dc.contributor.advisor |
Morshed, Prof. Dr. Mohammad Hasan |
|
dc.contributor.author |
Dey, Shishir Kumar |
|
dc.date.accessioned |
2018-05-20T07:28:39Z |
|
dc.date.available |
2018-05-20T07:28:39Z |
|
dc.date.copyright |
2016 |
|
dc.date.issued |
2016-11 |
|
dc.identifier.other |
ID 1553512 |
|
dc.identifier.uri |
http://hdl.handle.net/20.500.12228/123 |
|
dc.description |
This thesis is submitted to the Department of Chemistry, Khulna University of Engineering & Technology in partial fulfillment of the requirements for the degree of Master of Science in Chemistry, November 2016. |
en_US |
dc.description |
Cataloged from PDF Version of Thesis. |
|
dc.description |
Includes bibliographical references (pages 99-103) |
|
dc.description.abstract |
Paracetamol in presence of Water, 80% Water + 20% n-Propanol, 20% Water + 80% n-
Propanol, 80% Water + 20% n-Butanol and 20% Water + 80% n-Butanol were studied
through the measurement of viscosity and density at different temperatures (298.15K to
323.15K) with an interval of 5K. The results were discussed on the basis of structure
making and breaking mechanism of paracetamol in aqueous and aqueous alcohols solution under experimental conditions. The apparent molar volumes increase with the rise of concentration of paracetamol for all the studied systems indicating the structure making interaction for all the studied systems. The limiting apparent molar volume (φv
0) or partial molar volume at infinite dilution of paracetamol are positive and increase when paracetamol content in the solvents increase.
The positive values of transfer apparent molar volume (Δφv)tra suggest the structure
making ability through hydrophilic-hydrophilic interactions between polar groups of
paracetamol and polar groups of alcohols-water. The values of limiting apparent molar
volume expansibilities (Eφ0) are positive and the values of (δEφ0/δT)p are small which
suggest the structure making property in these systems.
Viscosities increase with increasing of paracetamol concentration. The B-coefficients for
paracetamol in the studied systems are positive and thus suggest the presence of solutesolvent interactions or structure making properties. The values of D-coefficient are mainly negative showing weak solute-solute interactions.
The changes of free energies (ΔG#) are increased with the increase of concentration of
paracetamol and the values are positive for all the studied systems. It is also seen that the changes of free energies (ΔG#) of paracetamol in aqueous solutions of n-Propanol and n-Butanol increase very slowly with increasing solute concentration and decrease with increasing temperature. The values of enthalpy of activation (ΔH≠) indicate the interaction presence in solute-solvent through H-bonding. The entropy (ΔS≠) values are positive for all the systems and decrease with increase of paracetamol concentration.
The positive values of change of chemical potential (Δμ1 ≠ - Δμo≠) for all studied show greater contribution per mole of solute to free energy of activation for viscous flow of the
solution and are good agreement with the values of B-coefficient showing structure
making properties between solute and solvent. |
en_US |
dc.description.statementofresponsibility |
Shishir Kumar Dey |
|
dc.format.extent |
103 pages |
|
dc.language.iso |
en_US |
en_US |
dc.publisher |
Khulna University of Engineering & Technology (KUET), Khulna, Bangladesh |
en_US |
dc.rights |
Khulna University of Engineering & Technology (KUET) thesis/dissertation/internship reports are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. |
|
dc.subject |
Properties of Paracetamol |
en_US |
dc.subject |
Properties of Alcohols |
en_US |
dc.subject |
Viscosity |
en_US |
dc.subject |
Molarity |
en_US |
dc.title |
Volumetric and Viscometric Studies of Paracetamol in Aqueous Solution of Alcohols at Different Temperatures |
en_US |
dc.type |
Thesis |
en_US |
dc.description.degree |
Master of Science in Chemistry |
|
dc.contributor.department |
Department of Chemistry |
|