Academic literature on the topic 'Carbon monoxide – Absorption and adsorption'

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Journal articles on the topic "Carbon monoxide – Absorption and adsorption"

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Dunwell, M., Junhua Wang, Y. Yan, and B. Xu. "Surface enhanced spectroscopic investigations of adsorption of cations on electrochemical interfaces." Physical Chemistry Chemical Physics 19, no. 2 (2017): 971–75. http://dx.doi.org/10.1039/c6cp07207k.

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Cabrera, A. L., J. Espinosa-Gangas, Johan Jonsson-Akerman, and Ivan K. Schuller. "Kinetics of subsurface hydrogen adsorbed on niobium: Thermal desorption studies." Journal of Materials Research 17, no. 10 (October 2002): 2698–704. http://dx.doi.org/10.1557/jmr.2002.0390.

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The adsorption/absorption of hydrogen and the adsorption of carbon monoxide by niobium foils, at room temperature, was studied using thermal desorption spectroscopy. Two hydrogen desorption peaks were observed with a maximum at 404 and 471 K. The first hydrogen desorption peak is regarded as hydrogen desorbing from surface sites while the second peak, which represents desorption from surface sites stronger bound to the surface, also has a component—due to its tailing to higher temperatures—of hydrogen diffusing from subsurface sites. Carbon monoxide adsorption was used to determine the number of surface sites, since it does not penetrate below the surface. Two carbon monoxide desorption peaks are observed in these experiments: at 425 and 608 K. The first peak is regarded as the adsorption of molecular carbon monoxide, and the second, as carbon monoxide dissociated on the niobium surface. The crystallographic orientation of the foils was determined by x-ray diffraction and showed a preferential (110) orientation of the untreated foil due to the effect of cold rolling. This preferential orientation decreased after hydrogen/heat treatment, appearing strong also in the (200) and (211) orientations. This change in texture of the foils is mainly due to the effect of heat treatment and not to hydrogen adsorption/desorption cycling. The kinetics of hydrogen and CO desorption is compared with that of Pd and Pd alloys.
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Wadayama, T., K. Abe, and H. Osano. "Infrared reflection absorption study of carbon monoxide adsorption on Pd/Cu(111)." Applied Surface Science 253, no. 5 (December 2006): 2540–46. http://dx.doi.org/10.1016/j.apsusc.2006.05.014.

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Lyons, K. J., J. Xie, W. J. Mitchell, and W. H. Weinberg. "Adsorption of carbon monoxide on Ir(110) investigated by infrared reflection-absorption spectroscopy." Surface Science 325, no. 1-2 (February 1995): 85–92. http://dx.doi.org/10.1016/0039-6028(94)00729-2.

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Rakic, Vesna, Vera Dondur, and Radmila Hercigonja. "FTIR study of carbon monoxide adsorption on ion-exchanged X, Y and mordenite type zeolites." Journal of the Serbian Chemical Society 68, no. 4-5 (2003): 409–16. http://dx.doi.org/10.2298/jsc0305409r.

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In this work Fourier transform infrared (FTIR) study has been applied to study the adsorption of carbon monoxide on transition metal (Mn2+, Co2 Ni2+) ion-exchanged zeolites type Y, X and mordenites. The adsorption of CO at room temperature produces overlapping IR absorption bands in the 2120?2200 cm-1 region. The frequency of the band around 2200 cm-1 is found to be dependent not only on the charge-balancing transition metal cation but also on the framework composition. The frequencies of the band near 1600 cm-1 was found to be dependent on the Si/Al ratio of the investigated zeolites.
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Wadayama, T., H. Yoshida, S. Oda, and N. Todoroki. "Infrared Reflection Absorption Study for Carbon Monoxide Adsorption on Chromium Deposited Cu(100) Surfaces." MATERIALS TRANSACTIONS 50, no. 4 (2009): 819–24. http://dx.doi.org/10.2320/matertrans.mra2008442.

