Zeolites have been extensively studied for years in different areas of chemical industry, such as shape selective catalysis, ion-exchange, and gas adsorption and separation. Generally, zeolites are prepared from solvothermal synthesis in the presence of a large amounts of solvents such as water and alcohols in sealed autoclaves under autogenous pressure. Water has been regarded as essential to synthesize zeolites for fast mass transfer of reactants, but it occupies a large space in autoclaves, which greatly reduces the yield of zeolite products. Furthermore, polluted wastes and relatively high pressure due to the presence of water solvent in the synthesis also leads to environmental and safety issues. Recently, inspired by great benefits of solvent-free synthesis, including the environmental concerns, energy consumption, safety, and economic cost, researchers continually challenge the rationale of the solvent and reconsider the age-old question "Do we actually need solvents at all in zeolite synthesis?" In this Account, we briefly summarize our efforts to rationally synthesize zeolites via a solvent-free route. Our research demonstrates that a series of silica, aluminosilicate, and aluminophosphate-based zeolites can be successfully prepared by mixing, grinding, and heating starting solid materials under solvent-free conditions. Combining an organotemplate-free synthesis with a solvent-free approach maximizes the advantages resulting in a more sustainable synthetic route, which avoids using toxic and costly organic templates and the formation of harmful gases by calcination of organic templates at high temperature. Furthermore, new insights into the solvent-free crystallization process of zeolites have been provided by modern techniques such as NMR and UV-Raman spectroscopy, which should be helpful in designing new zeolite structures and developing novel routes for synthesis of zeolites. The role of water and the vital intermediates during the crystallization of zeolites have been proposed and verified. In addition to a significant reduction in liquid wastes and a remarkable increase in zeolite yields, the solvent-free synthesis of zeolites exhibits more unprecedented benefits, including (i) the formation of hierarchical micro-, meso-, and macrostructures, which benefit the mass transfer in the reactions, (ii) rapid synthesis at higher temperatures, which greatly improve the space-time yields of zeolites, and (iii) construction of a novel catalytic system for encapsulation of metal nanoparticles and metal oxide particles within zeolite crystals synergistically combining the advantages of catalytic metal nanoparticles and metal oxide particles (high activity) and zeolites (shape selectivity). We believe that the concept of "solvent-free synthesis of zeolites" would open a door for deep understanding of zeolite crystallization and the design of efficient zeolitic catalysts.
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http://dx.doi.org/10.1021/acs.accounts.8b00057 | DOI Listing |
Org Biomol Chem
January 2025
Natural and Medical Sciences Research Center, University of Nizwa, P.O. Box 33, Postal Code 616, Birkat Al Mauz, Nizwa, Sultanate of Oman.
The [3 + 2] cycloaddition of dicyanoepoxides with benzylidene Meldrum's acid under microwave irradiation and solvent-free conditions was explored for the synthesis of trioxaspirodecanes. This method presents a highly diastereo- and regioselective route to spiro cycloadducts, delivering similar stereoselectivity to conventional reflux in toluene but with shorter reaction times and improved yields.
View Article and Find Full Text PDFAcc Chem Res
January 2025
School of Engineering, Westlake University, Hangzhou 310024, Zhejiang Province, China.
ConspectusCovalent triazine frameworks (CTFs) are a novel class of nitrogen-rich conjugated porous organic materials constructed by robust and functional triazine linkages, which possess unique structures and excellent physicochemical properties. They have demonstrated broad application prospects in gas/molecular adsorption and separation, catalysis, energy conversion and storage, etc. In particular, crystalline CTFs with well-defined periodic molecular network structures and regular pore channels can maximize the utilization of the features of CTFs and promote a deep understanding of the structure-property relationship.
View Article and Find Full Text PDFJ Biotechnol
January 2025
Department of Chemistry, Sapienza University of Rome, P.le A. Moro 5, Rome 00185, Italy. Electronic address:
This study explores the immobilization of lipase from Candida rugosa (CRL) on hemp tea waste to catalyze the esterification of oleic acid with primary aliphatic C2-C12 alcohols in a solvent-free system. The immobilization method employed was adsorption, chosen for its simplicity, low cost, and ability to preserve enzyme activity. The esterification of undecanoic acid, lauric acid, and oleic acid with alcohols of varying chain lengths (ethanol, 1-propanol, 1-butanol, 1-octanol, 1-decanol, and 1-dodecanol) was studied.
View Article and Find Full Text PDFDoping in pure materials causes vital alterations in opto-electrical and physicochemical characteristics, which enable the produced doped material to be highly efficient and effective. The current work focused on the synthesis of C/N-co-doped-ZnO nanorods a facile, eco-friendly, and solvent-free mechano-thermal approach. The synthesized C/N-co-doped ZnO nanorods were employed for the photocatalytic decay of methylene blue (MB) and brilliant cresyl blue (BCB) dyes, and their degradation capability was compared with that of pure ZnO nanoparticles prepared a precipitation approach.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Chemical Sciences, Indian Institute of Science Education and Research Kolkata (IISER Kolkata), Campus Rd, Mohanpur, Haringhata Farm, West Bengal 741246, India.
Utilization of carbon dioxide (CO) as a C1 feedstock to synthesize value-added chemicals using a catalyst made from earth-abundant elements and under mild conditions is a sustainable approach toward carbon neutrality but difficult to achieve. Herein, the CoAlO/AlO composite catalyst is developed and used for the light-driven epoxide to value-added cyclic carbonate conversion using CO. CoAlO/AlO composite catalysts (% Co-AlO) are prepared by calcining cobalt-incorporated Al-oxy-hydroxide at 500 °C under an air atmosphere.
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