Please use this identifier to cite or link to this item: https://repositorio.inpa.gov.br/handle/1/18729
Title: Black carbon increases cation exchange capacity in soils
Authors: Liang, Biqing
Lehmann, Johannes
Solomon, D.
Kinyangi, James M.
Grossman, Julie M.
O'Neill, Brendan E.
Skjemstad, Jan O.
Thies, Janice E.
Luizão, Flávio Jesus
Petersen, James B.
Neves, Eduardo Goés
Keywords: Carbon
Ion Exchange
Microscopic Examination
Ph Effects
Positive Ions
Spectroscopic Analysis
Biogeochemical Processes
Black Carbon
Cation Exchange Capacity (cec)
Scanning Transmission X-ray Microscopy (stxm)
Soil Surveys
Carbon
Ion Exchange
Microscopic Examination
Ph Effects
Positive Ions
Soil Surveys
Spectroscopic Analysis
Biogeochemistry
Black Carbon
Ion Exchange
Organic Carbon
Oxidation
Soil Nutrient
Soil Organic Matter
Amazon River
Brasil
South America
Bacteria (microorganisms)
Fungi
Issue Date: 2006
metadata.dc.publisher.journal: Soil Science Society of America Journal
metadata.dc.relation.ispartof: Volume 70, Número 5, Pags. 1719-1730
Abstract: Black Carbon (BC) may significantly affect nutrient retention and play a key role in a wide range of biogeochemical processes in soils, especially for nutrient cycling. Anthrosols from the Brazilian Amazon (ages between 600 and 8700 yr BP) with high contents of biomass-derived BC had greater potential cation exchange capacity (CEC measured at pH 7) per unit organic C than adjacent soils with low BC contents. Synchrotron-based near edge X-ray absorption fine structure (NEXAFS) spectroscopy coupled with scanning transmission X-ray microscopy (STXM) techniques explained the source of the higher surface charge of BC compared with non-BC by mapping cross-sectional areas of BC particles with diameters of 10 to 50 μm for C forms. The largest cross-sectional areas consisted of highly aromatic or only slightly oxidized organic C most likely originating from the BC itself with a characteristic peak at 286.1 eV, which could not be found in humic substance extracts, bacteria or fungi. Oxidation significantly increased from the core of BC particles to their surfaces as shown by the ratio of carboxyl-C/aromatic-C. Spotted and non-continuous distribution patterns of highly oxidized C functional groups with distinctly different chemical signatures on BC particle surfaces (peak shift at 286.1 eV to a higher energy of 286.7 eV) indicated that non-BC may be adsorbed on the surfaces of BC particles creating highly oxidized surface. As a consequence of both oxidation of the BC particles themselves and adsorption of organic matter to BC surfaces, the charge density (potential CEC per unit surface area) was greater in BC-rich Anthrosols than adjacent soils. Additionally, a high specific surface area was attributable to the presence of BC, which may contribute to the high CEC found in soils that are rich in BC. © Soil Science Society of America.
metadata.dc.identifier.doi: 10.2136/sssaj2005.0383
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