{"title":"Nanobubbles in Bulk Solution and Electrosprayed Microdroplets Accelerate Chemical Reactions","authors":"Bincy Binny, George Joseph, Andre R. Venter","doi":"10.1021/jasms.6c00359","DOIUrl":null,"url":null,"abstract":"<p>Bulk\r\nnanobubbles (NBs) are metastable gas-filled voids in solution,\r\nwith diameters of nearly 200 nm that exhibit long lifetimes and large\r\nsurface-to-volume ratios. Recent studies have shown that chemical\r\nreactions are significantly accelerated within sprayed microdroplets\r\nduring electrospray ionization mass spectrometry (ESI-MS). Although\r\nseveral factors, such as partial solvation of reagents, electric fields,\r\nordered orientation, and pH, have been implicated in the acceleration\r\nin microdroplets, the primary governing factor remains unclear and\r\ndependent on the system. Similar processes occur on the nanobubble–liquid\r\ninterface, leading to enhanced reaction rates when they are present\r\nin bulk solution. We demonstrate reaction rate acceleration by deliberately\r\nadding NBs to the bulk solution and microdroplets by considering two\r\nmodel systems: the Katritzky transamination reaction and the reaction\r\nbetween CO<sub>2</sub> and <em>N</em>,<em>N</em>-dibutyl-1,3-propane\r\ndiamine (DBPA). N<sub>2</sub> and CO<sub>2</sub> nanobubbles were\r\ngenerated using sonication, pressure cycling (PC), or the Tesla valve\r\n(TV) and delivered as bulk or spray solvents. The Katritzky reaction\r\nin bulk solution with NB-enriched solvent systems was examined by\r\nmass spectrometry under nonaccelerating electrospray conditions. The\r\nacceleration factor (AF) for the reaction doubled compared with the\r\ncontrol. On the other hand, the microdroplet accelerated the Katritzky\r\nreaction, with N<sub>2</sub> NB producing a further six-fold acceleration\r\ncompared to the microdroplet control. For the reaction of the diamine\r\nDBPA with N<sub>2</sub> nebulization, CO<sub>2</sub> reagent delivery\r\nby NB resulted in acceleration factors between 2 and 50 compared to\r\nthe microdroplet reaction control, depending on the solvent fraction,\r\nwherein bubbles were generated. With CO<sub>2</sub>, nebulization\r\nwhere ample reagent is already present, the addition of NBs produced\r\na further two-to-five-fold acceleration factor depending on the solvent\r\nfraction in which NBs were generated, indicating a NB catalytic effect.\r\nOur findings show that NBs improve reaction kinetics by acting both\r\nas improved reagent delivery vehicles and/or as catalysts. Catalytic\r\nactivity is a consequence of increased liquid–air interfacial\r\nsurface area and improved reagent transport in bulk solution and within\r\nmicrodroplets.</p>","PeriodicalId":672,"journal":{"name":"Journal of the American Society for Mass Spectrometry","volume":"37 10","pages":"2609–2617"},"PeriodicalIF":2.9000,"publicationDate":"2026-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Society for Mass Spectrometry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jasms.6c00359","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/9 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Bulk
nanobubbles (NBs) are metastable gas-filled voids in solution,
with diameters of nearly 200 nm that exhibit long lifetimes and large
surface-to-volume ratios. Recent studies have shown that chemical
reactions are significantly accelerated within sprayed microdroplets
during electrospray ionization mass spectrometry (ESI-MS). Although
several factors, such as partial solvation of reagents, electric fields,
ordered orientation, and pH, have been implicated in the acceleration
in microdroplets, the primary governing factor remains unclear and
dependent on the system. Similar processes occur on the nanobubble–liquid
interface, leading to enhanced reaction rates when they are present
in bulk solution. We demonstrate reaction rate acceleration by deliberately
adding NBs to the bulk solution and microdroplets by considering two
model systems: the Katritzky transamination reaction and the reaction
between CO2 and N,N-dibutyl-1,3-propane
diamine (DBPA). N2 and CO2 nanobubbles were
generated using sonication, pressure cycling (PC), or the Tesla valve
(TV) and delivered as bulk or spray solvents. The Katritzky reaction
in bulk solution with NB-enriched solvent systems was examined by
mass spectrometry under nonaccelerating electrospray conditions. The
acceleration factor (AF) for the reaction doubled compared with the
control. On the other hand, the microdroplet accelerated the Katritzky
reaction, with N2 NB producing a further six-fold acceleration
compared to the microdroplet control. For the reaction of the diamine
DBPA with N2 nebulization, CO2 reagent delivery
by NB resulted in acceleration factors between 2 and 50 compared to
the microdroplet reaction control, depending on the solvent fraction,
wherein bubbles were generated. With CO2, nebulization
where ample reagent is already present, the addition of NBs produced
a further two-to-five-fold acceleration factor depending on the solvent
fraction in which NBs were generated, indicating a NB catalytic effect.
Our findings show that NBs improve reaction kinetics by acting both
as improved reagent delivery vehicles and/or as catalysts. Catalytic
activity is a consequence of increased liquid–air interfacial
surface area and improved reagent transport in bulk solution and within
microdroplets.
期刊介绍:
The Journal of the American Society for Mass Spectrometry presents research papers covering all aspects of mass spectrometry, incorporating coverage of fields of scientific inquiry in which mass spectrometry can play a role.
Comprehensive in scope, the journal publishes papers on both fundamentals and applications of mass spectrometry. Fundamental subjects include instrumentation principles, design, and demonstration, structures and chemical properties of gas-phase ions, studies of thermodynamic properties, ion spectroscopy, chemical kinetics, mechanisms of ionization, theories of ion fragmentation, cluster ions, and potential energy surfaces. In addition to full papers, the journal offers Communications, Application Notes, and Accounts and Perspectives