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Removal of Cu(II) and Fe(III) from aqueous solutions by dead sulfate reducing bacteria

Hong’en QUAN, He BAI, Yang HAN, Yong KANG, Jiao SUN

《化学科学与工程前沿（英文）》 2013年 第7卷 第2期   页码 177-184 doi: 10.1007/s11705-013-1324-7

摘要： The biosorption properties of dead sulfate reducing bacteria (SRB) for the removal of Cu(II) and Fe(III) from aqueous solutions was studied. The effects of the biosorbent concentration, the initial pH value and the temperature on the biosorption of Cu(II) and Fe(III) by the SRB were investigated. FTIR analysis verified that the hydroxyl, carbonyl and amine functional groups of the SRB biosorbent were involved in the biosorption process. For both Cu(II) and Fe(III), an increase in the SRB biosorbent concentration resulted in an increase in the removal percentage but a decrease in the amount of specific metal biosorption. The maximum specific metal biosorption was 93.25 mg?g at pH 4.5 for Cu(II) and 88.29 mg?g at pH 3.5 for Fe(III). The temperature did not have a significant effect on biosorption. In a binary metal system, the specific biosorption capacity for the target metal decreased when another metal ion was added. For both the single metal and binary metal systems, the biosorption of Cu(II) and Fe(III) onto a SRB biosorbent was better represented by a Langmuir model than by a Freundlich model.

关键词： sulfate reducing bacteria     biosorption     Cu(II)     Fe(III)    

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Advances in Fe(III) bioreduction and its application prospect for groundwater remediation: A review

Yu Jiang, Beidou Xi, Rui Li, Mingxiao Li, Zheng Xu, Yuning Yang, Shaobo Gao

《环境科学与工程前沿（英文）》 2019年 第13卷 第6期 doi: 10.1007/s11783-019-1173-9

摘要： Microbial Fe(III) reduction is closely related to the fate of pollutants. Bioavailability of crystalline Fe(III) oxide is restricted due to thermodynamics. Amorphous Fe(III) (hydro)oxides are more bioavailable. Enrichment and incubation of Fe(III) reducing bacteria are significant. Microbial Fe(III) reduction is a significant driving force for the biogeochemical cycles of C, O, P, S, N, and dominates the natural bio-purification of contaminants in groundwater (e.g., petroleum hydrocarbons, chlorinated ethane, and chromium). In this review, the mechanisms and environmental significance of Fe(III) (hydro)oxides bioreduction are summarized. Compared with crystalline Fe(III) (hydro)oxides, amorphous Fe(III) (hydro)oxides are more bioavailable. Ligand and electron shuttle both play an important role in microbial Fe(III) reduction. The restrictive factors of Fe(III) (hydro)oxides bioreduction should be further investigated to reveal the characteristics and mechanisms of the process. It will improve the bioavailability of crystalline Fe(III) (hydro)oxides and accelerate the anaerobic oxidation efficiency of the reduction state pollutants. Furthermore, the approach to extract, culture, and incubate the functional Fe(III) reducing bacteria from actual complicated environment, and applying it to the bioremediation of organic, ammonia, and heavy metals contaminated groundwater will become a research topic in the future. There are a broad application prospects of Fe(III) (hydro)oxides bioreduction to groundwater bioremediation, which includes the in situ injection and permeable reactive barriers and the innovative Kariz wells system. The study provides an important reference for the treatment of reduced pollutants in contaminated groundwater.

关键词： Microbial Fe(III) reduction     Mechanism     Groundwater contamination     Remediation    

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Enhanced degradation of trichloroethene by calcium peroxide activated with Fe(III) in the presence of

Xiang ZHANG,Xiaogang GU,Shuguang LU,Zhouwei MIAO,Minhui XU,Xiaori FU,Muhammad DANISH,Mark L. BRUSSEAU,Zhaofu QIU,Qian SUI

