齐齐哈尔大学学报(自然科学版)
齊齊哈爾大學學報(自然科學版)
제제합이대학학보(자연과학판)
JOURNAL OF QIQIHAR UNIVERSITY(NATURAL SCIENCE EDITION)
2014年
3期
1-4,10
,共5页
张莹莹%郭祥峰%贾丽华%高连斌%吴平
張瑩瑩%郭祥峰%賈麗華%高連斌%吳平
장형형%곽상봉%가려화%고련빈%오평
表面活性剂%临界胶束浓度%胶束化热力学
錶麵活性劑%臨界膠束濃度%膠束化熱力學
표면활성제%림계효속농도%효속화열역학
surfactant%critical micelle concentration%thermodynamic function of micellization
在298.2 K下,用吊环法测定了烷基二甲基苄基氯化铵水溶液的表面张力,结果表明,随着该类表面活性剂的疏水基链长从12增加到18个碳原子,其临界胶束浓度(CMC)从9.1 mmol/L降低至0.053 mmol/L;其在溶液表面的饱和吸附量(Γmax)减小,吸附效率(pC20)增大。还用电导率法研究了该类表面活性剂在不同温度下的CMC及胶束化热力学函数,在298.2~318.2 K,CMC随着温度的升高而增大;胶束形成的自由能0m?G 均为负值,表明该表面活性剂溶液胶束化过程是自发的;胶束形成的主要驱动力是熵。
在298.2 K下,用弔環法測定瞭烷基二甲基芐基氯化銨水溶液的錶麵張力,結果錶明,隨著該類錶麵活性劑的疏水基鏈長從12增加到18箇碳原子,其臨界膠束濃度(CMC)從9.1 mmol/L降低至0.053 mmol/L;其在溶液錶麵的飽和吸附量(Γmax)減小,吸附效率(pC20)增大。還用電導率法研究瞭該類錶麵活性劑在不同溫度下的CMC及膠束化熱力學函數,在298.2~318.2 K,CMC隨著溫度的升高而增大;膠束形成的自由能0m?G 均為負值,錶明該錶麵活性劑溶液膠束化過程是自髮的;膠束形成的主要驅動力是熵。
재298.2 K하,용조배법측정료완기이갑기변기록화안수용액적표면장력,결과표명,수착해류표면활성제적소수기련장종12증가도18개탄원자,기림계효속농도(CMC)종9.1 mmol/L강저지0.053 mmol/L;기재용액표면적포화흡부량(Γmax)감소,흡부효솔(pC20)증대。환용전도솔법연구료해류표면활성제재불동온도하적CMC급효속화열역학함수,재298.2~318.2 K,CMC수착온도적승고이증대;효속형성적자유능0m?G 균위부치,표명해표면활성제용액효속화과정시자발적;효속형성적주요구동력시적。
By the ring method, the surface tension of alkyldimethylbenzylammonium chloride(BAC-n)was measured in aqueous solution at 298.2 K. The results show that the hydrophobic carbon chain lengths increase from 12 to 18, their CMCs decrease from 9.1 mmol/L to 0.053 mmol/L. Meanwhile the values of adsorption amount (Γmax ) decrease, and adsorption efficiency(pC20)increases. The critical micelle concentrations(CMCs)at the temperature range of 298.2 ~ 318.2 K were measured by the conductivity method, and the values of CMC of BAC-n increase with increasing the temperature. Furthermore, the thermodynamic functions of micellization were obtained. The values of micellization free energies( 0m?G )show negative sign, which means the process of micellization is a spontaneous process. And the process of micellization of BAC-n in aqueous solution is mainly driven by the entropy.