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Taal Volcano is one of the most active volcanoes in the Philippines. The magnetotelluric 3D forward analyses indicate the existence of a large high resistivity anomaly (∼100 Ω·m) with a volume of at least 3 km × 3 km × 3 km, which is capped by a conductive layer (∼10 Ω·m), beneath the Main Crater. This high resistivity anomaly is hypothesized to be a large hydrothermal reservoir, consisting of the aggregate of interconnected cracks in rigid and dense host rocks, which are filled with hydrothermal fluids coming from a magma batch below the reservoir. The hydrothermal fluids are considered partly in gas phase and liquid phase. The presence of such a large hydrothermal reservoir and the stagnant magma below may have influences on the volcano’s activity. Two possibilities are presented. First, the 30 January 1911 explosion event was a magmatic hydrothermal eruption rather than a base-surge associated with a phreato-magmatic eruption. Second, the earlier proposed four eruption series may be better interpreted by two cycles, each consisting of series of summit and flank eruptions.  相似文献   
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Chain‐growth condensation polymerization of p‐aminobenzoic acid esters 1 bearing a tri(ethylene glycol) monomethyl ether side chain on the nitrogen atom was investigated by using lithium 1,1,1,3,3,3‐hexamethyldisilazide (LiHMDS) as a base. The methyl ester monomer 1a afforded polymer with low molecular weight and a broad molecular weight distribution, whereas the polymerization of the phenyl ester monomer 1b at ?20 °C yielded polymer with controlled molecular weight (Mn = 2800–13,400) and low polydispersity (Mw/Mn = 1.10–1.15). Block copolymerization of 1b and 4‐(octylamino)benzoic acid methyl ester ( 2 ) was further investigated. We found that block copolymer of poly 1b and poly 2 with defined molecular weight and low polydispersity was obtained when the polymerization of 1b was initiated with equimolar LiHMDS at ?20 °C and continued at ?50 °C, followed by addition of 2 and equimolar LiHMDS at ?10 °C. Spherical aggregates were formed when a solution of poly 1b in THF was dropped on a glass plate and dried at room temperature, although the block copolymer of poly 1b and poly 2 did not afford similar aggregates under the same conditions. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1357–1363, 2010  相似文献   
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The synthesis of a variety of organotin compounds with 1H, 1H, 2H, 2H‐perfluorooctyl groups is reported, together with an improved method for the corresponding distannoxane. Unique properties of this compound are disclosed in terms of fluorophilicity and activity as a Lewis acid catalyst in comparison with other mono‐nuclear derivatives. A new criterion for obtaining high solubility in fluorocarbon solvents is presented. Copyright © 2003 John Wiley & Sons, Ltd.  相似文献   
116.
The heterogeneous higher order structure and molecular motion in a single crystalline film of a vinylidene fluoride (VDF) and trifluoroethylene (TrFE) copolymer with 73 mol % VDF was investigated with the 1H–13C cross‐polarization/magic‐angle spinning NMR technique. A transient oscillation was observed in plots of the 13C peak intensity versus the contact time for the CH2, CHF, and CF2 groups. On the basis of the extended cross‐relaxation theory of spin diffusion, we determined that the oscillation behavior was caused by the TrFE‐rich segments in the chain and that the crystal consisted of VDF‐rich and TrFE‐rich domains. The former had TrFE‐rich segments in VDF and TrFE fractions of 0.24 and 0.27, respectively, and the latter had VDF‐rich segments in a VDF fraction of 0.49. The spin–lattice relaxation time T1ρH in the rotating frame for each group was minimal in the three temperature regions of β, αb, and αc (↑) on heating and in the two temperature regions of α1D and αc (↓) on cooling. The αc (↑) and αc (↓) processes depended on the first‐order ferroelectric phase‐transition regions on heating and cooling, respectively. The motional modes for the other processes were confirmed by the T1ρH minimum behavior of the VDF and TrFE groups in the TrFE‐rich domain and the VDF‐rich segments in the VDF‐rich domain. The β and αb processes were attributed to the flip–flop motion of the TrFE‐rich segments and the competitive motion of the TrFE‐ and VDF‐rich segments in the ferroelectric phase, respectively. The α1D process was due to the one‐dimensional diffusion motion of the conformational defects along the chain in the paraelectric phase, accompanied by the trans and gauche transformation of the VDF conformers of ttg+tg? and g+tg?tt. The effect of the competitive motion of the TrFE‐rich segment on the thermal stability of the VDF‐rich segment in the chain near the Curie temperature was examined. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 1026–1037, 2002  相似文献   
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Naturally occurring pyrazines fit well the theory that conformity to the TCS rule gives a stable molecular system. Thus, many pyrazines so far synthesized and those in nature which are energetically very stable molecules can be synthetically quite accessible. The TCS rule applies very well to the construction route of pyrazine rings.  相似文献   
120.
A device that produces a low-energy and largely spin polarized RI beam based on the atomic beam resonance method (RIABR) has been developed. We have performed measurements of stopping and drifting an incoming RI ion beam in a gas chamber, extraction of the ions into a vacuum region, and neutralization of the extracted low-energy ion beam. The drift efficiency of RI ions in a gas and the extraction efficiency at a Laval-type glass nozzle were found to be 0.72±0.04 and 0.033, respectively. The result of the experiment for the neutralization is also discussed.  相似文献   
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