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Optimization of methyl orange removal from aqueous solution by response surface methodology using spent

Liangzhi LI,Xiaolin LI,Ci YAN,Weiqiang GUO,Tianyi YANG,Jiaolong FU,Jiaoyan TANG,Cuiying HU

《环境科学与工程前沿（英文）》 2014年 第8卷 第4期   页码 496-502 doi: 10.1007/s11783-013-0578-0

摘要： The effective disposal of redundant tea waste is crucial to environmental protection and comprehensive utilization of trash resources. In this work, the removal of methyl orange (MO) from aqueous solution using spent tea leaves as the sorbent was investigated in a batch experiment. First, the effects of various parameters such as temperature, adsorption time, dose of spent tea leaves, and initial concentration of MO were investigated. Then, the response surface methodology (RSM), based on Box–Behnken design, was employed to obtain the optimum adsorption conditions. The optimal conditions could be obtained at an initial concentration of MO of 9.75 mg·L , temperature of 35.3°C, contact time of 63.8 min, and an adsorbent dosage 3.90 g·L . Under the optimized conditions, the maximal removal of MO was 58.2%. The results indicate that spent tea leaves could be used as an effective and economical adsorbent in the removal of MO from aqueous solution.

关键词： spent tea leaves     adsorption     response surface methodology     methyl orange (MO)    

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Photocatalytic degradation of methyl orange using ZnO/TiO composites

Ming GE , Changsheng GUO , Xingwang ZHU , Lili MA , Wei HU , Yuqiu WANG , Zhenan HAN ,

《环境科学与工程前沿（英文）》 2009年 第3卷 第3期   页码 271-280 doi: 10.1007/s11783-009-0035-2

摘要： ZnO/TiO composites were synthesized by using the solvothermal method and ultrasonic precipitation followed by heat treatment in order to investigate their photocatalytic degradation of methyl orange (MO) in aqueous suspension under UV irradiation. The composition and surface structure of the catalyst were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and transmission electron microscopy (TEM). The degradation efficiencies of MO at various pH values were obtained. The highest degradation efficiencies were obtained before 30min and after 60min at pH 11.0 and pH 2.0, respectively. A sample analysis was conducted using liquid chromatography coupled with electrospray ionization ion-trap mass spectrometry. Six intermediates were found during the photocatalytic degradation process of quinonoid MO. The degradation pathway of quinonoid MO was also proposed.

关键词： photocatalytic degradation     methyl orange     ZnO/TiO2 composites     high performance liquid chromatography mass spectrometry (HPLC-MS)    

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Synthesis of TiO2 nano-particles and their photocatalytic activity for formaldehyde and methyl orange

XIAO Xinyan, ZHANG Huiping, CHEN Huanqin, LIAO Dongliang

《化学科学与工程前沿（英文）》 2007年 第1卷 第2期   页码 178-183 doi: 10.1007/s11705-007-0033-5

摘要： TiO nano-particles were synthesized by sol-gel technique and characterized by X-ray diffractometer (XRD) and transmission electron microscope (TEM). Their photocatalytic activities for formaldehyde (FA) and methyl orange (MO) degradation were tested using degradation rate (η) as an evaluation index. Based on the orthogonal test results, the optimal condition for TiO preparation was obtained. Results showed that particle sizes were in the range of 10 40 nm, and that prepared TiO had better photocatalytic activity than P25. A simplified model was developed to evaluate the apparent quantum efficiency (Φapp) of this photocatalytic reaction system.

