Determination of Trace Cobalt in Water by Reversed Flow Injection Spectrophotometry

2014 ◽  
Vol 955-959 ◽  
pp. 1276-1279
Author(s):  
Ling Su ◽  
Heng Shen Xie
Keyword(s):  
Flow Injection ◽  
Affecting Factors ◽  
Industrial Waste Water ◽  
Buffer Solution ◽  
Relative Standard ◽  
Relationship Of ◽  
The Relationship ◽  
Catalytic Effects ◽  
Coexisting Ions

A method for determination of cobalt in water by flow injection spectrophotometry based on the catalytic effects of cobalt on the oxidation reaction of arsenazo III by potassium bichromate in HAc-NaAc buffer solution of pH 4.6 was established. The relationship of the reduced absorbency to the concentration of cobalt was good linearity and the maximum absorption peak located at 550 nm. The affecting factors on the strength of absorption including acidity, dosage, temperature, coexisting ions and so on, and the optimal conditions of the reaction in the system were investigated. Calibration graphs were linear for ranges of 0 to 20 μg/mL and a detection limit of 0.3 μg/mL cobalt was achieved. The proposed method was successfully applied to the analyses of industrial waste water samples, with relative standard deviation of less than 1.5% and the recoveries are 95.1% to 96.8%for the determination of cobalt.

Determination of Formaldehyde Based on the Fading Reaction of Bordeaux R by Flow Injection Spectrophotometry

2012 ◽  
Vol 610-613 ◽  
pp. 436-439
Author(s):  
Ling Su ◽  
Wei Wei ◽  
Jia Liang Guo ◽  
Zhen Liu ◽  
Lu Sheng Liu
Keyword(s):  
Flow Injection ◽  
Optimal Conditions ◽  
Affecting Factors ◽  
Sulfuric Acid Medium ◽  
Relative Standard ◽  
Relationship Of ◽  
The Relationship ◽  
Catalytic Effects ◽  
Coexisting Ions

A method for determination of formaldehyde by flow injection spectrophotometry based on the catalytic effects of formaldehyde on the oxidation reaction of Bordeaux R by potassium chlorate in sulfuric acid medium was established. The relationship of the reduced absorbency to the concentration of formaldehyde was good linearity and the maximum absorption peak located at 520nm. The affecting factors on the strength of absorption including acidity, dosage, temperature, coexisting ions and so on, and the optimal conditions of the reaction in the system were investigated. Calibration graphs were linear for ranges of 0 to 3.0 mg l−1 and a detection limit of 2×10-8 g ml−1 formaldehyde was achieved. The proposed method was successfully applied to the analyses of environmental samples, with relative standard deviation of less than 1.6% and the recoveries are 93.6 % to 94.5% for the determination of formaldehyde.

Determination of Formaldehyde Based on the Fading Reaction of Methyl Orange by Reversed Flow Injection Spectrophotometry

2013 ◽  
Vol 295-298 ◽  
pp. 479-482
Author(s):  
Ling Su ◽  
Jia Liang Guo ◽  
Zhen Liu ◽  
Lu Sheng Liu ◽  
Wei Wei
Keyword(s):  
Methyl Orange ◽  
Indoor Air ◽  
Flow Injection ◽  
Affecting Factors ◽  
Sulfuric Acid Medium ◽  
Relative Standard ◽  
Relationship Of ◽  
The Relationship ◽  
Catalytic Effects

A rapid method for determination of formaldehyde in paint and indoor air by flow injection spectrophotometry based on the catalytic effects of formaldehyde on the oxidation reaction of methyl orange by potassium bromate in sulfuric acid medium was established. The relationship of the reduced absorbency to the concentration of formaldehyde was good linearity and the maximum absorption peak located at 508 nm. The affecting factors on the strength of absorption including temperature, acidity, dosage, coexisting ions and so on, and the optimal conditions of the reaction in the system were investigated. Calibration graphs were linear for ranges of 0 to 1.0 mg/L and a detection limit of 1.1×10-8 g/mL formaldehyde was achieved. The proposed method was successfully applied to the analyses of paint and indoor air samples, with relative standard deviation of less than 1.8% and the recoveries are 94.6％ to 106.2％for the determination of formaldehyde.

