Enhancement of alkali- and oxidation-modified biochars derived from water hyacinth for ammonium adsorption capacity

Abstract

ABSTRACTWastewater containing high concentrations of ammonium-nitrogen (NH4+-N) is considered a major concern because its untreated discharge has a variety of adverse effects on the environment and human health. Adsorption using biochars is an easy and cost-effective wastewater treatment method. However, aquatic plants such as water hyacinth for biochar feedstock are considered unsuitable for adsorbent use due to limited NH4+-N adsorption capacity. In this study, biochar made from water hyacinth was modified with potassium hydroxide (KOH) and hydrogen peroxide (H2O2) to obtain highly efficient adsorbent. This study aimed to enhance NH4+-N adsorption capacity by KOH- and H2O2-treatments and identify NH4+-N adsorption mechanism of the modified biochars derived from water hyacinth. The NH4+-N adsorption of all biochars was dependent on the initial solution pH increasing from pH 2 to 4, then relatively constant from pH 4 to 8. Pseudo-second-order model and Langmuir model were found to be the best fit for NH4+-N adsorption data. The maximum NH4+-N adsorption capacity of biochars increased about 8 times (17.1 mg g−1) and 10 times (21.5 mg g−1) after KOH- and H2O2-modification, respectively, compared to pristine biochar (2.14 mg g−1). The main NH4+-N adsorption mechanisms were suggested as cation exchange for both biochars particularly KOH-modified biochar, and hydrogen bonding by oxygen-containing surface functional groups for H2O2-modified biochar. This study suggested that aquatic plant-based biochar, which has been considered difficult to use, had potential as a promising alternative adsorbent for removing NH4+-N from wastewater through modification.KEY WORDS: Adsorption isothermadsorption kineticscarboxylic groupcation exchange capacityFTIR Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThe work was supported by the Science and Technology Research Partnership for Sustainable Development [JPMJSA2005].