Anca Peter, Camelia Nicula, Anca Mihaly Cozmuta, Goran Drazic, Antonio Peñas, Stefania Silvi, Leonard Mihaly Cozmuta
The increase in the polymer-based materials needs has induced along the waste accumulation, thus argued higher interest in recycling. The study aims to assess the structural, morphological, mechanical resistance, physical–chemical and biochemical characteristics, as well as the preservative role during the curd cheese storage of a recycled polylactic acid (PLA)-based film modified with Ag-graphene-TiO2 nanostructured composite, obtained by recovering the composite from the used film, followed by its incorporation in new PLA. The breaking load of the recycled film was 24% lower than that of the new film and 10% higher than of the neat PLA. Differential scanning calorimetry (DSC) showed changes of the recycled PLA’s surface tension and crystallization degree in a greater extent than in the newly prepared film, revealing better incorporation of the recovered composite into the PLA matrix. Fourier transformed infrared spectroscopy showed the formation of C–O–Ti bridges between composite and PLA both in new and recycled film. Oxygen transmission rate (OTR) of the new and recycled film decreased by 33% and 45%, respectively, in comparison with reference PLA. The curd cheese was successfully stored in the recycled packaging; the organoleptic characteristics of cheese wrapped in recycled film were superior in comparison with the new film. The variation of fat and protein contents and mass loss was the lowest when the recycled film was used as packaging material. The study successfully showed the possibility to recover and recycle the used PLA-based films modified with inorganic nanocomposites.
{"title":"Polylactic Acid-Based Film Modified with Nano-Ag-Graphene-TiO2: New Film versus Recycled Film","authors":"Anca Peter, Camelia Nicula, Anca Mihaly Cozmuta, Goran Drazic, Antonio Peñas, Stefania Silvi, Leonard Mihaly Cozmuta","doi":"10.1155/2023/9937270","DOIUrl":"https://doi.org/10.1155/2023/9937270","url":null,"abstract":"The increase in the polymer-based materials needs has induced along the waste accumulation, thus argued higher interest in recycling. The study aims to assess the structural, morphological, mechanical resistance, physical–chemical and biochemical characteristics, as well as the preservative role during the curd cheese storage of a recycled polylactic acid (PLA)-based film modified with Ag-graphene-TiO<sub>2</sub> nanostructured composite, obtained by recovering the composite from the used film, followed by its incorporation in new PLA. The breaking load of the recycled film was 24% lower than that of the new film and 10% higher than of the neat PLA. Differential scanning calorimetry (DSC) showed changes of the recycled PLA’s surface tension and crystallization degree in a greater extent than in the newly prepared film, revealing better incorporation of the recovered composite into the PLA matrix. Fourier transformed infrared spectroscopy showed the formation of C–O–Ti bridges between composite and PLA both in new and recycled film. Oxygen transmission rate (OTR) of the new and recycled film decreased by 33% and 45%, respectively, in comparison with reference PLA. The curd cheese was successfully stored in the recycled packaging; the organoleptic characteristics of cheese wrapped in recycled film were superior in comparison with the new film. The variation of fat and protein contents and mass loss was the lowest when the recycled film was used as packaging material. The study successfully showed the possibility to recover and recycle the used PLA-based films modified with inorganic nanocomposites.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":"17 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2023-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138541378","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}
Eun Joo Shin, Ye Jin Song, Yang Sook Jung, Imjoo Jung, Sunhee Lee
Reversible deformation structure fabricated by 4D printing can be applied in various fields, such as actuators, intelligent mechanisms, and soft robots. In this study, 4D filaments for use in fused deposition modeling (FDM) 3D printers were fabricated by melt extrusion process mixing polylactic acid (PLA) and soft actuator grade thermoplastic polyurethane (TPU) 75 Shore A. The morphological (scanning electron microscopy, atomic force microscopy), chemical (Fourier transform infrared), thermal (differential scanning calorimetry, dynamic mechanical analysis, thermogravimetric analysis), mechanical (Instron), and WAXS properties of the prepared TPU/PLA blend (5 : 5, 7 : 3, 9 : 1) filaments were investigated. Filaments of 4D auxetic reentrant TPU/PLA samples were 3D printed, and their shape-memory characteristics were assessed at temperatures of 60°C (corresponding to the glass transition temperature of PLA), 70°C, 80°C (matching the melting temperature of the soft segment of TPU), and 90°C. The properties of TPU/PLA samples differ based on the PLA to TPU ratio, with an increase in TPU content resulting in a higher shape setting temperature but a shorter shape recovery time. For the TPU/PLA 5 : 5 sample, setting at 70°C and recovering at 85°C is the most suitable condition for shape recovery, whereas for the TPU/PLA 7 : 3 sample the best conditions are setting at 80°C and recovering at 95°C. In the case of TPU/PLA 9 : 1, shape setting is possible at 90°C, and shape recovery is fastest at 95°C. A 4D structure of TPU/PLA could be achieved based on shape memory testing by temperature stimulation of 3D printed auxetic c TPU/PLA samples.
