| Literature DB >> 34173877 |
Heba Elbasiouny1, Marwa Darwesh1, Hala Elbeltagy1, Fatma G Abo-Alhamd1, Ahlam A Amer1, Mariam A Elsegaiy1, Israa A Khattab1, Esraa A Elsharawy1, Fathy Ebehiry2, Hassan El-Ramady3, Eric C Brevik4.
Abstract
Treatment of water contaminated with heavy metals is challenging. Heavy metals are non-degradable, persistent in the environment, have a high dispersion capacity by water, can bioaccumulate, and represent risks to human and environmental health. Conventional treatment methods have disadvantages; however, adsorption in biomass is a highly promising method with high efficiency and low cost that avoids many of the disadvantages of conventional methods. Black tea (BT) wastes and water hyacinth (WH) have attracted attention for their ability to remove heavy metals from wastewater. Utilizing these approaches can remove contaminants and effectively manage problematic invasive species and wastes. The conventional uses of BT and WH were efficient for removing heavy metals from wastewater. Due to the unique and distinct properties and advantages of biochar and nano-forms of biosorbents, the use of BT and WH in these forms is promising to achieve sustainable heavy metals removal from wastewater. However, more study is needed to confirm preliminary results.Entities:
Keywords: Biochar; Polluted wastewater; Wastes; Wastewater treatment
Mesh:
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Year: 2021 PMID: 34173877 PMCID: PMC8233605 DOI: 10.1007/s10661-021-09236-2
Source DB: PubMed Journal: Environ Monit Assess ISSN: 0167-6369 Impact factor: 2.513
Fig. 1SEM micrographs of BT biochar a before and b after Cd adsorption (Pal & Maiti, 2019)
Comparisons of heavy metals removal efficiency/adsorption capacity of water hyacinth and black tea waste
| Metal(s) | Removal efficiency/sorption capacity | Material(s) | Reference |
|---|---|---|---|
| Cd and Cu | Removal efficiency was 15.9% for Cu and 91.4% for Cd | Water hyacinth roots | Zheng et al. ( |
| Cr | Removal efficiency ranged from 25–72% to 35–96% | Water hyacinth | Bandara et al. ( |
| Cr | Removed 80% from standard solution and 99% from water after 20 days at 0.5 ppm | Water hyacinth | Saha et al. ( |
| As | Water hyacinth roots removed up to 50 mg As g−1 after exposure of 1500 mg As l−1 to 30 g of dried roots over a 24-h time period. | Water hyacinth roots | Al Rmalli et al. ( |
| As | Maximum removal was 37% with 0.1 g of biomasses and an As(V) concentration of 0.1 mg | Water hyacinth | Romero-Guzmán et al. ( |
| Cd, Cu, Pb, and Zn | Removed 61% of Cd, 59% of Cu, 49% of Pb, and 42% of Zn; removal efficiencies were 98% for Cd, 99% for Cu, 98% for Pb, and 84% for Zn | Water hyacinth | Sekomo et al. ( |
| Cr | Maximum removal was 13.05 mg/g, 26.74 mg/g, and 39.21 mg/g for stems, roots, and leaves, respectively, at pH 1; removal efficiencies of 31.5%, 40%, and 34%, respectively | Water hyacinth | Aggarwal and Arora ( |
| Cu | Removal efficiency from an aqueous solution containing various concentrations of Cu (1.5, 2.5, and 5.5 mg/L) was 97.3% over 21 days | Water hyacinth | Mokhtar et al. ( |
| Cd and Cu | Removal of Cd and Cu ranged from 87.69 to 95.59% and 6.67 to 35.48% in pharmaceutical wastewater. Average bioconcentration factors for Cd and Cu were 583.83 and 734.41, respectively. | Water hyacinth | Ajayi and Ogunbayo ( |
| Cr, Cu, and Zn | Maximum reduction of 94.78% for Cr, 96.88% for Zn, and 94.44% for Cu | Water hyacinth | Mahmood et al. ( |
| Cd | Maximum Cd(II) removal efficiency of 92.45%. Immobilization efficiency was 89.3%, and bioaccumulation capacity was 13.81 mg g−1 | Water hyacinth with algal cells | Shen et al. ( |
| Cu | The sorption capacity of Cu was 22.7mg g−1 at an initial pH of 5.5. | Water hyacinth roots | Zheng et al. ( |
| Cr | The removal efficiency was 95% of Cr(VI) from a solution at neutral pH. | Water hyacinth biochar+30% Zno | Yu et al. ( |
| Cr | Maximum removal of 99.3% of Cr(VI); 197.5 mg g-1 Cr at 120 mg L−1 initial Cr concentration | Tea waste biochar | Khalil et al. ( |
| F | The fluoride removal efficiency was 91.79% and 98.29% for TWB and CMB, respectively | Tea waste biochar and chemically modified biochar | Roy et al. ( |
| Pb | Removal rate for alkali treated green tea (GT) was 98.54%, GT was 64.18%, and GT residue was 70.73% at 50 mg/L of Pb | Alkali treated GT residue, GT, and GT residue | Yang and Cui ( |
| Pb and Cd | Adsorption efficiency for Pb was 125 mg g−1 (72%) and Cd 142.9 mg g−1 (72.14%) at pH 8 | Residual tea waste | Joshi et al. ( |
| Cd, Co, and Zn | Adsorption capacity for metals was 15.39 mg g−1 for Co, 13.77 mg g−1 for Cd, and 12.24 mg g−1 for Zn | Black tea waste | Mohammed ( |
| Ni and Zn | Maximum capacity of 90.91 mg Ni/g and 166.67 mg Zn/g at pH 5, contact time 250 min, and 20 g L-1 adsorbent concentration | Black tea waste | Malakahmad et al. ( |
| Cd, Pb, and Ni | 94–100% removal for Pb, 86% for Ni, and 77% for Cd | Tea waste | Mahvi et al. ( |
| As | Optimum arsenic removal was 92.5% at pH 7 | Tea waste | Shaikh et al. ( |
Fig. 2SEM micrographs of WH biochar surfaces at several magnifications (Allam et al., 2020)
Fig. 3TEM micrographs of biochar surfaces created with black tea wastes at 500 °C
Fig. 4TEM micrographs of biochar surfaces created with water hyacinth wastes at 500 °C
Fig. 5TEM micrographs of a black tea nano-biochar and b water hyacinth nano-biochar surfaces. Both biochars were created at 500 °C