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1.
This paper focuses on the influence of temperature conditions and the clay contents on enhancement of mechanical characterization of polypropylene (PP) nanocomposites. The nanocomposites were prepared using the melt mixing technique in a co-rotating intermeshing twin screw extruder followed by injection moulding. Nanocomposites properties such as impact strength and ultimate tensile strength, yield strength, failure strain, Young’s modulus and toughness are calculated. The addition of clay to PP matrix was showed remarkable enhancement in mechanical properties at the temperature of 25 oC and 120 °C. Nearly 36 % and 160 % increase in the Young’s modulus and about 45 % and 62 % increase in the impact strength were observed at both room temperature (RT) and high temperature (HT), respectively. But, the tensile strength was not affected much. The basal spacing of clay in the composites was measured by X-ray diffraction (XRD). Scanning electron microscopy (SEM) was used to assess the surface morphology of the fractured surfaces and dispersion of the nanoclay.  相似文献   

2.
Present research investigates the mechanical properties of jute-coir fiber reinforced hybrid polypropylene (PP) composite with fiber loading variation and observes the effect of chemical treatment of fiber on property enhancement of the composites. Composites were manufactured using hot press machine at four levels of fiber loading (5, 10, 15 and 20 wt%). Fiber ratio’s were varied (jute:coir=1:1, 3:1 and 1:3) for 20 % fiber loaded composites. Both jute and coir fiber was treated using 5 % and 10 % NaOH solutions. Composites were also prepared using treated fiber with jute-coir fiber ratio of 3:1. Tensile, flexural, impact and hardness tests and Fourier transform infrared spectroscopic analysis were conducted for characterization of the composites. Tensile test of composite showed a decreasing trend of tensile strength and increasing trend of the Young’s modulus with increase in fiber loading. During flexural, impact and hardness tests, the flexural strength, flexural modulus, impact strength and hardness values were found to be increased with increase in fiber loading. All these properties enhanced with the enhancement of jute content except impact strength. 5 % NaOH treatment provided an improving trend of properties whereas, 10 % NaOH treatment showed the reverse one. The FTIR analysis of the composites indicated decrease of hemicelluloses and lignin content with alkali treatment.  相似文献   

3.
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   

4.
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   

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.
PLA/LPCL/HPCL blend fibers composed of poly (lactic acid) (PLA), low molecular weight poly (ɛ-caprolactone) (LPCL), and high molecular weight poly (ɛ-caprolactone) (HPCL) were prepared by melt blending and spinning for bioabsorbable filament sutures. The effects of blending time and blend composition on the X-ray diffraction patterns and tensile properties of PLA/LPCL/HPCL blend fibers were characterized by WAXD and UTM. In addition, the effect ofin vitro degradation on the weight loss and tensile properties of the blend fibers hydrolyzed during immersion in a phosphate buffer solution at pH 7.4 and 37°C for 1–8 weeks was investigated. The peak intensities of PLA/LPCL/HPCL blend fibers in X-ray diffraction patterns decreased with an increase of blending time and LPCL contents in the blend fibers. The weight loss of PLA/LPCL/HPCL blend fibers increased with an increase of blending time, LPCL contents, and hydrolysis time while the tensile strength and modulus of the blend fibers decreased. The tensile strength and modulus of the blend fibers were also found to be increased with an increase of HPCL contents in the blend fibers. The optimum conditions to prepare PLA/LPCL/HPCL blend fibers for bioabsorbable sutures are LPCL contents of 5 wt%, HPCL contents of 35 wt%, and blending time of 30 min. The strength retention of the PLA/LPCL/HPCL blend fiber prepared under optimum conditions was about 93.5% even at hydrolysis time of 2 weeks.  相似文献   

7.
Maleated castor oil (MACO) was prepared and was used as biomodifier in unsaturated polyester resin (UPE)/fly ash composites. The prepared MACO was characterized for its molecular weight and viscosity. MACO was blended with UPE in three different ratios like 5, 10 and 15 wt%. Fly ash was incorporated in the blend matrix (10 wt%) and curing was done by free radical polymerization. MACO was polymerized and crosslinked with UPE in situ during the formation of the composites. The cured matrix therefore formed an interpenetrating polymer network and the enhancement in properties was significant. Incorporation of 5 wt% MACO was most effective compared to 10 and 15 wt%, when the impact strength increased by 52% without any loss in modulus. The glass transition temperature also shifted to a higher temperature indicating strong intercomponent bonding in this set of composites.  相似文献   

