Raymond Gorte

Last updated
Russell Pearce and Elizabeth Crimian Heuer Professor

Raymond J. Gorte
Born (1954-06-27) June 27, 1954 (age 69)
Nationality American
Alma mater University of Minnesota
University of Wisconsin
Known for Catalysis, Characterization, Fuel Cells
AwardsPaul H. Emmett Award (1999), AIChE Wilhelm Award (2009), National Academy of Engineering (2018)
Scientific career
Fields Chemical Engineer
Institutions University of Pennsylvania
Doctoral advisor Lanny D. Schmidt
External videos
Nuvola apps kaboodle.svg "Ray Gorte: What do we know about solid acidity?" "LRSM Science Café: Raymond J. Gorte "Automotive Emissions-Control Systems: How Does It Work and What Did Volkswagen Do?"

Raymond John Gorte is an American chemical engineer, currently the Russel Pearce and Elizabeth Crimian Heuer Endowed Professor of Chemical and Biomolecular Engineering (CBE) and Materials Science & Engineering (MSE) at the University of Pennsylvania. Throughout his career at the University of Pennsylvania and the University of Minnesota, he has advanced the study of fuel cells and catalysts including heterogeneous metals and zeolite materials. He is a member of the U.S. National Academy of Engineering. [1]

Contents

Early life and education

Gorte was born in Wisconsin and grew up in Manitowoc, Wisconsin.[ citation needed ] In 1976, he earned a Bachelor of Science in chemical engineering from the University of Wisconsin-Madison. He completed his Ph.D. in chemical engineering at the University of Minnesota in 1981 with advisor Lanny D. Schmidt on the topic of platinum catalysis of nitric oxide decomposition. His thesis was published in 1981 with the title, "The Kinetic Interaction of Nitric-Oxide with Single Crystal Platinum". [2]

Professor of chemical engineering

Gorte joined the University of Pennsylvania's Department of Chemical and Biomolecular Engineering in Philadelphia in 1981. He was promoted to associate professor in 1987, and professor in 1993. He is a member of the Penn Center for Energy Innovation, the Laboratory for Research on the Structure of Matter (LRSM), and the Catalysis Center for Energy Innovation. [3]

Fuel cells

Gorte's research in solid oxide fuel cells addresses the design of electrodes and applications in hydrocarbon oxidation. In 2000 he published an article in Nature with John Vohs describing the oxidation of methane and higher hydrocarbons with a composite anode of copper and ceria that achieves viable power densities while producing carbon dioxide and water. [4]

Solid acids

The design, synthesis, and utilization of solid acids such as amorphous silica-alumina, ZSM-5, or synthetic faujasite relies on an understanding of the chemical site of acidity. Gorte has proposed a description of solid acidity based on a thermochemical cycle including the proton affinity, the interaction energy, and the enthalpy of adsorption. Gorte has also developed a method for quantifying acid site concentration based on alkylamine decomposition by the Hoffmann elimination reaction occurring by temperature programmed desorption (TPD). He has recently extended this to a highly precise method of "reactive gas chromatography". [5]

Catalytic chemistry

Gorte's research in catalyst design has led to research projects on numerous applications and chemistries. He has published papers on the water-gas-shift reaction catalyzed by supported metals such as ceria-supported Pt, Pd and Rh. [6] Other applications include:

Works

Gorte has authored more than 400 journal articles on catalysis, surface chemistry, and fuels cells which includes:

With his Advisor

At Univ. of Pennsylvania

Honors

Gorte has received awards for his contributions to research, education and service, many of which highlight his interest in fuel cells and catalysis and the problems associated with characterization and fundamental mechanisms and kinetics. In 2018, Gorte was elected a member of the National Academy of Engineering. His election citation stated:

For fundamental contributions and their applications to heterogeneous catalysts and solid state electrochemical devices..

