全文获取类型
收费全文 | 148篇 |
免费 | 1篇 |
专业分类
化学 | 73篇 |
晶体学 | 1篇 |
力学 | 9篇 |
数学 | 25篇 |
物理学 | 41篇 |
出版年
2023年 | 1篇 |
2022年 | 3篇 |
2021年 | 5篇 |
2020年 | 2篇 |
2019年 | 1篇 |
2018年 | 2篇 |
2017年 | 1篇 |
2016年 | 6篇 |
2015年 | 3篇 |
2014年 | 2篇 |
2013年 | 7篇 |
2012年 | 3篇 |
2011年 | 12篇 |
2010年 | 4篇 |
2009年 | 5篇 |
2008年 | 11篇 |
2007年 | 6篇 |
2006年 | 5篇 |
2005年 | 6篇 |
2004年 | 8篇 |
2003年 | 1篇 |
2001年 | 1篇 |
2000年 | 6篇 |
1999年 | 4篇 |
1998年 | 3篇 |
1997年 | 2篇 |
1996年 | 2篇 |
1994年 | 1篇 |
1993年 | 3篇 |
1992年 | 1篇 |
1991年 | 2篇 |
1990年 | 1篇 |
1989年 | 3篇 |
1988年 | 1篇 |
1987年 | 3篇 |
1985年 | 1篇 |
1984年 | 1篇 |
1981年 | 2篇 |
1980年 | 1篇 |
1978年 | 2篇 |
1976年 | 1篇 |
1974年 | 2篇 |
1970年 | 2篇 |
1968年 | 2篇 |
1967年 | 2篇 |
1963年 | 1篇 |
1962年 | 2篇 |
1961年 | 1篇 |
1907年 | 2篇 |
排序方式: 共有149条查询结果,搜索用时 15 毫秒
71.
T.M. Schmidt C. Bianchini M.M.C. Forte S.C. Amico A. Voronoff R.C.F. Gonalves 《Polymer Testing》2006,25(8):1044-1051
The use of polyester (PET) fibre ropes in mooring applications for deep water oil platforms implies the use of terminations, e.g. the spliced eye, which demands specialized manual labour and is time consuming. This research evaluates the technical viability of substituting these terminations with a resin socketing procedure, which consists of introducing a simple-end rope in a hollow metallic device having a conical shape (i.e. a socket) and pouring into it a thermoset resin that, once cured, fastens the rope extremity. PET ropes (10 or 48 mm diameter) were socketed and evaluated under tensile testing. The curing and viscoelastic behaviour of various epoxy resin systems were monitored with DSC and DMA. The performance of socketed PET ropes was suitable for the intended application, showing failure loads similar to those of unsocketed ropes, being particularly dependant on resin type, socket conicity and resin/fibre volumetric ratio in it. 相似文献
72.
Beatrice Bocca Marcelo Enrique Conti Anna Pino Daniela Mattei Giovanni Forte 《International journal of environmental analytical chemistry》2013,93(15):1111-1123
A simple and convenient method for the digestion of animal tissues, lichens, and plants for 33 metals measured by sector field inductively coupled plasma mass spectrometry (SF-ICP-MS) was described. Microwave-assisted acid digestions were performed at atmospheric pressure by means of a multi-samples rotor designed for processing a large number of samples at once in screw-capped disposable polystyrene liners. The digested samples were filled up to final volume directly in the polystyrene liners ready for elemental quantification. Seven certified reference materials, namely BCR 184 (bovine muscle), BCR 186 (pig kidney), DORM-2 (dogfish muscle), BCR 422 (cod muscle), BCR 62 (olive leaves), BCR 100 (beech leaves), and BCR 482 (lichen) were analysed to verify the accuracy of the method. The linearity range, limit of quantification, precision, and recovery by addition of non-certified elements were also assessed. All elements, with the exception of Hg in BCR 184 and As in BCR 186, were above the quantification limit and blank concentrations, and good agreement existed between found and target values in bovine muscle, pig kidney, and cod muscle. Significant deviations were observed for Al, Co, Cr, Mn, and Ni in dogfish muscle and for Ca, Cr, Fe, and Hg in lichens and plants. The proposed digestion procedure offers a low contamination risk, simplicity, speed, low cost, and applicability in routine analysis, and the SF-ICP-MS method allowed metals from a fraction of ng?g?1 to hundreds of µg?g?1 to be quantified in one analytical run. 相似文献
73.
Separation of seven organic and inorganic arsenical species, i.e., inorganic arsenite (As III) and arsenate (As V), monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), arsenobetaine (AsBet), arsenocholine (AsCh) and p-arsanilic acid (pAs) was carried out by capillary electrophoresis (CE) equipped with one of two different optical path cells, i.e., either the standard detection interface (SDI) or the high sensitive detection cell (HSDC). Separation, identification and quantification of the As species were performed by means of a capillary silica column with an alkaline borate buffer at pH 9.3 and direct UV detection at 192 nm. This methodological approach was tested with the abovementioned types of cells, and the results of the two modes were compared. In both cases, good separation was obtained, and also, repeatability in terms of migration times and peak areas was rather satisfactory. With regard to sensitivity, the HSDC allowed peak areas to be obtained, which were ca. 50 times greater than those afforded by the former cell. This also led to a substantial improvement in the limits of detection (LoDs); by a factor of 9 in the case of AsCh. 相似文献
74.
