Performance of cobalt oxide/carbon cloth composite electrode in energy generation from dairy wastewater using microbial fuel cells

Abstract

The use of non-noble metal catalyst as electrode for energy harvesting device have drawn great deal of attention owing to its distinct features. In this work, cobalt oxide has been directly fabricated on carbon cloth substrates using simple cost effective Successive Ionic Layer Adsorption and Reaction. Cobalt oxide synthesized from Co (II) nitrate and NaOH was used as the electrode for generation of electricity from dairy wastes using Microbial Fuel Cells (MFC). Electrochemical characteristics such as cyclic voltammetry have been carried out for the cobalt oxide/carbon cloth and the obtained results are found to be a good alternative for platinum catalyst. A current of 0.15 mA was obtained at an external resistance of 2 kΏ. A single cell prototype of double chamber MFC is designed and the performance analysis is carried out in this work.

Introduction

Microbial Fuel Cells (MFC) is an alternative energy source that produces electricity in a bioelectrochemical way [1,2,3,4,5,6]. Because of this, the MFC finds applications in various fields like powering a low power sensor and wastewater treatment of industrial effluents, among others. The catalyst plays a vital role in the MFCs for improving their power density and current density [7,8,9,10]. Materials, like metal oxides and activated carbon, are all used as the coating materials for electrodes to improve the performance of MFCs [11]. Many modified stainless steel anode materials have been reported, e.g., zinc-cobalt coated in mild steel [12, 13], graphene oxide modified anode [14], polyaniline modified stainless steel anode [15], and polypyrrole coated anode for corrosion resistance [16] which give some limited performance than the carbon electrode materials. Stainless steel electrodes have the drawback of high internal resistance and corrosion effect. On the other hand, activated carbon materials have also been used for the anode and cathode electrode from various forms of the waste materials like the rubber tires [17], sewage sludge [18], etc. Modified carbon materials show good result than the bare carbon electrodes [19, 20]. Metal oxide coated with carbon material provides improvement in the performance of the MFCs. Platinum coated with carbon is one of the most successful combinations of the metal oxides with good electrochemical behavior. Platinum utilized as catalyst in the MFC can be supplanted by non-noble metals such as metal oxides [21, 22] which are inexpensive substitutes to platinum. However, the use of platinum in electrode material is costly than other metal oxides. Many metals such as nickel, graphene, Fe, Zn and Co are coated in the carbon electrode of the MFC. Cobalt oxide is one of the low cost metal oxides and has the ability to increase its surface area when coated on the electrode. This electrode is employed for the treatment of dairy waste and also improves the power density and current density of MFC. Synthesis of cobalt oxide for the oxygen reduction reaction in the cathode was depicted by Xia e al [23]. for a single chamber MFC and only used in the cathode side. In this work, cobalt oxide is coated on carbon cloth for both anode and cathode electrodes in double chamber MFC.

Industrial effluent like dairy waste water is treated in MFC to produce the electricity. Dairy waste water is rich in organic substrate which is a much suitable wastewater for the production of electricity. In addition, potassium ferricyanide is added in the cathode side of the MFC as an electron acceptor for improving the voltage output as investigated by others [24]. The concentration of the potassium ferricyanide is varied to investigate the output performance of the dairy based – Double Chamber MFC (DB-DCMFC) [7].

Materials and methods

MFC construction

The DB-DCMFC is constructed with plexiglass with a dimension of 6 × 12 × 8 cm with a total volume of 500 mL. The schematic of the DB-DCMFC is shown in Fig. S1 in Supplemental Information. Both the electrodes for the anode and cathode are made up of carbon cloth and copper wire is attached to the cloth. Cobalt oxide is coated with the carbon cloth and utilized in both anode and cathode side of the MFC. The two chambers are provided with inlet and outlet paths for refilling and releasing the wastewater after use. Nitrogen gas is purged into the anodic chamber to ensure anaerobic environment and it is airtight to make sure that air will not oxidize the electrons on the anode side.

The two chambers of the MFC are separated by Nafion membrane which is also called Proton Exchange Membrane and is used to allow only the hydrogen ions into the cathode chamber. Here the carbon cloth coated with cobalt oxide is directly utilized in the inoculum from the dairy wastewater for acquiring the electrons. The block diagram of the MFC process is shown in Fig. S2.

