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961.
借助多功能动态生理检测仪、现场道路交通噪声信号采集系统及室内道路交通噪声信号回放系统等精密仪器设备,研究了道路交通噪声对人体心电的短时影响,并运用统计学、时间序列理论对噪声影响心电指标的规律进行了分析,提出了一种解释道路交通噪声影响人体心电指标规律及确定噪声安全阈值的理论方法。结果表明,不同噪声声压级对心电低频(LF)、高频(HF)之比(LF/HF)时间序列的自相关系数衰减速率影响不同,声压级越高,LF/HF时间序列的自相关系数衰减到0.500时的速率越慢,经历的延迟期越长;当道路交通噪声超过43dB时,有可能对人体心电状态造成潜在的影响。 相似文献
962.
水力停留时间对MBR中溶解性微生物产物生成的影响 总被引:1,自引:0,他引:1
考察水力停留时间(HRT)对MBR中膜污染的主要污染物——溶解性微生物产物(SMP)生成的影响。结果表明,在装置稳定运行期间,MBR中SMP随运行时间出现累积。与HRT为8 h相比,HRT为12 h时,SMP在MBR中平均累积量要少10.1%,SMP中多糖含量平均高7 mg/L左右,而蛋白质含量平均低45.6%。SMP的平均粒径随装置运行呈下降趋势,并且HRT较短有利于粒径较小的SMP生成,从而堵塞膜孔;HRT较长有利于粒径较大的SMP生成,从而形成凝胶层,两种情况导致膜污染的机制不同。 相似文献
963.
构建了双室微生物燃料电池(MFC),并应用于污水BOD的检测。优化了MFC型BOD传感器的检测条件,分析了传感器进行污水BOD检测的特征。结果表明,以A2/O污水处理工艺中厌氧段污泥进行接种,双室MFC型BOD传感器2周内完成启动,所产电流达到稳定。传感器的最佳检测条件为外接电阻500Ω,添加缓冲溶液并维持待测水样pH为7.0,添加35 mg/L的L-半胱氨酸作为吸氧剂维持阳极室厌氧环境,阴极室富氧水流量为20 mL/min。利用MFC产生的电流峰值准确检测污水水样BOD浓度,传感器检测范围为10~50 mg/L,检测时间小于3 h;利用MFC产生的电荷量准确检测污水水样BOD浓度,检测范围为10~100 mg/L,检测时间小于10 h。利用MFC电流峰值和电荷量检测污水水样BOD浓度,偏差均小于15%,传感器运行稳定,寿命较长。 相似文献
964.
为了从一些具有代表性的监测时段数据中快速而直观地反映太原市大气环境状况,运用特征分析法对太原市中心城区7个监测点的16个时间点位的样本数据联系性进行了分析。借助MATLAB软件对其进行可视化,得到各监测点的时间点优化分组。通过对7个优化分组综合比选,提出了能整体反映春季典型天气条件下太原市大气环境状况的优化时段点位,分别为7:00、12:00、14:00、15:00、18:00、19:00和22:00。将5 d相同或相似天气状况的优化时段点位进行对比,得到的结果一致,体现了代表性。太原市总体优化时段点位数据由反映各区域状况的各监测点优化时段点数据平均值或乘以相应的权重得出。 相似文献
965.
