<?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">JMMCE</journal-id><journal-title-group><journal-title>Journal of Minerals and Materials Characterization and Engineering</journal-title></journal-title-group><issn pub-type="epub">2327-4077</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jmmce.2015.31002</article-id><article-id pub-id-type="publisher-id">JMMCE-52920</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><subject> Engineering</subject></subj-group></article-categories><title-group><article-title>
 
 
  Chemical Characterization of Auriferous Ores from the Brazilian State of Paraiba
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>arcelo</surname><given-names>Rodrigues do Nascimento</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>Artur</surname><given-names>M. G. Lourenço</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Instituto Federal de Educa&amp;amp;ccedil&amp;amp;atildeo, Ciência e Tecnologia da Paraíba, Laboratório de Flota&amp;amp;ccedil&amp;amp;atildeo, Campina Grande,
Brazil</addr-line></aff><aff id="aff2"><addr-line>Universidade Federal de Campina Grande, Programa de Pós-Gradua&amp;amp;ccedil&amp;amp;atildeo em Engenharia Civil, Campina
Grande, Brazil</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>marceloquimica@gmail.com(ARDN)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>26</day><month>12</month><year>2014</year></pub-date><volume>03</volume><issue>01</issue><fpage>9</fpage><lpage>14</lpage><history><date date-type="received"><day>18</day>	<month>October</month>	<year>2014</year></date><date date-type="rev-recd"><day>20</day>	<month>November</month>	<year>2014</year>	</date><date date-type="accepted"><day>1</day>	<month>December</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>
 
 
  One of the most important problems facing the gold industry is that the placer and free milling gold ores are almost terminating. Hence, the use of refractory ores has been increased during the recent years. In general, gold refractory ores occurs in various types of deposits associated with a range of minerals. Among the refractory ores, the sulfide type is the most common. The methodology employed in the mining process depends on the mode of occurrence of the ore and on the particle size, shape and degree of purity of the auriferous species. We have undertaken a mineralogical investigation of a representative sample of a complex gold mining ore collected in the municipality of Princesa Isabel, Paraiba, Brazil, using X-ray fluorescence spectrometry, X-ray diffractometry, infrared spectroscopy, inductively coupled plasma-atomic emission spectrometry and the Fire Assay. The results showed that the arsenic content of the ore was closely related to the gold content, and that the occurrence of “invisible gold” was associated primarily with pyrite and secondarily with arsenopyrite. The sulfur content of the ore was directly related to its refractoriness. It is concluded that gold mineralization in the study area is mainly of the gold-quartz-sulfide veins (lode gold), while the gold found in the mini-fractures of the deposits is probably associated with the hydrothermal processes that occurred in the region.
 
</p></abstract><kwd-group><kwd>Auriferous Ore</kwd><kwd> Chemical Characterization</kwd><kwd> X-Ray Fluorescence Spectrometry</kwd><kwd> X-Ray  Diffractometry</kwd><kwd> Inductively Coupled Plasma-Atomic Emission Spectrometry</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>In Cachoeira de Minas, gold occurs primarily in auriferous quartz veins, the distinguishing feature of which is the absence or scarcity of hydrothermal alterations in the host rock. In addition, minor occurrences of gold can be found in sulfide-rich shear zones created by hydrothermal alterations where no mining is performed. The dis- tribution of these different zones is determined by the tectonic and metamorphic architecture of the Forma&#231;&#227;o Salinas (distal unit of the Maca&#250;bas Group in the Ara&#231;ua&#237; basin). Thus, the gold mineralization in Paraiba is represented mainly by quartz-gold-sulfide veins (lode gold), with primary gold located in rocks of Riacho Gravat&#225; complex. The secondary source is the quartz veins and alluvial deposits, and the gold found in the micro- fractures of these veins is probably associated with hydrothermal processes that occurred in the area [<xref ref-type="bibr" rid="scirp.52920-ref3">3</xref>] .