10342
Amberlite™ IRN77 hydrogen form
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About This Item
Prodotti consigliati
Forma fisica
beads
Crosslinking
8 % cross-linked
Confezionamento
bucket of 500 g
Parametri
121 °C max. temp.
Umidità
49-55%
tecniche
LPLC: suitable
Matrice
styrene-divinylbenzene (gel)
Gruppo funzionale matrice
SCX
Dimensione particelle
600-700 μm
pH di lavoro
0-14
Capacità
1.9 meq/mL by wetted bed volume
Tecnica di separazione
cation exchange
Descrizione generale
Amberlite™ IRN77 is a strong acid cation exchange resin.
As Nuclear Grade, a minimum of 99% of the available exchange sites are in the hydrogen form.
Strongly acidic cation exchange resin for water treatment, RAD waste treatment, decontamination.
Applicazioni
Amberlite™ IRN77 was used as cation exchanger to determine the sorption activity towards Cs(I) and Sr(II) using isothermal titration calorimetry and solution-depletion methods.
Note legali
Amberlite is a trademark of DuPont de Nemours, Inc.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Water research, 38(7), 1911-1921 (2004-03-18)
This study investigated the production of high-purity water in the primary coolant of a nuclear power plant via the continuous electrodeionization (CEDI) process, using ion exchange resins as ion-conducting media between ion exchange membranes. The effectiveness of this method was
Environmental science and pollution research international, 21(15), 9334-9343 (2014-04-15)
Sorption performance of cation-exchange resins Amberlite® IRN77 and Amberlite™ IRN9652 toward Cs(I) and Sr(II) has been tested in single-component aqueous solutions and simulated waste effluents containing other monovalent (Effluent 1) or divalent (Effluent 2) metal cations, as well as nitrate
Nature communications, 11(1), 1792-1792 (2020-04-15)
Continuous cancer growth is driven by subsets of self-renewing malignant cells. Targeting of uncontrolled self-renewal through inhibition of stem cell-related signaling pathways has proven challenging. Here, we show that cancer cells can be selectively deprived of self-renewal ability by interfering
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