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Polycyclic aromatic hydrocarbons as byproducts of carbon-based fuel combustion are an important group of pollutants with wide distribution in the environment. Polycyclic aromatic hydrocarbons are known as toxic compounds for almost all organisms. Different plant species can uptake polycyclic aromatic hydrocarbons by roots and translocate them to various aerial parts. The aim of this study is to investigate the uptake, translocation, and accumulation of pyrene and phenanthrene in maize under controlled conditions. Seeds were cultivated in perlite containing 25, 50, 75, and 100 ppm of phenanthrene and pyrene, and their concentrations in the roots and shoots of the plants were measured using high-performance liquid chromatography technique after 7, 14, and 21 days. The results revealed that phenanthrene naturally existed in maize and its concentration showed a time-dependent decrease in shoots and roots. In contrast, the concentration of pyrene was increased in the roots and reduced in the shoots. Although pyrene had higher uptake than phenanthrene in roots of maize, the translocation factor value for pyrene was lower than for phenanthrene. According to these findings, phenanthrene could be metabolized in maize in the shoot and root tissues, but pyrene had more tendency to be accumulated in roots.
相似文献This study investigated the characteristics of iron corrosion scales in pipes at tube well, overhead tank, and consumers’ end in older untreated water distribution system in Peshawar city, Pakistan. Effect of water quality conditions on corrosion scales and that of scales on drinking water quality in such systems was also assessed by undertaking a comparison with new piped distribution systems. The scales were analyzed for chemical composition and morphology using X-ray diffraction (XRD), inductively coupled plasma (ICP), and a scanning electron microscope (SEM), while water quality was examined for physicochemical and biological characteristics. The main crystalline phases of corrosion scales were goethite, magnetite, siderite, and quartz. From tube well to consumers’ end, goethite increased from 36 up to 48%, quartz declined from 22 to 15%, while magnetite fluctuated and siderite disappeared. Elemental composition of scales showed the deposition of Zn, Al, Mn, Cr, Pb, Cu, As, and Cd with Zn (13.9 g/kg) and Al (3.6 g/kg) in highest proportion. The SEM analysis illustrated the presence of microbial communities indicating the formation of biofilms in the corrosion scales. The significant difference (P <?0.05) in levels of dissolved oxygen (DO), Cl?, SiO44?, electrical conductivity (EC), SO42?, NO3?, alkalinity, hardness, and trace metals between old (DS-O) and new piped systems indicated their role in corrosion scale formation/destabilization and the effect of scale dissolution on water quality. In DS-O, EC, Cu, and Mn were significantly higher (P?<?0.05), whereas turbidity, EC, DO, and SiO44? significantly increased from source to consumers’ end implying a higher dissolution of scales and lowered corrosion rates in DS-O to utilize SiO44? and DO for iron oxidation.
相似文献Date palm waste–derived biochar (DBC) was produced through pyrolysis (600 °C) and modified with zeolite (Z-DBC), silica (S-DBC), or nano-zerovalent iron (nZVI-DBC) to design efficient sorbents. The pristine and engineered biochars were characterized by SEM, XRD, BET, TGA, CHNS-O, and FTIR to investigate the surface, structural, and mineralogical composition. The nZVI-DBC exhibited lowest pH (6.15) and highest surface area (220.92 m2 g−1), carbon (80.55%), nitrogen (3.78%), and hydrogen (11.09%) contents compared with other biochars. Isotherm sorption data for chlortetracycline (CTC) removal from aqueous solutions was described well by Langmuir and Redlich–Peterson isotherms showing the highest fitness (R2 values in the range of 0.88–0.98 and 0.88–0.99, respectively). Langmuir predicted maximum CTC adsorption capacity was in order of nZVI-DBC (89.05 mg g−1) > S-DBC (45.57 mg g−1) > Z-DBC (30.42 mg g−1) > DBC (28.19 mg g−1). Kinetics adsorption data was best described by power function model (R2 = 0.93–0.99), followed by interaparticle diffusion (R2 = 0.85–0.96) model. The nZVI-DBC performed outclass by removing 98% of CTC, followed by S-DBC (68%), Z-DBC (35%), and DBC (36%). Chemisorption, H-bonding, and interaparticle diffusion were the operating mechanisms for CTC adsorption onto DBC, S-DBC, and Z-DBC, while π-π electron donor–accepter interactions and redox reactions augmented these mechanisms for highest CTC adsorption onto nZVI-DBC. Therefore, nZVI-DBC may serve as an efficient green technology for the removal of CTC from aqueous solutions and to reduce surface date palm waste pollution.
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