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101.
阿什河水系枯水期氮污染特征与同位素源解析 总被引:1,自引:0,他引:1
在阿什河水系设置20个采样点,采用水质监测技术和稳定氮同位素示踪技术,研究了枯水期阿什河氮污染特征和硝酸盐氮污染来源。结果表明:(1)阿什河枯水期大部分采样点氨氮浓度较低,大部分区域达到或优于《地表水环境质量标准》(GB3838—2002)中Ⅲ类。上游河段硝酸盐氮浓度较低,中游河段较高,到下游河段略有降低。总氮浓度较高,最高达19.4mg/L。(2)阿什河水系采样点15 N的丰度(δ15 N)主要处于0.11%~0.21%、0.42%~0.78%、0.83%~0.88%和1.09%~1.26%。稳定15 N同位素示踪解析阿什河硝酸盐氮污染来源表明,阿什河上游污染源主要为大气沉降、土壤有机氮和人工化肥;中游主要受畜禽养殖污水和生活污水污染;下游主要受城镇生活污水和工业废水影响。 相似文献
102.
农药混配制剂环境风险评估现状与展望 总被引:1,自引:0,他引:1
本文综述了欧洲和美国农药混配制剂的环境风险评估方法。详细介绍了欧洲食品安全局(EFSA)评估体系中的2种方法,即,基础的"整体测试法"和近年来提倡的"基于组分的方法"。"基于组分的方法"的特点是以浓度加和模型(CA模型)作为默认假设进行初级评估,以独立作用模型(IA模型)等作为高级评估手段的农药混配制剂环境风险评估方法。此外,本文还介绍了模型偏差率(MDR)、毒性相似度及毒力单元(TU)等概念以及混配制剂风险评估流程。本文的目的旨在为建立我国农药混配制剂的环境风险评估方法体系提供参考。 相似文献
103.
焦化厂环境粉尘中多环芳烃污染危害分析 总被引:4,自引:0,他引:4
分别采集某焦化厂办公区、新厂地面站、炼焦一车问、焦炉炉顶、老厂地面站环境中的粉尘样品,通过超声波萃取和高效液相的方法,测定了总悬浮颗粒物(TSP)、可吸入颗粒物(PM10)、苯并[a]芘(BaP)以及美国EPA优控的14种PAHs的浓度,并对照我国环境空气质量标准(GB3095—1996),分析了焦化厂环境粉尘中多环芳烃的污染状况。由分析可知,焦化厂环境中总悬浮颗粒物TSP的浓度(除了老厂地面站)、可吸入颗粒物PM10的浓度、苯并[a]芘的浓度均超过国家环境空气质量标准规定的限值。通过计算粉尘中多种PAHs相对于苯并[a]芘的等效浓度可知,粉尘中多种PAHs的共同作用,大大提高了粉尘的毒性。 相似文献
104.
厌氧膨胀床处理低浓度污水的污泥颗粒和生物活性变化 总被引:1,自引:0,他引:1
污泥的聚集形态和活性,是影响厌氧反应器处理效率的关键因素。通过对厌氧膨胀床反应器(anaerobicex—pandedblanketreactor,AEBR)处理低浓度城镇污水在启动和稳定运行期的污泥活性研究,AEBR在启动运行期内,接种颗粒污泥为适应低浓度基质条件,污泥粒径经历从大变小,再重新颗粒化粒径变大的过程。在运行期第103天,粒径小于1000μm污泥的体积比达到44.7%,平均粒径为952μm,到运行期第173天,粒径小于1000μm污泥的体积比降为28%,平均粒径达1179μm,污泥重新颗粒化完成。颗粒污泥适应新的环境后,单位重量污泥的最大比产甲烷活性(specificmetha.nogensisactivity,SMA)值和胞外聚合物含量增加,分别达到112mLCH4/(gVSS·d)和215mg/gVSS。在处理实际城镇污水的AEBR反应器内,辅酶F420含量可以有效指示污泥样品的产甲烷活性,AEBR反应器不同高度位置的污泥活性不一样,反应器底部污泥活性低于中上部区域污泥的活性。 相似文献
105.
106.
Shigekazu Hirao Hiromi Yamazawa Jun Moriizumi 《Journal of environmental radioactivity》2010,101(11):974-984
When used with an atmospheric transport model, the 222Rn flux distribution estimated in our previous study using soil transport theory caused underestimation of atmospheric 222Rn concentrations as compared with measurements in East Asia. In this study, we applied a Bayesian synthesis inverse method to produce revised estimates of the annual 222Rn flux density in Asia by using atmospheric 222Rn concentrations measured at seven sites in East Asia. The Bayesian synthesis inverse method requires a prior estimate of the flux distribution and its uncertainties. The atmospheric transport model MM5/HIRAT and our previous estimate of the 222Rn flux distribution as the prior value were used to generate new flux estimates for the eastern half of the Eurasian continent dividing into 10 regions.The 222Rn flux densities estimated using the Bayesian inversion technique were generally higher than the prior flux densities. The area-weighted average 222Rn flux density for Asia was estimated to be 33.0 mBq m−2 s−1, which is substantially higher than the prior value (16.7 mBq m−2 s−1). The estimated 222Rn flux densities decrease with increasing latitude as follows: Southeast Asia (36.7 mBq m−2 s−1); East Asia (28.6 mBq m−2 s−1) including China, Korean Peninsula and Japan; and Siberia (14.1 mBq m−2 s−1). Increase of the newly estimated fluxes in Southeast Asia, China, Japan, and the southern part of Eastern Siberia from the prior ones contributed most significantly to improved agreement of the model-calculated concentrations with the atmospheric measurements. The sensitivity analysis of prior flux errors and effects of locally exhaled 222Rn showed that the estimated fluxes in Northern and Central China, Korea, Japan, and the southern part of Eastern Siberia were robust, but that in Central Asia had a large uncertainty. 相似文献
107.
