scholarly journals TITANIUM OXIDE-OXIFLUORIDE SYNTHESIS AND STUDY OF ITS PHOTOCATALYTIC PROPERTIES

2021 ◽  
Vol 445 (1) ◽  
pp. 151-156
Author(s):  
M. Zh. Zhurinov ◽  
A. Z. Abilmagzhanov ◽  
N. S. Ivanov ◽  
B. B. Teltayev ◽  
A. E. Nurtazina
Keyword(s):  
Ultraviolet Radiation ◽  
Titanium Oxide ◽  
Calibration Graph ◽  
Muffle Furnace ◽  
Solution Ph ◽  
Research Article ◽  
Titanium Compound ◽  
Operating Wavelength ◽  
Metatitanic Acid

The research article discusses a new method for the photocatalyst synthesis based on a mixture of titanium oxide - titanium oxyfluoride. The synthesis was performed by dissolving titanium metal in an acidified solution of ammonium bifluoride, followed by oxidation to the highest oxidation state and hydrolysis with ammonia to obtain metatitanic acid. The decomposition of metatitanic acid was carried out in a muffle furnace at a temperature of 380°C. It was found that during the precipitation of metatitanic acid, the titanium compound with the fluoride ion also passes into the precipitate, which, after calcination, transforms into titanium oxyfluoride. Photocatalytic activity was determined by the oxidation reaction of the methyl orange dye upon irradiation with ultraviolet radiation. The source of ultraviolet radiation was a DRT-125 lamp with a wavelength in the range of 200-400 nm. Suspensions containing 60 mg/L of the dye and various contents of the photocatalyst in the concentration range of 1-7 g/L were subjected to oxidation. The construction of the calibration graph and the determination of the concentrations were carried out on an SF-2000 spectrophotometer at a wavelength of 466.4 nm. The operating wavelength was determined by scanning the solution in the wavelength range of 200-800 nm. It was found that as a result of oxidation, the solution pH shifts to the acidic side to 3.5, which leads to a shift in the wavelength of the maximum absorption; in this regard, the solutions pH was adjusted to the same values.

Determination of diltiazem based on the reduction of Cu(II)–BCA complexes in micellar medium

2010 ◽  
Vol 88 (6) ◽  
pp. 533-539 ◽  
Author(s):  
Larissa Zuppardo Lacerda Sabino ◽  
Daniele Cestari Marino ◽  
Horacio Dorigan Moya
Keyword(s):  
Standard Deviation ◽  
Relative Standard Deviation ◽  
Confidence Level ◽  
Limit Of Detection ◽  
Calibration Graph ◽  
Micellar Medium ◽  
Solution Ph ◽  
Simple Method ◽  
Relative Standard

A simple method was developed for determining microquantities of diltiazem, based on the reduction of copper(II) in buffered solution (pH 7.0) and the use of a micellar medium containing 4,4′-dicarboxy-2,2′-biquinoline acid. The copper(I) produced reacts with 4,4′-dicarboxy-2,2′-biquinoline acid and the complexes formed are spectrophotometrically measured at 558 nm. A typical calibration graph shows good linearity (r = 0.993) from 20 to 100 μg mL–1 of diltiazem. The limit of detection and relative standard deviation were calculated as 12 μg mL–1 (99% confidence level) and 3.5% (40 μg mL–1; n = 6), respectively, with a mean recovery value of 96.5% found in pharmaceutical dosages. A straightforward and effective way to recycle the reagents is addressed. The hazardous aspects of the Cu(I)–BCA reaction are presented as well.

Non-enzymatic determination of purine nucleotides using a carbon dot modified glassy carbon electrode

2019 ◽  
Vol 11 (30) ◽  
pp. 3866-3873 ◽  
Author(s):  
R. Karthikeyan ◽  
D. James Nelson ◽  
S. Abraham John
Keyword(s):  
Glassy Carbon ◽  
Low Cost ◽  
Phosphate Buffer Solution ◽  
Purine Nucleotides ◽  
Buffer Solution ◽  
Solution Ph ◽  
Carbon Dot ◽  
Enzymatic Determination ◽  
Sensitive Determination

