The adsorption of cytochrome c on to zeolite crystals and membranes with different chemical composition and structure was studied. The structure and texture of zeolite materials were identified by X-ray diffraction (XRD) and scanning electron microscopy (FESEM), while the variation of protein conformation was studied by Fourier transform infrared attenuated total reflectance (FTIR-ATR) analysis. In order to separate the influence of zeolite structures from the effect of composite membranes, a through analysis of the cytochrome c adsorption was performed on different crystals by varying several experimental parameters such as: pH value, protein amount, zeolite structures and chemical compositions. It is shown that the electrostatic type of interaction seems to be of the utmost importance to govern the immobilization, while the zeolite Brönsted acidity of the support is the subordinate parameter which differentiates the adsorption performances of different zeolite structures (that distinct for chemical composition of the framework).
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http://dx.doi.org/10.1016/j.colsurfb.2008.12.019 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Lab of Applied Biocatalysis, National Engineering Research Center of Wheat and Corn Further Processing, School of Food Science and Engineering, South China University of Technology, No. 381 Wushan Road, Guangzhou 510640, Guangdong China.
Biomineralization of enzymes inside rigid metal-organic frameworks (MOFs) is appealing due to its biocompatibility and simplicity. However, this strategy has hitherto been limited to microporous MOFs, leading to low apparent enzymatic activity. In this study, polysaccharide sodium alginate is introduced during the biomineralization of enzymes in zeolitic imidazolate frameworks (ZIFs) to competitively coordinate with metal ions, which endows the encapsulated enzyme with a 7-fold higher activity than that in microporous ZIFs.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Université de Caen Normandie, ENSICAEN, CNRS, LCS, 14000 Caen, France.
Germanium is known to occupy tetrahedral sites by substituting silicon in germanosilicate zeolites. In this study, we present pioneering findings regarding the synthesis of zeolites with an MFI structure (GeMFI) incorporating a high germanium amount (16% Ge). Remarkably, the germanium atoms feature a slight electron deficiency with respect to GeO, and the typical coordination number of 4, as usually reported for the germanosilicate zeolites, is exceeded, giving rise to Ge dimers in a double-bridge configuration.
View Article and Find Full Text PDFInorg Chem
January 2025
State Key Laboratory of Molecular & Process Engineering, SINOPEC Research Institute of Petroleum Processing, Beijing 100083, China.
The ZSM-5 zeolite is the key active component in high-severity fluid catalytic cracking (FCC) catalysts and is routinely activated by phosphorus compounds in industrial production. To date, however, the detailed structure and function of the introduced phosphorus still remain ambiguous, which hampers the rational design of highly efficient catalysts. In this work, using advanced solid-state NMR techniques, we have quantitatively identified a total of seven types of P-containing complexes in P-modified ZSM-5 zeolite and clearly revealed their structure, location, and catalytic role.
View Article and Find Full Text PDFHeliyon
January 2025
Department of Nanotechnology, Faculty of New Sciences and Technologies, Semnan University, Semnan, Iran.
This study details the synthesis of a novel ternary nanocomposite composed of MnFeO, FeVO, and modified zeolite, achieved through a two-step process. The initial step involved the hydrothermal synthesis of the MnFeO/FeVO composite, followed by its application onto modified zeolite using ultrasonic waves. The synthesized nanocomposite was thoroughly characterized using a range of analytical techniques.
View Article and Find Full Text PDFNanoscale
January 2025
Department of Chemistry, Shahid Beheshti University, G. C., 1983963113, Evin, Tehran, Iran.
Metal tellurides, known for their superior electrical conductivity and excellent electrochemical properties, are promising candidates for supercapacitor applications. This study introduces a novel method involving a metal-organic framework hybrid to synthesize CoTe@CoFeTe double-shelled nanocubes. Initially, zeolitic imidazolate framework-67 (ZIF67) and CoFe Prussian blue analog (PBA) nanocubes are synthesized through an anion-exchange reaction with [Fe(CN)] ions.
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