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1.
2.
Spin-lattice relaxation mechanisms in kaolinite have been reinvestigated by magic-angle spinning (MAS) of the sample. MAS is useful to distinguish between relaxation mechanisms: the direct relaxation rate caused by the dipole-dipole interaction with electron spins is not affected by spinning while the spin diffusion-assisted relaxation rate is. Spin diffusion plays a dominant role in 1H relaxation. MAS causes only a slight change in the relaxation behavior, because the dipolar coupling between 1H spins is strong. 29Si relaxes directly through the dipole-dipole interaction with electron spins under spinning conditions higher than 2 kHz. A spin diffusion effect has been clearly observed in the 29Si relaxation of relatively pure samples under static and slow-spinning conditions. 27Al relaxes through three mechanisms: phonon-coupled quadrupole interaction, spin diffusion and dipole-dipole interaction with electron spins. The first mechanism is dominant, while the last is negligibly small. Spin diffusion between 27Al spins is suppressed completely at a spinning rate of 2.5 kHz. We have analyzed the relaxation behavior theoretically and discussed quantitatively. Concentrations of paramagnetic impurities, electron spin-lattice relaxation times and spin diffusion rates have been estimated. 相似文献
3.
T. Nagaishi S. Ishiyama M. Matsumoto S. Yoshinaga 《Journal of Thermal Analysis and Calorimetry》1984,29(1):121-129
The reactions between ammonium sulphate and three metal oxides (Cr2O3, MnO2 and Fe2O3) were studied. It was confirmed by X-ray diffraction and chemical analysis that stable reaction intermediates were formed consecutively in the course of the reactions.These were (NH4)3M(SO4)3 and NH4M(SO4)2 for Cr2O3 and Fe2O3 and (NH4)2Mn2(SO4)3 for MnO2. The thermal decompositions of these intermediates and of the metal sulphates were carried out. The contracting-volume equation was valid for the decomposition of all the intermediates. The Arrhenius parameters were determined.
Zusammenfassung Es wurden die Reaktionen zwischen Ammoniumsulfat und drei Metalloxiden (Cr2O3, MnO2 und Fe2O3) untersucht. Durch Röntgendiffraktion und chemische Analyse wurde bestätigt, dass im Verlaufe der Reaktion stabile Zwischenprodukte gebildet werden. Es handelt sich dabei um (NH4)3M(SO4)3 und NH4M(SO4)2 im Falle von Cr2O3 und Fe2O3 und um (NH4)2Mn2(SO4)3 im Falle von MnO2. Diese Zwischenprodukte und die Metallsulfate wurden thermisch zersetzt. Die Volumenkontraktionsgleichung war für die Zersetzung all dieser Zwischenprodukte gültig. Die Arrheniusparameter wurden bestimmt.
Cr2O3, MnO2 Fe2O3. , . , (NH4)3M(SO4)3 NH4M(SO4)2, (NH4)2Mn2(SO4)3. . . .相似文献
4.
Tsugikazu Tomono Etsuo Hasegawa Eishun Tsuchida 《Journal of polymer science. Part A, Polymer chemistry》1974,12(5):953-965
Active hydrogen compounds such as hydroquinone (HQ), cyclohexanone (CH), acetophenone (AP), and 4,4′-methylene bis-N-methylaniline (MNA) polymerized with formaldehyde (F) and secondary diamines to produce Mannich base polyamine polymers. The HQ-containing polymers were oxidized to benzoquinone (BQ)-containing polymers and their redox properties were investigated in the desulfurization of hydrogen sulfide. 相似文献
5.
Hirokazu Morisawa Takashi Utagawa Takeshi Miyoshi Fumihiro Yoshinaga Akihiro Yamazaki Koji Mitsugi 《Tetrahedron letters》1980,21(5):479-482
An enzymatic transarabinosylation between 2-chlorohypoxanthine and 1-β--arabinofuranosyluracil gave 9-β--arabinofuranosyl-2-chlorohypoxanthine which was chemically converted to 9-β--arabinofuranosylguanine and its derivatives. 相似文献
6.
