Effects of relative humidity on carbonation kinetics and strength development of carbonated wollastonite composites containing sodium tripolyphosphate

Abstract

Assessing the impact of relative humidity (RH) on carbonation kinetics is crucial for the sustainable and high-strength advancement of CO₂-activated Ca-bearing materials incorporating phase-controlling additives. This work focuses on the carbonation kinetics, mechanical properties, and microstructure evolution of carbonated wollastonite composites containing sodium tripolyphosphate (STPP) when exposed to various RH levels. Results show that RH plays an important role during the carbonation of wollastonite, functioning both as a reaction material and accelerating role for wollastonite carbonation. The carbonation rate and the phase transition reaction of poorly crystalline CaCO₃ is accelerated at RH ranging from 70% to 95%, favouring to cementitious behaviour of CaCO₃ and results in denser microstructure, especially for 85% RH. The carbonation reaction is composed of two distinct stages, namely, wollastonite dissolution and precipitation of the stage-1 and ion-diffusion controlling of stage-2. Among them, the addition of STPP prolong the carbonation duration of stage-1. The degree of carbonation (DOC) of the internal layer sample is higher than that of the outermost layer sample. CaCO₃ and silica gel are evenly distributed indirectly, which reduces the elastic modulus at 85 % RH. However, regardless of RH, the cementitious efficiency of poorly crystalline CaCO₃ is the highest, followed by calcite and silica gel. Consequently, STPP modified carbonated wollastonite shows highest strength when exposed to 85% RH (67.3 MPa at 7 days). Our study provides a unique way toward developing the STPP-containing carbonated wollastonite system for high performance carbonated materials.