<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JMP</journal-id><journal-title-group><journal-title>Journal of Modern Physics</journal-title></journal-title-group><issn pub-type="epub">2153-1196</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jmp.2013.42032</article-id><article-id pub-id-type="publisher-id">JMP-28319</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  On the Usage of the Faraday Effect as an Authentication Technique for Vegetable Oils
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>.</surname><given-names>I. Abu-Taha</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>M.</surname><given-names>A. Halasa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>M.</surname><given-names>M. Abu-Samreh</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Physics Department, College of Science and Technology, Al-Quds University, Jerusalem, Palestine</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>mabutaha@science.alquds.edu(.IA)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>05</day><month>02</month><year>2013</year></pub-date><volume>04</volume><issue>02</issue><fpage>230</fpage><lpage>235</lpage><history><date date-type="received"><day>October</day>	<month>3,</month>	<year>2012</year></date><date date-type="rev-recd"><day>November</day>	<month>15,</month>	<year>2012</year>	</date><date date-type="accepted"><day>November</day>	<month>29,</month>	<year>2012</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   In this study we report on the measurements of the Verdet constant for olive and other vegetable oils. Study of samples stored for different periods at different storage conditions showed that each olive oil sample has a Verdet constant value depending on: production year, history of the sample (i.e. storage conditions) and geographical region. Photo and auto oxidations are found to have reverse effects on the value of the measured Verdet constant, on the one hand, photo-oxidation tends to decrease the Verdet constant, but on the other hand auto-oxidation tends to increase it. It is known that oils stored in room light had significantly lower tocopherol, carotenoid, and chlorophyll contents than did the same oils kept in the dark. For other vegetable oil samples, each vegetable oil was found to have a distinct Verdet constant value. Thus it is possible to differentiate vegetable oils making use of their respective Verdet constants. Preliminary results indicated the possibility to detect olive oil adulteration using the Faraday Effect, i.e. the effect could be suggested as a food authentication technique if calibration curves and standard Verdet constants values could be prepared for comparison with those of samples under investigation. 
 
</p></abstract><kwd-group><kwd>Olive Oil; Oil Content; Oil Adulteration; Photo-Oxidation; Auto-Oxidation; Magneto-Optics; Food Authentication</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Food authentication techniques have been evolving continually to deal with global market demands. Analytical techniques have been developed or modified to give plausible solutions to possible adulteration at each stage of production. Oils and fats constitute one of the three major classes of food products, the others being proteins and carbohydrates. Consumers are demanding food products that combine a pleasant flavor with nutritional benefits. On the basis of the expanding market for vegetable oils, their authenticity has become an important subject from both a commercial and a health perspective. The difference between the price of olive oil and other edible oils, for example, can mean that large amounts of money can be made by adding cheaper oils to virgin olive oil, i.e. adulteration. This harmful act constitutes a health hazard, and an example, was the toxic oil syndrome resulting from consumption of olive oil spiked with aniline-denatured rapeseed oil that affected more than 20,000 people [<xref ref-type="bibr" rid="scirp.28319-ref1">1</xref>].</p><p>Most of the current work on edible oil adulteration is based on chromatographic analysis. High performance liquid chromatography (HPLC) [<xref ref-type="bibr" rid="scirp.28319-ref2">2</xref>] and high resolution gas chromatography (HRGC) [<xref ref-type="bibr" rid="scirp.28319-ref3">3</xref>] analysis have been applied to the quantification of fatty acids, triglycerols, sterols, tocopherols and hydrocarbons. HPLC has been used increasingly over the last decade and it is still the most widely used technique. However, these seperative techniques have been complemented with or substituted by, many other modern techniques, such as supercritical fluid chromatography (SFC) [<xref ref-type="bibr" rid="scirp.28319-ref4">4</xref>], Chiral chromatography, silver ion chromatography, stable carbon isotope ratio analysis (SCIRA) [5,6], mass spectrometry (MS), nuclear magnetic resonance spectrometry (NMR) [<xref ref-type="bibr" rid="scirp.28319-ref7">7</xref>], near-infrared spectroscopy (NIR) [<xref ref-type="bibr" rid="scirp.28319-ref8">8</xref>], Fourier transform infrared spectroscopy (FT-IR) and FT-Raman spectroscopy [<xref ref-type="bibr" rid="scirp.28319-ref9">9</xref>].