Effects of Acid Modulators on the Microwave-Assisted Synthesis of Cr/Sn Metal-Organic Frameworks

• Published in: Polymers Vol. 14; no. 18; p. 3826
• Main Authors: Mao, Wei, Huang, Renting, Xu, Hao, Wang, Hao, Huang, Yi, Huang, Shurong, Zhou, Jinghong
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-09-2022; MDPI
• Subjects: Acetic acid; Analysis; bimetallic MIL-101 (Cr, Sn); Bimetals; Catalytic activity; Catalytic converters; Chromium; Contact angle; Conversion; Crystal structure; Crystals; Defects; Glucose; Hydrochloric acid; Hydroxymethylfurfural; Ligands; Metal-organic frameworks; microwave synthesis; Microwaves; Modulators; Morphology; Nanoparticles; Nitrates; Organic acids; Particle size; Particle size distribution; Reagents; Saline water; Structural stability; Structure; Thermogravimetric analysis; China; Germany; United States > US; Japan
• ISSN: 2073-4360; 2073-4360
• DOI: 10.3390/polym14183826

Metal-organic frameworks (MOFs) have attracted remarkable attention for their distinguished structural designability. Precisely controlling the particle size and improving the structural stability of MOF nanoparticles influence their catalytic activity significantly. In this study, six acids (nitric, hydrochloric, formic, acetic, succinic, and citric acids) were used as modulators to prepare bimetallic MIL-101 (Cr, Sn) (MIL stands for Materials of Institut Lavoisier) via a microwave-assisted hydrothermal method. Changes in volumetric, structural, stability, and catalytic properties, size, and shape of MIL-101 (Cr, Sn) were examined using scanning electron microscopy, X-ray diffraction, thermogravimetric analysis, and N2 adsorption–desorption measurements. All modulators altered the MOF properties. Compared with other samples, acetic acid as a modulator mildly altered the MOF morphology by narrowing their particle size distribution, enhancing the specific surface area, and significantly improving their water and thermal stabilities. The addition of acetic acid was suitable for the catalytic conversion of glucose to 5-hydroxymethylfurfural (5-HMF), achieving a 43.1% 5-HMF yield with 91.4% glucose conversion in a mixed solution of γ-valerolactone and saturated salt water at 150 °C after 30 min.