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Adsorption property of direct fast black onto acid-thermal modified sepiolite and optimization of adsorptionconditions using Box-Behnken response surface methodology

Chengyuan SU, Weiguang LI, Yong WANG

《环境科学与工程前沿（英文）》 2013年 第7卷 第4期   页码 503-511 doi: 10.1007/s11783-012-0477-9

摘要： The adsorption of direct fast black onto acid-thermal modified sepiolite was investigated. Batch adsorption experiments were performed to evaluate the influences of experimental parameters such as initial dye concentration, initial solution pH and adsorbent dosage on the adsorption process. The three-factor and three-level Box-Behnken response surface methodology (RSM) was utilized for modeling and optimization of the adsorption conditions for direct fast black onto the acid-thermal modified sepiolite. The raw sepiolite was converted to acid-thermal modified sepiolite, and changes in the fourier transform infrared spectrum (FTIR) adsorption bands of the sample were noted at 3435 cm and 1427 cm . The zeolitic water disappeared and the purity of sepiolite was improved by acid-thermal modification. The decolorization rate of direct fast black adsorbed increased from 68.2% to 98.9% on acid-thermal modified sepiolite as the initial solution pH decreased from 10 to 2. When the adsorbent dosage reached to 2.5 g·L , 2.0 g·L , 1.5 g·L and 1.0 g·L , the decolorization rate was 90.3%, 86.7%, 61.0% and 29.8%, respectively. When initial dye concentration increased from 25 to 200 mg·L , the decolorization rate decreased from 91.9% to 60.0%. The RSM results showed that the interaction between adsorbent dosage and pH to be a significant factor. The optimum conditions were as follows: the adsorbent dosage 1.99 g·L , pH 4.22, and reaction time 5.2 h. Under these conditions, the decolorization rate was 95.1%. The three dimensional fluorescence spectra of direct fast black before and after treatment showed that the direct fast black was almost all adsorbed by the acid-thermal modified sepiolite.

关键词： direct fast black     acid-thermal modified sepiolite     adsorption     response surface methodology    

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Parametric study on the mixed solvent synthesis of ZIF-8 nano- and micro-particles for CO adsorption:A response surface study

Alireza Hadi, Javad Karimi-Sabet, Abolfazl Dastbaz

《化学科学与工程前沿（英文）》 2020年 第14卷 第4期   页码 579-594 doi: 10.1007/s11705-018-1770-3

摘要： The room temperature synthesis of ZIF-8 micro- and nano-particles was investigated using a mixed methanol-water solvent system. ZIF-8 particles of good quality and high crystallinity were obtained. Response surface methodology was used to determine the effect of the synthesis conditions on the ZIF-8 yield, particle size distribution, and mean particle size. The ligand/metal salt molar ratio followed by the amount of sodium formate (the deprotonating agent) and then the amount of water (i.e., the composition of the mixed solvent) respectively had the largest effects on both the ZIF-8 yield and particle size. Results showed that mixing of solvents with different strengths in producing ZIF-8 crystals is a practical method to size-controlled synthesis of ZIF-8 particles. This method is more favorable for industrial-scale ZIF-8 synthesis than using excess amounts of ligands or chemical additives (like sodium formate). In addition, ZIF-8 samples with different mean particle sizes (100, 500, and 1000 nm) were used for CO adsorption and the mid-sized ZIF-8 particles had the highest adsorption capacity.

关键词： metal organic frameworks     zeolitic imidazolate frameworks     ZIF-8     response surface methodology     Box Behnken design     CO adsorption    

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Insight into the effect of surface carboxyl and amino groups on the adsorption of titanium dioxide for

Wenlong Zhang, Xuyang Zhao, Lin Zhang, Jinwei Zhu, Shanshan Li, Ping Hu, Jiangtao Feng, Wei Yan

《化学科学与工程前沿（英文）》 2021年 第15卷 第5期   页码 1147-1157 doi: 10.1007/s11705-020-1978-x

摘要： In this study, TiO functionalized with organic groups were prepared to study the effect of carboxyl and amino groups on the adsorption behavior of TiO for the removal of acid red G (ARG) as an anionic dye from aqueous solution. TiO was successfully modified with carboxyl and amino groups by using the hydrolysis method with oxalic acid (OAD, with two carboxyl groups), ethylenediamine (EDA, with two amino groups) and DL-alanine (DLA, with one carboxyl group and one amino group) at low temperature (65 °C) and labeled as OAD-TiO , EDA-TiO and DLA-TiO , respectively. The ARG uptake by the functionalized TiO samples was largely dependent on the functional groups. The interaction between ARG and the functional organic groups on the TiO samples plays an important role in the adsorption process, which leads to the excellent adsorption performance (higher capacity and faster adsorption rate) of the functionalized TiO samples than that of P25 (commercial TiO without modification). Furthermore, there is no obvious loss of the adsorption capacity for the functionalized TiO even after 5 adsorption-desorption cycles, which indicated the good reusability of the modified TiO samples for anionic dye removal from aqueous solution.