Selective and sensitive determination of one of the purine nucleotides, inosine (INO) using a low cost carbon dot (CD) modified glassy carbon (GC) electrode in 0.2 M phosphate buffer solution (pH 7.2) was demonstrated in this paper.

scholarly journals Determination of Finasteride in Tablets by High Performance Liquid Chromatography

2007 ◽  
Vol 4 (1) ◽  
pp. 109-116 ◽  
Author(s):  
K. Basavaiah ◽  
B. C. Somashekar
Keyword(s):  
High Performance ◽  
Internal Standard ◽  
High Performance Liquid Chromatographic ◽  
Reversed Phase ◽  
Calibration Graph ◽  
Official Method ◽  
Pharmaceutical Dosage Forms ◽  
Bulk Drug ◽  
Liquid Chromatographic

A rapid, highly sensitive high performance liquid chromatographic method has been developed for the determination of finasteride(FNS) in bulk drug and in tablets. FNS was eluted from a ODS C18reversed phase column at laboratory temperature (30 ± 2°C) with a mobile phase consisting of methanol and water (80+20) at a flow rate of 1 mL min-1with UV detection at 225 nm. The retention time was ∼ 6.1 min and each analysis took not more than 10 min. Quantitation was achieved by measurement of peak area without using any internal standard. Calibration graph was linear from 2.0 to 30 μg mL-1with limits of detection (LOD) and quantification (LOQ) being 0.2 and 0.6 μg mL-1, respectively. The method was validated according to the current ICH guidelines. Within-day co efficients of variation (CV) ranged from 0.31 to 0.69% and between-day CV were in the range 1.2-3.2%. Recovery of FNS from the pharmaceutical dosage forms ranged from 97.89 – 102.9 with CV of 1.41-4.13%. The developed method was compared with the official method for FNS determination in its tablet forms.

scholarly journals Rapid Production of Graphite Without Contamination for Biomedical AMS

Radiocarbon ◽  
1992 ◽  
Vol 34 (3) ◽  
pp. 344-350 ◽  
Author(s):  
John S. Vogel
Keyword(s):  
Isotopic Fractionation ◽  
Cross Contamination ◽  
Biological Variability ◽  
Muffle Furnace ◽  
New Class ◽  
Large Numbers ◽  
Rapid Production ◽  
Disposable Plastic ◽  
Single Reaction

The application of AMS to the detection of 14C makes possible a new class of sensitive experiments in molecular biology. Such experiments inherently produce large numbers of samples for the determination of biological variability in molecular interactions. The samples vary in 14C concentration over many orders of magnitude. We added TiH2 to aid the reduction of CO2 by zinc in a sealed tube to reproducibly make graphite without sample cross-contamination. The CO2 is transferred from a combustion tube to the reaction tube through a disposable plastic manifold. The sealed tubes are heated to a single-reaction temperature in a muffle furnace. The process is complete within 5 h. Bulk isotopic fractionation in the finished graphite is less than 0.5%.

Utilization of open pit burned household waste ash – a feasibility study in Dhaka

2014 ◽  
Vol 32 (5) ◽  
pp. 397-405
Author(s):  
Md. Obaidul Haque ◽  
Ahmed Sharif
Keyword(s):  
Room Temperature ◽  
Raw Materials ◽  
Bottom Ash ◽  
Open Pit ◽  
Household Waste ◽  
Chemical Compositions ◽  
Muffle Furnace ◽  
Clay Bricks ◽  
Peripheral Area

Informal incineration or open pit burning of waste materials is a common practice in the peripheral area of Dhaka, one of the fastest growing mega-cities in the world. This study deals with the effect of open pit burned (i.e. open burned) household waste bottom ash on fired clay bricks. Between 0 to 50% (by weight) of open pit burned household waste bottom ash was mixed with clay to make bricks. The molded specimens were air-dried at room temperature for 24 h and then oven dried at 100 °C for another 24 h to remove the water. The raw bricks were fired in a muffle furnace to a designated temperature (800, 900 and 1000 °C, respectively). The firing behaviour (mechanical strength, water absorption and shrinkage) was determined. The microstructures, phase compositions and leachates were evaluated for bricks manufactured at different firing temperatures. These results demonstrate that open pit burned ash can be recycled in clay bricks. This study also presents physical observations of the incinerated ash particles and determination of the chemical compositions of the raw materials by wet analysis. Open pit burned ash can be introduced easily into bricks up to 20% wt. The concentrations of hazardous components in the leachates were below the standard threshold for inert waste category landfill and their environmental risk during their use-life step can be considered negligible.

