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How polymer additives reduce the pour point of hydrocarbon solvents containing wax crystals

机译:聚合物添加剂如何降低含蜡晶体的烃类溶剂的倾点

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We have investigated how four different pour point depressant (PPD) polymers affect the pour point transition in mixtures of a single pure wax in a solvent. We used either n-eicosane (C20), CH3(CH2)(18)CH3, n-tetracosane (C24), CH3(CH2)(22)CH3 or n-hexatriacontane (C36), CH3(CH2)(34)CH3 as the wax component with either n-heptane or toluene as the solvent component. For all wax-solvent combinations, the measured variation of wax solubility with temperature is well predicted by ideal solution theory. The variation of pour point temperature as a function of the overall wax concentration is quantitatively modelled using the idea that, for each overall wax concentration, the pour point occurs at a temperature at which a critical volume fraction phi* of wax crystals has precipitated. Close to the pour point temperature, extraction and examination of the wax crystals show they consist of polydisperse, irregularly-shaped platelets with axial ratios (h/d, where h is the plate thickness and d is the plate long dimension) in the range 0.005-0.05. It is found that the measured phi* values corresponding to the pour point transitions are weakly correlated with the wax crystal axial ratios (h/d) for all wax-solvent-PPD polymer combinations. These results indicate that the pour point transition occurs at a volume fraction larger than the value at which the volumes of rotation of the platelet crystals overlap, i.e., 2.5(h/d) < phi* < 11(h/d). PPD polymers work, in part, by increasing the wax crystal axial ratio (h/d), thereby increasing phi* and reducing the pour point temperature. Since the PPD's ability to modify the wax crystal shape relies on its adsorption to the crystal-solution surface, it is anticipated and observed experimentally that optimum PPD efficacy is correlated with the difference between the wax and the polymer solubility boundary temperatures. This finding and the mechanistic insight gained here provide the basis for a simple and rapid screening test to identify candidate species likely to be effective PPDs for particular wax systems.
机译:我们已经研究了四种不同的降凝剂(PPD)聚合物如何影响单一纯蜡在溶剂中的混合物中的凝点转变。我们使用了正二十烷(C20),CH3(CH2)(18)CH3,正十四烷(C24),CH3(CH2)(22)CH3或正六aco烷(C36),CH3(CH2)(34)CH3作为蜡组分,正庚烷或甲苯作为溶剂组分。对于所有蜡-溶剂组合,通过理想的溶液理论可以很好地预测蜡的溶解度随温度的变化。倾点温度随总蜡浓度的变化可通过以下想法定量建模:对于每个总蜡浓度,倾点发生在蜡晶体的临界体积分数phi *沉淀的温度下。接近倾点温度,蜡晶体的萃取和检查表明它们由多分散的不规则形状的薄片组成,轴向比率(h / d,其中h为板厚,d为板长尺寸)在0.005范围内-0.05。发现对于所有蜡-溶剂-PPD聚合物组合,对应于倾点转变的测得的phi *值与蜡晶体轴向比(h / d)弱相关。这些结果表明,倾点转变发生的体积分数大于血小板晶体的旋转体积重叠的值,即2.5(h / d)<phi * <11(h / d)。 PPD聚合物部分地通过增加蜡晶轴向比率(h / d)起作用,从而增加phi *并降低倾点温度。由于PPD改变蜡晶体形状的能力取决于其对晶体溶液表面的吸附,因此可以预料并通过实验观察到,最佳PPD功效与蜡和聚合物溶解度边界温度之间的差异相关。该发现和在此获得的机理见解为简单,快速的筛选测试提供了基础,以鉴定可能对特定蜡体系有效的PPD的候选物质。

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