| Literature DB >> 27638318 |
Christopher Chibueze Azubuike1, Chioma Blaise Chikere2, Gideon Chijioke Okpokwasili2.
Abstract
Environmental pollution has been on the rise in the past few decades owing to increased human activities on energy reservoirs, unsafe agricultural practices and rapid industrialization. Amongst the pollutants that are of environmental and public health concerns due to their toxicities are: heavy metals, nuclear wastes, pesticides, green house gases, and hydrocarbons. Remediation of polluted sites using microbial process (bioremediation) has proven effective and reliable due to its eco-friendly features. Bioremediation can either be carried out ex situ or in situ, depending on several factors, which include but not limited to cost, site characteristics, type and concentration of pollutants. Generally, ex situ techniques apparently are more expensive compared to in situ techniques as a result of additional cost attributable to excavation. However, cost of on-site installation of equipment, and inability to effectively visualize and control the subsurface of polluted sites are of major concerns when carrying out in situ bioremediation. Therefore, choosing appropriate bioremediation technique, which will effectively reduce pollutant concentrations to an innocuous state, is crucial for a successful bioremediation project. Furthermore, the two major approaches to enhance bioremediation are biostimulation and bioaugmentation provided that environmental factors, which determine the success of bioremediation, are maintained at optimal range. This review provides more insight into the two major bioremediation techniques, their principles, advantages, limitations and prospects.Entities:
Keywords: Bioremediation; Environment; Pollutants; Techniques
Mesh:
Substances:
Year: 2016 PMID: 27638318 PMCID: PMC5026719 DOI: 10.1007/s11274-016-2137-x
Source DB: PubMed Journal: World J Microbiol Biotechnol ISSN: 0959-3993 Impact factor: 3.312
Fig. 1Bioremediation techniques. The divergence of each technique is hypothetical; therefore, the left to right order of internal nodes are not the order of evolution (technique development). Permeable reactive barrier (PBR) is not the arbitrary tree root. It is a physical remediation technique with some elements of bioremediation, hence the early hypothetical divergence
Some pollutants removed by bioreactor-based bioremediation
| Type/mode of bioreactor operation | Nature of sample | Nature of pollutant | Initial concentration | % Removal | References |
|---|---|---|---|---|---|
| Stir tank bioreactor (2.5 L) | Crude oil polluted sediment | Total petroleum and polyaromatic hydrocarbons | 19 and 3.1 ppm respectively | 82–97 | Chikere et al. ( |
| Stir tank bioreactor/batch (1.5 L) | Waste lubricating oil | Saturated and aromatic hydrocarbons | 80–86 g/L | 62–69 | Bhattacharya et al. ( |
| Expanded granular sludge bed (EGSB) reactor (1.4 L) | Laundry wastewater | Linear alkylbenze sulfonate (LAS) | 7.0 g TVS/L | 92.9 | Delforno et al. ( |
| Anaerobic sludge blanket/continuous-flow (3.3 L) | Synthetic BTEX-contaminated water | Benzene, toluene, ethylbeneze, and xylene (BTEX) | 50 g VSS/L | 51–86 | Firmino et al. ( |
| Packed-bed reactor (PBR, 1.25 L) | Amines | Mixture of sulfonated amines (4-aminobenzene sulfonic acid and 4-amino naphthalene sulfonic acid) | 50 mg/L | Juárez-Ramírez et al. ( | |
| Roller slurry bioreactor (1 L) | Contaminated soil | 2,4-Dichlorophenoxyacetic Acid | 200–500 mg/kg | 97–100 | Mustafa et al. ( |
| Packed bed biofilter (100 cm × 5 cm) | Pharmaceutical sludge | Xylene vapour | 0.2–1.2 g/m3 | 95–99 | Saravanan et al. ( |
| Submerged attached growth bioreactors (SAGBs, 61 cm × 61 cm × 46 cm) | Effluent | Total nitrogen | 48–53 | Shannon et al. ( | |
