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Quenching rates

Ion implantation (qv) has a large (10 K/s) effective quench rate (64). This surface treatment technique allows a wide variety of atomic species to be introduced into the surface. Sputtering and evaporation methods are other very slow approaches to making amorphous films, atom by atom. The processes involve deposition of a vapor onto a cold substrate. The buildup rate (20 p.m/h) is also sensitive to deposition conditions, including the presence of impurity atoms which can faciUtate the formation of an amorphous stmcture. An approach used for metal—metalloid amorphous alloys is chemical deposition and electro deposition. [Pg.337]

The writing process, that is, the transition crystalline — amorphous, is caused by briefly (<50 100 ns) heating up the selected storage area (diameter (( )) ca 0.5—1 Hm) by a laser pulse to a temperature above the melting point of the memory layer (Eig. 15, Record), such that the film locally melts. When cooled faster than a critical quench rate (10 -10 ° K/s), the formation of crystalline nuclei is suppressed and the melted area sohdifies into the amorphous (glass-like) state. [Pg.149]

Tensile Properties. Tensile properties of nylon-6 and nylon-6,6 yams shown in Table 1 are a function of polymer molecular weight, fiber spinning speed, quenching rate, and draw ratio. The degree of crystallinity and crystal and amorphous orientation obtained by modifying elements of the melt-spinning process have been related to the tenacity of nylon fiber (23,27). [Pg.247]

Any refractory material that does not decompose or vaporize can be used for melt spraying. Particles do not coalesce within the spray. The temperature of the particles and the extent to which they melt depend on the flame temperature, which can be controlled by the fueLoxidizer ratio or electrical input, gas flow rate, residence time of the particle in the heat zone, the particle-size distribution of the powders, and the melting point and thermal conductivity of the particle. Quenching rates are very high, and the time required for the molten particle to soHdify after impingement is typically to... [Pg.45]

Heat transfer between gas and sohds is exceedingly hard to measure because it is so rapid. Although the coefficient is low, the available surface area and the relative specific heat of solid to gas are so large that temperature equilibration occurs almost instantaneously. Experiments on injection of argon plasmas into fluidized beds have shown quenching rates of up to fifty million degrees Kelvin per second. Thus, in a properly designed bed, gas to solids heat transfer is not normally a matter of concern. [Pg.40]

Hamiltonian does not give rise to any crystalline order in the system. By employing models hke this, the quench-rate and chain-length dependence of the glass transition temperature, as well as time-temperature superposition, similar to experiments [23], were investigated in detail. [Pg.502]

The advantage of the simulations compared to the experiments is that the correspondence between the tracer diffusion coefficient and the internal states of the chains can be investigated without additional assumptions. In order to perform a more complete analysis of the data one has to look at the quench-rate and chain-length dependence of the glass transition temperature for a given density [43]. A detailed discussion of these effects is far beyond the scope of this review. Here we just want to discuss a characteristic quantity which one can analyze in this context. [Pg.502]

Since quench rates in simulations typically are artificially high, this leads to a special problem for comparison with experiment as well as to the question whether there is a more general way to determine the glass transition temperature from the structure of the system. The experimental definition of viscosity is certainly not apphcable to simulations. [Pg.503]

In the present case, = 1.1x10 M- s i, a typical value for the reaction of aminoacid moieties with 1O2 (Michaeli Feitelson, 1994 Bisby et al., 1999). By comparison with the total quenching rate constant, kfi = 2.7x10 M- s-i, it can be concluded that almost 60% of the interaction with 1O2 is through physical quenching and about 40% of the reactive moieties of GA are oxidized by 1O2. [Pg.15]

Of course, the issue of producing the aperiodic state in the laboratory would also involve estimating whether corresponding quenching rates can be experimentally achieved. [Pg.108]

Both energy and electron transfer quenchers have been employed to show that the quenching rates of the fullerene triplet state are decreased as a function of the size of the dendrimer shell [36]. These results further demonstrate that fullerene is an excellent functional group to probe the accessibility of a dendrimer core by external molecules. [Pg.93]

