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1.
为提高高烈度地震区隧道抗震性能,以某铁路隧道为研究背景,分析3种抗减震措施下隧道不同监测点隧道拱顶沉降、边墙收敛、衬砌结构PGA及最小安全系数,通过对比分析得到最优抗减震措施。结果表明:相比于工况1,工况2隧道拱顶沉降减小10.54%~81.10%,边墙收敛减小13.92%~78.77%,衬砌结构PGA减小31.42%~72.02%,最小安全系数增加18.04%~66.13%;相比于工况1,工况3结构拱顶沉降减小3.04%~18.02%,边墙收敛减小4.70%~32.00%,PGA增加13.95%~27.48%,最小安全系数增加7.49%~30.99%;工况4即“减震层+SFRC衬砌”刚柔并济法,相比于工况1,隧道拱顶沉降减小18.46%~83.98%,结构边墙收敛减小17.54%~85.47%,PGA减小30.00%~69.98%,最小安全系数增加47.95%~83.56%;4种工况抗减震性能由高到低依次为:工况4>工况2>工况3>工况1。研究结果可为隧道软硬围岩交接段抗震设防提供理论参考。 相似文献
2.
Secondary containment (bunds, drip trays, interceptors/sumps) is an integral part of many chemical, petrochemical, as well as agricultural, food and pharmaceutical facilities. Bunds are the built-in cases for accidental liquid substance spillage where there is a hazard that a substance could leak into the surroundings and the potential of health or environmental damage. The authors focus on the cases installed in large-volume atmospheric tanks storing hazardous chemicals in liquid form, where the bund failure occurred. In the first part of the study, a database of these accidents was created, numbering a total of 15 items. Attention was paid to the course of the accident, its causes and consequences. Several basic representative scenarios of bund failure have also been developed. The second part of the study is devoted mainly to the measures against the bund failure, such as risk assessment, technical and organizational measures. The aim of this study is to provide readers (including experts in the field of safety engineering, maintenance experts and building designers) with the information that can subsequently be used in the risk assessment of bund failure, possibly also for planning the construction of new bunds, or revitalization and maintenance of the existing ones. 相似文献
3.
Roukaya Bouyakhsass Soukaina Bouaouda Abdeslam Taleb Abdelaziz Madinzi Michel Baudu Salah Souabi 《环境质量管理》2023,32(4):237-246
The estimation of leachate quantities produced in landfills is necessary to dimension the treatment plants allowing to reduce the polluting load of these effluents and consequently avoid their negative impacts on the environment. Different leachate quantification methods were used in this study to assess the leachate volume produced at the Oum Azza landfill. The water balance method give comparable estimations of leachate production to the Ouled Berjal landfill ratio. The first method showed average values between 487 and 495 m3/day for 2015, 2018, and 2019, and at the same time, the second method gave values between 470 and 477 m3/day for the same years. In contrast, the World Bank ratio showed high values that vary between 2260 and 2295 m3/day for 2015, 2018, and 2019. The on-site data and the statistical analysis showed us that the World Bank ratio is not adapted for the estimation of the leachates produced in Oum Azza landfill, while the water balance and the ratio of Ouled Berjal landfill allowed to give comparable results to reality. 相似文献
4.
Tienan Ju Mei Lei Guanghui Guo Jinglun Xi Yang Zhang Yuan Xu Qijia Lou 《Frontiers of Environmental Science & Engineering》2023,17(1):8
5.
分析了我国居住建筑室内PM_(2.5)污染水平,总结了现阶段PM_(2.5)的研究方法,主要包括理论分析法、数值模拟法和实验测试法。指出室外源是室内PM_(2.5)的主要污染来源,而室内烟草烟雾、烹饪及人员活动也会严重影响室内PM_(2.5)浓度。针对目前研究中存在的问题,提出了标定典型建筑在不同影响因素下的I/O比范围、研究家具和家电的颗粒物释放状况、加强农村室内外空气颗粒物污染调查等建议。 相似文献
6.
