Repetitive liquefactions in angular and subangular gravels from an alluvial fan, in the case of two earthquakes with accelerations lower than that of a former which had caused liquefaction some months before, are described. The liquefaction took place from the surface, down to a depth of approximately 10 m. Water laden with sediments spouted out for some tens of minutes after the strong motion ceased. Knowledge of the grain size distribution of the sediments inside the body of the alluvial fan roughly defines the areas of the fan prone to future liquefaction. Non-repetitive liquefaction in overconsolidated fine fluvio-lacustrine sand of glacial origin at the unusual depth of 14 m to 16 m is also described. From the observation of sand lifted up for 10 m inside a large diameter well, and of that which spouted out from several microvents, it was estimated that extra-pore pressure was close to lithostatic conditions. Nevertheless, modeling of intrinsic pore pressure buildup on the DESRA2 programme gives lower values than the experimental one. Geotechnical characteristics of the 12 m-thick sandy stratum indicate that the upper part is unusually soft, either due to water circulation or past repetitive liquefactions which prevented reconsolidation. It is suggested that excess pore pressure generated by the earthquake was also due to redistribution of pressure from adjacent sediments.

抄録全体を表示

 The stability of

‒tetrahydrocannabinol acetate (‒THC‒OAc) and ‒tetrahydrocannabinol acetate (‒THC‒OAc) in -liquid during storage was investigated. ‒THC‒OAc liquids in cartridges were stored at ℃ or 30℃ for 28 days. The relative concentrations of cannabinoids in the liquids were measured by gas chromatography with flame ionization detection. ‒THC‒OAc decreased during storage at either temperature. ‒THC, a minor impurity, also decreased. ‒THC‒OAc liquid in a cartridge was stored at ℃ for 57 days. The concentration of ‒THC‒OAc and ‒THC, a minor impurity, did not change during that time. Cannabinol acetate increased in all liquids, and unknown products were also detected by gas chromatography/mass spectrometry (GC/MS). The ‒THC‒OAc and ‒THC‒OAc liquids were subjected to GC/MS to detect representative diluents, glycerol, propylene glycol, and polyethylene glycol 400, but none of these were detected.

抄録全体を表示

One method currently being considered for the disposal of high level radio-active waste is burial in the seabed. When a hot object is buried in soil, the temperature of the soil adjacent to the object is raised and there is transient heat flow away from the object. The rise in the temperature of the soil causes excess pore pressures to be generated and transient pore water diffusion also takes place. A finite element formulation of the coupled heat flow and consolidation problem is presented. The computer implementation of this formulation is found to compare favourably with analytical solutions based on the same physical principles.

抄録全体を表示

From the fronds of Polystichum tripteron (KUNZE) P_R. a new norcarotenoid glycoside was isolated and shown to be (R, , R)--hydroxy-megastigma-, -dien-3-one--O-β--glucoside. The fronds of Dennstaedtia wilfordii (MOORE) CHRIST. contain the same glucoside.

抄録全体を表示

In view of the significant role of the water film effect in flow failure for a liquefied sandy deposit, the mechanism of water film generation is numerically studied based on a 1-dimensional model test. The process of water film growth and decay can be simulated to a certain extent by a simple consolidation analysis, which indicates that only a small difference in permeability in layered sand is enough for a water film to develop. A 1 G shaking table test for a two-dimensional slope model with an arc of silt within a saturated sand is then addressed to discuss the dilatancy effect exerted in sheared sand during flow failure. It is possible that, once the water film is formed, the transmission of shear stress through it is interrupted, leaving the sand below free from the dilatancy ; this eventually allows the water film to stay without being absorbed during flow failure. The result of another shaking table test for a trapezoidal slope with horizontal silt seams indicate that water films beneath the seams enable the soil mass above them to laterally flow along water films very gently inclined even after shaking. If a silt seam breaks due to excessive pressure in the water film, it triggers re-liquefaction in the upper sand and leads to further instability.

抄録全体を表示

Syntheses of , , , , , -hexahydro-, -methano--methylthiazolo [, -] azocine (III) and , , , , , -hexahydro-, -methano--methylthiazolo [, -] azocine (IV) are described. Thiazolization of 2-azabicyclo [3. 3. 1] nonan--one (V) gave the 2-aminothiazole (VII), which was converted into III by deamination, hydrolysis of the benzoyl group and Esch-weiler-Clarke N-methylation. The 2-hydroxyl derivative (XIII) was also synthesized. On the other hand, compound (IV) was synthesized by cyclization of the olefinic urethane (XXI) with phenylselenenyl chloride, as a key step. Deselenation of XXII with triphenyltin hydride followed by reduction gave IV. The urethane (XXI) was prepared from the 2-aminothiazole (XVIIa), which was obtained by condensation of the bromodiketone (XVI) and thiourea.

