Energy Dispersive X-ray Fluorescence Spectrometer Research Articles

Analytical Techniques for Detecting Rare Earth Elements in Geological Ores: Laser-Induced Breakdown Spectroscopy (LIBS), MFA-LIBS, Thermal LIBS, Laser Ablation Time-of-Flight Mass Spectrometry, Energy-Dispersive X-ray Spectroscopy, Energy-Dispersive X-ray Fluorescence Spectrometer, and Inductively Coupled Plasma Optical Emission Spectroscopy

Rare earth elements (REEs) hold significant industrial, scientific, and modern technological worth. This study focused on detecting and quantifying REEs in various geological ore samples. These samples were collected from different REE-bearing locations recommended by geological experts. The analysis was conducted using laser-induced breakdown spectroscopy (LIBS) and laser ablation time-of-flight mass spectrometry (LA-TOF-MS). In this work, LIBS methodology was employed using three different configurations: standard LIBS, LIBS with an applied magnetic field, and LIBS with both an applied magnetic field and target sample heating within an optimal temperature range. Elements from the REE group, specifically lanthanum (La), cerium (Ce), and neodymium (Nd), were identified and quantified. To detect, quantify, and validate the results from LIBS and LA-TOF-MS, we utilized an array of analytical techniques—Energy-Dispersive X-ray Spectroscopy (EDX), Energy-Dispersive X-ray Fluorescence Spectrometer (ED-XRF), and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). Interestingly, the quantitative results for REEs (La, Ce, and Nd) in the ore samples obtained using the LIBS technique with various configurations were found to be in agreement with those from LA-TOF-MS, EDX, XRF, and ICP-OES. In addition, LIBS enables detailed microchemical imaging, allowing the map of the spatial distribution of elements within the mineral–ore matrix. The high-resolution microscale elemental mapping of REEs was accomplished using the emission lines Ce (II) at 446.0 nm, La (II) at 492.1 nm, and Nd (II) at 388.8 nm. By integrating multiple analytical techniques, our study enabled the construction of a complete elemental distribution map, providing new insights into the geochemical processes and mineral composition of rare earth ores, while advancing geochemistry and contributing valuable data for rare earth resource exploration.

Exploring soil pollution patterns in Ghana's northeastern mining zone using machine learning models

This study assessed the pollution status and effectiveness of machine learning models in predicting pollution indices in soils from a mining area in Northeastern Ghana. 552 soil samples were analysed with an Energy Dispersive X-ray Fluorescence (ED-XRF) spectrometer for their elemental concentrations. Four pollution indices; Nemerow Integrated Pollution Index (NIPI), degree of contamination (Cdeg), modified degree of contamination (mCdeg) and Pollution Load Index (PLI). Additionally, the Multivariate Adaptive Regression Splines (MARS) machine learning approach were used. The high CV%, skewness, and kurtosis values show a high degree of variability and uneven distribution patterns which denotes dispersed hotspots that can be interpreted as an influence of gold anomalies and illegal mining activities in the area. V (120.86 mg/L), Cr (242.42 mg/L), Co (30.92 mg/L) Ba (337.62 mg/L), and Zn (35.42 mg/L) recorded values higher than the global and regional contaminant thresholds. The NIPI shows that 46.74% and 26.81% of samples are slightly and moderately polluted respectively. The Cdeg analysis supports these findings, with 36.96% and 41.49% of samples classified as having “moderate” to “considerable” contamination, respectively. The PLI indicates progressive soil quality deterioration (43.84%) of samples reflecting substantial environmental disturbance. The pollution indices show the effect of illegal mining on Shaega, Buin and other areas in the eastern boundary of the study. The MARS models developed for the study demonstrated high predictive capabilities with an R2 value of 0.9665 for model 1 (NIPI), and RMSE and MAE values of 0.8227 and 0.4287 respectively. For model 2 (Cdeg), R2 value of 0.9863, RMSE and MAE of 1.0416 and 0.6181, respectively. Model 3 (mCdeg) produced an R2 value of 0.9844, RMSE and MAE of 0.1225 and 0.0670. These findings suggest MARS models can be an integral tool for soil quality analysis in cooperation with pollution indices. The study suggests that remedial and legislative measures be implemented to address the issue of illegal mining in the area.

