<?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">AJAC</journal-id><journal-title-group><journal-title>American Journal of Analytical Chemistry</journal-title></journal-title-group><issn pub-type="epub">2156-8251</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ajac.2015.65048</article-id><article-id pub-id-type="publisher-id">AJAC-55977</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Chemistry&amp;Materials Science</subject></subj-group></article-categories><title-group><article-title>
 
 
  Impact of Different Grinding Aids on Standard Deviation in X-Ray Fluorescence Analysis of Cement Raw Meal
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>ndrew</surname><given-names>Aondoaver Tyopine</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>Aondo</surname><given-names>Joseph Wangum</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Edwin</surname><given-names>Ameh Idoko</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Chemistry/Biochemistry/Molecular Biology, Faculty of Science and Technology, Federal University Ndufu Alike, Ikwo, Nigeria</addr-line></aff><aff id="aff3"><addr-line>Department of Chemistry, College of Sciences, Federal University of Agriculture, Makurdi, Nigeria</addr-line></aff><aff id="aff2"><addr-line>Department of Chemistry, Faculty of Sciences, Benue State University, Makurdi, Nigeria</addr-line></aff><pub-date pub-type="epub"><day>31</day><month>03</month><year>2015</year></pub-date><volume>06</volume><issue>05</issue><fpage>492</fpage><lpage>494</lpage><history><date date-type="received"><day>1</day>	<month>March</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>22</month>	<year>April</year>	</date><date date-type="accepted"><day>27</day>	<month>April</month>	<year>2015</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>
 
 
  X-ray fluorescence (XRF) analysis utilizes particle size which is resulted from milling of a material. The milling ensures uniform and fine grained powder. The finer and more uniform the particle size is, the better the result and easier it is for material quality control. To ensure uniformity in particle size and finer powder, a comparative analysis was conducted with different grinding aids and pressed pellet method was used in obtaining analysis results. Pressed pellets of cement raw meal sample milled with different grinding aids (graphite, aspirin and lithium borate) were subjected to XRF. Graphite produced better particle size uniformity with a corresponding standard deviation that made quality control of raw meal easier and better than aspirin and lithium borate.
 
</p></abstract><kwd-group><kwd>X-Ray Fluorescence</kwd><kwd> Pressed Pellets</kwd><kwd> Standard Deviation</kwd><kwd> Grinding Aid</kwd><kwd> Particle Size Uniformity</kwd><kwd> Comparative Analysis</kwd><kwd> Cement Raw Meal</kwd><kwd> Quality Control</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>X-ray fluorescence (XRF) has wide industrial application. It is applied in the cement industry for quality control of material since accurate and rapid determinations are critical. XRF is known for rapid and accurate analysis. However its problems include absorption, mineralogical variations among samples and particle size effects which often influence the intensities of analytical lines [<xref ref-type="bibr" rid="scirp.55977-ref1">1</xref>] .</p><p>XRF is best applied to materials where the compositional variation is small. This makes quality control of cement easier. Small variations in composition, reproducibility and accuracy of XRF analysis are affected by uniformity of particle size and size of powder grain of samples.</p><p>The reproducible and accurate results in XRF analysis require proper sample preparation in order to minimize intensity variations in the particle size distribution. Intensity increases with decrease in particle size [<xref ref-type="bibr" rid="scirp.55977-ref2">2</xref>] , because there is more penetration of incident X-ray. To achieve consistency in uniformity of particle size with a view to effective quality control, finer grinding is achieved with grinding aid.</p><p>There are studies on particle size effects on XRF where angle of intensity of incident X-rays was shown to be dependent on particle size [<xref ref-type="bibr" rid="scirp.55977-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.55977-ref4">4</xref>] , but this research focuses on studying the effect of particle size on standard deviation from XRF analysis of cement raw meal samples in quality control. Therefore the research aims to: compare particle size distribution when cement raw meal is ground with graphite, lithium borate and aspirin as grinding aids and to establish which grinding aid would produce the least standard deviation suitable for easier and better cement raw meal quality control.