Preparation and Properties of Nano-Hydroxyapatite Modified Nylon Composites

2009 ◽  
Vol 87-88 ◽  
pp. 228-232
Author(s):  
Li Yun Zheng ◽  
Zhi Min Liu ◽  
Ya Jun Zhao
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Body Fluid ◽  
Moisture Absorption ◽  
In Situ Polymerization ◽  
Average Molecular Weight ◽  
Ultrasonic Dispersion ◽  
Infrared Spectrometer

To enhance the mechanical property and the bioactivity of composites, nano-hydroxyapatite (n-HA) modified monomer casting nylon-6 (n-HA/N) composites were prepared by in situ polymerization. During the synthesis of n-HA/N composite, the n-HA and caprolactam were mixed, melt and placed in the field of ultrasonic radiation. The differences between composite with ultrasonic and without ultrasonic were investigated. The tensile strength and the viscosity average molecular weight of the nylon matrix were measured. The results show that the molecular weight of the nylon matrix decreased firstly and it had the lowest value when the content of nano-hydroxyapatite was 1.6 wt.%. After that the molecular weight increased and then it began to decrease when it reached the highest value. But the tensile strength of the n-HA/N composite were improved. The ultrasonic dispersion made the n-HA more evenly dispersed in the nylon and increased the mechanical properties of the n-HA/N composites significantly. The bioactivity and moisture absorption of n-HA/N composites in simulated body fluid (SBF) were examined and compared to pure nylon. What's more, Fourier transform infrared spectrometer was used to characterize the structure of the materials formed on the surface of the composite. The results showed that moisture absorption of the n-HA/N composites was lower than that of the pure nylon. After composites impregnated 16 days in SBF, a layer of carbon hydroxyapatite (CHA) with weak crystalline was formed on the surface of sample. This phenomenon showed that the n-HA/N composites have good bioactivity.

Preparation and Properties of the Polystyrene/Alumina Nanocomposites

2012 ◽  
Vol 557-559 ◽  
pp. 519-522
Author(s):  
Xu Man Wang ◽  
Cai Ning Zhang
Keyword(s):  
Molecular Weight ◽  
Thermal Resistance ◽  
Coupling Agent ◽  
Silane Coupling Agent ◽  
In Situ Polymerization ◽  
Average Molecular Weight ◽  
Experimental Results ◽  
Solvent Resistance ◽  
Silane Coupling

Silane coupling agent KH-570 was applied to modify the surface capability of the alumina (Al2O3). The modified Al2O3were dispersed in styrene. The in-situ polymerization was used to prepare the polystyrene/alumina (PS/Al2O3) composites, in which azodiisobutyronitrile (AIBN) was used as initiator. FTIR, DSC and TG were applied to characterize the prepared composites. The solvent resistance, thermal resistance of the composites and the average molecular weight of PS in PS/Al2O3nanocomposites were studied. The experimental results demonstrated that the solvent resistance of PS/Al2O3nanocomposites was improved by the adding of Al2O3nanoparticles. The thermal resistance of the composites increased with the increasing of the Al2O3content. Meanwhile, the molecular weight of PS in the composites increased with the increasing of the Al2O3content.

Synthesis of Biodegradable β-TCP/PLGA Composites Using Microwave Energy

2006 ◽  
Vol 510-511 ◽  
pp. 758-761 ◽  
Author(s):  
Hyeong Ho Jin ◽  
Sang Ho Min ◽  
Kyu Hong Hwang ◽  
Ik Min Park ◽  
Hong Chae Park ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Young’S Modulus ◽  
Tricalcium Phosphate ◽  
Bending Strength ◽  
In Situ Polymerization ◽  
Young's Modulus ◽  
Microwave Energy ◽  
Microstructure And Mechanical Properties

