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Netzsch 404 Pegasus

This model was found in 112 unique locations in 21 countries, where it was mentioned from 2004 until recently.

  • differential scanning calorimeter
  • tester
  • apparatus
  • calorimeter
locations where this model was found
112
countries where the model is used
21
related research fields
44
first year this model was mentioned
2004

About the Netzsch 404 Pegasus

Questpair Analytics found the Netzsch 404 Pegasus at 112 research organisations and laboratories in 21 countries, in publications from 2004 until recently. It is used most in General Materials Science, Condensed Matter Physics and Mechanics of Materials.

Usage over time

Mentions per year, 2004–2020

Mentions peaked in 2019.

Research fields

44 related research fields

The Netzsch 404 Pegasus is used by scientists in research fields such as General Materials Science, Condensed Matter Physics, Mechanics of Materials, General Chemistry and Mechanical Engineering.

  • General Materials Science
  • Condensed Matter Physics
  • Mechanics of Materials
  • General Chemistry
  • Mechanical Engineering
  • Electronic, Optical and Magnetic Materials
  • Materials Chemistry
  • General Physics and Astronomy
  • Electrical and Electronic Engineering
  • Metals and Alloys
  • General Chemical Engineering
  • General Biochemistry, Genetics and Molecular Biology
  • Ceramics and Composites
  • General Engineering
  • Physical and Theoretical Chemistry
  • Inorganic Chemistry
  • Physics and Astronomy (miscellaneous)
  • Catalysis
  • Colloid and Surface Chemistry
  • Biochemistry
  • Surfaces, Coatings and Films
  • Organic Chemistry
  • Instrumentation
  • Chemistry (miscellaneous)
  • General Medicine
  • Applied Microbiology and Biotechnology
  • Molecular Biology
  • General Immunology and Microbiology
  • Pharmaceutical Science
  • Industrial and Manufacturing Engineering
  • + 14 more

Organisations using this equipment

The model was found at 112 locations in 21 countries.

112 locations in 21 countries
OrganisationInstrumentCityCountry
Chengdu University
Netzsch 404CChengduChina
California Institute of Technology
Netzsch 404CPasadenaUnited States
University of Wollongong
Netzsch 404CWollongongAustralia
Technical University of Denmark
Netzsch 404CRoskildeDenmark
University of Aberdeen
Netzsch 404CAberdeenUnited Kingdom
Institute of Machine Tools and Manufacturing
Netzsch 404CZürichSwitzerland
13–18 of 112

Research that uses the Netzsch 404 Pegasus

Only abstracts that are published under Creative Commons Attribution 4.0 are shown on this page.

Entropy Determination of Single-Phase High Entropy Alloys with Different Crystal Structures over a Wide Temperature Range

We determined the entropy of high entropy alloys by investigating single-crystalline nickel and five high entropy alloys: two fcc-alloys, two bcc-alloys and one hcp-alloy. Since the configurational entropy of these single-phase alloys differs from alloys using a base element, it is important to quantify the entropy. Using differential scanning calorimetry, cp-measurements are carried out from −170 °C to the materials’ solidus temperatures TS. From these experiments, we determined the thermal entropy and compared it to the configurational entropy for each of the studied alloys. We applied the rule of mixture to predict molar heat capacities of the alloys at room temperature, which were in good agreement with the Dulong-Petit law. The molar heat capacity of the studied alloys was about three times the universal gas constant, hence the thermal entropy was the major contribution to total entropy. The configurational entropy, due to the chemical composition and number of components, contributes less on the absolute scale. Thermal entropy has approximately equal values for all alloys tested by DSC, while the crystal structure shows a small effect in their order. Finally, the contributions of entropy and enthalpy to the Gibbs free energy was calculated and examined and it was found that the stabilization of the solid solution phase in high entropy alloys was mostly caused by increased configurational entropy.

Sebastian Haas, Mike Mosbacher, Oleg Senkov, Michael Feuerbacher, Jens Freudenberger, Senol Gezgin, Rainer Völkl, Uwe Glatzel. Entropy, 20 (9), 654, 2018.

