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Optimal aeration area of cathode electrode in the batch type of microbial fuel cells with non-woven interface

Wang CT, Ubando AT, Wan ML, Ong Tang RC

Chemosphere, 2023 Oct;337:139257.
PMID: 37343634 DOI: 10.1016/j.chemosphere.2023.139257

Microbial fuel cells (MFCs) are based on the biochemical reaction of microorganisms to decompose organic wastewater for converting chemical energy into power energy. MFCs are considered an environmentally friendly technology that is gaining popularity due to their simultaneous digestion and energy production abilities. To enhance its real application in wastewater treatment, this study proposes to use a non-woven material for replacing the usage of expensive membranes in MFCs. In addition, the study aims to consider a series of different aeration areas of cathode electrodes for finding an optional design. Results have shown that the adoption of non-woven with 0.45 μm can effectively prohibit the diffusion of oxygen into the anode chamber. Moreover, the non-woven material played an important role as an interface between the anode and cathode, enhancing the MFC performance. The usage of suitable non-woven material can replace the role of the membrane when applied in real wastewater applications. The results have shown that the case study where a combination of a 50% aeration area of the cathode electrodes with 25% exposure of the cathode plate in the air yielded relatively better aeration in terms of a higher current density of 250 mA/m2, higher power density of 220 mW/m2, and higher open voltage circuit of 0.4 V, compared to other case studies considered. These results indicate the optimal aeration configuration for MFCs applied in commercial wastewater treatment in the future.

Matched MeSH terms: Oxygen/chemistry
Fulltext Exploiting the oxygen inhibitory effect on UV curing in microfabrication: a modified lithography technique

Alvankarian J, Majlis BY

PLoS One, 2015;10(3):e0119658.
PMID: 25747514 DOI: 10.1371/journal.pone.0119658

Rapid prototyping (RP) of microfluidic channels in liquid photopolymers using standard lithography (SL) involves multiple deposition steps and curing by ultraviolet (UV) light for the construction of a microstructure layer. In this work, the conflicting effect of oxygen diffusion and UV curing of liquid polyurethane methacrylate (PUMA) is investigated in microfabrication and utilized to reduce the deposition steps and to obtain a monolithic product. The conventional fabrication process is altered to control for the best use of the oxygen presence in polymerization. A novel and modified lithography technique is introduced in which a single step of PUMA coating and two steps of UV exposure are used to create a microchannel. The first exposure is maskless and incorporates oxygen diffusion into PUMA for inhibition of the polymerization of a thin layer from the top surface while the UV rays penetrate the photopolymer. The second exposure is for transferring the patterns of the microfluidic channels from the contact photomask onto the uncured material. The UV curing of PUMA as the main substrate in the presence of oxygen is characterized analytically and experimentally. A few typical elastomeric microstructures are manufactured. It is demonstrated that the obtained heights of the fabricated structures in PUMA are associated with the oxygen concentration and the UV dose. The proposed technique is promising for the RP of molds and microfluidic channels in terms of shorter processing time, fewer fabrication steps and creation of microstructure layers with higher integrity.

Matched MeSH terms: Oxygen/chemistry*
Stabilized sanitary landfill leachate treatment using anionic resin: treatment optimization by response surface methodology

Bashir MJ, Aziz HA, Yusoff MS, Aziz SQ, Mohajeri S

J Hazard Mater, 2010 Oct 15;182(1-3):115-22.
PMID: 20580491 DOI: 10.1016/j.jhazmat.2010.06.005

The treatability of stabilized sanitary landfill leachate via synthetic anion exchange resin (INDION FFIP MB) was investigated. An ideal experimental design was conducted based on central composite design using a response surface methodology to assess individual and interactive effects of critical operational variables (i.e., anionic dosage; contact time; shaking speed) and pH on treatment performance in terms of color, chemical oxygen demand (COD), suspended solid (SS), and turbidity removal efficiencies. Optimum operational conditions were established as 30.9 cm(3) anionic dosage, 90 min contact time, 150 rpm shaking speed, and pH 3.1. Under these conditions, the color, COD, SS, and turbidity removal efficiencies of 91.5, 70.3, 93.1, and 92.4% were experimentally attained and were found to fit well with the prediction model. According to these results, stabilized leachate treatment using INDION FFIP MB could be an effective alternative in the administration of color, COD, SS, and turbidity problems of landfill leachates.