{"title":"Manufacturing of Filament for 4D Printing through Polyether-Type TPU/PLA Blend","authors":"Eun Joo Shin, Ye Jin Song, Yang Sook Jung, Imjoo Jung, Sunhee Lee","doi":"10.1155/2023/4875625","DOIUrl":"https://doi.org/10.1155/2023/4875625","url":null,"abstract":"Reversible deformation structure fabricated by 4D printing can be applied in various fields, such as actuators, intelligent mechanisms, and soft robots. In this study, 4D filaments for use in fused deposition modeling (FDM) 3D printers were fabricated by melt extrusion process mixing polylactic acid (PLA) and soft actuator grade thermoplastic polyurethane (TPU) 75 Shore A. The morphological (scanning electron microscopy, atomic force microscopy), chemical (Fourier transform infrared), thermal (differential scanning calorimetry, dynamic mechanical analysis, thermogravimetric analysis), mechanical (Instron), and WAXS properties of the prepared TPU/PLA blend (5 : 5, 7 : 3, 9 : 1) filaments were investigated. Filaments of 4D auxetic reentrant TPU/PLA samples were 3D printed, and their shape-memory characteristics were assessed at temperatures of 60°C (corresponding to the glass transition temperature of PLA), 70°C, 80°C (matching the melting temperature of the soft segment of TPU), and 90°C. The properties of TPU/PLA samples differ based on the PLA to TPU ratio, with an increase in TPU content resulting in a higher shape setting temperature but a shorter shape recovery time. For the TPU/PLA 5 : 5 sample, setting at 70°C and recovering at 85°C is the most suitable condition for shape recovery, whereas for the TPU/PLA 7 : 3 sample the best conditions are setting at 80°C and recovering at 95°C. In the case of TPU/PLA 9 : 1, shape setting is possible at 90°C, and shape recovery is fastest at 95°C. A 4D structure of TPU/PLA could be achieved based on shape memory testing by temperature stimulation of 3D printed auxetic c TPU/PLA samples.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":"112 22","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135136936","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}
Rubber mixing is an important link in the production of rubber products. Computational fluid dynamics (CFD) simulation is often used to explore the effect of rubber mixing parameters on rubber mixing effect. Previous CFD-based rubber mixing simulation studies did not consider the impact of using 2D or 3D numerical calculation models on the numerical simulation results. In order to investigate the differences between 2D and 3D numerical computational models in rubber compounding CFD simulation problems, in this paper, we compare and analyze the results obtained from 2D and 3D computational models under different rotational speed conditions to investigate the differences between the models in the numerical simulation of rubber compounding. Three different experimental speeds of the rubber mixer—39, 44, and 49 r/min—were set during the study using 2D and 3D asynchronous rotor models with a speed ratio of 1.15, respectively. The rubber was processed using the Bird–Carreau model. The phase interface between rubber and air was calculated using the volume of fluid (VOF) method. The numerical simulation results of different models show that the rotational speed set to 49 r/min shows the best dispersion distribution effect; the mixing effect and speed change rule obtained by the 2D model are consistent with the results obtained by the 3D model. The performance of the results of the two models is consistent when exploring the numerical simulation of rubber compounding.