Biodegradable β-tricalcium phosphate (β-TCP)/poly (lactide-co-glycolide) (PLGA) composites were synthesized by in situ polymerization with microwave energy. The influence of the β-TCP content in β-TCP/PLGA composites on the molecular weight, crystallinity, microstructure, and mechanical properties was investigated. As the molecular weight of composites decreased, the β-TCP content increased up to 10 wt%, while further raising of the β-TCP content above 10%, the molecular weight increased with increasing β-TCP content. This behavior may be ascribed to the superheating effect or nonthermal effect induced by microwave energy. It was found that the bending strength and Young’s modulus of the β-TCP/PLGA composites were proportional to the molecular weight of PLGA. The bending strength of the β-TCP/PLGA composites ranged from 18 to 38 MPa, while Young’s modulus was in the range from 2 to 6 GPa.

scholarly journals Preparation and Property of Bio-Polyimide/Halloysite Nanocomposite Based on 2,5-Furandicarboxylic Acid

Polymers ◽  
2021 ◽  
Vol 13 (23) ◽  
pp. 4057
Author(s):  
Yingxia Chen ◽  
Shuya Fan ◽  
Xibin Yi ◽  
Bing Li ◽  
Shiwei Chen ◽  
...  
Keyword(s):  
Tensile Strength ◽  
Young’S Modulus ◽  
Water Resistance ◽  
Moisture Absorption ◽  
In Situ Polymerization ◽  
Young's Modulus ◽  
Polyimide Film ◽  
Nanocomposite Films ◽  
Furandicarboxylic Acid

Bio-based polyimide (PI)/halloysite nanotube (HNT) nanocomposites based on 2,5-furandicarboxylic acid were prepared by in situ polymerization. The pristine HNTs were modified by tetraethoxysilane (TEOS) and 4,4′-oxybisbenzenamine (ODA). The bio-based PI/HNT nanocomposite film exhibited lower moisture absorption than pure bio-based polyimide, showing that the water resistance of the bio-based polyimide film was improved. The thermal stability and glass transition temperature (Tg) of PI/HNTs nanocomposites were improved with the addition of modified HNTs. Both the tensile strength and Young’s modulus of bio-based PI/HNTs nanocomposite films were enhanced. A 37.7% increase in tensile strength and a 75.1% increase in Young’s modulus of bio-based PI/HNTs nanocomposite films, with 1 wt% of the modified HNTs, were achieved. The result confirmed that 2,5-furandicarboxylic acid could replace the oil-based material effectively, thus reducing pollution and protecting the environment. Finally, a preparation mechanism to prepare bio-based PI/HNTs nanocomposite is proposed.

scholarly journals Integrating Nano-Cu2O@ZrP into In Situ Polymerized Polyethylene Terephthalate (PET) Fibers with Enhanced Mechanical Properties and Antibacterial Activities

Polymers ◽  
2019 ◽  
Vol 11 (1) ◽  
pp. 113 ◽  
Author(s):  
Jialiang Zhou ◽  
Xiang Fei ◽  
Congqi Li ◽  
Senlong Yu ◽  
Zexu Hu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Polyethylene Terephthalate ◽  
In Situ Polymerization ◽  
Antibacterial Activities ◽  
Polymerization Process ◽  
Gel Chromatography ◽  
Blending Method ◽  
Pet Fibers

The approach of in situ polymerization modification has proven to be an effective route for introducing functions for polyester materials. In this work, Cu2O@ZrP nanosheets with excellent dispersity and high antibacterial activity were integrated into in situ polymerized polyethylene terephthalate (PET) fibers, revealing an enhanced mechanical performance in comparison with the PET fibers fabricated directly via a traditional melt blending method. Additionally, such an in situ polymerized PET/Cu2O@ZrP fibers displayed highly enhanced mechanical properties; and great antibacterial activities against multi-types of bacterium, including S. aureus, E. coli and C. albicans. For the as-obtained two types of PET/Cu2O@ZrP fibers, we have detailed their molecular weight (detailed molecular weight) and dispersibility of nano-Cu2O@ZrP and fibers crystallinity was investigated by Gel chromatography (GPC), Scanning electron microscope (SEM), and X-ray diffractometer (XRD), respectively. The results showed that the aggregation of the nano-Cu2O@ZrP in the resultant PET matrix could be effectively prevented during its in situ polymerization process, hence we attribute its highly enhanced mechanical properties to its superior dispersion of nano-Cu2O@ZrP.