</p></sec><sec id="s2"><title>2. Sample Preparation</title><p>10 g cement raw meal sample was ground with grinding aid for 130 seconds at 1200 rpm. The sieve results in <xref ref-type="table" rid="table1">Table 1</xref> shows residue by way of sieve analysis using 45 &#181;m sieve mesh (BS140-1). A total of nine (9) cement raw meal samples each weighing 10 g with varying combinations of grinding aid were milled using a Pfaff grinding machine for 130 secs at 1200 rpm. The resulting powders were pelletized into circular discs. Each disc pellet was analyzed using XRF analyzer (ARL 9900 oasis) and the standard deviations per grinding aid combination were generated.</p><p>The grinding aids were graphite (98%, purchased from blue sea Nigeria Ltd.), lithium borate (99%, purchased from FLS Germany) and aspirin was purchased from king size pharmaceuticals Nigeria Ltd.</p></sec><sec id="s3"><title>3. Results and Discussion</title><p><xref ref-type="table" rid="table1">Table 1</xref> shows the particle distribution by way of sieve residue using 45 &#181;m sieve mesh. Cement raw meal ground with aspirin gave least residue followed by graphite and lithium borate having the highest residue. This means there is better particle uniformity and finer powder with aspirin than graphite and lithium borate when used independently or combined.</p><p>Tables 2-4 show standard deviation in lime saturation factor (LSF) derived from chemical analysis of cement raw meal ground with various grinding aids.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Percentage residue on 45 &#181;m sieve mesh</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Grinding aid</th><th align="center" valign="middle" >Initial sample weight</th><th align="center" valign="middle" >Final residue weight</th><th align="center" valign="middle" >% residue</th></tr></thead><tr><td align="center" valign="middle" >Graphite and lithium borate</td><td align="center" valign="middle" >10 g</td><td align="center" valign="middle" >1.27 g</td><td align="center" valign="middle" >12.70</td></tr><tr><td align="center" valign="middle" >Aspirin and lithium borate</td><td align="center" valign="middle" >10 g</td><td align="center" valign="middle" >0.94 g</td><td align="center" valign="middle" >9.40</td></tr><tr><td align="center" valign="middle" >Lithium borate</td><td align="center" valign="middle" >10 g</td><td align="center" valign="middle" >2.96 g</td><td align="center" valign="middle" >29.60</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Standard deviation from XRF analysis of sample ground with graphite and lithium borate</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >1</th><th align="center" valign="middle" >2</th><th align="center" valign="middle" >3</th><th align="center" valign="middle" >AV</th></tr></thead><tr><td align="center" valign="middle" >SiO<sub>2</sub></td><td align="center" valign="middle" >13.62</td><td align="center" valign="middle" >13.69</td><td align="center" valign="middle" >13.65</td><td align="center" valign="middle" >13.65</td></tr><tr><td align="center" valign="middle" >Al<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >4.00</td><td align="center" valign="middle" >4.00</td><td align="center" valign="middle" >3.98</td><td align="center" valign="middle" >3.99</td></tr><tr><td align="center" valign="middle" >Fl<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >1.86</td><td align="center" valign="middle" >1.88</td><td align="center" valign="middle" >1.87</td><td align="center" valign="middle" >1.87</td></tr><tr><td align="center" valign="middle" >CaO</td><td align="center" valign="middle" >41.72</td><td align="center" valign="middle" >41.69</td><td align="center" valign="middle" >41.70</td><td align="center" valign="middle" >41.70</td></tr><tr><td align="center" valign="middle" >LSF</td><td align="center" valign="middle" >94.70</td><td align="center" valign="middle" >94.14</td><td align="center" valign="middle" >94.53</td><td align="center" valign="middle" >94.46</td></tr><tr><td align="center" valign="middle" >SD</td><td align="center" valign="middle"  colspan="4"  >0.27</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Standard deviation from XRF analysis of sample ground with aspirin and lithium borate</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >1</th><th align="center" valign="middle" >2</th><th align="center" valign="middle" >3</th><th align="center" valign="middle" >AV</th></tr></thead><tr><td align="center" valign="middle" >SiO<sub>2</sub></td><td align="center" valign="middle" >12.91</td><td align="center" valign="middle" >12.95</td><td align="center" valign="middle" >12.94</td><td align="center" valign="middle" >12.93</td></tr><tr><td align="center" valign="middle" >Al<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >4.18</td><td align="center" valign="middle" >4.20</td><td align="center" valign="middle" >4.20</td><td align="center" valign="middle" >4.19</td></tr><tr><td align="center" valign="middle" >Fl<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >1.86</td><td align="center" valign="middle" >1.88</td><td align="center" valign="middle" >1.87</td><td