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1.
We have prepared a series of polypropylene/exfoliated graphene (PP/EG) nanocomposite films via efficient meltcompounding and compression, and investigated their morphology, structures, thermal transition behavior, thermal stability, electrical and mechanical properties as a function of EG content. For the purpose, EG, which is composed of disordered graphene platelets as reinforcing nanoscale fillers, is prepared by the oxidation/exfoliation process of natural graphite flakes. SEM images and X-ray diffraction data confirm that the graphene platelets of EG are well dispersed in PP matrix for the nanocomposites with EG contents less than 1.0 wt%. It is found that thermo-oxidative degradation of PP/EG nanocomposites is noticeably retarded with the increasing of EG content. Electrical resistivity of the nanocomposite films was dramatically changed from ∼1016 to ∼106 Ω·cm by forming electrical percolation threshold at an certain EG content between 1 and 3 wt%. Tensile drawing experiments demonstrate that yielding strength and initial modulus of PP/EG nanocomposite films are highly improved with the increment of EG content.  相似文献   

2.
The development of high tenacity, high modulus monofilaments from Polypropylene/Clay nanocomposite has been investigated. Pure sodium montmorillonite nanoclay was modified using hexadecyl trimethyl ammonium bromide (HTAB) via an ion exchange reaction. Pure and modified clay were characterized through X-ray diffraction, FTIR and TGA. The modified clay was melt blended with polypropylene (PP) in presence of a swelling agent. Composite filaments from PP/Clay nanocomposite were prepared at different weight percentages of nanoclay and the spinning and drawing conditions were optimized. The filaments were characterized for their mechanical, morphological and thermal properties. The composite PP filaments with modified clay showed improved tensile strength, modulus and reduced elongation at break. The composite filaments with unmodified clay did not show any improvement in tensile strength but the modulus improved. The sharp and narrow X-ray diffraction peaks of PP/nanoclay composite filaments indicate increase in crystallinity in presence of modified clay at small loadings (0.5%). The improved thermal stability was observed in filaments with modified as well as unmodified clays.  相似文献   

3.
Jute fabrics (hessian cloth) reinforced polypropylene (PP) matrix composites (45 wt% fiber) were fabricated by compression molding. Jute fabrics were treated with 2-hydroxyethyl methacrylate (HEMA) using ultraviolet radiation in order to improve the mechanical properties of the composites. Concentration of HEMA, soaking time and radiation dose were optimized. It was found that 15% HEMA in methanol along with photoinitiator Darocur-1173 (2 %), 10 min soaking time and 20th pass of radiation rendered better performance. Urea of different concentrations (0.5–2 %) was incorporated with 15 % HEMA to monitor its effect on the properties and 1 % urea revealed the best results. For the improvement of the properties, jute fabrics were treated with potassium permanganate (KMnO4) solution in acetone of different concentrations (0.02, 0.03, 0.05, and 0.5 %) at different soaking times (1, 2, 3, and 5 min) before the composite fabrication. Optimized jute fabrics (jute fabrics treated with 0.03 % KMnO4) were again treated with HEMA (15 %) solution along with urea (1 %) and promising improvement of mechanical properties of the composites was observed. Scanning electron microscopy, water uptake, soil degradation and thermal aging of the treated and untreated composites were also performed.  相似文献   

4.
We prepared long carbon fiber (LCF)-reinforced thermoplastic composites using a compatibilizer of itaconic acid grafted polypropylene (PP-g-IA). We confirmed the structure of PP-g-IA and investigated the compatibilizing effects of PPg- IA on LCF/polypropylene composites. The tensile strength, tensile moduli, flexural strength, and flexural moduli of the composites increased with increasing PP-g-IA content in the thermoplastic composites. Using single pull-out analyzing system, we found PP-g-IA improved interfacial strength between the carbon fiber and PP matrix. The thermal properties of the composites were measured by thermogravimetric analysis (TGA). We could observe that LCF enhanced the mechanical properties and thermal decomposition temperature of the polypropylene (PP) composites, compared with neat PP. The fractured surfaces of PP/PP-g-IA/LCF composites showed that PP-g-IA was effective for improving the interfacial adhesion between LCF and PP matrix.  相似文献   

