Use of Solid Acids in Carbonate Based Carbon Capture Systems

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Description
In order to develop a new approach to carbon capture using carbonate brines and solid acids, this research project begins the development of a theoretical basis for solid acid based capture systems and experimental work to test the validity of

In order to develop a new approach to carbon capture using carbonate brines and solid acids, this research project begins the development of a theoretical basis for solid acid based capture systems and experimental work to test the validity of the theory. It appears that solid acids behave like weak acids and are able to increase the concentration of carbon dioxide above a solution compared to what would be achievable without solid acids. Experimental work aimed to show that solid acids behave as indicated by theory. Experiments partially validated the theory through demonstrating desorption of carbon dioxide from a carbonate brine. The regeneration of the solid acid with the help of a strong acid was only partially successful due to instability of the solid acid in the presence of a strong acid. The experimental work used activated.
Date Created
2024
Agent

Mathematical Modeling of Moisture Swing Sorption in Ion-Exchange Resins (IER) for Passive Direct Air Capture of CO2

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Description
The cost of capturing carbon dioxide (CO2) from ambient air needs to be greatly reduced if it is to contribute significantly to mitigating climate change. Ion-exchange resin (IER) with quaternary ammonium cation binds CO2 when dry and releases it when

The cost of capturing carbon dioxide (CO2) from ambient air needs to be greatly reduced if it is to contribute significantly to mitigating climate change. Ion-exchange resin (IER) with quaternary ammonium cation binds CO2 when dry and releases it when wet without supplemental energy, making the process attractive for economical Direct Air Capture (DAC). In this study, a design case basis was developed for a system of collectors capable of capturing 1000 tons/day of CO2 via moisture swing sorption. The model uses varying weather parameters such as temperature, wind speed, and relative humidity to understand the impact of weather on the sorbent loading, cycle time (capture and regeneration), and net water loss. Two independent isotherm models, namely Flory Huggins and the modified Langmuir isotherm model were used to estimate the water and CO2 loading of the resin respectively as a function of relative humidity. The capture model suggests a higher capture rate during the summer and daytime (in a diurnal cycle) as the relative humidity is lower. A design optimization model was developed to minimize the capture time and maximize the sorbent loading. The crude rate production and the net water loss can help conduct an economic analysis to determine the cost of carbon capture.
Date Created
2023
Agent

Functional Materials for the Direct Air Capture of Carbon Dioxide

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Description
The excessive use of fossil fuels over the last few centuries has led to unprecedented changes in climate and a steady increase in the average surface global temperatures. Direct Air Capture(DAC) aims to capture CO2 directly from the atmosphere and

The excessive use of fossil fuels over the last few centuries has led to unprecedented changes in climate and a steady increase in the average surface global temperatures. Direct Air Capture(DAC) aims to capture CO2 directly from the atmosphere and alleviate some of the adverse effects of climate change. This dissertation focuses on methodologies to make advanced functional materials that show good potential to be used as DAC sorbents. Details on sorbent material synthesis and post-synthesis methods to obtain high surface area morphologies are described in detail. First, by incorporating K2CO3 into activated carbon (AC) fiber felts, the sorption kinetics was significantly improved by increasing the surface area of K2CO3 in contact with air. The AC-K2CO3 fiber composite felts are flexible, cheap, easy to manufacture, chemically stable, and show excellent DAC capacity and (de)sorption rates, with stable performance up to ten cycles. The best composite felts collected an average of 478 µmol of CO2 per gram of composite during 4 h of exposure to ambient (24% RH) air that had a CO2 concentration of 400-450 ppm over 10 cycles. Secondly, incorporating the amino acid L-arginine (L-Arg) into a poly(vinyl alcohol) (PVA) nanofiber support structure, created porous substrates with very high surface areas of L-Arg available for CO2 sorption. The bio-inspired PVA-Arg nanofiber composites are flexible and show excellent DAC performance compared to bulk L-Arg. The nanofiber composites are fabricated from an electrospinning process using an aqueous polymer solution. High ambient humidity levels improve sorption performance significantly. The best performing nanofiber composite collected 542 µmol of CO2 per gram of composite during 2 h of exposure to ambient, high humidity (100% RH) air that had a CO2 concentration of 400-450 ppm. Finally, poly(vinyl guanidine) (PVG) polymer was synthesized and tested for sorption performance. The fabrication of PVG nanofibers, divinyl benzene crosslinked PVG beads and glutaraldehyde crosslinked PVG were demonstrated. The sorption performance of the fabricated sorbents were tested with the glutaraldehyde crosslinked PVG having a dynamic sorption capacity of over 1 mmol of CO2 per gram of polymer in 3 h. The sorption capability of liquid PVG was also explored.
Date Created
2024
Agent

