Adsorption Separation of R-22, R-32 and R-125 Fluorocarbons using 4A Molecular Sieve Zeolite

2016 ◽  
Vol 1 (13) ◽  
pp. 3718-3722 ◽  
Author(s):  
DarshikaK. J. A. Wanigarathna ◽  
Jiajian Gao ◽  
Tetsuo Takanami ◽  
Qichun Zhang ◽  
Bin Liu

2010 ◽  
Vol 27 (3) ◽  
pp. 752-758 ◽  
Author(s):  
Muthanna Jabbar Ahmed ◽  
Abdul Halim Abdul Karim Mohammed ◽  
Abdul Amir Hassan Kadhum


Author(s):  
Douglas L. Dorset ◽  
Andrew K. Massalski

Matrix porin, the ompF gene product of E. coli, has been the object of a electron crystallographic study of its pore geometry in an attempt to understand its function as a membrane molecular sieve. Three polymorphic forms have been found for two-dimensional crystals reconstituted in phospholipid, two hexagonal forms with different lipid content and an orthorhombic form coexisting with and similar to the hexagonal form found after lipid loss. In projection these have been shown to retain the same three-fold pore triplet geometry and analyses of three-dimensional data reveal that the small hexagonal and orthorhombic polymorphs have similar structure as well as unit cell spacings.



Author(s):  
Douglas R. Keene ◽  
B. Kerry Maddox ◽  
Marie B. Spurgin ◽  
Lynn Y. Sakai ◽  
Robert W. Glanville

A mouse monoclonal antibody was used to identify beaded aggregates found in guanidine extracts of human amnion as assemblies of fibrillin molecules. These aggregates were also shown to be a major component of extracellular matrix microfibrils. We further demonstrated that the periodicity of these aggregates can be increased when subjected to mechanical stress.Human amnion was extracted with guanidine and the extracted material purified using ion exchange and molecular sieve chromatography. A high molecular weight fraction was precipitated by dialyzing against dilute acetic acid. Part of the precipitate was suspended in 0.2 M ammonium bicarbonate buffer and rotary shadowed. A second portion was resuspended in culture medium containing antibody which recognizes matrix microfibrils, diluted 1:5 in ammonium bicarbonate and reacted for 120 minutes at room temperature. Antibody labeled precipitate was washed by repeated pelleting and resuspension in buffer and then incubated in Janssen GAM 5 nm gold conjugate for 60 minutes at room temperature.



1977 ◽  
Author(s):  
Richard L. Miller ◽  
Clarence F. Theis ◽  
Roger L. Stork ◽  
Kenneth G. Ikels


1978 ◽  
Author(s):  
Roger L. Stork ◽  
Clarence F. Theis ◽  
Kenneth G. Ikels ◽  
Richard L. Miller


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