Identification and Thermal Stability of Copper(I) Sulfate

1972 ◽  
Vol 50 (23) ◽  
pp. 3872-3875 ◽  
Author(s):  
Kim Vo Van ◽  
Fathi Habashi
Keyword(s):  
Thermal Stability ◽  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Thermogravimetric Analysis ◽  
Diffraction Pattern ◽  
Chemical Processes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thermal Stability Of

Anhydrous CU2SO4 was prepared and its X-ray diffraction pattern was established. Differential thermal analysis, thermogravimetric analysis, and X-ray diffraction methods were used to study the effect of heating in different atmospheres. The formation of CU2SO4 as an intermediate in chemical processes has been discussed.

Study of Thermal Behaviour of EPDM/SBR Blends and Carbon Nanocoatings Deposited by Sputtering

2021 ◽  
Vol 875 ◽  
pp. 116-120
Author(s):  
Muhammad Alamgir ◽  
Faizan Ali Ghauri ◽  
Waheed Qamar Khan ◽  
Sajawal Rasheed ◽  
Muhammad Sarfraz Nawaz ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Weight Loss ◽  
Thermogravimetric Analysis ◽  
Thermal Behavior ◽  
Thermal Behaviour ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thermal Stability Of

In this study, the effect of SBR concentration (10 Phr, 20 Phr & 30 Phr ) on the thermal behavior of EPDM/SBR blends was studied. Thermogravimetric analysis (TGA) was used to check weight loss of samples as function of temperature by heating upto 600°C. X-ray diffraction (XRD) was performed to determine quality and % crystallinity of the elastomer blends. It was seen that % crystallinity improved with an increase in the content of SBR in EPDM/SBR blends. TGA revealed that the thermal stability of EPDM/SBR blends has improved by 17% than neat EPDM. Carbon nano-coatings produced by sputtering have no beneficial influence on thermal behaviour of elastomers.

Thermal Stability vs. Crystallization of the Lithiumsilicate Glasses with Addition Zirconium Dioxide and Titanium Dioxide

2008 ◽  
Vol 39-40 ◽  
pp. 399-401
Author(s):  
Viliam Pavlík ◽  
Eugen Jóna ◽  
Martina Sapietová ◽  
Soňa Šnircová
Keyword(s):  
Activation Energy ◽  
Thermal Stability ◽  
Thermal Analysis ◽  
Titanium Dioxide ◽  
Differential Thermal Analysis ◽  
Structural Analysis ◽  
Zirconium Dioxide ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Relationship

The glasses with composition of Li2O . 2 SiO2 . n ZrO2 . n TiO2 (where n = 0; 0.015; 0.031; 0.050; 0.075; 0.1; 0.15; 0.2) were prepared and the relationship between structural and selected parameters of thermal stability vs. crystallization has been studied by differential thermal analysis. Structural analysis was provided by X–ray diffraction. The order of thermal stability vs. crystallization representing of activation energy of studied glass systems which increase with higher addition both oxides. The same order was obtained from the values of XRD. On the comparison the glasses with zero addition titanium dioxide their activation energy was much higher.

Amorphization of rapidly quenched quasicrystalline Al-transition metal alloys by the addition of Si

1986 ◽  
Vol 1 (3) ◽  
pp. 415-419 ◽  
Author(s):  
R.A. Dunlap ◽  
K. Dini
Keyword(s):  
Thermal Stability ◽  
Thermal Analysis ◽  
Metal Alloys ◽  
Icosahedral Symmetry ◽  
Quench Rate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transition Metal Alloys ◽  
Rapidly Solidified ◽  
Thermal Stability Of

The structure and thermal stability of rapidly solidified Al-Cr-Si, Al-Mn-Si, Al-Fe-Si, Al-Co-Si, and Al-Ni-Si alloys have been investigated using x-ray diffraction and thermal analysis measurements. Each series of alloys shows a region of stoichiometry that yields icosahedral symmetry and a region that yields an amorphous phase. Thermal and structural properties of these alloys are reported as a function of stoichiometry and quench rate.

ADSORPTION OF CYCLOHEXANE AND BENZENE ON MIXED HYDROXIDES AND OXIDES OF MAGNESIUM AND ALUMINIUM

1966 ◽  
Vol 44 (8) ◽  
pp. 877-884 ◽  
Author(s):  
R. I. Razouk ◽  
Sh. Nashed ◽  
F. N. Antonious
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Thermogravimetric Analysis ◽  
Surface Area ◽  
Structural Changes ◽  
Mixed Oxides ◽  
X Ray Diffraction ◽  
Oxide Systems ◽  
X Ray ◽  
Characteristic Lines

