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The statistics of liquid-to-crystal nucleation are measured for clathrate-forming mixtures of tetrahydrofuran (THF) and water using an automatic lag time apparatus (ALTA).
We provide here data from several series of measurements of the stochastic nature of THF water hydrate formation using an automatic lag time apparatus.
The optimum of a clearly defined irreversible drying process for the finite time transition of a and a connection between the process time, apparatus price and the optimal process intensity are pointed out.
A radial capillary suction time apparatus, and the filter paper used by it, are investigated in various ways to obtain the capillary suction pressure P, the water porosity ϵ of the filter paper, and the water saturation sw(r) in the filter paper as a function of the radial distance r from the suspension to be filtered.
In contrast with conventional experiments for ranking the performance of kinetic hydrate inhibitors (KHIs), the high pressure automated lag time apparatus (HP-ALTA) is not limited by the stochasticity of hydrate formation because it can make large numbers of formation measurements rapidly.
The second generation High Pressure Automated Lag Time Apparatus (HP ALTA MkII) was used to measure the nucleation curves of Structure II (sII)–forming methane propane mixed gas hydrates on the surface of a quasi free water droplet suspended in involatile hydrocarbon oil, squalane.
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Besides intrinsic origins (like blood or air), which affect the transversal relaxation time, apparatus-specific sources (insufficient field homogeneity) can also lead to signal decay in the MR gradient echo images.
The following thermal profile was used on an ABI Prism 7000 SDS Real-Time apparatus (Applied Biosystems): 30 min at 45°C for reverse transcription; 2 min at 95°C to inactivate the reverse transcriptase and activate the DNA polymerase; and then 40 amplification cycles of 15 s at 95°C and 1 min at 60°C each.
RNA from all samples, were amplified by RRT-PCR assay, run in an ABI Prism 7000 SDS Real-Time apparatus (Applied Biosystems) using the Superscript III Platinum One-step qRT-PCR kit (Invitrogen).
The RNA was amplified using a real-time RT-PCR assay and an ABI Prism 7500 SDS Real-Time apparatus (Applied Biosystems, Foster City, CA) using the QuantiTect kit (Qiagen, Hilden, Germany).
At the time, that apparatus was a weak one for the United States and they needed her score.
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