Groundwater Geochemistry. Группа авторов. Читать онлайн. Newlib. NEWLIB.NET

Автор: Группа авторов
Издательство: John Wiley & Sons Limited
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Жанр произведения: Биология
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isbn: 9781119709701
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(Marg 2011; Talabi and Kayode 2019).

      4.6.1 Oxidation

      The oxidation method includes the use of an oxidizing agent (Cl2, ClO2, O3, H2O2, NH2Cl, MnO4, FeO42−, etc.) to eliminate heavy metals from water (Sharma et al. 2007; Mondal et al. 2013; Bora and Dutta 2019). Investigation of the photochemical and photocatalytic oxidation process includes the oxidation of heavy metals using UV radiation, O2, etc. for the removal of dissolved pollutants. UV/solar radiation assists to develop the hydroxyl radicals during the photolysis of iron and iron hydroxide (fe(OH)3), hydroxyl radicals and O2 oxidizes the toxic metals like As(III) to As(V). The presence of these radicals, the oxidation reaction becomes faster (Yoon and Lee 2005; Sharma et al. 2007). On the other hand, the photocatalytic reaction is carried out in the presence of TiO2 for oxidation of the heavy metals (Miller et al. 2011).

Schematic illustration of conventional different conventional methods to decontaminate water from heavy metals.

      4.6.2 Coagulation‐Flocculation

      The coagulation and flocculation method has been investigated to eliminate the toxic metal pollution from contaminated water (Abouri et al. 2019; Bora and Dutta 2019). In this process, the coagulant is incorporated into the contaminated water and then forms the floc, which has the potential to eliminate heavy metals from the water. The positively charged coagulants such as aluminium and iron salts, which are widely used for heavy metal like As removal, help to decrease the negative charge of colloids. The larger particles (floc) form due to agglomeration of the particles, which settle down in water due to the influence of gravity (Choong et al. 2007). The formed floc helps to precipitate out the soluble heavy metals from the water and the solution can be filtered rapidly. Several reported coagulants like aluminium, ferrous sulphate, and ferric chloride result in the formation of amorphous metal hydroxide precipitates that are more suitable to eliminate toxic metals from contaminated water (Pallier et al. 2010). At lower pH, the colloidal substances with negative charges can be coagulated, but the cationic ion cannot be eliminated and at higher pH, the turbidity removal decreases and the cationic removal is favoured.

      4.6.3 Phytoremediation

      The phytoremediation process is based on the use of plants for the removal of toxic metals from the environment and it is even used to clean up contaminated air, soil, and water. It consists of several steps like phytoextraction, phytoming, phytostabilisation, rhizofiltration, and phytovolatilization (Dickinson et al. 2009; Behera 2014). Over the last decades, several researchers have been using various types of plants like Pteris Vittata, Vetiver grass, for remediation of toxic metals through the phytoremediation process (Hosamane 2012). The disadvantage of this process is that the plants adsorb high levels of toxic metals, which contaminate food crops and require more time to eliminate heavy metals from soil and water.

      4.6.4 Membrane Filtration

      The electrodialysis (ED) process carries out the separation of ions across charged membranes from one solution to another solution following an electric field as the driving force. Mostly, ion‐exchange membranes (cationic and anionic) are used in ED processes. It has been widely used for the production of drinking water, process water from brackish water and seawater, treatment of industrial effluents, recovery of useful materials from effluents, salt production, and for heavy metal wastewater treatment.

      According to the literature, the RO (reverse osmosis) process is a very old and famous method thought of as the best method to remove arsenic from water. The RO membrane has extremely small pores (<0.001 μm). The RO membrane process can achieve a high rejection of low molecular mass compound and ions. The cellulose acetate RO membrane was been investigated for the first time in the 1980s, and has a 90% As removal efficiency with the RO system with 400 psi high pressure. However, Akin et al. have investigated the RO operational parameters. A semi‐permeable membrane is used, which allows the fluid that is being purified to pass through it, while rejecting the contaminants. It accounts for more than 20% of the world's desalination capacity (Shahalam et al. 2002). RO is an alternative option for wastewater treatment in chemical and environmental engineering. The major problem with RO is the high power consumption due to the pumping pressures, and the restoration of the membranes.

      4.6.5 Ion Exchange

      The ion exchange method has been employed to eliminate both cationic and anionic impurities from water. It has many advantages, such as high treatment capacity, high removal efficiency, and fast kinetics (Rahimizadeh and Liaghatb 2015). The resin used may be either synthetic or natural solid resin (synthetic resins are comparatively more effective) (Alyüz and Veli 2009). As the solution containing heavy metal passes through the cations column, metal ions are exchanged for the hydrogen ions on the resin. The uptake of heavy metal ions by ion‐exchange resins is affected by certain variables such as pH, temperature, initial metal concentration, and contact time (Gode and Pehlivan 2006). Ionic charge also plays an important role in the ion‐exchange process. In contrast to resin, natural zeolites also exhibit good cation exchange capacities for heavy metal ions under different experimental conditions. Clinoptilolite is one of the most frequently studied natural zeolites that has received extensive attention due to its selectivity for heavy metals (Doula 2009). Although there are many reports on the use of zeolites and montmorillonites as ion‐exchange resin to decontaminate heavy metal, they are limited at present compared with the synthetic resins and the application of zeolites is on the laboratory experimental scale.

      4.6.6 Electrokinetics Remediation