Category Archives: Automotive

A prison tale (fiction) by R. E. Buxbaum

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I’m writing from the Michigan Department of Corrections; Mail-stop 5678 E, Jackson, MI, awaiting trial on auto-related charges. So, legally speaking, I’m still innocent, if not quite free. So, here’s my  story, and my bargain. The whole situation, it seems, is more comical than criminal. At its source, at bottom, all I was trying to do was take care of some left over issues from unofficial jobs I was doing for the city. For his honor, the mayor. That’s K.K., Kwamie Kilpatrick, the ex-mayor to you, but always his honor to me; great guy. Anyway, cars that fall in the river aren’t that unusual in this town, and it’s not like I planned to smuggle anything to Canada. You’ll notice my case doesn’t involve theft, or injuring anyone but myself. Just trespass, though I wouldn’t mind a short prison stay if it can be arranged. Sort of like Shawshank redemption.

Anyway, my minor crime was committed a week ago, Thursday, and involved a Dodge Viper. One that I own, straight-up, with a partner and the bank: a yellow, convertible viper costing some $220,000 when new. Beautiful machine; tinted glass, and capable of doing 180 mph without breaking a sweat. I use it, or did, to take care of errands for his honor. He tips nice, and helps out when I’m in a jam, so I did get paid for the work, but for the most part, it’s like I’m like a patriot-servant to the city. I’m using my own car for city business. In better days, those errands included taking judges for the occasional joy ride, to the airport or lunch, plus other deliveries. Not generally on the water, like last Thursday, and yes that’s me, waving in the photo. Shame about the car.

As to how I got the viper, I got it at the dealer on Woodward, just over the 8 mile bridge, and paid for it mostly myself, with a loan from First Federal. At the time I had a good job running errands for his honor, as I mentioned. Now I’m so of unemployed. What sort of errands? The sort of ones you’d want to run in a viper, Duh. Aside from driving judges to meetings, there were girl errands; some boy errands; some money errands. Occasionally a disposal — nothing illegal, but embarrassing maybe. When you’re disposing of city property, you don’t look too carefully at the item. When you’re carrying something big, or someone’s wife or girlfriend, or a lot of money, it’s nice to be able to move quickly. Judges and senators like to move fast too, behind tinted windows. They still do.

Anyway, after his honor goes to prison (real shame, that), and my job becomes near-ended. There’s still some errands to to, but not so many, and I’ll grant that the viper has become more of a liability than an asset. Not that there’s insurance fraud behind me ending up in the river, just good-ole fun, and maybe a little reckless driving. I’m owing like 165k still on the machine, and my brother and I came up with this great plan for a movie — no fraud intended. There’s this great spot that we know by Zug Island, where the Rouge meets the Detroit river. It’s pretty well deserted, with a pier and a boat ramp. We used it all the time, back in the day for meetings and such. No-one goes there because of the smells. There’s always an oil slick and the water there will dissolve most anything metal. The Zug Island folks make sure of there are no cameras or loiterers either — just so no-one steals their secrets. Anyway, my brother and I figured that, if I got the viper up to about 30- 40 mph on the pier we could sail it out over the rocks and garbage into the river, land softly in the water, and make for a great movie. We never planned to file an insurance claim like we’d lost the car or it was stolen. Anyway, the water’s only about 8′ below the end of the pier, so it’s sort of like a high-dive. I figured I’d get out of the sinking car swim up to the boat ramp, and walk to my brother’s car on the street. The car would dissolve to rust in a week; the water’s pretty nasty there. He’d film the whole thing. I’d dry off; we’d drive home, have a beer or two, then sell the film. Probably pull the rust out of the river in a week, just to keep everything in it’s pure, pristine state. Though, now that I think of it, insurance might still cover most of the value of the car. You never know.

So the first part goes OK. We drive to the pier about 9:00 PM, Thursday, just as the sun’s setting. There’s that good, reddish light over the Windsor skyline, and the pier is empty. There are two winos off far from my intended route. My brother and I take down the top and line up the vehicle so I avoid unwanted bumps and garbage as I sail out on my way to glory. And, with a shot of Jack, and a wave to my brother (It’s on the film), I go shooting out down the pier and over the water. Fine. No bumps, no rocks. Nice flight. No soft landing, though. The car hits water like a pumpkin on concrete. Ouch! The thing bends in the middle sealing the door shut and me inside. There’s hardly any spring to the seats anyway, and what little there once was is lost. My back gets twisted into the steering wheel. I can barely turn and I can’t quite get out. Then, about 5 minutes later, the air bag goes off. Guess they didn’t design for this accident. My back, is now twisted into the sat-back, and I’m in pain.

I think it’s some sort of Sprite Healey fracture like Kevin Everett got last year. I can walk, thanks, but it needs medical attention that I’m not likely to get on Medicaid. Anyway, like I said, I’m trapped inside the vehicle, and suppose I’d be dead if the car sank like we planned, bit it don’t sink. The thing floats. Like, forever. The car weighs like two tons and it floats! Who knew. I’m carried by my momentum and by some random Rouge current out past Zug Island into the main channel between Detroit and Windsor where I’m almost run down by an ore boat. Anyway, the yellow metal Viper-dingy I’m in gets noticed by the boat lookout and by some fishermen, but no one helps. Everyone’s seems to think it’s really funny. They’re all taking pictures, and texting, and calling their friends. And everyone is laughing but me. It’s funny, like a fart in a space suit. Meanwhile my brother’s been driving along by the river, filming everything and hoping I get out and can somehow swim to safety, and I keep floating off to Canada. Finally, someone calls the coast guard, but when the come, it turns out I’m in Canadian waters. So the Canadians come, and they’re all think it’s a boot. I’m a celebrity with pictures of me in my car floating all over the internet. And well, here I am, a relatively innocent man, with a junked car and a bad back. And I’m ready to make a deal. I’ll admit it looks like I was planning to defraud someone, but there’s no evidence. I’ll admit to trespass if you like, but not fraud or endangerment. There was no one there to endange, and no one endangered, except of me. And I won’t press charges (little joke).

