Nadka Tzankova Dintcheva

Prof. Nadka Tzankova Dintcheva

Department of Engineering, University of Palermo, 90128 Palermo, Italy
orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 April 2021 in Polymers
Verified
Journal Article
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ABAlberto Di Bartolo
Alberto Di Bartolo
Giulia InfurnaGiulia Infurna
Giulia Infurna
Nadka Tzankova DintchevaNadka Tzankova Dintcheva
Nadka Tzankova Dintcheva
The European Union is working towards the 2050 net-zero emissions goal and tackling the ever-growing environmental and sustainability crisis by implementing the European Green Deal. The shift towards a more sustainable society is intertwined with the production, use, and disposal of plastic in the European economy. Emissions generated by plastic production, plastic waste, littering and leakage in nature, insufficient recycling, are some of the issues addressed by the European Commission. Adoption of bioplastics–plastics that are biodegradable, bio-based, or both–is under assessment as one way to decouple society from the use of fossil resources, and to mitigate specific environmental risks related to plastic waste. In this work, we aim at reviewing the field of bioplastics, including standards and life cycle assessment studies, and discuss some of the challenges that can be currently identified with the adoption of these materials.

4 October 2022 in Polymers
Verified
Journal Article
Open access
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EMElisabetta Morici
Elisabetta Morici
Nadka Tzankova DintchevaNadka Tzankova Dintcheva
Nadka Tzankova Dintcheva
Thermoset materials and their composites are characterized by a long life cycle with their main applications in aircrafts, wind turbines and constructions as insulating materials. Considering the importance of recovery and valorization of these materials at their end-of-life, avoiding landfilling, the interest concerning their recycling grows continuously. The thermoset materials and their composites, to be successfully recovered and valorized, must degrade their three-dimensional structures and recover the mono-oligomers and/or fillers. The thermoset materials could successfully degrade through thermal treatment at different temperatures (for example, above 1000 °C for incineration, ca. 500 °C for oxidation/combustion of organic constituents, etc.), chemical degradation by catalyst, irradiation with or without the presence of water, alcohol, etc., and mechanical recycling, obtaining fine particles that are useful as filler and/or reinforcement additives. Among these recycling methods, this mini-review focuses on the formulation and recovery method of innovative thermoset with in-build recyclability, i.e., materials having chemical links that could be degraded on-demand or containing dynamic covalent bonds to have re-processable and/or recyclable thermoset. This issue could be considered the future perspective in developing novel thermoset materials. The aim of this review is to get an overview of the state of the art in thermoset recycling and of the most commonly used thermoset composites, recovering valuable reinforcing fibers. Additionally, in this work, we also report not only known recycling routes for thermoset and thermoset-based composites, but also new and novel formulating strategies for producing thermosets with built-in recyclability, i.e., containing chemical-triggered on-demand links. This mini-review is also a valuable guide for educational purposes for students and specialized technicians in polymer production and recycling.

1 March 2008 in Polymer
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Journal Article
Closed access
GFGiovanni Filippone
Giovanni Filippone
Nadka Tzankova DintchevaNadka Tzankova Dintcheva
Nadka Tzankova Dintcheva
DAD. Acierno
D. Acierno
Francesco Paolo La MantiaFrancesco Paolo La Mantia
Francesco Paolo La Mantia

5 March 2018 in Materials
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Rossella ArrigoRossella Arrigo
Rossella Arrigo
Rosalia TeresiRosalia Teresi
Rosalia Teresi
CGCristian Gambarotti
Cristian Gambarotti
Filippo ParisiFilippo Parisi
Filippo Parisi
Giuseppe LazzaraGiuseppe Lazzara
Giuseppe Lazzara
Nadka Tzankova DintchevaNadka Tzankova Dintcheva
Nadka Tzankova Dintcheva
The aim of this work is the investigation of the effect of ultrasound treatment on the structural characteristics of carbon nanotubes (CNTs) and the consequent influence that the shortening induced by sonication exerts on the morphology, rheological behaviour and thermo-oxidative resistance of ultra-high molecular weight polyethylene (UHMWPE)-based nanocomposites. First, CNTs have been subjected to sonication for different time intervals and the performed spectroscopic and morphological analyses reveal that a dramatic decrease of the CNT’s original length occurs with increased sonication time. The reduction of the initial length of CNTs strongly affects the nanocomposite rheological behaviour, which progressively changes from solid-like to liquid-like as the CNT sonication time increases. The study of the thermo-oxidative behaviour of the investigated nanocomposites reveals that the CNT sonication has a detrimental effect on the thermo-oxidative stability of nanocomposites, especially for long exposure times. The worsening of the thermo-oxidative resistance of sonicated CNT-containing nanocomposites could be attributed to the lower thermal conductivity of low-aspect-ratio CNTs, which causes the increase of the local temperature at the polymer/nanofillers interphase, with the consequent acceleration of the degradative phenomena.

4 November 2021 in ACS Sustainable Chemistry & Engineering
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Journal Article
Open access
Salvatore MarulloSalvatore Marullo
Salvatore Marullo
Carla RizzoCarla Rizzo
Carla Rizzo
Nadka Tzankova DintchevaNadka Tzankova Dintcheva
Nadka Tzankova Dintcheva
Francesca D'AnnaFrancesca D'Anna
Francesca D'Anna
Chemical recycling to monomers is one of the key strategies in tackling the issues deriving from persistent plastic pollution in the environment, and poly(ethylene terephthalate) (PET) is among the most used polymers in modern society. In this context, we herein describe the glycolysis of PET to bis-hydroxyethyl terephthalate (BHET), promoted by basic cholinium salts differing for the anions, also comprising amino acid anions. We investigated the optimal reaction conditions, finding that the best-performing catalyst is [Ch][Gly], in the presence of which a conversion of 85% and a yield of 51% are achieved at 150 °C after 6 h, from PET deriving from a clear water bottle. We used our protocol to carry out the glycolysis of PET deriving from different postconsumer waste, like opaque and colored bottles and food packages, finding that the performance is better in the former compared with the latter starting materials.

1 September 2009 in Polymer Degradation and Stability
Verified
Journal Article
Closed access
Nadka Tzankova DintchevaNadka Tzankova Dintcheva
Nadka Tzankova Dintcheva
SAS. Al-Malaika
S. Al-Malaika
Francesco Paolo La MantiaFrancesco Paolo La Mantia
Francesco Paolo La Mantia