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Books on the topic 'Catalyse plasma'

Author: Grafiati

Published: 25 May 2024

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1

Tu, Xin, J. Christopher Whitehead, and Tomohiro Nozaki, eds. Plasma Catalysis. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-05189-1.

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2

Parvulescu, Vasile I., Monica Magureanu, and Petr Lukes, eds. Plasma Chemistry and Catalysis in Gases and Liquids. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527649525.

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3

Winter, Lea. Upgrading Carbon and Nitrogen to Fuels and Chemicals Using Heterogeneous and Plasma Catalysis. [New York, N.Y.?]: [publisher not identified], 2020.

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4

service), SpringerLink (Online, ed. Molecular Catalysts for Energy Conversion. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009.

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5

Weidler, Natascha. Plasma-enhanced chemical vapor deposition of cobalt-based catalysts for the oxygen evolution reaction. Darmstadt: Universitäts- und Landesbibliothek Darmstadt, 2017.

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6

Plasma Catalysis. MDPI, 2019. http://dx.doi.org/10.3390/books978-3-03897-751-3.

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7

Tu, Xin, J. Christopher Whitehead, and Tomohiro Nozaki. Plasma Catalysis: Fundamentals and Applications. Springer, 2019.

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8

Parvulescu, Vasile I., Monica Magureanu, and Petr Lukes. Plasma Chemistry and Catalysis in Gases and Liquids. Wiley & Sons, Incorporated, John, 2013.

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9

Parvulescu, Vasile I., Monica Magureanu, and Petr Lukes. Plasma Chemistry and Catalysis in Gases and Liquids. Wiley & Sons, Incorporated, John, 2012.

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10

Parvulescu, Vasile I., Monica Magureanu, and Petr Lukes. Plasma Chemistry and Catalysis in Gases and Liquids. Wiley-VCH Verlag GmbH, 2012.

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11

Parvulescu, Vasile I., Monica Magureanu, and Petr Lukes. Plasma Chemistry and Catalysis in Gases and Liquids. Wiley & Sons, Incorporated, John, 2012.

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12

Parvulescu, Vasile I., Monica Magureanu, and Petr Lukes. Plasma Chemistry and Catalysis in Gases and Liquids. Wiley & Sons, Limited, John, 2012.

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13

Plasma-Catalysis for Environmental and Energy-Related Applications. MDPI, 2022. http://dx.doi.org/10.3390/books978-3-0365-2782-6.

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14

Kaneko, Masao, and Tatsuhiro Okada. Molecular Catalysts for Energy Conversion. Springer, 2010.

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15

Vernon, Hilary. Phenylketonuria. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0064.

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Abstract:

Phenylketonuria is an autosomal recessive biochemical disorder most often resulting from a deficiency of phenylalanine hydroxylase, the enzyme which catalyzes the conversion of phenylalanine to tyrosine. The remainder of the cases are caused by abnormalities in the phenylalanine hydroxylase cofactor, tetrahydrobiopterin. Phenylketonuria can be divided into three subgroups based on the elevation of plasma phenylalanine in the untreated state: “classical,” “variant,” and “benign.” Untreated individuals with classical phenylketonuria develop neurocognitive abnormalities including seizures, microcephaly, and severe intellectual disability. Other clinical effects include a musty body odor, eczema, and reduced skin pigmentation. Treatment, which includes dietary restriction of phenylalanine, supplementation with synthetic protein, and, in some cases, administration of a synthetic form of tetrahydrobiopterin, is successful in preventing the long-term consequences of phenylketonuria.

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