Category Archives: Robert Buxbaum

Crime: US vs UK and Canada

The US has a lot of guns and a lot of murders compared to England, Canada, and most of Europe. This is something Piers Morgan likes to point out to Americans who then struggle to defend the wisdom of gun ownership and the 2nd Amendment: “How do you justify 4.8 murders/year per 100,000 population when there are only 1.6/year per 100,000 in Canada, 1.2/year per 100,000 in the UK, and 1.0/year per 100,000 in Australia — countries with few murders and tough anti-gun laws?,” he asks. What Piers doesn’t mention, is that these anti-gun countries have far higher contact crime (assault) rates than the US, see below.

Contact Crime Per Country

Contact crime rates for 17 industrialized countries. From the Dutch Ministry of Justice. Click here for details about the survey and a breakdown of crimes.

The differences narrow somewhat when considering most violent crimes, but we still have far fewer than Canada and the UK. Canada has 963/year per 100,000 “most violent crimes,” while the US has 420/year per 100,000. “Most violent crimes” here are counted as: “murder and non-negligent manslaughter,” “forcible rape,” “robbery,” and “aggravated assault” (FBI values). England and Wales classify crimes somewhat differently, but have about two times the US rate, 775/year per 100,000, if “most violent crimes” are defined as: “violence against the person, with injury,” “most serious sexual crime,” and “robbery.”

It is possible that the presence of guns protects Americans from general crime while making murder more common, but it’s also possible that gun ownership is a murder deterrent too. Our murder rate is 1/5 that of Mexico, 1/4 that of Brazil, and 1/3 that of Russia; all countries with strong anti-gun laws but a violent populous. Perhaps the US (Texan) penchant for guns is what keeps Mexican gangs on their, gun-control side of the border. Then again, it’s possible that guns neither increase nor decrease murder rates, so that changing our laws would not have any major effect. Switzerland (a country with famously high gun ownership) has far fewer murders than the US and about 1/2 the rate of the UK: 0.7 murders/ year per 100,000. Japan, a country with low gun ownership has hardly any crime of any sort — not even littering. As in the zen buddhist joke, change comes from within.

Homicide rate per country

Homicide rate per country

One major theory for US violence was that drugs and poverty were the causes. Remove these by stricter anti-drug laws and government welfare, and the violent crime would go away. Sorry to say, it has not happened; worse yet, murder rates are highest in cities like Detroit where welfare is a way of life, and where a fairly high fraction of the population is in prison for drugs.

I suspect that our welfare payments have hurt Detroit as much as they’ve helped, and that Detroit’s higher living wage, has made it hard for people to find honest work. Stiff drug penalties have not helped Detroit either, and may contribute to making crimes more violent. As Thomas More pointed out in the 1500s, if you are going to prison for many years for a small crime, you’re more likely to use force to avoid risk capture. Perhaps penalties would work better if they were smaller.

Charity can help a city, i think, and so can good architecture. I’m on the board of two charities that try to do positive things, and I plant trees in Detroit (sometimes).

R. E. Buxbaum, July 10, 2013. To make money, I sell hydrogen generators: stuff I invented, mostly.

Chemist v Chemical Engineer joke

What’s the difference between a chemist and a chemical engineer?

 

How much they make.

 

I made up this joke up as there were no other chemical engineer jokes I knew. It’s an OK double entente that’s pretty true — both in terms of product produced and the amount of salary (there’s probably a cause-and-effect relation here). Typical of these puns, this joke ignores the internal differences in methodologies and background (see my post, How is Chemical engineering?). If you like, here’s another engineering joke,  a chemistry joke, and a dwarf joke.

R.E. Buxbaum –  June 28, 2013.

What’s Holding Gilroy on the Roof

We recently put a sculpture on our roof: Gilroy, or “Mr Hydrogen.” It’s a larger version of a creepy face sculpture I’d made some moths ago. Like it, and my saber-toothed tiger, the eyes follow you. A worry about this version: is there enough keeping it from blowing down on the cars? Anyone who puts up a large structure must address this worry, but I’m a professional engineer with a PhD from Princeton, so my answer is a bit different from most.

Gilroy (Mr Hydrogen) sculpture on roof of REB Research & Consulting. The eyes follow you.

