Accelerated carbonation curing (ACC) as well as partial replacement of cement with natural minerals are examples of many previous approaches, which aimed to produce cementitious products with better properties and environmental amicabilities. In this regard, the present study investigates CO₂ uptake of carbonation-cured cement blended with ground Saudi Arabian volcanic ash (VA). Paste samples with cement replacement of 20%, 30%, 40%, and 50% by mass were prepared and carbonation-cured after initial curing of 24 h. A compressive strength test, X-ray diffractometry (XRD), and thermogravimetry were performed. Although pozzolanic reaction of VA hardly occurred, unlike other pozzolana in blended cement, the results revealed that incorporation of VA as a supplementary cementitious material significantly enhanced the compressive strength and diffusion of CO₂ in the matrix. This increased the CO₂ uptake capacity of cement, reducing the net CO₂ emission upon carbonation curing.

Blast furnace slag, an industrial by-product, is emerging as a potential raw material to synthesize hydroxyapatite and zeolite. In this study, the effects of temperature on the hydrothermal synthesis of hydroxyapatite-zeolite from blast furnace slag were investigated. Specimens were synthesized at different temperatures (room temperature, 50, 90, 120, or 150 °C). The synthesized specimens were analyzed qualitatively and quantitatively via X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), BET/BJH, and scanning electron microscopy/energy dispersive using X-ray analysis (SEM/EDX). It was found that the hydroxyapatite phase was synthesized at all the reaction temperatures, while faujasite type zeolite appeared in the specimens synthesized at 90 and 120 °C. Moreover, faujasite was replaced by hydroxysodalite in the specimens synthesized at 150 °C. Additionally, the crystals of the hydroxyapatite tended to become larger and total crystallinity increased as the reaction temperature increased.

Chlorine is a critical element with respect to the use of fossil fuel, recycling of industrial wastes, and water purification. Chlorine could form toxic chemical compounds, corrode pipe systems and boilers, and contaminate surface and ground waters. Calcium aluminate-layered double hydroxides are one of the most promising materials to remove chlorides due to the chemisorption mechanism, since the phases have positively charged interlayers. Many studies on the synthesis and the characterization of calcium aluminate-layered double hydroxides have been extensively conducted, whereas few studies have been conducted on the chloride removal characteristics of the phases. The state-of-the-art studies on the synthesis methods and the structural characteristics of CaAl-LDH phases, the underlying mechanism on the removal of chlorides, and the potential removal rate and the capacity in the present study were thoroughly reviewed.

The growing importance of electromagnetic interference (EMI) shielding composites in civil engineering has garnered increasing attention. Conductive cement-based composites, incorporating various conductive fillers, such as carbon nanotubes (CNTs), carbon fibers (CFs), and graphene nanoplatelets (GNPs), provide effective solutions due to their high electrical conductivity. While previous studies have primarily focused on improving the overall shielding effectiveness, this research emphasizes balancing the reflection and absorption properties. The experimental results demonstrate an EMI shielding performance exceeding 50 dB, revealing that filler size (nano, micro, or macro) and shape (platelet or fiber) significantly influence both reflection and absorption characteristics. Based on a comprehensive evaluation of the shielding properties, this study highlights the need to consider factors such as reflection versus absorption losses and filler shape or type when optimizing filler content to develop effective cement-based EMI shielding composites.

The phase changes in alkali-activated slag samples when exposed to supercritical carbonation were evaluated. Ground granulated blast furnace slag was activated with five different activators. The NaOH, Na₂SiO₃, CaO, Na₂SO₄, and MgO were used as activators. C-S-H is identified as the main reaction product in all samples along with other minor reaction products. The X-ray diffractograms showed the complete decalcification of C-S-H and the formation of CaCO₃ polymorphs such as calcite, aragonite, and vaterite. The thermal decomposition of carbonated samples indicates a broader range of CO₂ decomposition. Formation of highly cross-linked aluminosilicate gel and a reduction in unreacted slag content upon carbonation is observed through ²⁹Si and ²⁷Al NMR spectroscopy. The observations indicate complete decalcification of C-S-H with formation of highly cross-linked aluminosilicates upon sCO₂ carbonation. A 20–30% CO₂ consumption per reacted slag under supercritical conditions is observed.