Abstract
This paper studied the adsorption of chemical oxygen demand (COD), oil and turbidity of the produced water (PW) which accompanies the production and reconnaissance of oil after treating utilizing powdered activated carbon (PAC), clinoptilolite natural zeolite (CNZ) and synthetic zeolite type X (XSZ). Moreover, the paper deals with the comparison of pollutant removal over different adsorbents. Adsorption was executed in a batch adsorption system. The effects of adsorbent dosage, time, pH, oil concentration and temperature were studied in order to find the best operating conditions. The adsorption isotherm models of Langmuir, Freundlich and Temkin were investigated. Using pseudo-first-order and pseudo-second-order kinetic models, the kinetics of oil sorption and the shift in COD content on PAC and CNZ were investigated. At a PAC adsorbent dose of 0.25 g/100 mL, maximum oil removal efficiencies (99.57, 95.87 and 99.84 percent), COD and total petroleum hydrocarbon (TPH) were identified. Moreover, when zeolite X was used at a concentration of 0.25 g/100 mL, the highest turbidity removal efficiency (99.97%) was achieved. It is not dissimilar to what you would get with PAC (99.65 percent). In comparison with zeolites, the findings showed that adsorption over PAC is the most powerful method for removing organic contaminants from PW. In addition, recycling of the consumed adsorbents was carried out in this study to see whether the adsorbents could be reused. Chemical and thermal treatment will effectively regenerate and reuse powdered activated carbon and zeolites that have been eaten.
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Introduction
Produced water (PW) is the largest stream of wastewater generated by the petroleum industry during oil and gas field exploration and production and contains a wide range of hydrocarbons in free, dispersed and dissolved forms (Al-Ghouti et al. 2019). PW has a complex compound (organic and inorganic), such as grease, dissolved and dispersed oil, formation solids, scale products, heavy metals, waxes, radionuclides, dissolved oxygen, treating chemicals, dissolved gases, salts and microorganisms (Igunnu and Chen 2014). 250 million barrels of water per day is generated from gas and oil fields, and greater than 40% of it is discharged to the environment globally (Hedar 2018), the discharge of PW may lead to severe pollution of surface, soil and underground water, and the hazard comes from the absence of appropriate treatment. Therefore, many technologies for the purification of PW are utilized (Show 2021) and can be divided into biological, chemical or physical methods (Fakhru’l-Razi 2009). Microbial degradation (Quintana et al. 2005), filtration (Guo et al. 2018), chemical oxidation (Zhu et al. 2020), electrochemical oxidation (Nidheesh et al. 2020), coagulation (Khader et al. 2018) and membrane separation (Xiao et al. 2010) may be suitable technologies for the elimination of environmental pollution. However, these techniques have their own limitations such as high cost, generation of secondary pollutants and poor removal efficiency (Gupta et al. 2012; Han 2007). Adsorption is considered the most significant traditional techniques for purification and reclamation of produced water (Zhao 2015), including the elimination of biological, organic and inorganic pollutants that are insoluble and soluble in water for meeting the environmental standards at least cost (Rashed 2013), so has been introduced as an environmental-friendly and cost-effective and economic method. It can replace other conventional methods for the treatment of pollutants in the wastewater (Kim et al. 2018; Albayati et al. 2020). Hence, it can be utilized in a wide range of applications and gives the removal efficiency over to 99%, ease of separation of the targeted compounds from the dilute solution, simplicity of design and operation, insensitive to toxic materials and the possibility of recovery of the adsorbed materials easily by different methods (desorbing agents, leaching employing chemical reagents, biological processes and thermal treatment) (Alardhi et al. 2020).
In the adsorption process, several types of adsorbents such as activated carbons, zeolites, activated alumina or low-cost materials (limestone, rice husk ash, peat, etc.) can be used. Activated carbon is considered the most widely used adsorbent (Babel and Kurniawan 2003). AC is an amorphous, microcrystalline and non-graphical solid with certain properties, including high thermal stability, high light stability, porous and solid structure, high mechanical stability, a high surface-to-volume ratio and high pureness. Furthermore, since AC has a high capacity for adsorption of various species, it can be used as an adsorbent to remove ions and organic contaminants from wastewater (Jhadhav 2015).
