Displaying publications 101 - 120 of 150 in total

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  1. Solar photocatalytic degradation of mono azo methyl orange and diazo reactive green 19 in single and binary dye solutions: adsorbability vs photodegradation rate
    Ong SA, Min OM, Ho LN, Wong YS
    Environ Sci Pollut Res Int, 2013 May;20(5):3405-13.
    PMID: 23114839 DOI: 10.1007/s11356-012-1286-1
    The objective of this study was to examine the effects of adsorbability and number of sulfonate group on solar photocatalytic degradation of mono azo methyl orange (MO) and diazo Reactive Green 19 (RG19) in single and binary dye solutions. The adsorption capacity of MO and RG19 onto the TiO₂ was 16.9 and 26.8 mg/g, respectively, in single dye solution, and reduced to 5.0 and 23.1 mg/g, respectively, in the binary dye solution. The data obtained for photocatalytic degradation of MO and RG19 in single and binary dye solution were well fitted with the Langmuir-Hinshelwood kinetic model. The pseudo-first-order rate constants of diazo RG19 were significant higher than the mono azo MO either in single or binary dye solutions. The higher number of sulfonate group in RG19 contributed to better adsorption capacity onto the surface of TiO₂ than MO indicating greater photocatalytic degradation rate.
    Matched MeSH terms: Azo Compounds/chemistry*
  2. Characterization of TiO(2)-chitosan/glass photocatalyst for the removal of a monoazo dye via photodegradation-adsorption process
    Zainal Z, Hui LK, Hussein MZ, Abdullah AH, Hamadneh IM
    J Hazard Mater, 2009 May 15;164(1):138-45.
    PMID: 18809254 DOI: 10.1016/j.jhazmat.2008.07.154
    In this paper, the newly explored TiO(2)-Chitosan/Glass was suggested as a promising alternative material to conventional means of wastewater treatment. Characterization of TiO(2)-Chitosan/Glass photocatalyst was studied with SEM-EDX, XRD, and Fourier transform infrared spectroscopy (FTIR) analysis. The combination effect of photodegradation-adsorption process for the removal of methyl orange (MO), an acid dye of the monoazo series occur promisingly when four layers of TiO(2)-Chitosan/Glass photocatalyst was used for MO removal. Approximately, 87.0% of total MO removal was achieved. The reactive -NH(2), -OH, and metal oxide contents in the prepared photocatalyst responsible for the photodegradation-adsorption effect were confirmed by FTIR study. Similarly, MO removal behavior was well supported by SEM-EDX and XRD analysis. Significant dependence of MO removal on the TiO(2)-Chitosan loading can be explained in terms of relationship between quantum yield of photocatalytic reactions and photocatalyst structure/activity. Hence, the research work done thus far suggests a new method, having both the advantages of photodegradation-adsorption process in the abatement of various wastewater pollutants.
    Matched MeSH terms: Azo Compounds/isolation & purification*
  3. Preparation and characterization of tungsten-loaded titanium dioxide photocatalyst for enhanced dye degradation
    Saepurahman, Abdullah MA, Chong FK
    J Hazard Mater, 2010 Apr 15;176(1-3):451-8.
    PMID: 19969415 DOI: 10.1016/j.jhazmat.2009.11.050
    Tungsten-loaded TiO(2) photocatalyst has been successfully prepared and characterized. TEM analysis showed that the photocatalysts were nanosize with the tungsten species forming layers of coverage on the surface of TiO(2), but not in clustered form. This was confirmed by XRD and FT-Raman analyses where tungsten species were well dispersed at lower loading (<6.5 mol%), but were in crystalline WO(3) at higher loadings (>12 mol%). In addition, loading with tungsten could stabilize the anatase phase from transforming into inactive rutile phase and did not shift the optical absorption to the visible region as shown by DRUV-vis analysis. PZC value of TiO(2) was found at 6.4, but the presence of tungsten at 6.5 mol% WO(3), decreased the PZC value to 3. Tungsten-loaded TiO(2) was superior to unmodified TiO(2) with 2-fold increase in degradation rate of methylene blue, and equally effective for the degradation of different class of dyes such as methyl violet and methyl orange at 1 mol% WO(3) loading.
    Matched MeSH terms: Azo Compounds/chemistry
  4. Adsorption of direct dye on palm ash: kinetic and equilibrium modeling
    Ahmad AA, Hameed BH, Aziz N
    J Hazard Mater, 2007 Mar 6;141(1):70-6.