Matched MeSH terms: Oxygen/chemistry
Molecular dynamics study of anhydrous lamellar structures of synthetic glycolipids: effects of chain branching and disaccharide headgroup

Achari VM, Nguan HS, Heidelberg T, Bryce RA, Hashim R

J Phys Chem B, 2012 Sep 27;116(38):11626-34.
PMID: 22967067

Glycolipids form materials of considerable potential for a wide range of surfactant and thin film applications. Understanding the effect of glycolipid covalent structure on the properties of their thermotropic and lyotropic assemblies is a key step toward rational design of new glycolipid-based materials. Here, we perform molecular dynamics simulations of anhydrous bilayers of dodecyl β-maltoside, dodecyl β-cellobioside, dodecyl β-isomaltoside, and a C(12)C(10) branched β-maltoside. Specifically, we examine the consequences of chain branching and headgroup identity on the structure and dynamics of the lamellar assemblies. Chain branching of the glycolipid leads to measurable differences in the dimensions and interactions of the lamellar assembly, as well as a more fluid-like hydrophobic chain region. Substitution of the maltosyl headgroup of βMal-C(12) by an isomaltosyl moiety leads to a significant decrease in bilayer spacing as well as a markedly altered pattern of inter-headgroup hydrogen bonding. The distinctive simulated structures of the two regioisomers provide insight into the difference of ~90 °C in their observed clearing temperatures. For all four simulated glycolipid systems, with the exception of the sn-2 chain of the branched maltoside, the alkyl chains are ordered and exhibit a distinct tilt, consistent with recent crystallographic analysis of a branched chain Guerbet glycoside. These insights into structure-property relationships from simulation provide an important molecular basis for future design of synthetic glycolipid materials.

Matched MeSH terms: Oxygen/chemistry
Treatment of pulp and paper mill wastewater by polyacrylamide (PAM) in polymer induced flocculation

Wong SS, Teng TT, Ahmad AL, Zuhairi A, Najafpour G

J Hazard Mater, 2006 Jul 31;135(1-3):378-88.
PMID: 16431022

The flocculation performances of nine cationic and anionic polyacrylamides with different molecular weights and different charge densities in the treatment of pulp and paper mill wastewater have been studied. The experiments were carried out in jar tests with the polyacrylamide dosages range of 0.5-15 mg l(-1), rapid mixing at 200 rpm for 2 min, followed by slow mixing at 40 rpm for 15 min and settling time of 30 min. The effectiveness of the polyacrylamides was measured based on the reduction of turbidity, the removal of total suspended solids (TSS) and the reduction of chemical oxygen demand (COD). Cationic polyacrlyamide Organopol 5415 with very high molecular weight and low charge density is found to give the highest flocculation efficiency in the treatment of the paper mill wastewater. It can achieve 95% of turbidity reduction, 98% of TSS removal, 93% of COD reduction and sludge volume index (SVI) of 14 ml g(-1) at the optimum dosage of 5 mg l(-1). SVI values of less than 70 m lg(-1) are found for all polyacrylamide at their respective optimum dosage. Based on the cost evaluation, the use of the polyacrylamides is economically feasible to treat the pulp and paper mill wastewaters. This result suggests that single-polymer system can be used alone in the coagulation-flocculation process due to the efficiency of the polyacrylamide. Sedimentation of the sludge by gravity thickening with settling time of 30 min is possible based on the settling characteristics of the sludge produced by Organopol 5415 that can achieve 91% water recovery and 99% TSS removal after 30 min settling.

