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101.
单层网壳结构等效静风荷载分布估计 总被引:1,自引:1,他引:0
单层网壳对外荷载分布极为敏感,且稳定问题是其结构设计中的主要问题,因此风荷载分布的估计对其结构静力抗风分析非常重要。但目前常采用的等效静风荷载分布并不能有效反映其脉动分量对结构稳定性的可能不利影响。首先简单回顾了目前单层网壳抗风分析的方法,并介绍了一种基于风洞试验的有效风荷载分布估计方案。随后从稳定分析角度提出了一种新方法,可用来简单高效地估计单层网壳的有效风荷载分布,同时还可就风荷载的影响进行保守分析。最后,分别采用单层球面和柱面网壳作为算例,基于风洞试验结果,比较了不同估计方法在分析这类结构极限承载能力及稳定性问题时的效率,表明了所提出方法在单层网壳稳定分析中估计有效风荷载分布时的优点。 相似文献
102.
Hideki Shige Toshitsugu Ishikawa Michio Suzukawa Masato Nishiwaki Takeshi Yamashita Kei Nakajima Toshimitsu Ito Kenji Higashi Makoto Ayaori Atsushi Yonemura Paul Nestel Haruo Nakamura 《Lipids》1998,33(12):1169-1175
The effects of vitamin E on cholesteryl ester (CE) metabolism in 1774 cells were examined. Pretreatment of 1774 cells with
vitamin E at concentrations above 50 μM significantly decreased acetylated low density lipoprotein (LDL)-induced incorporation
of [14C]oleate into CF in cells in a dose-dependent manner. This was partly due to vitamin E Also significantly inhibiting the uptake
of [3H]CE-labeled acetylated LDL by 1774 cells. A trend existed toward suppression of acyl-CoA:cholesterol acyltransferase (ACAT)
activity in the cell lysate at high vitamin E concentration, but there was no effect on hydrolysis of CE. These data indicate
that vitamin E reduces the uptake of modified LDL and suppresses ACAT activity, resulting in less cholesterol esterification
in macrophages; a novel mechanism underlying the antiatherogenic properties of vitamin E. 相似文献
103.
Chemiluminescence (CL) analysis was used for determining the oxidation layer formed by the irradiation of polypropylene for medical supplies. The depth of the oxidation layer from the surface depended on dose rate and increased with decreasing dose rate. The oxidation occurred remarkably at a region near the surface area of the film where the diffusion of oxygen is more sufficient. On the contrary, there was very little oxidation in the interior portion. The oxidation layers of polypropylene samples irradiated with electron beam showed U-shaped profiles in the cross-section of film as did as a sample irradiated with γ-rays. However, the degree of oxidation by irradiation with electron beam was very small; CL intensity at the surface area was only one-third that for the γ-irradiated samples. 相似文献
104.
105.
