Abstract: A collapsed composition is described which is substantially composed of microcrystallites collectively of the formula:M.sub.2m.sup.2+ Al.sub.2-p M.sub.p.sup.3+ T.sub.r O.sub.7+r.swhere M.sup.2+ is a divalent metal, M.sup.3+ is a trivalent metal, and T is vanadium, tungsten, or molybdenum.The microcrystallites are so small as to be undetectable through conventional x-ray diffraction techniques, yet high resolution electron microscopy reveals that a substantial portion of the microcrystallites are composed of a solid solution having aluminum oxide molecularly dispersed in a divalent metal monoxide crystal structure. Another portion of the microcrystallites are constituted by a spinel phase. The collapsed composition is suitable as a sulfur oxide absorbent, having comparatively high capacity and comparatively fast absorption and desorption rates. The collapsed composition may be produced by heat treating a layered mixed hydroxide clay having interlayer anions in monometalate form.

Abstract: A transition metal electrocatalyst surface (e.g. a porous surface of finely divided Group VIII or Group I-B metal with an attached current collector) is modified by a sulfur treatment, using an oxidized sulfur species of average sulfur oxidation state of about 4 or less, e.g. SO.sub.2 dissolved in aqueous acid. Treatment of the transition metal with SO.sub.2 or the like typically provides up to 100% coverage of the surface electrocatalyst sites with chemisorbed sulfur-containing species and perhaps subsurface effects as well, but washing or other non-electrochemical techniques can remove 5-90% (e.g. 25-70%) of the chemisorbed SO.sub.2 or the like from the surface, leaving substantially only a very strongly bound form of the sulfur-containing species. The strongly bound sulfur-containing species can then be reduced to form a highly beneficial, selectively-improving pattern of sites containing reduced -S (e.g. sulfur or sulfide) on the electrocatalyst surface.

Abstract: A transition metal electrocatalyst surface (e.g. a porous surface of finely divided Group VIII or Group I-B metal with an attached current collector) is modified by a sulfur treatment, using an oxidized sulfur species of average sulfur oxidation state of about 4 or less, e.g. SO.sub.2 dissolved in aqueous acid. Treatment of the transition metal with SO.sub.2 or the like typically provides up to 100% coverage of the surface electrocatalyst sites with chemisorbed sulfur-containing species and perhaps subsurface effects as well, but washing or other non-electrochemical techniques can remove 5-90% (e.g. 25-70%) of the chemisorbed SO.sub.2 or the like from the surface, leaving substantially only a very strongly bound form of the sulfur-containing species. The strongly bound sulfur-containing species can then be reduced to form a highly beneficial, selectivity-improving pattern of sites containing reduced --S (e.g. sulfur or sulfide) on the electrocatalyst surface.