Matched MeSH terms: Oxygen/chemistry
The study of dipole moment of some substituted acetic acids in an electronically excited state

Murthy MB, Daya Sagar BS, Patil RL

Spectrochim Acta A Mol Biomol Spectrosc, 2003 Apr;59(6):1277-80.
PMID: 12659896

The electronic absorption spectra of eight substituted acetic acids have been measured at room temperature in several solvents. The ground state dipole moments are evaluated experimentally for these molecules. These ground state values are used in conjunction with the spectral results to evaluate their first electronically excited state dipole moments. For all the molecules investigated here the dipole moments in the excited state are higher than their ground state values.

Matched MeSH terms: Oxygen/chemistry
Feasibility study of sequencing batch reactor system for upgrading wastewater treatment in Malaysia

Al-Shididi S, Henze M, Ujang Z

Water Sci Technol, 2003;48(11-12):327-35.
PMID: 14753553

The objective of this study was to assess the feasibility of the Sequencing Batch Reactor (SBR) system for implementation in Malaysia. Theoretical, field, laboratory investigations, and modelling simulations have been carried out. The results of the study indicated that the SBR system was robust, relatively cost-effective, and efficient under Malaysian conditions. However, the SBR system requires highly skilled operators and continuous monitoring. This paper also attempted to identify operating conditions for the SBR system, which optimise both the removal efficiencies and the removal rates. The removal efficiencies could reach 90-96% for COD, up to 92% for TN, and 95% for SS. An approach to estimate a full operational cycle time, to estimate the de-sludging rate, and to control the biomass in the sludge has also been developed. About 4 hours react time was obtained, as 2.25 hours of nitrification with aerated slow fill and 1.75 hour of denitrification with HAc addition as an additional carbon source. Inefficient settling was one of the problems that affect the SBR effluent quality. The settling time was one hour for achieving Standard B (effluent quality) and 2 hours for Standard A.

Matched MeSH terms: Oxygen/chemistry
Enhanced rhamnolipid production by Pseudomonas aeruginosa USM-AR2 via fed-batch cultivation based on maximum substrate uptake rate

Noh NA, Salleh SM, Yahya AR

Lett Appl Microbiol, 2014 Jun;58(6):617-23.
PMID: 24698293 DOI: 10.1111/lam.12236

A fed-batch strategy was established based on the maximum substrate uptake rate (MSUR) of Pseudomonas aeruginosa USM-AR2 grown in diesel to produce rhamnolipid. This strategy matches the substrate feed rates with the substrate demand based on the real-time measurements of dissolved oxygen (DO). The MSUR was estimated by determining the time required for consumption of a known amount of diesel. The MSUR trend paralleled the biomass profile of Ps. aeruginosa USM-AR2, where the MSUR increased throughout the exponential phase indicating active substrate utilization and then decreased when cells entered stationary phase. Rhamnolipid yield on diesel was enhanced from 0·047 (g/g) in batch to 0·110 (g/g) in pulse-pause fed-batch and 0·123 (g/g) in MSUR fed-batch. Rhamnolipid yield on biomass was also improved from 0·421 (g/g) in batch, 3·098 (g/g) in pulse-pause fed-batch to 3·471 (g/g) using MSUR-based strategy. Volumetric productivity increased from 0·029 g l(-1) h(-1) in batch, 0·054 g l(-1) h(-1) in pulse-pause fed-batch to 0·076 g l(-1) h(-1) in MSUR fed-batch.

Matched MeSH terms: Oxygen/chemistry
Reactive Black 5 as electron donor and/or electron acceptor in dual chamber of solar photocatalytic fuel cell

Khalik WF, Ho LN, Ong SA, Voon CH, Wong YS, Yusuf SY, et al.

