A method for rapid reaction optimisation in continuous-flow microfluidic reactors using online Raman spectroscopic detection

The Analyst ◽  
2005 ◽  
Vol 130 (1) ◽  
pp. 46 ◽  
Author(s):  
Shee-Ann Leung ◽  
Richard F. Winkle ◽  
Robert C. R. Wootton ◽  
Andrew J. deMello
1976 ◽  
Vol 40 (5) ◽  
pp. 707-714 ◽  
Author(s):  
R. A. Klocke

The rate of exchange of bicarbonate and chloride ions across the red cell membrane was studied in a continuous flow rapid reaction apparatus at 37 degrees C. A transmembrane gradient both ions was produced by mixture of cells suspended in a solution of one ion with an isosmotic solution of the other ion. Carbonic anhydrase activity was inhibited by acetazolamide to prevent changes in CO2 concentration during the experiments. Chloride and bicarbonate efflux from cells were studied in separate experiments at each experimental pH. Using a least squares technique, values of chloride and bicarbonate permeabilities were fitted to each pair of independent experiments. Chloride permeability averaged 1.1 (+/- 0.2 SD) X 10–4 cm/s and was not affected by change in pH. Recovered bicarbonate permeabilities varied widely, always remaining at least fivefold greater than chloride permeability. While bicarbonate permeability could not be accurately characterized, it appears to be greater than chloride permeability. Analysis of CO2 transfer with the estimated permeabilities indicates that the bicarbonate-chloride exchange by itself probably does not limit CO2 transfer.


1965 ◽  
Vol 208 (4) ◽  
pp. 801-811 ◽  
Author(s):  
H. P. Constantine ◽  
Margot R. Craw ◽  
R. E. Forster

A CO2 electrode was adapted for use in a continuous-flow rapid-reaction apparatus to measure the kinetics of the hydration-dehydration reactions of CO2. The dehydration constant of the reaction was found to be 80 sec–1 at 37 C. Red blood cell suspensions were mixed with bicarbonate solutions to alter suddenly the Pco2 around the cells from 42 to 57, and from 3 to 37 mm Hg. The velocity constants for the hydration of CO2 inside the cell were 236 and 772 sec–1, respectively, as compared with the uncatalyzed rate of 0.11 sec–1. These uninhibited rates are 0.16 and 0.54 the potential catalyzed rate in the cell, suggesting that some other process is rate limiting. In the presence of 0.25 g/liter acetazolamide, the velocity constants decreased to 28 and 65 sec–1, respectively.


2011 ◽  
Vol 7 ◽  
pp. 1360-1371 ◽  
Author(s):  
Charlotte Wiles ◽  
Paul Watts

Whilst microwave heating has been widely demonstrated as a synthetically useful tool for rapid reaction screening, a microwave-absorbing solvent is often required in order to achieve efficient reactant heating. In comparison, microreactors can be readily heated and pressurised in order to “super-heat” the reaction mixture, meaning that microwave-transparent solvents can also be employed. To demonstrate the advantages associated with microreaction technology a series of SNAr reactions were performed under continuous flow by following previously developed microwave protocols as a starting point for the investigation. By this approach, an automated microreaction platform (Labtrix® S1) was employed for the continuous flow synthesis of diaryl ethers at 195 °C and 25 bar, affording a reduction in reaction time from tens of minutes to 60 s when compared with a stopped-flow microwave reactor.


2021 ◽  
Author(s):  
Marco P. Cardoso Marques ◽  
Alvaro Lorente-Arevalo ◽  
Juan M. Bolivar

Lab on a Chip ◽  
2012 ◽  
Vol 12 (20) ◽  
pp. 4168 ◽  
Author(s):  
Ryan D. Sochol ◽  
Song Li ◽  
Luke P. Lee ◽  
Liwei Lin

2020 ◽  
Vol 5 (7) ◽  
pp. 1300-1310 ◽  
Author(s):  
Florian Menzel ◽  
Thomas Klein ◽  
Thomas Ziegler ◽  
Jochen M. Neumaier

This paper presents the development of milli- and microfluidic reactors made of polyether ether ketone (PEEK) and 3D-printed equipment for a complete continuous flow system.


2020 ◽  
Vol 22 (19) ◽  
pp. 6437-6443
Author(s):  
Cheng-Kou Liu ◽  
Meng-Yi Chen ◽  
Xin-Xin Lin ◽  
Zheng Fang ◽  
Kai Guo

A catalyst-, oxidant-, acidic solvent- and quaternary ammonium salt-free electrochemical para-selective hydroxylation of N-arylamides at rt in batch and continuous-flow was developed.


Sign in / Sign up

Export Citation Format

Share Document