| Membrane bioreactor (MBR, 8 L) | Coal gasification wastewater | Naphthalene and total nitrogen | 10–200 mg/L | 48–98 | Xu et al. ( |
| Sequencing batch reactors (SBR, 2.5 L) | Engineered nanomaterials (ENMs) | Nano fullerenes (nC60) and nanosilver | >90 % | Yang et al. ( | |
| Miniature membrane bioreactor (mMBR)/continuous | Brominated flame retardants (BFR) | Dibromoeopentyl glycol (DBNPG) | 50 | Zangi-Kotler et al. ( | |
| Sequence batch reactor (1.5 L) | Contaminated soil | Carbofuran | 20 mg/kg | 88–97 | Plangklang and Alissara Reungsang ( |
| Glass jar paddle-type impeller reactor (2 L) | Contaminated soil | 2,4,6-trinitophenylmethylnitramine (tetryl) | 1,00,000 mg/kg | 99.9 | Fuller et al. ( |
aPilot study
Some plants with phytoremediation potentials
| Plant | Nature of pollutant | Initial concentration | Mechanism of removal | % Removal | Reference |
|---|---|---|---|---|---|
|
| Gasoline | 2,07,800 mg/kg TPH | Biosurfactant enhanced rhizodegradation | 93.5 | Almansoory et al. ( |
|
| Brominated diphenyl ethers (BDE-47) | 5 μg/gdw | Biostimulated degradation | 58.2 | Chen et al. ( |
|
| As, Cu, Pb, Zn | 5–2153 mg/kg | Bioaugmented rhizoaccumulation | 19–65 | Mesa et al. ( |
|
| Cd and Zn | 78.9 and 66.6 kBq/dm3 respectively | Rhizofiltration | 100 | Dürešová et al. ( |
|
| Heavy metals (Fe, Zn, Cd, Cu, B, and Cr) | 0.02–20 mg/L | Rhizofiltration | 99.3 | Elias et al. ( |
|
| PAHs | 229.67 ± 15.56 μg/g | Rhizodegradation | 58.47 | Gregorio et al. ( |
|
| Pb | 5–200 mg/kg | Rhizofiltration | 50–100 | Ignatius et al. ( |
|
| Anthracene and fluoranthene | 50 mg/kg | Phytostimulationa | 85.9–99.5 | Somtrakoon et al. ( |
|
| Diesel | 1–5 wt% | Rhizodegradation | 90–98 | Dadrasnia and Agamuthu ( |
|
| Polychlorinated biphenyls | 6.260 ± 9.3 10−3 μg/g | Biostimulated rhizodegradation | 91.5 | Gregorio et al. ( |
|
| Ni | 25–150 μM | Phytoaccumulation | 25–60 | Iori et al. ( |
|
| TPH | 33,215.16 mg/kg | Phytoextraction and phytostimulation | 87 | Moreira et al. ( |
|
| Silver nanoparticles and Ag+ | 0.01–100 mg/L | Phytoaccumulation | 20–70 | Wang et al. ( |
|
| Pb | 1.0–10 mg/L | Rhizofiltration | Yadav et al. ( |
PAHs polyaromatic hydrocarbons, TPH total petroleum hydrocarbon
aHypothetical, needs further investigation
Some pollutants removed by permeable reactive barriers (PRBs) technique
| Reactive material | Nature of pollutant | Initial concentration | Mechanism of pollutant removal | % Removal | References |
|---|---|---|---|---|---|
| Clay | Cs-137 | 105 Bq/m3 | Sorption | De Pourcq et al. ( | |
| Oxygen reactive compound and clinoptilolite | NH4–N | 5–11 mg/L | Ion exchange and biological nitrification | >99 | Huang et al. ( |
| Natural pyrite (FeS2) | Cr(VI) | 10–100 mg/L | Sorption | 27–100 | Liu et al. ( |
| Zero-valent iron coupled with polyhydroxybutyrate | 1, 2-dichloroethane | 10 mg/L | Biological degradation | 20–80 | Baric et al. ( |
| Mixture of zero-valent iron, Zeolite and activated carbon | Landfill leachate | 55–94 | Zhou et al. ( | ||
| Bio-barrier ( | Polyaromatic hydrocarbons | 100 μM | Biodegradation | >80 | Ferreira et al. ( |
| Bio-barrier ( | Orange G dye | 150 mg/L | Biodegradation | 97 | Folch et al. ( |
| Organic substrates and zero-valent iron (ZVI) | Heavy Metals (Al, Zn and Cu) | 15, 20 and 1.2 mg/L | Precipitation | >95 | Gibert et al. ( |
| Granular oxygen-capturing materials (ZVI powder, sodium citrate and inorganic salts) and granular activated carbon | Nitrate and nitrite | 40 mg/L | Biodegradation | >94 | Liu et al. ( |
| Bioaugumented Bio-barrier ( | Benzene, toluene, ethylbenze and xylene (BTEX) | 100 mg/L | Biodegradation | 84–97 | Xin et al. ( |
| Granular iron | Chlorinated volatile organic compounds (VOC) | Degradation | Vogan et al. ( |
aPilot-scale study