scholarly journals New Spectrophotometric Method for Determination of Cadmium

2009 ◽  
Vol 6 (s1) ◽  
pp. S496-S500
Author(s):  
K. S. Parikh ◽  
R. M. Patel ◽  
K. N. Patel
Keyword(s):  
Stability Constant ◽  
Spectrophotometric Method ◽  
Basic Medium ◽  
Buffer Solution ◽  
Solution Ph ◽  
Yellow Colour ◽  
Maximum Absorbance ◽  
The Stability

The reagent 2-hydroxy-4-n-butoxy-5-bromopropiophenone thiosemicarbazone (HBBrPT) has been used for the determination of Cd(II) by using spectrophotometric method. The reagent HBBrPT gave an intense yellow colour with Cd(II) solution in basic medium. The maximum absorbance was observed at 440 nm, in basic buffer solution (pH 10.00). The molor absorptivity and Sandell’s sensitivity of Cd(II)-HBBrPT complex were 4035 mol-1cm-1and 0.02765 μg cm-2respectively. The stability constant of 1:2 Cd(II)-HBBrPT complex was 8.46×106. The effect of various iron was also studied.

scholarly journals Sensitive and fast determination of papaverine by adsorptive stripping voltammetry on renewable mercury film electrode

2013 ◽  
Vol 11 (5) ◽  
pp. 736-741 ◽  
Author(s):  
Robert Piech ◽  
Beata Paczosa-Bator
Keyword(s):  
Mercury Electrode ◽  
Stripping Voltammetry ◽  
Differential Pulse ◽  
Calibration Graph ◽  
Adsorptive Stripping Voltammetry ◽  
Film Electrode ◽  
Mercury Film Electrode ◽  
Mercury Film ◽  
Preconcentration Time

AbstractThe renewable mercury film electrode, applied for the determination of papaverine traces using differential pulse adsorptive stripping voltammetry (DP AdSV) is presented. The calibration graph obtained for papaverine is linear from 1.25 nM (0.42 µg L−1) to 95 nM (32.2 µg L−1) for a preconcentration time of 60 s, with correlation coefficient of 0.998. For the renewable mercury electrode (Hg(Ag)FE) with a surface area of 9.1 mm2 the detection limit for a preconcentration time of 60 s is 0.7 nM (0.24 µg L−1). The repeatability of the method at a concentration level of the analyte as low as 17 µg L−1, expressed as RSD is 3.3% (n=5). The proposed method was successfully applied and validated by studying the recovery of papaverine from drugs, urine and synthetic solution.

scholarly journals Nitroso-R-salt as a sensitive spectrophotometric reagent for the determination of paracetamol in pharmaceutical preparations

2009 ◽  
Vol 6 (3) ◽  
pp. 570-577
Author(s):  
Baghdad Science Journal
Keyword(s):  
Aqueous Solution ◽  
Statistical Difference ◽  
Pharmaceutical Preparations ◽  
Molar Absorptivity ◽  
Calibration Graph ◽  
Subsequent Reaction ◽  
Experimental Conditions ◽  
Colored Complex ◽  
British Pharmacopoeia

Nitroso-R-salt is proposed as a sensitive spectrophotometric reagent for the determination of paracetamol in aqueous solution. The method is based on the reaction of paracetamol with iron(III) and subsequent reaction with nitroso-R-salt to yield a green colored complex with maximum absorption at 720 nm. Optimization of the experimental conditions was described. The calibration graph was linear in the concentration range of 0.1 – 2.0 ?g mL-1 paracetamol with a molar absorptivity of 6.9 × 104 L mol-1 cm-1. The method was successfully applied to the determination of paracetamol in pharmaceutical preparations without any interference from common excipients. The method has been statistically evaluated with British Pharmacopoeia method and no statistical difference between methods was found at the 95% confidence level.

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