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241119s2024 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.4c03166
|2 doi
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|a eng
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|a Xue, Tao
|e verfasserin
|4 aut
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|a Development of Monolithic Hyper-Cross-Linked Polystyrene-Supported Ultrasmall Nano-Ag Catalysts for Enhanced NaBH4-Mediated Dye Degradation
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|c 2024
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|a Text
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|a Date Revised 03.12.2024
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a Synthesizing catalyst supports with appropriate compositions and structures is crucial for reducing the sizes of metal nanoparticles and enhancing their catalytic activities. In this work, a series of monolithic hyper-cross-linked supports (HCP-CC) with hierarchical pores were synthesized. The monolithic structure facilitated easy operation in catalytic reactions, while the composition and structure of HCP-CC could be tailored simultaneously by utilizing the functional cross-linking agent cyanogen chloride. Furthermore, in situ loading of nano-Ag into HCP-CC resulted in the hybrid catalyst HCP-CC-Ag. The synergy of confinement and coordination effect controlled and limited the size of nano-Ag to approximately 3 nm, classifying them as ultrasmall nanoparticles, which ensured outstanding catalytic activity. This hybrid catalyst could improve the reaction rate constant to 0.423 min-1; it efficiently promoted the degradation of organic dye and exhibited great universality and recyclability, making it a potential heterogeneous catalyst for dye wastewater treatment
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|a Journal Article
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|a Li, Hui
|e verfasserin
|4 aut
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|a Wang, Yuying
|e verfasserin
|4 aut
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|a Miao, Han
|e verfasserin
|4 aut
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|a Li, Xinxin
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1985
|g 40(2024), 48 vom: 03. Dez., Seite 25460-25470
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnas
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|g volume:40
|g year:2024
|g number:48
|g day:03
|g month:12
|g pages:25460-25470
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|u http://dx.doi.org/10.1021/acs.langmuir.4c03166
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