Quantitative Bulk and Trace Element X-Ray Mapping Using Multiple Detectors

X-ray mapping using energy dispersive spectroscopy or wavelength dispersive spectroscopy is a very popular characterisation tool for determining the elemental distribution in materials. Furthermore, quantitative X-ray mapping has become a very powerful technique enabling reliable quantitative results that can be an order of magnitude better than traditional analysis. Quantitative X-ray mapping is also far superior to regions of interest X-ray maps where low levels of an element or elemental overlaps are present. The one major drawback with X-ray mapping is the time required to obtain a high resolution X-ray map with good statistics at low levels of concentration. The use of multi-detectors, and just developed dual turret detectors for X-ray mapping, allows improvement in performance at low levels without compromising quantification quality and precision of traces, even in the presence of overlaps. However, for quantitative X-ray mapping to work properly, the characteristics of each detector must be accurately determined so that the final quantification of the individual detectors can be summed. To accomplish this effectively, the full spectrum at each pixel for each energy dispersive detector should be saved. As a final check for consistency between detectors, a technique was developed that involves assigning a different red-green-blue colour for each detector for the same element. By doing this, when we combine the three maps of the same element, we should obtain a grey scale map that indicates total correlation between the three detectors at the most critical final stage of quantification. To reduce contrast noise and further improve the quality of quantitative X-ray mapping images, a filter referred to as a “speckle filter” has been developed that allows the eye to see a more correct elemental concentration relationship.     

Soft X-ray spectromicroscopy on solid-stabilized emulsions

Oil–water emulsions stabilized by solids have been imaged with sub-100 nm spatial resolution and analyzed spectroscopically using a scanning transmission X-ray microscope. The emulsions are stabilized by particle heterocoagulate cages surrounding the oil droplets. These cages form due to the interaction of negatively charged clay mineral particles (sodium montmorillonite, Wyoming) and positively charged particles of calcium/aluminum layered double hydroxide (LDH). The emulsions were studied at atmospheric pressure, without any pretreatment using carbon K and calcium L X-ray absorption edges. Oil- and calcium-rich LDH were separately mapped, and the clay mineral dispersions were also imaged. Applying X-ray absorption-edge contrast, oil could be distinguished from water in the emulsion near the carbon K absorption edge (284 eV, 4.4 nm). Spectromicroscopy near the calcium L absorption edge (346 eV, 3.6 nm) allowed the structural details of heterocoagulate formation to be revealed. Received: 11 December 1998 Accepted in revised form: 10 January 1999     

Detector Calibration and Measurement of Fundamental Parameters for X-Ray Spectrometry

Energy-dispersive X-ray spectrometry offers the opportunity for a fast and reliable determination of the composition of a specimen. For fundamental parameter based quantification, detailed knowledge of the X-ray generation cross sections and of the detection system’s efficiency is required. The detection efficiency is determined comparing the measured and calculated spectrum of undispersed synchrotron radiation (SR) from the electron storage ring BESSY II in the spectral range from 0.1 keV to 100 keV. Alternatively, monochromatized SR in the spectral range from 0.1 keV to 60 keV is used to determine the detection efficiency with a typical relative uncertainty of 1% to 2% by direct comparison with a reference detector. Employing well-calibrated detectors and monochromatized SR of well-known radiant power and high spectral purity, fluorescence yields have been investigated and resonant Raman scattering was studied as an example of a basic effect creating spectral background.     

Synchrotron radiation FTIR imaging in minutes: a first step towards real-time cell imaging

FTIR microscopy with a focal plane array (FPA) of detectors enables routine chemical imaging on individual cells in only a few minutes. The brilliance of synchrotron radiation (SR) IR sources may enhance the signal obtained from such small biosamples containing small amounts of organic matter. We investigated individual cells obtained from a cell culture specifically developed for transmission FTIR imaging using either a Globar or an SR source coupled to the same instrumentation. SR-IR source focussing was optimized to control the energy distribution on the FPA of detectors. Here we show that accessing the IR absorption distribution from all the organic contents of cells at 1 × 1 μm pixel resolution was possible only with high circulating current (≥1.2 A) illuminating a limited number of the FPA’s detectors to increase the signal-to-noise ratio of IR images. Finally, a high-current SR ring is mandatory for collecting FTIR images of biosamples with a high contrast in minutes.     