关键词： prepared     photocatalytic activity     apparent     photocatalytic     orthogonal    

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Mayenite supported perovskite monoliths for catalytic combustion of methyl methacrylate

Zekai ZHANG, Zhijian KONG, Huayan LIU, Yinfei CHEN

《化学科学与工程前沿（英文）》 2014年 第8卷 第1期   页码 87-94 doi: 10.1007/s11705-014-1410-5

摘要： To improve their thermal stability, La Sr MnO cordierite monoliths are washcoated with mayenite, which is a novel Al-based material with the crystal structure of 12MO·7Al O (M= Ca, Sr). The monoliths are characterized by means of nitrogen adsorption/desorption, scanning electron microscopy, and X-ray diffraction. Catalytic performances of the monoliths are tested for methyl methacrylate combustion. The results show that mayenite obviously improves both the physic-chemical properties and the catalytic performance of the monoliths. Because mayenite improves the dispersity of La Sr MnO and also prevents the interaction between La Sr MnO and cordierite or -Al O , both crystal structure and surface morphology of La Sr MnO phase can thereby be stable on the mayenite surface even at high temperature up to 1050 oC. Under the given reaction conditions, La Sr MnO monolith washcoated with 12SrO·7Al O shows the best catalytic activity for methyl methacrylate combustion among all the tested monoliths.

关键词： mayenite     perovskite     catalytic combustion     methyl methacrylate     monolith    

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HPLC determination of glyoxal in aldehyde solution with 3-methyl-2-benzothiazolinone hydrazone

Yamei ZHU, Xiaoli YAO, Shaohui CHEN, Qun CUI, Haiyan WANG

《化学科学与工程前沿（英文）》 2011年 第5卷 第1期   页码 117-121 doi: 10.1007/s11705-010-0535-4

摘要： Based on the absorption property of a diazine that can be formed by reaction of glyoxal and 3-methyl-2-benzothiazolinone hydrazone (MBTH) in the Ultraviolet-visible (UV-vis) spectral region, a HPLC method was developed for the determination of glyoxal in acetaldehyde solution. Glyoxal was derivatised from MBTH and the derivatives (diazine) were analyzed by HPLC for identification and quantification. The determination was performed on a ZORBAX Eclipse XDB-C18 column (4.6 × 250 mm, 5 mm) at 35°C with an injection volume of 10 mL, using a mixture of acetonitrile-water solvent (99∶5, v∶v) as a mobile phase with a flow rate of 0.8 mL·min . The proper derivative reaction conditions were the temperature of 70°C, MBTH to carbonyl molar ratio of 12, and reaction time of 110 min. The glyoxal diazine was a yellow dye with a maximum molar absorptivity at 401 nm and its retention time was 5.2 min under optimal HPLC conditions. The standard curve for glyoxal had a strong linear relationship with a regression coefficient ( = 0.999) in the range of 0.002–0.020 g·L . The analysis of glyoxal in an oxidising solution gave accurate results with a relative standard deviation (RSD) value of 0.55%. The average relative recovery was 102%. This efficient HPLC technique is also proposed for detecting other dicarbonyl compounds besides glyoxal.

关键词： HPLC     glyoxal     3-methyl-2-benzothiazolinone hydrazone     diazine     dicarbonyl compounds    

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Polymerization of methyl methacrylate catalyzed by mono-/bis-salicylaldiminato nickel(II) complexes and

Jihong LU, Danfeng ZHANG, Qian CHEN, Buwei YU

《化学科学与工程前沿（英文）》 2011年 第5卷 第1期   页码 19-25 doi: 10.1007/s11705-010-0546-1

摘要： Two types of salicylaldiminato-based nickel complexes, mono-ligated Ni(II) complexes ([O-C H - - C(H)=N-Ar]Ni(PPh )(Ph) ( ), [O-(3,5-Br )C H - -C(H)=N-Ar]Ni(PPh )(Ph) ( ), [O-(3- -Bu)C H - -C(H)=N-Ar]Ni(PPh )(Ph) ( )) and bis-ligated Ni(II) complexes ([O-(3,5-Br )C H - -C(H)=N-Ar] Ni ( ), [O-(3,5-Br )C H - -C(H)=N-2-C H (PhO)] Ni ( ), Ar=2,6-C H ( -Pr) ) were synthesized and characterized by Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance (NMR), mass spectrography (MS) and elemental analysis (EA). In the presence of methylaluminoxane (MAO) as cocatalyst, all the nickel complexes exhibited high activities for the polymerization of methyl methacrylate (MMA) and syndiotactic-rich poly(methyl methacrylate) (PMMA) was obtained. The complexes with less bulky substituents on salicylaldiminato framework possessed higher activities, while with the same salicylaldiminato, the mono-ligated nickel complexes showed higher catalytic activity than bis-ligated ones.

