Effects of polypropylene-g-dibutyl maleate on mechanical and rheological properties of PP/PA6 blends

e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Duxin Li ◽  
Baoli Ou ◽  
Demin Jia
Keyword(s):  
Electron Microscopy ◽  
Morphological Properties ◽  
Scanning Calorimetry ◽  
Flow Activation Energy ◽  
Rheological Measurements ◽  
Transmission Electron ◽  
End Groups ◽  
Reactive Groups ◽  
Flow Activation ◽  
Dibutyl Maleate

AbstractThe effects of polypropylene-grafted-dibutyl maleate (PP-g-DBM) used as compatibilizer on mechanical, rheological and morphological properties of polypropylene (PP) and nylon 6 (PA6) blends was systematically investigated in this paper. The results of Molau test, solvent extraction and differential scanning calorimetry (DSC) indicated the formation of PP-g-PA6 in vicinity of interfaces during melting extrusion. Owing to the reaction between the reactive groups of PPg- DBM and amine (-NH2) end groups of PA6, the tensile and impact strength of the PP-g-DBM compatibilized PP/PA6 blends were much higher than that of the uncompatibilized PP/PA6 blends. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) results indicated that the domain sizes of the dispersed phase in the compatibilized PP/PA6 blends decreased and the interfaces become more indistinct, which indicated a clear compatibiliting effect was induced by the PP-g-DBM in the immiscible PP/PA6 blends, i.e. the PP-g-DBM was an effective compatibilizer for the PP/PA6 blends. In addition, the rheological measurements showed the PP-g-DBM compatibilized PP/PA6 blends possessed higher pseudo plasticity, melt viscosity and flow activation energy.

scholarly journals Study on Structure, Thermal Behavior, and Viscoelastic Properties of Nanodiamond-Reinforced Poly (vinyl alcohol) Nanocomposites

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1426
Author(s):  
Tomáš Remiš ◽  
Petr Bělský ◽  
Tomáš Kovářík ◽  
Jaroslav Kadlec ◽  
Mina Ghafouri Azar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Mechanical Analysis ◽  
Single Step ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Primary Particles ◽  
Solution Casting Method ◽  
Average Size

In this work, advanced polymer nanocomposites comprising of polyvinyl alcohol (PVA) and nanodiamonds (NDs) were developed using a single-step solution-casting method. The properties of the prepared PVA/NDs nanocomposites were investigated using Raman spectroscopy, small- and wide-angle X-ray scattering (SAXS/WAXS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). It was revealed that the tensile strength improved dramatically with increasing ND content in the PVA matrix, suggesting a strong interaction between the NDs and the PVA. SEM, TEM, and SAXS showed that NDs were present in the form of agglomerates with an average size of ~60 nm with primary particles of diameter ~5 nm. These results showed that NDs could act as a good nanofiller for PVA in terms of improving its stability and mechanical properties.

scholarly journals Age Hardening of Extruded AA 6005A Aluminium Alloy Powders

Materials ◽  
2019 ◽  
Vol 12 (14) ◽  
pp. 2316
Author(s):  
Feijoo ◽  
Cabeza ◽  
Merino ◽  
Pena ◽  
Rey
Keyword(s):  
Electron Microscopy ◽  
Heating Temperature ◽  
Hot Extrusion ◽  
Atomic Ratio ◽  
Age Hardening ◽  
Al Alloy ◽  
Ingot Metallurgy ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Peak Aging

Pre-alloyed micron-sized 6005A Al alloy (AA 6005A) powders, with a Mg/Si atomic ratio of 0.75, obtained by high pressure inert gas atomization were consolidated by uniaxial cold pressing at 200 MPa into cylindrical Al containers and hot extruded at 450, 480 and 500 °C with an extrusion rate of 7:1, followed by artificial T6 precipitation hardening. Ageing conditions were varied between 170 °C and 190 °C and times of 6, 7 and 8 hours. The microstructure of the extruded profiles was analysed using X-Ray diffractometry (XRD), light optical microscopy (LOM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Differential scanning calorimetry (DSC) was used to study the possible phase transformations. After our results, the peak-aging hardness condition was achieved at 180 °C for 6 h. Mechanical properties of the powder metallurgy (P/M) aluminium alloys consolidated by hot extrusion were superior to those of the extruded profiles of wrought alloy using conventional ingot metallurgy (I/M) billets. AA 6005A wrought P/M alloy via T6 heat treatment shown yield stress of 317 MPa and elongation of 21% at the extrusion pre-heating temperature of 500 °C.

scholarly journals An Efficient and Novel Ammonia Sensor Based on Polypyrrole/Tin Oxide/MWCNT Nanocomposite

