Removal of methylene red from aqueous solution by adsorption on treated and untreated red Kotta powder
In the present work, the building waste material Red Kotta was treated with sulphuric acid and formaldehyde and used as an adsorbent for the removal of Methylene red from aqueous solution. The adsorption characteristics of Methylene red dye on untreated and treated Red Kotta powder was evaluated as a function of pH, adsorbent dose, initial concentration of adsorbate, contact time and temperature. The effective adsorption was found to be in pH range 2 to7, adsorbent dose 1gm to 5 gm, initial concentration (100ppm to 500ppm) and temperature range (283K to 313K). The results show that Red Kotta powder holds a great potential in removal of Methylene red dye from industrial wastewater.
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Syntheses and spectroscopic characterizations of some vanillin schiff bases as potential metal chelators
New vanillin Schiff bases (A1-A6) have been prepared. The Schiff bases were synthesized via condensation of vanillin with various substituted anilines. Compounds A1-A4 came out as crystals of different colours while A5-A6 were obtained as thick viscous liquid. The organic compounds were characterized by IR spectra, UV/Visible spectra and melting points measurements. Purity of the new compounds was revealed by their sharp melting points. The coordination feasibility of the compounds was tested using compound A1 with Zn2+, Cu2+, Co2+ and Ni2+ salts.
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Synthesis, spectroscopic characterization and In-vitro antibacterial properties of some metal(II) complexes of schiff bases containing aminoindane moiety
New VO(IV), Mn(II), Co(II) and Ni(II) complexes of the Schiff bases, 2-[(2,3-dihydro-1H-inden-4-ylimino)methyl]-5-nitrophenol (HL1) and 3-[2,4-dihydro-1H-inden-4-ylimino) methyl]napthalen-2-ol (HL2) have been synthesized and characterized by elemental analysis, molar conductance, infrared and electronic spectral measurements. The purity of the ligands is confirmed by microanalyses and 1HNMR. The IR spectra show that the ligands are bidentate coordinating via azomethine N and napthalenol/phenol O atoms, and the metal complexes of HL1 exhibit geometric isomerism being in the Cis-form with a lone vC=N band. The metal complexes all assume a 4-coordinate tetrahedral/square planar geometry with exception of the VO(IV) complex which is 5-coordinate square-pyramidal as corroborated by electronic spectra. None is an electrolyte in nitromethane. The Schiff base, HL2, and its metal complexes have higher molar absorptivities of the ligand bands than HL1 and its metal complexes; due to a closer metal to ligand overlap, a consequence of extended conjugation in the naphthalene ring. The in-vitro antibacterial activities of these complexes and their Schiff bases against Staphylococcus aureus, Bacillus cereus, Escherichia coli, Proteus mirabilis, Klebsiella oxytoca and Pseudomonas aeruginosa shows that HL1 and its metal complexes are more active than HL2 and its metal complexes, and the latter compounds have selective inactivity against Bacillus cereus and Klebsiella oxytoca. It is note worthy that [CoL1]2 exhibited broad-spectrum antibacterial activity like the antibiotic ciprofloxacin (26.0-30.5 mm), although with smaller inhibitory zones in the range 12.5-17.0 mm.
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Ethanol stem extract of costus lucanusianus as a novel ecofriendly corrosion inhibitor for mild steel and aluminium in HCl
Corrosion inhibition of ethanol stem extract of Costus lucanusianus (ESECL) was studied on mild steel and aluminium by weight loss method. The constituents of the extract identified by Gas Chromatography-Mass Spectroscopy (GC-MS) were forty one (41) compounds with 13-Octadecenal, (Z)-(14.39 %) and 9-Octadecenoic acid, 12-hydroxy-, methyl ester, [R-(Z)]- (11.49 %) as the major compounds. Weight loss method revealed that as the concentration of inhibitor increased, the corrosion rate decreased and inhibition efficiency increased. Maximum corrosion inhibition efficiencies of 91% and 85% were obtained in 1 g/l concentration at low temperatures for mild steel and aluminium, respectively. The adsorption followed physisorption mechanism. Positive values of ?H suggested that the process was endothermic, and negative values of ?S suggested a decrease in the disorderliness of the system from thermodynamic approach. The adsorption model showed that Freundlich adsorption isotherm was the best fit for the process.
