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121.
Research on Chemical Intermediates - Iron-nanoparticle-impregnated activated carbon (IrAC) nanocomposite was synthesized as a new vanadium adsorbent. The vanadium adsorption rate for commercial...  相似文献   
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In this study, polyaniline-co-poly(o-toluidine)/graphene oxide nanosheets composite was electrodeposited on the surface of a stainless steel wire as a new coating for headspace solid-phase microextraction of benzene, toluene, ethylbenzene and xylenes (BTEX) with gas chromatography–mass spectrometry. The characteristics of the new coating were evaluated by the scanning electron microscopy and Fourier transform infrared spectroscopy. To study the coating performance, the influence of various parameters such as deposition potential and time, concentration of the monomers and GONSs, desorption temperature and time, extraction temperature and time and ionic strength on BTEX extraction efficiency was investigated. At the optimum conditions, the linear ranges and detection limits (S/N?=?3) were found 0.01–50 and 0.001–0.05 ng mL?1, respectively. The intra-day and inter-day relative standard deviations (RSDs) at 0.5 ng mL?1 concentration level (n?=?5) using a single-fiber were from 5.4 to 8.3 and 7.5 to 10.3%, respectively. The fiber-to-fiber RSDs % (n?=?3) was between 8.4 and 12.5%. Finally, the development method was applied to the analysis of various real samples.  相似文献   
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The 1 : 1 intermediates generated by addition of isoquinoline to isocyanates were trapped by diphenyl phosphonate to yield diphenyl [2‐(aminocarbonyl)‐1,2‐dihydroisoquinolin‐1‐yl]phosphonates in good yields under solvent‐free conditions.  相似文献   
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SPE joined with dispersive liquid–liquid microextraction based on solidification of floating organic drop (DLLME‐SFO) as a novel technique combined with GC with electron‐capture detection has been developed as a preconcentration technique for the determination of organochlorine pesticides (OCPs) in water samples. Aqueous samples were loaded onto multiwalled carbon nanotubes as sorbent. After the elution of the desired compounds from the sorbent by using acetone, the DLLME‐SFO technique was performed on the obtained solution. Variables affecting the performance of both steps such as sample solution flow rate, breakthrough volume, type and volume of the elution, type and volume of extraction solvent and salt addition were studied and optimized. The new method provided an ultra enrichment factor (8280–28221) for nine OCPs. The calibration curves were linear in the range of 0.5–1000 ng/L, and the LODs ranged from 0.1–0.39 ng/L. The RSD, for 0.01 μg/L of OCPs, was in the range of 1.39–13.50% (n = 7). The recoveries of method in water samples were 70–113%.  相似文献   
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In this work, iron nanoparticles were impregnated onto a commercial activated carbon surface to produce a novel adsorbent called iron-activated carbon nanocomposite (I-AC). Commercial activated carbon (CAC) and I-AC were used for vanadium separation in a fixed-bed column. The effects of various operating parameters such as inlet vanadium ion concentration, adsorbent dose and volumetric flow rate on vanadium separation performance of CAC were investigated. The performance of both adsorbents was compared in three adsorption/desorption cycles. The experimental breakthrough curves of vanadium ions in the fixed-bed column were modeled using the film-pore-surface diffusion model (FPSDM). The four mass transfer parameters characterizing this model, namely the external mass-transfer coefficient (k f ), pore and surface diffusion coefficients (D p and D s ), and axial dispersion coefficient (D L ) were evaluated through the model. Modelling and experimental results showed that the I-AC nanocomposite has a better performance for vanadium separation in comparison to AC. Sensitivity analysis on the FPSDM showed that the pore and surface diffusion, external mass transfer and axial dispersion play a significant role in vanadium separation using the I-AC. On the other hand, surface diffusion resulted to be relatively less important when CAC was used.  相似文献   
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In this work development of 68Ga-ethyl cysteinate dimer (68Ga-ECD) a 68Ga tracer for possible cerebral blood flow based on 99mTc ECD homolog is reported. 68Ga-ECD was prepared using generator-based 68GaCl3 and ECD at optimized conditions. Quality control, stability, partition co-efficient and the biodistribution of the tracer (by tissue counting and PET/CT in rats) was studied. Significant metabolism of the lipophilic tracer into water soluble metabolite(s) led to urinary excretion of the tracer, un-comparable to that of homologous 99mTc-compound. Cardiac uptake of the complex suggests formation of a possible lipophil cationic complex and/or metabolite.  相似文献   
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