The need for innovative solutions in energy storage and sustainable chemistry, ionic liquids have emerged as the go to materials. One of our hottest product is 1-Methyl-1-propylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([C3C1Pyrr][TFSI]), an ionic liquid that stands out for its exceptional properties and versatile applications.

What Makes [C3C1Pyrr][TFSI] Unique?

This ionic liquid is composed entirely of ions and exists in the liquid state at temperatures below 100°C. Its defining feature—a pyrrolidinium cation paired with a bis(trifluoromethylsulfonyl)imide anion. This particular ionic liquid has a wide electrical window, as well as excellent chemical and thermal stability. These characteristics make [C3C1Pyrr][TFSI] an ideal candidate for cutting-edge applications, including:

Advanced Lithium-Ion Batteries: The non-flammable nature and wide electrochemical stability window of 1-Methyl-1-propylpyrrolidinium bis(trifluoromethylsulfonyl)imide

  • Lithium Ion Batteries: address critical safety concerns in current lithium-ion batteries, offering a safer alternative to traditional organic electrolytes.
  • Replacement for traditional Solvents: Its low volatility and high ionic conductivity allow [C3C1Pyrr][TFSI] to serve as an environmentally friendly solvent in chemical synthesis and material processing.
  • High-Performance Capacitors: The ionic liquid’s ability to operate across a broad temperature range supports the development of energy-efficient and durable supercapacitors.

Key Benefits

  1. Thermal Stability: [C3C1Pyrr][TFSI] remains stable at elevated temperatures, ensuring reliability in high-demand applications.
  2. Non-Flammability: Its inherent safety reduces the risk of combustion, making it suitable for safer battery technologies.
  3. Customizable Properties: The ionic liquid can be tuned to meet specific needs by adjusting its formulation or blending with compatible materials.

Pioneering Research and Innovations

Recent studies have highlighted the potential of [C3C1Pyrr][TFSI] in energy storage. For example, research published in Batteries showcases how binary mixtures of this ionic liquid with lithium salts enhance ionic conductivity while maintaining safety and stability at varying temperatures. These breakthroughs underscore its role in paving the way for next-generation lithium batteries with superior performance metrics. (Batteries 2024, 10, 319. https://doi.org/10.3390/batteries10090319)

Summary of Research Paper

The paper titled “Pyrrolidinium-Based Ionic Liquids as Advanced Non-Aqueous Electrolytes for Safer Next Generation Lithium Batteries” provides a comprehensive analysis of [C3C1Pyrr][TFSI] and its mixtures with lithium salts. Key findings include:

  • Enhanced Thermal and Electrochemical Stability: The ionic liquid offers a wide liquid range, reducing risks such as crystallization at low temperatures and flammability, which are common with conventional electrolytes.
  • Ionic Conductivity: Mixtures with lithium bis(trifluoromethylsulfonyl)imide ([Li][TFSI]) exhibit ionic conductivities ranging from 0.4 S/m to 0.1 S/m at room temperature, making them highly efficient for lithium-ion battery applications.
  • Amorphous Behavior: The addition of lithium salts increased the amorphous nature of the mixtures, which improves ionic mobility and storage capabilities.

These findings place [C3C1Pyrr][TFSI] as a promising candidate for enhancing the safety and performance of lithium-ion batteries, with potential applications in other areas of green technology.

Real-World Applications

  1. Energy Storage Systems: [C3C1Pyrr][TFSI] is pivotal in creating safer, longer-lasting lithium-ion batteries that can power everything from electric vehicles to renewable energy grids.
  2. Industrial Processes: Its ability to dissolve a wide range of organic, inorganic, and polymeric substances makes it invaluable in specialized chemical industries.
  3. Sustainable Technologies: The ionic liquid contributes to greener manufacturing processes by replacing volatile organic solvents, thereby reducing environmental impact.

Why Choose RoCo for [C3C1Pyrr][TFSI]?

At RoCo, we’re committed to providing high-quality materials that meet the demands of advanced scientific and industrial applications. Our [C3C1Pyrr][TFSI] stands out for its high purity and consistent performance, backed by rigorous quality control and cutting-edge research.

Join the Innovation Revolution

The future of energy and material science is here. Whether you’re developing safer batteries, exploring sustainable solvents, or driving advancements in green chemistry, 1-Methyl-1-propylpyrrolidinium bis(trifluoromethylsulfonyl)imide is your key to success. Explore its possibilities and redefine the boundaries of innovation with RoCo.

 

Lithium-ion batteries are foundational to the global transition toward electrification, powering everything from smartphones and electric vehicles (EVs) to grid-scale energy storage systems. However, safety and longevity remain persistent challenges; one key limitation is the performance of the solid electrolyte interphase (SEI) layer. At RoCo®, we focus on ionic liquids and advanced electrolyte additives and materials engineered to address these critical pain points.

The SEI Layer: A Crucial Performance Limiter: The SEI layer, typically 10–50 nm thick, forms during the first few charge cycles and is a protective barrier on the anode. A well-formed SEI must exhibit low ionic resistivity (<10 Ω·cm²), elasticity to withstand anode volume changes, and chemical stability to prevent electrolyte decomposition. Failures in SEI performance are linked to lithium dendrite growth, capacity fades (10–20% over 500 cycles), and thermal runaway beyond 100°C.

Advanced Additive Chemistry: RoCo® has developed an ionic liquid SEI additive, a vinyl triazolium-based electro-polymerizable ionic liquid. It offers an electrochemical window of 0–5 V and a bulk ionic conductivity of ~10⁻³ S/cm. It is non-flammable and forms a high-quality SEI layer with no detectable flash point, addressing multiple safety and performance concerns. When combined with vinylene carbonate (VC), which polymerizes at low voltages, the resulting SEI shows a 30% impedance reduction measured via cyclic voltammetry (CV) over 10 cycles at a 1 mV/s scan rate. (See Triazolium Products).

