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1.
粘度法研究高分子溶液行为的实验改进(Ⅱ)   总被引:13,自引:0,他引:13  
高分子在粘度计毛细管管壁上的吸附不仅会导致毛细管有效管径减小,而且可以导致毛细管界面性质发生显著改变,具体表现为测定高分子溶液流过时间t之前和之后纯溶剂的流过时间t0和t0′与高分子溶液流过时间t对浓度作图外推到浓度为零时的值t0^*并不一致。不同温度时聚乙烯吡咯烷酮(PVP)水溶液粘度测定结果表明,当吸附讷发子显著改变了毛细管界面性质时,需要将高分子溶液粘度测定方法由t/t0′改为t/t0^*。经过改进的粘度测定方法不仅更加普适合理,而且更加简单有效。  相似文献   

2.
聚氧化乙烯水溶液粘度的测定   总被引:3,自引:0,他引:3  
测定了不同分子量聚氧化乙烯(PEO)在水溶液中的粘度,发现在低浓度区高分子溶液比浓粘度出现负偏离。用高分子溶液流过时间对浓度作图的外推值t0^*重新计算相对粘度,则高分子溶液比浓粘度与浓度之间满足线性关系。不同分子量PEO水溶液流过时间对浓度作图的外推值t0^*是完全一致的。利用纯溶剂在粘度计中流过时间的改变确定了高分子在毛细管管壁上吸附层的厚度,发现PEO在毛细管管壁上吸附层厚度与分子量无关。  相似文献   

3.
测定了不同分子量聚氧化乙烯(PEO)在水和苯溶剂中的粘度,发现在低浓度区PEO水溶液的比浓粘度出现负偏离, PEO苯溶液比浓粘度与浓度之间依旧满足线性关系.表面张力测定结果表明, PEO分子显著降低了水的表面张力,而苯的表面张力则不受影响.PEO水溶液和纯溶剂水表面张力的不同干扰了高分子溶液和溶剂在粘度计中流过时间的测量,导致低浓度区PEO水溶液比浓粘度出现负偏离.利用PEO水溶液和水表面张力测定结果,结合乌式粘度计的几何尺寸,定量分析了PEO水溶液和纯溶剂水表面张力的差异对粘度测量结果的影响,计算结果与实验结果基本相符.如果用PEO水溶液流过时间对浓度作图的外推值t0*计算相对粘度,可以完全消除PEO水溶液和水表面张力差异对粘度测量的影响.  相似文献   

4.
利用高分子溶液流过时间测量之前和之后纯溶剂流过时间的变化不仅再次证实了极低浓度区高分子溶液反常粘度行为的起源和校正方法,而且找到了定量研究粘度计毛细管管壁上高分子吸附层厚度的实验方法。研究结果表明,溶剂的性质对高分子吸附层厚度有着显著影响。  相似文献   

5.
在288.15-328.15 K温度范围内,测量了不同浓度的氨基酸离子液体[C_2mim][Ala]水溶液的密度和粘度,根据J ones-Dole方程得到了较大正值的粘度B系数并且dB/dT0。借助Feakins理论,计算了溶质对溶液粘滞流动活化自由能贡献Δμ_2~(≠0),根据Δμ_2~(≠0)随温度的线性变化,进而得到流动活化熵ΔS_2~(≠0)和活化焓ΔH_2~(≠0);在E yring液体粘度的过渡态理论基础上,提出了预测离子液体[C_2mim][Ala]水溶液粘度的半经验新方法,其预测值与相应的实验值很好的一致。  相似文献   

