scholarly journals Biobased Terpene Derivatives: Stiff and Biocompatible Compounds to Tune Biodegradability and Properties of Poly(butylene succinate)

Polymers ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 161
Author(s):  
Reza Zeinali ◽  
Luis J. del Valle ◽  
Lourdes Franco ◽  
Ibraheem Yousef ◽  
Jeroen Rintjema ◽  
...  
Keyword(s):  
Biomedical Applications ◽  
Tensile Modulus ◽  
Contact Angles ◽  
Butylene Succinate ◽  
Thermally Induced ◽  
Blend Films ◽  
Weight Losses ◽  
Chain Stiffness ◽  
Limonene Oxide ◽  
Terpene Derivatives

Different copolymers incorporating terpene oxide units (e.g., limonene oxide) have been evaluated considering thermal properties, degradability, and biocompatibility. Thus, polycarbonates and polyesters derived from aromatic, monocyclic and bicyclic anhydrides have been considered. Furthermore, ring substitution with myrcene terpene has been evaluated. All polymers were amorphous when evaluated directly from synthesis. However, spherulites could be observed after the slow evaporation of diluted chloroform solutions of polylimonene carbonate, with all isopropene units possessing an R configuration. This feature was surprising considering the reported information that suggested only the racemic polymer was able to crystallize. All polymers were thermally stable and showed a dependence of the maximum degradation rate temperature (from 242 °C to 342 °C) with the type of terpene oxide. The graduation of glass transition temperatures (from 44 °C to 172 °C) was also observed, being higher than those corresponding to the unsubstituted polymers. The chain stiffness of the studied polymers hindered both hydrolytic and enzymatic degradation while a higher rate was detected when an oxidative medium was assayed (e.g., weight losses around 12% after 21 days of exposure). All samples were biocompatible according to the adhesion and proliferation tests performed with fibroblast cells. Hydrophobic and mechanically consistent films (i.e., contact angles between 90° and 110°) were obtained after the evaporation of chloroform from the solutions, having different ratios of the studied biobased polyterpenes and poly(butylene succinate) (PBS). The blend films were comparable in tensile modulus and tensile strength with the pure PBS (e.g., values of 330 MPa and 7 MPa were determined for samples incorporating 30 wt.% of poly(PA-LO), the copolyester derived from limonene oxide and phthalic anhydride. Blends were degradable, biocompatible and appropriate to produce oriented-pore and random-pore scaffolds via a thermally-induced phase separation (TIPS) method and using 1,4-dioxane as solvent. The best results were attained with the blend composed of 70 wt.% PBS and 30 wt.% poly(PA-LO). In summary, the studied biobased terpene derivatives showed promising properties to be used in a blended form for biomedical applications such as scaffolds for tissue engineering.

Chitosan/Polyethylene Oxide (PEO) Filled Carbonized Wood Fiber Conductive Composite Film

2020 ◽  
Vol 1010 ◽  
pp. 638-644
Author(s):  
Mohd Pisal Mohd Hanif ◽  
Abd Jalil Jalilah ◽  
Mohd Fadzil Hanim Anisah ◽  
Arumugam Tilagavathy
Keyword(s):  
Electrical Conductivity ◽  
Tensile Strength ◽  
Polyethylene Oxide ◽  
Biomedical Applications ◽  
Wood Fiber ◽  
Conductive Polymer ◽  
Renewable Resource ◽  
Blend Films ◽  
Conductive Composite Film ◽  
Carbonized Wood

Biopolymer-based conductive polymer composites (CPCs) would open up various possibilities in biomedical applications owing to ease of processing, renewable resource and environmentally friendly. However, low mechanical properties are a major issue for their applications. In this study, the investigated the conductivity of chitosan/ PEO blend films filled with carbonized wood fiber (CWF) prepared by solution casting. The effect of CWF was also investigated on tensile properties and their morphological surfaces. The tensile results from different ratios of chitosan/PEO blend films without CWF show that the tensile strength and modulus increased with the increase of chitosan content and chitosan/PEO blend film with 70/30 ratio exhibited the best combination of tensile strength and flexibility. However, a reduction of tensile strength was observed when CWF amount was increased while the modulus of the tensile shows an increment. The film also exhibited higher electrical conductivity as compared to low chitosan ratio. The addition of CWF greatly enhanced the conductivity three-fold from 10-10 to 10-6 S/cm. The electrical conductivity continued to increase with the increase of CWF up to 30wt%. The surface morphology by Scanning Electron Microscopy (SEM) exhibits the absence of phase separation for the blends indicating good miscibility between the PEO and chitosan. Incorporation of CWF into the blend films at 5wt% showed agglomeration. However, the increase of CWF created larger agglomerations that formed conductive pathways resulting in improved conductivity. FTIR analysis suggested that intermolecular interactions occurred between chitosan and PEO while CWF interacts more with the protons of PEO.