As shown in Figure 1, the experimental data collected under the following conditions—a 2-hour soak at open-circuit voltage (OCV), lithium wire used as both reference and counter electrodes, and a graphite working electrode scanned at 1 mV/s over 10 cycles—demonstrate the superior performance of RoCo®‘s TzVmO2FS. Compared to vinylene carbonate (VC) and fluorinated VC (VC-F), the vinyl triazolium system exhibited lower reductive current and narrower hysteresis in cyclic voltammetry, indicating more efficient and stable SEI formation.

Broader Electrochemical Solutions RoCo® offers a suite of electrolyte and additive solutions:

  • Ionic liquid-based electrolytes (e.g., imidazolium, pyrrolidinium salts) deliver 10–15 mS/cm conductivity at 25°C and stability up to 4.5 V coupled with traditional carbonate solvents.
  • Solid-state battery polymers, including Polydiallyldimethylpyrrolidinium-based systems, provide >20 MPa tensile strength and high ionic transport available in FSI and TFSI anions.
  • High-purity lithium salts (>99.9%) such as LiPF₆, Li-FSI, and Li-TFSI enhance SEI stability and system energy density (target >300 Wh/kg).

Multifunctional Role of Additives RoCo® has designed multifunctional additives that serve essential roles in commercial and research battery systems:

  1. SEI Formers: Reduce initial capacity loss (<5%) and increase Coulombic efficiency (>99.5%).
  2. Cathode Protection Agents: Prevent oxidative decomposition at high voltages.
  3. Salt Stabilizers: Suppress decomposition of LiPF₆ into reactive phosphine/fluorine gases.
  4. Fire Retardants & Overcharge Protectors: Improve thermal safety by incorporating various ionic liquids into electrolyte chemistry.
  5. Lithium Deposition Modifiers: Promote uniform Li plating.
  6. Corrosion Inhibitors: Extend metal component life.
  7. Solvation Enhancers: Increase ion mobility.
  8. Wetting Agents/Viscosity Modifiers: Improve electrolyte penetration.

Conclusion RoCo®’s cutting-edge electrolyte additives and materials significantly improve battery performance, safety, and longevity. Through innovations like vinyl triazolium and complementary solutions, we support the transition to safer, higher-performance lithium-ion and solid-state batteries. Contact RoCo® for custom materials and technical consultation to optimize your next-generation energy storage applications.

 

As the CEO of RoCo, a small research company focused on ionic liquids of just four dedicated individuals, this holiday season offers the perfect moment to pause and reflect on a year that has been as challenging as it has been rewarding. When 2024 began, I truly believed that RoCo might not survive. Broken equipment, financial uncertainty, and personal health struggles loomed large. But today, as I look back, I see a year defined by resilience, growth, and the incredible power of relationships.

Navigating a World in Crisis

This year wasn’t just shaped by internal challenges; the world around us felt heavy. The ongoing war in Ukraine and the devastating conflict in Gaza reminded us daily of the fragility of peace and the interconnectedness of global systems. These crises reverberated through the supply chain, created economic pressures, and made us acutely aware of our own vulnerabilities. Yet, they also underscored the importance of our work. As a company rooted in innovation and sustainability, we feel a deep responsibility to contribute solutions to global challenges, no matter how small our role may seem.

The Challenges of January

Closer to home, we faced uncertainty. Equipment failures and mounting financial pressures cast a long shadow, and I wasn’t sure we’d make it through the first quarter. Yet, even in those dark times, our team’s unwavering commitment was a light. Ken Medlin, our laboratory manager, exemplified this spirit. His steadfast belief in RoCo’s mission—and in me—gave me the strength to keep going. Leadership isn’t about never feeling doubt; it’s about showing up even when doubt is overwhelming.

A Pivotal February

February brought a lifeline: a major sale of ionic liquids. This single event gave us the breathing room to push forward. Without it, I’m not sure we would have survived. That sale wasn’t just about numbers; it was a validation of the hard work and trust that defines RoCo.

Turning Points and Triumphs

As the year progressed, optimism—a trait both my greatest strength and occasional fault—proved invaluable. We secured two NASA subaward contracts for the development of groundbreaking ionic liquid technologies. Our sales tripled year over year, bolstered by strong relationships with major corporations and our trusted partner, IoLiTec GmbH.

We also welcomed Clarissa Crafton, a talented Carnegie Mellon graduate, to our team, strengthening our capabilities in polymer recycling. Her fresh perspective and expertise brought new energy to our work. Additionally, we maximized our laboratory space, expanding into new services and securing funding from the Mattress Recycling Council to explore innovative recycling processes.

The Power of Relationships

If there’s a single theme that defines 2024, it’s this: relationships matter. Our partnerships with Rochester Institute of Technology and Prof. Carlos Diaz have been instrumental in our success. Collaborating with Faraday and being part of the USRIA cohort opened new doors, reaffirming that strong connections are the foundation of any journey. Whether it’s with team members, partners, or customers, these bonds make every struggle and success worthwhile.

Investing in the Future

With the momentum we built, we invested in new equipment, including state-of-the-art Differential Scanning Calorimetry and Thermogravimetric Analysis units. These tools will allow us to continue pushing the boundaries of innovation, particularly in carbon composites using our ionic liquid technologies.

Looking Ahead

When 2024 began, I feared for the future—not just for RoCo, but for the world. The conflicts in Ukraine and Gaza, economic uncertainty, and global polarization weighed heavily on my mind. Yet, through it all, I’ve found hope. These challenges have taught me that even in the darkest moments, there is light to be found in the strength of a committed team, the support of valued partners, and the resilience of an idea worth fighting for.

