International Journal of Polymer Analysis and Characterization最新文献

{"title":"Experimental evaluation and numerical comparisons of pine tree leaves, graphene oxide loaded, and E-glass fiber reinforced sandwich composites","authors":"","doi":"10.1080/1023666X.2024.2371426","DOIUrl":"10.1080/1023666X.2024.2371426","url":null,"abstract":"<div><p>The research aim is to develop pure epoxy composites (PEC), PTL-reinforced epoxy composites (PTLEC), PTL-loaded and E-glass fiber- incorporated epoxy composites (PTLEIEC), and PTL- and E-glass fabric and graphene oxide-incorporated epoxy composites (PTLEIEGO) were fabricated through an open molding hand layup technique, and structural, mechanical, and thermal stability were carried out and results were compared. Functional groups such as OH, -C-H, C=O, C=C, and C-OH, were found in PTL. Similarly, the OH, C-H, Si-O-Si, C=O, and C-H present in the PTLEIEGO composites were found through Fourier transform infrared spectroscopy (FTIR). The crystal plane orientations (110) and (220) in the PTLEIEGO composites were found through XRD. The surface morphology and elemental compositions of PTLEIEGO composites were found through field emissions electron microscopy (FESEM) and found the presence of different organic and inorganic elemental compositions such as C, O, Si, Ca, Zn, K, and Br as 77.85, 20.78, 0.33, 0.45, 0.05, 0.05, and 0.50 wt.% through energy dispersive X-ray (EDX) spectroscopy. The DSC and TGA were carried out and found the thermal stability of the composites and the onset melting temperature was found to 353.1˚ C. The maximum tensile strength of PTL, PEC, PTLEC, PTLEIEC, and PTLEIEGO composites was found to be 1.25 MPa, 25 ± 0.5 MPa, 55 ± 0.5 MPa, 93 ± 0.5 MPa, and 120 ± 0.5 MPa as per ASTM D 638. The tensile strength was improved from 1.25 MPa for PTL to 120 ± 0.5 MPa for PTLEIEGO. The FEM results revealed a minimum error of 0 % and a maximum error of 21.38 % compared to the experimental results. The maximum shore D hardness of PEC, PTLEC, PTLEIEC, and PTLEIEGO composites was found to be 55 ± 0.5 SHN, 59 ± 0.5 SHN, 76.1 ± 0.5 SHN, and 81.4 ± 0.5 SHN, respectively, as per ASTM D2240. The flexural strengths of PEC, PTLEC, PTLEIEC, and PTLEIGO composites were found to be 37 ± 0.5 MPa, 43 ± 0.5 MPa, 94 ± 0.5 MPa, and 131 ± 0.5 MPa, respectively, as per ASTM D 790. The new composites would be employed in low-strength structural applications such as panels, cabins, doors, and laptop stands.<span>Highlights<ol><li><span><p>The tensile strength of PTL, PEC, PTLEC, PTLEIEC, and PTLEIEGO were found to be 1.25, 25 ± 0.5, 55 ± 0.5, 93 ± 0.5, and 120 ± 0.5 MPa, respectively.</p></span></li><li><span><p>The tensile strength of the experimental results was compared with FEM results.</p></span></li><li><span><p>The shore D hardness of PEC, PTLEC, PTLEIEC, and PTLEIGO was determined to be 55 ± 0.5, 59 ± 0.5, 76.1 ± 0.5, and 81. 4 ± 0.5 SHN, respectively.</p></span></li><li><span><p>The novel composite would be employed in low-strength structural applications such as panels, cabins, doors, and laptop stands.</p></span></li></ol></span></p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 6","pages":"Pages 363-384"},"PeriodicalIF":1.7,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141509285","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Influence of the processing parameters on the degradation of poly(lactic acid) (PLA) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and modification of their molecular weight using chain extenders","authors":"Adrian Boborodea ,&nbsp;F. Cordenier ,&nbsp;C. Lemenu ,&nbsp;L. Panarisi ,&nbsp;P. Le Maître ,&nbsp;S. Denis ,&nbsp;P. De Groote","doi":"10.1080/1023666X.2024.2369901","DOIUrl":"10.1080/1023666X.2024.2369901","url":null,"abstract":"<div><p>Poly(lactic acid) (PLA) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) exhibit valuable mechanical properties like high stiffness and tensile strength but are sensitive to processing parameters. The influence of these parameters was evaluated by measuring the variation of melt viscosity during processing. For all experiments, in the absence