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921.
重金属污染土壤植物修复及进展 总被引:4,自引:0,他引:4
土壤污染是当今面临的一个重要环境问题。常规的土壤污染物理化学治理技术 ,如客土换土法、冲洗法、热处理、固化、玻璃化、动电修复法等 ,由于其技术要求高或经济成本高昂 ,对土壤结构的扰动破坏较严重 ,因而 ,大规模推广应用存在较大问题。重金属超累积植物的不断发现 ,使人们认识到有可能利用植物于土壤污染的治理修复。自 2 0世纪 90年代起 ,植物修复成为环境污染治理研究领域的一个前沿性课题。研究表明 ,通过植物的吸收、挥发、根滤、稳定等作用 ,可以净化土壤或水体中金属污染物 ,达到净化环境的目的。近 10年来 ,在超累积植物的找寻培育、植物根际微生物共存体系研究、植物对重金属的耐忍性、超量吸收及其解毒机制以及植物修复的工艺技术方面已有不少研究 ,并取得长足的进展 ,现代分子生物学的发展以及基因工程技术的应用有可能使植物修复技术取得根本性的突破。 相似文献
922.
Trace metal emissions from co-combustion of refuse derived and packaging derived fuels in a circulating fluidized bed boiler 总被引:3,自引:0,他引:3
Helena Manninen Annikki Perkiö Juha Palonena Karl Peltola Juhanl Ruuskanen 《Chemosphere》1996,32(12):2457-2469
Energy recovery from refuse derived fuels (RDF) and packaging derived fuels (PDF) is one option in integrated waste management. Nine RDF and PDF co-combustion tests with peat and coal in a circulating fluidized bed boiler were carried out in this work. Heavy metal emissions in flue gas and fly ash were measured. Multivariate data analyses were used to find out the most important parameters affecting metal emissions in the flue gas.
The results showed that total heavy metal emissions were low. Although RDF and PDF had more heavy metals than peat and coal, the multivariate data analysis showed that an increase of the RDF or PDF share in the fuel mixture up to 20% did not correlate directly with the metal emissions in the flue gas. Distribution of Cd, Cu, Zn and Sn between flue gas and fly ash correlated with each other. Injection of limestone to bind sulphur and chlorine did not have a significant effect on heavy metal emissions in the flue gas. Heavy metals concentrated on the fly ash, but all fly ashes passed the EPA-TCLP tests. 相似文献
923.
924.
稀土金属具有一些特殊的性能,这使得其对碳质材料还原NO的反应可能表现出特殊的催化效果,而此方面的研究没有报道.为了研究稀土金属对活性炭还原NO反应的催化效果,采用浸渍法制备了负载氧化镧的活性炭颗粒(La/C),并在无氧的固定床反应器中进行了程序升温反应和等温反应,考察了气体流量、NO的入口浓度、反应温度和氧化镧负载量对反应活性的影响,同时对反应机理和动力学进行了初步探讨.研究结果表明负载氧化镧的活性炭还原NO的反应是一级反应.由于炭表面3%(质量分数)的氧化镧的存在,C-NO反应的起始反应温度从500 ℃降低到300 ℃,反应活性大大提高,反应活化能从88.95 kJ/mol降低到51.05 kJ/mol.氧化镧的负载量对反应活性有重要影响,但负载量的大量增加对反应活性的提高效果甚微,最佳负载量为1.5%.La/C体系在反应中较稳定,而反应温度的升高对其稳定性不利. 相似文献
925.
机械工业废水中重金属离子的处理工艺研究 总被引:4,自引:0,他引:4
研究了过氧化钙处理剂对机械工业废水中重金属离子锰、铜、锌、铬的处理工艺,以及过滤方法对重金属离子去除率的影响。处理的最佳条件为:过氧化钙用量0.1%~0.2%,处理时间30min,处理温度为室温,处理过程中不需调整pH。 相似文献
926.
Metal complexation by natural ligands is important for metal transport and distribution in surface and ground water. The goal of the work was to study the ligand exchange rate for two important metal ions in natural aquatic systems (Al, Fe) was determined using EDTA and natural organic matter (NOM) of humic type as ligands. After adding EDTA to a solution containing metal-NOM complexes, these complexes dissociated and metal-EDTA complexes were formed. Metal-NOM complexes were separated from metal-EDTA complexes with the help of size-exclusion chromatography and detected by on-line inductively coupled plasma-mass spectrometry (ICP-MS). Injecting the samples into the system over time after addition of EDTA allowed us to measure the rate of the exchange of NOM by EDTA. The experiments could be well described with a first-order rate law assuming that the dissociation of the metal-NOM complexes is the rate-determining step. The exchange rate of Fe was found to be faster than that of Al. This corresponds well with the exchange rate of water molecules from the coordination sphere of the metal ions, which is also faster for Fe than for Al. Furthermore, the UV and the fluorescence signal of the chromatograms were measured. The results indicate that no disaggregation of NOM molecules took place, although about 75-85% of the aggregate-forming metal ions exchanged NOM by EDTA in their coordination sphere. This suggests clearly the fundamental role of NOM in colloidal transport of metals and in their bioavailability. 相似文献
927.
Pesavento M Biesuz R Profumo A Soldi T 《Environmental science and pollution research international》2003,10(5):317-320
SCOPE: The detection and investigation of metal ions bound in strong complexes in natural waters is a difficult task, due to low concentration of the metal ions themselves, and also of the strong ligands, which, moreover, are often not of a well-defined composition. Here, a method is proposed for the investigation of the speciation of metal ions in natural waters. OBJECTIVE AND METHOD: It is based on the sorption of metal ions on strongly sorbing ion exchange resins, i.e. complexing resins. For this reason the method is called Resin Titration. It has been shown in previous investigations that the concentration of metal ion totally sorbed by a particular resin, and its reaction coefficient in the solution phase in the presence of the resin, can be determined from the sorption data using a simple relationship. Here, a data treatment (the Ruzic linearization method) is proposed for also determining the concentration of the ligands responsible for the complex in equilibrium with the resin. RESULTS: The method was applied to data obtained by Resin Titration of a freshwater and a seawater. Copper(II) and aluminium(III) were considered, using Chelex 100 as a titrant, due to its strong sorbing properties towards these metal ions. The results were: the total metal concentration in equilibrium with the resin, the side reaction coefficients, and the concentration of ligands. In all these cases the ligands forming very strong complexes were found to be at concentration lower than that of the metals. CONCLUSION: The Ruzic linearization method allows the determination of the concentration of the ligands forming very strong complexes in equilibrium with Chelex 100. The reaction coefficient was better determined by the calculation method previously proposed for RT. The ligands responsible for the strong complexes were found to be at low concentration, often lower than that of the metal ions considered. The metal in the original sample is partly bound to these ligands, since the complexes are very strong. Only a part of the metal is linked to weaker ligands, or free. 相似文献
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930.