FTIR imaging investigation in MIR and in an enlarged MIR-NIR spectral range

The study of polished cross sections is a well-assessed and practical method to investigate the stratigraphy of paintings and multilayer polychromies on works of art, in general. Analyses on cross sections allow us to characterize, at once, all the layers in the stratigraphy, giving information about the artists technique, the number of layers and their composition and sometimes about the conservation history of the artefact. In this paper, the application of an imaging detector focal plane array (FPA) coupled to an infrared (IR) microscope has been studied, focusing on the characteristics and potential of the different working methodologies (attenuated total reflectance (ATR) and total reflection). FPA detector coupled with ATR crystal can “localize” IR information coming from a 30 × 30μm sample area, in a 64 × 64 dot matrix detector. In particular, an innovative analysis methodology has been tested for the total reflectance measurements in order to obtain maximum information with single measurements. Micro-infrared total reflection measurements have been carried out in an extended IR range (from 1,000 to 5,266 cm⁻¹) exploiting the broad spectral response of mercury cadmium telluride detector in order to include overtones and combination bands from near-infrared spectral range without any modification of the standard mid-infrared micro-FT instrumentation. The potentialities of this new approach have been successfully transferred in the imaging/mapping investigations with a minimal tuning of the apparatus. Results obtained on a polished cross section coming from a modern painting and on a micro-sample of a wood polychromy from an undated historic polyptic are shown for demonstration.     

Deposition and Characterization of Metastable Cu3N Layers for Applications in Optical Data Storage

 Cu₃N films for optical data storage were deposited on Si(100) wafers and 0.6 mm thick polycarbonate DVD base material discs at a temperature of 50 °C by reactive magnetron sputtering. A copper target was sputtered in rf mode in a nitrogen plasma. For basic investigations concerning the composition and structure of Cu₃N, Si wafers were used as substrate material. To study the suitability of Cu₃N as an optical data storage medium under technical conditions, Cu₃N/Al bilayers were deposited on polycarbonate discs. The composition and structure of the films were investigated by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The decomposition of Cu₃N into metallic copper and nitrogen was induced and characterized with a dynamic tester consisting of an optical microscope with an integrated high power laser diode. The change in reflectivity induced by the laser pulses was measured by a high sensitivity photo detector. Optimized Cu₃N films could be decomposed into metallic copper at pulse lengths of 200 ns. The reflectivity change from 3.2% to 33.2% for completely transformed areas and to 12% for single bits as well as the maximum write data rate of 3.3 Mbit/s demonstrated the suitability of Cu₃N for write once optical data storage. Especially the carrier to noise ratio of 41 dB shows an increase of a factor of 3 for this novel material as compared to conventional optical data storage media.     

Benefits of X-Ray Spectrum Simulation at low Energies

 There are particular benefits in spectrum simulation for the interpretation of characteristic X-ray peaks below about 2 keV in energy, where peak overlaps, a sloping background and changing detector efficiency make it difficult to measure true peak intensities. Despite these difficulties, we have shown that a useful accuracy of simulation is possible without major revision of the existing theory, allowing the electron microprobe user to compare on-line a measured spectrum with one synthesised from an assumed sample composition. As part of a wider study, we have used a database of X-ray spectra from 150 samples of known composition to confirm the accuracy of simulation over the energy range from 0.28–1.9 keV, finding an RMS error of better than 8%. The database included 181 Kα, Lα and Mα peaks from elements of atomic number 6–77, excited by beam voltages from 5–30 kV. Central to the method is the use of the ratio of (Peak Intensity)/(Total Background Intensity), which allows spectra to be compared from instruments of differing collection efficiency, thereby easing the collection of data over a wide range of conditions. Examples are given to illustrate the use of the simulator in helping to choose the best conditions for analysis, and as an aid in interpreting the spectra so obtained. Both modes of operation are iterative in nature and require a fast and accurate simulator that is easy to use. Further development will be guided by experience in its use.     