    PMID: 16887263
    Palm ash, an agriculture waste residue from palm-oil industry in Malaysia, was investigated as a replacement for the current expensive methods of removing direct blue 71 dye from an aqueous solution. The experimental data were analyzed by the Langmuir and Freundlich models of adsorption. Equilibrium data fitted well with Freundlich model in the range of 50-600mg/L. The equilibrium adsorption capacity of the palm ash was determined with the Langmuir equation and found to be 400.01mg dye per gram adsorbent at 30 degrees C. The rates of adsorption were found to conform to the pseudo-second-order kinetics with good correlation. The results indicate that the palm ash could be employed as a low-cost alternative to commercial activated carbon.
    Matched MeSH terms: Azo Compounds/chemistry*
  5. Electrochemical-assisted photodegradation of dye on TiO2 thin films: investigation on the effect of operational parameters
    Zainal Z, Lee CY, Hussein MZ, Kassim A, Yusof NA
    J Hazard Mater, 2005 Feb 14;118(1-3):197-203.
    PMID: 15721544
    Electrochemical-assisted photodegradation of methyl orange has been investigated using TiO2 thin films. The films were prepared by sol-gel dip-coating method. Several operational parameters to achieve optimum efficiency of this electrochemical-assisted photodegradation system have been tested. Photoelectrochemical degradation was studied using different light sources and light intensity. The light sources chosen ranged from ultraviolet to visible light. The effect of agitation of the solution at different speeds has also been studied. Slight improvement of photodegradation rate was observed by applying higher agitation speed. Investigation on the electrode after repeated usages show the electrode can be reused up to 20 times with percentage of deficiency less than 15%. The study on the effect of solution temperature indicated that the activation energy of the methyl orange degradation is 18.63 kJ mol(-1).
    Matched MeSH terms: Azo Compounds/chemistry*
  6. Adsorption of methyl orange from aqueous solution onto calcined Lapindo volcanic mud
    Jalil AA, Triwahyono S, Adam SH, Rahim ND, Aziz MA, Hairom NH, et al.
    J Hazard Mater, 2010 Sep 15;181(1-3):755-62.
    PMID: 20538408 DOI: 10.1016/j.jhazmat.2010.05.078
    In this study, calcined Lapindo volcanic mud (LVM) was used as an adsorbent to remove an anionic dye, methyl orange (MO), from an aqueous solution by the batch adsorption technique. Various conditions were evaluated, including initial dye concentration, adsorbent dosage, contact time, solution pH, and temperature. The adsorption kinetics and equilibrium isotherms of the LVM were studied using pseudo-first-order and -second-order kinetic equations, as well as the Freundlich and Langmuir models. The experimental data obtained with LVM fits best to the Langmuir isotherm model and exhibited a maximum adsorption capacity (q(max)) of 333.3 mg g(-1); the data followed the second-order equation. The intraparticle diffusion studies revealed that the adsorption rates were not controlled only by the diffusion step. The thermodynamic parameters, such as the changes in enthalpy, entropy, and Gibbs free energy, showed that the adsorption is endothermic, random and spontaneous at high temperature. The results indicate that LVM adsorbs MO efficiently and could be utilized as a low-cost alternative adsorbent for the removal of anionic dyes in wastewater treatment.
    Matched MeSH terms: Azo Compounds/isolation & purification*
  7. A simple method to screen for azo-dye-degrading bacteria
    Syed MA, Sim HK, Khalid A, Shukor MY
    J Environ Biol, 2009 Jan;30(1):89-92.
    PMID: 20112868
    A stab-culture method was adapted to screen for azo dyes-decolorizing bacteria from soil and water samples. Decolorized azo dye in the lower portion of the solid media indicates the presence of anaerobic azo dyes-decolorizing bacteria, while aerobic decolorizing bacteria decolorizes the surface portion of the solid media. Of twenty soil samples tested, one soil sample shows positive results for the decolourisation of two azo dyes; Biebrich scarlet (BS) and Direct blue 71 (DB) under anaerobic conditions. A gram negative and oxidase negative bacterial isolate was found to be the principal azo dyes degrader The isolate was identified by using the Biolog identification system as Serratia marcescens.
