About the Mineral Carbonation Session
Mineral carbonation is an innovative approach in the realm of carbon capture and storage (CCS) technologies, offering a promising avenue for mitigating the impact of anthropogenic carbon dioxide (CO2) emissions on climate change. This process leverages the Earth's natural carbon cycle, where over geological timescales; CO2 reacts with certain metal oxides or silicate minerals to form solid carbonates. In contemporary applications, researchers are actively exploring mineral carbonation as a means to permanently sequester CO2 emissions from industrial processes and power plants. The fundamental reaction involves the combination of CO2 with minerals such as serpentine, olivine, or basalt. This union leads to the creation of stable carbonates, essentially transforming gaseous CO2 into a solid state. This conversion not only removes CO2 from the atmosphere but also contributes to the long-term storage of this greenhouse gas. The choice of minerals is crucial, and on-going research is focused on identifying optimal candidates that facilitate efficient and economically viable mineral carbonation. The potential of mineral carbonation lies in its capacity to provide a scalable and sustainable solution for carbon capture and storage. As efforts intensify to address climate change, enhancing the efficiency of this process is a primary objective. Researchers are exploring methods to accelerate the mineral carbonation reaction, optimize mineral sources, and streamline the overall sequestration process. Successful developments in these areas could position mineral carbonation as a robust tool in the global fight against rising CO2 levels and climate change, contributing significantly to a more sustainable and environmentally conscious future.
Topics Covered in Mineral Carbonation
Nano-Silica from Serpentine Carbonation
Carbonation in Nanoconfined Pores
Nanometer-Thick Passivation Layers
Nanoscale Carbonate Nucleation Imaging
Nano-Immobilized Carbonic Anhydrase
Precipitated Nano-Calcium Carbonate
Related Scientific Sessions at World Nano 2027
Why Attend the Mineral Carbonation Conference 2027
Earn CPD Credit
Participants can earn 1 CPD credit for each hour of attendance.
Present Your Research
Oral and poster slots for original Mineral Carbonation work, reviewed by the scientific committee.
Network Globally
Meet nanotechnologists, researchers, scientists and engineers from around the world across three days.
Abstract Book Included
In-person and virtual registrations include an electronic copy of the abstract book.
Learn from Keynotes
Plenary lectures from leading voices shaping Mineral Carbonation research and practice.
Hybrid Flexibility
Attend in person in Singapore or join virtually — same programme, same certificate.
Join World Nano 2027 for the Mineral Carbonation track
Oral and poster slots for your work — in person in Singapore or online. Not presenting? Attend as a delegate to learn from the field.
Mineral Carbonation Conference 2027 — FAQs
What is the Mineral Carbonation track at World Nano 2027?
The Mineral Carbonation track is a dedicated stream within World Nano 2027 covering the latest research, innovation, and best practice in Mineral Carbonation. It brings together researchers, educators, and practitioners for oral presentations, posters, and discussion.
Who should attend the Mineral Carbonation sessions?
Nanotechnology researchers, scientists and engineers, educators and students with an interest in Mineral Carbonation are all welcome — whether presenting or attending.
Can I present my research in the Mineral Carbonation track?
Yes. Submit an abstract for oral or poster presentation. All submissions are peer-reviewed by the scientific committee.
Is virtual attendance available for Mineral Carbonation sessions?
Yes. World Nano 2027 is a hybrid conference — attend the Mineral Carbonation track in person in Singapore or join live online, with on-demand access afterward.
Join the World Nano 2027 delegation
Singapore · March 18–20, 2027· Hybrid · in-person & virtual
Attend without presenting.