Gilroy (Mr Hydrogen) sculpture on roof of REB Research & Consulting. The eyes follow you. Aim is that it should withstand 50 mph winds.

The main force on most any structure is the wind (the pyramids are classic exceptions). Wind force is generally proportional to the exposed area and to the wind-speed squared: something called form-drag or quadratic drag. Since force is related to wind-speed, I start with some good statistics for wind speed, shown in the figure below for Detroit where we are.

The highest Detroit wind speeds are typically only 16 mph, but every few years the winds are seen to reach 23 mph. These are low relative to many locations: Detroit has does not get hurricanes and rarely gets tornadoes. Despite this, I’ve decided to brace the sculpture to withstand winds of 50 mph, or 22.3 m/s. On the unlikely chance there is a tornado, I figure there would be so much other flotsam that I would not have to answer about losing my head. (For why Detroit does not get hurricanes or tornadoes, see here. If you want to know why tornadoes lift things, see here).

The maximum area Gilroy presents is 1.5 m2. The wind force is calculated by multiplying this area by the kinetic energy loss per second 1/2ρv2, times a form factor.  F= (Area)*ƒ* 1/2ρv2, where ρ is the density of air, 1.29Kg/m3, and v is velocity, 22.3 m/s. The form factor, ƒ, is about 1.25 for this shape: ƒ is found to be 1.15 for a flat plane, and 1.1 to 1.3 a rough sphere or ski-jumper. F = 1.5*1.25* (1/2 *1.29*22.32) = 603 Nt = 134 lb.; pressure is this divided by area. Since the weight is only about 40 lbs, I find I have to tie down the sculpture. I’ve done that with a 150 lb rope, tying it to a steel vent pipe.

Wind speed for Detroit month by month. Used to calculate the force. From http://weatherspark.com/averages/30042/Detroit-Michigan-United-States

Wind speed for Detroit month by month. Used to calculate the force. From http://weatherspark.com/averages/30042/Detroit-Michigan-United-States

It is possible that there’s a viscous lift force too, but it is likely to be small given the blunt shape and the flow Reynolds number: 3190. There is also the worry that Gilroy might fall apart from vibration. Gilroy is made of 3/4″ plywood, treated for outdoor use and then painted, but the plywood is held together with 25 steel screws 4″ long x 1/4″ OD. Screws like this will easily hold 134 lbs of steady wind force, but a vibrating wind will cause fatigue in the metal (bend a wire often enough and it falls apart). I figure I can leave Gilroy up for a year or so without worry, but will then go up to replace the screws and check if I have to bring him/ it down.

In the meantime, I’ll want to add a sign under the sculpture: “REB Research, home of Mr Hydrogen” I want to keep things surreal, but want to be safe and make sales.

by Robert E. Buxbaum, June 21, 2013

What’s the quality of your home insulation

By Dr. Robert E. Buxbaum, June 3, 2013

It’s common to have companies call during dinner offering to blow extra insulation into the walls and attic of your home. Those who’ve added this insulation find a small decrease in their heating and cooling bills, but generally wonder if they got their money’s worth, or perhaps if they need yet-more insulation to get the full benefit. Here’s a simple approach to comparing your home heat bill to the ideal your home can reasonably reach.

The rate of heat transfer through a wall, Qw, is proportional to the temperature difference, ∆T, to the area, A, and to the average thermal conductivity of the wall, k; it is inversely proportional to the wall thickness, ∂;

Qw = ∆T A k /∂.

For home insulation, we re-write this as Qw = ∆T A/Rw where Rw is the thermal resistance of the wall, measured (in the US) as °F/BTU/hr-ft2. Rw = ∂/k.

Lets assume that your home’s outer wall thickness is nominally 6″ thick (0.5 foot). With the best available insulation, perfectly applied, the heat loss will be somewhat higher than if the space was filled with still air, k=.024 BTU/fthr°F, a result based on molecular dynamics. For a 6″ wall, the R value, will always be less than .5/.024 = 20.8 °F/BTU/hr-ft2.. It will be much less if there are holes or air infiltration, but for practical construction with joists and sills, an Rw value of 15 or 16 is probably about as good as you’ll get with 6″ walls.