What with all the publicity, I figure you want to press more than just trespass, and what I was thinking of is reckless driving. I’ll admit to that with no contest. Looked at the right way, that’s like a 60 day sentence, maybe 90 days, and that’s just fine with me. I don’t have the cleanest record, but it’s not like I’ve done this before. I think it would be fair if I got 60 to 90-days of incarceration with medical benefits and job rehabilitation. I’d like to learn a new trade, like auto repair. That’s a win-win for everyone. You close the case, and I get cured and put my job skills to work just as soon as I get out. But I really need the medical though. My health insurance doesn’t cover injury-in-performance-of-a-crime — it’s right there on page 28. And Medicare is garbage. Next time you get insurance, your honor, make sure to read the contract.

Anyway, you have the tape and the pictures, and can check with my brother. We have plenty of people who will testify for us, even folks in congress and in the police department. They’ll all tell you, we’re just a couple of good fellows, somewhat down on our luck, waiting to get out and go straight. Thanks for your help, and God-bless.

R. E. Buxbaum. Sept 30, 2015. Some weeks ago, I wrote an essay, “What is comedy.” So I thought I’d try writing one. Tell me how you think I did. No one in the story is meant to be anyone real, except for “his honor,’ who’s meant to be a fictional version of His Honor.

my electric cart of the future

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Buxbaum and Sperka cart of future

Buxbaum and Sperka show off the (shopping) cart of future, Oak Park parade July 4, 2015.

A Roman chariot did quite well with only 1 horse-power, while the average US car requires 100 horses. Part of the problem is that our cars weigh more than a chariot and go faster, 80 mph vs of 25 mph. But most city applications don’t need all that weight nor all of that speed. 20-25 mph is fine for round-town errands, and should be particularly suited to use by young drivers and seniors.

To show what can be done with a light vehicle that only has to go 20 mph, I made this modified shopping cart, and fitted it with a small, 1 hp motor. I call it the cart-of the future and paraded around with it at our last 4th of July parade. It’s high off the ground for safety, reasonably wide for stability, and has the shopping cart cage and seat-belts for safety. There is also speed control. We went pretty slow in the parade, but here’s a link to a video of the cart zipping down the street at 17.5 mph.

In the 2 months since this picture was taken, I’ve modified the cart to have a chain drive and a rear-wheel differential — helpful for turning. My next modification, if I get to it, will be to switch to hydrogen power via a fuel cell. One of the main products we make is hydrogen generators, and I’m hoping to use the cart to advertise the advantages of hydrogen power.

Robert E. Buxbaum, August 28, 2015. I’m the one in the beige suit.

The mass of a car and its mpg.

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Back when I was an assistant professor at Michigan State University, MSU, they had a mileage olympics between the various engineering schools. Michigan State’s car got over 800 mpg, and lost soundly. By contrast, my current car, a Saab 9,2 gets about 30 miles per gallon on the highway, about average for US cars, and 22 to 23 mpg in the city in the summer. That’s about 1/40th the gas mileage of the Michigan State car, or about 2/3 the mileage of the 1978 VW rabbit I drove as a young professor, or the same as a Model A Ford. Why so low? My basic answer: the current car weighs a lot more.

As a first step to analyzing the energy drain of my car, or MSU’s, the energy content of gasoline is about 123 MJ/gallon. Thus, if my engine was 27% efficient (reasonably likely) and I got 22.5 mpg (36 km/gallon) driving around town, that would mean I was using about .922 MJ/km of gasoline energy. Now all I need to know is where is this energy going (the MSU car got double this efficiency, but went 40 times further).

The first energy sink I considered was rolling drag. To measure this without the fancy equipment we had at MSU, I put my car in neutral on a flat surface at 22 mph and measured how long it took for the speed to drop to 19.5 mph. From this time, 14.5 sec, and the speed drop, I calculated that the car had a rolling drag of 1.4% of its weight (if you had college physics you should be able to repeat this calculation). Since I and the car weigh about 1700 kg, or 3790 lb, the drag is 53 lb or 233 Nt (the MSU car had far less, perhaps 8 lb). For any friction, the loss per km is F•x, or 233 kJ/km for my vehicle in the summer, independent of speed. This is significant, but clearly there are other energy sinks involved. In winter, the rolling drag is about 50% higher: the effect of gooey grease, I guess.

The next energy sink is air resistance. This is calculated by multiplying the frontal area of the car by the density of air, times 1/2 the speed squared (the kinetic energy imparted to the air). There is also a form factor, measured on a wind tunnel. For my car this factor was 0.28, similar to the MSU car. That is, for both cars, the equivalent of only 28% of the air in front of the car is accelerated to the car’s speed. Based on this and the density of air in the summer, I calculate that, at 20 mph, air drag was about 5.3 lbs for my car. At 40 mph it’s 21 lbs (95 Nt), and it’s 65 lbs (295 Nt) at 70 mph. Given that my city driving is mostly at <40 mph, I expect that only 95 kJ/km is used to fight air friction in the city. That is, less than 10% of my gas energy in the city or about 30% on the highway. (The MSU car had less because of a smaller front area, and because it drove at about 25 mph)

The next energy sink was the energy used to speed up from a stop — or, if you like, the energy lost to the brakes when I slow down. This energy is proportional to the mass of the car, and to velocity squared or kinetic energy. It’s also inversely proportional to the distance between stops. For a 1700 kg car+ driver who travels at 38 mph on city streets (17 m/s) and stops, or slows every 500m, I calculate that the start-stop energy per km is 2 (1/2 m v2 ) = 1700•(17)2  = 491 kJ/km. This is more than the other two losses combined and would seem to explain the majority cause of my low gas mileage in the city.

