scholarly journals The application of oscillating chemical reactions to analytical determinations

2013 ◽  
Vol 11 (7) ◽  
pp. 1023-1031 ◽  
Author(s):  
Jie Ren ◽  
Xiaoyan Zhang ◽  
Jinzhang Gao ◽  
Wu Yang

AbstractOscillating chemical reactions, which are far from equilibrium, are extremely sensitive to certain species and may provide new analytical methods using the regular oscillations as well as the non-equilibrium stationary state after system bifurcation. This review of their application to analytical chemistry from 2005 to 2012 includes other appropriate references. Both organic and inorganic analytes are included.

Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5297
Author(s):  
Kayla M. Billiard ◽  
Amanda R. Dershem ◽  
Emanuela Gionfriddo

Implementing green analytical methodologies has been one of the main objectives of the analytical chemistry community for the past two decades. Sample preparation and extraction procedures are two parts of analytical method development that can be best adapted to meet the principles of green analytical chemistry. The goal of transitioning to green analytical chemistry is to establish new methods that perform comparably—or superiorly—to traditional methods. The use of assessment tools to provide an objective and concise evaluation of the analytical methods’ adherence to the principles of green analytical chemistry is critical to achieving this goal. In this review, we describe various sample preparation and extraction methods that can be used to increase the greenness of a given analytical method. We gave special emphasis to modern microextraction technologies and their important contributions to the development of new green analytical methods. Several manuscripts in which the greenness of a solid-phase microextraction (SPME) technique was compared to other sample preparation strategies using the Green Analytical Procedure Index (GAPI), a green assessment tool, were reviewed.


1983 ◽  
Vol 101 ◽  
pp. 245-252
Author(s):  
P. F. Winkler ◽  
C. R. Canizares ◽  
B. C. Bromley

High resolution X-ray spectroscopy of the brightest knot of emission in the Puppis A supernova remnant shows that it is made up of ionizing plasma, far from equilibrium. Flux measurements in several X-ray lines enable us to determine the non-equilibrium conditions: electron temperature, ion populations, and time since the knot was heated by the supernova shock. Imaging and spectroscopic data from the Einstein Observatory together suggest that this knot is a cloud of density about 10 cm−3 which has recently been shocked to a temperature 7 × 106 K. Radio and optical data on the region appear consistent with this picture.


Author(s):  
Guanchen Li ◽  
Michael R. von Spakovsky

Conventional first principle approaches for studying non-equilibrium or far-from-equilibrium processes all depend on the mechanics of individual particles or quantum states and as a result, require too many details of the mechanical features of the system to easily or even practically arrive at the value of a macroscopic property. In contrast, thermodynamics, which has been extremely successful in the stable equilibrium realm, provides an approach for determining a macroscopic property without going into the mechanical details. Nonetheless, such a phenomenological approach is not generally applicable to a non-equilibrium process except in the near-equilibrium realm and under the limiting local equilibrium and continuum assumptions, both of which prevent its application across all scales. To address these drawbacks, steepest-entropy-ascent quantum thermodynamics (SEAQT) can be used. It provides an ensemble-based, thermodynamics, first principles approach applicable to the entire non-equilibrium realm even that far-from-equilibrium and does so with a single kinematics and dynamics able to cross all temporal and spatial scales. Based on prior developments by the authors, this paper applies SEAQT to the study of mass and heat diffusion. Specifically, the study focuses on the thermodynamic features of far-from-equilibrium state evolution. Two kinds of size effects on the evolution trajectory, i.e., concentration and volume effects, are discussed.


Entropy ◽  
2019 ◽  
Vol 21 (2) ◽  
pp. 179 ◽  
Author(s):  
Ramon Álvarez-Estrada

We review and improve previous work on non-equilibrium classical and quantum statistical systems, subject to potentials, without ab initio dissipation. We treat classical closed three-dimensional many-particle interacting systems without any “heat bath” ( h b ), evolving through the Liouville equation for the non-equilibrium classical distribution W c , with initial states describing thermal equilibrium at large distances but non-equilibrium at finite distances. We use Boltzmann’s Gaussian classical equilibrium distribution W c , e q , as weight function to generate orthogonal polynomials ( H n ’s) in momenta. The moments of W c , implied by the H n ’s, fulfill a non-equilibrium hierarchy. Under long-term approximations, the lowest moment dominates the evolution towards thermal equilibrium. A non-increasing Liapunov function characterizes the long-term evolution towards equilibrium. Non-equilibrium chemical reactions involving two and three particles in a h b are studied classically and quantum-mechanically (by using Wigner functions W). Difficulties related to the non-positivity of W are bypassed. Equilibrium Wigner functions W e q generate orthogonal polynomials, which yield non-equilibrium moments of W and hierarchies. In regimes typical of chemical reactions (short thermal wavelength and long times), non-equilibrium hierarchies yield approximate Smoluchowski-like equations displaying dissipation and quantum effects. The study of three-particle chemical reactions is new.


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