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1.
研究混合胺溶液吸收二氧化碳(CO2)的反应机理对低碳环保具有重要意义.本文以碳酸钙(CaCO3)为催化剂,在Eley-Rideal模型下通过Gaussian09软件模拟计算乙醇胺(MEA)+CO2反应机理,,同时计算混合胺溶液体系乙醇胺(MEA)+二乙醇胺(DEA)/2-氨基-2-甲基-1-丙醇(AMP)/N-甲基二乙醇胺(MDEA)吸收CO2中经实验证明的协同效应.本文在CCSD(T)/6-311++G(d,p)水平上计算在两性离子机理下中间步骤的自由能和几何振动频率.模拟结果表明,在固体催化剂CaCO3作用下,反应活化能降低了14.9%,但是自由能没有降低.混合胺盐能量(MEA-DEA-CO2,MEA-AMP-CO2)低于MEA-CO2-MEA能量,差距分别为-18.25%和-14.5%,而MEA-MDEA-CO2体系能量与单一溶液体系差距仅为-5.88%.这表明二级胺,空间位阻胺的协同效应大于三级胺. 相似文献
2.
Heavy-metal fractionation and distribution in soil profiles short-term-irrigated with sewage wastewater 总被引:1,自引:0,他引:1
Six soil profiles irrigated and non-irrigated with sewage wastewater were investigated for soil pH, electrical conductivity (EC), organic matter (OM), and CaCO3. The distributions and chemical fractions of Cu, Zn, Cd, and Pb, and their lability were also studied. The results indicated that pH, EC, OM, and CaCO3, as well as metal fractionation in soil profiles were affected by wastewater irrigation, especially in the surface layer. The surface layer (0-15 cm) irrigated with wastewater exhibited a 0.6 unit decrease in soil pH, a 40.6% decrease in CaCO3, and a 200% increase in EC as compared with that of the non-irrigated soil. The soil OM increased from 0.04% to 0.35% in the surface layer. The irrigation of soil with wastewater resulted in transformation of metals from the carbonate fraction (CARB) towards the exchangeable (EXCH), Fe-Mn oxide (ERO), and organic (OM) fraction for Zn, towards the EXCH, the OM, and residual fraction for Cu, and towards the exchangeable (EXCH) fraction for Cd. It was concluded that the use of sewage wastewater led to salt accumulation and an increase in the readily labile fraction of Zn, Cu, and Cd in the surface layer. Therefore, this reason may limit the use of wastewater under arid and semi-arid conditions. 相似文献
3.
《Chemistry and Ecology》2008,24(2):147-156
The main objective of this study was to investigate the efficiency of different substrates to reduce the extraction of heavy metals concentration in a heavily contaminated soil. Two contaminated soils by Cu and Zn were used to evaluate the effectiveness of eight substrates (calcium carbonate, bentonite, kaolinite, charcoal, manganese oxide, iron oxide, zeolite, phosphate) to reduce metal availability and to study the change of metals speciation in different forms using sequential extraction technique (single step). Sequential extraction technique (single step, 0.11 M acetic acid, HONH3Cl, H2O2+NH4OAc, Aqua regia) was applied on contaminated soils after and before treatment to evaluate metals speciation. Results indicate that the most effective treatments in decreasing available metal concentrations were calcium carbonate, zeolite and manganese or iron oxide. Metal sequential fractionations indicate that the exchangeable fraction of Cu and Zn in contaminated soils can be transformed into unavailable forms after chemical remediation. 相似文献
4.
微生物诱导碳酸盐沉淀(MICP)可将游离的重金属离子转化为稳定的矿化物,在修复土壤重金属污染方面具有广阔的应用前景.本研究从铜陵矿区周边土壤中筛选得到1株产脲酶且耐镉矿化菌株CZW-1,16S rDNA鉴定为芽孢杆菌(Bacillus sp.),并将其利用于添加外源Ca2+的矿化固结Cd2+实验中.通过扫描电镜(SEM)、傅立叶红外光谱(FT-IR)以及X射线衍射(XRD)对矿化产物进行表征和分析.结果表明,添加一定浓度的Ca2+可促进细菌的生长,其最佳浓度为20 mmol·L-1.且Ca2+的添加可提高细菌的最小抑制浓度和促进脲酶活性,提高对Cd2+的矿化率,加钙前后的矿化率由68.93%提高到75.95%.通过对矿化物的定性分析,可知加钙前后的矿物沉淀由单一CdCO3变为CdCO3和CaCO3的复合沉淀,其表面也由严密紧实变成填满了小颗粒CdCO3的多孔状. 相似文献
5.
Co-present Pb(II) accelerates the oxidation of organic contaminants by permanganate: Role of Pb(III)
Lei Dong Pin Xie Xin Zhang Junlian Qiao Dandan Rao Yuankui Sun Xiaohong Guan 《Frontiers of Environmental Science & Engineering》2022,16(8):109
6.