Self-assembled monolayer gold electrode for surfactant analysis

A gold electrode coated with a self-assembled monolayer of octane-thiol (SAM/Au) has been used as an amperometric detector for the determination of surfactants. This detector operated in the presence of a high percentage of organic solvent and was adapted to an HPLC System. At the SAM/Au, the electrochemical response of an electroactive tracer (potassium ferricyanide) was completely inhibited, but, in the presence of a cationic surfactant, the electrochemical reduction was progressively restored. In flow injection analysis, using the SAM/Au in an amperometric flow-through detector polarised at 0.0 V vs Ag/AgCl, a linear response (i=f{[surfactant]}) was observed for cationic surfactants e.g. cetylpyridinium chloride in the concentration range 2 × 10⁻⁶–1 × 10⁻³ M. The electrochemical data along with the determination of the ion pair stoichiometry between the redox tracer and the surfactant suggest an electrochemical response related to ion pair formation and governed by electron transfer by tunneling effect. Received: 28 January 1997 / Accepted: 7 March 1997     

The Observation of Strong Absorption of the Yttrium Lα Line in Sialon Ceramics

 β-sialon ceramics sintered with yttria additives have been studied with the use of an electron probe X-ray analysis (EPMA). Sialon ceramics were prepared from a carbothermally derived β-sialon powder and then sintered in a nitrogen atmosphere with yttria admixture. The above process was followed by annealing in flowing nitrogen. Scanning electron microscope (SEM) observations have shown that the sintered material contains a glassy phase (Y-Si-Al-O-N) on the grain boundaries. X-ray diffraction (XRD) after annealing in nitrogen revealed the presence of a considerable amount of yttrium aluminium garnet (YAG). The higher voltage of 30 kV was used in order to excite the yttrium K_α radiation (14.96 keV) at an appropriate overvoltage ratio because in some phases of the material, the disappearance of the yttrium L_α line has been observed during EPMA examination at an accelerating voltage of 15 kV in energy dispersive spectra (EDS). The intensity of the yttrium K_α line was sufficiently high, while the Y L_α line was not seen in the ED spectrum. Because the position of the yttrium L_α line (1.922 keV) is very close to the Si (K) absorption edge (1.84 keV), the strong absorption at this edge is probably responsible for the effect. This result should be considered as a serious warning in the case of EPMA (EDS) studies on compounds or mixtures suspected to contain both silicon and yttrium, because at electrons energies lower than 15 keV, the presence of yttrium in materials can go unnoticed. In wavelength dispersive spectra (WDS) obtained at 15 keV the intensity of the yttrium L_α line was also very low but measurable.     

Quantitative determination of large structures by small-angle light scattering

A new small-angle light scattering camera has been developed. In contrast to conventional detection the present system is based on a recently developed two-dimensional charge-coupled-device chip made by Thomson (France). The advantage of this chip is its excellent linear response and very low dark signal even at room temperature. The best linearity was obtained by leading each pixel signal through the same amplifying system. The optical system covered a diffraction angular region from about 1° to 15° (q = 0.2–2.6 μm⁻¹). The camera was calibrated with grids and pinholes and was tested with polymer latex particles in solution and with spherulites from polymer films. Received: 06 December 1999 Accepted: 04 February 2000     

Immunochemical analysis of 3-phenoxybenzoic acid,a biomarker of forestry worker exposure to pyrethroid insecticides

Pyrethroid insecticides widely used in forestry, agricultural, industrial, and residential applications have potential for human exposure. Short sample preparation time and sensitive, economical high-throughput assays are needed for biomonitoring studies that analyze a large number of samples. An enzyme-linked immunosorbent assay (ELISA) was used for determining 3-phenoxybenzoic acid (3-PBA), a general urinary biomarker of exposure to some pyrethroid insecticides. A mixed-mode solid-phase extraction reduced interferences from acid hydrolyzed urine and gave 110 ± 6% recoveries from spiked samples. The method limit of quantification was 2 μg/L. Urine samples were collected from forestry workers that harvest pine cone seeds where pyrethroid insecticides were applied at ten different orchards. At least four samples for each worker were collected in a 1-week period. The 3-PBA in workers classified as high, low, or no exposure based on job analysis over all sampling days was 6.40 ± 9.60 (n = 200), 5.27 ± 5.39 (n = 52), and 3.56 ± 2.64 ng/mL (n = 34), respectively. Pair-wise comparison of the differences in least squares means of 3-PBA concentrations among groups only showed a significant difference between high and no exposure. Although this difference was not significant when 3-PBA excretion was normalized by creatinine excretion, the general trend was still apparent. No significant differences were observed among days or orchards. This ELISA method using a 96-well plate was performed as a high-throughput tool for analyzing around 300 urine samples measured in triplicate to provide data for workers exposure assessment.     

