首页> 外文期刊>Journal of Chemistry >Study on Treatment of Salicylhydroxamic Acid Wastewater from Tungsten Molybdenum Mineral Processing
【24h】

Study on Treatment of Salicylhydroxamic Acid Wastewater from Tungsten Molybdenum Mineral Processing

机译:钨钼矿物加工治疗水杨羟肟酸废水的研究

获取原文
       

摘要

Salicylhydroxamic acid is an excellent collector of oxidizing ore, and it has an efficient collection performance for tungsten molybdenum ore. However, the utilization ratio of salicylhydroxamic acid is relatively low in the flotation process, and a large amount of flotation wastewater discharged might cause damage to the water environment. This study mainly compared the effects of natural sunlight degradation, ozonation, and Fenton oxidation processes on the treatment of salicylchydroxamic acid wastewater from W–Mo mineral processing. The results showed after 30 hours degradation by natural sunlight, the CODcr removal rate of wastewater was only 25.99%. When the initial pH was 8, the dosage of O3 was 1.3?mg/L and the reaction time was 60 minutes; O3 oxidation could remove 40.37% CODcr from wastewater, and the BOD5/CODcr value increased to higher than 0.3 after 15?min reaction. Under the Fenton oxidation conditions such as initial pH 3, H2O2 dosage 0.96?g/L, and the molar ratio of H2O2 to Fe2+ 2?:?1, 90.43% CODcr could be removed from flotation wastewater after 90?min reaction, and the BOD5/CODcr value was obviously improved. Fenton oxidation was a high efficient processing technology for salicylhydroxamic acid wastewater, and the effluent could meet the discharge and reuse emission standard requirements in China.
机译:水杨羟肟酸是氧化矿石的优异收集器,具有钨钼矿石的有效收集性能。然而,水杨酰胺酸的利用率在浮选过程中相对较低,并且排出的大量浮选废水可能会导致水环境损坏。本研究主要比较自然阳光降解,臭氧化和芬顿氧化方法对W-Mo矿物加工的水杨酰基酸废水的影响。通过自然阳光降解30小时后,结果表明,废水的CODCR去除率仅为25.99%。当初始pH为8时,O 3的剂量为1.3?mg / L,反应时间为60分钟; O3氧化可以从废水中除去40.37%CODCR,并且在15℃反应后,BOD5 / CODCR值增加至高于0.3。在芬顿氧化条件下,例如初始pH 3,H 2 O 2剂量0.96·g / L,以及H 2 O 2至Fe 2 + 2的摩尔比?:1,90.43%CodCr可以在90〜min反应后从浮选废水中除去, BOD5 / CODCR值明显改善。芬顿氧化是水杨羟肟酸废水的高效加工技术,流出物可以满足中国的排放量和再利用排放标准要求。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号