The Preparation and Property Research on Laponite-Poly (L-Lactide) Composite Film

2013 ◽  
Vol 750-752 ◽  
pp. 1919-1923 ◽  
Author(s):  
Guo Xian Zhou ◽  
Ming Wei Yuan ◽  
Lin Jiang ◽  
Ming Long Yuan ◽  
Hong Li Li

The laponite-poly (L-lactide) composite films are prepared by the method of solution blending with polylactide (PLA) and laponite. The result shows that the homogeneous and smooth composite film is prepared with 1, 4-dioxane. Thermogravimetry analysis (TG) and tensile strength studies demonstrate that the thermal stability and tensile strength are improved with the laponite added. The scanning electron microscopy (SEM) measurement indicates that the pores of composite films get uniform and network structure is more and more compact with compared to pure PLA film. The present study reveals that the laponite as a complexing agent can improve the mechanical properties and thermal stability of PLA.

2013 ◽  
Vol 706-708 ◽  
pp. 340-343 ◽  
Author(s):  
Hong Li Li ◽  
Guo Xian Zhou ◽  
Yu Kai Shan ◽  
Ming Long Yuan

Abatract: The poly (L-lactide)/laponite composite films are prepared by the method of solution blending with polylactide (PLA) and laponite. The results show that when laponite content was lower than 0.2 %( mass w/w), laponite can be uniform dispersed in PLA and the composed material had good stability. Fourier transform infrared spectroscopy (FTIR) study demonstrates that PLA was successfully incorporated with laponite by Si-O bond. The mechanical measurement reveals that the tensile strength of PLA/laponite composite film has been increased with compared to pure PLA. The water contact angle (WCA) tests indicate that the hydrophobicity of the laponite modified PLA films can be improved. The present study reveals that the laponite as a complexing agent can improve the mechanical properties and hydrophilicity of PLA.


2013 ◽  
Vol 467 ◽  
pp. 3-7
Author(s):  
Hui Fen Yang ◽  
Lin Fei Lu ◽  
Bei Ping Jiang ◽  
Jin Long Zhang

Based on analyzing of chemical composition, mineral composition and thermal stability of red mud, preparation of ceramisite, using anthracite added as foaming agent, was investigated. Internal structure was observed by scanning electron microscopy (SEM). The results showed the bulk density of ceramisite was obviously reduced by anthracite added. The ceramisite with bulk density of 1.30g/cm3, water absorption rate£ ̈WAR£©of 2.98% and cylinder compressive strength £ ̈CCS£©of 9.48 MPa was obtained when weight ratio of red mud/waste glass/bentonites/anthracite was at 73:15:11:1. Majority of porosity in ceramisite was closed based on SEM. The porosity of ceramisite was much higher when anthracite was added as foaming agent than only calcite in red mud was used as foaming agent. The bulk density of the former was lower than that of the latter.


2018 ◽  
Vol 930 ◽  
pp. 224-229
Author(s):  
Marcos Antônio Guerra ◽  
Jeferson Prado Swerts ◽  
Mei Abe Funcia ◽  
Neide Aparecida Mariano ◽  
Maria Gabriela Nogueira Campos

Polyethylene terephthalate (PET) fiber is a very versatile fiber that can be produced with different properties, such as antimicrobial activity. This study aims to synthesize antimicrobial PET filaments incorporated with silver nanoparticles immobilized in silica (NPAg-Si) by bulk additive method. Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray (EDX) characterized the obtained filaments at concentrations (w/w) of 0.008%, 0.016%, 0.032%, 0.047% and 0.063% NPAg-Si, in order to identify the nanoparticles and analyze their dispersion in the polymeric matrix. Moreover, thermogravimetric analysis (TGA) was carry out to confirm the presence and concentration of the silver nanoparticles in the filaments as well as the thermal stability of the nanocomposites. The bulk addition method was efficient to produce PET-Silver filaments with silver nanoparticles homogeneously dispersed in the PET matrix.


2013 ◽  
Vol 334-335 ◽  
pp. 60-64 ◽  
Author(s):  
Mohammad Reza Loghman-Estark ◽  
Reza Shoja Razavi ◽  
Hossein Edris

Scandia, yttria doped zirconia ((ZrO2)0.96(REO1.5)0.04(RE=Sc3+, Y3+)) nanoparticles were prepared by the modified sol-gel method. The microstructure of the products was characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Raman spectroscopy. Thermal stabillity of SYSZ nanocrystals were also investigated. The SYSZ nanocrystals synthesized with EGM:Zr+4mole ratio 4:1, calcined at 700°C, have average diameter of ~20 nm.


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Lokesh R. Rane ◽  
Niranjan R. Savadekar ◽  
Pravin G. Kadam ◽  
Shashank T. Mhaske

The purpose of this study is to improve the performance properties of K-carrageenan (K-CRG) by utilizing nanosilica (NSI) as the reinforcing agent. The composite films were prepared by solution casting method. NSI was added up to 1.5% in the K-CRG matrix. The prepared films were characterized for mechanical (tensile strength, tensile modulus, and elongation at break), thermal (differential scanning calorimetry, thermogravimetric analysis), barrier (water vapour transmission rate), morphological (scanning electron microscopy), contact angle, and crystallinity properties. Tensile strength, tensile modulus, and crystallinity were found to have increased by 13.8, 15, and 48% whereas water vapour transmission rate was found to have decreased by 48% for 0.5% NSI loaded K-CRG composite films. NSI was found to have formed aggregates for concentrations above 0.5% as confirmed by scanning electron microscopy. Melting temperature, enthalpy of melting, and degradation temperature of K-CRG increased with increase in concentration of NSI in K-CRG. Contact angle also increased with increase in concentration of NSI in K-CRG, indicating the decrease in hydrophilicity of the films improving its water resistance properties. This knowledge of the composite film could make beneficial contributions to the food and pharmaceutical packaging applications.


