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排序方式: 共有161条查询结果,搜索用时 31 毫秒
1.
三峡库区滑坡地带岩石特性的研究 总被引:1,自引:0,他引:1
针对三峡库区组成滑坡岩层的主要岩石——泥质岩、灰岩、砂岩,通过显微镜观察、X射线分析显微镜的定量分析及室内岩石力学强度试验,对各岩石的特性进行了分析。显微镜及X射线定量分析结果表明风化较弱的泥质岩基本上含有石英与钙质矿物,后者由于易溶于水而导致岩石的孔隙率增加。孔隙的一部分连接形成了裂缝, 从而使岩石的强度下降。各岩石的单轴压缩试验结果表明砂岩的强度最高,发生了风化的泥质砂岩的强度最低。在饱和状态下紫红色泥岩及风化了的泥质砂岩的单轴压缩强度降低最显著,比自然干燥状态下降低了大约50%, 推测是受粘土矿物含量的影响。所有岩石都表现出在峰值强度之前应力与应变几乎呈线性关系,而峰值强度之后应力急剧下降的脆性特征。这种在饱和状态下岩石强度大幅度下降与脆性特征表明在治理滑坡时需要采取十分周密及复杂的预防措施。 相似文献
2.
Ken’ichiro Matsumoto Yuko Arai Rina Nagao Takaaki Murata Kazuma Takase Hideo Nakashita Seiichi Taguchi Hiroaki Shimada Yoshiharu Doi 《Journal of Polymers and the Environment》2006,14(4):369-374
In this paper, the photosynthetic production of short-chain-length/medium-chain-length polyhydroxyalkanoate (PHA) copolymers is reported. The wild-type and highly active doubly mutated PHA synthase 1 (S325T/Q481K, abbreviated ST/QK) genes from Pseudomonas sp. 61-3 were introduced into Arabidopsis thaliana. Peroxisome targeting signal 1 (PTS1) was used to target PHA synthases into the peroxisome to synthesize PHA from the intermediates of the β-oxidation pathway. The transgenic Arabidopsis produced PHA copolymers consisting of 40–57 mol% 3-hydroxybutyrate, 21–49 mol% 3-hydroxyvalerate, 8–18 mol% 3-hydroxyhexanoate, and 2–8 mol% 3-hydroxyoctanoate. The maximum PHA contents were 220μ g/g cell dry weight (cdw) in leaves, and 36μ g/g cdw in stems, respectively. The expression of the ST/QK mutated PHA synthase in leaves gene did not lead to significant difference in PHA content and monomer composition of PHAs, compared to the wild-type PHA synthase gene, suggesting that the supply of monomers may be a rate-determining step of PHA biosynthesis in the peroxisome. However, in stems, there were significant differences dependent on whether the wild-type or ST/QK mutated PHA synthase was expressed. These results suggest that tissue-specific monomer availability is important in determining the final mol% composition of PHA copolymers produced by the peroxisome in plants. 相似文献
3.
Michie Naito Claire Radcliffe Yuji Wada Takashi Hoshino Xiongmin Liu Mitsuru Arai Masamitsu Tamura 《Journal of Loss Prevention in the Process Industries》2005,18(4-6):469-473
The Japanese government is planning to introduce DME as a substituted energy for oil and LNG. Introduction of DME could contribute greatly to both the prevention of global warming and the formation of resource-recycling societies. In these circumstances, a safety assessment of DME is very important when DME is used on a large scale. There is a possibility that prolonged exposure in air induces autoxidation to produce explosive organic peroxides during transportation and storage of DME. Therefore, the reactivity of DME with oxygen and the mechanism of the autoxidation were investigated. Accelerating Rate Calorimetry (ARC) was used to evaluate the thermal stability of DME and DIPE, a known peroxide producers, under adiabatic and various atmospheric conditions. In ARC studies of DME under oxygen, exothermic decompositions were detected although its self-heating rate was low in comparison with DIPE. Oven storage tests were carried out and iodimetry was used to measure the concentration of peroxides produced from DME in comparison with DIPE and DEE. However, no products could be found for DME either by GC/MS or by iodimetry, while some evidence of autoxidation of both DEE and DIPE were obtained from these experiments. 相似文献
4.
Polychlorinated dibenzo-p-dioxins and dibenzofurans in paddy soils and river sediments in Akita, Japan 总被引:1,自引:0,他引:1
Paddy soils and sediments from the Yoneshirogawa, Omonogawa, and Koyoshigawa River Basins in Akita were analyzed for polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs). The levels and compositions in those samples including soils from non-agricultural areas (non-agricultural soils) were investigated using isomer-specific analysis to determine characteristic sources. The PCDD/PCDF compositions in the samples were compared with respect to possible sources. The PCDD/PCDF concentrations in paddy soils were much higher than those in the non-agricultural soils and much higher than those found in other parts of Japan. Although PCDD/PCDFs were ubiquitous in sediments from river sources to mouths of the respective river basins, those concentrations were much lower than those from paddy soils and non-agricultural soils, and from other parts of Japan. Comparison of PCDD/PCDF homologues and isomer compositions for samples indicated that compositions of paddy soils and sediments, except for those from river sources, had similar characteristics to PCDD/PCDFs originating from impurities in herbicides, 2,4,6-trichlorophenyl 4-nitrophenyl ether (CNP) and pentachlorophenol (PCP), and that compositions of river-source sediments and non-agricultural soils resembled those of atmospheric depositions. Results of statistical analyses suggest that PCDD/PCDF contamination of paddy soils and sediments is attributable mainly to three sources: CNP, PCP, and atmospheric deposition. Results of this study also demonstrate that CNP and PCP are not only important contaminants of local areas of Japan, but that they exist throughout Akita, in northern Japan. We therefore conclude that PCDD/PCDF pollution caused by those compounds has a widespread influence on paddy soils and river sediments in Japan. 相似文献
5.
