Aluminum electrode modified with manganese hexacyanoferrate as a chemical sensor for hydrogen peroxide

Talanta ◽  
2001 ◽  
Vol 55 (2) ◽  
pp. 395-402 ◽  
Author(s):  
A Eftekhari
2000 ◽  
Vol 404 (2) ◽  
pp. 213-221 ◽  
Author(s):  
Samina S Khan ◽  
Eunsook S Jin ◽  
Neso Sojic ◽  
Paul Pantano

Author(s):  
Savita Dubey ◽  
Amita Joshi ◽  
Rashmi Trivedi ◽  
Parmesh Kumar Chaudhari ◽  
Dharm Pal ◽  
...  

Abstract In the current scenario treatment of industrial waste water is big challenge especially waste water that contain high organic load. Hydrogen peroxide assisted electrocoagulation (EC) process provides better result to treat highly polluted wastewater as compared to EC alone. However, hydrogen peroxide is well known as a strong oxidant, which cast a potential threat to human health. To overcome this problem hydrogen peroxide has been used here for treatment of wastewater in small quantity, and that consume during the process. Therefore the harmful effect of hydrogen peroxide in human and aquatic life could be minimized. This work is an attempt to treat biodigester effluent (BDE) using H2O2 assisted EC processes with respect to chemical oxygen demand (COD) and color reductions. To perform this experiment both iron and aluminum electrodes are used as an electrode material in the presence of H2O2. In case of iron electrode the maximum COD and color reduction efficiency of 98.3 and 83.6% was achieved at the cost of 1.5 Wh/dm3 energy consumption while maximum COD and color removal efficiency of 96.8 and 77.1% with 1.7 Wh/dm3 of energy consumption was observed in the aluminum electrode based EC process. A part from this conventional biological process (i.e., activated sludge treatment, ponds, and lagoon etc.) and physiochemical treatment process (i.e., coagulation, adsorption) provided treatment efficiency of 40–80% hence hydrogen peroxide assisted EC process should a better choice to treat distillery effluent. Furthermore, hybrid EC process was also performed with iron used as anode and aluminum as cathode in the presence of H2O2. Iron electrode based peroxi-EC process provided better result at optimum operating conditions; current density of 114 A/m2, initial COD concentration of 12,000 mg/dm3, initial pH of 7.3, H2O2 concentration of 120 mg/dm3, stirring speed of 120 rpm and electrolysis time of 90 min. The cost estimated for operation is 1.56 US $/m3. Finally, sludge analysis and cost optimization are also incorporated in this article.


Author(s):  
Višnja Oreščanin ◽  
Robert Kollar ◽  
Dražen Vratarić ◽  
Karlo Nadj ◽  
Gordana Medunić ◽  
...  

The work was development and application of the purification system suitable for the treatment of groundwater used for human consumption as well as watering of the plants in the system for the hydroponic cultivation of tomatoes. For that purpose the well water from the 60 m deep water layer situated near the city of Županja (Eastern Croatia) was processed. Most of the measured parameters exceeded upper permissible limit (UPL) for drinking water. The concentrations of the parameters color, turbidity, iron, manganese, arsenic, phosphates, chemical oxygen demand and ammonia were as follows 292±20 mg/PtCo, 21±5 NTU, 1.72±0.34 mg/L, 0.075±0.014 mg/L, 0.074±0.011 mg/L, 10.4±1.7 mg/L, 37±1 mg/L and 1.2±0.1 mg/L, respectively. Due to the complex composition of the treated water, the purification system required the combination of electrochemical treatment, using iron and aluminum electrode plates with simultaneous ozonation followed by post treatment with hydrogen peroxide and ozone. The electrocoagulation/ozonation approach was used for the removal of heavy metals, color, turbidity, phosphates and partially organic matter while the rest of the organic contaminants and ammonia were removed by the treatment with hydrogen peroxide and ozone. Following the combined electrochemical treatment and post treatment with hydrogen peroxide and ozone all measured parameters in the treated water were in agreement with regulated values. The combined treatment resulted in total removal of arsenic, color, turbidity, ammonia and organic contaminants while the removal of other parameters of interest was up to 97.98%.


2021 ◽  
Vol 6 (1) ◽  
pp. 1
Author(s):  
Arwa Laroussi ◽  
Noureddine Raouafi ◽  
Vladimir Mirsky

The fast and selective determination of hydrogen peroxide (H2O2) is of importance not only because of strong interest in this widely applied analyte, but also because of the development of enzymatic biosensors for glucose or other metabolites where the sensor for H2O2 can be used as the transducer. Here, we report on an electrocatalytical amperometric sensor for the detection of H2O2. It is a sensor that consists of a gold electrode covered by a self-assembled monolayer (SAM) with immobilized p-benzoquinone. To provide highly stable immobilization of p-benzoquinone at the distance of effective electron tunneling, a new anchor compound—1,3-dimercaptopropan-2-ol—was synthesized and used for preparation of the SAM. Due to two thiol groups binding gold surface, this compound provides high stability of the SAM. The surface concentration of p-benzoquinone obtained from cyclic voltammetry is 2.5 ± 0.2 × 10−10 mol·cm−2. Cyclic voltammetry and chronoamperometry experiments proved that the immobilized benzoquinone exhibited high electrocatalytic activity towards the decomposition of H2O2. Depending on the used potential range, different sensing modes can be realized. For example, one can measure electrochemical response due to the oxidation of H2O2 at anodic potentials, or due to the reduction of oxygen formed during oxidative decomposition of H2O2. Also, amperometric response at fixed potential of +0.4 V vs. Ag/AgCl corresponding to the oxidation of benzoquinone to hydroquinone was studied. The sensor exhibited a linear response over a concentration range of 0.1–2 mM with a low detection limit of 4.24 µM. The reproducibility of three different electrodes prepared was examined at the H2O2 concentration range from 0.1 till 3 mM, which resulted in a relative standard deviation below 4.2%.


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