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431.
PCBs污染土壤的CaO诱导低温热处理脱氯研究   总被引:1,自引:0,他引:1  
研究了低温热处理脱氯技术对废弃电容器封存点附近污染土壤中多氯联苯脱氯的效果,考察反应温度、反应时间及CaO添加比例对PCBs去除率、脱氯率的影响以及反应前后土壤中污染物的组分变化。实验土样中PCBs浓度为107.7 mg/g,属于罕见高浓度PCBs污染土壤。当反应温度为400℃、停留时间4h、CaO添加比例为10%,PCBs的去除率为87.7%,脱氯率为85.3%。土壤样品中五氯联苯和四氯联苯反应后含量降低或未检出,部分反应后样品检出一氯联苯和联苯,说明在CaO诱导PCBs低温热处理脱氯反应中存在逐步脱氯/加氢反应途径。  相似文献   
432.
利用Fe(Ⅱ)EDTA络合吸收-铁粉间歇还原再生脱除NO并回收氨资源的方法,实验研究了铁粉还原再生Fe(Ⅱ)(NO)EDTA的过程及其影响因素。结果表明,以0.015 mol/L的Fe(Ⅱ)EDTA做吸收剂,在起始p H 5.5、温度323K条件下吸收400×10-6~500×10-6的NO,脱除率95%以上;铁粉还原再生Fe(Ⅱ)(NO)EDTA过程可用缩芯模型阐释;铁粉添加量与搅拌强度直接决定了铁粉质点数量,是影响反应的重要因素;实验中Fe(Ⅱ)(NO)EDTA络合液150 m L,氧气含量为5%时,搅拌速度900 r/min、粒径为0.12 mm的铁粉浓度5.3 g/L、温度353 K、p H=6为最适宜再生条件。  相似文献   
433.
Concentrations of heavy metals (As, Cd, Pb, Cu, Ni, Fe, Mn, and Zn) in market vegetables and fishes in Beijing, China, are investigated, and their health risk to local consumers is evaluated by calculating the target hazard quotient (THQ). The heavy metal concentrations in vegetables and fishes ranged from not detectable (ND) to 0.21 mg/kg fresh weight (f.w.) (As), ND to 0.10 mg/kg f.w. (Cd), and n.d to 0.57 mg/kg f.w. (Pb), with average concentrations of 0.17, 0.04, and 0.24 mg/kg f.w., respectively. The measured concentrations of As, Cd, Pb, Cu, Ni, Fe, Mn, and Zn are generally lower than the safety limits given by the Chinese regulation safety and quality standards of agriculture products (GB2762-2012). As, Cd, and Pb contaminations are found in vegetables and fishes. The exceeding standard rates are 19 % for As, 3 % for Cd, and 25 % for Pb. Pb contaminations are found quite focused on the fish samples from traditional agri-product markets. The paper further analyzed the health risk of heavy metals in vegetables and fishes respectively from supermarkets and traditional agri-product markets; the results showed that the fishes of traditional agri-product markets have higher health risk, while the supermarkets have vegetables of higher heavy metal risk, and the supervision should be strengthened in the fish supply channels in traditional agri-product markets.  相似文献   
434.
Nitrous oxide (N2O), a strong greenhouse gas, can be produced by ammonium-oxidizing bacteria (AOB) as a by-product of ammonium oxidation and can potentially be formed in all types of nitrification processes. However, partial nitritation has been reported to cause significantly higher N2O emissions than complete nitrification. In the study presented here, the mechanisms and factors that drive N2O formation by AOB were investigated with respect to different operational strategies to achieve nitrite accumulation base on combined evaluation of oxygen uptake rate (OUR) and N2O formation rate. On the one hand, N2O formation during partial nitritation and nitrification in a continuously stirred tank reactor (CSTR) with continuous aerobic conditions was observed. On the other hand, the effect of intermittent aeration on N2O formation during nitrification was investigated. The presence of nitrite, the extend of sludge-specific ammonium loading, low oxygen concentration, and transition from aerobic to anoxic conditions significantly increased N2O formation in this reactor independently from each other, indicating that different formation pathways, supposedly via nitrite or hydroxylamine, were active.  相似文献   
435.
