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1

Salzer, Reiner. "Schwingungsspektroskopie im Nahen Infrarot." Zeitschrift für Chemie 26, no. 8 (August 31, 2010): 275–84. http://dx.doi.org/10.1002/zfch.19860260803.

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2

Gerstendörfer-Hart, Barbara. "Sekundenschnell vernetzt im nahen Infrarot." adhäsion KLEBEN & DICHTEN 56, no. 3 (March 2012): 36–39. http://dx.doi.org/10.1365/s35145-012-0097-3.

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3

Fabian, J. "Polymethinfarbstoffe mit Lichtabsorption im Nahen Infrarot." Journal f�r Praktische Chemie 333, no. 2 (1991): 197–222. http://dx.doi.org/10.1002/prac.19913330202.

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4

Kunz, Manfred H. "Spektroskopische Strukturgruppenbestimmung von Kohlenwasserstoffen im nahen Infrarot." Zeitschrift für Chemie 5, no. 9 (September 2, 2010): 333–38. http://dx.doi.org/10.1002/zfch.19650050904.

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5

Funovics, M. "Optische Bildgebung von Fluoreszenz im nahen Infrarot." Der Radiologe 47, no. 1 (January 2007): 53–61. http://dx.doi.org/10.1007/s00117-006-1452-x.

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6

Lederhose, Paul, Zhijun Chen, Rouven Müller, James P. Blinco, Si Wu, and Christopher Barner-Kowollik. "Lichtgesteuerte Kupplungsreaktionen im nahen Infrarot mittels Aufkonvertierungs-Nanopartikeln." Angewandte Chemie 128, no. 40 (August 25, 2016): 12382–86. http://dx.doi.org/10.1002/ange.201606425.

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7

Song, Chunyu, and Reinhard Otto. "Schnellbestimmung von wertbestimmenden Komponenten in Wurstwaren mittels Nahe-Infrarot-Transmissionsspektroskopie." Zeitschrift f�r Lebensmittel-Untersuchung und -Forschung 201, no. 3 (May 1995): 226–29. http://dx.doi.org/10.1007/bf01192993.

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8

Rurack, Knut, Matthias Kollmannsberger, and Jörg Daub. "Molekulares Schalten im nahen Infrarot (NIR) mit einem funktionalisierten Bordipyrromethen-Farbstoff." Angewandte Chemie 113, no. 2 (January 19, 2001): 396–99. http://dx.doi.org/10.1002/1521-3757(20010119)113:2<396::aid-ange396>3.0.co;2-w.

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9

Burfeindt, J., B. Gondokusumo, and H. D. Ließ. "Angewandte optische Untersuchungen im nahen Infrarot- und Rotbereich an Humanvollblut; Anwendungsbeispiele- - Applied Optical Studies on Human Blood Using Infrared and Red Light; Application Examples." Biomedizinische Technik/Biomedical Engineering 30, no. 1-2 (1985): 18–23. http://dx.doi.org/10.1515/bmte.1985.30.1-2.18.

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10

Uhlemann, J., E. Töpfer, R. Freyer, A. Weck-Heimann, and R. Entzeroth. "Spektrales Transmissions- und Absorptionsverhalten lebender Standardzellen im Bereich des visuellen und nahen infraroten Lichtes." Biomedizinische Technik/Biomedical Engineering 42, s2 (1997): 494–95. http://dx.doi.org/10.1515/bmte.1997.42.s2.494.

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11

Molaei, M., F. Salari Bardsiri, A. R. Bahador, and M. Karimipour. "One-pot microwave assisted approach for synthesis of CdSe/CdS core-shell quantum dots (QDs) and investigating optical properties." Modern Physics Letters B 30, no. 07 (March 20, 2016): 1650074. http://dx.doi.org/10.1142/s0217984916500743.

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In this work, CdSe QDs were synthesized using a microwave assisted method and chemical reaction between NaHSe, CdSO4 at the presence of TGA as capping molecule. Thereafter without CdSe extraction, CdS shell was grown subsequently around CdSe cores by a reaction based on the heat sensitivity of Na2S2O3 dissociation. Synthesized QDs were characterized by means of X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), UV–Vis and photoluminescence (PL) spectroscopy. All of these analyzes confirmed formation of CdSe QDs and successfully growth of CdS shell on surface of CdSe to forming CdSe/CdS core-shell structure.
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12

Molaei, M., F. Sarhani, F. Salari Bardsiri, and M. Karmipour. "CdSe/ZnS core–shell QDs: Synthesis and investigating optical properties." Modern Physics Letters B 30, no. 08 (March 30, 2016): 1650093. http://dx.doi.org/10.1142/s0217984916500937.

