scholarly journals Thermal behaviour study of solid state compounds of manganese (II), zinc (II) and lead (II) with cinnamic acid

1998 ◽  
Vol 23 (0) ◽  
pp. 09-16
Author(s):  
Marco Aurélio da Silva CARVALHO FILHO ◽  
Massao IONASHIRO

Compounds of cinnamic acid with manganese, zinc and lead have been prepared in aqueous solution. Thermogravimetry, derivative thermogravimetry (TG, DTG), differential scanning calorimetry (DSC), X-ray diffraction and complexometry have been used in the characterization as well as in the study of the thermal stability and interpretation concerning the thermal decomposition.

1998 ◽  
Vol 23 (0) ◽  
pp. 91-98 ◽  
Author(s):  
Ana Glauce ZAINA CHIARETTO ◽  
Marco Aurélio da Silva CARVALHO FILHO ◽  
Nedja Suely FERNANDES ◽  
Massao IONASHIRO

Solid state compounds of general formula ML2.nH2O [where M is Mg, Ca, Sr or Ba; L is cinnamate (C6H5 -CH=CH-COO-) and n = 2, 4, 0.8, 3 respectively], have been synthetized. Thermogravimetry (TG), derivative thermogravimetry (DTG), differential scanning calorimetry (DSC) and X-ray diffraction powder patterns have been used to characterize and to study the thermal stability and thermal decomposition of these compounds.


1999 ◽  
Vol 24 (0) ◽  
pp. 29-44 ◽  
Author(s):  
Maria Ines Gonçalves LELES ◽  
Cristo Bladimiros MELIOS ◽  
Lázaro Moscardini D’ASSUNÇÃO ◽  
Massao IONASHIRO

Solid Ln-OHCO3-DMCP compounds, where Ln represents lanthanides (III) and yttrium (III) ions and DMCP is the anion 4-dimethylaminocinnamylidenepyruvate, have been prepared. Thermogravimetry, derivative thermogravimetry (TG, DTG), differential scanning calorimetry (DSC), x-Ray diffraction powder patterns and elemental analysis have been used to characterize the compounds. The thermal stability as well as the thermal decomposition of these compounds were studied using an alumina crucible in an air atmosphere.


2000 ◽  
Vol 25 (0) ◽  
pp. 9-17 ◽  
Author(s):  
Marisa CHAHUD ◽  
Marco Aurélio da Silva CARVALHO FILHO ◽  
Nedja Suely FERNANDES ◽  
Massao IONASHIRO

Solid dithizonates of Hg(I), Ag(I) and Bi(III) have been prepared. Thermogravimetry (TG), derivative thermogravimetry (DTG), differential scanning calorimetry (DSC), X ray diffraction powder patterns and elemental analysis have been used to characterize and to study the thermal stability and thermal decomposition of the dithizone and of these dithizonates.


2019 ◽  
pp. 089270571987919
Author(s):  
Volodymyr Krasinskyi ◽  
Ivan Gajdos ◽  
Oleh Suberlyak ◽  
Viktoria Antoniuk ◽  
Tomasz Jachowicz

The structure and thermal characteristics of nanocomposites based on polyvinyl alcohol (PVA) and montmorillonite (MMT) intercalated with polyvinylpyrrolidone were investigated by X-ray diffraction analysis and differential scanning calorimetry. The modification of PVA with intercalated MMT reduces the degree of crystallinity of the resulting nanocomposites but significantly increases their thermal stability. Under ultrasound, the intercalated MMT was completely distributed in a PVA solution and formed a monocrystalline structure. Films based on PVA with modified MMT were cross-linked at 110°C in the presence of 5 wt% acrylic acid and 0.5 wt% Ferrous(II) sulfate as an initiator. The formed films have a homogeneous cross-linked structure.


2015 ◽  
Vol 13 ◽  
pp. 37-41
Author(s):  
Bogdan Viorel Neamţu ◽  
Traian Florin Marinca ◽  
Horea Florin Chicinaş ◽  
Ionel Chicinaş ◽  
Olivier Isnard

Result of research concerning the influence of milling conditions on the amorphisation of the Fe75Si20B5 (at.%) alloy is presented. Amorphous powder of Fe75Si20B5 (at.%) was prepared by dry and wet mechanical alloying (MA) route starting from a mixture of Fe, Si and B elemental powders. The mixture was wet/dry milled up to 50 hours. Benzene, oleic acid and ethanol were used as process control agents (PCA) in order to investigate the influence of their chemical composition on the powder amorphisation. The evolution of the powder crystalline structure, thermal stability and magnetic properties were investigated by X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetry (TG) as well as magnetic measurements versus temperature and field. It is proved that the chemical composition of the PCA (especially the carbon content) plays an important role in the amorphisation process induced by wet MA.


e-Polymers ◽  
2017 ◽  
Vol 17 (5) ◽  
pp. 409-416 ◽  
Author(s):  
Yottha Srithep ◽  
Dutchanee Pholharn

AbstractPoly(l-lactide) (PLLA)/poly(d-lactide) (50/50) with plasticizer contents ranging from 2% to 16% w/w were prepared by melt blending using an internal mixer. Wide-angle X-ray diffraction, Fourier transform infrared spectroscopy and differential scanning calorimetry results confirmed that complete stereocomplex polylactide crystallites without any homocrystallites were produced. Compared to neat PLLA, the melting temperature of the stereocomplex polylactide and its plasticized samples was approximately 55°C higher. Higher plasticizer contents decreased glass transition temperature of the stereocomplex, which implied higher flexibility and enhanced the crystallization rate. However, the plasticizer in the stereocomplex reduced the thermal stability.


2013 ◽  
Vol 46 (4) ◽  
pp. 980-992 ◽  
Author(s):  
Tarek M. Madkour ◽  
Sahar K. Mohamed

The morphology, crystallinity and X-ray diffraction of speciality heterocyclic and aromatic based polyurethane and poly(urethane–urea) elastomers synthesized via a one-shot polymerization method were studied. The samples were chain extended by mixtures of aliphatic diols and furanic or aromatic diamine chain extenders. Small-angle X-ray scattering (SAXS) measurements confirmed the results obtained by differential scanning calorimetry (DSC) and revealed the presence of phases with sharp phase boundaries. The SAXS patterns are best fitted with a model that consists of liquid-like ordered polydisperse spheres. Most of the samples were shown to be poorly crystalline, but some soft-phase crystals do exist and these melted at about 353 K as confirmed by DSC and temperature-dependent wide-angle X-ray diffraction. Annealing at 273 K did not affect the thermal stability but influenced the morphology of the samples. The effect of annealing on the samples of poly(urethane–urea) extended using diamine chain extenders was smaller than that for polyurethane samples, which indicates a much higher thermal stability of the poly(urethane–urea) samples owing to the formation of bidentate hydrogen-bond networks across the urea groups.


2000 ◽  
Vol 25 (0) ◽  
pp. 31-39 ◽  
Author(s):  
Egon SCHNITZLER ◽  
Wilson COSTA ◽  
Cristo Bladimiros MELIOS ◽  
Maria Ines Gonçalves LELES ◽  
Massao IONASHIRO

Solid state compounds of general formula M(DMCP)2.nH2O, where M represents Mg, Ca, Sr, Ba, and DMCP is 4-dimethylaminocinnamylidenepyruvate, and n = 1, except for Ca, where n = 2.5, have been prepared. Thermogravimetry, derivative thermogravimetry (TG, DTG), differential scanning calorimetry (DSC), X-ray diffraction powder patterns and complexometry were used to characterize and to study the thermal decomposition of these compounds.


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