首页> 美国卫生研究院文献>Environmental Engineering Science >Fenton Oxidation Kinetics and Intermediates of Nonylphenol Ethoxylates
【2h】

Fenton Oxidation Kinetics and Intermediates of Nonylphenol Ethoxylates

机译:Fenton氧化动力学和壬基酚乙氧基化物的中间体

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Removal of nonylphenol ethoxylates (NPEOs) in aqueous solution by Fenton oxidation process was studied in a laboratory-scale batch reactor. Operating parameters, including initial pH temperature, hydrogen peroxide, and ferrous ion dosage, were thoroughly investigated. Maximum NPEOs reduction of 84% was achieved within 6 min, under an initial pH of 3.0, 25°C, an H2O2 dosage of 9.74×10−3 M, and a molar ratio of [H2O2]/[Fe2+] of 3. A modified pseudo-first-order kinetic model was found to well represent experimental results. Correlations of reaction rate constants and operational parameters were established based on experimental data. Results indicated that the Fenton oxidation rate and removal efficiency were more dependent on the dosage of H2O2 than Fe2+, and the apparent activation energy (ΔE) was 17.5 kJ/mol. High-performance liquid chromatography and gas chromatograph mass spectrometer analytical results indicated degradation of NPEOs obtained within the first 2 min stepwise occurred by ethoxyl (EO) unit shortening. Long-chain NPEOs mixture demonstrated a higher degradation rate than shorter-chain ones. Nonylphenol (NP), short-chain NPEOs, and NP carboxyethoxylates were identified as the primary intermediates, which were mostly further degraded.
机译:在实验室规模的间歇反应器中研究了通过Fenton氧化工艺去除水溶液中的壬基酚乙氧基化物(NPEO)。彻底研究了包括初始pH温度,过氧化氢和亚铁离子剂量在内的操作参数。在初始pH为3.0、25°C,H2O2剂量为9.74×10 -3 M,摩尔比为[H2O2] /的情况下,在6 min内,NPEOs的最大减少量达到了84%。 [Fe 2 + ]为3。发现改进的伪一级动力学模型很好地代表了实验结果。基于实验数据建立了反应速率常数与操作参数的相关性。结果表明,Fenton的氧化速率和去除效率比Fe 2 + 对H2O2的依赖性更大,表观活化能(ΔE)为17.5 kJ / mol。高效液相色谱和气相色谱质谱仪的分析结果表明,在最初的2分钟内,由于乙氧基(EO)单元的缩短,所获得的NPEO逐步降解。长链NPEOs混合物显示出比短链NPEOs更高的降解率。壬基酚(NP),短链NPEO和NP羧乙氧基化物被确定为主要中间体,它们大多会进一步降解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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