scholarly journals Review of Hanson et al. Measurement Report: Sulfuric Acid Nucleation and Experimental Conditions in a Photolytic Flow Reactor

2020 ◽  
Author(s):  
Anonymous
2021 ◽  
Vol 21 (3) ◽  
pp. 1987-2001
Author(s):  
David R. Hanson ◽  
Seakh Menheer ◽  
Michael Wentzel ◽  
Joan Kunz

Abstract. Nucleation rates involving sulfuric acid and water measured in a photolytic flow reactor have decreased considerably over a time period of several years. Results show that the system – flow reactor, gas supplies and lines, flow meters, valves, H2SO4 photo-oxidant sources – has reached a baseline stability that yields nucleation information such as cluster free energies. The baseline nucleation rate is punctuated by temporary bursts that in many instances are linked to cylinder changes, delineating this source of potential contaminants. Diagnostics were performed to better understand the system, including growth studies to assess H2SO4 levels, chemiluminescent NO and NOx detection to assess the HONO source, and deployment of a second particle detector to assess the nanoparticle detection system. The growth of seed particles shows trends consistent with the sizes of nucleated particles and provides an anchor for calculated H2SO4 concentrations. The chemiluminescent detector revealed that small amounts of NO are present in the HONO source, ∼ 10 % of HONO. The second condensation-type particle counter indicates that the nanoparticle mobility sizing system has a bias at low sulfuric acid levels. The measured and modeled nucleation rates represent upper limits to nucleation in the binary homogeneous system, H2SO4-H2O, as contaminants might act to enhance nucleation rates and ion-mediated nucleation may contribute. Nonetheless, the experimental nucleation rates, which have decreased by an order of magnitude or larger since our first publication, extrapolate to some of the lowest rates reported in experiments with photolytic H2SO4. Results from experiments with varying water content and with ammonia addition are also presented and have also decreased by an order of magnitude from our previous work; revised energetics of clusters in this three-component system are derived which differ from our previous energetics mainly in the five-acid and larger clusters.


2020 ◽  
Author(s):  
David Roy Hanson ◽  
Seakh Menheer ◽  
Michael Wentzel ◽  
Joan Kunz

Abstract. Nucleation involving sulfuric acid and water has been studied in a photolytic flow reactor over a time period of several years. Results show that the system – flow reactor, gas supplies and lines, flow meters, valves, H2SO4 photo-oxidant sources – has a baseline stability that yields nucleation information such as cluster free energies. The baseline nucleation rate is punctuated by temporary bursts that in many instances are linked to cylinder changes, delineating this source of potential contaminants. Diagnostics were performed to better understand the system include growth studies to assess H2SO4 levels, chemiluminescent NO and NOx detection to assess the HONO source, and deployment of a second particle detector to assess the nanoparticle detection system. The growth studies show trends consistent with calculated H2SO4 levels and also provide an anchor for H2SO4 concentrations. The chemiluminescent detector revealed that small amounts of NO are present in the HONO source, ∼10 % of HONO. The second, condensation-type particle counter indicates that the nanoparticle sizing system has a bias at low sulfuric acid levels. Modeling studies yield nucleation rates as a function of sulfuric acid concentration that probably represent upper limits to nucleation in the binary system, H2SO4-H2O, as contaminants might act to enhance nucleation rates or ion-mediated nucleation may contribute. Nonetheless, the experimental nucleation rates are some of the lowest reported so far in experiments where sulfuric acid is photolytically-generated. Results from experiments with varying water content and with ammonia addition are also described. The energetics of clusters in this three component system reveal a challenging interplay between the components (e.g. previously reported ion-mediated and homogeneous rates are unintentionally similar) and experiments indicate water plays a significant role in nucleation involving sulfuric acid and ammonia.


2016 ◽  
Author(s):  
Coty N. Jen ◽  
Jun Zhao ◽  
Peter H. McMurry ◽  
David R. Hanson

Abstract. Chemical ionization (CI) mass spectrometers are used to study atmospheric nucleation by detecting clusters produced by reactions of sulfuric acid and various basic gases. These instruments typically use nitrate to deprotonate and thus chemically ionize the clusters. In this study, we compare cluster concentrations measured using either nitrate or acetate. Clusters were formed in a flow reactor from vapors of sulfuric acid and dimethylamine, ethylene diamine, tetramethylethylene diamine, or butanediamine (also known as putrescine). These comparisons show that nitrate is unable to chemically ionize clusters with high base content. In addition, we vary the ion-molecule reaction time to probe ion processes which include proton-transfer, ion-molecule clustering, and decomposition of ions. Ion decomposition upon deprotonation by acetate/nitrate was observed. More studies are needed to quantify to what extent ion decomposition affects observed cluster content and concentrations, especially those chemically ionized with acetate since it deprotonates more types of clusters than nitrate. Model calculations of the neutral and ion cluster formation pathways are also presented to better identify the cluster types that are not efficiently deprotonated by nitrate. Comparison of model and measured clusters indicate that sulfuric acid dimer with two diamines and sulfuric acid trimer with two or more base molecules are not efficiently chemical ionized by nitrate. We conclude that acetate CI provides better information on cluster abundancies and their base content than nitrate CI.


