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Gas chromatographic measurements of infinite dilution diffusion coefficients of volatile liquids in amorphous polymers at elevated temperatures

机译:高温下无定形聚合物中挥发性液体的无限稀释扩散系数的气相色谱测量

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AbstractMeasurements were made of infinite dilution diffusion coefficients of volatile liquids in amorphous polymers at elevated temperatures, using inverse gas chromatography. The liquids used were benzene, toluene, ethylbenzene, andn‐decane. The polymers used were polystyrene and poly(vinyl acetate), and temperatures ranged from 30°C to 120°C above the glass transition temperatures of the polymers. Packed chromatographic columns were used to obtain data of the variation of the plate height with the average gas velocity, which was then used to determine diffusion coefficients with the aid of the van Deemter equation. In the present investigation, we have used different sizes of glass beads (0.3, 0.5, 0.6, and 1.0 mm in diameter), depending on the system temperature and the polymer/solute pair chosen. An attempt was made to correlate on the diffusion coefficient D measured at various temperaturesT, using inDζ as ordinate and 1/(K22+T−Tg2)/Tc (hereafter referred to as the reciprocal of reduced free volume temperature, 1/TRF) as abscissa, in which ζ =M1/2/T 1/2cV 1/3c,Mbeing the molecular weight,Tcthe critical temperature, andVcthe critical volume of the solute,K22is a free volume parameter of the polymer, andTg2is the glass transition temperature of the polymer. It has been found that such plots give rise to two linear regions having different slopes, separated by a critical value of 1/TRF. The critical value of 1/TRFis found to be insensitive to the type of solute and the type of polymer used. We have concluded that the infinite dilution diffusion coefficient of volatile liquids in amorphous polymers is controlled predominatly by the free volume of polymer above a critical value of 1/TRF, but energy effects are significant below the critical value of this parameter. In order to apply the generalized relationships in conjunction with gas chromatographic measurements, the results of this study indicate that, for values of 1/TRFlarger than a critical value, which is approximately 4.8, the following expression, InDζ = α +b/TRF, may be used to predict infinite dilution diffusion coefficients of volatile liquids in amorpous polymers at elevated temperatures, in which α is a constant, independent of the type of solute, andbis approximately a constant for a given polymer in the free volume region, independent of the type of solute. More experimental studies are needed, particularly for temperatures higher than those reported in this study, to corroborate and/or extend the correlations
机译:摘要采用逆气相色谱法测定了无定形聚合物中挥发性液体在高温下的无限稀释扩散系数。使用的液体是苯、甲苯、乙苯和癸烷。使用的聚合物是聚苯乙烯和聚醋酸乙烯酯,温度范围为比聚合物的玻璃化转变温度高30°C至120°C。填充色谱柱用于获得板高度随平均气速变化的数据,然后借助van Deemter方程确定扩散系数。在本研究中,我们使用了不同尺寸的玻璃珠(直径为 0.3、0.5、0.6 和 1.0 毫米),具体取决于系统温度和所选的聚合物/溶质对。尝试将不同温度下测得的扩散系数D相关联,以inDζ为纵坐标,以1/[(K22+T−Tg2)/Tc](以下称为降低的自由体积温度的倒数,1/TRF)为横坐标,其中ζ=M1/2/T 1/2cV 1/3c,M为分子量,Tc为临界温度,Vc为溶质的临界体积,K22是聚合物的自由体积参数,Tg2是聚合物的玻璃化转变温度。已经发现,这样的图产生了两个具有不同斜率的线性区域,以1/TRF的临界值分隔。发现 1/TRFs 的临界值对溶质类型和所用聚合物类型不敏感。我们得出的结论是,非晶态聚合物中挥发性液体的无限稀释扩散系数主要由聚合物的自由体积控制,临界值高于 1/TRF,但能量效应低于该参数的临界值是显着的。为了将广义关系与气相色谱测量相结合,本研究的结果表明,对于1/TRF大于临界值(约4.8)的值,以下表达式InDζ = α +b/TRF可用于预测高温下挥发性液体在离水聚合物中的无限稀释扩散系数, 其中α是一个常数,与溶质的类型无关,并且之二是自由体积区域中给定聚合物的近似常数,与溶质的类型无关。需要更多的实验研究,特别是对于高于本研究中报告的温度,以证实和/或扩展相关性

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