The Interaction Effect of the Design Parameters on the Water Absorption of the Hemp-Reinforced Biocarbon-Filled Bio-Epoxy Composites

Natural fiber-reinforced composites perform poorly when exposed to moisture. Biocarbon has been proven to improve the water-absorbing behavior of natural fiber composites. However, the interaction effect of the design parameters on the biocarbon-filled hemp fiber-reinforced bioepoxy composites has not been studied. In this study, the effects of the design parameters (pyrolysis temperature, biocarbon particle size, and filler loading) on the water absorptivity and water diffusivity of hemp-reinforced biopolymer composites have been investigated. Biocarbon from the pyrolysis of hemp and switchgrass was produced at 450, 550, and 650 degrees C. Composite samples with 10 wt.%, 15 wt.%, and 20 wt.% of biocarbon fillers of sizes below 50, 75, and 100 microns were used. The hemp fiber in polymer composites showed a significant influence in its water uptake behavior with the value of water absorptivity 2.41 x 10(-6) g/m(2).s(1/2). The incorporation of biocarbon fillers in the hemp biopolymer composites reduces the average water absorptivity by 44.17% and diffusivity by 42.02%. At the optimized conditions, the value of water absorptivity with hemp biocarbon and switchgrass biocarbon fillers was found to be 0.72 x 10(-6) g/m(2).s(1/2) and 0.73 x 10(-6) g/m(2).s(1/2), respectively. The biocarbon at 650 degrees C showed the least composite thickness swelling due to its higher porosity and lower surface area. Biocarbon-filled hemp composites showed higher flexural strength and energy at the break due to the enhanced mechanical interlocking between the filler particles and the matrix materials. Smaller filler particle size lowered the composite's water diffusivity, whereas the larger particle size of the biocarbon fillers in composites minimizes the water absorption. Additionally, higher filler loading results in weaker composite tensile energy at the break due to the filler agglomeration, reduced polymer-filler interactions, reduced polymer chain mobility, and inadequate dispersion of the filler.