89 resultados para 989.2:37


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作为研究土壤侵蚀垂直分布的新方法 ,较详细地描述了稳定性稀土元素 (REE)示踪法的原理与操作技术 ;通过实例说明了诸如示踪元素的选择原则、施放量的计算、施放方法及其注意事项等实际应用中可能遇到的各种问题的解决办法 ;给出了该方法的精度计算公式。

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The activities/properties of two molecules with identical formula but different configuration states of the asymmetric atoms are different. Thus, usually the common topological indices are not suitable. In this study, the chiral topological indices were obtained by extending A(mi) indices suggested by our laboratory and molecular connectivity indices. The modified topologial indices have been used for the studies on D2 for dopamine receptor and a receptor activities of fourteen N-alkylated 3-(3-hydroxypyenyl)-piperidines. It has been observed that selected variables possess low correlations. The results obtained by using multiple regression analysis and artificial neural networks are satisfactory.

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The plateau modulus of polyphenylquinoxaline (PPQ-E) films has been obtained by from their dynamic mechanical properties curves. Using these data, the entanglement density of PPQ-E films, 2.37 X 10(26) m(-3) Or 0.39mmol/cm(3),has been estimated. The deformation mechanism of polyphenylquinoxaline (crazing mechanism,or shear yielding mechanism, or both), can be predicted according to entanglement density values. The changes in morphology of PPQ-E films during tensile deformation have been observed by Polarized Light Microscope. The result shows that crazing first appears in the tensile process, then shear yielding appears. It needs to point out that the craze is terminated by micro-shear band and the direction of craze in shear band is also changed,which prevents the craze growth into crack and avoid the failure of material. This result is in accordance with the prediction on the basis of the entanglement density data. The morphology and structure of crazes in PPB-E thin film have been determined by TEM. The craze morphology of PPQ-E is mainly fibril craze consisting of micro-fibrils and micro-voids,the interface between bulk and craze is distinct. Multiply crazes, blunting of craze tip and shear deformation zone are also observed. This result reflects the accordance of entanglement density and the morphology and structure of crazes.

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电喷雾串联质谱快速分析人参皂甙混合物周雨莫文俊刘淑莹*(中国科学院长春应用化学研究所130022)在天然产物的化学成分研究中,混合物的分离和各组分的结构鉴定一直是困扰我们的难题。通常的化学成分分析,涉及到提取、分离等多个步骤,最后才能通过NMR、MS…

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Like 6-phenoxy-5,12-naphthacenequinone (1), 6-[4-(2-( 8-hydroxyphenyl) isopropyl)phenoxy]-5, 12-naphthacenequinone (2) and 6-naphthyloxynaphthacenequinone (6) showed normal photochromism, The relative initial rates of trans to ana photoconversion were in the order: 1, 100; 2, 37; 6, 21, 6-[4-(Phenylazo)phenoxyl-5,12-naphthacenequinone (3), 6-[4-(p-ethoxyphenylazo) phenoxy]-5,12-naphthacenequinone (4), 6-[4-(p-nitrophenylazo)phenoxy]-5,12-naph cenequinone (5) had only slight W-induced photochromism for the phenoxynaphthacenequinone photochrome. 6-(2-Nitrosonaphthyloxy)-5,12-naphthacenequinone (7) exhibited no photochromism and underwent irreversible photoreaction.

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Using a recently developed laser light-scattering (LLS) procedure, we accomplished the characterization of a broadly distributed unfractionated phenolphthalein poly(aryl ether ketone) (PEK-C) in CHCl3 at 25 degrees C. The laplace inversion of precisely measured intensity-intensity time correlation function from dynamic LLS leads us first to an estimate of the characteristic line-width distribution G(Gamma) and then to the translational diffusion coefficient distribution G(D). By using a previously established calibration of D (cm(2)/s) = 2.37 X 10(-4)M(-0.57), were able to convert G(D) into a differential weight distribution f(w)(M). The weight-average molecular weight M(w) calculated from f(w)(M) agrees well with that directly measured in static LLS. Our results indicate that both the calibration and LLS procedure used in this study are ready to be applied as a routine method for the characterization of the molecular weight distribution of PEK-C. (C) 1996 John Wiley & Sons, Inc.

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Five different molecular weight phenolphthalein poly(aryl ether ketone) (PEK-C) fractions in CHCl3 were studied by static and dynamic laser light scattering(LLS). The dynamic LLS revealed that the PEK-C samples contain some large polymer clusters. These large clusters can be removed by filtering the solution with a 0.1-mu m filter. We found that the persistence length of PEK-C in CHCl3 at 25 degrees C is similar to 2 nm and the Flory characteristic ratio, C-infinity is similar to 25. Our results showed that [R(g)(2)](1/2)(z) = (3.50+/-0.20) x 10(-2)M(w)(0.54+/-0.01) and [D] = (2.37+/-0.05) x 10(-4)M(w)(-0.55+/-0.01), with [R(g)(2)](1/2)(z), M(w), and [D] being the z-average radius of gyration, the weight-average molecular weight, and the z-average translational diffusion coefficient, respectively. A combination of static and dynamic LLS results enabled us to determine D = (2.20+/-0.10) x 10(-4)M(-0.555+/-0.015), where D and M correspond to monodisperse species. Using this calibration between D and M,we have determined molecular weight distributions of five PEK-C fractions from their corresponding translational diffusion coefficient distribution.

