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Hemolymph buffer curves were measured with a micro-pH-electrode (MI-4152; Microelectrodes Inc., Bedford, U.S.A). in a gas diffusion chamber [ 130] at 20°C.
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In addition, in order to accelerate the gas diffusion process, the donor chamber was aerated.
The mathematical model based on the experimental design has been built, and a general solution has been obtained by considering gas diffusion from the gas chamber to the core, under the pressure difference.
Gas slippage and gas diffusion mainly influence the gas rate at later production time, especially the Knudsen diffusion dominates the flow behavior in the formation linear period.
This paper describes the development, testing, validation, and initial use of a diffusion chamber specifically designed to measure inert gas diffusivity on firn cores.
A small cell makes it easy to control gas diffusion homogeneity and turbulences in comparison to larger gas chamber.
Ammonia and COD removal rates by single-chamber MFC were significantly improved by doubling the gas diffusion area [ 22].
Two different silver-based cathode designs (a gas diffusion electrode and a flooded cathode) and three different separator designs (a porous separator, a stirred separator chamber, and a redox-flow separator) are compared.
A solid plate was used for the anode frame, while the cathode chamber was bolted with a hollow side plate allowing for one side of the gas diffusion cathode to be exposed to air.
Using the diffusion chamber and the microfluorometric set-up described above, a 10 μl sample was equilibrated with gas mixtures of different PCO2 (0.135–5.50 kPa).
The diffusion chamber provided an artificial barrier against larger lymphocytes and macrophages, while allowing passage of smaller nutrients, gases, and insulin.
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