Using atomic force spectroscopy, we investigated the adhesion-promoting ability of chromium. An intermediate layer of chromium can overcome the low adhesion between metal films and silicon dioxide. For the first time, we quantitatively studied this experimentally well known fact. We compared the adhesion between chromium and different substrates such as gold, silver, mica, and silicon dioxide and, beyond that, the adhesion between silicon dioxide and the same substrates. To avoid additional effects due to water, we chose ethanol as a nonpolar solvent. Taking the interfacial energies of the surfaces with the liquid into account eliminates the direct influence of the fluid medium on the adhesion of the solid material. The results we obtained corroborate the experimental fact of higher adhesion of chromium with the chosen substrates, as well as substantiate the value of chromium as an adhesion promoter. The adhesion of chromium-coated probes on gold, silicon dioxide, and mica is higher than the adhesion of silicon dioxide probes on the same substrates. 相似文献
Infrared and Raman spectra of atactic PMMA and infrared spectra of stereoregular PMMA and of its four deuterated derivatives , were measured. They were used to assign the bands of stretching and deformation vibrations of CH2, CCH3 and OCH3 groups in the infrared and Raman spectra and to discuss the effect of stereoregularity on these bands in the infrared spectra. 相似文献
Regioisomerically pure 1,3-sn-diacylglycerols are conveniently prepared in high yields (>80%) and in large quantities by enzymatic esterification of glycerol
in the presence of various 1,3-selective lipases(Chromobacterium viscosum, Rhizopus delemar, Rhizomucor miehei) and a variety of different acyl donors like free fatty acids, fatty acid alkyl esters and vinyl esters. All reactions are
carried out in aprotic organic solvents of low water content, namelyn-hexane, diethyl ether or tBuOMe. The creation of an artificial interphase between the solvent-immiscible hydrophilic glycerol
and the hydrophobic reaction media by the adsorption of glycerol onto a solid support prior to use was essential for the success
of these transformations. The effects of reaction conditions and the regioselectivities of the lipases on the product yields
are described in detail. 相似文献
Summary
13c T1 of some polymers has been measured at various temperatures. This relaxation is sensitive to other motions than those determining the proton relaxation. The T1's of polyethylene and poly(ethylene-vinylacetate) show minima which correspond to second moments of 108 s–2 and 4·108 s–2, respectively, in contrary to the theoretical value of 4·109 s–2. The reason is a strongly restricted motion — e. g. torsional oscillation — which cannot average out completely the dipolar interaction. In poly(methylmethacrylate) and in poly(vinylacetate) a decrease of the restriction with increasing temperature has been observed.Presented at the 22nd Microsymposium, Characterization of Structure and Dynamics of Macromolecular Systems by NMR Methods, Prague, CSSR, July 20–23, 1981 相似文献
Two different types of mullite could be determined in differently coloured fragments of South American bauxites: − Mullites, occuring in light bauxite fragments with low impurity contents (Σ wt % (Fe2O3 + TiO2) 2.5), and cell dimensions close to that of 3/2 mullite, the b parameter being slightly shorter. − Mullites, occurring in grey to dark grey, and in brown bauxite fragments, with high impurity contents (Σ wt % (Fe2O3 + TiO2) 4,0) and a and c cell dimensions close to those of 2/1 mullite. The b constant of these mullites is slightly expanded with respect to impurity free mullites. Increasing impurity contents in mullite are linearly correlated with a b expansion. The expansion was structurally explained with a substitution of Al3+ by Fe3+ and Ti4+ at octahedral lattice sites, which causes stretching of the AlO6 octahedra along to the elastic Al1---DD bond in mullites which is 30° to either side of b. The substitution-produced expansion is superimposed by an expansion due to the change of the structural state of mullite from the 3/2 to the 2/1 type. The greatest variation in any cell parameter with the change of the structural state is the a constant. 相似文献
Illinois No. 6 coal and its reductive methylation and butylation products have been studied by magnetic resonance techniques. Conventional CP-MAS13Cn.m.r. spectroscopy indicates that 62% of the carbon atoms in the coal are aromatic and that about 6% of the carbon atoms are carbonyl. Esters are more abundant than carboxylic acids. The resonances of methoxy groups and other novel etheric carbon atoms are apparent in the high field region. Dipolar dephasing experiments suggest that methyl carbon atoms constitute no more than 16% of the carbon, methylene and methine carbon atoms about 14% and quaternary aliphatic carbon atoms about 2%. The dipolar dephasing experiments in conjunction with previous work also permit estimates of the hydrogen atom distribution. The THF-insoluble products obtained in the reductive alkylation reactions with13C-enriched alkylating agents contain paramagnetic and ferromagnetic substances that adversely influence the solid state n.m.r. spectra. However, good 13C n.m.r. spectra were obtained after these substances were extracted with aqueous hydrochloric acid. The O:C alkylation ratios are 1.2 and 1.0 for methylation and butylation, respectively. Dipolar dephasing experiments establish that the decay constants of functional groups in the whole coal and of C- and O-methyl-13C and C- and O-butyl-1 -13C nuclei in the labelled coal molecules are very similar to those of reference compounds. These findings suggest that the decay constants measured for the 13C nuclei in coals and coal-derived solids provide reliable information about their degree of substitution. 相似文献
Summary Living polystyrene microparticles with average particle diameters varying between 0.5 and 3.8 m were obtained via sec-butyl lithium-initated anionic polymerization of styrene in n-hexane diluent when polystyrene-block-poly(4-trimethyl-silylstyrene) was added as dispersing agent. The influence of block copolymer molecular architecture and concentration as well as polymerization temperature, monomer concentration and THF addition on polystyrene particle size, molecular weight and molecular weight distribution were investigated. In comparison to anionic styrene polymerization in cyclohexane solution, the anionic styrene dispersion polymerization in n-hexane was markedly slower. 相似文献
Glycidyl carbamate chemistry combines the excellent properties of polyurethanes with the crosslinking chemistry of epoxy resins.
Glycidyl carbamate functional oligomers were synthesized by the reaction of polyfunctional isocyanate oligomers and glycidol.
The oligomers were formulated into coatings with several amine functional crosslinkers at varying stoichiometric ratios and
cured at different temperatures. Properties such as solvent resistance, hardness, and impact resistance were dependent on
the composition and cure conditions. Most coatings had an excellent combination of properties. Studies were carried out to
determine the kinetics of the curing reaction of the glycidyl carbamate functional oligomers with multifunctional and model
amines. Detailed kinetic analysis of the curing reactions was also undertaken. The results indicated that the glycidyl carbamate
functional group is more reactive than a glycidyl ether group.
Presented at the 82nd Annual Meeting of the Federation of Societies for Coatings Technology, on October 27–29, 2004, in Chicago,
IL. 相似文献