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681.
为研究狭长空间内细水雾幕对顶棚射流火焰的抑制效果,通过全尺寸试验研究不同工作压力对射流火焰蔓延形态、雾幕隔热效果及烟气沉降的影响。研究结果表明:随着工作压力的增加,雾滴的动量随之增大,雾幕对射流火焰的扰动作用增强,强化雾幕对射流火焰的阻挡效果;同时,雾幕的隔热效率有明显改善,2.5 MPa时的细水雾幕的隔热效率可达0.75。然而,过大的工作压力会造成烟气层的沉降,工作压力大于2.0 MPa时保护区内烟气层高度低于1.8 m。因此,应综合考虑细水雾幕对射流火焰和烟气的作用,选择适当的工作压力。 相似文献
682.
为明确作用于采空区的复合惰气的竞争吸附,进行不同温度、压力及组分下烟煤对N2、O2、CO2多元气体竞争吸附分子的模拟研究。研究结果表明:当注入压力达到3 MPa后,竞争吸附效果不再明显,为高压注入提供一定的理论基础;随着CO2分压的增大,O2吸附量降低速度逐渐平缓,初步确定最佳注入配比范围为2∶1至3∶1,为进一步结合实际工程中成本等因素确定最佳注入配比提供参考;等量吸附热受吸附条件的影响较小,仅与吸附质本身有关;随着CO2分压的增大,范德华能升高56.9%,分子内能升高78.7%,静电能升高67.2%,CO2对整个系统内的吸附作用强度及吸附量有着较大的影响;随着CO2分压增大,N2竞争吸附能力逐渐弱于O2,竞争吸附能力大小顺序为CO2>O2>N2。 相似文献
683.
大气细颗粒物(PM2.5)中的非极性化合物包括多环芳烃(PAHs)和正构烷烃(n-alkanes)等,通常用于识别污染来源,且对人体健康和环境有很重要的影响.为探究广西背景点PM2.5中非极性有机气溶胶的污染特征及来源,于2017年11月至2018年10月,对野外采集的PM2.5样品分析了其中17种多环芳烃和20种正构烷烃.结果表明,多环芳烃和正构烷烃全年的平均值分别为(4.28±4.25)ng·m-3和(13.7±14.72)ng·m-3;季节变化规律均是:冬季[(7.86±5.19)ng·m-3和(27.51±16.9)ng·m-3]>春季[(2.73±1.76)ng·m-3和(7.64±4.71)ng·m-3]>秋季[(2.34±1.45)ng·m-3和(7.01±4.55)ng·m-3]>夏季[(1.91±1.67)ng·... 相似文献
684.
Nicolas A.O. Morin Patrik L. Andersson Sarah E. Hale Hans Peter H. Arp 《环境科学学报(英文版)》2017,29(12):115-132
Flame retardants in commercial products eventually make their way into the waste stream.Herein the presence of flame retardants in Norwegian landfills, incineration facilities and recycling sorting/defragmenting facilities is investigated. These facilities handled waste electrical and electronic equipment(WEEE), vehicles, digestate, glass, combustibles, bottom ash and fly ash. The flame retardants considered included polybrominated diphenyl ethers(∑BDE-10) as well as dechlorane plus, polybrominated biphenyls, hexabromobenzene,pentabromotoluene and pentabromoethylbenzene(collectively referred to as ∑FR-7). Plastic,WEEE and vehicles contained the largest amount of flame retardants(∑BDE-10: 45,000–210,000 μg/kg; ∑FR-7: 300–13,000 μg/kg). It was hypothesized leachate and air concentrations from facilities that sort/defragment WEEE and vehicles would be the highest. This was supported for total air phase concentrations(∑BDE-10: 9000–195,000 pg/m~3 WEEE/vehicle facilities, 80–900 pg/m~3 in incineration/sorting and landfill sites), but not for water leachate concentrations(e.g., ∑BDE-10: 15–3500 ng/L in WEEE/Vehicle facilities and 1–250 ng/L in landfill sites). Landfill leachate exhibited similar concentrations as WEEE/vehicle sorting and defragmenting facility leachate. To better account for concentrations in leachates at the different facilities, waste-water partitioning coefficients, Kwastewere measured(for the first time to our knowledge for flame retardants). WEEE and plastic waste had elevated Kwastecompared to other wastes, likely because flame retardants are directly added to these materials. The results of this study have implications for the development of strategies to reduce exposure and environmental emissions of flame retardants in waste and recycled products through improved waste management practices. 相似文献
685.
Alternative brominated flame retardants (BFRs) have become prevalent as a consequence of restrictions on the use of polybrominated diphenyl ethers (PBDEs). For risk assessment of these alternatives, knowledge of their metabolism via cytochrome P450 enzymes is needed. We have previously proved that density functional theory (DFT) is able to predict the metabolism of PBDEs by revealing the molecular mechanisms. In the current study, the reactivity of 1,2-bis(2,4,6-tribromophenoxy)ethane and structurally similar chemicals with the Compound I model representing the active site of P450 enzymes was investigated. The DFT calculations delineated reaction pathways which lead to reasonable explanations for products that were detected by wet experiments, meanwhile intermediates which cannot be determined were also proposed. Results showed that alkyl hydrogen abstraction will lead to bis(2,4,6-tribromophenoxy)ethanol, which may undergo hydrolysis yielding 2,4,6-tribromophenol, a neurotoxic compound. In addition, a general pattern of oxidation reactivity regarding the 2,4,6-tribromophenyl moiety was observed among several model compounds. Our study has provided insights for convenient evaluation of the metabolism of other structurally similar BFRs. 相似文献
686.