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Wadayama, Toshimasa, Hirosato Yoshida, Naoto Todoroki, and Shogo Oda. "Carbon Monoxide Adsorption on Ni/Pt(111) Surfaces Investigated by Infrared Reflection Absorption Spectroscopy." e-Journal of Surface Science and Nanotechnology 7 (2009): 230–33. http://dx.doi.org/10.1380/ejssnt.2009.230.

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Wadayama, T., H. Osano, K. Murakami, T. Maeyama, and H. Yoshida. "Infrared reflection absorption study of carbon monoxide adsorption on Fe-deposited Pt(111) surface." Journal of Physics: Conference Series 100, no. 1 (March 1, 2008): 012007. http://dx.doi.org/10.1088/1742-6596/100/1/012007.

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Wadayama, Toshimasa, Hiroshi Osano, Toshiaki Maeyama, Hirosato Yoshida, Koji Murakami, Naoki Todoroki, and Shogo Oda. "Infrared Reflection−Absorption Study of Carbon Monoxide Adsorption on Fe/Pt(111) Bimetallic Surfaces." Journal of Physical Chemistry C 112, no. 24 (May 21, 2008): 8944–50. http://dx.doi.org/10.1021/jp712095w.

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Lei, S. Y., S. Luan, and H. Yu. "Co-doped phosphorene: Enhanced sensitivity of CO gas sensing." International Journal of Modern Physics B 32, no. 06 (February 26, 2018): 1850068. http://dx.doi.org/10.1142/s0217979218500686.

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First-principle calculation was carried out to systematically investigate carbon monoxide (CO) adsorption on pristine and cobalt (Co)-doped phosphorenes (Co-bP). Whether or not CO is adsorped, pristine phosphorene is a direct-band-gap semiconductor. However, the bandgap of Co-bP experiences direct-to-indirect transition after CO molecule adsorption, which will affect optical absorption considerably, implying that Co doping can enhance the sensitivity of phosphorene as a CO gas sensor. Moreover, Co doping can improve an adsorption energy of CO to 1.31 eV, as compared with pristine phosphorene (0.12 eV), also indicating that Co-bP is energetically favorable for CO gas sensing.
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Dissertations / Theses on the topic "Carbon monoxide – Absorption and adsorption"

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Christiaen, Anne-Claire. "Adsorption of water and carbon monoxide on Cu₂O(111) single crystal surfaces." Thesis, This resource online, 1994. http://scholar.lib.vt.edu/theses/available/etd-11102009-020324/.

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Winski, David Nathaniel. "Design and construction of a polarization modulated infrared reflection absorption spectrometer and validation with carbon monoxide adsorption on a platinum (100) surface." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 96 p, 2009. http://proquest.umi.com/pqdweb?did=1889078511&sid=1&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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Feltovich, Susanne D. "Influence of solvent on the infared spectrum of carbon monoxide adsorbed on platinum electrodes." Thesis, This resource online, 1993. http://scholar.lib.vt.edu/theses/available/etd-09292009-020247/.

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Canard, Gabriel. "Matériaux hybrides organiques-inorganiques incorporant des métallocorroles de cobalt(III) : application à l'adsorption sélective du monoxyde de carbone." Dijon, 2004. http://www.theses.fr/2004DIJOS046.

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Repper, Stephen. "Carbon monoxide absorption by copper(I) containing ionic liquids." Thesis, University of Sheffield, 2014. http://etheses.whiterose.ac.uk/7674/.

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Kennedy, Sinead A. "Infrared studies of adsorption on model catalysts." Thesis, University of Reading, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.250661.

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Chamberlain, Jeffrey P. "The adsorption of carbon monoxide on silicon and gallium arsenide surfaces." Diss., Georgia Institute of Technology, 1993. http://hdl.handle.net/1853/29799.

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Kalimtgis, Konstandinos. "ADSORPTION OF TRICHLOROETHYLENE AND CARBON TETRACHLORIDE ON SYNTHETIC AND NATURAL ADSORBENTS." Thesis, The University of Arizona, 1985. http://hdl.handle.net/10150/275355.