Chemosphere, 2018 Jul;202:467-475.
PMID: 29579681 DOI: 10.1016/j.chemosphere.2018.03.113

The role of azo dye Reactive Black 5 (RB5) as an electron donor and/or electron acceptor could be distinguished in dual chamber of photocatalytic fuel cell (PFC). The introduction of RB5 in anode chamber increased the voltage generation in the system since degradation of RB5 might produce electrons which also would transfer through external circuit to the cathode chamber. The removal efficiency of RB5 with open and closed circuit was 8.5% and 13.6%, respectively and removal efficiency for open circuit was low due to the fact that recombination of electron-hole pairs might happen in anode chamber since without connection to the cathode, electron cannot be transferred. The degradation of RB5 in cathode chamber with absence of oxygen showed that electrons from anode chamber was accepted by dye molecules to break its azo bond. The presence of oxygen in cathode chamber would improve the oxygen reduction rate which occurred at Platinum-loaded carbon (Pt/C) cathode electrode. The Voc, Jsc and Pmax for different condition of ultrapure water at cathode chamber also affected their fill factor. The transportation of protons to cathode chamber through Nafion membrane could decrease the pH of ultrapure water in cathode chamber and undergo hydrogen evolution reaction in the absence of oxygen which then increased degradation rate of RB5 as well as its electricity generation.

Matched MeSH terms: Oxygen/chemistry
Estimating the refractive index of oxygenated and deoxygenated hemoglobin using genetic algorithm - support vector regression model

Alade IO, Bagudu A, Oyehan TA, Rahman MAA, Saleh TA, Olatunji SO

Comput Methods Programs Biomed, 2018 Sep;163:135-142.
PMID: 30119848 DOI: 10.1016/j.cmpb.2018.05.029

BACKGROUND AND OBJECTIVES: The refractive index of hemoglobin plays important role in hematology due to its strong correlation with the pathophysiology of different diseases. Measurement of the real part of the refractive index remains a challenge due to strong absorption of the hemoglobin especially at relevant high physiological concentrations. So far, only a few studies on direct measurement of refractive index have been reported and there are no firm agreements on the reported values of refractive index of hemoglobin due to measurement artifacts. In addition, it is time consuming, laborious and expensive to perform several experiments to obtain the refractive index of hemoglobin. In this work, we proposed a very rapid and accurate computational intelligent approach using Genetic Algorithm/Support Vector Regression models to estimate the real part of the refractive index for oxygenated and deoxygenated hemoglobin samples.
METHODS: These models utilized experimental data of wavelengths and hemoglobin concentrations in building highly accurate Genetic Algorithm/Support Vector Regression model (GA-SVR).
RESULTS: The developed methodology showed high accuracy as indicated by the low root mean square error values of 4.65 × 10-4 and 4.62 × 10-4 for oxygenated and deoxygenated hemoglobin, respectively. In addition, the models exhibited 99.85 and 99.84% correlation coefficients (r) for the oxygenated and deoxygenated hemoglobin, thus, validating the strong agreement between the predicted and the experimental results CONCLUSIONS: Due to the accuracy and relative simplicity of the proposed models, we envisage that these models would serve as important references for future studies on optical properties of blood.

Matched MeSH terms: Oxygen/chemistry*
Stability of folic acid under several parameters

Gazzali AM, Lobry M, Colombeau L, Acherar S, Azaïs H, Mordon S, et al.

Eur J Pharm Sci, 2016 Oct 10;93:419-30.
PMID: 27575880 DOI: 10.1016/j.ejps.2016.08.045

Folic acid is a small molecule, also known as vitamin B9. It is an essential compound involved in important biochemical processes. It is widely used as a vector for targeted treatment and diagnosis especially in cancer therapeutics. Nevertheless, not many authors address the problem of folic acid degradation. Several researchers reported their observations concerning its denaturation, but they generally only took into account one parameter (pH, temperature, light or O2etc.). In this review, we will focus on five main parameters (assessed individually or in conjunction with one or several others) that have to be taken into account to avoid the degradation of folic acid: light, temperature, concentration, oxygen and pH, which are the most cited in the literature. Scrupulous bibliographic research enabled us to determine two additional degradation factors that are the influence of singlet oxygen and electron beam on folic acid stability, which are not considered as among the prime factors. Although these two factors are not commonly present as compared to the others, singlet oxygen and electron beams intervene in new therapeutic technologies and must be taken in consideration for further applications such photodynamic or X-rays therapies.