5.
Chemical treatment is an often-followed route to improve the physical and mechanical properties of natural fiber reinforced polymer matrix composites. In this study, the effect of chemical treatment on physical and mechanical properties of jute fiber reinforced polypropylene (PP) biocomposites with different fiber loading (5, 10, 15, and 20 wt%) were investigated. Before being manufactured jute fiber/PP composite, raw jute fiber was chemically treated with succinic anhydride for the chemical reaction with cellulose hydroxyl group of fiber and to increase adhesion and compatibility to the polymer matrix. Jute fiber/PP composites were fabricated using high voltage hot compression technique. Fourier Transform Infrared spectroscopy (FTIR) and Scanning Electron Microscopy (SEM) tests were employed to evaluate the morphological properties of composite. Succinic anhydride underwent a chemical reaction with raw jute fiber which was confirmed through FTIR results. SEM micrographs of the fractured surface area were taken to study the fiber/matrix interface adhesion and compatibility. Reduced fiber agglomeration and improved interfacial bonding was observed under SEM in the case of treated jute fiber/PP composites. The mechanical properties of jute/PP composite in terms of Tensile strength and Young’s modulus was found to be increased with fiber loading up to 15 wt% and decreased at 20 wt%. Conversely, flexural strength and flexural modulus increased with fiber loading up to 10 wt% and start decreasing at 15 wt%. The treated jute/PP composite samples had higher hardness (Rockwell) and lower water absorption value compared to that of the untreated ones.  相似文献   

6.
This study examined the thermal and mechanical properties of polypropylene filaments reinforced with multi-walled carbon nanotubes (MWNTs). The MWNTs were functionalized with maleic anhydride polypropylene to increase the interfacial interactions between the CNTs and polypropylene. PP/MWNT composites with different concentrations of MWNTs were prepared by melt compounding using a twin screw extruder. The composites of the filament were then post drawn and heat treated. Tensile tests showed increased strength with the addition of only 0.1 wt% while there were only slight changes in elongation. The thermal properties were also slightly enhanced by the MWNTs.  相似文献   

7.
Bidirectional PP/jute yarn eco-composites were fabricated via environment friendly commingling technique and its long term durability/life time was monitored as an effect of accelerated solar ageing on its mechanical properties (tensile & flexural). Accelerated solar ageing promoted the thermal oxidation of PP thus resulting in deterioration of its properties, however; MAPP and KMnO4 treated commingled composites showed much better stability towards thermal oxidation brought about by the solar concentrator, compared to untreated sample and neat polypropylene. This increased resistivity of treated composites (especially MAPP and KMnO4) towards thermal oxidation brought about by the solar concentrator is due to the increased interfacial adhesion between the matrix and jute yarn owing to chemical modifications. The significance of effective stress transfer between the PP matrix and reinforcing jute yarns is evident from the increased tear resistance of PP/jute yarn commingled composites with increasing fibre content and also with different chemical treatments.  相似文献   

8.
In this work, the effect of organosolv lignin on properties of polypropylene (PP)/chitosan composites was investigated. Mechanical and thermal properties of the composites were analyzed by means of ASTM D 638-91, ASTM D 256, thermogravimetry analysis (TGA) and differential scanning calorimetry (DSC). Tensile strength and elongation at break of the PP composites decreased upon the presence of chitosan filler, but Young’s modulus improved. Impact strength was found to increase with the maximum value at 30 php of filler loading. At a similar loading, treated PP/chitosan composites were found to have higher tensile strength, elongation at break, Young’s modulus as well as impact strength than untreated composites. Furthermore, the presence of organosolv lignin imparted a plasticizing effect. Thermal properties of the treated PP/chitosan composites were better as compared with the untreated PP/chitosan composites; although the chemical treatment did not alter the thermal degradation mechanism. In addition, the obtained results were comparable to results from previous studies. This finding implied that the organosolv lignin could be a potential reagent to replace its synthetic counterpart.  相似文献   