To everyone who has been part of our journey—our team, partners, and customers—thank you. As we step into 2025, I look forward to continuing this incredible journey together.

What challenges have you overcome this year? Who has been your greatest support?

Happy holidays to all,
Batool Nulwala
CEO, RoCo

Ionic liquids have transformative potential across industries, particularly in green solvents and liquid electrolytes development. Our advances in polymer composites and ionic liquids have been lately focused on developing sustainable polymer recycling solutions.

First, ionic liquids are not liquids in the traditional sense. Yes, they flow, but something that flows doesn’t make it a liquid. The name ionic liquids has caught on, so we will stick with it. However, I want to clarify that they should not be considered, treated or thought of as liquids. Ionic liquids are highly ordered, flowing solids. I want to clarify this before jumping into applications. They are just the coolest class of materials there are.

Figure: 1: As the chain length of the ionic liquid increases specific structures are formed mainly due to segregation.

Di Cola’s work on 1-alkyl-3-methyl imidazolium Cl salts shows nanometer-scale structures, as observed using X-ray diffraction. The size of these structures depends on the length of the alkyl chains. This supports molecular simulations that suggest alkyl chains tend to group and then likely form clusters of ionic moieties, resulting in nanostructures. The size of these structures changes with temperature. However, above its glass transition temperature Tg , the behavior becomes very complex. These findings offer insights into room-temperature ionic liquids’ unique physical and chemical properties.

It is well known that ionic interactions are orders of magnitude stronger than Van der Waals interactions and it gives insight into the very low vapor pressure of these materials. That said as these are very strong interactions, we can design systems that improve materials’ properties overall and open a new frontier in material science. At RoCo, we enjoy working with ionic liquids; the structural flexibility of these materials excites us.

Indeed, ionic liquids reshape industrial processes by offering non-toxic, sustainable, and highly effective solutions for persistent corrosion prevention and polymer recycling challenges. Dr. Hunaid Nulwala and Ms. Nulwala recently shared their technical work about RoCo® and LumiShield at the Rochester Institute of Technology. The polymer work was carried out in collaboration with Prof. Carlos Diaz, with funding from the US Department of Energy, to create the next generation of compatibilizers. These ionic liquid solvents have transformative potential across industries, particularly in green solvents and liquid electrolytes development.

Our advances in polymer composites and ionic liquids structure support sustainable polymer recycling solutions.

Collaboration with the Rochester Institute of Technology has been pivotal for our entrepreneurship initiatives to commercialize sustainable solutions. Lets now look at the problem of polymeric blends.

The Problem: Polymers Don’t Mix — An Entropy and Enthalpy Perspective

The immiscibility of most polymers is a balance play between entropy and enthalpy contributions, as described by the Gibbs free energy of mixing:

∆𝐺𝑚𝑖𝑥 = ∆𝐻𝑚𝑖𝑥 − 𝑇∆𝑆𝑚𝑖𝑥
Where:
∆𝐺𝑚𝑖𝑥: Gibbs free energy of mixing
∆𝐻𝑚𝑖𝑥 : Enthalpy of mixing
∆𝑆𝑚𝑖𝑥: Entropy of mixing
𝑇: Temperature

For polymers to mix, they must be negative. However, in most cases, this condition is not met due to the following factors:

1. Low Entropy of Mixing ∆𝑆𝑚𝑖𝑥:

Entropy is the measure of randomness or disorder in a system. For small
molecules, mixing significantly increases entropy because the molecules can distribute freely among one another. This is not the case with polymers. Polymers are bound together so they are difficult to mix. Couple that with the size and the volume they occupy. What this means is that they have few configurations to mix. Hence, there is a very low Entropy of mixing.

Basically, the entropy gained from mixing polymers is negligible due to their size and restricted configurational freedom.

2. Positive Enthalpy of Mixing ∆𝐻𝑚𝑖𝑥

Interactions between polymer molecules when they mix. For most polymers ∆𝐻𝑚𝑖𝑥 The enthalpy of mixing represents the energy change associated with the is positive due to Incompatible Intermolecular Interactions, as most polymers have weak interactions (Van der Waals forces) between their chains. These weaker interactions do not compensate for the energy required to break the stronger self- interactions and the solvent bonds within each polymer type. The bottom line is that both Entropy and Enthalpy favor phase separation.
The combination of a negligible entropy gains and a positive enthalpy of mixing leads to a situation where is positive. This makes the mixing of polymers thermodynamically unfavorable, and they remain immiscible.

Even when we look at similar molecules, such as High-Density Polyethylene (HDPE) and Polypropylene (PP), they are not miscible with each other. Overcoming immiscibility is a multi-billion-dollar opportunity.

Implications in Industry

The immiscibility of polymers is a critical challenge in composites, recycling and materials science. In recycling, it limits the ability to reuse mixed polymer waste. One way is to make the interfaces ionic, thus improving the use of ionic bonds and phase segregation to make polymeric blends that provide significant value.

Polymer Recycling with Reactive Ionic Liquids: The ionic liquids developed at RoCo have improved mixed PP/HDPE systems, overcoming both tensile and impact properties. These ionic liquids have transformative potential across industries, particularly in green solvents and liquid electrolytes development. Our advances in polymer composites and ionic liquid’s structure support sustainable polymer recycling solutions.

To build on the theme of ionic liquid as a compatibilizer, RoCo technology works by introducing ionic interaction at the interface of the phase separation and also modifies the polymers.

Figure 2: Introducing Ionic moieties at the interface significantly improves the phase separation strength.

Our initial results show that using reactive ionic liquid improves both tensile strength and properties. Our study used 0.5 wt.% ionic liquid, which improved the impact and tensile properties.

improvement in both impact and tensile properties

Figure 3: We see improvement in both impact and tensile properties.