关键词： amino group     carboxylic group     titanium dioxide     ARG     adsorption    

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Immobilization of NZVI in polydopamine surface-modified biochar for adsorption and degradation of tetracycline

Xiangyu Wang, Weitao Lian, Xin Sun, Jun Ma, Ping Ning

《环境科学与工程前沿（英文）》 2018年 第12卷 第4期 doi: 10.1007/s11783-018-1066-3

摘要：

Novel method for polydopamine (PDA) modified biochar (BC) with immobilized NZVI.

PDA/NZVI@BC exhibits significantly enhanced activity for tetracycline (TC) removal.

TC removal efficiency was increased by 55.9% compared with that of pristine NZVI.

The mechanism of tetracycline removal by PDA/NZVI@BC was proposed.

关键词： Biochar     Polydopamine     NZVI     Modification     Tetracycline    

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A density functional theory study of the adsorption of Hg and HgCl2 on a CaO(001) surface

GUO Xin, ZHENG Chuguang, LU Nanxia

《能源前沿（英文）》 2007年 第1卷 第1期   页码 101-104 doi: 10.1007/s11708-007-0011-0

摘要： The adsorption of mercury and mercury chloride on a CaO(001) surface was investigated by the density functional theory (DFT) by using CaO cluster embedded in an electrostatic field represented by 178 point charges at the crystal CaO lattice positions. For the mercury molecular axis normal to the surface, the mercury can only coordinate to the O anion and has a very weak binding energy of 19.649 kJ/mol. When the mercury chloride molecular axis is vertical to the surface, the Cl atom coordinates to the Ca cation and has a binding energy of 23.699 kJ/mol. When the mercury chloride molecular axis is parallel to the surface, the Hg atom coordinates to the O anion and has a binding energy of 87.829 kJ/mol, which means that the parallel geometry is more stable than the vertical one. The present calculations show that CaO injection could substantially reduce gaseous mercury chloride, but have no apparent effect on the mercury, which is compatible with the available experimental results. This research will provide valuable information for optimizing and selecting a sorbent for the trace element in flue gas.

关键词： mercury chloride     mercury molecular     surface     cluster     electrostatic    

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of malachite green from aqueous solution by sorption on hydrilla verticillata biomass using response surface

R. RAJESHKANNAN, N. RAJAMOHAN, M. RAJASIMMAN

《化学科学与工程前沿（英文）》 2009年 第3卷 第2期   页码 146-154 doi: 10.1007/s11705-009-0007-x

摘要： In the present study, the effect of adsorbent dose, pH, temperature, initial dye concentration and contact time on malachite green removal from an aqueous medium using hydrilla verticillata biomass has been investigated. The central composite face-centered experimental design (CFCD) in response surface methodology (RSM) was used for designing the experiments as well as for full response surface estimation. The optimum conditions for maximum removal of malachite green from an aqueous solution of 75.52 mg/L were as follows: adsorbent dose (11.14 g/L), pH (8.4), temperature (48.4°C) and contact time (194.5 min). This was evidenced by the higher value of coefficient of determination ( =0.9158).

关键词： response surface methodology     hydrilla verticillata     malachite green     adsorption     central composite design    

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Adsorption of toluene, ethylbenzene and xylene isomers on multi-walled carbon nanotubes oxidized by different

