Abstract: A method of reducing scale formation in an aqueous solution using an electrolysis apparatus which has, in an electrolysis chamber, at least two electrodes and a bipolar electrode between the two electrodes includes feeding an aqueous solution to the electrolysis chamber, applying either a DC potential to the two electrodes so that one electrode is an anode and the other electrode is a cathode and reversing the polarity of the electrodes at intervals so that the composition of the aqueous solution remains essentially unchanged, or applying an AC potential to the two electrodes, producing, after the aqueous solution has passed through the electrolysis chamber, a treated aqueous solution having a significantly reduced tendency to form scale.
Type:
Grant
Filed:
April 14, 1999
Date of Patent:
July 10, 2001
Inventors:
Andreas Weissenbacher, Jürgen Johann, Ernst Oberhauser, Helmut Irauschek
Abstract: It is an object of the present invention to provide a corrosion resistance test process, wherein the estimation of the corrosion resistance of an article formed of a metal material and a coating can be carried out synthetically and in a short time. In carrying out a corrosion resistance test, the article is immersed into an electrolytic solution and then, a voltage is applied to the metal material to carry out a metal material corroding step and a coating peeling-off step alternatively and repeatedly. The voltage applied to the metal material is a superimposed voltage Vd+Va resulting from superimposition of a DC voltage Vd and an AC voltage Va. A voltage condition of Vd<0 and Vd+Va>0 is established at the metal material corroding step, while a voltage condition of Vd<0 and Vd+Va<0 is established at the coating peeling-off step.
Abstract: There is provided manganese dioxide to be suitably used for alkaline manganese batteries and manganese batteries to make them excellent both in the initial performance and the storability. There is also provided a method of manufacturing such manganese dioxide. The electrolytic manganese dioxide has a BET specific surface area of less than 30 m.sup.2 /g (preferably less than 27 m.sup.2 /g) and a suspensiveness of less than 50 mg/liter. A method of manufacturing electrolytic manganese dioxide may be a suspension method, wherein manganese oxide is suspended at a rate of 0.01 to 0.2 g/liter in an electrolytic bath containing sulfuric acid at a concentration of 0.4 to 0.55 mol/liter and electrolyzed to produce electrolytic manganese dioxide with an anodic current density of 0.4 to 3.0 A/dm.sup.2 and an electrolytic temperature of 93.degree. to 103.degree. C., the relationship between the anodic current density and the electrolytic temperature being expressed by 103.gtoreq.y.gtoreq.1.67x+92.
Abstract: The present invention provides a method for preparing irreversible linear aggregates (fibrils) of metal oxide powders by utilizing static or pulsed DC electrical fields across a relatively non-conducting liquid solvent in which organometal compounds or silicon alkoxides have been dissolved. The electric field is applied to the relatively non-conducting solution throughout the particle formation and growth process promoting the formation of either linear aggregates (fibrils) or spherical shaped particles as desired. Thus the present invention provides a physical method for altering the size, shape and porosity of precursor hydrous metal oxide or hydrous silicon oxide powders for the development of advanced ceramics with improved strength and insulating capacity.
Type:
Grant
Filed:
June 9, 1994
Date of Patent:
February 18, 1997
Assignee:
Martin Marietta Energy Systems, Inc.
Inventors:
Michael T. Harris, Osman A. Basaran, Warren G. Sisson, Ronald R. Brunson
Abstract: The method of removing sulfurous compounds (organic and inorganic) from any fluid (gas or liquid) phase by contacting said fluid (gas or liquid) with the reactive metal to form a metal sulfide recovering said fluid (gas or liquid) free from said sulfurous compound and containing compounds free from sulfur and recovering electrochemically said reactive metal from said sulfur to return said metal to elemental form to release elemental sulfur, said separating being done at temperatures above melting point of sulfur.