A chelating cellulose adsorbent for the removal of Cu(II) from aqueous solutions

2006 ◽  
Vol 99 (6) ◽  
pp. 2888-2897 ◽  
Author(s):  
D. W. O'Connell ◽  
C. Birkinshaw ◽  
T. F. O'Dwyer
Keyword(s):  
Aqueous Solutions ◽  
Cellulose Adsorbent

scholarly journals Removal of Lead(II) Ions from Aqueous Solutions Using a Modified Cellulose Adsorbent

2006 ◽  
Vol 24 (4) ◽  
pp. 337-348 ◽  
Author(s):  
David W. O'Connell ◽  
Colin Birkinshaw ◽  
Thomas F. O'Dwyer
Keyword(s):  
Aqueous Solutions ◽  
Cellulose Adsorbent ◽  
Modified Cellulose

Removal and Recovery of Chromium(III) from Aqueous Solutions by a Spheroidal Cellulose Adsorbent

2001 ◽  
Vol 73 (3) ◽  
pp. 322-328 ◽  
Author(s):  
Minghua Liu ◽  
Hong Zhang ◽  
Xinshen Zhang ◽  
Yun Deng ◽  
Weiguo Liu ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Cellulose Adsorbent ◽  
Removal And Recovery

A modified cellulose adsorbent for the removal of nickel(II) from aqueous solutions

2006 ◽  
Vol 81 (11) ◽  
pp. 1820-1828 ◽  
Author(s):  
David W O'Connell ◽  
Colin Birkinshaw ◽  
Thomas F O'Dwyer
Keyword(s):  
Aqueous Solutions ◽  
Cellulose Adsorbent ◽  
Modified Cellulose

Ultrathin frozen sections of yeast without aldehyde prefixation

1978 ◽  
Vol 36 (2) ◽  
pp. 58-59
Author(s):  
K. J. Böhm ◽  
a. E. Unger
Keyword(s):  
Aqueous Solutions ◽  
Biological Material ◽  
Yeast Cells ◽  
Frozen Sections ◽  
Good Preservation ◽  
Ultrathin Frozen Sections

During the last years it was shown that also by means of cryo-ultra-microtomy a good preservation of substructural details of biological material was possible. However the specimen generally was prefixed in these cases with aldehydes.Preparing ultrathin frozen sections of chemically non-prefixed material commonly was linked up to considerable technical and manual expense and the results were not always satisfying. Furthermore, it seems to be impossible to carry out cytochemical investigations by means of treating sections of unfixed biological material with aqueous solutions.We therefore tried to overcome these difficulties by preparing yeast cells (S. cerevisiae) in the following manner:

Imaging polymers, proteins and dna in aqueous solutions with the atomic force microscope

1989 ◽  
Vol 47 ◽  
pp. 32-33
Author(s):  
S.A.C. Gould ◽  
B. Drake ◽  
C.B. Prater ◽  
A.L. Weisenhorn ◽  
S.M. Lindsay ◽  
...  
Keyword(s):  
Amino Acids ◽  
Dna Sequencing ◽  
Aqueous Solutions ◽  
Atomic Force Microscope ◽  
Piezoelectric Crystal ◽  
Atomic Force ◽  
Structure Of Molecules ◽  
Optical Lever

The atomic force microscope (AFM) is an instrument that can be used to image many samples of interest in biology and medicine. Images of polymerized amino acids, polyalanine and polyphenylalanine demonstrate the potential of the AFM for revealing the structure of molecules. Images of the protein fibrinogen which agree with TEM images demonstrate that the AFM can provide topographical data on larger molecules. Finally, images of DNA suggest the AFM may soon provide an easier and faster technique for DNA sequencing.The AFM consists of a microfabricated SiO2 triangular shaped cantilever with a diamond tip affixed at the elbow to act as a probe. The sample is mounted on a electronically driven piezoelectric crystal. It is then placed in contact with the tip and scanned. The topography of the surface causes minute deflections in the 100 μm long cantilever which are detected using an optical lever.

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