scholarly journals Superiority of Cellulose Non-Solvent Chemical Modification over Solvent-Involving Treatment: Application in Polymer Composite (part II)

Materials ◽  
2020 ◽  
Vol 13 (13) ◽  
pp. 2901 ◽  
Author(s):  
Stefan Cichosz ◽  
Anna Masek

The following article debates on the properties of cellulose-filled ethylene-norbornene copolymer (EN) composites. Natural fibers employed in this study have been modified via two different approaches: solvent-involving (S) and newly developed non-solvent (NS). The second type of the treatment is fully eco-friendly and was carried out in the planetary mill without incorporation of any additional, waste-generating substances. Composite samples have been investigated with the use of spectroscopic methods (FT-IR), differential scanning calorimetry (DSC), static mechanical analysis, and surface-free energy measurements. It has been proved that the possible filler-polymer matrix interaction changes may occur due to the performed modifications. The highest reinforcement was evidenced for the composite sample filled with cellulose treated via a NS approach—TS = (34 ± 2) MPa, Eb = (380 ± 20)%. Additionally, a surface free energy polar part exhibited a significant increase for the same type of modification. Consequently, this could indicate easier wetting of the material which may contribute to the degradation process enhancement. Successfully developed cellulose-filled ethylene-norbornene copolymer composite compromises the rules of green chemistry and sustainable development by taking an advantage of renewable natural resources. This bio-inspired material may become an eco-friendly alternative for commonly used polymer blends.

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).


Materials ◽  
2020 ◽  
Vol 13 (24) ◽  
pp. 5789
Author(s):  
Olga Mysiukiewicz ◽  
Mateusz Barczewski ◽  
Arkadiusz Kloziński

Polylactide-based composites filled with waste fillers due to their sustainability are a subject of many current papers, in which their structural, mechanical, and thermal properties are evaluated. However, few studies focus on their behavior in low temperatures. In this paper, dynamic and quasi-static mechanical properties of polylactide-based composites filled with 10 wt% of linseed cake (a by-product of mechanical oil extraction from linseed) were evaluated at room temperature and at −40 °C by means of dynamic mechanical analysis (DMA), Charpy’s impact strength test and uniaxial tensile test. It was found that the effect of plasticization provided by the oil contained in the filler at room temperature is significantly reduced in sub-zero conditions due to solidification of the oil around −18 °C, as it was shown by differential scanning calorimetry (DSC) and DMA, but the overall mechanical performance of the polylactide-based composites was sufficient to enable their use in low-temperature applications.


2018 ◽  
Vol 23 (1) ◽  
pp. 3-11
Author(s):  
Anna Wiśniewska ◽  
Gabriela Chwalik ◽  
Sylwia Łagan

The evaluation of a degradation process of polyethylene (PE) in in vitro conditions under the influence of X-rays (X) and an in-cubation in two solutions simulating the environment of a living organism (SBF – simulated body fluid) was carried out. A dose corresponding to 10 standard X-ray pictures of the skeletal system as well as Ringer's and saline solutions at 40°C were used in the study. The paper presents the results of the influence of the 12-month studies on the selected surface properties of the material: surface wettability and abrasiveness. The value of surface free energy (SFE) was determined on the basis of the wetting angle measurements. The conductivity of the incubation fluids was also analyzed. The obtained results indicate that the adopted dose of X-ray radiation has no significant effect on the wettability of the surface of polyethylene. The nature of the surface layer of polyethylene did not change as a result of the 12-month incubation and remained hydrophilic. For the samples incubated in both immersion fluids, a decrease in surface free energy (SFE) was observed. For both the irradiated material and the control group, no significant changes in the mass of the samples and the conductivity of the incubation fluids were found, which indicates the stability of polyethylene. However, the abrasion value increased by approximately 26%. With the passage of the incubation time, a decrease in the value of this parameter was observed for the polyethylene subjected to radiation. No significant changes were found for the control group.


2019 ◽  
Vol 73 (1) ◽  
pp. 13-24 ◽  
Author(s):  
Ivan Stefanovic ◽  
Jasmina Dostanic ◽  
Davor Loncarevic ◽  
Dana Vasiljevic-Radovic ◽  
Sanja Ostojic ◽  
...  

