Effects of Fe and Al ions during hydrogen sulphide (H2S)-induced corrosion of tetracalcium aluminoferrite (C4AF) and tricalcium aluminate (C3A)
Creators
- 1. State Key Laboratory of Geo-mechanics and Geo-technical Engineering, Institute of Rock and Soil Mechanics, Chinese Academy of Sciences, Wuhan, Hubei 430071 (China)
- 2. School of New Energy and Materials, Southwest Petroleum University, Chengdu, Sichuan 610500 (China)
- 3. State Key Laboratory of Oil & Gas Reservoir Geology and Exploitation, Southwest Petroleum University, Chengdu, Sichuan 610500 (China)
- 4. Engineering Technology Research Institute, PetroChina Southwest Oil & Gas Field Company, Guanghan, Sichuan 618300 (China)
- 5. The State Key Laboratory of Safety and Health for Metal Mines, Maanshan, Anhui 243000 (China)
Description
Highlights: • Based on multiple investigations, the effects of Fe and Al ions in C4AF and C3A corroded by H2S were clarified. • In C4AF, Fe ions acted as catalysts for elemental S oxidisation under an H2S-rich corrosion condition. • AlOx moieties in C3A were modified by H2S, resulting in microstructure degradation. With high concentration and toxic H2S gas found in sewage facilities, it has ultra-high leakage risk and great environment impact, once the sealing material failure. In this study, hydrogen sulphide (H2S)-induced corrosion effects of tetracalcium aluminoferrite (C4AF) and tricalcium aluminate (C3A) phases of cement were evaluated during the initial stages of reaction. Both phase changes and bond structures were examined by techniques including Fourier transform infrared spectroscopy (FTIR). The results indicate that corrosion occurred through a stepwise reaction promoted by Fe ions. The effects of Fe and Al ions were further quantitatively investigated by X-ray photoelectron spectroscopy (XPS) and 27Al solid-state nuclear magnetic resonance (SSNMR). Compared with hydrated samples, the Fe ions were changed with Fe(II) ions increasing and Fe(III) ions reducing, and the AlOx group was observed to be transformed form AlO4 to AlO6 after H2S corrosion. Changes obtained will be benefit the further development of hazardous H2S control material and risk management operations.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2020.123928Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2020.123928;
- PII
- S030438942031918X;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 403
- Journal Page Range
- vp.
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54024810
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S46: INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND TECHNOLOGY;
- Descriptors DEI
- ALUMINATES; ALUMINIUM IONS; CATALYSTS; CEMENTS; CORROSION; ECOLOGICAL CONCENTRATION; FOURIER TRANSFORM SPECTROMETERS; HYDROGEN SULFIDES; INFRARED SPECTRA; IRON IONS; MICROSTRUCTURE; NUCLEAR MAGNETIC RESONANCE; RISK ASSESSMENT; SEWAGE; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALUMINIUM COMPOUNDS; BUILDING MATERIALS; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; ELECTRON SPECTROSCOPY; HYDROGEN COMPOUNDS; IONS; MAGNETIC RESONANCE; MATERIALS; MEASURING INSTRUMENTS; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; RESONANCE; SPECTRA; SPECTROMETERS; SPECTROSCOPY; SULFIDES; SULFUR COMPOUNDS; WASTES
Optional Information
- Copyright
- Copyright (c) 2020 Elsevier B.V. All rights reserved.