Xiang ZHANG Xiaogang GU Shuguang LU Zhouwei MIAO Minhui XU Xiaori FU Muhammad DANISH Mark L. BRUSSEAU Zhaofu QIU Qian SUI 《Frontiers of Environmental Science & Engineering》2016,10(3):502-512
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 H2O2 generation. The generation of HO? and O2-? 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 O2-? 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-, HCO3-, 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. 相似文献
7.
Caiyan Qu Lushan Li Fan Feng Kainian Jiang Xing Wu Muchuan Qin Jia Tang Xi Tang Ruiyang Xiao Di Wu Chongjian Tang 《Frontiers of Environmental Science & Engineering》2023,17(9):115
8.
Zecong Yu Keke Xiao Yuwei Zhu Mei Sun Sha Liang Jingping Hu Huijie Hou Bingchuan Liu Jiakuan Yang 《Frontiers of Environmental Science & Engineering》2022,16(6):80
9.
Jing Ding Wanyi Seow Jizhong Zhou Raymond Jianxiong Zeng Jun Gu Yan Zhou 《Frontiers of Environmental Science & Engineering》2021,15(1):7
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11.
Sodium-jarosite is a type of industrial waste that results from hydrometallurgy and inorganic chemical production. The iron content of jarosite residue may be utilized to produce theoretically the ferrous materials. The difficulty in production of high quality poly-ferric sulfate (PFS) is how to remove impurities contained in jarosite residue. This paper proposes a novel method for disposing sodium-jarosite which can be used to synthesize PFS, a very important reagent for treating waste water. The method consists of a two-step leaching experimental procedures. The first step, pre-leaching process, is to remove impurity metals by strictly controlling the leaching conditions. The acid concentration of acidic water was adjusted according to the content of impurity metals in sodium-jarosite and the leaching temperature was controlled at 25°C. The second step is to decompose sodium-jarosite to provide enough ferric ions for synthesizing PFS, the concentrated sulfuric acid consumption was 0.8 mL·g-1 sodium-jarosite and the leaching temperature was above 60°C. In the experiment, decomposing iron from sulfate sodium-jarosite can take the place of ferric martials for synthesizing PFS. Results show that the PFS synthesized from sodium-jarosite had a high poly-iron complex Fe4.67(SO4)6(OH)2·20H2O. Further, the PFS product’s specifications satisfied the national standard of China. 相似文献
12.
Hongmei ZHU Weiying CHEN Xuguang JIANG Jianhua YAN Yong CHI 《Frontiers of Environmental Science & Engineering》2015,9(2):230
Under both pyrolysis and combustion condition, HCl removal efficiency for medical waste with Ca-based additives was semi-quantitatively studied by means of TG-FTIR. Additionally, the difference of HCl removal efficiency for PVC and medical waste was compared. Experimental results showed that: 1) Thermal degradation of medical waste mainly took place in two steps under both pyrolysis and combustion condition; 2) HCl emitted at both two steps and HCl concentration increased with the increased of Cl ratio in the medical waste; 3) for the same additive, HCl concentration decreased with the increased of additives amount, that is to say, HCl removal efficiency of medical waste increased as the increased of Ca/Cl molar ratio. Fourth, when Ca(OH)2 was used as additive, HCl removal efficiency for medical waste combustion was a little higher than that for medical waste pyrolysis, but either CaCO3 or CaO was used as additive, it was just opposite, more specifically, when CaCO3 was used as additive with Ca/Cl=1.3, HCl removal efficiency was 5.49% under pyrolysis condition, but that was only 4.24% under combustion condition. Fifth, under the same Ca/Cl molar ratio, HCl removal efficiency for PVC was higher than that for medical waste under both pyrolysis and combustion condition, more specifically, when Ca(OH)2 was used as additive with Ca/Cl=1, HCl removal efficiency was 64.51% for PVC, but that was only 27.66% for medical waste pyrolysis with 4% Cl under pyrolysis condition. 相似文献
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14.
Liqin JI Xue BAI Lincheng ZHOU Hanchang SHI Wei CHEN Zulin HUA 《Frontiers of Environmental Science & Engineering》2013,7(3):442-450
A simple solvothermal method was used to prepare monodisperse magnetite (Fe3O4) nanoparticles attached onto graphene oxide (GO) sheets as adsorbents to remove tetrabromobisphenol A (TBBPA) from an aqueous solution. These Fe3O4/GO (MGO) nanocomposites were characterized by transmission electron microscopy. The adsorption capacity at different initial pH, contact duration, and temperature were evaluated. The kinetics of adsorption was found to fit the pseudo-second-order model perfectly. The adsorption isotherm well fitted the Langmuir model, and the theoretical maximum of adsorption capacity calculated by the Langmuir model was 27.26 mg?g-1. The adsorption thermodynamics of TBBPA on the MGO nanocomposites was determined at 303 K, 313 K, and 323 K, respectively. The results indicated that the adsorption was spontaneous and endothermic. The MGO nanocomposites were conveniently separated from the media by an external magnetic field within several seconds, and then regenerated in 0.2 M NaOH solution. Thus, the MGO nanocomposites are a promising candidate for TBBPA removal from wastewater. 相似文献
15.