The sum of the above losses is 0.819 MJ/km, and I’m willing to accept that the rest of the energy loss (100 kJ/km or so) is due to engine idling (the efficiency is zero then); to air conditioning and headlights; and to times when I have a passenger or lots of stuff in the car. It all adds up. When I go for long drives on the highway, this start-stop loss is no longer relevant. Though the air drag is greater, the net result is a mileage improvement. Brief rides on the highway, by contrast, hardly help my mileage. Though I slow down less often, maybe every 2 km, I go faster, so the energy loss per km is the same.

I find that the two major drags on my gas mileage are proportional to the weight of the car, and that is currently half-again the weight of my VW rabbit (only 1900 lbs, 900 kg). The MSU car was far lighter still, about 200 lbs with the driver, and it never stopped till the gas ran out. My suggestion, if you want the best gas milage, buy one light cars on the road. The Mitsubishi Mirage, for example, weighs 1000 kg, gets 35 mpg in the city.

A very aerodynamic, very big car. It's beautiful art, but likely gets lousy mileage -- especially in the city.

A very aerodynamic, very big car. It’s beautiful art, but likely gets lousy mileage — especially in the city.

Short of buying a lighter car, you have few good options to improve gas mileage. One thought is to use better grease or oil; synthetic oil, like Mobil 1 helps, I’m told (I’ve not checked it). Alternately, some months ago, I tried adding hydrogen and water to the engine. This helps too (5% -10%), likely by improving ignition and reducing idling vacuum loss. Another option is fancy valving, as on the Fiat 500. If you’re willing to buy a new car, and not just a new engine, a good option is a hybrid or battery car with regenerative breaking to recover the energy normally lost to the breaks. Alternately, a car powered with hydrogen fuel cells, — an option with advantages over batteries, or with a gasoline-powered fuel cell. 

Robert E. Buxbaum; July 29, 2015 I make hydrogen generators and purifiers. Here’s a link to my company site. Here’s something I wrote about Peter Cooper, an industrialist who made the first practical steam locomotive, the Tom Thumb: the key innovation here: making it lighter by using a forced air, fire-tube boiler.

Statistics of death and taxes — death on tax day

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Strange as it seems, Americans tend to die in road accidents on tax-day. This deadly day is April 15 most years, but on some years April 15th falls out on a weekend and the fatal tax day shifts to April 16 or 17. Whatever weekday it is, about 8% more people die on the road on tax day than on the same weekday a week earlier or a week later; data courtesy of the US highway safety bureau and two statisticians, Redelmeier and Yarnell, 2014.

Forest plot of individuals in fatal road crashes over 30 years. X-axis shows relative increase in risk on tax days compared to control days expressed as odds ratio. Y-axis denotes subgroup (results for full cohort in final row). Column data are counts of individuals in crashes. Analytic results expressed with 95% confidence intervals setting control days as referent. Results show increased risk on tax day for full cohort, similar increase for 25 of 27 subgroups, and all confidence intervals overlapping main analysis. Recall that odds ratios are reliable estimates of relative risk when event rates are low from an individual driver’s perspective.

Forest plot of individuals in fatal road crashes for the 30 years to 2008  on US highways (Redelmeier and Yarnell, 2014). X-axis shows relative increase in risk on tax days compared to control days expressed as odds ratio. Y-axis denotes subgroup (results for full cohort in final row). Column data are counts of individuals in crashes (there are twice as many control days as tax days). Analytic results are 95% confidence intervals based on control days as referent. Dividing the experimental subjects into groups is a key trick of experimental design.

To confirm that the relation isn’t a fluke, the result of well-timed ice storms or football games, the traffic death data was down into subgroups by time, age, region etc– see figure. Each groups showed more deaths than on the average of the day a week before and after.

The cause appears unrelated to paying the tax bill, as such. The increase is near equal for men and women; with alcohol and without, and for those over 18 and under (presumably those under 18 don’t pay taxes). The death increase isn’t concentrated at midnight either, as might be expected if the cause were people rushing to the post office. The consistency through all groups suggests this is not a quirk of non-normal data, nor a fluke but a direct result of  tax-day itself.Redelmeier and Yarnell suggest that stress — the stress of thinking of taxes — is the cause.

Though stress seems a plausible explanation, I’d like to see if other stress-related deaths are more common on tax day — heart attack or stroke. I have not done this, I’m sorry to say, and neither have they. General US death data is not tabulated day by day. I’ve done a quick study of Canadian tax-day deaths though (unpublished) and I’ve found that, for Canadians, Canadian tax day is even more deadly than US tax day is for Americans. Perhaps heart attack and stroke data is available day by day in Canada (?).

Robert Buxbaum, December 12, 2014. I write about all sorts of stuff. Here’s my suggested, low stress income tax structure, and a way to reduce/ eliminate income taxes: tariffs– they worked till the Civil war. Here’s my thought on why old people have more fatal car accidents per mile driven.

Seniors are not bad drivers.

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Seniors cause accidents, but need to get places too

Seniors are often made fun of for confusion and speeding, but it’s not clear they speed, and it is clear they need to get places. Would reduced speed limits help them arrive alive?

Seniors have more accidents per-mile traveled than middle age drivers. As shown on the chart below, older Canadians, 75+, get into seven times more fatal accidents per mile than 35 to 55 year olds. At first glance, this would suggest they are bad drivers who should be kept from the road, or at least made to drive slower. But I’m not so sure they are bad drivers, and am pretty certain that lower speed limits should not be generally imposed. I suspect that a lot of the problem comes from the a per-mile basis comparison with folks who drive long distances on the same superhighways instead of longer, leisurely drives on country roads. I suspect that, on a per-hour basis, the seniors would look a lot safer, and on a per highway-mile basis they might look identical to younger drivers.

Canadian Vehicle Survey, 2001, Statistics Canada, includes drivers of light duty vehicles.

