225 resultados para 0.9-percent Saline
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本文探讨了焙烧温度对催化剂结构及氨氧化活性的影响。得出:La_(0.9)Sr_(0.1)NiO_(3-λ)在1223K后分解,生成具有K_2NiF_4结构的La_2NiO_4相,NiO相和LaNiO_3相。催化活性相主要是具有钙钛矿结构的组分。最佳活性相在1273K形成。
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本文讨论了LnVO_4:Eu(Ln_(0.9)Eu_(0.1)VO_4,Ln=La~(3+)、Gd~(3+)、Y~(3+)、Sc'+和Lu_(3+))多晶粉末中Eu~(3+)离子~5D_0→~7F_2电偶跃迁(618.4nm)发光与化学组成、晶体结构和R—O键强之间的变化规律。
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本文介绍自行合成的LaxBa_(1-x)SnO_3(x=0~0.2)的结构、电学性质、温敏性质和气敏性质,其结构均为立方晶体,晶胞参数随镧含量的增加而减少.La_(0.1)Ba_(0.9)SnO_3在室温至600℃温区内,电阻随温度升高而线性下降,有可能用作温敏元件.当La_(0.1)Ba_(0.9)SnO_3作成旁热式气敏元件时,有可能用于(10~10000)10~(-6)乙醇蒸汽的检测,而不受煤气、液化汽、汽油和烟的干扰.
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The present work is devoted to the studies on relationship of structure and activity of Sn-Mo oxides by using XRD, ESR, IR, XPS, TEM and SEM. Eight samples with Mo/(Mo + Sn) rations: 0.0, 0.1, 0.2, 0.4, 0.6, 0.8, 0.9, 1.0 were prepared. On the basis of structure characterization, Sn-Mo oxides can be divided into three groups: Catalysts I with Mo/(Mo + So) less-than-or-equal-to 0.2, Catalysts II with 0.2 < Mo/(Mo + Sn) < 0.8, and catalysts III with Mo/(Mo + Sn) greater-than-or-equal-to 0.8. The solid solution of Mo5+ in tin oxide was formed and the cation vacancy was formed in catalysts I. The solid solution of Sn4+ in molybdenum oxide was formed in catalysts III. The lattice oxygen in catalysts III has higher mobility and reactivity than that in catalysts I. The catalysts III showed higher activity but lower selectivity than that of catalysts I.
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The crystal structure of [Mn(thiamine)Cl2(H2O)]2[thiamine]2Cl4.2H2O has been determined by X-ray diffraction methods. The compound contains a cyclic dimer of a complex cation with two thiamine ligands bridged by two Mn(II) ions across a crystallographic center of symmetry. Each Mn(II) is coordinated by two chloride atoms, a water molecule, a N(1') atom of the pyrimidine from a thiamine and an O(53) atom of the hydroxyethyl side chain from another thiamine. There are two free-base thiamine molecules related by a center of symmetry in the unit cell, which form a base-pair through the hydrogen bonds. Both the independent thiamine molecules in the asymmetric unit assume the common F conformation with phi-T = 10.0(9) and 3.6(10) and phi-P = 85.6(7) and 79.6(7), respectively. The compound provides a possible model for a metal-bridged enzyme-coenzyme complex in thiamine catalysis. Crystallographic data: triclinic, space group P1BAR, a = 12.441(4), b = 13.572(4), c = 11.267(3) angstrom, alpha = 103.15(2), beta 89.03(3), gamma = 115.64(2)-degrees, Z = 1, D(calc) = 1.524 g cm-3, and R = 0.050 for 3019 observed reflections with I > 3-sigma(I).
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采用蒸发溶液法从磷酸溶液中生长出一系列Ce_xGd_yTb_(1-x-y)P_5O_(14)晶体.测定了它们的结构.它们属于单斜晶系,空间群P2_(1/c).测定了Ce_(0.9)Gd_(0.1)P_5O_(14)、Ce_(0.9)Tb_(0.1)P_5O_(14)和La_(0.8)Gd_(0.1)Tb_(0.1)P_5O_(14)等晶体的光谱.首次观察到,将Gd加入Ce_xTb_(1-x)P_5O_(14)晶体中形成.Ce_xGd_yTb_(1-x-y)P_5O_(14)时阻碍了Ce~(3+)→Tb~(3+)的能量传递,导致Ce~(3+)的发射峰增强,Tb~(3+)的~5D_4—~F_J发射峰减弱、而~5D_3—~7F_J发射峰增强.