Election Citation, National Academy of Engineering, 2018 [22]

Other awards and honors include: [23]

Related Research Articles

<span class="mw-page-title-main">Catalysis</span> Process of increasing the rate of a chemical reaction

Catalysis is the increase in rate of a chemical reaction due to an added substance known as a catalyst. Catalysts are not consumed by the reaction and remain unchanged after it. If the reaction is rapid and the catalyst recycles quickly, very small amounts of catalyst often suffice; mixing, surface area, and temperature are important factors in reaction rate. Catalysts generally react with one or more reactants to form intermediates that subsequently give the final reaction product, in the process of regenerating the catalyst.

<span class="mw-page-title-main">Surface science</span> Study of physical and chemical phenomena that occur at the interface of two phases

Surface science is the study of physical and chemical phenomena that occur at the interface of two phases, including solid–liquid interfaces, solid–gas interfaces, solid–vacuum interfaces, and liquid–gas interfaces. It includes the fields of surface chemistry and surface physics. Some related practical applications are classed as surface engineering. The science encompasses concepts such as heterogeneous catalysis, semiconductor device fabrication, fuel cells, self-assembled monolayers, and adhesives. Surface science is closely related to interface and colloid science. Interfacial chemistry and physics are common subjects for both. The methods are different. In addition, interface and colloid science studies macroscopic phenomena that occur in heterogeneous systems due to peculiarities of interfaces.

Zeolite is a family of several microporous, crystalline aluminosilicate materials commonly used as commercial adsorbents and catalysts. They mainly consist of silicon, aluminium, oxygen, and have the general formula Mn+
1/n
(AlO
2
)
(SiO
2
)
x
・yH
2
O
where Mn+
1/n
is either a metal ion or H+. These positive ions can be exchanged for others in a contacting electrolyte solution. H+
exchanged zeolites are particularly useful as solid acid catalysts.

<span class="mw-page-title-main">Adsorption</span> Phenomenon of surface adhesion

Adsorption is the adhesion of atoms, ions or molecules from a gas, liquid or dissolved solid to a surface. This process creates a film of the adsorbate on the surface of the adsorbent. This process differs from absorption, in which a fluid is dissolved by or permeates a liquid or solid. While adsorption does often precede absorption, which involves the transfer of the absorbate into the volume of the absorbent material, alternatively, adsorption is distinctly a surface phenomenon, wherein the adsorbate does not penetrate through the material surface and into the bulk of the adsorbent. The term sorption encompasses both adsorption and absorption, and desorption is the reverse of sorption.

<span class="mw-page-title-main">Activated carbon</span> Form of carbon processed to have small, low-volume pores that increase the surface area

Activated carbon, also called activated charcoal, is a form of carbon commonly used to filter contaminants from water and air, among many other uses. It is processed (activated) to have small, low-volume pores that increase the surface area available for adsorption or chemical reactions. Activation is analogous to making popcorn from dried corn kernels: popcorn is light, fluffy, and its kernels have a high surface-area-to-volume ratio. Activated is sometimes replaced by active.

<span class="mw-page-title-main">Heterogeneous catalysis</span> Type of catalysis involving reactants & catalysts in different phases of matter

Heterogeneous catalysis is catalysis where the phase of catalysts differs from that of the reactants or products. The process contrasts with homogeneous catalysis where the reactants, products and catalyst exist in the same phase. Phase distinguishes between not only solid, liquid, and gas components, but also immiscible mixtures, or anywhere an interface is present.

Desorption is the physical process where adsorbed atoms or molecules are released from a surface into the surrounding vacuum or fluid. This occurs when a molecule gains enough energy to overcome the activation barrier and the binding energy that keep it attached to the surface.

The water–gas shift reaction (WGSR) describes the reaction of carbon monoxide and water vapor to form carbon dioxide and hydrogen:

<span class="mw-page-title-main">Cerium(IV) oxide</span> Chemical compound

Cerium(IV) oxide, also known as ceric oxide, ceric dioxide, ceria, cerium oxide or cerium dioxide, is an oxide of the rare-earth metal cerium. It is a pale yellow-white powder with the chemical formula CeO2. It is an important commercial product and an intermediate in the purification of the element from the ores. The distinctive property of this material is its reversible conversion to a non-stoichiometric oxide.

