Silicalite-1 zeolites are widely applied in gas adsorption, catalysis, and separation due to their excellent hydrothermal stability and unique pore structure. However, traditional preparation methods have inherent drawbacks such as high pollution, high cost, etc. Therefore, this work proposed a green and efficient route for preparing Silicalite-1 zeolite by adding NHF (F/Si = 0.1) and seeds (10 wt%) in a much shorter time (8 h) in a low-template system (TPA/Si = 0.007). It was found that NHF is beneficial for inhibiting the formation of SiO. The S-1 seeds could drastically induce the formation of the zeolite skeleton structure. Noteworthy, the morphology of zeolites was determined by the relative content of NHF and seeds. The crystal morphology is determined by the higher content of the two substances; however, when the content is similar, the crystal morphology is determined by NHF. The results showed that simultaneous control of NHF and seeds can suppress SiO formation, can improve the relative crystallinity of products, and can be precisely regulated via the synergistic effect of both in zeolite morphology. This work not only provides new ideas for regulating the morphology of silicate-1 crystals but also offers a new path for industrial large-scale production of low-cost and efficient zeolites.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10779753 | PMC |
http://dx.doi.org/10.3390/ma17010266 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Changchun Institute of Applied Chemistry Chinese Academy of Sciences: Chang Chun Institute of Applied Chemistry Chinese Academy of Sciences, State Key Laboratory of Rare Earth Resource Utilization, CHINA.
Chemical conversion of CO2 is providing an opportunity to mitigate the global warming induced by the overconsumption of fossil fuel. Cu has been regarded as one of the most powerful contenders in catalyzing CO2 conversion, yet the precise manipulation of its surface state and the nearby chemical environment continues to pose a formidable challenge. In this work, we report a high-efficiency catalyst by utilizing CeO2 and pure silicon zeolite (S1) to co-activate Cu species.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
January 2025
School of Chemical and Biological Engineering, Seoul National University, 1, Gwanak-ro, Gwanak-gu, Seoul 08826, South Korea.
The crystal structure of a highly loaded complex of silicalite-1 (SL-1) with eight mol-ecules of -xylene per unit cell has been solved by single-crystal X-ray diffraction. In the crystal, four symmetrical SiO·2CH subunits per unit cell are observed. The -xylene mol-ecules sit at two different positions within the SL-1 channels.
View Article and Find Full Text PDFSmall
December 2024
Institute of Materials, China Academy of Engineering Physics, Jiangyou, Sichuan, 621908, P. R. China.
The construction, use, and maintenance of tritium-related equipment will inevitably produce tritium-containing radioactive waste gas, and the production of efficient catalysts for tritium removal remains a difficult problem. Herein, silicalite-1 zeolite with entrapped Pt nanoclusters is skillfully post-oxidized at an appropriate temperature, building highly active Pt─O sites on the nanoclusters to achieve efficient oxidation of hydrogen isotopes at low temperatures. The designed Pt─O sites can directly participate in the oxidation reaction of hydrogen isotopes.
View Article and Find Full Text PDFNano Lett
December 2024
Department of Chemistry, College of Sciences, Northeastern University, Shenyang, Liaoning 110819, China.
The performance of blue devices utilizing perovskite quantum dots (PQDs) has lagged remarkably behind that of green light-emitting diodes because of low luminescence quantum yields and poor spectral stability. Here, benefiting from the rapid and short diffusion paths within the nanosized silicalite-1 (N-Si-1) zeolite (∼40 nm) channels, CsPbBr PQDs encapsulated within N-Si-1 show a high dispersion with an ultrasmall particle size of ∼2.38 nm and a blue emission of 474 nm with a high photoluminescence quantum yield (PLQY) of 44.
View Article and Find Full Text PDFNano Lett
December 2024
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States of America.
Polymers can be used to augment the properties of microporous materials, affording enhanced processability, stability, and compatibility. Manipulating polymers to target specific properties, however, requires detailed knowledge of how different polymers and microporous materials interact. Here, we report a study of the thermodynamics of polyethylene glycol (PEG) intrusion into a representative hydrophobic zeolite (silicalite-1) and metal-organic framework [ZIF-67; Co(2-methylimidazolate)] in water, both of which can be formed into colloidally stable aqueous dispersions─termed "microporous water"─with dry, guest-accessible pore networks.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!