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991.
在热重分析仪上,以1 000℃预煅烧5h铜渣为催化剂,在氧气气氛下,进行生物质的催化气化实验.在预煅烧铜渣/生物质(质量比)为0.5~2.5范围内,考察铜渣的催化性能.实验结果表明,在所研究的比例范围内,生物质热解阶段和气化阶段的最大失重速率呈现先增大后减小的趋势,且在比例为2时都达到最大值.研究表明,铜渣中的铁氧化物在气化过程中被还原为金属Fe和FeO,而生成的FeO与SiO2反应生成Fe2SiO4.在铜渣与生物质混合催化气化反应中,金属Fe从铜渣中的铁氧化物中被还原出来而提供了活性位,表明铜渣因含有易还原的铁元素而具有催化作用.  相似文献   
992.
膜生物反应器(MBR)是一种高效的污水处理工艺,而微生物燃料电池(MFC)能利用NO-3作为电子受体进行脱氮。为解决膜生物反应器(MBR)脱氮效率低和膜污染问题,建立了一套能够进行脱氮、有效抑制膜污染的一体式MFC-好氧MBR新工艺。以开路MFC-MBR反应器为对照,对耦合系统中污水处理效果、膜污染情况进行研究。研究表明,2套系统的COD去除率均超过88%,对NH4-N的去除均达到99%。闭路MFC-MBR系统TN去除率达到69.4%,高于开路系统的55.3%。混合液的MLVSS/MLSS稳定在88%左右,同时耦合系统能够改善污泥混合液的性质,zeta电位的绝对值和粘度较开路系统有所减少,污泥颗粒平均体积粒径(233.482μm)较开路系统(94.877μm)有明显增加,膜清洗周期延长了41.17%。  相似文献   
993.
构建了双室微生物燃料电池(MFC),并应用于污水BOD的检测。优化了MFC型BOD传感器的检测条件,分析了传感器进行污水BOD检测的特征。结果表明,以A2/O污水处理工艺中厌氧段污泥进行接种,双室MFC型BOD传感器2周内完成启动,所产电流达到稳定。传感器的最佳检测条件为外接电阻500Ω,添加缓冲溶液并维持待测水样pH为7.0,添加35 mg/L的L-半胱氨酸作为吸氧剂维持阳极室厌氧环境,阴极室富氧水流量为20 mL/min。利用MFC产生的电流峰值准确检测污水水样BOD浓度,传感器检测范围为10~50 mg/L,检测时间小于3 h;利用MFC产生的电荷量准确检测污水水样BOD浓度,检测范围为10~100 mg/L,检测时间小于10 h。利用MFC电流峰值和电荷量检测污水水样BOD浓度,偏差均小于15%,传感器运行稳定,寿命较长。  相似文献   
994.
阴极催化性能及材料对微生物燃料电池(microbial fuel cells,MFCs)的产电特性及制造成本有很大影响。本研究选用金属铂(Pt)、活性炭作为催化剂、聚四氟乙烯(PTFE)和道康宁1-2577作为阴极的扩散层、碳布和不锈钢网作为阴极的基体材料制备得4种阴极,分别考察了相应MFC的产电性能和阴极特性。结果表明,采用传统Pt催化剂+PTFE扩散层+碳布制备成的阴极(Pt-PTC),MFC的最大输出电压为560 mV,最大功率密度为808 mW/m2,而采用活性炭+道康宁1-2577+不锈钢网制备成的阴极(AC-DCS),MFC的最大输出电压为510 mV,最大功率密度为726 mW/m2,两者的MFC产电性能极为接近。SEM结果表明,活性炭催化层表面和道康宁1-2577扩散层分别比Pt催化层及PTFE扩散层的更均匀光滑。阴极线性伏安测定结果表明,AC-DCS与Pt-PTC的电化学氧化性能较为接近。AC-DCS阴极成本仅为Pt-PTC的1/300左右,是一种低成本扩大化生产MFC阴极的新方法。  相似文献   
995.
脱氮副球菌YF1微生物燃料电池生物阴极脱氮和产电   总被引:1,自引:0,他引:1  
以脱氮副球菌YF1构建纯种生物阴极微生物燃料电池(microbial fuel cell,MFC)进行脱氮和产电机理的研究。研究结果发现,阴极碳氮比、pH值对产电和脱氮效率有明显影响。当MFC的阴极运行条件pH值为8.0,碳氮比为20时,运行时间15 h时,脱氮率高达100%,输出电压为150 mV。上述结果表明,微生物燃料电池运行过程中,细菌降解硝酸根的机理为将硝酸根还原为N2或者直接将其作为自身的营养物质而利用。循环伏安(CV)与扫描电镜(SEM)的结果表明,在微生物燃料电池运行中,副球菌YF1通过接触导电作为产电的电子供体。  相似文献   
996.