Etsuo Watanabe Shunsuke Tokimatsu Kenzo Toyama Isao Karube Hideaki Matsuoka Shuichi Suzuki 《Analytica chimica acta》1984
A multielectrode enzyme sensor for the simultaneous determination of adenosine-5′-phosphate (AMP), inosine-5′-phosphate (IMP), inosine (HXR) and hypoxanthine (HX)in fish meat was developed by assembling four enzyme sensors for AMP, IMP, HXR and HX in a flow cell. These compounds were determined from oxygen consumption according to the following reactions: AMP IMP HXR HX Uric acid where AD is AMP deaminase, NT is 5′-nucleotidase, NP is nucleoside phosphorylase and XO is xanthine oxidase. Enzymes were covalently bound to a membrane prepared from cellulose triacetate, 1,8-diamino-4-aminomethyloctane and glutaraldehyde. Sensors for HX, HXR, IMP and AMP were prepared by attaching membranes of XO, XONP, XO NPNT, and of XONPNT and AD, respectively, to four oxygen electrodes. Samples extracted from sea bass, bream, flounder, abalone and arkshell were analyzed within 5 min, from the simultaneous response curves of the four electrodes. Results obtained by the multisensor system were in good agreement with those determined by each single electrode. 相似文献
7.
Ogawa Y Ogawa K Kokufuta E 《Langmuir : the ACS journal of surfaces and colloids》2004,20(7):2546-2552
Polyampholyte gels were prepared by free radical polymerization of aqueous monomer solutions with the following composition: 69% N-isopropylacrylamide (thermosensitive neutral monomer), 1% N,N'-methylenebisacrylamide (cross-linker), 15% 1-vinylimidazole (cationic monomer), and either 15% acrylic acid (AAc, anionic monomer) or poly(acrylic acid) (PAAc, polyanion). We thus obtained two sorts of polyampholyte gels; that is, G1 with immobilized PAAc and G2 with randomly copolymerized AAc. The equilibrium swelling ratio (Qe) was studied as a function of the pH, NaCl concentration, and temperature. Also studied was the kinetics of swelling and shrinking in response to a sudden pH change. The significant results obtained were as follows: (i) A fully collapsed state was observed at pH 4.5-9.0 for G1 and at pH 4.5-7.0 for G2. (ii) Below and above these pH ranges, both gels were in a swollen state; therefore, an isoelectric point (pI) appeared in a wide pH range. (iii) At alkaline pH regions where a hysteresis was observed in the Qe versus pH curves of G1 and G2 as the pH was first increased then decreased, G1 exhibited very slow swelling-shrinking kinetics. (iv) An increase in the NaCl concentration allowed the gel to swell at pH approximately pI (antipolyelectrolyte behavior) but to shrink at pHs below and above the pI range (polyelectrolyte behavior). (v) The magnitude of the salt-induced shrinking of G1 is smaller than that of G2 at pH 10 and at NaCl concentrations > 0.01 M. (vi) At pH 10, an increase in the temperature from 35 to 50 degrees C led to a shrinking change of G1 but not of G2. These results were found to be explicable in terms of a different distribution of negative charges within the polyampholyte gel network. 相似文献
8.
Inorganic-organic hybrids have been synthesized by incorporation of the inorganic component of Ti(OC2H5)4 into the organic polymer of ethyl cellulose. The inorganic-organic hybrids did not dissolve in toluene used as a solvent for the starting materials. The ethanol was formed as a by-product of the alcoholysis condensation reaction between Ti(OC2H5)4 and ethyl cellulose. These results suggest that ethoxy groups of Ti(OC2H5)4 react with hydroxy groups of ethyl cellulose to form cross-linking bonds of –O–Ti–O–. The reaction of Ti(OC2H5)4 with ethyl cellulose was further investigated by Fourier transform infrared (FT-IR) spectroscopy. The FT-IR spectroscopic experiments revealed that the Ti–O bond state of Ti(OC2H5)4 was changed by refluxing a toluene solution of Ti(OC2H5)4 with ethyl cellulose. The inorganic-organic hybrids have an interesting dielectric property; their dielectric constant is higher than that of ethyl cellulose and that of a simple mixture of TiO2 and ethyl cellulose. 相似文献
9.
The title hydride and its deuteride were successfully synthesized. The crystal structure of the deuteride was determined by time-of-flight neutron powder diffraction. BaAlD(5) crystallizes with a new orthorhombic structure in space group Pna2(1) (No. 33), cell parameters a = 9.194(1) A, b = 7.0403(9) A, and c = 5.1061(6) A, Z = 4. BaAlH(5) is the first example that contains one-dimensional zigzag chains of [AlH(6)] along the crystallographic c axis. 相似文献
10.
The chiral separation ability of unmodified and di- and trimethylated -, β- and γ-cyclodextrins (CDs) as chiral selectors in capillary zone electrophoresis was investigated in the presence of urea derivatives using twelve dansylamino acids as model solutes. The addition of these urea derivatives (unsubstituted, methyl-, ethyl- and 1,3-dimethylureas) produced dramatic enhancement in the enantioselectivity of unmodified β-CD but also reduced the enantioselectivities of the other CDs. 相似文献