Archive for the ‘technique’ Category

Kamikaze cookery

Wednesday, October 8th, 2008

There’s a new weekly cooking show you shouldn’t miss. It’s about cooking and science, or “Kamikaze cookery” to be more precise. And there’s a good dash of humor as well which doesn’t hurt. The first episode out is on how to cook that perfect steak (it’s embedded below, but on their site you can watch it at a better resolution). I’ve covered the topic before in my post on DIY sous-vide, but their video is much more entertaining :) They use a vacuum cleaner to suck out the air and a blow torch for the Maillard reaction! There is also a blog accompanying the videos. Hereby recommended!

Ten tips for practical molecular gastronomy, part 9

Saturday, May 31st, 2008

9. Keep a written record of what you do!

Wouldn’t it be a pity if you couldn’t recreate that perfect concoction you made last week, simply because you forgot how you did it? Last year I made a vegetable soup to which I added garam masala and pepper. I was cooking ad lib, adding a little of this and that without taking notes… Which is annoying, because it turned out very nice! It had a remarkable aftertaste which gave me a somewhat dry feeling on the back of the tongue and it reminded me of mangoes. Even immediately after the meal I wasn’t able to recall all the ingredients.

As an undergraduate student I took an organic chemistry lab course, and I remember we were told not to use post it notes or small pieces of paper for taking notes. Everything should be recorded in a proper journal or - if necessary - small note books. Having finished my Ph.D. a couple of years later, I can only testify to this. Everything you do - be it in the lab or in the kitchen - should be recorded immediately in a journal. It’s amazing how something that was obvious one day, slips your mind a week or month later.

There is a wonderful Donald Duck story by Volker Reiche entitled “The soul of science” (the original appeared in 1981 in the Dutch Donald Duck magazine). At a point “Professor Duck”, who actually works as a janitor in a lab, utters the words “Careful notes are the soul of science” as he is caught experimenting. This is true also for the kitchen and experimental cooking. A German translation of the story was reprinted in the article “Das Leiden des cand. chem. Donald Duck” (open access) in case you want to read the whole story.


Careful notes are also the soul of kitchen science!

When taking notes it’s essential that you are able to re-cook the dish yourself. But if no one else is, the notes are of limited value. The biggest source of uncertainty in the kitchen is the widespread use of volume for measuring powders. This can best be illustrated by the question: How much does a cup of flour weigh?

I bumped into this when I began baking no-knead bread (recipe). I converted the recipe to metric units using an online calculator, but the no-knead bread wasn’t a huge success. The problem was that there is no simple answer to the question “How much does a cup of flour weigh?”. Cooking conversion online states that a cup of all-purpose flour weighs 99 g. King Arthur Mills claim that all their flours weigh 113 g/cup. USDA states 125 g/cup and Gold Medal 130 g/cup. Some cookbooks have settled at 140 g/cup (apparently because this is about half way between a loosely and densly packed cup) and if the flour is hard packed you can reach 160 g/cup. In other words - when following a recipe you would need to know how the volume of flour was measured in order to use exactly the same amount of flour. Some recipes call for “spoon and level” or “scoop and level”, but many do not include any information about this.

My recommendation is to weigh all dry ingredients (and preferably also the wet ingredients). A normal digital kitchen scale typically has a resolution of 1 g with an accuracy of +/- 5 g and they are quite affordable. Weighing liquids is also far more accurate than the average volume measurement in the kitchen. If the scale has a “tara” function it’s also much faster as you can zero the display after each ingredient you add. It shouldn’t come as a surprise that I’m not the only chemist advocating weight measurements in kitchen. And it’s not difficult finding other sites in favor of weight measurements either.