Deaths per billion km. Canadian Vehicle Survey, 2001, Statistics Canada, includes light duty vehicles.

Another source of misunderstanding, I find, is that comparisons tend to overlook how very low the accident rates are. The fatal accent rate for 75+ year old drivers sounds high when you report it as 20 deaths per billion km. But that’s 50,000,000 km between fatalities, or roughly one fatality for each 1300 drives around the earth. In absolute terms it’s nothing to worry about. Old folks driving provides far fewer deaths per km than 12-29 year olds walking, and fewer deaths per km than for 16-19 year olds driving.

When starting to research this essay, I thought I’d find that the high death rates were the result of bad reaction times for the elderly. I half expected to find that reduced speed limits for them helped. I’ve not found any data directly related to reduced speeds, but now think that lowered speed limits would not help them any more than anyone else. I note that seniors drive for pleasure more than younger folks and do a lot more short errand drives too — to the stores, for example. These are places where accidents are more common. By contrast, 40 to 70 year olds drive more miles on roads that are relatively safe.

Don't walk, especially if you're old.

Don’t walk, especially if you’re old. Netherlands data, 2001-2005 fatalities per billion km.

The Netherlands data above suggest that any proposed solution should not involve getting seniors out of their cars. Not only do seniors find walking difficult, statistics suggest walking is 8 to 10 times more dangerous than driving, and bicycling is little better. A far better solution, I suspect, is reduced speeds for everyone on rural roads. If you’re zipping along a one-lane road at the posted 40, 55, or 60 mph and someone backs out of a driveway, you’re toast. The high posted speeds on these roads pose a particular danger to bicyclists and motorcyclists of all ages – and these are folks who I suspect drive a lot on the rural roads. I suspect that a 5 mph reduction would do quite a lot.

For automobiles on super-highways, it may be worthwhile to increase the speed limits. As things are now, the accident fatality rates are near zero, and the main problem may be the time wasted behind the wheel – driving from place to place. I suspect that an automobile speed limit raise to 80 mph would make sense on most US and Canadian superhighways; it’s already higher on the Autobahn in Germany.

Robert Buxbaum, November 24, 2014. Expect an essay about death on tax-day, coming soon. I’ve also written about marijuana, and about ADHD.

Hydrogen cars and buses are better than Tesla

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Hydrogen fueled cars and buses are as clean to drive as battery vehicles and have better range and faster fueling times. Cost-wise, a hydrogen fuel tank is far cheaper and lighter than an equivalent battery and lasts far longer. Hydrogen is likely safer because the tanks do not carry their oxidant in them. And the price of hydrogen is relatively low, about that of gasoline on a per-mile basis: far lower than batteries when the cost of battery wear-out is included. Both Presidents Clinton and Bush preferred hydrogen over batteries, but the current administration favors batteries. Perhaps history will show them correct, but I think otherwise. Currently, there is not a hydrogen bus, car, or boat making runs at Disney’s Experimental Community of Tomorrow (EPCOT), nor is there an electric bus car or boat. I suspect it’s a mistake, at least convening the lack of a hydrogen vehicle. 

The best hydrogen vehicles on the road have more range than the best electric vehicle, and fuel faster. The hydrogen powered, Honda Clarity debuted in 2008. It has a 270 mile range and takes 3-5 minutes to fuel with hydrogen at 350 atm, 5150 psi. By contrast, the Tesla S-sedan that debuted in 2012 claims only a 208 mile range for its standard, 60kWh configuration (the EPA claims: 190 miles) and requires three hours to charge using their fastest charger, 20 kW.

What limits the range of battery vehicles is that the stacks are very heavy and expensive. Despite using modern lithium-ion technology, Tesla’s 60 kWh battery weighs 1050 lbs including internal cooling, and adds another 250 lbs to the car for extra structural support. The Clarity fuel system weighs a lot less. The hydrogen cylinders weigh 150 lb and require a fuel cell stack (30 lb) and a smaller lithium-ion battery for start-up (90 lb). The net effect is that the Clarity weighs 3582 lbs vs 4647 lbs for the Tesla S. This extra weight of the Tesla seems to hurt its mileage by about 10%. The Tesla gets about 3.3 mi/kWh or 0.19 mile/lb of battery versus 60 miles/kg of hydrogen for the Clarity suggesting  3.6 mi/kWh at typical efficiencies. 

High pressure hydrogen tanks are smaller than batteries and cheaper per unit range. The higher the pressure the smaller the tank. The current Clarity fuels with 350 atm, 5,150 psi hydrogen, and the next generation (shown below) will use higher pressure to save space. But even with 335 atm hydrogen (5000 psi) a Clarity could fuel a 270 mile range with four, 8″ diameter tanks (ID), 4′ long. I don’t know how Honda makes its hydrogen tanks, but suitable tanks might be made from 0.065″ Maranging (aged) stainless steel (UTS = 350,000 psi, density 8 g/cc), surrounded by 0.1″ of aramid fiber (UTS = 250,000 psi, density = 1.6 g/cc). With this construction, each tank would weigh 14.0 kg (30.5 lbs) empty, and hold 11,400 standard liters, 1.14 kg (2.5 lb) of hydrogen at pressure. These tanks could cost $1500 total; the 270 mile range is 40% more Than the Tesla S at about 1/10 the cost of current Tesla S batteries The current price of a replacement Tesla battery pack is $12,000, subsidized by DoE; without the subsidy, the likely price would be $40,000.

Next generation Honda fuel cell vehicle prototype at the 2014 Detroit Auto Show.

Next generation Honda fuel cell vehicle prototype at the 2014 Detroit Auto Show.

