Relevant bibliographies by topics / Cell volume regulation

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Cell volume regulation'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 February 2022

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Journal articles on the topic "Cell volume regulation"

1

Völkl, H., M. Paulmichl, and F. Lang. "Cell Volume Regulation in Renal Cortical Cells." Kidney and Blood Pressure Research 11, no. 3-5 (1988): 158–73. http://dx.doi.org/10.1159/000173160.

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Macknight, Anthony D. C. "Principles of Cell Volume Regulation." Kidney and Blood Pressure Research 11, no. 3-5 (1988): 114–41. http://dx.doi.org/10.1159/000173158.

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Graf, J., P. Haddad, D. Haeussinger, and F. Lang. "Cell Volume Regulation in Liver." Kidney and Blood Pressure Research 11, no. 3-5 (1988): 202–20. http://dx.doi.org/10.1159/000173163.

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Deutsch, Carol, and Sherwin C. Lee. "Cell Volume Regulation in Lymphocytes." Kidney and Blood Pressure Research 11, no. 3-5 (1988): 260–76. http://dx.doi.org/10.1159/000173166.

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Lewis, Rebecca, Claire H. Feetham, and Richard Barrett-Jolley. "Cell Volume Regulation in Chondrocytes." Cellular Physiology and Biochemistry 28, no. 6 (2011): 1111–22. http://dx.doi.org/10.1159/000335847.

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Hoffmann, Else K. "Cell Swelling and Volume Regulation." Canadian Journal of Physiology and Pharmacology 70, S1 (1992): S310—S313. http://dx.doi.org/10.1139/y92-277.

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The extracellular space in the brain is typically 20% of the tissue volume and is reduced to at least half its size under conditions of neural insult. Whether there is a minimum size to the extracellular space was discussed. A general model for cell volume regulation was presented, followed by a discussion on how many of the generally involved mechanisms are identified in neural cells and (or) in astrocytes. There seems to be clear evidence suggesting that parallel K+ and Cl− channels mediate regulatory volume decrease in primary cultures of astrocytes, and a stretch-activated cation channel h
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Civan, M. M. "Overview of cell volume regulation." Experimental Eye Research 55 (September 1992): 126. http://dx.doi.org/10.1016/0014-4835(92)90655-c.

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Wang, Meng, Yaowei Yang, Lichun Han, Feng Xu, and Fei Li. "Cell mechanical microenvironment for cell volume regulation." Journal of Cellular Physiology 235, no. 5 (2019): 4070–81. http://dx.doi.org/10.1002/jcp.29341.

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Gómez-Angelats, Mireia, Carl D. Bortner, and John A. Cidlowski. "Cell volume regulation in immune cell apoptosis." Cell and Tissue Research 301, no. 1 (2000): 33–42. http://dx.doi.org/10.1007/s004410000216.

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Okada, Y. "Volume-sensitive chloride channels and cell volume regulation." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 126 (July 2000): 111. http://dx.doi.org/10.1016/s1095-6433(00)80220-2.

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Dissertations / Theses on the topic "Cell volume regulation"

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Khalbuss, Walid E. "Electrophysiology, Cell Calcium, and Mechanisms of Hepatocyte Volume Regulation." Digital Commons @ East Tennessee State University, 1990. https://dc.etsu.edu/etd/2709.

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The electrophysiologic technique (Reuss, L., Proc. Natl. Acad. Sci. USA 82:6014, 1985) was modified to measure changes in steady-state hepatocyte volume during osmotic stress. Hepatocytes in mouse liver slices were loaded with tetramethylammonium ion (TMA$\sp{+}$) during transient exposure of cells to nystatin. Intracellular TMA$\sp{+}$ activity (a$\sp{\rm i}\sb{\rm TMA}$) was measured with TMA$\sp{+}$-sensitive, double-barreled microelectrodes. Loading hepatocytes with TMA$\sp{+}$ did not change their membrane potential (V$\sb{\rm m}$), and under steady-state conditions a$\sp{\rm i}\sb{\rm TM
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Terashima, Keisuke. "Modeling Cl[-] homeostasis and volume regulation of the cardiac cell." Kyoto University, 2007. http://hdl.handle.net/2433/135908.

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Richard, Samantha. "Development of Cell Volume Regulatory Mechanisms During Oocyte Growth and Meiotic Maturation." Thesis, Université d'Ottawa / University of Ottawa, 2017. http://hdl.handle.net/10393/37022.

