Annealing Effects in Conventionally Cast and Homogenized Al-Zn-Mg(-Sc-Zr) Alloy

2017 ◽  
Vol 380 ◽  
pp. 167-172
Author(s):  
Martin Vlach ◽  
Veronika Kodetova ◽  
Bohumil Smola ◽  
Hana Kudrnova ◽  
Tomáš Kekule
Keyword(s):  
Electron Microscopy ◽  
Supersaturated Solid Solution ◽  
Microstructure Development ◽  
Scanning Calorimetry ◽  
Zr Addition ◽  
Annealing Effects ◽  
Positive Effect ◽  
Scanning Electron ◽  
Zr Alloy ◽  
Conventionally Cast

Al-based alloys are very preferred for automotive manufacture to produce lightweight vehicles. The positive effect of Sc,Zr-addition on the mechanical properties in Al-based alloys is generally known. Microstructure, mechanical, electrical and thermal properties of the conventionally cast and homogenized Al–Zn–Mg alloy with and without Sc,Zr-addition during isochronal annealing were studied. The electrical resistometry and microhardness together with differential scanning calorimetry measurements were compared to microstructure development that was observed by optical microscopy and transmission and scanning electron microscopy. It was observed that the Sc,Zr-content in the alloy after casting is not homogeneously distributed but concentrated in randomly localized matrix regions and together with Zn and Mg in the particles at grain boundaries. However, the hardening effect after annealing above 280 °C lightly reflects the Sc,Zr-addition. The distinct changes in resistivity and microhardness as well as in heat flow of the alloys studied are mainly caused by formation/dissolution of the Guinier-Preston zones and subsequent precipitation of the metastable particles from the Al–Zn–Mg system. The eutectic Zn,Mg-containing phase partly disappeared during the annealing above ~ 390 °C. Melting of the Zn,Mg-containing phase was observed at ~ 475 °C. The decomposition sequence of the supersaturated solid solution of the studied alloys is compatible with the decomposition sequence of the Al–Zn–Mg system minimally up to ~ 380 °C.

scholarly journals Characteristics of Reconstituted Collagen Fibers from Chicken Keel Cartilage Depends on Salt Type for Removal of Proteoglycans

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3538
Author(s):  
Anna Pudło ◽  
Szymon Juchniewicz ◽  
Wiesław Kopeć
Keyword(s):  
Electron Microscopy ◽  
Rheological Properties ◽  
Thermal Denaturation ◽  
Surface Structures ◽  
Scanning Calorimetry ◽  
Cartilage Extracellular Matrix ◽  
Oscillatory Rheometry ◽  
Freeze Dried ◽  
Basic Features ◽  
Scanning Electron

The aim of the presented research was to obtain reconstituted atelocollagen fibers after extraction from poultry cartilage using the pepsin-acidic method in order to remove telopeptides from the tropocollagen. Firstly, we examined the extraction of collagen from the cartilage extracellular matrix (ECM) after proteoglycans (PG) had been removed by the action of salts, i.e., NaCl or chaotropic MgCl2. Additionally, the effects of the salt type used for PG and hyaluronic acid removal on the properties of self-assembled fibers in solutions at pH 7.4 and freeze-dried matrices were investigated. The basic features of the obtained fibers were characterized, including thermal properties using scanning calorimetry, rheological properties using dynamic oscillatory rheometry, and the structure by scanning electron microscopy. The fibers obtained after PG removal with both analyzed types of salts had similar thermal denaturation characteristics. However, the fibers after PG removal with NaCl, in contrast to those obtained after MgCl2 treatment, showed different rheological properties during gelatinization and smaller diameter size. Moreover, the degree of fibrillogenesis of collagens after NaCl treatment was complete compared to that with MgCl2, which was only partial (70%). The structures of fibers after lyophilization were fundamentally different. The matrices obtained after NaCl pretreatment form regular scaffolds in contrast to the thin, surface structures of the cartilage matrix after proteoglycans removal using MgCl2.