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Rohmann, Christoph. "Carbon monoxide adsorption onto the metal oxides of α-Al2O3 and TiO2." Thesis, University of Auckland, 2011. http://hdl.handle.net/2292/9552.

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The aim of this study is to elucidate surface properties of α-Al2O3 and TiO2, such as; the number and accessibility of adsorption sites, forces governing the interaction of the surface with adsorbates and surface relaxation and reconstruction, using a combination of theory and experiment. Carbon monoxide was used as a probe molecule and its adsorption onto both clean and hydroxylated (0001) surfaces of α-Al2O3 was modelled using Density Functional Theory (DFT). Adsorption of CO onto α-Al2O3 and TiO2 (anatase and rutile) powders was investigated experimentally using infrared spectroscopy. In addition, Reflection-Absorption Infrared Spectroscopy (RAIRS) experiments were conducted to study the adsorption and photo-oxidation of CO to CO2 over the rutile TiO2(110) single crystal surface. Computational modelling of the adsorption of CO onto both dry and hydroxylated a-Al2O3(0001) surfaces was undertaken to investigate changes in binding conformations, surface relaxation effects & CO vibrational frequencies, with increasing adsorbate coverage. The adsorption of CO onto the (0001) surface begins with the C of CO approaching an Al adsorption site in a perpendicular fashion. Upon CO adsorption onto the dry and hydroxylated surfaces significant surface relaxations were noted, which were enhanced at hydroxylated surfaces. Generally, as the surface coverage increases, the CO adsorption energy and the CO vibrational frequency both decrease, except for highly hydroxylated surfaces, which do not tend to adsorb CO at all (?), as the surface hydroxylation causes the free Al adsorption sites to retreat into the bulk material. CO adsorption onto α-Al2O3 and TiO2 (anatase and rutile) powders have been studied by Fourier Transform Infrared (FTIR) spectroscopy to determine the CO vibrational frequency and heats of adsorption in order to compare those to the computed CO adsorption energies of the dry and hydroxylated (0001) surfaces of a-Al2O3 as well as to previously reported findings. The CO vibrational frequency was blue shifted (a shift to higher wavenumbers indicating a strengthening of the CO bond) compared to the free molecule in all cases, revealing a CO heat of adsorption being greatest for anatase followed by rutile while a-Al2O3 is exhibiting the weakest binding at the investigated powders. Reflection-Absorption Infrared Spectroscopy (RAIRS) has been successfully conducted for the first time to identify the CO adsorption site on well defined metal oxide single crystal surface, the (110) surface of TiO2 in this case. Therefore it is now possible to assign peaks observed on powder samples exactly to a crystal plane, enabling better comparison of computational and experimental results. RAIRS results revealed the presence of irreversibly adsorbed CO on top of five fold coordinated surface Ti atoms at 110K. Upon UV irradiation in the presence of molecular oxygen, a second band (attributed to physisorbed CO2) appeared and increased in intensity over time, while the CO adsorption band decreased. This photo-oxidation process (of CO to CO2) occurred.
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Predescu, Ligia. "Adsorption of nitrogen, methane, and carbon monoxide on aluminosilicate and aluminophosphate molecular sieves." Thesis, University of Ottawa (Canada), 1996. http://hdl.handle.net/10393/10115.

