The production rate of industrial and agricultural waste is increasing due to population growth. Soil is the most important receiver of industrial and agricultural waste. Contaminants such as heavy metals in various waste after reception by the soil, immediately become part of the cycle that has different impacts on the environment. Geopolymer, as a chemical stabilizer has the potential to stabilize heavy metals in the soil. In this research, several geopolymers for the stabilization of heavy metals in soil were synthesized. Silicon dioxide (SiO2) and aluminosilicate (Al2SiO4) must be used to produce the geopolymers. Rice husk ash was used as the SiO2 source. Also, Iranian zeolite and sepiolite, and red clay soil were utilized as the source of Al2SiO4. The synthesized geopolymers were investigated for the adsorption of nickel and cadmium. Also, batch and column studies of using geopolymers for the chemical stabilization of heavy metals in soil were conducted. The results revealed a high adsorption capacity of the geopolymers. The zeolite, sepiolite, and red clay geopolymer-soil samples adsorbed 100% of the heavy metals (i.e., Ni and Cd) at a concentration of 100 ppm. The zeolite geopolymer adsorbent adsorbed 57% and 96% of Ni and Cd at a concentration of 1000 ppm, respectively. In general, it was concluded that the use of geopolymer compounds in soils with high heavy metal adsorption capacity could be an efficient approach to prevent groundwater resource pollution.

Nitrate is the most common contaminant in groundwater in Korea, as well as across the world. Reduction of nitrate to ammonia is one of the options available to remediate groundwater. In this study, nitrate in groundwater was removed using a zero-valent iron (ZVI) containing biochar synthesized by co-pyrolyzing iron oxide and sawdust biomass. Among the various biogases generated during the pyrolysis of biomass, CO and H₂ act as reducing agents to transform iron oxides to ZVI. Approximately 71% of nitrate was reduced to ammonium by ZVI-biochar at initial pH 2.0, and the reduction decreased sharply by the increase in pH. The mass of nitrate-N decreased is exactly same with the mass of ammonia-N formed. However, ammonium remained in the aqueous phase after reduction by ZVI-biochar, and the total nitrogen was not lowered. Acid-washed zeolite adsorbed most ammonium reduced by the ZVI-biochar and maintained the pH to acidic condition to facilitate the reduction of nitrate. The results of this study imply that nitrate-contaminated groundwater can be properly treated within the guidelines of water quality by synthesized ZVI-containing biochar.

This work investigated the impact of pyrolysis medium and catalyst on the production of bio-BTX (benzene, toluene, and xylene) from Quercus Mongolica (Q. Mongolica) via catalytic pyrolysis. Two different pyrolysis media (N₂ and CH₄) and five different zeolite catalysts (HY, HBeta, HZSM-5, 1 wt% Ni/HZSM-5, and 1 wt% Ga/HZSM-5) were considered for the Q. Mongolica pyrolysis. The HZSM-5 yielded more BTX than the HY and HBeta due to its strong acidity. The employment of CH₄ as the pyrolysis medium improved the BTX yield (e.g., 2.7 times higher total BTX yield in CH₄ than in N₂) and resulted in low coke yield (e.g., 5.27% for N₂-pyrolysis and 2.57% for CH₄-pyrolysis) because the CH₄-drived hydrogen simulated a hydropyrolysis condition and facilitated dehydroaromatization reaction. CH₄ also led to direct coupling, Diels-Alder, and co-aromatization reactions during the pyrolysis, contributing to enhancing the BTX yield. The addition of Ga to the HZSM-5 could further increase the BTX yield by means of facilitating hydrocracking/demethylation and methyl radical formation from CH₄ assisting the generation of >C2 alkenes that could be further converted into BTX on acid sites of the HZSM-5.