<span class="mw-page-title-main">Phosphotungstic acid</span> Chemical compound

Phosphotungstic acid (PTA) or tungstophosphoric acid (TPA), is a heteropoly acid with the chemical formula H3PW12O40]. It forms hydrates H3[PW12O40nH2O. It is normally isolated as the n = 24 hydrate but can be desiccated to the hexahydrate (n = 6). EPTA is the name of ethanolic phosphotungstic acid, its alcohol solution used in biology. It has the appearance of small, colorless-grayish or slightly yellow-green crystals, with melting point 89 °C (24 H2O hydrate). It is odorless and soluble in water (200 g/100 ml). It is not especially toxic, but is a mild acidic irritant. The compound is known by a variety of names and acronyms (see 'other names' section of infobox).

<span class="mw-page-title-main">Metal–organic framework</span> Class of chemical substance

Metal–organic frameworks (MOFs) are a class of compounds consisting of metal clusters coordinated to organic ligands to form one-, two-, or three-dimensional structures. The organic ligands included are sometimes referred to as "struts" or "linkers", one example being 1,4-benzenedicarboxylic acid (BDC).

Reactive flash volatilization (RFV) is a chemical process that rapidly converts nonvolatile solids and liquids to volatile compounds by thermal decomposition for integration with catalytic chemistries.

<span class="mw-page-title-main">Lanny D. Schmidt</span> American physical chemist (1938–2020)

Lanny D. Schmidt was an American chemist, inventor, author, and Regents Professor of Chemical Engineering and Materials Science at the University of Minnesota. He is well known for his extensive work in surface science, detailed chemistry (microkinetics), chemical reaction engineering, catalysis, and renewable energy. He is also well known for mentoring over a hundred graduate students and his work on millisecond reactors and reactive flash volatilization.

Transition metal oxides are compounds composed of oxygen atoms bound to transition metals. They are commonly utilized for their catalytic activity and semiconducting properties. Transition metal oxides are also frequently used as pigments in paints and plastics, most notably titanium dioxide. Transition metal oxides have a wide variety of surface structures which affect the surface energy of these compounds and influence their chemical properties. The relative acidity and basicity of the atoms present on the surface of metal oxides are also affected by the coordination of the metal cation and oxygen anion, which alter the catalytic properties of these compounds. For this reason, structural defects in transition metal oxides greatly influence their catalytic properties. The acidic and basic sites on the surface of metal oxides are commonly characterized via infrared spectroscopy, calorimetry among other techniques. Transition metal oxides can also undergo photo-assisted adsorption and desorption that alter their electrical conductivity. One of the more researched properties of these compounds is their response to electromagnetic radiation, which makes them useful catalysts for redox reactions, isotope exchange and specialized surfaces.

<span class="mw-page-title-main">Grigoriy Yablonsky</span>

Grigoriy Yablonsky is an expert in the area of chemical kinetics and chemical engineering, particularly in catalytic technology of complete and selective oxidation, which is one of the main driving forces of sustainable development.

<span class="mw-page-title-main">Cu Y Zeolite</span>

Cu-Y zeolites are copper-containing high-silica derivatives of the faujasite mineral group which in turn is a member of the zeolite family. Cu-Y zeolites are synthesized through aqueous or gaseous ionic exchange unlike the naturally occurring faujasites: faujasite-Ca, faujasite-Mg, and faujasite-Na. The exchanged copper atom can vary in oxidation states, but the most studied Cu-Y zeolite variants include Cu(I) or Cu(II) cations. Due to their high catalytic potential, they are utilized as desulfurization agents and in the production of nitrogen gas from nitrogen monoxide.

