首页> 外文会议>World Congress of Soil Science >Depth profiling of soil clay-xanthan complexes using step-scan mid-infrared photoacoustic spectroscopy
【24h】

Depth profiling of soil clay-xanthan complexes using step-scan mid-infrared photoacoustic spectroscopy

机译:利用阶梯式中红外光声光谱检查土壤粘土 - 黄原声复合物的深度分析

获取原文

摘要

Many soil micro-organisms produce extracellular polysaccharides (EPS); former studies demonstrate that EPS are produced in soil and are closely associated with the surrounding clay particles, and the formed clay-EPS complexes play an important role insoil biogeochemistry. In the present study, experimental clay-xanthan complexes were prepared as models for the soil/biota interface, and the step-scan function of FTIR-PAS technique was initially applied to in situ explore the characteristics of surface layers. The variances of depth profiling spectra of montmorilllonite are higher than that of kaolin, and more xanthan information was observed in the depth profiling spectra of montmorillonite, which was specifically verified by absorption in the region of 600-1200 cm~(-1) .The xanthan structure changed significantly due to the interaction between xanthan functional group and clay surface. The surface of montmorillonite is more hydrophilic than that of kaolin as indicated by absorption at 1640 cm~(-1); montmorillonite seems to interact more easily with hydrophilic xanthan and a much broader surface layer was observed through depth profiling PAS spectra (9.8 mum vs 3.8 mum). The thicker surface layer resulted in stronger water retention capability, and may provide a basis for interpreting the variance of soil quality.
机译:许多土壤微生物产生细胞外多糖(EPS);前研究表明,EPS在土壤中产生,与周围的粘土颗粒密切相关,并且形成的粘土复合物发挥着重要作用的生物地球化学。在本研究中,制备实验性粘土 - 黄原料配合物作为土壤/生物达界面的模型,并且最初施加FTIR-PAS技术的阶梯扫描功能探索表面层的特性。 Montmorillonite的深度分析光谱的差异高于高岭土的差异,并且在蒙脱石的深度分析光谱中观察到更多的黄原烷信息,在600-1200cm〜(-1)区域中的吸收具体验证。由于黄原官能团和粘土表面之间的相互作用,黄原坦结构显着变化。 Montmorillonite的表面比在1640cm〜(-1)的吸收所示的那样高于高岭土的水平更亲水; Montmorillonite似乎更容易与亲水X原样相互作用,并且通过深度分析PAS谱(9.8毫米与3.8毫米)观察到更宽的表面层。较厚的表面层导致保水能力较强,并且可以为解释土壤质量方差提供依据。

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