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description
weakly acidic cation exchange resin
Quality Level
form
beads
packaging
pkg of 1000 g
parameter
120 °C Na+ form max. temp.
80 °C H+ form max. temp.
moisture
55-65%
technique(s)
LPLC: suitable
matrix
crosslinked polystyrene (highly porous)
matrix active group
iminodiacetic acid functional group
particle size
16-45 mesh
operating pH
4-10
capacity
0.35 meq/mL by wetted bed volume (calcium)
1.2 meq/g by dry weight (calcium)
separation technique
affinity
General description
Application
Chelating resin for metal recovery, wastewater treatment, brine purification, etc.
Diaion CR11 was used to prepare phosphate buffer, required to measure rate constants of the reactions of hypochlorite with L-Arg and taurine by stopped-flow spectrophotometry.[3]
Legal Information
Diaion is a registered trademark of Mitsubishi Chemical Corp.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Sofia A Cavaco et al.
Journal of hazardous materials, 169(1-3), 516-523 (2009-05-02)
In this study two chelating resins containing iminodiacetic acid groups (Amberlite IRC 748 and Diaion CR 11) and a chelating resin based on sulfonic and diphosphonic acid groups (Diphonix) were investigated in order to separate Cr(III) from industrial effluents produced
Sofia A Cavaco et al.
Journal of hazardous materials, 144(3), 634-638 (2007-03-06)
Effluent discharged from the chromium electroplating industry contains a large number of metals, including chromium, copper, nickel, zinc, manganese and lead. The ion exchange process is an alternative technique for application in the treatment of industrial wastewater containing heavy metals
C Zhang et al.
The Journal of biological chemistry, 276(29), 27159-27165 (2001-05-26)
The myeloperoxidase-derived oxidant hypochlorous acid (HOCl) is thought to contribute to endothelial dysfunction, but the mechanisms underlying this inhibitory effect are unknown. The present study tested the hypothesis that HOCl and L-arginine (L-Arg) react to form novel compounds that adversely
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