Conclusion:

Ionic liquids offer significant advantages as a compatibilizer. However, this technology is nascent, and RoCo will keep working on this to take it to the market. These ionic liquid solvents have transformative potential across industries, particularly in green solvents and liquid electrolytes development.

If you develop battery technology, the Mattress Recycling Council (MRC), together with RoCo®, is looking for battery researchers and manufacturers interested in decreasing their carbon footprint in energy storage devices and incorporating state-of-the-art electrolytes and battery salts.

A Sustainable Solution for High-Performance Batteries
In the quest for sustainable and efficient energy storage solutions, recent research led by Dr. Ram Gupta at Pittsburg State University’s National Institute for Materials Advancement (NIMA) funded by MRC has demonstrated that carbon derived from recycled mattress components serves as an excellent feedstock for battery and supercapacitor electrodes. This is a promising alternative to traditional graphite, which has a high carbon footprint.

Innovative Carbon Production Process
The process involves carbonizing mattress foam at temperatures below 900°C, significantly lower than the 3000°C typically required for graphite production. This innovative process recycles mattress foam into a high-performance,high-surface-area electrode material. The carbon derived from this process yields carbon with excellent energy storage and retention properties. The work carried out at NIMA has shown that carbon is comparable in performance to conventional materials, making it a viable and eco-friendly alternative.

Electrochemical Stability and Efficiency
The research highlights the electrochemical stability of devices made from recycled mattress materials. Tested devices show stability up to 10,000 charge-discharge cycles and nearly 100% Coulombic efficiency. The use of different electrolytes, including aqueous and organic, has further enhanced the performance of these devices.

Applications in Li-S Batteries
One of the most significant advancements from this research is the development of lithium-sulfur (Li-S) batteries using carbon derived from recycled mattressmaterials. Li-S batteries offer a theoretical specific energy of around 2600 Wh/kg, five times higher than conventional Li-ion batteries. The carbon-based materials help mitigate common issues such as the shuttling effect and volume expansion, enhancing the overall performance and stability of Li-S batteries.

Carbon Blade to Develop Renewable Energy-Powered, Zero-Waste CO2 Removal Systems utilizing RoCo® IP. 

Dateline: PITTSBURGH, PA,  November 6, 2023

RoCo®, an advanced materials company, has recently sold its innovative Direct Air Capture (DAC) technology to Carbon Blade, a California-based firm. The revolutionary DAC technology allows solvent regeneration without heat, which fosters the creation of smaller, renewable energy-powered modules. This represents a significant stride forward in carbon dioxide removal (CDR).

 

Carbon Blade is a climate technology company creating devices to transform global perspectives on CDR. The company is developing innovative, containerized, small-footprint systems that can be deployed virtually anywhere. Powered entirely by renewable energy, these systems will facilitate the capture and removal of CO2 without the need for energy-intensive, centralized removal facilities that require expensive support infrastructure to transport the captured CO2 to sequestration sites. According to Josh Franklin, CEO of Carbon Blade, “The acquisition of this technology is key to achieving our goal of being a disrupter and a price leader in the CDR space.”

 

“The sale of its intellectual property demonstrates RoCo’s® continued dedication to promoting innovative solutions that reduce the cost of carbon capture and contribute to environmental conservation,” said Batool Nulwala, CEO of RoCo®. Furthermore, the company believes this sale will allow both companies to focus on their core competencies, as Carbon Blade is better suited for scaling up the technology.

RoCo®, headquartered in Pittsburgh, PA, is a leading materials technology innovator focused on developing and scaling sustainable technologies that promote clean air, clean water, clean energy, and a better environment for future generations.

 

Carbon Blade is a California-based climate technology company that develops hardware solutions to capture CO2 directly from the air as a climate mitigation strategy. We believe climate action is the existential challenge for our generation, and the reduction of CO2 concentrations in the atmosphere, both from decarbonization and CDR, is key to success in this endeavor. As such, we develop renewable energy-powered, cost-efficient CDR solutions that can lower atmospheric CO2 concentrations at scale.

 

Media Contact Information:

For RoCo®:

www.roco.global

Phone: 724-315-9170

Email: [email protected]

 

For Carbon-Blade:

www.carbon-blade.com

Phone: 773-531-8526

Email: [email protected]

Polypropylene Recycling

For decades, we have been hearing about recycling, especially plastics. Education on recycling for most of us in our 40s started in elementary school, with programs, ads, etc., promoting its benefits and how you can help mitigate the effects of climate change. Unfortunately, we are now learning that most plastics are not recycled. We now know that media and corporations lied to us about the recycling programs they created, doping us into using more plastics than needed.

Polyethylene (PE) and polypropylene (PP) are the most used polymers. Over 80 million metric tons of PP were made in 2021, and less than 2% was recycled. A study published by Greenpeace found that no plastics, including soda bottles which are the most common items, meet the requirements to be called “recyclable.” Over 827,000 tons are collected annually from American households, and almost all of it is sent to landfills.

Proper recycling reduces carbon dioxide and other greenhouse gas emissions that lead to climate change. Increasing the PP recycling rate to 50% would mean taking 7.5 million cars off U.S. highways, avoiding 34,607,544 tons of CO2 emitted annually.  That said, PP is a difficult polymer to recycle.

RoCo is committed to finding a solution by developing innovative technologies that will aid in the upcycling of PP. The most common containment observed in PP is PE. We are currently working on an ionic compatibilizer that is halide free, non-toxic, and miscible with polyolefins. This ionic compatibilizer overcomes phase separation.  Our work is promising and has already demonstrated that a small amount of ionic compatibilizer ~0.5 wt.% significantly improves mechanical and impact properties and overcomes the stiffness-impact trade-off observed in PP contaminated with PE. The ionic nature of the compatibilizer provides an interface to form highly miscible domains resulting in overcoming phase separation.

