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The interface water concentration decreased significantly on addition of DHPC to each detergent.
Vibration/hydrostatic pressure may not play significant role in draining the interface water through CPF liner.
Moreover, the effects of interface, water cement ratio, volume fraction ratio of fine aggregate to coarse aggregate, air voids, CTE of coarse aggregate and elastic modulus of cement paste on the CTE are analyzed.
Dynamically, the aluminate-silicate chains, calcium ions and functional hydroxyl groups establish the "cages", and strongly prevent the freely diffusion of the interface water molecules, stabilizing the connections between CSH and GO structures.
For combined phospholipid and detergent concentration of 50 mM the interface water concentration decreased, as measured by ESR of the spin-probes, from 38.5 M/L of interface volume in SDS alone to 9 M/L when the phospholipid was present at 0.7 mole fraction.
Water molecules are defined as interface water molecules if they are less than 3.5 Å from the atoms of the two components of a complex, as in [21].
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The LC-ESI-MS/MS device was adjusted with a PicoTip Emitter (New Objective, Woburn, MA) fitted on a Z-spray nanoESI interface (Waters).
Aqueous humor flow is tangent to the interface water-tamponade and this may induce the deformation of the interface.
For LC-MS analysis, 4 μl of extracted sample was injected onto a UPLC-QTOF-MS system equipped with an ESI interface (Waters Q-TOF XevoTM: Waters MS Technologies, Manchester, UK) operating in negative and positive ion modes.
For LC/MS analysis, 4 μl of extracted sample was injected into a Xevo™ QTOF in combination with the Waters Acquity UPLC System and equipped with an ESI interface (Waters MS Technologies, Manchester, UK) operating in negative ion mode.
The compounds were analyzed by a UPLC-MS/MS with ACQUITY I-Class UPLC and a XEVO TQD triple quadrupole mass spectrometer that was equipped with an electrospray ionization (ESI) interface (Waters Corp., Milford, MA, USA).
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