4.7 Article

Preparation and Characterization of TiO2-Coated Hollow Glass Beads for Functionalization of Deproteinized Natural Rubber Latex via UVA-Activated Photocatalytic Degradation

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POLYMERS
卷 15, 期 19, 页码 -

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MDPI
DOI: 10.3390/polym15193885

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natural rubber latex; low-molecular-weight natural rubber latex; photochemical degradation process; titanium dioxide

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In this study, the photochemical degradation method was used to modify the properties of natural rubber. TiO2-coated hollow glass beads (TiO2-HGBs) were introduced as photocatalysts to functionalize deproteinized natural rubber (DPNR). The molecular weight of DPNR was significantly reduced and functional groups were successfully incorporated. Remarkably, TiO2-HGBs maintained their performance after multiple cycles of reuse, showing great potential for the advanced functionalization of natural rubber.
The photochemical degradation of natural rubber (NR) is a prevalent method used to modify its inherent properties. Natural rubber, predominantly derived from the Hevea Brasiliensis tree, exhibits an exceptionally high molecular weight (MW), often reaching a million daltons (Da). This high MW restricts its solubility in various solvents and its reactivity with polar compounds, thereby constraining its versatile applications. In our previous work, we employed TiO2 in its powdered form as a photocatalyst for the functionalization of NR latex. However, the post-process separation and reuse of this powder present substantial challenges. In this present study, we aimed to functionalize deproteinized NR (DPNR) latex. We systematically reduced its MW via photochemical degradation under UVA irradiation facilitated by H2O2. To enhance the efficiency of the degradation process, we introduced TiO2-coated hollow glass beads (TiO2-HGBs) as photocatalysts. This approach offers the advantage of easy collection and repeated reuse. The modified DPNR showed a reduction in its number-average MW from 9.48 x 10(5) to 0.28 x 10(5) Da and incorporated functional groups, including hydroxyl, carbonyl, and epoxide. Remarkably, the TiO2-HGBs maintained their performance over seven cycles of reuse. Due to their superior efficacy, TiO2-HGBs stand out as promising photocatalysts for the advanced functionalization of NR across various practical applications.

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