Characterization of sub-50-nm line array structures with angle-resolved multiple wavelength scatterometry

2008 ◽  
Author(s):  
Michael Kotelyanskii ◽  
Fei Shen ◽  
Gary Jiang ◽  
Benjamin Bunday
Keyword(s):  
Multiple Wavelength ◽  
Line Array ◽  
Array Structures

Optical characterization of thin films non-uniform in thickness by a multiple-wavelength reflectance method

2002 ◽  
Vol 34 (1) ◽  
pp. 660-663 ◽  
Author(s):  
M. Ohlídal ◽  
I. Ohlídal ◽  
D. Franta ◽  
T. Králík ◽  
M. Jákl ◽  
...  
Keyword(s):  
Thin Films ◽  
Optical Characterization ◽  
Multiple Wavelength

Characterization of Copper Line Array Erosion with Picosecond Ultrasonics

2007 ◽  
Author(s):  
Nicolas Pic ◽  
Karim Bennedine ◽  
Guray Tas ◽  
Dario Alliata ◽  
Jana Clerico ◽  
...  
Keyword(s):  
Copper Line ◽  
Line Array ◽  
Picosecond Ultrasonics

Optical characterization of MEMS deformable mirror array structures

2001 ◽  
Author(s):  
Soe-Mie F. Nee ◽  
Lewis F. DeSandre ◽  
Thomas G. Bifano ◽  
Linda F. Johnson ◽  
Mark B. Moran
Keyword(s):  
Optical Characterization ◽  
Deformable Mirror ◽  
Array Structures

Morphological Characterization of Mycobacteriophage R1

1974 ◽  
Vol 32 ◽  
pp. 254-255
Author(s):  
B. L. Soloff ◽  
T. A. Rado
Keyword(s):  
Carbon Source ◽  
Stationary Phase ◽  
Growth Phase ◽  
Minimal Medium ◽  
Morphological Characterization ◽  
Logarithmic Growth Phase ◽  
Complete Lysis ◽  
Lysogenic Culture ◽  
Logarithmic Growth

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.

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