Poly(vinyl alcohol)/graphene oxide nanocomposites prepared by in situ polymerization with enhanced mechanical properties and water vapor barrier properties

RSC Advances ◽  
2016 ◽  
Vol 6 (55) ◽  
pp. 49448-49458 ◽  
Author(s):  
Jiaojiao Ma ◽  
Ying Li ◽  
Xiande Yin ◽  
Yu Xu ◽  
Jia Yue ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Graphene Oxide ◽  
Vinyl Alcohol ◽  
In Situ Polymerization ◽  
Barrier Properties ◽  
Poly Vinyl Alcohol ◽  
Water Vapor Barrier ◽  
One Step ◽  
Polymerization Method

A novel and one-stepin situpolymerization method for preparing the poly(vinyl alcohol) (PVA)/graphene oxide (GO) nanocomposites.

Synthesis and Characterizations of Poly(Butylene Succinate) Copolyester

2014 ◽  
Vol 1015 ◽  
pp. 381-384
Author(s):  
Li Liu ◽  
Li Hai Cai ◽  
Dan Liu ◽  
Jun Xu ◽  
Bao Hua Guo
Keyword(s):  
Mechanical Properties ◽  
Polymer Matrix ◽  
Crystallization Temperature ◽  
In Situ Polymerization ◽  
Nucleating Agent ◽  
Single Fiber ◽  
Butylene Succinate ◽  
Crystallization Behaviors ◽  
Polymerization Method

The poly (butylene succinate) (PBS) and 3 wt% attapulgite (ATP) reinforced PBS/ATP nanocomposites with 1,6-hexanediol were fabricated using an in situ polymerization method. The crystallization behaviors indicated that ATP had effectively acted as nucleating agent, resulting in the enhancement on the crystallization temperature. The SEM results showed a superior interfacial linkage between ATP and PBS. Also, ATP could disperse as a single fiber and embed in the polymer matrix, which resulted in the improved mechanical properties.

Preparation and properties of poly (vinyl alcohol)/sodium caseinate blend films crosslinked with glutaraldehyde and glyoxal

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Bedriye Ucpinar Durmaz ◽  
Ayse Aytac
Keyword(s):  
Water Vapor ◽  
Vinyl Alcohol ◽  
Sodium Caseinate ◽  
Barrier Properties ◽  
Poly Vinyl Alcohol ◽  
Infrared Analysis ◽  
Crosslinking Reaction ◽  
Water Contact ◽  
Casting Technique ◽  
Water Vapor Barrier

Abstract Bio-based films containing poly (vinyl alcohol)/casein have poor mechanical and water vapor barrier properties that limit their use in packaging application. Some properties such as water resistance and tensile strength can be increased by the cross-linking process. For this reason, poly(vinyl alcohol)/sodium caseinate (PVA/SC) blends were crosslinked by adding glutaraldehyde (GLA) and glyoxal (GL) at different ratios in this work. The films were prepared by solution casting technique. Fourier transform infrared analysis (FTIR) confirmed the crosslinking reaction between the components. As a result of the crosslinking, the thicknesses, water vapor barrier properties and water contact angle values of the films have increased. The total soluble matters (TSM) of PVA/SC film decreased with increasing amounts of crosslinkers and GLA crosslinked films exhibited lower TSM. The addition of GLA and GL resulted in more strengthened films as verified by the tensile test. On the other hand, GLA crosslinked films were more flexible than un-crosslinked and GL crosslinked PVA/SC films. The hydrophilic PVA/SC film became more hydrophobic with the increasing amounts of crosslinkers. With the crosslinking, the PVA/SC film became more thermally stable. In conclusion, the crosslinked PVA/SC films were obtained with suitable properties for packaging applications.

scholarly journals Regulation Mechanism of Graphene Oxide on the Structure and Mechanical Properties of Bio-Based Gel-Spun Lignin/Poly (Vinyl Alcohol) Fibers