It therefore puzzles me why recipes that call for the following are still so abundant:

1 pack of instant yeast
1 envelope unflavored gelatin
1 gelatin sheet (see comment #4-5)
1 sachet powdered pectin
1 tablespoon liquid pectin
1 stick of butter
… and the list goes on

The only exception to the general advice on weighing ingredients is when very small quantities are used. This could be spices, food coloring or hydrocolloids. With normal kitchen scales, you’ll be better of using volume measurements for amounts less than 5 g (equal to a teaspoon if measuring water). Otherweise it’s worthwhile mentioning that scales with a 0.1 g and 0.01 g readout are getting cheaper and cheaper.

*

There is a summary of the “10 tips for practical molecular gastronomy” posts. The collection of books (favorite, molecular gastronomy, aroma/taste, reference/technique, food chemistry) and links (people/chefs/blogs, webresources, institutions, articles and audio/video) at khymos.org might also be of interest.

Hydrocolloid recipe collection v.2

Wednesday, May 21st, 2008

Texture - A hydrocolloid recipe collection
It’s a pleasure for me to announce that an updated version of the hydrocolloid recipe collection is available for free download as a pdf file (73 pages, 1.8 Mb).

What’s new?
Several new recipes have been added (now counting more than 220 in total), including recipes with cornstarch, guar gum, gum arabic, konjac and locust bean gum. All in all 14 different hydrocolloids are included (plus lecithin which technically isn’t a hydrocolloid). In each section recipes are now sorted according to the amount of hydrocolloid used. The appendix has been updated with tables for comparison of hydrocolloid properties, hydrocolloid densities and synergies. The perhaps biggest change is that all recipes have been indexed according both to the texture/appearance of the resulting dish and according to the hydrocolloid used. Let’s say you want to make spheres, this index will show you which hydrocolloids can be used (that’s right - there are other possiblities than sodium alginate) and list the example recipes.

Foreword
A hydrocolloid can simply be defined as a substance that forms a gel in contact with water. Such substances include both polysaccharides and proteins which are capable of one or more of the following: thickening and gelling aqueous solutions, stabilizing foams, emulsions and dispersions and preventing crystallization of saturated water or sugar solutions.

In the recent years there has been a tremendous interest in molecular gastronomy. Part of this interest has been directed towards the “new” hydrocolloids. The term “new” includes hydrocolloids such as gellan and xanthan which are a result of relatively recent research, but also hydrocolloids such as agar which has been unknown in western cooking, but used in Asia for decades. One fortunate consequence of the increased interest in molecular gastronomy and hydrocolloids is that hydrocolloids that were previously only available to the food industry have become available in small quantities at a reasonable price. A less fortunate consequence however is that many have come to regard molecular gastronomy as synonymous with the use of hydrocolloids to prepare foams and spheres. I should therefore emphasize that molecular gastronomy is not limited to the use of hydrocolloids and that it is not the intention of this collection of recipes to define molecular gastronomy.

Along with the increased interest in hydrocolloids for texture modification there is a growing scepticism to using “chemicals” in the kitchen. Many have come to view hydrocolloids as unnatural and even unhealthy ingredients. It should therefore be stressed that the hydrocolloids described in this collection are all of biological origin. All have been purified, some have been processed, but nevertheless the raw material used is of either marine, plant, animal or microbial origin. Furthermore hydrocolloids can contribute significantly to the public health as they allow the reduction of fat and/or sugar content without loosing the desired mouth feel. The hydrocolloids themselves have a low calorific value and are generally used at very low concentrations.

One major challenge (at least for an amateur cook) is to find recipes and directions to utilize the “new” hydrocolloids. When purchasing hydrocolloids, typically only a few recipes are included. Personally I like to browse several recipes to get an idea of the different possibilities when cooking. Therefore I have collected a number of recipes which utilize hydrocolloids ranging from agar to xanthan. In addition to these some recipes with lecithin (not technically a hydrocolloid) have been included. Recipes for foams that do not call for addition of hydrocolloids have also been included for completeness. Some cornstarch recipes have been included to illustrate it’s properties at different consentrations. Recipes where flour is the only hydrocolloid do not fall within the scope of this collection as these are sufficiently covered by other cook books.