关键词： late transition metal catalyst     methyl methacrylate     polymerization     salicylaldiminato nickel complexes     methylaluminoxane     syndiotactic structure    

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Accelerated degradation of orange G over a widepH range in the presence of FeVO

Xiaoxia Ou, Jianfang Yan, Fengjie Zhang, Chunhua Zhang

《环境科学与工程前沿（英文）》 2018年 第12卷 第1期 doi: 10.1007/s11783-018-1013-3

摘要： In this study, FeVO was prepared andused as Fenton-like catalyst to degrade orange G (OG) dye. The removalof OG in an aqueous solution containing 0.5 g·L FeVO and 15 mmol·L hydrogen peroxide at pH 7.0 reached 93.2%. Similar rates were achievedat pH 5.7 ( = 0.0471 min ), pH 7.0 ( = 0.0438 min ), and pH 7.7 ( = 0.0434 min ). The FeVO catalyst successfullyovercomes the problem faced in the heterogeneous Fenton process, i.e.,the narrow working pH range. The data for the removal of OG in FeVO systems containing H O conform to the Langmuir–Hinshelwood model ( = 0.9988),indicating that adsorption and surface reaction are the two basicmechanisms for OG removal in the FeVO –H O system. Furthermore, the irradiationof FeVO by visible light significantly increasesthe degradation rate of OG, which is attributed to the enhanced ratesof the iron cycles and vanadium cycles.

关键词： Azo dye     Degradation     FeVO4     Kinetics     Advanced oxidation processes    

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Efficient degradation of orange II by ZnMn

Qingzhuo Ni, Hao Cheng, Jianfeng Ma, Yong Kong, Sridhar Komarneni

《化学科学与工程前沿（英文）》 2020年 第14卷 第6期   页码 956-966 doi: 10.1007/s11705-019-1907-z

摘要： A ZnMn O catalyst has been synthesized via a sucrose-aided combustion method and characterized by various analytical techniques. It is composed of numerous nanoparticles (15–110 nm) assembled into a porous structure with a specific surface area (SSA) of 19.1 m ·g . Its catalytic activity has been investigated for the degradation of orange II dye using three different systems, i.e., the photocatalysis system with visible light, the chemocatalysis system with bisulfite, and the photo-chemical catalysis system with both visible light and bisulfite. The last system exhibits the maximum degradation efficiency of 90%, much higher than the photocatalysis system (15%) and the chemocatalysis system (67%). The recycling experiments indicate that the ZnMn O catalyst has high stability and reusability and is thus a green and eximious catalyst. Furthermore, the potential degradation mechanisms applicable to the three systems are discussed with relevant theoretical analysis and scavenging experiments for radicals. The active species such as Mn(III), O , h , e , SO and HO are proposed to be responsible for the excellent degradation results in the photo-chemical catalysis system with the ZnMn O catalyst.

关键词： ZnMn2O4     photo-chemical catalysis     bisulfite     dye degradation    

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Carbon-coated Ni-Co alloy catalysts: preparation and performance for aqueous phase hydrodeoxygenation of methyl