Research on compatibility and surface of high impact bio-based polyamide

2021 ◽  
pp. 095400832110055
Author(s):  
Yang Wang ◽  
Yuhui Zhang ◽  
Yuhan Xu ◽  
Xiucai Liu ◽  
Weihong Guo
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Scanning Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Crystallization Behavior ◽  
High Impact ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Scanning Electron

The super-tough bio-based nylon was prepared by melt extrusion. In order to improve the compatibility between bio-based nylon and elastomer, the elastomer POE was grafted with maleic anhydride. Scanning Electron Microscopy (SEM) and Thermogravimetric Analysis (TGA) were used to study the compatibility and micro-distribution between super-tough bio-based nylon and toughened elastomers. The results of mechanical strength experiments show that the 20% content of POE-g-MAH has the best toughening effect. After toughening, the toughness of the super-tough nylon was significantly improved. The notched impact strength was 88 kJ/m2 increasing by 1700%, which was in line with the industrial super-tough nylon. X-ray Diffraction (XRD) and Differential Scanning Calorimetry (DSC) were used to study the crystallization behavior of bio-based PA56, and the effect of bio-based PA56 with high crystallinity on mechanical properties was analyzed from the microstructure.

scholarly journals Effect of the dispersion of the chromophore on the optical performances of polarizers from polyethylene and 5”-thio- (3-butyl)nonyl-2,2’:5’,2”-terthiophene

e-Polymers ◽  
2002 ◽  
Vol 2 (1) ◽  
Author(s):  
Andrea Pucci ◽  
Letizia Moretto ◽  
Giacomo Ruggeri ◽  
Francesco Ciardelli
Keyword(s):  
Electron Microscopy ◽  
Molecular Weight ◽  
Scanning Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Melting Point ◽  
Drawing Ratio ◽  
Scanning Calorimetry ◽  
Affine Deformation ◽  
Ultra High Molecular Weight ◽  
Scanning Electron

AbstractA new polyethylene-compatible terthiophene chromophore, 5”-thio-(3- butyl)nonyl-2,2’:5’,2”-terthiophene, with melting point lower than 0°C was prepared and used for linear polarizers based on ultra-high-molecular-weight polyethylene (UHMWPE). Differential scanning calorimetry and scanning electron microscopy indicate that the new chromophore is dispersed uniformly in films of UHMWPE obtained by casting from solution. The films show excellent dichroic properties (dichroic ratio 30) at rather low drawing ratio (≈ 20) . Moreover, qualitative agreement is observed with the Ward pseudo-affine deformation scheme.

scholarly journals Development of an Oxcarbazepine Solid Dispersion Using Skimmed Milk to Improve the Solubility and Dissolution Profile

2019 ◽  
Vol 11 (05) ◽  
Author(s):  
M. Shah ◽  
D. Patel
Keyword(s):  
Electron Microscopy ◽  
Solid Dispersion ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Infra Red ◽  
Crystalline Nature ◽  
Skimmed Milk ◽  
Scanning Electron

Oxcarbazepine has low solubility and low oral bioavailability, so it’s a challenge to formulate suitable dosage form. In this present investigation, to improve the dissolution rate and solubility, skimmed milk is used as a carrier. Physical mixers were prepared using various drugs to carrier ratio and spray drying technology was used to develop solid dispersion with the carrier. Various techniques were used to characterize the solid dispersion immediately after they were made which includes differential scanning calorimetry, scanning electron microscopy, fourier transform infra- red spectroscopy, X-ray diffraction and in-vitro dissolution profiles. The differential scanning calorimetry thermograms of raw drug indicated of its anhydrous crystalline nature. In thermograms of solid dispersion, the characteristic peak was absent suggesting the change from crystalline nature to amorphous form. X-ray diffraction confirmed those results. X-ray diffraction results of raw drug showed highly intense peak characteristic of its crystalline nature where solid dispersion showed less intense, more diffused peak indicating the change in crystalline form. Fourier transforms infra-red spectroscopy studies showed there was no interaction between drug and carrier. Scanning electron microscopy support the amorphous nature of mixer. The whole formulation showed distinct enhancement in the drug release behavior and solubility. The optimum oxcarbazepine to skimmed milk ratio 1:3 enhances the in-vitro drug release by 3.5 fold and also show distinct increase in solubility. It was concluded that for improvement of solubility of poorly water soluble oxcarbazepine, skimmed milk powder as a carrier can be utilize very well.

