816 resultados para 857
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对乙胺丁醇 (EMB)在玻碳电极上的阳极伏安行为进行了研究 ,发现在 0 .0 39mol LNa2 HPO4溶液中于1 0 4V(vs.Ag AgCl)左右产生一个与EMB浓度 3~ 1 0 0 0mg L呈良好的线性关系的阳极氧化峰 ;大多数金属离子和药剂辅料及生化有机物质不干扰测定。方法用于药剂和加标人尿中EMB的测定 ,获得满意结果
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A method for the determination of impurity elements in high purity cadmium by inductively coupled plasma mass spectrometry was developed. The spectral interference arising from Cd was discussed and the magnitude of interference by the polyatomic ion of Cd was compared. The effect of the high concentration Cd on the analyte signal was studied. The results showed that Cd possessed both significant suppression effects on the light mass elements signal and enhancement effects on the heavy mass elements signal,and the effects can be corrected by the use of internal standard elements. In this paper, Y and Bi was employed for the light mass elements and the heavy mass elements,respectively. As, Be, Co, Cu, Ga, Ge, Mn, Mo, Pb, Ni, Sr, Au, Tl, Th, V and U in high purity cadmium were determined. Detection limits are 0.005-0.052 mu g L-1,and the recoveries of standard addition are 82%-108%.
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The crystallization behaviors, dynamic mechanical properties, tensile, and morphology features of polyamide1010 (PA1010) blends with the high-impact polystyrene (HIPS) were examined at a wide composition range. Both unmodified and maleicanhydride-(MA)-grafted HIPS (HIPS-g-MA) were used. It was found that the domain size of HIPS-g-MA was much smaller than that of HIPS at the same compositions in the blends. The mechanical performances of PA1010-HIPS-g-MA blends were enhanced much more than that of PA1010-HIPS blends. The crystallization temperature of PA1010 shifted towards higher temperature as HIPS-g-MA increased from 20 to 50% in the blends. For the blends with a dispersed PA phase (less than or equal to 35 wt %), the T-c of PA1010 shifted towards lower temperature, from 178 to 83 degrees C. An additional transition was detected at a temperature located between the T-g's of PA1010 and PS. It was associated with the interphase relaxation peak. Its intensity increased with increasing content of PA1010, and the maximum occurred at the composition of PA1010-HIPS-g-MA 80/20. (C) 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 857-865, 1999.
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采用电感耦合等离子体质谱法测定高纯镉中的杂质元素。讨论了镉基体的谱线干扰,比较了镉基体产生的多原子离子的干扰程度,该干扰按Cdh、CdO、CdO2、CdAr、CdOH和CdOH2顺序递减。研究了不同浓度镉基体对分析物信号的抑制或增强效应,镉的浓度大于0.25·L-1时,对质量数小于100的分析物的信号强度产生抑制,而对质量数大于150的分析物的信号强度产生增强,采用89Y和209Bi作内标分别克服基体的抑制和增强效应。测定了高纯镉的As、Be、Co、Cu、Ga、Ge、Mn、Mo、Pb、Ni、Sr、Au、Tl、Th、V和U等16个杂质元素,方法的检测限0.005~0.052μg·L-1,标准加入回收率82%~108%。
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The Nd-III ion in hexa-mu-chloro-1:2 kappa(2)Cl;1:3 kappa(2)Cl;1:4 kappa(2)Cl-hexachloro-2 kappa(2)Cl,3 kappa(2)Cl,4 kappa(2)Cl- [1 (eta(6))- toluene] trialuminiumneodymium has distorted pentagonal bipyramidal coordination geometry. Five Cl atoms form the equatorial plane, and the toluene ring and the sixth Cl atom occupy the apical sites. The average Nd-C(eta(6)) and Nd-Cl distances are 2.926 (5) and 2.857 (1) Angstrom, respectively.
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本文报道一种新型透射式红外光谱电化学池的设计制作。应用盐片加工技术,采用内参比点设置等方法。使该池达到30μm的厚度,且具有十分良好的电化学性能。
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The single crystal of heteropoly blue, HsSiMo12O40.12H2O, the reduced product of molybdenum-silicon heteropoly acid, was prepared by electrochemical reduction and evaporation in nitrogen atmosphere. The Crystal structure of the product was determined. The heteropoly blue H8SiMo12O40.12H2O, Crystallizes space group P1BAR a = 1.3769 (3) nm, b = 1.4346 (4) nm, c = 1.4134 (4) nm, alpha = 120.47 (2)-degrees, beta = 110.70 (2)-degrees, gamma = 66.11 (2)-degrees, Z = 2, R = 0.0608. The heteropoly blue anion was determined to have Keggin Structure and alpha-isomer and it remained the structure of the unreduced heteropoly acid anion. But the distortion of the structure and the changes of bond length and bond angle take place obviously. The four Mo5+ Positions were determined in the structure.