Determination of Chromium(VI) in Waste Water by Reversed Flow Injection Spectrophotometry

2011 ◽  
Vol 356-360 ◽  
pp. 939-942
Author(s):  
Ling Su ◽  
Heng Shen Xie
Keyword(s):  
Waste Water ◽  
Flow Injection ◽  
Sodium Periodate ◽  
Industrial Waste Water ◽  
Reversed Flow ◽  
Chromium Vi ◽  
Sulfuric Acid Medium ◽  
Relative Standard ◽  
Catalytic Effects

A method for determination of Chromium(VI) by reversed flow injection spectrophotometry based on the catalytic effects of chromium on the oxidation reaction of methylene blue by sodium periodate in sulfuric acid medium is established. Effects of concentration of reagents and other conditions have been optimized. Calibration graphs are linear for ranges of 0 to 1.0mgl−1. A detection limit of 0.007mgl−1 chromium is achieved. The proposed method is successfully applied to the analyses of industrial waste water and electroplating waste liquor, with relative standard deviation of less than 1.5% and the recoveries are 92.9％ to 97.5％for the determination of chromium.

scholarly journals Spectrophotometric flow injection system for determination of Zn2+ in ophthalmic formulations using Alizarin red S

2018 ◽  
Vol 34 (2) ◽  
pp. 67
Author(s):  
Orlando Fatibello-Filho ◽  
Heberth Juliano Vieira
Keyword(s):  
Flow Injection ◽  
Sampling Rate ◽  
Alizarin Red S ◽  
Injection System ◽  
Borate Buffer Solution ◽  
Buffer Solution ◽  
Solution Ph ◽  
Alizarin Red ◽  
Relative Standard

A spectrophotometric flow injection method for the determination of Zn(II) in ophthalmic formulations was developed. In this work, Zn(II) ion was complexed with Alizarin red S in borate buffer solution (pH 9.0) and the chromophore produced was monitored at 520 nm. The analytical curve was linear in the Zn(II) concentration range from 6.05 x 10-6 to 1.50 x 10-4 mol L-1 with a detection limit of 3.60 x 10-6 mol L-1. Recoveries ranged from 96.3 to 105 % and a relative standard deviation of 1.2 % (n = 10) for 5.5x10-5 mol L-1 Zn(II) reference solution were obtained. The sampling rate was 60 h-1 and the results obtained of Zn(II) in ophthalmic products using this procedure are in close agreement with those obtained using a comparative spectrophotometric procedure at 95 % confidence level.

scholarly journals Determination of Phosphine Residues in Whole Grains and Soybeans by Ion Chromatography via Conversion to Phosphate

1998 ◽  
Vol 81 (6) ◽  
pp. 1190-1201 ◽  
Author(s):  
Marvin Carlson ◽  
Richard D Thompson
Keyword(s):  
Colorimetric Method ◽  
Whole Grains ◽  
Aluminum Phosphide ◽  
Precision Data ◽  
Relative Standard ◽  
Suppressed Conductivity Detection ◽  
Phosphine Residues ◽  
Relationship Of ◽  
The Relationship

Abstract An ion chromatographic (IC) method was developed for determining phosphine (PH3) in whole grains (barley, corn, oats, rice, rye, and wheat) and soybeans. The method converts phosphine to phosphate (i.e., orthophosphate) and isolates the phosphate by IC with eluent-suppressed conductivity detection. Recoveries of unbound phosphine by the method were similar to those obtained by an established colorimetric method for 7 different products fortified at 3 levels. Mean recoveries were low (i.e., 30-60%) and varied with product type and level of fortification. Recoveries of PH3 from previously fumigated products fortified with aluminum phosphide ranged from 19.0% for barley fortified at 0.734 ppm to 88.3% for corn fortified at 1.691 ppm. Precision data from 3 products based on replicate analyses (n = 4 or 5) gave relative standard deviations of 1.78-4.66% for mean laboratory-fumigated PH3 levels of 0.679-1.309 ppm. Estimated limits of detection (LOD) and quantitation (LOQ) for PH3 were 0.010 μg/g (10 ppb) and 0.0275 μg/g (27.5 ppb) at signal-to-noise ratios (S/N) of 4:1 and 10:1, respectively. These values were also determined for a nonchemically suppressed IC system with LOD of 0.02 μg/g (20 ppb) and LOQ of 0.055 μg/g (55 ppb) at S/N of 4:1 and 10:1, respectively. Phosphate response was linear over the concentration range equivalent to 0.30-10.0 fig P/mL, with a mean correlation coefficient of 0.9988 based on replicate standard curves. The relationship of product composition to recovery from various products was also examined.