The differences in distribution of geometric isomers of unsaturated PC hydroperoxides generated by free radical oxidation
were compared, as corresponding hydroxy analogs, in heterogeneous liposomes and in a homogeneous methanol solution by using
HPLC with UV detection due to the presence of conjugated dienes. Identification of fractionated peak components was carried
out by GC-MS. When the oxidation of 1-palmitoyl-2-linoleoyl-sn-glycero-3-phosphocholine, PC(16∶0/18∶2), was initiated in liposomes by a hydrophilic azo radical initiator, and in a methanol
solution by a hydrophobic azo radical initiator, there was no significant difference in the relative percentages of 1-palmitoyl-2-(9-hydroxy-trans-10,trans-12-octadecadienoyl)-sn-glycero-3-phosphocholine (9-t,t-OH PC) and 1-palmitoyl-2-(13-hydroxy-trans-9,trans-11-octadecadienoyl)-sn-glycero-3-phosphocholine (13-t,t-OH PC) between the PC oxidized in liposomes and in the methanol solution. For the oxidation of 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine, PC(16∶0/20∶4), the relative percentage of 1-palmitoyl-2-(5-hydroxy-trans-6,cis-8,11,14-eicosatetraenoyl)-sn-glycero-3-phosphocholine (5-OH PC) was significantly higher (P<0.01) than that of 1-palmitoyl-2-(15-hydroxy-cis-5,8,11,trans-13-eicosatetraenoyl)-sn-glycero-3-phosphocholine (15-OH PC) in liposomes. For the homogeneous methanol solution of PC(16∶0/20∶4), the relative percentage
of 5-OH PC was close to that of 15-OH PC. For the PC(16∶0/20∶4) oxidized in bulk with added pentamethylchromanol, the individual
amount of 15-OH PC, 1-palmitoyl-2-(11-hydroxy-cis-5,8trans-12,cis-14-eicosatetraenoyl)-sn-glycero-3-phosphocholine (11-OH PC), 1-palmitoyl-2-(12-hydroxy-cis-5,8,trans-10,cis-14-eicosatetraenoyl)-sn-glycero-3-phosphocholine (12-OH PC), 1-palmitoyl-2-(8-hydroxy-cis-5,trans-9,cis-11,14-eicosatetraenoyl)-sn-glycero-3-phosphocholine (8-OH PC), 1-palmitoyl-2-(9-hydroxy-cis-5,trans-7,cis-11,14-eicosatetraenoyl)-sn-glycero-3-phosphocholine (9-OH PC), and 5-OH PC were close to each other compared to the corresponding values in liposomes
and in methanol solution. The results obtained by gel permeation chromatography of the PC liposomes containing hydrophilic
2,2′-azobis-2-amidinopropane) dihydrochloride (AAPH) suggest that the AAPH added to the liposomes of PC(16∶0/20∶4) was partitioned
into the water phase and out of the hydrophobic region of the fatty acyl moieties of the PC. These results confirm that the
distance that exists in the bis-allylic carbons of the unsaturated fatty acyl moieties of PC from the interface between the
hydrophilic region of PC and the water phases played an important role in influencing hydrogen abstraction to form a symmetrical
distribution of hydroperoxide isomers in both the heterogeneous liposomes and the homogeneous methanol solution. 相似文献
106.
Kenji Hatanaka Masashi Katsuyama Hideki Takagi 《Journal of the American Ceramic Society》2003,86(1):135-140
The fatigue tests under push-pull completely reversed loading and pulsating loading were performed for silicon nitride ceramics at elevated temperatures. Then the effects of stress wave form, stress rate, and cyclic understressing on fatigue strength, and cyclic straining behavior, were examined. The cycle-number-based fatigue life is found to be shorter under trapezoidal stress wave loading than under triangular stress wave loading, and to become shorter with increasing hold time under the trapezoidal stress wave loading. Meanwhile, the equivalent time-based life curve, which is estimated from the concept of slow crack growth, almost agrees with the static fatigue life curve in the short and intermediate life regions, showing the small cyclic stress effect and the dominant stress-imposing period effect on cyclic fatigue life. The fatigue strength increased in stepwise stress amplitude increasing test, where stress amplitude is increased stepwise every given number of stress cycles, at 1100° and 1200°C. Occurrence of cyclic strengthening was proved through a gradual decrease in strain amplitude during a pulsating loading test at 1200°C in this material, corresponding to the above cyclic understressing effect on fatigue strength. 相似文献
107.
Sterol composition of 19 vegetable oils 总被引:6,自引:4,他引:6
The unsaponifiables from 19 vegetable oils were divided into a sterol and three other fractions by thin-layer chromatography.
All except olive and palm kernel oils gave the sterol fraction in a large quantity. Compositions of the sterol fractions were
determined by gas liquid chromatography. Identification of each sterol was carried out by gas liquid chromatography and combined
gas chromatograph-mass spectrometry. Campesterol, stigmasterol and β-sitosterol were present in all oils, and a minor amount
of cholesterol in majority of the oils. Brassicasterol occurrence was widespread but its content was extremely small in oils
other than rapeseed oil. Other sterols, presumably δ7-stigmastenol and δ5- and δ7-avenasterol were detected in most of the oils. 相似文献
108.