Because of their cost-effectiveness, zeolites are one of the most widely used adsorbents in water treatment (Pandey et al. 2020). Natural zeolites are mineral crystalline aluminosilicates and hydrated alkali and alkaline earth metals with a tridimensional lattice that are divided into two types (clinoptilolite, analcime, limonite, phillipsite, mordenite) and artificial zeolites (Malekmohammadi et al. 2016). Clinoptilolite is the most abundant of the more than 40 natural zeolite species, and its low cost, high specific surface area and high ion exchange capability make it a popular choice for water and wastewater treatment (Hamidpour et al. 2010; Yang et al. 2011). The synthetic zeolites are usually obtained from the chemical reaction between sodium silicate, Na2SiO3, and sodium aluminate, NaAlO2, under varying conditions of temperature, pressure and reaction time. Raw materials such as fly ash, perlite, clay minerals and obsidian, in addition to pure chemical reagents, can be used in the synthesis of zeolites (Bandura et al. 2017).
Some researchers studied the ability the AC and zeolites (natural and synthetic) in the treatment of pollutants from wastewater. Pandey et al. (2020) applied the clinoptilolite zeolite, molybdenum sulfide (MoS2) and MoS2–clinoptilolite composite to treat lead (Pb) in industrial mining wastewater. Al-Haddad et al. (2007) used the natural zeolite (clinoptilolite), manufactured synthetic zeolite and activated carbon to treat ammonia from refinery wastewater. Payne and Abdel-Fattah 2004 compared and evaluated the performance of activated carbon and natural zeolites (clinoptilolite and chabazite) and synthetic zeolites (Faujasite (13X) and Linde type A (5A) in the treatment of Pb2 + by using batch adsorption. Bandura et al. (2016) utilized synthetic zeolites (Na-P1 and Na-X) and natural zeolites (clinoptilolite and diatomite) to reduce (Benzene, Toluene, Xylene) BTX from gas streams. Malekmohammadi et al. (2016) studied the efficiency of adsorbents (zeolite, silica and activated carbon) in the treatment of pollutants (COD, phosphate, iron, ammonium and turbidity). Vega et al. (2018) applied the faujasite zeolite type X to remove heavy metals, water hardness, ammoniacal nitrogen and COD. Daoud (2020) evaluated the ability mixture of natural zeolite and granular activated carbon in treatment of Fe, Cu, Zn and Pb from landfill leachate-contaminated groundwater. Paliulis (2016) tested the chemically modified and natural zeolite consisting of mordenite and clinoptilolite minerals in the reduction of formaldehyde by the adsorption process. El-Naas et al. (2010) evaluated the performance of locally prepared date-pit activated carbon for the removal of COD from petroleum refinery wastewater. Malik (2004) used the mahogany sawdust to develop carbon adsorbent for the reduction of direct dyes from textile wastewater. Nekoo and Fatemi (2013) employed Granular activated carbon for the removal of COD. However, there is no researcher appearing the simultaneous treatment of oil content, COD, TPH contents and turbidity in produced water by unmodified activated carbon and zeolites (natural and synthetic).
The aim of this study is to investigate the ability of several adsorbents (activated carbon, natural zeolites and synthetic zeolite type X) and the comparison between them in the treatment of produced water (removal of oil content, COD, TPH contents and turbidity). The reduction of these contaminated is necessary to meet the requirements set by the Iraqi Central Organization for Standardization and Quality Control and World Health Organization (WHO). In addition, the adsorption kinetics, isotherm behaviors were studied and the thermodynamic parameters were calculated as well.
Materials and methods
Materials
Natural zeolite (clinoptilolite) utilizing in this work was supplied from Atcholding Company Iran, and powdered activated carbon and synthetic zeolite type X were purchased from Sigma-Aldrich Company. Before carrying out the experiments, the two types of zeolite were washed several time with distilled water and then dried in an oven at 110 °C for 24 h. Sodium hydroxide [NaOH, purity ≥ 97%] and hydrochloric acid (HCl, purity ≥ 98%)] were obtained from Sigma-Aldrich Company. The crude oil (light oil) and clay (bentonite) were supplied from the Petroleum Research and Development Center in the Oil Ministry of Iraq. The X-ray fluorescence method was utilized to determine the chemical composition of adsorbents, and the Brunauer–Emmet–Teller method was used to determine the surface area of the adsorbents. The values of other properties were determined as well, and the results are summarized in Table S1.
Synthetic produced water
Chemicals were added to 1000 mL distilled water, such as clay materials (bentonite 4 g), crude oil (light oil 0.1 g) and salt (NaCl 100 g), to prepare the synthetic produced water in order to adjust the properties of the PW for this research. The oil value and synthetic PW turbidity were set to become equivalent to the parameters (oil content, turbidity and salt content) of the natural PW which was taken from the Southern Oil Company in Basra, Iraq. The light oil and bentonite were mixed with distilled water by stirred for 15 min at high speed (27,000 rpm) to obtain a regular diffusion of light oil and bentonite. The characteristics of the synthetic PW utilized in this research are summarized in Table S2.