    Matched MeSH terms: Azo Compounds/metabolism*
  8. Determination of para-arsanilic acid with improved diazotization reaction using differential pulse cathodic stripping voltammetry in aqueous system
    Misni M, Sathishkumar P, Ahamad R, MohdYusoff AR
    Environ Technol, 2015;36(17):2249-54.
    PMID: 25749108 DOI: 10.1080/09593330.2015.1025105
    Para-arsanilic acid (p-ASA) has been widely used in the poultry industry to promote growth and prevent dysentery. It is excreted unchanged in the manure and released into non-target sites causing organoarsenic pollution risk to the environment and living system. Therefore, simple and effective analytical strategies are demanded for determining the samples that contain p-ASA. However, direct determination of both p-ASA and ortho-arsanilic acid (o-ASA) using differential pulse cathodic stripping voltammetry (DPCSV) gives the similar voltammograms that directly hamper the analysis used by the DPCSV technique. In this study, a method to determine and differentiate p-ASA from o-ASA via diazotization and coupling reaction of the amine groups followed by the direct DPCSV determination of diazo compounds is presented. The diazotization reaction carried out at pH 1.5 and 0 ± 1°C for 10 min showed two reduction peaks in DPCSV at-70 mV and -440 mV vs. Ag/AgCl (KCl 3 M). However, when the diazotization reaction was performed at pH 12.5 and 0 ± 1°C for 40 min, a coloured azo compound was produced and the DPCSV showed only one reduction peak that appeared at -600 mV vs. Ag/AgCl (3 M of KCl). The results of this study show that only p-ASA compound gave a reduction peak, whereas o-ASA compound did not give any peak. The detection limit of p-ASA was found to be 4 × 10(-8 )M. As a result, the proposed electro-analytical technique might be a good candidate to determine and differentiate the p-ASA present in the poultry and environmental samples.
    Matched MeSH terms: Azo Compounds/analysis
  9. Fulltext Enhancement of Treatment Efficiency of Recalcitrant Wastewater Containing Textile Dyes Using a Newly Developed Iron Zeolite Socony Mobil-5 Heterogeneous Catalyst
    Ahmad M, Asghar A, Abdul Raman AA, Wan Daud WM
    PLoS One, 2015;10(10):e0141348.
    PMID: 26517827 DOI: 10.1371/journal.pone.0141348
    Fenton oxidation, an advanced oxidation process, is an efficient method for the treatment of recalcitrant wastewaters. Unfortunately, it utilizes H2O2 and iron-based homogeneous catalysts, which lead to the formation of high volumes of sludge and secondary pollutants. To overcome these problems, an alternate option is the usage of heterogeneous catalyst. In this study, a heterogeneous catalyst was developed to provide an alternative solution for homogeneous Fenton oxidation. Iron Zeolite Socony Mobile-5 (Fe-ZSM-5) was synthesized using a new two-step process. Next, the catalyst was characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy, fourier transform infrared spectroscopy, and Brunauer-Emmett-Teller analysis and tested against a model wastewater containing the azo dye Acid Blue 113. Results showed that the loading of iron particles reduced the surface area of the catalyst from 293.59 to 243.93 m2/g; meanwhile, the average particle size of the loaded material was 12.29 nm. Furthermore, efficiency of the developed catalyst was evaluated by performing heterogeneous Fenton oxidation. Taguchi method was coupled with principal component analysis in order to assess and optimize mineralization efficiency. Experimental results showed that under optimized conditions, over 99.7% degradation and 77% mineralization was obtained, with a 90% reduction in the consumption of the developed catalyst. Furthermore, the developed catalyst was stable and reusable, with less than 2% leaching observed under optimized conditions. Thus, the present study proved that newly developed catalyst has enhanced the oxidation process and reduced the chemicals consumption.
    Matched MeSH terms: Azo Compounds/chemistry*
  10. Biosorption and biodegradation of Acid Orange 7 by Enterococcus faecalis strain ZL: optimization by response surface methodological approach
    Lim CK, Bay HH, Aris A, Abdul Majid Z, Ibrahim Z
    Environ Sci Pollut Res Int, 2013 Jul;20(7):5056-66.