Fei YU, Jie MA, Yanqing WU

《环境科学与工程前沿（英文）》 2012年 第6卷 第3期   页码 320-329 doi: 10.1007/s11783-011-0340-4

摘要： Multi-walled carbon nanotubes (MWCNTs) were fabricated and oxidized by different concentrations of sodium hypochlorite (NaOCl) solutions. The untreated MWCNTs and modified MWCNTs were employed as adsorbents to study their characterizations and adsorption performance of toluene, ethylbenzene and xylene isomers (TEX) in an aqueous solution. The physicochemical properties of MWCNTs were greatly affected after oxidation, which influences TEX adsorption capacity. The 3% NaOCl-oxidized MWCNTs shows the greatest enhancement in TEX adsorption, followed by the 30% NaOCl. More interestingly, the 15% NaOCl-oxidized MWCNTs has lower adsorption capacities than untreated MWCNTs. The adsorption mechanism of TEX on treated MWCNTs is attributed to the combined action of hydrophobic interaction, π-π bonding interaction between the aromatic ring of TEX and the oxygen-containing functional groups of MWCNTs and electrostatic interaction. 3% NaOCl solution could not only introduce much oxygen-containing functional groups on MWCNTs, but also lead to less damage for the pore structure. This suggests that the CNTs-3% NaOCl is efficient adsorbent for TEX and that they may possess good potential for TEX removal in wastewater treatment.

关键词： adsorption     toluene     ethylbenzene and xylene isomers (TEX)     multi-walled carbon nanotube     surface oxidation    

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Preparation of a novel anion exchange group modified hyper-crosslinked resin for the effective adsorption

Qing ZHOU, Mengqiao WANG, Aimin LI, Chendong SHUANG, Mancheng ZHANG, Xiaohan LIU, Liuyan WU

《环境科学与工程前沿（英文）》 2013年 第7卷 第3期   页码 412-419 doi: 10.1007/s11783-013-0483-6

摘要： A novel hyper-crosslinked resin (MENQ) modified with an anion exchange group was prepared using divinylbenzene (DVB) and methyl acrylate (MA) as comonomers via four steps: suspension polymerization, post-crosslinking, ammonolysis and alkylation reactions. The obtained resin had both a high specific surface area (793.34 m ·g ) and a large exchange capacity (strong base anion exchange capacity, SEC: 0.74 mmol·g , weak base anion exchange capacity, WEC: 0.45 mmol·g ). XAD-4 was selected as an adsorbent for comparison to investigate the adsorption behavior of tetracycline (TC) and humic acid (HA) onto the adsorbents. The results revealed that MENQ could effectively remove both TC and HA. The adsorption capacity of XAD-4 for TC was similar to that of MENQ, but XAD-4 exhibited poor performance for the adsorption of HA. The adsorption isotherms of TC and HA were well-fitted with the Freundlich model, which indicated the existence of heterogeneous adsorption through cation-π bonding and π–π interactions. The optimal solution condition for the adsorption of TC was at a pH of 5–6, whereas the adsorption of HA was enhanced with increasing pH of the solution.

关键词： high surface area     adsorption     anion exchange     micropollutant     dissolved organic matters    

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New insights into mercury removal mechanism on CeO

Ling Li, Yu He, Xia Lu

《环境科学与工程前沿（英文）》 2018年 第12卷 第2期 doi: 10.1007/s11783-018-1007-1

摘要： First-principles calculations were performed to investigate the mechanism of Hg adsorption and oxidation on CeO (111). Surface oxygen activated by the reduction of Ce to Ce was vital to Hg adsorption and oxidation processes. Hg was fully oxidized by the surface lattice oxygen on CeO (111), without using any other oxidizing agents. HCl could dissociate and react with the Hg adatom on CeO (111) to form adsorbed Hg–Cl or Cl–Hg–Cl groups, which promoted the desorption of oxidized Hg and prevented CeO catalyst deactivation. In contrast, O–H and H–O–H groups formed during HCl adsorption consumed the active surface oxygen and prohibited Hg oxidation. The consumed surface oxygen was replenished by adding O into the flue gas. We proposed that oxidized Hg desorption and maintenance of sufficient active surface oxygen were the rate-determining steps of Hg removal on CeO -based catalysts. We believe that our thorough understanding and new insights into the mechanism of the Hg removal process will help provide guidelines for developing novel CeO -based catalysts and enhance the Hg removal efficiency.