《环境科学与工程前沿（英文）》 2016年 第10卷 第3期   页码 502-512 doi: 10.1007/s11783-016-0838-x

摘要： Trichloroethene (TCE) degradation by Fe(III)-activated calcium peroxide (CP) in the presence of citric acid (CA) in aqueous solution was investigated. The results demonstrated that the presence of CA enhanced TCE degradation significantly by increasing the concentration of soluble Fe(III) and promoting H O generation. The generation of HO? and O ? in both the CP/Fe(III) and CP/Fe(III)/CA systems was confirmed with chemical probes. The results of radical scavenging tests showed that TCE degradation was due predominantly to direct oxidation by HO?, while O ? strengthened the generation of HO? by promoting Fe(III) transformation in the CP/Fe(III)/CA system. Acidic pH conditions were favorable for TCE degradation, and the TCE degradation rate decreased with increasing pH. The presence of Cl , HCO , and humic acid (HA) inhibited TCE degradation to different extents for the CP/Fe(III)/CA system. Analysis of Cl production suggested that TCE degradation in the CP/Fe(III)/CA system occurred through a dechlorination process. In summary, this study provided detailed information for the application of CA-enhanced Fe(III)-activated calcium peroxide for treating TCE contaminated groundwater.

关键词： calcium peroxide     trichloroethene (TCE)     citric acid     ferric ion     free radicals     oxidation    

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Approaching the commercial threshold of solar water splitting toward hydrogen by III-nitrides nanowires

《能源前沿（英文）》 doi: 10.1007/s11708-023-0870-z

摘要： Approaching the commercial threshold of solar water splitting toward hydrogen by III-nitrides nanowires

关键词： threshold solar water     splitting hydrogen III    

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Self-assembled bright luminescent hierarchical materials from a tripodal benzoate antenna and heptadentate Eu(III) and Tb(III) cyclen complexes

Aramballi J. Savyasachi, David F. Caffrey, Kevin Byrne, Gerard Tobin, Bruno D'Agostino, Wolfgang Schmitt, Thorfinnur Gunnlaugsson

《化学科学与工程前沿（英文）》 2019年 第13卷 第1期   页码 171-184 doi: 10.1007/s11705-018-1762-3

摘要：

The europium heptadentate coordinatively unsaturated (Eu(III)) and the terbium (Tb(III)) 1,4,7,10-tetraazacyclododecane (cyclen) complexes 1 and 2 were used in conjunction with ligand 3 (1,3,5-benzene-trisethynylbenzoate) to form the supramolecular self-assembly structures 4 and 5; this being investigated in both the solid and the solution state. The resulting self-assemblies gave rise to metal centered emission (both in the solid and solution) upon excitation of 3, confirming its role as a sensitizing antenna. Drop-cased examples of ligand 3, and the solid forms of 4 and 5, formed from both organic and mixture of organic-aqueous solutions, were analyzed using Scanning Electron Microscopy, which showed significant changes in morphology; the ligand giving rise to one dimensional structures, while both 4 and 5 formed amorphous materials that were highly dense solid networks containing nanoporous features. The surface area (216 and 119 m2·g−1 for 4 and 5 respectively) and the ability of these porous materials to capture and store gases such as N2 investigated at 77 K. The self-assembly formation was also investigated in diluted solution by monitoring the various photophysical properties of 3–5. This demonstrated that the most stable structures were that consisting of a single antennae 3 and three complexes of 1 or 2 (e.g., 4 and 5) in solution. By monitoring the excited state lifetimes of the Eu(III) and Tb(III) ions in H2O and D2O respectively, we showed that their hydration states (the q-value) changed from ~2 to 0, upon formation of the assemblies, indicating that the three benzoates of 3 coordinated directly to the each of the three lanthanide centers. Finally we demonstrate that this hierarchically porous materials can be used for the sensing of organic solvents as the emission is highly depended on the solvent environment; the lanthanide emission being quenched in the presence of acetonitrile and THF, but greatly enhanced in the presence of methanol.