2021 ◽  
Author(s):  
Yanhong Jin ◽  
Yuanyuan Jing ◽  
Wenxin Hu ◽  
Jiaxian Lin ◽  
Yu Cheng ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Graphene Oxide ◽  
Young’S Modulus ◽  
Vinyl Alcohol ◽  
Young's Modulus ◽  
Lignin Content ◽  
Poly Vinyl Alcohol ◽  
Regulation Mechanism ◽  
Composite Fibers

Abstract Lignin has been used as a sustainable and eco-friendly filler in composite fibers. However, lignin aggregation occurred at high lignin content, which significantly hindered the further enhancement of fiber performance. The incorporation of graphene oxide (GO) enhanced the mechanical properties of the lignin/poly(vinyl alcohol) (PVA) fibers and affected their structure. With the GO content increasing from 0 to 0.2%, the tensile strength of 5% lignin/PVA fibers increased from 491 MPa to 631 MPa, and Young's modulus increased from 5.91 GPa to 6.61 GPa. GO reinforced 30% lignin/PVA fibers also showed the same trend. The tensile strength increased from 455 MPa to 553 MPa, and Young's modulus increased from 5.39 GPa to 7 GPa. The best mechanical performance was observed in PVA fibers containing 5% lignin and 0.2% GO, which had an average tensile strength of 631 MPa and a Young’s modulus of 6.61 GPa. The toughness values of these fibers are between 9.9-15.6 J/g, and the fibrillar and ductile fracture microstructure were observed. Structure analysis of fibers showed that GO reinforced 5% lignin/PVA fibers had higher crystallinity, and evidence of hydrogen bonding among GO, lignin, and PVA in the gel fibers was revealed. Further, water resistance and swelling behavior of composite PVA fibers were studied to further evidence the structure change of composite fibers.

Physico-mechanical properties of graphene oxide/poly(vinyl alcohol) composites

2019 ◽  
Vol 297 (3) ◽  
pp. 485-491 ◽  
Author(s):  
Tatiana V. Panova ◽  
Anna A. Efimova ◽  
Aleksandr V. Efimov ◽  
Anna K. Berkovich
Keyword(s):  
Mechanical Properties ◽  
Graphene Oxide ◽  
Vinyl Alcohol ◽  
Poly Vinyl Alcohol

scholarly journals Effects of Immobilized Ionic Liquid on Properties of Biodegradable Polycaprolactone/LDH Nanocomposites Prepared by In Situ Polymerization and Melt-Blending Techniques

Nanomaterials ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 969
Author(s):  
Sonia Bujok ◽  
Jiří Hodan ◽  
Hynek Beneš
Keyword(s):  
Ionic Liquid ◽  
Water Vapor ◽  
Ring Opening ◽  
In Situ Polymerization ◽  
High Capacity ◽  
Barrier Properties ◽  
Melt Blending ◽  
Water Vapor Barrier ◽  
Double Hydroxides

The high capacity of calcinated layered double hydroxides (LDH) to immobilize various active molecules together with their inherent gas/vapor impermeability make these nanoparticles highly promising to be applied as nanofillers for biodegradable polyester packaging. Herein, trihexyl(tetradecyl)phosphonium decanoate ionic liquid (IL) was immobilized on the surface of calcinated LDH. Thus, the synthesized nanoparticles were used for the preparation of polycaprolactone (PCL)/LDH nanocomposites. Two different methods of nanocomposite preparation were used and compared: microwave-assisted in situ ring opening polymerization (ROP) of ε-caprolactone (εCL) and melt-blending. The in situ ROP of εCL in the presence of LDH nanoparticles with the immobilized IL led to homogenous nanofiller dispersion in the PCL matrix promoting formation of large PCL crystallites, which resulted in the improved mechanical, thermal and gas/water vapor barrier properties of the final nanocomposite. The surface-bonded IL thus acted as nanofiller surfactant, compatibilizer, as well as thermal stabilizer of the PCL/LDH nanocomposites. Contrary to that, the melt-blending caused a partial degradation of the immobilized IL and led to the production of PCL nanocomposites with a heterogenous nanofiller dispersion having inferior mechanical and gas/water vapor barrier properties.

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