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51.
Marzena Biaek Krystyna Czaja Aleksandra Reszka 《Journal of polymer science. Part A, Polymer chemistry》2005,43(22):5562-5570
Ethylene polymerization and its copolymerization with 1‐hexene with a set of supported metallocene catalysts were studied. As a carrier, the complex of magnesium chloride with tetrahydrofuran, which was previously pretreated with a triisobutylaluminium (TIBA), was used. The investigated metallocene compound differs in the metal type (Zr or Ti), the nature of the alkyl substituent in the cyclopentadienyl ring, and the type of ligand (Cp or Ind). The effect of catalyst composition on the anchored metal content, catalyst activity, comonomer reactivity, and polymer properties was investigated. The results obtained with supported catalysts were compared with those obtained with their homogeneous counterparts under the same (co)polymerization conditions. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5562–5570, 2005 相似文献
52.
Investigations into the compositional heterogeneity of ethylene/1-hexene copolymers obtained with various zirconocene/MAO catalysts, either homogeneous or supported on inorganic carriers such as a complex of magnesium chloride with tetrahydrofuran or methyl alcohol, were conducted. The dependence between metallocene structure, as well as catalyst immobilization, and the compositional heterogeneity of the related products was investigated. It was found that the heterogeneity of copolymers is determined by the metallocene catalyst structure. The amount of peaks on the DSC thermograms of copolymers and their division increase with the increase of bulkiness of the ligand in the catalytic system. The immobilization of the investigated catalysts on the magnesium carrier leads to an increase of the copolymer's compositional heterogeneity. However, the modification of the MgCl2 carrier by tetrahydrofuran or methyl alcohol seems to not have any influence on the copolymers’ CCD. 相似文献
53.
pH‐Responsive Non‐Ionic Diblock Copolymers: Ionization of Carboxylic Acid End‐Groups Induces an Order–Order Morphological Transition 下载免费PDF全文
Joseph R. Lovett Dr. Nicholas J. Warren Dr. Liam P. D. Ratcliffe Dr. Marzena K. Kocik Prof. Steven P. Armes 《Angewandte Chemie (International ed. in English)》2015,54(4):1279-1283
A carboxylic acid based reversible additionfragmentation transfer (RAFT) agent is used to prepare gels composed of worm‐like diblock copolymers using two non‐ionic monomers, glycerol monomethacrylate (GMA) and 2‐hydroxypropyl methacrylate (HPMA). Ionization of the carboxylic acid end‐group on the PGMA stabilizer block induces a worm‐to‐sphere transition, which in turn causes immediate degelation. This morphological transition is fully reversible as determined by TEM and rheology studies and occurs because of a subtle change in the packing parameter for the copolymer chains. A control experiment where the methyl ester derivative of the RAFT agent is used to prepare the same diblock copolymer confirms that no pH‐responsive behavior occurs in this case. This end‐group ionization approach is important for the design of new pH‐responsive copolymer nano‐objects as, unlike polyacids or polybases, only a minimal amount of added base (or acid) is required to drive the morphological transition. 相似文献
54.
An automatic sequential injection system, combining monosegmented flow analysis, sequential injection analysis and sequential injection titration is proposed for acidity determination. The system enables controllable sample dilution and generation of standards of required concentration in a monosegmented sequential injection manner, sequential injection titration of the prepared solutions, data collecting, and handling. It has been tested on spectrophotometric determination of acetic, citric and phosphoric acids with sodium hydroxide used as a titrant and phenolphthalein or thymolphthalein (in the case of phosphoric acid determination) as indicators. Accuracy better than |4.4|% (RE) and repeatability better than 2.9% (RSD) have been obtained. It has been applied to the determination of total acidity in vinegars and various soft drinks. The system provides low sample (less than 0.3 mL) consumption. On average, analysis of a sample takes several minutes. 相似文献
55.
Jasiewicz B Wojciechowska-Nowak M Boczoń W Wyrzykiewicz E 《European journal of mass spectrometry (Chichester, England)》2011,17(3):227-235
The electron-ionization mass spectra (EI-MS) of oxo- and thio-derivatives of minor tobacco alkaloids and structurally similar piperidine alkaloids, i.e. thiocotinine (1), 2'-oxo-N-methylanabasine (2), 2'-thio-N- methylanabasine (3), 2'-oxoanabasamine (4) and 2'-thioanabasamine (5) are discussed and general fragmentation routes of their molecular cations are proposed. Comparison of the data obtained for 1 with the EI-MS data of metameric metabolites of nicotine: 3'-hydroxycotinine, (A) and 5'-hydroxycotinine, (B) allows a differentiation between these metamers. The data will be useful for the identification of metabolites of alkaloids of these types in biological matrices. 相似文献
56.