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In this work, CdSe quantum dots (QDs) were synthesized using a microwave activated reaction between NaHSe and CdSO4 in the presence of thioglycolic acid (TGA) as capping molecule and then using a one-pot method, ZnS shell was grown subsequently around CdSe cores by a room temperature reaction based on the photo-sensitivity of Na2S2O3 dissociation. Synthesized QDs were characterized by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), UV-visible (UV-Vis) and photoluminescence (PL) spectroscopy. All these analyses confirmed the formation of CdSe QDs and successful growth of ZnS shell around CdSe cores.
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13

Andreeva, N. V., K. V. Zotov, V. I. Yusupov, and A. V. Belyavsky. "Hydrogen Sulfide Donor NaHS Protects Mesenchymal Stem and Melanoma Cells from the Negative Effects of Infrared Laser Irradiation." Molecular Biology 53, no. 2 (March 2019): 286–90. http://dx.doi.org/10.1134/s002689331902002x.

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14

Junek, Hans, Georg Uray, and Gerhard Zuschnig. "Aminophenyl-pentafulven-6,6-dicarbonitrile-farbstoffe mit absorptionen bis in den nahen infrarot-bereich. synthesen mit nitrilen, LXXVI11LXXV. Mitteilung: M. Mittelbach, Mh. Chem., 118, 617 (1987)." Dyes and Pigments 9, no. 2 (January 1988): 137–52. http://dx.doi.org/10.1016/0143-7208(88)80013-5.

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15

Krauß, M., G. Pöhlmann, H. Bär, H. R. Figulla, and G. Grohmann. "Zur Makro- und Mikrozirkulation am Vorfuß unter verschiedenen Kompressionsdrücken bei gesunden Probandinnen." Phlebologie 29, no. 05 (May 2000): 114–23. http://dx.doi.org/10.1055/s-0037-1617334.

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ZusammenfassungZielstellung und Methoden: Das Ziel dieser Studie bestand in der Untersuchung der Makro- und Mikrozirkulation am Fuß bei Gesunden unter dosierter Kompression des Beines. Die Makro- und Mikrozirkulation wurden mit Doppler-Ultraschall-Knöchelarteriendruck- Messung und Nahe-Infrarot-Rot-Remissions-Photoplethysmographie (NIRP) bzw. mit Laser-Doppler-Flowmetrie (LDF), transkutaner Sauerstoff- (tcpO2) bzw. Kohlendioxidpartialdruckmessung (tcpCO2) und NIRP an 13 weiblichen Probanden, mittleres Alter 33,4 ± 16,8 Jahre, unter Ruhebedingungen vor und nach jeweils 5-minütiger Kompression mit 10, 20, 30, 40 bzw. 50 Torr gemessen. Ergebnisse: Der Knöchelarteriendruck sowie tcpO2 und tcpCO2 blieben unverändert. Ein signifikanter Abfall zeigte sich mit steigendem Kompressionsdruck oberhalb 20 Torr beim LDF-Flux (p <0,01) und Hämatokrit (p <0,05). Der mit NIRP bestimmte periphere Mikrozirkulations- Koeffizient pMC verminderte sich signifikant (p <0,05) oberhalb 10 Torr Kompressionsdruck. Die spektrale Maßzahl MLFo veränderte sich kaum, während die Maßzahl MLFv signifikant (p <0,05 bzw. 0,01) anstieg. Der Pulsquotient PQ fiel signifikant (p <0,05) ab bei signifikanten (p <0,01) Rückgang von Gipfelzeit TG und Wendepunktzeit TW oberhalb von 10 bzw. 30 Torr. Schlußfolgerung: Bei Gesunden tritt unter Kompression bis 50 Torr keine Verschlechterung der Makrozirkulation auf, während sich die Mikrozirkulation komperessionsbedingt ändert.
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16

Usery, E. Lynn. "GeoAI for Topographic Mapping Feature Extraction to Knowledge Graph." Abstracts of the ICA 2 (October 9, 2020): 1. http://dx.doi.org/10.5194/ica-abs-2-39-2020.

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Abstract. The U.S Geological Survey is exploring the use of machine learning and geospatial artificial intelligence (GeoAI) for topographic mapping tasks. These automated tasks include extracting topographic features such as hydrography, transportation, vegetation canopy, urban 3D structures, and others from raw data including lidar point clouds, color and near infrared images, historic topographic maps, and Web sources of existing geospatial resources. Current (2020) work includes extracting hydrography from elevation data, and geomorphic features with geographic names from historical topographical maps using Deep Learning. Extracted features are included in a geographic information system (GIS), supporting topographic mapping and modeling activities, and as semantic entities in a graph data model, building a knowledge graph for topographic data. These GIS datasets and topographic knowledge graphs can be used in automated topographic mapping processes and artificial intelligence routines that develop data for hydrologic, biologic, and geologic models that form part of the USGS EarthMap vision.
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17

Franco-Molina, Moisés Armides, Silvia Elena Santana-Krímskaya, Diana Ginette Zarate-Triviño, Pablo Zapata-Benavides, Sara Paola Hernández-Martínez, Fernanda Cervantes-Wong, and Cristina Rodríguez-Padilla. "Bovine Dialyzable Leukocyte Extract IMMUNEPOTENT CRP: Evaluation of Biological Activity of the Modified Product." Applied Sciences 11, no. 8 (April 14, 2021): 3505. http://dx.doi.org/10.3390/app11083505.

