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Impact of Municipal Water Characteristics on Corrosion of Steel and Copper PipingPrasad, Harsha 28 April 2016 (has links)
This research evaluated corrosion and scale deposition in steel and copper pipe sections from apartment complexes located in Rhode Island (RI), Massachusetts (MA), and Maryland (MD). Piping samples from these locations had corroded at an accelerated rate and consisted of HVAC piping, and domestic copper pipes. Pipes were analyzed by scanning electron microscopy (SEM) and electron dispersive spectroscopy (EDS) to quantify the elemental composition of the samples. The water chemistry of each system was compared to the elemental data to determine correlations. Particular elements from the EDS analysis in comparison to the water quality parameters, Langelier Saturation Index, and Larson Skold indices exhibited inverse and direct correlations. The deposition of corrosion product and scales occurred in all systems that had implemented corrosion control in the form of pH adjustment and inhibitors to prevent infrastructure degradation. Although measures were taken to prevent corrosion, the current practices were not effective at the current dosing rate showing that the municipalities could consider other options such phosphate blend inhibitors and lime as effective corrosion control mechanisms.
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Mineraliseringar utmed REE-linjen i sydvästra BergslagenLinnros, Henrik January 2014 (has links)
This paper briefly summarizes Bergslagen as a bedrock province in order to give background to the genesis and presence of REE-bearing minerals (short for Rare Earth Elements) in the region. These mineralizations mainly occur along the REE-line, a line aproximately a hundred kilometers in length between Norberg in the north and Nora in the south with a width of a few kilometers. Situated in the southwest of Bergslagen it is currently one of only a few places in Sweden where REE-bearing iron oxide mineralizations are potentially economically viable for mining. Ore microscopy has been conducted in order to characterize an ore sample from Myrbacksfältet, one of few sulphide rich iron oxide mineralizations within the REE-line. Additionally, an electron microscope analysis of a sample from Stålklockan, a suspected REE-bearing mineralization also within the REE-line was confirmed by EDS (short for Energy Dispersive Spectrum) analysis. An interactive map has been made of the REE- line to aid with visualization in an attempt to collect all known geospatial-, mineral- and bedrock information in one place. The map is available in PDF format in conjunction with this text. A static version of this map is presented under 4.1 (REE-linjen). / Berggrundsprovinsen Bergslagens regionala geologi beskrivs inledningsvis för att ge bakgrund till de fyndigheter av REE-förande mineral (eng. Rare Earth Elements; Sällsynta jordartsmetaller) som förekommer utmed en ungefär hundra kilometer lång och ett par kilometer bred zon. Detta geografiskt och mineralogiskt avgränsade område kallas REE-linjen och ligger i sydvästra Bergslagen. I detta område mellan Norberg i norr och Nora i söder finns idag några av de få potentiellt ekonomiskt brytbara fyndigheterna av REE-förande mineral i Sverige vilket har gjort en kartkonstruktion vari spatiell-, mineralogisk-, och berggrundsdata över området finns sammanställd meningsfull. En sådan karta har gjorts i ArcGIS och presenteras i interaktivt PDF format i anslutning till texten. Malmmikroskopisk karaktärisering av en sulfidrik järnmalm från Myrbacksfältet i REE-linjen, såväl som en elektronmikroskopisk EDS (Energy Dispersive Spectrum) analys av ett prov från Stålklockan i Riddarhyttans malmfält har genomförts.
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Vikingatida förgyllningstekniker : En studie av förgyllningstekniker tillämpade på föremål från Birka med SEM-EDSPatriksdotter, Amanda January 2019 (has links)
Studies with primary focus on Viking age gilding techniques in Scandinavia has not been carried out since the sixties. During the past 50 years knowledge about prehistoric gilding techniques and traces of them in the archeological material, as well as the usage of natural sciences within archaeology, has developed considerably. The aim of this thesis was to revisit the topic of gilding and shed new light on Viking age metalworking in Scandinavia with focus on gilding techniques. The second aim was to determine the possibilities and limitations of the study of gilding with a non-destructive methodology. The surfaces of 13 metal objects, four of which are indigenous and the rest are imported goods, were analyzed with SEM-EDS. The chemical compositions of the gilded layers as well as the underlying silver- or copper alloys were analyzed. Furthermore, observations of micro morphological structures were carried out on the gilt surfaces. Interpretations of both chemical compositions and micro morphology were carried out in order to identify what technique or techniques have been used for gilding. The results show that two of artefacts have not been gilded at all, five of them have been fire gilded and the results of the remaining six objects are inconclusive mainly due to lacking reference data. It can be concluded that further research regarding the aging of gilt surfaces on gilded artefacts, more specifically the loss of mercury in fire gilded surfaces over time, needs to be carried out.