8.
Octamethyl-POSS and Octaphenyl-POSS reinforced polypropylene nanocomposite monofilaments were prepared by melt blending route. It was observed that incorporation of Octamethyl-POSS and Octaphenyl-POSS in polypropylene show improvement in mechanical as well as thermal properties. Octaphenyl POSS/PP nanocomposites show significant increase in thermal stability even at very low concentration as compared to neat polymer matrix. An increase of 100 and 140 °C was observed in thermal degradation temperature at 5 wt% loss and maximum degradation over neat PP filaments respectively at low OP-POSS loadings (<5 wt%). Both Octamethyl-POSS and Octaphenyl-POSS act as lubricating agents facilitating drawing which results in improvement in orientation as well as mechanical properties.  相似文献   

9.
In the present study, nanocomposites films formed by hydroxyethyl cellulose (HEC) and graphene oxide (GO) were synthesized and characterized. Compared with pure hydroxyethyl cellulose film, the thermal stability and mechanical properties of the composite materials were significantly improved. When the graphene loading was only 1.0 wt%, the maximum weight loss temperature increased 11.14 °C. The tensile strength and Young’s modulus of HEC/GO nanocomposites films were increased by 30.28 and 75.63 % compared to the pure HEC films, with only 1.0 wt% GO. The X-ray diffraction and Fouriertransform infrared spectroscop showed that GO sheets were completely exfoliated in the HEC matrix and suggested the presence of the weak interaction between HEC and GO sheets because of large number of oxygen-containing hydrophilic functional groups on the surface and edge of GO sheets. Furthermore, the well-dispersed GO nanosheets in the films can be inferred from the SEM and Halpin-Tsai model analysis. On the other hand, the composite films showed improved barrier properties against oxygen. This simple process for preparation of HEC/GO films is attractive for potential development of high-performance films for packing applications.  相似文献   

10.
The objective of this investigation was to evaluate the mechanical, thermal stability and viscoelastic behaviors of experimental PP composites made from wheat straw and PP-g-MA coupling agent. Four levels of wheat straw, 10, 20, 25 and 30 wt % and two levels of coupling agent, 0 and 3 % wt were mixed with PP in rotary type mixer and injection molding process, respectively. Tensile characteristics and impact strength, thermal gravity and dynamic mechanical and thermal analysis of the samples were evaluated. Based on the results, it was observed that the tensile properties increased and impact strength decreased with the increase in the fiber loading from 10 % to 30 %. Further, the composites treated with PP-g-MA exhibited improved mechanical properties which confirmed efficient fiber-matrix adhesion. DMT analysis showed that the PP composites made of 30 % wheat straw containing 3 % PP-g-MA showed the highest E’ and lowest tan δ than the untreated ones. Also, the thermal stability of wheat straw was lower than PP and as filler content in the composites increased, the thermal stability decreased and the ash content increased.  相似文献   

11.
A simple method based on the combination of the intercalation from solution and melt-processing preparation methods was used to prepare highly exfoliated and compatible thermoplastic starch (TPS) and montmorillonite clay (MMT) nanocomposites. The effects of the MMT content on the thermal, structural, and mechanical properties of the nanocomposites were investigated. XRD diffraction was used to investigate the MMT exfoliation/intercalation degrees in the TPS matrix. Data from thermogravimetric analysis and differential scanning calorimetry revealed that the addition of MMT increased the thermal stabilities of TPS nanocomposites. Young's modulus and tensile strength increased from 8.0 to 23.8 MPa and 1.5 to 2.8 MPa with an increasing MMT content from 0 to 5 wt% without diminishing their flexibility. The improvement in such properties can be attributed to the good dispersion/exfoliation of MMT in the TPS matrix. Combining both methods, it was possible to obtain homogenous and transparent nanocomposites with excellent thermal and mechanical properties for application as packaging materials.  相似文献   