Flow injection spectrofluorimetric determination of iron(III) in water using salicylic acid

2010 ◽  
Vol 64 (4) ◽  
Author(s):  
Adem Asan ◽  
Muberra Andac ◽  
Ibrahim Isildak
Keyword(s):  
Salicylic Acid ◽  
Flow Injection ◽  
Limit Of Detection ◽  
Sampling Rate ◽  
Linear Calibration ◽  
Fluorimetric Determination ◽  
Buffer Solution ◽  
Quenching Effect ◽  
Relative Standard

AbstractA simple and fast flow injection fluorescence quenching method for the determination of iron in water has been developed. Fluorimetric determination is based on the measurement of the quenching effect of iron on salicylic acid fluorescence. An emission peak of salicylic acid in aqueous solution occurs at 409 nm with excitation at 299 nm. The carrier solution used was 2 × 10−6 mol L−1 salicylic acid in 0.1 mol L−1 NH4+/NH3 buffer solution at pH 8.5. Linear calibration was obtained for 5–100 μg L−1 iron(III) and the relative standard deviation was 1.25 % (n = 5) for a 20 μL injection volume iron(III). The limit of detection was 0.3 μg L−1 and the sampling rate was 60 h−1. The effect of interferences from various metals and anions commonly present in water was also studied. The method was successfully applied to the determination of low levels of iron in real samples (river, sea, and spring waters).

scholarly journals Spectrophotometric flow injection system for determination of Zn2+ in ophthalmic formulations using Alizarin red S

2009 ◽  
Vol 34 (2) ◽  
pp. 67-72 ◽  
Author(s):  
Orlando Fatibello-Filho ◽  
Heberth Juliano Vieira
Keyword(s):  
Flow Injection ◽  
Sampling Rate ◽  
Alizarin Red S ◽  
Injection System ◽  
Borate Buffer Solution ◽  
Buffer Solution ◽  
Solution Ph ◽  
Alizarin Red ◽  
Relative Standard

A spectrophotometric flow injection method for the determination of Zn(II) in ophthalmic formulations was developed. In this work, Zn(II) ion was complexed with Alizarin red S in borate buffer solution (pH 9.0) and the chromophore produced was monitored at 520 nm. The analytical curve was linear in the Zn(II) concentration range from 6.05 x 10-6 to 1.50 x 10-4 mol L-1 with a detection limit of 3.60 x 10-6 mol L-1. Recoveries ranged from 96.3 to 105 % and a relative standard deviation of 1.2 % (n = 10) for 5.5x10-5 mol L-1 Zn(II) reference solution were obtained. The sampling rate was 60 h-1 and the results obtained of Zn(II) in ophthalmic products using this procedure are in close agreement with those obtained using a comparative spectrophotometric procedure at 95 % confidence level.