{"title":"Simulation Method for Rubber Compounding under Isothermal Partial Filling Conditions","authors":"Guolin Wang, Jingshixiong Wang, Haichao Zhou, Chen Liang","doi":"10.1155/2023/6062543","DOIUrl":"https://doi.org/10.1155/2023/6062543","url":null,"abstract":"Rubber mixing is an important link in the production of rubber products. Computational fluid dynamics (CFD) simulation is often used to explore the effect of rubber mixing parameters on rubber mixing effect. Previous CFD-based rubber mixing simulation studies did not consider the impact of using 2D or 3D numerical calculation models on the numerical simulation results. In order to investigate the differences between 2D and 3D numerical computational models in rubber compounding CFD simulation problems, in this paper, we compare and analyze the results obtained from 2D and 3D computational models under different rotational speed conditions to investigate the differences between the models in the numerical simulation of rubber compounding. Three different experimental speeds of the rubber mixer—39, 44, and 49 r/min—were set during the study using 2D and 3D asynchronous rotor models with a speed ratio of 1.15, respectively. The rubber was processed using the Bird–Carreau model. The phase interface between rubber and air was calculated using the volume of fluid (VOF) method. The numerical simulation results of different models show that the rotational speed set to 49 r/min shows the best dispersion distribution effect; the mixing effect and speed change rule obtained by the 2D model are consistent with the results obtained by the 3D model. The performance of the results of the two models is consistent when exploring the numerical simulation of rubber compounding.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":"18 8","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135819045","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}
The shape memory (SM) polymers with superior SM properties were successfully fabricated based on melt blending of natural rubber (NR) and ethylene octene copolymer (EOC) at various crystallinity of EOC phase. The differential scanning calorimetry analysis, mechanical properties, temperature scanning stress relaxation, and shape memory properties were studied. Results revealed that the mechanical and thermal properties of the prepared NR/EOC blends improved as a function of amount of ethylene fraction in the EOC phase. The ethylene segment of EOC in the NR/EOC blend is triggered as a stimulus-sensitive domain. The shape memory properties in terms of shape fixity and shape recovery efficiencies of the blends tended to increase with the increasing of crystalline segments in the blends. The shape memory properties of the prepared blends substantially exceed the best performance (close to 100%) by blending the NR/EOC at 50/50 parts by weight, having 62%–80% of ethylene content in the EOC phase, which corresponds to approximately 3°–16° of crystallinity of EOC phase in the blends.
{"title":"Thermo-Responsive Shape Memory Thermoplastic Elastomer Based on Natural Rubber and Ethylene Octene Copolymer Blends","authors":"Ekwipoo Kalkornsurapranee, Adisak Keereerak, Nussana Lehman, Akarapong Tuljittraporn, Jobish Johns, Nattapon Uthaipan","doi":"10.1155/2023/7276854","DOIUrl":"https://doi.org/10.1155/2023/7276854","url":null,"abstract":"The shape memory (SM) polymers with superior SM properties were successfully fabricated based on melt blending of natural rubber (NR) and ethylene octene copolymer (EOC) at various crystallinity of EOC phase. The differential scanning calorimetry analysis, mechanical properties, temperature scanning stress relaxation, and shape memory properties were studied. Results revealed that the mechanical and thermal properties of the prepared NR/EOC blends improved as a function of amount of ethylene fraction in the EOC phase. The ethylene segment of EOC in the NR/EOC blend is triggered as a stimulus-sensitive domain. The shape memory properties in terms of shape fixity and shape recovery efficiencies of the blends tended to increase with the increasing of crystalline segments in the blends. The shape memory properties of the prepared blends substantially exceed the best performance (close to 100%) by blending the NR/EOC at 50/50 parts by weight, having 62%–80% of ethylene content in the EOC phase, which corresponds to approximately 3°–16° of crystallinity of EOC phase in the blends.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":"100 ","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136018835","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}