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Utilização da técnica de fluorescência de raios X por dispersão em energia (EDXRF) na avaliação do material particulado em suspensão na cidade de Limeira - SP / Using energy dispersive X ray fluorescence (EDXRF) technique to evaluate the suspended particulate matter from Limeira city, State of São Paulo, BrazilMoraes, Liz Mary Bueno de 31 August 2009 (has links)
O objetivo principal deste trabalho foi avaliar a composição química do material particulado em suspensão na atmosfera na cidade de Limeira/SP, pela técnica de fluorescência de raios X dispersiva em energia (EDXRF). Um amostrador tipo stacker foi utilizado para coletar particulados fino (partículas com diâmetro aerodinâmico entre 2,5 e 10 \'mü\'m) e grosso (partículas maiores que 10 \'mü\'m), utilizando filtros de policarbmüonato de 47 mm de diâmetro e com diâmetros de poro de 0,4 e 8 \'mü\'m, respectivamente. As amostras foram coletadas em 2006 (de janeiro a dezembro), 2008 (de janeiro a abril e de julho a dezembro) e 2009 (de janeiro a março). Na excitação da técnica de EDXRF utilizou-se um tubo de Mo com filtro de Fe (análise sob vácuo) para a determinação dos elementos do Al ao Ca, e com filtro de Zr (análise sob ar atmosférico) para determinação do Sc ao Zn e também do Pb. Para a detecção dos raios X utilizou-se um detector semicondutor de Si(Li) acoplado a um analisador multicanal, com um tempo de aquisição de 300 s. Os espectros de raios X foram interpretados através do programa AXIL e a para a quantificação dos elementos químicos fez-se o uso da metodologia dos parâmetros fundamentais. Realizou-se também microanálises nas amostras utilizando-se um microscópio eletrônico de varredura acoplado a um sistema de fluorescência de raios X por dispersão em energia (SEM/EDS) para a caracterização química e morfológica das partículas coletadas no material particulado em suspensão. Determinou-se também a concentração de negro de fumo (black carbon) utilizando a técnica de reflectância. Embora a amostragem não tenha sido suficiente para indicar a contribuição de cada fonte de emissão, a metodologia de análise de agrupamento possibilitou a identificar duas principais fontes para o material particulado em suspensão: poeira de solo e resíduos de queima de cana-de-açúcar / The main objective of this work was to evaluate the chemical composition of the suspended particulate matter from the atmosphere of the city of Limeira, State of São Paulo, by energy dispersive X-ray fluorescence (EDXRF) technique. A stacker filter sampler was used to collect the fine (particles with aerodynamic diameter between 2.5 and 10 \'mü\'m) and the gross particulates (particles larger than 10 \'mü\'m) employing 47 mm polycarbonate filters, with 0.4 and 8 \'mü\'m pore diameters, respectively. Samples were collected in 2006 (from January to December), 2008 (from January to April and from July to December), and 2009 (from January to March). The EDXRF excitation was carried out using a Mo X-ray tube with Fe filter (analysis under vacuum) to determine elements from Al to Ca, and with Zr filter (analysis under air atmosphere) to determine from Sc to Zn and also Pb. A Si(Li) semiconductor detector coupled to a multichannel analyzer was used for X-ray detection, with 300 s acquisition time. The X-ray spectra were deconvoluted by the AXIL software, and fundamental parameters methodology was adopted for quantification. Samples microanalysis by scanning electron microscope, connected to an energy dispersive X-ray fluorescence system (SEM/EDS) was carried out for chemical and morphological characterization of collected particles in the suspended particulate matter. Black carbon content was also evaluated by reflectance. Despite the fact that the sampling was not enough to indicate the contribution of each emission source, grouping analysis statistical method allowed to identify two main sources of the particulate matter in suspension: dust soil and sugar cane burning residues
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Malmmikroskopi, SEM-EDS- undersökning och framställning av polerprov från en sektion av Lovisagruvans sulfidmalm, Bergslagen / Ore Microscopy, SEM-EDS and Preparation of Polished Samples from a Section of the Lovisagruvan Sulphide Ore, BergslagenGhaderidosst, Joanna January 2019 (has links)