Tensile and flammability characterizations of corn straw slagging/high-density polyethylene composites

2019 ◽  
Vol 33 (11) ◽  
pp. 1466-1477
Author(s):  
Qingfa Zhang ◽  
Wenyu Lu ◽  
Liang Zhou ◽  
Donghong Zhang ◽  
Hongzhen Cai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Tensile Strength ◽  
Flame Retardant ◽  
High Density Polyethylene ◽  
Oxygen Index ◽  
High Density ◽  
Corn Straw ◽  
Scanning Calorimetry ◽  
Scanning Electron

Biocomposites were prepared with corn straw slagging (CSS) and high-density polyethylene (HDPE) at four loading levels (10, 20, 30, and 40 wt%) by extrusion method. CSS/HDPE composites were tested by tension, oxygen index meter, differential scanning calorimetry, X-ray diffraction, and the scanning electron microscopy. The scanning electron microscopy showed that CSS was dispersed uniformly in the HDPE matrix and strong interfacial interaction was achieved, which had an important influence on the tensile strength of the composites. The tensile strength of the composites could be improved with proper increase of CSS and reached maximum value at 30 wt% content. Furthermore, the addition of CSS played an important role in improving the flame-retardant ability of CSS/HDPE composites, and the limited oxygen index was 31.26% at 40 wt% content, good flame-retardant effect achieved.

Influence of Cementitious Capillary Crystalline Waterproofing Material on the Water Impermeability and Microstructure of Concrete

2019 ◽  
Vol 953 ◽  
pp. 209-214
Author(s):  
Yi Teng Zhang ◽  
Lian Zuo ◽  
Jin Chao Yang ◽  
Wei Xia Zhao ◽  
Xiang Xiong Zeng
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Cement Matrix ◽  
Hardened Cement ◽  
Hydration Products ◽  
Hardened Cement Paste ◽  
Scanning Calorimetry ◽  
Chinese Standard ◽  
Scanning Electron

The main objective of this study is to investigate the effect of cementitious capillary crystalline waterproofing (CCCW) material on the water impermeability and microstructure of concrete. The water impermeability of concrete covered with or without CCCW material was tested according to the Chinese standard GB 18445-2012. The results indicate that concretes coated with CCCW material showed much higher water impermeability than blank ones, and the ratio of water impermeability pressure between them reached 275. The samples obtained in various depths of hardened cement paste specimens with or without CCCW coating were analyzed through scanning electron microscopy (SEM) and thermogravimetry-differential scanning calorimetry (TG-DSC), to study the differences in microstructure and hydration products. The results present that after a 28-day standard curing, there were lots of ettringite crystals and CaCO3 formed in the paste in 1 cm from the coating, but the action depth of the CCCW coating could not reach 3 cm. The ettringite and CaCO3 is precipitated in the pore structure of cement matrix and filling the voids, which leads to the significant enhancement in water impermeability.

Preparation of Chitosan-Polycaprolactone (PCL) Composite Nanofiber as Potential for Annulus Fibrosus Regeneration

2020 ◽  
Vol 840 ◽  
pp. 368-376 ◽  
Author(s):  
Nur Rofiqoh Eviana Putri ◽  
Dhimas Agung Kurniawan ◽  
Bintang Adi Pradana ◽  
Nadya Alfa Cahaya Imani ◽  
Yuni Kusumastuti
Keyword(s):  
Electron Microscopy ◽  
Annulus Fibrosus ◽  
Composite Nanofibers ◽  
Synthetic Polymer ◽  
Medical Applications ◽  
Scanning Calorimetry ◽  
Composite Nanofiber ◽  
Remarkable Result ◽  
Ivd Degeneration ◽  
Scanning Electron