Mechanical Property Improvement of Poly(Butylene Succinate) by Reinforcing with Modified Fumed Silica

2014 ◽  
Vol 1025-1026 ◽  
pp. 215-220 ◽  
Author(s):  
Sasirada Weerasunthorn ◽  
Pranut Potiyaraj
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Impact Strength ◽  
Flexural Strength ◽  
Fumed Silica ◽  
Tensile Modulus ◽  
Silica Particles ◽  
Melt Mixing ◽  
Butylene Succinate ◽  
Ir Spectrophotometry

Fumed silica particles (SiO2) were directly added into poly (butylene succinate) (PBS) by melt mixing process. The effects of amount of fumed silica particles on mechanical properties of PBS/fumed silica composites, those are tensile strength, tensile modulus, impact strength as well as flexural strength, were investigated. It was found that the mechanical properties decreased with increasing fumed silica loading (0-3 wt%). In order to increase polymer-filler interaction, fumed silica was treated with 3-glycidyloxypropyl trimethoxysilane (GPMS), and its structure was analyzed by FT-IR spectrophotometry. The PBS/modified was found to possess better tensile strength, tensile modulus, impact strength and flexural strength that those of PBS/fumed silica composites.

scholarly journals Polypropylene/Lignin/POSS Nanocomposites: Thermal and Wettability Properties, Application in Water Remediation

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3950
Author(s):  
Abeer Alassod ◽  
Syed Rashedul Islam ◽  
Mina Shahriari Khalaji ◽  
Rogers Tusiime ◽  
Wanzhen Huang ◽  
...  
Keyword(s):  
Organic Liquid ◽  
Contact Angles ◽  
Water Remediation ◽  
Scanning Calorimetry ◽  
Water Contact ◽  
Thermally Induced ◽  
Dsc Measurements ◽  
Infrared Measurement ◽  
Oligomeric Silsesquioxane ◽  
Tga And Dsc

Compositing is an interesting strategy that has always been employed to introduce or enhance desired functionalities in material systems. In this paper, sponges containing polypropylene, lignin, and octavinyl-polyhedral oligomeric silsesquioxane (OV-POSS) were successfully prepared via an easy and elegant strategy called thermally induced phase separation (TIPS). To fully explore the behaviour of different components of prepared sponges, properties were characterized by a thermogravimetric analyser (TGA), differential scanning calorimetry (DSC), Fourier transform infrared measurement (FTIR), and scanning electron microscopy (SEM). Furthermore, wettability properties toward an organic liquid and oil were investigated. The FTIR analysis confirmed the chemical modification of the components. TGA and DSC measurements revealed thermal stability was much better with an increase in OV-POSS content. OV-POSS modified sponges exhibited ultra-hydrophobicity and high oleophilicity with water contact angles of more than 125°. The SEM revealed that POSS molecules acted as a support for reduced surface roughness. Moreover, OV-POSS-based blend sponges showed higher sorption capacities compared with other blend sponges without OV-POSS. The new blend sponges demonstrated a potential for use as sorbent engineering materials in water remediation.

Novel Alginate Frankincense Oil Blend Films for Biomedical Applications

2019 ◽  
Vol 90 (2) ◽  
pp. 303-312
Author(s):  
Mona A. Saied ◽  
Nagwa A. Kamel ◽  
Azza A. Ward ◽  
Amal E. Abd El-kader
Keyword(s):  
Biomedical Applications ◽  
Blend Films ◽  
Oil Blend

Poly(lactic acid)/poly(butylene-succinate-co-adipate) (PLA/PBSA) blend films containing thymol as alternative to synthetic preservatives for active packaging of bread

2020 ◽  
Vol 25 ◽  
pp. 100515 ◽  
Author(s):  
Panitee Suwanamornlert ◽  
Noppadon Kerddonfag ◽  
Amporn Sane ◽  
Wannee Chinsirikul ◽  
Weibiao Zhou ◽  
...  
Keyword(s):  
Lactic Acid ◽  
Active Packaging ◽  
Poly Lactic Acid ◽  
Butylene Succinate ◽  
Blend Films

scholarly journals Shape-Memory Polymers for Biomedical Applications

2008 ◽  
Vol 54 ◽  
pp. 96-102 ◽  
Author(s):  
Andreas Lendlein ◽  
Marc Behl
Keyword(s):  
Shape Memory ◽  
Material Properties ◽  
Biomedical Applications ◽  
Traditional Approach ◽  
Shape Change ◽  
Shape Memory Polymers ◽  
Thermally Induced ◽  
Wide Range ◽  
Multifunctional Polymers ◽  
Suitable Process

