Atomic absorption spectrophotometric determination of selected elements in ferromanganese nodules from the Pacific, Atlantic, and Indian Oceans

DOI

Twenty-one samples of deep-sea ferromanganese nodules collected from the Pacific, Atlantic, and Indian oceans were supplied by the Lamont-Doherty Geological Observatory of Columbia University and the Hawaii Institute of Geophysics, University of Hawaii. The air-dried manganese nodules were crushed with the aid of a ceramic mortar and pestle, and sorted according to particle size using a set of U.S. standard mesh sieves. Powdered nodules (100/150 ?m) in particle diameter) were dried overnight at 450°C in a Lindberg furnace, and the weight loss of the sample was measured for H2O concentration determination. Exactly 500 mg of the dehydrated samples were acid-digested in a pressurized Teflonbomb and the contents were diluted to 100 ml with 0.5 M boric acid solution. Five replicates of each nodule specimen were digested and stored in polyethylene bottle. Four aliquots of the acid-digested sample were pipetted into separate beakers to which aqueous thallium standards were added successively with Eppendorf micropipettes. Each sample solution was adjusted to pH 10.8, and the wash solution was added to the separatory funnel. Five milliliters of a 1% APDC solution and 10 ml of MIBK were pipetted into each separatory funnel. The funnels were mounted on a Kraft Model S-500 mechanical shaker and shaken at a maximum amplitude for 10 min. A Perkin-EImer 603 atomic absorption spectrophotometer equipped with Westinghouse single-element hollow cathode lamps was used together with an air-acetylene oxidizing flame and a 10-cm single slot burner for all the measurements. Thallium was determined in the APDC-MIBK extract as soon as possible after the extraction step was completed, using the primary wavelength (276.8 nm), a 16 mA lamp current, and a slit setting at 4. Other metals such as Mn, Fe, Cu, Ni, and Co were measured directly in a portion of the acid-digested samples without carrying out the solvent extraction preconcentration step.

From 1983 until 1989 NOAA-NCEI compiled the NOAA-MMS Marine Minerals Geochemical Database from journal articles, technical reports and unpublished sources from other institutions. At the time it was the most extended data compilation on ferromanganese deposits world wide. Initially published in a proprietary format incompatible with present day standards it was jointly decided by AWI and NOAA to transcribe this legacy data into PANGAEA. This transfer is augmented by a careful checking of the original sources when available and the encoding of ancillary information (sample description, method of analysis...) not present in the NOAA-MMS database.--This table is digitized from Table 1, pp. 289-290 of the linked publication.

Identifier
DOI https://doi.org/10.1594/PANGAEA.946414
Related Identifier https://doi.org/10.7289/V52Z13FT
Related Identifier https://doi.org/10.7289/V53X84KN
Metadata Access https://ws.pangaea.de/oai/provider?verb=GetRecord&metadataPrefix=datacite4&identifier=oai:pangaea.de:doi:10.1594/PANGAEA.946414
Provenance
Creator Iskowitz, J M; Lee, John Jong-Hae; Zeitlin, Harry; Fernando, Quintus
Publisher PANGAEA
Publication Year 2022
Rights Creative Commons Attribution 4.0 International; https://creativecommons.org/licenses/by/4.0/
OpenAccess true
Representation
Resource Type Dataset
Format text/tab-separated-values
Size 208 data points
Discipline Earth System Research
Spatial Coverage (-7.188W, -54.500S, 44.767E, 45.972N); Pacific Ocean; Pacific Oean; Indian Ocean; Atlantic Ocean; South Atlantic Ocean
Temporal Coverage Begin 1959-11-27T00:00:00Z
Temporal Coverage End 1977-06-29T00:00:00Z