Characterization and acid leaching beneficiation studies of Anka (Zamfara State, Nigeria) copper ore deposit

The chemical and mineralogical characterization of the Anka copper was examined and its susceptibility to H2SO4 acid leaching was assessed. A crude sample of the ore, weighing 5 kg, was sourced from the mines, communiated, homogenized, and characterised the crude sample. A 100 g fraction of the crushed sample was subjected to fractional sieve analysis and each sieve retained was chemically analysed. The leaching process was carried out on 100 g of -125+90 µm sieve size fraction using H2SO4 acid and the resulting product was chemically analyzed. The characterization result reveals 42.271% CuO using the energy dispersive x-ray fluorescence spectrometer and the x-ray diffractometer shows that the ore is mainly composed of Cu-carbonate hydroxide in the form of malachite mineral. The scanning electron microscope micrograph suggests that the ore contains dispersed grains of sodium aluminium silicate and copper carbonate hydroxide in a silica-dominated matrix. The ore's liberation size was determined to be at the sieve size of -125+90 μm. Finally, the ore was discovered to be responsive to the H2SO4 acid leaching operation, leading to an enrichment of the feed from 42.27% Cu to a pregnant solution of 52.51% Cu and the residue from the leaching was analyzed to be 4.69% Cu.

Assessment of marine and urban-industrial environmental impact on stone acting as the base of a quaternary bronze sculpture

This work investigates the influence of a marine and urban-industrial environment on the deterioration of a funerary memorial in Getxo (Basque Country, Spain). The sculpture and artificial stone materials as well as their degradation products were characterised via a multi-analytical approach. An in situ characterisation of the bronze statue and its artificial limestone base was carried out with portable Energy Dispersive X-Ray Fluorescence (ED-XRF) and Raman spectrometers. In addition, several samples of white crusts as well as metal runoff crusts and biological patina were collected and some of them were prepared as cross-sections. High Resolution Micro-X-ray fluorescence and micro-Raman spectroscopy were used as non-destructive methods to detect original and degradation compounds. The test of soluble salts was also carried out on the samples and ion chromatography was employed in the laboratory. Exclusively calcite salt-efflorescences were found at the monument side with ED-XRF and Raman spectroscopy. While their morphology was compact at unsheltered sites, they showed a lamellar structure at sheltered locations, whose increased volume strongly influences the destruction of the memorial. The spectroscopic characterization of metal runoff showed that its excessive occurrence on the memorial surface was due to the dissolution of the copper-alloy caused by chemical reactivity with the surrounding acidic atmosphere. The formation of brochantite Cu4(SO4)(OH)6, posnjakite Cu4(SO4)(OH)6·(H2O), langite Cu4(SO4)(OH)6·2(H2O), or malachite Cu2(CO3)(OH)2 was favored exclusively in metal runoff crusts at unsheltered locations. However, much thinner crusts collected at sheltered sites showed a different composition, with copper species such as moolooite (Cu(C2O4)·nH2O) and atacamite Cu2Cl(OH)3. The soluble salt extraction showed a variable concentration of soluble ions depending on the area where the samples come from. The sample from north west sheltered location showed the highest content of sulfate, nitrate and chloride compounds. In addition, the concentration of fluoride and nitrate reflects the impact of contamination of surrounding industries.

Determination of Transmission Factors and γ-Ray Linear Attenuation Coefficients of Some Construction Materials Mixed with Ulexite and Borax

In the study, transmission factors (T) and linear attenuation coefficients (μ) of some construction materials (briquette, sand, marble, paint, adobe, soil, and lime) mixed with ulexite and borax are measured with energy dispersive X-ray fluorescence spectrometer for 59.5 keV energy by using a Si(Li) detector. Ulexite and borax were added to the samples at a rate of 25, 50, and 75 percent. Results are presented and discussed in this paper. Measurements made on these construction materials with technological importance will create new use areas

Characterizations and solubility profile of novel senary SiO2–CaO–Na2O–P2O5–CaF2–SrO glass structure modified with Nb2O5

