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In this work, a new stir cake sorptive extraction (SCSE) using polymeric ionic liquid monolith as sorbent was prepared. The sorbent was obtained by in situ copolymerization of an ionic liquid, 1-allyl-3-methylimidazolium bis[(trifluoro methyl)sulfonyl]imide (AMII) and divinylbenzene (DB) in the presence of N,N-dimethylformamide. The influence of the content of ionic liquid and the porogen in the polymerization mixture on extraction performance was studied thoroughly. The physicochemical properties of the polymeric ionic liquid were characterized by infrared spectroscopy, elemental analysis, scanning electron microscopy and mercury intrusion porosimetry. The usefulness of SCSE–AMIIDB was demonstrated by the enrichment of trace benzimidazole anthelmintics. Several parameters affecting the extraction efficiency were investigated, and under the optimized conditions, a simple and effective method for the determination of trace benzimidazoles residues in water, milk and honey samples was established by coupling SCSE–AMIIDB with high performance liquid chromatography/diode array detection (SCSE–AMIIDB–HPLC/DAD). Results indicated that the limits of detection (S/N = 3) for target compounds were 0.020–0.072 μg L−1, 0.035–0.10 μg L−1 and 0.026–0.076 μg L−1 in water, milk and honey samples, respectively. In addition, an acceptable reproducibility was achieved by evaluating the repeatability and intermediate precision with relative standard deviations (RSD) of less than 9% and 11%, respectively. Finally, the established AMII–SCSE–HPLC/DAD method was successfully applied for the determination of benzimidazoles residues in milk, honey and environmental water samples. Recoveries obtained for the determination of benzimidazole anthelmintics in spiking samples ranged from 70.2% to 117.6%, with RSD below 12% in all cases. 相似文献
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Nonlinear Dynamics - An integrable extension of the Kadomtsev–Petviashvili (KP) and Davey–Stewartson (DS) equations is investigated in this paper. We will refer to this integrable... 相似文献
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Xiaojia Huang Yulei Wang Dongxing Yuan Xiaojing Li Shuyu Nong 《Analytical and bioanalytical chemistry》2013,405(7):2185-2193
A novel porous monolith has been prepared and used as a sorbent in stir-cake-sorptive extraction (SCSE). The monolithic material was prepared by in-situ copolymerization of allyl thiourea (AT) and divinylbenzene (DB) in the presence of dimethylformamide as a porogen solvent. To optimize the polymerization conditions, different monoliths with different ratios of functional monomer to porogenic solvent were prepared, and their extraction efficiency was investigated in detail. The monolith was characterized by elemental analysis, scanning electron microscopy, mercury intrusion porosimetry, and infrared spectroscopy. Analysis of polar phenols in environmental water samples by a combination of ATDB-SCSE and HPLC with diode-array detection was selected as a model for the practical application of the new sorbent. Several extraction conditions, including extraction and desorption time, pH, and ionic strength of the sample matrix were optimized. The results showed that the new monolith had high affinity for polar phenols and could be used to extract them effectively. Under the optimum conditions, low detection (S/N?=?3) and quantification (S/N?=?10) limits were achieved for the phenols, within the ranges 0.18–0.90 and 0.59–2.97 μg L?1, respectively. The linearity of the method was good, and the method enabled simple, practical, and low-cost extraction of these analytes. The distribution coefficients between ATDB and water (K ATDB/W) were calculated for the phenolic compounds and compared with K O/W. Finally, the proposed method was successfully applied to the determination of the compounds in three environmental water samples, with acceptable recovery and satisfactory repeatability. Figure
HPLC chromatograms of real water sample treated with ATDB-SCSE (a) and spiked water sample treated with ATDB-SCSE (b) 相似文献
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We report the observation of in-plane anisotropic magnetoresistance and planar Hall effect in non-magnetic HfTe5 thin layers.The observed anisotropic magnetoresistance as well as its sign is strongly dependent on the critical resistivity anomaly temperature Tp.Below Tp,the anisotropic magnetoresistance is negative with large negative magnetoresistance.When the in-plane magnetic field is perpendicular to the current,the negative longitudinal magnetoresistance reaches its maximum.The negative longitudinal magnetoresistance effect in HfTe5 thin layers is dramatically different from that induced by the chiral anomaly as observed in Weyl and Dirac semimetals.One potential underlying origin may be attributed to the reduced spin scattering,which arises from the in-plane magnetic field driven coupling between the top and bottom surface states.Our findings provide valuable insights for the anisotropic magnetoresistance effect in topological electronic systems and the device potential of HfTe5 in spintronics and quantum sensing. 相似文献
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确定了广义超特殊P-群G的自同构群的结构.设|G|=p2n+m,|ζG|=pm,其中n≥1,m≥2,AutfG是AutG中平凡地作用在Frat G上的元素形成的正规子群,则(1)当G的幂指数是pm时,(i)如果p是奇素数,那么Aut G/AutfG≌Z(p_1)pm-2,并且AutfG/Inn G≌Sp(2n,p)×zp.(ii)如果p=2,那么AutG=AutfG(若m=2)或者AutG/AutfG≌Z2m-3×z2(若m≥3),并且AutfG/InnG≌Sp(2n,2)× z2.(2)当G的幂指数是pm+1时,(i)如果p是奇素数,那么AutG=<θ>×AutfG,其中p的阶是(p-1)pm-1,且AutfG/InnG≌K(×)Sp(2n-2,p),其中K是p2n-1阶超特殊p-群.(ii)如果p=2,那么Aut G=<θ1,θ2>(×) AutfG,其中<θ1,θ2>=<θ1>×<θ2>≌Z2m-2×Z2,并且AutfG/InnG≌K(×)Sp(2n-2,2),其中K是22n-1阶初等Abel 2-群.特别地,当n=1时,AutfG/InnG≌Zp. 相似文献
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Dr. Yueqing Wang Dr. Xiaohai Yang Dr. Guoqiang Ding Dr. Hongyan Zheng Xianqing Li Prof. Yongwang Li Prof. Yulei Zhu 《ChemCatChem》2019,11(8):2118-2125
One-step catalytic conversion of fructose to furfuryl alcohol (FOL) is not only a challenge task but also to open a new pathway for conversion of hexose into useful chemicals. The favorable yield (41.6 %) of FOL can be directly obtained from fructose over the tandem of HY zeolite and Pd/Al2O3. However, the Pd/montmorillonite (Pd/MMT) was deactivated for production of FOL. The proportion of available Pd active sites (i. e. facets, corners and edges) vary with different supports, and the strong metal support interaction (SMSI) plays the pivotal role on the catalytic performance. For Al2O3 support, exposure of Pd (111) plane allows the hydroxymethylfurfural (HMF) to bind on the Pd (111) surface via planar arrangement. In this stance, the aldehyde group of HMF is readily eliminated by decarbonylation. Conversely, for Pd/MMT, the decarbonylation is completely inhibited due to the HMF absorbs on corner sites in perpendicular orientation. The XPS studies indicate that the density electron of Pd nanoparticles (NPs) could be manipulated by various supports, and the electron-donating effect of Al2O3 was observed. The collaborative effects between available sites and density electron of Pd are observed with respect to the different binding modes of HMF on the surface of Pd. The electronegative Pd NPs facilitate the decarbonylation of HMF as a consequence of the different adsorption strength between furan ring and aldehyde group. 相似文献