关键词： Elemental mercury removal     Surface adsorption     Ceria     First-principles calculations    

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Occurrence of bisphenol A in surface and drinking waters and its physicochemical removal technologies

Liping LIANG,Jing ZHANG,Pian FENG,Cong LI,Yuying HUANG,Bingzhi DONG,Lina LI,Xiaohong GUAN

《环境科学与工程前沿（英文）》 2015年 第9卷 第1期   页码 16-38 doi: 10.1007/s11783-014-0697-2

摘要： Bisphenol A (BPA), an endocrine disrupting compound, has caused wide public concerns due to its wide occurrence in environment and harmful effects. BPA has been detected in many surface waters and drinking water with the maximum concentrations up to tens of μg·L . The physicochemical technology options in eliminating BPA can be divided into four categories: oxidation, advanced oxidation, adsorption and membrane filtration. Each removal option has its own limitation and merits in removing BPA. Oxidation and advanced oxidation generally can remove BPA efficiently while they also have some drawbacks, such as high cost, the generation of a variety of transformation products that are even more toxic than the parent compound and difficult to be mineralized. Only few advanced oxidation methods have been reported to be able to mineralize BPA completely. Therefore, it is important not only to identify the major initial transformation products but also to assess their estrogenic activity relative to the parent compounds when oxidation methods are employed to remove BPA. Without formation of harmful by-products, physical separation methods such as activated carbon adsorption and membrane processes are able to remove BPA in water effluents and thus have potential as BPA removal technologies. However, the necessary regeneration of activated carbon and the low BPA removal efficiency when the membrane became saturated may limit the application of activated carbon adsorption and membrane processes for BPA removal. Hybrid processes, e.g. combining adsorption and biologic process or combining membrane and oxidation process, which can achieve simultaneous physical separation and degradation of BPA, will be highly preferred in future.

关键词： Bisphenol A (BPA)     occurrence     conventional oxidation     advanced oxidation     adsorption     membrane filtration    

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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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矿物浮选吸附平衡模型构建与应用：精准解析矿物 表面离子 / 药剂特征吸附

高雅,付心壮,韩海生,王丽,岳彤,孙伟

《中国工程科学》 2023年 第25卷 第6期   页码 248-258 doi: 10.15302/J-SSCAE-2023.07.020

摘要：

矿物浮选吸附平衡模型是准确描述矿物浮选过程中所涉及的矿物表面离子 / 药剂吸附平衡的数学模型，首次实现了矿物表面位点与浮选药剂吸附作用亲和性的量化解析。传统浮选理论对矿物表面作用位点缺乏科学描述，难以阐明浮选药剂的吸附作用能力及平衡状态，新浮选药剂体系开发多以“试错法”“复配法”等经验性方法为主。药剂选择性吸附作为浮选作业的核心机制，若不能准确预测其在各矿物表面的吸附行为，将严重限制浮选工艺智能化控制的发展。本文详细论述了矿物浮选吸附平衡模型的构建原理，以赤铁矿 ‒ 石英和一水硬铝石 ‒ 高岭石两个浮选体系为例，通过对少量实验数据的拟合计算，解析出矿物表面活性位点密度Ns、加 / 去质子反应常数Kt1/Kt2、药剂吸附常数Kf等矿物浮选特征常数。将解析的矿物浮选特征常数代入到平衡模型中，预测出各条件下矿物表面电性、离子及浮选药剂的吸附量，通过零电点、实验及测试等方法验证了可靠性，形成了矿物浮选过程预测系统的内核算法。该算法对各条件下每种矿物药剂吸附的初步准确预测，可在一定程度上反映其可浮性趋势，有助于缩短浮选工艺开发周期，对矿物表面药剂吸附机理研究、浮选药剂分子设计、浮选工艺流程优化及智能控制等具有重要意义。

关键词： 矿物加工；浮选机理；矿物浮选吸附平衡模型；可浮性预测；矿物浮选特征常数    

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Fabrication, characterization and evaluation of mesoporous activated carbons from agricultural waste: Jerusalem artichoke stalk as an example

Lei YU,Chen TU,Yongming LUO

《环境科学与工程前沿（英文）》 2015年 第9卷 第2期   页码 206-215 doi: 10.1007/s11783-014-0631-7

摘要： This work explores the feasibility of Jerusalem artichoke stem (JAS), an agricultural waste, as an alternative precursor for fabrication of mesoporous activated carbon (MAC) via conventional ZnCl activation. The as-prepared JAS-MACs were characterized by thermogravimetric, nitrogen gas adsorption isotherm and high resolution scanning electron microscopy analysis. The interacting effects of chemical dosage, activation temperature and time on the mesoporosity, mesopore volume and carbon yield were investigated, and further optimized by response surface methodology (RSM). The Brunauer-Emmett-Teller surface area, mesoporosity and mesopore volume of the JAS-MAC prepared under optimum condition were identified to be 1631 m ·g , 90.16% and 1.11 cm ·g , respectively. Compared with commercial activated carbons, this carbon exhibited a comparable monolayer adsorption capacity of 374.5 mg·g for Methylene Blue dye. The findings suggest that RSM could be an effective approach for optimizing the pore structure of fabricated activated carbons.