2015 ◽  
Vol 69 (5) ◽  
Author(s):  
Melinda Mojzesová ◽  
Mária Mečiarová ◽  
Ambroz Almássy ◽  
Roger Marti ◽  
Radovan Šebesta

AbstractNon-standard experimental conditions can often enhance organocatalytic reactions considerably. The current study explores the effectiveness of a range of non-standard reaction conditions for the asymmetric organocatalytic 1,3-dipolar cycloaddition of a nitrone with α,β-unsaturated aldehydes. The influence of ionic liquids, high-pressure conditions, ultrasound, microwave irradiation and ballmilling was tested as well as the flow process. Because of the low reactivity of the nitrone and unsaturated aldehydes in the 1,3-dipolar cycloaddition, cycloadducts were isolated in only moderate yields from the majority of experiments. However, high diastereo- and enantioselectivities were observed in ionic liquids under solvent-free conditions and in the flow reactor.


1955 ◽  
Vol 38 (5) ◽  
pp. 581-598 ◽  
Author(s):  
Margaret R. McDonald

The proteolytic activity of dilute solutions of clystalline trypsin is destroyed by x-rays, the amount of inactivation being an exponential function of the radiation dose. The reaction yield increases steadily with increasing concentration of trypsin, varying, as the concentration of enzyme is increased from 1 to 300 µM, from 0.068 to 0.958 micromole of trypsin per liter inactivated per 1000 r with 0.005 N hydrochloric acid as the solvent, from 0.273 to 0.866 with 0.005 N sulfuric acid as the solvent, and from 0.343 to 0.844 with 0.005 N nitric acid as the solvent. When the reaction yields are plotted as a function of the initial concentration of trypsin, they fall on a curve given by the expression Y α XK, in which Y is the reaction yield, X is the concentration of trypsin, and K is a constant equal to 0.46, 0.20, and 0.16, respectively, with 0.005 N hydrochloric, sulfuric, and nitric acids as solvents. The differences between the reaction yields found with chloride and sulfate ions in I to 10 µM trypsin solutions are significant only in the pH range from 2 to 4. The amount of inactivation obtained with a given dose of x-rays depends on the pH of the solution being irradiated and the nature of the solvent. The reaction yield-pH curve is a symmetrical one, with minimum yields at about pH 7. Buffers such as acetate, citrate, borate and barbiturate, and other organic molecules such as ethanol and glucose, in concentrations as low as 20 µM, inhibit the inactivation of trypsin by x-radiation. Sigmoid inactivation-dose curves instead of exponential ones are obtained in the presence of ethanol. The reaction yields for the inactivation of trypsin solutions by x-rays are approximately 1.5 times greater when the irradiation is done at 26°C. than when it is done at 5°C., when 0.005 N hydrochloric acid is the solvent. The dependence on temperature is less when 0.005 N sulfuric acid is used, and is negligible with 0.005 N nitric acid. The difficulties involved in interpreting radiation effects in aqueous systems, and in comparing the results obtained under different experimental conditions, are discussed.


The relative concentrations of hydrogen atoms were measured during the oscillatory ignition of hydrogen in a well stirred flow reactor. Comparisons were made with the experimental concentration—time profiles of the hydroxyl radical obtained previously under similar experimental conditions. The predicted concentration profiles obtained from numerical analysis of a thermokinetic model were also compared with the experimental results. Experiments were performed in a 600 cm 3 Pyrex glass, jet-stirred reactor with the reactants, 2H 2 + O 2 , at a total pressure of 16 Torr ( ca . 2132.8 Pa) and at a vessel temperature of 753 K. The mean residence time was 1.2 s. Oscillatory ignition was established at a period of 3 s in which high radical concentrations were attained and in which the temperature rise was almost adiabatic. The concentration-time profile of hydrogen atoms was obtained by a resonance enhanced multiphoton ionization (rempi) which was induced by a laser pulse at energies in the vicinity of 364 nm, with ion collection at a stainless steel probe inserted into the reactor. Supplementary studies were made to characterize the signals and to identify effects of the probe within the reaction volume. A measurement of the relative concentrations of hydrogen atoms was obtained from an integration of the area of the rempi spectrum determined over the laser wavelength range 363.8-364.6 nm. The spectrum was measured at successive times in the oscillatory cycle by imposing a variable delay on the laser firing signal. The results show that, during oscillatory ignition, the maximum concentration of hydrogen atoms was reached and a sharp decay was already well advanced before that of the hydroxyl radicals was attained. The numerical analysis was in very good quantitative accord with this experimental result. The phase difference of the cyclic variation in the H atoms relative to that of OH radicals is a key feature of the kinetic mechanisms which control the oscillatory oxidation of hydrogen.