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本文提出了用电感耦合等离子体原子发射光谱(ICP—AES)法直接测定混合稀土铜合金中13个非稀土和稀土元素。选用了合适的分析线对及ICP光源的工作参数。探讨了观察高度、功率、酸度、载气和基体量的变化对被测元素谱线强度的影响。不用化学分离,可一次同时测定La、Ce、pr、Nd、Sm、Sn、Zn、Fe、Al、Ni、Pb,Mg和Mn。测定范围(%):La_2O_3:0.096~6.4;CeO_2:0.24~16;Pr_6O_(11):0.0384~2.56;Nd_2O_3:0.096~6.4;Sn:0.096~3.2;Mg、Mn、Fe,Sm_2O_3:0.024~1.6;Zn:0.396~6.7;Pb:0.092~6.4;Ni:0.096~3.2;Al:0.0384~1.28。相对标准偏差±3.0~9.1%;回收率85~116%满足冶炼上的要求,得到了满意的结果。
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本文以1-丁烯在水蒸汽存在下选择性氧化制甲乙酮为典型反应,利用 XRD,ESR,IR,XPS,TEM 和 SEM 研究了 Sn-Mo 氧化物的结构与活性的关系.制备了8个样品,A,B,C,D,E,F,G 和 H 的 Mo/(Mo+Sn)分别为0,0.1,0.2,0.4,0.6,0.8,0.9,1.0.根据结构特征,可将 Sn-Mo 氧化物分为三组:第Ⅰ组 Mo/(Mo+Sn)≤0.2;第Ⅱ组0.2
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Marine bacterium Vibrio sp. F-6, utilizing agarose as a carbon source to produce agarases, was isolated from seawater samples taken from Qingdao, China. Two agarases (AG-a and AG-b) were purified to a homogeneity from the cultural supernatant of Vibrio sp. F-6 through ammonium sulfate precipitation, Q-Sepharose FF chromatography, and Sephacryl S-100 gel filtration. Molecular weights of agarases were estimated to be 54.0 kDa (AG-a) and 34.5 kDa (AG-b) by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The optimum pH values for AG-a and AG-b were about 7.0 and 9.0, respectively. AG-a was stable in the pH range of 4.0-9.0 and AG-b was stable in the pH range of 4.0-10.0. The optimum temperatures of AG-a and AG-b were 40 and 55 degrees C, respectively. AG-a was stable at temperature below 50 degrees C. AG-b was stable at temperature below 60 degrees C. Zn2+, Mg2+ or Ca2+ increased AG-a activity, while Mn2+, Cu2+ or Ca2+ increased AG-b activity. However, Ag+, Hg2+, Fe3+, EDTA and SDS inhibited AG-a and AG-b activities. The main hydrolysates of agarose by AG-a were neoagarotetraose and neoagarohexaose. The main hydrolysates of agarose by AG-b were neoagarooctaose and neoagarohexaose. When the mixture of AG-a and AG-b were used, agarose was mainly degraded into neoagarobiose.
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Sargassum muticum is important in maintaining the structure and function of littoral ecosystems, and is used in aquaculture and alginate production, however, little is known about its population genetic attributes. In this study, random amplified polymorphic DNA (RAPD) and inter-simple sequence repeat (ISSR) markers were used to investigate the genetic structure of four populations of S. muticum and one outgroup of S. fusiforme (Harv.) Setchell from Shandong peninsula of China. The selected 24 RAPD primers and 19 ISSR primers amplified 164 loci and 122 loci, respectively. Estimates of genetic diversity with different indicators (P%, percentage of polymorphic loci; H, the expected heterozygosity; I, Shannon's information index) revealed low or moderate level of genetic variations within each S. muticum population, and a high level of genetic differentiations were determined with pairwise unbiased genetic distance (D) and fixation index (F-ST ) among the populations. The Mantel test showed that two types of matrices of D and F-ST were highly correlated whether from RAPD (r = 0.9706, P = 0.009) or ISSR data (r = 0.9161, P = 0.009). Analysis of molecular variance (AMOVA) was conducted to apportion the variations among and within the S. muticum populations. It indicated that variations among populations were higher than those within populations, being 55.82% verse 44.18% by RAPD and 55.21% verse 44.79% by ISSR, respectively. Furthermore, the Mantel test suggested that genetic differentiations among populations were related to the geographical distances (r > 0.6), namely, conformed to the IBD (isolation by distance) model, as expected from UPGMA (unweighted pair group method with arithmetic averages) cluster analysis. On the whole, the high genetic structuring among the four S. muticum populations along the distant locations was clearly indicated in RAPD and ISSR analyses (r > 0.9, P < 0.05) in our study.
