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401.
建立了气相色谱法(GC)和高效液相色谱法(HPLC)测定水中苦味酸的分析方法,并对2种方法进行比较。GC法检出限为0.000 4 mg/L,线性范围为0.0~0.050 mg/L,加标回收率为92.3%~94.1%,相对标准偏差为4.6%~8.9%。HPLC法检出限为0.02 mg/L,线性范围为0.10~5.00 mg/L,加标回收率为93.7%~96.5%,相对标准偏差为1.3%~2.0%。2种方法相比,GC法灵敏度较高,可用于痕量分析,但操作烦琐,不能有效地将苦味酸与硝基酚类干扰物分离;而HPLC法虽然灵敏度较差些,但简单、快速、稳定性好、准确度高,可有效地将苦味酸与硝基酚类干扰物分离。 相似文献
402.
采用离子交换树脂XAD-7吸附-毛细管柱气相色谱法测定工作场所空气中乙二醇,结果表明,该方法在0 mg/L~1 116 mg/L范围内线性良好,方法检出限为0.88 mg/L,当采样体积为7.5 L时,最低检出质量浓度为0.11 mg/m3。乙二醇标准溶液测定结果的RSD为1.3%,空白加标回收率为80.1%~107%,方法的采集效率为98.0%。 相似文献
403.
通过试验,讨论盐析效应、顶空的平衡温度和平衡时间、水样的p H值、色谱条件等对顶空-气相色谱法测定环境水体中吡啶准确度的影响。优化上述条件后,方法在0 mg/L~3.95 mg/L范围内线性良好,检出限可达0.016 mg/L,测定下限为0.064 mg/L。用该方法对地表水和生活污水做3个质量浓度水平的加标回收试验,测定6次结果的RSD为1.7%~5.7%,回收率为93.9%~113%。 相似文献
404.
气相色谱法测定废气中非甲烷总烃,国内外相关标准选用的标准气体各不相同,通过试验考察各标准气体对测定的影响,并比对相关文献信息。结果表明:甲烷和丙烷(浓度以碳计)在填充柱气相色谱仪和毛细管柱气相色谱仪FID检测器上的响应无明显差异,而采用甲烷作为标准气体,分析时间短,工作效率高。 相似文献
405.
建立固体吸附/热脱附-气相色谱法测定环境空气中苯系物的不确定度评定方法,分析测定过程中不确定度的来源,进行各不确定度分量的评估,并给出合成相对标准不确定度和扩展不确定度。 相似文献
406.
排导槽是泥石流治理常用的工程措施,泥石流若在槽内淤积,将极大影响排导槽防治效果。目前国内现行规范中没有关于排导槽淤积情况计算的相关条款,导致排导槽被泥石流淤埋的工程事故时有发生。鉴于此,分析了排导槽淤堵的常见原因,对现有的一些排导槽淤积验算公式进行了分析和整理,提出了一套基于槽宽验算、槽内泥深及流速验算等公式的排导槽防淤设计验算方法。该方法在雅(安)泸(沽)高速公路沿线某泥石流沟V型排导槽淤埋事故的处理中进行了应用,重建的排导槽经受了2011年6月17日特大暴雨形成的泥石流的考验,说明该方法实施效果良好,可供相关研究与设计参考。 相似文献
407.
《Journal of environmental science and health. Part. B》2013,48(5-6):845-860
Abstract A field experiment was performed to evaluate water and nutrient balances in paddy rice culture operations during 2001–2002. The water balance analysis indicated that about half (50–60%) of the total outflow was lost by surface drainage, with the remainder occurring by evapotranspiration (490–530 mm). The surface drainage from paddy fields was mainly caused by rainfall and forced-drainage, and in particular, the runoff during early rice culture periods depends more on the forced-drainage due to fertilization practices. Most of the total phosphorus (T-P) inflow was supplied by fertilization at transplanting, while the total nitrogen (T-N) inflow was supplied by the three fertilizations, precipitation, and from the upper paddy field, which comprised 13–33% of the total inflow. Although most of the nutrient outflow was attributed to plant uptake, nutrient loss by surface drainage was substantial, comprising 20% for T-N and 10% for T-P. Water and nutrient balances indicate that reduction of surface drainage from paddy rice fields is imperative for nonpoint source pollution control. The simplified computer model, PADDIMOD, was developed to simulate water and nutrient (T-N and T-P) behavior in the paddy rice field. The model predicts daily ponded water depth, surface drainage, and nutrient concentrations. It was formulated with a few equations and simplified assumptions, but its application and a model fitness test indicated that the simulation results reasonably matched the observed data. It is a simple and convenient planning model that could be used to evaluate BMPs of paddy rice fields alone or in combination with other complex watershed models. Application of the PADDIMOD to other paddy rice fields with different agricultural environments might require further calibration and validation. 相似文献
408.
Short chain chlorinated paraffins (SCCPs) are a group of persistent organic pollutants (POPs) of increasing concern, but are to date not widely investigated in the environment, largely due to the challenges involved in their quantification. Here, SCCPs were quantified in marine sediments from the Firth of Clyde, Scotland, by gas chromatography with electron capture negative ionisation mass spectrometry (GC-ECNIMS) and through carbon skeleton analysis by gas chromatography with flame ionisation detection (GC-FID), and the analytical challenges encountered are discussed. Concentrations in the sediments ranged from 0.4 to 69 μg kg−1 when determined by GC-ECNIMS, and from 5.6 to 379 μg kg−1 when determined by GC-FID. For 8 out of 11 samples, analysis by GC-FID gave higher results than analysis by GC-ECNIMS. Unexpected aspects of the analysis, such as the presence of high concentrations of longer chain chlorinated paraffins in the samples, are also presented. 相似文献
409.
The applicability of three different Silphenylene Silicone co-polymer (Si-Arylene) GC stationary phases (J&W Scientific DB-5ms, Varian VF-5ms, and VF-Xms) has been evaluated for the separation of all 136 tetra- through the octa- chlorinated dibenzo-p-dioxins (PCDD) and chlorinated dibenzofurans (PCDF) from closely eluting isomers using gas chromatography/high resolution mass spectrometry (GC/HRMS). Their relative performance data are compared to the “conventional” 5% diphenyl 95% dimethylpolysiloxane GC column (Supelco Equity-5) and to each other based on absolute retention times, visualized mass chromatograms, and the separation of 2,3,7,8-substituted isomers. VF-Xms GC column was able to demonstrate a better performance towards separation of 2,3,7,8-substituted PCDD/PCDF compared to other Si-Arylene GC columns tested, where only 2,3,4,7,8-PnCDF can not be resolved from 1,2,3,6,9-PnCDF and 2,3,4,6,7,8-/1,2,3,6,8,9-HxCDF and 1,2,3,7,8,9-/1,2,3,4,8,9-HxCDF can be at least partially resolved. These data suggest that the development of a single GC column for the separation of all 17 2,3,7,8-substituted dioxins and furans is feasible, which therefore could be used as a standard tool for the PCDD/PCDF methods globally including USEPA methods 1613b, 8290A, 8280B, European Standard Method EN 1948, Canadian methods DFPCB-E3418, EPS 1/RM/19, Japanese methods JIS K0311 and JIS K0312. Having one specific GC column to separate all 2,3,7,8-substituted PCDD/PCDF will significantly improve the data quality, comparability by the various methods and assessment techniques while simultaneously leading to a more cost and time efficient operation. 相似文献
410.