Molecular vapor osmometry

Hydroxyl number and molecular weight are normally determined by end-group analysis, by titration with acetic, phthaUc, or pyromellitic anhydride (264). Eor lower molecular weights (higher hydroxyl numbers), E- and C-nmr methods have been developed (265). Molecular weight deterrninations based on coUigative properties, eg, vapor-phase osmometry, or on molecular size, eg, size exclusion chromatography, are less useful because they do not measure the hydroxyl content. 

Among the techniques employed to estimate the average molecular weight distribution of polymers are end-group analysis, dilute solution viscosity, reduction in vapor pressure, ebuUiometry, cryoscopy, vapor pressure osmometry, fractionation, hplc, phase distribution chromatography, field flow fractionation, and gel-permeation chromatography (gpc). For routine analysis of SBR polymers, gpc is widely accepted. Table 1 lists a number of physical properties of SBR (random) compared to natural mbber, solution polybutadiene, and SB block copolymer. 

The molecular weights and molecular weight distributions (MWD) of phenolic oligomers have been evaluated using gel permeation chromatography (GPC),23,24 NMR spectroscopy,25 vapor pressure osmometry (VPO),26 intrinsic viscosity,27 and more recently matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS).28... 

However, because of the high price, MALDI-TOF mass spectrometers have not come into wide use. Vapor pressure osmometry (VPO), an old and traditional method for estimating molecular weight, is useful in the field of CPO chemistry. The experimental error of this measurement is approximately 10% however, the obtained data are sufficiently useful to estimate the number of porphyrins in a molecule. 

Vapor Pressure Osmometry - The number average molecular weights of polymers with Mn < 20,000 were determined using "Model 232A Molecular Weight Apparatus, Wescan Instruments, Inc., 3018 Scott Blvd., Santa Clara, CA 95050". Toluene was used as solvent and the instrument was calibrated using polystyrene of Mn 9,000 and 20,400. 

The number average molecular weights, Mq, of the polymers obtained in Table II ranged from 1300 to 3900 as determined by vapor nressure osmometry (VPO), and they were further characterized by - -H- and C-NMR spectrometry at ambient temperature and at 90°C, as well as by IR spectroscopy. The homopolymers of isopropenylferro-cene were found to have the expected structure, P, shown below, obtained by polymerization through the isopropenyl units, as indicated by spectroscopic characterization ... 

Molecular weights of the products as measured with vapor pressure osmometry were in good agreement with the calculated ones. Interestingly, resins based on hexahydrophthalic anhydride and diisopropanolamine with tertiary amines as functional groups are soluble in water without quaternization of the... 

GPC was calibrated with polystyrene standards. M was also determined by vapor pressure osmometry (VPO) on a Wescan model 233 molecular weight apparatus at a current setting of 50pamp in toluene... 

What principle is used in the determination of molecular weight by vapor pressure osmometry ... 

Table XVII. Reproducibility of Molecular Weight Determinations by Vapor-Phase Osmometry (Butarez CTL Lot 18)...

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