Currently hydrogen is more expensive than electricity per energy value, but my company has technology to make it cheaply and more cleanly than electricity. My company, REB Research makes hydrogen generators that produce ultra pure hydrogen by steam reforming wow alcohol in a membrane reactor. A standard generator, suitable to a small fueling station outputs 9.5 kg of hydrogen per day, consuming 69 gal of methanol-water. At 80¢/gal for methanol-water, and 12¢/kWh for electricity, the output hydrogen costs $2.50/kg. A car owner who drove 120,000 miles would spend $5,000 on hydrogen fuel. For that distance, a Tesla owner would spend only $4400 on electricity, but would have to spend another $12,000 to replace the battery. Tesla batteries have a 120,000 mile life, and the range decreases with age. 

For a bus or truck at EPCOT, the advantages of hydrogen grow fast. A typical bus is expected to travel much further than 120,000 miles, and is expected to operate for 18 hour shifts in stop-go operation getting perhaps 1/4 the miles/kWh of a sedan. The charge time and range advantages of hydrogen build up fast. it’s common to build a hydrogen bus with five 20 foot x 8″ tanks. Fueled at 5000 psi., such buses will have a range of 420 miles between fill-ups, and a total tank weight and cost of about 600 lbs and $4000 respectively. By comparison, the range for an electric bus is unlikely to exceed 300 miles, and even this will require a 6000 lb., 360 kWh lithium-ion battery that takes 4.5 hours to charge assuming an 80 kW charger (200 Amps at 400 V for example). That’s excessive compared to 10-20 minutes for fueling with hydrogen.

While my hydrogen generators are not cheap: for the one above, about $500,000 including the cost of a compressor, the cost of an 80 kW DC is similar if you include the cost to run a 200 Amp, 400 V power line. Tesla has shown there are a lot of people who value clean, futuristic transport if that comes with comfort and style. A hydrogen car can meet that handily, and can provide the extra comforts of longer range and faster refueling.

Robert E. Buxbaum, February 12, 2014 (Lincoln’s birthday). Here’s an essay on Lincoln’s Gettysburg address, on the safety of batteries, and on battery cost vs hydrogen. My company, REB Research makes hydrogen generators and purifiers; we also consult.

My failed process for wood to green gasoline

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Most researchers publish the results of their successful projects, and ignore the rest. It’s an understandable failing given the cost and work to publish and the general sense that the project that flops indicated a loser – researcher. Still, it’s a shame, and I’d like to break from it here to describe a worthwhile project of mine that failed — turning wood into green gasoline. You may come to believe the project worthwhile too, and figure that you might learn from my story some pathways to avoid if you decide to try it. Besides I figure that it’s an interesting tale. All success stories are similar, I find; failure can come in many ways.

Failure can come from incorrect thinking – assumptions that are wrong. One basis of my thinking was the observation that gasoline, for the most part, was crude-oil that had been fluffed up with hydrogen. The density you buy weighs about 5.5 lb/gallon while crude oil weighs 9 lb/gallon. The difference is hydrogen. Perhaps wood too could be turned into gasoline if hydrogen were added. Another insight was that the structure of wood was the structure of a long chain -alcohol,  —(CHOH)-(CHOH)-(CHOH)—. My company had long experience breaking alcohols to make hydrogen. I figured we could do something similar with wood, fluffing up the wood by breaking the long-chain alcohols to short ones.

A possible first reaction step would be to break a C-O-C bond, a ketone bond, with hydrogen:

—(CHOH)-(CH2O)-(CHOH)— + H2 –>  —(CHOH)-CH2OH + CH2OH—

The next reaction step, I imagined was de-oxygenation:

—(CHOH)-CH2OH  +  H2 –>  —(CHOH)-CH3  + H2O

At this point, we are well on the way to making gasoline, or making a gasoline-relevant alcohol like C6H11-OH. The reactions I wanted were exothermic, meaning they would probably “go” — in actuality -∆G is the determinate of reaction favorability, but usually a -∆H and -∆G go together. Of course there are other reactions that I could have worried about –Ones that produce nasty goop. Among these:

–(CHOH)-(CH2O)-(CHOH)—  –> –(CO)-(C)-(CHOH)— + H2O +H2

I didn’t worry about these reactions because I figured I could outrun them using the right combination of a high hydrogen pressure, the right (low) temperature and the right catalyst. I may have been wrong. Then again, perhaps I picked the wrong catalyst – Fe2O3/ rust, or the wrong set of conditions. I picked Fe2O3 because it was cheap and active.

I convinced myself that Fe2O3 was sufficiently specific to get the product to a good 5-6 carbon compounds for gasoline. Wood celluloses are composed of five and six-carbon ring structure, and the cost of wood is very low per energy. What could go wrong? I figured that starting with these 5-6 carbon ring structures, virtually guaranteed getting high octane products. With the low cost and all the heat energy of the wood, wood + H2 seemed like a winning way to store and transport energy. If i got 6 carbon alcohols and similar compounds they’d have high-octane and the right vapor pressures and the products should be soluble in ordinary gasoline.

And the price was right; gasoline was about $3.50/ gallon, while wood was essentially free.  Hydrogen isn’t that expensive, even using electrolysis, and membrane reactors (a major product of our company) had the potential to make it cheaper. Wood + Hydrogen seemed like the cheaper version of syngas: CO +H2, and rust is similar to normal Fischer Tropsch catalyst. My costs would be low, and I’d expected to get better conversion since I should get fewer low molecular weight products like methane, ethane and methanol. Everything fundamental looked like it was in my favor.

With all the fundamentals in place, I figured my only problem would be to design a reasonably cheap reactor. At first I considered a fluidized bed reactor, but decided on a packed bed reactor instead, 8″ long by 3/4″ OD. This was a tube, filled with wood chips and iron oxide as a catalyst. I introduced high pressure hydrogen via a 150 psi hydrogen + 5% He mix. I hoped to see gasoline and water come out the other end. (I had the hydrogen – helium mix left over from a previous experiment, and was paying rental; otherwise I would have used pure hydrogen). I used heat tape and a controller to keep the temperature near-constant.