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A new fermentative hydrogen-producing bacterium was isolated from mangrove sludge and identified as Pantoea agglomerans using light microscopic examination, Biolog test and 16S rRNA gene sequence analysis. The isolated bacterium, designated as P. agglomerans BH-18, is a new strain that has never been optimized as a potential hydrogen-producing bacterium. In this study, the culture conditions and the hydrogen-producing ability of P. agglomerans BH-18 were examined. The strain was a salt-tolerant facultative anaerobe with the initial optimum pH value at 8.0-9.0 and temperature at 30 degrees C on cell growth. During fermentation, hydrogen started to evolve when cell growth entered late-exponential phase and was mainly produced in the stationary phase. The strain was able to produce hydrogen over a wide range of initial pH from 5 to 10, with an optimum initial pH of 6. The level of hydrogen production was affected by the initial glucose concentration, and the optimum value was found to be 10 g glucose/l. The maximum hydrogen-producing yield (2246 ml/l) and overall hydrogen production rate (160 ml/l/h) were obtained at an initial glucose concentration of 10 g/l and an initial pH value of 7.2 in marine culture conditions. In particular, the level of hydrogen production was also affected by the salt concentration. Hydrogen production reached a higher level in fresh culture conditions than in marine ones. In marine conditions, hydrogen productivity was 108 ml/l/h at an initial glucose concentration of 20 g/l and pH value of 7.2, whereas, it increased by 27% in fresh conditions. In addition, this strain could produce hydrogen using glucose and many other carbon sources such as fructose, sucrose, sorbitol and so on. As a result, it is possible that P. agglomerans BH-18 is used for biohydrogen production and biological treatment of mariculture wastewater and marine organic waste. (C) 2008 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
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The variolitic andesite from the Susong County in the Dabie Mountains implies that it was erupted in water. The mineralogy of the varioles is primarily radiate plagioclase (albite sind oligoclase), with little pyroxene, hornblende and quartz (derived from alteration). The pyroxene, hornblende and quartz are in the interstices between plagiocalse. The matrix consists of glass, hornblende, chlorite, epidote and zoisite. It is clearly subjected an extensive alteration. The andesite has an uncommon chemical composition. The SiO2 content is about 56.8%, TiO2 = 0.9%, MgO = 6.4%, Fe2O3 (tot) = 6.7%similar to 7.6%, 100Mg/(Mg + Fe) = 64.1 similar to 66.2. Mg-# is significantly high. The andesite has high abundances of large-lithophile trace elements (e.g. K, Ba. Sr, LREE), e.g. La/Nb = 5.56 similar to 6.07, low abundances of high-strength-field elements (HFSE e.g. Ta, Nb, P, Ti), particularly Ta and Nb strongly depleted. These are consistent with the characteristics of subduction-related magmas. In the spider diagram of trace elements, from Ce to right hand, the abundances of elements decrease quickly, showing a character of the continental margins. There has a strong punishment of light-rare-earth elements, with a significant diffraction of REEs (the mean value of (La/Yb)(N) is 32.84). No Eu anomaly, but there are anomaly high (La/Yb)(N) = 28.63 similar to 36.74, (La/Y)(N) = 70.33 similar to 82.4. The elements Y and Yb are depleted greatly, Y<20
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Suspended Particulate Matter (SPM) concentrations at various levels within the water column, together with salinity and temperature, were measured using water samples collected from six stations across the Straits of Dover. The sampling programme covered a 16-month period, undertaken during 23 cruises. On the basis of the spatial variability in the concentrations, the water bodies are divided by several boundaries, controlled by tidal and wind conditions. Within the water column, SPM concentrations were higher near the sea bed than in the surface waters. Throughout the cross-section, maximum concentrations occurred adjacent to the coastlines. Temporal variability in the SPM concentration exists on daily and seasonal scales within the coastal waters (4.2 to 74.5 mg L-1): resuspension processes, in response to semi-diurnal tidal cycles (with a period of around 12.4 h) and spring-neap cycles (with a period of 15 days) make significant contributions. Distinctive seasonal/annual concentration changes have also been observed. In the offshore waters, such variability is much less significant (0.9 to 6.0 mg L-1). In the summer the English Coastal Zone is associated with relatively high SPM concentrations: the Central Zone has a low and stable SPM concentration between these zones, there is a Transitional Zone, where there is a rapid response of SPM concentration to wind forcing. Finally, the French Coastal Zone is characterized by variable (sometimes high) SPM concentrations. Because of the zonation, SPM fluxes within the Dover Strait are controlled by different transport mechanisms. Within the Central Zone, the flux can be represented by the product of mean water discharges and SPM concentrations. However, within the coastal zones fluctuations in SPM concentrations on various time-scales must be considered. In order to calculate the maximum and minimum SPM fluxes, 10 cells were divided in the strait. A simple modelling calculation has been proposed for this complex area. The effect of spring-neap tidal cycles and seasonal changes can contribute significantly to the overall flux, which is of the order of 20 x 10(6) t.yr(-1) (through the Dover Strait, towards the North Sea). Such an estimate is higher than most obtained previously. (C) 2000 Ifremer/CNRS/IRD/Editions scientifiques et medicales Elsevier SAS.