To show you how to evaluate your home, I’ll now calculate the R value of my walls based on the size of my ranch-style home (in Michigan) and our heat bills. I’ll first do this in a simplified calculation, ignoring windows, and will then repeat the calculation including the windows. Windows are found to be very important. I strongly suggest window curtains to save heat and air conditioning,

The outer wall of my home is 190 feet long, and extends about 11 feet above ground to the roof. Multiplying these dimensions gives an outer wall area of 2090 ft2. I could now add the roof area, 1750 ft2 (it’s the same as the area of the house), but since the roof is more heavily insulated than the walls, I’ll estimate that it behaves like 1410 ft2 of normal wall. I calculate there are 3500 ftof effective above-ground area for heat loss. This is the area that companies keep offering to insulate.

Between December 2011 and February 2012, our home was about 72°F inside, and the outside temperature was about 28°F. Thus, the average temperature difference between the inside and outside was about 45°F; I estimate the rate of heat loss from the above-ground part of my house, Qu = 3500 * 45/R = 157,500/Rw.

Our house has a basement too, something that no one has yet offered to insulate. While the below-ground temperature gradient is smaller, it’s less-well insulated. Our basement walls are cinderblock covered with 2″ of styrofoam plus wall-board. Our basement floor is even less well insulated: it’s just cement poured on pea-gravel. I estimate the below-ground R value is no more than 1/2 of whatever the above ground value is; thus, for calculating QB, I’ll assume a resistance of Rw/2.

The below-ground area equals the square footage of our house, 1750 ft2 but the walls extend down only about 5 feet below ground. The basement walls are thus 950 ft2 in area (5 x 190 = 950). Adding the 1750 ft2 floor area, we find a total below-ground area of 2700 ft2.

The temperature difference between the basement and the wet dirt is only about 25°F in the winter. Assuming the thermal resistance is Rw/2, I estimate the rate of heat loss from the basement, QB = 2700*25*(2/Rw) = 135,000/Rw. It appears that nearly as much heat leaves through the basement as above ground!

Between December and February 2012, our home used an average of 597 cubic feet of gas per day or 25497 BTU/hour (heat value = 1025 BTU/ ft3). QU+ Q= 292,500/Rw. Ignoring windows, I estimate Rw of my home = 292,500/25497 = 11.47.

We now add the windows. Our house has 230 ft2 of windows, most covered by curtains and/or plastic. Because of the curtains and plastic, they would have an R value of 3 except that black-body radiation tends to be very significant. I estimate our windows have an R value of 1.5; the heat loss through the windows is thus QW= 230*45/1.5 = 6900 BTU/hr, about 27% of the total. The R value for our walls is now re-estimated to be 292,500/(25497-6900) = 15.7; this is about as good as I can expect given the fixed thickness of our walls and the fact that I can not easily get an insulation conductivity lower than still air. I thus find that there will be little or no benefit to adding more above-ground wall insulation to my house.

To save heat energy, I might want to coat our windows in partially reflective plastic or draw the curtains to follow the sun. Also, since nearly half the heat left from the basement, I may want to lay a thicker carpet, or lay a reflective under-layer (a space blanket) beneath the carpet.

To improve on the above estimate, I could consider our furnace efficiency; it is perhaps only 85-90% efficient, with still-warm air leaving up the chimney. There is also some heat lost through the door being opened, and through hot water being poured down the drain. As a first guess, these heat losses are balanced by the heat added by electric usage, by the body-heat of people in the house, and by solar radiation that entered through the windows (not much for Michigan in winter). I still see no reason to add more above-ground insulation. Now that I’ve analyzed my home, it’s time for you to analyze yours.

How is Chemical Engineering?

I’m sometimes asked about chemical engineering by high-schoolers with some science aptitude. Typically they are trying to decide between a major in chemistry or chemical engineering. They’ve typically figured out that chemical engineering must be some practical version of chemistry, but can’t quite figure out how that could be engineering. My key answer here is: unit operations.