Efficient maximization of coloration by modification in morphology of electrodeposited NiO thin films prepared with different surfactants

In this paper, we report on the nickel oxide (NiO) thin films potentiostatically electrodeposited onto indium-doped tin oxide-coated glass substrates by using two types of organic surfactants: (1) non-ionic: polyethylene glycol (PEG), polyvinylpyrrolidone (PVP) and (2) anionic: sodium dodecyl sulfate (SDS). An aqueous solution containing nickel sulfate precursor and potassium hydroxide buffer was used to grow the samples. The effect of organic surfactants on its structural, morphological, wettability, optical, electrochromic, and in situ colorimetry were studied using X-ray diffraction, scanning electron microscopy, contact angle, FT-IR spectroscopy, optical transmittance, cyclic voltammetry, and CIE system of colorimetry. X-ray diffraction patterns show that the films are polycrystalline, consisting of NiO cubic phase. A nanoporous structure with pore diameter of about 150–200 nm was observed for pure NiO. The films deposited with the aid of organic surfactants exhibits various surface morphological feature. PVP-mediated NiO thin film shows noodle-like morphology with well-defined surface area whereas, an ordered pore structure composed of channels of uniform diameter of about 60–80 nm was observed for PEG. A compact and smooth surface with nanoporous structure stem from SDS helps for improved electrochromic performance compared with that of NiO deposits from surfactant-free solution. Wetting behavior shows, transformation from hydrophilic to superhydrophilic nature of NiO thin films deposited with organic surfactant, which helps for much more paths for electrolyte access. The surfactant-mediated NiO produce high color/bleach transmittance difference up to 57% at 630 nm. On oxidation of NiO/SDS, the CIELAB 1931 2° color space coordinates show the transition from colorless to the deep brown state (L* = 84.41, a* = −0.33, b* = 4.41, and L* = 43.78, a* = 7.15, b* = 13.69), with steady decrease in relative luminance. The highest coloration efficiency of 54 cm² C⁻¹ with an excellent reversibility of 97% was observed for NiO/SDS thin films.     

Electrochemical kinetic study about cobalt electrodeposition onto GCE and HOPG substrates from sulfate sodium solutions

In the present work, we analyze the electrodeposition of cobalt by electrochemical techniques onto GCE (system I) and HOPG (system II) electrodes from sulfate solutions. Cyclic voltammetry and current transient measurements were used to obtain the nucleation and growth mechanism. The results clearly showed that electrodeposition of cobalt is a diffusion-controlled process with a typical 3D nucleation mechanism in both substrates. The average ΔG calculated for the stable nucleus formation was 1.97 × 10⁻²⁰ J nuclei⁻¹ and 3.58 × 10⁻²⁰ J nuclei⁻¹ for system I and system II, respectively. The scanning electron microscope (SEM) images indicated similar nucleation and growth processes on GCE and HOPG substrates at same overpotential with a homogeneous disperse cobalt clusters. X-ray energy-dispersive spectroscopy (EDS) was performed in order to ensure that the clusters formed are cobalt. The nuclei’s size obtained was dependent of the overpotential applied; at lower overpotentials, the growth rate of the cobalt clusters diminishes when their number increases due to the strongly reduced concentration of cobalt ions because of their consumption by a larger number of growing particles. A theoretical quantum study employing PM6 method suggests that Na⁺ adsorbed deactivate the local surface occasionating the formation of disperse cobalt clusters on carbon electrodes.     

The new X-ray mapping: X-ray spectrum imaging above 100 kHz output count rate with the silicon drift detector.

Electron-excited X-ray mapping is a key operational mode of the scanning electron microscope (SEM) equipped with energy dispersive X-ray spectrometry (EDS). The popularity of X-ray mapping persists despite the significant time penalty due to the relatively low output count rates, typically less than 25 kHz, that can be processed with the conventional EDS. The silicon drift detector (SDD) uses the same measurement physics, but modifications to the detector structure permit operation at a factor of 5-10 times higher than conventional EDS for the same resolution. Output count rates as high as 500 kHz can be achieved with 217 eV energy resolution (at MnKalpha). Such extraordinarily high count rates make possible X-ray mapping through the method of X-ray spectrum imaging, in which a complete spectrum is captured at each pixel of the scan. Useful compositional data can be captured in less than 200 s with a pixel density of 160 x 120. Applications to alloy and rock microstructures, ultrapure materials with rare inclusions, and aggregate particles with complex chemistry illustrate new approaches to characterization made practical by high-speed X-ray mapping with the SDD.Note: The Siegbahn notation for characteristic X-rays is commonly used in the field of electron beam X-ray spectrometry and will be used in this article. The equivalent IUPAC notation is indicated in parentheses at the first use.In this article, the following arbitrary definitions will be used when referring to concentration (C) ranges: major: C > 0.1 (10 wt%), minor: 0.01 相似文献   