This work is focused on preparation of poly(urethane-siloxane)/titanium-dioxide nanocompo-sites (PUSNs) with enhanced features. PUSNs were prepared by the in situ polymerization re-action using titanium-dioxide as a nano-filler in different amounts (1, 2, 3 and 5 wt.%) with respect to the poly(urethane-siloxane) (PUS) matrix. PUS copolymer was based on ?,?-dihy-droxy-ethoxypropyl-poly(dimethylsiloxane), 4,4?-methylenediphenyldiisocyanate and 1,4-bu-tanediole. In order to investigate the influence of TiO2 content on the structure, UV resistance, thermal properties, hydrophobicity and morphology of the prepared PUSNs, FTIR spectro-scopy, UV-Vis diffuse-reflectance spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), contact angle measurements, surface free energy (SFE) analysis, water absorption, scanning electron microscopy (SEM) and atomic force microscopy (AFM) were performed. The PUSNs showed excellent UV resistance, high hydrophobicity, low surface free energy and also higher thermal stability and rougher surface and cross-section relief structure as compared to the pure PUS copolymer. Based on the obtained results it can be concluded that prepared PUSNs could be potentially used as protective coatings.


2019 ◽  
Vol 3 (1) ◽  
pp. 6 ◽  
Author(s):  
Mohd Radzi Mohd Hafiezal ◽  
Abdan Khalina ◽  
Zainal Abidin Zurina ◽  
Md Deros Mohd Azaman ◽  
Zin Mohd Hanafee

This purpose of this paper was to reveal characteristics of a composite structure containing carbon fiber as a reinforcement and blended synthetic epoxy/bio-epoxy derived from crude jatropha oil as resin and compared with fully synthetic epoxy. The composite structure was prepared by the vacuum-assisted resin transfer molding technique and was left to cure for 24 h at room temperature. Both were characterized for their thermal, chemical, and flammable characteristics. The incorporation of jatropha bio-epoxy into the matrix significantly improved the thermal stability between 288–365 °C as obtained by thermogravimetric analysis (TGA) test. Dynamic mechanical analysis (DMA) curves showed slight diminution of performances and Tg from DMA tests confirmed well with the trend of Tg obtain by differential scanning calorimetry (DSC) curves. On the other hand, the flammability property was rated horizontal burning (HB) which was the same as the fully synthetic composite, but the duration to self-extinguish was halved for the composite with jatropha bio-epoxy. Fourier transform infrared attenuated total reflectance (FT-IR/ATR) was conducted to determine the difference of functional groups’ spectrum due to bonding type existing on both specimens. Overall, the composite specimen with blended bio-epoxy exhibited better thermal stability, comparable flammability characteristics, and performances. The aim of this paper was to introduce bio-based epoxy as a potential alternative epoxy and to compete with synthetic epoxy so as to minimize the footprint of non-renewable composite.


2020 ◽  
pp. 002199832097829
Author(s):  
Renato P Melo ◽  
Marcelo P da Rosa ◽  
Paulo H Beck ◽  
Lucas GP Tienne ◽  
Maria de Fátima V Marques

The use of cellulosic fibers from different natural sources as fillers in polymer matrices to improve their properties has been extensively studied in the last years. It is mainly due to the vast availability of natural fibers as well as their biodegradability. The purpose of this present work was to extract cellulose, silica, and cellulose-silica fillers – these last called “hybrids” – from rice husk through delignification and subsequent oxidation and, then, prepare composites with polyamide 6 and improve mainly its thermal-mechanical properties. The content of 10 wt.% of fillers was inserted in PA 6 matrix. Infrared spectroscopy pointed the main characteristic peaks of cellulose and silica of hybrids, as thermogravimetric analysis showed high thermal stability of fillers, allowing their incorporation in PA-6 matrix by extrusion method. Thermo dynamic-mechanical analysis showed, in a general overview, a significant improvement of mechanical properties of composites, as elastic modulus, compared with neat polyamide-6, mainly the one with 2.5 wt% of silica and 7.5% of cellulose. This last also showed increasing of degree of crystallinity, measured by differential scanning calorimetry, showing the extraction efficiency of fillers from rice husk as well as the potential application of composites as structural components in automotive parts.


Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2330 ◽  
Author(s):  
Yufei Liu ◽  
Min He ◽  
Daohai Zhang ◽  
Qian Zhao ◽  
Yang Li ◽  
...  

P(N-phenylmaleimide-alt-styrene) (P(NPMI-alt-St)) and P(N-(4-carboxyphenyl)maleimide-alt-styrene) (P(CPMI-alt-St)) were designed and synthesized via free radical copolymerization. Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance spectroscopy (1H NMR and 13C NMR), gel permeation chromatography (GPC), and differential scanning calorimetry (DSC) were used to confirm the structure of P(NPMI-alt-St) and P(CPMI-alt-St). Next, the effect of P(CPMI-alt-St) on the heat deflection temperature (HDT) of nylon 6 was studied. In comparison to the PA6/P(NPMI-alt-St) blend, with the addition of 10 wt %, the HDT value of the PA6/P(CPMI-alt-St) blend increased by 15.7 °C, and the glass transition temperature (Tg) by Dynamic mechanical analysis (DMA) increased 2.3 °C. According to the analysis of DMA, dynamic viscosity, and the SEM of PA6 and its blends, P(CPMI-alt-St) promoted its compatibility with PA6, and promoted the storage modulus and dynamic viscosity of the blends. Thus, the introduction of 4-carboxyl can significantly improve the effect of P(CPMI-alt-St) on the heat resistance modification of nylon 6.