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Oral Bioavailability Enhancement and Anti-Fatigue Assessment of the Andrographolide Loaded Solid Dispersion

Andrographolide (AG), a major diterpene lactone isolated from Andrographis paniculata (Burm. f.) Nees (Acanthaceae), possesses a wide spectrum of biological activities. However, its poor water solubility and low bioavailability limit its clinical application. Therefore, this study aimed to develop a solid dispersion (SD) formulation to increase the aqueous solubility and dissolution rate of AG. Different drug-polymer ratios were used to prepare various SDs. The optimized formulation was characterized for differential scanning calorimetry, Fourier transform infrared spectroscopy, and powder X-ray diffraction. The analysis indicated that the optimized SD enhanced AG solubility and dissolution rates by changing AG crystallinity to an amorphous state. The dissolution behaviors of the optimum SD composed of an AG-polyvinylpyrrolidone K30-Kolliphor EL ratio of 1:7:1 (w/w/w) resulted in the highest accumulated dissolution (approximately 80%). Pharmacokinetic studies revealed that Cmax/dose and the AUC/dose increased by 3.7-fold and 3.0-fold, respectively, compared with AG suspension. Furthermore, pretreatment using the optimized AG-SD significantly increased the swimming time to exhaustion by 1.7-fold and decreased the plasma ammonia level by 71.5%, compared with the vehicle group. In conclusion, the optimized AG-SD formulation appeared to effectively improve its dissolution rate and oral bioavailability. Moreover, the optimized AG-SD provides a promising treatment against physical fatigue.

Ching-Chi Yen, Yu-Kai Liang, Chao-Pei Cheng, Mei-Chich Hsu, Yu-Tse Wu. International Journal of Molecular Sciences, 21 (7), 2506, 2020.

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The Structural Evolution of Al86Ni9La5 Glassy Ribbons during Milling at Room and Cryogenic Temperatures

Melt-spun metallic Al86Ni9La5 glassy ribbons solidified at different circumferential speeds (Sc) were subjected to high-energy ball milling at room and cryogenic temperatures. Crystallization induced by milling was found in the Al86Ni9La5 solidified at lower circumferential speed (Sc = 14.7 m/s), while the Al86Ni9La5 with Sc = 36.6 m/s kept amorphous. Besides, a trend of structural rejuvenation during milling process was observed, as the onset temperatures (Tx1, Tx2) and the crystallization enthalpies (ΔH1, ΔH2) first decreased and then increased along with the milling time. We explored the structural origin of crystallization by ab initio molecular dynamic simulations and found that the tricapped trigonal prism (TTP) Ni-centered clusters with a higher frequency in samples solidified at a lower cooling rate, which tend to link into medium-range orders (MROs), may promote crystallization by initiating the shear bands during milling. Based on the deformation mechanism and crush of metallic glasses, we presented a qualitative model to explain the structural rejuvenation during milling.

Zhicheng Yan, Yan Liu, Shaopeng Pan, Yihua Hu, Jing Pang, Weimin Wang. Materials, 11 (10), 1956, 2018.

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Effect of Cooling Rate on Phase and Crystal Morphology Transitions of CaO–SiO2-Based Systems and CaO–Al2O3-Based Systems

The phase and crystal morphology transitions of two typical types of mold fluxes were investigated fundamentally using differential scanning calorimetry (DSC) and confocal scanning laser microscopy (CSLM) techniques. For the traditional CaO–SiO2–CaF2-based mold flux, different cooling rates can change the phases and the crystal morphologies. Faceted cuspidine and CaSiO3 are co-precipitated when the cooling rate is less than 50 °C·min−1. The phases transform from Ca4Si2O7F2 and CaSiO3 to Ca4Si2O7F2 at the cooling rate of 50 °C·min−1. Cuspidine shows four different morphologies: faceted shape, fine stripe, fine stripe dendrite, and flocculent dendrite. The crystalline phases of CaAl2O4 and Ca3B2O6 are co-precipitated in the CaO–Al2O3-based mold flux. Neither the phases nor the crystal morphologies change in the low cooling rate range (5 °C·min−1 to 50 °C·min−1). With decreasing temperature, the morphology of CaAl2O4 firstly becomes dendritic, and then the dendritic quality gradually changes to a large-mesh blocky shape at the cooling rates of 100 °C·min−1, 200 °C·min−1, and 500 °C·min−1. Different cooling rates do not show an obvious impact on the morphology transition of CaAl2O4. The strong crystallization ability and large rate of crystallization affect the control of the heat transfer of the CaO–Al2O3-based mold flux during casting. The big morphology difference between primary crystals of the CaO–SiO2–CaF2-based mold flux and the CaO–Al2O3-based mold flux is probably one of the biggest factors limiting lubrication between the CaO–Al2O3-based mold flux and high-Al steel during casting.