12.
Blends of poly(butylene terephthalate) (PBT)/thermoplastic polyurethane (TPU) were prepared by melt compounding. The miscibility, crystallization behaviors and toughening mechanism of the PBT/TPU blends were studied. Dynamic mechanical analysis results demonstrated that PBT was immiscible with TPU. Differential scanning calorimetry and wide angle X-ray diffraction results showed that the crystallinity of PBT decreased with increasing TPU content. Furthermore, blending with TPU did not modify the crystal structure of PBT. The small angle X-ray scattering results indicated that the crystal layer thickness decreased and the amorphous layer thickness increased with increasing TPU content, indicating that TPU mainly resided in the interlamellar region of PBT spherulites in the blends. An obvious improvement in toughness of PBT was achieved with addition of TPU. Neat PBT had elongation at break and impact strength of about 15 % and 2.9 kJ/m2, respectively. However, the elongation at break and impact strength of the 70/30 PBT/TPU blend reached 410 % and 62.9 kJ/m2, respectively. The morphology of the PBT/TPU blends after tensile and impact tests was investigated, and the corresponding toughening mechanism is discussed. It was found that the PBT showed obvious shear yielding in the blend during the tensile and impact tests, which induced dissipation of energy and, therefore, led to the improvement in toughness of the PBT/TPU blends.  相似文献   

13.
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   

14.
The main objective of this research was to study the effect of fiber content variation and stearic acid (SA) treatment on the fundamental properties of unidirectional coir fiber (CF) reinforced polypropylene (PP) composites. Several percentages of filler contents were used (10–40 wt %) in order to gain insights into the effect of filler content on the properties of the composites. Coir/PP composites were fabricated by compression molding, and the properties of composites were studied by physico-mechanical and thermal properties. The results from mechanical properties such as tensile strength (TS), tensile modulus (TM) and impact strength (IS) of the CF/PP composites were found to be increased with increasing fiber content, reached an optimum and thereafter decreased with further increase in fiber content. Treatment of the coir with SA as the coupling agent enhanced the mechanical properties, crystallization temperature and crystallinity of virgin PP and water desorption of the resulting composites, resulting from the improved adhesion between the CF and PP matrix. Scanning electron micrographs (SEM) of the tensile fractured samples showed improved adhesion between fiber and matrix upon treatment with SA. Interfacial shear strength (IFSS) of the composites was measured by single fiber fragmentation test (SFFT).  相似文献   

15.
Melt-processed blends of zein and polyvinylpyrrolidone (PVP) of varying molecular weights (55K, 360K and 1.3M) were compared based on mechanical and thermal properties. Generally, all samples stored at 50% RH exhibited a slight improvement in tensile strength, with the PVP360K samples showing the greatest improvement. At the higher levels of PVP, samples stored at 70% RH showed a decrease in tensile strength. Elongation was also more significantly impacted at higher humidity, with the higher levels of PVP causing greater elongation increases. Differential scanning calorimetry data for the blends showed single Tg values intermediate between the zein and PVP controls. Kinetic thermogravimetric data suggested a multi-step degradation interaction for the zein/PVP blends. Scanning electron microscope imaging of compression molded samples showed homogeneous surface contours for even the 20% PVP1.3M blend. Melt-processed blends of zein with polyvinylpyrrolidone of various molecular weights appear to be compatible. This work represents the first melt-processed blend of zein with PVP to generate a compatible blend.  相似文献   

16.
This research evaluates the miscibility and performance of polypropylene (PP)/polybutylene succinate (PBS) and PP/polylactic acid (PLA) blend and natural-flour-filled, PP/PLA and PP/PBS blend bio-composites. The melting temperature (T m ) and glass transition temperature (T g ) of pure PP, PBS and PLA showed a single peak but differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) presented two peaks for the T m and T g of the PP/PBS and PP/PLA blends. These results indicated that the PP/PBS and PP/PLA blend systems existed as immiscible blends. These results were also confirmed by the scanning electron microscopy (SEM) micrographs of the tensile fracture surface of the PP/PBS and PP/ PLA blends. At a PP/PBS and PP/PLA blend ratio of 70/30, the tensile and flexural strengths of bamboo flour (BF)- and wood flour (WF)-filled, PP/PBS and PP/PLA blend bio-composites were similar to those of BF- and WF-filled, PP and PBS bio-composites. In addition, these strengths of maleic anhydride-grafted PP (MAPP)- and acrylic acid-grafted PP (AAPP)-treated, BF- and WF-filled, PP/PBS and PP/PLA blend bio-composites were higher than those of non-treated bio-composites.  相似文献   

