Wednesday, May 6, 2020
Optimization And Enhancement Of Hybrid Cooling System
OPTIMIZATION AND ENHANCEMENT OF HYBRID COOLING SYSTEM Makkala Anil kumar 1, D. Muralidhar Yadav 2, M.Mastanaiah3 1M.Tech Student, 2 Associate Professor, 3 Professor Department of Mechanical Engineering DR.SAMUEL GEORGE INSTITUTE OF ENGINEERING AND TECHNOLOGY MARKAPURAM-523316, PRAKASAM DIST, ANDHRA PRADESH ABSTRACT An alternative is to use air as the cooling medium but their performance drops in hot weather conditions. Maximization of overall efficiency is as vital as the cost and availability of water. Therefore there is a need to integrate the technologies of air cooled and water cooled condensers. This paper will focus on parallel condensing where steam from the turbine is ducted in parallel to both air cooled and water cooled condensers. To optimize the parallel condensing capacities of air cooled and water cooled condensers considering parameters such as ambient temperature, pressure, availability of water, fan power, pumping costs. Keywords: Optimization; Enhancement; Hybrid Cooling System; 1.0 INTRODUCTION Exhaust steam from the steam turbine is separated into two streams. One stream flows into a water cooled surface condenser while the other is directed to an air-cooled condenser. The heated cooling water is cooled as it flows through a cooling tower, where air is forced through the tower by mechanical or natural draft. Fig .1 Condensate from the water cooled andShow MoreRelatedInformation Technology : A New Generation Of Sql1596 Words à |à 7 Pageswhen needed, such as mission-critical transactional workloads. The two methodologies Hybrid automated decision making supports SQL and NoSQL IBM Informix determines if you are dealing with a JSON Collection or a SQL tables and processes the operations appropriately. Thus IBM Informixââ¬â¢s ability to access JSON documents and/or SQL tables within the popular MongoDB APIs provides the foundation for a single hybrid application to span all of the enterprise data. 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Forensic Toxicology and Dermal Sensitization â⬠MyAssignmenthelp.com
Question: Discuss about the Forensic Toxicology and Dermal Sensitization. Answer: As a toxicologist assigned to determine whether a novel chemical has the capability of dermal sensitization production, I will use the following steps to explain how I would test for dermal sensitization. In undertaking this task, I will also present an explanation for the model/test system I would further provide a brief description of how the test is run and how the results are interpreted. To undertake this assignment, I have chosen the Guinea Pig Maximization Model because it is easy to use and has been previously effective in testing the production of dermal sensitization. GPMT Overview At least ten animals are utilized in treatment cohort and a minimum of 5 animals are used in control cohort/twenty-test and ten-control animals. Induction is then undertaken originally on skin of shoulder area with 3 intradermal injections on day zero. Control animals also receive 3 intradermal injections, however, only vehicle is utilized in place of test substance. Five to seven days later animal skin is smeared with 0.50 mL of ten percent sodium-lauryl-sulfate in Vaseline. This painting is done to create a local irritation, twenty-four hours later, test substance is applied for 48 hours under occlusion (Varns et al., 2016)). Challenge is then undertaken on twentieth-twenty-second day with reapplication of patches for twenty-four hours and assessment of results done at 48 hours and 72 hours following challenge. Magnusson and Kligman grading scale is then utilized for evaluation. Zero equal no observable change, one equals discrete/patchy erythema, two equals moderate and confluent erythema while three indicates intense erythema and swelling. Aim: To establish the sensitizing prospective of a test article when it is dermally applied. The test conforms to the established OECD Guideline 406 and EPA-OCSPP 870.2600 standards. Principle: The contact dermal sensitization remains an immunological procedure whereby a host animal, via recurrent skin-exposure, needs a particular allergic-sensitivity to a substance. Guinea Pig Maximization (GPMT) model will have the contact dermal sensitivity being demonstrated as a surged erythema. Test Overview: The following sections generally details briefly how the Guinea Pig Maximization Model is used to undertake and interpret the dermal sensitization test and results respectively. Typical Testing Time: Approximately ten wees encompassing pre-test, central test and reporting times. Induction Stage: In the 1st induction stage, it will encompass a manifold intradermal injections to test using twenty animals. I will use an adjuvant (fifty percent Freunds Complete Adjuvant; FCA), the test article (TA) alongside the mixture of TA and FCA. I will administer the mixture to the dorsum (clipped free of hair) in duplicate 0.10-ml injections (Sato, Yuta Kusaka, 2017). I will select TA concentration that does not yield local ulceration/necrosis. The TA concentration I choose will also be free from systemic toxicity. I will then treat Ten Vehicle Group animals identically with an exemption of replacing vehicle for the TA. I will then examine the treated sites of every animal and score them at twenty-four-and forty-eight hours following the injections (Hamada, Bruze, Zimerson, Isaksson Engfeldt, 2017). After 7 days, I will apply the 2nd induction which is applied administered topically via the application of a TA-saturated two-centimeter by four-centimeter section of the Whatman No. one filter paper over the past already injected intradermal sites clipped free of hair for forty-eight hours as an obstructed exposure. I will tolerate TA concentration in the similar manner, however, this time using the vehicle. I will then examine the treated sites of every animal and score them at forty-eight hours following patch application. Challenge Phase: After the fourteenth day following the topical induction, I will topically challenge the animals in both Vehicle Group and TA Group over a twenty-four, occluded exposure. I will do this by applying a two-centimeter by 2-centimeter section of Whatman number one filter paper saturated with the uppermost non-irritating TA concentration on left flank. I will apply vehicle in similar manner as TA. And I will also apply patch to right flank of every animal. I will then examine and score the challenge sites after twenty-four hours and forty-eight hours following the removal of patch (Lewandowski Cohen, 2016). Interpretation: I will regard a score of one/greater than 1 for redness in the GPMT a positive response. I will determine sensitization prospective on the basis of proportion of the animals showcasing a positive reaction. A 6-animal screening study is appropriate in determination of the suitable induction (topical and intradermal) and challenge (topical) concentrations. References Hamada, H., Bruze, M., Zimerson, E., Isaksson, M., Engfeldt, M. (2017). Factors Affecting the Concentration of Diphenylmethane-4, 4-Diisocyanate in Freunds Complete Adjuvant. Can They Affect the Outcome of the Guinea-Pig Maximization Test?. Journal of Clinical Experimental Dermatology Research, 8(4). Lewandowski, T. A., Cohen, J. M. (2016). Skin sensitization risk assessment: Considering available data for weight of evidence assessments. Regulatory toxicology and pharmacology: RTP, 82, 186-187. Sato, K., Yuta, K., Kusaka, Y. (2017). Skin Sensitization Model Based on Only Animal Data by Qualitative Structure-Toxicity Relationships (QSTR) Approach. In Allergy and Immunotoxicology in Occupational Health (pp. 93-101). Springer Singapore. Varns, K., Finnema, S. J., Stepanov, V., Takano, A., Tth, M., Svedberg, M., ... Halldin, C. (2016). Neurokinin-3 Receptor Binding in Guinea Pig, Monkey, and Human Brain: In Vitro and in Vivo Imaging Using the Novel Radioligand,[18F] Lu AF10628. International Journal of Neuropsychopharmacology, 19(8).
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