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Considering the difficulties associated with the experimental determination of binary mixture adsorption isotherms, pure-gas adsorption information becomes vital in the prediction of these isotherms and the corresponding phase equilibria necessary in the design of adsorptive separation units. Experimental equilibrium isotherms describing the adsorption of pure N$\rm\sb2,\ CH\sb4,$ and CO in a natural aluminosilicate molecular sieve (clinoptilolite from Cuba) and two synthetic small-pore aluminophosphate molecular sieves (AlPO$\sb4$-17 and AlPO$\sb4$-18) have been determined using the volumetric method at 40$\sp\circ$C over a pressure range up to about 1000 mm Hg, and subsequently fitted with the Langmuir and Flory-Huggins Vacancy Solution Theory equations. Additional Langmuir and FH-VST fits of equilibrium isotherms previously measured over the same pressure range at room temperature and 40$\sp\circ$C to describe the equilibrium adsorption of the same three adsorbates in two aluminosilicate molecular sieves (natural clinoptilolite from Turkey and zeolite 5A), as well as in a medium-pore aluminophosphate molecular sieve AlPO$\sb4$-11 were also obtained. The Freundlich equation was found to yield a better fit than either the Langmuir or FH-VST equations for the experimental adsorption isotherms of N$\sb2$ and CO on AlPO$\sb4$-17. The higher observed capacities of the aluminosilicate molecular sieves, compared to the aluminophosphates, were attributed to the energetic heterogeneity conferred by the presence of framework-charge compensating cations. The model parameters obtained by fitting the experimental pure-component adsorption isotherms permitted the prediction of the mixture adsorption phase diagrams and the binary adsorption isotherms by the Extended Langmuir Model and the Flory-Huggins Vacancy Solution Model for the three possible binary mixtures at 101.3 kPa total pressure and the pure-component adsorption temperatures investigated. The Ideal Adsorbed Solution Theory was also applied with the explanation of the behaviour predicted by each model for each adsorption system was attempted. (Abstract shortened by UMI.)
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Books on the topic "Carbon monoxide – Absorption and adsorption"

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Adsorption by carbons. Amsterdam: Elsevier, 2008.

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Nelson, T. P. Full-scale carbon adsorption applications study. Cincinnati, OH: U.S. Environmental Protection Agency, Hazardous Waste Engineering Research Laboratory, 1985.

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Nelson, T. P. Full-scale carbon adsorption applications study. Cincinnati, OH: U.S. Environmental Protection Agency, Hazardous Waste Engineering Research Laboratory, 1985.

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Nelson, T. P. Full-scale carbon adsorption applications study. Cincinnati, OH: U.S. Environmental Protection Agency, Hazardous Waste Engineering Research Laboratory, 1985.

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Nelson, T. P. Full-scale carbon adsorption applications study. Cincinnati, OH: U.S. Environmental Protection Agency, Hazardous Waste Engineering Research Laboratory, 1985.

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Nelson, T. P. Full-scale carbon adsorption applications study. Cincinnati, OH: U.S. Environmental Protection Agency, Hazardous Waste Engineering Research Laboratory, 1985.

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Lupașcu, Tudor. Cărbuni activi din materii prime vegetale. [Chișinău]: Știința, 2004.

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Mei ceng xi fu te zheng ji chu qi ji li. Beijing Shi: Ke xue chu ban she, 2013.

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Edwards, John C. Mathematical model of absorption of carbon dioxide by rescue breathing apparatus scrubber. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1987.

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Rikuiki seitaikei no tanso dōtai: Chikyū kankyō e no shisutemu apurōchi. Kyōto-shi: Kyōto Daigaku Gakujutsu Shuppankai, 2013.

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Book chapters on the topic "Carbon monoxide – Absorption and adsorption"

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Knözinger, H. "Adsorption of Carbon Monoxide on Catalyst Surfaces: Oxides, Sulfides and Zeolites." In Adsorption on Ordered Surfaces of Ionic Solids and Thin Films, 257–67. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78632-7_23.

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Rodriguez, René R., Wade J. Tornquist, Francis Guillaume, and Gregory L. Griffin. "Vibrational Spectroscopic Studies of Adsorbate Competition During Carbon Monoxide Adsorption on Platinum Electrodes." In ACS Symposium Series, 369–82. Washington, DC: American Chemical Society, 1988. http://dx.doi.org/10.1021/bk-1988-0378.ch025.

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Bardi, U., and G. Rovida. "Adsorption and Dissociation of Carbon Monoxide on Co(1120)." In Structure and Reactivity of Surfaces, 49–57. Elsevier, 1989. http://dx.doi.org/10.1016/s0167-2991(08)60669-2.

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"Absorption, Adsorption and Membrane Based Separation Processes for CO2 Capture." In Carbon Capture and Storage, 1–2. Apple Academic Press, 2014. http://dx.doi.org/10.1201/b16845-2.