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Dialyzable leukocyte extracts are clinically used under different commercial names (IMMUNEPOTENT CRP®, IMMODIN®, Transferon®) to modulate the immune response altered by pathological conditions such as cancer, inflammation, and viral infections. The purpose of this study is to improve the production process of bovine dialyzable leukocyte extract without decreasing its biological activities (antioxidant, anti-inflammatory, and antitumoral). Our product modification consists of adding a dry heating step in the production process. In this study, we evaluated and compared the chemical composition (bromatological analysis), physical structure (infrared spectroscopy, X-ray diffraction, SEM, and zeta potential) and biological function of the dialyzable leukocyte extracts obtained from fresh and dry bovine spleens. Our results showed that the use of a drying step in the production process of the bovine dialyzable leukocyte extract (bDLE) did not affect its antioxidant and anti-inflammatory effects and it improved its antitumor properties. We suggest that this process modification could be applied to other biological products, such as dialyzable leukocyte extracts derived from other sources, in order to improve its functionality and formulation.
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18

Wrenn, Courtney. "Nebulae (emission / absorption)." Culture and Cosmos 16, no. 1 and 2 (October 2012): 439–42. http://dx.doi.org/10.46472/cc.01216.0273.

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My presentation consists of a collage on panel. Using colour laser copies of nebulae, the dual composition recombines torn pieces of several nebular images. Optically entangled from light colour patterns, the focus of each nebula resembles the opposing behaviour of absorption and emission nebula. The collages include false colour composite astronomical images to extend the visualization beyond the limits of the human eye. The subtleties of infrared and x-ray interpreted light appear to observe extra-dimensions that we intellectually understand. The layered torn paper creates forms for visual experience/contemplation. The pseudonym, scrapworm, names the allegory of my creative process. This identity is a human perspective on witnessing the passage of time and figuratively identifies with more subtle entanglements of living systems dynamics. I have recently been working with astronomical data acquired by space telescopes in my fine art collage work. The nebulae collages seek to create discourse on the time-bending implied by transmitting optical data through deep space (as related to the limit the of speed of light as well as emerging paradigms on the electric universe, quantum dynamics, and null physics).
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19

Pastore, Tereza Cristina Monteiro, Jez Willian Batista Braga, Vera Terezinha Rauber Coradin, Washington Luiz Esteves Magalhães, Esmeralda Yoshico Arakaki Okino, José Arlete Alves Camargos, Graciela Inês Bonzon de Muñiz, Otávio Augusto Bressan, and Fabrice Davrieux. "Near infrared spectroscopy (NIRS) as a potential tool for monitoring trade of similar woods: Discrimination of true mahogany, cedar, andiroba, and curupixá." Holzforschung 65, no. 1 (January 1, 2011): 73–80. http://dx.doi.org/10.1515/hf.2011.010.

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Abstract Mahogany is one of the most valuable woods and was widely used until it was included in Appendix II of the Convention on International Trade in Endangered Species as endangered species. Mahogany wood sometimes is traded under different names. Also, some similar woods belonging to the Meliaceae family are traded as “mahogany” or as being of a “mahogany pattern”. To investigate the feasibility of the use of near infrared spectroscopy for wood discrimination, the mahogany (Swietenia macrophylla King.), andiroba or crabwood (Carapa guianensis Aubl.), cedar (Cedrela odorata L.), and curupixá (Micropholis melinoniana Pierre) woods were examined. Four discrimination models based on partial least squares-discriminant analysis were developed based on a calibration set composed of 88 samples and a test set with 44 samples. Each model corresponds to the discrimination of a wood species from the others. Optimization of the model was performed by means of the OPUS® software followed by statistical analysis software (Matlab®). The observed root mean square errors of predictions were 0.14, 0.09, 0.12, and 0.06 for discriminations of mahogany, cedar, andiroba, and curupixá, respectively. The separations of the species obtained based on the difference in the predicted values was at least 0.38. This makes it possible to perform safe discriminations with a very low probability of misclassifying a sample. This method can be considered accurate and fast.
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20

Kyzas, George, Evi Christodoulou, and Dimitrios Bikiaris. "Basic Dye Removal with Sorption onto Low-Cost Natural Textile Fibers." Processes 6, no. 9 (September 14, 2018): 166. http://dx.doi.org/10.3390/pr6090166.