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The ability of oocytes and early cleavage-stage embryos to regulate their volume is essential to avoid developmental arrests at in vivo-osmolarities. This is accomplished primarily via GLYT1-mediated glycine transport into the cells. GLYT1 activity has previously been shown to be absent in freshly isolated oocytes but becomes activated ~3-4 hours after oocyte maturation has been initiated either by isolation from ovarian follicles in vitro or following an ovulatory stimulus in vivo. GLYT1 activity then persists until the 4-cell stage of preimplantation embryo development. GLYT1 has been shown
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Hughes, Alexandra. "Mechanisms of volume regulation in murine choroid plexus epithelial cells." Thesis, University of Manchester, 2010. https://www.research.manchester.ac.uk/portal/en/theses/mechanisms-of-volume-regulation-in-murine-choroid-plexus-epithelial-cells(66cb068e-0e38-4773-83ca-a7867aaff66c).html.

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The choroid plexuses are largely responsible for cerebrospinal fluid (CSF) secretion and therefore play a fundamental role in brain homeostasis. The membrane proteins involved in CSF secretion are not fully known. Several electroneutral transporters have been identified by molecular methods in choroid plexus epithelial cells but there is a lack of functional data to support their expression making it impossible to elucidate their role in CSF secretion fully. The activity of many of these transporters can be observed in cell volume regulation. Thus, the main aim of the present study was to dete
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Harvey, Victoria Louise. "Ion channels & volume regulation in the nervous system cell line, CAD." Thesis, University of Huddersfield, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289402.

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Mauritz, Jakob Martin Andreas. "Homeostasis and volume regulation in the Plasmodium falciparum infected red blood cell." Thesis, University of Cambridge, 2011. https://www.repository.cam.ac.uk/handle/1810/240497.

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The thesis reports on the application of advanced microanalytical techniques to answer a fundamental open question on the homeostasis of Plasmodium falciparum infected red blood cells, namely how infected cells retain their integrity for the duration of the parasite asexual reproduction cycle. The volume and shape changes of infected cells were measured and characterized at femtolitre resolution throughout the intraerythrocytic cycle using confocal microscopy. Fluorescence lifetime imaging and electron probe X-ray microanalysis were applied for the quantification of intracellular haemoglobin a
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Richards, Tiffany. "Cell volume regulation and organic osmolytes in post-compaction stage mouse embryos." Thesis, University of Ottawa (Canada), 2009. http://hdl.handle.net/10393/28374.

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It has previously been shown that high osmolarity is detrimental to cleavage-stage mouse embryo development in vitro, and that the presence of several organic osmolytes can provide protection against the detrimental effects of raised osmolarity. Whether the same is true for post-compaction stage embryos is unknown. In the present work, it was found that mouse post-compaction stage embryo development was inhibited by raised osmolarity. However, inhibition of embryo development from the 8-cell to the blastocyst stage occurred only at much higher osmolarities than that which inhibited development
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Ernest, Nola Jean. "The role of chloride in the volume regulation of human glioma cells." Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2007. http://www.mhsl.uab.edu/dt/2007p/ernest.pdf.

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Basavappa, Srisaila. "Hypoosmotically-activated anion permeability in the human neuroblastoma cell line CHP-100." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318761.

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Butt, Omar Iqbal. "Regulation of biomechanical properties of cells in circulation by angiotensin II." The Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=osu1155735506.

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Books on the topic "Cell volume regulation"

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Farlinger, Christopher M. The influence of skeletal muscle cell volume on the regulation of carbohydrate uptake and muscle metabolism. Brock University, Faculty of Applied Health Sciences, 2007.

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1943-, Okada Yasunobu, ed. Cell volume regulation: The molecular mechanism and volume sensing machinery : proceedings of the 23rd Taniguichi Foundation Biophysics Symposium held in Okazaki, Japan, 17-21 November 1997. Elsevier, 1998.

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Douglas, Ian James. Volume regulation in acinar cells isolated from the rat lacrimal gland. University of Manchester, 1996.

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Florian, Lang, ed. Cell volume regulation. Karger, 1998.

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W, Beyenbach Klaus, ed. Cell volume regulation. Karger, 1990.

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Cell volume regulation. Karger, 1990.

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Lang, F., ed. Cell Volume Regulation. S. Karger AG, 1998. http://dx.doi.org/10.1159/isbn.978-3-318-00337-6.

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Cell Volume Regulation (Comparative Physiology). S. Karger AG (Switzerland), 1990.

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Beyenbach. Cell Volume Regulation (Molecular Comparative Physiology). Hart Associates, 1990.

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Lang, F. Mechanisms And Significance of Cell Volume Regulation. S. Karger AG (Switzerland), 2006.

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Book chapters on the topic "Cell volume regulation"

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Sachs, John R. "Cell Volume Regulation." In Molecular Biology of Membrane Transport Disorders. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1143-0_19.

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Spring, Kenneth R. "Epithelial Cell Volume Regulation." In Mechanics of Swelling. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84619-9_22.

