- 【Updated on May 12, 2025】 Integration of CiNii Dissertations and CiNii Books into CiNii Research
- Trial version of CiNii Research Knowledge Graph Search feature is available on CiNii Labs
- 【Updated on June 30, 2025】Suspension and deletion of data provided by Nikkei BP
- Regarding the recording of “Research Data” and “Evidence Data”
Reactive Crystallization of Dolomite by CO<sub>2</sub> Microbubble Injection into Concentrated Brine
-
- TSUCHIYA Yuko
- College of Industrial Technology, Nihon University
-
- WADA Yoshinari
- College of Industrial Technology, Nihon University Faculty of Engineering, Chiba Institute of Technology
-
- MASAOKA Koji
- College of Industrial Technology, Nihon University The Salt Industry Center of Japan, Research Institute of Salt and Sea Water Science
-
- SATO Toshiyuki
- College of Industrial Technology, Nihon University
-
- OKADA Masaki
- College of Industrial Technology, Nihon University
-
- HIAKI Toshihiko
- College of Industrial Technology, Nihon University
-
- ONOE Kaoru
- Faculty of Engineering, Chiba Institute of Technology
-
- MATSUMOTO Masakazu
- College of Industrial Technology, Nihon University
Bibliographic Information
- Other Title
-
- 製塩苦汁へのCO<sub>2</sub>マイクロバブルの導入によるドロマイトの反応晶析
- Reactive Crystallization of Dolomite by CO₂ Microbubble Injection into Concentrated Brine
Search this article
Description
In this study, utilizing the minute gas-liquid interfaces around CO2 microbubbles as novel reaction fields where the crystal nucleation proceeds predominantly, a crystallization technique that enables the synthesis of dolomite(CaMg(CO3)2)fine particles with a Mg/Ca ratio of 1.0 was developed. In the regions around the gas-liquid interfaces of CO2 microbubbles, the local increase in the concentrations of Ca2+, Mg2+, and CO32- because of the electric charge on microbubble surface and the acceleration of CO2 mass transfer are caused by minimizing the bubble size. CO2 microbubbles with an average bubble size of 40 μm were continuously supplied to the concentrated brine coming from salt manufacture discharge in Japan using a self-supporting bubble generator, and CaMg(CO3)2 was crystallized within a reaction time of 120 min. The CO2 flow rate varied in the range between 1.49 and 23.8 mmol/(l・min). For comparison, the reactive crystallization with the injection of CO2 bubbles at dbbl of 200, 300, 800 or 2000 μm was performed using a dispersing bubble generator. The results indicated that minimizing the bubble formation and increasing the CO2 flow rate can achieve the high-yield crystallization of CaMg(CO3)2 fine particles with a higher Mg/Ca ratio.
Journal
-
- Bulletin of the Society of Sea Water Science, Japan
-
Bulletin of the Society of Sea Water Science, Japan 71 (2), 103-109, 2017
The Society of Sea Water Science, Japan
- Tweet
Details 詳細情報について
-
- CRID
- 1390282763050647296
-
- NII Article ID
- 130007490740
-
- NII Book ID
- AN0018645X
-
- ISSN
- 21859213
- 03694550
-
- NDL BIB ID
- 028113880
-
- Text Lang
- en
-
- Data Source
-
- JaLC
- NDL Search
- CiNii Articles
-
- Abstract License Flag
- Disallowed