The solubility/degradability of bioactive glasses play crucial role in bone tissue engineering applications owing to the release of ions from their structure, which exert therapeutic effects on tissues. The present study evaluates the findings of a detailed investigation on the main features and solubility behaviors of newly formulated Nb incorporated glasses (Nb-BGs). New glass formulation in SiO2–CaO–Na2O–P2O5–CaF2–SrO–xNb2O5 (x: 0.0, 0.5, 1.0, and 1.5 mol. %) system was successfully synthesized by melt-quenching technique. Glass composition was verified with Energy Dispersive X-ray Fluorescence spectrometer analysis and its amorphous nature, functional groups of the matrix and morphological features were identified via X-Ray diffraction analyses, Fourier Transform Infrared Spectroscopy and Scanning Electron Microscope analysis, respectively. Network connectivity (NC) of the Nb-BGs was assessed with respect to the role of Nb2O5 in the glass matrix as network former, modifier, or both. In order to evaluate the in vitro solubility of Nb-BGs, released concentrations of particular ions from the glass compositions were determined at certain time points and comprehensively discussed with several mathematical models such as zero-order, first-order, second-order, Higuchi, and Korsmeyer-Peppas for the first time. Results showed that the incorporation of Nb2O5 (up to 1.5 mol. %) increased the density, oxygen density as well as NC values of newly formulated glasses. Si, Na and Ca ions which play a main role in well-defined Hench's mechanism followed mostly second-order release kinetics for all glasses in the mathematical models studied. When the Nb content increase (to 1.5 mol. %) in glass composition, the release mechanism of Si ion according to Korsmeyer-Peppas model shifts from the diffusion mechanism to an erosion-dominant release mechanism.

Fabrication and characterization of new Fe3O4@SiO2@TiO2-CPTS-HBAP (FST-CH) nanoparticles for photocatalytic degradation and adsorption removal of rhodamine B dye in the aquatic environment

In this study, Fe3O4@SiO2@TiO2-CPTS-HBAP (FST-CH) nanoparticle was prepared for the simultaneous adsorption and photocatalytic degradation of aromatic chemical pollutants (Rhodamine B dye) in aqueous solution. FST-CH nanoparticle was characterized using scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), Energy Dispersive X-Ray (EDX) Fluorescence Spectrometer and X-Ray Diffraction (XRD) spectroscopy. The photocatalytic activity of rhodamine B dye (RhB) was evaluated with a Kerman UV 8/18 vertical roller photoreactor. About 56% of RhB in aqueous medium was adsorbed by FST-CH nanoparticles with only 45 min of stirring in the dark, and about 77.01% was degraded or converted to other structures under the photoreactor for 120 min. The photocatalytic degradation of RhB (apparent rate constant: 0.0026 mg dm−3 min−1) occurred by a pseudo-second order reaction. In addition, the recovery of the prepared magnetic FST-CH nanoparticle by an external magnetic field, exhibiting good magnetic response and reusability, shows that the obtained magnetic FST-CH nanoparticle is stable and maintains high degradation ratio and catalyst recovery even after four cycles. Thus, the prepared FST-CH nanoparticle can be highly recommended for its use in potential applications of water decontamination.

Analysis the Metal Composition of Fish Samples Collected From Karacaören II Dam Lake

The objective of this study was to analyze the metal content in the organs of Oncorhynchus mykiss, commonly known as rainbow trout, at 12 different locations within the cages located in Karacaören II Dam Lake. The metal contents in fish samples were analyzed using a PANalytical Epsilon5 energy dispersive X-ray fluorescence (EDXRF) spectrometer. We will analyze the findings by displaying the fluctuating metal concentrations in various internal organs over the seasons.

Quantitative analysis of iodine and bromine in soil using an energy-dispersive X-ray fluorescence spectrometer with three-dimensional polarized optics.

A nondestructive and simple method for the determination of bromine and iodine in soil was investigated using an energy-dispersive X-ray fluorescence spectrometer equipped with three-dimensional polarized optics. Using a gadolinium X-ray tube and Mo and Al2O3 as optimal secondary target materials, K-lines were detected for bromine and iodine. The minimum detection limits for bromine and iodine were calculated using JSAC0411, a certified reference material of soil for metal composition analysis, and were 0.77mg/kg for bromine and 2.3mg/kg for iodine at a measurement time of 600s. The results of the determination of bromine and iodine in soil samples by the standard addition method were 256 ± 8mg/kg for iodine and 67.9 ± 1.3mg/kg for bromine with JSAC0411, which were in close agreement with the results measured by inductively coupled plasma mass spectrometry (ICP-MS) after alkaline extraction with tetramethylammonium hydroxide (TMAH) solution. The method developed in this study is an excellent technique for direct analysis of soil by X-ray fluorescence analysis without any pretreatment such as alkaline extraction. It is expected to be a practical analytical method for elucidating the dynamics of bromine and iodine in agricultural land and soil.