2020 ◽  
Vol 32 (6) ◽  
pp. 1505-1510
Author(s):  
Ahmad Husain ◽  
Mohd Urooj Shariq ◽  
Anees Ahmad
Keyword(s):  
Electron Microscopy ◽  
Tin Oxide ◽  
Charge Carriers ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
Ammonia Sensing ◽  
Transmission Electron ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

In present study, the synthesis and characterization of a novel polypyrrole (PPy)/tin oxide (SnO2)/MWCNT nanocomposite along with pristine polypyrrole is reported. These materials have been studied for their structural and morphological properties by FT-IR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. PPy/SnO2/MWCNT nanocomposite has been converted into a pellet-shaped sensor, and its ammonia sensing studies were carried out by calculating the variation in the DC electrical conductivity at different concentration of ammonia ranging from 10 to 1500 ppm. The sensing response of the sensor was determined at 1500, 1000, 500, 200, 100 and 10 ppm and found to be 70.4, 66.1, 62.2, 55.4, 50.8 and 39.7%, respectively The sensor showed a complete reversibility at lower concentrations along with excellent selectivity and stability. Finally, a sensing mechanism was also proposed involving polarons (charge carriers) of polypyrrole and lone pairs of ammonia molecules

scholarly journals Energetic Films Realized by Encapsulating Copper Azide in Silicon-Based Carbon Nanotube Arrays with Higher Electrostatic Safety

Micromachines ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 575 ◽  
Author(s):  
Xuwen Liu ◽  
Yan Hu ◽  
Hai Wei ◽  
Bingwen Chen ◽  
Yinghua Ye ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Porous Alumina ◽  
Chemical Vapor ◽  
Exothermic Peak ◽  
Alumina Film ◽  
Scanning Calorimetry ◽  
Micro Electro Mechanical Systems ◽  
Transmission Electron ◽  
Anodic Oxidation Method ◽  
Silicon Based

Since copper azide (Cu(N3)2) has high electrostatic sensitivity and is difficult to be practically applied, silicon-based Cu(N3)2@carbon nanotubes (CNTs) composite energetic films with higher electrostatic safety were fabricated, which can be compatible with micro-electro mechanical systems (MEMS). First, a silicon-based porous alumina film was prepared by a modified two-step anodic oxidation method. Next, CNTs were grown in pores of the silicon-based porous alumina film by chemical vapor deposition. Then, copper nanoparticles were deposited in CNTs by electrochemical deposition and oxidized to Cu(N3)2 by gaseous hydrogen azide. The morphology and composition of the prepared silicon-based Cu(N3)2@CNTs energetic films were characterized by field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD), respectively. The electrostatic sensitivity of the composite energetic film was tested by the Bruceton method. The thermal decomposition kinetics of the composite energetic films were studied by differential scanning calorimetry (DSC). The results show that the exothermic peak of the silicon-based Cu(N3)2@CNTs composite energetic film is at the temperature of 210.95 °C, its electrostatic sensitivity is significantly less than that of Cu(N3)2 and its 50% ignition energy is about 4.0 mJ. The energetic film shows good electric explosion characteristics and is successfully ignited by laser.

Reactions in Metal-Metalloid Multilayers

1993 ◽  
Vol 311 ◽  
Author(s):  
Robert Sinclair ◽  
Toyohiko J. Konno
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Reactive Systems ◽  
Nucleation And Growth ◽  
In Situ Observation ◽  
Scanning Calorimetry ◽  
Compound Formation ◽  
Transmission Electron

ABSTRACTWe have studied the reactions at metal-metalloid interfaces using high resolution transmission electron microscopy, including in situ observation, and differential scanning calorimetry. There is contrasting behavior depending on the affinity for interaction or segregation. For reactive systems, compound formation ultimately results, but this can be preceded by solidstate amorphization. For non-reactive systems, crystallization of the metalloid is often achieved with nucleation and growth mediated by the metal phase.

Preparation and Property of Al87Ce3Ni8.5Mn1.5 Nanophase Amorphous Composites

2011 ◽  
Vol 412 ◽  
pp. 263-266
Author(s):  
Hong Wei Zhang ◽  
Li Li Zhang ◽  
Feng Rui Zhai ◽  
Jia Jin Tian ◽  
Can Bang Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
Volume Fraction ◽  
Material Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures

The higher mechanical strength of Al87Ce3Ni8.5Mn1.5 nanophase amorphous composites has been obtained with two methods. The first nanophase amorphous composites are directly produced by the single roller spin quenching technology. The method taken for the second nanophase amorphous composites is at first to obtain amorphous single-phase alloy, followed by annealed at different temperatures .The formative condition, the microstructure, the particle size, the volume fraction of α-Al phase and microhardness of nanophase amorphous composites etc have been investigated and compared by X-ray diffraction (XRD) and transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The microstructure of composites produced by the second method is higher than the former, the fabricated material structure of the system is more uniform and the process is easier to control.