Maria Flytzani-Stephanopoulos was a Greek chemical engineer and, at the time of her death, had been the Robert and Marcy Haber Endowed Professor in Energy Sustainability and a distinguished professor at Tufts University. Flytzani-Stephanopoulos had also been the Raytheon Professor of Pollution Prevention at Tufts. She published more than 160 scientific articles with over 14,000 citations as of April 2018. She was a Fellow of AIChE, the American Association for the Advancement of Science and American Institute of Chemical Engineers. She lived in the Greater Boston Area with her husband, Professor Gregory Stephanopoulos of MIT.

Dionisios G. Vlachos is an American chemical engineer, the Allan & Myra Ferguson Endowed Chair Professor of Chemical Engineering at the University of Delaware and director of the Catalysis Center for Energy Innovation, a U.S. Department of Energy - Energy Frontiers Research Center. Throughout his career at University of Delaware and the University of Minnesota, he has advanced the study of catalysts and reaction engineering including catalytic applications in biomass utilization, alkane conversion and zeolites. He is a fellow of the American Association for the Advancement of Science and recipient of the Wilhelm Award of the American Institute of Chemical Engineers (2011).

In chemistry, catalytic resonance theory was developed to describe the kinetics of reaction acceleration using dynamic catalyst surfaces. Catalytic reactions occurring on surfaces that undergo variation in surface binding energy and/or entropy exhibit overall increase in reaction rate when the surface binding energy frequencies are comparable to the natural frequencies of the surface reaction, adsorption, and desorption.

<span class="mw-page-title-main">Samarium(III) nitrate</span> Chemical compound

Samarium(III) nitrate is an odorless, white-colored chemical compound with the formula Sm(NO3)3. It forms the hexahydrate, which decomposes at 50°C to the anhydrous form. When further heated to 420°C, it is converted to the oxynitrate, and at 680°C it decomposes to form samarium(III) oxide.

