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in-cites, July 2003
Citing URL: http://www.in-cites.com/scientists/MichaelJerryAntal.html
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An
essay by:
Michael Jerry Antal, Jr., Ph.D. |
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ccording to a recent in-cites analysis, Dr. Michael J. Antal Jr.
of the University of Hawaii at Manoa entered the top 1% of scientists
in the field of Engineering in the ISI
Essential
Science Indicators
Web product, with 27
papers cited a total of 479 times. In the essay below, Dr. Antal
discusses his journey from student to highly cited scientist. Dr.
Antal is the Coral Industries Distinguished Professor in the
University of Hawaii at Manoa’s School of Ocean Earth Science &
Technology.
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I belong to the generation whose earliest childhood memories
include the Korean conflict, the Space Race, nuclear energy, and
nuclear bomb shelters. Like many of my generation who grew up in
Einstein’s shadow (my home was only a bike ride from his), those
influences evoked in my thought a keen interest in physics, chemistry,
and mathematics. My first year in college was marked by the arrival of
a state-of-the-art General Electric mainframe computer that enabled
numerical solutions of difficult physics problems, and e-mail to girl
friends at Mount Holyoke College. My Ph.D. research centered on
numerical solutions to Schrodinger’s Equation applied to a
charge-exchange problem in atomic scattering theory.
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...soon the USA would be forced to fight wars over oil in the Mideast if it did not develop renewable
alternatives.
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While in graduate school I learned that the computer had
applications beyond physics. In their jarring book Limits to Growth,
Donella Meadows and her coworkers at MIT used innovative numerical
simulations to predict Malthusian scenarios scheduled to debut at the
beginning of the 21st century. Their predictions became the
subject of heated discussions both inside and outside the classroom.
Unknown to many of us at that time, more than a decade prior to the
publication of Limits to Growth, M. King Hubbert of the U.S.
Geological Survey had used numerical models based on solutions of the
logistics equation to predict the year that U.S. oil production would
peak. Hubbert’s prediction proved to be true. Moreover, the year of
publication of Limits to Growth nearly coincided with the peak
in U.S. oil production. Fortunately for us now, the predictions of
Donella Meadows and her coworkers were less reliable than the
projections of M. King Hubbert.
In spite of these disturbing mathematical prognostications, young
physicists like myself could feel some optimism about the future.
Nuclear energy promised power "too cheap to meter" (prior to
the event at Three Mile Island), thermonuclear energy seemed to be
just around the corner, and prescient futurists proclaimed the
hydrogen economy as the panacea for all problems associated with
fossil fuels and their environmental impacts. At that time the Los
Alamos Scientific Laboratory (LASL) was a hotbed of research in
nuclear and hydrogen energy (high-temperature gas-cooled nuclear
reactors suited for producing hydrogen by thermochemical water
splitting cycles), as well as nuclear fusion (especially laser fusion)
research. I was delighted when Los Alamos offered me a position in its
thermonuclear weapons physics group. My first job was to develop
software to simulate fast charged particle transport in thermonuclear
plasmas by numerical solution of the Boltzmann equation. The addition
of my software to existing code caused the package to exceed the
storage limits of the most powerful computers of that era. A computer
simulation ran all night and its output was studied for days
thereafter.
There were no serious shortages of gasoline at Los Alamos during
the "first energy crisis" of 1973. In my free time I
followed the energy literature and was deeply impressed by an article
in Science concerning the magnitude of the renewable American
biomass resource. My reading led me to conclude that renewable
hydrogen could be produced from biomass by a steam reforming process
similar to that used in the manufacture of hydrogen from methane.
During the winter of 1974, I obtained special permission to attend the
first international meeting on Hydrogen Energy that was organized and
chaired by Dr. Mel Bowman, who was then Associate CMB Division Leader.
A few months later I garnered significant support from the U.S.
Environmental Protection Agency to pursue my ideas on hydrogen
production from biomass in collaboration with my colleague Dr. Bowman.