关键词： self-assembly     supramolecular chemistry     lanthanides     Eu(III) and Tb(III) complexes     luminescence     metallostars    

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III族氮化物材料和设备的未来技术及用途

Shuji Nakamura

《工程（英文）》 2015年 第1卷 第2期   页码 161-161 doi: 10.15302/J-ENG-2015059

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Group III metabotropic glutamate receptors and drug addiction

null

《医学前沿（英文）》 2013年 第7卷 第4期   页码 445-451 doi: 10.1007/s11684-013-0291-1

摘要：

Neuroadaptations of glutamatergic transmission in the limbic reward circuitry are linked to persistent drug addiction. Accumulating data have demonstrated roles of ionotropic glutamate receptors and group I and II metabotropic glutamate receptors (mGluRs) in this event. Emerging evidence also identifies Gαi/o-coupled group III mGluRs (mGluR4/7/8 subtypes enriched in the limbic system) as direct substrates of drugs of abuse and active regulators of drug action. Auto- and heteroreceptors of mGluR4/7/8 reside predominantly on nerve terminals of glutamatergic corticostriatal and GABAergic striatopallidal pathways, respectively. These presynaptic receptors regulate basal and/or phasic release of respective transmitters to maintain basal ganglia homeostasis. In response to operant administration of common addictive drugs, such as psychostimulants (cocaine and amphetamine), alcohol and opiates, limbic group III mGluRs undergo drastic adaptations to contribute to the enduring remodeling of excitatory synapses and to usually suppress drug seeking behavior. As a result, a loss-of-function mutation (knockout) of individual group III receptor subtypes often promotes drug seeking. This review summarizes the data from recent studies on three group III receptor subtypes (mGluR4/7/8) expressed in the basal ganglia and analyzes their roles in the regulation of dopamine and glutamate signaling in the striatum and their participation in the addictive properties of three major classes of drugs (psychostimulants, alcohol, and opiates).

关键词： group III metabotropic glutamate receptors     cocaine     amphetamine     alcohol     opiate    

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Preparation of manganese (III) acetylacetonate nanoparticles via an environmentally benign route

M. S. Shalaby, H. Abdallah

《化学科学与工程前沿（英文）》 2013年 第7卷 第3期   页码 329-337 doi: 10.1007/s11705-013-1339-0

摘要： With the hope of overcoming the generation of hazardous materials to human health and environment, serious and great endeavor have been made in catalyst fabrication using green chemistry technology. In this paper, the manganese (III) acetylacetonate nanoparticles with diameters of about 146 nm were prepared by a simple and environmentally benign route based on hydrolysis of KMnO followed by reaction with acetylacetone in rapid stirring rate or ultrasonication. The as-prepared samples were characterized by X-ray diffraction, energy dispersive X-ray fluorescence (EDIX), Fourier transfer infrared spectroscopy and scanning electron microscope. Various parameters were investigated, and the pure and stable crystals of manganese (III) acetylacetonate could be obtained in 98% conversion at a molar ratio 7∶1 of acetylacetone to KMnO and 75°C after 60 min. We further proposed a mathematical model, and the predicted results from model were in good agreement with experimental results.

关键词： green chemistry     manganese (III) acetylacetonate     reaction conversion     Mathematical model    

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Exposure-response of Cr(III)-organic complexes to Saccharomyces cerevisiae

Nivedita CHATTERJEE, Zejiao LUO,

《环境科学与工程前沿（英文）》 2010年 第4卷 第2期   页码 196-202 doi: 10.1007/s11783-010-0008-5

摘要： Hexavalent chromium [Cr(VI)] bioreduction produces soluble Cr(III)-organic complexes. The Cr(III)-organic complexes are relatively stable once they are formed, and no data about their toxicity were reported. Therefore, this study aims to investigate the bioavailability and toxicity of the soluble Cr(III)-organic complexes. L-1 wild type yeast strain was chosen as the model organism and Cr(III)-citrate was selected as the representative compound of the Cr(III)-organic complexes. The short-term chronic aquatic toxicity tests of the Cr(III)-citrate was explored by measuring growth inhibition, direct viable cell count, dry biomass, biosorption, and the amount of CO production. Cr(III)-citrate exerted a toxicity of 51mg/L with an , which was calculated from the percent growth inhibition. These toxicity data would be helpful to define the toxic potential of the organo-chromium-III compounds in the environment.