Historical and geographical aspects of the increasing perfluorooctanoate and perfluorooctane sulfonate contamination in human serum in Japan 总被引:1,自引:0,他引:1
Harada K Koizumi A Saito N Inoue K Yoshinaga T Date C Fujii S Hachiya N Hirosawa I Koda S Kusaka Y Murata K Omae K Shimbo S Takenaka K Takeshita T Todoriki H Wada Y Watanabe T Ikeda M 《Chemosphere》2007,66(2):293-301
Perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) have recently received attention due to their widespread contamination in the environment, as well as in wildlife and humans. We measured the PFOS and PFOA concentrations in historically recorded human serum samples at an age range between 20 and 59 years collected in Kyoto, 20 persons per each time point (n=100), and also the PFOS and PFOA concentrations in human serum samples at an age range between 20 and 59 years from 10 locations throughout Japan (n=200). The historical samples collected from 1983 to 1999 demonstrated that the PFOA concentrations in males and females from Kyoto have increased 4.4-fold and 4.3-fold at a rate of increase of 0.49 ng/ml/year and 0.42 ng/ml/year, respectively. In contrast, serum concentrations of PFOS reached a plateau in the late 1980s. There are also regional differences in both the PFOS and PFOA serum concentrations. The concentrations in serum [geometric mean (geometric standard deviation)] (ng/ml) in 2003-2004 ranged from 7.6(1.6) in the town of Matsuoka in Fukui prefecture to 27.8(1.6) in Kyoto city, and ranged from 2.3(1.5) in Matsuoka to 14.5(1.3) in Osaka city for PFOS and PFOA, respectively. 相似文献
6.
Morey Burnham Zhao Ma Joanna Endter‐Wada Tim Bardsley 《Journal of the American Water Resources Association》2016,52(6):1366-1384
In the Wasatch Range Metropolitan Area of Northern Utah, water management decision makers confront multiple forms of uncertainty and risk. Adapting to these uncertainties and risks is critical for maintaining the long‐term sustainability of the region's water supply. This study draws on interview data to assess the major challenges climatic and social changes pose to Utah's water future, as well as potential solutions. The study identifies the water management adaptation decision‐making space shaped by the interacting institutional, social, economic, political, and biophysical processes that enable and constrain sustainable water management. The study finds water managers and other water actors see challenges related to reallocating water, including equitable water transfers and stakeholder cooperation, addressing population growth, and locating additional water supplies, as more problematic than the challenges posed by climate change. Furthermore, there is significant disagreement between water actors over how to best adapt to both climatic and social changes. This study concludes with a discussion of the path dependencies that present challenges to adaptive water management decision making, as well as opportunities for the pursuit of a new water management paradigm based on soft‐path solutions. Such knowledge is useful for understanding the institutional and social adaptations needed for water management to successfully address future uncertainties and risks. 相似文献
7.
Teru Yamamoto Kazuo Higashino Tamae Abe Takumi Takasuga Hiroaki Takemori Roland Weber Yuko Sasaki 《Environmental science and pollution research international》2018,25(32):31874-31884
Studies on the formation of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) during the electrolysis of sodium chloride solution (brine) using graphite or titanium electrodes were carried out at a laboratory scale. High concentrations of PCDFs but no PCDDs were formed in tests using graphite electrodes. With titanium electrodes, PCDFs were only formed when tar pitch was added and mainly originated from the dibenzofuran present in the tar. For the first time, a detailed assessment of the formation of mono- to octachlorinated PCDD/PCDF from tar pitch was investigated. The assessment included of the chlorination steps proved that PCDFs were formed by successive lateral chlorinated from dibenzofuran to MonoCDFs, DiCDFs, and TriCDFs to form the typical known “chlorine pattern” of TetraCDF to OctaCDF with a dominance of 1,2,7,8- and 2,3,7,8-TetraCDFs, 1,2,3,7,8-PentaCDF, and 1,2,3,4,7,8-HexaCDF as marker congeners. The final homologue distributions depended on reaction time and reaction temperature. In addition, electrolysis with non-chlorinated dibenzo-p-dioxins, dibenzofuran, and biphenyl was carried out. As a result, PCDDs, PCDFs, and PCB were formed at comparable yields. Congener patterns in soil samples from a PCDD/F-contaminated site where chlor-alkali electrolysis had been operated for decades in Japan had identical isomer distribution demonstrating the source and contamination potential and risk of these processes. Therefore, sites where in the past 120 years chlor-alkali electrolysis has been operated or where residues from chlor-alkali production or other chlorine using industries have been disposed should be assessed for their pollution level and exposure relevance. The assessment of total organohalogen content revealed that PCDF is only a small fraction of organohalogens in the contaminated soils. For an appropriate risk assessment, also other chlorinated aromatic compounds such as PCBs or PCNs need to be considered. 相似文献
8.
