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1.
The GPC elution behaviour of a polymer was studied when a solution of another polymer in a liquid was used as an eluent. In ternary systems containing two polymers, GPC results are influenced by the thermodynamics of polymer incompatibility. The incompatibility manifests itself both in the slope of the dependence of elution volume upon the concentration of injected polymer and in the shift of elution volumes extrapolated to zero concentration. Experimental data for systems containing poly(styrene) and poly(methyl methacrylate) have been accounted for qualitatively by theoretical views on coil shrinkage resulting from polymer incompatibility. The concentration effects of the injected polymer and the polymer in the mobile phase on elution volume are compared; further parameters affecting the separation in the systems with polymer solution as eluent are discussed. 相似文献
2.
Radical copolymerization of styrene with benzalacetophenone or benzalacetone in bulk or in suspension yielded copolymers with as much as 10 wt% of carbonyl monomer. They were characterized by GPC, viscometry and spectroscopy. Photolysis of copolymers was investigated in benzene at 313 nm. Quantum yields for main chain scissions were about 0.005 and the life-time of the triplet state was 5 nsec. Photo-oxidation in films was followed by monitoring the decrease in molecular weight and by i.r. and emission spectra. Quantum yield for main chain scission in films was about 0.0002. During photooxidation in film, the molecular weight distribution widened. A new i.r.-band appeared at 3580 cm?1 and the carbonyl band was spread between 1700 and 1800 cm?1. In the emission spectra, the vibrational resolved emission (typical of the carbonyl chromophore) disappeared. 相似文献
3.
Summary Coupling of full adsorption-desorption and size-exclusion chromatography (FAD-SEC) has been applied to the separation and
molecular characterization of three- and four-component polymer blends. The method is based on the full adsorption of alln orn−1 components of the polymer blend in a specially designed FAD minicolumn. By appropriate eluent switching the adsorbed polymers
are desorbed stepwise from the FAD minicolumn into an on-line SEC column for molecular characterization. It is shown that
the desorption isotherms of particular blend components give valuable information about the appropriate displacer composition.
The exact position of the desorption isotherms depends, however, both on the amount of polymer adsorbed and in the presence
of other, chemically different, polymers within FAD column. The nature and composition of the displacer must, therfore, be
adjusted if the intervals between the desorption of particular blend components are to be large enough to prevent displacement
overlap.
Presented at: Balaton Symposium on High-Performance Separation Methods, Siófok, Hungary, September 3–5, 1997. 相似文献
4.
A new method of HPLC column retentivity testing utilizes polymeric probes instead of conventional sets of low molar mass substances. The procedure allows at least semiquantitative, separate and independent evaluation of adsorption and partition properties of column packings. In this present work, the method is applied for comparison of the polar interactivities of selected silica gel C18 HPLC columns. It is shown that free silanols which remained on the surface of the end-capped silica C18 column packings are accessible for interaction with highly polar macromolecules. High molar mass polymeric test probes are adsorbed on the surface silanols and their retention volumes increase. As result, deviations from regular size-exclusion chromatographic (SEC) behavior are observed. The extent of retention volume changes depends on both the nature of polymer probes and on column packing type. Adsorption of macromolecules can be suppressed by addition of a highly polar substance to the mobile phase. The amount of polar additive which is needed to attain regular SEC elution of the polymer probe depends on the column packing type and can be used as a characteristic of silanophilic column interactivity. Courses of dependences of retention volumes on sizes of macromolecules indicate the presence of "U-turn" adsorption which allows two and more silanols situated among C18 groups to be occupied simultaneously with the same macromolecule. 相似文献
5.
The ring opening polymerization of L-lactide was studied in bulk using stannous octoate as initiator. In some experiments, triphenylphosphine, a Lewis base was also used as co-initiator. The polymerization was carried out at 130°C up to 29 h. The monomer was used after recrystallizing three times with dry toluene. Experiments were carried out using a wide range of monomer to initiator ratio. The averages and distributions of molar masses of resulting PLA have been determined by means of size exclusion chromatography, SEC. It is shown that the (mode, process) procedure of dispersion of the catalyst in polymerization system affects the molar mass distribution of the product as is evidenced by the bimodality or even trimodality observed in the SEC chromatograms. 相似文献
6.
7.
Summary Brief pressure changes take often place within a liquid chromatography column, e.g., during sample injection. It is shown
that pressure jumps may cause local changes in the composition of a mixed effluent and the rise of system peaks in the chromatogram.
This is a consequence of the dependence of sorption equilibrium on pressure. 相似文献
8.
M. Berek 《Zeitschrift für Physik A Hadrons and Nuclei》1926,36(9-10):675-688
9.
10.
M. Berek K. Männchen W. Schäfer und H. S. Patterson 《Fresenius' Journal of Analytical Chemistry》1938,113(7-8):283-284
Ohne Zusammenfassung 相似文献