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91.
北京典型道路交通环境机动车黑碳排放与浓度特征研究   总被引:3,自引:2,他引:1  
本研究对2009年北京市典型道路(北四环中路西段)进行实际交通流监测和调研,分析了总车流量、车型构成和平均速度的日变化规律.应用北京机动车排放因子模型(EMBEV模型)和颗粒物黑碳排放的研究数据,计算该路段的黑碳平均排放因子和排放强度.根据同期观测的气象数据,应用AERMOD模型对道路黑碳排放进行了扩散模拟,并根据城市背景站点和道路边站点的监测数据对模拟结果进行了验证.研究表明,该路段黑碳平均排放因子与重型柴油车在总车流中所占比例呈现出极强的相关性,由于北京市实行货车区域限行制度,日间时段总车流的平均黑碳排放因子为(9.3±1.2)mg·km-1·veh-1,而夜间时段上升至(29.5±11.1)mg·km-1·veh-1.全天时均黑碳排放强度为17.9~115.3g·km-1·h-1,其中早(7:00—9:00)晚(17:00—19:00)高峰时段的黑碳排放强度分别为(106.1±13.0)g·km-1·h-1和(102.6±6.2)g·km-1·h-1.基于同期监测数据验证,AERMOD模型的模拟效果较好.模拟时段的道路黑碳排放对道路边监测点的平均浓度贡献为(2.8±3.5)μg·m-3.由于局地气象条件差异,日间和夜间的机动车排放对道路边黑碳的模拟浓度存在显著差异.日间时段,小型客车排放对道路边站点的黑碳浓度贡献最高,达(1.07±1.57)μg·m-3;其次为公交车,达(0.58±0.85)μg·m-3.夜间时段货车比例明显上升,其黑碳排放占主导地位,贡献浓度(2.44±2.31)μg·m-3.  相似文献   
92.
The responses of sulfur (S) uptake assimilation-related genes' expression in roots of two rice cultivars to cadmium (Cd), bensulfuron-methyl (BSM) and their co-contamination (Cd+BSM) were investigated by gene-chip microarray analysis and quantitative real-time PCR (QRT-PCR) technology. Treatments of Cd and Cd+BSM induced expression of sulfate transporter and permease genes, and promoted sulfate uptake in rice roots. Cd+BSM could alleviate Cd toxicity to cv. Fengmeizhan seedlings, probably due to Cd+BSM promoting greater S absorption by seedlings. Cd and Cd+BSM induced expression of sulfate assimilation-related genes, and thus activated the sulfur assimilation pathway. Cd and Cd+BSM induced expression of phytochelatin synthase and metallothionein genes, and induced expression of glutathione S-transferases (GSTs), glutathione synthase (GS) and S- containing antioxidation enzyme genes, which detoxified Cd2+. It is suggested that (to cope with the toxicity of Cd, BSM and their co-contamination) the S uptake and assimilation pathway was activated in rice roots by increased expression of related genes, thus enhancing the supply of organic S for synthesis of Cd or BSM resistance-related substances.  相似文献   
93.
The photocatalytic degradation of methylene blue(MB) over Fe-doped CaTiO3 under UV-visible light was investigated. The as-prepared samples were characterized using X-ray diffraction(XRD), scanning electron microscope(SEM) equipped with an energy dispersive spectrometer(EDS) system, Fourier transform infrared spectra(FT-IR), and UV-visible diffuse reflectance spectroscopy(DRS). The results show that the doping with Fe significantly promoted the light absorption ability of CaTiO3 in the visible light region. The Fe-doped CaTiO3 exhibited higher photocatalytic activity than CaTiO3 for the degradation of MB.However, the photocatalytic activity of the Fe-doped CaTiO3 was greatly influenced by the calcination temperature during the preparation process. The Fe-doped CaTiO3 prepared at500°C exhibited the best photocatalytic activity, with degradation of almost 100% MB(10 ppm)under UV-visible light for 180 min.  相似文献   
94.
Higher concentrations of Hg can be emitted from coal pyrolysis or gasification than from coal combustion, especially elemental Hg. Highly efficient Hg removal technology from coal-derived fuel gas is thus of great importance. Based on the very excellent Hg removal ability of Pd and the high adsorption abilities of activated carbon(AC) for H2 S and Hg, a series of Pd/AC sorbents was prepared by using pore volume impregnation, and their performance in capturing Hg and H2 S from coal-derived fuel gas was investigated using a laboratory-scale fixed-bed reactor. The effects of loading amount, reaction temperature and reaction atmosphere on Hg removal from coal-derived fuel gas were studied. The sorbents were characterized by N2 adsorption, X-ray diffraction(XRD) and X-ray photoelectron spectroscopy(XPS). The results indicated that the efficiency of Hg removal increased with the increasing of Pd loading amount, but the effective utilization rate of the active component Pd decreased significantly at the same time. High temperature had a negative influence on the Hg removal. The efficiency of Hg removal in the N2-H2S-H2-CO-Hg atmosphere(simulated coal gas) was higher than that in N2-H2S-Hg and N2-Hg atmospheres, which showed that H2 and CO, with their reducing capacity, could benefit promote the removal of Hg. The XPS results suggested that there were two different ways of capturing Hg over sorbents in N2-H2S-Hg and N2-Hg atmospheres.  相似文献   
95.
