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Littérature scientifique sur le sujet « Active probes »

Auteur : Grafiati

Publié le 1 mars 2025

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Articles de revues sur le sujet "Active probes"

Birring, Anmol. « Optimizing Probe Active Aperture for Phased Array Weld Inspections ». Materials Evaluation 79, n^o 8 (1 août 2021) : 797–804. http://dx.doi.org/10.32548/2021.me-04220.

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Phased array ultrasonic testing (PAUT) has become a popular nondestructive technique for weld inspections in piping, pressure vessels, and other components such as turbines. This technique can be used both in manual and automated modes. PAUT is more attractive than conventional angle-beam ultrasonic testing (UT), as it sweeps the beam through a range of angles and presents a cross-sectional image of the area of interest. Other displays are also available depending on the software. Unlike traditional A-scan instruments, which require the reconstruction of B- and C-scan images from raster scanning, a phased array image is much simpler to produce from line scans and easier to interpret. Engineering codes have incorporated phased array technology and provide steps for standardization, scanning, and alternate acceptance criteria based on fracture mechanics. The basis of fracture mechanics is accurate defect sizing. There is, however, no guidance in codes and standards on the selection and setup of phased array probes for accurate sizing. Just like conventional probes, phased array probes have a beam spread that depends on the probe’s active aperture and frequency. Smaller phased array probes, when used for thicker sections, result in poor focusing, large beam spread, and poor discontinuity definition. This means low resolution and oversizing. Accurate sizing for fracture mechanics acceptance criteria requires probes with high resolution. In this paper, guidance is provided for the selection of phased array probes and setup parameters to improve resolution, definition, and sizing of discontinuities.

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Anson, Christopher E., Tina J. Baldwin, Colin S. Creaser, Mark A. Fey et G. Richard Stephenson. « IR-Active Organometallic pH Probes ». Organometallics 15, n^o 5 (janvier 1996) : 1451–56. http://dx.doi.org/10.1021/om950589o.

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Tschirret-Guth, Richard A., Katalin F. Medzihradszky et Paul R. Ortiz de Montellano. « Trifluoromethyldiazirinylphenyldiazenes : New Hemoprotein Active-Site Probes ». Journal of the American Chemical Society 121, n^o 20 (mai 1999) : 4731–37. http://dx.doi.org/10.1021/ja990351h.

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Glasmachers, A. « Active miniature radio frequency field probe ». Advances in Radio Science 1 (5 mai 2003) : 161–64. http://dx.doi.org/10.5194/ars-1-161-2003.

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Abstract. For the measuring of the electromagnetic interference (e.g. on men) of RF fields produced by mobile communication equipment field probes are required with high spatial resolution and high sensitivity. Available passive probes show good results with respect to bandwidth and low field distortion, but do not provide the required sensitivity and dynamic range. A significant limitation for active miniature probes is the power supply problem, because batteries cannot be used. Therefore the effect of high impedance connection lines is examined by a numerical field simulation. Different approaches for the design of an active probe are discussed, a favourable solution with a logarithmic demodulator is implemented and measuring results are presented.

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Szalkowski, Marcin, Karolina Sulowska, Martin Jönsson-Niedziółka, Kamil Wiwatowski, Joanna Niedziółka-Jönsson, Sebastian Maćkowski et Dawid Piątkowski. « Photochemical Printing of Plasmonically Active Silver Nanostructures ». International Journal of Molecular Sciences 21, n^o 6 (16 mars 2020) : 2006. http://dx.doi.org/10.3390/ijms21062006.

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In this paper, we demonstrate plasmonic substrates prepared on demand, using a straightforward technique, based on laser-induced photochemical reduction of silver compounds on a glass substrate. Importantly, the presented technique does not impose any restrictions regarding the shape and length of the metallic pattern. Plasmonic interactions have been probed using both Stokes and anti-Stokes types of emitters that served as photoluminescence probes. For both cases, we observed a pronounced increase of the photoluminescence intensity for emitters deposited on silver patterns. By studying the absorption and emission dynamics, we identified the mechanisms responsible for emission enhancement and the position of the plasmonic resonance.

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Devanesan, Prabhakar D., et Albert M. Bobst. « Spin probes as mechanistic inhibitors and active site probes of thymidylate synthetase ». Journal of Medicinal Chemistry 29, n^o 7 (juillet 1986) : 1237–42. http://dx.doi.org/10.1021/jm00157a021.

