کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
148402 456411 2013 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Comparison of enhanced microsphere transport in an iron-oxide-coated porous medium by pre-adsorbed and co-depositing organic matter
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Comparison of enhanced microsphere transport in an iron-oxide-coated porous medium by pre-adsorbed and co-depositing organic matter
چکیده انگلیسی


• Pre-adsorbed OM limited initial colloid deposition rate.
• Co-depositing OM enhanced declining rates during transient colloid deposition.
• Site blocking by OM was the primary colloidal mobility-enhancing mechanism.
• Pre-adsorbed and co-deposited OM had comparable blocking capacity.
• A numerical model was developed to simulate co-deposition of colloid and OM.

The effects of two types of organic matter (OM) (humic acid and protein) on colloid transport in porous media were investigated with column experiments and numerical modeling. Colloid deposition was explored in double-pulse experiments (DPEs) by injecting a pulse of OM to allow its pre-adsorption to iron-oxide-coated sand, followed by a pulse of latex microspheres. These experiments were compared with single-pulse experiments (SPEs), where one mixed pulse of OM and microspheres was introduced to the column. The experimental results show that pre-adsorbed and co-depositing OM may, respectively, limit initial and transient colloid deposition. The DPE results can be interpreted with an existing colloid transport model (random sequential adsorption: RSA). SPE results were interpreted with an extended RSA model (RSAE) that couples the process of OM co-deposition and blocking to colloid transport by introducing a conversion factor (Kconv) that reflects the blocking efficiency of OM. The calculations with the verified model suggest a comparable site blocking capacity of pre-adsorbed and co-depositing OM with a blocking capacity that differs for different sources of OM. Traditionally described as a modification of the chemistry of the overall deposition surface for the suspended particles, OM adsorption can also be interpreted as blocking local colloid attachment sites by the OM. This second interpretation may be more useful in describing nanoparticle deposition where the particle size is comparable to the length scale where a molecule of OM modifies the deposition surface.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Engineering Journal - Volume 230, 15 August 2013, Pages 537–546
نویسندگان
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