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铁尾矿地砖的制备及其机理分析 总被引:2,自引:0,他引:2
简要介绍了唐山地区铁矿尾矿制备铁尾矿砖的试验研究,并设计制备铁尾矿砖生产工艺流程和最佳配比。研究结果表明,以铁尾矿为主要材料,通过掺加适量的水泥、粉煤灰、粗骨料和一定的外加剂,经常温常压养护28天后,抗压强度可达到28.30MPa,抗折强度为5.63MPa,同时长期性能研究也表明可以制备出合格的铁尾矿地砖。为铁尾矿大量资源化利用辊供了一条新的徐径.同时还对铁尾砖的微观机理作了初步研究。 相似文献
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目的解决在较强的噪声环境下最大二阶循环平稳盲解卷积(MaximumSecond OrderCyclostationary Blind Deconvolution,CYCBD)算法在滚动轴承故障特征提取时效果欠佳的问题,为滚转尾翼导弹的尾翼滚动轴承故障诊断提供方法参考。方法提出一种利用麻雀搜索算法(SparrowSearchAlgorithm,SSA)优化CYCBD算法的方法,将CYCBD算法解卷积的包络谱熵作为SSA寻优的适应度函数,利用SSA高效地寻找出合适的循环频率以及滤波器长度,选择自适应参数后,再使用CYCBD算法有效解卷得到周期脉冲特征。结果同时对比SSA优化CYCBD前后进行故障特征提取的包络谱图,CYCBD的噪声幅值不超过0.13 m/s^(2),峰值不超过0.29 m/s^(2),用SSA优化CYCBD的噪声幅值不超过0.08 m/s^(2),峰值不超过0.32 m/s^(2),故障频率成分更加突显,无论是噪声幅度,还是峰值幅度特性,均较CYCBD有了较大改善。结论仿真实验验证了SSA优化CYCBD方法能够更加清晰地辨识到故障特征频率及其倍频成分,其具有良好的工程应用前景。 相似文献
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天津中心城区环境空气挥发性有机物污染特征分析 总被引:9,自引:7,他引:9
为研究天津中心城区挥发性有机物的污染特征,在天津中心城区布点26个,分别对春、夏、秋、冬四季进行了系统采样.天津中心城区共检出挥发性有机物80余种,检出率大于80%的物质主要为烷烃、苯系物和卤代烃.天津中心城区挥发性有机物总浓度(体积分数,下同)季节变化特征为:春季(110.43×10-9)>秋季(93.73×10-9)>冬季(73.37×10-9)>夏季(60.43×10-9).统计结果表明,城区挥发性有机物总浓度主要集中在30×10-9~90×10-9之间,在此区间4个季节的样品百分比均在50%以上.天津中心城区不同季节VOCs组成存在一定差异.含氧有机物和烷烃是VOCs主要组成物质,两者浓度百分比之和4个季节均在50%以上.对苯系物和卤代烃这两类主要污染物,进行了季节变化分析. 相似文献
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为了深入了解工业园区恶臭污染情况、保障工业园区工作人员的工作环境安全,以珠海市某工业园区为分析对象,采集园区内涉及8种行业类型、14个工业恶臭源的主要工艺流程中通过有组织方式排放的恶臭废气,分析了14个排放源的恶臭VOCs排放特征,测定了感官臭气浓度,应用理论臭气强度法确定了各排放源的特征恶臭物质,并对各排放源的恶臭废气进行了致癌和非致癌风险评估.结果表明:①14个排放源排放的物质种类相同、含量差异较大,纤维和电池制造及烃类、酸酐、酯类和溶剂合成的恶臭VOCs排放以烷烯烃为主;炼油源、PTA合成源和乳胶合成源废气中苯及苯系物含量最高;酯类化合物是活性炭加工、树脂合成源和喷涂源废气排放的主要物质;陶瓷制造源和添加剂合成源排放的废气以羰基化合物和硫化物为主;②14个排放源的废气均具有较为强烈的感官刺激性,润滑油添加剂合成和乳胶类合成排放的废气感官刺激性最严重.其中,添加剂合成源的特征恶臭物质为乙硫醇、乙硫醚、正丁醇和甲苯,乳胶合成源的特征恶臭物质为苯乙烯、丙苯、异丙苯、丙烯酸丁酯和1,3-丁二烯;③14个排放源恶臭废气的终生致癌风险LCR值范围为3. 06×10-7~1. 06×10-2,其中炼油源、PTA合成源、酯类合成源和乳胶合成源排放废气存在较大潜在风险;非致癌风险HI总值范围为0. 02~51. 66,其中乳胶合成、酯类合成、炼油、PTA合成和纤维制造存在一定的非致癌健康风险.乳胶合成源、酸酐合成源和树脂合成源厂界均存在潜在致癌风险. 相似文献
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为了识别恶臭污染源排放特征以及了解不同行业恶臭物质排放差异,对恶臭污染排放源指纹谱指标物质进行了筛选,并依据筛选结果对6家典型恶臭排放企业进行样品采集及分析,绘制了各家企业的指纹谱图.结果表明:①通过物质嗅觉阈值与AMGE(ambient multimedia environmental goals,周围环境目标值)和RfC(reference concentration,健康风险参考浓度)对比以及结合国内外恶臭标准受控物质和现有的标准检测方法,最终确定了包括三甲胺、硫化氢、甲硫醇等典型恶臭物质在内的19种物质作为指纹谱指标物质.②依据我国现行的标准监测分析方法对19种恶臭指标物进行检测,初步得到了各家企业的恶臭物质指纹谱数据,绘制了各家企业的指纹谱图.③指纹谱成分分析结果显示,污水处理厂主要的恶臭物质是硫化氢,ρ(硫化氢)为44.566 mg/m3;涂料企业ρ(甲基乙基酮)、ρ(丁醛)和ρ(乙酸乙酯)较高,分别为39.037、28.757、27.840 mg/m3;制药企业ρ(丙醛)较高,为4.791 mg/m3;汽车和家具制造企业ρ(二甲苯)较高,分别为15.209和2.081 mg/m3.④应用分歧系数法分析不同企业指纹谱之间的相似程度,分析结果显示,分歧系数在0.331~0.809之间,不同企业之间指纹谱存在较大差异.研究显示,建立恶臭污染排放源指纹谱可进行恶臭源排放特征识别,为恶臭污染溯源提供基础数据和科学依据. 相似文献
8.