In addition, we have observed a 30% improvement in mechanical properties in glass-fibered filled PP. If we successfully commercialize this technology, it will improve recycling rates and provide upcycled PP in the market. Based on our initial estimates, the ionic compatibilizer cost will be much lower per Kg of polymer, providing a cost-effective methodology compared to the current block copolymer approach.

Polypropylene does not like to be mixed with other polymers. Small amounts of contaminants impact PP properties dramatically.

We are working on this goal to develop ionic compatibilizers which make PP resilient to contaminants. This results in upcycling of PP upon recycling. This would allow us to engage with industry leaders and fast-track the commercialization of this technology.

If you are interested in learning more, please contact us at [email protected] for more information.

Climate change is the biggest challenge facing humanity. The global implications are already becoming clear with an increase in wildfires in the Northwest United States, record-breaking heat waves worldwide, and, most recently, the devastating flooding in Pakistan. Drastic changes must be made to mitigate the impact of climate change and eliminate the amount of CO2 emitted into the atmosphere. To do this, an executive order was signed to make the Federal government carbon-neutral and achieve net zero greenhouse gas emissions by 2050 and carbon capture is a must.

RoCo is a vision-driven company focused on developing technologies that can reduce the impact of climate change. We have been at the forefront of developing new materials technologies to capture carbon from the point of source (large scale) and direct air capture. Recently, RoCo spun off Carbon Blade, focusing on CO2 for Direct Air Capture (DAC).

RoCo has developed a highly effective Water-Lean Low Viscosity Solvent to capture CO2 from the large industrial sector. For conventional carbon capture applications, hazardous pollutants are also part of the mix that must be removed. This includes sulfur dioxide (SOx) and nitrogen oxide (NOx), which need to be removed before capturing CO2. The cost of implementing emission control technologies for the removal of SOx and NOx is substantial and can be even more concerning for applications that require high removal efficiency. This leads to a significant impact on the overall economics of the carbon capture processes. One potential solution is demonstrating carbon capture technologies with significant ancillary environmental benefits. If successful, it would result in decreasing the cost of CO2 capture significantly. However, there is little understanding and quantification of the co-benefit pollutant reductions.

Our newest project is focused on developing technology to further this gap. SBIR-DOE-SC0022623 funds this project. Under this project, the RoCo team aims to understand and quantify the co-benefit pollutant (NOx and SOx) reductions and evaluate their impact on water-lean solvents. The study will provide crucial information for practical process design and more accurate economic analysis that are the foundation for the development, scale-up, and commercialization of RoCo’s solvent technology. RoCo has developed high-performance, water-lean solvents which have a low viscosity. We have identified promising solvent systems with exceptionally low viscosity and two times the working capacity of traditional solvents. RoCo is working on conducting tests at a lab scale under simulated flue gas containing 4% (NGCC) or 15% CO2 (PC), capable of reaching > 95% capture efficiency with SOx and NOx to quantify the auxiliary benefits and reduced the overall cost of capture.

RoCo’s goal is to scale up and implement this technology on a commercial scale for large point source capture sites such as power plants, the metals industry, the cement industry, etc. If successful, this water-lean solvent can further reduce the cost by $5.0/ton of CO2 captured, according to preliminary cost-benefit analysis. The proposed work is essential and would help to determine whether separate emission control units are needed upon implementing the technology, which may lead to an additional cost saving of $600/kW in capital cost and almost $7/kW-year in operating costs.

Partnering with RoCo:

If you are interested in our water-lean solvent technology or our qualification method for carbon removal efficiency, please contact us at [email protected] for more information.

Ionic liquids (ILs) are conductive liquids with no or little vapor pressure. ILs form dynamic structures within the liquid state, and these structures exist within an equilibrium at a specific condition. As the conditions change, either by exposure to external stimuli and environmental changes (humidity, gas composition, etc.), these materials’ conductivity also varies, thus providing materials-based sensors which can be fabricated into sensing devices.

Diagram, schematic Description automatically generated

Figure 1: a) chemical structure of allyltriphenylphosphium-bis(trifluoromethyl)sulfonyl)amide (AllylPh3P-TFSI). B)The crystal structure of (AllylPh3P-TFSI) shows that the phenyl rings mainly interact with the CF3 of the TSFI anion. The anion and cation are separated, creating spaces between them. AllylPh3P-TFSI was created mainly to accommodate the flow of ions through the channels. X-Ray structure was obtained by Dr. Damodaran Achary of the University of Pittsburgh

RoCo has been conducting ionic liquids research for many years for several applications, including batteries, carbon capture, polymer compatibilizer, and solvent. Figure 1 shows the chemical structure of allyltriphenylphosphium-bis(trifluoromethyl)sulfonyl)amide. This IL was specifically developed for gas absorption applications and studied extensively by the researchers at RoCo. On the right, single-crystal X-Ray data of this ionic liquid is shown. The IL here is different as the anion and cation are separated due to steric hindrance, forming ionic channels where polar gas molecules can reside and be used for sensor applications. This material can also be used as a high-temperature battery electrolyte as well.

There is significant interest in electronic skin sensors or wearable thin-film sensors. These sensors can be placed directly on the skin to measure body parameters such as body temperature, heartbeat, sweat composition, etc. These sensors are now used in various applications such as healthcare, sports, robotics and prosthetics, and the military. Ionic liquid-based skin sensors are an emerging type of pressure sensor capable of perceiving external stimuli of pressure, strain, and torsion and turning them into electrical signals. These ionic liquid sensors can be encapsulated in silicones and can be worn directly. When connected with smart devices, it effectively expands the ability of human beings to perceive and evaluate the external environment. It is essential to point out that ionic liquids can be polymerized and converted into membranes, coatings, thus further widening their applicability. When ionic material is impregnated into textile fibers, it can provide skin sensors with high permeability, wearable comfort, wears resistance, and anti-bacterial properties.