An Experimental Examination on the Determination of γ-ray Shielding Parameters of Some Dielectric Materials

In this study, γ-ray shielding parameters (transmission factors (TF), linear attenuation coefficients (μ), mass attenuation coefficients (μ⁄ρ), mean free path ("λ" ), radiation protection efficiency (RPE), half-value layer (HVL), and tenth value layer (TVL)) were measured of some dielectric materials (amber, plexiglass, organic glass, quartz, bakelite, NaCl, porcelain, and marble). The absorption measurements were done by EDXRFS (Energy Dispersive X-ray Fluorescence Spectrometer). The study aims to create new areas of use thanks to the measurements and calculations to be made on these technologically important dielectric materials. According to the results obtained, amber is the best gamma ray shielding material, while quartz is not suitable for gamma ray shielding.

DEVELOPMENT OF A REFERENCE SAMPLE FOR RAPID ANALYSIS OF AN ELEMENTAL COMPOSITION OF MEDICINAL PLANT RAW MATERIALS

Objective: Development and validation of a technique for preparation of a reference sample for elemental microanalysis using the XRF technique in terms of repeatability, reproducibility, and optimization of the technique for rapid determination of the elemental composition of medicinal plants based on X-ray fluorescence analysis. Methods: Samples: fresh shoots of Kalanchoe daigremontiana, ready reference sample "Birch Leaf" LB-1 (A. P. Vinogradov Institute of Geochemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russia), and IAEA reference sample SRM 2976 (IAEA, MEL, Monaco). The dispersed fraction was analyzed using a Master Sizer 2000 instrument (Malvern Panalytical, Worcestershire, UK). Elemental analysis using an energy dispersive X-ray fluorescence spectrometer EDX-7000 Shimadzu (Shimadzu Corporation, Kyoto, Japan), GZ-AAS using an Agilent instrument, model 240Z AA instrument (Agilent Technologies, Inc., Santa Clara, USA) with electrothermal atomization and Zeeman background correction, and ICP-MS using an Agilent 7500 CE instrument (Agilent Technologies, Inc., Santa Clara, USA). Results: By the LALLS method, they were separated by the maximum distribution, which was 63 microns, and a minor fraction of 39 microns. This indicates sufficient homogeneity in the sample. Further, homogeneity was proved by the XRF method by measuring six independent samples obtained by the quartering method. Also, the elemental composition of the reference samples was determined: completely dried, homogenized before sifting, and homogenized after sifting. Further, the obtained reference sample of K. daigremontiana was compared with reference samples: IAEA SRM 2976 and "birch leaf methods: ICP-MS, GZ-AAS, XRF. Conclusion: The reference sample will allow for rapid analysis of medicinal plant raw materials. Standardization of medicinal plants by the content of microelements will allow observing species differences as well as adjusting the concentrations of microelements for therapeutic purposes using medicinal plants.

When one equals two: Chemometrics turns Mössbauer spectrometer into X-ray fluorescence one

Here we explore the feasibility of using classical Mössbauer spectroscopy setup in scattering geometry to assess the elemental composition of samples using characteristic X-ray fluorescence. Even though, the scintillation detector of Mössbauer spectrometer yields rather low spectral resolution spectra, this can be effectively compensated using chemometric data processing. This hypothesis was first checked with simulated spectra of steel samples and afterwards was confirmed with real experiments. The results of Ti, Cr, Mn, Ni, Nb and Mo quantification in real steel samples obtained from Mössbauer spectrometer were compared with those obtained with commercial energy dispersive X-ray fluorescence (EDXRF) spectrometer. In case of Ti, Cr and Ni the accuracy attained with Mössbauer spectrometer was similar to that of an ordinary commercial EDXRF device.

Distribution of silicon in different organ of bamboo (Gigantochloa apus (Schult. & Schult.) Kubz ex Munro)

Bamboo is one of the plants that accumulates large amounts of silicon (Si) and potentially be utilized as a source of Si. Si plays a role in reducing abiotic and biotic stresses. This study aims to analyze the Si content in ash from various bamboo plant organs (leaves, stems and roots). Bamboo was taken from Klaten Regency, Central Java. The process of making ash used manual burning, followed by ashing using a furnace at 600 °C in temperature. Bamboo plant ash was analyzed using the AOAC method and confirmed by Energy Dispersive X-Ray Fluorescence Spectrometer (ED XRF), Scanning Electron Microscope (SEM) instruments and mapping to determine the composition of the oxide and SiO2 content. Analysis using the AOAC method showed that SiO2 content in bamboo leaf ash (76.88%) was higher than bamboo stem ash (48.43%) and bamboo root ash (56.28%). The results of ED XRF, SEM analysis and mapping showed that the main composition of bamboo plant ash was SiO2. SiO2 content of bamboo leaf ash (22.89%; 80.28%) was higher than bamboo stem ash (12.36%; 39.17%) and bamboo root ash (11.82%; 61.57%), respectively. The higher Si content in bamboo leaf ash was related to Si deposition in the leaf epidermis.