Chirality is one of the most common and significant phenomenon in nature, and epoxy resin is one of the most widely used and researched thermosetting resins, however the influences of chiral carbon in epoxy group on the performances of the cured epoxy resins have ever been hardly studied, therefore it is crucial and meaningful to explore the structure–function relationship of chirality and performance of epoxy resins. Herein, from the analysis of synthesis mechanism, the different chiral configuration with high percent enantiomeric excess (>99%) and racemic bisphenol A epoxy resins were simply prepared by controlling the chirality of epichlorohydrin. The apparent activation energy of the curing process with D230 was calculated by Kissinger method and Flynn–Wall–Ozawa method, respectively, and both results indicate that chirality have no effect on the curing reaction. We found that the secondary structure of epoxy monomer is untouched by its chirality, and they are all right helix structure. For this reason, the thermal stability, glass transition temperature, and thermomechanical properties of diverse chiral epoxy resins cured by D230 have no significant difference. Nevertheless, it was found that the optical rotation activity of chiral epoxy resins can be partially maintained after curing reaction, it manifests the cured products of chiral epoxy resins possesses the possibility of application in the field of polarized materials.
{"title":"Preparation of Chiral Epoxy Resins and the Optically Active Cured Products","authors":"Xinyuan Tang, Ming Hu, Xiaoran Liu, Yanyun Li, Junying Zhang, Jue Cheng","doi":"10.1155/2023/6612220","DOIUrl":"https://doi.org/10.1155/2023/6612220","url":null,"abstract":"Chirality is one of the most common and significant phenomenon in nature, and epoxy resin is one of the most widely used and researched thermosetting resins, however the influences of chiral carbon in epoxy group on the performances of the cured epoxy resins have ever been hardly studied, therefore it is crucial and meaningful to explore the structure–function relationship of chirality and performance of epoxy resins. Herein, from the analysis of synthesis mechanism, the different chiral configuration with high percent enantiomeric excess (>99%) and racemic bisphenol A epoxy resins were simply prepared by controlling the chirality of epichlorohydrin. The apparent activation energy of the curing process with D230 was calculated by Kissinger method and Flynn–Wall–Ozawa method, respectively, and both results indicate that chirality have no effect on the curing reaction. We found that the secondary structure of epoxy monomer is untouched by its chirality, and they are all right helix structure. For this reason, the thermal stability, glass transition temperature, and thermomechanical properties of diverse chiral epoxy resins cured by D230 have no significant difference. Nevertheless, it was found that the optical rotation activity of chiral epoxy resins can be partially maintained after curing reaction, it manifests the cured products of chiral epoxy resins possesses the possibility of application in the field of polarized materials.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":"468 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135766168","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}
The increasing concerns about solid waste disposal have led to the development of innovative strategies for repurposing waste materials. This paper describes a simple solution casting process for recycling postconsumed footwear leather fiber (PCF) into a biocomposite film reinforced with graphene oxide (GO) and polyvinylpyrrolidone (PVP). PVP was utilized as a compatibilizer to strengthen the interfacial bonding of GO and leather fiber via π–π interactions. UV–visible spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis, and scanning electron microscopy were used to examine the material dispersibility bonding between GO and PCF, structural properties, thermal properties, and surface morphology of the biocomposite films, respectively. Compared to pure PCF film, the oxygen transmission rate of the prepared biocomposite films is elevated by 64% as well as the biodegradability rate is intensified up to 60%. In addition, the film’s tensile strengths are raised by 216%, while their elongation at break is increased by 164.64% as compared with PCF. The versatility of these eco-friendly and biodegradable composite films extends to its possible applications in packaging and interior design. The outcomes of the research reveal the viability of manufacturing affordable and sustainable biocomposites through the utilization of waste leather from consumed footwear.