I detta arbete har polerprov framställts för att därefter undersökas med malm- och svepelektronmikroskopi (SEM) med energidispersiv röntgenspektroskopisk analys (EDS). Med dessa metoder har mineralsammansättning, strukturer och texturer identifierats och undersökts. De undersökta proverna kommer från borrkärnor genom malmzonen i Lovisagruvan i Bergslagen, södra Mellansverige. Malmen är en tabulär, silverförande Zn-Pb-sulfidmineralisering. De kombinerade undersökningarna av polerproven visar att de huvudsakligen består av zinkblände, blyglans, kvarts, mikroklin, granat, amfibol och pyrit, vilka karakteriseras av texturer som visar på omkristallisation, heterogen deformation och lokal remobilisering. De uppvisar småskaliga texturer som sannolikt är direkt relaterade till uppkomsten av s.k. kulmalmstextur. De ingående mineralens inbördes relationer tyder på att blyglans och zinkblände bildades samtidigt och därefter, under regionalmetamorfa förhållanden, tillväxte pyrit och granat som porfyroblaster. Majoriteten av texturerna och strukturerna är sekundära och visar på en kraftig senare överprägling av malmen genom metamorfos och flerfasig deformation under olika tryck- och temperaturförhållanden. / In this project polished sections have been prepared for study by means of ore and scanning electron microscopy (SEM) with energy dispersive x-ray spectroscopy (EDS). The application of these methods allows mineralogy, structures and textures to be characterized. This was done within the EU H2020-funded project X-Mine. The studied samples are from drill cores transecting the ore zone of the Lovisa mine (Lovisagruvan), which is located in Örebro County in the Bergslagen ore province, south central Sweden. Here, a tabular, stratiform silver-bearing Zn-Pb sulphide ore is mined. Studies of the polished ore sections show that the samples mainly contain sphalerite, galena, quartz, microcline, garnet, amphibole and pyrite, characterized by textures of recrystallisation, heterogeneous deformation and localized remobilization. The studied samples from the main ore and exhibit textures directly related to the formation off the so-called ball ore. The textural interrelationships of the major minerals indicate that galena and sphalerite formed penecontemporaneously, and then under regional metamorphic conditions, pyrite and garnet formed as porphyroblasts. The majority of the present textures and structures are secondary, representing different stages of metamorphism and deformation under variable P-T-conditions, post-dating original ore formation. / Real-Time Mineral X-Ray Analysis for Efficient and Sustainable Mining, H2020 X-Mine, Projekt-id: 730270
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Caracterização química multitécnicas de tintas artísticas brasileiras, um estudo de caso / Multi-technique chemical characterization of Brazilian artistic paints, a case studyMarcelo Miyada Redigolo 30 November 2018 (has links)
O presente trabalho apresenta a caracterização química de tintas artísticas brasileiras. Diferente de outras matrizes, os materiais de arte fabricados no Brasil não apresentam informações na literatura que auxiliem em sua conservação e restauração. Amostras de tintas acrílicas e a óleo, nacionais e importadas, foram analisadas pelas técnicas espectroscópicas Raman e infravermelho por transformada de Fourier (FTIR), pirólise acoplada a cromatografia a gás e espectrometria de massas (Py-GC/MS) e microscopia eletrônica de varredura acoplada a espectrometria de fluorescência de raios X (SEM-EDS). Resultados de análise indicam que tintas acrílicas brasileiras são compostas por poliestireno (PS), diferentemente das importadas, compostas por polimetilmetacrilato (PMMA). Enquanto as tintas a óleo apresentam composição semelhante (óleo de linhaça), brasileiras e importadas. Duas pinturas do acervo da Pinacoteca do Estado de São Paulo foram selecionadas para um estudo de caso. As obras apresentam a formação de exsudatos em sua superfície, o que demanda a caracterização química como etapa anterior ao desenvolvimento de uma metodologia de restauração. A obra \"Mandala da saudade\", de Sara Goldman-Belz, é composta por tinta spray (alkyd) e a obra \"Três pessoas\", de Marina Saleme, por tinta a óleo. Os resultados de análise apresentam um primeiro passo no estabelecimento de um banco de dados de materiais artísticos fabricados no Brasil para fins de restauração e perícia criminal de obras de arte. / The current work presents the chemical characterization of Brazilian artistic paints. Differently from other matrices, art materials produced in Brazil lack for information in literature that help in their conservation and restoration. Acrylic and oil paint samples, Brazilian and imported, were analyzed by Raman and Fourier transform infrared (FTIR) spectroscopies, pyrolysis coupled with gas chromatography and mass spectrometry (Py-GC/MS) and scanning electron microscopy coupled with x-ray fluorescence spectrometry (SEM-EDS). Results indicate that Brazilian acrylic paints are composed of polystyrene (PS), differently from imported ones, composed of polymethyl methacrylate (PMMA). Whereas, oil paints present similar composition (linseed oil), Brazilian and imported. Two paintings from the collection of Pinacoteca do Estado de São Paulo were selected for a case study. Both works of art present formation of exudates on their surface, which demands chemical characterization as a previous step to the development of a restoration methodology. The painting \"Mandala da saudade\", by Sara Goldman-Belz, is composed of spray paint (alkyd) and the painting \"Três pessoas\", by Marina Saleme, is composed of oil paint. Results presented in this thesis are the first step towards the establishment of a database for artistic materials produced in Brazil for purposes of art restoration and forensic science.