Jiwan SINGH Yoon-Young CHANG Jae-Kyu YANG Seon-Hong KANG Janardhan Reddy KODURU 《Frontiers of Environmental Science & Engineering》2016,10(4):9
Phenol removal by n/m Fe in the presence of H2O2 was highly effective.
Increasing the amounts of n/m Fe and H2O2?increased the phenol removal rate.
Phenol removal was decreased with an increase in the concentration of phenol.
The natural pH (6.9) of the solution was highly effective for phenol removal.
The pseudo-first-order kinetics was best fitted for the degradation of phenol.
The study investigates the magnetic separation of Fe from automobile shredder residue (ASR) (<0.25 mm) and its application for phenol degradation in water. The magnetically separated Fe was subjected to an ultrasonically assisted acid treatment, and the degradation of phenol in an aqueous solution using nano/micro-size Fe (n/m Fe) was investigated in an effort to evaluate the possibility of utilizing n/m Fe to remove phenol from wastewater. The prepared n/m Fe was analyzed by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The effects of the dosages of n/mFe, pH, concentration of phenol and amount of H2O2 on phenol removal were evaluated. The results confirm that the phenol degradation rate was improved with an increase in the dosages of n/mFe and H2O2; however, the rate is reduced when the phenol concentration is higher. The degradation of phenol by n/mFe followed the pseudo-first-order kinetics. The value of the reaction rate constant (k) was increased as the amounts of n/m Fe and H2O2 increased. Conversely, the value of k was reduced when the concentration of phenol was increased. The probable mechanism behind the degradation of phenol by n/m Fe is the oxidation of phenol through hydroxyl radicals which are produced during the reaction between H2O2 and n/m Fe. 相似文献
16.
Giovanni Cagnetta Kunlun Zhang Qiwu Zhang Jun Huang Gang Yu 《Frontiers of Environmental Science & Engineering》2019,13(1):11
17.
Yanxiao Si Fang Zhang Hong Chen Guanghe Li Haichuan Zhang Dun Liu 《Frontiers of Environmental Science & Engineering》2021,15(6):112
18.
石灰性土壤环境中缺锌机理的探讨 总被引:3,自引:0,他引:3
作者认为石灰性土壤中锌活性较低的原因,是由于碳酸盐导致土壤pH上升,在较高pH条件下氧化铁对锌的强烈固定,造成了大量专性吸附状态的氧化铁结合态锌及部份碳酸盐结合态锌,使交换态的有效锌含量很低,同时还证明:自然的石灰性土壤中,松结有机态锌与碳酸盐结合态是活性锌的直接给源,外源加入的锌仅为松结右机态锌。此外,石灰性土壤中各主要土壤的化学组份对外源锌的固定量高伛顺序为:氧化铁>有机质>粘土矿物>碳酸盐>氧化锰:对土壤中原有锌的固定作用大小依次为:粘土矿物>氧化铁>有机质>氧化锰>碳酸盐。 相似文献
19.
Xiaoyan SHI Kebin HE Weiwei SONG Xingtong WANG Jihua TAN 《Frontiers of Environmental Science & Engineering》2012,6(4):463-469
The effects of a diesel oxidation catalytic (DOC) converter on diesel engine emissions were investigated on a diesel bench at various loads for two steady-state speeds using diesel fuel and B20. The DOC was very effective in hydrocarbon (HC) and CO oxidation. Approximately 90%–95% reduction in CO and 36%–70% reduction in HC were realized using the DOC. Special attention was focused on the effects of the DOC on elemental carbon (EC) and organic carbon (OC) fractions in fine particles (PM2.5) emitted from the diesel engine. The carbonaceous compositions of PM2.5 were analyzed by the method of thermal/optical reflectance (TOR). The results showed that total carbon (TC), OC and EC emissions for PM2.5 from diesel fuel were generally reduced by the DOC. For diesel fuel, TC emissions decreased 22%–32% after the DOC depending on operating modes. The decrease in TC was attributed to 35%–97% decrease in OC and 3%–65% decrease in EC emissions. At low load, a significant increase in the OC/EC ratio of PM2.5 was observed after the DOC. The effect of the DOC on the carbonaceous compositions in PM2.5 from B20 showed different trends compared to diesel fuel. At low load, a slight increase in EC emissions and a significant decrease in OC/EC ratio of PM2.5 after DOC were observed for B20. 相似文献
20.
Yali Chang Jianwei Cao Wenfeng Song Zhi Wang Chenyang Xu Mengzhuo Long 《Frontiers of Environmental Science & Engineering》2023,17(10):128