For about six months I devoted my mornings to thermonuclear weapons
physics research, and my afternoons to chemical engineering activities
centered on hydrogen production by the thermochemical gasification of
biomass. Unfortunately, the leadership of Los Alamos was not
comfortable with my widespread interests, and they made their
disapproval known to me. I was glad when Princeton University offered
me a tenure-track position in the energy sciences within its
Department of Mechanical and Aerospace Engineering. I took a part of
my EPA sponsored research program with me to Princeton when I left Los
Alamos in 1975.
At Princeton, Dr. Martin Summerfield enjoyed an international
reputation for his work in solid rocket fuel propellants. I was
fortunate that he offered me space in his laboratory to pursue my
research. As a result of my interactions with him, his staff, and his
students, I realized the need to understand the effects of
temperature, pressure, and heating rate on the products of biomass
pyrolysis and gasification. Furthermore, I needed a fundamental
understanding of both solid phase and gas phase transformations. In
collaboration with Dr. Henry Friedman—a past President of the North
American Thermal Analysis Society—my students and I employed
thermogravimetric analysis (TGA) and differential scanning calorimetry
(DSC) to study the pyrolytic behavior of whole biomass substrates
(e.g., oak wood) and representative model compounds (e.g., cellulose
and levoglucosan). Likewise, Dr. Maitland Jones, Jr.—author of a
highly regarded organic chemistry textbook and one of Princeton’s
most beloved professors—generously worked with me and my students to
develop a better understanding of the gas phase pyrolysis behavior of
tarry vapors and their model compounds (e.g., 1,3 dioxolane and
glycerol). I also developed an interest in chemical applications of
high temperature solar energy. Research projects in this field took me
to the 1 MWth solar furnace in the French Pyrenees, and a
smaller furnace on the Georgia Tech campus. Unfortunately, some of the
senior faculty in my department—and their corporate sponsors—strongly
disapproved of my interests. They felt that I should focus my
attention on shale oil and other fossil fuels. This conflict was
resolved when the University of Hawaii (UH) received an unexpected
gift of $800,000 from the Texas oil magnate David Chalmers to endow a
Chair in Renewable Energy. I was delighted to accept the Coral
Industries Chair of Renewable Energy Resources when it was offered to
me in the spring of 1981, and I moved my laboratory and students to
the Manoa campus on 1 January 1982.
During my last year at Princeton, I had a memorable experience. The
editor of a widely read journal of the middle-Atlantic states asked me
to write a feature article on renewable energy. I was promised a
substantial honorarium. To ensure that I was on the right track, I
sent installments of the article as I wrote it to an assistant editor
for his review. Each installment was greeted with enthusiasm and
compliments. I concluded the article with the prediction that soon the
USA would be forced to fight wars over oil in the Mideast if it did
not develop renewable alternatives. The editor of the journal did not
like my conclusion, and demanded that I rewrite it. Dutifully I
deleted all unpleasant references to war and the urgent need for
energy conservation, but my faux pas in the first draft had poisoned
the well: the editor refused to publish my article.
During the following two decades my work at UH matured and came to
focus on four principal fields of application.
- Hydrogen from biomass. My initial interest at Los Alamos in the
steam reforming of biomass evolved into studies of biomass
gasification in supercritical water. We learned that carbon
catalysts enabled the complete gasification of biomass feedstocks
in supercritical water. Furthermore, the gas was unusually rich in
hydrogen, and available at a very high pressure. But an economic
prognosis by the National Renewable Energy Laboratory (NREL)
indicated that hydrogen produced by our process would cost more
than four times the current cost of oil, and funding for this work
ceased. Nevertheless, my former student, Professor Yukihiko
Matsumura of the University of Hiroshima, together with another
former student, Dr. Tomoaki Minowa of AIST in Japan, organized an
international research effort including workers from the
Netherlands and the USA on this topic. Furthermore, following my
lead German researchers at the Forschungszentrum Karlsruhe built a
pilot plant ("VERENA") to demonstrate supercritical
water gasification of biomass. Unfortunately, recently the
Japanese have confirmed the dismal economics of the process, and
the Germans have encountered difficult engineering hurdles in
their work.