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Caracterização química multitécnicas de tintas artísticas brasileiras, um estudo de caso / Multi-technique chemical characterization of Brazilian artistic paints, a case studyRedigolo, Marcelo Miyada 30 November 2018 (has links)
O presente trabalho apresenta a caracterização química de tintas artísticas brasileiras. Diferente de outras matrizes, os materiais de arte fabricados no Brasil não apresentam informações na literatura que auxiliem em sua conservação e restauração. Amostras de tintas acrílicas e a óleo, nacionais e importadas, foram analisadas pelas técnicas espectroscópicas Raman e infravermelho por transformada de Fourier (FTIR), pirólise acoplada a cromatografia a gás e espectrometria de massas (Py-GC/MS) e microscopia eletrônica de varredura acoplada a espectrometria de fluorescência de raios X (SEM-EDS). Resultados de análise indicam que tintas acrílicas brasileiras são compostas por poliestireno (PS), diferentemente das importadas, compostas por polimetilmetacrilato (PMMA). Enquanto as tintas a óleo apresentam composição semelhante (óleo de linhaça), brasileiras e importadas. Duas pinturas do acervo da Pinacoteca do Estado de São Paulo foram selecionadas para um estudo de caso. As obras apresentam a formação de exsudatos em sua superfície, o que demanda a caracterização química como etapa anterior ao desenvolvimento de uma metodologia de restauração. A obra \"Mandala da saudade\", de Sara Goldman-Belz, é composta por tinta spray (alkyd) e a obra \"Três pessoas\", de Marina Saleme, por tinta a óleo. Os resultados de análise apresentam um primeiro passo no estabelecimento de um banco de dados de materiais artísticos fabricados no Brasil para fins de restauração e perícia criminal de obras de arte. / The current work presents the chemical characterization of Brazilian artistic paints. Differently from other matrices, art materials produced in Brazil lack for information in literature that help in their conservation and restoration. Acrylic and oil paint samples, Brazilian and imported, were analyzed by Raman and Fourier transform infrared (FTIR) spectroscopies, pyrolysis coupled with gas chromatography and mass spectrometry (Py-GC/MS) and scanning electron microscopy coupled with x-ray fluorescence spectrometry (SEM-EDS). Results indicate that Brazilian acrylic paints are composed of polystyrene (PS), differently from imported ones, composed of polymethyl methacrylate (PMMA). Whereas, oil paints present similar composition (linseed oil), Brazilian and imported. Two paintings from the collection of Pinacoteca do Estado de São Paulo were selected for a case study. Both works of art present formation of exudates on their surface, which demands chemical characterization as a previous step to the development of a restoration methodology. The painting \"Mandala da saudade\", by Sara Goldman-Belz, is composed of spray paint (alkyd) and the painting \"Três pessoas\", by Marina Saleme, is composed of oil paint. Results presented in this thesis are the first step towards the establishment of a database for artistic materials produced in Brazil for purposes of art restoration and forensic science.