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本研究运用RAPD和ISSR两种分子标记技术,对采自山东半岛4个不同地理位置的鼠尾藻(Sargassum thunbergii)和海黍子(S. muticum)种群进行了遗传多样性和遗传结构的研究,从而对其种群间的地理隔离、基因流动水平及其影响因素做出估计和判断,为马尾藻自然资源的保护和开发提供依据。在室内对鼠尾藻有性生殖幼苗的早期发育和生长进行了研究,了解其繁殖生物学特性,为鼠尾藻人工种苗的培育提供依据。主要研究结果如下: 对4个鼠尾藻(S. thunbergii)地理种群的遗传多样性研究中,筛选出了28条RAPD 引物和19条ISSR引物,分别扩增产生了174和125个位点。选用的三种不同指标,即多态位点比率(P%,percentage of polymorphic loci),平均预期杂合度(H,the expected heterozygosity)和 Shannon's 信息多样性指数(I,Shannon's information index),均可反映出鼠尾藻种群内部的遗传多样性呈较低水平。而群体间遗传距离(D,Nei’s unbiased genetic distance)矩阵和固定化指数(FST,the fixation index)矩阵均反映出群体间高度的遗传分化。通过分子变异分析(AMOVA,Analysis of molecular variance)来区分来自种群内部和种群之间的遗传变异,揭示出多数的遗传变异(57.57% 或59.52%)来自于鼠尾藻种群之间。另外,Mantel分析表明,4个鼠尾藻种群间的遗传分化与地理距离呈正相关(r>0.5),遵循传统的IBD(isolation by distance)模式,UPGMA(unweighted pair group method with arithmetic averages)聚类分析也反映出相似的结果。 对4个海黍子(S. muticum)地理种群遗传结构的研究中,筛选出的24条RAPD 引物和19条ISSR引物分别扩增出164和122个位点。遗传多样性评估结果表明,海黍子种群内部存在较低或者中等水平的遗传多样性,而D矩阵和FST 矩阵均显示种群间存在高水平的遗传分化。并且,发现D和FST 矩阵在RAPD和ISSR分析中均具有高且显著的相关性。AMOVA分析显示,种群之间的遗传变异高于种群内部。Mantel分析和UPGMA聚类分析均发现海黍子种群间的遗传分化遵循IBD模式,即与地理隔离呈正相关(r>0.6)。 并且,RAPD和ISSR分析的结果高度一致(r>0.9,P<0.05),均揭示4个海黍子种群之间存在高度的遗传分化。 对鼠尾藻有性生殖幼苗早期生长发育的研究结果表明,其早期发育过程属于马尾藻科(Sargassaceae)中典型的“8核1卵”型。在一定条件下培养两个月后,产生了1~2个小叶,幼苗的长度达2~3毫米。生长实验发现,温度(10, 15, 20, 25℃)和光照强度(9, 18, 44, 88 µEm-2s-1)对培养第一周幼苗的生长均有显著的影响(ANOVA, P<0.01)。在两个月的培养中,幼苗对温度和光强的耐受范围较宽,在10℃~25℃,9~88 µEm-2s-1条件下均可生长,最适温度和光强为25℃,44 µEm-2s-1;低温(10℃)对幼苗的生长有显著抑制。不同光质对幼苗生长的影响显著(P<0.01),相同光强条件下,蓝光和白光相比较,蓝光显然不能满足鼠尾藻幼苗早期生长的需要。