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Tomassen, Sebastian F. B., Hugo R. de Jonge, and Ben C. Tilly. "Cell Volume Regulation in Intestinal Epithelial Cells." In Cell Volume and Signaling. Springer US, 2004. http://dx.doi.org/10.1007/0-387-23752-6_31.

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Bortner, Carl D., Francis M. Hughes, and John A. Cidlowski. "Cell Volume Regulation, Ions, and Apoptosis." In Programmed Cell Death. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-0072-2_7.

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Lang, F., M. Paulmichl, H. Voelkl, E. Gstrein, and F. Friedrich. "ELECTROPHYSIOLOGY OF CELL VOLUME REGULATION." In Molecular Nephrology, edited by Walter G. Guder and Zoran Kovačević. De Gruyter, 1987. http://dx.doi.org/10.1515/9783110884746-022.

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Hoffmann, E. K., L. O. Simonsen, and I. H. Lambert. "Cell Volume Regulation: Intracellular Transmission." In Advances in Comparative and Environmental Physiology. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-77124-8_7.

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Friedrich, B., I. Matskevich, and F. Lang. "Cell Volume Regulatory Mechanisms." In Mechanisms and Significance of Cell Volume Regulation. KARGER, 2006. http://dx.doi.org/10.1159/000096284.

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Spring, K. R. "Control of Epithelial Cell Volume." In Endocrine Regulation of Electrolyte Balance. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71405-4_2.

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Wehner, Frank. "Cell Volume-Regulated Cation Channels." In Mechanisms and Significance of Cell Volume Regulation. KARGER, 2006. http://dx.doi.org/10.1159/000096315.

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Browning, Joseph A., J. Clive Ellory, and John S. Gibson. "Pathophysiology of Red Cell Volume." In Mechanisms and Significance of Cell Volume Regulation. KARGER, 2006. http://dx.doi.org/10.1159/000096327.

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Conference papers on the topic "Cell volume regulation"

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Chen, Zhihong, and Chun-xue Bai. "Impaired Migration And Cell Volume Regulation In Aquaporin 5-Deficient SPC-A1 Cells." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a5067.

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Hulme, Paul, Simon Chi, Dominic Young, John Matyas, and Neil A. Duncan. "Enzymatic Digestion Technique Influences Regulatory Volume Decrease of Isolated Bovine Chondrocytes." In ASME 2002 International Mechanical Engineering Congress and Exposition. ASMEDC, 2002. http://dx.doi.org/10.1115/imece2002-32671.

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Cell volume regulation has been observed in almost all cell types examined to date. When cells are exposed to hypotonic solutions a quick increase in volume is followed by a more gradual return, termed regulatory volume decrease (RVD). The mechanism associated with RVD depends upon cell type and species, but in bovine chondrocytes the non-selective osmolyte channels are mainly responsible [1]. In a chondrocyte, volume control is critical for the maintenance of metabolism, and biosynthesis. Volume fluctuations can be due to changes in hydrostatic pressure, fluid flows, deformation, and extracel
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Teitel, J. M., A. Shore, and J. McBarron. "REGULATION OF INTERLEUKIN-2 (IL-2) PRODUCTION BY ENDOTHELIAL CELL (EC) DERIVED SUBSTANCES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642865.

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We recently reported that vascular EC support the staphylococcal protein A (SPA)-induced production of IL-2 by T cells, and furthermore do so synergistically with monocytes. We have now assessed the contributions of EC membrane-associated and secreted factors to these functions. IL-2 was measured by either human tonsil blast of CTLL cell assay. Separation of EC from T cells by a permeable membrane (.45μ pore size) prevented IL-2 production. Consistent with this, supernatant from resting EC (ECs) was also unable to induce IL-2 generation. In addition, neither a crude EC plasma membrane preparat
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Anderson, Everett B., Katherine E. Ayers, Luke Dalton, and Mark Schiller. "Large Scale Energy Storage Using MW-Size PEM Electrolysis." In ASME 2014 12th International Conference on Fuel Cell Science, Engineering and Technology collocated with the ASME 2014 8th International Conference on Energy Sustainability. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/fuelcell2014-6398.

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With the ever-increasing addition of wind and solar renewable energy to the traditional electric grid, the need for energy storage also grows. A recent study projects the value of energy storage for wind and solar integration worldwide to exceed $30 Billion by 2023 [1]. Hydrogen from electrolysis is a promising technology for renewable energy capture as it has the capability to store massive amounts of energy in a relatively small volume. In addition, electrolysis can also provide ancillary services to the grid such as frequency regulation and load shifting resulting in multiple value streams.
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Moghaddam, Saeed, Eakkachai Pengwang, Kevin Lin, Rich Masel, and Mark Shannon. "Fuel Cell-Based MEMS Power Source." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-68425.

