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Herein, we describe the preparation of patterned photoresponsive hydrogels by using a facile method. This polymer‐network hydrogel coating consists of N‐isopropylacrylamide (NIPAAM), cross‐linking agent tripropylene glycol diacrylate (TPGDA), and a new photochromic spiropyran monoacrylate. In a pre‐study, a linear NIPAAM copolymer (without TPGDA) that contained the spiropyran dye was synthesised, which showed relatively fast photoswitching behaviour. Subsequently, the photopolymerisation of a similar monomer mixture that included TPGDA afforded freestanding hydrogel polymer networks. The light‐induced isomerisation of protonated merocyanine into neutral spiropyran under slightly acidic conditions resulted in macroscopic changes in the hydrophilicity of the entire polymer film, that is, shrinkage of the hydrogel. The degree of shrinkage could be controlled by changing the chemical composition of the acrylate mixture. After these pre‐studies, a hydrogel film with spatially modulated cross‐link density was fabricated through polymerisation‐induced diffusion, by using a patterned photomask. The resulting smooth patterned hydrogel coating swelled in slightly acidic media and the swelling was higher in the regions with lower cross‐linking densities, thus yielding a corrugated surface. Upon exposure to visible light, the surface topography flattened again, thus showing that a hydrogel coating could be created, the topography of which could be controlled by light irradiation.  相似文献   
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Résumé Le procédé de séparation des isotopes de l'hydrogène par chromatographie en lit mobile présenté est un procédé continu.Le principe en est le suivant: dans une colonne verticale, un lit mobile de silicagel descend par gravité. Le mélange à séparer (protium/deutérium) est introduit au milieu de cette colonne. La séparation du mélange en ses deux constituants s'effectue par échange à contre-courant entre la phase gazeuse et la phase adsorbée. Le protium, moins adsorbé, est soutiré en tête de colonne, le deutérium est soutiré en pied. Le reflux en bas de colonne est obtenu de 2 façons différentes qui dépendent du type de désorption employé: désorption du silicagel par élévation de températuré et élution du deuté rium, par de l'hélium désorption du silicagel par élévation de température et déplacement du deutérium, par de l'azote.Dans le ler cas, les gaz produits sont dilués dans l'hélium, dans le 2ème cas ils sortent non dilués. Le silicagel est remonté en tête de colonne par un transport pneumatique. L'expérimentation présentée à été faite avec gaz de déplacement azote.
Summary The preparation-process of hydrogen isotopes by chromatography in a moving bed in a continuous process is described.The principle is as follows: In a vertical column silicagel flows downward, by gravity, in a moving bed. The gaseous mixture to be separated (protium/deuterium) is introduced into the central portion of this column. Separation of the mixture into its two constituents is achieved by a counter-current exchange between the gaseous phase and the adsorbed phase. Protium less adsorbed is withdrawn at the top, deuterium is withdrawn at the bottom. The reflux is produced, at the bottom of the column, by two differents means, depending on the type of desorption used: Silicagel-desorption by rise of temperature and deuterium-elution by helium or displacing of deuterium by nitrogen.The gases produced are mixed with helium (1st case), or not (2nd case). Silicagel is carried again onto the top of the column by pneumatic transport. The experiments presented were carried out by means of nitrogen as displacing gas.
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We consider a recent branch-and-bound algorithm of the authors for nonconvex quadratic programming. The algorithm is characterized by its use of semidefinite relaxations within a finite branching scheme. In this paper, we specialize the algorithm to the box-constrained case and study its implementation, which is shown to be a state-of-the-art method for globally solving box-constrained nonconvex quadratic programs. S. Burer was supported in part by NSF Grants CCR-0203426 and CCF-0545514.  相似文献   
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Existing global optimization techniques for nonconvex quadratic programming (QP) branch by recursively partitioning the convex feasible set and thus generate an infinite number of branch-and-bound nodes. An open question of theoretical interest is how to develop a finite branch-and-bound algorithm for nonconvex QP. One idea, which guarantees a finite number of branching decisions, is to enforce the first-order Karush-Kuhn-Tucker (KKT) conditions through branching. In addition, such an approach naturally yields linear programming (LP) relaxations at each node. However, the LP relaxations are unbounded, a fact that precludes their use. In this paper, we propose and study semidefinite programming relaxations, which are bounded and hence suitable for use with finite KKT-branching. Computational results demonstrate the practical effectiveness of the method, with a particular highlight being that only a small number of nodes are required. This author was supported in part by NSF Grants CCR-0203426 and CCF-0545514.  相似文献   
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Surface-mounted metal–organic frameworks (SURMOFs) are crystalline films of MOFs and have garnered a great deal of attention in the past years. So far, thin-film MOF research has been mainly focused on the synthesis and the exploration of potential applications of these materials, while a detailed understanding of their growth is still lacking. In this report evidence is provided for the inter-grown nature of surface-mounted thin films of Zn-ZIF-8 (SURZIF-8; ZIF=zeolitic imidazolate framework). Two distinct SURZIF-8 thin films have been made through layer-by-layer (LBL) growth after applying 20 and 50 LBL cycles. They have been characterized with atomic force microscopy (AFM) and Raman micro-spectroscopy. A detailed analysis of the Raman mapping data, inter alia using principal component analysis (PCA), revealed the existence of phase boundaries within the 20-cycle thin film, while the 50-cycle thin film is chemically more homogeneous. To further analyze these chemical heterogeneities, density functional theory (DFT) calculations were performed of three theoretical models providing spectroscopic fingerprints of the molecular vibrations associated with the Zn-ZIF-8 thin films. Based on these calculations and the experimental data distinct vibrational markers indicative for the presence of defects sites were identified.  相似文献   
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The ability to control the external porosity and to tune the dimensions of the macropore size on multiple length scales provides the possibility of tailoring the monolithic support structure towards separation performance. This paper discusses the properties of conventional polymer–monolithic stationary phases and its limitations regarding the effects of morphology on kinetic performance. Furthermore, guidelines to improve the macropore structure are discussed. The optimal monolithic macropore structure is characterized by high external porosity (while maintaining ultra‐high‐pressure stability), high structure homogeneity, polymer globule clusters in the submicron range, and macropores with a diameter tuned toward speed (small diameter in the 100–500 nm range using short beds) or efficiency (larger macropores in the range of 500 nm–1 μm allowing the use of longer column formats). Finally, promising approaches to control the morphology are discussed.  相似文献   
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