Preparation, characterization, and properties of polystyrene/Na-montmorillonite composites

2018 ◽  
Vol 32 (8) ◽  
pp. 1078-1091 ◽  
Author(s):  
Sibel Erol Dağ ◽  
Pınar Acar Bozkurt ◽  
Fatma Eroğlu ◽  
Meltem Çelik
Keyword(s):  
Electron Microscopy ◽  
Interlayer Spacing ◽  
Decomposition Temperature ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Sem Images ◽  
Specific Pore Volume ◽  
Transmission Electron ◽  
Thermal Stability Of

A series of polystyrene (PS)/unmodified Na-montmorillonite (Na-MMT) composites were prepared via in situ radical polymerization. The prepared composites were characterized using various techniques. The presence of various functional groups in the unmodified Na-MMT and PS/unmodified Na-MMT composite was confirmed by Fourier transform infrared spectroscopy. Morphology and particle size of prepared composites was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). According to the XRD and TEM results, the interlayer spacing of MMT layers was expanded. SEM images showed a spongy and porous-shaped morphology of composites. TEM revealed the Na-MMT intercalated in PS matrix. The thermal stability of PS/unmodified Na-MMT composites was significantly improved as compared to PS, which is confirmed using thermogravimetric analysis (TGA). The TGA curves indicated that the decomposition temperature of composites is higher at 24–51°C depending on the composition of the mixture than that of pure PS. The differential scanning calorimetry (DSC) results showed that the glass transition temperature of composites was higher as compared to PS. The moisture retention, water uptake, Brunauer–Emmett–Teller specific surface area, and specific pore volume of composites were also investigated. Water resistance of the composites can be greatly improved.

Methods of analysing morphology of kaolinites: relations between crystallographic and morphological properties

Clay Minerals ◽  
1986 ◽  
Vol 21 (1) ◽  
pp. 55-68 ◽  
Author(s):  
J.M. Cases ◽  
P. Cunin ◽  
Y. Grillett ◽  
C. Poinsignon ◽  
J. Yvon
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Surface Area ◽  
Lateral Surface ◽  
Morphological Properties ◽  
Surfactant Adsorption ◽  
Adsorption Calorimetry ◽  
Crystalline Sample ◽  
Transmission Electron ◽  
Total Specific Surface Area

AbstractA study was made of the extent to which the lateral surfaces contribute to the surface area of five kaolinites of different crystallinities. Methods used included the low-temperature adsorption of N2and Ar as measured by a volumetric technique coupled with microcalorimetry, the interpretation of the adsorption isotherms of alkyldodecylammonium ions, particle-size distribution curves, and shadowed transmission electron microscopy. With the exception of surfactant adsorption and adsorption calorimetry using Ar, these methods gave different and debatable results. For instance, specific lateral surface area values expressed as a percentage of total specific surface area varied from 17·0 to 40·4% for the most crystalline sample and from 12·0 to 54·3% for the least crystalline. It is shown that the decrease in crystallinity of samples is accompanied by a reduction in crystallite size from 0·8 to 0·08 µm and a decrease in lateral surface area from 34·0 to 12·0%.

scholarly journals Characterization of monoclonal IgG cryoglobulins: fine-structural and morphological analysis

Blood ◽  
1987 ◽  
Vol 69 (2) ◽  
pp. 677-681 ◽  
Author(s):  
DN Podell ◽  
CH Packman ◽  
J Maniloff ◽  
GN Abraham
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Morphological Analysis ◽  
Vascular Occlusion ◽  
Molecular Clusters ◽  
Morphological Properties ◽  
Transmission Electron ◽  
Thin Walled ◽  
Scanning Electron

Abstract The morphology of the amorphous, gelatinous, and crystalline varieties of monoclonal IgG cryoglobulins was analyzed by light and transmission and scanning electron microscopy. Each cryoglobulin had a characteristic fine structure that correlated with its gross morphology. Transmission electron microscopy showed that the amorphous precipitates were random and disorganized molecular clumps. In contrast, cryogels were thin-walled, well-organized, and hydrated strawlike clusters, whereas cryocrystals formed tightly compacted, highly structured molecular clusters. Crystals that formed in blood produced rouleaux, and analysis by scanning electron microscopy indicated that the crystals could form thick-walled, branching, macromolecular nets that could physically trap cells. The morphological properties provided visual impressions by which cryoglobulins could cause clinical disease secondary to vascular occlusion produced by self- associated IgG cryoglobulin molecules.

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