Calculating the aerodynamics of vertical axis wind turbines

2012 ◽  
Vol 34 (3) ◽  
pp. 169-184 ◽  
Author(s):  
Hoang Thi Bich Ngoc
Keyword(s):  
Wind Turbine ◽  
Incidence Angle ◽  
Vertical Axis ◽  
Rotor Blades ◽  
Vertical Axis Wind Turbine ◽  
Horizontal Axis Wind Turbine ◽  
Velocity Triangle ◽  
Relationship Of ◽  
The Relationship

Vertical axis wind turbine technology has been applied last years, very long after horizontal axis wind turbine technology. Aerodynamic problems of vertical axis wind machines are discussible. An important problem is the determination of the incidence law in the interaction between wind and rotor blades. The focus of the work is to establish equations of the incidence depending on the blade azimuth, and to solve them. From these results, aerodynamic torques and power can be calculated. The incidence angle is a parameter of velocity triangle, and both the factors depend not only on the blade azimuth but also on the ratio of rotational speed and horizontal speed. The built computational program allows theoretically selecting the relationship of geometric parameters of wind turbine in accordance with requirements on power, wind speed and installation conditions.

Tire Treadwear — A Comprehensive Evaluation of the Factors: Generic Type, Aspect Ratio, Tread Pattern, and Tread Composition Part I: Introduction and Details on the Organization of the Program

1986 ◽  
Vol 14 (4) ◽  
pp. 201-218 ◽  
Author(s):  
A. G. Veith
Keyword(s):  
Aspect Ratio ◽  
Comprehensive Evaluation ◽  
Test Method ◽  
Interactive Effects ◽  
Data Analyses ◽  
Main Effect ◽  
Systematic Determination ◽  
Relationship Of ◽  
The Relationship

Abstract This four-part series of papers addresses the problem of systematic determination of the influence of several tire factors on tire treadwear. Both the main effect of each factor and some of their interactive effects are included. The program was also structured to evaluate the influence of some external-to-tire conditions on the relationship of tire factors to treadwear. Part I describes the experimental design used to evaluate the effects on treadwear of generic tire type, aspect ratio, tread pattern (groove or void level), type of pattern (straight rib or block), and tread compound. Construction procedures and precautions used to obtain a valid and functional test method are included. Two guiding principles to be used in the data analyses of Parts II and III are discussed. These are the fractional groove and void concept, to characterize tread pattern geometry, and a demonstration of the equivalence of wear rate for identical compounds on whole tread or multi-section tread tires.

Knowledge management implementation in Indian automobile ancillary industries

2016 ◽  
Vol 11 (3) ◽  
pp. 802-810 ◽  
Author(s):  
Nitin Yashwant Patil ◽  
Ravi M. Warkhedkar
Keyword(s):  
Knowledge Management ◽  
Industrial Area ◽  
Total Quality ◽  
Limited Data ◽  
Interpretive Structural Modeling ◽  
Content Type ◽  
Relationship Of ◽  
Power And Dependence ◽  
The Relationship

Purpose In the past decade, much has been written about knowledge management (KM) in the manufacturing; however, less attention has been paid to the Indian automobile ancillary industries located in Chinchwad, Pune. It is suitable to find out the relationship of the factors of the study. It helps in identifying the hierarchy of factors to be taken, and interlinking of production department with KM improves the productivity of the industries. Categorization of these principles based on their driving power (principles which hold other principles) and dependence (principles which are dependent on other principles) has also been examined for KM implementation to study the driving power and dependence power of these principles. This paper aims to determine the roadmap of KM implementation and categorize KM principles based on their driving power for manufacturing industries with the use of the interpretive structural modeling (ISM)-based model. The results indicate that the principles possessing higher driving power, such as KM, inventory control, quality control, productivity and scheduling and their interlinking. The major contribution of this research lies in the development of contextual relationship among various identified factors of KM and determination of their driving and dependence power through a single systemic framework. Design/methodology/approach In this paper, author find out the suitability ISM for Indian Automobile industries to find the relation among the variables. Findings ISM model has been developed for the hierarchy of the identified KM. As ISM model results a hypothetical hierarchy which needs a proper quantitative analysis to evaluate their percentage effectiveness in the hierarchy. Research limitations/implications It is applied to automobile industries with limited number of variables that will show the dependence variable and driving variables and their interrelations. It can be applied other fields to fine the relationship of variables. Practical implications The ISM may be used in supply chain management and total quality management to find interlinking between the variables. Originality/value The limited data collected from Pimpri Chinchwad industrial area of Pune from Maharashtra state (India).

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