Abstract: A process for purifying an acidic technical-grade iron chloride solution formed from cyclone dust from the production of TiO.sub.2 in accordance with the chloride process by adjusting the pH with a first neutralizing agent and thereafter introducing the pH adjusted solution in a controlled manner into a solution containing a second neutralizing agent. In this process undesired ions which are to be separated, such as chromium, vanadium, zirconium and/or niobium, precipitate in the form of efficiently filterable hydroxides which can be separated industrially under economical conditions by filtration. The filter cake is non-hazardous and can safely be disposed of by dumping. Calcium carbonate is the preferred neutralizing agent, and the pH adjustment may also advantageously be effected by using scrap iron or by using iron sinters with reduction of any Fe(III) ions before the second neutralization step.

Abstract: The SO.sub.2 content of gases is catalytically reacted to form SO.sub.3. The SO.sub.3 -containing gases are cooled in a plurality of stages with a cooling fluid (A) before the SO.sub.3 is absorbed. The absorbing acid is cooled by a cooling fluid (B) which delivers heat to a consumer. To increase the temperature of the cooling fluid (B) or to reduce the expenditue and to prevent a temperature drop in the SO.sub.3 -containing gases below the dew point temperature, the SO.sub.3 -containing gases are cooled first by and indirect heat exchange and then by a second indirect heat exchange with a cooling fluid (A) to a temperature slightly above the dew point temperature of the SO.sub.3 -containing gases. The cooling fluid (A) is conducted in a closed cycle. The sulfuric acid circulated through the absorber is cooled by an indirect heat exchange with a liquid cooling fluid (B), which is conducted in a closed cycle.