Adsorption of precious metal ions onto electrochemically oxidized carbon fibers

Electrochemically oxidized carbon fibers (ECF) adsorbed a prodigious amount of Ag+ in contrast to oxygen plasma and nitric acid treated carbon fibers. The amount of adsorbed Ag+ reached 3700 mu mol/g after 5652 C/g of electro chemical oxidation. This value approaches the 4050 mu mol/g of Ag+ which ad sorbed onto steam-activated Kenaf-based carbon (with a surface area of 1284 m(2)/g determined by N-2/BET) under the same adsorption conditions. ECF ox idized to 9540 C/g adsorbed more than its own weight of Ag+ (12 608 mu mol/ g). These fibers exhibited a surface area of 115 m(2)/g (CO2-DR). Two diffe rent reactions occurred during Ag+ adsorption. These reactions were ion exc hange adsorption between Ag+ and acidic functions (carboxyl) and redox adso rption between Ag+ and reducing functions such as catechol groups on these electrochemically oxidized fibers (ECF). The redox capability was expressed by the reaction electric potential (E) using the Nernst equation. High res olution XPS C 1s spectra of ECFs (level of oxidation 5300 C/g), before and after Ag+ adsorption, showed that the carbon atoms present in phenolic, alc ohol or ether groups and those present in carbonyl or quinone groups increa sed after Ag+ adsorption. X-ray diffraction and X-ray photoelectron spectro scopy (XPS) Ag 3d spectra of the ECF showed that adsorbed Ag+ was reduced t o Ag-0 after both Ag+ adsorption and subsequent post-heat treatment of the fibers under N-2 at 550 degrees C for 30 min. Only about one-third as much Au3+ adsorption occurred versus the extent of electrochemical oxidation as was observed for Ag+. This ratio matches the requirement that three electro ns are required to convert Au3+ to Au-0 versus one to convert Ag+ to Ag. Hi gh resolution angle resolved XPS (ARXPS) Pd 3d and Pt 4+ spectra show that there are two different Pd oxidation states and three different Pt oxidatio n states present after adsorption of Pd2+ and Pt2+ onto ECF. The peak areas as a function of take off angle showed that substantial amounts of Pd-0 an d Pt-0 are present in addition to Pd2+ and Pt2+ and Pt4+ on the outermost s urface regions of oxidized fibers. (C) 1999 Elsevier Science Ltd. All right s reserved.