Seasonal and diurnal variations of atmospheric peroxyacetyl nitrate, peroxypropionyl nitrate, and carbon tetrachloride in Beijing 总被引:1,自引:0,他引:1
Gen Zhang Yujing Mu Junfeng Liu Chenglong Zhang Yuanyuan Zhang Yujie Zhang Hongxing Zhang 《环境科学学报(英文版)》2014,26(1):65-74
Atmospheric peroxyacetyl nitrate(PAN), peroxypropionyl nitrate(PPN), and carbon tetrachloride(CCl4) were measured from September 2010 to August 2011 in Beijing. PAN exhibited low values from mid-autumn to early spring(October to March) with monthly average concentrations ranging from 0.28 to 0.73 ppbV, and increased from early spring to summer(March to August), ranging from 1.37–3.79 ppbV. The monthly variation of PPN was similar to PAN, with low values(below detection limit to 0.18 ppbV) from mid-autumn to early spring, and a monthly maximum in September(1.14 ppbV). The monthly variation of CCl4was tightly related to the variation of temperature, exhibiting a minimum in winter(69.3 pptV) and a maximum of 180.6 pptV in summer. Due to weak solar intensity and short duration, PAN and O3showed no distinct diurnal patterns from morning to night during winter, whereas for other seasons, they both exhibited maximal values in the late afternoon(ca. 15:00 to 16:00 local time) and minimal values during early morning and midnight. Good linear correlations between PAN and PPN were found in autumn(R = 0.91), spring(R = 0.94), and summer(R = 0.81), with slopes of 0.130, 0.222, and 0.133, respectively, suggesting that anthropogenic hydrocarbons dominated the photochemical formation of PANs in Beijing. Positive correlation between PAN and O3 in summer with the low slopes( O3 / PAN) ranging from 9.92 to 18.0 indicated serious air pollution in Beijing, and strong negative correlation in winter reflected strong O3consumption by NO titration and less thermal decompositin of PAN. 相似文献
9.
Diversity of Soil Nematodes in Areas Polluted with Heavy Metals and Polycyclic Aromatic Hydrocarbons (PAHs) in Lanzhou,China 总被引:1,自引:0,他引:1
This study investigated the soil nematode community structure along the Yellow River in the Lanzhou area of China, and analyzed
the impact of heavy metals (Cd, Pb, Cr, Cu, and Zn) and polycyclic aromatic hydrocarbons (PAHs) on the nematode community.
Soil samples from five locations (named A–E), which were chosen for soil analysis, showed significant differences in their
heavy metal content (p < 0.01), as well as in the variety of nematodes (up to 41 genera) and families (up to 20) that were present. The different
samples also differed significantly in the total PAH content (p < 0.05), as well as the six types of PAH present. Sites A–C showed the most severe contamination with heavy metals and PAHs;
these sites had the lowest abundance of fungivores and omnivore/predators, but the proportion of bacteriovores was the highest
(p < 0.05). Site E, in contrast, showed only minor pollution with heavy metals and PAHs, and it contained the highest abundance
of plant parasites (p < 0.05). Several nematode ecological indicators were found to correlate with concentration of soil pollutants at all the
sites tested: the maturity index (MI, in addition to plant parasites), plant parasite index (PPI), ΣMI (including all the
soil nematodes), Shannon-Wiener diversity index (H′′), and Wasilewska index (WI). Disturbance to the soil environment was more severe when MI, ΣMI, and H′ values were lower. The results of the study show that the abundance and structure of the soil nematode communities in the
sampling locations were strongly influenced by levels of heavy metals and PAHs in the soil. They also show that the diversity
index H′ and the maturity index can be valuable tools for assessing the impact of pollutants on nematodes. 相似文献
10.
Investigation of 1,4-dioxane originating from incineration residues produced by incineration of municipal solid waste 总被引:1,自引:0,他引:1
Fujiwara T Tamada T Kurata Y Ono Y Kose T Ono Y Nishimura F Ohtoshi K 《Chemosphere》2008,71(5):894-901
As a groundwater contaminant, 1,4-dioxane is of considerable concern because of its toxicity, refractory nature to degradation, and rapid migration within an aquifer. Although landfill leachate has been reported to contain significant levels of 1,4-dioxane, the origin of 1,4-dioxane in leachate has not been clarified until now. In this study, the origins of 1,4-dioxane in landfill leachate were investigated at 38 landfill sites and three incineration plants in Japan. Extremely high levels of 1,4-dioxane 89 and 340 microg l(-1), were detected in leachate from two of the landfill sites sampled. Assessments of leachate and measurement of 1,4-dioxane in incineration residues revealed the most likely source of 1,4-dioxane in the leachate to be the fly ash produced by municipal solid waste incinerators. Effective removal of 1,4-dioxane in leachate from fly ash was achieved using heating dechlorination systems. Rapid leaching of 1,4-dioxane observed from fly ash in a sequential batch extraction indicated that the incorporation of a waste washing process could also be effective for the removal of 1,4-dioxane in fly ash. 相似文献