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Over the last several years, the trend of researchers has been to use some very low-cost materials as adsorbents. For this purpose, some already commercially used bast fibers were selected as potential adsorbent materials to remove basic dye from synthetic effluents. The adsorption of basic yellow 37 dye was studied using three different bast fibers under the names of flax, ramie, and kenaf. Their morphological structure was examined using several techniques such as scanning electron microscopy (SEM), crystallinity, X-Ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR), as well as those characterizations being a useful tool to propose a mechanism of the whole adsorption process. The adsorption evaluation was achieved by studying at first the pH (12) and temperature effects (25–55 °C). Two isotherm models (Langmuir and Freundlich) were also applied to the experimental equilibrium data revealing the superiority of ramie fibers (327, 435, and 460 mg·g−1 (25 °C) for kenaf, flax, and ramie, respectively). The crucial adsorbent’s dosage was found to be 0.1 g per litre for all fibers, while the completed desorption study (eluant’s pH and reuse cycles) also confirmed the strong potential of these kinds of fibers as adsorbents. The latter may be attributed to the cellulosic content.
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21

Bosi, Ferdinando, Andrew G. Christy, and Ulf Hålenius. "Crystal-chemical aspects of the roméite group, A2Sb2O6Y, of the pyrochlore supergroup." Mineralogical Magazine 81, no. 6 (December 2017): 1287–302. http://dx.doi.org/10.1180/minmag.2016.080.166.

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AbstractFour specimens of the roméite-group minerals oxyplumboroméite and fluorcalcioroméite from the Långban Mn-Fe deposit in Central Sweden were structurally and chemically characterized by single-crystal X-ray diffraction, electron microprobe analysis and infrared spectroscopy. The data obtained and those on additional roméite samples from literature show that the main structural variations within the roméite group are related to variations in the content of Pb2+, which is incorporated into the roméite structure via the substitution Pb2+→A2+ where A2+ = Ca, Mn and Sr. Additionally, the cation occupancy at the six-fold coordinated B site, which is associated with the heterovalent substitution BFe3+ + Y☐→BSb5++YO2-, can strongly affect structural parameters.Chemical formulae of the roméite minerals group are discussed. According to crystal-chemical information, the species associated with the name ‘kenoplumboroméite’, hydroxycalcioroméite and fluorcalcioroméite most closely approximate end-member compositions Pb2(SbFe3+)O6☐, Ca2(Sb5+Ti) O6(OH) and (CaNa)Sb2O6F, respectively. However, in accord with pyrochlore nomenclature rules, their names correspond to multiple end-members and are best described by the general formulae: (Pb,#)2(Sb,#)2O6☐, (Ca,#)2(Sb,#)2O6(OH) and (Ca,#)Sb2(O,#)6F, where ‘#’ indicates an unspecified charge-balancing chemical substituent, including vacancies.
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22

Willard, T. R., C. M. Peacock, and D. G. Shilling. "Photosynthesis as an Index of Turfgrass Growth Following Application of Herbicides." HortScience 25, no. 4 (April 1990): 451–53. http://dx.doi.org/10.21273/hortsci.25.4.451.

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The effects of sethoxydim, cloproxydim, and fluazifop on photosynthesis and growth of St. Augustinegrass [Stenotaphrum secundatum (Walt.) Kuntze `Floralawn'], bahiagrass (Paspalum notatum var. saurae Parodi `Pensacola'), and centipedegrass [Eremochloa ophiuroides (Munro.) Hack.] were evaluated to determine if photosynthesis could be used as a rapid, nondestructive measure of relative susceptibility. Field and greenhouse studies were conducted using infrared CO2 analysis to estimate photosynthesis. Under field conditions, St. Augustinegrass was susceptible to sethoxydim and fluazifop applications, as indicated by a 40% and 38% reduction in apparent photosynthesis, respectively. Bahiagrass incurred a respective 62% and 51% reduction in apparent photosynthesis from sethoxydim and fluazifop application. Growth of these species, as measured by foliage dry weight, was also inhibited by both herbicides. Centipedegrass growth was unaffected by sethoxydim, but was reduced 48% by fluazifop. Under greenhouse conditions, centipedegrass apparent photosynthesis was reduced by sethoxydim and cloproxydim (41% and 51%, respectively), while fluazifop caused a 71% reduction. Growth of centipedegrass was significantly reduced only by fluazifop (83%). These studies indicated that in vivo photosynthetic measurements may provide a sensitive, rapid, and nondestructive method for determining the susceptibility of turfgrasses to postemergence grass herbicides. chemical names used: 2-[1-(ethoxyimino)butyl]-5-[2-(ethylthio) propyl]-3-hydroxy-2-cyclohexen-l-one (sethoxydim); (E,E) -2-[1-[[(3-chloro-2-propenyl) oxy]imino]butyl] -5-[2-(ethylthio) propyl]-3-hydroxy-2-cyclohexen-l-one (cloproxydim); and butyl ester of 2-[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]-propanoate(fluazifop).
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23

Bonifazi, Giuseppe, Giuseppe Capobianco, and Silvia Serranti. "Hyperspectral Imaging and Hierarchical PLS-DA Applied to Asbestos Recognition in Construction and Demolition Waste." Applied Sciences 9, no. 21 (October 28, 2019): 4587. http://dx.doi.org/10.3390/app9214587.