采用牡蛎壳为曝气生物滤池填料,以含NaCl的生活污水为处理对象,在SBR操作条件下,系统考察进水NaCl浓度、曝气时间及进水pH值等对硝化性能的影响。结果表明,进水NaCl浓度为10~15 g/L时,平均氨氮去除率可稳定在97%以上;较高浓度NaCl对亚硝酸化菌活性影响较弱,对硝酸化菌活性影响较强,特别是在日曝气时间少于12 h时,其出水中亚硝氮的含率大于50%;当进水pH值在6~9变化时,反应器内pH值可稳定在6.5~7.5,硝化性能良好,表明牡蛎壳填料可为硝化反应提供碱度。 相似文献
108.
研究了UV/Fenton技术对高浓度金属清洗乳化油废水的处理效果,考察了亚铁与双氧水浓度、pH、反应时间和搅拌对COD去除效果的影响。实验结果表明,UV/Fenton技术对高浓度乳化油废水(COD平均浓度为35 000 mg/L)具有较高的去除效果,最佳工艺条件为:亚铁与双氧水浓度分别为2 400 mg/L和6 000 mg/L,pH为3,经过2 h反应,COD可降低至1 050 mg/L,去除率为97%。搅拌会降低COD的去除率。研究表明,UV/Fenton技术对高浓度乳化油废水具有很好的降解效果,且药品消耗较低,为目前此类高浓度有机废水的处理提供了技术参考。 相似文献
109.
110.
Siedlecka EM Stepnowski P 《Environmental science and pollution research international》2009,16(4):453-458
Background, aim, and scope Ionic liquids are regarded as essentially “green” chemicals because of their insignificant vapor pressure and, hence, are
a good alternative to the emissions of toxic conventional volatile solvents. Not only because of their attractive industrial
applications, but also due to their very high stability, ionic liquids could soon become persistent contaminants of technological
wastewaters and, moreover, break through into natural waters following classical treatment systems. The removal of harmful
organic pollutants has forced the development of new methodologies known as advanced oxidation processes (AOPs). Among them,
the Fenton and Fenton-like reactions are usually modified by the use of a higher hydrogen peroxide concentration and through
different catalysts. The aim of this study was to assess the effect of hydrogen peroxide concentration on degradation rates
in a Fenton-like system of alkylimidazolium ionic liquids with alkyl chains of varying length and 3-methyl-N-butylpyridinium chloride.
Materials and methods The ionic liquids were oxidized in dilute aqueous solution in the presence of two different concentrations of hydrogen peroxide.
All reactions were performed in the dark to prevent photoreduction of Fe(III). The concentrations of ionic liquids during
the process were monitored with high-performance liquid chromatography. Preliminary degradation pathways were studied with
the aid of 1H NMR.
Results Degradation of ionic liquids in this system was quite effective. Increasing the H2O2 concentration from 100 to 400 mM improved ionic liquid degradation from 57–84% to 87–100% after 60 min reaction time. Resistance
to degradation was weaker, the shorter the alkyl chain.
Discussion The compound omimCl was more resistant to oxidation then other compounds, which suggests that the oxidation rates of imidazolium
ionic liquids by OH· are structure-dependent and are correlated with the n-alkyl chain length substituted at the N-1-position. The level of degradation was dependent on the type of head group. Replacing
the imidazolium head group with pyridinium increased resistance to degradation. Nonetheless, lengthening the alkyl chain from
four to eight carbons lowered the rate of ionic liquid degradation to a greater extent than changing the head group from imidazolium
to pyridinium. 1H-NMR spectra show, in the first stage of degradation, that it is likely that radical attack is nonspecific,
with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack.
Conclusions The proposed method has proven to be an efficient and reliable method for the degradation of imidazolium ionic liquids by
a Fenton-like reagent deteriorated with lengthening n-alkyl substituents and by replacing the imidazolium head group with pyridinium. The enhanced resistance of 1-butyl-3-methylpyridinium
chloride when the resistance of imidazolium ionic liquids decreases with increasing H2O2 concentration is probably indicative of a change in the degradation mechanism in a vigorous Fenton-like system. H-NMR spectra
showed, in the first stage of degradation, that radical attack is nonspecific, with any one of the carbon atoms in the ring
and the n-alkyl chain being susceptible to attack.
Recommendations and perspectives Since ionic liquids are now one of the most promising alternative chemicals of the future, the degradation and waste management
studies should be integrated into a general development research of these chemicals. In the case of imidazolium and pyridinium
ionic liquids that are known to be resistant to bio- or thermal degradation, studies in the field of AOPs should assist the
future structural design as well as tailor the technological process of these chemicals 相似文献