共查询到20条相似文献,搜索用时 15 毫秒
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Removal of copper (II) and phenol from aqueous solution using porous carbons derived from hydrothermal chars 总被引:1,自引:0,他引:1
The feasibility of hydrothermal char (HTC), a byproduct from biomass hydrothermal liquefaction for bio-oil production, as raw material for preparation of porous carbons was investigated in the present study. The resultant HTC-derived porous carbons were characterized and utilized as adsorbents for copper (II) and phenol removal from aqueous solution. Compared with porous carbons using pyrolytic char as precursor, the HTC-derived porous carbons exhibited unique textural features, e.g., narrow pore size distribution, high surface area and large pore size. In addition, FT-IR analysis confirmed that substantial amount of ketene groups existed on the surface of the HTC-derived porous carbons. As the adsorbents, the copper (II) adsorption onto HTC-derived carbons was strongly affected by the pH value of the solution in comparison with phenol adsorption. The carbons derived from pinewood and rice husk HTC exhibited high adsorption capacity of 83.88 and 39.30 mg/g for phenol and 25.18 and 22.62 mg/g for copper (II), respectively. The adsorption data for copper (II) and phenol onto the carbon adsorbents could be well described by Langmuir and Freundlich models. In comparison with pinewood sawdust HTC-derived carbon, the adsorption onto rice husk HTC-derived carbon preferentially followed Freundlich model due to the presence of silica on the surface. 相似文献
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Eric Favre Quang Trong Nguyen Sophie Bruneau 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1996,65(3):221-228
The extraction of 1-butanol from fermentation broths by pervaporation offers potential for use in biotechnology. Various membrane materials have been screened for their suitability for this process. Polydimethylsiloxane (PDMS) membranes gave the best results in terms of flux and selectivity, with large variations depending on their nature and preparation. Selectivity was further increased by including either organophilic adorbents (cyclodextrins, zeolites), or oleyl alcohol in dense PDMS membranes. The predominance of driving force (i.e. activity gradient) on pervaporation extraction performances was shown by a comparative study on different binary aqueous solutions of alcohols. Water flux remained practically constant while the alcohol flux was linearly related to its feed concentration. The conclusions obtained with binary mixtures were consistent with those obtained with two model ternary solutions; the influence of salt on 1-butanol permeability was negligible, whereas ethanol had a strong effect. 相似文献
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利用铁炭内电解法处理酸性废水,研究了铁、炭、pH值、水力停留时间对此废水COD去除效果的影响。结果表明,通过铁炭内电解可使酸性废水COD去除率达83%。 相似文献
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Biofilter in water and wastewater treatment 总被引:1,自引:0,他引:1
Durgananda Singh Chaudhary Saravanamuthu Vigneswaran Huu-Hao Ngo Wang Geun Shim Hee Moon 《Korean Journal of Chemical Engineering》2003,20(6):1054-1065
Biofilter is one of the most important separation processes that can be employed to remove organic pollutants from air, water,
and wastewater. Even though, it has been used over a century, it is still difficult to explain theoretically all the biological
processes occurring in a biofilter. In this paper, the fundamental of biological processes involved in the biofilter is critically
reviewed together with the mathematical modeling approach. The important operating and design parameters are discussed in
detail with the typical values used for different applications. The most important parameter which governs this process is
the biomass attached to the medium. The relative merits of different methods adopted in the measurement of the biomass are
discussed. The laboratory-and full-scale applications of the biofilter in water and wastewater treatment are also presented.
Their performances in terms of specific pollutant removal are highlighted. 相似文献
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Alexander Hammerschmidt Nikolaos Boukis Elena Hauer Eckhard Dinjus Tommy Larsen 《Fuel》2011,90(2):555-562
The purpose of the work presented here is the production of liquid biofuels from wet organic waste matter in a continuous one-step catalytic process under hydrothermal conditions. The catalytic reaction of wet organic matter at near-critical water conditions (T > 300 °C, p > 22.1 MPa) is used to produce a mixture of combustible organics which can be used as liquid biofuel. In order to achieve a good product quality in a continuous one-step process, two catalysts were applied, a homogeneous potassium carbonate catalyst and a heterogeneous ZrO2 catalyst. In addition, the reaction mixture was recirculated. The continuous flow of concentrated waste biomass feed at low flow rates and recirculation of the hot reaction mixture were the most challenging obstacles to overcome. The scale of the plant (0.1 l reactor volume) allowed for a variation of the feed, reaction temperature, and recirculation rate in order to optimise the process conditions. Still, the product quantity obtained was sufficient to perform a analytical characterisation. The experimental results confirmed the feasibility of the process. Hydrothermal treatment of waste biomass, after dewatering, resulted in a biocrude oil of high calorific value. 相似文献