关键词： mesoporous activated carbon     response surface methodology     adsorption isotherm     agricultural wastes    

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Contributions of adsorption, bioreduction and desorption to uranium immobilization by extracellular polymeric

《环境科学与工程前沿（英文）》 2023年 第17卷 第9期 doi: 10.1007/s11783-023-1707-z

摘要：

● EPS immobilizes U(VI) via adsorption, bioreduction and desorption.

关键词： Adsorption     Bioreduction     Desorption     Kinetics     Isotherm     Uranium    

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Polypropylene microplastics alter the cadmium adsorption capacity on different soil solid fractions

《环境科学与工程前沿（英文）》 2022年 第16卷 第1期   页码 3-3 doi: 10.1007/s11783-021-1437-z

摘要：

Microplastics (MPs) are widely present in a variety of environmental media and have attracted more and more attention worldwide. However, the effect of MPs on the interaction between heavy metals and soil, especially in soil solid fraction level, is not well understood. In this study, batch experiments were performed to investigate the adsorption characteristics of Cd in bulk soil and three soil solid fractions (i.e. particulate organo matter (POM), organic-mineral compounds (OMC), and mineral) with or without polypropylene (PP) MPs.

关键词： Polypropylene microplastics     Cadmium     Adsorption     POM     OMC     Mineral    

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标题 作者 时间 类型 操作

Adsorption property of direct fast black onto acid-thermal modified sepiolite and optimization of adsorptionconditions using Box-Behnken response surface methodology

Chengyuan SU, Weiguang LI, Yong WANG

期刊论文

Parametric study on the mixed solvent synthesis of ZIF-8 nano- and micro-particles for CO adsorption:A response surface study

Alireza Hadi, Javad Karimi-Sabet, Abolfazl Dastbaz

期刊论文

Insight into the effect of surface carboxyl and amino groups on the adsorption of titanium dioxide for

Wenlong Zhang, Xuyang Zhao, Lin Zhang, Jinwei Zhu, Shanshan Li, Ping Hu, Jiangtao Feng, Wei Yan

期刊论文

Immobilization of NZVI in polydopamine surface-modified biochar for adsorption and degradation of tetracycline

Xiangyu Wang, Weitao Lian, Xin Sun, Jun Ma, Ping Ning

期刊论文

A density functional theory study of the adsorption of Hg and HgCl2 on a CaO(001) surface

GUO Xin, ZHENG Chuguang, LU Nanxia

期刊论文

of malachite green from aqueous solution by sorption on hydrilla verticillata biomass using response surface

R. RAJESHKANNAN, N. RAJAMOHAN, M. RAJASIMMAN

期刊论文

Adsorption of toluene, ethylbenzene and xylene isomers on multi-walled carbon nanotubes oxidized by different

Fei YU, Jie MA, Yanqing WU

期刊论文

Preparation of a novel anion exchange group modified hyper-crosslinked resin for the effective adsorption

Qing ZHOU, Mengqiao WANG, Aimin LI, Chendong SHUANG, Mancheng ZHANG, Xiaohan LIU, Liuyan WU

期刊论文

New insights into mercury removal mechanism on CeO

Ling Li, Yu He, Xia Lu

期刊论文

Occurrence of bisphenol A in surface and drinking waters and its physicochemical removal technologies

Liping LIANG,Jing ZHANG,Pian FENG,Cong LI,Yuying HUANG,Bingzhi DONG,Lina LI,Xiaohong GUAN

期刊论文

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

矿物浮选吸附平衡模型构建与应用：精准解析矿物 表面离子 / 药剂特征吸附

高雅,付心壮,韩海生,王丽,岳彤,孙伟

期刊论文

Fabrication, characterization and evaluation of mesoporous activated carbons from agricultural waste: Jerusalem artichoke stalk as an example

Lei YU,Chen TU,Yongming LUO

期刊论文

Contributions of adsorption, bioreduction and desorption to uranium immobilization by extracellular polymeric

期刊论文

Polypropylene microplastics alter the cadmium adsorption capacity on different soil solid fractions

期刊论文