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Solvent vapor annealing (SVA) is a widely used technique for controlling the morphology and ordering of block copolymer (BCP) films. [1] [2] [3] By controlling the block ratio (f = NA/N), spheres, cylinders, gyroids, and lamellae structures can be generated by forming a swollen and mobile layer of thin-film from added solvent vapor to facilitate the self-assembly of the polymer blocks. [4]
n-propyl bromide (nPB) based solvents for vapor degreasing, in comparison to other solvents for vapor degreasing, are environmentally friendly. nPB solvents are non flammable (no flashpoint), non chlorinated, U.S. EPA SNAP approved, non hazardous waste (per U.S. Department of Transportation), and non ozone layer depleting.
The vapor pressure lowering relative to pure solvent is = = =, which is proportional to the mole fraction of solute. If the solute dissociates in solution, then the number of moles of solute is increased by the van 't Hoff factor i {\displaystyle i} , which represents the true number of solute particles for each formula unit.
Original vapor pressure A nonvolatile solute lowers the solvent’s vapor pressure. In terms of chemical potential, at the boiling point, the liquid and gas phases have the same chemical potential. Adding a nonvolatile solute lowers the solvent’s chemical potential in the liquid phase, but the gas phase remains unaffected.
Raoult's law (/ ˈ r ɑː uː l z / law) is a relation of physical chemistry, with implications in thermodynamics.Proposed by French chemist François-Marie Raoult in 1887, [1] [2] it states that the partial pressure of each component of an ideal mixture of liquids is equal to the vapor pressure of the pure component (liquid or solid) multiplied by its mole fraction in the mixture.
Desorption atmospheric pressure photoionization (DAPPI) is an ambient ionization technique for mass spectrometry that uses hot solvent vapor for desorption in conjunction with photoionization. Ambient Ionization techniques allow for direct analysis of samples without pretreatment. [ 1 ]
Dynamic vapor sorption (DVS) is a gravimetric technique that measures how quickly and how much of a solvent is absorbed by a sample such as a dry powder absorbing water. It does this by varying the vapor concentration surrounding the sample and measuring the change in mass which this produces.
The relative activity of a species i, denoted a i, is defined [4] [5] as: = where μ i is the (molar) chemical potential of the species i under the conditions of interest, μ o i is the (molar) chemical potential of that species under some defined set of standard conditions, R is the gas constant, T is the thermodynamic temperature and e is the exponential constant.