375 resultados para Bibel, Levitikus, 13,2-46
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Sr2Mg(BO3)(2) thermoluminescence (TL) phosphor was synthesized by a high temperature solid state reaction and the effect of Li+, Bi3+, Gd3+ or Ti4+ as a codopant on TL of Sr2Mg(BO3)(2) : Dy was investigated. The results show that Li+ as a codopant improves the emission intensity of high temperature TL peak of Sr2Mg(BO3)(2) : Dy phosphor whereas the addition of Bi3+, Gd3+ or Ti3+ leads to the decrease of TL intensity. The TL emission bands of Sr2Mg(BO3)(2) : Dy phosphors with Li+, Bi3+, Gd3+ or Ti4+ as a codopant are situated at 480, 579, 662 and 755 nm, which were attributed to the characteristic F-4(9/2)-> H-6(15/2), F-4(9/2)-> H-6(13/2), F-4(9/2)-> H-6(11/2) and F-4(9/2)-> H-6(9/2) transitions of Dy3+ ion, consistent with the emission of Sr2Mg(BO3)(2) : Dy phosphors. The kinetics parameters of 234 degrees C TL peak of Sr2Mg(BO3)(2) Dy-0.04(3+), (Li-0.04(+)) phosphor with the values of trap depth E=1.1 eV, frequency factor s=6.3 x 10(9) s(-1) were estimated by a peak shape method, which obey the second order kinetics.
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Two orange phosphorescent iridium complex monomers, 9-hexyl-9-(iridium (III)bis(2-(4'-fluorophenyl)-4-phenylquinoline-N, C-2')(tetradecanedionate-11,13))-2,7-dibromofluorene (Br-PIr) and 9-hexyl-9-(iridium(III)bis(2-(4'-fluorophenyl)-4-methylquinoline-N, C-2')(tetradecanedionate-11,13))-2,7-dibromofluorene (Br-MIr), were successfully synthesized. The Suzuki polycondensation of 2,7-bis(trimethylene boronate)-9,9-dioctylfluorene with 2,7-dibromo-9,9-dioetylfluorene and Br-Plr or Br-MIr afforded two series of copolymers, PIrPFs and MIrPFs, in good yields, in which the concentrations of the phosphorescent moieties were kept small (0.5-3 mol % feed ratio) to realize incomplete energy transfer. The photoluminescence (PL) of the copolymers showed blue- and orange-emission peaks. A white-light-emitting diode with a configuration of indium tin oxide/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)/PIr05PF (0.5 mol % feed ratio of Br-PIr)/Ca/Al exhibited a luminous efficiency of 4.49 cd/A and a power efficiency of 2.35 lm/W at 6.0 V with Commission Internationale de L'Eclairage (CIE) coordinates of (0.46, 0.33). The CIE coordinates were improved to (0.34, 0.33) when copolymer MIr10PF (1.0 mol % feed ratio of Br-MIr) was employed as the white-emissive layer. The strong orange emission in the electroluminescence spectra in comparison with PL for these kinds of polymers was attributed to the additional contribution of charge trapping in the phosphorescent dopants.
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Rare earth ions (Eu3+ and Dy3+)-doped Gd-2(WO4)(3) phosphor films were prepared by a Pechini sol-gel process. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), atomic force microscopy (AFM) and photoluminescence (PL) spectra as well as lifetimes were used to characterize the resulting powders and films. The results of XRD indicate that the films begin to crystallize at 600degreesC and the crystallinity increases with the elevation of annealing temperatures. The film is uniform and crack-free, WO(4)(2-)mainly consists of closely packed fine particles with an average grain size of 80 nm. Owing to an energy transfer from 4 groups, the rare earth ions show their characteristic emissions in crystalline Gd-2(WO4)(3) phosphor films, i.e., D-5(J) -F-7(J), (J = 0, 1, 2, 3; J' = 0 1, 2, 3, 4, not in all cases) transitions for Eu3+ and F-4(9/2)-H-6(J) (J = 13/2, 15/2) transitions for D Y3+, with the hypersensitive transitions D-5(0)-F-7(2) (Eu3+) and F-4(9/2) - H-6(13/2) (Dy3+) being the most prominent groups, respectively.
