Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.776788
Title: Micellar properties in aqueous solution of a series of synthesised non-ionic detergents
Author: Macfarlane, Calum B.
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1964
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Abstract:
In the first part of the thesis a review of the chemistry of the polyoxyethylene type non-ionic detergents is given. The preparation by ethylene oxide polymerisation and other synthetic routes of the polyoxyethylene glycols and their monoalkyl ether condensates is reported and a resume made of the existing work on the formation and structure of the micelles of these detergents in aqueous solutions the effects of temperatures electrolytes 1, and solubilisates on these propertiess and their surface activity. The theory of the determination of molecular weights of both large and small particles by light-scatterings and the relationship between the viscosity of solutions of macromolecules and solute shape and solvations is outlined. Part 2 The synthesis of a series of non-ionic detergents, based on hexadecyl alcohols containing a definite oxyethylene chain length is described. The series has the general formula CH3(CH2)15(OCH2CH2)nOH, and six members having n 6a v. 70 90 12,E 15v and.21 respectively, have been prepared (for ease of handling the names of these compounds have been abbreviated to Hn6, Hn7,...Hn21). Some of their physical properties are reported. The critical micellar concentrations (cmc's.) of these materials in aqueous solution have been investigated using the Wilhelmy plate method for measuring surface tension; cm's. were determined from plots of surface tension; vs. log. concentration. Very small critical micellar concentrations were obtained. A light-scattering photometer has been constructed and calibrated. Using the Hn9 detergent and the results from the calibration of the photometers a statistical analysis of most of the errors in the measurement of molecular weight by light-scattering has been carried out and it is shown that the largest part of the error arises in the measurement of the turbidities of the solutions rather than from the measurement of the specific refractive index increment or depolarization.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.776788  DOI: Not available
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