9.
The Allyl-heptaisobutyl-polyhedral Oligomeric Silsesquioxane (AHO-POSS) grafted polypropylene (PP) nanocomposite monofilaments were prepared by γ-ray irradiation induced grafting. The structure and properties of physically blended and γ-ray irradiated AHO-POSS/PP nanocomposite filaments were investigated by FTIR, wide-angle X-ray diffraction (WAXD), Thermo-gravimetric Analysis and mechanical property studies. Chemical bonding of AHO-POSS with PP after γ-ray irradiation was confirmed by FT-IR spectroscopy. Grafting resulted in change in mechanical and thermal properties and the extent of change was critically dependent on loading of AHO-POSS in PP and radiation dose level. In general, tensile strength decreased almost continuously with increase in radiation dose whereas thermal stability increased upto a radiation dose of 5 kGy and then decreased. The loss in tensile strength was caused due to chain scission, cross linking and loss in orientation.  相似文献   

10.
Improvement of both the tensile and impact strength of the same polymeric material has always been a great challenge for the plastic industry. The study focuses on the effect of incorporation of calcium carbonate nanoparticles (0.3 wt% to 15 wt%) into three polypropylene (PP) based matrices viz. PP homopolymer, propylene-ethylene (PP-PE) copolymer and the blend of PP:PP-PE (30:70) to improve their impact behavior without hampering the tensile strength much. A loss in both the tensile and impact properties was observed in PP based nanocomposite. However, PP-PE based nanocomposites showed a significant improvement in impact strength (47 %) at 10 wt% loading with a loss of tensile strength by 22 %. To minimize this loss a blend of PP:PP-PE (30:70) was explored as a matrix. At 10 wt% loading, this matrix showed an improvement of 30 % in impact strength whereas the tensile loss was minimized to 10 %. Further, silane coupling agent which promoted good interfacial adhesion was used for best compositions. The variation of crystalline morphology of the nanocomposites with various formulations was analyzed using differential scanning calorimetry and X-ray diffraction.  相似文献   

11.
Aluminum particles (Al) were added to polypropylene (PP) in the presence of poly ethylene glycol (PEG) and polypropylene-graft-maleic anhydride to produce composites. The composites were then melt-spun into a mono filament and tested for tensile properties, diameter evenness and morphology. Melt rheological properties of Al/PP composites were studied in linear viscoelastic response regions. It was observed that level of dispersion of aluminum particles within a polypropylene composite fiber could be improved by incorporating polyethylene glycol. The improvement of dispersion led to an improvement in the fibers mechanical properties through a reduction of the coefficient of variation of fiber diameter.  相似文献   

12.
Natural fibers are largely divided into two categories depending on their origin: plant based and animal based. Plant based natural jute fiber reinforced polypropylene (PP) matrix composites (20 wt% fiber) were fabricated by compression molding. Bending strength (BS), bending modulus (BM), tensile strength (TS), Young’s modulus (YM), and impact strength (IS) of the composites were found 44.2 MPa, 2200 MPa, 41.3 MPa, 750 MPa and 12 kJ/m2, respectively. Animal based natural B. mori silk fiber reinforced polypropylene (PP) matrix composites (20 wt% fiber) were fabricated in the same way and the mechanical properties were compared over the silk based composites. TS, YM, BS, BM, IS of silk fiber reinforced polypropylene composites were found 55.6 MPa, 760 MPa, 57.1 MPa, 3320 MPa and 17 kJ/m2 respectively. Degradation of composites in soil was measured upto twelve weeks. It was found that plant based jute fiber/PP composite losses its strength more than animal based silk fiber/PP composite for the same period of time. The comparative study makes it clear that mechanical properties of silk/PP composites are greater than those values of jute/PP composites. But jute/PP composites are more degradable than silk/PP composites i.e., silk/PP composites retain their strength for a longer period than jute/PP composites.  相似文献   