All recipes have been changed to SI units which are the ones preferred by the scientific community (and hopefully soon by the cooks as well). In doing so there is always uncertainty related to the conversion of volume to weight, especially powders. As far as possible, brand names have been replaced by generic names. Almost all recipes have been edited and some have been shortened significantly. To allow easy comparison of recipes the amount of hydrocolloid used is also shown as mass percentages and the recipes are ranked in an ascending order. In some recipes, obvious mistakes have been corrected. But unfortunately, the recipes have not been tested, so there is no guarantee that they actually work as intended and that the directions are complete, accurate and correct. It appears as if some of the recipes are not optimized with regard to proper dispersion and hydration of the hydrocolloids which again will influence the amount of hydrocolloid used. It is therefore advisable to always consult other similar recipes or the table with the hydrocolloid properties. The recipes have been collected from various printed and electronic sources and every attempt has been made to give the source of the recipes.

Since recipes can neither be patented nor copyrighted, every reader should feel free to download, print, use, modify, and further develop the recipes contained in this compilation. The latest version will be available for download from the static Khymos site and will also be announced here. I would like to thank readers for giving me feedback and suggestions on how to improve the collection. Feedback, comments, corrections and new recipes are always welcome at webmaster (a t) khymos ( dot ) org.

TGRWT #8: White chocolate soufflé with caviar

Wednesday, January 30th, 2008

white-chocolate-caviar-2.jpg

As a late (but just in time for the deadline) response to TGRWT #8 which was announced by Chadzilla in December last year - here is finally my write up on a recipe and a little on the background of this flavor combination which has become a classic in molecular gastronomy.

Heston Blumenthal introduced it around 2002 at The Fat Duck. It’s well worth reading what Heston wrote about this combination back then. He describes how salt can help bring out the flavor of many desserts. At one point he tried caviar and white chocolate - the effect was stunning. He then wanted to find out why this combination was so successful:

I gave some caviar and chocolate to François Benzi, who works for Firmenich, the flavourings and perfumes company based in Geneva. He was so surprised at the way that the caviar and chocolate melded together that he excused himself for half an hour while he tried to discover the reason behind the success of this union.

When he returned, the response was that both the chocolate and caviar contain high levels of amines. These are a group of proteins that have broken down from their amino acid state but not so far as to become ammonia. Amines contribute to the desirable flavours that we find in cooked meats and cheeses, among other things.

Some might object to using caviar but remember that there is no need to turn to sturgeon caviar as this species is endangered. I used caviar from Capelin which costs less than $4/€3 for a box of 50 g. As I have never tasted the “real” stuff I’m not the right person to judge about similarity or difference in aroma. And in case you also wondered about the terminology - roe is the fully ripe egg masses of fish whereas caviar refers to processed, salted roe. I decided to make a soufflé and based the recipe loosely on one of the soufflé recipes in my Larousse Gastronomique.

white-chocolate-caviar-3.jpg

White chocolate soufflé with caviar
40 g white chocolate
30 g flour
1 dL milk
35 g caviar
3 eggs, separated
nutmeg

Melt chocolate on very low heat. Add 1/3 of the flour and stir, heating gently. Add a 1/3 of the milk and mix thoroughly. Add another 1/3 of the flour, then more milk and so on. Add finely ground nutmeg. Add 3 egg yolks and heat until right before the mixture sets (yeah - I admit - this is not very precise…). Then add the caviar. Beat egg whites stiff and fold them in. Pour into greased soufflé dish and bake at 220 °C for about 15 min.

Verdict: Aromas blend well together, but when eaten alone it’s perhaps a little bland. But I’m quite sure that it could be succesfully incorporated into a menu together with something acidic. The texture was nice, but the soufflé quickly falls together once it’s removed from the oven (I’ll have to post more on the chemistry of soufflés some other time - Hervé This has written a lot about this).