</p><p>This work attempts to employ Faraday effect as a sampling technique. It is a magneto-optical effect that deals with phenomena arising from the interaction between light and matter that occur in liquids, gases, as well as solids. When light propagates along the axis of a transparent medium of length L, the application of an axial magnetic field B to the medium causes a rotation <img src="12-7501028\bc1892b5-35c4-42df-96ec-c63099cbe74b.jpg" /> of the plane of polarization of the light beam such that [<xref ref-type="bibr" rid="scirp.28319-ref10">10</xref>]:</p><disp-formula id="scirp.28319-formula29697"><label>(1)</label><graphic position="anchor" xlink:href="12-7501028\faae9a8f-686c-4b85-a070-d87c1094fdd8.jpg"  xlink:type="simple"/></disp-formula><p>Here V is the Verdet constant, which measures the strength of the effect and has different values for different materials, and varies with the wavelength <img src="12-7501028\dcf68c3a-5ecd-42be-abf5-c03d67ef8af3.jpg" /> of the light used in the study [<xref ref-type="bibr" rid="scirp.28319-ref10">10</xref>]. The Faraday Effect is attributed to the symmetry breaking of the propagating lefthanded and right-handed circularly polarized light in the presence of the magnetic field, i.e., the index of refraction for light of the two polarizations becomes different in the presence of the field. A simple semi-classical approach that incorporates the essential physics and retains the right order of magnitude for the effect, the Verdet constant can be written as [11,12]:</p><disp-formula id="scirp.28319-formula29698"><label>(2)</label><graphic position="anchor" xlink:href="12-7501028\1d2e0b03-7c0a-4f69-a2cd-a6686347d425.jpg"  xlink:type="simple"/></disp-formula><p>where, e is the charge of the electron, m it’s mass, c is the speed of the light, <img src="12-7501028\8a29bcd6-e1a8-49b9-9116-eaed7fdbf3c8.jpg" />is the wavelength of the light beam, and n is the index of refraction of the medium. The dimensionless constant, K, measures the deviation of the Verdet constant from the value predicted by the simple semi-classical theory.</p><p>It is worth mentioning here that the Verdet constant and the wavelength dependence of the index of refraction relationship depend mainly on the nature of the medium, i.e. whether it is semiconducting, diamagnetic, paramagnetic ferromagnetic. Thus, correct calculations can be attained by making use of the quantum theory methods.</p><p>Accordingly, there are several analytical procedures that have been employed to identify and quantify the components of vegetable oils. In this work we propose the Faraday effect as a new nondestructive technique for testing vegetable oils through measurement of Verdet constant. To our knowledge there is no reported data in the literature on the measured values of Verdet constant for vegetable oils.</p></sec><sec id="s2"><title>2. Experimental</title><sec id="s2_1"><title>2.1. Set-Up and New Improvements</title><p>The basic setup of the Faraday Effect shown in <xref ref-type="fig" rid="fig1">Figure 1</xref> [<xref ref-type="bibr" rid="scirp.28319-ref13">13</xref>] was used with some improvements on the Faraday rotation-angle measurement and the detection scheme.</p><p>The normal procedure used [<xref ref-type="bibr" rid="scirp.28319-ref13">13</xref>] for calculating the Verdet constant employs measuring the rotation-angle directly using the circular scale of the analyzer graduated in degrees, and magnetic field value responsible for certain angle of rotation that causes light extinction. This method is totally dependent on the experimenter’s eye sight. Hence, the result is considered a crude measurement. An improvement on the experimental technique was found necessary and introduced to improve measurement sensitivity. The circular scale giving angle measurements in degrees is transferred to a linear micrometer scale. This is an achieved by introducing the new design shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>. The corresponding micrometer reading can be easily converted into more reliable and accurate angle measure.</p><p>As far as light extinction is concerned an improvement was added also by which a phase sensitive detection scheme in conjunction with a photocell is used, hence the measurement is carried out electronically avoiding possible error of insensitive human eye. This allows using lock-in amplifiers to detect AC signals, all the way down to a few nanovolts, hence, allowing an exact determination of the rotation angle. It is possible to make accurate measurements even when the small signal is obscured by noise sources many thousands of times larger and differentiates against stray light signals. The improved setup is exhibited as a complete experimental setup in <xref ref-type="fig" rid="fig3">Figure 3</xref>.