scholarly journals Flame Photometric Determination of Alkali Elements in Raw Materials and By-product of Blast Furnace

1956 ◽  
Vol 4 (3) ◽  
pp. 14-22
Author(s):  
Ryohei ISHIDA ◽  
Yoshimasa FUJISHIRO ◽  
Hayata MANAKA ◽  
Yujiro HASHIMOTO ◽  
Hironori KANEKO
1989 ◽  
Vol 46 (2) ◽  
pp. 83-85
Author(s):  
V. G. Amelin ◽  
P. A. Andreev

Author(s):  
V. A. Makarov ◽  
T. K. Savosteenko

The requirements for the content of hexavalent chromium in cements and raw materials for its manufacture are described. The problem with the utilization of dust from gas treatment plants of metallurgical plants at metallurgical enterprises is given. The influence of the chemical composition of the dust of gas cleaning plants of metallurgical plants on the determination of hexavalent chromium is established. A method for measuring the hexavalent chromium in the dust of gas cleaning plants of metallurgical plants by the photometric method is described. A method has been developed for extracting hexavalent chromium from dust at the cleaning units of metallurgical plants for subsequent photometric determination. An extraction method has been established to prevent underestimation of the hexavalent chromium content. The determination of hexavalent chromium was based on the formation of a blue-violet complex with diphenylcarbazide. Calibration was carried out on aque solutions with a known concentration of hexavalent chromium. For the preparation of calibration solutions, potassium dichromate of chemical purity was used. The concentration of hexavalent chromium in each calibration solution was carried out by a calculation method, overlapping the entire measurement range. The measurement of optical density was carried out on a photoelectric colorimeter type KFK-3, at a wavelength of 540 nm. Analysis of the obtained calibration dependence showed a good correlation. The calibration factor was calculated using the least square method. Extraction of hexavalent chromium from the sample to be analyzed was performed with water. The reducing effect of iron was eliminated with a solution of phosphoric acid. The developed technique is used when conducting certification control of dust from gas cleaning units of metallurgical plants, as well as during research.A validation procedure was carried out. Obtained acceptable limits of repeatability and reproducibility of the method.


Author(s):  
I.G. Muravyeva ◽  
D.N. Togobitskaya ◽  
N.G. Ivancha ◽  
A.S. Nesterov

The paper presents the concept of creating an expert system for selecting the optimal composition of a multicomponent domain mixture, the basis of which will be: models of physical and chemical transformations of iron-containing materials, technological criteria, models of loading and distribution of charge materials, taking into account the distribution of the components of the charge over the cross section of the blast furnace. The system being developed differs from the well-known, based on the determination of the forecast indicators blast furnace by varying the component composition of the raw materials using calculations of material - thermal balance of the process. A block diagram of the solution of the problem of choosing the optimal composition of the charge is given.


Author(s):  
M. I. Stukov ◽  
A. Yu. Chernavin ◽  
V. A. Kobelev ◽  
D. A. Chernavin ◽  
K. P. Ivashinenko

Information about character of burden materials behavior inside a blast furnace at its different horizons enables to increase control efficiency of BF heat running. The elaborated complex of methodologies for carbon materials and iron ore raw materials properties study enables to simulate their behavior at the horizon of iron ore materials reducing, in the viscoplastic zone, at the horizon of iron ore raw materials smelting and its interaction with coke filling. A vertical electric resistance shaft furnace with a tube carbon heater was used as a base equipment for simulation of burden behavior in the reduction zone and smelting zone, as well as for simulation of iron ore burden melt outflow through coke filling. Burden materials preparation to the experiment concluded in crushing of iron ore component followed by 3–5 mm fraction extraction and a mixing it with 3–5 mm fraction of brown coal semi-coke in relation 2:1 for further heating-reduction treatment. The heating-reduction treatment of the mixture charged in the electric furnace simulates the reducing zone and is carried out by a slow heating of the iron ore component and reducing agent mixture from 20 up to 980–1020 ºС. The methodology of determination of lump carbon materials combustibility in the highly heated air blast flow was developed for the complex of equipment based on the shaft electric resistance furnace and aimed at testing of burning process of carbon samples of technological fuels. The combustibility was determined under conditions of burnt sample heating in the temperature range from 500 up to 1500 °C with an accuracy of ±10 °С. The temperature of air blast flow (21 % vol. of oxygen at natural moisture) was set in the range from 120 up to 1200 °С and was kept with an accuracy of ±12 °С. The burnt sample mass, volume of air blast and its velocity was correlated to obtaining of complex non-dimensional Re factor (Reinolds number) more than 100, that guaranteed a reliable process running in the combustion area with no risk of transferring to gasification process. Based on GOST 26517–85 (“Iron ores, sinter and pellets”) a methodology was elaborated for determining of parameters of iron ore materials status in the viscoplastic zone. The methodology comprises heating of preliminary reduced sample of a tested iron ore material in an inert gas and determination of softening temperature and smelting end by a hard rod sinking into the material layer under external pressure action. The temperature at which the layer shrinkage reaches level of 2% during heating, was taken as the softening temperature of the iron ore material. The sinking of the rod into the material by 80% was taken as the temperature of the beginning of the material melting. The interval softening-melting was determined as the difference between melting temperature and softening temperature (at sample shrinkage by 2 %).


2019 ◽  
Vol 85 (10) ◽  
pp. 23-28
Author(s):  
F. S. Aliyeva ◽  
F. O. Mamedova ◽  
F. N. Bahmanova ◽  
Yu. A. Yusibov ◽  
F. M. Chyragov

Author(s):  
Jiří Zimák ◽  
Kristýna Dalajková ◽  
Roman Donocik ◽  
Petr Krist ◽  
Daniel Reif ◽  
...  
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