《化学科学与工程前沿（英文）》 2022年 第16卷 第3期   页码 443-460 doi: 10.1007/s11705-021-2079-1

摘要： Carbon-coated Ni, Co and Ni-Co alloy catalysts were prepared by the carbonization of the metal doped resorcinol-formaldehyde resins synthesized by the one-pot extended Stöber method. It was found that the introduction of Co remarkably reduced the carbon microsphere size. The metallic Ni, Co, and Ni-Co alloy particles (mainly 10–12 nm) were uniformly distributed in carbon microspheres. A charge transfer from Ni to Co appeared in the Ni-Co alloy. Compared with those of metallic Ni and Co, the d-band center of the Ni-Co alloy shifted away from and toward the Fermi level, respectively. In the in-situ aqueous phase hydrodeoxygenation of methyl palmitate with methanol as the hydrogen donor at 330 °C, the decarbonylation/decarboxylation pathway dominated on all catalysts. The Ni-Co@C catalysts gave higher activity than the Ni@C and Co@C catalysts, and the yields of n-pentadecane and n-C6–n-C16 reached 71.6% and 92.6%, respectively. The excellent performance of Ni-Co@C is attributed to the electronic interactions between Ni and Co and the small carbon microspheres. Due to the confinement effect of carbon, the metal particles showed high resistance to sintering under harsh hydrothermal conditions. Catalyst deactivation is due to the carbonaceous deposition, and the regeneration with CO2 recovered the catalyst reactivity.

关键词： Stöber method     carbon-coated Ni-Co alloy     in-situ hydrodeoxygenation     methyl palmitate     decarbonylation/decarboxylation    

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Acid Orange 7 degradation using methane as the sole carbon source and electron donor

《环境科学与工程前沿（英文）》 2022年 第16卷 第3期 doi: 10.1007/s11783-021-1468-5

摘要：

• AO7 degradation was coupled with anaerobic methane oxidation.

关键词： Azo dyes     AO7 degradation     Anaerobic methane oxidation     Microbial community     ANME-2d    

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Risk analysis methods of the water resources system under uncertainty

Zeying GUI,Chenglong ZHANG,Mo Li,Ping GUO

《农业科学与工程前沿（英文）》 2015年 第2卷 第3期   页码 205-215 doi: 10.15302/J-FASE-2015073

摘要： The main characteristic of the water resources system (WRS) is its great complexity and uncertainty, which makes it highly desirable to carry out a risk analysis of the WRS. The natural environmental, social economic conditions as well as limitations of human cognitive ability are possible sources of the uncertainties that need to be taken into account in the risk analysis process. In this paper the inherent stochastic uncertainty and cognitive subjective uncertainty of the WRS are discussed first, from both objective and subjective perspectives. Then the quantitative characterization methods of risk analysis are introduced, including three criteria (reliability, resiliency and vulnerability) and five basic optimization models (the expected risk value model, conditional value at risk model, chance-constrained risk model, minimizing probability of risk events model, and the multi-objective optimization model). Finally, this paper focuses on the various methods of risk analysis under uncertainty, which are summarized as random, fuzzy and mixed methods. A more comprehensive risk analysis methodology for the WRS is proposed based on the comparison of the advantages, disadvantages and applicable conditions of these three methods. This paper provides a decision support of risk analysis for researchers, policy makers and stakeholders of the WRS.

关键词： water resources system     evaluation criterion     optimization model     risk analysis method     uncertainty    

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Trend detection and stochastic simulation prediction of streamflow at Yingluoxia hydrological station, Heihe River Basin, China

Chenglong ZHANG,Mo LI,Ping GUO

《农业科学与工程前沿（英文）》 2017年 第4卷 第1期   页码 81-96 doi: 10.15302/J-FASE-2016112

摘要： Investigating long-term variation and prediction of streamflow are critical to regional water resource management and planning. Under the continuous influence of climate change and human activity, the trends of hydrologic time series are nonstationary, and consequently the established methods for hydrological frequency analysis are no longer applicable. Five methods, including the linear regression, nonlinear regression, change point analysis, wavelet analysis and Hilbert-Huang transformation, were first selected to detect and identify the deterministic and stochastic components of streamflow. The results indicated there was a significant long-term increasing trend. To test the applicability of these five methods, a comprehensive weighted index was then used to assess their performance. This index showed that the linear regression was the best method. Secondly, using the normality test for stochastic components separated by the linear regression method, a normal distribution requirement was satisfied. Next, the Monte Carlo stochastic simulation technique was used to simulate these stochastic components with normal distribution, and thus a new ensemble hydrological time series was obtained by combining the corresponding deterministic components. Finally, according to these outcomes, the streamflow at different frequencies in 2020 was predicted.

