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Thematische Bibliographien / Vitrification process

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Zeitschriftenartikel

Auswahl der wissenschaftlichen Literatur zum Thema „Vitrification process“

Autor: Grafiati

Veröffentlicht am 25. Mai 2024

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Zeitschriftenartikel zum Thema "Vitrification process"

1

Faltus, Milos, Alois Bilavcik, Stacy Denise Hammond Hammond, and Jiri Zamecnik. "Vitrification process control by DSC." Cryobiology 109 (December 2022): 23–24. http://dx.doi.org/10.1016/j.cryobiol.2022.11.074.

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2

Odagaki, Takashi, and Akira Yoshimori. "Localization transition in the vitrification process." Physica B: Condensed Matter 296, no. 1-3 (2001): 174–79. http://dx.doi.org/10.1016/s0921-4526(00)00796-1.

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3

Short, Rick, Nick Gribble, Edward Turner, and Andrew D. Riley. "Using the Vitrification Test Rig for Process Improvements on the Waste Vitrification Plants." Advances in Science and Technology 73 (October 2010): 176–82. http://dx.doi.org/10.4028/www.scientific.net/ast.73.176.

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The Vitrification Test Rig (VTR) is a full scale non-active waste vitrification plant (WVP), that replicates the lines used for immobilising highly active reprocessing waste at Sellafield in the UK. In the high level waste (HLW) vitrification process, liquid HLW is dried in a rotating tube furnace then mixed with an alkali borosilicate glass frit. This mixture is heated to form a homogeneous product glass that is poured, cooled and stored in steel canisters. The primary function of the VTR is to trial and develop methods to increase the efficiency of high level waste processing at the active WVP. Efficiency gains are mainly achieved by increasing the rate at which the immobilised product is created and by increasing the ratio of HLW to glass frit in the product. The VTR has also been used to investigate the chemistry of various process additions and conditions, the effects of potential fault scenarios, and the processing of dilute waste streams that will be received by WVP in the future. All of these areas have the potential to improve processing efficiency through the optimisation of process conditions and the minimisation of unplanned plant outages. This paper discusses several VTR campaigns that have led to overall improvements of WVP operation.

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4

Romero, M., and J. M. Rincón. "El proceso de vitrificación/cristalización controlada aplicado al reciclado de residuos industriales inorgánicos." Boletín de la Sociedad Española de Cerámica y Vidrio 39, no. 1 (2000): 155–63. http://dx.doi.org/10.3989/cyv.2000.v39.i1.884.

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5

Peymani, R., S. Najmabadi, H. Badrzadeh, T. M. Macaso, Z. Azadbadi, and A. Ahmady. "Comparison of two vitrification solutions on the outcome of vitrification/thaw process in a closed vitrification system, V-Kim." Fertility and Sterility 90 (September 2008): S286—S287. http://dx.doi.org/10.1016/j.fertnstert.2008.07.1105.

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6

F. N. C, Anyaegbunam. "Hazardous Waste Vitrification by Plasma Gasification Process." IOSR Journal of Environmental Science, Toxicology and Food Technology 8, no. 3 (2014): 15–19. http://dx.doi.org/10.9790/2402-08311519.

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7

Schug, Brett W., and Matthew J. Realff. "Analysis of waste vitrification product-process systems." Computers & Chemical Engineering 22, no. 6 (1998): 789–800. http://dx.doi.org/10.1016/s0098-1354(98)80002-1.

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8

Masrat-Un-Nisa, Asloob Ahmad Malik, Khursheed Ahmad Sofi, Arjuma Khatun, and Nahida Yousuf. "Recent Advancements in Vitrification Cryodevices for Gamete and Gonadal Tissue." Cryoletters 43, no. 3 (2022): 129–39. http://dx.doi.org/10.54680/fr22310110112.

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Cryopreservation of gametes and gonadal tissue is nowadays primarily accomplished through vitrification. Variables such as cooling rate, viscosity and volume of vitrification solution are critical in gamete vitrification. In addition, sample size and stepwise exposure are also crucial for gonadal tissue vitrification. Recently a class of cryodevices has been developed to reduce the volume of vitrification solution so as to achieve higher cooling rates. Vitrification devices are classified as "open" or "closed" depending on whether the medium comes into direct contact with liquid nitrogen during the process. Examples of the open cryodevices for gamete vitrification are Cryotop, Cryolock, open pulled straw (OPS), etc., and closed devices are Vitrisafe, CryoTip, and high security vitrification kit. Similarly, for tissue vitrification open cryodevices used are needles, cryovials and closed devices used are Cryotissue, ovarian tissue cryosystem, etc. Among all the gamete cryodevices, Cryotop is unique and the best-selling micro-volume storage device. Use of this device has resulted in the highest number of babies born after embryo or oocyte vitrification. Another novel device, Kitasato vitrification system, is a vitrification solution absorber, which is similar to Cryotop but differs in one way, as it possesses a porous membrane that absorbs extra solution from the gamete. This review provides an update on the recent use of cryodevices for gamete and gonadal tissue vitrification.

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9

Widjiati, Widjiati, Epy Muhammad Luqman, and Portia Sumarsono. "Comparison of Morula and Blastula Embryo Vitrification by Using Cryoprotectant Ethylene Glycol, Propanediol, DMSO and Insulin Transferrin Selenium." KnE Life Sciences 3, no. 6 (2017): 205. http://dx.doi.org/10.18502/kls.v3i6.1129.

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Vitrification is freezing method with low temperature (-196ºC) using high concentrations of cryoprotectants with a view to preventing the formation of ice crystals that can damage cells and decrease the viability of the embryo blastomeres. Embryos post warming which has low viability when transferred to a recipient will decrease the pregnancy rate. Intracellular cryoprotectants used in vitrification is ethylene glycol, propanediol, or DMSO. The third type of cryoprotectants has different capacities to protect the morula and blastocyst stage embryos. This study aims to decide the exact type of cryoprotectants in protecting the morula and blastocyst stage embryos when vitrification process. Research methods were divided into three groups of cryoprotectants that group treatment 1 (P1): Ethylene Glycol 30% + Sucrose 1 M + Insulin Transferrin Selenium 15 mL, group treatment 2 (P2): Propanediol 30% + Sucrose 1 M + Insulin Transferrin Selenium 15 mL, treatment Group 3 (P3): DMSO 30% + Sucrose 1 M + Insulin Transferrin Selenium 15 mL. The data obtained were analyzed by one-way ANOVA. Results of research that use Propanediol at the morula stage embryo vitrification is not significantly different from the Ethylene glycol but significantly different from DMSO. Then use Ethylene Glycol at the blastocyst stage embryo vitrification significantly different with Propanediol and DMSO and DMSO Propanediol but usage is no different. The conclusion of this study is Propanediol used as cryoprotectants in the vitrification process morula stage embryos, while ethylene glycol used as cryoprotectants the blastocyst stage embryo vitrification process.Keywords: vitrification; ethylene glycol; propanediol; DMSO; morula; blastocyst

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10

Odagaki, Takashi. "Non-Ergodicity and Non-Gaussianity in Vitrification Process." Progress of Theoretical Physics Supplement 126 (1997): 9–12. http://dx.doi.org/10.1143/ptps.126.9.

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