Interaction of Kaolinite with Calcite on Heating: III. Effect of Different Kaolinites

Clay Minerals ◽  
1988 ◽  
Vol 23 (2) ◽  
pp. 191-203 ◽  
Author(s):  
R. C. Mackenzie ◽  
L. Heller-Kallai ◽  
A. A. Rahman ◽  
H. M. Moir
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
High Temperature ◽  
Room Temperature ◽  
General Relationship ◽  
Experimental Conditions ◽  
Tentative Explanation ◽  
General Locality ◽  
Dta Curves

AbstractThe degree of distortion of the calcite endotherm on differential thermal analysis (DTA) curves for kaolinite-calcite mixtures depends on the kaolinite sample used as well as on the factors previously established. Although no two of the ten kaolinite samples employed, even if from the same general locality, produced identical effects under all experimental conditions, a general relationship between locality of origin and degree of distortion was noted. The crystalline species detected in the products of heating, after standing in air at room temperature, included portlandite, calcite, aragonite, vaterite and the high-temperature phases gehlenite, α′-Ca2SiO4, and 12CaO. 7Al2O3. The actual species present again depended on the kaolinite sample. Although the results cannot be directly related to the volatiles evolved along with water on dehydroxylation of the different kaolinites, a tentative explanation is offered on the basis of the effects of the volatiles on the surfaces of the particles present.

High-Temperature Modifications of Thorium Dicarbide

1964 ◽  
Vol 8 ◽  
pp. 78-85 ◽  
Author(s):  
P. K. Gantzel ◽  
S. Langer ◽  
N. L. Baldwin ◽  
F. L. Kester
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
High Temperature ◽  
Thermal Effects ◽  
Room Temperature ◽  
Thermal Analyses ◽  
Tetragonal Modification ◽  
X Ray ◽  
Space Groups ◽  
Heating And Cooling

AbstractThermal analyses of samples of thorium dicarbide in equilibrium with graphite show arrests which indicate phase transitions at 1427 ± 21°C arid 1481 ± 28°C. These thermal effects have been observed on heating and cooling both in standard thermal analysis and in differential thermal analysis using graphite as a reference material. The microstructure of thorium dicarbide samples shows the characteristic “herringbone” pattern of a material which has undergone a martensitic-type transition.A high-temperature X-ray investigation has revealed that the observed thermal arrests correspond to erystallographic transformations. The monodinic modification found at room temperature is stable to 1427°C, at which temperature a tetragonal modification with a0 = 4.235 ± 0.002Å and c0 = 5.408 ± 0.002Å is formed. At 1481°C, the tetragonal is transformed to cubic with a0 = 5.809 ± 0.002 Å. The best agreement between observed and calculated intensities has been obtained with C-C units of 1.5-Å assumed bond length in space groups P42/mmc and Pa3 for the tetragonal and cubic modifications, respectively.

Effect of experimental conditions on the differential thermal-analysis of karnallite type hydrates

1984 ◽  
Vol 49 (12) ◽  
pp. 2770-2775
Author(s):  
Vladimir Z. Poilov ◽  
Jana Ederová ◽  
Antonín Blažek
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Experimental Conditions

Article in Russian

scholarly journals X-Ray Investigations of the Low-Temperature Phases of the Organic Metals α- and β-(BEDT-TTF)2I3

1986 ◽  
Vol 41 (11) ◽  
pp. 1319-1324 ◽  
Author(s):  
H. Endres ◽  
H. J. Keller ◽  
R. Swietlik ◽  
D. Schweitzer ◽  
K. Angermund ◽  
...  
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Room Temperature ◽  
Unit Cell Volume ◽  
Unit Cell ◽  
Slight Variation ◽  
X Ray ◽  
Organic Metals ◽  
Β Phase ◽  
Α Phase

The structure of single crystals of the organic metals α- and β-(BEDT-TTF)2I3* was determined at 100 K, well below the phase transitions indicated by resistivity and thermopower measurements as well as by differential thermal analysis. In the α-phase no unusual change of the room temperature unit cell but a slight variation in the triiodide network and especially a more pronounced dimerization in one of the two donor stacks have been found. The β-phase develops a superstructure with a unit cell volume three times as large as that at room temperature and with pronounced distortions of the I3--ions.