13.
The bleached jute fabric (BJF) reinforced polypropylene (PP) composites with various contents of acrylic acid (AA)-treated BJF and un-AA-treated BJF were fabricated by compression moulding method at 190 °C. The AA-grafted BJF reinforced PP composites were then irradiated by γ-ray at various doses. The mechanical properties of neat PP (N-P), ungrafted-BJF and PP composites (UG-BJFPC), AA-grafted-BJF and PP composites (AA-BJFPC) and γ-ray cum AA-grafted-BJF and PP composites (γAA-BJFPC) show maximum tensile strength (TS) of 30, 46, 47 and 51 MPa, maximum flexural strength (FS) of 34, 49, 50 and 54 MPa and maximum Young’s modulus (E) of 280, 428, 436, and 680 MPa, respectively. The increase of TS, FS and E from UG-BJFPC are 2 %, 2 %, and 2 % for AA-BJFPC and 11 %, 10 % and 59 % for γAA-BJFPC. The TS, FS and E are found to increase with radiation dose up to 500Krad and then decrease. The water absorption (WA) for UG-BJFPC, AA-BJFPC and γAA-BJFPC is respectively about 14, 10 and 9 %, indicating a gradual development of hydrophobic character of the composites first by AA-treatment and then by γ-ray-treatment. AA treatment on jute fabric and gamma irradiation on composite result in significant change of morphology of the jute fabric composites surface and better mechanical bonding between fabric and polymer matrix, as a result improved mechanical properties are found.  相似文献   

14.
Plasticization and toughness of polylactide (PLA) are of interesting due to its poor machinability and brittleness. Here, low and high macromolecular weight of Poly(diethylene glycol adipate)s (L-PDEGA and H-PDEGA) were used to plasticize and toughen PLA simultaneously. The results showed that the mechanical properties of PLA remained almost unchanged when only 5 wt% L-PDEGA was added. However, H-PDEGA were effective in lowering the glass transition temperatures as well as in increasing the elongation at break and the impact strength. Compared with neat PLA, the crystallinity of PLA increased with increasing H-PDEGA content. When 20 wt% H-PDEGA was added, the impact strength and the elongation at break increased from 3.1 kJ/m2 and 5.6 % of neat PLA to 68.3 kJ/m2 to 272.4 %, respectively. Additionally, morphological study revealed that the fracture behavior of PLA had been changed from brittle to ductile after H-PDEGA incorporated. The results of rheological analysis showed that the storage modulus and complex viscosity in the melt state of the blends were decreased compared with that of neat PLA.  相似文献   

15.
Poly(ethylene terephthalate) (PET)/CaCO3 and PET/modified-CaCO3 (m-CaCO3) nanocomposites were prepared by melt blending. The morphology indicated that m-CaCO3 produced by reacting sodium oxalate and calcium chloride, was well dispersed in PET matrix and showed good interfacial interaction with PET compared to CaCO3. No significant differences in the thermal properties such as, glass transition, melting and degradation temperatures, of the nanocomposites were observed. The thermal shrinkage of PET at 120 °C was 10.8 %, while those of PET/CaCO3 and PET/m-CaCO3 nanocomposites were 2.9–5.2 % and 1.2–2.8 %, respectively depending on filler content. The tensile strength of PET/CaCO3 nanocomposite decreased with CaCO3 loading, whereas that of PET/m-CaCO3 nanocomposites at 0.5 wt% loading showed a 17 % improvement as compared to neat PET. The storage modulus at 120 °C increased from 1660 MPa for PET to 2350 MPa for PET/CaCO3 nanocomposite at 3 wt% loading, and 3230 MPa for PET/m-CaCO3 nanocomposite at 1 wt% loading.  相似文献   

16.
The present paper deals with improvement in disperse dyeability as well as imparting of cationic dyeablility to difficultly dyeable polypropylene by a melt blending technique. Isotactic polypropylene (PP) was blended with fibre grade polybutylene terephthalate (PBT), cationic dyeable polyethylene terephthalate (CDPET) and polystyrene (PS), individually. The resulting binary blends were spun and drawn into fibres at draw ratio 2, 2.5, and 3. The compatibility of blends, structural changes of fibres in terms of X-ray crystallinity, relative crystallinity, sonic modulus, birefringence and thermal stability were examined. The blended fibres were found to be disperse dyeable by the conventional method of high temperature and high pressure dyeing. And this dyeability increased with increase in the level of substitution. PP/CDPET blend also exhibited dyeablility with cationic dyes in addition to that with disperse dyes. The optimum level of blending was predicted keeping in view of tenacity and thermal stability of melt blend fibres. The wash fastness properties of the dyed fibres were found to be of high rate.  相似文献   