Controlling the temperature was key, I thought, to my aim of avoiding dehydration and the formation of new carbon-carbon bonds. At too high a temperature, the cellulose molecules would combine and lose water to form a brown high molecular weight tar called bio-oil, as well as methane and char. Bio-oil is formed the same way you form caramel from sugar, and as with sugar, it’s nothing you’d want to put in a car. If I operated at too low a temperature (or with the wrong catalyst) the reaction would be too slow, and the capital costs would be excessive. I could keep the temperature in the right (Goldilocks) temperature, I thought with the right catalyst and the right (high) hydrogen pressure.

No matter how I did this, I knew that I’d get some carbon-carbon bond formation, and perhaps a little char, but so long as it wasn’t too much it should be manageable. I figured I could hydrogenate the tar and remove the char at the end of the process. Most of the gasoline energy would come from the trees, and not the hydrogen, and there would be little hydrogen wasted forming methane. Trees would always be cheap: they grow quickly, and are great at capturing solar energy. Many cities pay for disposal of their tree waste, so perhaps a city would pay us to take their wood chips. With cheap wood, the economics would be good so long as used all the hydrogen I put in, and got some reasonable fraction of energy from the wood. 

i began my reaction at 150°C with 50 psi hydrogen. At these conditions, I saw no reaction; I then raised the temperature to 200°C, then raised the pressure to 100 psi (still nothing) and then tried 250°C, still at 100psi. By now we were producing water but it was impossible to tell if we were hydrogenating the cellulose to gasoline, or dehydrating the cellulose to bio-oil.

As it turned out we were getting something worse that bio-oil: bio-oil gunk. Instead of the nasty brown liquid that’s made when wood is cooked to dehydration (water removal, caramelization), I got something that was nastier than I’d imagined possible. The wood molecules did not form nice chains but combined to form acidic, aromatic gunk (aromatic in both senses: benzine-type molecules and smelly) that still contained unreacted wood as a sort of press-board. The gunk was corrosive and reactive; it probably contained phenol, and seemed bent on reacting to form a phenolic glue. I found the gunk was insoluble in most everything: water, gasoline, oil, methanol (the only exception was ethanol). As best I can tell, you can not react this gunk with hydrogen to make gasoline as it is non-volatile, and almost impossible to get out of my clogged reactor. Perhaps a fluidized bed would be would be better, but I’m afraid it would form wood clumps even there. 

I plan to try again, perhaps using higher pressure hydrogen and perhaps a liquid hydrogen carrier, to get the hydrogen to the core of the wood and speed the catalysis of the desired products. The key is finding a carrier that is not too expensive or that can be easily recovered.

Robert E. Buxbaum, Dec 13, 2013. Here’s something on a visit to my lab, on adding hydrogen to automobile engines, and on the right way to do science. And here’s my calculation for how much wood a woodchuck chucks if a woodchuck could chuck wood, (100 lbs/ night) plus why woodchucks do not chuck wood like beavers.

Thermodynamics of hydrogen generation

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Perhaps the simplest way to make hydrogen is by electrolysis: you run some current through water with a little sulfuric acid or KOH added, and for every two electrons transferred, you get a molecule of hydrogen from one electrode and half a molecule of oxygen from the other.

2 OH- –> 2e- + 1/2 O2 +H2O

2H2O + 2e- –>  H2 + 2OH-

The ratio between amps, seconds and mols of electrons (or hydrogen) is called the Faraday constant, F = 96500; 96500 amp-seconds transfers a mol of electrons. For hydrogen production, you need 2 mols of electrons for each mol of hydrogen, n= 2, so

it = 2F where and i is the current in amps, and t is the time in seconds and n is the number electrons per molecule of desired product. For hydrogen, t = 96500*2/i; in general, t = Fn/i.

96500 is a large number, and it takes a fair amount of time to make any substantial amount of hydrogen by electrolysis. At 1 amp, it takes 96500*2 = 193000 seconds, 2 days, to generate one mol of hydrogen (that’s 2 grams H2 or 22.4 liters, enough to fill a garment bag). We can reduce the time by using a higher current, but there are limits. At 25 amps, the maximum current of you can carry with house wiring it takes 2.14 hours to generate 2 grams. (You’ll have to rectify your electricity to DC or you’ll get a nasty H2 /O2 mix called Brown’s gas, While normal H2 isn’t that dangerous, Browns gas is a mix of H2 and O2 and is quite explosive. Here’s an essay I wrote on separating Browns gas).

Electrolysis takes a fair amount of electric energy too; the minimum energy needed to make hydrogen at a given temperature and pressure is called the reversible energy, or the Gibbs free energy ∆G of the reaction. ∆G = ∆H -T∆S, that is, ∆G equals the heat of hydrogen production ∆H – minus an entropy effect, T∆S. Since energy is the product of voltage current and time, Vit = ∆G, where ∆G is the Gibbs free energy measured in Joules and V,i, and t are measured Volts, Amps, and seconds respectively.

Since it = nF, we can rewrite the relationship as: V =∆G/nF for a process that has no energy losses, a reversible process. This is the form found in most thermodynamics textbooks; the value of V calculated this way is the minimum voltage to generate hydrogen, and the maximum voltage you could get in a fuel cell putting water back together.

To calculate this voltage, and the power requirements to make hydrogen, we use the Gibbs free energy for water formation found in Wikipedia, copied below (in my day, we used the CRC Handbook of Chemistry and Physics or a table in out P-chem book). You’ll notice that there are two different values for ∆G depending on whether the water is a gas or a liquid, and you’ll notice a small zero at the upper right (∆G°). This shows that the values are for an imaginary standard state: 20°C and 1 atm pressure. You can’t get 1 atm steam at 20°C, it’s an extrapolation; behavior at typical temperatures, 40°C and above is similar but not identical. I’ll leave it to a reader to send this voltage as a comment.