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Asbestos-Containing Materials (ACMs) are hazardous and prohibited to be sold or used as recycled materials. In the past, asbestos was widely used, together with cement, to produce “asbestos cement-based” products. During the recycling process of Construction and Demolition waste (C&DW), ACM must be collected and deposited separately from other wastes. One of the main aims of the recycling strategies applied to C&DW was thus to identify and separate ACM from C&DW (e.g., concrete and brick). However, to obtain a correct recovery of C&DW materials, control methodologies are necessary to evaluate the quality and the presence of harmful materials, such as ACM. HyperSpectral Imaging (HSI)-based sensing devices allow performing the full detection of materials constituting demolition waste. ACMs are, in fact, characterized by a spectral response that nakes them is different from the “simple” matrix of the material/s not embedding asbestos. The described HSI quality control approach is based on the utilization of a platform working in the short-wave infrared range (1000–2500 nm). The acquired hyperspectral images were analyzed by applying different chemometric methods: Principal Component Analysis for data exploration and hierarchical Partial Least-Square-Discriminant Analysis (PLS-DA) to build classification models. Following this approach, it was possible to set up a repeatable, reliable and efficient technique able to detect ACM presence inside a C&DW flow stream. Results showed that it is possible to discriminate and identify ACM inside C&DW. The recognition is potentially automatic, non-destructive and does not need any contact with the investigated products.
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24

Groves, Ethan, Skip Palenik, and Christopher S. Palenik. "A Generalized Approach to Forensic Dye Identification: Development and Utility of Reference Libraries." Journal of AOAC INTERNATIONAL 101, no. 5 (September 1, 2018): 1385–96. http://dx.doi.org/10.5740/jaoacint.18-0052.

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Abstract While color is arguably the most important optical property of evidential fibers, the actual dyestuffs responsible for its expression in them are, in forensic trace evidence examinations, rarely analyzed and still less often identified. This is due, primarily, to the exceedingly small quantities of dye present in a single fiber as well as to the fact that dye identification is a challenging analytical problem, even when large quantities are available for analysis. Among the practical reasons for this are the wide range of dyestuffs available (and the even larger number of trade names), the low total concentration of dyes in the finished product, the limited amount of sample typically available for analysis in forensic cases, and the complexity of the dye mixtures that may exist within a single fiber. Literature on the topic of dye analysis is often limited to a specific method, subset of dyestuffs, or an approach that is not applicable given the constraints of a forensic analysis. Here, we present a generalized approach to dye identification that (1) combines several robust analytical methods, (2) is broadly applicable to a wide range of dye chemistries, application classes, and fiber types, and (3) can be scaled down to forensic casework-sized samples. The approach is based on the development of a reference collection of 300 commercially relevant textile dyes that have been characterized by a variety of microanalytical methods (HPTLC, Raman microspectroscopy, infrared microspectroscopy, UV-Vis spectroscopy, and visible microspectrophotometry). Although there is no single approach that is applicable to all dyes on every type of fiber, a combination of these analytical methods has been applied using a reproducible approach that permits the use of reference libraries to constrain the identity of and, in many cases, identify the dye (or dyes) present in a textile fiber sample.
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Cámara, F., E. Bittarello, M. E. Ciriotti, F. Nestola, F. Radica, F. Massimi, C. Balestra, and R. Bracco. "As-bearing new mineral species from Valletta mine, Maira Valley, Piedmont, Italy: III. Canosioite, Ba2Fe3+(AsO4)2(OH), description and crystal structure." Mineralogical Magazine 81, no. 2 (April 2017): 305–17. http://dx.doi.org/10.1180/minmag.2016.080.097.