EPMA and X-Ray Diffraction of the Degraded Fuel Bundle from the Phebus FPT1 Test

 The degraded fuel rod bundle from the second Phebus test (FPT1) was examined at ITU, Karlsruhe. Metallographic and microprobe analysis of the degraded fuel pieces were carried out. The fuel samples from the upper bundle and cavity edge were porous and had remnants of thick oxidised cladding adhering to them. Electron microprobe analysis line scans across the cladding-fuel interface showed interdiffusion of U and Zr, with U diffusing down the grain boundaries of the oxidised cladding, while point analyses revealed noticeable amounts of Zr (1.5–4.2 wt%) in the UO₂ fuel. EPMA oxygen measurements revealed in the upper part of the bundle a superstoichiometry of x = 0.3–0.4 in UO _2 + x , indicating that fuel fragments in this position had undergone considerable oxidation. X-ray diffraction of the corium pool disclosed a deformed cubic fluorite lattice of UO₂. The lattice parameter of a = 5.2984 ? was considerably reduced compared with pure, stoichiometric UO₂ and was consistent with a lattice containing approximately 45 mol% ZrO₂ that had undergone little oxidation. The corium’s nominal composition of (U_0.5Zr_0.5) O₂ also corresponded to its observed single phase microstructure.     

Thermodynamic Investigation of Phase Equilibria in Metal Carbonate–Water–Carbon Dioxide Systems

 Solubility measurements as a function of temperature have been shown to be a powerful tool for the determination of thermodynamic properties of sparingly-soluble transition metal carbonates. In contrast to calorimetric methods, such as solution calorimetry or drop calorimetry, the evaluation of solubility data avoids many systematic errors, yielding the enthalpy of solution at 298.15 K with an estimated uncertainty of ±3 kJ · mol⁻¹. A comprehensive set of thermodynamic data for otavite (CdCO₃), smithsonite (ZnCO₃), hydrozincite (Zn₅(OH)₆(CO₃)₂), malachite (Cu₂(OH)₂CO₃), azurite (Cu₃(OH)₂(CO₃)₂), and siderite (FeCO₃) was derived. Literature values for the standard enthalpy of formation of malachite and azurite were disproved by these solubility experiments, and revised values are recommended. In the case of siderite, data for the standard enthalpy of formation given by various data bases deviate from each other by more than 10 kJ · mol⁻¹ which can be attributed to a discrepancy in the auxiliary data for the Fe²⁺ ion. A critical evaluation of solubility data from various literature sources results in an optimized value for the standard enthalpy of formation for siderite. The Davies approximation, the specific ion-interaction theory, and the Pitzer concept are used for the extrapolation of the solubility constants to zero ionic strength in order to obtain standard thermodynamic properties valid at infinite dilution, T = 298.15 K, and p = 10⁵ Pa. The application of these electrolyte models to both homogeneous and heterogeneous (solid-solute) equilibria in aqueous solution is reviewed.     

Li-cycling properties of nano-crystalline (Ni1 ? xZnx)Fe2O4 (0 ≤ x ≤ 1)

Sol–gel auto-combustion method is adopted to prepare solid solutions of nano-crystalline spinel oxides, (Ni_1 − x Zn _x )Fe₂O₄ (0 ≤ x ≤ 1).The phases are characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy, selected area electron diffraction, and Brunauer–Emmett–Teller surface area. The cubic lattice parameters, calculated by Rietveld refinement of XRD data by taking in to account the cationic distribution and affinity of Zn ions to tetrahedral sites, show almost Vegard’s law behavior. Galvanostatic cycling of the heat-treated electrodes of various compositions are carried in the voltage range 0.005–3 V vs. Li at 50 mAg⁻¹ up to 50 cycles. Phases with high Zn content x ≥ 0.6 showed initial two-phase Li-intercalation in to the structure. Second-cycle discharge capacities above 1,000 mAh g⁻¹ are observed for all x. However, drastic capacity fading occurs in all cases up to 10–15 cycles. The capacity fading between 10 and 50 cycles is found to be greater than 52% for x ≤ 0.4 and for x = 0.8. For x = 0.6 and x = 1, the respective values are 40% and 18% and a capacity of 570 and 835 mAh g⁻¹ is retained after 50 cycles. Cyclic voltammetry and ex situ transmission electron microscopy data elucidate the Li-cycling mechanism involving conversion reaction and Li–Zn alloying–dealloying reactions.     