Oxidative transformation of polybrominated diphenyl ether congeners (PBDEs) and of hydroxylated PBDEs (OH-PBDEs) 总被引:1,自引:0,他引:1
Moreira Bastos P Eriksson J Vidarson J Bergman A 《Environmental science and pollution research international》2008,15(7):606-613
BACKGROUND, AIM, AND SCOPE: The historical and widespread use of polybrominated diphenyl ethers (PBDEs) as flame retardants in consumer products worldwide has caused PBDEs to now be regarded as pervasive environmental contaminants. Most recently, hydroxylated PBDEs (OH-PBDEs) and methoxylated PBDEs (MeO-PBDEs) have emerged as environmentally relevant due to reports of their natural production and metabolism. An important parameter for assessing the environmental impact of a chemical substance is persistence. By formulating the concept that persistence is the result of the substance's physicochemical properties and chemical reactivity, Green and Bergman have proposed a new methodology to determine the inherent persistence of a chemical. If persistence could be predicted by straightforward methods, substances with this quality could be screened out before large-scale production/manufacturing begins. To provide data to implement this concept, we have developed new methodologies to study chemical transformations through photolysis; hydrolysis, substitution, and elimination; and via oxidation. This study has focused on adapting an oxidative reaction method to be applicable to non-water soluble organic pollutants. MATERIALS AND METHODS: PBDEs and one MeO-PBDE were dissolved in tetrahydrofuran/methanol and then diluted in alkaline water. The OH-PBDEs were dissolved in alkaline water prior to reaction. The oxidation degradation reaction was performed at 50 degrees C using potassium permanganate as described elsewhere. The pH was maintained at 7.6 with disodium hydrogen phosphate and barium hydrogen phosphate, the latter also serving as a trapping agent for manganate ions. The oxidation reactions were monitored by high-performance liquid chromatography and reaction rates were calculated. RESULTS: The OH-PBDEs have very fast oxidative transformation rates compared to the PBDEs. The reaction rates seem to be primarily dependent on substitution pattern of the pi-electron-donating bromine substituents and of bromine content. There are indications that further reactions of OH-PBDEs, e.g., methylation to the MeO-PBDEs, decrease the oxidation rates, and thereby generate more persistent substances. DISCUSSION: The resistance of PBDEs to oxidation, a major degradation pathway in air, should be further investigated, since these compounds do undergo long range transport. With slight modifications, the original method has been adapted to include a larger variety of chemical substances, and preliminary data are now available on the oxidative transformation rates for PBDEs and of OH-PBDEs. CONCLUSIONS: The original oxidation degradation method can now include non-water soluble compounds. This modification, using low concentrations of test chemicals, allows us to measure oxidative transformation rates, for some of the lower brominated DEs, data that can be used to assess their persistence in future model calculations. Oxidative transformation rates for PBDEs are slow compared to those for the OH-PBDEs. This suggests that OH-PBDEs, when released into the environment, undergo faster oxidative metabolism and excretion than the PBDEs. RECOMMENDATIONS AND PERSPECTIVES: To evaluate the modified method, more degradation reactions with non-water soluble compounds should be investigated. Recent studies show that OH-PBDEs are present in rats and in humans and, because of their activity as endocrine disruptors, determining their subsequent environmental fate is of importance. The resistance of PBDEs to oxidative degradation should be acknowledged as of possible future concern. Several other compound classes (such as polychlorinated biphenyls (PCBs), hydroxylated polychlorinated biphenyls (OH-PCBs), and pharmaceuticals) need to be subjected to this screening method to increase the database of transformation rates that can be used with this model. 相似文献
966.
Kwon KD Jo WK Lim HJ Jeong WS 《Environmental science and pollution research international》2008,15(6):521-526
BACKGROUND, AIM, AND SCOPE: To identify household products that may be potential sources of indoor air pollution, the chemical composition emitted from the products should be surveyed. Although this kind of survey has been conducted by certain research groups in Western Europe and the USA, there is still limited information in scientific literature. Moreover, chemical components and their proportions of household products are suspected to be different with different manufacturers. Consequently, the current study evaluated the emission composition for 42 liquid household products sold in Korea, focusing on five product classes (deodorizers, household cleaners, color removers, pesticides, and polishes). MATERIALS AND METHODS: The present study included two phase experiments. First, the chemical components and their proportions in household products were determined using a gas chromatograph and mass spectrometer system. For the 19 target compounds screened by the first phase of the experiment and other selection criteria, the second phase was done to identify their proportions in the purged-gas phase. RESULTS: The number of chemicals in the household products surveyed ranged from 9 to 113. Eight (product class of pesticides) to 17 (product class of cleaning products) compounds were detected in the purged-gas phase of each product class. Several compounds were identified in more than one product class. Six chemicals (acetone, ethanol, limonene, perchloroethylene (PCE), phenol, and 1-propanol) were identified in all five product classes. There were 13 analytes occurring with a frequency of more than 10% in the household products: limonene (76.2%), ethanol (71.4%), PCE (66.7%), phenol (40.5%), 1-propanol (35.7%), decane (33%), acetone (28.6%), toluene (19.0%), 2-butoxy ethanol (16.7%), o-xylene (16.7%), chlorobenzene (14.3%), ethylbenzene (11.9%), and hexane (11.9%). All of the 42 household products analyzed were found to contain one or more of the 19 compounds. DISCUSSION: The chemical composition varied broadly along with the product classes or product categories, and it was different from that reported in other studies abroad, although certain target chemicals were identified in both studies. This finding supports an assertion that chemical components emitted from household products may be different in different products and with different manufacturers. The chlorinated pollutants identified in the present study have not been reported to be components of cleaning products in papers published since the early 1990s. Limonene was identified as having the highest occurrence in the household products in the present study, although it was not detected in any of 67 household products sold in the U.S. CONCLUSIONS: The emission composition of selected household products was successfully examined by purge-and-trap analysis. Along with other exposure information such as use pattern of household products and the indoor climate, this composition data can be used to estimate personal exposure levels of building occupants. This exposure data can be employed to link environmental exposure to health risk. It is noteworthy that many liquid household products sold in Korea emitted several toxic aromatic and chlorinated organic compounds. Moreover, the current finding suggests that product types and manufacturers should be considered, when evaluating building occupants' exposure to chemical components emitted from household products. RECOMMENDATIONS AND PERSPECTIVES: The current findings can provide valuable information for the semiquantitative estimation of the population inhalation exposure to these compounds in indoor environments and for the selection of safer household products. However, although the chemical composition is known, the emissions of household products might include compounds formed during the use of the product or compounds not identified as ingredients by this study. Accordingly, further studies are required, and testing must be done to determine the actual composition being emitted. Similar to eco-labeling of shampoos, shower gels, and foam baths proposed by a previous study, eco-labeling of other household products is suggested. 相似文献
967.