of chain extenders, the decrease in melt viscosity clearly showed the degradation of polymers during processing. This is more pronounced for PHBV than PLA. In order to compensate for the degradation and, if possible, improve the melt strength of these bio-based polymers, two chain extenders have been evaluated: dicumyl peroxide (DCP) and a polymeric epoxy acrylate chain extender (Joncryl^® ADR 4400). DCP reacts quickly with PLA and PHBV, while the epoxy-acrylate chain extender shows slower kinetics. For the PLA, with both investigated chain extenders, an increase in the molecular weight as compared with the virgin polymer and eventually the apparition of an insoluble fraction due to branching and crosslinking are observed. In the case of PHBV, the degradation is compensated by using DCP, requiring short processing times. No significant increase in molecular weight was observed when using the polymeric epoxy acrylate chain extender, requiring longer residence times, although the apparition of a gel fraction suggests the presence of branching and crosslinking.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 6","pages":"Pages 347-362"},"PeriodicalIF":1.7,"publicationDate":"2024-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141881075","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Hybrid benzoxazines from natural bio-phenolics for enhanced thermal stability and hydrophobicity: a study on vermiculite reinforced composites with low dielectric constant","authors":"Subasri Appasamy ,&nbsp;Kavya Shanmugam ,&nbsp;Balaji Krishnasamy ,&nbsp;Hariharan Arumugam ,&nbsp;Alagar Muthukaruppan","doi":"10.1080/1023666X.2024.2349629","DOIUrl":"10.1080/1023666X.2024.2349629","url":null,"abstract":"<div><p>Two series of unsymmetrical hybrid benzoxazines were separately synthesized using combinations of natural bio-phenolic materials, namely cardanol (C) with eugenol (E), vanillin (V), and guaiacol (G) using diaminodiphenylmethane (ddm)/diaminodiphenyl ether (dde) through the well-known Mannich reaction. The synthesized hybrid benzoxazines have a cure temperature between 229 °C and 269 °C. Compared to previous synthesized benzoxazines, vanillin-based benzoxazines (C-dde-V and C-ddm-V) have a lower cure temperature. TGA results show that poly(C-ddm-V) and poly(C-dde-V), two hybrid polybenzoxazines, have superior thermal stability than the other hybrid polybenzoxazines. In order to develop polybenzoxazine composites, different wt% of GPTMS functionalized vermiculite was incorporated with poly(C-ddm-V). The properties of these composites were examined and contrasted with those of a neat matrix. The hybrid polybenzoxazines and composites water contact angle values vary from 136° to 144°, suggesting that all of the hybrid polybenzoxazines and composites have good hydrophobic behavior. On increasing the concentration of vermiculite, the dielectric constant value significantly decreased to a low dielectric constant.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 4","pages":"Pages 226-240"},"PeriodicalIF":1.9,"publicationDate":"2024-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141122896","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Preparation and luminescence properties of polypyrrole-thiophene derivatives","authors":"Pan Wang ,&nbsp;Jingjing Liu ,&nbsp;Xinrui Hou ,&nbsp;Zhixuan Chen","doi":"10.1080/1023666X.2024.2357397","DOIUrl":"https://doi.org/10.1080/1023666X.2024.2357397","url":null,"abstract":"<div><p>Four kinds of polypyrrole-thiophene derivatives (PPy-Th) are prepared via solution polycondensation using pyrrole, 3-acylpyrrole, and 2-thenaldehyde as monomers. The structure, molecular weight, micromorphology, thermal degradation, ultraviolet-visible absorption, and luminescence performance of the derivatives are investigated by fourier transform infrared (FTIR), hydrogen nuclear magnetic resonance (¹HNMR) spectroscopy, gel permeation chromatography (GPC), X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), ultraviolet-visible (UV-Vis), and fluorescence spectra. FTIR and ¹HNMR confirm that the derivatives have been successfully fabricated, and