Electrode preparation

A variety of materials is used as the electrodes in MFCs. In this present study carbon cloth electrode is used with the double chamber MFC using dairy wastewater as the influent. Cobalt oxide is coated on carbon cloth using Successive Ionic Layer Adsorption and Reaction (SILAR) technique and it is used as electrode in the DB-DCMFC. Initially 0.05 M of Co (II) nitrate was dissolved in 100 mL of double distilled water and stirred in magnetic stirrer until cobalt completely dissolves in water. Similarly, 0.05 M of NaOH is dissolved in 100 mL of double distilled water and stirred well using magnetic stirrer. Anionic solution (1 M) of Co (II) nitrate hexahydrate and cationic solution (1 M) of NaOH were coated in the carbon cloth material with the help of SILAR coating system for 25 cycles at a dip time interval of 40 s each in the Co (II) nitrate and NaOH. After 25 cycles of coating the carbon cloth, it turned into light brown color due to the cobalt coating on the carbon cloth. The loading of cobalt oxide after coating is 156 mg cm^− 2 by using weight gain method. The electrode preparation part is depicted in the block diagram as shown in Fig. S2.

Microorganisms and medium

Bacteria in the dairy wastewater are utilized as the biocatalysts for the generation of electricity. Dairy wastewater from the local dairy industry in Tiruchirappalli, Tamil Nadu, India is taken and analyzed for pH, Biological Oxygen Demand (BOD) and Chemical Oxygen Demand (COD). The pH range for this dairy waste water is from 7.0 to 8.5, COD ranges from 1200 to 1589 mg L^− 1, BOD ranges from 850 to 983 mg L^− 1 and total dissolved solids ranges from 1000 to 1200 mg L^− 1 at the room temperature.

Experimental conditions

In the two chamber of the DB-DCMFC, one chamber on the left hand side is chosen as the anode chamber, 270 mL dairy wastewater inoculum is filled with carbon cloth as the anode and the cathode chamber on the right hand side of the MFC is supplied with open air and potassium ferricyanide initially of 0.05 M added. After this operation, the catholyte concentration is varied and the output is recorded till the voltage is exhausted. Another setup of the same parameters for dairy wastewater with cobalt oxide coated carbon cloth is taken. The same procedures are repeated for this setup also. The hydrogen ions from the anode side will penetrate through the membrane and combine with the oxygen to produce water molecules. When the voltage level reduces, the chamber is refilled with the wastewater. The hardware setup of the DB-DCMFC is shown in Fig. S3.

Electrical measurements

The output voltage (V) of the MFC is measured using the precision multimeter and is noted for every 30 min. Both the open circuit voltage and closed circuit voltage with three different resistances values are measured respectively.

The power (P) and current (I) are calculated using Ohm’s law Eqs. (1) and (2).

$$ I=\frac{V}{R_{ext}} $$

(1)

$$ P=\frac{V^2}{R_{ext}} $$

(2)

Where R_ext is the external resistance connected to the circuit. The external resistances values are varied from 50 Ω to 2 kΩ and the output voltage values are recorded and utilized to draw the polarization curve. The power density and current density are calculated with the surface area of the electrode. The pH of the substrate is monitored time to time with the help of the pH meter to ensure the appropriate value of pH. The internal resistances are measured by the polarization slope method. The MFC will discharge the electrons until the organisms are present in the inoculum after which it is changed with fresh wastewater and the MFC takes an hour to attain the steady state.

Results and discussion

The dairy wastewater is loaded in the anode side of the double chamber MFC and potassium ferricyanide solution of 0.05 M intial concentration on the cathode side of the MFC. Both the electrodes are at equal distance from the membrane inside the chamber since the distance plays a significant factor for the change in power density [22]. The distance should be as much as low as possible to attain a higher power density. The maximum open circuit voltage obtained is 370 mV in the DB-DCMFC with plain carbon cloth as the anode on the second day of the operation. Fresh wastewater is replaced after it comes to the lowest point of voltage drop value of 60 mV. The open circuit potential of the modified carbon cloth electrode is 750 mV which is twice as much as the plain carbon cloth electrode. The open circuit characteristic of MFC is shown in the Fig. 1. After every 20 h of operation the voltage of the MFC is dropped. The wastewater is refilled with new inoculum in which the MFC reactor will take some time to regain to its higher point of voltage. The open circuit voltage is the total potential that the MFC can produce without any resistive load connected across the anode and cathode.

Fig. 1

Characteristics between open circuit potential (OCP) and time for plain carbon electrode and modified electrode

Characteristics at different loading rates

A curve based on changing the values of the external resistance is plotted with the function of voltage and current. The resitance value is varied from 50 Ω to 2 kΩ as shown in the Fig. 2 for both coated and non-coated carbon electrode. The value of resistance is changed in descending order because of the solidity of the voltage in the DB-DCMFC. The maximum current generation can be observed at the lower value of the resistance because of release of more electrons. The current and voltage curves against the resistance look inversely proportional to each other. The voltage starts increasing as the resistance increases and attains a value of 560 mV as shown in the Fig. 2 for the coated carbon cloth with a corresponding current value of 0.15 mA at closed circuit condition.

