Time constant analysis of tropospheric gas-phase chemistry
Literature Information
Time constants are often used to describe and categorize the time dependence of concentrations in chemically reactive systems. Though originally deduced for linear systems (defined as those that have chemical balance equations that are linear in the concentrations), they are also useful for non-linear problems. Here, the concept is reviewed for tropospheric gas-phase chemistry which is substantially non-linear due to the majority of bimolecular reactions introducing quadratic terms into the balance equations. Application to a simplified reaction scheme reveals that, in many cases, the time constants for the locally linearized equations provide a reasonable approximation to the global (as opposed to local in the above sense) temporal behaviour. For a simple CO, NOx, O3 and HOx chemistry, the range of time constants is characterized by one group of small values below 10 min separated by a substantial gap from longer term processes with time constants above 1 day. For NOx<1 ppb, an assignment of time constants to the relaxation of specific compounds is approximately possible. For NOx>1 ppb, in particular around the NOx mixing ratio that maximizes the OH concentration, the analysis indicates linearly unstable motion with an exponential increase on a time scale of weeks which is, however, unimportant under real atmospheric conditions. In this region, an assignment of time constants and compounds is not possible indicating the strong coupling between all compounds.
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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.










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