关键词： Cr(III)-organic complexes     Saccharomyces cerevisiae     toxicity     EC50     bioavailability    

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Studies on advanced water-cooled reactors beyond generation III for power generation

CHENG Xu

《能源前沿（英文）》 2007年 第1卷 第2期   页码 141-149 doi: 10.1007/s11708-007-0018-6

摘要： China s ambitious nuclear power program motivates the country s nuclear community to develop advanced reactor concepts beyond generation III to ensure a long-term, stable, and sustainable development of nuclear power. The paper discusses some main criteria for the selection of future water-cooled reactors by considering the specific Chinese situation. Based on the suggested selection criteria, two new types of water-cooled reactors are recommended for future Chinese nuclear power generation. The high conversion pressurized water reactor utilizes the present PWR technology to a large extent. With a conversion ratio of about 0.95, the fuel utilization is increased about 5 times. This significantly improves the sustainability of fuel resources. The supercritical water-cooled reactor has favorable features in economics, sustainability and technology availability. It is a logical extension of the generation III PWR technology in China. The status of international R&D work is reviewed. A new supercritical water-cooled reactor (SCWR) core structure (the mixed reactor core) and a new fuel assembly design (two-rows FA) are proposed. The preliminary analysis using a coupled neutron-physics/thermal-hydraulics method is carried out. It shows good feasibility for the new design proposal.

关键词： Chinese situation     selection     generation     water-cooled     feasibility    

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The performance of nitrate-reducing Fe(II) oxidation processes under variable initial Fe/N ratios: The

《环境科学与工程前沿（英文）》 2021年 第15卷 第4期 doi: 10.1007/s11783-020-1366-2

摘要：

•Bacterially-mediated coupled N and Fe processes examined in incubation experiments.

关键词： Denitrification     N2O emission     Fe(II) oxidation     Fe/N ratio     Fe minerals    

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Tianrun Xia County phase III 99.5 MW wind power engineering technology and green innovation

Xiaobo WANG

《工程管理前沿（英文）》 2019年 第6卷 第1期   页码 131-137 doi: 10.1007/s42524-019-0012-9

摘要：

关键词： low carbon design     green standard system     environmental protection     sustainable development     Tianrun Sijiao Town wind farm    

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III. Impact resistance property

Heming LIN, Dongming QI, Jian HAN, Zhiqi CAI, Minghua WU

《化学科学与工程前沿（英文）》 2009年 第3卷 第2期   页码 176-181 doi: 10.1007/s11705-009-0203-8

摘要： A novel phenolic rigid organic filler (KT) was used to modify isotactic polypropylene (iPP). The influence of KT particles on the impact resistance property of PP/KT specimens (with similar interparticles distance, 1.8 μm) was studied by notched izod impact tests. It was found that the brittle-ductile transition (BDT) of the PP/KT microcomposites took place at the filler content of about 4%, and the impact strength attains the maximum at 5% (with filler particles size of 1.5 μm), which is about 2.5 times that of unfilled iPP specimens. The impact fracture morphology was investigated by scanning electron microscopy (SEM). For the PP/KT specimens and the high-density polyethylene/KT (HDPE/KT) specimens in ductile fracture mode, many microfibers could be found on the whole impact fracture surface. It was the filler particles that induced the plastic deformation of interparticles ligament and hence improved the capability of iPP matrix on absorbing impact energy dramatically. The determinants on the BDT were further discussed on the basis of stress concentration and debonding resistance. It can be concluded that aside from the interparticle distance, the filler particles size also plays an important role in semicrystalline polymer toughening.

关键词： rigid organic filler     polypropylene     impact resistance    

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Cadmium removal mechanistic comparison of three Fe-based nanomaterials: Water-chemistry and roles ofFe dissolution

《环境科学与工程前沿（英文）》 2022年 第16卷 第12期 doi: 10.1007/s11783-022-1586-8

摘要：

● nZVI, S-nZVI, and nFeS were systematically compared for Cd(II) removal.

