He +8 位作者 Lin Chen Jie Shang Jiajia Wang Shuaijun Wang Huimin Song Jinqiang Zhang chaocheng zhao Shaobin Wang Hongqi Sun 《Chinese Chemical Letters》 SCIE CAS CSCD 2020年第10期2668-2672,共5页
Graphitic carbon nitride(g-C_(3)N_(4))as a metal-free candidate of photocatalyst has received worldwide attention because of its great potentials in solar light-induced degradation and hydrogen evolution,yet the indus... Graphitic carbon nitride(g-C_(3)N_(4))as a metal-free candidate of photocatalyst has received worldwide attention because of its great potentials in solar light-induced degradation and hydrogen evolution,yet the industrial application is seriously hindered by the small specific surface area and rapid recombination rate of carriers.Herein,we demonstrate that porous g-C_(3)N_(4)(HCl-CNU-X)can be prepared via the copolymerization of acidified melamine and a green bubble template(urea).Transmission electron microscopy and nitrogen sorption characterization results show that the prepared HCl-CNU-X possesses an in-plane porous structure and large specific surface area,enabling the exposure of more accessible active sites.As a result,HCl-CNU-X exhibits both enhanced photocatalytic tetracycline hydrochloride degradation and higher hydrogen evolution than bulk g-C_(3)N_(4).The boosted photocatalytic performance was ascribed to the formation of the porous structure,which dramatically promotes the separation of charge-carriers and facilitates the electron transfer.This work demonstrates that the acidification of nitrogen-rich precursors combined with a bubble-template can develop a new paradigm of highly porous photocatalysts for environmental remediation and water splitting. 展开更多
关键词 g-C_(3)N_(4) Porous structure Tetracycline hydrochloride Hydrogen evolution Acidification and bubble template Visible light
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Effect of calcination process on performance of 3DOM CeMnO3 catalysts
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作者 Xin Liu Xinyi Lv +2 位作者 Yongqiang Wang chaocheng zhao Fang Liu 《Journal of Rare Earths》 SCIE EI CAS CSCD 2021年第9期1073-1081,共9页
A series of 3DOM CeMnO3 perovskite catalysts were prepared by poly(methyl methacrylate)hardtemplating-excessive impregnation method at calcination temperature of x℃(x=600,700,800)and the heating rate of y℃/min(y=1,2... A series of 3DOM CeMnO3 perovskite catalysts were prepared by poly(methyl methacrylate)hardtemplating-excessive impregnation method at calcination temperature of x℃(x=600,700,800)and the heating rate of y℃/min(y=1,2,5,10).The samples were characterized by Brunauer-Emmett-Teller method,scanning electron microscopy,transmission electron microscopy,H2-temperature programmed reduction,X-ray photoelectron spectroscopy,X-ray diffraction,moreover,the effect of the calcination process on the catalytic activity of the samples were discussed by the catalytic combustion of toluene.The results show that the 3DOM CeMnO3 catalysts calcined at 600℃promote the formation of a perovskite structure,inhibit the reduction of the Mn4+species in the catalyst with high temperature.The catalyst expresses the complete macroporous structure,large specific surface area(38.8 m^(2)/g),higher adsorption oxygen concentration and Mn4+substance concentration,with a low T90%=172℃.By preparing the catalysts at different calcination heating rates,it can be concluded that the catalyst possesses a high concentration of adsorbed oxygen and a low reduction temperature and a large specific surface area(40.42 m^(2)/g)greatly promotes adsorption stage catalytic oxidation reaction and catalytic combustion of toluene at low temperature under the heating rate of 5℃/min.When the heating rate is 1℃/min,the catalyst has a complete macroporous structure(>250 nm),which is beneficial to the exchange of macromolecular substances during the catalytic reaction and the catalyst has a high concentration of lattice oxygen suitable for the catalysis of toluene in high temperature flue gas combustion. 展开更多
关键词 Three-dimensionally ordered macroporous Perovskite catalyst Calcination temperature Calcination heating rate Rare earths
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