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合成了HPW12、HSiW12杂多酸的一系列铯盐:CsxH3-xPW12(x=0~3),CsxH4-xSiW12(x=0~4).测定了它们的酸强度、pH滴定曲线、NH3-TPD、IR光谱和比表面积.以乙酸和正丁醇的酯化为探针反应,考察了催化剂的酸催化活性.实验发现,碱金属取代后,PW12系列的多数催化剂的酸强度提高,而SiW12系列的则降低,但对同一系列来说,由NH3-TPD测得的酸强度和酸量均随取代量增加而减小,pH滴定的结果与此类似,当x=2.5时,两系列催化剂的比表面积均存在一个极值.对乙酸和正丁醇的催化酯化活性只与总酸量有关,与表面积无关,属假液相反应.

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本文用核磁共振 (NMR)波谱和化学定磷法研究了 Ce(SO4) 2 对 5′-腺嘌呤核苷酸 (5′- AMP)及5′-鸟嘌呤核苷酸 (5′- GMP)的水解断裂作用。结果表明 :Ce(SO4) 2 在 37℃ ,酸性条件下使 5′- AMP断裂为腺嘌呤核苷 (A)及无机磷 ,使 5′- GMP断裂为鸟嘌呤核苷 (G)及无机磷 ,SO2 -4 浓度及酸强度对 5′- AMP及 5′- GMP的水解断裂程度有很大影响 ,并对其水解断裂机制进行了研究。

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研究了以Cu~(2+)为催化剂的Mo(V)-SCN~--ERB~+-PVA超高灵敏新显色体系及钼的分光光度测定条件。缔合物的吸收峰在580nm处,表观摩尔吸光系数ε=5.6×10~6L·mol~(-1)·cm~(-1)。Mo(Ⅵ)含量在0~0.3μg/25mL范围内符合比耳定律。初步研讨了显色反应的机理。结合离子交换分离,本法可成功地用于水样及麦饭石浸出液中痕量钼的测定。

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本文研究了伯胺N_(1923)与中性磷试剂(TBP,DBBP)的正庚烷溶液,从盐酸介质中对Cd(II)的协同萃取。用斜率法、等摩尔系列法确定协萃配合物的组成为(RN-H_3Cl)_2·CdCl_2·B,求得协萃反应的平衡常数分别为lgK_(12)(TBP)=2.13,lgK_(12)(DBBP)=2.37;有机相协萃配合物的生成常数分别为lgβ_(12)(TBP)=1.22,lgβ_(12)(DBBP)=1.41,计算了协萃反应的热力学函数,并对协萃配合物的IR,NMR谱进行了研究。

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The abundance and biomass of ciliated protozoa and copepod nauplii were investigated at 21 grid stations and two anchored stations in the Laizhou Bay, Bohai Sea, China in June 1998. Dilution incubations were carried out to investigate micro-zooplankton grazing pressure at the anchored stations during spring tide and neap tide. The dominant species were Tintinnopsis amoyensis, T. chinglanensis, T. pallida and aloricate ciliates. A total of 13 species of tintinnids were found. The total abundance of ciliates and nauplii ranged from 30 to 2390 ind l(-1) at grid stations. Tintinnopsis amoyensis was the only ciliate found at the anchored stations and in concentrations which varied from 0 to 6700 ind l(-1). The spatial distribution of ciliates was patchy. Tintinnopsis amoyensis and T. pallida were distributed in the Weihe River mouth and Xiaoqinghe River mouth respectively. The aloricate ciliates, T. chinglanensis and Codonellopsis ostenfeldi dominated offshore in sequence. The water mixing process may affect the spatial pattern of the dominant ciliate species. The abundance and biomass of copepod nauplii were in the range of 0-140 ind l(-1) and 0-7 mu g C l(-1) respectively, with the peak appearing at grid station 15. The total biomass of ciliates and copepod nauplii was in the range of 1(.)5-25 mu g C l(-1). Water column biomass of ciliates and nauplii varied from 2(.)37 to 52(.)3 mg C m(-2). At the anchored stations, the phytoplankton growth rates ranged from undetectable to 0 21 d(-1) and micro-zooplankton grazing rates from 0 13 to 0(.)57 d(-1). The grazing pressure of micro-zooplankton were 12 to 43% of the chlorophyll standing stock and 84 to 267% of the chlorophyll (C) 2000 Academic Press.

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建立了以十七烷酸甲酯为内标物,用毛细管气相色谱同时测定沙棘油中六种脂肪酸(棕榈酸、棕榈油酸、硬脂酸、油酸、亚油酸、亚麻酸)的方法。样品经氢氧化钾-甲醇皂化、三氟化硼-甲醇酯化后使生成相应的脂肪酸甲酯,以DM—FFAP毛细管柱分离,火焰离子化检测器测定。用保留时间定性,内标法定量。结果表明,在所选择的色谱条件下,上述脂肪酸在10min内获得较好的分离;六种脂肪酸的峰面积与其质量浓度有良好的线性关系,相关系数均大于0.9998;样品加标回收率(n=6)为92.1%~101.4%;相对标准偏差为2.37%~4.19%;最低检出限为4.0mg/L。该方法操作简便、快速、准确,适合批量样品的测定。