In the literature, several ionic liquids have been used for this application. 1-ethyl-3-methylimidazolium-tetrafluoroborate (EMIM BF4) has been used as a gelled electrolyte in wearable electronics. In addition to EMIM BF4, the gelled ionic liquid sensors based on a trihexyltetradecyl-phosphonium dicyanoamide have been used to evaluate real-time pH in sweat. Ionic liquid composites with carbon nanotubes and an ionic liquid ([EMIM]Tf2N) have also been used to sense surface temperature.

If you are working with ionic liquids, our knowledgeable team can support your developmental efforts by identifying the suitable ionic liquid and developing custom ionic liquid materials solutions. Contact us

 

Authors: Dan Soeder, Hunaid Nulwala, James Lawler, Daryl-Lynn Roberts

Team Carbon Blade is pioneering carbon capture and storage solution that provides stand-alone, small-footprint “Blade” (Direct Air Capture (DAC)) modules that combine wind-powered electrodialysis with bipolar membrane separation (EDBM) to remove CO2 from ambient air at less than $100/t CO2. The small footprint units can be deployed wherever underground or other CO2 storage or transport options exist, enabling a scalable solution.

Team Carbon Blade is a registered participant in the Elon Musk X-Prize carbon removal competition and comprises experts from all key disciplines relevant to developing and implementing a scalable solution to carbon capture and storage. These include advanced materials chemistry and physics, fluid dynamics, computational mechanics, energy technology commercialization, and geologic storage. Team bios are at the end of this article.

The CO2 bathtub is overflowing, and experts believe that drastic measures are necessary.

Continuous measurements of atmospheric carbon dioxide (CO2) began in 1957 on the flank of the Mauna Loa volcano in Hawaii at a trace gas observatory established by the U.S. National Oceanic and Atmospheric Administration (NOAA) and operated by the Scripps Institute of Oceanography. In 1976 a group from Scripps and NOAA decided to analyze trends in the measurements for any variations (Keeling et al., 1976). Figure 1 shows what is known as the “Keeling Curve” after this 1976 publication. This curve shows the CO2 concentration increase in parts per million in the atmosphere over time. These measurements have continued to the present day at about 160 stations across the globe.


Figure 1: The Keeling Curve of carbon dioxide levels in the atmosphere measured since 1957 at Mauna Loa in Hawaii. The sawtooth pattern represents seasonal changes in CO2 as northern hemisphere plants bloom in spring and go dormant in fall. The solid line up the center is the annual average trend.

Source: U.S. National Oceanic and Atmospheric Administration (NOAA) public domain

The Keeling Curve shows a steady increase in the concentration of CO2 in the atmosphere of nearly 100 parts per million (ppm) over the past 60 years. The sawtooth line represents the annual cycle of vegetation blooming in spring and absorbing CO2, then going dormant in the fall and ultimately returning the CO2 to the atmosphere. The solid, dark line located in the center is the average annual concentration trend. It is important to note that the average yearly concentration line is steepening with time.

What is causing this increasing concentration of atmospheric CO2? Some have suggested that natural sources such as volcanic eruptions might be responsible. Although volcanic eruptions may emit copious quantities of CO2 into the atmosphere, many large eruptions would be necessary to account for the upward slope. There is no evidence that any sustained mega-eruptions have occurred within this time frame. Most volcanoes erupt episodically, which would result in irregular, upward spikes on the Keeling Curve. Yet, it shows a relatively smooth and steady increase in average CO2 levels over time. Other proposed sources of GHG like forest fires, rotting vegetation, and even cattle flatulence would not produce the rapid anomaly shown in the Keeling Curve. In a balanced carbon cycle, carbon flows between Earth’s natural reservoirs – the ocean, soils, and vegetation – without rapid accumulation in the atmosphere.
Draft diagram of the carbon cycle.

Figure 2: The diagram shows the overall carbon cycle leading to the movement of carbon between land, atmosphere, and oceans. Yellow numbers are natural fluxes, and red is human contributions in gigatons of carbon per year. White numbers indicate stored carbon.

Source: “The Carbon Cycle.” Earth Observatory. NASA

However, burning fossil fuels such as coal, petroleum, and natural gas releases excess carbon that had been stored deep underground for millions of years. This carbon is not part of the atmospheric carbon cycle (Figure 2), and so once released, that process cannot fully reabsorb it. The trend of increased fossil fuel use since the Industrial Revolution (Figure 3) matches the increased CO2 concentrations in the atmosphere shown in Figure 1. These trends precisely explain the Keeling Curve anomaly.

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Figure 3: Global energy consumption from 1800 to 2019, showing the dominance of fossil fuels.

Source: Ritchie, H. “Energy” (open access) Published online at OurWorldInData.org.

CO2 is known as a “greenhouse gas” (GHG) because it absorbs infrared (heat) radiation. Specifically, higher concentrations of CO2 in the air absorb more heat and result in a warmer atmosphere. Since the early part of the 19th century, it has been acknowledged that shortwave infrared (I.R.) radiation from the sun penetrates the atmosphere and warms the Earth. The warm Earth, in turn, radiates heat back into space as longer wavelength I.R. CO2 and other GHGs absorb the longer I.R. wavelengths, warming the air from below. This is why air temperature decreases with altitude, and high mountain peaks are perpetually snow-covered.

