Reaction Dynamics and Chemical Pattern Formation in Capillary Tubes Resulting from the Competition Between Two Elementary Complex Formation Reactions

1996 ◽  
Vol 464 ◽  
Author(s):  
Anna L. Lin ◽  
Andrew Yen ◽  
Yong-Eun Lee Koo ◽  
Baruch Vilensky ◽  
Haim Taitelbaum ◽  
...  

AbstractA system of competing elementary reactions is investigated experimentally usingthe reaction of xylenol orange with Cr3+ in aqueous solution. The two reagents areinitially separated in a long, thin capillary tube and meet in the center, forming a reactionfront (s). The geometry of the reactor and the initial separation of the reagents makes the system effectively one-dimensional. Aqueous Cr3+ solution has a very rich chemistryand provides two different chemical Cr3+ reactants which compete to react with xylenolorange. Rich spatio-temporal patterns are observed experimentally and are explained by a reaction-diffusion model. Results from exact enumeration simulations predict that when the concentrations of the competing species are very different and the microscopic rate constants of the competing species are such that the majority species reaction rate is much faster than the reaction rate of the minority species, the reaction front splits into two distinct regions. The spatio-temporal patterns generated by theory and experiment agree quantitatively. Also in agreement with the theory are the experimental early time and asymptotic time global rate behaviors, which exhibit multiple crossovers.

1994 ◽  
Vol 366 ◽  
Author(s):  
Anna Lin ◽  
Andrew Yen ◽  
Yong-Eun Koo ◽  
Raoul Kopelman

ABSTRACTWe study a reaction-diffusion system within the confines of a thin capillary tube. Xylenol orange and Cr 3+ are introduced into a capillary tube from opposite ends and meet in the middle forming a reaction front. Unequal initial concentrations of the reactants causes the center of the reaction front to move in time. Characteristics of the front such as the width of the reaction zone, w, the position of the center of the front, xf, the global reaction rate, R, and the local reaction rate, r(xf,t) are determined by continuously monitoring the product concentration in space vs. time. We observe crossover of the global rate from classical to non-classical behavior and a splitting of the reaction front.


1995 ◽  
Vol 50 (12) ◽  
pp. 1147-1150 ◽  
Author(s):  
Gerold Baier ◽  
Peter Strasser ◽  
Ursula Kummer

Abstract We investigate the model of an enzymatic reaction with Michaelis-Menten kinetics and bell-shaped pH-dependence of the reaction rate. In the case of proton consumption the reaction can generate oscillations in a homogeneous reactor and turbulent spatio-temporal patterns in a reaction-diffusion environment. I n s t a b il it i e s in a S im p le E n z y m e R e a c tio n C a u s e d b y p H -D e p e n d e n c e *


2019 ◽  
Vol 38 (2) ◽  
pp. 239-254
Author(s):  
M.B. SINGH ◽  
◽  
NITIN KUMAR MISHRA ◽  

2010 ◽  
Vol 11 (4) ◽  
pp. 428-435 ◽  
Author(s):  
Wenhui KUANG ◽  
Quanqin SHAO ◽  
Jiyuan LIU ◽  
Chaoyang SUN

2019 ◽  
Vol 13 (12) ◽  
pp. e0007916 ◽  
Author(s):  
Yujuan Yue ◽  
Dongsheng Ren ◽  
Xiaobo Liu ◽  
Yujiao Wang ◽  
Qiyong Liu ◽  
...  

2020 ◽  
Vol 117 ◽  
pp. 106565
Author(s):  
Roxana Triguero-Ocaña ◽  
Joaquín Vicente ◽  
Pablo Palencia ◽  
Eduardo Laguna ◽  
Pelayo Acevedo

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