Effects of sulfate on biotite interfacial reactions under high temperature and high CO2 pressure. Issue 12 (6th March 2019)
- Record Type:
- Journal Article
- Title:
- Effects of sulfate on biotite interfacial reactions under high temperature and high CO2 pressure. Issue 12 (6th March 2019)
- Main Title:
- Effects of sulfate on biotite interfacial reactions under high temperature and high CO2 pressure
- Authors:
- Zhang, Lijie
Zhu, Yaguang
Wu, Xuanhao
Jun, Young-Shin - Abstract:
- Abstract : Anions affect water–biotite interfacial interactions to different extents and subsequently alter surface wettability. Abstract : To ensure the safety and efficiency of engineered subsurface operations, it is vital to understand impacts of aqueous chemistries on brine–mineral interactions in subsurface environments. In this study, using biotite as a model phyllosilicate, we investigated the effects of sulfate on its interfacial reactions under subsurface relevant conditions (95 °C and 102 atm of CO2 ). By making monodentate mononuclear complexes with biotite surface sites, 50 mM sulfate enhanced biotite dissolution by 40% compared to that without sulfate. However, sulfate at lower concentrations than 50 mM did not obviously affect biotite dissolution. In addition, sulfate did not impact secondary mineral precipitation. However, even without any discernible surface morphological change, sulfate adsorption made biotite surfaces more hydrophilic. To provide a more comprehensive perspective on environmentally-abundant ligands, we further comparatively examined the effects of various inorganic ( e.g., sulfate and phosphate) and organic ligands ( e.g., acetate, oxalate, and phosphonates) on biotite interfacial interactions and assessed their impacts on physico-chemical properties. We found that the presence of phosphate and phosphonates significantly promoted precipitation of Fe- and Al-bearing secondary minerals, but sulfate, acetate, and oxalate did not. BiotiteAbstract : Anions affect water–biotite interfacial interactions to different extents and subsequently alter surface wettability. Abstract : To ensure the safety and efficiency of engineered subsurface operations, it is vital to understand impacts of aqueous chemistries on brine–mineral interactions in subsurface environments. In this study, using biotite as a model phyllosilicate, we investigated the effects of sulfate on its interfacial reactions under subsurface relevant conditions (95 °C and 102 atm of CO2 ). By making monodentate mononuclear complexes with biotite surface sites, 50 mM sulfate enhanced biotite dissolution by 40% compared to that without sulfate. However, sulfate at lower concentrations than 50 mM did not obviously affect biotite dissolution. In addition, sulfate did not impact secondary mineral precipitation. However, even without any discernible surface morphological change, sulfate adsorption made biotite surfaces more hydrophilic. To provide a more comprehensive perspective on environmentally-abundant ligands, we further comparatively examined the effects of various inorganic ( e.g., sulfate and phosphate) and organic ligands ( e.g., acetate, oxalate, and phosphonates) on biotite interfacial interactions and assessed their impacts on physico-chemical properties. We found that the presence of phosphate and phosphonates significantly promoted precipitation of Fe- and Al-bearing secondary minerals, but sulfate, acetate, and oxalate did not. Biotite surface wettability was also altered as a result of changes in biotite surface functional groups and surface charges by ligand adsorption: sulfate, oxalate, phosphate, and phosphonate made biotite more hydrophilic, while acetate made it less hydrophilic. This study provides useful new insights into the effects of brine chemistries on brine–mineral interactions, enabling safer and more efficient engineered subsurface operations. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 21:Issue 12(2019)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 21:Issue 12(2019)
- Issue Display:
- Volume 21, Issue 12 (2019)
- Year:
- 2019
- Volume:
- 21
- Issue:
- 12
- Issue Sort Value:
- 2019-0021-0012-0000
- Page Start:
- 6381
- Page End:
- 6390
- Publication Date:
- 2019-03-06
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8cp07368f ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9678.xml