Most polymers used in clinical applications today are materials that have been developed originally for application areas other than biomedicine. On the other side, different biomedical applications are demanding different combinations of material properties and functionalities. Compared to the intrinsic material properties, a functionality is not given by nature but result from the combination of the polymer architecture and a suitable process. Examples for functionalities that play a prominent role in the development of multifunctional polymers for medical applications are biofunctionality (e.g. cell or tissue specificity), degradability, or shape-memory functionality. In this sense, an important aim for developing multifunctional polymers is tailoring of biomaterials for specific biomedical applications. Here the traditional approach, which is designing a single new homo- or copolymer, reaches its limits. The strategy, that is applied here, is the development of polymer systems whose macroscopic properties can be tailored over a wide range by variation of molecular parameters. The Shape-memory capability of a material is its ability to trigger a predefined shape change by exposure to an external stimulus. A change in shape initiated by heat is called thermally-induced shape-memory effect. Thermally, light-, and magnetically induced shape-memory polymers will be presented, that were developed especially for minimally invasive surgery and other biomedical applications. Furthermore triple-shape polymers will be introduced, that have the capability to perform two subsequent shape changes. Thus enabling more complex movements of a polymeric material.

Structural Control and Property Development of Silicone Polymers

2018 ◽  
Vol 45 (3) ◽  
pp. 129-136
Author(s):  
Hiroki Uehara ◽  
Takeshi Yamanobe ◽  
Eiichi Akiyama
Keyword(s):  
Structural Control ◽  
Main Chain ◽  
Tensile Modulus ◽  
Industrial Applications ◽  
Silicone Elastomer ◽  
Property Development ◽  
Blend Films ◽  
Dimethyl Siloxane ◽  
Silicone Polymers ◽  
Phenyl Rings

Typical silicones, including poly(dimethyl siloxane) (PDMS), are amorphous, but poly(tetramethyl-p-silphenylene-siloxane) (PTMPS) containing phenyl rings in the main chain is crystalline. A combination of in-situ X-ray and NMR measurements during heating of PTMPS indicates that the molecular motion of the phenyl rings exhibits remarkable anisotropy even in the molten state, suggesting rigidity of the PTMPS molecules. Therefore, a melt-drawing technique could be successfully applied to PTMPS. The obtained melt-drawn PTMPS membrane is transparent but exhibits an excellent tensile modulus and strength of 1.7 GPa and 20 MPa, which are enough for various industrial applications. Similar introduction of phenyl rings in the main chain is also effective for property development of silicone elastomer. Blend films of PTMPS and silicone elastomer exhibits the characteristic phase separation, depending on the blending compositions. Such blend films give the remarkably higher tensile strength than the original silicone elastomer, due to the crystalline component.

The Degradation of Poly (Butylene Succinate)/Natural Rubber Composites

2014 ◽  
Vol 934 ◽  
pp. 110-115
Author(s):  
Li Gao ◽  
Er Juan Zhi ◽  
Ping Li Wang ◽  
Jun Hui Ji
Keyword(s):  
Green Composites ◽  
X Ray Diffraction ◽  
Rubber Composites ◽  
Scanning Calorimetry ◽  
Butylene Succinate ◽  
X Ray ◽  
Weight Losses ◽  
Natural Rubber Composites ◽  
Degradation Test ◽  
Scanning Electron

In this study, poly (butylene succinate) (PBS)/nature rubber (NR) composites were prepared, and the effects of NR content on the biodegradability were evaluated by vermiculite-degradation test. X-ray Diffraction, differential scanning calorimetry (DSC), and scanning electron microscopy (SEM) were used to characterize the degraded blends. The weight losses of PBS/NR composites are higher than that of pure PBS, and increased with adding NR content. The weight loss of 30% NR content composite after 120 days is 16.84%. The XRD and DSC results show that the crystallinity of PBS/NR composites increase after buried in vermiculite. These results were confirmed using SEM observations by the presence of many large holes and more cracks in the degradation surface morphology of the increasing content of NR. It was observed that PBS/NR composites are green-composites or eco-materials.

Silk Fibroin/Hyaluronic Acid Blend Film with Good Water Stability and Cytocompatibility

2013 ◽  
Vol 377 ◽  
pp. 209-214
Author(s):  
Ling Shuang Wang ◽  
Shu Qin Yan ◽  
Ming Zhong Li
Keyword(s):  
Cell Proliferation ◽  
Hyaluronic Acid ◽  
Silk Fibroin ◽  
Biomedical Applications ◽  
Water Resistance ◽  
High Water ◽  
Casting Method ◽  
Blend Ratio ◽  
Blend Films

Stimulating cell proliferation is a challenge in the field of silk fibroin-based biomaterials. In this study, silk fibroin/hyaluronic acid blend films were prepared by a casting method using carbodiimide as a cross-linking agent. Carbodiimide induced silk fibroin to form Silk I crystal structure which was not affected by the presence of hyaluronic acid. The films showed high water resistance. In vitro, the performance of these films was assessed by seeding L929 cells. The results indicated that the silk fibroin/hyaluronic acid blend films with the blend ratio of 80/20 and 60/40 promoted cell proliferation compared with the pure silk fibroin or hyaluronic acid film. These results suggest that silk fibroin/hyaluronic acid blend films are water stable and cytocompatible materials which are expected to be useful in biomedical applications.

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