Kun Lv Lu Bai Boyu Song Xindong M Minmin Hou Jie Fu Yali Shi Yawei Wang Guibin Jiang 《环境科学学报(英文版)》2022,34(5):277-285
The production and application of organophosphate esters (OPEs) have dramatically increased in recent years due to their use as a replacement for brominated flame retardants. In this study, 13 OPEs (Σ13OPEs) were analyzed in indoor air samples from kitchens and living rooms in 14 residential homes in Beijing, China. The concentrations of Σ13OPEs in kitchen air samples (mean: 13 ng/m3) were significantly (p < 0.05) higher than in living room air samples (5.0 ng/m3). In addition, paired window surface organic film samples were collected and analyzed to investigate film-air partitioning, exhibiting a mean concentration of Σ13OPEs of 4100 ng/m2. The congener profiles showed that tris(2-chloroisopropyl) phosphate (TCPP) was the predominant compound in both window film samples (48%) and the corresponding indoor air sample (56%). The estimated daily intakes (EDI) of OPEs via indoor air inhalation were 2.8 and 1.4 ng/kg/day for infants and adults, respectively, both of which are below the reference dose values (RfDs). Overall, these findings indicate that OPEs in the indoor air environment of residential homes in Beijing are not likely to pose a health risk to the general population. 相似文献
687.
Green leaf volatiles (GLVs) emitted by plants after stress or damage induction are a major part of biogenic volatile organic compounds (BVOCs). Proton transfer reaction time-of-flight mass spectrometry (PTR-TOF-MS) is a high-resolution and sensitive technique for in situ GLV analyses, while its performance is dramatically influenced by humidity, electric field, etc. In this study the influence of gas humidity and the effect of reduced field (E/N) were examined in addition to measuring calibration curves for the GLVs. Calibration curves measured for seven of the GLVs in dry air were linear, with sensitivities ranging from 5 to 10 ncps/ppbv (normalized counts per second/parts per billion by volume). The sensitivities for most GLV analyses were found to increase by between 20% and 35% when the humidity of the sample gas was raised from 0% to 70% relative humidity (RH) at 21°C, with the exception of (E)-2-hexenol. Product ion branching ratios were also affected by humidity, with the relative abundance of the protonated molecular ions and higher mass fragment ions increasing with humidity. The effect of reduced field (E/N) on the fragmentation of GLVs was examined in the drift tube of the PTR-TOF-MS. The structurally similar GLVs are acutely susceptible to fragmentation following ionization and the fragmentation patterns are highly dependent on E/N. Overall the measured fragmentation patterns contain sufficient information to permit at least partial separation and identification of the isomeric GLVs by looking at differences in their fragmentation patterns at high and low E/N. 相似文献
688.
689.
以胃蛋白酶(蛋白质)、谷胱甘肽(氨基酸多肽)、葡萄糖(糖类)作为模型物质代表藻来源有机物,并以Fluka腐殖酸为对照,研究其耗氯量、三卤甲烷(主要是氯仿)、卤乙酸(主要是二氯乙酸(DCAA)、三氯乙酸(TCAA))的形成情况.结果显示4种模型物质在氯化后,其余氯在前2 h迅速降低,6 h后则下降速度渐缓;其中耗氯量最大的是谷胱甘肽(96 h:7.1 mg·mg-1(以每毫克碳计,下同)),其次是胃蛋白酶(96 h:4.2 mg·mg-1)、腐殖酸(96 h:3.0 mg·mg-1),而葡萄糖最小(96 h:0.7 mg·mg-1).4种模型物质氯仿、DCAA、TCAA的生成速度也是在起初的2 h较快,随后渐缓;但从单位碳的产量来看,腐殖酸和胃蛋白酶形成氯仿(96h: 15.1~55.2 μg·mg-1(以每毫克碳计,下同))、DCAA(96 h: 15.1~55.2 μg·mg-1)、TCAA(96h: 15.1~55.2 μg·mg-1)均较多,而谷胱甘肽、葡萄糖则相对较少(氯仿-96 h:2.5~5.1 μg·mg-1;DCAA-96 h:0.6~8.0 μg·mg-1;TCAA-96 h:0.12~3.8 μg·mg-1);而从前驱物特性来说,氯仿、TCAA的前驱物具有较高的芳香度(即高的SUV254值),而DCAA前驱物的SUV254相对较低.对于富含蛋白质、多肽、糖类等的富营养化饮用水源,则要格外注意饮用水中DCAA所带来的健康风险. 相似文献
690.
An experimental study has been conducted to investigate the effects of hydrogen addition on the fundamental propagation characteristics of methane/air premixed flames at different equivalence ratios in a venting duct. The hydrogen fraction in the methane–hydrogen mixture was varied from 0 to 1 at equivalence ratios of 0.8, 1.0 and 1.2. The results indicate that the tendency towards flame instability increased with the fraction of hydrogen, and the premixed hydrogen/methane flame underwent a complex shape change with the increasing hydrogen fraction. The tulip flame only formed when the fraction of hydrogen ranged from 0 to 50% at an equivalence ratio of 0.8. It was also found that the flame front speed and the overpressure increased significantly with the hydrogen fraction. For all equivalence ratios, the stoichiometric flame (Φ = 1.0) has the shortest time of flame propagation and the maximum overpressure. 相似文献