- Ethanol from lignocellulosic biomass. Our work with
supercritical water led us to the unexpected discovery that all of
the hemicellulose and about half of the lignin in lignocellulosic
biomass dissolves during a one to two minute exposure to liquid
water at 220 ºC. Working with Professor Lee Lynd at Dartmouth
College—an internationally recognized authority on fermentations—we
showed that the cellulosic residual of our hot liquid water
pretreatment was very well suited for enzymatic saccharification
followed by fermentation to ethanol. The yields of ethanol
obtained by Professor Lynd and his students were among the highest
ever reported. Late last year NREL announced that hot liquid water
appears to be the most attractive pretreatment process for ethanol
production. Nevertheless, NREL estimates that a commercial ethanol
from biomass refinery will cost more than $300 million.
- Chemicals from biomass. The novel acid- and base-catalyzed
reactions of sugars and fermentation products in hot liquid, and
supercritical water seemed to offer opportunities to produce a
variety of desired chemical building blocks from biomass. With
Professor Geoffrey Richards of the University of Montana—a
winner of the Anselme Payen Award of the American Chemical Society—we
shed new light on the reactions that form furfural from xylose and
hydroxymethyl furfural from glucose, fructose, and sucrose.
Similarly, with Maitland Jones we examined reactions that form
acrylic acid from lactic acid, and methacrylic acid from citric
acid. During the academic year 1990-91, Dr. Donald G. M. Anderson,
Gordon McKay Professor of Applied Mathematics at Harvard, hosted
my sabbatical, and together we developed detailed, mechanistic
kinetic models of the acid-catalyzed formation of ethene from
ethanol, propene from 1- and 2-propanol, and butene from
tert-butanol.
- Carbon from biomass. The MSE thesis of my student William Mok at
Princeton showed that increasing pressure strongly favors the
formation of carbon (charcoal) from biomass during pyrolysis. His
work with DSC and TGA continued via collaborations with Dr. Gabor
Varhegyi of the Research Laboratory of Materials and Environmental
Chemistry of the Hungarian Academy of Sciences, and Dr. Morten
Gronli of the Norwegian Technological University. Results of these
fundamental studies became the foundation of an effort to
dramatically improve the efficiency of charcoal production. We
built a pilot plant whose charcoal yields attained the limit set
by thermodynamics with a reaction time of about 70 minutes. This
work was patented and licensed, but a Kingsford engineer
complained to us about the energy input. Two years ago his
complaint caused me to initiate work on a pressurized, downdraft
biomass "gasifier" that would be operated to quickly
produce high yields of carbon from biomass. This "flash
carbonization" process has been successful beyond our wildest
dreams. Yields of carbon equal or exceed those of the high-yield
charcoal process, and reaction times have been reduced to as
little as 20 minutes. The UH has applied for patents on flash
carbonization and has already licensed it. We anticipate that the
production biomass carbons will eclipse that of fossil carbons
(coal) and will find many new applications. For example, one
current focus of my research is the development of a biocarbon
fuel cell (a "battery" that generates electricity by the
electrochemical oxidation of charcoal).
While at Princeton I invited M. King Hubbert to speak on his work.
During his seminar he used the same mathematical models that had
successfully predicted the peak of oil production in the USA to
predict that world oil production would peak shortly after the turn of
the century. Recently, Professor Kenneth S. Deffeyes (also of
Princeton) updated and refined the models of M. King Hubbert. In his
widely read book Hubbert’s Peak, Deffeyes predicts
that the peak in world oil production will occur next year. I am aware
of much evidence that corroborates his prediction. The adjustments
that will be required as demand for oil exceeds supply, following the
peak in world oil production, are beyond my ability to comprehend. I
hope that mankind’s progress in the development of renewable energy
will not be too little, too late.
In conclusion I thank my students, coworkers, and collaborators—many
of whom could not be mentioned in this essay because of space
limitations—for their inspiration and friendship. My work would not
have been possible without them.
Michael Jerry Antal, Jr., Ph.D.
School of Ocean Earth Science & Technology
University of Hawaii, Manoa
Oahu, Hawaii, USA
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in-cites, July 2003
Citing URL: http://www.in-cites.com/scientists/MichaelJerryAntal.html
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