</p></sec><sec id="s2_2"><title>2.2. Samples</title><p>Olive oil samples from different geographical parts of Palestine were collected over years ago for the various production years and stored at different storing condition. Some were stored at room light other in the dark, in plastic or glass containers; totally or partially filled. Tested oil samples were placed in ordinary glass tube 20 mm long, 5 mm internal diameter, then inserted through the hole drilled in the magnet poles. In addition to the olive oil samples, other different vegetable oil samples were bought for analysis from a local store. Adultered oil samples were prepared by mixing pure oil sample by different ratios of other oils.</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><p>A set of improvements on the conventional method allowed a sensitive measurement of the rotation angle. For example, parts of angles as small as 0.02 deg could be measured in the present work compared to the smallest measurable angle of 0.5 deg. in the conventional way. This enhanced the sensitivity to a level that minute rotation angles by the plane of polarization for vegetable oils could be monitored. The circular angle scale on the analyzer was changed to a linear sensitive easy to measure scale as could be seen in <xref ref-type="fig" rid="fig4">Figure 4</xref>.</p><p><xref ref-type="fig" rid="fig5">Figure 5</xref> shows the angle of rotation of the polarization plane as a function of the mean flux density for two olive oil samples taken from the same geographical region and stored in a plastic container in room light and having one year age difference.</p><p>It is seen that the Verdet constant decreases appreciably from 227 deg/(T∙m) for less older sample to 165 deg/ (T∙m) for older one. This indicates that the verdet constant value becomes less the larger the sample age is. The</p><p>oils stored in the dark mainly contained primary oxidation products while the oils kept in room light contained secondary oxidation products as confirmed by the K<sub>270</sub> values which exceeded the legal limits even after purification by means of alumina [<xref ref-type="bibr" rid="scirp.28319-ref14">14</xref>]. This is because the photo-oxidation takes place faster than the auto-oxidation. It is possible to conclude that the decrease of the Verdet constant in the samples exposed to light is due to the decrease in the concentration of tocopherol and carotenoid since chlorophylls disappear after 4 months of storage. This is in agreement with the Caponio et al., 2005 [<xref ref-type="bibr" rid="scirp.28319-ref15">15</xref>] results whose results had shown that oils stored in the light had significantly lower tocopherol, carotenoid and chlorophyll contents than did the same oils kept in the dark. On the contrary, the results for the samples taken from the same region but stored in glass containers in the dark have shown constant Verdet’s constant values for at least one year (see <xref ref-type="fig" rid="fig6">Figure 6</xref>).</p><p>This can be attributed to the interruption of both photo-oxidation and auto-oxidation since glass is impermeable to oxygen. This agrees with the result obtained by Kanavouras and Coutelieris, 2006 [<xref ref-type="bibr" rid="scirp.28319-ref16">16</xref>].</p><p>In <xref ref-type="fig" rid="fig7">Figure 7</xref>, the effect of storage in filled and unfilled containers was displayed. As it can be seen from the figure, the Verdet constant for samples stored in filled plastic container (V = 165 deg/(T∙m)) and a partially filled container (V = 123 deg/(T∙m)). The degradation in the Verdet constant for the oil in the partially filled container is attributed to the interaction of the oil with air layer on top of the oil in the container.</p><p>The results of oil samples taken from another geographical area Mid-southern region of the West-Bank, and stored in plastic container in room light kept with one</p><p>year age difference are shown in <xref ref-type="fig" rid="fig8">Figure 8</xref>. Their measured values of the Verdet constant decreased with exposure to light in a similar fashion the samples taken from the south area shown in <xref ref-type="fig" rid="fig5">Figure 5</xref>. <xref ref-type="fig" rid="fig9">Figure 9</xref> shows the angle of rotation of the polarization plane as a function of the mean flux density belonging to the Mid-Southern area olive oil samples stored in glass in the dark with one year age difference. Their results are consistent with those of <xref ref-type="fig" rid="fig6">Figure 6</xref>, i.e. the value of the Verdet constant does not change for at least one year.</p><p>The results of the investigated samples taken from the middle region of the west-bank are shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>0. Such results confirmed the previously reported results in which the value of the Verdet constant increases with storage in a plastic container in the dark.</p><p><xref ref-type="fig" rid="fig1">Figure 1</xref>1 displayed a set of curves of the investigated samples obtained from northern region of the west-bank. It was found that the value of their Verdet constant decreased from V = 182 deg/(T∙m) for the sample that is that is 3 years younger, i.e. to V = 132 deg/(T∙m) for the older sample. 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