Graphical user interface, chart Description automatically generatedMathematical climate models are complex simulations that represent the interactions of significant climate components (atmosphere, land surface, ocean, and sea ice), with a specific focus on Earth’s energy balance. These models predict that a warmer atmosphere leads to unstable climates by melting polar ice caps, altering ocean currents, and rising sea levels. Warm air holds more water vapor than cold air; thus, a warmer climate will result in more intense droughts along with more intense storms. Climate change is already occurring, as is evident in the climate data (Figure 4). Based on multiple sources of evidence, human-produced or “anthropogenic” GHG is the leading cause of climate change. An excellent resource to learn about climate change and GHG is the American Chemical Society’s climate toolkit.

Figure 4: change in temperature over time from different sources. Note that temperature has gone up from the 1960s and compared it to the data in Figure 1.

Source: (Muller 2013)

For the last century, human civilization and progress have thrived from readily available fossil fuels. Most electricity is generated by burning fossil fuels, and most vehicles run on liquid fuels like gasoline or diesel. Coal and natural gas are used directly in industrial processes ranging from steelmaking to cement manufacturing. Despite a significant push towards renewable energy (wind turbines and solar) and a sixty-year history of nuclear power deployment, the United States still obtains 80 percent of its primary energy from fossil fuels with the largest economy globally. The second-largest economy, China, obtains 86 percent of its energy from fossil fuels. Replacing these fuels with energy resources that emit zero GHG is an enormous challenge.

Addressing climate change is a complex problem and will require the incorporation of multiple solutions. The Intergovernmental Panel on Climate Change (IPCC) Special Report on Global Warming of 1.5 Degrees states that global emissions of GHGs must reach net-zero by 2050 to limit warming to 1.5 degrees C. This will mean switching to carbon-neutral or carbon-free energy sources, reducing CO2 emissions from other industrial processes, developing carbon-neutral or CO2 negative materials, and removing CO2 directly from the atmosphere.

Compared to the 34 billion metric tons of anthropogenic CO2 released globally to the atmosphere in 2020, the annual amount of CO2 captured and stored by all of humanity was only roughly 5 million metric tons in 2020. There are several ways by which this is currently accomplished. The CO2 generated from prominent industrial sources, such as power plants, can be captured at the source and stored/isolated from the atmosphere. This process is known as carbon capture and storage or CCS. CCS has not been implemented widely as the process is expensive. Still, the economics can be improved if a profitable use can be found for the captured CO2 (referred to as CCUS, for carbon capture “utilization” and storage). Ambient atmospheric GHG levels can be reduced by removing CO2 directly from the air with direct air capture or DAC (Kramer, 2018). DAC can be achieved biologically by planting trees or growing algae or mechanically by the chemical removal of CO2. Carbon dioxide captured by mechanical DAC must be stored similarly to CCS.

Current designs to capture CO2 at the source point (CCS) are bulky and limited to stationary sources of carbon dioxide, such as power plants. The two primary existing processes for separating CO2 from flue gases are chemical or cryogenic, although membrane separation may yield another potential approach (Songolzadeh et al., 2014). Chemical methods use amines to absorb carbon dioxide directly from the flue gas and release it elsewhere for storage by changing the pressure or temperature. The cryogenic process works by freezing the CO2 out of the air, converting it to solid “dry ice” at very cold temperatures (-109.3 °F or -78.5 °C). Neither approach is energy efficient– the energy cost for carbon capture is 15 percent or more of a power plant’s output and does not account for the cost associated with sequestration and transport.

Carbon dioxide at the moment has low commercial value, limiting the potential for utilization in CCUS. Industries that utilize the gas harvest it directly from CO2 wells in naturally occurring underground reservoirs at the cost of $30 to $40 per ton (Kramer, 2018). Depending on the method deployed, capturing carbon dioxide from flue gases costs about $100 to $200 per ton. This price disparity has hobbled CCUS. Currently, the primary use for captured CO2 is to re-pressurize depleted petroleum reservoirs for enhanced oil recovery (EOR) operations. EOR is done primarily because the CO2 is available for oilfield operations and receives a tax credit since the CO2 remains sequestered underground. However, more petroleum to be burned may offset any net carbon storage and does not help with the climate crisis at hand.

Another concern with the “utilization” component of CCUS is the challenge of transporting the captured carbon dioxide from the source to the use location. If a power plant is near an enhanced oil recovery area, then seamless transport can be achieved. For example, Petra Nova Project (CCUS) captures about 90 percent of the CO2 emissions from a coal-fired powerplant near Houston, Texas. It transports the gas via pipeline to Hilcorp’s West Ranch oil field, located near Vanderbilt, Texas, in EOR operations. Project plans call for the eventual sequestration of some 1.4 million metric tons of CO2 annually.

In contrast, direct air capture (DAC) systems have the potential advantage of removing CO2 directly from the atmosphere with no restriction to a specific CO2 source. A DAC system can be placed in an area with favorable geologic features for carbon storage, eliminating the need for dedicated transport pipelines.

The three main storage options for CO2 are 1) geologic storage deep underground, 2) terrestrial storage in soils, vegetation, or manufactured materials on the surface, and 3) ocean storage in deep seawater (Ajayi et al., 2019).

Geologic storage seeks to place CO2 deep underground to keep it isolated and stored for the long term. It is done by compressing CO2 into deep rocks. At elevated pressures, carbon dioxide forms what is known as a “supercritical fluid,” where the compressed gas transforms into a high-density liquid. The so-called “critical point” where this occurs for CO2 is 88 degrees F at 1070 psi (31 degrees C at 7.38 MPa). In rock formations under normal hydrostatic pressure gradients, the transformation occurs at depths of about 2,500 feet (800 m). At this point, a small increase in pressure will cause a significant increase in the density of the supercritical fluid. Thus, substantially more CO2 can be stored in rock formations as a supercritical fluid than gas. Depending on the geologic storage option under consideration, this can be important.