Sterols,methylsterols, and triterpene alcohols in threeTheaceae and some other vegetable oils 总被引:4,自引:0,他引:4
The unsaponifiables from threeTheaceae (Camellia japonica L.,Camellia Sasanqua Thunb., andThea sinensis L.) oils and alfalfa, garden balsam, and spinach seed oils and shea fat were separated into four fractions: sterols, 4-methylsterols,
triterpene alcohols, and less polar compounds by thin layer chromatography. While the sterol fraction was the major one for
the unsaponifiables from alfalfa and spinach seed oils, the triterpene alcohol fraction was predominant for the unsaponifiables
from all other oils. The sterol, 4-methylsterol, and triterpene alcohol fractions were analyzed by gas chromatography. All
the sterol fractions were alike in their compositions, consisting exclusively of Δ7-sterols, such as α-spinasterol and Δ7-stigmastenol as predominant components together with Δ7-avenasterol and 24-methylcholest-7-enol. Obtusifoliol, gramisterol (occasionally accompanied with cycloeucalenol), and citrostadienol,
together with several other unidentified components, were found in the 4-methylsterol fractions from all of the oils except
shea fat. The 4-methylsterol fraction from shea fat showed a characteristic composition containing a large proportion of unidentified
components which had relative retention time greater than that of citrostadienol, while no citrostadienol was detected. β-Amyrin,
lupeol, and butyospermol were major components of the triterpene alcohol fractions from most of the oils, but the fraction
from spinach seed oil contained cycloartenol and 24-methylene-cycloartanol as predominant components. There is a close similarity
in the compositions of unsaponifiables (sterols, 4-methylsterols, and triterpene alcohols) of the threeTheaceae oils. Two sterols, α-spinasterol and Δ7-stigmastenol, and five triterpene alcohols were isolated from tea seed oil. Moreover, five unidentified components beside
parkeol, butyrospermol, α-amyrin, and lupeol were isolated from the triterpene alcohol fraction of shea fat. 相似文献
109.
Takuya Honma Ikue Sasaki Nobuhiro Tamura Junichi Tatami Shinichiro Fujichika Katsutoshi Komeya Takeshi Meguro 《International Journal of Applied Ceramic Technology》2013,10(2):348-353
To fabricate functionally graded materials, a highly concentrated slurry of SiO2‐Mo system was prepared and centrifugal force was applied in an attempt to achieve a graded composition. Subsequently, we formed a homogeneous green body with compositional gradation by floc‐casting at 80°C, which was then fired at 1750°C for 10 min in Ar. The sintered body had compositional ratios of SiO2 and Mo as well as electrical conductivities that changed gradually along the direction of centrifugal force. The results demonstrate that centrifugation and control of slurry characteristics such as flocculation are effective in fabricating functionally graded SiO2‐Mo materials. 相似文献
110.
Yoshihiko Okada Kaori Sasaki Baiqian Zhong Hideki Ishida Takeshi Mitsuda 《Journal of the American Ceramic Society》1994,77(5):1319-1323
A mixture of CaO and silicic acid prepared with a Ca/Si ratio of 2.0 was hydrothermally synthesized at 80° to 200°C, and the thermal decomposition behavior of the products (C-S-H with Ca(OH)2 ) was analyzed using XRD, 29 Si MAS NMR, and the trimethylsililation method (TMS). It was found that the main silicate anion structure of C-S-H was a mixture of a dimer and a single-chain polymer (larger than Si5 O16 ) and that polymerization advanced with an increase of the synthesizing temperature. On heating, the products decomposed to form β-C2 S. It was found that the decomposition was gradual and that the-higher the temperature of hydrothermal synthesis, the lower was the temperature of the decomposition into β-C2 S. Although the decomposition proceeded to form a monomer (β-C2 S) from the polymer and dimer, this dimer was resistant to heat and did not decompose unless heated to above 400°C. 相似文献