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171.
有机磷阻燃剂(OPFRs)逐渐替代了危害较大的多溴联苯醚(PBDEs),因此使得人类及其他生物更易暴露于这种有机物中。有研究表明,部分有机磷酸酯具有致癌性,因而使人们对其毒性的问题也日益关注。本文概述了有机磷阻燃剂的环境暴露水平,总结了近年来从体外与体内实验2个方面动物毒性效应的研究。目前研究发现诸多地区的大气、土壤和水体中的有机磷阻燃剂总含量水平相对较低;仅高浓度暴露才会对不同动物体造成一定程度的损伤,而远大于环境浓度的低浓度暴露几乎无损伤效应。最后,对有机磷阻燃剂毒性效应的未来研究重点进行了展望。 相似文献
172.
Webber Wei-Po Lai Ying-Chih Chuang Angela Yu-Chen Lin 《Environmental science and pollution research international》2017,24(17):14595-14604
The influences of HCO3 ?, Cl?, and other components on the UV/TiO2 degradation of the antineoplastic agents ifosfamide (IFO) and cyclophosphamide (CP) were studied in this work. The results indicated that the presence of HCO3 ?, Cl?, NO3 ?, and SO4 2? in water bodies resulted in lower degradation efficiencies. The half-lives of IFO and CP were 1.2 and 1.1 min and increased 2.3–7.3 and 3.2–6.3 times, respectively, in the presence of the four anions (initial compound concentration = 100 μg/L, TiO2 loading =100 mg/L, anion concentration = 1000 mg/L, and pH = 8). Although the presence of HCO3 ? in the UV/TiO2/HCO3 ? system resulted in a lower degradation rate and less byproduct formation for IFO and CP, two newly identified byproducts, P11 (M.W. = 197) and P12 (M.W. = 101), were formed and detected, suggesting that additional pathways occurred during the reaction of ?CO3 ? in the system. The results also showed that ?CO3 ? likely induces a preferred ketonization pathway. Besides the inorganic anions HCO3 ?, Cl?, NO3 ?, and SO4 2?, the existence of dissolved organic matter in the water has a significant effect and inhibits CP degradation. Toxicity tests showed that higher toxicity occurred in the presence of HCO3 ? or Cl? during UV/TiO2 treatment and within 6 h of reaction time, implying that the effects of these two anions should not be ignored when photocatalytic treatment is applied to treat real wastewater. 相似文献
173.
The kinetics and mechanism for degradation of omethoate (OMT) by catalytic ozonation with Fe(III)-loaded activated carbon (Fe@AC) were investigated in this study with focus on identification of degradation byproducts. The rate constants of OMT reacting with ozone and hydroxyl radical (OH) were determined to be 0.04 and 5.3 × 108 M?1 s?1 at pH 7.5 and 20 °C, respectively. OMT was predominantly degraded by OH in the catalytic ozonation with Fe@AC. The high-molecular-weight degradation byproducts identified were O,O,O-trimethyl phosphoric ester (TMP), pyrrolidin-2-one, N-methyl-2-sulfanylacetamide, 2-(methylthio)acetamide, O,O,S-trimethylthiophosphate (STMP), and N-methyl-2-(methylthio)acetamide. Besides, low-molecular-weight organic acids and inorganic anions were also detected and quantified, including formic, acetic and oxalic acids as well as nitrate, sulfate and phosphate ions. In the catalytic ozonation, TMP and phosphate were two major P-containing byproducts resulting from OMT degradation. The toxicity of OMT solution gradually decreased during the catalytic ozonation, indicating that Fe@AC is a safe catalyst for OMT removal by ozone in water. 相似文献
174.
Pierluigi Caboni Giorgia Sarais Alberto Angioni Francesco Lai Fabrizio Dedola Paolo Cabras 《Journal of environmental science and health. Part. B》2013,48(6):598-605
The degradation of the main azadirachtoids on tomatoes was studied after greenhouse treatment. These experiments were carried out at 1 and 5× the concentration recommended by the manufacturer. In all experiments the deposition of azadirachtin A (AZA-A) was below the maximum residue level (MRL). Even if at the highest dose, AZA-A half-life time calculated as pseudo first order kinetic was 1.2 days in agreement with the recommended preharvest interval (PHI) of 3 days. Experiments with a model system showed that sunlight photodegradation is the main factor influencing the rate of disappearance of AZA-A after greenhouse treatment while tomato epicuticular waxes doubled the photodegradation rate of AZA-A in a commercial formulation. 相似文献
175.
实验采用经甲苯培养驯化而成的单一假单胞菌菌种,通过分析平板式生物膜反应器内,不同阶段假单胞细菌生物膜干重、厚度、活性生物量和生物种群分布的变化,研究生物膜特性与降解效率之间的关系。实验结果表明,在挂膜初期生物膜迅速生长,生物量以及生物膜干重增长很快,有利于甲苯及营养物质的传输,降解效率也快速提升。随着生物膜的生长,生物量及干重也逐步增加,厚度逐渐增加使传质阻力不断增大,生物膜上层微生物的有机底物供应不足,使生物膜上层结构稀疏,最终维持一个甲苯的总传输量与生化降解量的平衡,生物量的生长与衰亡也达到动态平衡,形成了一个较高且稳定的降解效率。 相似文献
176.
灵芝漆酶对直接蓝86的催化脱色性能 总被引:1,自引:0,他引:1
利用灵芝菌Ganoderma lucidum U-281漆酶对直接蓝86进行酶促氧化脱色,并对其降解机理进行了探讨。结果表明,染料-漆酶共反应体系在20~50℃及pH小于5.0范围内,直接蓝86均可脱色50%以上;漆酶对直接蓝86具有宽泛的浓度适应性,对300 mg/L的该染料仍具有耐受性。最优脱色工艺参数为温度40℃、pH 5.0、染料初始浓度200 mg/L、漆酶用量1 U/mL。在优化条件下,直接蓝863 h的脱色率达到54.54%,48 h脱色率达到91.54%。紫外-可见吸收光谱分析表明,漆酶的酶促氧化导致染料的分子结构产生了变化,是造成直接蓝86脱色的主要发生机制。 相似文献
177.
采用生物过滤法,以鸡粪堆肥和PE混合物为填料,在高气速条件下间歇式处理高负荷H2S废气。空床停留时间为20、15、10、6.7和5 s时,入口浓度3 000 mg/m3下的平均去除率分别为100%、100%、96.5%、89.2%和90.5%。高气速EBRT为5 s时,高入口负荷2 147 g/(m3.h)时的去除负荷为2 023 g/(m3.h),去除率达94%。采用Michaelis-Ment-en模型进行生物降解宏观动力学研究,其中Ks为550 mg/m3,Vm为6.8×104g/(m3.d)。结果表明,在实验温度17~24℃,湿度30%~50%下,生物过滤法间歇式处理高气速高负荷H2S的去除性能好。 相似文献
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