دانلود رایگان مقاله انگلیسی چهارچوب فلز-آلی آب-پایدار برای حذف مایع فلزات سنگین و ایزوتوپ های پرتوزا - الزویر 2018

عنوان فارسی
چهارچوب فلز-آلی آب-پایدار برای حذف مایع فلزات سنگین و ایزوتوپ های پرتوزا: بررسی
عنوان انگلیسی
Water-stable metal-organic frameworks for aqueous removal of heavy metals and radionuclides: A review
صفحات مقاله فارسی
0
صفحات مقاله انگلیسی
67
سال انتشار
2018
نشریه
الزویر - Elsevier
فرمت مقاله انگلیسی
PDF
نوع مقاله
ISI
نوع نگارش
مقالات مروری
رفرنس
دارد
پایگاه
اسکوپوس
کد محصول
E9467
رشته های مرتبط با این مقاله
شیمی، محیط زیست
گرایش های مرتبط با این مقاله
شیمی تجزیه، شیمی محیط زیست، آب و فاضلاب
مجله
Chemosphere
دانشگاه
Department of Environmental and Occupational Health - School of Public Health - Texas A&M University - College Station - USA
کلمات کلیدی
فلزات سنگین؛ رادیونوکلئید؛ چهارچوب فلزی-آلی؛ جذب؛ کاهش فوتوکاتالیستی؛ پاکسازی آلودگی
doi یا شناسه دیجیتال
https://doi.org/10.1016/j.chemosphere.2018.06.114
چکیده

Abstract


Heavy metals and radionuclides in water are a global environmental issue, which has been receiving considerable attention worldwide. Water-stable MOFs are green and recyclable materials to eliminate the environmental impacts caused by the hazardous heavy metal ions and radionuclides in water. This paper presents a systematical review on the current status of waterstable MOFs that capture and convert a wide range of heavy metal ions (e.g., As(III)/As(V), Pb(II), Hg(II), Cd(II), and Cr(III)/Cr(VI)) and radionuclides (e.g., U(VI), Se(IV)/Se(VI) and Cs(I)) in aqueous solution. Water-stable MOFs and MOF-based composites exhibit the superior adsorption capability for these metal species in water. Significantly, MOFs show high selectivity in capturing target metal ions even in the presence of multiple water constituents. Mechanisms involved in capturing metal ions are described. MOFs also have excellent catalytic performance (photocatalysis and catalytic reduction by formic acid) for Cr(VI) conversion to Cr(III). Future research is suggested to provide insightful guidance to enhance the performance of the MOFs in capturing target pollutants in aquatic environment.

نتیجه گیری

9. Conclusions and outlook


Water-stable MOFs and MOF-based composites are green materials that exhibited the superior adsorption ability for removing target metal species. The adsorptive processes were generally fitted well with pseudo-second-order kinetic and Langmuir isotherm models. Several dominated adsorptive mechanisms were proposed, including the strong coordination between heavy metals/radionuclides and the binding sites (e.g., hydroxyl, thiol, amide substituents and other oxygen-containing groups) of organic ligands of water-stable MOFs, electrostatic interactions, anion exchange or SC-SC transformation, and combined adsorption-reduction process. Additionally, these materials also showed the excellent visible light-driven photocatalytic performance for reducing Cr(VI) by forming reactive photo-generating electrons in the systems and by decreasing the recombination of electron-hole pairs. Also, MOFs could catalyze the reduction of Cr(VI) by formic acid effectively, which appears to be a green technology in sustainable water purification. The superior selectivity, good stability, and reusability of MOFs during the treatments, indicating the promising applications of these emerging techniques for treating water and wastewater contaminated with different kinds of heavy metal ions and radionuclides. There are still great challenges before applying MOFs in practical water treatment. The primary consideration is the upscale potential of synthesis, which has not been addressed adequately in literature. Nowadays, most of the MOFs are synthesized by solvothermal methods in organic solvents such as N,N’-dimethylformamide (DMF) and methanol. The impact of used solvent to the environment should be considered thoroughly. Negative effects of organics many be minimized by recycling the solvents. A progress is being in developing environmentally benign synthetic conditions of aqueous phase (Li et al., 2018) and solvent-free synthesis (Zou et al., 2016).


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