If you try to make this - note that white chocolate doesn’t behave excately like butter when you add the flour. It all got very thick, very fast - that’s why I started adding milk early. I also guess you have to be really careful when heating the whtie chocolate, but I didn’t do any stress tests here.

white-chocolate-caviar-1.jpg
This is what the mix looks like before I folded in the egg whites.

For my first attempt at this recipe I used 20 g flour and 15 g caviar. The result was that the caviar sedimented before the soufflé had set, besides the fact that one could hardly taste the caviar at all. On my second attempt however, there was enough flour to keep the caviar suspended until the soufflé set. And one could actually also taste the caviar.

white-chocolate-caviar-4.jpg

And now on to the chemistry behind:
I promised that I would come back with more information about the chemistry behind this pairing, but there isn’t very much information out there. There is one paper on aroma development in block-milk which used in the production of white chocolate. This paper lists a couple of volatiles, but only with their relative peak areas. Turning to caviar (or roe), there is a recent paper on flavor characterization of ripened cod roe, and this paper includes qualitative information about odor intensity.

Comparing the list of volatiles, the following volatiles which contribute substantially to the odor of ripened cod roe are also found in block milk (followed by odor thresholds in water, given in ppb, taken from this page):

2-butanone (50000 ppb)
2-methylbutanal (1 ppb)
3-methylbutanal (0.2-2 ppb)
pentanal (na)

Of these, the first has a high odor threshold, so it’s not likely to be an impact odorant in block-milk (and white chocolate). The methylbutanals however probably contribute to the overlapping aroma of roe and white chocolate. I didn’t find any threshold value for pentanal.

One group of compounds which was not mentioned in the paper on cod roe odor from 2004, but which was mentioned in a Russian paper from 1967 are amines (Golovnya: “Gas-chromatographic analysis of amines in volatile substances of salmon caviar”). Considering the fact that trimethylamine has a threshold in the range of 0.37-1.06 ppb, and that trimethylamine is found in block-milk suggests that it might contribute significantly to the odor of both white chocolate and roe. I guess the reason trimethylamine (and the whole range of other, closely related amines) is not found in the odor analysis in the 2004 paper has to do with the analytical method used.

The fact that amines are crucial is further supported by the Guardian article I quoted from in the beginning where Heston Blumenthal describes how he turned to François Benzi, a flavor chemist at Firmenich, to find out why white chocolate and caviar is such a good match. Benzi concludes that it is due to the presence of similar amines in white chocolate and caviar.

TGRWT #5: Grilled pork tenderloin with chocholate beef stock cream

Sunday, August 26th, 2007

chocolate-beef-stock-cream.jpg

This month’s TGRWT is hosted by Le Petite Boulanger, and the foods to pair are chocolate and meat. The recipe for the chocolate beef stock cream is inspired by the Iberian Ham Cream by Ferran Adrià/El Bulli (the recipe can be found on p. 21 in the hydrocolloid recipe collection). I used anis because it brings out the meatiness very well. After mixing in the olive oil I saw that the droplets were not properly dispersed. Addition of some lecithin which solved this problem.

Chocolate beef stock cream
100 g water
2 g beef stock powder
10 g chocolate (70%)
1/4 t anis, powdered
0.5 g xanthan
0.2 g lecithin
20 g olive oil
honey and chili oil to taste

Heat water to dilute beef stock and melt chocolate. Cool. Add xanthan and lecithin. Mix with immersion blender. Add olive oil. Mix until smooth texture. Sprinkle with chives.

Grilled pork tenderloin
pork tenderloin, cut in 3 cm thick pieces
oil
powdered anis
crushed garlic

Marinate meat with oil, garlic and anis mixture. Grill. Serve together with the chocolate meat broth cream.

pork-chocolate-beef-stock-cream.jpg

Verdict: The chocolate beef stock cream has very meaty and almost nutty flavour. Honey is important to round of the otherwise slightly bitter taste of the chocolate. Chili oil gives it a bite, but can be omitted.