6.
李晓东 《大学化学》2001,16(6):48-50
作为物理化学基础实验之一 ,粘度法是测定高分子化合物相对分子质量的一种简单易行的方法 ,其准确度能够满足许多情况下的要求。但在此实验中会遇到诸多对实验结果产生影响的因素 ,现在就我在用粘度法测定聚乙烯醇相对分子质量的实验中遇到的一些情况做一简单分析。1 实验过程  实验中所用仪器有三管粘度计 ,停表及恒温槽装置一套 ;试剂为聚乙烯醇水溶液。实验过程如下[1] 。  ①于 30 .0 0± 0 .0 5℃的条件下恒温待测液和蒸馏水。  ②向粘度计中加入 1 0mL聚乙烯醇水溶液 ,质量浓度为 5.50 0 g/L ,测定溶液自粘度计的中间管上…  相似文献   

7.
用NDJ-1型旋转粘度计测定了293.15~343.15 K温度范围内、醇胺质量分数介于30%~50%时, 二乙醇胺(Diethanolamine, DEA)-N-甲基二乙醇胺(N-methyldiethanolamine, MDEA)水溶液的粘度. 以Grunberg-Nissan方程和Weiland方程对DEA水溶液、MDEA水溶液和MDEA-DEA水溶液的粘度进行了预测. 在实验测定和理论预测的基础上, 阐明了醇胺水溶液的粘度与温度和醇胺浓度之间的关系.  相似文献   

8.
报道了二苯胺-4-重氮盐(DDS)与十二烷基硫酸钠(SDS)在水溶液中的相互作用.实验结果表明,体系粘度随SDS/DDS物质的量比(ξ)的变化而急增急降.当ξ=0~0.9时,二者形成沉淀,体系的粘度基本不变;当ξ=1.9~2.3时,沉淀溶解并伴随着体系粘度急增,最高粘度达初始值的2520倍;之后,随ξ的增大,体系粘度迅速下降至初始值.对DDS-SDS聚集体的微观结构与体系粘度的关系进行了初步讨论.同时发现体系粘度是光敏性的,紫外光照可使其迅速下降.  相似文献   

9.
阳离子Gemini表面活性剂与PVA相互作用;聚乙烯醇;粘度;表面张力  相似文献   

10.
研究了具有相同碳链不同羟基位置的两种丙二醇(1,2-丙二醇和1,3-丙二醇)和三种丁二醇(1,3-丁二醇、2,3-丁二醇和1,4-丁二醇)对其水溶液保湿性、粘度、动态表面张力和喷射性能的影响。实验结果表明,相同碳链的二元醇中含伯羟基多的二元醇保湿性较差;每种二元醇水溶液随着二元醇浓度增加,粘度逐渐增加,表面张力逐渐降低,仲羟基在分子发生相对滑动时更容易使分子缠绕,体现为溶液的粘度大,含-CH_3基团的醇分子疏水性相对较强,使醇分子更多的在气液界面排列,表现为溶液表面张力较低;高频喷射时,溶液粘度接近时,表面张力大的溶液在喷射时容易离开喷嘴,液滴尾部获得初速度大,容易获得良好的液滴形态。  相似文献   

11.
利用手持技术改进测定乙醇分子结构实验   总被引:1,自引:0,他引:1  
利用压强传感器代替排水集气法,改进测定乙醇分子结构实验的仪器装置,并探索最佳反应条件。另外,设计两个空白实验,结合压强变化曲线对实验误差进行相关讨论。  相似文献   

12.
13.
由于石化行业的生产需要,其材质的使用具有多样性和广泛性,经常会出现顾客委托的测试样品的一个或几个元素跨越光谱仪现有测试程序测量范围的情况。本法通过对光谱仪测试原理的认识,根据光谱仪的测试能力及标样的采集,实现了一个或几个元素测量范围的扩展,并对其测量的影响因素进行了研究。  相似文献   

14.
The oxygen quenching rate constants for singlet and triplet excited states of the dimethyl ester of mesoporphyrin IX increase with decreasing viscosity of the medium and reach a maximum at a viscosity of approximately 0.4 mPa·sec, after which the rate constants begin to decrease. The drop in rate constant with increasing fluidity of the medium may be related to a nonequilibrium character of the elementary act in the interaction of the reactants in the solvent cage. In viscous media such as isopropyl alcohol, isobutyl alcohol, and isoamyl alcohol, the reaction radius is greater than the sum of the radii of the reacting particles. The long-range character of these processes is due to the relatively weak dependence of the quenching probability on distance.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 25, No. 2, pp. 161–167, March–April, 1989.  相似文献   