抄録全体を表示

Circuit techniques to enhance the linearity of input-voltage-to-current (V/I) conversion and to increase the output impedance of a current source by compensating for the low intrinsic gain of a transistor were introduced to realize a high-frequency operational transconductance amplifier (OTA) for a low supply voltage using sub-100-nm CMOS processes. Applying these techniques, a MOS th-order Gm- linear-phase low-pass filter (LPF) was realized using a 65nm CMOS process. A simplified biquad LPF that can serve as a component of a th-order LPF was newly developed by replacing OTAs with resistors. As a result, the -3dB frequency bandwidth, group delay ripple, 3rd-order distortion, and 3rd-order input intercept point (IIP3) were 200MHz, 2.2%, ≤ -55dB with a 100MHz input, and +10.3dBm, respectively, all with a ±0.1Vp-p input signal at each input terminal in the pseudodifferential configuration. The LPF including an output buffer dissipated 60mW in the case of a 1.2V supply. Wide spurious-free dynamic range (SFDR) characteristics were confirmed up to high frequencies.

抄録全体を表示

Two new partially saturated tricyclic ring systems, , a, , , , 10, 10a, 11-octahydro-11-oxodibenz [, ] oxepins (3a and 3), and -thiepins (a and ) were synthesized. Compounds a and were desulfurized to give a pair of isomeric 2-methylbenzoylcyclohexanes (10a and 10). Deuterated a and (11a and 11) were prepared starting from butadiene- (12). The stereochemical features of 3a (trans), 3 (cis), a (trans) and (cis) are compared with those of 10a, 10, 11a and 11 on the basis of proton nuclear magnetic resonance data.

抄録全体を表示

2-Benzyl--chloro--mercapto-3 (2H)-pyridazinone (1) was heated in ethanol under reflux for 10 hours to form concurrently 2, -dibenzyldipyridazo [, - : ', '-]-1, -dithiin-1, (2H, H)-dione (Ia) (57% in yield) and 2, -dibenzyldipyridazo [, - : ', '-]-1, -dithiin-1, (2H, H)-dione (IIa) (14% in yield). Assignment of the two products to the corresponding structures is established by their physico-chemical constants and chemical behaviors. The concurrent formation of the dipyridazo [, - : ', '-]-1, -dithiin-1, (2H, H)-dione and the -1, (2H, H)-dione were observed in, not only heating -chloro--mercapto-3 (2H)-pyridazinones (1-3) in polar solvent, but warming -mercapto--chloro-3 (2H)-pyridazinones (-) in the presence of potassium carbonate in DMF. For the interpretation of the reaction, keto-thioketo carbenes as active intermediate species and a reversible interconversion among them are suggested on the basis of the fact that there was nonexistence of an equilibrium between the two compounds, such as Ia and IIa, under the reaction condition and a trapping keto-thioketo carbene species as 2-phenylimino--benzylpyridazo [, -]-1, 3-dithiol- (H)-one (IVa) (14% in yield) along with the major products, (Ia) and (IIa), was furnished by warming 1 with phenylisothiocyanate in the presence of triethylamine in dry benzene. On the contrary, participation of a reversible interconversion between Ia and IIa, to a considerable extent, with the concurrent formation of them in the case of benzylation of either Ib or IIb, by warming with benzylchloride in the presence of potassium carbonate in DMF at °, might not be neglected, because an attempted approach to an equilibrium between Ia and IIa in a similar reaction condition except the use of benzylchloride realized, whereas non-existence of an equilibrium between Ib and IIb in the similar reaction condition was observed.

抄録全体を表示

 We examined the stability of

-tetrahydrocannabinol acetate (-THC-OAc) and -tetrahydrocannabinol acetate (-THC-OAc) in -liquid products. Eight samples were heated at 30℃ for 28 days and one of them was heated at 70℃ for 2, , , 10, and 15 days. Residual ratios of -THC-OAc and -THC-OAc were evaluated by gas chromatography with flame ion detection and their degradation products were examined by gas chromatography/mass spectrometry (GC/MS). Some samples were tested for solubility in hexane and were submitted to GC/MS analysis to detect propylene glycol and glycerol. After a 28-day incubation at 30℃, -THC-OAc was slightly decomposed (residual ratio: .–.2%) but -THC-OAc was almost stable (residual ratio: 95.2–108.%). Heating at 70℃ decomposed not only -THC-OAc but also -THC-OAc. The decomposition proceeded rapidly in the initial 2 days then slowly until 15 days later. The degradation products, four putative one-oxygen-atom adducts and cannabinol, were detected but deacetylated products (-tetrahydrocannabinol and -tetrahydrocannabinol) were not detected. All the samples tested were completely dissolved in hexane differently from propylene glycol and glycerol. Propylene glycol and glycerol were not detected from the samples completely dissolved in hexane. This study indicated that deacetylation of -THC-OAc and -THC-OAc did not proceed when the sample did not contain propylene glycol and glycerol.

