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Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
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Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
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One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
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Catalysis

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The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
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Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
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Acetone Sensing and Catalytic Conversion by Pd-Loaded SnO2.

Pascal M Gschwend1, Florian M Schenk1, Alexander Gogos2,3

  • 1Particle Technology Laboratory, Department of Mechanical and Process Engineering, Institute of Energy and Process Engineering, ETH Zurich, Sonneggstrasse 3, CH-8092 Zurich, Switzerland.

Materials (Basel, Switzerland)
|October 23, 2021
PubMed
Summary

Adding palladium (Pd) to tin oxide (SnO2) enhances acetone gas sensors. Optimal performance for detecting acetone as a lipolysis marker occurs at low Pd levels and specific temperatures, around 200-262.5 °C.

Keywords:
breath sensorchemoresistivemetal oxiden-typenanoparticles

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Area of Science:

  • Materials Science
  • Chemical Engineering
  • Sensor Technology

Background:

  • Noble metal additives enhance metal oxide gas sensor performance.
  • Palladium (Pd) on tin oxide (SnO2) is a prominent combination.
  • Acetone detection via breath analysis is crucial for monitoring lipolysis.

Purpose of the Study:

  • To investigate the effect of varying palladium (Pd) quantities on nanostructured tin oxide (SnO2) gas sensors.
  • To determine the optimal operating temperature for acetone sensing.
  • To understand the relationship between Pd loading, operating temperature, and catalytic acetone oxidation.

Main Methods:

  • Photodeposition of different Pd quantities (0-3 mol%) onto nanostructured SnO2.
  • Evaluation of acetone sensing performance (sensitivity, response/recovery times) at various operating temperatures.
  • Analysis of catalytic oxidation of acetone using Pd-loaded SnO2 in a packed bed.

Main Results:

  • Pd addition can improve or degrade sensor performance based on loading and temperature.
  • Optimal Pd loading for acetone sensing is below 0.2 mol%.
  • Peak sensor performance is achieved at operating temperatures between 200-262.5 °C with approximately 50% acetone conversion.

Conclusions:

  • Optimized Pd loading and operating temperature are critical for effective acetone gas sensing.
  • Pd-loaded SnO2 sensors show promise for breath analysis applications.
  • Understanding the catalytic oxidation mechanism is key to sensor performance enhancement.