    PMID: 23334551 DOI: 10.1007/s11356-013-1476-5
    Reactive dyes account for one of the major sources of dye wastes in textile effluent. In this study, decolorization of the monoazo dye, Acid Orange 7 (AO7) by the Enterococcus faecalis strain ZL that isolated from a palm oil mill effluent treatment plant has been investigated. Decolorization efficiency of azo dye is greatly affected by the types of nutrients and the size of inoculum used. In this work, one-factor-at-a-time (method and response surface methodology (RSM) was applied to optimize these operational factors and also to study the combined interaction between them. Analysis of AO7 decolorization was done using Fourier transform infrared (FTIR) spectroscopy, desorption study, UV-Vis spectral analysis, field emission scanning electron microscopy (FESEM), and high performance liquid chromatography (HPLC). The optimum condition via RSM for the color removal of AO7 was found to be as follows: yeast extract, 0.1% w/v, glycerol concentration of 0.1% v/v, and inoculum density of 2.5% v/v at initial dye concentration of 100 mg/L at 37 °C. Decolorization efficiency of 98% was achieved in only 5 h. The kinetic of AO7 decolorization was found to be first order with respect to dye concentration with a k value of 0.87/h. FTIR, desorption study, UV-Vis spectral analysis, FESEM, and HPLC findings indicated that the decolorization of AO7 was mainly due to the biosorption as well as biodegradation of the bacterial cells. In addition, HPLC analyses also showed the formation of sulfanilic acid as a possible degradation product of AO7 under facultative anaerobic condition. This study explored the ability of E. faecalis strain ZL in decolorizing AO7 by biosorption as well as biodegradation process.
    Matched MeSH terms: Azo Compounds/analysis; Azo Compounds/metabolism*
  11. Fulltext Thermodynamic and spectroscopic investigation of interactions between reactive red 223 and reactive orange 122 anionic dyes and cetyltrimethyl ammonium bromide (CTAB) cationic surfactant in aqueous solution
    Irfan M, Usman M, Mansha A, Rasool N, Ibrahim M, Rana UA, et al.
    ScientificWorldJournal, 2014;2014:540975.
    PMID: 25243216 DOI: 10.1155/2014/540975
    The present study describes the conductometric and spectroscopic study of the interaction of reactive anionic dyes, namely, reactive red 223 and reactive orange 122 with the cationic surfactant cetyltrimethyl ammonium bromide (CTAB). In a systematic investigation, the electrical conductivity data was used to calculate various thermodynamic parameters such as free energy (ΔG), enthalpy (ΔH), and the entropy (ΔS) of solubilization. The trend of change in these thermodynamic quantities indicates toward the entropy driven solubilization process. Moreover, the results from spectroscopic data reveal high degree of solubilization, with strong interactions observed in the cases of both dyes and the CTAB. The spontaneous nature of solubilization and binding was evident from the observed negative values of free energies (ΔG p and ΔG b).
    Matched MeSH terms: Azo Compounds/analysis*; Azo Compounds/metabolism
  12. Decolourisation of Acid Orange 7 recalcitrant auto-oxidation coloured by-products using an acclimatised mixed bacterial culture
    Bay HH, Lim CK, Kee TC, Ware I, Chan GF, Shahir S, et al.
    Environ Sci Pollut Res Int, 2014 Mar;21(5):3891-906.
    PMID: 24293297 DOI: 10.1007/s11356-013-2331-4
    This study focuses on the biodegradation of recalcitrant, coloured compounds resulting from auto-oxidation of Acid Orange 7 (AO7) in a sequential facultative anaerobic-aerobic treatment system. A novel mixed bacterial culture, BAC-ZS, consisting of Brevibacillus panacihumi strain ZB1, Lysinibacillus fusiformis strain ZB2, and Enterococcus faecalis strain ZL bacteria were isolated from environmental samples. The acclimatisation of the mixed culture was carried out in an AO7 decolourised solution. The acclimatised mixed culture showed 98 % decolourisation within 2 h of facultative anaerobic treatment using yeast extract and glucose as co-substrate. Subsequent aerobic post treatment caused auto-oxidation reaction forming dark coloured compounds that reduced the percentage decolourisation to 73 %. Interestingly, further agitations of the mixed culture in the solution over a period of 48 h significantly decolourise the coloured compounds and increased the decolourisation percentage to 90 %. Analyses of the degradation compounds using UV-visible spectrophotometer, Fourier transform infrared spectroscopy (FTIR) and high performance liquid chromatography (HPLC) showed complete degradation of recalcitrant AO7 by the novel BAC-ZS. Phytotoxicity tests using Cucumis sativus confirmed the dye solution after post aerobic treatment were less toxic compared to the parent dye. The quantitative real-time PCR revealed that E. faecalis strain ZL was the dominant strain in the acclimatised mix culture.