Evidence has shown that polymorphisms of various genes known to be involved in estrogen biosynthesis and function are associated with estrogen-dependent diseases (EDDs). These genes include CYP17A1, estrogen receptor 1 (ESR1), and 2 (ESR2). Phthalates are considered estrogenic endocrine disruptors, and recent research has suggested that they may act as a risk factor for EDDs. However, extremely few studies have assessed the effects of gene–environment interaction on these diseases. We recruited 44 patients with endometriosis or adenomyosis, 36 patients with leiomyoma, and 69 healthy controls from a medical center in Taiwan between 2005 and 2007. Urine samples were collected and analyzed for seven phthalate metabolites using liquid chromatography tandem mass spectrometry. Peripheral lymphocytes were used for DNA extraction to determine the genotype of CYP17A1, ESR1, and ESR2. Compared to controls, patients with leiomyoma had significantly higher levels of total urinary mono-ethylhexyl phthalate (ΣMEHP) (52.1 vs. 29.6 μg/g creatinine, p?=?0.040), mono-n-butyl phthalate (MnBP) (75.4 vs. 51.3 μg/g creatinine, p?=?0.019), and monoethyl phthalate (MEP) (103.7 vs. 59.3 μg/g creatinine, p?=?0.031). In contrast, patients with endometriosis or adenomyosis showed a marginally increased level of urinary MEHP only. Subjects who were homozygous for both the ESR1 C allele (rs2234693) and CYP17A1 C allele (rs743572) showed a significantly increased risk for leiomyoma (OR?=?19.8; 95 % CI, 1.70; 231.5; p?=?0.017) relative to subjects with other genotypes of ESR1 and CYP17A1. These results were obtained after adjusting for age, cigarette smoking, MEHP level, GSTM1 genotype and other covariates. Our results suggested that both CYP17A1 and ESR1 polymorphisms may modulate the effects of phthalate exposure on the development of leiomyoma.  相似文献   
436.
437.
为解决水体因低碳氮比而导致脱氮效率差的问题,将颗粒聚己内酯(PCL)重新塑形为阶梯环状,研究其作为反硝化过程的生物膜载体与固相碳源的反硝化性能。结果表明,在静态实验中,平均反硝化速率为8.57 mg NO3-N/(L·h);反硝化过程为零级反应。连续填充床实验中,超过90%的硝酸盐可被去除,出水NO2-N质量浓度低于0.20 mg/L;出水NH3-N质量浓度略有上升;出水溶解性有机碳(DOC)先上升后降低至1 mg/L左右。电子扫描显微镜扫描显示,PCL阶梯环反应表面空隙率较高,表面生物膜以杆菌为主,反应后被明显腐蚀;液相色谱检测显示PCL阶梯环分子量反应前后略有下降,其结构未受到破坏;表明该材料适合作为反硝化反应的碳源的同时,又可以作为载体供微生物附着生长。  相似文献   
438.
餐厨垃圾中有机物大部分以大分子的形式存在,对其进行热处理,破坏大分子有机物的存在形式,将会影响其干式厌氧发酵的过程。实验对餐厨垃圾进行了热处理(100℃),处理后将其在含固率(TS)20%、接种率25%的条件下进行高温55℃厌氧发酵。实验结果表明,热处理后,餐厨垃圾的理化性质发生显著变化,累计产气量、TS和VS的去除率均增大。当热处理时间为15 min时,餐厨垃圾的SCOD值最高,为59.49 g/L,比未处理时提高了3.3倍。同样该条件下,累计产气量也最高,为2 782.8 m L,与未处理相比累积产气量提高58.30%,第二产气高峰比未处理提前3天。各发酵瓶发酵前后TS、VS去除率的变化趋势与累计产气量的变化基本一致,累计产气量越大,TS、VS的去除率越大。  相似文献   
439.
Effect of the addition of poly(ethylene glycol) terminated by benzoate (PEG-BA) on the crystallization behavior and dynamic mechanical properties of poly(l-lactic acid) PLLA is studied as compared with poly(ethylene glycol) (PEG-OH). It is found that PEG-BA is miscible with PLLA and shows good plasticizing effect. Because PEG-OH having the same degree of polymerization is immiscible with PLLA, the end group in PEG-BA, i.e., benzoate, plays an important role in the miscibility. Furthermore, PEG-BA does not induce the PLLA degradation at melt-processing, whereas PEG-OH leads to the hydrolysis degradation. Finally, the addition of PEG-BA pronounces the crystallization rate of PLLA at low crystallization temperatures and thus enhances the degree of crystallinity at conventional processing. Consequently, the temperature dependence of dynamic mechanical properties are similar to that for isotactic polypropylene.  相似文献   
440.
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