首页 | 本学科首页   官方微博 | 高级检索  
     检索      

肝素提取废水的GC-MS分析和处理研究
引用本文:解恒参,宗志敏,赵建军,刘彤,苏苓,魏贤勇.肝素提取废水的GC-MS分析和处理研究[J].环境工程学报,2009,3(12):2227-2231.
作者姓名:解恒参  宗志敏  赵建军  刘彤  苏苓  魏贤勇
作者单位:1. 徐州建筑职业技术学院科技与产业处,徐州,221116;中国矿业大学化工学院,徐州,221008
2. 中国矿业大学化工学院,徐州,221008
3. 徐州建筑职业技术学院科技与产业处,徐州,221116
基金项目:徐州建筑职业技术学院(国家级示范高职学院)院级科研基金项目(JYA308-19)
摘    要:肝素钠废水含有高浓度无机盐和大量有机污染物,对环境具有潜在的毒性且难以处理,已经受到环境工作者的关注。为了了解废水的主要成分和处理此类废水,本实验用GC-MS对废水进行了分析,并且利用芬顿试剂对其进行了处理,结果发现废水中有机物有26种,其中脂肪酸和芳香衍生物占有较大比例,处理后,有机成分只有3种;讨论了影响处理效果的因素和最佳的工艺条件,发现当pH 值为6.66,硫酸亚铁和过氧化氢的量分别为2.5 g/L和2.8‰ (v/v),搅拌速度为2 000 r/min, 搅拌时间为15 min时,COD的去除率可达到94.50%。

关 键 词:肝素钠废水  GC-MS分析  Fenton试剂
收稿时间:3/3/2009 12:00:00 AM

GC-MS analysis and treatment of heparin sodium wastewater
Xie Hengshen,Zong Zhimin,Zhao Jianjun,Liu Tong,Su Ling and Wei Xianyong.GC-MS analysis and treatment of heparin sodium wastewater[J].Techniques and Equipment for Environmental Pollution Control,2009,3(12):2227-2231.
Authors:Xie Hengshen  Zong Zhimin  Zhao Jianjun  Liu Tong  Su Ling and Wei Xianyong
Abstract:Owing to high chloride ion and many organic compounds,heparin sodium wastewater is potential toxicity to the environment and difficult to be treated. Fortunately,it has attracted attention by environmental re-searchers. The treated and untreated wastewaters were analyzed by GC-MS,the result indicated that the propor-tion of palmitic acid and isobutyl oetyl phthalate are higher,but after treated by Fenton reagent oxidation,they are not detected. At the same time,some main factors on the removal rate of COD,such as the amount of H_2O_2 and FeSO_4,pH value and stirring time and speed,were investigated one by one in the experiment. As a result,optimal technical conditions were obtained. The removal rate of COD can reach 94. 50% when pH value is 6.66,the amount of FeSO_4 and H_2O_2 is 2. 5 g/L and 2.8%o (v/v) respectively,stirring time is 15 minutes and stirring speed is 2 000 r/min.
Keywords:heparin sodium wastewater  GC-MS analysis  Fenton reagent
本文献已被 万方数据 等数据库收录!
点击此处可从《环境工程学报》浏览原始摘要信息
点击此处可从《环境工程学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号