</p></sec><sec id="s2"><title>2. Methodology</title><sec id="s2_1"><title>2.1. Sample Preparation</title><p>Samples of auriferous rock (100 kg) were collected in the region of Princesa Isabel, and subsequently crushed, ground in a disk mill and homogenized in stacks in order to obtain a representative sample of the study area. All transfer operations were carried out using an iron shovel. Screening assays were performed on 1.0 kg samples using standard Tyler sieves, with mesh openings of 0.600, 0.500, 0.300, 0.177, 0.104 and 0.074 mm, and a vi- bratory sieve shaker. A precision analytical scale with an accuracy of 1 mg was used to weigh the materials re- tained by the sieves.</p></sec><sec id="s2_2"><title>2.2. Chemical and Mineralogical Analyses</title><p>Samples were subjected to elemental analysis by X-ray fluorescence (XRF) spectrometry employing a RIX- 3000 instrument (Rigaku, Tokyo, Japan) equipped with a Rh X-ray tube and six analyzing crystals. Crystalline structure was evaluated using a model D-5000 X-ray diffractometer (Siemens, Berlin, Germany) with Cu-Kα as the source of monochromatic radiation. For all samples, scattering intensities were recorded at room temperature over the angular range 2θ = 10˚ - 90˚ with a step size of 0.03˚ and a step time of 1.0 s. Infrared spectra of samples in the form of vacuum-pressed KBr pellets were measured in the range 4000 - 400 cm<sup>−1</sup> using a Bomem (ABB-Bomem, Quebec, Canada) model MB-102 Fourier-transform infrared (FTIR) spectrometer. Rare earth elements were characterized by inductively coupled plasma-atomic emission spectrometry (ICP-AES) using an ARL model 35,000 instrument (Applied Research Laboratories, Austin, TX, USA). Gold and other noble metals were characterized by the Fire Assay method and atomic absorption spectrometry (AAS) employing an Analyst model 100 spectrometer (Perkin Elmer, Waltham, MA, USA). The limits of detection of the ICP-AES and Fire Assay/AAS techniques were 0.008 - 0.02 ppm for light elements and 0.005 ppm for gold, respectively.</p></sec></sec><sec id="s3"><title>3. Results</title><p>Particle size classification of the bulk sample (<xref ref-type="fig" rid="fig1">Figure 1</xref>) revealed p<sub>80</sub> and p<sub>50</sub> values of 0.485 and 0.265 mm, indicating that 80% and 50% of the particles, respectively, passed through the 32- and 48-mesh sieves. In addition, 90% of particles passed through the 28-mesh sieve, whereas only 14.9% passed through the 200-mesh sieve. The mean values of the quantity of material retained in each of the sieves reflect the efficiency of the grinding method since the mechanical properties of the minerals present in the sample are distinct. For example, the host rock is more brittle and has high iron content, whereas the gold-bearing rock (quartz) is very hard.</p><p>XRF analysis verified the heterogeneous composition of the sample and confirmed that the levels of silicon dioxide (from the quartz), aluminum oxide and iron oxide were high, as expected (<xref ref-type="table" rid="table1">Table 1</xref>). The refractoriness of the ore was explained by the presence of arsenic trioxide and sulfur trioxide, which contribute to the difficulty in treating and processing the gold associated with pyrite, arsenopyrite, and chalcopyrite.</p><p>ICP-AES analysis (<xref ref-type="table" rid="table1">Table 1</xref>) revealed that the sample contained various economically important metals such as Cu, Zn and Ni that could be recovered by flotation and/or leaching techniques. The presence of rare earth elements in the ore suggests the possibility of greater exploitation in the longer term, since these materials have a number of applications in the computer industry, industrial engineering, renewable energy sciences and medi- cine.</p><p>According to the Fire Assay/AAS method, the concentration of gold in the ore sample was 4.422 ppm (assay detection limit 0.005 ppm), a value that is below the limit of detection of XRF (10 ppm or 0.01%). In this type of mineral ore, the gold is typically dissolved in the interstices, primarily of pyrite and secondarily of arsenopyrite [<xref ref-type="bibr" rid="scirp.52920-ref4">4</xref>] .</p><p>Since every crystalline material has a specific and characteristic X-ray diffraction pattern, it was possible toidentify the substances present in the sample by comparison of the diffractograms with those published in the literature. The diffraction profile presented in <xref ref-type="fig" rid="fig2">Figure 2</xref> confirms the presence of gold in the study sample [<xref ref-type="bibr" rid="scirp.52920-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.52920-ref7">7</xref>] , and reveals the face-centered cubic structure of the crystalline material. Additionally, the less intense peak observed at 64.1˚ is typical of Fe<sub>2</sub>O<sub>3</sub> [<xref ref-type="bibr" rid="scirp.52920-ref8">8</xref>] .