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用 Siemens P4四圆衍射仪,测得了1,4-二丙氧基-2,3-二氰基萘的晶体结构。晶体属单斜晶系,空间群为 C2/C。晶格参数 a=14.987(3)A,b=10.527(2),c=11.755(2),β=118.98°(3),晶胞体积 V=1622.4(6)3,Z=4,Dc=1.205Kg/m~3,μ(MoK_α)=0.079mm~(-1),F(000)=624,T=293(2)K_o晶体结构应用直接法,解出最后的偏离因子 R=0.0554[1425个Ⅰ≥2σ(Ⅰ)衍射点]。结构分析表明,萘环的1,4和2,3位碳原子上的氢原子分别被丙氧基和氰基所取代,由于取代基的引入使萘环的结构有所改变。
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The polymerization of acrylonitrile initiated by organolanthanide complexes alone is studied for the first time. The effect df polymerization conditions on catalytic activity of the title complex and molecular weight of the polymers produced have been studied.
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用电导法研究了甲醇溶液中稀土硝酸盐及氯化物与穴醚[2,1,1]的配位作用,测定了1:1配合物的稳定常数lgK及摩尔电导ΛML。在甲醇溶液中,稀土氯化物与[2,1,1]配合物的稳定性大于硝酸盐的相应配合物。稀土硝酸盐与[2,1,1]配合物的稳定常数lgK随镧系收缩有明显的钆断效应。电导测定表明,在甲醇溶液中,稀土硝酸盐为弱电解质。轻稀土与[2,1,1]反应后为1:1型电解质,重稀土配合物则属1:2型电解质;稀土氯化物在甲醇中为1:1型电解质,所形成的配合物均为1:2型电解质。
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首次报道用稀土有机配合物作为单组份催化剂催化丙烯腈聚合。研究了聚合条件对标题化合物的催化活性和所得聚丙烯腈的分子量及其结构的影响。
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Two lanthanum(III) [2,2,2]cryptates, [LaCl[2,2,2](H2O)]Cl-2.H2O (1) and [La(CF3SO3)[2,2,2](DMF)] (CF3SO3)(2) (2) have been prepared by the reaction of LaCl3 and La(CF3SO3)(3) with [2,2,2]cryptand, respectively and their crystal structures have been determ
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本研究测定了2-乙基己基膦酸单2-乙基己基酯(HEH/EHP)与镧系元素镧、铈、镨、钕、钐、铕、钬、铒、镱、镥的1H、(13)C、(31)P核磁共振谱。对HEH/EHP的碳骨架进行了详细归属,并根据(31)PNMR谱峰的积分面积,推测了萃合物可能的配位络合比,(HEH/EHP与Ln(Ⅲ)之比)。对铕、镱、镥为6,对铒为5,对钬、钐为4。
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采用GPC法与[η]测定相结合的方法,研究了1,2-PB在薄通过程中分子量和分子量分布的变化。结果表明,同一类型的1,2-PB,当[η]>200mL/g时,随薄通次数的增加[η]下降,分子量分布向低分子量方向移动。[η]降到200mL/g左右时,尽管成倍增加薄通次数,[η]降低缓慢,並趋于稳定,[η]≈200mL/g时,在薄通过程中[η]变化极小。比较当日和放置30d后测定的薄通样品,结果表明,薄通样品在放置过程中会产生自由基结合,生成支链结构,致使流体力学体积降低。
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Introduced species often start with limited genetic variability, which is problematic for selective breeding. The problem of inbreeding can be exasperated by hermaphroditism. The bay scallop Argopecten irradians irradians is a hermaphroditic species that has been introduced to and now supports a major aquaculture industry in China. Positive response to selection for fast growth was observed in one of the less inbred stocks in a previous study. In this study, we evaluated selection for the second generation to determine if response to selection can be sustained in this introduced population of a hermaphroditic species. Response to selection, realized heritability for the second generation, cumulative (over two generations), current (for the second generation) and residual (from the first generation) genetic gains were estimated by comparing three different types of lines: SS (selected for two generation), SC (selected for the first generation only) and CC (unselected for two generations). The SS line grew significantly faster (P < 0.05) than the other two lines, indicating that the second generation selection for faster growth is still effective. Response to selection and realized heritability for the second generation were 0.612 +/- 0.101 and 0.349 +/- 0.057, respectively, which are similar to those observed for the first generation. The cumulative, current, and residual gains were 17.56 +/- 5.30%, 10.63 +/- 2.46%, and 6.25 +/- 3.13%, respectively. The sustained response to selection for the second generation observed here suggests that considerable genetic variability exists in this population and that future efforts on selective breeding are likely to be fruitful. (c) 2005 Elsevier B.V. All rights reserved.