GPC indicates that the derivatives belong to oligomers with narrow molecular weight distribution. For acyl-substituted derivatives, the microstructures are mainly lamellar accumulation. Furthermore, under ultraviolet excitation, the derivatives can produce blue or green light emission, corresponding to the transitions of large π electrons in the conjugated structure of the molecular chains. Especially, the maximum emission wavelengths and Stokes shifts of the acyl-substituted derivatives are markedly larger than that of the non-acyl-substituted derivatives. The fluorescence quantum yield and band gap of the PVT are 4.46% and 2.01 eV, respectively. The fabricated PPy-Th can be used as luminescent materials in the development and application of polymer light-emitting diodes.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 4","pages":"Pages 241-252"},"PeriodicalIF":1.9,"publicationDate":"2024-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141289564","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Enhancing poly(lactic acid)/maleated polypropylene blend with magnesium oxide catalyst: a reactive blending approach for improved mechanical properties","authors":"Iman Nikkhah Sokhanvar ,&nbsp;Narjes Sadat Karbalaei Ghomi ,&nbsp;Seyed Amin Mirmohammadi ,&nbsp;Afshar Alihosseini ,&nbsp;Robabeh Nasirian","doi":"10.1080/1023666X.2024.2357555","DOIUrl":"10.1080/1023666X.2024.2357555","url":null,"abstract":"<div><p>Some defects of polylactic acid (PLA), especially its poor mechanical properties, were modified using a minimum content of non-biodegradable maleated polypropylene (MAPP). To this end, first, the amount of MAPP was optimized, which was 20 wt.%. Second, MgO was used as a new catalyst to improve the exchange reactions between active groups in both polymers in a reactive blending process. Tensile and izod analyses showed that, compared to neat PLA, with a slight decrease in modulus and tensile strength, elongation at break, and impact resistance were improved in the presence of 20 and 0.1 wt.% of MAPP and MgO, respectively. This improvement in mechanical properties can be related to the exchange reactions between two polymers and the formation of PLA-MAPP block copolymers. MFI and WDCA analyses demonstrated the increase in melt flowability and surface hydrophilicity of the resulting blends, respectively. DSC analysis showed that the T_g values of both polymers approached each other in the presence of catalyst. Also, the elimination of cold crystallization of PLA and the decrease in the T_m and crystallinity of both polymers are clear reasons for the miscibility of the alloy. TEM displayed the proper dispersion of MgO nanoparticles within the polymer matrix, and in addition, the XRD test also proved the decrease in the crystallinity of both polymers and appropriate miscibility of the samples containing 20 and 0.1 wt.% of MAPP and MgO, respectively. These results can promise the design of a compound with the maximum amount of PLA for further use in various industries.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 4","pages":"Pages 253-268"},"PeriodicalIF":1.9,"publicationDate":"2024-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141100173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Synthesis of novel stimuli-responsive hydrogels based on polyurethane","authors":"Axel J. Cimas ,&nbsp;Francisco M. Pardini ,&nbsp;Javier I. Amalvy","doi":"10.1080/1023666X.2024.2346432","DOIUrl":"10.1080/1023666X.2024.2346432","url":null,"abstract":"<div><p>This article describes the study of a thermo-responsive hybrid systems based on polyurethane (PU) modified with sensitive acrylamide derivates. The hybrid systems were synthesized using PU and two acrylamide derivatives (<em>N</em>-isopropylacrylamide (NIPA) and <em>N</em>-isopropylmethacrylamide (NIPMA)) in different proportions. The systems were characterized using infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic light scattering (DLS). Water-uptake capacity and sedimentation rate were also determined. The results showed that the hybrids with 30% acrylamide derivate (AD) showed a T50 of