</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Particle size distribution of a representative sample of gold mining oreoriginating from Princesa Isabel, PB, Brazil</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2710267x6.png"/></fig><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Chemical profile of a representative sample of gold mining ore originating from Princesa Isabel, PB, Brazil</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="13"  >Oxides (%) determined by XRF analysis<sup>a</sup></th></tr></thead><tr><td align="center" valign="middle" >Al<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >SiO<sub>2</sub></td><td align="center" valign="middle" >Fe<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >PbO</td><td align="center" valign="middle" >SO<sub>3</sub></td><td align="center" valign="middle" >K<sub>2</sub>O</td><td align="center" valign="middle" >MnO</td><td align="center" valign="middle" >As<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >TiO<sub>2</sub></td><td align="center" valign="middle" >CaO</td><td align="center" valign="middle" >P<sub>2</sub>O<sub>5</sub></td><td align="center" valign="middle" >MgO</td><td align="center" valign="middle" >Cr<sub>2</sub>O<sub>3</sub></td></tr><tr><td align="center" valign="middle" >4.55</td><td align="center" valign="middle" >66.81</td><td align="center" valign="middle" >17.42</td><td align="center" valign="middle" >2.41</td><td align="center" valign="middle" >3.08</td><td align="center" valign="middle" >1.33</td><td align="center" valign="middle" >0.56</td><td align="center" valign="middle" >0.27</td><td align="center" valign="middle" >0.23</td><td align="center" valign="middle" >0.19</td><td align="center" valign="middle" >0.20</td><td align="center" valign="middle" >0.10</td><td align="center" valign="middle" >0.10</td></tr><tr><td align="center" valign="middle"  colspan="13"  >Metals (ppm) determined by Fire Assay/AAS and ICP-AES analysis</td></tr><tr><td align="center" valign="middle" >Zn</td><td align="center" valign="middle" >Zr</td><td align="center" valign="middle" >V</td><td align="center" valign="middle" >Cu</td><td align="center" valign="middle" >Mo</td><td align="center" valign="middle" >Ni</td><td align="center" valign="middle" >Rb</td><td align="center" valign="middle" >Tl</td><td align="center" valign="middle" >Zn</td><td align="center" valign="middle" >Sr</td><td align="center" valign="middle" >Ba</td><td align="center" valign="middle" >Au</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >194</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >71</td><td align="center" valign="middle" >280</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >82</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >194</td><td align="center" valign="middle" >75</td><td align="center" valign="middle" >195</td><td align="center" valign="middle" >4.42</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle"  colspan="13"  >Rare earth elements (ppm) determined by ICP-AES analysis</td></tr><tr><td align="center" valign="middle" >Ce</td><td align="center" valign="middle" >Gd</td><td align="center" valign="middle" >Hf</td><td align="center" valign="middle" >La</td><td align="center" valign="middle" >Nd</td><td align="center" valign="middle" >Pr</td><td align="center" valign="middle" >Sm</td><td align="center" valign="middle" >U</td><td align="center" valign="middle" >Yb</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >18</td><td align="center" valign="middle" >1.45</td><td align="center" valign="middle" >1.32</td><td align="center" valign="middle" >9.50</td><td align="center" valign="middle" >7.90</td><td align="center" valign="middle" >2.21</td><td align="center" valign="middle" >1.10</td><td align="center" valign="middle" >1.10</td><td align="center" valign="middle" >0.90</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p><sup>a</sup>Loss on Ignition (LOI) = 2.52%.</p><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> X-ray diffraction profile of a representative sample of gold mining ore originating from Princesa Isabel, PB, Brazil. Legend: Au (*); SiO<sub>2</sub> (+); Fe<sub>2</sub>O<sub>3</sub> (#)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2710267x7.png"/></fig><p>Information regarding the SiO<sub>2</sub> matrix could be obtained from the FTIR spectrum (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Based on detailed interpretations of the IR spectra of various silica-containing structures [<xref ref-type="bibr" rid="scirp.52920-ref9">9</xref>] - [<xref ref-type="bibr" rid="scirp.52920-ref11">11</xref>] , a band attributable to the asymmetric stretching mode of Si-O bonds in an [SiO<sub>4</sub>]<sup>2−</sup> tetrahedron was observed around 1080 cm<sup>−1</sup>. Although this band could be overlapping with another band corresponding to g-Al<sub>2</sub>O<sub>3</sub> [<xref ref-type="bibr" rid="scirp.52920-ref12">12</xref>] , the symmetric stretching modes of Si-O bonds could be readily observed at around 785 cm<sup>−1</sup>, and bands between 565 and 455 cm<sup>−1</sup> could be assigned to the deformation vibrations of Si-O-Si bonds.