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Sandoghdar, V., et J. Mlynek. « Prospects of apertureless SNOM with active probes ». Journal of Optics A : Pure and Applied Optics 1, n^o 4 (1 janvier 1999) : 523–30. http://dx.doi.org/10.1088/1464-4258/1/4/319.

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Kovalev, Yuri A. « Some active galactic nuclei as cosmological probes ». Space Science Reviews 74, n^o 3-4 (novembre 1995) : 475–79. http://dx.doi.org/10.1007/bf00751436.

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Tong, Jiaqi, Ting Hu, Anjun Qin, Jing Zhi Sun et Ben Zhong Tang. « Deciphering the binding behaviours of BSA using ionic AIE-active fluorescent probes ». Faraday Discussions 196 (2017) : 285–303. http://dx.doi.org/10.1039/c6fd00165c.

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The binding behaviours of a transport protein, bovine serum albumin (BSA), in its native, unfolding and refolding states have been probed by monitoring the emission changes of two exogenous AIE-active fluorescent probes, M2 and M3, which are designed to be anionic and cationic, respectively. Due to their AIE properties, both M2 and M3 display emission enhancement when bound to the hydrophobic cavity of BSA. The binding site of M2 and M3 is found to be subdomain IIA. Then, the BSA + M2 and BSA + M3 systems are utilized to fluorescently signal the conformation changes of BSA caused by various external stimuli, including thermally or chemically induced denaturation. The data confirmed the multi-step unfolding process and the existence of a molten-globule intermediate state. The unfolding process consists of the rearrangement of subdomain IIA, the exposure of a negatively charged binding site in domain I that prefers interacting with cationic species, and the transformation of the molten-globule intermediate into the final random coil. The anionic and cationic modifications of the probes enable us to observe that electrostatic interactions play a role in the folding and unfolding of BSA.

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Chen, Xinqi, Ming Sun et Huimin Ma. « Progress in Spectroscopic Probes with Cleavable Active Bonds ». Current Organic Chemistry 10, n^o 4 (1 mars 2006) : 477–89. http://dx.doi.org/10.2174/138527206776055312.

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Thèses sur le sujet "Active probes"

Walpole, C. S. J. « Active site probes for bacterial luciferase ». Thesis, University of Sussex, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356510.

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Sun, Zhenning. « Studies on fluorescent probes for the specific detection of reactive oxygen species and reactive nitrogen species in living cells ». View the Table of Contents & ; Abstract, 2006. http://sunzi.lib.hku.hk/hkuto/record/B36845395.

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Torun, Hamdi. « Micromachined membrane-based active probes for biomolecular force spectroscopy ». Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/39638.

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Atomic force microscope (AFM) is an invaluable tool for measurement of pico-Newton to nano-Newton levels of interaction forces in liquid. As such, it is widely used to measure single-molecular interaction forces through dynamic force spectroscopy. In this technique, the interaction force spectra between a specimen on the sharp tip of the cantilever and another specimen on the substrate is measured by repeatedly moving the cantilever in and out of contact with the substrate. By varying the loading rate and measuring the bond rupture force or bond lifetime give researchers information about the strength and dissociation rates of non-covalent bonds, which in turn determines the energy barriers to overcome. Commercially available cantilevers can resolve interaction forces as low as 5 pN with 1 kHz bandwidth in fluid. This resolution can be improved to 1 pN by using smaller cantilevers at the expense of microfabrication constraints and sophisticated detection systems. The pulling speed of the cantilever, which determines the loading rate of the bonds, is limited to the point where the hydrodynamic drag force becomes comparable to the level of the molecular interaction force. This level is around 10 um/s for most cantilevers while higher pulling speeds are required for complete understanding of force spectra. Thus, novel actuators that allow higher loading rates with minimal hydrodynamic drag forces on the cantilevers, and fast, sensitive force sensors with simple detection systems are highly desirable. This dissertation presents the research efforts for the development of membrane-based active probe structures with electrostatic actuation and integrated diffraction-based optical interferometric force detection for single-molecular force measurements. Design, microfabrication and characterization of the probes are explained in detail. A setup including optics and electronics for experimental characterization and biological experiments with the probes membranes is also presented. Finally, biological experiments are included in this dissertation. The "active" nature of the probe is because of the integrated, parallel-plate type electrostatic actuator. The actuation range of the membrane is controlled with the gap height between the membrane and the substrate. Within this range it is possible to actuate the membrane fast, with a speed limited by the membrane dynamics with negligible hydrodynamic drag. Actuating these membrane probes and using a cantilever coupled to the membrane, fast pulling experiments with an order of magnitude faster than achieved by regular AFM systems are demonstrated. The displacement noise spectral density for the probe was measured to be below 10 fm/rtHz for frequencies as low as 3 Hz with differential readout scheme. This noise floor provides a force sensitivity of 0.3 - 3 pN with 1 kHz bandwidth using membranes with spring constants of 1 - 10 N/m. This low inherent noise has a potential to probe wide range of biomolecules. The probes have been demonstrated for fast-pulling and high-resolution force sensing. Feasibility for high throughput parallel operation has been explored. Unique capabilities of the probes such as electrostatic spring constant tuning and thermal drift cancellation in AFM are also presented in this dissertation.

