疏水碳链长度对胺类捕收剂起泡性能的影响研究
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  • 英文篇名:Effect of Hydrophobic Carbon Chain Length on Properties of Monoamine Collector Foaming Abilities
  • 作者:高子蕙 ; 朱一民
  • 英文作者:Gao Zihui;Zhu Yimin;School of Resource and Civil Engineering,Northeastern University;National-Local Joint Engineering Research Center of Refractory Iron Ore Resources Efficient Utilization Technology;
  • 关键词:碳链长度 ; 泡沫性能 ; 胺类捕收剂 ; 表面张力 ; 黏度
  • 英文关键词:Carbon chain length;;Foam properties;;Amino group-containing collectors;;Surface tension;;Viscosity
  • 中文刊名:JSKS
  • 英文刊名:Metal Mine
  • 机构:东北大学资源与土木工程学院;难采选铁矿资源高效开发利用技术国家地方联合工程研究中心;
  • 出版日期:2019-02-15
  • 出版单位:金属矿山
  • 年:2019
  • 期:No.512
  • 基金:国家自然科学基金项目(编号:51774069)
  • 语种:中文;
  • 页:JSKS201902027
  • 页数:6
  • CN:02
  • ISSN:34-1055/TD
  • 分类号:135-140
摘要
为了研究疏水碳链中碳原子数目对胺类捕收剂起泡性能的影响,采用充气法对十二胺、十四胺和十六胺产生的泡沫体积、泡沫半衰期和泡沫大小分布等参数进行了测量。结果表明:在溶液p H=6.0时,具有最大发泡体积的捕收剂种类由高到低依次是十四胺>十六胺>十二胺;在药剂用量均为1.0 g/L时,起泡能力由强到弱为十四胺>十六胺>十二胺;随着捕收剂疏水碳链中碳原子数的增加,分子间的相互作用增强,溶液黏度增大,泡沫半衰期也大幅增加,t1/2由高到低依次是十六胺>十四胺>十二胺;气泡索特直径达到最小值时的药剂用量由低到高依次为十六胺<十四胺<十二胺;胺类捕收剂中疏水碳链越长,其最大发泡体积和CCC也更容易在低浓度下达到,在试验药剂用量范围内,药剂溶液黏度由低到高依次为:十二胺<十四胺<十六胺,药剂溶液黏度越大,产生的泡沫稳定性越好。
        In order to study the effect of the number of carbon atoms in the hydrophobic carbon chain on the perfor?mance of the amine collector foaming ability,the aeration method was used to capture the foam volume of dodecylamine,tetra?decylamine and hexadecylamine. The parameters such as foam half-life and foam size distribution were also measured. The re?sults show that the order of the agents has biggest foam volume at pH=6.0 from high to low is tetradecylamine>hexadecylam?ine>dodecylamine. As the number of carbon atoms in the hydrophobic carbon chain increases,the interaction between the molecules increases,and the viscosity of the solution increases,so that the half-life of the foam is also greatly increased. The order of t1/2 from large to small is hexadecylamine>tetradecylamine>dodecylamine. When the foam Sauter diameter reach the minimum number,the dosage of agents from low to high is tetradecylamine
引文
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