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Utilização da técnica de fluorescência de raios X por dispersão em energia (EDXRF) na avaliação do material particulado em suspensão na cidade de Limeira - SP / Using energy dispersive X ray fluorescence (EDXRF) technique to evaluate the suspended particulate matter from Limeira city, State of São Paulo, BrazilLiz Mary Bueno de Moraes 31 August 2009 (has links)
O objetivo principal deste trabalho foi avaliar a composição química do material particulado em suspensão na atmosfera na cidade de Limeira/SP, pela técnica de fluorescência de raios X dispersiva em energia (EDXRF). Um amostrador tipo stacker foi utilizado para coletar particulados fino (partículas com diâmetro aerodinâmico entre 2,5 e 10 \'mü\'m) e grosso (partículas maiores que 10 \'mü\'m), utilizando filtros de policarbmüonato de 47 mm de diâmetro e com diâmetros de poro de 0,4 e 8 \'mü\'m, respectivamente. As amostras foram coletadas em 2006 (de janeiro a dezembro), 2008 (de janeiro a abril e de julho a dezembro) e 2009 (de janeiro a março). Na excitação da técnica de EDXRF utilizou-se um tubo de Mo com filtro de Fe (análise sob vácuo) para a determinação dos elementos do Al ao Ca, e com filtro de Zr (análise sob ar atmosférico) para determinação do Sc ao Zn e também do Pb. Para a detecção dos raios X utilizou-se um detector semicondutor de Si(Li) acoplado a um analisador multicanal, com um tempo de aquisição de 300 s. Os espectros de raios X foram interpretados através do programa AXIL e a para a quantificação dos elementos químicos fez-se o uso da metodologia dos parâmetros fundamentais. Realizou-se também microanálises nas amostras utilizando-se um microscópio eletrônico de varredura acoplado a um sistema de fluorescência de raios X por dispersão em energia (SEM/EDS) para a caracterização química e morfológica das partículas coletadas no material particulado em suspensão. Determinou-se também a concentração de negro de fumo (black carbon) utilizando a técnica de reflectância. Embora a amostragem não tenha sido suficiente para indicar a contribuição de cada fonte de emissão, a metodologia de análise de agrupamento possibilitou a identificar duas principais fontes para o material particulado em suspensão: poeira de solo e resíduos de queima de cana-de-açúcar / The main objective of this work was to evaluate the chemical composition of the suspended particulate matter from the atmosphere of the city of Limeira, State of São Paulo, by energy dispersive X-ray fluorescence (EDXRF) technique. A stacker filter sampler was used to collect the fine (particles with aerodynamic diameter between 2.5 and 10 \'mü\'m) and the gross particulates (particles larger than 10 \'mü\'m) employing 47 mm polycarbonate filters, with 0.4 and 8 \'mü\'m pore diameters, respectively. Samples were collected in 2006 (from January to December), 2008 (from January to April and from July to December), and 2009 (from January to March). The EDXRF excitation was carried out using a Mo X-ray tube with Fe filter (analysis under vacuum) to determine elements from Al to Ca, and with Zr filter (analysis under air atmosphere) to determine from Sc to Zn and also Pb. A Si(Li) semiconductor detector coupled to a multichannel analyzer was used for X-ray detection, with 300 s acquisition time. The X-ray spectra were deconvoluted by the AXIL software, and fundamental parameters methodology was adopted for quantification. Samples microanalysis by scanning electron microscope, connected to an energy dispersive X-ray fluorescence system (SEM/EDS) was carried out for chemical and morphological characterization of collected particles in the suspended particulate matter. Black carbon content was also evaluated by reflectance. Despite the fact that the sampling was not enough to indicate the contribution of each emission source, grouping analysis statistical method allowed to identify two main sources of the particulate matter in suspension: dust soil and sugar cane burning residues
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Automated Mineral Analysis of Mine WasteBuckwalter-Davis, Martha 26 August 2013 (has links)
Mineral Liberation Analyzer (MLA) is an automated mineralogical system originally developed to characterize ore and mill feeds for the metallurgical processing industry. Its ability to quantitatively characterize solid and particulate material, including whole rock thin sections, waste rock, tailings, soil, and sediments, has led to increasing applications in other industries. The software uses back-scatter electron imagery and energy dispersive X-ray analysis to analyze each particle’s shape, size, and mineralogical information. Energy dispersive X-ray data are compared to a user-generated Mineral Reference Library consisting of known phases and corresponding EDS spectra to classify each particle. MLA is used in this study to provide quantitative assessments of mining-related environmental samples to answer questions regarding mineralogical controls on bioaccessibility, metal leaching/acid rock drainage potential, and anthropogenic influence.