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Schrag, Michael L. « Development of active site directed probes for cytochrome P450 / ». Thesis, Connect to this title online ; UW restricted, 1998. http://hdl.handle.net/1773/8153.

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Shelton, Thomas Earl. « Small Phosphomonoesters as Probes of Protein-Tyrosine Phosphatase Active Sites ». Thesis, Virginia Tech, 1999. http://hdl.handle.net/10919/44898.

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I evaluated the potential of isomers of the low molecular weight phosphomonoester naphthyl phosphate as general diagnostic substrates for differentiating between two families of protein phosphatases: the protein-tyrosine phosphatases [PTPs] and the dual-specificity protein phosphatases [DSPs]. Three PTPs, PTP-1B, Tc-PTPa, and PTP-H1, and three DSPs, Cdc-14, VHR, and IphP, were challenged in vitro with alpha-naphthyl phosphate and beta-naphthyl phosphate. Both the DSPs and PTPs readily hydrolyzed beta-naphthyl phosphate. As expected, the DSPs also hydrolyzed alpha-naphthyl phosphate at rates comparable to beta-naphthyl phosphate and two of the PTPs, PTP-1B and Tc-PTPa, hydrolyzed alpha-naphthyl phosphate at a rate one-tenth that of beta-naphthyl phosphate. However, PTP-H1 hydrolyzed both alpha- and beta- naphthyl phosphate at nearly equal rates. Intriguingly, when challenged with radiolabeled phosphoproteins, PTP-H1 was markedly less stringent, by a factor of 40- to 200- fold, than PTP-1B or Tc-PTPa in its selectivity for [32P]phosphotyrosyl- over [32P]phosphoseryl- proteins in vitro.

The DSPs and PTPs listed above also were challenged in vitro with free phosphoserine. Each displayed little or no activity towards free phosphoserine. However, the addition of a hydrophobic "handle" to form N-(cyclohexane carboxyl)-O-phospho-L-serine produced a derivative that was hydrolyzed by IphP at rates comparable to that of the avid substrates p-nitrophenyl phosphate and beta-naphthyl phosphate. VHR also hydrolyzed N-(cyclohexane carboxyl)-O-phospho-L-serine, though at a lower rate than IphP. Cdc14 displayed little activity towards N-(cyclohexane carboxyl)-O-phospho-L-serine.

The active site of VHR was mapped and amino acid residues potentially involved in binding N-(cyclohexane carboxyl)-O-phospho-L-serine were identified. The amino acid sequence of VHR was aligned with the amino acid sequences of IphP and Cdc14 to identify the nature of the corresponding residues in IphP and Cdcd14.

Low molecular weight phosphomonoesters have proven to be effective in vitro indicators of protein phosphatase activity. They also have shown potential as diagnostic substrates for specific subclasses of protein phosphatases. However, neither alpha- and beta- naphthyl phosphate nor N-(cyclohexane carboxyl)-O-phospho-L-serine proved to be universal discriminatory substrates for the functional subgroups within the family of protein-tyrosine phosphatases. Indeed, the probability of identifying such a substrate would appear to be relatively low.
Master of Science

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Meier, Jordan Leslie. « Synthetic active site probes for PKS and NRPS biosynthetic enzymes ». Diss., [La Jolla] : University of California, San Diego, 2009. http://wwwlib.umi.com/cr/ucsd/fullcit?p3359523.