Matched MeSH terms: Oxygen/chemistry
Potential of porous Co3O4 nanorods as cathode catalyst for oxygen reduction reaction in microbial fuel cells

Kumar R, Singh L, Zularisam AW, Hai FI

Bioresour Technol, 2016 Nov;220:537-542.
PMID: 27614156 DOI: 10.1016/j.biortech.2016.09.003

This study aims to investigate the potential of porous Co3O4 nanorods as the cathode catalyst for oxygen reduction reaction (ORR) in aqueous air cathode microbial fuel cells (MFCs). The porous Co3O4 nanorods were synthesized by a facile and cost-effective hydrothermal method. Three different concentrations (0.5mg/cm(2), 1mg/cm(2), and 2mg/cm(2)) of Co3O4 nanorods coated on graphite electrodes were used to test its performance in MFCs. The results showed that the addition of porous Co3O4 nanorods enhanced the electrocatalytic activity and ORR kinetics significantly and the overall resistance of the system was greatly reduced. Moreover, the MFC with a higher concentration of the catalyst achieved a maximum power density of 503±16mW/m(2), which was approximately five times higher than the bare graphite electrode. The improved catalytic activity of the cathodes could be due to the porous properties of Co3O4 nanorods that provided the higher number of active sites for oxygen.

Matched MeSH terms: Oxygen/chemistry*
Role of dissolved oxygen on the degradation mechanism of Reactive Green 19 and electricity generation in photocatalytic fuel cell

Lee SL, Ho LN, Ong SA, Wong YS, Voon CH, Khalik WF, et al.

Chemosphere, 2018 Mar;194:675-681.
PMID: 29247929 DOI: 10.1016/j.chemosphere.2017.11.166

In this study, a membraneless photocatalytic fuel cell with zinc oxide loaded carbon photoanode and platinum loaded carbon cathode was constructed to investigate the impact of dissolved oxygen on the mechanism of dye degradation and electricity generation of photocatalytic fuel cell. The photocatalytic fuel cell with high and low aeration rate, no aeration and nitrogen purged were investigated, respectively. The degradation rate of diazo dye Reactive Green 19 and the electricity generation was enhanced in photocatalytic fuel cell with higher dissolved oxygen concentration. However, the photocatalytic fuel cell was still able to perform 37% of decolorization in a slow rate (k = 0.033 h-1) under extremely low dissolved oxygen concentration (approximately 0.2 mg L-1) when nitrogen gas was introduced into the fuel cell throughout the 8 h. However, the change of the UV-Vis spectrum indicates that the intermediates of the dye could not be mineralized under insufficient dissolved oxygen level. In the aspect of electricity generation, the maximum short circuit current (0.0041 mA cm-2) and power density (0.00028 mW cm-2) of the air purged photocatalytic fuel cell was obviously higher than that with nitrogen purging (0.0015 mA cm-2and 0.00008 mW cm-2).

Matched MeSH terms: Oxygen/chemistry*
Fulltext QuadraPure-supported palladium nanocatalysts for microwave-promoted Suzuki cross-coupling reaction under aerobic condition

Liew KH, Loh PL, Juan JC, Yarmo MA, Yusop RM

ScientificWorldJournal, 2014;2014:796196.
PMID: 25054185 DOI: 10.1155/2014/796196

Cross-linked resin-captured palladium (XL-QPPd) was readily prepared by simple physical adsorption onto the high loading QuadraPure macroporous resin and a subsequent reduction process. To enhance the mechanical stability, entrapped palladium nanocatalysts were cross-linked with succinyl chloride. Both transmission electron microscopy images and X-ray diffraction analysis revealed that the palladium nanoparticles were well dispersed with diameters ranging in 4-10 nm. The catalyst performed good catalytic activity in microwave-promoted Suzuki cross-coupling reactions in water under aerobic condition with mild condition by using various aryl halides and phenylboronic acid. In addition, the catalyst showed an excellent recyclability without significant loss of catalytic activity.