Vacuum Carburization of Nanometer Tungsten Powder with Carbon Black

2007 ◽  
Vol 534-536 ◽  
pp. 165-168 ◽  
Author(s):  
Luo Ji ◽  
Lin Tao ◽  
Zhi Meng Guo ◽  
Cheng Chang Jia
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Surface Area ◽  
Tungsten Powder ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
X Ray Scattering ◽  
Vacuum Carburization ◽  
Dta Curves

Vacuum carburization of nanometer tungsten powder was investigated in a simple designed apparatus. An X-Y recorder was used to plot differential thermal analysis (DTA) curves to determine the starting temperature of carburization of four samples with different specific surface area. The product was characterized by X-ray Diffraction (XRD) and small angle X-ray scattering (SAXS). The results show that finer tungsten powder has lower starting temperature of carburization. Tungsten powder, the BET surface area of which is 32.97m2/g, was completely carburized to tungsten carbide at 1050°C, even though the starting temperature was 890°C. The particle was found to grow sharply before carburization.

A DTA Study on HVOF Thermally Sprayed WC–M Coatings

2007 ◽  
Vol 566 ◽  
pp. 155-160
Author(s):  
M. Heydarzadeh Sohi ◽  
Shahin Khameneh Asl ◽  
Kazuyuki Hokamoto ◽  
M. Rezvani
Keyword(s):  
Heat Treatment ◽  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
High Temperature ◽  
Amorphous Phase ◽  
Exothermic Reaction ◽  
Intermetallic Phase ◽  
Chemical Compositions ◽  
Crystalline Phases ◽  
Sprayed Coatings

Five types of tungsten carbide based powders with different chemical compositions (WC-12Co, WC-17Co, WC-10Ni, WC-10Co-4Cr and WC- 20Cr-7Ni) were deposited onto ST37 mild steel substrate using high velocity oxy fuel (HVOF) spray technique. The feedstock powders and sprayed coatings were studied by using X-ray diffraction (XRD), and differential thermal analyzing (DTA). The results were shown during HVOF thermal spraying, WC-M powders become partially melted before being sprayed on the surface of the substrate with supersonic speed. In these types of coatings, the crystallographic structures are normally non equilibrium, because the cooling rates of the deposited splats are very high due to the cold substrate acting as a thermal sink. These partially melted powders are then rapidly solidified to an amorphous phase. XRD analysis showed that the amorphous phase was existed in all of the as sprayed coatings. The amorphous phase in WC-12Co, WC-17Co and WC-10Ni coatings was transformed to crystalline phases by heat treatment at high temperature. Heat treatment of these coatings at high temperature also resulted in partially dissolution of WC particles and formation of new crystalline phases. In cobalt base coatings, the new phases were eta carbide phases like Co6W6C and Co3W3C but in WC-10Ni coating a NiW intermetallic phase was formed. Heat treatment of WC-10Co-4Cr and WC-20Cr-7Ni coatings did not change the amorphous phases in these coatings. Differential thermal analysis of cobalt containing coatings revealed an exothermic reaction at approximately 880°C. This exothermic reaction may be related to the transformation of the amorphous phase to eta phases. On the contrary, DTA analysis of feedstock powders of these coatings showed an endothermic reaction at approximately 1000°C. DTA analyses of nickel containing cermets also showed similar results. Differential thermal analysis of chromium containing cermets did not show any noticeable exothermic or endothermic reactions.

