首页> 外文期刊>Environmental Science & Technology >Adsorption of humic substances on goethite: Comparison between humic acids and fulvic acids
【24h】

Adsorption of humic substances on goethite: Comparison between humic acids and fulvic acids

机译:腐殖质在针铁矿上的吸附:腐殖酸和富里酸的比较

获取原文
获取原文并翻译 | 示例
       

摘要

The adsorption of humic acids (HA) to goethite (at pH 3 - 11) and the proton co-adsorption (at pH 4.0, 5.5, and 7.0) were measured, and the results were compared to those of fulvic acids (FA). Compared to FA, the adsorption of HA is stronger and more ionic strength dependent. The adsorption of both HA and FA decreases with increasing pH. The relative change of the adsorption with pH is bigger for HA than for FA at relatively low pH. At relatively high pH, it is the opposite. Protons are released at pH 4.0 and co-adsorbed at pH 5.5 and 7.0 upon the adsorption of both HA and FA. The observed pH dependency of HA and FA adsorption is in agreement with the proton co- adsorption data. Model calculations show that the adsorbed FA particles are on average located in the Stern layer, whereas the adsorbed HA particles protrude beyond the Stern layer. The closer location to the surface of the adsorbed FA leads to stronger electrostatic interactions between the FA particles and the surface, which explains the larger amount of protons released at low pH and co- adsorbed at high pH with each mass unit of FA adsorbed than that with HA adsorbed. The model also reveals that for FA a mean-field (smeared-out) approximation is reasonable, but for HA a patchwise approach is more appropriate at relatively low loading.
机译:测量了腐殖酸(HA)在针铁矿上的吸附(pH为3-11)和质子共吸附(pH为4.0、5.5和7.0),并将结果与​​黄腐酸(FA)进行了比较。与FA相比,HA的吸附更强,并且离子强度更高。 HA和FA的吸附均随pH值的增加而降低。在相对较低的pH值下,HA的pH值吸附相对变化要大于FA。在相对较高的pH下,情况恰恰相反。质子在pH 4.0时释放,并在HA和FA均吸附时在pH 5.5和7.0共同吸附。观察到的HA和FA吸附的pH依赖性与质子共吸附数据一致。模型计算表明,吸附的FA颗粒平均位于斯特恩层中,而吸附的HA颗粒则突出到斯特恩层之外。靠近被吸附的FA表面的位置会导致FA颗粒与表面之间更强的静电相互作用,这解释了在低pH下释放的质子和在高pH下与被吸附的FA的每个质量单位共吸附的质子要多于质子。 HA吸附。该模型还表明,对于FA,平均场(拖尾)近似是合理的,但是对于HA,在相对较低的负载下,逐块方法更合适。

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