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首页> 外文期刊>Fresenius Environmental Bulletin >MUTUAL RELATIONSHIP OF HENRY'S LAW CONSTANTS AND AQUEOUS PHASE CONCENTRATIONS FOR BENZENE,TOLUENE AND O-XYLENE AT 30 ° C
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MUTUAL RELATIONSHIP OF HENRY'S LAW CONSTANTS AND AQUEOUS PHASE CONCENTRATIONS FOR BENZENE,TOLUENE AND O-XYLENE AT 30 ° C

机译:30°C下苯,甲苯和邻二甲苯的亨利定律常数与水相浓度的相互关系

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摘要

Dimensionless Henry's law constant in water at 30 °C ranged from 0.272 ± 0.015 to 0.340 ± 0.008 for benzene as the equilibrium aqueous phase concentrations ranged from 0.546 ± 0.003 to 329 ± 1 mg/dm~3. A decrease in the Henry's law constant to 0.190 ± 0.002 was recorded be-tween 329 ± 1 and 1370 ± 3 mg/dm~3, but the results of the Dixon test at 1 % level of significance indicated that this value was a statistically significant outlier. Therefore Henry's law constant of benzene was independent on the dissolved aqueous phase of benzene and the average value of 0.312 ± 0.022 is recommended for practical purposes. For toluene, the equilibrium aqueous phase concentration ranged from 3.42 ± 0.05 to 420 ± 4 mg/dm~3 and dimen-sionless Henry's law constants varied between 0.170 ± 0.011 and 0.321 ± 0.007. In the case of o-xylene, equilib-rium aqueous phase concentrations ranged from 3.03 ± 0.03 to 123.9 ± 0.3 mg/dm~3 and Henry's law constants ranged from 0.120 ± 0.004 to 0.268 ± 0.008. Using Kruskal-Wallis analysis of variance by ranks and the Mack-Wolfe test for ordered alternatives, the Henry's law constant increased up to 6.78 ± 0.04 mg/dm~3 for toluene. For o-xylene, Henry's law constant was independent of dissolved concentration up to 6.96 ± 0.05 mg/dm~3. Henry's law constants decreased with increasing equilibrium aqueous phase concentration at higher values for toluene and o-xylene. Hydrogen bonding between water molecules and the aromatic hydrocarbon molecules provides a possible explanation for the observed trends.
机译:在30°C的水中,苯的无量纲亨利定律常数范围为0.272±0.015至0.340±0.008,而平衡水相浓度的范围为0.546±0.003至329±1 mg / dm〜3。在329±1和1370±3 mg / dm〜3之间记录到亨利定律常数降低到0.190±0.002,但在显着性水平为1%的Dixon测试结果中,该值具有统计学意义离群值。因此,苯的亨利定律常数与苯的溶解水相无关,建议实际应用的平均值为0.312±0.022。对于甲苯,平衡水相浓度范围为3.42±0.05至420±4 mg / dm〜3,无因次亨利定律常数在0.170±0.011至0.321±0.007之间变化。对于邻二甲苯,平衡水相浓度范围为3.03±0.03至123.9±0.3 mg / dm〜3,亨利定律常数范围为0.120±0.004至0.268±0.008。使用Kruskal-Wallis等级方差分析和Mack-Wolfe检验有序替代物,甲苯的亨利定律常数增加至6.78±0.04 mg / dm〜3。对于邻二甲苯,亨利定律常数与溶解浓度无关,最高为6.96±0.05 mg / dm〜3。在甲苯和邻二甲苯的较高值下,亨利定律常数随着平衡水相浓度的增加而降低。水分子和芳烃分子之间的氢键为观察到的趋势提供了可能的解释。

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  • 来源
    《Fresenius Environmental Bulletin 》 |2012年第1期| p.68-75| 共8页
  • 作者单位

    Environmental Health and Biotechnology Research Group, Division of Pharmaceutical Chemistry, Faculty of Pharmacy, P.O. Box 94, Rhodes University, Grahamstown 6140, South Africa;

    Environmental Health and Biotechnology Research Group, Division of Pharmaceutical Chemistry, Faculty of Pharmacy, P.O. Box 94, Rhodes University, Grahamstown 6140, South Africa;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    aromatic hydrocarbon; concentration dependence; volatilisation;

    机译:芳香烃浓度依赖性挥发;

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