17.
The Allyl-heptaisobutyl-polyhedral oligomeric silsesquioxane (AHO-POSS) grafted polypropylene (PP) was prepared by reactive extrusion and by physical blending routes. The structure and properties of physically blended and reactively blended POSS/PP nanocomposites were investigated by FTIR, wide-angle X-ray diffraction (WAXD), differential scanning calorimetry (DSC), thermogravimetric analysis, SEM, spherutlic growth and mechanical properties studies. Chemical bonding of POSS with PP in reactive extrusion was confirmed by FT-IR spectroscopy. DSC and TGA studies showed that the thermal stability of AHO-POSS/PP nanocomposite prepared by reactive extrusion improved significantly as compared to only physically blended nanocomposites. WAXD studies showed decrease in crystallinity of the AHO-POSS/PP nanocomposites prepared by reactive extrusion. SEM studies showed aggregation tendency in case of physically blended AHO-POSS/PP nanocomposites. Spherulite growth studies show reactive blending retards spherulite growth in PP polymer.  相似文献   

18.
In this study, in-situ polypropylene/polystyrene (PP/PS) blends were prepared via a reactive extrusion technique. Fourier transform infrared spectroscopy (FTIR) analysis confirmed the generation of polypropylene-grafted-polystyrene (PP-g-PS) copolymer in the reactive process. The morphology of the in-situ PP/PS blend tended to form a homogeneous structure, as observed by scanning electron microscopy (SEM). Owing to the introduction of PP-g-PS in the reactive extrusion, a remarkable enhancement of mechanical properties was achieved for the in-situ PP/PS blend. The elongation at break of the in-situ PP/PS blend with 15 wt% PS can reach 500 %, over 10 times higher than that of the normal PP/PS blend. Differential scanning calorimetry (DSC) showed an increased crystallization temperature of PP, which can be attributed to the heterogeneous nucleation effect of the PS and grafted PS. The analysis of wide angle X-ray diffraction (WAXD) indicated the development of beta crystals in the in-situ PP/PS blend.  相似文献   

19.
In this research, possibility of producing and processing antibacterial organic/inorganic nanocomposite polypropylene filament yarns for permanent antimicrobial efficiency has been investigated. First PP powder and inorganic nanocomposite filler were mixed in a twin screw extruder and modified masterbatch was produced. Continuous filament yarn was made by a pilot plant melt spinning machine from the blend of PP granule and various blending contents of the prepared masterbatch. Pure PP and all other combined samples showed acceptable spinnability at the spinning temperature of 240 °C and take-up speed of 2000 m/min. After producing as-spun filament yarns, samples were drawn, textured and finally weft knitted. Physical and structural properties of as-spun and drawn yarns with constant and variable draw ratios were investigated and also tensile and crimp properties of textured yarns were evaluated. Moreover, the DSC, SEM, FTIR techniques have been used for characterization of samples. Finally antibacterial efficiency of knitted samples was evaluated. The experimental results indicated that the maximum crystallinity reduction of modified drawn yarns has reached to 5 %. The observed improvement in the tensile properties of modified as-spun yarns compared to the pure PP was significant. Drawing process improved generally the tensile properties of as-spun yarns. Tensile properties of modified textured and drawn yarns were higher than the pure PP. An optimum of antibacterial activity has been observed in the sample containing 0.75 wt% of nano-filler. It is interesting that the optimum of tensile properties has been also obtained for the sample with maximum bioactivity.  相似文献   

20.
Siloxylated polypropylene fibers composed of polypropylene (PP) and aluminosiloxane (AS) were prepared by melt blending followed by spinning. The effects of blend compositions on the thermal behaviors, surface and tensile properties of PP/AS blend fibers were investigated by DSC, WAXD, SEM, static honestometer, etc. The heat of fusion of PP/AS blends decreased with increasing AS contents. In addition, the peak intensity of PP/AS blends in X-ray diffraction patterns decreased with increasing AS contents. It was observed that the silicone molecules exist and well distribute on the surface of siloxylated polypropylene fibers. From the results of the half-life period measurements, the anti-static properties of PP fibers siloxylated with AS was found to be significantly modified.  相似文献   

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