1990 ◽  
Vol 182 ◽  
Author(s):  
J. R. Phillips ◽  
P. Revesz ◽  
J. O. Olowolafe ◽  
J. W. Mayer

AbstractThe thermal stability of Co silicide on single crystal and polycrystalline Si has been investigated. Co films were evaporated onto (100) Si and undoped polycrystalline Si and annealed in vacuum. Resulting silicide films were examined using Rutherford backscattering spectroscopy, scanning electron microscopy, electron—induced x—ray spectroscopy, and sheet resistivity measurements. We find that CoSi2 on single crystal (100) Si remains stable through 1000ºC. In contact with undoped polycrystalline Si, intermixing begins at temperatures as low as 650ºC for 30min annealing. The Co silicide and Si layers are intermixed after 750ºC 30min annealing, giving islands of Si surrounded by silicide material, with both components extending from the surface down to the underlying oxide layer. The behavior of CoSi2 contrasts with results reported for TiSi2 which agglomerates on single crystal Si around 900ºC but is stable on polycrystalline silicon as high as 800ºC. Resistivity measurements show that the Co silicide remained interconnected despite massive incursion by Si into the silicide layer.


2011 ◽  
Vol 284-286 ◽  
pp. 253-256 ◽  
Author(s):  
Xiao Hua Wang ◽  
Ming Nie

The polyaniline(PANI)-poly(vinyl alcoho1)(PVA) composite film doped with HC1 was prepared with PVA as matrix. Effects of PVA content, film drying temperature on properties of PANI-PVA composite film were studied. Tensile strength, elasticity, conductivity and thermal stability of PVA, HC1-PANI or PANI-PVA were compared. Tensile strength and elasticity of PVA film were the largest, its conductivity was the least. The conductivity of PANI-PVA was the largest, tensile strength and elasticity of PANI-PVA are bigger than those of HC1-PANI. The order of their thermal stability is PVA> HC1-PANI > PANI-PVA before 260°C, the order of their thermal stability is HC1-PANI>PANI-PVA> PVA after 260°C.


2015 ◽  
Vol 819 ◽  
pp. 262-267
Author(s):  
Mohammad Mizanur Rahman Khan ◽  
Wan Ahmad Kamil Mahmood ◽  
Yee Keat Wee ◽  
Hanis binti Azizan

The comparison of the influence of CaO and CuO alone and combined CaO/CuO on the diameter, surface morphology and thermal stability of polyaniline (PANI) nanofibers is reported. The possible incorporation of CaO and CuO in PANI was revealed by both fourier transform infrared spectroscopy (FT-IR) and ultraviolet-visible spectroscopy (UV–vis). It was found that the diameter of PANI nanofibers varied for the addition of CaO and CuO alone compared to their combined use. Field emission scanning electron microscopy (FESEM) showed that the addition of CaO, CuO and CaO/CuO consistently produce composite material in nanofibers structures. This nanofibers shows regular and uniform surface morphology and without secondary growth and agglomeration of the primary nanofibers. Thermogravimetric analysis (TGA) data showed better thermal stability for all composite materials as compared to PANI nanofibers.


2011 ◽  
Vol 675-677 ◽  
pp. 295-298
Author(s):  
Liang Shao ◽  
Jian Hui Qiu ◽  
Ming Zhu Liu ◽  
Hui Xia Feng ◽  
Guo Hong Zhang ◽  
...  

New types of conducting composites using andalusite as an inorganic substrate and polyaniline as the conducting phase were prepared. The composites exhibited conductivities in the 0.14-2.08 S/cm range, depending on the amount of polyaniline. The thermal stability of andalusite/polyaniline composites were studied by thermogravimetric analysis. The resulting composites were also characterized by using FTIR spectroscopy and scanning electron microscopy.


2019 ◽  
Vol 32 (4) ◽  
pp. 418-428 ◽  
Author(s):  
Maryam Rasekh ◽  
Zahra Rafiee

Polyimide (PI)/Fe3O4 nanocomposites were successfully prepared via the thermal curing of different amounts of Fe3O4 nanoparticles (2, 4, 6 and 8 wt%) functionalized by 3-aminopropyltriethoxy silane as a coupling agent, containing the poly(amic acid) derived from 5-diamino- N-(4-(4,5-diphenyl-1H-imidazol)phenyl)benzamide and 3,3′,4,4′-benzophenonetetracarboxylic dianhydride. The effect of Fe3O4 nanoparticles on the structural, thermal and magnetic properties of nanocomposites was investigated. The Fourier transform infrared spectroscopy and scanning electron microscopy (SEM) results reveal that the surface of Fe3O4 nanoparticles is sufficiently compatible with PI through linkage of the coupling agent between Fe3O4 and the polymer. Also, the SEM image shows that Fe3O4 nanoparticles are dispersed uniformly in the polymer matrix, with a particle size of around 78 nm. The nanocomposites of 2 and 8 wt% exhibit the saturation magnetization values of 0.055 and 0.170 emu g− 1, respectively. The thermogravimetric analysis data show that the thermal stability of the nanocomposites is improved as compared to the pure PI.


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