关键词： Nano zero valent iron     Sulfided zero valent iron     FeS     Cd(II) immobilization     Fe dissolution    

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Synergistic effect of V and Fe in Ni/Fe/V ternary layered double hydroxides for efficient and durable

《化学科学与工程前沿（英文）》 2023年 第17卷 第1期   页码 102-115 doi: 10.1007/s11705-022-2179-6

摘要： High-performance and stable electrocatalysts are vital for the oxygen evolution reaction (OER). Herein, via a one-pot hydrothermal method, Ni/Fe/V ternary layered double hydroxides (NiFeV-LDH) derived from Ni foam are fabricated to work as highly active and durable electrocatalysts for OER. By changing the feeding ratio of Fe and V salts, the prepared ternary hydroxides were optimized. At an Fe:V ratio of 0.5:0.5, NiFeV-LDH exhibits outstanding OER activity superior to that of the binary hydroxides, requiring overpotentials of 269 and 274 mV at 50 mA·cm–2 in the linear sweep voltammetry and sampled current voltammetry measurements, respectively. Importantly, NiFeV-LDH shows extraordinary long-term stability (≥ 75 h) at an extremely high current density of 200 mA·cm–2. In contrast, the binary hydroxides present quick decay at 200 mA·cm–2 or even reduced current densities (150 and 100 mA·cm–2). The outstanding OER performance of NiFeV-LDH benefits from the synergistic effect of V and Fe while doping the third metal into bimetallic hydroxide layers: (a) Fe plays a crucial role as the active site; (b) electron-withdrawing V stabilizes the high valence state of Fe, thus accelerating the OER process; (c) V further offers great stabilization for the formed intermediate of FeOOH, thus achieving superior durability.

关键词： oxygen evolution reaction     electrocatalysts     ternary layered double hydroxides     long-term stability    

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标题 作者 时间 类型 操作

Removal of Cu(II) and Fe(III) from aqueous solutions by dead sulfate reducing bacteria

Hong’en QUAN, He BAI, Yang HAN, Yong KANG, Jiao SUN

期刊论文

Advances in Fe(III) bioreduction and its application prospect for groundwater remediation: A review

Yu Jiang, Beidou Xi, Rui Li, Mingxiao Li, Zheng Xu, Yuning Yang, Shaobo Gao

期刊论文

Enhanced degradation of trichloroethene by calcium peroxide activated with Fe(III) in the presence of

Xiang ZHANG,Xiaogang GU,Shuguang LU,Zhouwei MIAO,Minhui XU,Xiaori FU,Muhammad DANISH,Mark L. BRUSSEAU,Zhaofu QIU,Qian SUI

期刊论文

Approaching the commercial threshold of solar water splitting toward hydrogen by III-nitrides nanowires

期刊论文

Self-assembled bright luminescent hierarchical materials from a tripodal benzoate antenna and heptadentate Eu(III) and Tb(III) cyclen complexes

Aramballi J. Savyasachi, David F. Caffrey, Kevin Byrne, Gerard Tobin, Bruno D'Agostino, Wolfgang Schmitt, Thorfinnur Gunnlaugsson

期刊论文

III族氮化物材料和设备的未来技术及用途

Shuji Nakamura

期刊论文

Group III metabotropic glutamate receptors and drug addiction

null

期刊论文

Preparation of manganese (III) acetylacetonate nanoparticles via an environmentally benign route

M. S. Shalaby, H. Abdallah

期刊论文

Exposure-response of Cr(III)-organic complexes to Saccharomyces cerevisiae

Nivedita CHATTERJEE, Zejiao LUO,

期刊论文

Studies on advanced water-cooled reactors beyond generation III for power generation

CHENG Xu

期刊论文

The performance of nitrate-reducing Fe(II) oxidation processes under variable initial Fe/N ratios: The

期刊论文

Tianrun Xia County phase III 99.5 MW wind power engineering technology and green innovation

Xiaobo WANG

期刊论文

III. Impact resistance property

Heming LIN, Dongming QI, Jian HAN, Zhiqi CAI, Minghua WU

期刊论文

Cadmium removal mechanistic comparison of three Fe-based nanomaterials: Water-chemistry and roles ofFe dissolution

期刊论文

Synergistic effect of V and Fe in Ni/Fe/V ternary layered double hydroxides for efficient and durable

期刊论文