Seven mixed hydroxides of magnesium and aluminium were prepared, and phase and structural changes accompanying their dehydration were investigated by differential thermal analysis, thermogravimetric analysis, and X-ray diffraction techniques. The differential thermal analysis curves possess 2 peaks corresponding to those of parent hydroxides together with a new peak, and the thermogravimetric analysis curves show slight inflections. X-ray diffraction patterns of the mixed hydroxides possess the characteristic lines of the parent hydroxides together with three to five new intense lines which might indicate the formation of a double hydroxide. When the mixed hydroxides are progressively heated they give rise to products possessing patterns which first become diffuse and ultimately pass mainly into the spinel pattern.Adsorption isotherms of cyclohexane and benzene were measured on the mixed hydroxides and their dehydration products. Specific surface areas calculated by the application of the Brunauer, Emmett, Teller (B.E.T.) equation are in general in good agreement for the two adsorbates. The surface area increases with rise of dehydration temperature to a maximum at 500–600 °C and then decreases with further rise in temperature. This behavior is common to crystalline oxide systems and may be ascribed to the intermingling of decomposition, re-crystallization, and sintering processes. Variations in the molecular ratio of the mixed oxides (as much as 20-fold), and in the method of preparation, do not much alter the surface area.

Synthesis and Characterization of Polyaniline Copolymer

2012 ◽  
Vol 217-219 ◽  
pp. 551-554
Author(s):  
Ting Xi Li ◽  
Yu Hua Zhao ◽  
Qian Li ◽  
Cheng Qian Yuan ◽  
Quan Liang Chen ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Infrared Spectroscopy ◽  
Thermogravimetric Analysis ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
The Difference ◽  
Thermal Stability Of

Abstract. Polyaniline (PANI) and p-phenylenediamine (p-PDA)-aniline copolymer were prepared via a same microemulsion method. The structures of the PANI and p-PDA-aniline copolymer were characterized by infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermogravimetric analysis（TGA）. The results revealed the difference of synthesis and characterization between PANI and p-PDA-aniline copolymer. It was shown that structure of the copolymer is almost similar to that of PANI, but the p-PDA-aniline copolymer has a better crystallization than PANI, and the thermal stability of the copolymer is higher than that of pure PANI.

scholarly journals Study of structures and properties of ZnO-Sb2O3-P2O5-Na2O glasses

2014 ◽  
Vol 32 (3) ◽  
pp. 414-418 ◽  
Author(s):  
Yajun Qi ◽  
Zhiqiang Wang ◽  
Shangru Zhai ◽  
Shuwen Jiang ◽  
Hai Lin
Keyword(s):  
Thermal Stability ◽  
Thermal Analysis ◽  
Weight Loss ◽  
Deionized Water ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Good Thermal Stability ◽  
Structures And Properties ◽  
Thermal Stability Of

AbstractThe influence of ZnO substitution by 0–12 wt.% Na2O on the properties of ZnO-Sb2O3-P2O5-Na2O glasses has been investigated. The structure and properties of the glasses with the composition of (13.86-x)ZnO-57.93Sb2O3-28.21P2O5−x Na2O (x = 0–12 wt.%) were characterized by infrared spectra (IR), X-ray diffraction and differential thermal analysis (DTA). The results of IR indicated an increase in the intensity of symmetric vibrations of P-O-P bond, which was confirmed by the improvement of water durability with the increasing amount of Na2O in the range of 0–10 wt.%. Substitution of 10 wt.% Na2O led to the weight loss of the glass to 5.93 mg/cm−2 after immersion in deionized water at 50 °C for 24 h. The results of XRD showed that the ability of crystallization decreased, indicating the good thermal stability of the glass. The glass containing 8 wt.% Na2O had the best properties in every respect and might be an alternative to lead based glasses for the applications, providing further composition improvement.

The Effect of H3BO3 Microaddition on Microstructure of Ni/MgO Sintered Compact by Co-Precipitation Method

2013 ◽  
Vol 750 ◽  
pp. 168-171
Author(s):  
Ning Ning Zhou ◽  
Dong Ying Ju ◽  
Wan Yu Ding
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Thermogravimetric Analysis ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Sintered Compact ◽  
X Ray ◽  
Sintered Powder ◽  
Co2 Flow ◽  
Co Precipitation

In the present work, Ni/MgO powder was prepared by co-precipitation in which CO restore NiO to elemental subtance Ni due to C2O42- was decompose to CO and CO2 at 700°C. As the process of the second sintering, H3BO3 was added into the sintered powder of 700°C and was grinded. Then the powder of H3BO3 added was sintered at 800°C，so that the powder was refined, obviously. Thermogravimetric analysis (TGA) and differential thermal analysis(DTA) was carried out in CO2 flow at 10°C/min. X-ray diffraction (XRD) was carried out on a X-ray diffractometer operated at 20KV and 40mA. The microstructures and morphologies were studied by EPMA and XPS.

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