The most popular geologic storage options include the following:

  • Depleted conventional oil and gas fields: These held oil and natural gas underground over extended periods in porous rocks sealed within a geologic trap like a fold or an offset along a fault. If the integrity of the trap was not compromised during oilfield operations, the depleted field contains empty pore space that could potentially store CO2. Depleted fields have existing wells that can be used for injection, and the injected CO2 can often be used to recover additional oil from the reservoir. This has been done on old oilfields in Texas, Louisiana, and Wyoming. The economics require relatively high oil prices. However, there is a concern that the stored CO2 might leak out of the geologic reservoir and migrate back to the surface. Potential flow paths to the surface include a possible breach in the caprock from pressure cycling during oil production and leaks created by the deterioration of the materials used to construct wells, such as steel casing and downhole cement (Watson and Bachu, 2009).
  • Coal seams: The organic carbon that makes up the bulk of coal can adsorb or chemically attach itself to CO2, providing a significant amount of storage estimated to store 85-100 Gt of CO2. Coal seams that have not been mined because they are too deep or too thin are potential candidates for CO2 storage. Coal seam storage of CO2 has been investigated in the laboratory, but no large-scale field tests have been conducted.
  • Depleted gas shales: Organic-rich shales that have been hydraulically fractured (“fracked”) to produce natural gas may provide another option for CO2 storage once they are depleted (Levine et al., 2016). Like conventional oil and gas reservoirs, depleted shales would have existing wells and empty pore space for CO2, and like coal, the organic-rich shale would also adsorb a component of the gas. However, it is unclear when production companies would declare a shale gas well “depleted.” These are known to produce slow but steady amounts of natural gas for decades. In addition, the possible effects of fracking on the integrity of shale for CO2 storage are unknown. There have been laboratory experiments, but the shale gas industry vehemently opposes any field tests of CO2 injection into gas shales.
  • Deep saline aquifers: Porous rocks at great depths contain very salty water rather than the fresh groundwater obtained near the surface. This saltwater can hold CO2 in solution under high pressure. Dissolved CO2 requires less subsurface pore volume than gaseous or even supercritical CO2 to store the same amount. The downside is that drilling to the depths of these saltwater aquifers is expensive. Also, carbon dioxide forms a weak acid when dissolved in water, and the potential effects on wells and the rock formation itself are unclear.
  • Basaltic lava rocks: These rocks weather easily and release calcium and magnesium into a solution that reacts chemically with the CO2 and turns it into the solid carbonate minerals calcite and magnesite. A significant advantage of the mineralization process is that once converted, and the CO2 is essentially fixed. Basalts contain the correct minerals for providing Ca and Mg, but they are often highly fractured, and it is not clear how well the CO2 will be contained within the rock while undergoing the conversion to mineral form. However, the required residence time appears relatively short; field experiments in Iceland found that CO2 injected into basalt formed carbonates in as little as two years (Matter et al., 2016).

Terrestrial storage of CO2 seeks to store the gas in soils or vegetation or utilize CO2 in construction materials to keep it out of the atmosphere for an extended period. Storage in terrestrial ecosystems uses soils and biomass in forests to sequester CO2 as organic carbon (Litynski et al., 2006). Another option is to use biofuels to capture the CO2 from the air through plant growth and subsequently apply CCS when the fuel is burned to store the CO2. This is known as biofuel energy carbon capture and storage, or BECCS. Other ideas for terrestrial carbon storage include:

  • Concrete manufacturing is a major emitter of GHG, so using it to sequester CO2 can substantially offset these emissions. The material that holds concrete together is cement, made of calcium oxide (CaO) that reacts with CO2 as the concrete cures to form calcite. Several methods have been developed to introduce CO2 into the cement mixture to enhance this reaction, sequester the CO2, and make the concrete stronger. Once locked down in the concrete, the CO2 stays in place for long periods. Sealed greenhouses: Various exotic hardwoods and other desirable plant-based construction materials like bamboo could be grown quickly in greenhouses containing a CO2-enriched atmosphere. It is unclear if this approach can be scaled up to make much of a difference towards climate change.
  • Microbial conversion to methane: CO2, provided to cultures of anaerobic bacteria, is converted into methane gas. CO2 from the biomethane combustion could be captured and recycled or permanently sequestered in a BECCS system.
  • Microbial conversion of CO2 to valuable materials: Microbes can convert CO2 to calcite or create graphene, carbon fiber, carbon nanotubes, or other desirable materials from CO2.
  • Chemical conversion of CO2 to fuels or materials: Chemical engineering technology can convert CO2 into ethylene and other products or feedstock materials that are currently fossil sourced. The economics of these processes remains uncertain.

Ocean storage of CO2 involves injecting carbon dioxide into seawater at depths greater than one kilometer from ships, pipelines, or offshore platforms. The CO2 is supercritical with a density greater than water at these depths and will dissolve and disperse without coming to the surface (Herzog et al., 2000). However, given the concerns about ocean acidification by CO2 inputs from the atmosphere, major environmental impacts could be on deep-sea biota near concentrated CO2 injection points (Seibel and Walsh, 2003). Ocean storage remains in the research stage without any actual field tests (Ajayi et al., 2019).

The IPCC recommends that at least 10 billion tons of CO2 be removed annually to avoid the worst aspects of climate change (IPCC, 2018). We have released an overabundance of carbon into the atmosphere, and the proverbial bathtub is overflowing. Unfortunately, it will always be more cost-effective to pollute. So widespread and stringent carbon tax policies are necessary to facilitate more favorable economics for CCS, CCUS, and DAC systems, to stimulate further development and deployment. Market-based solutions, such as carbon fee and dividend policies, which distribute proceeds from carbon taxes back to the population, are growth-stimulating and equitable, representing a viable path to accomplishing this goal. The world has reached a point where urgent action in this direction is required to avoid massive economic damage and the further destruction of this priceless planet.