The preparation, molecular structure, and theoretical study of carbohydrazide (CHZ)

Carbohydrazide is prepared by reacting dimethyl carbonate with hydrazine hydrate. Its single crystal has been cultured with slow evaporation method. Its molecular structure and crystal structure have been determined by X-ray single crystal diffraction technique. The obtained results shows that the crystal belongs to Crystal system of Monoclinic, space group P2(1)/n with crystal parameters of a = 3.725(1), b = 8.834(2), c = 11.96(3), β = 91.97(1)°, V = 392.23(2) ³, Z = 4, D _c = 1.522 g/cm³, μ = 0.128 mm⁻¹, F0 0 0) = 192. Based on the crystal data, we have also carried quantum chemistry calculations on the title compound using the B3LYP and MP2 method with cc-pVTZ basis set. The calculation results further demonstrate the molecular structure of title compound and its coordination properties.     

Chemical deposition and characterization of thin polypyrrole films on glass plates: role of organosilane treatment

 Thin chloride-doped polypyrrole films (PPyCl) were deposited chemically onto untreated and silane-treated planar glass plates from aqueous solutions. The organosilanes used to treat the glass substrates were methyltriethoxysilane (Cl), propyltrimethoxysilane (C3), octyltrimethoxysilane (C8) and aminopropyltriethoxysilane (APS). The decreasing order of hydrophobic character of silane-treated glass slides, as measured by water contact angle measurements, was glass–APS ≅ glass–C8 > glass–C3 > glass–C1 > glass. X-ray photoelectron spectroscopy was used to determine the surface chemical composition of the glass plates before and following coating with the silane coupling agents and/or the PPy thin layer, respectively. The attenuation in intensity of the glass Na_{1 s} peak enabled the average thickness of the various organosilane overlayers to be estimated. Atomic force microscopy showed that the morphology of the organosilane overlayers was islandlike. The domains have a structure which depends upon the nature of the organosilane in question. Scanning electron microscope images showed that the morphology of the PPyCl thin films was homogeneous when coated onto glass–APS and glass–C8, but wrinkled at the surface of glass, glass–C1 and glass–C3 plates. Qualitative peel tests using 3M adhesive tape showed very good adhesion of PPyCl to the glass–APS substrate, whereas adhesion was fairly poor in the case of glass–PPy and PPy–alkylsilane–glass interfaces. The results of this multitechnique study suggest that hydrophobic interactions are important to obtain homogeneous and continuous thin PPy films, but Lewis acid–base interactions are the driving forces for strong and durable PPy–glass adhesion. Received: 3 January 2000/Accepted: 19 May 2000     

Mass spectrometry imaging with high resolution in mass and space (HR<Superscript>2</Superscript> MSI) for reliable investigation of drug compound distributions on the cellular level

Mass spectrometry (MS) imaging is a versatile method to analyze the spatial distribution of analytes in tissue sections. It provides unique features for the analysis of drug compounds in pharmacokinetic studies such as label-free detection and differentiation of compounds and metabolites. We have recently introduced a MS imaging method that combines high mass resolution and high spatial resolution in a single experiment, hence termed HR² MS imaging. In the present study, we applied this method to analyze the spatial distribution of the anti-cancer drugs imatinib and ifosfamide in individual mouse organs. The whole kidney of an animal dosed with imatinib was measured at 35 μm spatial resolution. Imatinib showed a well-defined distribution in the outer stripe of the outer medulla. This area was analyzed in more detail at 10 μm step size, which constitutes a tenfold increase in effective spatial resolution compared to previous studies of drug compounds. In parallel, ion images of phospholipids and heme were used to characterize the histological features of the tissue section and showed excellent agreement with histological staining of the kidney after MS imaging. Ifosfamide was analyzed in mouse kidney at 20 μm step size and was found to be accumulated in the inner medulla region. The identity of imatinib and ifosfamide was confirmed by on-tissue MS/MS measurements. All measurements including mass spectra from 10 μm pixels featured accurate mass (≤2 ppm root mean square) and mass resolving power of R = 30,000. Selected ion images were generated with a bin size of ∆m/z = 0.01 ensuring highly specific information. The ability of the method to cover larger areas was demonstrated by imaging a compound in the intestinal tract of a rat whole-body tissue section at 200 μm step size. The described method represents a major improvement in terms of spatial resolution and specificity for the analysis of drug compounds in tissue sections.