    Matched MeSH terms: Azo Compounds/metabolism*; Azo Compounds/toxicity
  13. Effect of degree of deacetylation of chitosan on adsorption capacity and reusability of chitosan/polyvinyl alcohol/TiO2 nano composite
    Habiba U, Joo TC, Siddique TA, Salleh A, Ang BC, Afifi AM
    Int J Biol Macromol, 2017 Nov;104(Pt A):1133-1142.
    PMID: 28690164 DOI: 10.1016/j.ijbiomac.2017.07.007
    The chitosan/polyvinyl alcohol/TiO2 composite was synthesized. Two different degrees of deacetylation of chitosan were prepared by hydrolysis to compare the effectiveness of them. The composite was analyzed via field emission scanning electron microscopy, Fourier transform infrared, X-ray diffraction, thermal gravimetric analysis, weight loss test and adsorption study. The FTIR and XRD results proved the interaction among chitosan, PVA and TiO2 without any chemical reaction. It was found that, chitosan with higher degree of deacetylation has better stability. Furthermore, it also showed that higher DD of chitosan required less time to reach equilibrium for methyl orange. The adsorption followed the pseudo-second-order kinetic model. The Langmuir and Freundlich isotherm models were fitted well for isotherm study. Adsorption capacity was higher for the composite containing chitosan with higher DD. The dye removal rate was independent of the dye's initial concentration. The adsorption capacity was increased with temperature and it was found from reusability test that the composite containing chitosan with higher DD is more reusable. It was notable that adsorption capacity was even after 15 runs. Therefore, chitosan/PVA/TiO2 composite can be a very useful material for dye removal.
    Matched MeSH terms: Azo Compounds
  14. Fulltext Free standing zirconia nanotubes formation and their photocatalytic properties
    Syahriza Ismail, Nurul Izza Soaid, Suriyati Mohamed Ansari, Nurulhuda Bashirom, Monna Rozana, Tan, Wai Kian, et al.
    Malaysian Journal of Microscopy, 2016;12(1):20-23.
    MyJurnal
    In the formation of ZrO2 (zirconia) nanotubes (ZNTs) by anodisation of zirconium, a balance between chemical etching at the surface of the nanotubes and inward growth inside the nanotubes is required. This can be achieved by using fluorinated organic electrolyte like ethylene glycol with the addition of small volume of oxidant. In this work, carbonate was selected as the oxidant and NH4F as the source of fluoride for chemical etching process. Two sets of electrolytes were studied EG/fluoride/Na2CO3 and EG/fluoride/K2CO3. It appears that in the presence of carbonate evolution of gas at the anode during the anodisation process was rather severe. The gas which is likely to be CO2 was found to weaken the adherence between the oxide film with the underlying Zr foil. This induced the formation of free standing ZNTs. High Resolution Transmission Electron Microscope (HRTEM) was used to investigate the crystallinity of the nanotubes where the majority crystal phase of ZNTs was tetragonal/cubic. The ZNTs were used as photocatalysts to oxidize methyl orange dye.
    Matched MeSH terms: Azo Compounds
  15. Fulltext Adsorption of acid dyes onto Zinc Chloride-Modified Cocoa (Theobroma Cacao) pod Husk-based carbon
    Nur Aqilah Zainal, Shariff Ibrahim, Borhannuddin Arifin
    Pertanika Journal of Science & Technology, 2017;25(103):129-138.
    MyJurnal
    An agricultural waste, the cocoa pod husk was chemically modified using a dehydrating agent, zinc chloride (ZnCl2), carbonised and used for the remediation of acid dyes in an aqueous solution. The targeted acid dyes are: (i) Acid Violet 17 (AV17); (ii) Acid Yellow 36 (AY36); and (iii) Acid Blue 29 (AB29). The physicochemical properties of the zinc chloride-modified cocoa pod husk-based carbon (ZCPHC) were characterised by ash content, bulk density, pH slurry, pHpzc and Field Emission Scanning Electron Microscopy (FESEM) and Energy Dispersive X-Ray (EDX) analysis. The bulk density and ash content of the prepared carbon is 0.55 g cm-1 and 7.0% respectively. The photograph of SEM shows distinct changes at the ZCPHC carbon surface as it has large pores formed due to ZnCl2 modification. The adsorption tests were performed in a batch adsorption system using an aqueous solution of the understudy acid dyes. The influence of pH and dose of an adsorbent on the acid dye uptake was investigated and discussed. The adsorption was in favour at acidic condition with maximum removal observed at pH 2. The removal efficiency of the aqueous acid dye solution increased with the increase in adsorbent dosage. The kinetic experiment showed equilibrium time is less than 40 minutes and the kinetic data for all three understudy acid dyes fitted well with the pseudo-second-order model with a correlation coefficient (R2) values above 0.98.
