Journal of Polymer & Composites Original Research Special issue
Development and Performance Evaluation of Polymer-Modified Geopolymer Composites Incorporating GGBS
Abstract
This research investigates the development and performance of geopolymer-based composite materials formulated using Ground Granulated Blast Furnace Slag (GGBS) as a reactive mineral component within an aluminosilicate polymer matrix. The study aims to create an eco-efficient and structurally sound inorganic polymer composite comparable to M35-grade concrete, produced entirely under ambient curing conditions. A series of mixes with varying GGBS replacement ratios (0–100%) was prepared, maintaining a constant binder content of 400 kg/m³ and an activator-to-binder ratio of 0.45. The polymerisation reaction between sodium hydroxide (NaOH) and sodium silicate (Na₂SiO₃) solutions facilitated the formation of a cross-linked aluminosilicate network, serving as a polymeric binder reinforced by calcium-rich GGBS particles. Mechanical testing, including compressive, flexural, and split tensile strength, as well as durability assessments such as water absorption and sorptivity, were conducted at 7, 14, and 28 days. Microstructural and spectroscopic analyses (FTIR, Raman, TGA/DTA, XRD) confirmed the development of a hybrid C–A–S–H/N–A–S–H composite gel structure, indicating strong interfacial bonding and matrix densification. The 28-day compressive strength increased from 28.8 MPa to 41.6 MPa with increasing GGBS content, while water absorption and sorptivity decreased by over 30%, demonstrating improved composite integrity and reduced permeability. The optimal mix (60–80% GGBS) delivered superior performance and sustainability, achieving nearly a 90% reduction in embodied carbon compared with OPC-based systems. Overall, this study advocates GGBS-based geopolymer concrete as a sustainable inorganic polymer composite that offers high mechanical performance, microstructural stability, and environmental compatibility for next-generation structural applications.
Keywords
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