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

Author:

Nijpanich Supinya1,Nimpaiboon Adun2ORCID,Rojruthai Porntip3ORCID,Park Jae-Hyeok4ORCID,Hagio Takeshi45ORCID,Ichino Ryoichi45ORCID,Sakdapipanich Jitladda1ORCID

Affiliation:

1. Department of Chemistry, Center of Excellence for Innovation in Chemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand

2. Rubber Technology Research Centre, Faculty of Science, Mahidol University, Nakhon Pathom 73170, Thailand

3. Division of Chemical Industrial Process and Environment, Faculty of Science, Energy and Environment, King Mongkut’s University of Technology North Bangkok, Rayong 21120, Thailand

4. Institute of Materials Innovation, Institutes of Innovation for Future Society, Nagoya University, Nagoya 464-8601, Japan

5. Department of Chemical Systems Engineering, Graduate School of Engineering, Nagoya University, Nagoya 464-8603, Japan

Abstract

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 × 105 to 0.28 × 105 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.

Funder

Mahidol University

National Research Council of Thailand

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

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