{"title":"Fabrication of Graphene Oxide Reinforced Biocomposite: Recycling of Postconsumed Footwear Leather","authors":"Rashedul Islam, Md Ashikur Rahaman Noyon, Thuhin Kumar Dey, Mamun Jamal, Rajasekar Rathanasamy, Moganapriya Chinnasamy, Md. Elias Uddin","doi":"10.1155/2023/3996687","DOIUrl":"https://doi.org/10.1155/2023/3996687","url":null,"abstract":"The increasing concerns about solid waste disposal have led to the development of innovative strategies for repurposing waste materials. This paper describes a simple solution casting process for recycling postconsumed footwear leather fiber (PCF) into a biocomposite film reinforced with graphene oxide (GO) and polyvinylpyrrolidone (PVP). PVP was utilized as a compatibilizer to strengthen the interfacial bonding of GO and leather fiber via π–π interactions. UV–visible spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis, and scanning electron microscopy were used to examine the material dispersibility bonding between GO and PCF, structural properties, thermal properties, and surface morphology of the biocomposite films, respectively. Compared to pure PCF film, the oxygen transmission rate of the prepared biocomposite films is elevated by 64% as well as the biodegradability rate is intensified up to 60%. In addition, the film’s tensile strengths are raised by 216%, while their elongation at break is increased by 164.64% as compared with PCF. The versatility of these eco-friendly and biodegradable composite films extends to its possible applications in packaging and interior design. The outcomes of the research reveal the viability of manufacturing affordable and sustainable biocomposites through the utilization of waste leather from consumed footwear.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":"96 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135385829","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}
Mahmood M. S. Abdullah, Hamad A. Al-Lohedan, Mohd Sajid Ali
Polyethylene terephthalate (PET) is one of the most widely used plastics in the world. Due to the large production and use of this plastic, its waste represents one of the most critical environmental problems. The purpose of this study is to convert PET waste into a valuable material. The consumed PET was transformed into a precursor to synthesize a polyionic liquid (PIL) that was used for dehydrating crude oil emulsions. To do so, the consumed PET was converted to bis(2-hydroxyethyl) terephthalate (BHET). First, BHET and tetraethylene glycol were reacted separately with thionyl chloride, obtaining the corresponding alkyl halides, bis(2-chloroethyl) terephthalate, BCET, and TEC, respectively. Next, the obtained alkyl halides, BCET and TEC, were reacted with 1,5-pentanediamine, yielding a polymer (BTP). Finally, BTP was reacted with acetic acid to produce the corresponding PIL (BTP–PIL). The structure and thermal stability of BTP–PIL were characterized using nuclear magnetic resonance spectroscopy and thermal gravimetric analysis. The dehydration performance of PIL and the original polymer was investigated using the bottle test method, including several factors such as demulsifier dose, brine content, temperature, and settling time. Results indicated that PIL achieved high performance in dehydrating crude oil emulsions.
{"title":"Performance of Plastic Waste-Based Polyionic Liquid toward the Dehydration of Crude Oil Emulsions","authors":"Mahmood M. S. Abdullah, Hamad A. Al-Lohedan, Mohd Sajid Ali","doi":"10.1155/2023/3740956","DOIUrl":"https://doi.org/10.1155/2023/3740956","url":null,"abstract":"Polyethylene terephthalate (PET) is one of the most widely used plastics in the world. Due to the large production and use of this plastic, its waste represents one of the most critical environmental problems. The purpose of this study is to convert PET waste into a valuable material. The consumed PET was transformed into a precursor to synthesize a polyionic liquid (PIL) that was used for dehydrating crude oil emulsions. To do so, the consumed PET was converted to bis(2-hydroxyethyl) terephthalate (BHET). First, BHET and tetraethylene glycol were reacted separately with thionyl chloride, obtaining the corresponding alkyl halides, bis(2-chloroethyl) terephthalate, BCET, and TEC, respectively. Next, the obtained alkyl halides, BCET and TEC, were reacted with 1,5-pentanediamine, yielding a polymer (BTP). Finally, BTP was reacted with acetic acid to produce the corresponding PIL (BTP–PIL). The structure and thermal stability of BTP–PIL were characterized using nuclear magnetic resonance spectroscopy and thermal gravimetric analysis. The dehydration performance of PIL and the original polymer was investigated using the bottle test method, including several factors such as demulsifier dose, brine content, temperature, and settling time. Results indicated that PIL achieved high performance in dehydrating crude oil emulsions.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":"13 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134885101","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}