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Viena, Vera, Elvitriana, Muhammad Nizar, Sari Wardani, and Suhendrayatna. "Preparation of Activated Carbon From Banana (Musa acuminate L.) peels for Carbon Monoxide Adsorption." In Proceedings of MICoMS 2017, 381–86. Emerald Publishing Limited, 2018. http://dx.doi.org/10.1108/978-1-78756-793-1-00087.

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Birdi, K. S. "Adsorption (on Solids) and Absorption (in Fluids) of Gases (CCS Procedures) (Surface Chemistry Aspects)." In Surface Chemistry of Carbon Capture, 31–72. CRC Press, 2019. http://dx.doi.org/10.1201/9781351116466-2.

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Birdi, K. S. "A Short Review of Different Carbon Dioxide (CO2) Capture Processes (Adsorption on Solids and Absorption in Fluids)." In Surface Chemistry of Carbon Capture, 113–41. CRC Press, 2019. http://dx.doi.org/10.1201/9781351116466-5.

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Bateman, J. E., and M. A. Chesters. "A Transmission Ftir Study of the Adsorption of Carbon Monoxide and Cyclohexane on Evaporated Silver Films." In Structure and Reactivity of Surfaces, 75–83. Elsevier, 1989. http://dx.doi.org/10.1016/s0167-2991(08)60672-2.

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Dovesi, R., C. Roetti, M. Causa, and C. Pisani. "AB Initio Study of the Periodic Carbon Monoxide Adsorption on the Basal Plane of Alpha-Alumina." In Structure and Reactivity of Surfaces, 385–93. Elsevier, 1989. http://dx.doi.org/10.1016/s0167-2991(08)60701-6.

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Jungsuttiwong, S., P. Khongpracha, T. N. Truong, and J. Limtrakul. "15-P-10-A theoretical study of adsorption of carbon monoxide on Ag-ZSM-5 zeolite." In Studies in Surface Science and Catalysis, 257. Elsevier, 2001. http://dx.doi.org/10.1016/s0167-2991(01)81549-4.

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Conference papers on the topic "Carbon monoxide – Absorption and adsorption"

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Rathi, Tejas, Vijay Rao Kumbhare, and Manoj Kumar Majumder. "Adsorption of Carbon Monoxide on Multilayered Graphene." In 2020 IEEE 7th Uttar Pradesh Section International Conference on Electrical, Electronics and Computer Engineering (UPCON). IEEE, 2020. http://dx.doi.org/10.1109/upcon50219.2020.9376429.

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Patel, Sanjay, and K. K. Pant. "Hydrogen Production for PEM Fuel Cells via Oxidative Steam Reforming of Methanol Using Cu-Al Catalysts Modified With Ce and Cr." In ASME 2006 4th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2006. http://dx.doi.org/10.1115/fuelcell2006-97209.

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The performance of Cu-Ce-Al-oxide and Cu-Cr-Al-oxide catalysts of varying compositions prepared by co-precipitation method was evaluated for the PEM fuel cell grade hydrogen production via oxidative steam reforming of methanol (OSRM). The limitations of partial oxidation and steam reforming of methanol for the hydrogen production for PEM fuel cell could be overcome using OSRM and can be performed auto-thermally with idealized reaction stoichiomatry. Catalysts surface area and pore volume were determined using N2 adsorption-desorption method. The final elemental compositions were determined using atomic absorption spectroscopy. Crystalline phases of catalyst samples were determined by X-ray diffraction (XRD) technique. Temperature programmed reduction (TPR) demonstrated that the incorporation of Ce improved the copper reducibility significantly compared to Cr promoter. The OSRM was carried out in a fixed bed catalytic reactor. Reaction temperature, contact-time (W/F) and oxygen to methanol (O/M) molar ratio varied from 200–300°C, 3–21 kgcat s mol−1 and 0–0.5 respectively. The steam to methanol (S/M) molar ratio = 1.4 and pressure = 1 atm were kept constant. Catalyst Cu-Ce-Al:30-10-60 exhibited 100% methanol conversion and 152 mmol s−1 kgcat−1 hydrogen production rate at 300°C with carbon monoxide formation as low as 1300 ppm, which reduces the load on preferential oxidation of CO to CO2 (PROX) significantly before feeding the hydrogen rich stream to the PEM fuel cell as a feed. The higher catalytic performance of Ce containing catalysts was attributed to the improved Cu reducibility, higher surface area, and better copper dispersion. Reaction parameters were optimized in order to maximize the hydrogen production and to keep the CO formation as low as possible. The time-on-stream stability test showed that the Cu-Ce-Al-oxide catalysts subjected to a moderate deactivation compared to Cu-Cr-Al-oxide catalysts. The amount of carbon deposited onto the catalysts was determined using TG/DTA thermogravimetric analyzer. C1s spectra were obtained by surface analysis of post reaction catalysts using X-ray photoelectron spectroscopy (XPS) to investigate the nature of coke deposited.
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Shimizu, Naofumi, Ken Matsuyama, and Iwao Hosako. "Absorption spectra of hydrogen chloride and carbon monoxide in smoke." In 2012 37th International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz 2012). IEEE, 2012. http://dx.doi.org/10.1109/irmmw-thz.2012.6380330.