Marzena Ciszak Stefano Euzzor Andrea Geltrude F. Tito Arecchi Riccardo Meucci 《Communications in Nonlinear Science & Numerical Simulation》2013,18(4):938-945
The synchronization in four forced FitzHugh–Nagumo (FHN) systems is studied, both experimentally and by numerical simulations of a model. We show that synchronization may be achieved either by coupling of systems through bidirectional diffusive interactions, by introducing a common noise to all systems or by combining both ingredients, noise and coupling together. Here we consider white and colored noises, showing that the colored noise is more efficient in synchronizing the systems respect to white noise. Moreover, a small addition of common noise allows the synchronization to occur at smaller values of the coupling strength. When the diffusive coupling in the absence of noise is considered, the system undergoes the transition to subthreshold oscillations, giving a spike suppression regime. We show that noise destroys the appearance of this dynamical regime induced by coupling. 相似文献
57.
Michael Armbruster Marzena Fügenschuh Christoph Helmberg Alexander Martin 《Mathematical Programming Computation》2012,4(3):275-306
While semidefinite relaxations are known to deliver good approximations for combinatorial optimization problems like graph bisection, their practical scope is mostly associated with small dense instances. For large sparse instances, cutting plane techniques are considered the method of choice. These are also applicable for semidefinite relaxations via the spectral bundle method, which allows to exploit structural properties like sparsity. In order to evaluate the relative strengths of linear and semidefinite approaches for large sparse instances, we set up a common branch-and-cut framework for linear and semidefinite relaxations of the minimum graph bisection problem. It incorporates separation algorithms for valid inequalities of the bisection cut polytope described in a recent study by the authors. While the problem specific cuts help to strengthen the linear relaxation significantly, the semidefinite bound profits much more from separating the cycle inequalities of the cut polytope on a slightly enlarged support. Extensive numerical experiments show that this semidefinite branch-and-cut approach without problem specific cuts is a superior choice to the classical simplex approach exploiting bisection specific inequalities on a clear majority of our large sparse test instances from VLSI design and numerical optimization. 相似文献
58.
The Use of Starch Drying Kinetics Curves for Experimental Determination of Its Specific Surface Area
The most popular method for the calculation of specific surface area is its determination from water vapour sorption isotherms. The study presented here has been designed for the purpose of optimisation and selection of the conditions of drying so as to allow the determination of specific surface area from plotted curves of the drying process. The results indicate that drying curves can be used as the basis for the determination of specific surface area, the values of which do not differ statistically significantly (α = 0.05) from those determined from isotherms of water vapour sorption (adsorption/desorption). 相似文献
59.
Marek T. Cegla Marzena Baran Agnieszka Czarny Marek Zylewski Joanna Potaczek Jeff Klenc Lucjan Strekowski 《Journal of heterocyclic chemistry》2011,48(3):720-723
Fused dihydrooxazoles are produced by the reaction of 8‐bromoteophylline (1), 6‐bromo‐2‐pyridone (7), or 2‐bromobenzimidazole (11) with an N‐substituted N‐(2,3‐epoxypropyl)amine. The product derived from 1 undergoes rearrangement to a fused dihydrooxazine while the fused dihydrooxazoles derived from 7 and 11 are stable. J. Heterocyclic Chem., (2011). 相似文献
60.
Robert Skorek Magdalena Jablonska Marzena Polowniak Andrzej Kita Piotr Janoska Franciszek Buhl 《Central European Journal of Chemistry》2012,10(1):71-84
In this study, more than 200 samples of drinking water from taps in the Silesian District (southern Poland) were analyzed. Concentrations of As, Bi, Cd, Co, Cr, Mo, Ni, Pb, Rb, Sb, Se, Te, Tl and V were measured using inductively coupled plasma-mass spectrometry technique (ICP-MS). The levels of the tested elements generally met European Union regulations. All analytical results were processed using computational methods, including the Pearson and Gini coefficients with the Lorenz curves, one-way ANOVA, the Kruskal-Wallis one-way analysis of variance, the Mann-Whitney U test, the variance correlation test and the Spearman’s test. In addition, Principal Component Analysis (PCA) with Varimax and Cluster Analysis with Ward’s Method were applied. It was shown, that some parameters (e.g. hardness and alkalinity) were highly correlated. The score plot described the degree of mineralization of water samples, so the origin of water could be easily determined. In turn, based on the created dendrogram, the division of samples into several groups (with soft, medium and highly mineralized water) could be deduced. 相似文献