کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1329680 1500083 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A novel porous anionic metal–organic framework with pillared double-layer structure for selective adsorption of dyes
ترجمه فارسی عنوان
یک چارچوب ارگانیک فلزی آنیونی متخلخل جدید با ساختار دو لایه پاره ای برای جذب رنگ انتخابی
کلمات کلیدی
چارچوب فلزی آلی آنیونی، ساختار دو لایه قرمز جذب انتخابی رنگها
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
چکیده انگلیسی


• An anionic metal-organic framework (BUT-201) has been synthesized and characterized.
• BUT-201 has a three-dimensional (3D) pillared double-layer structure.
• BUT-201 can selectively and rapidly adsorb cationic dyes.
• The adsorbed dyes can be gradually released in the methanol solution of LiNO3.

A novel porous anionic metal–organic framework, (Me2NH2)2[Zn2L1.5bpy]·2DMF (BUT-201; H4L=4,8-disulfonaphthalene-2,6-dicarboxylic acid; bpy=4,4-bipyridine; DMF=N,N-dimethylformamide), with pillared double-layer structure has been synthesized through the reaction of a sulfonated carboxylic acid ligand and Zn(NO3)2·6H2O with 4,4-bipyridine as a co-ligand. It is found that BUT-201 can rapidly adsorb cationic dyes with a smaller size such as Methylene Blue (MB) and Acriflavine Hydrochloride (AH) by substitution of guest (CH3)2NH2+, but has no adsorption towards the cationic dyes with a lager size such as Methylene Violet (MV), the anionic dyes like C. I. Acid Yellow 1 (AY1) and neutral dyes like C. I. Solvent Yellow 7 (SY7), respectively. The results show that the adsorption behavior of BUT-201 relates not only to the charge but also to the size/shape of dyes. Furthermore, the adsorbed dyes can be gradually released in the methanol solution of LiNO3.

A porous anionic metal–organic framework (BUT-201) can selectively adsorb the cationic dyes by cationic guest molecule substitution, and the adsorbed dyes can be gradually released in the methanol solution of LiNO3.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Solid State Chemistry - Volume 233, January 2016, Pages 143–149
نویسندگان
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