珠江口表层水中多环芳烃的分布特征及健康风险评估 总被引:1,自引:0,他引:1
分别于2015年2、5、8、11月在珠江八大入海口采集表层水体样品,应用固相萃取富集法对该区域表层水体中16种USEPA优控多环芳烃(PAHs)的时空分布特征进行分析,并利用终生致癌风险增量模型(ILCR)对该区域的饮水健康风险进行评价。结果表明:珠江口4个季度所采集的水样中,∑15PAHs的浓度范围为18.0~50.3 ng/L,含量处于中等水平。其中7种强致癌性∑7PAHs的浓度范围为1.53~3.73 ng/L,占∑15PAHs的5.89%~11.1%,∑15PAHs和∑7PAHs在枯水期(2、11月)样品中明显高于丰水期(5、8月)。就组成特征而言,各采样点PAHs以3、4环为主。珠江口表层水中非致癌类PAHs的危害商数值为0.99×10~(-5)~2.73×10~(-5),远低于USEPA规定的阈值(1);致癌类PAHs产生的健康风险为6.50×10~(-8)~2.37×10~(-7),其中Ba P导致的饮水途径健康风险最高,所有点位致癌类PAHs的健康风险均低于USEPA推荐的对致癌物质最大可接受风险水平(10~(-6)),表明珠江口表层水中PAHs尚不具备严重的致癌风险,但是仍然存在潜在的健康风险,需要重点控制和管理。 相似文献
7.
Erdal Yabalak Özkan Görmez Ahmet Murat Gizir 《Journal of environmental science and health. Part. B》2018,53(5):334-339
This study was conducted to investigate the degradation of propham, which is a compound that pollutes water and seriously threatens human health, by subcritical water oxidation and using H2O2 as an oxidising agent. The maximum total organic carbon removal rate of propham was obtained as 73.65% at 40 min of treatment time and 60 mM of H2O2 concentration and 373 K of temperature. In addition, response surface method based on the Box-Behnken design was applied to design the degradation experiments of propham for determination of the combined effects of process variables, namely temperature, concentration of oxidising agent and treatment time. The proposed quadratic model of propham degradation, which was examined with the analysis of variance, was used for navigating the design space. The R2 and adjusted R2 values of the model were determined as 0.9921 and 0.9819 respectively. It was shown that propham was effectively degraded, thus could be removed from the water by using an environmentally friendly method. 相似文献
8.
We show a substantive problem exists with the widely-used ratio of coefficients approach to calculating willingness to pay (WTP) from discrete choice models. The correctly calculated standard error for WTP using this approach is shown to be undefined. This occurs because the cost parameter's standard error implies some possibility the true parameter value is arbitrarily close to zero. We propose a simple yet elegant way to overcome this problem by reparameterizing the (negative) cost variable's coefficient using an exponential transformation to enforce the theoretically correct positive coefficient. With it the confidence interval for WTP is now finite and well behaved. 相似文献
9.
采用高效液相色谱-串联质谱(HPLC-MS/MS)检测,建立了地表水中13种药物及个人护理品的测定方法。水样用盐酸与氢氧化钠溶液调p H值至7.0左右,过固相萃取小柱进行富集,用14 m L甲醇洗脱。以C18柱为分离柱,0.01%甲酸的甲醇-0.01%甲酸水溶液为流动相,目标物在10 min内分离,在0.50~250μg/L范围内,13种化合物峰面积与内标物质峰面积之比与质量浓度的线性关系良好(0.99),检出限在0.05~0.5 ng/L范围内。基质加标实验结果表明,13种化合物在水中的回收率分别在56.2%~123.2%之间(加标水平5 ng/m L)和58.0%~107.8%(加标水平50 ng/m L),相对标准偏差在1.60%~19.9%(n=6)之间。应用该方法测定了从2条纳污河流采集的10份水样,结果表明,除美托诺尔和普洛萘尔未被检出外,其余11药物的检出频率在30%~100%之间。在13种目标物质中,咖啡因的检测浓度最高达287.5ng/L,舒必利次之,为277.5 ng/L。本方法快速、准确,适用于地表水中PPCPs类的快速测定。 相似文献
10.