2016 ◽  
Vol 16 (19) ◽  
pp. 12513-12529 ◽  
Author(s):  
Coty N. Jen ◽  
Jun Zhao ◽  
Peter H. McMurry ◽  
David R. Hanson

Abstract. Chemical ionization (CI) mass spectrometers are used to study atmospheric nucleation by detecting clusters produced by reactions of sulfuric acid and various basic gases. These instruments typically use nitrate to deprotonate and thus chemically ionize the clusters. In this study, we compare cluster concentrations measured using either nitrate or acetate. Clusters were formed in a flow reactor from vapors of sulfuric acid and dimethylamine, ethylene diamine, tetramethylethylene diamine, or butanediamine (also known as putrescine). These comparisons show that nitrate is unable to chemically ionize clusters with high base content. In addition, we vary the ion–molecule reaction time to probe ion processes which include proton-transfer, ion–molecule clustering, and decomposition of ions. Ion decomposition upon deprotonation by acetate/nitrate was observed. More studies are needed to quantify to what extent ion decomposition affects observed cluster content and concentrations, especially those chemically ionized with acetate since it deprotonates more types of clusters than nitrate.Model calculations of the neutral and ion cluster formation pathways are also presented to better identify the cluster types that are not efficiently deprotonated by nitrate. Comparison of model and measured clusters indicate that sulfuric acid dimers with two diamines and sulfuric acid trimers with two or more base molecules are not efficiently chemical ionized by nitrate. We conclude that acetate CI provides better information on cluster abundancies and their base content than nitrate CI.


1983 ◽  
Vol 38 (8) ◽  
pp. 896-908 ◽  
Author(s):  
K. Wörsdorfer ◽  
B. Reimann ◽  
P. Potzinger

Abstract The reactions of hydrogen atoms with silane and the methylated silanes - with the exception of tetramethylsilane -have been investigated in a fast flow reactor. Under our experimental conditions hydrogen abstraction from the Si-H bond is followed by combination of hydrogen atoms with the corresponding silyl radicals. The molecules formed in this way are activated by about 375 kJ/mol of vibrational energy. Two decomposition channels have been unequivocally identified, namely the elimination of molecular hydrogen and of methane, both with concomittant formation of the respective silylenes. In a subsequent step, silylene inserts into the substrate under formation of disilanes. With increasing degree of methylation. stabilization of the activated molecule competes with decomposition and dominates the kinetics in the case of trimethylsilane. With methyl -and dimethyl-silane, methyl radicals are observed as an additional reaction product. On the basis of RRKM calculations it is unlikely that they originate from a direct decomposition of the activated molecules.Absolute values for the room temperature rate constants of the abstraction reactions are given; for H+CH3SiH3, Arrhenius parameters have been determined.


1973 ◽  
Vol 19 (10) ◽  
pp. 1128-1134 ◽  
Author(s):  
Thomas E Hewitt ◽  
Harry L Pardue

Abstract We studied the kinetics of the reaction between cholesterol and sulfuric acid in acetic acid-acetic anhydride medium. Results have been used to establish near-optimal conditions for the fast kinetic determination of cholesterol in serum. The reaction rate measured during the first 20 s of the reaction is proportional to cholesterol concentration. There is good agreement (<2% deviation) between pseudo-first-order rate constants for cholesterol standards and sera. Recoveries of standard cholesterol added to sera range from 99% to 104% (average, 100.7%). Values for serum cholesterol by this kinetic determination tend to be somewhat lower than equilibrium values reported by local hospital laboratories. Whether bilirubin interferes depends on reaction conditions; under optimal conditions, each milligram of bilirubin is kinetically equivalent to about 1 mg of apparent cholesterol. Kinetic data are included to show how results are degraded by operating under nonoptimal conditions, and considerations involved in changing experimental conditions are discussed.


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