Wuppertal, Univ., Diss., 2002. / Computerdatei im Fernzugriff.

Wuppertal, Univ., Diss., 2002. / Computerdatei im Fernzugriff.

Wuppertal, Universiẗat, Diss., 2002.

München, Techn. University, Diss., 2003.

Zugl.: Dresden, Techn. Universiẗat, Diss., 2007.

No description available.

Techn. Universiẗat, Diss., 2000--Darmstadt.

Universiẗat, Diss., 2004--Bremen. / Erscheinungsjahr an der Haupttitelstelle: 2003.

HCl ist ein Nebenprodukt bei vielen organischen Chlorierungsprozessen. Die Aufarbeitung von HCl wäre wirtschaftlich sinnvoll. Eine der möglichen Optionen ist die Rückgewinnung des Chlors durch die katalytische HCl-Oxidation mit O2 (Deacon-Prozess). Das Hauptziel dieser Arbeit war es, die katalytische Aktivität von kupferchlorid-haltigen Schmelzen in Abhängigkeit von der Temperatur und dem Verhältnis der Reaktionsgase zu untersuchen. Dazu wurden Versuche unter stationären und instationären Reaktionsbedingungen im Temperaturintervall zwischen 400 und 500 °C durchgeführt. Für das bessere Verständnis des Katalysator-Systems wurde ein thermodynamisches Modell für das Stoffsystem MeCl-CuCl-CuCl2-CuO-HCl-H2O-Cl2-O2 (Me = Li, Na, K) erstellt. Weiterhin wurden mithilfe von kinetischen Untersuchungen Hinweise auf die Rolle der gelösten oxidischen Zwischenverbindungen im stufenweisen Reaktionsmechanismus gefunden. Mit den Versuchsergebnissen wurde gezeigt, dass die MeCl-CuCl-CuCl2-Schmelzen eine genügende katalytische Aktivität besitzen und damit eine Alternative zu den mit Feststoffträgern arbeitenden Katalysatoren darstellen. Zur Minderung von Korrosionsproblemen wurden mehrstufige Prozessführungen kritisch diskutiert.

The production of chlorate, chlorine and sodium hydroxiderelies heavily on electrical energy, so that savings in thisarea are always a pertinent issue. This can be brought aboutthrough increased mass transfer of reacting species to therespective electrodes, and through increased catalytic activityand uniformity of current density distribution at theseelectrodes. This thesis will present studies involvingmathematical modelling and experimental investigations of theseprocesses. They will show the effect that hydrodynamicbehaviour has on the total current density and cell voltages,along with the effects on current density distributions andindividual overpotentials atthe respective electrodes. Primary, secondary and psuedo-tertiary current densitydistribution models of a chlor-alkali anode are presented anddiscussed. It is shown that the secondary model presentsresults rather similar to the pseudo-tertiary model, when thecurrent density distribution is investigated, although thepotential distribution differs rather markedly. Furthermore, itis seen that an adequate description of the hydrodynamicsaround the anode is required if the potential distribution, andthereby the prevalence of side-reactions, is to be reasonablepredicted. A rigorous tertiary current density distribution model ofthe chlorate cell is also presented, which takes into accountthe developing hydrodynamic behaviour along the height of thecell. This shows that an increased flowrate gives more uniformcurrent density distributions. This is due to the fact that theincreased vertical flowrate of electrolyte replenishes ioncontent at the electrode surfaces, thus reducing concentrationoverpotentials. Furthermore, results from the model lead to theconclusion that it is the hypochlorite ion that partakes in themajor oxygen producing side-reaction. A real-scale cross-section of a segmented anode-cathode pairfrom a chlorate cell was designed and built in order to studythe current density distribution in industrial conditions.These experiments showed that increased flowrate brought aboutmore even current density distributions, reduced cell voltageand increased the total current density. An investigation ofthe hydrodynamic effects on the respective electrodeoverpotentials shows the anode reactions being more favoured byincreased flowrate. This leads to the conclusion that theuniform current density distribution, caused by increasedflowrate, occurs primarily through decreasing the concentrationoverpotential at the anode rather than by decreasing thebubble-induced ohmic drop at the cathode. Finally, results from experiments investigating thebubble-induced free convection from a small electrochemicalcell are presented. These experiments show that Laser DopplerVelocimetry is the most effective instrument for investigatingthe velocity profiles in bubble-containing electrochemicalsystems. The results also show that the flow can transform fromlaminar to turbulent behaviour on both the vertical andhorizontal planes, in electrochemical systems where bubbles areevolved.