968.
复杂地铁工程施工安全控制技术研究 总被引:8,自引:3,他引:5
北京地铁5号线崇文门站为国内首次在既有地铁隧道下方采用暗挖法施工的地铁车站,施工期间要保证既有地铁线路的正常运营,因此施工难度和风险极大。施工前对既有地铁结构进行了安全评估,根据评估结果并结合相关规范制定了既有线结构变形的安全控制标准。在施工风险分析的基础上,结合数值模拟计算确定了柱洞法施工方案,并辅以降水、超前大管幕和注浆等辅助技术措施,同时采用远程自动监测系统实时监控既有线的动态变化,对施工中既有线结构出现的异常变形进行了及时处理,最终地铁车站成功建成,并确保了既有地铁结构的安全和线路的正常运营。 相似文献
969.
970.
Temporal variability of groundwater chemistry in shallow and deep aquifers of Araihazar, Bangladesh 总被引:2,自引:0,他引:2
Dhar RK Zheng Y Stute M van Geen A Cheng Z Shanewaz M Shamsudduha M Hoque MA Rahman MW Ahmed KM 《Journal of contaminant hydrology》2008,99(1-4):97-111
Samples were collected every 2-4 weeks from a set of 37 monitoring wells over a period of 2-3 years in Araihazar, Bangladesh, to evaluate the temporal variability of groundwater composition for As and other constituents. The monitoring wells are grouped in 6 nests and span the 5-91 m depth range. Concentrations of As, Ca, Fe, K, Mg, Mn, Na, P, and S were measured by high-resolution ICPMS with a precision of 5% or better; concentrations of Cl were measured by ion chromatography. In shallow wells <30 m deep, As and P concentrations generally varied by <30%, whereas concentrations of the major ions (Na, K, Mg, Ca and Cl) and the redox-sensitive elements (Fe, Mn, and S) varied over time by up to +/-90%. In wells tapping the deeper aquifers >30 m often below clay layers concentrations of groundwater As were much lower and varied by <10%. The concentrations of major cations also varied by <10% in these deep aquifers. In contrast, the concentration of redox-sensitive constituents Fe, S, and Mn in deep aquifers varied by up to 97% over time. Thus, strong decoupling between variations in As and Fe concentrations is evident in groundwaters from shallow and deep aquifers. Comparison of the time series data with groundwater ages determined by (3)H/(3)He and (14)C dating shows that large seasonal or inter-annual variations in major cation and chloride concentrations are restricted to shallow aquifers and groundwater recharged <5 years ago. There is no corresponding change in As concentrations despite having significant variations of redox sensitive constituents in these very young waters. This is attributed to chemical buffering due to rapid equilibrium between solute and solid As. At two sites where the As content of groundwater in existing shallow wells averages 102 microg/L (range: <5 to 648 microg/L; n=118) and 272 microg/L (range: 10 to 485 microg/L; n=65), respectively, a systematic long-term decline in As concentrations lends support to the notion that flushing may slowly deplete an aquifer of As. Shallow aquifer water with >5 years (3)H/(3)He age show a constant As:P molar ratio of 9.6 over time, suggesting common mechanisms of mobilization. 相似文献