References

  1. "Raymond Gorte Elected to National Academy of Engineering". tufts.edu. Retrieved April 7, 2017.
  2. Gorte, Raymond John (1981). The Kinetic Interaction of Nitric-Oxide with Single Crystal Platinum (Ph.D). University of Minnesota. ProQuest   303136437.
  3. "Membership - Catalysis Center for Energy Innovation" . Retrieved 2 March 2018.
  4. Park, Seungdoo; Vohs, John M.; Gorte, Raymond J. (2000). "Direct oxidation of hydrocarbons in a solid-oxide fuel cell". Nature. 404 (6775): 265–267. Bibcode:2000Natur.404..265P. doi:10.1038/35005040. PMID   10749204. S2CID   4426984.
  5. Abdelrahman, Omar A.; Vinter, Katherine P.; Ren, Limin; Xu, Dandan; Gorte, Raymond J.; Tsapatsis, Michael; Dauenhauer, Paul J. (2017). "Simple Quantification of Zeolite Acid Site Density by Reactive Gas Chromatography". Catalysis Science & Technology. 7 (17): 3831–3841. doi:10.1039/C7CY01068K.
  6. 1 2 Bunluesin, T.; Gorte, R.J.; Graham, G.W. (1998). "Studies of the water-gas-shift reaction on ceria-supported Pt, Pd, and Rh: implications for oxygen-storage properties". Applied Catalysis B: Environmental. 15 (1–2): 107–114. doi: 10.1016/S0926-3373(97)00040-4 .
  7. Zafiris, G.S.; Gorte, R.J. (1993). "Evidence for a second CO oxidation mechanism on Rh/ceria". Journal of Catalysis. 143: 86–91. doi:10.1006/jcat.1993.1255.
  8. Wang, X.; Gorte, R.J. (2001). "Steam reforming of n-butane on Pd/ceria". Catalysis Letters. 73: 15–19. doi:10.1023/A:1009070118377. S2CID   92757001.
  9. Roy, Sounak; Mpourmpakis, Giannis; Hong, Do-Young; Vlachos, Dionisios G.; Bhan, A.; Gorte, R. J. (2012). "Mechanistic study of alcohol dehydration on γ-Al2O3". ACS Catalysis. 2 (9): 1846–1853. doi:10.1021/cs300176d.
  10. Gorte, R.; Schmidt, L.D. (1978). "Desorption Kinetics with Precursor Intermediates". Surface Science. 76 (2): 559–573. Bibcode:1978SurSc..76..559G. doi:10.1016/0039-6028(78)90114-0.
  11. Gorte, R.; Schmidt, L.D. (1979). "Temperature Programmed Desorption with Reaction". Applications of Surface Science. 3 (3): 381–389. Bibcode:1979ApSS....3..381G. doi:10.1016/0378-5963(79)90007-2.
  12. Gorte, R.J.; Schmidt, L.D. (1981). "Interactions Between NO and CO on Pt(111)". Surface Science. 111 (2): 260–278. Bibcode:1981SurSc.111..260G. doi:10.1016/0039-6028(80)90708-6.
  13. Gorte, R.J.; Schmidt, L.D.; Gland, John L. (1981). "Binding States and Decomposition of NO on Single Crystal Planes of Pt". Surface Science. 109 (2): 367–380. Bibcode:1981SurSc.109..367G. doi:10.1016/0039-6028(81)90494-5.
  14. Gorte, R. (1981). "The Electron Energy Loss Spectrum of Isocyanic Acid on the Pt(111) Surface". Journal of Catalysis. 67 (2): 387–391. doi:10.1016/0021-9517(81)90298-0.
  15. Parrillo, D.J.; Adamo, A.T.; Kokotailo, G.T.; Gorte, R.J. (1990). "Amine adsorption in H-ZSM-5". Applied Catalysis. 67: 107–118. doi:10.1016/S0166-9834(00)84435-8.
  16. Zafiris, G.S.; Gorte, R.J. (1993). "Evidence for low-temperature oxygen migration from ceria to Rh". Journal of Catalysis. 139 (2): 561–567. doi:10.1006/jcat.1993.1049.
  17. Parrillo, D.J.; Lee, C.; Gorte, R.J. (1994). "Heats of adsorption for ammonia and pyridine in H-ZSM-5: evidence for identical Brønsted-acid sites". Applied Catalysis A: General. 110: 67–74. doi:10.1016/0926-860X(94)80106-1.
  18. Farneth, W. E.; Gorte, R. J. (1995). "Methods for Characterizing Zeolite Acidity". Chemical Reviews. 95 (3): 615–635. doi:10.1021/cr00035a007.
  19. Gorte, R.J. (1999). "What do we know about the acidity of solid acids?". Catalysis Letters. 62: 1–13. doi:10.1023/A:1019010013989. S2CID   85547570.
  20. Park, Seungdoo; Vohs, John M.; Gorte, Raymond J. (2000). "Direct Oxidation of hydrocarbons in a solid oxide fuels cell". Nature. 404 (6775): 265–267. Bibcode:2000Natur.404..265P. doi:10.1038/35005040. PMID   10749204. S2CID   4426984.
  21. Atkinson, A.; Barnett, S.; Gorte, R. J.; Irvine, J. T. S.; McEvoy, A. J.; Mogensen, M.; Singhal, S. C.; Vohs, J. (2004). "Advanced anodes for high-temperature fuel cells". Nature Materials. 3 (1): 17–27. Bibcode:2004NatMa...3...17A. doi:10.1038/nmat1040. PMID   14704781. S2CID   40574890.
  22. "NAE Member - Raymond Gorte" . Retrieved 2 March 2018.
  23. "UPenn - Raymond Gorte" . Retrieved 2 March 2018.
  24. "Parravano Memorial Award" . Retrieved 2 March 2018.
  25. "AIChE Wilhelm Award". 2012-03-28. Retrieved 2 March 2018.