Matched MeSH terms: Oxygen/chemistry
Synthesis of oxygenated fuel additives via the solventless etherification of glycerol

Ayoub M, Khayoon MS, Abdullah AZ

Bioresour Technol, 2012 May;112:308-12.
PMID: 22437049 DOI: 10.1016/j.biortech.2012.02.103

The synthesis of oxygenated fuel additives via solvent freebase-catalyzed etherification of glycerol is reported. The products of glycerol etherification arediglycerol (DG) and triglycerol (TG) with DG being the favorable one. The catalytic activity of different homogeneous alkali catalysts (LiOH, NaOH, KOH and Na(2)CO(3)) was investigated during the glycerol etherification process. LiOH exhibited an excellent catalytic activity during this reaction, indicated by the complete glycerol conversion with a corresponding selectivity of 33% toward DG. The best reaction conditions were a reaction temperature of 240°C, a catalyst/glycerol mass ratio of 0.02 and a reaction time of 6h. The influences of various reaction variables such as nature of the catalyst, catalyst loading, reaction time and reaction temperature on glycerol etherification were elucidated. Industrially, the findings attained in this study might contribute towards promoting the biodiesel industry through utilization of its by-products.

Matched MeSH terms: Oxygen/chemistry*
Decomposition and biodegradability enhancement of textile wastewater using a combination of electron beam irradiation and activated sludge process

Mohd Nasir N, Teo Ming T, Ahmadun FR, Sobri S

Water Sci Technol, 2010;62(1):42-7.
PMID: 20595752 DOI: 10.2166/wst.2010.239

The research conducted a study on decomposition and biodegradability enhancement of textile wastewater using a combination of electron beam irradiation and activated sludge process. The purposes of this research are to remove pollutant through decomposition and to enhance the biodegradability of textile wastewater. The wastewater is treated using electron beam irradiation as a pre-treatment before undergo an activated sludge process. As a result, for non-irradiated wastewater, the COD removal was achieved to be between 70% and 79% after activated sludge process. The improvement of COD removal efficiency increased to 94% after irradiation of treated effluent at the dose of 50 kGy. Meanwhile, the BOD(5) removal efficiencies of non-irradiated and irradiated textile wastewater were reported to be between 80 and 87%, and 82 and 99.2%, respectively. The maximum BOD(5) removal efficiency was achieved at day 1 (HRT 5 days) of the process of an irradiated textile wastewater which is 99.2%. The biodegradability ratio of non-irradiated wastewater was reported to be between 0.34 and 0.61, while the value of biodegradability ratio of an irradiated wastewater increased to be between 0.87 and 0.96. The biodegradability enhancement of textile wastewater is increased with increasing the doses. Therefore, an electron beam radiation holds a greatest application of removing pollutants and also on enhancing the biodegradability of textile wastewater.

Matched MeSH terms: Oxygen/chemistry
Synthesis of fatty acid methyl ester from used vegetable cooking oil by solid reusable Mg 1-x Zn 1+x O2 catalyst

Olutoye MA, Hameed BH

Bioresour Technol, 2011 Feb;102(4):3819-26.
PMID: 21183335 DOI: 10.1016/j.biortech.2010.11.100

Fatty acid methyl ester was produced from used vegetable cooking oil using Mg(1-)(x) Zn(1+)(x)O(2) solid catalyst and the performance monitored in terms of ester content obtained. Used vegetable cooking oil was employed to reduce operation cost of biodiesel. The significant operating parameters which affect the overall yield of the process were studied. The highest ester content, 80%, was achieved with the catalyst during 4h 15 min reaction at 188°C with methanol to oil ratio of 9:1 and catalyst loading of 2.55 wt% oil. Also, transesterification of virgin oil gave higher yield with the heterogeneous catalyst and showed high selectivity towards ester production. The used vegetable cooking oil did not require any rigorous pretreatment. Catalyst stability was examined and there was no leaching of the active components, and its performance was as good at the fourth as at the first cycle.