Fig. 2

Characteristics of voltage and current with respect to resistance for non- coated and coated electrode

The value of voltage is low when the value of resistance is less due to the liberation of more electrons and a maximum current generation of 2.5 mA is obtained at the minimum value of resistance of 0.1 kΏ. The current as per the Ohm’s law starts decreasing as the resistance increases; it has a maximum current of 2.4 mA at very low resistance value. For this maximum current of 2.4 mA the closed circuit voltage is 146 mV was generated in the DB-DCMFC.

The polarization and the power density curves predict the essential influence in the performance of the DB-DCMFC. The curve drawn between the current density and the voltage is called as the polarization curve in which the value of the voltage is higher at lower current density. This shows that both the parameters are inversely proportional to each other. A peak value of 560 mV is obtained at the current density of 6.3 mA m^− 2 as shown in Fig. 3. Also the power density increases as the current density increases up to a critical value of 80 mW m^− 2 after which it starts decaying as shown in the Fig. 3. This shows that the power density will decay after certain value of current density.

Fig. 3

Plots of voltage and power density against current density

Electrochemical evaluation of electrodes

Bioelectrochemical behavior of MFC under variable loading conditions was determined by adopting Cyclic-voltammetry (CV). This evaluates the redox activities of the components involved in bio-chemical system in solution and the components bound to the bacteria in dairy wastewater. This is helpful in finding the electro-active species of the effluent. The CV for plain carbon cloth electrode and cobalt oxide coated carbon cloth electrode was analyzed as shown in Fig. 4. The electron transfer to the electrode is 60 mA for the modified electrode which is much higher than the bare carbon cloth electrode and it shows the oxidation peak at a potential of 0.5 V against Standard Calomel Electrode (SCE) and the reduction peak at 0.125 V against SCE. The scanning rate for the CV test is 0.10 V s^− 1. The oxidation and the reduction reactions improved because of the effective interaction between the cobalt oxide and carbon cloth electrode. This shows that the Co (II) nitrate shows good electrochemical activity over the electrode surface [20]. Table 1 compares different electrodes and their output current densities. In this DB-DCMFC shows some good current density value of 0.00064 mA cm^− 2 comparatively shown good performance with other form of electrode used in the MFC. The power density and the current showed a better improvement for the cobalt oxide coated carbon cloth electrode.

Fig. 4

Cyclic-voltammetry characteristics for plain carbon cloth and coated carbon cloth

Table 1 Comparison of output for different electrode setup

Influence of variation in potassium ferricyanide concentration

The change in catholyte concentration influences the value of power density due to the change in the kinetics of reaction occurring in the solution. Potassium ferricyanide is a good electron acceptor which increases the power generation. The concentration is varied as 0.5, 1.0 and 1.5 M along with phosphate buffer (K₂HPO₄ & KH₂PO₄) in equal molar volume. The test was conducted based on the variation in concentration of potassium ferricyanide and the pH is maintained to 7.5. The maximum open circuit voltages of the 0.5, 1.0 and 1.5 M are 650, 655 and 640 mV, respectively. For more than 1.5 M potassium ferricyanide concentration, the voltage is depleted.

The voltage level of the DB-DCMFC with various concentrations of the catholyte is in a decreasing fashion from the maximum value as the current density increases. For 0.1 M concentration of the potassium ferricyanide at the cathode side, a low value of current density at 2 mA m^− 2 with the peak voltage of 655 mV was observed as shown in Fig. 5. The voltage levels of 582 and 543 mV are obtained for 0.05 and 0.15 M concentrations, respectively. The peak power density observed in this type of design is 170 mW m^− 2 at a current density of 590 mA m^− 2 for the catholyte concentration of 0.1 M as shown in Fig. 6.

Fig. 5

Polarization curve for different concentrations of pottasium ferricyanide catholyte

Fig. 6

Power density characteristics against current denstiy for different concentrations of pottasium ferricyanide catholyte

Conclusions

A two-chamber MFC with metal oxide modified electrodes in dairy wastewater was investigated. This study showed that some non-negligible amount of energy could in fact be recovered, and this could perhaps have been further increased with more aggressive process management. However, in addition to the generation and recovery of electric energy, MFCs have some additional advantages over traditional biological treatment processes, whether aerobic or anaerobic.

A comparison is made between the plain carbon cloth electrode and cobalt oxide coated carbon cloth electrode. Cobalt oxide coated in the carbon electrode improved the power density of the MFC. In this type of MFC the voltage produced is 630 mV by a single cell of the MFC. This paper gives the method to generate electricity from dairy wastes and the performance improvement of the double chamber MFC with respect to the power density and voltage. The performance of this MFC can be improved in the future by improving the MFC output to an increased level for different low power applications.