Omar Faruk, Yang Yang, Jiangliang Zhang, Junxin Yu, Jiaojiao Lv, Weichao Lv, Yueying Du, Jindan Wu, Dongming Qi
Ultrahigh molecular weight polyethylene (UHMWPE) fiber is widely recognized for its exceptional properties, including high strength-to-weight ratio, toughness, and chemical resistance, making it a preferred material for reinforcement in various applications. However, its low melting point, surface inertness, and weak adhesion to polymer matrices have limited its potential use in some fields. Researchers have addressed these shortcomings by focusing on surface modifications through physical treatment or chemical coating, thereby enhancing the versatility of materials in numerous UHMWPE fiber composites. By improving the tribological and interfacial properties of UHMWPE, various applications can be explored, including prosthetic joints, energy-absorbing road safety systems, microelectromechanical system devices, and protective materials for defense and personal thermal management. This review provides a comprehensive overview of the remarkable performance of UHMWPE and its composites, providing insights into its wide array of applications.
{"title":"A Comprehensive Review of Ultrahigh Molecular Weight Polyethylene Fibers for Applications Based on Their Different Preparation Techniques","authors":"Omar Faruk, Yang Yang, Jiangliang Zhang, Junxin Yu, Jiaojiao Lv, Weichao Lv, Yueying Du, Jindan Wu, Dongming Qi","doi":"10.1155/2023/6656692","DOIUrl":"https://doi.org/10.1155/2023/6656692","url":null,"abstract":"Ultrahigh molecular weight polyethylene (UHMWPE) fiber is widely recognized for its exceptional properties, including high strength-to-weight ratio, toughness, and chemical resistance, making it a preferred material for reinforcement in various applications. However, its low melting point, surface inertness, and weak adhesion to polymer matrices have limited its potential use in some fields. Researchers have addressed these shortcomings by focusing on surface modifications through physical treatment or chemical coating, thereby enhancing the versatility of materials in numerous UHMWPE fiber composites. By improving the tribological and interfacial properties of UHMWPE, various applications can be explored, including prosthetic joints, energy-absorbing road safety systems, microelectromechanical system devices, and protective materials for defense and personal thermal management. This review provides a comprehensive overview of the remarkable performance of UHMWPE and its composites, providing insights into its wide array of applications.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":"4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135063340","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}
Hananeh Hamedfar, Tayebeh Zivari-Ghader, A. Akbarzadeh, S. Davaran
In addition to being a lipid-lowering medication, atorvastatin (ATV) is an anti-inflammatory agent. When there is a bone defect or inflammation of adjacent tissues, it aids in bone repair. This study aimed to develop a chitosan–alginate (CS/ALG)–tripolyphosphate (TPP)–ATV hybrid hydrogel as a drug delivery system, using a tissue engineering scaffold for the first time. For this purpose, a CS/ALG hydrogel crosslinked with TPP was developed. The delivery profile of ATV and its physicochemical properties such as particle size and hydrogel swelling percentage were determined. The structure and morphology of the hydrogels were analyzed using Fourier transform infrared spectroscopy and scanning electron microscopy. As a result, an alginate–chitosan hydrogel with a TPP crosslinker was prepared. The results revealed that drug loading was nearly complete, and the first hour revealed a 25% explosive release. The drug was gradually released over 10 hr at approximately 35%. The amount of crosslinker used significantly influenced the encapsulation gain and release profiles. Owing to its high porosity and swelling, the CS/ALG hydrogel crosslinked with PPT is an ideal scaffold for loading drugs, macromolecules, and cells.