Tissue engineering has shown a remarkable result in medical applications. Further exploration, these multidisciplinary fields are also given a possibility as an alternative medication for intervertebral disc (IVD) degeneration. Focusing on the annulus fibrous repair, to improve the mechanical properties of biomaterials, a composite made of chitosan and polycaprolactone (PCL) was developed in this present study. Due to its tuneable properties, the electrospinning-based method was used in the experiment to create the chitosan/PCL composite. Varies concentration of PCL (11, 12, and 13 wt%) and a different ratio of precursors chitosan to PCL (1:1; 1:3; 1:5) were used to optimize the composition of natural and synthetic polymer in the composite nanofibers. The obtained nanofibers were then characterized using Scanning Electron Microscopy (SEM) to observe the morphology, swelling test, Fourier Transform Infrared (FTIR) spectroscopy, and Differential Scanning Calorimetry (DSC). The results show that the increasing concentration and composition of PCL could form the more homogeneous and larger diameter of nanofiber with fewer beads compare to the lower composition of PCL nanofiber. Meanwhile, the swelling percentage decreases by increasing the amount of PCL. FTIR results also show that all samples of composite nanofibers contain both chitosan and PCL.

scholarly journals DESIGN AND DEVELOPMENT OF RILPIVIRINE NANOPARTICLE CONTAINING CHITOSAN USING IONIC GELATION METHOD FOR HIV INFECTIONS

2020 ◽  
pp. 113-118
Author(s):  
MONTUKUMAR PATEL ◽  
NIRAV V. PATEL ◽  
TEJAS B. PATEL
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
In Vitro Release ◽  
Amorphous State ◽  
Hiv Infections ◽  
Spherical Particles ◽  
Ionic Gelation ◽  
Scanning Calorimetry ◽  
Scanning Electron

Objective: The primary objective of the current research was to prepare rilpivirine loaded Nanoparticles containing Chitosan using the ionic gelation method for HIV infections. Methods: The nanoparticles of rilpivirine were prepared using the ionic gelation technique. Further, nanoparticles were characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and in vitro drug release. Results: The optimized nanoparticles were found with a particle size of 130.30±5.29 nm (mean±SD) and entrapment efficiency (% EE) of 77.10±0.50%. Scanning electron microscopy technique exposed spherical particles with uniform size. It was observed that the nanoparticles created showed the absence of the crystalline nature of the drug and its switch to the amorphous state. Results showed that more than 45% of the pure drug is released in 50 min and after 90 min almost about 95% of the drug is released. Conclusion: The research study concluded that the in vitro release profile of nanoparticles was found to be sustained up to 24 hr. Sustained release of the rilpivirine could improve patient obedience to drug regimens, growing action effectiveness. 

Effects of Thermal Treatment on the Morphology and Properties of CSM/Poly(Urethane-Isocyanurate) Composites Formed by SRIM Process

2008 ◽  
Vol 575-578 ◽  
pp. 941-946
Author(s):  
Hong Yan Tang ◽  
Ji Hui Wang ◽  
Guo Qiang Gao ◽  
Wen Xing Chen
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Mechanical Property ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Treatment Time ◽  
Microphase Separation ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Scanning Electron

Fiberglass continuous strand mat(CSM)/poly(urethane-isocyanurate) composites were formed by SRIM process, treated under different conditions and then characterized based on dynamic mechanical thermal analysis (DMTA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) ,transmission electron microscopy (TEM) and the mechanical property tests. The results show that the mechanical properties of the composites could be increased with improving the degree of microphase separation. At a given temperature (120°C), the degree of microphase separation is the highest for 4h and decreases gradually with prolonging treatment time. For a given time (4h), the well microphase-separated morphology is obtained and the degree of microphase mixing is increased at 120°C and 140°C treatments, respectively. The degree of microphase separation of the composites decreases with enhancing the temperature to 140°C.

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