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Influence of post harvest processing conditions on yield and quality of Curcuma longa (L.) ground rhizomes produced in Benin
Studies were carried out to evaluate the effect of post harvest processing conditions on yield and quality of Curcuma longa (L.) rhizomes infusettes. A material balance was determined for four production processes including or not peeling and blanching. Sliced and dried rhizomes were packaged on tea bags and the products quality was monitored using reference methods. Production yields ranged from 38.39 to 76.87% with higher values obtained from unpeeled and blanched rhizomes. The moisture content varyed from 3.15 to 3.75 % m/m with a significant difference (P< 0.05) between the peeled and blanched samples which got lower values compared to the others. Microbiological analyses revealed that all samples were of satisfactory quality. Phytochemical screening showed that the presence or absence of metabolites was not influenced by these processing conditions. Peel removal caused mass loss of 33% without blanching but the tea bags obtained from this process had higher intensity of yellow-orange color. Peeling, blanching and drying were operations that affect not only the yield but also the quality of Curcuma longa (L.) rhizomes infusettes.
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Mineralogical and elemental analysis of hendrina fly ash
Coal is the major source of electricity in South Africa and a large volume of coal fly ash waste is generated by the thermal fired power stations which have become a serious environmental issue because of the problem of the disposal. The aim of this research is to assess the quality and beneficiation of the coal fly ash samples. The fly ash sample was characterized using analytical techniques such as X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy. The morphology of the fly ash is spherical and the XRD identified mullite, gypsum, magnetite, lime, quartz and hematite mineral phases. The elemental composition of the fly ash using XRF containing major elements: SiO2, Al2O3, Fe2O3, CaO, while the minor elements are P2O5, SO3, MgO, NaO, TiO2, and V2O5. The result shows that the coal fly ash sample is class C ash with high pozzolanic properties that is suitable to be used for making concrete or cement.
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New spectrophotometric methods for the determination of Entacapone in bulk and pharmaceutical dosage forms
Two simple and sensitive spectrophotometric methods (Method A& Method B) in the visible region have been developed for determination of Entacapone in bulk and pharmaceutical formulations. Method A is based on Oxidation of Entacapone with Fe(III) under controlled experimental conditions followed by complex formation between Fe(II) and bathophenanthroline to give red colored complex which can be measured at 535 nm. Method B (p-nitroaniline) is based on electrophilic aromatic substitution to form brown colored complex which can be measured at 470 nm. The color obeyed Beer’s law in the concentration range of 2-10 ?g/ml for Method A and 10-50 ?g/ml for Method B respectively. When Pharmaceutical formulations (Tablets) containing Entacapone were analyzed, the results obtained by proposed methods are in good agreement with labeled amounts. Recovery in both methods was 98%-102%.