A study was performed selecting one protected forest and an adjacent degraded forest ecosystem to quantify the impact of forest degradation on soil inorganic nitrogen, fine root production, nitrification, N-mineralization and microbial biomass N. There were marked seasonal variations of all the parameters in the upper 0–10 and lower 10–20 cm depths. The seasonal trend of net nitrification and net N-mineralization was reverse of that for inorganic nitrogen and microbial biomass N. Net nitrification, net N-mineralization and fine root biomass values were highest in both forests during rainy season. On contrary, inorganic nitrogen and microbial biomass N were highest during summer season. There was a marked impact of forest degradation on inorganic nitrogen, fine root production nitrification, N-mineralization and microbial biomass observed. Soil properties also varied with soil depth. Fine root biomass, nitrification, N-mineralization and microbial biomass N decreased significantly in higher soil depth. Degradation causes decline in mean seasonal fine root biomass in upper layer and in lower depth by 37% and 27%, respectively. The mean seasonal net nitrification and N-mineralization in upper depth decreased by 42% and 37%, respectively and in lower depth by 42.21% and 39% respectively. Similarly microbial biomass N also decreased by 31.16% in upper layer 33.19% in lower layer.  相似文献   
997.
The abundance and biomass of phytoplankton and zooplankton proved to noticeably decrease after the water passed through the cooling system of the Beloyarsk Nuclear Power Plant: the phytoplankton perished by 38% (65 metric tons per day), and the zooplankton, by 55% (6 t/day). In the period between 1985 and 1991, the concentration of60Co in the plankton of water intake and discharge canals varied from 120 to 1400 Bq/kg dry weight, and that of137Cs, from 150 to 1040 Bq/kg dry weight, which is commensurable with the content of radionuclides in the plants and grounds of the Beloyarsk reservoir. In 1985, it was noted that the plankton passing through the cooling system of the nuclear power plant became enriched with Ca, Fe, Mg, Mn, Co, Cs, Cu, Mo, Ni, Pb, Si, Sn, Ti, V, and W.  相似文献   
998.
The main solid waste product from coal-fired power stations is pulverised fuel ash (PFA), which can be enriched in toxic elements. Disposal of PFA by dry (in landfills) or wet (by slurrying) disposal methods can release these elements into the environment. Thereafter, the contaminants can be taken up by biota such as Eichhornia crassipes, a common aquatic plant, which has the ability to accumulate elements from water. This study investigates the uptake of Cd, Cu, Ni and Zn by E. crassipes grown in leachates and slurries prepared from two different PFA samples. PFA samples were obtained from Indraprastha Power Station (IPP Stn.) in New Delhi, India and the Ratcliffe-on-Soar Power Station in the UK. E. crassipes grown in PFA leachates and slurries at 1:5 and 1:50 solid:liquid (PFA:deionised water) ratios show that the plant has a very high accumulation capacity for Cd, Cu, Ni and Zn from both leachates and slurries and the uptake of these metals is stronger in the roots than in the tops of the plant. Metal accumulation, as shown by the accumulation factor (AF) values, is higher from both leachates and slurries for plants grown in the 1:50 (PFA:DIW) ratios than in the 1:5 ratios, initial metal concentrations being higher in the 1:5 ratios than in the 1:50 ratios. Lower metal accumulation in the plants grown in slurries than in leachates is related to the high turbidity of growth medium in slurries resulting in ash particles adhering to the root surfaces thus reducing the surface area of metal absorption. Eichhornia plants are able to reduce the pH of all leachates, especially the highly alkaline Ratcliffe leachates to near neutral conditions. Accumulation of Cd and Zn by the plant is higher from the lower pH IPP leachates than the Ratcliffe leachates, indicating that these metals are more soluble and bioavailable in the acidic medium. However, accumulation of Cu and Ni is independent of the pH of the leachates, indicating that other factors, such as metal species, presence of complexing agents in the growth solutions, and effects of competing metal ions may be contributory factors towards the metal uptake and accumulation by the plant.  相似文献   
999.
This study was aimed at establishing the feasibility of microalgae biomass acquisition from waters of the Vistula Lagoon with the use of an installation operating in the fractional–technical scale, and at determining the effectiveness of biogas production from the acquired substrate. Depending on the technological solution of the concentration process, the degree of aquatic biomass hydration ranged from 99.6 to 97.90%. The quantity of biogas produced during methane fermentation fitted within the range of 243.9 to 395.2 dm3/kg d.m.. The values achieved were found to depend directly on the concentration of organic matter in the acquired water biomass and on system’s loading with a feedstock of organic compounds. The content of methane in a gaseous mixture ranged from 41.4 to 61.9%. The biomass produced was predominated by taxa belonging to Cyanoprokaryota, Bacillarophyceae, and Chlorophyta.  相似文献   
1000.
Safe and reliable metal hydride canisters (MHCs) for the use of hydrogen storage at low pressure can be applied to supply small fuel cell vehicles or scooters with hydrogen fuel. However, greater cost-effectiveness of hydrogen gas is obviously necessary to the successful promotion of hydrogen fuel cell scooters in the market. In this study, we use the net present value (NPV) method to evaluate the feasibility of an investment project on the supply of purified hydrogen in a pulp company at Hualien, Taiwan. The purified hydrogen can be separated from waste hydrogen by using pressure swing adsorption (PSA) technology and then be stored in MHCs. Under some assumptions of improved parameters about hydrogen production cost and hydrogen gas price, the discounted payback period of hydrogen purification and storage project in our study can be less than 10 years and the unit cost of hydrogen gas can be close to the price of gasoline. Moreover, the unit cost of hydrogen gas in our study can be lower than the cost from other sources of hydrogen.  相似文献   
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