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AbstractThe new mineral species canosioite, ideally Ba2Fe3+(AsO4)2(OH), has been discovered in the dump of Valletta mine, Maira Valley, Cuneo Province, Piedmont, Italy. Its origin is probably related to the reaction between ore minerals and hydrothermal fluids. It occurs in reddish-brown granules, subhedral millimetre-size crystals, with a pale yellow streak and vitreous lustre. Canosioite is associated with aegirine, baryte, calcite, hematite, bronze Mn-bearing muscovite, unidentified Mn oxides and unidentified arsenates. Canosioite is biaxial (+) with a 2Vmeas= 84(2)°. It is weakly pleochroic withX= brownish yellow,Y= brown,Z= reddish brown,Z>Y>X. Canosioite is monoclinic,P21/m, witha= 7.8642(4),b= 6.1083(3),c= 9.1670(5) Å, β = 112.874(6)°,V= 405.73(4) Å3andZ= 2. Calculated density is 4.943 g cm–3. The seven strongest diffraction lines of the observed powder X-ray diffraction pattern are [din Å, (I) (hkl)]: 3.713 (18)(111), 3.304 (100)(211̄), 3.058 (31)(020), 3.047 (59)(103̄), 2.801 (73)(112), 2.337 (24)(220), 2.158 (24)(123̄). Electron microprobe analyses gave (wt.%): Na2O 0.06, MgO 0.43, CaO 0.02, NiO 0.02, CuO 0.03, SrO 0.42, BaO 49.36, PbO 1.69, Al2O31.25, Mn2O33.89, Fe2O36.95, Sb2O30.01, SiO20.03, P2O50.02, V2O510.88, As2O524.64, SO3 0.01, F 0.02, H2O1.61 was calculated on the basis of 1 (OH,F,H2O) group per formula unit. Infrared spectroscopy confirmed the presence of OH. The empirical formula calculated on the basis of 9 O apfu, is (Ba1.92Pb0.05Sr0.02Na0.01)∑2.00(Fe0.523+Mn0.293+Al0.15Mg0.06)∑1.02[(As0.64V0.36)∑1.00O4]2[(OH0.92F0.01)(H2O)0.07]and the ideal formula is Ba2Fe3+(AsO4)2(OH). The crystal structure was solved by direct methods and found to be isostructural to that of arsenbrackebuschite. The structure model was refined (R1= 2.6%) on the basis of 1245 observed reflections. Canosioite is named after the small municipality of Canosio, where the type locality, the Valletta mine, is situated. The new mineral and name were approved by the International Mineralogical Association Commission on New Minerals and Mineral Names (IMA2015-030).
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"Karl Storz: Fluoreszenzbildgebung für die offene Chirurgie." kma - Klinik Management aktuell 21, no. 09 (September 2016): 53. http://dx.doi.org/10.1055/s-0036-1578470.

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27

Vag, T., T. Schramm, I. Hilger, and WA Kaiser. "Identifikation molekularer Marker für die Bildgebung der Tumorangiogenese im nahen Infrarot-Bereich." RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren 178, S 1 (2006). http://dx.doi.org/10.1055/s-2006-941128.

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28

Dullin, C., M. Zientkowska, J. Missbach-Güntner, F. Alves, LF Tietze, and E. Grabbe. "Bildfusion zwischen Flächendetektor basierter Volumen-Computer Tomographie und Fluoreszenzbildgebung im nahen Infrarot-Bereich." RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren 178, no. 11 (January 2, 2007). http://dx.doi.org/10.1055/s-2006-956194.

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29

Zscherpel, U., E. Brunner, and B. Staudte. "Wasseradsorption an Kieselgel - quantitative Aussagen aus Spektren in diffuser Reflexion im nahen Infrarot." Zeitschrift für Physikalische Chemie 271, no. 1 (January 1, 1990). http://dx.doi.org/10.1515/zpch-1990-01116.

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30

Zscherpel, U., E. Brunner, and B. Staudte. "Wasseradsorption an Kieselgel - quantitative Aussagen aus Spektren in diffuser Reflexion im nahen Infrarot." Zeitschrift für Physikalische Chemie 271, no. 1 (January 1, 1990). http://dx.doi.org/10.1515/zpch-1990-271116.

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31

Kozak, Halyna, Zdenek Remes, Alexander Kromka, and Martin Ledinsky. "Optical characterisation of organosilane-modified nanocrystalline diamond films." Chemical Papers 65, no. 1 (January 1, 2011). http://dx.doi.org/10.2478/s11696-010-0095-6.

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AbstractWe report on an optical characterisation of nanocrystalline diamond films photochemically functionalised with the organosilane-coupling agent, N 1-(3-(trimethoxysilyl)propyl)hexane-1,6-diamine (alternative names: N-(6-aminohexyl)aminopropyl-trimethoxysilane, (3-(6-aminohexylamino)propyl) trimetoxysilane, AHAPS). The presence and homogeneity of the organosilane layers were detected by fluorescence microscopy and infrared reflectance-absorbance spectroscopy. The results indicated that a homogeneous surface coverage with organosilane layers was achieved on diamond surfaces which were modified either by hydrogen or by oxygen plasma treatment. The functionalised nanocrystalline diamonds present a promising solution in future biosensor applications.
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32

Braun, Frank, Robert Schalk, Jochen Brunner, Hanns Simon Eckhardt, Michael Theuer, Ute Veith, Steffen Hennig, et al. "Nicht-invasive Prozesssonde zur Inline-Ramananalyse durch optische Schaugläser." tm - Technisches Messen 83, no. 10 (January 28, 2016). http://dx.doi.org/10.1515/teme-2016-0011.