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通过电化学还原的方法得到钼硅杂多酸的还原产物杂多蓝单晶H_8SiMo_(12)O_(40)·12H_2O.测完了它的晶体结构.晶体空间群属PI.α=1.3769(3)nm,b=1.4346(4)nm,c=1.4134(4)nm;α=120.47(2)°,β=110.70(2)°,γ=66.11(2)°;Z=2;R=0.0608.确证杂多蓝阴离子呈现Keggin结构和α-异构体特征,基本保持未还原杂多酸阴离子的结构.但是在结构畸变程度、键角和键长的变化以及结晶水的分布上有明显不同.同时确定了杂多蓝阴离子结构中4个Mo~(5+)离子的位置.
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A pattern recognition protein (PRP), lipopolysaccharide and beta-1,3-glucan binding protein (LGBP) cDNA was cloned from the haemocyte of Chinese shrimp Fenneropenaeus chinensis by the techniques of homology cloning and RACE. Analysis of nucleotide sequence revealed that the full-length cDNA of 1,275 bp has an open reading frame of 1,098 bp encoding a protein of 366 amino acids including a 17 amino acid signal peptide. Sequence comparison of the deduced amino acid sequence of F. chinensis LGBP showed a high identity of 94%, 90%, 87%, 72% and 63% with Penaeus monodon BGBP, Litopenaeus stylirostris LGBP, Marsupenaeu japonicus BGBP, Homarus gammarus BGBP and Pacifastacus leniusculus LGBP, respectively. The calculated molecular mass of the mature protein is 39,857 Da with a deduced pI of 4.39. Two putative integrin binding motifs, RGD (Arg-Gly-Asp) and a potential recognition motif for beta-1,3-linkage of polysaccharides were observed in LGBP sequence. RT-PCR analysis showed that LGBP gene expresses in haemocyte and hepatopancreas only, but not in other tissues. Capillary electrophoresis RT-PCR method was used to quantify the variation of mRNA transcription level during artificial infection with heat-killed Vibrio anguillarum and Staphylococcus aureusin. A significant enhancement of LGBP transcription was appeared at 6 h post-injection in response to bacterial infection. These results have provided useful information to understand the function of LGBP in shrimp.
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The noble gas nuclide abundances and isotopic ratios of the upmost layer of Fe-Mn crusts from the western and central Pacific Ocean have been determined. The results indicate that the He and Ar nuclide abundances and isotopic ratios can be classified into two types: low He-3/He-4 type and high He-3/He-4 type. The low He-3/He-4 type is characterized by high He-4 abundances of 191x10(-9) cm(3.)STP(.)g(-1) on average, with variable He-4, Ne-20 and Ar-40 abundances in the range (42.8-421)x10(-9) cm(3.)STP(.)g(-1), (5.40-141)x10(-9)cm(3.)STP(.)g(-1), and (773-10976)x10(-9) cm(3.)STP(.)g(-1), respectively. The high He-3/He-4 samples are characterized by low He-4 abundances of 11.7x10(-9) cm(3.)STP(.)g(-1) on average, with He-4, Ne-20 and Ar-40 abundances in the range of (7.57-17.4)x10(-9) cm(3.)STP(.)g(-1), (110.4-25.5)x10(-9) cm(3.)STP(.)g(-1) and (5354-9050)x10(-9) cm(3.)STP(.)g(-1), respectively. The low He-3/He-4 samples have He-3/He-4 ratios (with RIRA ratios of 2.04-2.92) which are lower than those of MORB (R/R-A=8 +/- 1) and Ar-40/Ar-36 ratios (447-543) which are higher than those of air (295.5). The high He-3/He-4 samples have He-3/He-4 ratios (with R/R-A ratios of 10.4-12.0) slightly higher than those of MORB (R/R-A=8 +/- 1) and Ar-40/Ar-36 ratios (293-299) very similar to those of air (295.5). The Ne isotopic ratios (Ne-20/Ne-22 and Ne-21/Ne-22 ratios of 10.3-10.9 and 0.02774-0.03039, respectively) and the Ar-38/Ar-36 ratios (0.1886-0.1963) have narrow ranges which are very similar to those of air (the Ne-20/Ne-22, Ne-21/Ne-22, Ar-38/Ar-36 ratios of 9.80, 0.029 and 0.187, respectively), and cannot be