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961.
962.
Risky Ayu Kristanti Masahiro Kanbe Tadashi Toyam Yasuhiro Tanak Yueqin Tang Xiaolei Wu Kazuhiro Mori 《环境科学学报(英文版)》2012,24(5):800-807
We investigated the biodegradation of 2-nitrophenol (2-NP), 4-nitrophenol (4-NP), and 2,4-dinitrophenol (2,4-DNP) in the rhizosphere of Spirodela polyrrhiza plants by conducting degradation experiments with three river water samples supplemented with each nitrophenol (NP). We then isolated NP-degrading bacteria both from the S. polyrrhiza roots and from the river water. In the river water samples, removal of the three NP was accelerated in the presence of S. polyrrhiza plants. The three NPs persisted in an autoclaved solution with sterile plants suggests that NP removal was accelerated largely by bacterial NP biodegradation rather than by adsorption and uptake by the plants. We isolated 8 strains of NP-degrading bacteria: 6 strains from the S. polyrrhiza roots and 2 strains from river water without the plants. The 2-NP- and 2,4-DNP-degrading bacteria were isolated only from the S. polyrrhiza roots. The 4-NPdegrading bacteria different from those isolated from the river water samples were also found on S. polyrrhiza roots. The 2-NP- and 4-NP-degrading strains isolated from the roots utilized the corresponding NP (0.5 mmol/L) as the sole carbon and energy source. The 2,4-DNP-degrading strains isolated from the roots showed substantial 2,4-DNP-degrading activity, but the presence of other carbon and energy sources was required for their growth. The isolated NP-degrading bacteria from the roots must have contributed to the accelerated degradation of the three NPs in the rhizosphere of S. polyrrhiza. Our results suggested that rhizoremediation with S. polyrrhiza may be effective for NP-contaminated surface water. 相似文献
963.
964.
生物可降解络合剂聚天冬氨酸治理土壤重金属污染 总被引:5,自引:0,他引:5
土壤重金属污染会产生严重的生态环境问题,土壤淋洗技术可达到土壤修复的目的,其中络合剂的选择是达到安全、有效修复效果的关键.聚天冬氨酸(PASP)可生物降解,对环境安全.文章选择PASP作为重金属的络合剂,研究其修复土壤重金属污染的效果.结果表明,PASP对金属离子Cd、Zn和Ca均有较好的提取率,均超过50%,并且络合剂/重金属的摩尔比越高,提取效果越好,受pH的影响就越少,提取速率开始比较快,而后趋于平缓.在PASP络合物的形态分布中,在pH较低阶段,PASP-Cd络合物所占的比例较大,随着pH的升高,PASP-Zn和PASP-Ca的比例增加,同时微生物对聚天冬氨酸的降解作用对治理效果产生负面影响.PASP可作为环保型的络合剂,达到修复土壤重金属污染的目的. 相似文献
965.
生态系统的数据结构不同于商用数据结构。本文参考美国LTERN的Sevilleta站生态系统的数据管理模式,结合中国科学院封丘农业生态实验站的实际情况,着重介绍了生态系统的数据文档文件的特点、结构和应用,而这些都是研究生态系统数据管理的最基础工作。 相似文献
966.
不同染料化合物在天然锰矿界面的脱色特性 总被引:41,自引:0,他引:41
本文考察了染料化合物在天然锰矿界面脱色特性,并探讨溶液pH值、环境温度、不 照射及颗粒物浓度和粒径对脱色效果的影响。实验表明,溶液pH值是影响染料脱色效果的最主要因素,光照对不同染料化合物脱色有不同程度的影响。颗粒物浓度升高及粒径降低有利于染料脱色,温度升高,直接耐晒红F3B脱色率提高,将不同温度下,该染料脱色率随时间的变化按一级反应动力学方程模拟,再依据阿累尼乌斯方程,求得直接耐晒红F3B在天然 相似文献
967.