15.
The spectral-polarization characteristics of absorption and phosphorescence of molecules of the initial form of nitro-substituted indolinospirobenzothiopyran were studied in oriented polyethylene films and in solutions with different polarity. An oscillator model of the electron transitions responsible for the formation of absorption and luminescence spectra was suggested. It was established that the principal differences in the spectral and photophysical properties of the compound studied and its oxygen-containing analog are associated with the fact that the electronegativity of the S atom is lower than that of the O atom. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1143–1146, June, 1997.  相似文献   

16.

The heats of detonation of 20 simple high explosives and explosive mixtures were determined by means of an adiabatic detonation calorimeter designed by the authors. The results indicated that the performance of the instrument was reliable and the experimental data were very accurate. For explosive mixtures, there was a linear accumulative relationship between the heats of detonation of the explosive mixture and its components. Accordingly, the heats of detonation of explosive mixtures could be calculated directly from the heats of detonation of simple explosives and the characteristic heats of other components. The experiments showed that the gold or brass shell of the cylindrical charge could be substituted by a thick-walled porcelain shell, which had the advantage of cheapness.

  相似文献   

17.
实验教学目的是从解决实际问题出发,以实验技术训练和实验设计思想培养为目标。介绍了将单一的物质分配系数测定实验改进为综合实验,提高了实验效果及实验资源利用率。  相似文献   

18.
The compositions of the neutral diterpenoids of the oleoresins of five species of conifers growing in the Transcarpathia have been studied. It has been found that the oleoresins ofAbies alba M.,Larix decidua M., andPicea excelsa L. contain more than 50% of neutral diterpenoids. The group and qualitative compositions of the oxygen-containing diterpenoids have been determined. In the oleoresins ofAbies alba,Picea excelsa, andPicea abies tertiary alcohols — cis-abienol and isocembrol — predominate, while inLarix decidua the main component is the hydroxy ester larixyl acetate. Primary alcohols related to the resin acids have been found in all the oleoresins investigated. Features of the distribution of diterpenoids according to the species of conifers have been revealed. The results obtained are necessary for the chemotaxonomy of conifers of the family Pinceae.Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Translated from Khimiya Prirodynkh Soedinenii, No. 6, pp. 812–816, November–December, 1988.  相似文献   

19.
Sets of hydrogen molecule equivalents have been developed which permit the calculation of hydrogenation of different types of carbon-carbon bonds from ab initio total energies (3-21G and 6-31G* basis sets, and, to a more limited extent, for MP2/6-31G* data) of reactants and products. The calculated enthalpies of hydrogenation are in good agreement with experiment for unstrained molecules, with average errors on the order of 2 kcal/mol. The 6-31G* equivalents allow the enthalpies for strained molecules to be calculated accurately, but the 3-21G equivalents do not. The equivalents for both basis sets have been tested by calculating the enthalpies of hydrogenation of carbon-carbon bonds in nitrogen- and oxygen-containing organic molecules, free radicals, and classical carbocations. The results are in good agreement with experiment in most cases.  相似文献   

20.
非那雄胺能抑制5α-还原酶的活性,明显降低二氢睾酮水平,是一种治疗良性前列腺增生的有效药品。该合成工艺以甾烯酮酸为原料,将其与氯化亚砜反应,无须分离即与叔丁胺反应得17β-酰胺化合物,再氧化开环,环合,氢化,脱氢合成了非那雄胺。经元素分析、IR、1HNMR、13CNMR、MS分析表征了其结构。该法无须使用昂贵的2,2-二吡啶二硫化物和剧毒药品苯亚硒酸酐,且以乙酸铵代替氨气,降低了对设备的要求和腐蚀,更适用于工业生产。  相似文献   

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