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Thesis (Ph. D.)--University of California, San Diego, 2009.
Title from first page of PDF file (viewed July 7, 2009). Available via ProQuest Digital Dissertations. Vita. Includes bibliographical references.

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Peng, Tao, et 彭濤. « Rhodol fluorophores and fluorescent probes for the detection and imaging of reactive oxygen species ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B41757920.

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Peng, Tao. « Rhodol fluorophores and fluorescent probes for the detection and imaging of reactive oxygen species ». Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B41757920.

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Sun, Zhenning, et 孫振宁. « Studies on fluorescent probes for the specific detection of reactive oxygen species and reactive nitrogen species in living cells ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B38677490.

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Sharp, Jonathan Oliver. « Synthesis of redox-active probes for the multiplex detection of DNA ». Thesis, University of Bath, 2013. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607450.

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The research presented within this thesis is concerned with the design and synthesis of redox-active derivatives for the use as labels for DNA probes to be used in a commercial DNA detection assay. Chapter 1: Introduces the area of electrochemical DNA sensing, the methods used and the transducer derivatives used. Also included within this chapter is the discussion on the use of ferrocene and its derivatives as redox-active transducer moieties and their use in a DNA sensing capacity. Chapter 2: Introduces the sponsoring company, Atlas genetics, and the DNA detection assay they are developing for use in a point of care device (POC). The chapter also details the design, synthesis and electrochemical analysis via differential pulse voltammetry of mono-ferrocenyl derivatives for the use as redox-active labels for DNA sensing. The chapter outlines the development of labels containing a variety of functionality as well as possessing a range of oxidation potentials from 95 to 610 mV (vs Ag/AgCl). Chapter 3: Introduces and details the sensitivity issues between mono-ferrocenyl and di-ferrocenyl labels and the effect this could have on the commercial DNA detection assay. Within this chapter there are the details of the design, synthesis and electrochemical analysis via differential pulse voltammetry of the di-ferrocenyl labels. The chapter shows the synthesis of di-ferrocenyl labels containing a wide range of functionality on both the ferrocene core as well as the linker unit, with the labels processing a range of oxidation potentials from 242 to 500 mV (vs. Ag/AgCl). Chapter 4: Discusses the use of the labels designed and synthesised in chapters 2 and 3 in the commercial DNA detection assay developed by Atlas genetics. The development of the labels used as DNA probes in the DNA detection assay and their ability to be used in multiplex DNA detection assays are also described. Demonstrated within this chapter is the use of the labels synthesised in this thesis that give both a duplex between two different probes and also the development of a triplex assay using three different labels to detect for two different target DNAs as well as provide an internal control. Chapter 5: Introduces the synthetic methods towards the synthesis of 2-oxazolines and discusses their use within ring-opening reactions. This chapter details the optimisation of the ring-opening reaction of phenyl-2-oxazoline with a range of carboxylic acid derivatives. The synthesis of a range of 2-oxazolines with various functionality aimed towards the analytical detection of carboxylic acids through the direct conjugation with 2-oxazolines. The ring-opening reaction was found to tolerate a wide range of carboxylic acid derivatives as well as a variety of functionality on the 2-oxazolines such as ferrocene-2-oxazolines and also 3,5 – bis(trifluoromethyl)phenyl-2-oxazoline. The use of ferrocene-2-oxazoline allowed for the electrochemical detection of carboxylic acids and the 3,5 – bis(trifluoromethyl)phenyl-2-oxazoline allows for thedetection of carboxylic acids through its ring-opened form via 19F NMR. These two functionalised 2-oxazolines were used to further analyse the reactions viability as a possible analytical tool for the detection of carboxylic acids by carring out the ring-opening reaction conditions for the detection of ibuprofen from an over the counter tablet.

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Livres sur le sujet "Active probes"

Hong, Suk ho. Designing Active Site-Directed Covalent Probes for Tyrosine Phosphatases. [New York, N.Y.?] : [publisher not identified], 2022.

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Paul, Kolodziej, et United States. National Aeronautics and Space Administration., dir. Dual active surface heat flux gage probe. [Washington, DC] : National Aeronautics and Space Administration, 1995.

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Xia, Fangzhou, Ivo W. Rangelow et Kamal Youcef-Toumi. Active Probe Atomic Force Microscopy. Cham : Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-44233-9.

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Eisenkraft, Arthur. Active physics. Armonk, N.Y : It's About Time, 1998.