Mei Leng, Feifei Lai, Jiangling Li. Materials, 12 (1), 62, 2018.

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Crystallization Products and Structural Characterization of CaO-SiO2-Based Mold Fluxes with Varying Al2O3/SiO2 Ratios

During the casting of high aluminum steel, the dramatic increase in the Al2O3/SiO2 ratio is inevitable, resulting in significant changes of the crystallization behavior, which would result in heat transfer and lubrication problems. Crystallization products and structure characterization of glassy CaO-SiO2-based mold fluxes with different Al2O3/SiO2 ratios were experimentally investigated using a differential scanning calorimetry technique and Raman spectroscopy. With increasing Al2O3/SiO2 ratios, the following results were obtained. The crystallization temperature and the crystallization products are changed. With increasing Al2O3/SiO2 ratios from 0.088 to 0.151, the crystallization temperature first increases greatly from 1152 °C to 1354 °C, and then moderately increases. The crystallization ability of the mold flux is strengthened. The species of the precipitated crystalline phase change from two kinds, i.e., Ca4Si2O7F2 and Ca2SiO4, to four kinds, i.e., Ca4Si2O7F2, Ca2SiO4, 2CaO·Al2O3·SiO2 and Ca12Al14O32F2, the crystallization ability of Ca4Si2O7F2 is gradually attenuated, but other species show the opposite trend. The results of Raman spectroscopy indicate that Al3+ mainly acts as a network former by the information of [AlO4]-tetrahedral structural units, which can connect with [SiO4]-tetrahedral by the formation of new bridge oxygen of Al–O–Si linkage, but there is no formation of Al–O–Al linkage. The linkage of Al–O–Si increases and that of Si–O–Si decreases. The polymerization degree of the network and the average number of bridging oxygens decrease. Further, the relatively strong Si–O–Si linkage gradually decreases and the relatively weak Al–O–Si gradually increases. The change of the crystalline phase was interpreted from the phase diagram and structure.

Yuxiang Gao, Mei Leng, Yangfan Chen, Zhichao Chen, Jiangling Li. Materials, 12 (2), 206, 2019.

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Synthesis and Characterization of K and Eu Binary Phosphides

The synthesis, structural characterization, and optical properties of the binary Zintl phases of α-EuP3, β-EuP3, EuP2, and α-K4P6 are reported in this study. These crystal structures demonstrate the versatility of P fragments with dimensionality varying from 0D (P6 rings in α-K4P6) to 1D chains (EuP2) to 2D layers (both EuP3). EuP2 is isostructural to previously reported SrP2 and BaP2 compounds. The thermal stabilities of the EuP2 and both EuP3 phases were determined using differential scanning calorimetry (DSC), with melting temperatures of 1086 K for the diphosphide and 1143 K for the triphosphides. Diffuse reflectance spectroscopy indicated that EuP2 is an indirect semiconductor with a direct bandgap of 1.12(5) eV and a smaller indirect one, less than 1 eV. Both EuP3 compounds had bandgaps smaller than 1 eV.

Juli-Anna Dolyniuk, Justin Mark, Shannon Lee, Nhon Tran, Kirill Kovnir. Materials, 12 (2), 251, 2019.

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Thermoelectric Properties of Scandium Sesquitelluride

Rare-earth (RE) tellurides have been studied extensively for use in high-temperature thermoelectric applications. Specifically, lanthanum and praseodymium-based compounds with the Th3P4 structure type have demonstrated dimensionless thermoelectric figures of merit (zT) up to 1.7 at 1200 K. Scandium, while not part of the lanthanide series, is considered a RE element due to its chemical similarity. However, little is known about the thermoelectric properties of the tellurides of scandium. Here, we synthesized scandium sesquitelluride (Sc2Te3) using a mechanochemical approach and formed sintered compacts through spark plasma sintering (SPS). Temperature-dependent thermoelectric properties were measured from 300–1100 K. Sc2Te3 exhibited a peak zT = 0.3 over the broad range of 500–750 K due to an appreciable power factor and low-lattice thermal conductivity in the mid-temperature range.

Dean Cheikh, Kathleen Lee, Wanyue Peng, Alexandra Zevalkink, Jean-Pierre Fleurial, Sabah Bux. Materials, 12 (5), 734, 2019.

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