Batch adsorption methods
The experiments of batch adsorption were executed in a 150-ml conical glass flask filled with 100 ml PW, and 0.03–0.3 g adsorbents were added to the water. The glass flask was placed onto a mechanistic shaker instrument (Water Bath Shaker Heidolph Unimax 1010 model) used to mix the PW with adsorbents and set at 200 rpm speed. In order to follow the concentration of the residual pollutant, the sample withdrawn by pipette and then put in a centrifugal instrument for 10 min at 4500 rpm. Then, the adsorbent was separated from the sorbate. Figure 1 shows a schematic view of an experimental apparatus including the shaker water bath model (WisdBath) and centrifuge.
The pollutants remaining in the treated water were analyzed by using special analytical instruments for each pollutants using (Oil Content Analyzer) HORIBA instrument model OCMA-350 to measure oil content in PW. The turbidity meter that used in the measurements of the samples turbidities during the experiments was Lovibond Turb Direct model/serial number12/1805 with a measurement unit NTU (nephlometric turbidity unit), and COD was measured by using COD instrument model Lovibond SN11/25370. Adsorption time ranged from 10 to 90 min and the pH range was 2–10. The pH meter used in this work allows measuring pH, EC (conductivity) and TDS (model MW801). Various concentrations of oil (Co = 50 – 1000 ppm) and COD (Co = 1357 – 26,890 ppm) at 25 °C were applied to studied the adsorption isotherm models. And the range of temperature from 10 to 55 °C was applied to conduct the adsorption experiments thermodynamic. The percentage of removal efficiency and the amount of pollutant adsorbed by the adsorbents were calculated by the following equations:
where Co and Ce are the initial and equilibrium concentrations of pollutants in PW, respectively; qe is the amount of pollutant adsorbed at equilibrium, V is the volume of solution and m is the mass of the adsorbents utilized.
Results and discussion
The effects of adsorbents dose on the oil, COD removal efficiencies and decrease in turbidity are illustrated in Figure S1. As shown, the removal efficiency increases with an increase in the adsorbent dose up to 0.25 g. This can be explained by the introduction of more binding/sorption sites and larger specific surface area. However, further increase in the dose of adsorbent (> 0.25 g) does not result in additional removal, and it remains almost constant or decreasing, which could be attributed to saturation of the binding sites (Mohan and Gandhimathi 2009). The initial oil and COD concentrations of the PW were 100 ppm and 2508 ppm, respectively. Depending on dosage addition studies, it was discovered that using 0.03–0.3 g/100 mL PAC and CNZ at pH = 7, for 30 min, it is capable of adsorbing up to 87.2 percent of the initial oil content, 79.1% of the initial COD content and 98.15 percent of the initial turbidity (at 0.3 g PAC dose /100 mL). At 0.3 g CNZ dose/100 mL addition, the removal efficiency reached up to 74.6% for the oil, 49.92% for the COD and 98.85% for the turbidity.
At 100 ppm oil concentration and 1357 ppm COD concentration, the effect of time on the adsorption of pollutants (oil, COD and turbidity) by PAC and CNZ was studied, and the results are shown in Figure S2.
Figure S2 shows that the removal efficiency increasing with increased time and the adsorption included two important phases; the primary quick uptake phase was followed by a relatively slow uptake phase before reached to equilibrium. This can be explained due to the availability of a large number of vacant surface sites for adsorption, but with increased time, fewer available sites on the adsorbent surface for adsorption were hard to be occupied because of the repulsive forces between the molecules of organic pollutant on adsorbents. The adsorption reached the equilibrium within approximately 60 min and 50 min when PAC and CNZ adsorbents were used with oil removal efficiencies reaching up to 94.8% and 77.7% for PAC and CNZ, respectively. The COD removal efficiencies reached up to 87.4% and 53.18% for PAC and CNZ, respectively, while the turbidity removal efficiencies reached up to 98.96% for PAC and 99.53% for CNZ.