approximately 360 °C indicating that thermal degradation decreased with the addition of NIPA and NIPMA. Additionally, the incorporation of AD increases the glass transition temperature from −34 to −22 °C when 30% AD was used. The hybrids with 30% AD showed a variation in the diameters (above 60%) when the temperature was decreased from 50 to 22 °C. These changes were attributed to the hydrophilic → hydrophobic transition that occurs when measuring below and above the low critical solution temperature (LCST) of the polymer. Furthermore, the extra methyl group in the structure of NIPMA makes the collapse less pronounced than in NIPA, decreasing the relative diameter change by 10%. Sedimentation tests showed that the addition of the hybrid hydrogels in the sand increased the time of decantation by 60%. So, the combination of two thermo-responsive polymers to alter the hydrophilic/hydrophobic balance allows these polymers to modify their conformation at a specific temperature and could be potentially useful as self-suspending support agents or drug delivery systems.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 4","pages":"Pages 213-225"},"PeriodicalIF":1.9,"publicationDate":"2024-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141122091","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Evaluation of poly(2-hydroxyethyl methacrylate) and poly(N-hydroxyethyl acrylamide) cryogels as potential quercetin release matrices","authors":"Cahit Özbilenler ,&nbsp;Elvan Yilmaz ,&nbsp;Ergül Mutlu Altundağ","doi":"10.1080/1023666X.2024.2349628","DOIUrl":"10.1080/1023666X.2024.2349628","url":null,"abstract":"<div><p>Fabrication of a suitable drug delivery system forms an attractive strategy to overcome the low bioavailability of quercetin. Poly(2-hydroxyethyl methacrylate–<em>co</em>-N-hydroxyethyl acrylamide), P(HEMA-<em>co</em>-HEAA) copolymer samples, and homopolymers of 2-hydroxyethyl methacrylate (PHEMA) and N-hydroxyethyl acrylamide (PHEAA) offer potential as quercetin delivery matrices owing to their favorable properties rendered in this study. Free radical polymerization applied under cryogenic conditions produced the polymer gels. The homopolymers and copolymers are noncytotoxic, porous, soft cryogels with surfaces resistant to protein and HCT-116 cancer cell adhesion. <em>In vitro,</em> quercetin release studies from samples reveal swelling-controlled, zero-order drug release at pH = 7.4 and 37 °C with high cumulative release percentages ranging from 92.03% to 94.82%. The durability of the cryogels and limited quercetin release at pH = 2.0 indicate that these cryogels are promising matrices for successfully delivering quercetin to the small intestine, where its primary absorption occurs.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 3","pages":"Pages 189-212"},"PeriodicalIF":1.9,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140985778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Studies of thermal decomposition of poly(vinyl chloride) composition with cadmium yellow and stearic acid","authors":"Magdalena Tworek ,&nbsp;Edwin Makarewicz ,&nbsp;Iryna Shyychuk ,&nbsp;Joanna Kowalik ,&nbsp;Anna Zalewska ,&nbsp;Jolanta Tomaszewska","doi":"10.1080/1023666X.2024.2346857","DOIUrl":"10.1080/1023666X.2024.2346857","url":null,"abstract":"<div><p>The article presents research on the thermal decomposition of individual ingredients and compositions that are physical mixtures of emulsion poly(vinyl chloride) (PVC), cadmium yellow, and stearic acid. The results of the tests were TG, DTA, and DTG graphs. From their course, the initial decomposition temperatures, maximum decomposition rate, and final temperatures were determined, and changes in the mass of samples and the values of thermal effects were calculated. The influence of pigment and stearic acid on the thermal decomposition of PVC was investigated. Cadmium yellow, modified in an alkaline medium and containing hydroxyl groups, was also used for the tests. It was found that the presence of both pigment and stearic acid had a retarding effect on the initiation of thermal decomposition of PVC. The addition of CdS modified in an alkaline environment had a more or less similar effect on the initial decomposition temperature of PVC. Depending on the composition of the polymer and the value of the final temperature, different values of thermal effects and the amount of products formed were indicated.