differentiated into different groups. The noble gas nuclide abundances and isotopic ratios, together with their regional variability, suggest that the noble gases in the Fe-Mn crusts originate primarily from the lower mantle. The low He-3/He-4 type and high He-3/He-4 type samples have noble gas characteristics similar to those of HIMU (High U/Pb Mantle)- and EM (Enriched Mantle)-type mantle material, respectively. The low He-3/He-4 type samples with HIMU-type noble gas isotopic ratios occur in the Magellan Seamounts, Marcus-Wake Seamounts, Marshall Island Chain and the Mid-Pacific Seamounts whereas the high He-3/He-4 type samples with EM-type noble gas isotopic ratios occur in the Line Island Chain. This difference in noble gas characteristics of these crust types implies that the Magellan Seamounts, Marcus-Wake Seamounts, Marshall Island Chain, and the Mid-Pacific Seamounts originated from HIMU-type lower mantle material whereas the Line Island Chain originated from EM-type lower mantle material. This finding is consistent with variations in the Pb-isotope and trace element signatures in the seamount lavas. Differences in the mantle surce may therefore be responsible for variations in the noble gas abundances and isotopic ratios in the Fe-Mn crusts. Mantle degassing appears to be the principal factor controlling noble gas isotopic abundances in Fe-Mn crusts. Decay of radioactive isotopes has a negligible influence on the nuclide abundances and isotopic ratios of noble gases in these crusts on the timescale of their formation.
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选择青海湖地区的次生芨芨草草地为研究对象,以围栏内封育和围栏外自由放牧的草地做对照,研究了围栏内外土壤种子库的萌发状况、密度和数量、物种多样性,以及土壤种子库与地上植被的关系。结果表明,围栏内外土壤种子库的萌发趋势非常相似,但是萌发种子累计数量不同;围栏内外土壤种子库中萌发种子的平均密度分别为3660和2460粒·m-2,围栏内萌发种子数比围栏外提高了48.8%;围栏内外土壤种子库的物种多样性指数差异较大,围栏内外丰富度指数R1分别为17和13,R2为3.693和2.832,丰富度围栏内大于围栏外,多样性指数和丰富度指数具有相同的规律,均匀度指数围栏内外分别为0.812和0.857,则是围栏外大于围栏内。围栏内外地上植被群落组成存在显著差异,围栏内的封育草地的物种丰富度和多样性指数均大于围栏外的放牧草地,而均匀度指数则呈相反趋势。
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在高寒矮嵩草 (K obresia humilis)草甸地区以太阳短波辐射为背景 ,建立了人工增强 U V- B辐射的实验装置 ,每天增补 15 .8k J· m- 2 的辐射剂量 ,模拟平流层臭氧破坏约 5 %时近地表面太阳 UV- B辐射的增强。观测表明 :UV- B辐射的增强对麻花艽 (Gentiana straminea)植物的光合作用无明显的抑制或伤害作用。相反 ,在早晨补充UV- B辐射的短时间内 ,叶片的 Pn 随 Gs的增大而有所提高。随 UV- B辐射时间的延长 ,约在 11∶ 30~ 12∶ 30 ,Pn和Gs有所降低。U V- B辐射时间进一步延长后 (约 14∶ 0 0以后 ) ,处理和对照组叶片 Pn和 Gs的差异趋向不明显。增强太阳 UV- B辐射后 ,麻花艽叶片的光合色素并无明显变化 ,U V-B 吸收物质的含量也无明显变化。麻花艽叶片厚度的直接测量表明: 增强UV -B 辐射能明显提高叶片的厚度。叶片厚度的增加可补偿增强UV -B 辐射后引起的光合色素的光降解, 改善单位叶面积为基础的光合速率, 是高原植物对强UV-B 辐射的一种适应方式。
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A rapid and sensitive liquid chromatography-atmospheric pressure chemical ionization mass spectrometry (HPLC-APCI-MS) assay for the determination of five pharmacologically active compounds (PAC) extracted from the traditional Chinese medicine, Rhodiola , namely salidroside, tyrosol, rhodionin, gallic acid, and ethyl gallate has been developed. In this method, PAC could be baseline separated and detected with DAD at 275 nm. The validation of the method, including sensitivity, linearity, repeatability, and recovery, was examined. The linear calibration curves were acquired with correlation coefficient >0.999 and the limits of detection LOD (at a signal-to-noise ratio=3:1) were between 0.058 and 1.500 mu mol/L. It was found, that the amounts of PAC varied with different species of Rhodiola . The established method is rapid and reproducible for the separation of five natural pharmacologically active compounds from extracts of Rhodiola with satisfactory results.