The Impact of Direct Ionization by Beam Electrons on the Electron Kinetics of the Beam Discharge Plasma in Molecular Hydrogen

Icing/snowing/frosting is ubiquitous in nature and industrial processes, and the accretion of ice mostly leads to catastrophic consequences. The existing understanding of icing is still limited, particularly for aircraft icing, where direct observation of the freezing dynamics is inaccessible. In this work, we investigate experimentally the impact and freezing of a water drop onto the supercooled substrate at extremely low vapor pressure, to mimic an aircraft passing through clouds at a relatively high altitude, engendering icing upon collisions with pendant drops. Special attention is focused on the ice coverage induced by an impinging drop, from the perimeter pointing outward along the radial direction. We observed two freezing regimes: (I) spread-recoil-freeze at the substrate temperature of Ts = −15.4 ± 0.2 °C and (II) spread (incomplete)-freeze at the substrate temperature of Ts = −22.1 ± 0.2 °C. The ice coverage is approximately one order of magnitude larger than the frozen drop itself, and counterintuitively, larger supercooling yields smaller ice coverage in the range of interest. We attribute the variation of ice coverage to the kinetics of vapor diffusion in the two regimes. This fundamental understanding benefits the design of new anti-icing technologies for aircraft.

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Morphology and crystallization kinetics of Rubber-modified Nylon 6 Prepared by Anionic In-situ Polymerization

Science and Engineering of Composite Materials ◽

10.1515/secm-2020-0020 ◽

2020 ◽

Vol 27 (1) ◽

pp. 204-215

Author(s):

Hongkai Zhao ◽

Dengchao Zhang ◽

Yingshuang Li

Keyword(s):

Crystallization Kinetics ◽

In Situ Polymerization ◽

Good Description ◽

Nylon 6 ◽

Avrami Equation ◽

Infrared Analysis ◽

Chain Segment ◽

The Impact ◽

Kinetics Of

AbstractIn this work, we modified nylon 6 with liquid rubber by in-situ polymerization. The infrared analysis suggested that HDI urea diketone is successfully blocked by caprolactam after grafting on hydroxyl of HTPB, and the rubber-modified nylon copolymer is generated by the anionic polymerization. The impact section analysis indicated the rubber-modified nylon 6 resin exhibited an alpha crystal form.With an increase in the rubber content, nylon 6 was more likely to generate stable α crystal. Avrami equation was a good description of the non-isothermal crystallization kinetics of nylon-6 and rubber-modified nylon-6 resin. Moreover, it is found that the initial crystallization temperature of nylon-6 chain segment decreased due to the flexible rubber chain segment. n value of rubber-modified nylon-6 indicated that its growth was the coexistence of two-dimensional discoid and three-dimensional spherulite growth. Finally, the addition of the rubber accelerated the crystallization rate of nylon 6.

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Single entity electrochemistry and the electron transfer kinetics of hydrazine oxidation

Nano Research ◽

10.1007/s12274-021-3353-8 ◽

2021 ◽

Cited By ~ 1

Author(s):

Ruiyang Miao ◽

Lidong Shao ◽

Richard G. Compton

Keyword(s):

Electron Transfer ◽

Bulk Solution ◽

Relative Contribution ◽

Rate Determining Step ◽

Multistep Process ◽

Ph Range ◽

Electro Catalytic Oxidation ◽

Single Particle Impact ◽

The Impact ◽

Kinetics Of

AbstractThe mechanism and kinetics of the electro-catalytic oxidation of hydrazine by graphene oxide platelets randomly decorated with palladium nanoparticles are deduced using single particle impact electrochemical measurements in buffered aqueous solutions across the pH range 2–11. Both hydrazine, N2H4, and protonated hydrazine N2H5+ are shown to be electroactive following Butler-Volmer kinetics, of which the relative contribution is strongly pH-dependent. The negligible interconversion between N2H4 and N2H5+ due to the sufficiently short timescale of the impact voltammetry, allows the analysis of the two electron transfer rates from impact signals thus reflecting the composition of the bulk solution at the pH in question. In this way the rate determining step in the oxidation of each specie is deduced to be a one electron step in which no protons are released and so likely corresponds to the initial formation of a very short-lived radical cation either in solution or adsorbed on the platelet. Overall the work establishes a generic method for the elucidation of the rate determining electron transfer in a multistep process free from any complexity imposed by preceding or following chemical reactions which occur on the timescale of conventional voltammetry.

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Dissecting the impact of target-binding kinetics of protein binders on tumor localization

iScience ◽

10.1016/j.isci.2021.102104 ◽

2021 ◽

Vol 24 (2) ◽

pp. 102104

Author(s):

Yunjin Song ◽

Hoibin Jeong ◽

Song-Rae Kim ◽

Yiseul Ryu ◽

Jonghwi Baek ◽

...

Keyword(s):

Binding Kinetics ◽

Tumor Localization ◽

Protein Binders ◽

Target Binding ◽

The Impact ◽

Kinetics Of

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A Study of the Impact of Graphite on the Kinetics of SPS in Nano- and Submicron WC-10%Co Powder Compositions

Ceramics ◽

10.3390/ceramics4020025 ◽

2021 ◽

Vol 4 (2) ◽

pp. 331-363

Author(s):

Eugeniy Lantcev ◽

Aleksey Nokhrin ◽

Nataliya Malekhonova ◽

Maksim Boldin ◽

Vladimir Chuvil'deev ◽

...

Keyword(s):

Activation Energy ◽

Solid Phase ◽

Continuous Heating ◽

Diffusion Creep ◽

Hard Alloys ◽

Fine Grained ◽

Plasma Sintering ◽

Spark Plasma ◽

The Impact ◽

Kinetics Of

This study investigates the impact of carbon on the kinetics of the spark plasma sintering (SPS) of nano- and submicron powders WC-10wt.%Co. Carbon, in the form of graphite, was introduced into powders by mixing. The activation energy of solid-phase sintering was determined for the conditions of isothermal and continuous heating. It has been demonstrated that increasing the carbon content leads to a decrease in the fraction of η-phase particles and a shift of the shrinkage curve towards lower heating temperatures. It has been established that increasing the graphite content in nano- and submicron powders has no significant effect on the SPS activation energy for “mid-range” heating temperatures, QS(I). The value of QS(I) is close to the activation energy of grain-boundary diffusion in cobalt. It has been demonstrated that increasing the content of graphite leads to a significant decrease in the SPS activation energy, QS(II), for “higher-range” heating temperatures due to lower concentration of tungsten atoms in cobalt-based γ-phase. It has been established that the sintering kinetics of fine-grained WC-Co hard alloys is limited by the intensity of diffusion creep of cobalt (Coble creep).

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