The pH plays an essential role in the adsorption of oil, COD and turbidity by PAC and CNZ adsorbents, and it affects the surface properties and binding sites present on the surface of the adsorbents (Ibrahim et al. 2009). In this experiment, optimal adsorbent dose was mixed with 100 mL of PW at pH values that ranged from 2 to 10. The optimal times of 50 and 60 min were set during the experiments. The desired pH values of PW were obtained using 0.1 N HCl and 0.1 N NaOH. In Figure S3, it can be noted that the removal efficiency of pollutants increases with decreasing in the pH. The maximum oil removal was 97.85% and 83.9%, the COD removal was 93.78% and 60.12% and the removal of turbidity was 99.48% and 99.8% at pH = 2 for PAC and CNZ adsorbents, respectively. High efficiency was obtained at low pH; this is due to the electrostatic attractions between the organic pollutants molecules and protonated binding sites on the surface of the adsorbent. This results in high removal efficiency at pH = 2 (Chiou and Li 2003).
The influences of oil concentrations (Co = 50 −100 ppm) and COD concentrations (Co = 1357 − 26,890 ppm) on the adsorption of oil and COD and turbidity on PAC and CNZ adsorbents were investigated at the equilibrium time. Figure S4 shows that the oil removal percentage decreased from 99.58 to 80.43% over PAC and from 84.8 to 71.02% over CNZ. The COD removal decreased from 95.87 to 67.15% over PAC and from 63.74 to 29.02% over CNZ. The turbidity removal decreased from 99.65 to 62.36 and from 99.91 to 73.24% over PAC and CNZ, respectively. These results refer that the adsorption of pollutants are affected by the concentration because it provides the major driving force to overcome mass transfer limitations between the adsorbent and adsorbate (Younis et al. 2015). At low concentrations, occupation of active binding sites involves adsorption, and it is a quick process, but at high concentrations, the active binding sites became saturated and more mass transfer from the liquid to solid phase happened by valence forces through participation, exchange of electrons and the complex forming which is a relatively slow process (Ho and McKay 1999).
One of the most important factors which could have a significant impact on the oil and COD removal and on decrease in the turbidity from produced water is the temperature. Figure S5 shows that the oil, COD and turbidity removal efficiency increased on increasing the temperature from 15 to 55 °C at high oil and COD concentrations. The increase in the oil removal percentage is due to the decrease in the viscosity of oil, where with the decreases in oil viscosity, the oil uptake of the sorbent increases (Li. 2013). Furthermore, as the temperature rises, the rate of diffusion of adsorbate molecules across the external boundary layer and into the internal pores of the adsorbent particles increases due to a decrease in solution viscosity. As a result, a change in temperature will alter the adsorbent's equilibrium capacity for a specific adsorbate (Ya-Li et al. 2008). However, at low concentration there was no change in the removal efficiency when the temperature increased because the effect of temperature at low concentration hardly can be observed.
Adsorption isotherm models
The adsorption isotherm provides a relation between the total mass of adsorbed adsorbate per unit mass of sorbent at constant ambient conditions. In order to develop adsorption isotherms, adsorption experiments were performed. In these experiments, the amount of adsorbent was kept constant, while the initial concentration of the adsorbate was varied. Langmuir adsorption isotherm and Freundlich adsorption isotherm are the most common isotherms which are used for adsorption studies (Metcalf & Eddy et al. 2003). The equilibrium data were correlated utilized Langmuir Eq. (3), Freundlich Eq. (4) and Temkin Eq. (5) isotherms.
where qe is the amount of the substance adsorbed at equilibrium per amount of adsorbent; qmax is the saturation monolayer adsorption capacity, Ceq is the equilibrium concentration, b is the Langmuir equilibrium adsorption constant, Kf and n are the Freundlich constants and bT is the Temkin equilibrium adsorption constant.
The parameters of the isotherm models (Langmuir, Freundlich and Temkin) are given in Table S3. A comparison between the correlation coefficients R2 obtained from Langmuir, Freundlich and Temkin models indicates that the experimental data fit well to the Freundlich model. As well, 0 < 1/n < 1 refers that the adsorption of pollutants (oil and COD) by PAC and CNZ is an appropriate process. Similar results have been obtained by Abdelwahab et al. (2021).
Adsorption thermodynamics
Figure S6 shows with increasing the temperature that the adsorption capacity of oil and COD by PAC and CNZ increased, demonstrating the adsorption process endothermic nature, which is further illustrated from the calculated positive value of ΔHo. As shown in Table S4, the positive value of ΔSo indicates the reversible characteristic of the adsorption of oil and COD over PAC and CNZ. ΔGo values were positive indicating that the adsorption process led to an increase in Gibbs free energy. Positive ΔGo values of oil and COD over CNZ indicate the non-spontaneity of the adsorption process, and the negative ΔGo value of oil and COD over PAC indicates the adsorption process was spontaneous.