Contract Design and Enforcement in Carbon Management

Description

To mitigate climate change, carbon needs to be removed from the atmosphere and stored for thousands of years. Currently, carbon removal and storage are voluntarily procured, and longevity of storage is inconsistently defined and regulated. Clauses can be added to

To mitigate climate change, carbon needs to be removed from the atmosphere and stored for thousands of years. Currently, carbon removal and storage are voluntarily procured, and longevity of storage is inconsistently defined and regulated. Clauses can be added to procurement contracts to require long-term management and increase the durability of storage. Well-designed and properly enforced contracts can pave the way to future regulation for long-term carbon management.

Date Created
2023-05
Agent

A conceptual framework for the certification of carbon sequestration

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Description

This document details a conceptual Framework for the Certification of Carbon Sequestration (FCCS). It is based on a system designed to support negative emissions. It provides the minimum requirements for the development of carbon sequestration standards and certificates of carbon

This document details a conceptual Framework for the Certification of Carbon Sequestration (FCCS). It is based on a system designed to support negative emissions. It provides the minimum requirements for the development of carbon sequestration standards and certificates of carbon sequestration. It allows the certification of standards so that they in turn produce certification of removed carbon that authenticates durability and verifiability. The framework (i) identifies an organizational structure for the certification system, (ii) clarifies the responsibility of participating entities, (iii) provides certificate designs and usages, (iv) details the requirements to develop measurement protocols, (v) provides mechanisms to support a long-term industry, and (vi) outlines a vision towards durable storage.

Date Created
2022-12-05
Agent

Experimental Characterization of Sorbents for Direct Air Capture of Carbon Dioxide

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Description
Climate change poses a serious challenge humankind. Society’s reliance on fossil fuels raises atmospheric CO2 concentrations causing global warming. Already, the planet has warmed by 1.1 °C making it nearly impossible to heed the advice of the IPCC (2022) and

Climate change poses a serious challenge humankind. Society’s reliance on fossil fuels raises atmospheric CO2 concentrations causing global warming. Already, the planet has warmed by 1.1 °C making it nearly impossible to heed the advice of the IPCC (2022) and prevent warming in excess of 1.5 °C by 2050. Even the current excess of CO2 in the atmosphere poses significant risks. Direct air capture (DAC) of CO2 offers one of the most scalable options to the drawdown of carbon. DAC can collect CO2 that is already diluted into the atmosphere for disposal or utilization. Central to most DAC are sorbents, i.e., materials that bind and release CO2 in a capture and release cycle. There are sorbents that cycle through a temperature swing. Others use a moisture swing, or a pressure swing or combinations of all of them. Since DAC is still a nascent technology, advancement of sorbents is an important part of DAC development. There is a nearly infinite combination of possible sorbents and form factors of sorbents that can be deployed in many different variations of DAC. Our goal is to develop a methodology for characterizing sorbents to facilitate rational choices among different options. Good sorbent characteristics include high capacity, fast sorption and desorption kinetics, low energy need for unloading, and longevity. This work presents the development of a systematic approach to evaluate sorbents from the milligram to tonne scale focusing on the important characteristics mentioned above. The work identified a good temperature swing sorbent whose characterization moved from the mg to kg scale without loss in performance. This work represents a first step in systematizing sorbent characterization for rational sorbent development programs.
Date Created
2022
Agent

The socio-economic and technical context for Direct Air Capture in decarbonization pathways

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Description

Workshop report on socio-economic and technical discussions Direct Air Capture as a technology for the climate transition.

Date Created
2022-01-19
Agent

Carbon Removal Accounting Methodologies: How to rethink the system for negative carbon emissions

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Description

We analyze current approaches to carbon accounting for removed carbon sold on carbon markets, focusing on carbon crediting under the framing of a remaining carbon budget, the issue of durability, and approaches to accounting methodologies. We explore the topic of

We analyze current approaches to carbon accounting for removed carbon sold on carbon markets, focusing on carbon crediting under the framing of a remaining carbon budget, the issue of durability, and approaches to accounting methodologies. We explore the topic of mixing carbon with other problems in developing carbon accounting methodologies and highlight the open policy questions. We conclude with a suggested framework for accounting for carbon removal accounting that simplifies climate action and enables a world with negative carbon emissions.