Crystal Growth in Amorphous Binary Alloys of Zr-Ni System

2007 ◽  
Vol 26-28 ◽  
pp. 675-678 ◽  
Author(s):  
Takeshi Fukami ◽  
I. Noda ◽  
M. Asada ◽  
D. Okai ◽  
T. Yamasaki
Keyword(s):  
Activation Energy ◽  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Crystal Growth ◽  
Crystallization Process ◽  
Isothermal Annealing ◽  
Binary Alloys ◽  
Isothermal Condition ◽  
Amorphous State ◽  
Dta Curves

A crystallization process in an amorphous state under isothermal condition is examined for binary alloys ZrNi and ZrNi2 by differential thermal analysis (DTA). Time dependence of DTA curves is measured at several constant temperatures just below crystallization temperature. The fraction of crystallized volume in amorphous state and its time evolution during isothermal annealing are measured. These data are analyzed by the Johnson-Mehl–Avrami formula. The Avrami exponent is 2.4±0.1 for ZrNi and 3~4 depending on the set temperature for ZrNi2. The activation energy for crystallization of amorphous ZrNi and ZrNi2 was estimated by plots of lnt1/2 vs. 1/T.

Liquid Crystals in Binary Systems of Lead Decanoate with Zinc or Cadmium Decanoate

2000 ◽  
Vol 55 (11-12) ◽  
pp. 899-901
Author(s):  
Mirnaya T. A. ◽  
L. S. Sudovtsova ◽  
G. G. Yaremchuk
Keyword(s):  
Phase Transition ◽  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Room Temperature ◽  
Binary Systems ◽  
Crystal Formation ◽  
Liquid Region ◽  
Polarization Microscopy ◽  
Isotropic Liquid ◽  
Phase Transition Temperatures

Abstract The phase transition temperatures were determined by differential thermal analysis and hot stage polarization microscopy between room temperature and the isotropic liquid region for the binary systems of lead (II) decanoate with zinc (II) or cadmium (II) decanoate. The boundaries of the liquid crystal formation in these systems were found.

Differential thermal analysis of linear chain mercury compounds

1983 ◽  
Vol 61 (1) ◽  
pp. 71-75 ◽  
Author(s):  
D. Chartier ◽  
W. R. Datars ◽  
R. J. Gillespie
Keyword(s):  
Thermal Analysis ◽  
Thermal Decomposition ◽  
Differential Thermal Analysis ◽  
Single Crystals ◽  
Temperature Interval ◽  
Room Temperature ◽  
Linear Chain ◽  
Disorder Transition ◽  
Mercury Compounds

Differential thermal analysis of powders and single crystals of Hg3-δAsF6 is reported for the temperature interval 100 to 500 K. There is an endotherm at 234 K, corresponding to the melting of mercury during warming, but no exotherm at this temperature during cooling. The amount of mercury detected during warming is 1.3 ± 0.4% of the mercury in a sample. This is greater than the amount of mercury expected from simple contraction of the lattice from room temperature. These results are explained by the presence of a phase of dispersed, solid mercury in the sample. Mercury is formed at the order–disorder transition of the mercury chains and melts at 235 K. Mercury in samples with some decomposition showed a freezing exotherm after supercooling at 18 K. There is irreversible thermal decomposition of Hg3-δAsF6 above 400 K.

scholarly journals DTA/TG analysis of mechanochemicaly activated sodium carbonate

2021 ◽  
pp. 47-55
Author(s):  
Nataša Đorđević ◽  
Slavica Mihajlović ◽  
Gvozden Jovanović ◽  
Branislav Marković
Keyword(s):  
Carbon Dioxide ◽  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Relaxation Time ◽  
Environmental Protection ◽  
Sodium Carbonate ◽  
Room Temperature ◽  
Tg Analysis ◽  
Relaxation Period ◽  
Sorption Characteristics

Sodium carbonate is a material that is very good sorbent of carbon dioxide from the atmosphere, and it is a reason of it is increasing importance in environmental protection. In order to improve it is sorption characteristics, activation of Na2CO3 was performed by mechanochemical procedure and monitoring of changes during the relaxation time. This research is based on differential thermal analysis with thermogravimetry, in order to determine the changes that occurred on the activated samples during the relaxation period under controlled conditions. Sodium carbonate was activated for 2 and 7 minutes in a vibro mill, and then the activated samples were deposited in at room temperature and atmosphere of carbon dioxide at a humidity of 95% for 96h.

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