989 resultados para 157-955
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目录
- 1.1 化合物的生成焓,反应焓及燃烧热
- 1.2 热化学定律
- 1.3 热力学平衡与自由能,化学平衡与反应自由能
- 1.4 质量作用定律及可逆反应的平衡常数
- 1.5 平衡常数和标准反应自由能的关系
- 1.6 温度和压力对平衡常数的影响
- 1.7 绝热火焰温度计算
- 1.8 化学动力学中采用的几个基本概念和定义
- 1.9 反应的分类
- 1.10 阿累尼乌斯(Arrhenius)定律
- 1.11 双分子反应碰撞理论
- 1.12 反应分子数及反应级数
- 1.13 影响化学反应的因素
- 1.14 链锁反应
- 5.1 燃烧波的两种形式――缓燃(或火焰正常传播)及爆震
- 5.3 马兰特和利-恰及利耶的简化分析法
- 5.4 层流火焰传播速度的无量纲分析法
- 5.5 泽尔多维奇和弗朗克-卡门涅茨基的分区近似解
- 5.6 分区近似解的改进
- 5.7 精确解
- 5.8 物理化学参数对S1的影响及对火焰厚度的影响
- 5.9 火焰传播界限
- 5.10 用层流火焰传播速度计算化学动力参数的方法
- 5.11 火焰的基本性质及火焰的几何学
- 5.12 本生灯火焰稳定的条件
- 5.13 层流火焰传播速度的实验测定
- 5.14 单组元燃料滴燃烧
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Cephalopod remains (beaks, bodies, and parts of bodies) were collected from the stomachs of 157 sperm whales (Physeter macrocephalus) taken off central California (lat. 37°-39°N). At least 24 species representing 14 families were identified. Frequencies of occurrence of the six most numerous taxa were Moroteuthis robusta 72.0%, Gonatopsis borealis 66.2%, Histioteuthis dofleini 36.9%, Galiteuthis spp. (including G. phyllura and G. pacifica) 36.3%, Octopoteuthis deletron 35.0%, and Vampyroteuthis infernalis 27.4%. One find of two Mesonychoteuthis hamiltoni beaks strongly suggests transequatorial migration by one large male sperm whale. (PDF file contains 18 pages.)
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Finantza bazterketa gaur egun orduan eta garrantzia handiagoa duan errealitatea da. Hau dela eta, finantza bazterketaren kontzeptua, zergati posibleak eta egungo egoera aztertuko dituzte. Ondoren banku etikoetan zentratuko dira, finantza bazterketari aurre egiteko bide bat baita. Aurrekarien gainbegiraketa labur bat egin ostean, oro har banku etikoak Europan duen egoera eta Espainian, zehazki, duen garrantzia aztertuko dute, gogoeta batzuekin amaituz.
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157 p. : il., graf.
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157 p.
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Die 24. Sitzung des Komitees für Fische und Fischerzeugnisse wurde vom 5. bis 9. Juni 2000 erstmalig in Ålesund, Norwegen, durchgeführt. Die Tagung wurde von 140 Delegierten und Beobachtern aus 43 Mitgliedsstaaten und 3 internationalen Organisationen (EU, A.C.P. Generalsekretariat und Internationale Vereinigung der Fischinspektoren, IAFI) sowie FAO- und WHO-Personal (4) besucht. Die größten Delegationen stellten Frankreich (6), Kanada (6), Thailand (7), USA (10), Marokko (13) und Norwegen als Gastgeber (16). Die deutsche Delegation wurde von Dr. Achim Viereck (BML) geleitet. Weitere Mitglieder waren Dr. Jörg Oehlenschläger (BFAFi, Sprecher), Dr. Reinhard Schubring (BFAFi), Dr. Günter Klein (BgVV) und Dr. Matthias Keller (Bundesverband der deutschen Fischindustrie und des Fischgroßhandels). Die Sitzung, die von Peter Gullestad, dem norwegischen Generaldirektor für Fischerei, eröffnet wurde, leitete Dr. Bjorn Rothe Knudtsen, Regionaldirektor des norwegischen Direktorats für Fischerei und Aquakultur, Trondheim.