Polymers ◽  
2021 ◽  
Vol 13 (17) ◽  
pp. 2963
Author(s):  
Sukannika Tubtimsri ◽  
Yotsanan Weerapol

Ternary solid solutions composed of nifedipine (NDP), amino methacrylate copolymer (AMCP), and polysorbate (PS) 20, 60, or 65 were prepared using a solvent evaporation method. The dissolution profiles of NDP were used to study the effect of the addition of polysorbate based on hydrophilic properties. A solid solution of NDP and AMCP was recently developed; however, the dissolution of NDP was <70%. In the present study, polysorbate was added to improve the dissolution of the drug by altering its hydrophilicity. The suitable formulation contained NDP and AMCP at a ratio of 1:4 and polysorbate at a concentration of 0.1%, 0.3%, or 0.6%. Differential scanning calorimetry and powder X-ray diffraction were used to examine the solid solutions. No peak representing crystalline NDP was observed in any solid solution samples, suggesting that the drug was molecularly dispersed in AMCP. The NDP dissolution from NDP powder and solid solution without PS were 16.82% and 58.19%, respectively. The highest dissolution of NDP of approximately 95.25% was noted at 120 min for the formulation containing 0.6% PS20. Linear correlations were observed between the surface free energy and percentages of dissolved NDP (R2 = 0.7115–0.9315). Cellular uptake across Caco-2 was selected to determine the drug permeability. The percentages of cellular uptake from the NDP powder, solid solution without and with PS20 were 0.25%, 3.60%, and 7.27%, respectively.


Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 655
Author(s):  
Cristian Sánchez-Rodríguez ◽  
María-Dolores Avilés ◽  
Ramón Pamies ◽  
Francisco-José Carrión-Vilches ◽  
José Sanes ◽  
...  

Polylactic acid (PLA)-based nanocomposites were prepared by twin-screw extrusion. Graphene oxide (GO) and an ionic liquid (IL) were used as additives separately and simultaneously. The characterization of the samples was carried out by means of Fourier transform infrared (FT-IR) and Raman spectroscopies, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The viscoelastic behavior was determined using dynamic mechanical analysis (DMA) and rheological measurements. IL acted as internal lubricant increasing the mobility of PLA chains in the solid and rubbery states; however, the effect was less dominant when the composites were melted. When GO and IL were included, the viscosity of the nanocomposites at high temperatures presented a quasi-Newtonian behavior and, therefore, the processability of PLA was highly improved.


Molecules ◽  
2020 ◽  
Vol 25 (6) ◽  
pp. 1279 ◽  
Author(s):  
Stefan Cichosz ◽  
Anna Masek

A recently developed cellulose hybrid chemical treatment consists of two steps: solvent exchange (with ethanol or hexane) and chemical grafting of maleic anhydride (MA) on the surface of fibers. It induces a significant decrease in cellulose moisture content and causes some changes in the thermal resistance of analyzed blend samples, as well as surface properties. The thermal characteristics of ethylene-norbornene copolymer (TOPAS) blends filled with hybrid chemically modified cellulose fibers (UFC100) have been widely described on the basis of differential scanning calorimetry and thermogravimetric analysis. Higher thermal stability is observed for the materials filled with the fibers which were dried before any of the treatments carried out. Dried cellulose filled samples start to degrade at approximately 330 °C while undried UFC100 specimens begin to degrade around 320 °C. Interestingly, the most elevated thermal resistance was detected for samples filled with cellulose altered only with solvents (both ethanol and hexane). In order to support the supposed thermal resistance trends of prepared blend materials, apparent activation energies assigned to cellulose degradation (EA1) and polymer matrix decomposition (EA2) have been calculated and presented in the article. It may be evidenced that apparent activation energies assigned to the first decomposition step are higher in case of the systems filled with UFC100 dried prior to the modification process. Moreover, the results have been enriched using surface free energy analysis of the polymer blends. The surface free energy polar part (Ep) raises considering samples filled with not dried UFC100. On the other hand, when cellulose fibers are dried prior to the modification process, then the blend sample’s dispersive part of surface free energy is increased with respect to that containing unmodified fiber. As polymer blend Ep exhibits higher values reflecting enhanced material degradation potential, the cellulose fibers employment leads to more eco-friendly production and responsible waste management. This is in accordance with the rules of sustainable development.


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