{"title":"Physicochemical Characteristics of Chitosan–Alginate Scaffold Containing Atorvastatin","authors":"Hananeh Hamedfar, Tayebeh Zivari-Ghader, A. Akbarzadeh, S. Davaran","doi":"10.1155/2023/9452164","DOIUrl":"https://doi.org/10.1155/2023/9452164","url":null,"abstract":"In addition to being a lipid-lowering medication, atorvastatin (ATV) is an anti-inflammatory agent. When there is a bone defect or inflammation of adjacent tissues, it aids in bone repair. This study aimed to develop a chitosan–alginate (CS/ALG)–tripolyphosphate (TPP)–ATV hybrid hydrogel as a drug delivery system, using a tissue engineering scaffold for the first time. For this purpose, a CS/ALG hydrogel crosslinked with TPP was developed. The delivery profile of ATV and its physicochemical properties such as particle size and hydrogel swelling percentage were determined. The structure and morphology of the hydrogels were analyzed using Fourier transform infrared spectroscopy and scanning electron microscopy. As a result, an alginate–chitosan hydrogel with a TPP crosslinker was prepared. The results revealed that drug loading was nearly complete, and the first hour revealed a 25% explosive release. The drug was gradually released over 10 hr at approximately 35%. The amount of crosslinker used significantly influenced the encapsulation gain and release profiles. Owing to its high porosity and swelling, the CS/ALG hydrogel crosslinked with PPT is an ideal scaffold for loading drugs, macromolecules, and cells.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2023-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49078186","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}
Lion Sundermann, Sebastian Leineweber, B. Klie, Heike Wittek, T. Ebel, B. Reitz, Kathrin Ottink, Matthias Graf, Tobias Lankenau, L. Overmeyer, U. Giese
The additive manufacturing (AM) of elastomeric parts based on high-viscosity reinforced rubbers has increasingly become a topic of scientific research in recent years. In addition to the viscosity, which is several decades higher during processing than the viscosities of thermoplastics, the flowability of the compound after the printing process and the necessary chemical crosslinking of the printed component play a decisive role in producing an elastic, high-quality, and geometrically stable part. After the first technological achievements using the so-called additive manufacturing of elastomers (AME) process, the knowledge gained has to be transferred first to concrete industrial parts. Therefore, in this study, the cure kinetics of a conventional rubber compound are tailored to match the specific requirements for scorch safety in the additive manufacturing of an industrial 2-component rod seal based on an acrylonitrile butadiene rubber O-ring in combination with a thermoplastic polyurethane as the base body. Experimental tests on a test rig for rod seals demonstrate the functionality of this additively manufactured 2-component rod seal.
{"title":"Tailoring the Curing Kinetics of NBR-Based Rubber Compounds for Additive Manufacturing of Rod Seals","authors":"Lion Sundermann, Sebastian Leineweber, B. Klie, Heike Wittek, T. Ebel, B. Reitz, Kathrin Ottink, Matthias Graf, Tobias Lankenau, L. Overmeyer, U. Giese","doi":"10.1155/2023/7343194","DOIUrl":"https://doi.org/10.1155/2023/7343194","url":null,"abstract":"The additive manufacturing (AM) of elastomeric parts based on high-viscosity reinforced rubbers has increasingly become a topic of scientific research in recent years. In addition to the viscosity, which is several decades higher during processing than the viscosities of thermoplastics, the flowability of the compound after the printing process and the necessary chemical crosslinking of the printed component play a decisive role in producing an elastic, high-quality, and geometrically stable part. After the first technological achievements using the so-called additive manufacturing of elastomers (AME) process, the knowledge gained has to be transferred first to concrete industrial parts. Therefore, in this study, the cure kinetics of a conventional rubber compound are tailored to match the specific requirements for scorch safety in the additive manufacturing of an industrial 2-component rod seal based on an acrylonitrile butadiene rubber O-ring in combination with a thermoplastic polyurethane as the base body. Experimental tests on a test rig for rod seals demonstrate the functionality of this additively manufactured 2-component rod seal.","PeriodicalId":7372,"journal":{"name":"Advances in Polymer Technology","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2023-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44489409","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}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：