Related Experiment Video
Updated: Aug 29, 2025

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
Published on: April 8, 2020
Clusteromics IV: The Role of Nitric Acid in Atmospheric Cluster Formation
1Department of Chemistry, Aarhus University, Langelandsgade 140, 8000 Aarhus C, Denmark.
Abstract:
Nitric acid (NA) has previously been shown to affect atmospheric new particle formation; however, its role still remains highly uncertain. Through the employment of state-of-the-art quantum chemical methods, we study the (acid)1-2(base)1-2 and (acid)3(base)2 clusters containing at least one nitric acid (NA) and sulfuric acid (SA) or methanesulfonic acid (MSA) with bases ammonia (A), methylamine (MA), dimethylamine (DMA), trimethylamine (TMA), and ethylenediamine (EDA). The initial cluster configurations are generated using the ABCluster program. PM7 and ωB97X-D/6-31++G(d,p) calculations are used to reduce the number of relevant configurations. The thermochemical parameters are calculated at the ωB97X-D/6-31++G(d,p) level of theory with the quasi-harmonic approximation, and the final single-point energies are calculated with high-level DLPNO-CCSD(T0)/aug-cc-pVTZ calculations. The enhancing effect from the presence of nitric acid on cluster formation is studied using the calculated thermochemical data and cluster dynamics simulations. We find that when NA is in excess compared with the other acids, it has a substantial enhancing effect on the cluster formation potential.
Related Concept Videos
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
2° Amines to N-Nitrosamines: Reaction with NaNO2
Preparation of Carboxylic Acids: Hydrolysis of Nitriles
Rate-Determining Steps
In a multistep reaction mechanism, one of the elementary steps progresses significantly slower than the others. This slowest step is called the rate-limiting step (or rate-determining step). A reaction cannot proceed faster than its slowest step, and hence, the rate-determining step limits the overall reaction rate.
The concept of rate-determining step can be understood from the analogy of a 4-lane freeway with a short-stretch of traffic-bottleneck caused due to...
Nitriles to Carboxylic Acids: Hydrolysis

