رئوس مطالب

  • چکیده
  • مقدمه
  • 1. بخش تجربی
  • 1.2 روش‌ها و مواد
  • 2.2 تهیه‌ HKUST-1 [Cu3(BTC)2]
  • 3.2 شناسایی
  • 4.2 اندازه‌گیری‌های وزن‌سنجی
  • 2. بحث و نتیجه‌گیری
  • 1.3 مطالعه ساختاری HKUST-1
  • 2.3 مقایسه‌ روش‌های سولووترمال و الکتروشیمیایی
  • 3.3 شناسایی ماده
  • 4.3 پایداری حرارتی
  • 5.3 آنالیزهای تخلخل و مساحت سطح
  • 6.3 آنالیز مورفولوژیکی HKUST-1
  • 7.3 اندازه‌گیری مادون قرمز
  • 8.3 اندازه‌گیری ذخیره‌سازی متان
  • نتیجه‌گیری کلی

Abstract

A comparison synthetic strategy of Metal-Organic Frameworks, namely, Hongkong University of Techhnology-1 {HKUST-1[Cu3(BTC)]2} (BTC = 1,3,5-benzene-tri-carboxylate) through solvothermal and electrochemical method in ethanol:water (1:1) has been conducted. The obtained material was analyzed using powder X-ray diffraction, Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), Thermo-Gravimetric Analysis (TGA) and Surface Area Analysis (SAA). While the voltage in the electrochemical method are varied, ranging from 12 to 15 Volt. The results show that at 15 V the texture of the material has the best degree of crystallinity and comparable with solvothermal product. This indicated from XRD data and supported by the SEM image to view the morphology. The thermal stability of the synthesized compounds is up to 320 °C. The shape of the nitrogen sorption isotherm of the compound corresponds to type I of the IUPAC adsorption isotherm classification for microporous materials with BET surface area of 629.2 and 324.3 m²/g (for solvothermal and electrochemical product respectively) and promising for gas storage application. Herein, the methane storage capacities of these compounds are also tested.


Conclusions

HKUST-1 has been successfully synthesized through an efficient and environmentally friendly electrochemical method. Methane uptake experiment of the corresponding product (at 15 V, RT in the solvent mixture EtOH: H2O /1:1) showed higher capacity than the solvothermal product and reached up to 11 %wt at 20 Psi (1,38 Bar) according to gravimetric analysis.

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