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Concise Dictionary of Materials Science Part 9 ppt

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single-domain particle Magnetic particle whose minimum linear size is smaller than the domain wall thickness; because of this, it consists of one magnetic domain.. Thus, in a single-dom

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silica Silicon dioxide SiO2 Interatomic bond in silica is partially covalent and

partially ionic ( see electronegativity ) It has three polymorphic modifica-tions: cristobalite, tridymite, and quartz, with the transformation

temper-atures 1470 (cristobalite ↔ tridymite) and 867°C (tridymite ↔ quartz)

In all of the modifications, Si atoms are arranged at the centers of tetra-hedra formed by O atoms

simple lattice See primitive lattice

single crystal Body consisting of one crystal only There are no grain boundaries

in single crystals, although subboundaries and sometimes twin boundaries

can be found

single-domain particle Magnetic particle whose minimum linear size is smaller

than the domain wall thickness; because of this, it consists of one magnetic domain If several domains were present in such a particle, the particle’s free energy would be increased In the particle, the energy of the magnetic

poles at its surface is the lowest in the case of the largest pole spacing Thus, in a single-domain particle of an elongated shape, the orientation

of its magnetization vector is determined not only by its magnetic crys-talline anisotropy, but also by its shape anisotropy If elongated

single-domain particles are oriented predominately along the same direction in

a body, the latter possesses a magnetic texture and excellent hard-magnetic

properties

single slip Dislocation glide motion over a single slip system characterized by

the maximum Schmid factor.

sintering Procedure for manufacturing dense articles from porous particulate

compacts (porosity in green compacts usually is between 25 and 50 vol%) resulting from spontaneous bonding of adjacent particles The main driv-ing force for sinterdriv-ing is a decrease of an excess free energy associated with the phase boundaries Sintering is fulfilled by firing the compacts

at high temperatures (up to ∼0.9 Tm), and is always accompanied by their shrinkage and densification (i.e., a decrease in porosity) Shrinkage evolves primarily through coalescence of neighboring particles under the influence of the capillary force in the neck between the particles The

pore healing also contributes to shrinkage Densification during sintering

is accomplished by both the surface diffusion and the grain-boundary diffusion It is essential for densification that the pores remain at the grain boundaries, because the pores inside the grains can be eliminated by slow bulk diffusion only, whereas the grain-boundary pores “dissolve,” via the splitting out of vacancies and their motion to sinks, by much more rapid

grain-boundary diffusion Thus, the theoretical density can be achieved

in cases in which the abnormal grain growth is suppressed and the rate

of normal grain growth is low (for details of microstructure evolution in

the course of sintering, see solid-state sintering) Sintering can be accel -erated in the presence of a liquid phase (see liquid-phase sintering) or by pressure application during firing (see hot pressing)

size distribution Histogram displaying the frequency of grains (or particles) of

different sizes The shape of grain size distribution after normal grain

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silica Silicon dioxide SiO2 Interatomic bond in silica is partially covalent and

partially ionic ( see electronegativity ) It has three polymorphic modifica-tions: cristobalite, tridymite, and quartz, with the transformation

temper-atures 1470 (cristobalite ↔ tridymite) and 867°C (tridymite ↔ quartz)

In all of the modifications, Si atoms are arranged at the centers of tetra-hedra formed by O atoms

simple lattice See primitive lattice

single crystal Body consisting of one crystal only There are no grain boundaries

in single crystals, although subboundaries and sometimes twin boundaries

can be found

single-domain particle Magnetic particle whose minimum linear size is smaller

than the domain wall thickness; because of this, it consists of one magnetic domain If several domains were present in such a particle, the particle’s free energy would be increased In the particle, the energy of the magnetic

poles at its surface is the lowest in the case of the largest pole spacing Thus, in a single-domain particle of an elongated shape, the orientation

of its magnetization vector is determined not only by its magnetic crys-talline anisotropy, but also by its shape anisotropy If elongated

single-domain particles are oriented predominately along the same direction in

a body, the latter possesses a magnetic texture and excellent hard-magnetic

properties

single slip Dislocation glide motion over a single slip system characterized by

the maximum Schmid factor.

sintering Procedure for manufacturing dense articles from porous particulate

compacts (porosity in green compacts usually is between 25 and 50 vol%) resulting from spontaneous bonding of adjacent particles The main driv-ing force for sinterdriv-ing is a decrease of an excess free energy associated with the phase boundaries Sintering is fulfilled by firing the compacts

at high temperatures (up to ∼0.9 Tm), and is always accompanied by their shrinkage and densification (i.e., a decrease in porosity) Shrinkage evolves primarily through coalescence of neighboring particles under the influence of the capillary force in the neck between the particles The

pore healing also contributes to shrinkage Densification during sintering

is accomplished by both the surface diffusion and the grain-boundary diffusion It is essential for densification that the pores remain at the grain boundaries, because the pores inside the grains can be eliminated by slow bulk diffusion only, whereas the grain-boundary pores “dissolve,” via the splitting out of vacancies and their motion to sinks, by much more rapid

grain-boundary diffusion Thus, the theoretical density can be achieved

in cases in which the abnormal grain growth is suppressed and the rate

of normal grain growth is low (for details of microstructure evolution in

the course of sintering, see solid-state sintering) Sintering can be accel -erated in the presence of a liquid phase (see liquid-phase sintering) or by pressure application during firing (see hot pressing)

size distribution Histogram displaying the frequency of grains (or particles) of

different sizes The shape of grain size distribution after normal grain

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Taylor factor Quantity averaging the influence of various grain orientations on

the resolved shear stress, τr, in a polycrystal:

σ = Mτr

(M is the Taylor factor, and σ is the flow stress) The averaging is fulfilled

under the supposition that the deformations of the polycrystal and its grains are compatible Reciprocal Taylor factor can be used for polycrys

-tals instead of Schmid factor, whose magnitude is defined for a single grain only In a nontextured polycrystal with FCC structure, reciprocal

Taylor factor is 0.327

temper carbon In malleable irons, graphite clusters varying in shape from flake

aggregates to distorted nodules

tempered martensite Microconstituent occurring in quenched steels upon the

tempering treatment at low temperatures Due to the precipitation of ε -carbides, the lattice of tempered martensite is characterized by a tetra-gonality corresponding to 0.2 wt% carbon dissolved in the martensite

See steel martensite

tempering of steel martensite Alterations in the phase composition under the

influence of tempering treatment They are the following Up to ∼200°

C, as-quenched martensite decomposes into tempered martensite and ε-

(or η-) carbide (in low- to medium-carbon steels) or χ-carbide (in

high-carbon steels) Above ∼300°C, cementite precipitates from the tempered martensite, whereas the latter becomes ferrite and the ε- and η- (χ-)

carbides dissolve In steels alloyed with carbide-formers, the alloying elements inhibit the carbon diffusion and displace all the previously

men-tioned phase transitions to higher temperatures In addition, at tempera-tures ∼600°C, the diffusion of the substitutional alloying elements becomes possible, which leads to the occurrence of special carbides

accompanied by cementite dissolution The phase transformations described are accompanied by the following microstructural changes in martensite and ferrite Crystallites of tempered martensite retain the shape

of as-quenched martensite Ferrite grains, occurring from tempered

mar-tensite, do not change their elongated shape and substructure until

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