关键词： Monte Carlo     nonstationary     trend detection     streamflow prediction     decomposition and ensemble     Yingluoxia    

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Synthesis of porous carbon from orange peel waste for effective volatile organic compounds adsorption

《化学科学与工程前沿（英文）》 2023年 第17卷 第7期   页码 942-953 doi: 10.1007/s11705-022-2264-x

摘要： Volatile organic compounds have posed a serious threat to the environment and human health, which require urgent and effective removal. In recent years, the preparation of porous carbon from biomass waste for volatile organic compounds adsorption has attracted increasing attention as a very cost-effective and promising technology. In this study, porous carbon was synthesized from orange peel by urea-assisted hydrothermal carbonization and KOH activation. The role of typical components (cellulose, hemicellulose, and lignin) in pore development and volatile organic compounds adsorption was investigated. Among the three components, hemicellulose was the major contributor to high porosity and abundant micropores in porous carbon. Higher hemicellulose content led to more abundant –COOR, amine-N, and pyrrolic/pyridonic-N in the derived hydrochar, which were favorable for porosity formation during activation. In this case, the toluene adsorption capacity of the porous carbon improved from 382.8 to 485.3 mg·g–1. Unlike hemicellulose, cellulose reduced the >C=O, amine-N, and pyrrolic/pyridonic-N content of the hydrochar, which caused porosity deterioration and worse toluene adsorption performance. Lignin bestowed the hydrochar with slightly increased –COOR, pyrrolic/pyridonic-N, and graphitic-N, and reduced >C=O, resulting in comparatively poor porosity and more abundant micropores. In general, the obtained porous carbon possessed abundant micropores and high specific surface area, with the highest up to 2882 m2·g–1. This study can provide guidance for selecting suitable biomass waste to synthesize porous carbon with better porosity for efficient volatile organic compounds adsorption.

关键词： biomass waste     porous carbon     feedstock composition     urea-assisted hydrothermal carbonization     toluene adsorption     N-doped hydrochar    

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Efficient hydrothermal deoxygenation of methyl palmitate to diesel-like hydrocarbons on carbon encapsulated

《化学科学与工程前沿（英文）》 2023年 第17卷 第2期   页码 139-155 doi: 10.1007/s11705-022-2217-4

摘要： Porous carbon-encapsulated Ni and Ni–Sn intermetallic compound catalysts were prepared by the one-pot extended Stöber method followed by carbonization and tested for in-situ hydrothermal deoxygenation of methyl palmitate with methanol as the hydrogen donor. During the catalyst preparation, Sn doping reduces the size of carbon spheres, and the formation of Ni–Sn intermetallic compounds restrain the graphitization, contributing to larger pore volume and pore diameter. Consequently, a more facile mass transfer occurs in carbon-encapsulated Ni–Sn intermetallic compound catalysts than in carbon-encapsulated Ni catalysts. During the in-situ hydrothermal deoxygenation, the synergism between Ni and Sn favors palmitic acid hydrogenation to a highly reactive hexadecanal that easily either decarbonylate to n-pentadecane or is hydrogenated to hexadecanol. At high reaction temperature, hexadecanol undergoes dehydrogenation–decarbonylation, generating n-pentadecane. Also, the C–C bond hydrolysis and methanation are suppressed on Ni–Sn intermetallic compounds, favorable for increasing the carbon yield and reducing the H2 consumption. The n-pentadecane and n-hexadecane yields reached 88.1% and 92.8% on carbon-encapsulated Ni3Sn2 intermetallic compound at 330 °C. After washing and H2 reduction, the carbon-encapsulated Ni3Sn2 intermetallic compound remains stable during three recycling cycles. This is ascribed to the carbon confinement that effectively suppresses the sintering and loss of metal particles under harsh hydrothermal conditions.

