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Featured researches published by Jan Kalfus.


Composite Interfaces | 2010

Effect of Particle Size on the Thermal Stability and Flammability of Mg(OH)2/EVA Nanocomposites

Jan Kalfus; J. Jancar

The effect of the Mg(OH)2 particle size on the thermal degradation and flammability of a model nanocomposite is presented. In order to investigate the effect of particle size on the flammability and thermal stability of materials intended for cable coatings, the ethylene–vinyl acetate copolymer (EVA) was filled with two types of magnesium hydroxide (Mg(OH)2) with the average particle size 20 nm and 2000 nm. The thermogravimetric experiments performed under nitrogen and air atmosphere did not reveal any substantial effect of particle size on the mechanisms and kinetics of Mg(OH)2 decomposition. Both types of Mg(OH)2, at temperatures above 350°C, decomposed endothermally to MgO and H2O. At the same filler volume fraction, composites with the larger Mg(OH)2 particles exhibited greater value of the limiting oxygen index (LOI) compared to Mg(OH)2 nanocomposites. It is proposed that the reduction of Mg(OH)2 particle size below 200 nm results in the catalytic effect of Mg2+ to become more prominent compared to coarser particles. In the case of nano-sized Mg(OH)2, a large portion of polymer matrix is in direct contact with filler surface due to the high specific surface area of the filler used. Large filler–matrix contact area most probably resulted in the surface-induced catalytic effects of the Mg2+ ion on degradation of polyolefins, already described in the literature, accelerating thermal degradation of EVA matrix. This process acts against the flame retarding effect of the Mg(OH)2 thermal decomposition. Furthermore, larger filler surface of nano-filler led to the indispensable change of the deformation response of EVA compared to the micro-filled composite.


Journal of Polymer Science Part B | 2007

Relaxation Processes in PVAc-HA Nanocomposites

Jan Kalfus; J. Jancar


Polymer Degradation and Stability | 2008

Degradation of polypropylene impact-copolymer during processing

Jiří Tocháček; Josef Jančář; Jan Kalfus; Petra Zbořilová; Zdeněk Buráň


Composites Science and Technology | 2008

Reinforcing mechanisms in amorphous polymer nano-composites

Jan Kalfus; J. Jancar


Polymer Composites | 2007

Elastic Response of Nanocomposite Poly(vinylacetate)- hydroxyapatite With Varying Particle Shape

Jan Kalfus; J. Jancar


Polymer | 2007

Immobilization of polyvinylacetate macromolecules on hydroxyapatite nanoparticles

Jan Kalfus; J. Jancar


Polymer Composites | 2007

Viscoelastic response of nanocomposite poly(vinyl acetate)-hydroxyapatite with varying particle shape—Dynamic strain softening and modulus recovery

Jan Kalfus; J. Jancar


Polymer Engineering and Science | 2008

Effect of Weakly Interacting Nanofiller on the Morphology and Viscoelastic Response of Polyolefins

Jan Kalfus; J. Jancar; J. Kucera


Polymer Degradation and Stability | 2011

Processing stability of polypropylene impact-copolymer during multiple extrusion – Effect of polymerization technology

Jiří Tocháček; Josef Jančář; Jan Kalfus; Soňa Hermanová


Polymer Degradation and Stability | 2009

Effect of multiple extrusion on molecular structure of polypropylene impact copolymer

Soňa Hermanová; Jiří Tocháček; Josef Jančář; Jan Kalfus

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J. Jancar

Brno University of Technology

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Jiří Tocháček

Brno University of Technology

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Josef Jančář

Brno University of Technology

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Soňa Hermanová

Institute of Chemical Technology in Prague

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R. Balkova

Brno University of Technology

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