Matched MeSH terms: Oxygen/chemistry*
Trends in the use of Fenton, electro-Fenton and photo-Fenton for the treatment of landfill leachate

Umar M, Aziz HA, Yusoff MS

Waste Manag, 2010 Nov;30(11):2113-21.
PMID: 20675113 DOI: 10.1016/j.wasman.2010.07.003

Advanced oxidation processes (AOPs) such as Fenton, electro-Fenton and photo-Fenton have been applied effectively to remove refractory organics from landfill leachate. The Fenton reaction is based on the addition of hydrogen peroxide to the wastewater or leachate in the presence of ferrous salt as a catalyst. The use of this technique has proved to be one of the best compromises for landfill leachate treatment because of its environmental and economical advantages. Fenton process has been used successfully to mineralize wide range of organic constituents present in landfill leachate particularly those recalcitrant to biological degradation. The present study reviews the use of Fenton and related processes in terms of their increased application to landfill leachate. The effects of various operating parameters and their optimum ranges for maximum COD and color removal are reviewed with the conclusion that the Fenton and related processes are effective and competitive with other technologies for degradation of both raw and pre-treated landfill leachate.

Matched MeSH terms: Oxygen/chemistry
Treatment of p-nitrophenol in an adsorbent-supplemented sequencing batch reactor

Loo YM, Lim PE, Seng CE

Environ Technol, 2010 Apr 14;31(5):479-87.
PMID: 20480823 DOI: 10.1080/09593330903514482

The objective of this research was to evaluate the treatment ofp-nitrophenol (PNP) as a sole organic carbon source using a sequencing batch reactor (SBR) with the addition of adsorbent. Two types of adsorbents, namely powdered activated carbon (PAC) and pyrolysed rice husk (PRH) were used in this study. Two identical SBRs, each with a working volume of 10 L, were operated with fill, react, settle, draw and idle periods in the ratio of 2:8:1:0.75:0.25 for a cycle time of 12 h. The results showed that, without the addition of adsorbent, increasing the influent PNP concentration to 200 mg/L resulted in the deterioration of chemical oxygen demand (COD) removal efficiency and PNP removal efficiency in the SBRs. Improvement in the performance of the SBR was observed with the addition of PAC. When the dosage of 1.0 g PAC/cycle was applied, COD removal of 95% and almost complete removal of PNP were achieved at the influent PNP concentration of 300 mg/L. The kinetic study showed that the rates of COD and PNP removal can be described by the first-order kinetics. The enhancement of performance in the PAC-supplemented SBR was postulated to be due to the initial adsorption of PNP by the freshly added and the bioregenerated PAC, thus reducing the inhibition on the microorganisms. The PRH was found to be ineffective because of its relatively low adsorption capacity for PNP, compared with that of PAC.

Matched MeSH terms: Oxygen/chemistry
Hexavalent chromium adsorption on impregnated palm shell activated carbon with polyethyleneimine

Owlad M, Aroua MK, Wan Daud WM

Bioresour Technol, 2010 Jul;101(14):5098-103.
PMID: 20156679 DOI: 10.1016/j.biortech.2010.01.135

Removal of Cr(VI) ions from aqueous solution was investigated using modified palm shell activated carbon. Low Molecular Weight Polyethyleneimine (LMW PEI) was used for impregnation purpose. The maximum amount of LMW PEI adsorbed on activated carbon was determined to be approximately 228.2mg/g carbon. The adsorption experiments were carried out in a batch system using potassium dichromate K(2)Cr(2)O(7) as the source of Cr(VI) in the synthetic waste water and modified palm shell activated carbon as the adsorbent. The effects of pH, concentration of Cr(VI) and PEI loaded on activated carbon were studied. The adsorption data were found to fit well with the Freundlich isotherm model. This modified Palm shell activated carbon showed high adsorption capacity for chromium ions.

Matched MeSH terms: Oxygen/chemistry

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