增强多氯联苯(PCBs)的水溶性是强化PCBs微生物降解的主要控制因素之一,本研究选取了PCB5(2,3-CB)和PCB31(2,4',5-CB)作为低氯代PCBs的典型代表,以曲拉通100(TX-100)、吐温80(Tween 80)、鼠李糖脂粗提物(RL crude)3种表面活性剂和β-环糊精( HPCD)联合Burkholderia xenoνorans LB400构建PCBs好氧降解体系,测试了它们对PCB5和PCB31的溶出率及微生物生长的影响.结果表明,TX-100(CMC=194 mg·L-1)、 Tween 80(CMC=13.1 mg·L-1)、 RL crude(CMC=50 mg·L-1)浓度在1~7 CMC 时和 HPCD 浓度在500~1500 mg·L-1时对 PCB5和 PCB31溶出率分别达到54.7%~100%、59.8%~100%;10.5%~40.8%、6.8%~31.6%;10.3%~19.9%、3.3%~11.6%和19.5%~34.2%、4.2%~10.7%. TX-100浓度在1~7 CMC时对B. xenoνorans LB400生长的抑制率达到30.3%~45.8%,而Tween 80浓度在0.1~1 CMC时对其生长的抑制率为10.0%~15.4%; RL crude 本身能作为底物促进 LB400的生长,而 HPCD 对其生长无明显影响. B. xenoνorans LB400对PCB31(5 mg·L-1)的降解效率在添加表面活性剂后有不同程度的提高:TX-100,23.7%~65.5%; Tween 80,14.6%~44.3%;RL crude,9.6%~27.2%;HPCD,15.3%~20.7%;而表面活性剂对PCB5(10 mg·L-1)的降解效率则无明显影响.表面活性剂主要通过增大溶液中PCBs-表面活性剂的胶束浓度来提高LB400对PCBs的降解效率,在水溶液培养体系中当设置TX-100和Tween 80浓度分别在1和7 CMC时,PCB31的降解效率达到100%和81.7%,而此时B. xenoνorans LB400生长的抑制率为30.3%和5.4%.  相似文献   
96.
根据《中华人民共和国环境影响评价法》的有关条款,探讨了建设项目环境影响后评价的定义、适用对象、工作内容、工作程序。同时,结合多年的环境管理经验,分析了典型行业环境影响后评价的重点,并指出了目前中国建设项目环境影响后评价存在的问题,提出了改进和完善的建议。实践表明,开展环境影响后评价有助于提高环境管理决策水平。  相似文献   
97.
概括了循环经济工业园区规划环境影响评价的框架思路。归纳总结了规划环评的主要内容,并以山西省长治市襄垣富阳循环经济工业园区为例,对规划环评指标体系的构建进行探讨。  相似文献   
98.
畜牧养殖业最大的污染物就是畜禽粪便,在畜禽养殖也实施清洁生产技术十分必要,将粪便在产生的环节上降低污染物的产生和排放,结合具体实例,按照企业清洁生产审核程序要求,对一家生猪养殖场进行清洁生产审核,对生态发酵床技术在规模化养猪场的应用进行深入研究,从技术、环境、经济三个方面阐述这项清洁生产技术的示范作用。  相似文献   
99.
为分析施工情境中危险识别注意资源动态投入分配规律,基于动态时间规整算法,挖掘危险识别注视轨迹序列,以表征注意资源投入分配变化,并采用k-means聚类、注视熵、Needleman-Wunsch全局序列对齐算法和统计等方法,深入挖掘注意资源在危险目标中投入和分配等时空变化规律。研究结果表明:当事人危险识别各阶段注意资源呈现从显著目标到高危目标的投入变化趋势,危险识别注意资源分配随情境复杂因素呈现零散、均匀的空间特征,分配无序程度提高。  相似文献   
100.
The selective catalytic reduction(SCR) activities of the MoO_3 doped V/WTi catalysts prepared by the incipient wetness impregnation method at low temperature were investigated.The results showed that the addition of MoO_3 could enhance the NO_ xconversion at low temperature and the best SCR activity was obtained when the dosage of MoO_3 reached5 wt.%. The NH3-TPD and DRIFTS experiments indicated that the addition of MoO_3 changed the type and number of acid sites on the surface of catalysts and reaction activities of acid sites were altered at the same time. The redox capacity and amount of active oxygen species got improved for V3Mo5/WTi catalyst, which could be confirmed by the H_2-TPR and transient response experiments. Water vapor inhibited the NO_xconversion at low temperature. Deposition of ammonium sulfate or bisulfate might be main reason for the loss of catalytic activity in the presence of SO_2 at low temperature. Choosing the suitable NH_3/NO ratio and elevation of reaction temperature both could weaken the influence of SO_2 on the SCR activity of the V3Mo5/WTi catalyst. Thermal treatment of the deactivated catalyst at350°C could get the low temperature activity recovered. The decrease of GHSV improved the de NO_x efficiency at low temperature and we speculated that the rational technological process and operation parameters could contribute to the application of this kind of catalysts in real industrial environment.  相似文献   
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