scholarly journals Monomer Selection for In Situ Polymerization Infusion Manufacture of Natural-Fiber Reinforced Thermoplastic-Matrix Marine Composites

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 2928
Author(s):  
Yang Qin ◽  
John Summerscales ◽  
Jasper Graham-Jones ◽  
Maozhou Meng ◽  
Richard Pemberton
Keyword(s):  
Mechanical Properties ◽  
Moisture Absorption ◽  
Natural Fiber ◽  
In Situ Polymerization ◽  
Synthetic Fiber ◽  
Thermoplastic Composites ◽  
Processing Temperature ◽  
Primary Focus ◽  
The Cost

Awareness of environmental issues has led to increasing interest from composite researchers in using “greener” materials to replace synthetic fiber reinforcements and petrochemical polymer matrices. Natural fiber bio-based thermoplastic composites could be an appropriate choice with advantages including reducing environmental impacts, using renewable resources and being recyclable. The choice of polymer matrix will significantly affect the cost, manufacturing process, mechanical properties and durability of the composite system. The criteria for appropriate monomers are based on the processing temperature and viscosity, polymer mechanical properties, recyclability, etc. This review considers the selection of thermoplastic monomers suitable for in situ polymerization during resin, now monomer, infusion under flexible tooling (RIFT, now MIFT), with a primary focus on marine composite applications. Given the systems currently available, methyl methacrylate (MMA) may be the most suitable monomer, especially for marine composites. MMA has low process temperatures, a long open window for infusion, and low moisture absorption. However, end-of-life recovery may be limited to matrix depolymerization. Bio-based MMA is likely to become commercially available in a few years. Polylactide (PLA) is an alternative infusible monomer, but the relatively high processing temperature may require expensive consumable materials and could compromise natural fiber properties.

scholarly journals Melt- vs. Non-Melt Blending of Complexly Processable Ultra-High Molecular Weight Polyethylene/Cellulose Nanofiber Bionanocomposite

Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 404
Author(s):  
Nur Sharmila Sharip ◽  
Hidayah Ariffin ◽  
Tengku Arisyah Tengku Yasim-Anuar ◽  
Yoshito Andou ◽  
Yuki Shirosaki ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Yield Strength ◽  
Young’S Modulus ◽  
High Molecular Weight ◽  
Melt Processing ◽  
Cellulose Nanofiber ◽  
Melt Blending ◽  
Ultra High Molecular Weight

The major hurdle in melt-processing of ultra-high molecular weight polyethylene (UHMWPE) nanocomposite lies on the high melt viscosity of the UHMWPE, which may contribute to poor dispersion and distribution of the nanofiller. In this study, UHMWPE/cellulose nanofiber (UHMWPE/CNF) bionanocomposites were prepared by two different blending methods: (i) melt blending at 150 °C in a triple screw kneading extruder, and (ii) non-melt blending by ethanol mixing at room temperature. Results showed that melt-processing of UHMWPE without CNF (MB-UHMWPE/0) exhibited an increment in yield strength and Young’s modulus by 15% and 25%, respectively, compared to the Neat-UHMWPE. Tensile strength was however reduced by almost half. Ethanol mixed sample without CNF (EM-UHMWPE/0) on the other hand showed slight decrement in all mechanical properties tested. At 0.5% CNF inclusion, the mechanical properties of melt-blended bionanocomposites (MB-UHMWPE/0.5) were improved as compared to Neat-UHMWPE. It was also found that the yield strength, elongation at break, Young’s modulus, toughness and crystallinity of MB-UHMWPE/0.5 were higher by 28%, 61%, 47%, 45% and 11%, respectively, as compared to the ethanol mixing sample (EM-UHMWPE/0.5). Despite the reduction in tensile strength of MB-UHMWPE/0.5, the value i.e., 28.4 ± 1.0 MPa surpassed the minimum requirement of standard specification for fabricated UHMWPE in surgical implant application. Overall, melt-blending processing is more suitable for the preparation of UHMWPE/CNF bionanocomposites as exhibited by their characteristics presented herein. A better mechanical interlocking between UHMWPE and CNF at high temperature mixing with kneading was evident through FE-SEM observation, explains the higher mechanical properties of MB-UHMWPE/0.5 as compared to EM-UHMWPE/0.5.