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This paper describes a study of the effects of hydrothermal dewatering of raw tropical peat from Pontianak, West Kalimantan-Indonesia, on the amounts of organic compounds released into wastewater and gaseous products. Hydrothermal upgrading and dewatering of the peat was carried out in a batch-type autoclave reactor at temperatures between 150 and 380 °C at a maximum pressure of 25.1 MPa for 30 min. It was found that the extent of decomposition of organics during hydrothermal dewatering depended on temperature increase.Wastewater from hydrothermal dewatering was found to contain organic carbon (TOC) ranging from 800 ppm at low temperatures, to 7504 ppm at high temperatures. A number of sugars and furans were detected in the wastewater at 250 °C, and organic acids and alcohols at all temperatures. Phenol and phenolic derivatives were observed at 250 °C, and significant amounts of CO2, CO and H2 were detected at all temperatures studied; CH4 was detected only at 380 °C, but at this temperature CO2 was no longer detected.A simplified schematic diagram of the decomposition behavior of tropical peat in the hydrothermal dewatering process is discussed with respect to the change in the concentration of organics in wastewater and gaseous products as determined by TOC, GC, GC–MS and 13C NMR analyses of the solids produced. 相似文献
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电解阳极间接氧化法处理制药废水的研究 总被引:4,自引:3,他引:4
通过在废水中加入NaCl电解质,考察了电解阳极间接氧化法制药废水的处理效果。实验分析了废水中电解质NaCl对制药废水电解过程中CODCr、色度去除的影响,并对不同用量NaCl电解效果进行了对比。另外还用电解质Na2SO4、NaNO3作了对比实验来说明NaCl产生的电解阳极间接氧化的存在。最后对甲红霉素废水进行中试实验,结果表明,NaCl电解产生的NaClO具有极强的氧化性,促进了CODCr的去除,同时还发现,废水中氨氮的存在不利于废水CODCr的去除。 相似文献
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介绍了应用铁屑内电解、中和混凝、兼氧、接触氧化工艺处理医药化工废水的工程实例。长期的运行结果表明,该工艺处理效果稳定、耐冲击负荷,并对工艺各处理阶段的成功之处作了总结。 相似文献
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Ammonium nitrate wastewater treatment by coupled membrane electrolysis and electrodialysis 总被引:2,自引:0,他引:2
E. Gain S. Laborie Ph. Viers M. Rakib G. Durand D. Hartmann 《Journal of Applied Electrochemistry》2002,32(9):969-975
A process coupling membrane electrolysis and electrodialysis is implemented to treat ammonium nitrate wastewater. Membrane electrolysis produces ammonia and nitric acid while electrodialysis reconcentrates the depleted salt solution. Ammonia is removed continuously by in situ stripping; thus allowing gas production with a constant current efficiency (about 70%). Nitric acid up to 8 mol L–1 is obtained. The current efficiency of acid production depends on nitric acid concentration. When this concentration varies from 1 to 8 mol L–1 the average current efficiency is about 58%. Electrodialysis produces a rejected stream containing less than 3 × 10–3 mol L–1 of ammonium nitrate. 相似文献
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A novel Ni/carbon catalyst recently developed by the authors was used to gasify organic compounds dissolved in the wastewater with TOC concentration from 0.2 to 2%. The process removes the organic compounds by gasifying them into high calorific gases like methane and hydrogen. The investigations were focused on the efficiency of the Ni/carbon catalyst in terms of carbon conversion, conversion of big organic molecules, and catalyst deactivation due to sintering. The preliminary results showed that up to 99% carbon conversion can be achieved at 360 °C, and 20 MPa. A conversion mechanism was suggested which consists of: first, decomposition of big molecules to small molecules on the metal surface, steam gasification of small molecules to produce CO and H2 followed by CO methanation and CO shift reaction to produce CH4 and CO2. The catalyst was found to be highly active and stable and no sintering was observed even after 100 h of reaction time. 相似文献
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内电解法处理印染废水的效果研究与分析 总被引:14,自引:0,他引:14
印染废水成分复杂、色度高、CODCr高且难降解,对环境造成较大污染。印染废水处理一般采用生化一混凝沉淀法、混凝气浮法、化学氧化及活性炭吸附法等,但这些方法存在运行费用较高、不易管理等缺点。内电解的基本原理是利用铁屑中的铁和炭组分构成微小原电池的正极和负极,以充入的废水为电解质溶液,发生氧化-还原反应,形成原电池。利用内电解对印染废水进行预处理,脱色率可达75%。90%,CODCr去除率达55%左右。另外还可提高废水的可生化性,废水的BOD5/CODCr值从原来的0.23提高到0.57,为后续生化处理和处理后达标排放奠定了基础,且运行成本低,易于管理。 相似文献
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分别以平板Ti/SnO_2网状电极和石墨为阳极和阴极,制作隔膜和无隔膜电解反应器并对比处理500mg/L自配氨氮溶液。在处理水量为3.6 L,电流密度为10 m A/cm2,有效阳极面积为1 440 cm~2,电流为0.8 A,反应时间70 min条件下,出水氨氮分别为74、222 mg/L,去除率分别为85.2%、55.6%;当两种反应器吨水电耗均为10.5k W·h时,出水氨氮分别为74、153 mg/L,去除率分别为85.2%、69.4%。在出水氨氮相同时,隔膜电解反应器在吨水电耗、电流效率以及反应速率方面均优于无隔膜电解反应器。 相似文献
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Characterization and application of chars produced from pinewood pyrolysis and hydrothermal treatment 总被引:4,自引:0,他引:4
Two types of pinewood chars, hydrothermal char (H300) and pyrolytic char (P700) from biomass-to-energy conversion were characterized and used as adsorbent for the copper removal from aqueous solution. The result showed that the pinewood underwent a deeper carbonization during pyrolysis process and more activated sites available and stable carbon-oxygen complex existed after hydrothermal treatment. Comparing with raw pinewood, hydrothermal treatment increased 95% total oxygen-containing groups (carboxylic, lactone and phenolic group) while 56% oxygen-containing groups decreased after pyrolysis process. SEM analysis indicated that both hydrothermal and pyrolytic processes developed rough surface with new cavities on the chars, and the BET surface area were 21 and 29 m2/g for H300 and P700, respectively. Although H300 had lower surface area, its adsorption capacity for copper was much higher than P700 since ion-exchange reaction was the predominant removal mechanism by H300, while physical adsorption dominated by P700. The adsorption data could be well described by Langmuir isotherm model for copper onto both H300 and P700. 相似文献