align="center" valign="middle" >1.87</td></tr><tr><td align="center" valign="middle" >CaO</td><td align="center" valign="middle" >40.80</td><td align="center" valign="middle" >40.72</td><td align="center" valign="middle" >40.92</td><td align="center" valign="middle" >40.81</td></tr><tr><td align="center" valign="middle" >LSF</td><td align="center" valign="middle" >96.52</td><td align="center" valign="middle" >95.60</td><td align="center" valign="middle" >96.60</td><td align="center" valign="middle" >96.24</td></tr><tr><td align="center" valign="middle" >SD</td><td align="center" valign="middle"  colspan="4"  >0.57</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Standard deviation from XRF analysis of sample ground with lithium borate</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >1</th><th align="center" valign="middle" >2</th><th align="center" valign="middle" >3</th><th align="center" valign="middle" >AV</th></tr></thead><tr><td align="center" valign="middle" >SiO<sub>2</sub></td><td align="center" valign="middle" >14.67</td><td align="center" valign="middle" >14.73</td><td align="center" valign="middle" >14.85</td><td align="center" valign="middle" >14.75</td></tr><tr><td align="center" valign="middle" >Al<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >4.26</td><td align="center" valign="middle" >4.28</td><td align="center" valign="middle" >4.25</td><td align="center" valign="middle" >4.26</td></tr><tr><td align="center" valign="middle" >Fl<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >1.84</td><td align="center" valign="middle" >1.85</td><td align="center" valign="middle" >1.84</td><td align="center" valign="middle" >1.84</td></tr><tr><td align="center" valign="middle" >CaO</td><td align="center" valign="middle" >43.13</td><td align="center" valign="middle" >43.14</td><td align="center" valign="middle" >42.94</td><td align="center" valign="middle" >43.07</td></tr><tr><td align="center" valign="middle" >LSF</td><td align="center" valign="middle" >91.18</td><td align="center" valign="middle" >90.87</td><td align="center" valign="middle" >89.36</td><td align="center" valign="middle" >90.47</td></tr><tr><td align="center" valign="middle" >SD</td><td align="center" valign="middle"  colspan="4"  >0.68</td></tr></tbody></table></table-wrap><p>Sieve analysis as shown in <xref ref-type="table" rid="table1">Table 1</xref> revealed that finer particles could be achieved when aspirin is used with lithium borate. It gave 9.40% residue on 45 &#181;m. This is least when compared to graphite with lithium borate and lithium borate alone. The impact of using aspirin with lithium borate translates into a lower standard deviation as shown in <xref ref-type="table" rid="table3">Table 3</xref> when compared to that obtained when using only lithium borate as grinding aid revealed in <xref ref-type="table" rid="table4">Table 4</xref>. However it is not a good choice for industrial quality control of cement raw meal where speed is required. It had rough surface when pressed into a pellet and had high breakage frequency before few could be analyzed. Its rough surface produced higher standard deviation than that of graphite with lithium borate (<xref ref-type="table" rid="table2">Table 2</xref>). Cement meal pellet produced with graphite and lithium borate produced 12.70% residue on 45 &#181;m which is less than that produced by lithium borate alone (<xref ref-type="table" rid="table1">Table 1</xref>). Both of them produced smooth surface and robust pellets which supports speed of sample preparation. However graphite with lithium borate yielded least standard deviation (<xref ref-type="table" rid="table2">Table 2</xref>). This may be attributed to non stickiness of sample particles when ground with graphite-lithium borate grinding aid mixture which minimizes scattering of reflected rays from surface of pellet.</p></sec><sec id="s4"><title>4. Conclusion</title><p>Graphite with lithium borate gave a consistent lower standard deviation from analysis of a number of samples as compared with lithium borate. The implication is that there was less material adjustment during quality control. Cement control process parameters improved and quality control with the grinding aid mixture produced larger tons of material with consistent composition and consequently better quality.</p></sec><sec id="s5"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.55977-ref1"><label>1</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Bradner</surname><given-names> D.W. </given-names></name>,<etal>et al</etal>. (<year>1999</year>)<article-title>Analysis of Limestone and Dolomites by X-Ray Fluorescence</article-title><source> Rigaku Journal</source><volume> 16</volume>,<fpage> 16</fpage>-<lpage>18</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.55977-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Burnstein, F. (1962) Particle Size and Mineralogical Effects in Mining Applications of X-Ray Analysis. 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