scholarly journals Preparation, Thermal, and Thermo-Mechanical Characterization of Polymeric Blends Based on Di(meth)acrylate Monomers

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 878
Author(s):  
Krystyna Wnuczek ◽  
Andrzej Puszka ◽  
Łukasz Klapiszewski ◽  
Beata Podkościelna

This study presents the preparation and the thermo-mechanical characteristics of polymeric blends based on di(meth)acrylates monomers. Bisphenol A glycerolate diacrylate (BPA.GDA) or ethylene glycol dimethacrylate (EGDMA) were used as crosslinking monomers. Methyl methacrylate (MMA) was used as an active solvent in both copolymerization approaches. Commercial polycarbonate (PC) was used as a modifying soluble additive. The preparation of blends and method of polymerization by using UV initiator (Irqacure® 651) was proposed. Two parallel sets of MMA-based materials were obtained. The first included more harmless linear hydrocarbons (EGDMA + MMA), whereas the second included the usually used aromatic copolymers (BPA.GDA + MMA). The influence of different amounts of PC on the physicochemical properties was discussed in detail. Chemical structures of the copolymers were confirmed by attenuated total reflection–Fourier transform infrared (ATR/FT-IR) spectroscopy. Thermo-mechanical properties of the synthesized materials were investigated by means of differential scanning calorimetry (DSC), thermogravimetric (TG/DTG) analyses, and dynamic mechanical analysis (DMA). The hardness of the obtained materials was also tested. In order to evaluate the surface of the materials, their images were obtained with the use of atomic force microscopy (AFM).

2020 ◽  
Vol 234 (2) ◽  
pp. 171-199
Author(s):  
Abd El-Aziz El-Sayed Fouda ◽  
El-Sayed Gmal Zaki ◽  
Mohamed Ahmed Khalifa

AbstractSome surfactants were synthesized, its chemical structures were checked using Fourier transform infrared spectroscopic (FT-IR). The investigation of inhibition efficiency (IE%) for dissolution of (LCS) in 1.0 M HCl with and without various concentrations of these compounds were done using electrochemical and non-electrochemical methods. Measured data depends on temperature, concentration, and nature of the substance. These compounds were adsorbed on LCS surface following Temkin isotherm. Polarization studies illustrated that these surfactants act as mixed inhibitors (anodic and cathodic). The effect of these inhibitors on LCS surface morphology’s was detected by Scanning Electron Microscope (SEM), ATR-IR (Attenuated total reflection Infra-red) and Atomic Force Microscopy (AFM) techniques. The parameters in an activated state of LCS were studied and estimated. All data techniques were compatible and matched.


2013 ◽  
Vol 27 (11) ◽  
pp. 1350073
Author(s):  
M. P. BINITHA ◽  
P. P. PRADYUMNAN

Single crystals of copper succinate dihydrate (CSD) with triclinic structure were grown in silica gel medium. The functional groups in the crystal were analyzed by FT-IR Spectroscopy. Atomic Force Microscopy (AFM) revealed the striations on the surface of grown crystals, which were incorporated during its time of growth. Thermal degradation studies have been carried out by Differential Scanning Calorimetry (DSC). Dielectric constant and AC conductivity have been estimated as a function of frequency at different temperatures.


2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Hohyoun Jang ◽  
Jaeseong Ha ◽  
Jiho Yoo ◽  
Jaeseung Pyo ◽  
Kunyoung Choi ◽  
...  

The purpose of this study was to enhance the scratch resistance of polycarbonate copolymer by using 3,3′-dibenzoyl-4,4′-dihydroxybiphenyl (DBHP) monomer, containing benzoyl moieties on the ortho positions. DBHP monomer was synthesized from 4,4′-dihydroxybiphenyl and benzoyl chloride, followed by the Friedel-Craft rearrangement reaction with AlCl3. The polymerizations were conducted following the low-temperature procedure, which is carried out in methylene chloride by using triphosgene, triethylamine, bisphenol-A, and DBHP. The chemical structures of the polycarbonate copolymers were confirmed by1H-NMR. The thermal properties of copolymers were investigated by thermogravimetric analysis and differential scanning calorimetry, and also surface morphologies were assessed by atomic force microscopy. The scratch resistance of homopolymer film (100 μm) changed from 6B to 1B, and the contact angle of a sessile water drop onto the homopolymer film also increased.


Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1069 ◽  
Author(s):  
Gabriele Nanni ◽  
José A. Heredia-Guerrero ◽  
Uttam C. Paul ◽  
Silvia Dante ◽  
Gianvito Caputo ◽  
...  

Poly(furfuryl alcohol) (PFA) is a bioresin synthesized from furfuryl alcohol (FA) that is derived from renewable saccharide-rich biomass. In this study, we compounded this bioresin with polycaprolactone (PCL) for the first time, introducing new functional polymer blends. Although PCL is biodegradable, its production relies on petroleum precursors such as cyclohexanone oils. With the method proposed herein, this dependence on petroleum-derived precursors/monomers is reduced by using PFA without significantly modifying some important properties of the PCL. Polymer blend films were produced by simple solvent casting. The blends were characterized in terms of surface topography by atomic force microscopy (AFM), chemical interactions between PCL and PFA by attenuated total reflection-Fourier transform infrared (ATR-FTIR), crystallinity by XRD, thermal properties by differential scanning calorimetry (DSC), and mechanical properties by tensile tests and biocompatibility by direct and indirect toxicity tests. PFA was found to improve the gas barrier properties of PCL without compromising its mechanical properties, and it demonstrated sustained antioxidant effect with excellent biocompatibility. Our results indicate that these new blends can be potentially used in diverse applications ranging from food packing to biomedical devices.


2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Xiaozhou Su ◽  
Lei Li ◽  
Weihan Huang

Complex nanomicelles were prepared by sericin and type A gelatin with molecular weight of 5789 Da and 128664 Da separately. The assembling conditions were as follows: mass ratio (sericin/gelatin) was 1 : 1, protein concentration was 0.5%, temperature was 35°C, and assembling time was 18 hours. Scanning electron microscopy (SEM), atomic force microscopy (AFM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), and dynamic light scattering (DLS) were conducted to observe and characterize the complex nanomicelles. Results showed that the complex sericin/gelatin micelles was a kind of nanospindle micelles. The micelles had high electrochemical stability, thermal stability, antidilution stability, and storage stability.


2020 ◽  
Vol 21 (17) ◽  
pp. 6154
Author(s):  
Barbara Gieroba ◽  
Anna Sroka-Bartnicka ◽  
Paulina Kazimierczak ◽  
Grzegorz Kalisz ◽  
Izabela S. Pieta ◽  
...  

In order to determine the effect of different gelation temperatures (80 °C and 90 °C) on the structural arrangements in 1,3-β-d-glucan (curdlan) matrices, spectroscopic and microscopic approaches were chosen. Attenuated total reflection Fourier transform infrared spectroscopy (ATR FT-IR) and Raman spectroscopy are well-established techniques that enable the identification of functional groups in organic molecules based on their vibration modes. X-ray photoelectron spectroscopy (XPS) is a quantitative analytical method utilized in the surface study, which provided information about the elemental and chemical composition with high surface sensitivity. Contact angle goniometer was applied to evaluate surface wettability and surface free energy of the matrices. In turn, the surface topography characterization was obtained with the use of atomic force microscopy (AFM) and scanning electron microscopy (SEM). Described techniques may facilitate the optimization, modification, and design of manufacturing processes (such as the temperature of gelation in the case of the studied 1,3-β-d-glucan) of the organic polysaccharide matrices so as to obtain biomaterials with desired characteristics and wide range of biomedical applications, e.g., entrapment of drugs or production of biomaterials for tissue regeneration. This study shows that the 1,3-β-d-glucan polymer sample gelled at 80 °C has a distinctly different structure than the matrix gelled at 90 °C.