城市工业区周边土壤-水稻系统中重金属的迁移累积特征 总被引:7,自引:0,他引:7
对H市工业区土壤-稻米-谷壳体系中重金属的迁移累积特征进行分析,结果显示,不同重金属元素的迁移累积特征不同,Cd易于从土壤中向稻谷籽实迁移,而Cu,Zn,Cr,Ni,As和Hg等迁移能力则较弱.水稻籽实中不同重金属在稻米和谷壳之间的分配规律不同.营养元素Cu和Zn有向稻米迁移累积的趋势,而有毒有害重金属Pb,Cd,Cr,Ni和As则主要累积于谷壳中,Cr和Nj在稻米和谷壳之间的分配较均衡.重金属在稻米中的累积能力为:Cd>Zn>Ni>Cu>Pb>Cr>Hg>As,而在谷壳中则为:Cd>Pb>Ni>Zn>Cr>Cu>As>Hg. 相似文献
968.
五种农药对三唑酮光解的影响 总被引:8,自引:0,他引:8
本文研究了氯氰菊酸,溴氰菊酯,多菌灵,γ-六六六及辛硫磷等五种农药对杀菌剂三唑酮光化学降解的影响,当三唑酮分别与这五种农药以等剂量混合光照后,三唑酮的光解速度加快1.44-2.42倍,表现了较强的光敏降解效应,其敏化光解效率我照时间延长而逐渐提高,当三唑酮分别与这五种农药以2:1剂量比混合光照后,仅溴氰菊酯.多菌灵表现敏化降解效应,而氯氰菊酯,γ-六六六及辛硫磷则显示光猝灭降解效应,五种农药对三唑 相似文献
969.
Yu Y Huang Q Wang Z Zhang K Tang C Cui J Feng J Peng X 《Journal of environmental monitoring : JEM》2011,13(4):871-878
The occurrence and behavior of β-blockers, antiepileptic drug carbamazepine and its metabolites, X-ray contrast agent iopromide, natural and synthetic hormones, and several groups of hormone-like personal care products (PCPs), including antiseptics (triclocarban, triclosan, and 2-phenylphenol), parabens and bisphenol A, were investigated in municipal wastewater, sewage sludge, and urban river water of the Pearl River Delta, South China. The pharmaceuticals, natural hormones and PCPs were ubiquitously detected in the raw wastewater from a sewage treatment plant (STP). Only triclocarban and triclosan were detected at significant amounts in the dewatered sludge. Iopromide and the PCPs were greatly removed/transformed from the aqueous phase of the wastewater. The β-blockers were only moderately removed/transformed. Carbamazepine passed through the STP almost unchanged. Biodegradation was the dominant process for elimination/transformation of the pharmaceuticals, hormones, and most PCPs in the STP. However, sorption also played an important role in the fate of triclocarban with nearly 50% of the mass load entering the STP ended up and persisted in the dewatered sludge. The pharmaceuticals, estrone, and PCPs were also widely detected in the Pearl River at Guangzhou. Bisphenol A had the highest concentration. The pharmaceutical concentrations in the Pearl River were higher in March than in May, most likely due to less dilution by lower precipitation. The omnipresence and high levels of the pharmaceuticals and PCPs in the Pearl River may be associated with direct discharge of untreated wastewater and pose potential risks to the ecological system. 相似文献
970.
Using the ionic liquid(IL)1-octyl-3-methylimidazolium hexafluorophosphate as the extractant and methanol as the dispersion solvent,a dispersive liquid–liquid microextraction method was developed to extract silver nanoparticles(AgN Ps)from environmental water samples.Parameters that influenced the extraction efficiency such as IL concentration,pH and extraction time were optimized.Under the optimized conditions,the highest extraction efficiency for AgN Ps was above 90% with an enrichment factor of 90.The extracted AgN Ps in the IL phase were identified by transmission electron microscopy and ultraviolet–visible spectroscopy,and quantified by inductively coupled plasma mass spectrometry after microwave digestion,with a detection limit of 0.01 μg/L.The spiked recovery of AgN Ps was 84.4% with a relative standard deviation(RSD)of 3.8%(n = 6)at a spiked level of 5 μg/L,and 89.7% with a RSD of 2.2%(n = 6)at a spiked level of 300 μg/L,respectively.Commonly existed environmental ions had a very limited influence on the extraction efficiency.The developed method was successfully applied to the analysis of Ag NPs in river water,lake water,and the influent and effluent of a wastewater treatment plant,with recoveries in the range of 71.0%–90.9% at spiking levels of 0.11–4.7 μg/L. 相似文献