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A brief discussion is presented on the current situation regarding world fisheries and the future role of aquaculture. The various components involved in fisheries, and affecting all changes in fisheries through time, include the biology of the species involved, environment, technology/engineering and socio-economics. The importance of education in fisheries and aquaculture development is also examined
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An examination is made of the requirements for the commercial propagation of carp and tilapia in Nigeria. It is concluded that the operation of a successful Fish Hatchery and fry production system will depend on the following factors: 1) Correct initial planning for intended production (both species and intended numbers); 2) Design of the appropriate facilities to enable required production; 3) Selection of top calibre, dedicated and experienced hatchery staff; and, 4) The ethical responsibility taken by the hatchery management to produce only the highest quality seed under the best possible conditions. Purchasing farmers are dependent on this
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Effects of flame stretch on the laminar burning velocities of near-limit fuel-lean methane/air flames have been studied experimentally using a microgravity environment to minimize the complications of buoyancy. Outwardly propagating spherical flames were employed to assess the sensitivities of the laminar burning velocity to flame stretch, represented by Markstein lengths, and the fundamental laminar burning velocities of unstretched flames. Resulting data were reported for methane/air mixtures at ambient temperature and pressure, over the specific range of equivalence ratio that extended from 0.512 (the microgravity flammability limit found in the combustion chamber) to 0.601. Present measurements of unstretched laminar burning velocities were in good agreement with the unique existing microgravity data set at all measured equivalence ratios. Most of previous 1-g experiments using a variety of experimental techniques, however, appeared to give significantly higher burning velocities than the microgravity results. Furthermore, the burning velocities predicted by three chemical reaction mechanisms, which have been tuned primarily under off-limit conditions, were also considerably higher than the present experimental data. Additional results of the present investigation were derived for the overall activation energy and corresponding Zeldovich numbers, and the variation of the global flame Lewis numbers with equivalence ratio. The implications of these results were discussed. 2010 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
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针对大飞机壁板用的铝合金板料AA6056进行激光弯曲过程的试验研究.试验选用厚度为1.0 mm和2.5 mm的薄板,采用多组不同的工艺参数进行对比分析.采用直径0.1 mm的镍铬.镍硅热电偶作为温度传感器,YOKOGAWA MV200型便携式记录仪测量板料表面的温度;使用MV.1300UM CCD拍摄板料激光弯曲变形的过程,通过自行开发的实时采集软件记录并进行图像处理,最终得到了板料激光弯曲变形过程的实测曲线.试验结果为该过程的数值模拟提供了更为精确的验证依据,为深入研究板料激光弯曲过程奠定了试验基础.
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The synthesis of a sterically tailored ligand array (M)_2((C_5H_2-2-Si(CH_3)_3-4-C(CH_3)_3)S_2i(CH_3)_2]("M_2Bp") (M = Li, 16; K, 19) is described. Transmetallation of Li_2Bp with YCl_3(THF)_3 affords exclusively the C_2 symmetric product rac-[BpY(µ_2-Cl)_2Li(THF)_2], 20. A X-ray crystal structure of 20 has been determined; triclinic, P1, a= 13.110 (8), b = 17.163 (15), c = 20.623 (14) Å, α = 104.02 (7), β = 99.38 (5), γ = 100.24 (6)° , Z = 4, R = 0.056. Transmetallation of K_2Bp with YCl_3(THF)_3 affords the halide free complex rac-BpYCl, 23. The corresponding rac-BpLaCl, 28, is prepared in an anlogous manner. In all cases the achiral meso isomer is not obtained since only for the racemic isomers are the unfavorable steric interactions between the Si(CH3)_3 groups in the narrow portion of the [Cp-M'-Cp] wedge avoided. Alkylation of 20 or 23 with LiCH(Si(CH_3)_3)_2 affords rac-BpYCH(Si(CH_3)_3)_2, 26 in good yield. Alkylation of 28 with LiCH(Si(CH_3)_3)_2 affords rac-BpLaCH(Si(CH_3)_3)_2 29. Hydrogenation of 26 cleanly affords the bridging hydride species [BpY(µ_2-H)]_2, 27, as the homochiral (R,R) and (S,S) dimeric pairs. 26 is an efficient initiator for the polymerization of ethylene to high molecular weight linear polyethylene. 27 catalyzes the polymerization of propylene (25% v/v in methylcyclohexane) and neat samples of 1-butene, 1-pentene, 1-hexene to moderately high molecular weight polymers: polypropylene (M_n = 4,200, PDI 2.32, T_m 157 °C); poly-1-butene (M_n = 8,500, PDI 3.44, T_m 105 °C); poly-1-pentene (M_n = 20,000, PDI 1.99, T_m 73 °C); poly-1-hexene (M_n = 24,000, PDI 1.75, T_m < 25 °C). ^(13)C NMR spectra at the pentad analysis level indicates that the degree of isotacticity is 99% mmmm for all polymer samples. 27 is the first single component iso-specific α-olefin polymerization catalyst. The presumed origins of the high isospecificity are presented.
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The propellane alkaloids comprise a large class of natural products that possess varying degrees of structural complexity and biological activity. The earliest of these to be isolated was acutumine, a chlorinated alkaloid that has been shown to exhibit selective T-cell cytotoxicity and antiamnesic properties. Alternatively, the hasubanan family of natural products has garnered considerable attention from the synthetic community in part due to its structural similarities to morphine. While these alkaloids have been the subject of numerous synthetic studies over the last forty years, very few enantioselective total syntheses have been reported to date.
As part of a research program directed towards the synthesis of various alkaloid natural products, we have developed a unified strategy for the preparation of the hasubanan and acutumine alkaloids. Specifically, a highly diastereoselective 1,2-addition of organometallic reagents to benzoquinone-derived tert-butanesulfinimines was established, which provides access to enantioenriched 4-aminocyclohexadienone products. This methodology enabled the enantioselective construction of functionalized dihydroindolones, which were found to undergo intramolecular Friedel-Crafts conjugate additions to furnish the propellane cores of several hasubanan alkaloids. As a result of these studies, the first enantioselective total syntheses of 8-demethoxyrunanine and cepharatines A, C, and D were accomplished in 9-11 steps from commercially available starting materials.
More recent efforts have focused on applying the sulfinimine methodology to the synthesis of a more structurally complex propellane alkaloid, acutumine. Extensive studies have determined that a properly functionalized dihydroindolone undergoes a photochemical [2+2] cycloaddition followed by a lactone fragmentation/Dieckmann cyclization to establish the carbocyclic framework of the natural product. The preparation of more appropriately oxidized propellane intermediates is currently under investigation, and is anticipated to facilitate our synthetic endeavors toward acutumine.