Liquid H2O formation ∆G° = -237.14
Gaseous H2O formation ∆G° = -228.61

The reversible voltage for creating liquid water in a reversible fuel cell is found to be -237,140/(2 x 96,500) = -1.23V. We find that 1.23 Volts is about the minimum voltage you need to do electrolysis at 0°C because you need liquid water to carry the current; -1.18 V is about the maximum voltage you can get in a fuel cell because they operate at higher temperature with oxygen pressures significantly below 1 atm. (typically). The minus sign is kept for accounting; it differentiates the power out case (fuel cells) from power in (electrolysis). It is typical to find that fuel cells operate at lower voltages, between about .5V and 1.0V depending on the fuel cell and the power load.

Most electrolysis is done at voltages above about 1.48 V. Just as fuel cells always give off heat (they are exothermic), electrolysis will absorb heat if run reversibly. That is, electrolysis can act as a refrigerator if run reversibly. but electrolysis is not a very good refrigerator (the refrigerator ability is tied up in the entropy term mentioned above). To do electrolysis at reasonably fast rates, people give up on refrigeration (sucking heat from the environment) and provide all the entropy needed for electrolysis in the electricity they supply. This is to say, they operate at V’ were nFV’ ≥ ∆H, the enthalpy of water formation. Since ∆H is greater than ∆G, V’ the voltage for electrolysis is higher than V. Based on the enthalpy of liquid water formation,  −285.8 kJ/mol we find V’ = 1.48 V at zero degrees. The figure below shows that, for any reasonably fast rate of hydrogen production, operation must be at 1.48V or above.

Electrolyzer performance; C-Pt catalyst on a thin, nafion membrane

Electrolyzer performance; C-Pt catalyst on a thin, nafion membrane

If you figure out the energy that this voltage and amperage represents (shown below) you’re likely to come to a conclusion I came to several years ago: that it’s far better to generate large amounts of hydrogen chemically, ideally from membrane reactors like my company makes.

The electric power to make each 2 grams of hydrogen at 1.5 volts is 1.5 V x 193000 Amp-s = 289,500 J = .080 kWh’s, or 0.9¢ at current rates, but filling a car takes 20 kg, or 10,000 times as much. That’s 800 kW-hr, or $90 at current rates. The electricity is twice as expensive as current gasoline and the infrastructure cost is staggering too: a station that fuels ten cars per hour would require 8 MW, far more power than any normal distributor could provide.

By contrast, methanol costs about 2/3 as much as gasoline, and it’s easy to deliver many giga-joules of methanol energy to a gas station by truck. Our company’s membrane reactor hydrogen generators would convert methanol-water to hydrogen efficiently by the reaction CH3OH + H2O –> 3H2 + CO2. This is not to say that electrolysis isn’t worthwhile for lower demand applications: see, e.g.: gas chromatography, and electric generator cooling. Here’s how membrane reactors work.

R. E. Buxbaum July 1, 2013; Those who want to show off, should post the temperature and pressure corrections to my calculations for the reversible voltage of typical fuel cells and electrolysis.

Camless valves and the Fiat-500

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One of my favorite automobile engine ideas is the use of camless, electronic valves. It’s an idea whose advantages have been known for 100 years or more, and it’s finally going to be used on a mainstream, commercial car — on this year’s Fiat 500s. Fiat is not going entirely camless, but the plan is to replace the cams on the air intake valves with solenoids. A normal car engine uses cams and lifters to operate the poppet valves used to control the air intake and exhaust. Replacing these cams and lifters saves some weight, and allows the Fiat-500 to operate more efficiently at low power by allowing the engine to use less combustion energy to suck vacuum. The Fiat 500 semi-camless technology is called Multiair: it’s licensed from Valeo (France), and appeared as an option on the 2010 Alfa Romeo.

How this saves mpg is as follows: at low power (idling etc.), the air intake of a normal car engine is restricted creating a fairly high vacuum. The vacuum restriction requires energy to draw and reduces the efficiency of the engine by decreasing the effective compression ratio. It’s needed to insure that the car does not produce too much NOx when idling. In a previous post, I showed that the rate of energy wasted by drawing this vacuum was the vacuum pressure times the engine volume and the rpm rate; I also mentioned some classic ways to reduce this loss (exhaust recycle and adding water).

Valeo’s/Fiat’s semi-camless design does nothing to increase the effective compression ratio at low power, but it reduces the amount of power lost to vacuum by allowing the intake air pressure to be higher, even at low power demand. A computer reduces the amount of air entering the engine by reducing the amount of time that the intake valve is open. The higher air pressure means there is less vacuum penalty, both when the valve is open even when the valve is closed. On the Alfa Romeo, the 1.4 liter Multiair engine option got 8% better gas mileage (39 mpg vs 36 mpg) and 10% more power (168 hp vs 153 hp) than the 1.4 liter cam-driven engine.

David Bowes shows off his latest camless engines at NAMES, April 2013.

David Bowes shows off his latest camless engines at NAMES, April 2013.

Fiat used a similar technology in the 1970s with variable valve timing (VVT), but that involved heavy cams and levers, and proved to be unreliable. In the US, some fine engineers had been working on solenoids, e.g. David Bowes, pictured above with one of his solenoidal engines (he’s a sometime manufacturer for REB Research). Dave has built engines with many cycles that would be impractical without solenoids, and has done particularly nice work reducing the electric use of the solenoid.

Durability may be a problem here too, as there is no other obvious reason that Fiat has not gone completely camless, and has not put a solenoid-controlled valve on the exhaust too. One likely reason Fiat didn’t do this is that solenoidal valves tend to be unreliable at the higher temperatures found in exhaust. If so, perhaps they are unreliable on the intake too. A car operated at 1000-4000 rpm will see on the order of 100,000,000 cycles in 25,000 miles. No solenoid we’ve used has lasted that many cycles, even at low temperatures, but most customers expect their cars to go more than 25,000 miles without needing major engine service.

