Removal of lead ions (Pb2+) from water and wastewater: a review on the low-cost adsorbents.

The presence of lead compounds in the environment is an issue. In particular, supply water consumption has been reported to be a significant source of human exposure to lead compounds, which can pose an elevated risk to humans. Due to its toxicity, the International Agency for Research on Cancer and the US Environmental Protection Agency (USEPA) have classified lead (Pb) and its compounds as probable human carcinogens. The European Community Directive and World Health Organization have set the maximum acceptable lead limits in tap water as 10 µg/L. The USEPA has a guideline value of 15 µg/L in drinking water. Removal of lead ions from water and wastewater is of great importance from regulatory and health perspectives. To date, several hundred publications have been reported on the removal of lead ions from an aqueous solution. This study reviewed the research findings on the low-cost removal of lead ions using different types of adsorbents. The research achievements to date and the limitations were investigated. Different types of adsorbents were compared with respect to adsorption capacity, removal performances, sorbent dose, optimum pH, temperature, initial concentration, and contact time. The best adsorbents and the scopes of improvements were identified. The adsorption capacity of natural materials, industrial byproducts, agricultural waste, forest waste, and biotechnology-based adsorbents were in the ranges of 0.8-333.3 mg/g, 2.5-524.0 mg/g, 0.7-2079 mg/g, 0.4-769.2 mg/g, and 7.6-526.0 mg/g, respectively. The removal efficiency for these adsorbents was in the range of 13.6-100%. Future research to improve these adsorbents might assist in developing low-cost adsorbents for mass-scale applications.

Removal of Pb2+ from water using the carbon nanotube-g-poly[(sodium methacrylate)-co- 2-(methacryloyloxy)ethyl acetoacetate]: experimental investigation and modeling.

A solid polymer, poly[(sodium methacrylate)-co-2-(methacryloyloxy)ethyl acetoacetate], p(MAA-co-MEAA) was synthesized and then grafted onto carbon nanotubes to prepare poly(MAA-co-MEAA)-grafted carbon nanotubes [CNT-g-p(MAA-co-MEAA)]. NMR, TGA, and FT-IR characterized the synthesized polymers and adsorbents. SEM-EDX was used to investigate the surface characteristics of the adsorbents. Pb2+ was removed from the aqueous solution using the CNT-g-p(MAA-co-MEAA). A batch adsorption experiment was performed at different Pb2+ concentrations (1, 10, 25, 50 mg/L), pH (4 and 6.75), temperature (25 and 35 °C), and contact periods (1, 5, 20, 60, and 1440 min) to study the adsorption kinetics and isotherm. The adsorbent dose of 2.5 g/L could effectively lower the initial Pb2+ concentration of 1000 to 2 ppb. The maximum adsorption capacity of the adsorbent was found to be 1178 mg/g. In addition, the adsorbents have been shown to effectively reduce the coexisting metal ion concentrations from industrial wastewater, which indicated the potential of the proposed adsorbent in removing metal ions from coexisting metals containing wastewater. To predict the adsorption efficiency of Pb2+, various linear, non-linear, and neural network models were established. An additional data set, not incorporated in model training, was used to validate the models. A number of models showed excellent performance with R2 in the range of 0.89-0.98. In model validation studies, the correlation coefficients (r) ranged from 0.94 to 0.99. The novel adsorbent and models will most likely aid in the development of a robust treatment technique for removing Pb2+ ions from water and wastewater.

Predicting risk and loss of disability-adjusted life years (DALY) from selected disinfection byproducts in multiple water supply sources in Saudi Arabia.

Disinfection byproducts (DBPs) in drinking water is an issue in many countries. Many DBPs are possible or probable human carcinogens while few DBPs pose cyto- and genotoxic effects to the mammalian cells. The populations are likely to consume DBPs with drinking water throughout their lifetimes. A number of DBPs are regulated in many countries to protect humans. In this study, human exposure, risk and disability-adjusted life years (DALY) were predicted from DBPs in multiple water supply systems, including groundwater (GW), desalinated water (DW) and blend water (BW). The averages of lifetime excess cancer risks from GW, DW and BW were 4.15 × 10-6, 1.75 × 10-5 and 2.59 × 10-5 respectively. The populations in age groups of 0 - <2, 2-16 and >16 years contributed 25.4-25.7%, 28.6-29.6% and 45.0-45.7% to the total risks respectively. The DALY from GW, DW and BW were estimated to be 5.8, 27.0 and 39.9 years, respectively while the corresponding financial burdens were US$ 0.63, 2.93 and 4.34 million respectively. The findings are likely to assist in selecting the supply water sources to better control human exposure and risk from DBPs.

Human exposure and risk of trihalomethanes during continuous showering events.

Exposure to disinfection byproducts (DBPs) in municipal water mainly occurs through ingestion, inhalation during showering, house cleaning and dermal permeation. While showering, the air-phase DBPs [e.g., trihalomethanes (THMs)] can pose risk to humans through inhalation pathway. In assessing inhalation risk during showering, current approaches assume negligible initial concentrations of air-phase THMs in shower stalls, which may not be realistic in places with common shower stalls (e.g., gymnasiums). The time difference between successive showering events in these places is likely to be minimal, resulting in significant initial concentrations of THMs due to prior showering events. In this study, exposure to air-phase THMs during the successive showering events were predicted. In the 2nd showering event, averages of chronic daily intake (CDI), cancer risk (CR) and hazard index (HI) were 1.82, 1.83 and 1.85 times the CDI, CR and HI in the first event, respectively. In the 3rd event, these were 2.50, 2.54 and 2.58 times, respectively. The increasing trends of CDI, CR and HI were observed for up to the 9th event (5.06, 4.98 and 5.60 times, respectively). By widening the time-gap between the successive showering events, reducing showering duration and enhancing ventilation, human exposure and risk can be controlled.

Highly porous carboxylated activated carbon from jute stick for removal of Pb2+ from aqueous solution.

Drinking water is a potential source of human exposure to lead (Pb2+), which can induce several health effects upon exposure to low dose for a long period. In particular, the children and young populations are the vulnerable groups. Removal of Pb2+ from drinking water using an inexpensive adsorbent is a challenge. In this research, activated carbon adsorbent was developed using jute stick, an agricultural by-product. Following carboxylic acid functionalization, the jute stick activated carbon (JSAC) was applied for Pb2+ removal from aqueous solution. The carboxylated JSAC (JSAC-COO-) was characterized using several techniques. The surface area of the JSAC-COO- was 615.3 m2/g. The JSAC-COO- was tested for variable concentrations of Pb2+ (10 and 25 mg/L) at different pH (4.0 and 7.0), temperature (15 °C and 27 °C), and contact periods (1, 5, 10, 15, 30, and 60 min). Up to 99.8% removal of Pb2+ was achieved for these concentrations of Pb2+ within 15 min of contact time. The adsorption process followed standard kinetics, and the adsorption capacity was > 25.0 mg Pb2+/g of JSAC-COO-. The JSAC-COO- can be used for fast and easy removal of Pb2+ from aqueous solution, which has the potential for domestic and industrial applications.