کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
645562 | 1457144 | 2015 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Adsorption isotherms and kinetics of water vapor on novel adsorbents MIL-101(Cr)@GO with super-high capacity
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
جریان سیال و فرایندهای انتقال
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
A novel composite (MIL-101@GO) of MIL-101 (Cr) and graphite oxide (GO) with high water vapor capacity for adsorption heat pumps (AHPs) was developed in this work. A series of composites MIL-101@GO with varied GO loading were synthesized using a hydrothermal method, and characterized by N2 adsorption test, SEM, XRD, thermal gravimetric analysis. The adsorption isotherms and kinetics of water vapor over the composites were determined by gravimetric method. Regeneration performance of the composites was evaluated in multiple adsorption-desorption cycles. Results showed that MIL-101@GO possessed a super-high adsorption capacity for water vapor up to 1.58Â g/g, which was attributed to its ultrahigh Langmuir specific surface area (5188Â m2/g) and pore volume (1.78Â cm3/g). The isosteric heat of water vapor adsorption on MIL-101@GO was calculated to be in the range of 44-56Â kJ/mol, slightly higher than that on MIL-101 (44-53Â kJ/mol). Diffusion coefficients of water vapor over MIL-101@GO composites were ranged from 0.133Â ÃÂ 10â10 to 4.485Â ÃÂ 10â10Â cm2/s at 298-313Â K. Additionally, six consecutive adsorption-desorption cycles suggesting that the synthesized MIL-101@GO had excellent reversibility and stability for water vapor adsorption. These superior water vapor adsorption/desorption performances make MIL-101@GO a promising candidate as the water vapor adsorbent for AHPs process.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Thermal Engineering - Volume 84, 5 June 2015, Pages 118-125
Journal: Applied Thermal Engineering - Volume 84, 5 June 2015, Pages 118-125
نویسندگان
Jian Yan, Ying Yu, Chen Ma, Jing Xiao, Qibin Xia, Yingwei Li, Zhong Li,