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测定了管藻目绿藻刺松藻和假根羽藻的叶状体、叶绿体及类囊体膜的吸收光谱和低温荧光光谱,并同软丝藻等5种非管藻目绿藻和菠菜进行了比较。证实绿藻普遍缺少作为高等植物 PSI 标志的 730nm 的低温长波荧光,其长波发射峰在 710 ~ 715nm 以及 695nm 荧光也不明显。采用和的 PAGE 法从刺松藻、假根羽藻、软丝藻和菠菜中分别得到 11 种、11 种、7 种和 9 种色素蛋白复合物,并测定了各复合物的分子量、Chl a/b、叶绿素的分布、多肽组成和结构关系,以及吸收光谱、低温荧光发射和激发光谱等各种光谱特性。刺松藻和假根羽藻的 CPIa_(1-2) 复合物的荧光发射主峰分别在 698、690 和 685nm,软丝藻 CPIa 在 715nm,菠菜 CPIa_(1-2) 分别在 729 和 722nm。两种管藻目绿藻的 LHCI 与 CII 的结合程度较菠菜和软丝藻更紧密,其 CPI 复合物中仍含有一定量的,710 ~ 715nm 荧光呈隐现状态。用二次 PAGE 法将刺松藻和假根羽藻的 CPIa 和 CIP 再分离,得到 PSI 的捕光复合 LHCI,为管藻黄素-Chl a/b-蛋白复合物, Chl a/b=1.2,含有 27.5、26.2、26 和 24.5kDa 四种多肽,77K 荧光峰在 682 ~ 683nm。LHCI 没有发射高等植物 730nm 荧光的相应组分是管藻目绿藻缺少 730nm 荧光的主要原因。核心复合物 CCI 含有 67 和 56kDa 两种多肽,与软丝藻和菠菜相似,但 3 种藻类核心复合物的 77K 荧光峰在 715nm,而菠菜在 720nm。刺松藻和假根羽藻有 LHCI 存在时,715nm 荧光峰不明显,随着 LHCI 的解离,荧光逐渐显现。刺松藻 PSI 中与 CCI 结合最紧密的是 LHCI 的 27.5 和 24.5kDa 多肽,两个 26 kDa 多肽的结合较为松散。用差速离心法对刺松藻、假根羽藻、软丝藻及菠菜的 PSI 颗粒进行了初步的分离。PSI 粗提物的 77K 长波荧光发射峰分别在 710、712、713 和 730nm,与 PAGE 法得到的结果相符。刺松藻和假根羽藻的 PSII 核心复合物 CPa 与菠菜相同,都含有两个 33kDa 核心多肽及 40 ~ 47 kDa 的内天线蛋白。从两种管藻目绿藻中首次分离到 6 种 LHCII 捕光复合物,其中 LHCP_(1-3),四种都是管藻黄素- Chl a/b-蛋白复合物, Chl a/b=0.7 ~ 0.9。刺松藻和假根羽藻中含量最高、最稳定的捕光复合物是分子量最大的 LHCP_1 由 34.4、31.5、29.5、28.1 和 26.5kDa 多肽构成,其中 34.4 和 31.5kDa 多肽在菠菜和软丝藻中没有对应组分。LHCP_1 再分离结果表明,分子量较小的捕光复合物都是 LHCP_1 的组成部分,但分子量最小的 Fca_1 和 Fca_2 与其它复合物的关系尚不确定。31.5 和 29.5 kDa 多肽是 LHCP_1 的核心,34.4、28.1 和 26.5kDa 多肽位于外侧;整个 LHCP_1 以 28.1 和 26.5kDa 多肽与 CCII 紧密结合,构成 PSII。根据刺松藻和假根羽藻光系统结构及其特异性的研究结果,提出了一个管藻目绿藻 PSI 和 PSII 色素蛋白复合物结构关系模型,并与高等植物的模型做了比较。讨论了光合作用两个光系统结构和特性的进化过程,指出 730nm 低温荧光峰不能作为管藻目乃至非管藻目绿藻 PSI 的表征。管藻目绿藻同杂色藻类在这方面有相似性。