Hydrogen Peroxide Photolysis in Acidic Aqueous Solutions Containing Chloride Ions. I. Chemical Mechanism

2003 ◽  
Vol 107 (9) ◽  
pp. 1313-1324 ◽  
Author(s):  
Xiao-Ying Yu ◽  
John R. Barker
1986 ◽  
Vol 51 (11) ◽  
pp. 2437-2443
Author(s):  
František Kopecký ◽  
Mária Vojteková ◽  
Milan Pešák

The conventional activity of chloride ions was measured by an ion-selective electrode at 25 °C in aqueous solutions of benflurone, i.e. 5-(2-(N,N-dimethylamino)ethoxy)-7-oxo-7H-benzo(c)fluorene hydrochloride, without or with additions of KCl. These results suggest a gradual association of benflurone; the formation of a hetero-associate, (BH+)2Cl-, followed by higher associates was evaluated in the measured range up to 0.1 mol l-1.


1984 ◽  
Vol 49 (10) ◽  
pp. 2222-2230 ◽  
Author(s):  
Viliam Múčka ◽  
Rostislav Silber

The catalytic and physico-chemical properties of low-temperature nickel-silver catalysts with nickel oxide concentrations up to 43.8% (m/m) are examined via decomposition of hydrogen peroxide in aqueous solution. The mixed catalysts prepared at 250°C are composed of partly decomposed silver carbonate or oxide and nickel carbonate or hydroxide decomposed to a low degree only and exhibiting a very defective crystal structure. The activity of these catalysts is determined by the surface concentration of silver ions, which is affected by the nickel component present. The latter also contributes to the thermal stability of the catalytic centres of the silver component, viz. the Ag+ ions. The concentration of these ions varies with the temperature of the catalyst treatment, the activity varies qualitatively in the same manner, and the system approaches the Ag-NiO composition. The catalytic centres are very susceptible to poisoning by chloride ions. A previous exposition of the catalyst to a gamma dose of 10 kGy from a 60Co source has no measurable effect on the physico-chemical properties of the system.


1994 ◽  
Vol 59 (6) ◽  
pp. 1311-1318 ◽  
Author(s):  
Ladislav Svoboda ◽  
Petr Vořechovský

The properties of cellulose chelating ion exchangers Ostsorb have been studied in the sorption of cadmium and lead from aqueous solutions. The Cd(II) and Pb(II) ions are trapped by the Ostsorb OXIN and Ostsorb DETA ion exchangers most effectively in neutral and alkaline media but at these conditions formation of stable hydrolytic products of both metals competes with the exchange equilibria. From this point of view, Ostsorb DTTA appears to be a more suitable sorbent since it traps the Pb(II) and Cd(II) ions in acidic media already. Chloride ions interfere with the sorption of the two metals by Ostsorb DTTA whereas the ionic strength adjusted by the addition of sodium perchlorate does not affect the exchange capacity of this ion exchanger.


1970 ◽  
Vol 48 (18) ◽  
pp. 2948-2948
Author(s):  
C. E. Burchill ◽  
I. S. Ginns

not available


1979 ◽  
Vol 18 (7) ◽  
pp. 1971-1973 ◽  
Author(s):  
Mark M. Morrison ◽  
Julian L Roberts ◽  
Donald T. Sawyer

2009 ◽  
Vol 113 (48) ◽  
pp. 15843-15850 ◽  
Author(s):  
Marcel D. Baer ◽  
I-Feng William Kuo ◽  
Hendrik Bluhm ◽  
Sutapa Ghosal

1955 ◽  
Vol 3 (4) ◽  
pp. 379 ◽  
Author(s):  
W. V. Mayneord ◽  
W. Anderson ◽  
H. D. Evans ◽  
D. Rosen

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