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IRON ZIRCONATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52933-62-7

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52933-62-7 Usage

Chemical Properties

reacted product, -200 mesh with 99.7% purity [CER91]

Check Digit Verification of cas no

The CAS Registry Mumber 52933-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,3 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52933-62:
(7*5)+(6*2)+(5*9)+(4*3)+(3*3)+(2*6)+(1*2)=127
127 % 10 = 7
So 52933-62-7 is a valid CAS Registry Number.
InChI:InChI=1/Fe.O.Zr/q+3;-2;+4

52933-62-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name iron(3+),oxygen(2-),zirconium(4+)

1.2 Other means of identification

Product number -
Other names Iron zirconate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52933-62-7 SDS

52933-62-7Upstream product

52933-62-7Downstream Products

52933-62-7Relevant academic research and scientific papers

The influence of thermal treatment on phase development in ZrO2-Fe2O3 and HfO2-Fe2O3 systems

Tefani,Greta,Nomura,Trojko,Musi

, p. 151 - 160 (2001)

The effects of thermal treatment (500, 600, 800 and 1100°C) of the amorphous precursors of ZrO2-Fe2O3 and HfO2-Fe2O3 systems, coprecipitated from aqueous solutions of the corresponding salts, were studied at room temperature (RT) by X-ray powder diffraction (XRD) and, in some cases, by laser Raman spectroscopy. The incorporation of Fe3+ ions partially stabilized the high temperature polymorphs of zirconia (ZrO2) and hafnia (HfO2). The stabilization of the cubic polymorphs of ZrO2 and HfO2 occurred in the solid solutions with an Fe2O3 content of ≥10 mol%. The presence of Fe3+ ions above their solid solubility limit caused the transition of metastable polymorphs of ZrO2 and HfO2 to monoclinic polymorphs. The terminal solid solubility limit of Fe2O3 in ZrO2, as estimated at RT, was ~33 mol% after calcination at 600°C, ~9 mol% after calcination at 800°C and ~2 mol% after calcination at 1100°C. After the same thermal treatment, the terminal solid solubility limits of Fe2O3 in HfO2 proved to be very similar only a little smaller. The unit-cell volume of the cubic polymorphs of ZrO2 and HfO2, determined by powder-pattern-fitting methods, decreased linearly with the increase in iron content, but the rate of decrease was greater in the ZrO2 polymorph. The thermal behavior of the amorphous precursors was also followed by differential thermal analysis and thermogravimetric analysis. The crystallization temperature of both systems increased with an increase in the Fe2O3 content, from 405 to 730°C in the ZrO2-Fe2O3 system, and from 520 to 720°C in the HfO2-Fe2O3 system. The results indicated that the amorphous precursors with more than 30 mol% of Fe2O3 were single co-gels. The status of the Fe3+ ions in the ZrO2-type lattice and the process of their segregation into the α-Fe2O3-phase were examined by57Fe Mo?ssbauer spectroscopy. Significantly lower values of the hyperfine magnetic fields compared to that of α-Fe2O3 indicated the incorporation of Zr4+ ions into the α-Fe2O3 lattice, the amount of which decreased with the increasing temperature of treatment.

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