Antonio Bartolotta Claudia Forte Marco Geppi Domenico Minniti Giuseppe Visalli 《Solid state nuclear magnetic resonance》1997,8(4):231-239
1H-, 13C-, 23Na-solid state NMR measurements have been used to characterise the morphology and the dynamics of several NaSCN-PEO mixtures. Selective 13C-MAS experiments allowed to determine the composition of the (PEO)nNaSCN samples in terms of the different phases present, as well as the real stoichiometry of the crystalline complex. 1H- and 13C-spin-lattice relaxation times provided estimates of the dimensions of the different domains and gave information on the dynamics of the polymer chains. 23Na-MAS spectra and 2D nutation experiments allowed to individuate the presence of different environments for the sodium cations on the basis of their quadrupolar interactions. 相似文献
75.
76.
A new water-soluble uranyl-salophen complex incorporating two glucose units has been synthesized. This neutral derivative shows noteworthy binding affinity for fluoride in water thanks to the Lewis acid-base interaction occurring between the metal and the anion. Such interaction is strong enough to overcome the high hydration enthalpy of fluoride. Moreover this complex effectively binds hydrogen phosphate and exhibits remarkably strong association for nucleotide polyanions ADP(3-) and ATP(4-). 相似文献
77.
Ab initio calculations including electron correlation are still extremely costly, except for the smallest atoms and molecules. Therefore, our purpose in the present study is to employ a bond-order correlation approach to obtain, via equilibrium molecular energies, molecular dissociation energies and heats of formation for some 20 molecules containing C, H, and O atoms, with a maximum number of electrons of around 40. Finally, it is important in the proposed procedure to include electron correlation effects in the basis set choice when determining thermodynamic properties. With the optimum choice of basis set, the average percentage error for some 20 molecules is approximately 20% for heats of formation. For molecular dissociation energies the average error is much smaller: ~0.4%. 相似文献
78.
The action of the orthogonal group \(O(2)\) on the space of plane elasticity tensors has been the subject of some recent investigations. It is shown here that the approach based on the “harmonic decomposition” technique, which is also used in a three-dimensional setting, gives a unified perspective on this issue. We construct explicit relationships between invariants and quantities derived from such an approach and what was found earlier by Tsai and Pagano and, more recently, through the “polar method” and the use of complex variables. 相似文献
79.
Francesca F. Slejko Riccardo Petrini Anna Lutman Claudia Forte 《Isotopes in environmental and health studies》2019,55(1):56-69
The origin of a resurgent hexavalent chromium contamination in groundwater from a phreatic aquifer in the Friuli Venezia Giulia Region plain was investigated by chromium isotopic systematics. The area underwent a severe Cr(VI) contamination by industrial effluents in 1997, when Cr(VI) concentration in groundwater reached 4500?µg/L. In subsequent years the contamination naturally attenuated, totally disappearing in 2003. A renewal of water contamination was observed in 2008, Cr(VI) reaching 1560?µg/L. The δ53Cr value in groundwater and extracts from sediments was measured in 2009–2011, and it ranges between ?3.21 and +0.21‰ and between ?4.71 and +1.26‰, respectively. Due to the lack of geogenic Cr-sources, these data are interpreted as evidence of the subsequent oxidation through Mn-oxides of the Cr(III) hosted in the aquifer and originated by the reduction of the original industrial chromates. Cr(III) is characterized by negative δ53Cr, starting from the δ53Cr value around zero of Cr(VI) in industrial effluents. Oxidation liberates soluble Cr(VI) which is transported by groundwater and permeated soils. The complex Cr-isotopic vs. concentration distribution reflects both the new Cr(VI) reduction and dilution processes in the aquifer system. From an environmental point of view, the data raise concerns regarding the potential impact of past Cr(VI)-contamination. 相似文献
80.
G. Forte G.M. Lombardo G.G.N. Angilella R. Pucci R. Vilardi 《Physics letters. A》2008,372(40):6168-6174
We have followed a ‘molecular’ approach to study impurity effects in graphene. This is thought as the limiting case of an infinitely large cluster of benzene rings. Therefore, we study several carbon clusters, with increasing size, from phenalene, including three benzene rings, up to coronene 61, with 61 benzene rings. The impurities considered were a chemisorbed H atom, a vacancy, and a substitutional proton. We performed HF and UHF calculations using the STO-3G basis set. With increasing cluster size in the absence of impurities, we find a decreasing energy gap, here defined as the HOMO-LUMO difference. In the case of H chemisorption or a vacancy, the gap does not decrease appreciably, whereas it is substantially reduced in the case of a substitutional proton. The presence of an impurity invariably induces an increase of the density of states near the HOMO level. We find a zero mode only in the case of a substitutional proton. In agreement with experiments, we find that both the chemisorbed H, the substitutional proton, and the C atom near a vacancy acquire a magnetic moment. The relevance of graphene clusters for the design of novel electronic devices is also discussed. 相似文献