Six tailings samples from the New Calumet Mine in Quebec, Canada, were analyzed using MLA. Gastric Pb bioaccessibility testing and total metal content performed on these samples indicated that Pb bioaccessibility in the <250 micron size fraction was not directly correlated with the total Pb concentration. This suggested that there were mineralogical and/or physical controls on bioaccessibility. MLA was used to quantify the relative proportions of cerussite, a highly bioaccessible Pb carbonate, and galena, a lower bioaccessibility Pb sulfide. Liberation and particle size were also analyzed as controls on bioaccessibility. Sample GD-VEG1 (highest bioaccessibility) has the highest ratio of cerussite to galena, the smallest particle size, and the most liberated Pb-bearing particles.
The New Calumet tailings were also analyzed using static testing, a suite of laboratory tests used by environmental scientists and mine operators to operationally define acid rock drainage and metal leaching potential. Modal mineralogy obtained from MLA analysis was used to calculate neutralization potential (NP) and acid potential (AP), taking into account the presence of iron carbonate minerals and iron-bearing sulfides other than pyrite. Results are within several units of those obtained by static testing.
Two Ni-impacted soil samples collected from the region of Kalgoorlie, Australia were characterized using MLA. Previous studies had focused on bioaccessibility and sequential extraction testing and minor mineralogical work. Preliminary XANES characterization conflicted with mineralogy predicted from sequential extraction and EMPA and MLA were used to quantitatively characterize major Ni-bearing phases and resolve previous discrepancies. / Thesis (Master, Geological Sciences & Geological Engineering) -- Queen's University, 2013-08-24 08:13:18.722
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The effect of latent fingerprint processing on the recovery of gunshot primer residue particles from latex glovesJenquine, Kelsie Lynn 12 June 2019 (has links)
Gunshot primer residue (P-GSR) is released from the openings of a firearm when it is discharged12,13. P-GSR is made of microscopic particles that are considered characteristic of being derived from firearm ammunition when composed of barium (Ba), lead (Pb), and antimony (Sb) and have the correct morphology4. Morphology describes the shape of the P-GSR particle, which can be spherical, irregularly shaped, and must be non-crystalline. Forensic labs are commonly requested to test for the presence of P-GSR on evidential items, such as hands, clothing, vehicles, and gloves, in order to provide circumstantial evidence showing that they were, in some way, possibly involved with a shooting. Occasionally these evidential items are also expected to undergo fingerprint processing to potentially link someone to a crime. Latex gloves are often utilized in the commission of a crime with the impression that fingerprints cannot be left behind, however latent prints can often be developed on this non-porous material. Due to the evidential value of fingerprints and in order to ensure that potential prints are not damaged during P-GSR collection, latent print development is routinely performed first. Considering that P-GSR particles are easily dislodged, it is possible that some loss of P-GSR may occur during latent print processing.
The purpose of this study was to evaluate the effect of processing a non-porous item for latent fingerprints on the subsequent recovery and detection of P-GSR. Latex gloves were worn during the discharge of either a pistol or a revolver and then processed for latent prints by undergoing cyanoacrylate fuming followed by either white powder or yellow dye. The latex gloves were then sampled for P-GSR using aluminum stubs containing an adhesive coating which were dabbed over the gloves until they loss their tackiness. The stubs were then carbon coated using a Denton Vacuum Desk IV in order to prevent charging in the analytical instrument. Utilizing a JEOL JSM-6460LV Scanning Electron Microscope (JEOL USA Inc., Peabody, MA coupled with an EDAX Apollo X Analyzer (EDAX Inc., Mahwah, NJ) and EDAX Genesis GSR Software, the stubs were processed for three-component particles characteristic of P-GSR.
It was determined that P-GSR can still be recovered on latex gloves after undergoing latent print processing involving cyanoacrylate fuming followed by either white powder or yellow dye processing. Three-component particles were found on both the interior and exterior of the latex gloves after being processed for latent prints. On average, 33 P-GSR particles were found on the exterior of the gloves and four P-GSR particles were found on the interior of the gloves. Although significantly less were found on the interior of the gloves (<10), it is recommended that both sides of gloves be stubbed when collecting P-GSR for the greatest chances of collecting three-component particles if they are in fact present on a pair of gloves.
Although more particles were found on the gloves that were not processed for latent prints, a sufficient number of particles (≥3 particles) were consistently found on the latex gloves after undergoing latent print processing to provide a positive P-GSR result according to the Massachusetts State Police Crime Lab guidelines for P-GSR analysis. Therefore, this research shows that latex gloves can first be processed for latent prints and then subsequently be processed for P-GSR effectively in order to try and obtain both forms of evidence for a case.
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