抄録全体を表示

The apogalanthamine analogs - and -bromo-, , , -tetrahydrodibenz [, ] azocines (a and a) and their methylenedioxy derivatives ( and ) were prepared by photolysis of the hydrochlorides of the respective N-benzyl-β-phenethylamines (a, and a, ) substituted with both iodine and bromine atoms. The dibenz [, ] azocines a and were also obtained by thermal syntheses from the biphenyl compounds 17a and 17, respectively.

抄録全体を表示

-Amino--mercapto-1, 3-dimethyluracil (2) was prepared by the treatment of , -diamino-1, 3-dimethyluracil (1) with liquid H₂S and pyridine in a sealed steel tube at 60° for 20 h. Thiazolo[, -]pyrimidinediones 3a, were obtained from 2 by cyclization with HCO₂H and AcOH.Under stringent conditions, however, 1 was converted into the , -dihydrodipyrimido[, - : ', '-][1, ]thiazine derivtive a.The structure of a was confirmed by spectral (nuclear magnetic resonance and mass spectra) data and by comparison with a sample which was prepared from 2 and -hydroxy-1, 3-dimethyluracil.Benzylation of a gave 1, 3, , -tetramethyl--benzyl (or p-bromobenzyl)-, -dihydrodipyrimido[, - : ', '-][1, ]thiazine-2, , , -(1H, 3H, H)-tetrone (, ) and 1, 3, , -tetramethyl--benzyl (or p-bromobenzyl)-, -dihydropyrrolo[3, 2- : , -']dipyrimidine-2, , , -(1H, 3H, H)-tetrone (a, ).

抄録全体を表示

11-Amino-, a, , , , 10, 10a, 11-octahydrodibebenzo[, ]thiepines (a-) and -oxepines (a-) were synthesized by the Leuckart reaction of , a, , , , 10, 10a, 11-octahydro-11-oxodibenzo[, ]thiepines (1a, )and -oxepines (2a, ) followed by hydrolysis of the reaction products a- and a-, respectively. The four diastereomers, cis(a-H, 10a-H)-cis(10a-H, 11-H) a and a, cis(a-H, 10a-H)-trans(10a-H, 11-H) and , trans(a-H, 10a-H)-trans(10a-H, 11a-H) and , and trans(a-H, 10a-H)-cis(10a-H, 11-H) and , were isolated and their configurations and conformations were elucidated by chemical methods together with ¹H-nuclear magnetic resonance spectroscopic and X-ray crystallographic analyses.

抄録全体を表示

A biosynthetic pathway for (

)-methyl cinnamate formation was evaluated in Tricholoma matsutake by tracer experiments using

13C

- and ²H-labeled precursors. One hundred percent selective

13C

incorporation was observed when L-[1,2,3,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

, ^15/N]phenylalanine was converted to (

E

)-[1,2,3,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

]cinnamate and (

E

)-[1,2,3,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

]methyl cinnamate. Similarly, 100% selective

13C

incorporation was observed when (

E

)-[1,2,3,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

]cinnamate was converted to (

E

)-[1,2,3,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

]methyl cinnamate. In contrast, the ²H incorporation selectivities were 82.1% and 81.

4

% when L-[2,3,

4

,

5

,

6

,

7

,

7

,

8

-

2H₈

]phenylalanine was converted to (

E

)-[2,3,

4

,

5

,

6

,

7

,

8

-

2H₇

]cinnamate and (

E

)-[2,3,

4

,

5

,

6

,

7

,

8

-

2H₇

]methyl cinnamate, respectively. Thus, T. matsutake synthesizes (

E

)-methyl cinnamate from L-phenylalanine via (

E

)-cinnamate. (

E

)-cinnamate was likely formed through two pathways: one was major and the other was a minor.

抄録全体を表示

In this study the field feasibility of an innovative thermal technique to improve the performance of prefabricated vertical drains (PVD) used in conjunction with the preloading ground improvement method is investigated. For this purpose, two identical .0 m high full-scale test embankments for preloading were constructed over the soft Bangkok clay where a conventional PVD system was installed underneath one embankment and a novel prefabricated vertical thermo-drain (PVTD) system was utilized for the other. The PVTD unit consists of a U-tube made of cross-linked polyethylene plastic (PEX) that is attached to a conventional PVD unit. Preheated water at about 90° is circulated through the attached U-tube to raise the soil temperature underneath the PVTD embankment. The behavior of the two test embankments were compared in terms of excess pore water pressure and consolidation results. The comparison shows the advantage of a PVTD system over a conventional PVD system. The rate of consolidation increases significantly in the PVTD system due to the temperature effect on the hydraulic conductivity. Moreover, the embankment with the PVTD system generates more settlement due to the thermally induced irreversible contraction of saturated normally consolidated soft Bangkok clay.

抄録全体を表示