We use solenoidal pumps in our hydrogen generators too, but increase the operating live by operating the solenoid at only 50 cycles/minute — maximum, rather than 1000- 4000. This should allow our products to work for 10 years at least without needing major service. Performance car customers may be willing to stand for more-frequent service, but the company can’t expect ordinary customers to go back to the days where Fiat stood for “Fix It Again Tony.”

Hydrogen versus Battery Power

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There are two major green energy choices that people are considering to power small-to-medium size, mobile applications like cars and next generation, drone airplanes: rechargeable, lithium-ion batteries and hydrogen /fuel cells. Neither choice is an energy source as such, but rather a clean energy carrier. That is, batteries and fuel cells are ways to store and concentrate energy from other sources, like solar or nuclear plants for use on the mobile platform.

Of these two, rechargeable batteries are the more familiar: they are used in computers, cell phones, automobiles, and the ill-fated, Boeing Dreamliner. Fuel cells are less familiar but not totally new: they are used to power most submarines and spy-planes, and find public use in the occasional, ‘educational’ toy. Fuel cells provided electricity for the last 30 years of space missions, and continue to power the international space station when the station is in the dark of night (about half the time). Batteries have low energy density (energy per mass or volume) but charging them is cheap and easy. Home electricity costs about 12¢/kWhr and is available in every home and shop. A cheap transformer and rectifier is all you needed to turn the alternating current electricity into DC to recharge a battery virtually anywhere. If not for the cost and weight of the batteries, the time to charge the battery (usually and hour or two), batteries would be the obvious option.

Two obvious problems with batteries are the low speed of charge and the annoyance of having to change the battery every 500 charges or so. If one runs an EV battery 3/4 of the way down and charges it every week, the battery will last 8 years. Further, battery charging takes 1-2 hours. These numbers are acceptable if you use the car only occasionally, but they get more annoying the more you use the car. By contrast, the tanks used to hold gasoline or hydrogen fill in a matter of minutes and last for decades or many thousands of fill-cycles.

Another problem with batteries is range. The weight-energy density of batteries is about 1/20 that of gasoline and about 1/10 that of hydrogen, and this affects range. While gasoline stores about 2.5 kWhr/kg including the weight of the gas tank, current Li-Ion batteries store far less than this, about 0.15 kWhr/kg. The energy density of hydrogen gas is nearly that of gasoline when the efficiency effect is included. A 100 kg of hydrogen tank at 10,000 psi will hold 8 kg of hydrogen, or enough to travel about 350 miles in a fuel-cell car. This is about as far as a gasoline car goes carrying 60 kg of tank + gasoline. This seems acceptable for long range and short-range travel, while the travel range with eVs is more limited, and will likely remain that way, see below.

The volumetric energy density of compressed hydrogen/ fuel cell systems is higher than for any battery scenario. And hydrogen tanks are far cheaper than batteries. From Battery University. http://batteryuniversity.com/learn/article/will_the_fuel_cell_have_a_second_life

The volumetric energy density of compressed hydrogen/ fuel cell systems is higher than for any battery scenario. And hydrogen tanks are far cheaper than batteries. From Battery University. http://batteryuniversity.com/learn/article/will_the_fuel_cell_have_a_second_life

Cost is perhaps the least understood problem with batteries. While electricity is cheap (cheaper than gasoline) battery power is expensive because of the high cost and limited life of batteries. Lithium-Ion batteries cost about $2000/kWhr, and give an effective 500 charge/discharge cycles; their physical life can be extended by not fully charging them, but it’s the same 500 cycles. The effective cost of the battery is thus $4/kWhr (The battery university site calculates $24/kWhr, but that seems overly pessimistic). Combined with the cost of electricity, and the losses in charging, the net cost of Li-Ion battery power is about $4.18/kWhr, several times the price of gasoline, even including the low efficiency of gasoline engines.

Hydrogen prices are much lower than battery prices, and nearly as low as gasoline, when you add in the effect of the high efficiency fuel cell engine. Hydrogen can be made on-site and compressed to 10,000 psi for less cost than gasoline, and certainly less cost than battery power. If one makes hydrogen by electrolysis of water, the cost is approximately 24¢/kWhr including the cost of the electrolysis unit.While the hydrogen tank is more expensive than a gasoline tank, it is much cheaper than a battery because the technology is simpler. Fuel cells are expensive though, and only about 50% efficient. As a result, the as-used cost of electrolysis hydrogen in a fuel cell car is about 48¢/kWhr. That’s far cheaper than battery power, but still not cheap enough to encourage the sale of FC vehicles with the current technology.

My company, REB Research provides another option for hydrogen generation: The use of a membrane reactor to make it from cheap, easy to transport liquids like methanol. Our technology can be used to make hydrogen either at the station or on-board the car. The cost of hydrogen made this way is far cheaper than from electrolysis because most of the energy comes from the methanol, and this energy is cheaper than electricity.

In our membrane reactors methanol-water (65-75% Methanol), is compressed to 350 psi, heated to 350°C, and reacted to produce hydrogen that is purified as it is made. CH3OH + H2O –> 3H2 + CO2, with the hydrogen extracted through a membrane within the reactor.

The hydrogen can be compressed to 10,000 psi and stored in a tank on board an automobile or airplane, or one can choose to run this process on-board the vehicle and generate it from liquid fuel as-needed. On-board generation provides a saving of weight, cost, and safety since you can carry methanol-water easily in a cheap tank at low pressure. The energy density of methanol-water is about 1/2 that of gasoline, but the fuel cell is about twice as efficient as a gasoline engine making the overall volumetric energy density about the same. Not including the fuel cell, the cost of energy made this way is somewhat lower than the cost of gasoline, about 25¢/kWhr; since methanol is cheaper than gasoline on a per-energy basis. Methanol is made from natural gas, coal, or trees — non-imported, low cost sources. And, best yet, trees are renewable.