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Recycling is time consuming and the time available for housework may determine the intensity of recycling activities. In this study, we conducted a survey of 546 Japanese households and asked them their daily practice of five varieties of recycling activities: (1) choice of refill products, (2) use of own shopping bags, (3) sorting of recycled papers from burnable waste, (4) use of own drinking bottles when going out, and (5) use of recycle boxes prepared at the grocery store. We also asked households to record their behavior for two successive days. By combining recycling activity data and diary data, we estimate a multivariate probit model to empirically examine whether time available for housework determines the intensity of five varieties of recycling activities. The empirical result demonstrates that an individual that can allocate sufficient time for housework tends to purchase refill products. He or she also tends to bring their own shopping bags for grocery shopping. We also find that the size of house and the number of family members determine the likelihood of recycling. A housewife living with many family members in a large house is more likely to engage in time-consuming recycling activities.  相似文献   
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Journal of Material Cycles and Waste Management - Polyamide 66 was efficiently depolymerized and chemically converted by treatment with supercritical MeOH in the presence of glycolic acid. The...  相似文献   
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H-ZSM-5 zeolite-supported gallium oxides were studied as aromatization catalysts for polyolefin pyrolysate. The catalysts were prepared by a conventional physical mixing method with a gallium content of 1.0 and 4.5 wt% and were reduced in flowing hydrogen at 585°C. To test their activity, a polyolefin sample was pyrolyzed and passed over a heated catalyst layer; the product was analyzed by gas chromatography/mass spectrometry. A continuous-flow fixed-bed reactor was used for aromatization of a model gas of polyolefin pyrolysate. For chlorine-free sources at 450°C, the catalyst with only 1.0 wt% gallium exhibited activity comparable to a gallium silicate catalyst. For chlorine-contaminated sources, the catalyst with 4.5 wt% gallium sustained catalytic activity for long periods. From the activity test results, it was found that zeolite-supported gallium catalysts prepared by the physical mixing method are suitable for converting polyolefin into aromatic hydrocarbons.  相似文献   
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Recent climate modeling studies have concluded that cumulative carbon emissions determine temperature increase, regardless of emission pathways. Accordingly, the optimal emission pathway can be determined from a socioeconomic standpoint. To access the path dependence of socioeconomic impacts for cumulative carbon emissions, we used a computable general equilibrium model to analyze impacts on major socioeconomic indicators on a global scale for 30–50 pathways with different emission reduction starting years, different subsequent emission pathways, and three different cumulative 2100 emission scenarios (emissions that meet the 2 °C target, the 2 °C target emissions plus 10 %, and emissions producing radiative forcing of 4.5 W/m2). The results show that even with identical cumulative emission figures, the resulting socioeconomic impacts vary by the pathway realized. For the United Nations 2 °C target, for example, (a) the 95 % confidence interval of cumulative global gross domestic product (GDP) is 1355–1363 trillion US dollars (2010–2100, discount rate = 5 %), (b) the cumulative GDP of pathways with later emission reduction starting years grows weaker (5 % significance level), and (c) emissions in 2100 have a moderate negative correlation with cumulative GDP. These results suggest that GDP loss is minimized with pathways with earlier emission reduction followed by more moderate reduction rates to achieve lower emission levels. Consequently, we suggest an early emission peak to meet the stringent target. In our model setting, it is desirable for emissions to peak by 2020 to reduce mitigation cost and by 2030 at the latest to meet the 2 °C target.  相似文献   
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The aqueous monochlorophenols were degraded by contact glow discharge electrolysis (CGDE), in which plasma was generated in a localized zone between an electrolytic solution and an anode. With the decay of monochlorophenols, the amount of total organic carbon (TOC) also decreased smoothly, indicating that carbon atoms of benzene nucleus could be eventually converted to inorganic carbons. Meanwhile, it was also clarified that chlorine atoms in the organics were liberated as chloride ions. In addition, it was revealed that the disappearance of monochlorophenols obeyed the first-order rate law, depending on the isomeric structures.  相似文献   
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80·2 Per cent of 111 Down syndrome pregnancies had amniotic fluid (AF) alpha fetoprotein (AFP) levels on or below the median and 10·8 per cent at or below 0·5 MoM compared with 41·9 and 1·4 per cent of controls. These differences were even more striking when the gestational age was < 18 weeks compared with ⩾ 18 weeks. No such association was seen for other chromosome abnormalities including trisomy 18,45,X and mosaics, 47,XXY, 47,XXX, and other structural abnormalities and triploidy, even when high levels due to defects such as omphalocele and cystic hygroma were excluded. All cases of trisomy 13 and 80 per cent with 47,XYY had AF-AFP levels above the median. Selection of cases for karyotyping by a low level of AF-AFP would clearly fail to detect aneuploidies other than Down syndrome and is not recommended. A possible weak association between low maternal serum (MS) and AF-AFPs in Down syndrome was most evident at < 18 weeks, suggesting that MS screening between 16 and 18 weeks may be the most informative time.  相似文献   
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Decomposition of aqueous monofluorophenols (MFPs) was investigated by contact glow discharge electrolysis (CGDE). During CGDE, both MFPs and the corresponding total organic carbon (TOC) in water were consumed smoothly, suggesting that carbon atoms of benzene nucleus could be eventually mineralized to inorganic carbon (IC). And all the fluorine atoms in the MFPs were equally converted to fluoride ions. Based on the primary intermediates from each starting materials, it showed that aromatic hydroxylation preferentially occurred at the para-or ortho-position to the phenolic OH group of each MFPs. The disappearance of both MFPs and TOC followed the first-order rate law. The apparent rate constants for the decay of MFPs were independent from the pKa values of MFPs.  相似文献   
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