Resumo:
以1,2-苯并-3,4-二氢咔唑-9-乙基苯磺酸酯为衍生化试剂,在充氮的气氛下对鱼油进行皂化处理,所得皂化产物经正己烷萃取处理后进行柱前衍生化,再以HPLC/MS分离和鉴定。通过对长链脂肪酸分子的标记处理,其衍生物分子在质谱分析中呈现出双键位置的规范信息。通过建立模型计算式,借助不饱和脂肪酸的分子离子峰和特征碎片离子峰的质量数,计算不饱和的碳碳双键位置。共鉴定出23种脂肪酸。结果表明深海鱼油主要由C12-C22的脂肪酸组成,多不饱和脂肪酸含量占67.08%(峰面积百分比,下同),其中C16∶19-十六碳烯酸(11.7%);C16∶44,7,10,13-十六碳四烯酸(2.91%);C18∶112-十八碳烯酸(11.1%);C18∶46,9,12,15-十八碳四烯酸(3.62%);C20∶113-二十碳烯酸(1.21%);C20∶55,8,11,14,17-二十碳五烯酸(16.71%);C22∶62,5,8,11,14,17-二十二碳六烯酸(10.53%)。所建立的方法为不饱和脂肪酸碳链中双键位置的确定提供了新的技术手段。
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为了解青海省春小麦收割后田间堆放期间产量和品质的变化,选择近年育成的春小麦品种“高原205”(白粒,易穗发芽)、“高原115”(紫黑色小麦)、“高原448”(红粒)和“高原314”(白粒)以及曾为青海省主栽品种的“青春533”(红粒)为材料,收割后以农民常用的田间堆放方式进行堆放,每隔9d对其进行采样,测定产量、SDS沉淀值和降落数值的变化。结果表明,随着堆放时间的延长,收获产量逐步下降,平均产量从第1次采样(Od)时的504g/m^2减少到63d后的384g/m^2,收获产量平均值与取样时间直线回归F值为20.91,大于F0.01(6.90);SDS沉淀值变化较小,F值为0.90,小于F0.05(2.13);降落数值在取样时间点上差异极显著.F值等于46,72,大于F0.01(2.87)。高原205的降落数值一直呈现下降趋势,而高原448、高原115、高原314和青春533的变化是在O~18d间上升,然后下降。总体而言,田间堆放对收获产量和品质不利。
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在自然生长状态下 ,用测定在黄头鹡鸰(Motacillacitreola)成鸟产卵期性腺及输卵管蛋的质量变化的方法 ,研究了它们在产卵期间的能量投入及其分配形式 .产卵期 ,雌鸟用于性腺增长和卵形成的能量预算为 6 6 2 4~71 19kJ ,其中用于蛋白质和脂肪的能量分别为 40 42kJ和 2 5 82~ 30 78kJ,占总能量预算的 5 6 8%~ 6 1 0 %和36 3%~ 46 5 % .用于繁殖蛋白的能量分配为 :输卵管 2 77kJ ,卵黄蛋白 12 80kJ ,卵白蛋白 2 4 85kJ.雌鸟耗能最大的是第 0d~ +1d ,达 (13 2 8~ 14 2 6 )kJ/d .产卵期雄鸟耗能 (用于性腺增长 ) 7 98kJ,雌雄亲鸟用于卵的形成和性腺增长共投入能量 74 2 2~ 79 17kJ.雌鸟耗能为雄鸟的 8 3倍~ 8 9倍。
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对13万年以来洛川黄土-古土壤序列中固定铵态氮进行了分析。末次间冰期S1占土壤中固定铵态氮含量最高,其次为冰后期S0古土壤,末次冰期形成的马兰黄土最低;而且,固定铵态氮的分布在马兰黄土中也能体现出三次小的低-高值的波动特征。洛川黄土13万年以来固定铵态氮的分布与磁化率和<2μm组分的分布相似。在此基础上,利用马兰黄土中粒度与固定铵态氮的相关关系,计算了S1古土壤中固定铵的分布,并与实测结果进行了对比,推测S1古土壤中固定铵态氮有轻微的损失,尽管如此,S1古土壤中固定铵态氮含量仍然高于黄土。鉴于黄土-古土壤序列中固定铵态氮的分布与粉尘粒度有密切的关系,能与气候变化较好地对应,它可视为反映黄土高原区东亚冬季风强,弱周期性变化较好的替代性指标。