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ZusammenfassungTrotz der bekannten Vorteile der Raman-Spektroskopie, wie bspw. eine höhere chemische Selektivität gegenüber Messmethoden im nahen Infrarot (NIR) oder die im Vergleich zum mittleren Infrarotbereich (MIR) niedrigen Matrixeinflüsse des Wassermoleküls, ist diese optische Messtechnik in der Online-Prozessanalysentechnik nicht weit verbreitet. Ein wesentliches Problem besteht in einem oftmals kostenintensiven Nachrüsten einer Messstelle durch den Einbau sogenannter Immersionssonden in eine produktführende Rohrleitung oder einen Behälter. Eine praktikable Alternative stellt das hier entwickelte neuartige Sondensystem dar, welches eine Strahlführung über Linsen mit relativ großen Durchmessern beinhaltet, da dieses an vorhandene Schauglasarmaturen angekoppelt werden kann. Mit diesem robusten Sondenaufbau sind Brennweiten weit über 25 mm möglich, welche Echtzeit-Messungen von außerhalb der produktführenden Leitungen durch optische Schaugläser gestatten. Die dadurch entstehenden Messoptionen werden exemplarisch am Nachweis von Ethanol durch Schaugläser unterschiedlicher Dicken sowie bei einer quantitativen Echtzeit-Verfolgung eines Propylencarbonat-Wasser-Gemisches durch eine Schauglasarmatur (Nenndruck PN 16, Nennweite DN 50) im Technikumsmaßstab untersucht. Die vorgestellte Raman-Sonde hat durch einfache Adaption an bereits vorhandene Armaturen industrieller Anlagen das Potential einer preiswerten und kontaktlosen Inline-Messlösung mit hoher Standzeit in der Prozessanalysentechnik (PAT).
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Huang, Min-Fu, José Luis, Alison da Silva, Juliana Rocha, Tatjana Lima, Marcus Scotti, Luciana Scotti, et al. "Synthesis, in silico Study and Antileishmanial Evaluation of New Selenides Derived from 7-Chloro-quinoline and N-Phenylacetamides." Journal of the Brazilian Chemical Society, 2021. http://dx.doi.org/10.21577/0103-5053.20200223.

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This study describes a virtual screening performed for two series of selenides (28 compounds), derived from N-phenylacetamides chlorides and 7-chloro-quinoline, to determine their potential for leishmanicidal activity against Leishmania amazonensis and Leishmania donovani. Seven compounds were predicted as potential leishmanicides; therefore, they were synthesized from elemental selenium, as a precursor for the production of NaHSe, and subsequent reactions with 4,7-dichloro-quinoline and N-phenylacetamides chlorides were performed. The compounds were characterized by infrared (IR), 1H and 13C nuclear magnetic resonance (NMR), and sent for in vitro cytotoxicity tests against L. amazonensis and were found to be active and selective, and two compounds presented half-maximal inhibitory concentrations (IC50) of 5.67 and 10.81 µg mL-1. They also presented good interaction energies in the docking study, suggesting that may exert their effects by inhibiting the N-myristoyltransferase and O-acetylserine sulfhydrylase enzymes in parasites.
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Pais, Aurélio de Jesus Rodrigues, Natasha Sofia Ribeiro, and Rubens Manoel dos Santos. "Mapping floristic communities in Southern Africa savannas, Mozambique." Rodriguésia 72 (2021). http://dx.doi.org/10.1590/2175-7860202172010.

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Abstract The present study was carried out in Limpopo National Park (LNP) with the objective to map floristic communities that occur inside the park. Three (3) Landsat 8 satellite images were obtained by Operational Land Imager (OLI) and Thermal Infrared Sensor (TIRS) tools and were pre-processed and classified, culminating in six (6) types of land use and cover. The floristic survey consisted of stratified sampling in three (3) main LNP landscapes types, namely landscape of limestone soils, landscape of rhyolite shallow soils and landscape of deep sandy soils. The final map presents 13 floristic communities identified by the names of greatest value of ecological importance (IVI) species. The community of Terminalia sericea / Combretum apiculatum / Guibourtia conjugata / Colophospermum mopane presented a larger occurrence area. Colophospermum mopane was the most representative species among the mapped communities, mostly occurring in association with other species. The overall accuracy was 74% and the Kappa index was 68%, thus giving a good rating. The mapping also showed that human occupied areas are larger than some floristic communities areas, so we suggest that these smaller communities, should be given priority actions for their conservation, especially those without human occupation.
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Morekhure-Mphahlele, Refilwe, Walter W. Focke, and Wiebke Grote. "Characterisation of vumba and ubumba clays used for cosmetic purposes." South African Journal of Science Volume 113, Number 3/4 (March 29, 2017). http://dx.doi.org/10.17159/sajs.2017/20160105.