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 3","pages":"Pages 172-188"},"PeriodicalIF":1.9,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140996807","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Preparation and opto-electrical characterization of poly(ethylene oxide) based polymer blends for electrochemical applications","authors":"Samartharama B. N. ,&nbsp;N. Nagaiah ,&nbsp;Ambika M. R. ,&nbsp;Demappa T. ,&nbsp;Swaroop K Acharya","doi":"10.1080/1023666X.2024.2336308","DOIUrl":"10.1080/1023666X.2024.2336308","url":null,"abstract":"<div><p>Solid polymer electrolyte blends with varied compositions of poly(ethylene oxide) (PEO)/carboxymethyl cellulose (Na-CMC) in 10/90, 50/50, and 90/10 compositions have been successfully prepared by means of the solution cast technique at room temperature. The modification of the structural, optical, and electrical properties of the prepared blend samples was studied by employing XRD, FTIR, UV-Vis, and electrical impedance spectroscopy methods. X-ray diffraction studies revealed that the crystalline nature gradually transforms into amorphous as the Na-CMC content increases in the sample. The variation of bands noticed in the Fourier transform infrared spectroscope characteristic spectrum of the blends reveals the formation of complexes between the individual polymers. The analysis of optical properties using a UV-Vis spectrometer in the wavelength range of 900–1100nm, shows a gradual decrease in the optical indirect energy band gap with an increase in Na-CMC content in the blend. The study of the electrical properties of the blend carried out in the frequency range 50 Hz–1MHz and temperature range 303K–338K, using an electrical impedance analyzer reveals that, the dielectric constant and loss decrease with the rise in frequency, exhibiting the usual behavior of the polymers. AC conductivity is found to increase with an increase in temperature. The highest value of ionic conductivity is found to be 6.06 × 10⁻³Scm⁻¹ for the blend with a 10/90 composition.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 3","pages":"Pages 157-171"},"PeriodicalIF":1.9,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140597848","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Synthesis and properties of functional methacrylic copolymers","authors":"Tamara G. Oberti ,&nbsp;M. Laura Mosca ,&nbsp;Adolfo Pesce ,&nbsp;Fernando Amarilla ,&nbsp;Maria Susana Cortizo","doi":"10.1080/1023666X.2024.2312492","DOIUrl":"10.1080/1023666X.2024.2312492","url":null,"abstract":"<div><p>In the present work, a family of functionalized statistical copolymers was synthesized by radical polymerization from a varied composition of benzyl methacrylate (BzMA) and N,N-dimethylaminoethyl methacrylate (DMAEMA) comonomers using 2,2’-azobisisobutyronitrile (AIBN) as initiator. The characterization, identification, and composition analysis of each copolymer were carried out by spectroscopic methods (FTIR and 1H-NMR). Then, different properties were evaluated: molecular size was determined by measurement of intrinsic viscosity [η] in THF at 25 °C and glass transition temperature (Tg) analyzed by differential scanning calorimetry. Films were prepared by the solvent casting method from selected samples with different compositions and their mechanical properties were analyzed by tensile tests. It was observed that the composition of the functionalized copolymers substantially affects their macromolecular and mechanical properties, evidencing greater flexibility when the DMAEMA content in the copolymer increased.</p></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 2","pages":"Pages 146-155"},"PeriodicalIF":1.9,"publicationDate":"2024-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139903326","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}