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Guo, Jian-qiang, Li Wang, Zeyong Wang, and Jinglong Li. "Study of instrument measurement of carbon monoxide concentration by absorption spectrum." In Sixth International Symposium on Precision Engineering Measurements and Instrumentation. SPIE, 2010. http://dx.doi.org/10.1117/12.885712.

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Yuliusman, Mega Puspita Sari, and Azmia Rizka Nafisah. "Modification of low-density polyethylene based activated carbon using titanium dioxide for carbon monoxide and hydrocarbon adsorption." In PROCEEDINGS OF THE 5TH INTERNATIONAL SYMPOSIUM ON APPLIED CHEMISTRY 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5134592.

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Shanying Zhu, Youping Chen, Gang Zhang, and Jiming Sa. "An optical fiber sensor based on absorption spectroscopy for carbon monoxide detection." In 2010 International Conference on Computer Design and Applications (ICCDA 2010). IEEE, 2010. http://dx.doi.org/10.1109/iccda.2010.5541304.

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Briggs, Ryan M., Clifford Frez, Siamak Forouhar, Randy D. May, and Gary A. Ruff. "Portable 4.6 µm Laser Absorption Spectrometer for Carbon Monoxide Monitoring and Fire Detection." In 43rd International Conference on Environmental Systems. Reston, Virginia: American Institute of Aeronautics and Astronautics, 2013. http://dx.doi.org/10.2514/6.2013-3474.

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Henderson, Angus, Pam Roper, Roy D. Mead, James R. Gord, Gregory J. Fiechtner, and George E. Tietz. "Carbon monoxide absorption spectroscopy using a diode-pumped continuous wave optical parametric oscillator." In Laser Applications to Chemical and Environmental Analysis. Washington, D.C.: OSA, 2001. http://dx.doi.org/10.1364/lacea.2000.pd3.

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Zhang, Jingchao, Suxia Cao, and Lijun Guan. "Carbon Monoxide Gas Sensor Based on Cavity Enhanced Absorption Spectroscopy and Harmonic Detection." In 2009 Symposium on Photonics and Optoelectronics. IEEE eXpress Conference Publishing, 2009. http://dx.doi.org/10.1109/sopo.2009.5230315.

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He, Yu-kai, Ru-lin Wang, and Yu-qiang Yang. "A Novel Carbon Monoxide Detection System Based on Infrared Absorption Used in Mine." In 2006 International Conference on Machine Learning and Cybernetics. IEEE, 2006. http://dx.doi.org/10.1109/icmlc.2006.258392.

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Reports on the topic "Carbon monoxide – Absorption and adsorption"

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VanderWiel, David P. A kinetic study on the adsorption and reaction of hydrogen over silica-supported ruthenium and silver-ruthenium catalysts during the hydrogenation of carbon monoxide. Office of Scientific and Technical Information (OSTI), February 1999. http://dx.doi.org/10.2172/348889.

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