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Eisenkraft, Arthur. Active physics. Armonk, N.Y : It's About Time, 1998.

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Brownell, Judi. Building active listening skills. Englewood Cliffs, N.J : Prentice-Hall, 1986.

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Cussler, Clive. Night probe ! New York : Bantam Books, 2014.

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Atrill, Peter. Management accounting : An active learning approach. Oxford, OX, UK : Blackwell Business, 1994.

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Kathleen, McKinney, Heyl Barbara Sherman 1942- et McKinney Kathleen, dir. Sociology through active learning : Student exercises. 2^e éd. Thousand Oaks, Calif : Pine Forge Press, 2009.

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Chapitres de livres sur le sujet "Active probes"

Undén, A., et T. Bartfai. « Peptides as active probes ». Dans Interface between Chemistry and Biochemistry, 229–55. Basel : Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-9061-8_11.

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Heber-Katz, Ellen, et Hildegund C. J. Ertl. « Peptides as Molecular Probes of Immune Responses ». Dans Biologically Active Peptides, 269–87. Boca Raton : CRC Press, 2023. http://dx.doi.org/10.1201/9781003419853-13.

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Xia, Fangzhou, Ivo W. Rangelow et Kamal Youcef-Toumi. « Nanofabrication of AFM Cantilever Probes ». Dans Active Probe Atomic Force Microscopy, 109–50. Cham : Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-44233-9_5.

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Szuszkiewicz, Ewa. « Active Galactic Nuclei as Cosmological Probes ». Dans QSO Absorption Lines, 401–2. Berlin, Heidelberg : Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-540-49458-4_87.

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Rangelow, Ivo W., et Matias Holz. « Active Scanning Probes in Nanostructure Fabrication ». Dans 21st Century Nanoscience – A Handbook, 18–1. Boca Raton, Florida : CRC Press, [2020] : CRC Press, 2019. http://dx.doi.org/10.1201/9780367341558-18.

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Gunes, Mehmet H., et Kamil Sarac. « Analyzing Router Responsiveness to Active Measurement Probes ». Dans Lecture Notes in Computer Science, 23–32. Berlin, Heidelberg : Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-00975-4_3.

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Kaminsky, L. S., R. S. Obach et M. J. Fasco. « Cytochrome P450 : Probes of Active Site Residues ». Dans Cytochrome P450, 183–94. Berlin, Heidelberg : Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-77763-9_12.

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Schneider, Kurt. « Active Probes Synergy in Experience-Based Process Improvement ». Dans Product Focused Software Process Improvement, 6–19. Berlin, Heidelberg : Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-540-45051-1_5.

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Wilson, Andrew S. « Extended Emission-Line Regions as Probes of Nuclear Activity in Galaxies ». Dans Physics of Active Galactic Nuclei, 307–24. Berlin, Heidelberg : Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-77566-6_74.

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Langmuir, Margaret E., Jun-Rui Yang, Karen A. LeCompte et Ralph E. Durand. « New Thiol Active Fluorophores for Intracellular Thiols and Glutathione Measurement ». Dans Fluorescence Microscopy and Fluorescent Probes, 229–33. Boston, MA : Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1866-6_34.

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Actes de conférences sur le sujet "Active probes"

Basov, Dmitri N. « Nano-optical probes of Van der Waals interfaces ». Dans Active Photonic Platforms (APP) 2024, sous la direction de Ganapathi S. Subramania et Stavroula Foteinopoulou, 20. SPIE, 2024. http://dx.doi.org/10.1117/12.3027547.

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Poβner, Lucas, Florian Wilhelmy, Jeremy Ranke, Michael Wallenta, Uwe Pliquett, Matthias Laukner, Thomas Knösche, Erdem Güresir et Konstantin Weise. « Comparison of Active and Passive Shielded 4-Point Probes for Impedance Spectroscopy of Brain Tissue ». Dans 2024 International Workshop on Impedance Spectroscopy (IWIS), 54–55. IEEE, 2024. https://doi.org/10.1109/iwis63047.2024.10847233.

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Hills, M. D., D. T. Kewley, J. M. Bower et G. T. A. Kovacs. « Active SOI-Based Neural Probes ». Dans 2002 Solid-State, Actuators, and Microsystems Workshop. San Diego, CA USA : Transducer Research Foundation, Inc., 2002. http://dx.doi.org/10.31438/trf.hh2002.49.