</p></sec><sec id="s4"><title>4. Discussion</title><p>In the recovery of gold from auriferous rock, the particle size at which the metal lies represents a key factor in determining the overall efficiency of the process. In this context, the crushing and grinding steps are extremely important since they determine the range of particle sizes generated from the ores. According to the literature [<xref ref-type="bibr" rid="scirp.52920-ref3">3</xref>] , 80% of gold can be collected on sieves ranging between 100 and 400 mesh. Hence, the aim of a particle size- study is to establish sieve sizes that allow the selection of particles with a high degree of release, thereby facilitating the separation of particles of interest from the gangue. Although ball mills are normally employed in grinding in gold mining operations [<xref ref-type="bibr" rid="scirp.52920-ref13">13</xref>] , a disk mill was used in the present study because the sample rocks ex-</p><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Fourier-Transform infrared spectrum of a representative sample of gold mining ore originating from Princesa Isabel, PB, Brazil</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2710267x8.png"/></fig><p>hibited elevated hardness owing to the presence of quartz.</p><p>It may be inferred from the results presented herein that the gold in ores from the state of Paraiba is associated predominantly with pyrite, arsenopyrite and sulfide. Refractory ores of this type generally require treatment involving roasting, bacterial oxidation or fine grinding. The mechanism of incorporation of submicroscopic particles of gold into sulfides has not yet been elucidated, but it has been suggested that gold is assimilated as sulfide by chemisorption onto surfaces that are Fe-deficient and As-rich, where it exists as a metastable solid solution [<xref ref-type="bibr" rid="scirp.52920-ref14">14</xref>] . Simon et al. [<xref ref-type="bibr" rid="scirp.52920-ref15">15</xref>] demonstrated that gold was present in the structure of arsenopyrite as microinclusions of Au<sup>0</sup> and Au<sup>1+</sup>, while Au<sup>0</sup> concentrated in fine pyrite at lower temperatures. Cabri et al. [<xref ref-type="bibr" rid="scirp.52920-ref16">16</xref>] confirmed that gold is present in arsenopyrite either as microparticles of Au<sup>0</sup> or in the form of covalently linked Au<sup>1+</sup>. These ores can become more reactive if the crystal lattice energy is reduced, and this can be achieved through mechanical grinding and/or vibration techniques. In this case, the reduction of the activation energy of the reaction is attributed to microcracks and structural defects.</p><p>In the last decade, numerous studies have been performed with the purpose of augmenting gold recovery and developing cleaner technologies, but few studies have focused on understanding the mineralogy of the deposits in which gold can be found. Knowledge of the composition of the rocks that encase the precious metal can contribute to the reduction in operational and production costs. In this context, our study provides essential data regarding a representative sample of auriferous ore from the state of Paraiba.</p></sec><sec id="s5"><title>5. Conclusion</title><p>It is concluded that the submicroscopic gold particles incorporated into the crystal lattice of pyrite and arsenopyrite are progressive released as inclusions and fractures, and the presence of such particles is the main factor responsible for the refractoriness of the auriferous ore from Princesa Isabel, PB, Brazil. This information is of considerable importance since, in ores containing pyrite and arsenopyrite, the fine particles of gold are occluded and disseminated among the sulfide minerals and cannot be released solely by mechanical grinding. The flotation concentrates of this type of gold ore are usually pre-treated by pyrometallurgical or hydrometallurgical methods.</p></sec><sec id="s6"><title>Acknowledgements</title><p>The authors wish to thank the Conselho Nacional de Desenvolvimento Cient&#237;fico e Tecnol&#243;gico (CNPq; grant no. 550261/2010-9) for financial support and the miners from Princesa Isabel for assistance with sample collection.</p></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.52920-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ojeda, M.W., Perino, E. and Ruiz, M.C. (2009) Gold Extraction by Chlorination Using a Pyrometallurgical Process. Minerals Engineering, 22, 409-411. 
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