Porter and Wilkinson(56) measured the rates of quenching for a variety of triplet donors with triplet acceptors at room temperature in fluid solution by flash photolysis. The appearance of the triplet-triplet absorption spectrum of the acceptor and the simultaneous disappearance of the donor triplet-triplet absorption spectrum provided unequivocal evidence for the triplet-triplet energy transfer process. Table 6.5 provides some of the quenching rate constants reported in this classic paper. [Pg.150]

It should be noted that this expression is a general one that can be used for any photochemical reaction that can be quenched. It is commonly called the Stern-Volmer equation. This equation predicts that if the proposed mechanism is correct, the data, when plotted as 4>a0/4>a vs. [Q], should be linear with an intercept equal to unity and a slope equal to kqr. Linear plots were indeed observed out to large d>°/d> values. Assuming a value of 5 x 10 M 1 sec-1 for the quenching rate constant,(7) the data presented in Table 4.1 were obtained. [Pg.375]

Quenching rate constants for dienes and quadricyclenes have similar sensitivities to the electronic and structural features of the excited aromatic hydrocarbon. However, during this process quadricyclene isomerizes to nor-boraadiene with a quantum yield of 0.52, whereas dienes usually remain unchanged/10 Hammond has suggested that vibrational energy which is partitioned to the acceptor upon internal conversion of the exciplex can lead to isomerization(10a,103) ... [Pg.457]

Singlet Oxygen Quenching Rate Constants for Carotenoids in Benzene... [Pg.285]

Second-Order Quenching Rate Constants for the Quenching of 102 by Carotenoids in Unilamellar DPPC Liposomes, Benzene, and Triton X-100/405 Micelles... [Pg.288]

Kuimova, MK, Yahioglu, G, and Ogilby, PR, 2009. Singlet oxygen in a cell Spatially dependent lifetimes and quenching rate constants. J Am Chem Soc 131, 332-340. [Pg.346]


See other pages where Quenching rates is mentioned: [Pg.3010]    [Pg.366]    [Pg.314]    [Pg.335]    [Pg.335]    [Pg.336]    [Pg.336]    [Pg.398]    [Pg.237]    [Pg.390]    [Pg.502]    [Pg.503]    [Pg.1183]    [Pg.237]    [Pg.221]    [Pg.222]    [Pg.1276]    [Pg.71]    [Pg.79]    [Pg.278]    [Pg.167]    [Pg.14]    [Pg.144]    [Pg.192]    [Pg.175]    [Pg.176]    [Pg.257]    [Pg.389]    [Pg.247]    [Pg.248]    [Pg.248]    [Pg.290]    [Pg.301]   
See also in sourсe #XX -- [ Pg.19 ]

See also in sourсe #XX -- [ Pg.191 , Pg.194 , Pg.195 ]

See also in sourсe #XX -- [ Pg.375 ]

See also in sourсe #XX -- [ Pg.310 , Pg.314 ]




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Bimolecular-quenching rate constants

Critical quenching rate

Diffusion-corrected quenching rate

Flame pressure, quenching rate

Fluorescence quenching rate constant

Halides, quenching rate constant

Marcus electron transfer rate quenching

Mean quenching rate

Monomer quenching rate constants

Photoinitiator quenching rate constants

Quench rate technique

Quench rate, kinetic

Quench rates

Quench rates

Quenching Rates and Mechanisms

Quenching rate INDEX

Quenching rate constant

Quenching rate constants, free energy

Quenching rate constants, free energy dependence

Quenching rate constants, pyrene

Quenching rate laser flash photolysis

Quenching rate mechanism

Quenching rate model

Quenching rate temperature dependence

Quenching rate triplet carbenes

Rate long-component quenching

Relaxation Processes. Radiative Lifetimes and Quenching Rates

Self-quenching rates

Singlet oxygen quenching rate constants

Stem-Volmer quenching rate

Stem-Volmer quenching rate constants

Stern-Volmer quenching rates

The Rates of Specific Quenching Channels

The Stern-Volmer Equation for Determination of Quenching Rate

Total Quenching Rate Constants

Triplet quenching rate

Triplet quenching rate constants

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