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Heisig, Sven, W. Steffens et Egbert Oesterschulze. « Optical active gallium arsenide probes for scanning probe microscopy ». Dans SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, sous la direction de Suganda Jutamulia et Toshimitsu Asakura. SPIE, 1998. http://dx.doi.org/10.1117/12.326832.

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Peltre, Gabriel, Helene Senechal, Jean-Pierre Sutra, Francois-Xavier Desvaux, Helene Chardin et Pascal Poncet. « Peptides used as probes for detecting rare proteins and allergens ». Dans XIth Conference Biologically Active Peptides. Prague : Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2009. http://dx.doi.org/10.1135/css200911104.

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Mittal, Surbhi, Ji Zhang, David Pommerenke, James L. Drewniak, Kuifeng Hu et Xiaopeng Dong. « Active probes for creating H-field probes for flat frequency response ». Dans 2009 IEEE International Symposium on Electromagnetic Compatibility - EMC 2009. IEEE, 2009. http://dx.doi.org/10.1109/isemc.2009.5284635.

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Kim, Kihyun, Namgon Kim, Sung-Hyun Hwang, Taeyoon Seo, Yong-Kweon Kim et Youngwoo Kwon. « Microwave active integrated probes for biomedical applications ». Dans 2013 Asia Pacific Microwave Conference - (APMC 2013). IEEE, 2013. http://dx.doi.org/10.1109/apmc.2013.6695151.

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Youngwoo Kwon, Kihyun Kim, Sung-Hyun Hwang, Taeyoon Seo et Yong-Kweon Kim. « Active integrated probes for tumor detection and ablation ». Dans 2014 IEEE/MTT-S International Microwave Symposium - MTT 2014. IEEE, 2014. http://dx.doi.org/10.1109/mwsym.2014.6848647.

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Shakouri, M. S., H. Matsuura, B. A. Auld et D. M. Bloom. « Active Probes for Millimeter-Wave On-Wafer Measurements ». Dans 38th ARFTG Conference Digest. IEEE, 1991. http://dx.doi.org/10.1109/arftg.1991.324039.

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Majidi-Ahy, R., et D. M. Bloom. « 120-GHz Active Wafer Probes for Picosecond Device Measurement ». Dans Picosecond Electronics and Optoelectronics. Washington, D.C. : Optica Publishing Group, 1989. http://dx.doi.org/10.1364/peo.1989.hsmt31.

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We have developed frequency-multiplier and harmonic mixer active wafer probes for picosecond device measurements to 120 GHz. All-electronic 100 GHz on-wafer frequency-response measurements have been demonstrated using these probes.

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Rapports d'organisations sur le sujet "Active probes"

Newcomb, N. High-Speed Active Integrators for Magnetic Probes. Office of Scientific and Technical Information (OSTI), octobre 2020. http://dx.doi.org/10.2172/1673199.

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Berezovsky, Jesse. Final report : Mapping Interactions in Hybrid Systems with Active Scanning Probes. Office of Scientific and Technical Information (OSTI), septembre 2017. http://dx.doi.org/10.2172/1395561.

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Pinnick, Ronald G., J. D. Pendleton et Gorden Videen. Response Characteristics of Active Scattering Aerosol Spectrometer Probes Made by Particle Measuring Systems. Fort Belvoir, VA : Defense Technical Information Center, mars 2000. http://dx.doi.org/10.21236/ada376912.

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Blackmond, D. G., I. Wender, R. Oukaci et J. Wang. Probe molecule studies : Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), juillet 1992. http://dx.doi.org/10.2172/7154553.

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Blackmond, D. G., I. Wender, R. Oukaci et J. Wang. Probe molecule studies : Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), décembre 1992. http://dx.doi.org/10.2172/6758736.

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Blackmond, D. G. Probe molecule studies : Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), avril 1992. http://dx.doi.org/10.2172/5100318.

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Blackmond, D. G., et I. Wender. Probe molecule studies : Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), juillet 1991. http://dx.doi.org/10.2172/5262741.

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Blackmond, D. G., et I. Wender. Probe molecule studies : Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), septembre 1991. http://dx.doi.org/10.2172/6128128.

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Blackmond, D. G., I. Wender, R. Oukaci et J. Wang. Probe molecule studies : Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), octobre 1992. http://dx.doi.org/10.2172/6873487.

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Blackmond, D. G. Probe molecule studies : Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), décembre 1991. http://dx.doi.org/10.2172/5389426.

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