Analysis of adsorption kinetics
The kinetics of oil and COD adsorption over PAC and CNZ were studied at 25 °C. The two types of kinetics models, pseudo-first-order and pseudo-second-order, were applied in experiments adsorption to determine the model that fits the data (Febrianto et al. 2009). The linear forms of the equations can be written as in Eqs. (6) and (7).
where qt is the amount of pollutants adsorbed at a given time (mg/g), qe is the amount of pollutants adsorbed at equilibrium (mg/g), k1 is the rate constant of pseudo-first-order (1/min) and k2 is the rate constant of pseudo-second-order (g/mg min).
Table S5 lists the pseudo-first- and pseudo-second-order kinetic models parameters values from them plots Fig. 8 reveal that the latter model fits the data well as compared to the former model. The R2 value for the pseudo-second-order kinetic model was higher than that of pseudo-first-order kinetic model.
The best operational conditions of adsorption for removal oil, turbidity, chemical oxygen demand (COD) and total petroleum hydrocarbon (TPH)
On the basis of data summarized in Tables S6 and S7, it can be seen that good results were achieved for treatment of PW by monitoring the turbidity, oil, TPH and COD removal efficiencies by using natural and synthetic adsorbents. Tables S6 and S7 show the maximum removal efficiency of oil, COD and TPH by using PAC. At the same time, both types of zeolites exhibited high decrease in turbidity. Furthermore, the zeolites were less effective than PAC for removal of organic pollutants by batch adsorption. The lowest COD removal efficiency was observed over CNZ. Also the concentration of pollutants was within the regulatory limit by using PAC adsorbent. This is due to the difference in the adsorbents surface area. PAC has a larger surface area than the CNZ.
Desorption studies
The desorption step is deemed one of the most significant features of the adsorption process, which can decrease the cost of the process. Wherefore, adsorbents reuse experiments were conducted. Electric thermal treatment was applied for CNZ and XSZ at 700 °C, whereas the chemical treatment for PAC was utilized after each run, and then, those were reused in the next run under the same conditions. The results obtained with regenerated and recycled adsorbents are shown in Table S8. This means that adsorbents can be regenerated and reused efficiently.
Conclusions
Batch adsorption experiments for the adsorption of chemical oxygen demand (COD), oil and turbidity from produced water (PW) have been executed utilizing powdered activated carbon (PAC) and clinoptilolite natural zeolite (CNZ) adsorbents. Batch experiment showed that the oil, COD and turbidity removal efficiencies increase on increasing the contact time, adsorbents dosage and temperature, and decrease with the increase in pH and initial oil and COD concentrations. The adsorption experiments appeared that Freundlich isotherm model and a pseudo-second-order kinetic model were best fitted for adsorption of oil and COD over adsorbents and have high correlation value. At optimum parameters in adsorption process, the best removal efficiencies of oil, COD, TPH and turbidity were 99.58%, 95.87%, 99.84% and 99.65% over PAC. In case of CNZ, those were 84.8%, 63.74%, 85.06% and 99.91%, and in case of XSZ, the values were to 91.08%, 80.32%, 93.57% and 99.97%, respectively. The results show that PAC can be used with higher effectiveness for oil, COD and TPH removal from POW but XSZ exhibited the best efficiency in turbidity reduction. PAC, CNZ and XSZ can be well regenerated and can be effectively reused for the treatment of PW. Scale-up and pilot plant experiments are required for commercialization of experimental results in order to provide a complete picture of the feasibility of industrial applications.
Abbreviations
- CNZ:
-
Clinoptilolite natural zeolite
- COD:
-
Chemical oxygen demand
- PAC:
-
Powdered activated carbon
- PW:
-
Produced water
- TDS:
-
Total dissolved solid
- TPH:
-
Total petroleum hydrocarbon
- WHO:
-
Word Health Organization
- XSZ:
-
Synthetic zeolite type X
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Acknowledgements
The authors would like to say thanks to the staff of Petroleum Research and Development Center of Oil Ministry of Iraq and the staff of University of Isfahan for their support during conducting this work.
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All authors, including Eman Hashim Khader, Thamer Jassim Mohammed, Nourollah Mirghaffari, Ali Dawood Salman, Juzsakova Tatjána, Abdullah Adnan Thamer, state that they do not have a conflict of interest.
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Khader, E.H., Mohammed, T.J., Mirghaffari, N. et al. Removal of organic pollutants from produced water by batch adsorption treatment. Clean Techn Environ Policy 24, 713–720 (2022). https://doi.org/10.1007/s10098-021-02159-z
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DOI: https://doi.org/10.1007/s10098-021-02159-z