关键词： extended Stöber method     carbon encapsulated Ni–Sn intermetallic compounds     confinement     in-situ hydrothermal deoxygenation     hydrogenation     decarbonylation    

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铝合金板材拉伸变形时橘皮成因的研究进展

马鸣图,杨红亚,吴娥梅,金庆生

《中国工程科学》 2014年 第16卷 第1期   页码 4-13

摘要：

本文对铝合金板材拉伸变形时橘皮成因的研究进展进行了评述。首先展示了有无橘皮板材在各种检测仪器下拉伸变形前后的表面形貌、表面滑移带、粗糙度和拉伸断口的形貌，并展示了纳米硬度的测量结果和表征。进一步介绍了最近关于橘皮形成的电子背散射衍射技术（EBSD）的研究成果和X射线对有无橘皮样品的织构测量结果，结合样品的显微组织和力学性能深入分析了橘皮的成因。一系列的结果表明，拉伸变形以后表面橘皮的出现与拉伸变形过程中产生的织构密切相关，而织构的生成又与拉伸过程中晶粒变形的不均匀性有关；晶粒的大小将明显影响变形的不均匀性和织构的生成，粗晶粒比细晶粒更容易产生不均匀变形、晶粒转动和织构，从而导致拉伸变形后生成表面橘皮。由此介绍了粗晶粒和细晶粒拉伸变形后表面状态的示意模型，同时建议对橘皮的形成进行进一步的研究和分析，以完善橘皮成因的定量描述。

关键词： 橘皮成因     力学性能     拉伸断口     纳米硬度     EBSD     X射线    

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标题 作者 时间 类型 操作

Optimization of methyl orange removal from aqueous solution by response surface methodology using spent

Liangzhi LI,Xiaolin LI,Ci YAN,Weiqiang GUO,Tianyi YANG,Jiaolong FU,Jiaoyan TANG,Cuiying HU

期刊论文

Photocatalytic degradation of methyl orange using ZnO/TiO composites

Ming GE , Changsheng GUO , Xingwang ZHU , Lili MA , Wei HU , Yuqiu WANG , Zhenan HAN ,

期刊论文

Synthesis of TiO2 nano-particles and their photocatalytic activity for formaldehyde and methyl orange

XIAO Xinyan, ZHANG Huiping, CHEN Huanqin, LIAO Dongliang

期刊论文

Mayenite supported perovskite monoliths for catalytic combustion of methyl methacrylate

Zekai ZHANG, Zhijian KONG, Huayan LIU, Yinfei CHEN

期刊论文

HPLC determination of glyoxal in aldehyde solution with 3-methyl-2-benzothiazolinone hydrazone

Yamei ZHU, Xiaoli YAO, Shaohui CHEN, Qun CUI, Haiyan WANG

期刊论文

Polymerization of methyl methacrylate catalyzed by mono-/bis-salicylaldiminato nickel(II) complexes and

Jihong LU, Danfeng ZHANG, Qian CHEN, Buwei YU

期刊论文

Accelerated degradation of orange G over a widepH range in the presence of FeVO

Xiaoxia Ou, Jianfang Yan, Fengjie Zhang, Chunhua Zhang

期刊论文

Efficient degradation of orange II by ZnMn

Qingzhuo Ni, Hao Cheng, Jianfeng Ma, Yong Kong, Sridhar Komarneni

期刊论文

Carbon-coated Ni-Co alloy catalysts: preparation and performance for aqueous phase hydrodeoxygenation of methyl

期刊论文

Acid Orange 7 degradation using methane as the sole carbon source and electron donor

期刊论文

Risk analysis methods of the water resources system under uncertainty

Zeying GUI,Chenglong ZHANG,Mo Li,Ping GUO

期刊论文

Trend detection and stochastic simulation prediction of streamflow at Yingluoxia hydrological station, Heihe River Basin, China

Chenglong ZHANG,Mo LI,Ping GUO

期刊论文

Synthesis of porous carbon from orange peel waste for effective volatile organic compounds adsorption

期刊论文

Efficient hydrothermal deoxygenation of methyl palmitate to diesel-like hydrocarbons on carbon encapsulated

期刊论文

铝合金板材拉伸变形时橘皮成因的研究进展

马鸣图,杨红亚,吴娥梅,金庆生

期刊论文