Repellents play a key role in preventing mosquito-borne diseases such as malaria by reducing
human-vector contact. The general mechanism of action relies on providing a repelling vapour
around the applied area on the skin. Thus, the proper evaporation rate and consistency of the
composition of the released vapour are factors determining the performance of repellent
formulations. The formulation should evaporate fast enough to provide a sufficient level of
repellence during its life time. However, if evaporation proceeds too fast, then it will be
depleted rapidly so that activity is lost within a short period of time, which makes the repellent
inefficient.
Several controlled-release approaches have been developed to improve both the protection time
and level. However, these techniques have inherent drawbacks from the industrial point of
view. Moreover, these techniques mostly focus only on reducing the release rate, while the
consistency of the vapour composition has not been addressed.
In the present study, a novel approach towards controlling the evaporation behaviour of
repellents is proposed. It is based on engineering the molecular interactions in order to design
negative pseudo-azeotrope formulations. Negative pseudo-azeotrope mixtures are less volatile
than the pure parent components and they do not undergo separation during evaporation. The feasibility of the idea was investigated by studying the molecular structure of generally
available repellents. Among known molecular interactions, hydrogen bonding has the most
likely impact on the formation of azeotropes and in particular pseudo-azeotropes. Thus,
established repellents were classified based on their chemical structures and their capability to
take part in hydrogen bonding. Next, a simple spectroscopic method for anticipating pseudoazeotropes
formation was developed. Binary compositions of nonanoic acid and ethyl
butylacetylaminopropionate (IR3535) showed a potential for forming pseudo-azeotrope
mixtures. Hence R3535 and nonanoic acid were selected as model compounds to test the
hypothesis.
An experimental technique to confirm pseudo-azeotrope formation and to locate the
composition of the probable pseudo-azeotrope point was required. To this end, an oven test
was designed. The temporal mass loss, under an isothermal program, of a series of evaporating
mixtures was measured. Simultaneously, the Fourier transform infrared (FTIR) spectra of the
liquid remaining was recorded. Inverse analysis techniques were used to determine the
composition of remaining liquid mixtures from the recorded FTIR spectra. The oven tests
revealed that, as vaporisation progressed, the composition of the liquid remaining and the
emitted vapour converged to a fixed IR3535 content of ca. 75 mol%. Mixtures close to this
composition also featured the lowest volatility. Oven test also showed that the composition of
the liquid mixtures diverged from the fixed IR3535 content of ca. 10 mol%. Mixtures close to
this composition featured the highest volatility. These observations showed that IR3535 and
nonanoic acid forms two pseudo-azeotrope compositions, i.e. a negative pseudo-azeotrope at
an IR3535 content of ca. 75 mol%, and a positive pseudo-azeotrope at IR3535 content of ca.
10 mol%.
Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were applied
to check these results. TGA confirmed that the negative pseudo-azeotrope mixture is less
volatile while the positive pseudo-azeotrope is more volatile than the parent compounds. The
DSC results revealed that in comparison with the pure compounds, negative pseudo-azeotrope
had a lower boiling point onset while the positive pseudo-azeotrope had a higher boiling point.
Although negative pseudo-azeotrope repellent formulations have the desired lower constant
release rate, their repellent activity needed to be tested. This is due to the fact that mixing the ingredients to formulate a negative pseudo-azeotrope results in interactions among the
components. As a consequence, the inherent repellence effect of the compounds might have
been impaired in the mixture.
The modified arm-in-cage test was used to test the repellence of the controlled-release repellent
formulation i.e. the negative pseudo-azeotrope of the IR3535 + nonanoic acid system. Results
showed that the mixture featured improved performance with respect to both repellence
efficacy and persistence. Moreover, the negative pseudo-azeotrope also exhibited a knock
down effect, even resulting in mortality of most of the test mosquitoes.
The presence of two pseudo-azeotrope points at different composition in the IR3535 +
nonanoic acid system is a rare occurrence, analogous to double azeotropy. Thus, molecular
simulation techniques were used to explore the nature of system and the interactions
responsible for this unique behaviour. Gibbs-Monte Carlo simulation results suggest that
variations in the sizes of the molecular clusters present in the liquid at various compositions
might be responsible. They revealed that IR3535 and nonanoic acid in neat form are both highly
structured liquids. The break-down in the structure of IR3535 at high concentrations of the acid
may be the origin of increased evaporation rate and formation of the positive pseudo-azeotrope.
On the other hand, negative pseudo-azeotrope may be resulted from formation of bulkier
clusters at the ration of 3:1 (IR3535: nonanoic acid). / Thesis (PhD (Chemical Technology))--University of Pretoria, 2016. / English / PhD (Chemical Technology) / Unrestricted
Identifer | oai:union.ndltd.org:netd.ac.za/oai:union.ndltd.org:up/oai:repository.up.ac.za:2263/81873 |
Date | January 2016 |
Creators | Izadi, Homa |
Contributors | Focke, Walter Wilhelm, homaizadi@gmail.com |
Publisher | University of Pretoria |
Source Sets | South African National ETD Portal |
Language | English |
Detected Language | English |
Type | Thesis |
Rights | © 2021 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. |
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