Antitoxic activity of spruce cone extract in acute lead acetate poisoning in experiment

Introduction. Lead contamination is continuing worldwide. The development of new effective drugs for lead poisoning is an urgent task. The aim of the work is to evaluate the effectiveness of dry aqueous extract of spruce cones in lead poisoning. Materials and methods. The experiment was carried out on 24 white mongrel rats of both sexes. Animals of the studied groups were administered aqueous solution of lead acetate. The animals of the third group were treated with the extract of cones of common spruce (extract) by intragastric administration 3 times a week for a month. Animals of the fourth group were treated with polypheman by intragastric administration 3 times a week for a month. The elemental composition of tissue samples of animals of the studied groups was determined on energy dispersive X-ray fluorescence spectrometer QUANT’X. The free radical reaction with 2,2-diphenyl-1-picrylhydrazyl was used to determine the antioxidant activity of the extract. Results. In groups of animals injected with lead acetate solution and treated with the extract and the comparison preparation polyphepan, a decrease in lead content in bones and brain tissues was observed compared to the content in animals injected with lead acetate solution without treatment. No effect of the extract on the motor function of the intestine was revealed. When determining the antiradical activity, it was found that the extract showed a pronounced ability to bind free radicals, comparable to the known antioxidant rutin. Discussion. The use of the extract allows effective excretion of lead and prevents its deposition in bone tissue. Due to the ability of procyanidins to penetrate the blood-brain barrier, the extract is effective in brain damage caused by lead. The extract will also be effective in relieving oxidative stress resulting from lead poisoning. Conclusion. The dry aqueous extract of cones of common spruce shows the ability to reduce the lead content in bones and brain tissues in comparison with the group that did not receive treatment for lead acetate poisoning. The extract is able not only to effectively reduce the lead content in the body, but also to fight the consequences of poisoning, due to its pronounced antiradical activity.

On the Methodology of the Quantitative Analysis of Fe–Cr–Mn–Mo–N–C Steels Reinforced with Oxide and Nitride Particles Using an Energy Dispersive X-Ray Fluorescence Spectrometer BRA-135F

On the Methodology of the Quantitative Analysis of Fe–Cr–Mn–Mo–N–C Steels Reinforced with Oxide and Nitride Particles Using an Energy Dispersive X-Ray Fluorescence Spectrometer BRA-135F

X-ray fluorescent method for the analysis of trace elements in bio-materials with correction of the matrix effect.

A method for correcting the matrix effect by measuring the intensity of fluorescent radiation and its absorption by the sample material in the same x-ray optical scheme is proposed. The use of a complex secondary Ag-Ge emitter as a primary radiation source provides a low detection limit for a wide range of chemical elements from Ca (Z = 20) to Mo (Z = 42) in the K-series and from Cd (Z = 48) to Bi (Z = 83) in the L-series. To measure the absorption, the radiation of an additional secondary emitter is used, of which the wavelengthcan be varied in the range from 0.633 to 3.38 Å, depending on the measured impurity. An example of determining the mass fraction of an impurity in a sample of unknown composition prepared from a mixture of state standard samples of aqueous solutions is given. The x-ray optical scheme was assembled on the basis of a portable Energy Dispersive X-ray Fluorescence(EDXRF) spectrometer. The method is designed to study materials with a base consisting of chemical elements with a low atomic number.

