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The energy landscape is changing worldwide, with a drastic reduction in sulfur dioxide (precursor to sulfuric acid, H2SO4) emitted from fossil fuel combustion. As a result, acid-base chemistry leading to new particle formation (NPF) from sulfuric acid is decreasing. At the same time, photooxidation of biogenic organosulfur compounds leading to the formation of H2SO4 and methanesulfonic acid (MSA) is expected to become more important. Aqueous solutions of alkanolamines have been proposed as carbon capture technology media to store carbon dioxide from stack plumes before release into the atmosphere. It is therefore expected that some of the alkanolamines will be released, making it critical to understand their atmospheric fates including their role in new particle formation and growth. We expanded our experimental studies of nucleation from the reaction of MSA with simple amines to the multifunctional alkanolamines, including mononethanolamine (HO(CH2)2NH2; MEA) and 4-aminobutanol (HO(CH2)4NH2; 4AB). Experiments were performed in a 1-m borosilicate flow reactor under dry conditions as well as in presence of water. These two systems were shown to produce sub-10 nm particles with MSA extremely efficiently. Surprisingly, the presence of water did not enhance NPF, in contrast to the drastic effect water had on small alkylamine reactions with MSA. This is likely due to the fact that MEA and 4AB have an -OH group that provides additional H-bond interactions within the cluster. Sampling of the chemical composition of these small nanoparticles with high resolution and high transmission was possible down to 3-4 nm using a novel high-flow differential mobility analyzer (half-mini DMA) interfaced to a thermal chemical ionization mass spectrometer (TDCIMS). There was no size dependence for the acid-to-base molar ratio (1:1) for either amine. Integration of these data with preliminary results obtained for a simple C4 alkylamine (butylamine) and a C4 diamine (putrescine) will be discussed in the context of developing a molecular structure-reactivity scheme for new particle formation from MSA and amines of varying structures.
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Probing sub-10nm nanoparticle chemical composition from reactions of methansulfonic acid with multifunctional amines using thermal desorption chemical ionization mass spectrometry (TDCIMS)
(1) Introduction. Although new particle formation (NPF) constitutes an important process in air, there are large uncertainties regarding which species participate in the formation of the first nanoclusters. Acid-base reactions are known generate new particles, with methanesulfonic acid (MSA) from the photooxidation of biogenic organosulfur compounds becoming more important with time relative to sulfuric acid as fossil-fuel related sources of the latter decline. Simultaneously, the use of alkanolamines in carbon capture and storage (CCS) is expected to result in increased atmospheric concentrations of these bases. This study applied a unique mass spectrometry method to examine the chemical composition of 2-10 nm particles from the MSA reaction with monoethanolamine and 4-aminobutanol, the most efficient system for NPF from MSA examined to date. (2) Methods. Thermal desorption chemical ionization mass spectrometry (TDCIMS, HToF mass analyzer, Tofwerk AG) was used to measure the size and acid-to-base molar ratios of nanoparticles formed from the reaction of MSA with multifunctional amines. A high-flow differential mobility analyzer (half-mini DMA, SEADM) was interfaced with the TDCIMS, which provides a high mobility resolution and high particle transmission in the diameter range 2-10 nm, where chemical composition measurements are the most challenging due to the very small amount of mass. With this novel combination of techniques we were able to examine MSA-amine systems either from nanoparticles exiting the outlet of a flow reactor or nanoclusters generated via electrospray. (3) Preliminary Data. These experiments show that MSA-driven acid-base reactions with monethanolamine or 4-aminobutanol are even more efficient in NPF than that of simple alkylamines, exhibiting to date the highest nanoparticle formation rates measured in laboratory flow tube studies. The observed enhancement is rooted in the presence of an -OH group on the parent molecules, which initiates a H-bond network throughout the nanoclusters. In these systems, water had only a minimal enhancing effect. We demonstrated that the nanoparticles formed in both systems are neutral (i.e. contain as much acid as base molecules) in the range 2-10 nm. This contrasts with MSA reactions from previous studies on the smallest alkylamine, methylamine, where particles smaller than 9 nm were more acidic. Investigations of reactions of MSA with a diamine (1,4-diaminobutane) showed a similar pattern of neutral particles across the diameter range studied and experiments with larger alkylamine, butylamine, are underway to probe the relationship between structure- and NPF potential from MSA. These findings highlight that there is no “one size-fits-all” regarding NPF from MSA reactions with amines and illustrates the need for studies of more complex amines to fully characterize the NPF potential of this atmospherically relevant strong acid. (4) Novel Aspect. The combination of TDCIMS with a novel particle sizing system provided the chemical composition of 2-10 nm particles.
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- Award ID(s):
- 1928252
- PAR ID:
- 10521385
- Publisher / Repository:
- ASMS 2024 Anaheim
- Date Published:
- Format(s):
- Medium: X
- Location:
- ASMS 2024 Anaheim
- Sponsoring Org:
- National Science Foundation
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