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Polyphenol constituents of different extract of Lepidium .sativum seed by High-Performance Liquid Chromatography (HPLC) against pathogenic microorganism
Lepidium sativum Polyphenol constituents of (aqueous, ethyl acetate and petroleum ether) seed extracts were examined by HPLC, the aqueous extract contained 17 compounds were 3,4,5-trihydroxybenzoic acid (gallic acid), 3(3,4-Dihydroxycinnamoyl)quinate (Chlorogenic acid), (2R,3S)-2-(3,4Dihydroxphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol (Catechin), 1,3,7-Trimethylpurine-2,6-dione (caffeine), 3,4-Dihydroxycinnamic acid (Coffeic acid), 4-Hydroxy-3,5-dimethoxy benzoic acid (Syringic acid), Rutin, Benzene-1,2-diol (Pyro catechol), 4,4,5,5,6,6-Hexahydroxydiphenic acid 2,6,2,6-dilactone (Ellagic acid), 4-Hydroxycinnamic (Coumaric acid), 4-Hydroxy-3-methoxy benzaldehyde (Vanillin), hydroxycinnamic acid (Ferulic acid), 5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one(Naringenin), Proply 3,4.5-trihydroxybenzoate(PropylGallate),4`.7-DihdroxyisoFlavone, 2-(3,4dihyoxyphenyl-3.5.7-trihydroxy-4H-chromen-4-one, (Quercetin), (2E)-3-phenylprop-2-enoic acid (Cinnamic Acid). The Lepidium sativum ethyl acetate and petroleum ether seed extract contained 13 compounds were 3,4,5-trihydroxy benzoic acid (gallic acid), 3(3,4-Dihydroxycinnamoyl)quinate (Chlorogenic acid), (2R,3S)-2-(3,4Dihydroxphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol(Catechin),1,3,7-Trimethylpurine-2,6dione(caffeine), 4-Hydroxy-3,5-dimethoxybenzoic acid (Syringic acid), Rutin, 4,4,5,5,6,6-Hexahydroxydiphenic acid 2,6,2,6-dilactone (Ellagic acid),4-Hydroxycinnamic (Coumaric acid), 4-Hydroxy-3-methoxy benzaldehyde (Vanillin), hydroxycinnamic acid (Ferulic acid), 5,7-Dihydroxy-2-(4-hydroxyphenyl)chromn-4-one (Naringenin), 2-(3,4-dihyoxyphenyl-3.5.7-trihydroxy-4H-chromen-4-one,(Quercetin) (2E)-3-phenylprop-2-enoic acid (Cinnamic Acid). The four type of different pathogenic bacteria ( Salmonella typhimurium, Pseudomonas aeruginosa, Escherichia coli, and Bacillus cereus0, treated with different seed extract of Lepidium sativum ( Aqueous, ethyl acetate, petroleum ether) by Mueller Hinton Agar and measuring inhibition zone (diameter mm), show that there were significant differences among bacteria and different method of extract. All different Lepidium sativum seed extract (aqueous, ethyl acetate, and petroleum ether) have high activity against Candida albicans fungus. The study was conducted to identify the Lepidium sativum polyphenol Compound and the activity against bacteria and fungi
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Synthesis, characterization and antimicrobial evaluation of mixed ligand complexes of Ni(ii) and Co(ii) 1,2,3-triazole with thiocyanate
The metal complexes of Co2+ and Ni2+ 1,2,3-triazole mixed ligand have been synthesized. The synthesized complexes in different ratios have been characterized by element chemical analysis, molar conductance and Uv-visible and FTIR spectroscopic studies. IR spectra data suggests the involvement of sulphur and nitrogen in coordination to the central metal ions. On the basis of spectral studies and elemental analysis, a tetrahedral geometry was assigned for the nickel complexes while dimerization was suspected for cobalt(II) complexes. The free ligand and metal complexes were tested in vitro against a number of microorganisms (fungi and bacteria) in order to assess their microbial properties. They are found to be proactive against fungi and bacteria upon the metal complexes, nickel complexes performed better than the cobalt complees.
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Precipitation of barium sulphate from sulphate-rich acid mine drainage
Sulphate-rich acid mine drainage (AMD) generated by some mining industries is a serious issue to water treatment industry operators and the South African government. The aim of carrying this study is to reduce if not completely remove the high concentration of sulphate in the AMD by using reagent grade chemical barium chloride. Precipitation technique was used to synthesize barium sulphate from sulphate-rich acid mine water with the addition of barium chloride solution to form a white precipitate. The precipitate formed was characterized using analytical techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HTREM), Fourier transform infra-red (FTIR) spectroscopy and Brunauer-Emmett-Teller (BET). Synthesized barium sulphate was compared with reagent grade synthesized BaSO4 was characterize with XRD to identify the mineral phase, while SEM and HRTEM revealed similar morphology and the BET surface area for both synthesized and reagent grade barium sulphate crystals were determined to be 7.7 m2/g and 68 m2/g. The results from this study shows that sulphate in the acid mine water can be used to synthesize barium sulphate.
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