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Preparation and properties of carmine radish cellulose/nano-Cu composite porous material and its application for catalytic degradation of organic dyes

Journal 2026 · IF 8.7 · 发表于 2026 年 8 月 24 日
作者: Zhu Xiong,Huisheng Huang,Fenggui Chen,Shuying Kong,Fulan Zhang
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摘要

Transforming agricultural waste into functional catalysts addresses both environmental and resource challenges. Specifically, cellulose from discarded carmine radish residue (CRC) was made into a porous support for copper nanoparticles (Cu NPs). Inherent brittleness limits cellulose-based materials' practical use, so hexamethylene diisocyanate (HDI) was introduced as a covalent crosslinker. This approach replaces partial interchain hydrogen bonds with urethane linkages, building a resilient three-dimensional (3D) network in the CRC matrix. FTIR, XRD and 2D-WAXS verified the crosslinking, while low-field NMR showed the chemical network accounted for roughly 66.77% of the system. Mechanical properties were notably enhanced: compressive modulus rose from 30 kPa to 130 kPa, compressive strength stayed at 80 kPa, and compressive strain increased from approximately 62% to 81%. Molecular dynamics simulations confirmed cohesive energy dropped from 101.83 kJ mol −1 to 56.27 kJ mol −1 , explaining improved energy dissipation. The toughened CRC scaffold was loaded with ∼35 nm Cu NPs to form a CRC/nano-Cu composite. When applied to catalytic dye degradation using NaBH 4 , the composite achieved near-complete degradation of methylene blue (MB) within 25 min. This performance dramatically outperforms the non-catalytic reaction, which only achieved 29% degradation after 240 min. Furthermore, electrostatic interactions driven by the electron-rich Cu surface conferred strong charge-selectivity for cationic dyes, while the composite retained robust reusability over 5 cycles and high activity under severe ionic interference. This work offers a novel strategy for high-value biomass waste utilization and a mechanism for designing strong bio-based catalytic materials by enhancing energy dissipation through covalent crosslinking.

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