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Abstract Two traditional cosmetic clays bear similar names in different local South African languages: vumba (Tshivenda) and ubumba (isiZulu). The wet clays are applied topically for cosmetic purposes by the respective indigenous peoples. Six samples from two South African provinces were characterised using X-ray diffraction, X-ray fluorescence spectroscopy, Fourier transform infrared spectroscopy, thermal gravimetric analysis and scanning electron microscopy. It was found that the samples differed widely with respect to mineralogy and chemical composition. This finding raises the possibility that texture characteristics during application on the skin override composition effects. Of concern is the high levels of quartz found in all the samples as it might pose a health hazard; the lowest value for quartz was 11 wt% for vumba, while values for ubumba ranged from 26 wt% to 85 wt%. All samples contained varying amounts of silicates in the form of smectite, kaolin, chlorite and plagioclase. Minor amounts of anatase and rutile were present in some samples. Three samples also contained goethite. All samples were essentially free from the toxic elements As, Pb, Hg, Cd, Se and Sb. However, they did contain low levels of chromium and heavy metals such as Cu, Zn and Ni. The pH values of ubumba slurries were slightly basic, while those of a vumba slurry were slightly acidic.
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36

Hasrawati, A., Irsan Rizaldi, Deisy Febrianti, A. Mumtihanah Mursyid, and Neneng Amelia Bakri. "PREPARATION AND CHARACTERIZATION OF THYMOQUINONE NANOPARTICLES PEGYLATED AS DRUG DELIVERY SYSTEM." Universal Journal of Pharmaceutical Research, January 15, 2021. http://dx.doi.org/10.22270/ujpr.v5i6.506.

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Objective: Thymoquinone is a main component of Black Cumin (Nigella sativa Linn.) with various pharmacological activities, but has poor stability and bioavailability. The purpose of this study was to carry out the preparation and characterization of timoquinone nanoparticles PEGylation. Methods: The Thymoquinone nanoparticles (TQ-NP) were made with PEGylation using PEG 6000 with the concentrations on each preparation of 3 mM (A), 4 mM (B), and 5 mM (C) then were evaluated by the parameter of yield percentage Entrapment Efficiency (EE) and Drug Loading (DL), drug release, size and distribution particle, morphological analysis and Fourier Transform-Infrared spectrophotometer (FTIR). Results: Thymoquinone nanoparticle was PEGylated with PEG 6000 has the highest efficiency entrapment of 99.9718±0.029% in formula A, with the capacity of drug loading 0,66%. Formulation A release 99.9718±0.029% of Thymoquinone at 50 minutes. The morphological observations with Scanning Electron Microscope (SEM) showed spherical nanoparticles morphology. Peer Review History: Received 11 September 2020; Revised 5 Decembe; Accepted 3 January, Available online 15 January 2021 UJPR follows the most transparent and toughest ‘Advanced OPEN peer review’ system. The identity of the authors and, reviewers will be known to each other. This transparent process will help to eradicate any possible malicious/purposeful interference by any person (publishing staff, reviewer, editor, author, etc) during peer review. As a result of this unique system, all reviewers will get their due recognition and respect, once their names are published in the papers. We expect that, by publishing peer review reports with published papers, will be helpful to many authors for drafting their article according to the specifications. Auhors will remove any error of their article and they will improve their article(s) according to the previous reports displayed with published article(s). The main purpose of it is ‘to improve the quality of a candidate manuscript’. Our reviewers check the ‘strength and weakness of a manuscript honestly’. There will increase in the perfection, and transparency. Received file: Comments of reviewer(s): Average Peer review marks at initial stage: 6.0/10 Average Peer review marks at publication stage: 8.0/10 Reviewer(s) detail: Dr. Evren Alğin Yapar, Turkish Medicines and Medical Devices Agency, Turkiye, evren.yapar@yahoo.com Dr. Sally A. El-Zahaby, Pharos University in Alexandria, Egypt, sally.elzahaby@yahoo.com Similar Articles: ABACAVIR LOADED NANOPARTICLES: PREPARATION, PHYSICOCHEMICAL CHARACTERIZATION AND IN VITRO EVALUATION LONG CHAIN POLYMERIC CARBOHYDRATE DEPENDENT NANOCOMPOSITES IN TISSUE ENGINEERING EFFECT OF PEGYLATED EDGE ACTIVATOR ON SPAN 60 BASED- NANOVESICLES: COMPARISON BETWEEN MYRJ 52 AND MYRJ 59
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