    Matched MeSH terms: Azo Compounds
  16. Design, Synthesis, SAR Study, Antimicrobial and Anticancer Evaluation of Novel 2-Mercaptobenzimidazole Azomethine Derivatives
    Tahlan S, Narasimhan B, Lim SM, Ramasamy K, Mani V, Shah SAA
    Mini Rev Med Chem, 2020;20(15):1559-1571.
    PMID: 30179132 DOI: 10.2174/1389557518666180903151849
    BACKGROUND: Various analogues of benzimidazole are found to be biologically and therapeutically potent against several ailments. Benzimidazole when attached with heterocyclic rings has shown wide range of potential activities. So, from the above provided facts, we altered benzimidazole derivatives so that more potent antagonists could be developed. In the search for a new category of antimicrobial and anticancer agents, novel azomethine of 2-mercaptobenzimidazole derived from 3-(2- (1H-benzo[d]imidazol-2-ylthio)acetamido)benzohydrazide were synthesized.

    RESULTS AND DISCUSSION: The synthesized analogues were characterized by FT-IR, 1H/13C-NMR and MS studies as well C, H, N analysis. All synthesized compounds were evaluated for in vitro antibacterial activity against Gram-positive (B. subtilis), Gram-negative (E. coli, P. aeruginosa, K. pneumoniae and S. typhi) strains and in vitro antifungal activity against C. albicans and A. niger strains by serial dilution method, the minimum inhibitory concentration (MIC) described in μM/ml. The in vitro anticancer activity of synthesized compounds was determined against human colorectal carcinoma cell line (HCT- 116) using 5-fluorouracil as standard drug.

    CONCLUSION: In general, most of the synthesized derivatives exhibited significant antimicrobial and anticancer activities. Compounds 8, 10, 15, 16, 17, 20 and 22 showed significant antimicrobial activity towards tested bacterial and fungal strains and compound 26 exhibited significant anticancer activity.

    Matched MeSH terms: Azo Compounds/chemical synthesis; Azo Compounds/pharmacology; Azo Compounds/chemistry*
  17. Fulltext Removal of methyl orange dye by manganese/aluminium-layered double hydroxide
    Mamat, M., Abdullah, M.A.A., Jaafar, A.M., Soh, S.K.C., Lee, C.E.
    ASM Science Journal, 2018;11(101):105-113.
    MyJurnal
    As textile production flourishes nowadays, the amount of dyed wastewater entering the
    water body has also increased. Dyes could have serious negative impacts to the environment
    and also the human health, hence, they need to be removed from the water body. In this
    study, layered double hydroxide (LDH) of manganese/aluminium (MnAl) was synthesised
    to be used as a potential adsorbent to remove methyl orange (MO) dye due to its unique
    lamellar structure which provides LDH with high anion adsorption and exchange ability.
    MnAl was synthesized by using co-precipitation method and characterized by powder X-ray
    diffraction (PXRD), Fourier-Transform Infrared Spectroscopy (FTIR), Inductively coupled
    plasma atomic emission spectroscopy (ICP-AES) and Carbon, Hydrogen, Nitrogen, Sulphur
    (CHNS) elemental analysers, and Accelerated Surface Area and Porosity Analyzer (ASAP).
    Adsorption studies were conducted at different contact times and dosages of MnAl to evaluate
    the performance of MnAl in removing MO from water. Kinetic and isotherm models were
    tested using pseudo-first order, pseudo-second order, Langmuir isotherm and Freundlich
    isotherm. MnAl LDH was found to be perfectly fitted into pseudo-second order and Langmuir
    isotherm.
    Matched MeSH terms: Azo Compounds
  18. Fulltext Isolation and characterization of a molybdenum-reducing and Orange G-decolorizing Enterobacter sp. strain Zeid-6 in soils from Sudan
    Othman, A.R., Rahman, M.F., Shukor, M.Y., Abu Zeid, I.M., Ariffin, F.
    Bioremediation Science and Technology Research, 2015;3(2):13-19.