17.
Natural rubber and styrene butadiene rubber (NR/SBR) reinforced with both short nylon fibers and nanoclay (Cloisite 15A) nanocomposites were prepared in an internal and a two roll-mill mixer by a three-step mixing process. The effects of fiber loading and different loading of nanoclay (1, 3 and 5 wt. %) were studied on the microstructure and mechanical properties of the nanocomposites. The adhesion between the fiber and the matrix was improved by the addition of a dry bonding system consisting of resorcinol, hexamethylene tetramine and hydrated silica (HRH). This silicate clay layers was used in place of hydrated silica in a HRH bonding system for SBR/NR-short nylon fiber composite. Nanoclay was also used as a reinforcing filler in the matrix-short fiber hybrid composite. The cure and scorch times of the composites decreased while cure rate increased when the short fiber and nanoclay were added. The mechanical properties of the composites showed improvement in both longitudinal and transverse directions with increasing short fiber and nanoclay content. The structure of the nanocomposites was characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM). X-ray diffraction results of nanocomposites indicated that the interlayer distance of silicate layers increased. The mechanical properties of nanocomposites (tensile, hardness and tear strength) are examined and the outcome of these results is discussed in this paper.  相似文献   

18.
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   

19.
PLA/PLA-g-ABS blends were prepared and evaluated for mechanical properties performance. Firstly, carboxylic acid functionalized ABS particles were synthesized by grafting polymethacrylic acid (PMAA) onto ABS particle surface using potassium persulfate as an initiator. The reaction was followed by FTIR analysis. The resultant carboxylated ABS was melt mixed with virgin PLA in an internal mixer to obtain PLA/PLA-g-ABS blends. The obtained PLA/PLA-g-ABS blends were subject to injection molding to obtain specimens for testing evaluation. It was found that impact resistance values significantly outperformed neat PLA by 60 %, 87 %, and 150 % for PLA/PLA-g-ABS 10 wt%, PLA/PLA-g-ABS 20 wt%, and PLA/PLA-g-ABS 30 wt%, respectively. A significant increase in impact strength was contributable to ABS rubber which exhibited even dispersion and good interfacial adhesion. The impact strength was dependent on the percent loading of PLAg-ABS; the more the PLA/PLA-g-ABS the higher the impact strength value. In a similar manner, tensile strength increases when loaded with PLA/PLA-g-ABS albeit at lesser effect. Considering the percent elongation, a massive increase in percent elongation was recorded in case of PLA/PLA-g-ABS 20 wt% and PLA/PLA-g-ABS 30 wt%, implying that these blends were extremely flexible and tough when compared to neat PLA, control, and PLA/PLA-g-ABS 10 wt%.  相似文献   

20.
In this study, PLA/PC blends were prepared in order to investigate the effects of the addition of PC loading level into PLA matrix on the mechanical properties of these blends. After that, PLA/PC (70/30), which has the lowest tensile strength value, was selected as a control sample for the compatibilization study. Commercial styrene-acrylic multi-functional-epoxide oligomeric agent (SAmfE), styrene maleic anhydride copolymer (SMA), tetrasilanol phenyl polyhedral oligomeric silsesquioxane (T-POSS) and glycidyl isooctyl-polyhedral oligomeric silsesquioxane (G-POSS) were used as compatibilizers for PLA/PC blends. The variation of mechanical, thermal, structural and morphological properties were examined by conducting tensile tests, dynamic mechanical analyses, differential scanning calorimetry, Fourier Transform IR and scanning electron microscope analyses. Tensile test results showed that the tensile strength and elongation at break values of the PLA/PC blend compatibilized with SAmfE were higher than those of the other blends. DSC analyses revealed that Tg and Tm values of the blends were not significantly affected by compatibilizer but, degree of crystallinity was found to be sensitive to compatibilizer type. DMA results showed that the best mechanical properties were obtained for the PLA/PC/SAmfE blend. When all of the results evaluated, it was found that the SAmfE is the most effective compatibilizer among the using compatibilizer types for PLA/PC blends.  相似文献   

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