scholarly journals Effect of Na- and Organo-Modified Montmorillonite/Essential Oil Nanohybrids on the Kinetics of the In Situ Radical Polymerization of Styrene

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 474
Author(s):  
Ioannis S. Tsagkalias ◽  
Alexandra Loukidi ◽  
Stella Chatzimichailidou ◽  
Constantinos E. Salmas ◽  
Aris E. Giannakas ◽  
...  
Keyword(s):  
Essential Oil ◽  
Radical Polymerization ◽  
Food Packaging ◽  
In Situ Polymerization ◽  
Average Molecular Weight ◽  
Monomer Conversion ◽  
Hydroxyl Groups ◽  
Modified Montmorillonite ◽  
Kinetics Of

The great concern about the use of hazardous additives in food packaging materials has shown the way to new bio-based materials, such as nanoclays incorporating bioactive essential oils (EO). One of the still unresolved issues is the proper incorporation of these materials into a polymeric matrix. The in situ polymerization seems to be a promising technique, not requiring high temperatures or toxic solvents. Therefore, in this study, the bulk radical polymerization of styrene was investigated in the presence of sodium montmorillonite (NaMMT) and organo-modified montmorillonite (orgMMT) including thyme (TO), oregano (OO), and basil (BO) essential oil. It was found that the hydroxyl groups present in the main ingredients of TO and OO may participate in side retardation reactions leading to lower polymerization rates (measured gravimetrically by the variation of monomer conversion with time) accompanied by higher polymer average molecular weight (measured via GPC). The use of BO did not seem to affect significantly the polymerization kinetics and polymer MWD. These results were verified from independent experiments using model compounds, thymol, carvacrol and estragol instead of the clays. Partially intercalated structures were revealed from XRD scans. The glass transition temperature (from DSC) and the thermal stability (from TGA) of the nanocomposites formed were slightly increased from 95 to 98 °C and from 435 to 445 °C, respectively. Finally, better dispersion was observed when orgMMT was added instead of NaMMT.

Test Methods for Mechanical Properties of Structural Adhesives

2010 ◽  
Vol 97-101 ◽  
pp. 814-817 ◽  
Author(s):  
Jun Deng
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Shear Strength ◽  
Elastic Modulus ◽  
Butt Joint ◽  
Test Methods ◽  
Joint Specimen ◽  
Lap Shear ◽  
Better Than

One of the greatest drawbacks to predicting the behaviour of bonded joints has been the lack of reliable data on the mechanical properties of adhesives. In this study, methods for determining mechanical properties of structural adhesive were discussed. The Young’s modulus, Poisson’s ratio and tensile strength of the adhesive were tested by dogbone specimens (bulk form) and butt joint specimens (in situ form). The shear modulus and shear strength were test by V-notched specimens (bulk form) and thick adherend lap-shear (TALS) joint specimens (in situ form). The test results show that the elastic modulus provided by the manufacturer is too low, the dogbone specimen is better than the butt joint specimen to test the tensile strength and elastic modulus and the TALS joint specimen is better than the V-notched specimen to test the shear strength.

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.

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