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The increasing demand for high energy density power sources driven by advancements in portable electronics and MEMS devices has generated significant interest in development of micro fuel cells. One of the major challenges in development of hydrogen micro fuel cells is the fabrication and integration of auxiliary systems for generation and delivery of fuel to the membrane electrode assembly (MEA). In this paper, we report the development of a millimeter-scale (3×3×1 mm3) micro fuel cell with on-board fuel and control system. Hydrogen is generated in the device through reaction between water an
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Chiu, Justin N. W., and Viktoria Martin. "Industrial Surplus Heat Storage in Smart Cities." In ASME 2015 9th International Conference on Energy Sustainability collocated with the ASME 2015 Power Conference, the ASME 2015 13th International Conference on Fuel Cell Science, Engineering and Technology, and the ASME 2015 Nuclear Forum. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/es2015-49535.

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Surplus heat generated from industrial sectors amounts to between 20% and 50% of the total industrial energy input. Smart reuse of surplus heat resulted from industrial sectors and power generation companies is an opportunity to improve the overall energy efficiency through more efficient use the primary energy sources. A potential solution to tackle this issue is through use of thermal energy storage (TES) to match user demand to that of the generated surplus heat. A mobile TES (M-TES) concept of transportation of industrial surplus heat from production sites to end customers has shown promis
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Zhu, Qingfu, Ziyu Zhu, and Mei He. "3D Additive Manufacturing and Micro-Assembly for Transfection of 3D-Cultured Cells and Tissues." In ASME 2018 13th International Manufacturing Science and Engineering Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/msec2018-6567.

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3D additive manufacturing, namely 3D printing, has been increasingly needed in the fabrication of biological materials and devices. Compared to traditional fabrication, direct 3D digital transformation simplifies the manufacturing process and enhances capability in geometric fabrication. In this paper, we demonstrated a rapid and low-cost 3D printing approach for “lego” assembly of micro-structured parts as an electro-transfection device. Electro-transfection is an essential equipment for engineering and regulating cell biological functions. Nevertheless, existing platforms are mainly employed
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Xie, Jianwen, Weidong Fan, and Jianwen Zhang. "Study of Gas Temperature Characteristics at the Bottom of the Platen Heaters of Boiler Employing Shenhua Bituminous Coal Based on Two-Level Air Staging Combustion System." In ASME 2017 Power Conference Joint With ICOPE-17 collocated with the ASME 2017 11th International Conference on Energy Sustainability, the ASME 2017 15th International Conference on Fuel Cell Science, Engineering and Technology, and the ASME 2017 Nuclear Forum. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/power-icope2017-3118.

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A 600MW tangentially fired sub-critical boiler with the volume heat load of 87.6kW/m3 at the case of BMCR was not originally equipped with the separated over fire air (SOFA) system. Shenhua bituminous coal with low ash fusion point and strong slagging characteristics is employed as its design coal. To prevent serious slagging on its platen heaters, it is necessary to employ 80% Shenhua bituminous coal with low ash fusion temperature blending 20% Shenhua bituminous coal with high ash fusion temperature. However, NOx emission value at the furnace exit reaches more than 370mg/m3 (O2 = 6%). In ord
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Khan, Munir, Yexiang Xiao, Bengt Sunde´n, and Jinliang Yuan. "Analysis of Multiphase Transport Phenomena in PEMFCS by Incorporating Microscopic Model for Catalyst Layer Structures." In ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-65142.

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The catalyst layer (CL) in polymer electrolyte membrane (PEM) fuel cells is one of the key components regulating the overall performance of the cell. In PEM fuel cells, there are two CLs having identical composition for hydrogen oxidation (HO) and oxygen reduction (OR) reactions. There are four phases inside the CL, namely: carbon, Pt particles, ionomer and voids. In this work, a micro-model of the cathode CL has been developed mathematically using finite volume (FV) technique to investigate the transport phenomena of reactants and product species, ions and electrons by incorporating the above
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Sapra, Harsh D., Youri Linden, Wim van Sluijs, Milinko Godjevac, and Klaas Visser. "Experimental Investigations of Hydrogen-Natural Gas Engines for Maritime Applications." In ASME 2018 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/icef2018-9615.

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A novel ship propulsion concept employs natural gas to reduce ship emissions and improve overall ship propulsion efficiency. This concept proposes a serial integration of Solid Oxide Fuel Cell (SOFC) and a natural gas engine, while anode-off gas (gas at the fuel cell exhaust) is used in the natural gas engine. This study focusses on SOFC-gas engine integration by experimentally analyzing the effects of adding hydrogen, which is the main combustible component of the fuel cell anode-off gas, in marine natural gas engines. The overall challenge is to employ the anode-off gas to improve the perfor
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