If I were a chemist trying to make an interesting product, beer or whisky say, I might start with sugar, barley, water and yeast, plus perhaps some hops and tablets of nutrients and antimicrobial. After a few hours of work, I’d have 5 gallons of beer fermenting, and after a month I’d have beer that I could either drink or batch-distill into whisky. If I ran the cost numbers, I’d find that my supplies cost as much to make as buying the product in a store; the value of my time was thus zero and would not be any higher if I were to scale up production: I’m a chemist.

The key to making my time more valuable is unit operations. I need to scale up production and use less costly materials. Corn costs less than sugar but has to be enzyme processed into a form that can be fermented. Essentially, I have to cook a large batch of corn at the right temperatures (near boiling) and then add enzymes from the beer or from sprouted corn and then hold the temperature for an hour or more. Sounds simple, but requires good heat control, good heating, and good mixing, otherwise the enzymes will die or won’t work or the corn will burn and stick to the bottom of the pot. These are all unit operations; you’ll learn more about them in chemical engineering.

Reactor design is a classical unit operation. Do I react in large batches, or in a continuous fermentor. How do I hold on to the catalyst (enzymes); what is the contact time; these are the issues of reactor engineering, and while different catalysts and reactions have different properties and rates, the analysis is more-or-less the same.

Another issue is solid-liquid separation, in this case filtration of the dregs. When made in small batches, the bottoms of the beer barrel, the dregs, were let to settle and then washed down the sink. At larger scales, settling will take too long and will still leave a beer that is cloudy. Further, the dregs are too valuable to waste. At larger scales, you’ll want to filter the beer and will want to do something to the residue. Centrifugal filtration is typically used and the residue is typically dried and sold as animal feed. Centrifugal filtration is another unit operation.

Distillation is another classical unit operation. An important part here is avoiding hangover-producing higher alcohols and nasty tasting, “fusel oils.” There are tricks here that are more-or-less worth doing depending on the product you want. Typically, you start with a simple processes and equipment and keep tweaking them until the product and costs are want you want. At the end, typically, the process equipment looks more like a refinery than like a kitchen: chemical engineering equipment is fairly different from the small batch equipment that was used as the chemist.

The same approach to making things and scaling them up also applied in management situations, by the way, and many of my chemical engineering friends have become managers.

Robert Buxbaum is now on the board of a new charity

I’m now on the board of directors for two non-profits (lucky me), plus for my own hydrogen company, REB Research. My first charity seat is for The Jewish Heritage Foundation; it’s really one rabbi who takes donations to make tapes about topics he finds interesting. He then gives away or sells the tapes. We meet once a year to go over the finances and decide what his salary ought to be — basically we rubber stamp.

The second board seat, one I’ve been elected/appointed to just this week, is with a group call “The First Covenant Foundation” they’re semi-religious, trying to get people to behave decently. The first covenant is the one with Noah — God won’t destroy the earth but we have to behave sort-of OK. It’s certainly worthwhile to get people to keep to this minimal standard: no murder, no bestiality, don’t eat the limbs off of living creatures… Then again, if God has trouble keeping folks to this standard, I’m not sure how effective the 1st covenant will be. So far they’ve done nothing illegal or immoral that I’ve seen, so that’s good. Unlike with my first my board position, my contract with first covenant includes a sanity clause. They’re more inclusive that way; as expected, the Jewish heritage group didn’t believe in any sanity clause.

As for REB Research, our aims are simpler: to make and sell good hydrogen-related products, to make money, to pay our workers and creditors, and to develop our workers through training associated with the making and selling of good hydrogen products. Simple enough. My board meets 3 or 4 times a year over pizza; the salary of board members is the pizza. So far we haven’t done anything illegal either, that I know of — and we’re even making money.

Here are the Princeton PhD group of 1980. I’m the hairy bearded fellow at right who’s looking the wrong way. My thesis advisor, Ernest Johnson is the suited fellow just left of center. Dave Ollis is in front of me, and Joe Calo is in front of him, etc. Visit my Facebook page to see how my friends tagged themselves. 35 years ago!
Princeton Chemical Engineering Grad-students, late 1970s. My thesis advisor is the tall fellow at center; I'm the bearded fellow at right looking the wrong way.

Princeton Chemical Engineering Grad-students, late 1970s. My thesis advisor is the tall fellow at center; I’m the bearded fellow at right looking the wrong way.