Gabriela Borcia

Dr. Gabriela Borcia

orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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25 May 2023 in Polymers
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Journal Article
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EBEmma Bîrleanu
Emma Bîrleanu
IMIlarion MIHAILA
Ilarion MIHAILA
Ionut TOPALAIonut TOPALA
Ionut TOPALA
CBCatalin Borcia
Catalin Borcia
GBGabriela Borcia
Gabriela Borcia
Atmospheric-pressure plasma (APP) has advantages for enhancing the adhesion of polymers and has to provide uniform, efficient treatment, which also limits the recovery effect of treated surfaces. This study investigates the effects of APP treatment on polymers that have no oxygen bonded in their structure and varying crystallinity, aiming to assess the maximum level of modification and the post-treatment stability of non-polar polymers based on their initial structure parameters, including the crystalline–amorphous structure. An APP reactor simulating continuous processing operating in air is employed, and the polymers are analyzed using contact angle measurement, XPS, AFM, and XRD. APP treatment significantly enhances the hydrophilic character of the polymers, with semicrystalline polymers exhibiting adhesion work values of approximately 105 mJ/m2 and 110 mJ/m2 for 0.5 s and 1.0 s exposure, respectively, while amorphous polymers reach approximately 128 mJ/m2. The maximum average oxygen uptake is around 30%. Short treatment times induce the roughening of the semicrystalline polymer surfaces, while the amorphous polymer surfaces become smoother. The polymers exhibit a limit to their modification level, with 0.5 s exposure being optimal for significant surface property changes. The treated surfaces remain remarkably stable, with the contact angle only reverting by a few degrees toward that of the untreated state.

31 October 2007 in Applied Physics A
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CBCatalin Borcia
Catalin Borcia
GBGabriela Borcia
Gabriela Borcia
NDN. Dumitrascu
N. Dumitrascu

12 June 2001 in Journal of Applied Polymer Science
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Journal Article
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NDN. Dumitrascu
N. Dumitrascu
GBGabriela Borcia
Gabriela Borcia
GPG. Popa
G. Popa

5 February 2013 in Plasma Chemistry and Plasma Processing
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Journal Article
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SCSilvia Alina Chiper
Silvia Alina Chiper
GBGabriela Borcia
Gabriela Borcia

20 October 2023 in Polymers
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Journal Article
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SCSilvia Alina Chiper
Silvia Alina Chiper
GBGabriela Borcia
Gabriela Borcia
This study’s aim is a comparison of the plasma-induced effects on polymers exposed in helium and argon gaseous environments in a pulsed dielectric barrier discharge at atmospheric pressure. Cellulose-based and synthetic polymers are tested with regard to a range of parameters, such as wettability, adhesion, surface energy and polarity, the oxygen amount in their structure, and surface morphology. The surface properties are analyzed by contact angle measurements, X-ray photoelectron spectroscopy, and scanning electron microscopy images. The results point to the efficient and remarkably stable modifications of the plasma-exposed surfaces, such as their enhanced adhesion, surface energy, and oxygen incorporation. Additionally, plasma provides significant oxygen uptake in cellulose-based materials that bear already prior to treatment a high amount of oxygen in their structure. The comparison between the properties of the non-permeable, homogeneous, smooth-surface synthetic polymer and those of the loosely packed, porous, heterogeneous cellulose-based polymers points to the different rates of plasma-induced modification, whereby a progressive alteration of cellulosic surface properties over much larger ranges of exposure durations is noted. Present experimental conditions ensure mild treatments on such sensitive material, such as paper, and this is without alterations of the surface morphology and the physical degradation of the material over a large range of treatment duration.

24 April 2008 in Journal of Biomedical Materials Research Part B: Applied Biomaterials
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NDNicoleta Dumitrascu
Nicoleta Dumitrascu
CBCatalin Borcia
Catalin Borcia
GBGabriela Borcia
Gabriela Borcia