Total organic halogens (TOX) analysis in ether solutions

1990 ◽  
Vol 24 (9) ◽  
pp. 1173-1176 ◽  
Author(s):  
P Le Cloirec ◽  
R.M Lelacheur ◽  
J.D Johnson ◽  
R.F Christman
2002 ◽  
Vol 2 (5-6) ◽  
pp. 509-514 ◽  
Author(s):  
H. Pourmoghaddas ◽  
A.A. Stevens

The effects of bromide ion, pH and reaction time on the formation of four trihalomethanes, nine haloacetic acids and total organic halogens in chlorinated drinking water have been investigated. In this extensive study, the relationship of total trihalomethanes and total haloacetic acids with total organic halogen have been evaluated. The study determined the concentration range of nine haloacetic acids and four trihalomethanes as a percentage of total organic halogen. The results showed that the percentage of total organic halogen made up of total trihalomethanes plus total haloacetic acids significantly increases with increasing bromide ion concentrations and pH. These observations suggest that both a higher bromide concentration and pH cause the formation of mainly brominated trihalomethanes with the reduction of haloacetic acids which could be identified and quantified by current USEPA methods.


2012 ◽  
Vol 27 (4) ◽  
pp. 707-713 ◽  
Author(s):  
Jukka Pekka lsoaho ◽  
Suvi Tarkkanen ◽  
Raimo Alen ◽  
Juha Fiskari

Abstract Softwood-based kraft mill bleaching effluents from the initial bleaching stages D0 and E1 (the bleaching sequence being D0E 1D 1 E2D2) were treated by the oxidative Fenton method (H20rFeS04) to decompose organic pollutants contammg adsorbable organic halogens (AOX). Experiments designed using the Taguchi method were applied to predict the process conditions that would result in a cost-effective and adequate removal of AOX. In addition to the composition and concentration of the reagents (H202 and Fe2+), the main process parameters selected were temperature and reaction time, while pH was adj usted to an approximate value of 4 (the volumetric ratio of the mixed effluents D0:E 1 was 3 :2). The results indicated that an AOX removal of about 70% for this mixture ( corresponding to about 50% for the mill) was achieved when the eftluent samples were treated for 60 min at 70°C with H202 and Fe2+ at a concentration of 1 600 mg/1 and 28 mg/1, respectively.


2009 ◽  
Vol 81 (2) ◽  
pp. 178-183 ◽  
Author(s):  
Qing-fu Zeng ◽  
Jie Fu ◽  
Yin-tao Shi ◽  
Dong-sheng Xia ◽  
Hai-liang Zhu

1991 ◽  
Vol 24 (3-4) ◽  
pp. 373-383 ◽  
Author(s):  
A. Grimvall ◽  
H. Borén ◽  
S. Jonsson ◽  
S. Karlsson ◽  
R. Sävenhed

The long-term fate of chlorophenols and adsorbable organic halogens (AOX) was studied in two large recipients of bleach-plant effluents: Lake Vättern in Sweden and the Baltic Sea. The study showed that there is a long-distance transport (>100 km) of chloroguaiacols from bleach-plants to remote parts of receiving waters. However, there was no evidence of several-year-long accumulation of chloro-organics in the water-phase. A simple water-exchange model for Lake Vättern showed that the cumulated bleach-plant discharges from the past 35 years would have increased the AOX concentration in the lake by more than 100 µg Cl/l, if no AOX had been removed from the water by evaporation, sedimentation or degradation. However, the observed AOX concentration in Lake Vättern averaged only about 15 µg Cl/l, which was less than the average AOX concentration (32 µg Cl/l) in the “unpolluted” tributaries of the lake. Similar investigations in the Baltic Sea showed that non-point sources, including natural halogenation processes, accounted for a substantial fraction of the AOX in the open sea. The presence of 2,4,6-trichlorophenol in precipitation and “unpolluted” surface waters showed that non-point sources may also make a considerable contribution to the background levels of compounds normally regarded as indicators of bleach-plant effluents.


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