Date Created
2022-11-01
Agent

Numerical Simulation of Moisture Swing Absorption Model for Carbon Dioxide Capture

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Description
The current level of carbon dioxide in ambient air is increasing and reinforcing the severity of global warming. Several techniques have been developed to capture the gas directly from the air. Moisture swing absorption (MSA) is a mechanism through

The current level of carbon dioxide in ambient air is increasing and reinforcing the severity of global warming. Several techniques have been developed to capture the gas directly from the air. Moisture swing absorption (MSA) is a mechanism through which a reactive surface, namely resin beads, absorbs carbon dioxide when dry and releases it when wet. The ionic complexity of the surface of the bead interacts with CO2 when H2O contents are low, and CO2 diffuses as bicarbonate or carbonate. Hence, diffusion-drift-reaction equations describe the moving species behavior MS sorbent. A numerical model has been developed previously applying finite difference scheme (FDS) to estimate the evolution of species concentrations over uniform time and space intervals. The methodology was based on a specific membrane and bead geometry. In this study, FDS was employed again with modifications over the boundary conditions. Neumann boundary condition was replaced by Robin boundary condition which enforced diffusion and drift fluxes at the center of the sorbent. Furthermore, the generic equations were approximated by another numerical scheme, Finite volume scheme (FVS), which discretizes the spatial domain into cells that conserves the mass of species within. The model was predicted to reduce the total carbon mass loss within the system. Both schemes were accommodated with a simulated model of isolated chamber that contained arbitrary sorbent. Moreover, to derive the outcomes of absorption/desorption cycles and validate the performance of FVS, Langmuir curve was utilized to obtain CO2 saturation in the sorbent and examine two scenarios: one by varying the partial pressure of CO2 (PCO2) in the chamber at constant H2O (PH2O), or changing PH2O at constant PCO2. The results from FDS approximation, when adjusting the center with Robin boundary condition, show 0.11% lower carbon mass gain than when applying Neumann boundary condition. On the other hand, FVS minimizes the mass loss by 0.3% lower than the original total carbon mass and achieves sorbent saturation without any adjustment. Moreover, the isotherm curve demonstrates that increasing PH2O reduces CO2 saturation and is dependent on the linear and non-linear correlations used to estimate water concentration on the surface.
Date Created
2021
Agent

Occurrence and Speciation of Bromine and Iodine in Drinking Water Sources

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Description

Halogens in drinking water sources, such as bromine (Br) and iodine (I) pose no direct health risk, but are critical precursors in formation of cyto- and genotoxic brominated and iodinated (Br-/I-) DBPs. However, few spatial or historic datasets exist for

Halogens in drinking water sources, such as bromine (Br) and iodine (I) pose no direct health risk, but are critical precursors in formation of cyto- and genotoxic brominated and iodinated (Br-/I-) DBPs. However, few spatial or historic datasets exist for bromine and iodine species in drinking water sources. This dissertation aims to quantify and understand the occurrence and speciation of Br and I in groundwater and surface water serving as source waters for drinking water treatment plants (DWTPs). Aggregation of data from >9000 non-drinking water sampling locations in USA collected from 1930-2017 on halides (bromide (Br-) and iodide (I-)) determined that Br- concentrations were 50 μg/L and 100 μg/L; and I- concentrations were 12 μg/L and 13 μg/L in surface and groundwater respectively. Although, these locations were not drinking water sources, this first of its kind analysis provides potential bounds for Br- and I-. To focus specifically on DWTP sources, a nationwide survey of >250 drinking water sources was conducted between 2018-2020. Br- ion is the only bromine specie, whereas both inorganic (iodide and iodate ions) and organic iodine occur. I- concentrations ranged from 1-250 μg/L and are 4 to 100 times lower than Br- concentrations (10-7800 μg/L, median=80 μg/L). No strong correlation exists between bromide and iodide occurrence (R<0.5, p<0.005). I- was detected in 50% of the samples (75th percentile=5 μg/L) and IO3- was detected in 40% (75th percentile=3 μg/L) of all the samples. To quantify iodine species, tandem ion chromatography and inductively coupled plasma mass spectrometry was applied for the first time in drinking water sources. I- and IO3- peaks were well resolved and have minimum detection limit of 0.4 μg/L and 0.7 μg/L respectively. Organic iodine (Org-I) peaks in select drinking water samples from the nationwide survey were partically resolved ranging from <5 to 40 μg/L. This dissertation provides updated nationwide Br- survey and first ever national I species survey. The data generated through this dissertation will be useful to further Br-/I-DBP formation and toxicity research by providing relevant drinking water sources information. Future research targeting Br- and I- removal is advocated for managing Br-/I-DBPs in watersheds.

Date Created
2021
Agent