2013 ◽  
Vol 1453 ◽  
Author(s):  
Bonifacio Alvarado-Tenorio ◽  
Angel Romo-Uribe ◽  
Patrick T. Mather

ABSTRACTShape memory nanocomposites were produced following a simple one-step synthesis route initiated by a series of molar mixtures of POSS thiol nanocages and pentaerythritol tetrakis (3mercaptopropionate), and a diacrylate polycaprolactone (PCL) with Mn=3,000 g/mol. Simultaneous wide- and small- angle X ray scattering (WAXS/SAXS), differential scanning calorimetry (DSC) and atomic force microscopy (AFM) experiments were carried out and results were correlated on microstructure. Molecular identification was performed by Fourier transformed infrared (FTIR-ATR). Thermomechanical shape memory cycles revealed that the nanocomposites achieved excellent shape recovery (99%) and shape fixity (100%) parameters. Dynamic mechanical analysis showed that elastomeric modulus decrease in function of the POSS thiol molar concentration and this result is correlated with the decrease in average crosslink density (ν). WAXS studies revealed orthorhombic crystallites for PCL combined with an amorphous POSS phase when the molar concentration of POSS was low (2.5%, 5%, 10%). However, increasing the molar concentration of POSS thiol until 20%, a broad and weak reflection centered around 2θ =7.9° which corresponded to imperfect POSS crystals. At the nanoscale, SAXS analysis showed lamellar nanostructure formation for all POSS/polycaprolactone crosslinked networks. Strikingly, induced anisotropic orientation of polycaprolactone lamellar nanostructure was observed when the concentration of POSS increased to 10 and 20 mol%.


2013 ◽  
Vol 11 (4) ◽  
pp. 542-553 ◽  
Author(s):  
Mihaela Mândru ◽  
Constantin Ciobanu ◽  
Stelian Vlad ◽  
Maria Butnaru ◽  
Laurent Lebrun ◽  
...  

AbstractThis paper is focused on the preparation and physicochemical characterization of two poly(ester ether urethane)s with rifampicin in their matrix and different molar concentrations of urethane groups. The polyurethanes with rifampicin were processed as asymmetrical microporous membranes by a phase inversion method and characterized by attenuated total reflection — Fourier transform infrared (ATR-FTIR) spectroscopy and differential scanning calorimetry (DSC). The influence of the surface morphology in the release of drug compounds was analyzed by scanning electron microscopy (SEM), atomic force microscopy (AFM), contact angle, and water uptake. The release of rifampicin depends on the molar concentration of urethane groups and also on the surface morphology of the polyurethane membranes. The antibacterial activity was evaluated with S. Epidermidis RP 62 A and P. Aeruginosa ATCC 1544. Finally, the biocompatibility of the polyurethane membranes was studied with human dermal fibroblasts (HDF) to evaluate the potential biomedical applications.


Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1292 ◽  
Author(s):  
Jia-Wun Li ◽  
Hsun-Tsing Lee ◽  
Hui-An Tsai ◽  
Maw-Cherng Suen ◽  
Chih-Wei Chiu

In this study, novel biodegradable long-segment fluorine-containing polyurethane (PU) was synthesized using 4,4′-diphenylmethane diisocyanate (MDI) and 1H,1H,10H,10H-perfluor-1,10-decanediol (PFD) as hard segment, and polycaprolactone diol (PCL) as a biodegradable soft segment. Nuclear magnetic resonance (NMR) was used to perform 1H NMR, 19F NMR, 19F–19F COSY, 1H–19F COSY, and HMBC analyses on the PFD/PU structures. The results, together with those from Fourier transform infrared spectroscopy (FTIR), verified that the PFD/PUs had been successfully synthesized. Additionally, the soft segment and PFD were changed, after which FTIR and XPS peak-differentiation-imitating analyses were employed to examine the relationship of the hydrogen bonding reaction between the PFD chain extender and PU. Subsequently, atomic force microscopy was used to investigate the changes in the microphase structure between the PFD chain extender and PU, after which the effects of the thermal properties between them were investigated through thermogravimetric analysis, differential scanning calorimetry, and dynamic mechanical analysis. Finally, the effects of the PFD chain extender on the mechanical properties of the PU were investigated through a tensile strength test.


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