    MyJurnal
    Chemical toxins and organic contaminants such as hydrocarbons and dyes are major global
    contaminants with countless tones of those chemicals are created yearly with a significant
    amount release to the environment. In this work we screen the ability of a molybdenum-reducing
    bacterium isolated from contaminated soil to decolorize various azo and triphenyl methane dyes
    independent of molybdenum reduction. Biochemical analysis resulted in a tentative identification
    of the bacterium as Enterobacter sp. strain Zeid-6. The bacterium was able to decolorize the azo
    dye Orange G. The bacterium reduces molybdate to Mo-blue optimally at pH between 5.5 and
    8.0 and temperatures of between 30 and 37 oC. Other requirements include a phosphate
    concentration of 5 mM and a molybdate concentration of 20 mM. The absorption spectrum of the
    Mo-blue produced was similar to previous Mo-reducing bacterium, and closely resembles a
    reduced phosphomolybdate. Molybdenum reduction was inhibited by copper, lead, mercury and
    silver which showed 36.8, 16.9, 64.9 and 67.6% inhibition to Mo-reducing activity of
    Enterobacter sp. strain Zeid-6, respectively. The resultant molybdenum blue spectrum closely
    resembles the spectrum of molybdenum blue from the phosphate determination method. The
    ability of this bacterium to detoxify molybdenum and decolorize azo dye makes this bacterium
    an important tool for bioremediation.
    Matched MeSH terms: Azo Compounds
  19. Evaluation on the Photocatalytic Degradation Activity of Reactive Blue 4 using Pure Anatase Nano-TiO2
    Joon Ching Juan, Sze Nee Goh, Ta Yeong Wu, Emy Marlina Samsudin, Tan Tong Ling, Sharifah Bee Abd. Hamid
    Sains Malaysiana, 2015;44:1011-1019.
    Disposal of dye wastewater into water streams without treatment endangers human and marine lives. This work focused on the second largest class of textile dyes after azo dyes due to its high resistivity to biodegradation and high toxicity. The photocatalytic degradation of Reactive Blue 4 (RB4), an anthraquinone dye, has been investigated using pure anatase nano titanium (IV) oxide (TiO2). The dye molecules were fully degraded and the addition of hydrogen peroxide (H2O2) enhanced the photodegradation efficiency. It is found that the degradation as the hydroxyl radicals in the bulk solution is sufficient for complete mineralisation. The disappearance of the dye follows pseudo-first-order kinetics. The effect of pH, amount of photocatalyst, UV-light intensity, light source and concentration of hydrogen peroxide was ascertained.
    Matched MeSH terms: Azo Compounds
  20. Characteristics and performance of a mesoporous cerium-aluminum-silver mixed oxide for removal of methyl Violet Dye
    Phatai P, Srisomang R
    Sains Malaysiana, 2016;45:1477-1485.
    In this study, the adsorption efficiency of methyl violet (MV) dye onto Ce0.3Al0.7 and Ce0.3Al0.7Agx (x = 0.1, 0.3 & 0.5) mixed oxides was investigated. The properties of mixed oxide were determined by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), N2 adsorption-desorption isotherm, diffuse reflectance UV-vis spectroscopy (UV-vis DRS) and X-ray absorption near edge structure (XANES). Characterization showed that synthesized mixed oxide with fluorite has a pure cubic structure of a mesoporous nature and a small grain size with rough surface. Batch adsorption experiments were used to study parameters including contact time and initial dye concentration. The results showed that these parameters affected the degree of MV dye adsorption. The dye adsorption of mixed oxides attained equilibrium at 120 min. The equilibrium adsorption data were analyzed using Langmuir, Freundlich and Temkin isotherms. The adsorption behavior of MV dye onto Ce0.3Al0.7 was found to follow the Langmuir isotherm (R2 = 0.9951), providing a maximum monolayer adsorptive capacity of 2.35 mg/g. Alternatively, the adsorption of MV dye onto Ce0.3Al0.7Ag0.1 (R2 = 0.7839), Ce0.3Al0.7Ag0.3 (R2 = 0.9301) and Ce0.3Al0.7Ag0.5 (R2 = 0.9396) followed the Freundlich isotherm. The possible adsorption mechanisms of MV dyes onto the Ce0.3Al0.7 and Ce0.3Al0.7Agx were also discussed.
    Matched MeSH terms: Azo Compounds
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