Chemical Compositions of Chinese Glazed Tiles from an Imperial Mausoleum of the Liao Dynasty

Glazed tiles are characteristic architectural ceramics traditionally used in ancient Chinese royal buildings. Studies on their chemical compositions have provided valuable information regarding their compositional classifications and the provenances of their raw materials. Existing studies have mainly focused on the Yuan dynasty (1271–1368 AD) or later. Research on earlier ages is limited because of a lack of samples. In this study, we used an energy-dispersive X-ray fluorescence spectrometer to analyze the chemical compositions of 18 glazed tiles unearthed from an imperial mausoleum (the Xinli site) from the Liao dynasty (969–982 AD). The glazes of the tiles had a SiO2–Al2O3–PbO ternary oxidic system and the bodies of the tiles had a SiO2–Al2O3 binary oxidic system. Certain compositional differences were observed among the samples with different types of decorations. Compared with samples from the Yuan dynasty and later periods, the Xinli samples had higher SiO2 and Al2O3 contents and lower PbO and CuO contents in the tile glazes. The tile bodies of the Xinli samples had compositions similar to those of tile bodies from the Qing dynasty (1616–1912 AD). We speculated that the Xinli samples with different decorations came from different kiln sites.

Portable EDXRF spectrometer: determination of linearity, LOD, LOQ, and working range for the analysis of base and precious metals in liquid matrices

Utilizing a portable energy dispersive X-ray fluorescence (EDXRF) spectrometer and certified reference materials, this study aimed to determine the linearity, limit of detection (LOD), limit of quantification (LOQ), and working range of the method for quantitative analysis of base and precious metals in liquid matrices. As the EDXRF method lacks standardization and is highly susceptible to matrix effects, these calculations play a crucial role in the analytical validation process. The obtained R2 values in this study exceeded 0.99, and the residuals exhibited a random distribution pattern. The LOD and LOQ values were determined to be exceptionally low, approaching the resolution limit of the spectrometer. Consequently, our calculations confirmed the analytical validation of the portable EDXRF method for analyzing elements in liquid matrices. The utilization of portable EDXRF equipment in quantitative measurements of elements in liquid matrices represents an innovative approach, unveiling new areas of application for this type of instrument.

Art and technique of Cuojinyin: Two belt hooks from luoyang of eastern zhou dynasty

Cuojinyin is an inlay technique for delicately decorating the surface of bronze and iron wares. It takes advantage of the ductility of gold and silver to perfectly embed them into prepared grooves on the surface of bronze and iron wares without traces of using adhesives. This paper presents preliminary analyses of two belt hooks with cuojinyin decoration excavated from Luoyang, the capital of Eastern Zhou, dated to the Warring States Period. Non-destructive analytical methods including Ultra-Depth Three-Dimensional Microscope and energy dispersive X-ray fluorescence spectrometer (XRF) were conducted to obtain analytical data and reconstruct the manufacturing process. Several interesting technical features were observed such as the secondary casting of tin–lead alloy, the elemental composition of which is totally different from the bronze surface, and the chasing marks inside the casted grooves for gold and silver inlay. The aesthetic orientation and technical details of cuojinyin not only indicate inspirations from the nomadic world and the long distance interaction across the Eurasia, but also reflect the long developed local tradition in ancient China laid in bronze mold casting technology and turquoise inlay.

Sumaki Höyük (Batman, Türkiye) Neolitik Yerleşiminde Bulunan Bazalt Parçalarının Çok Perspektifli Jeokimyasal ve Mineralojik Analizi

This study aims to determine the provenance of grinding stone tools unearthed from the Neolithic phases of Sumaki Höyük settlement using a portable Energy Dispersive X-ray Fluorescence Spectrometer (P-EDXRF) and X-ray Diffraction spectrometer (XRD). Sumaki Höyük is located in the Lower Garzan Basin of Batman province, Turkey. The settlement is dated to 9084 - 8123 cal BP. Grinding stone tools in this settlement are usually made of basalt. Albeit at low amounts, limestone was also used in the production of grinding stones. The Lower Garzan Basin, located to the east of Diyarbakır Basin, is surrounded by Mount Kıradağı and Mount Raman to the west and the Garzan and Kentalan Anticlinal to the east with Kıradağı extending in a northwest-southeast direction. The basalt flow occurred in the Quaternary period. Samples collected from different parts of the Neolithic phase of Sumaki Höyük and the Kıradağı basalt flows were analyzed using P-EDXRF to determine their chemical composition. The same samples were also analyzed using XRD to determine their mineral composition. P-EDXRF and XRD analyses reveal that the samples from Sumaki Höyük and Kıradağı are in good accordance with each other. It is therefore understood that the basalt stone tools used in the settlement were taken from the Kıradağı basalts. Data gathered on the characteristics of potential source locations provide an insight into the settlement strategy and mobility of Neolithic communities.