Takashi Yamamoto Yasufumi Kai Hiroaki Nakauchi Toshiaki Abuku Yukio Noma 《Environmental science and pollution research international》2014,21(12):7557-7566
A series of treatment experiments were carried out to evaluate the applicability of a high-temperature melting treatment (GeoMelt process) to the destruction of polychlorinated naphthalene (PCN) formulation. We started with 10-kg-scale experiments in which a small melting furnace was used and then scaled up to a 1-t-scale experiment in which a melting furnace that resembled an actual treatment system was used. These runs were evaluated whether destruction efficiency (DE) of total PCNs was more than 99.999 % and whether concentrations of PCNs and polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDDs/DFs) in vitrified materials, emission gas, and scrubber water were below the target levels. Because DE values and the target levels of PCNs and PCDDs/DFs in these runs were satisfactory, then we carried out a demonstrative experiment using the actual treatment system and confirmed destruction of PCNs. Based on good results of the demonstrative experiment, stock of PCN formulation was successfully treated continuously. 相似文献
9.
Keigo Akimoto Fuminori Sano Takashi Homma Kenichi Wada Miyuki Nagashima Junichiro Oda 《Sustainability Science》2012,7(2):157-168
This study focuses on analyses of greenhouse gas (GHG) emission reductions, from the perspective of interrelationships among
time points and countries, in order to seek effective reductions. We assessed GHG emission reduction potentials and costs
in 2020 and 2030 by country and sector, using a GHG emission reduction-assessment model of high resolution regarding region
and technology, and of high consistency with intertemporal, interregional, and intersectoral relationships. Global GHG emission
reduction potentials relative to baseline emissions in 2020 are 8.4, 14.7, and 18.9 GtCO2eq. at costs below 20, 50, and 100 $/tCO2eq., corresponding to +19, −2, and −7 %, respectively, relative to 2005. The emission reduction potential for 2030 is greater
than that for 2020, mainly because many energy supply and energy-intensive technologies have long lifetimes and more of the
current key facilities will be extant in 2020 than in 2030. The emission reduction potentials in 2030 are 12.6, 22.0, and
26.6 GtCO2eq. at costs below 20, 50, and 100 $/tCO2eq., corresponding to +19, −2, and −7 %, respectively, relative to 2005. The emission reduction potential for 2030 is greater
than that for 2020, mainly because many energy supply and energy-intensive technologies have long lifetimes and more of the
current key facilities will be extant in 2020 than in 2030. The emission reduction potentials in 2030 are 12.6, 22.0, and
26.6 GtCO2eq. at costs below 20, 50, and 100 /tCO2eq., corresponding to +33, +8, and −3 %, respectively, relative to 2005. Global emission reduction potentials at a cost below
50 $/tCO2eq. for nuclear power and carbon capture and storage are 2.3 and 2.2 GtCO2eq., respectively, relative to baseline emissions in 2030. Longer-term perspectives on GHG emission reductions toward 2030
will yield more cost-effective reduction scenarios for 2020 as well. 相似文献
10.
We need to ensure the sustainable management of advanced materials, such as purified silicon, that contribute to a low-carbon
society. Because a drastic increase in the demand for photovoltaic (PV) systems is tightening the supply of silicon for PV
cells, the sustainability of silicon feedstock needs to be explored. For this purpose, a material flow analysis of silicon
in Japan from 1996 to 2006 is presented in this paper. Our analysis finds that rapid growth in demand for polycrystalline
silicon (pc-silicon) and single crystalline silicon (sc-silicon) has changed the structure of the purified silicon supply.
The strong demand for purified silicon for solar cells is responsible for this change. While off-grade silicon obtained as
a by-product of electronic-grade silicon (EG-Si) covered the demand for solar sells before 2000, pc-silicon is currently produced
independently for solar cells via an energy-intensive process. Analysis of the resource effective-use index (REI), which indicates
how effectively purified silicon is used, shows progress in the effective use of pc- and sc-silicon. REI analysis indicates
that the effective use of pc-silicon is reaching a maximum, while the effective use of sc-silicon is advancing, with a corresponding
increase in price. To ensure a sustainable supply of silicon feedstock, this paper proposes four solutions: (1) production
of solar-grade pc-silicon by a less costly and less energy-consuming method; (2) reduction in the amount of crystalline silicon
per watt in solar cells; (3) acceleration of the development and deployment of other solar cell types; and (4) reuse and recycling
of solar cells in the future. 相似文献