Since ocular aberrations above the Zernike fourth order are relatively insignificant in normal eyes, current scanning lasers with a beam diameter of 1.0 mm or less are theoretically capable of eliminating most higher-order aberrations.
Rate coefficients of the reaction of hydroxyl (OH) radicals with
CH3OCH3 (k
1) and
CH3OC(CH3)3
(k
2) over
an extended temperature range are reported. Measurements were
performed using a laser photolysis−laser-induced fluorescence technique under slow flow conditions at a total
pressure of 740 ± 10 Torr. Arrhenius
plots of the data exhibited significant curvature and were fitted in
the form of k(T) =
AT
B
exp(−C/T). The
resulting modified Arrhenius expressions (error limits ±2σ) that
best described these extended temperature
measurements and prior low-temperature measurements were (in units of
cm3 molecule-1
s-1)
k
1(295−650
K) = (1.05 ± 0.10) ×
10-17
T
2.0
exp[(328 ± 32)/T] and
k
2(293−750 K) = (1.15 ± 0.11) ×
10-17
T
2.04
exp[(266 ± 41)/T]. Comparison of our measurements for
k
1 with previous, overlapping
low-temperature
measurements indicated generally good agreement. Our measurements
for k
2, although consistent with
previous
room temperature measurements, exhibited a larger temperature
dependence than previously reported. High-temperature oxidation mechanisms for these oxygenated fuel components
are proposed. Support for the
mechanisms is presented in the form of product analysis studies in
high-temperature tubular flow reactors.
For CH3OC(CH3)3,
these studies suggest that H abstraction from the tert-butyl
group is an important high-temperature oxidation pathway.
A refracting system consisting of two lenses is designed to transform an annular Gaussian laser beam into a circular Bessel beam. The slopes of the input and output surfaces fit well with a sixth-order polynomial. A smooth variation of the radii of curvature of the resulting aspheric surfaces is very attractive for easy machining of the surfaces. The diffraction-free length for the designed system is 59.4735 m at 633 nm.
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