You can get an impression of the texture from this video:

Hydrocolloid recipe collection

Tuesday, August 14th, 2007

I’m happy to finally announce the first edition of a recipe collection devoted mainly to hydrocolloids. Totaling 111 recipes, it’s available for download as a pdf file (29 pages, 433 kB).

Update: The collection has been revised and is now available for download (more than 220 recipe, 73 pages, 1.8 Mb).

The following text is from the introduction I’ve written to the recipe collection:

A hydrocolloid can simply be defined as a substance that forms a gel in contact with water. Such substances include both polysaccharides and proteins which are capable of one or more of the following: thickening and gelling aqueous solutions, stabilizing foams, emulsions and dispersions and preventing crystallization of saturated water or sugar solutions.

In the recent years there has been a tremendous interest in molecular gastronomy. Part of this interest has been directed towards the “new” hydrocolloids. The term “new” includes hydrocolloids such as xanthan which is a result of relatively recent research, but also hydrocolloids such as agar which has been unknown in western cooking, but used in Asia for decades. One fortunate consequence of the increased interest in molecular gastronomy and hydrocolloids is that hydrocolloids that were previously only available to the food industry have become available in small quantities at a reasonable price. A less fortunate consequence however is that many have come to regard molecular gastronomy as synonymous with the use of hydrocolloids to prepare foams and spheres. I should therefore emphasize that molecular gastronomy is not limited to the use of hydrocolloids and that it is not the intention of this collection of recipes to define molecular gastronomy.

One major challenge (at least for an amateur cook) is to find recipes and directions to utilize the “new” hydrocolloids. When purchasing hydrocolloids, typically only a few recipes are included. Personally I like to browse several recipes to get an idea of the different possibilities when cooking. Therefore I have collected more than 100 recipes which utilize hydrocolloids ranging from agar to xanthan. In addition to these some recipes with lecithin (not technically a hydrocolloid) have been included. Recipes for espumas that do not call for addition of gelatin or other thickening agents have also been included for completeness.
All recipes have been changed to SI units which are the ones preferred by the scientific community (and hopefully soon by the cooks as well). As far as possible, brand names have been replaced by generic names. Most of the recipes have been edited and some have been shortened significantly. In some recipes, obvious mistakes have been corrected. But unfortunately, the recipes have not been tested, so there is no guarantee that they actually work as intended and that the directions are complete, accurate and correct. The recipes have been collected from various printed and electronic sources and every attempt has been made to give the source of the recipes.

Since recipes can neither be patented nor copyrighted, every reader should feel free to download, print, use, modify, distribute and further develop the recipes contained in this compilation. The latest version will be available for download from http://khymos.org/recipe-collection.php and will also be announced at http://blog.khymos.org. Feedback, comments, corrections and new recipes are welcome at recipe.at.khymos.dot.org.

Martin Lersch
Oslo, August 2007

Banana marshmallows with parsley (v 1.5)

Saturday, June 23rd, 2007

parsley-fresh-dried.jpg

For TGRWT #2 I made banana marshmallows with parsley. The texture came out nice, but the initially fresh parsley flavour had become grassy/hay-like over night. The litterature I referred to last time suggested that the off-flavour is produced by oxidation of unsaturated fatty acids or polyenes. There are several strategies to avoid this. The first would be not to mince the parsley as finely as I did last time to avoid exposure to the air’s oxygen. If the oxidation is enzymatic, blanching would be helpful. And it would also be worthwhile to see if addition of lemon juice (vitamin C and citric acid, are both antioxidants) would have any effect (however, on second thought this would be strange since parsley already has a lot of vitamin C!). Mirko Junge commented last time that freeze dried parsley would possibly retain more of the freshness and he most generously provided me with several samples of freeze dried parsley. I decided to proceed with the following six types of parsley for my marshmallows:

  1. fresh parsley leaves, chopped to pieces of about 2-3 mm (picture above, left)
  2. parsley leaves, blanched for 30 sec, chopped to pieces of about 2-3 mm
  3. parsley leaves, sprinkled with lemon jucie, chopped to pieces of about 2-3 mm
  4. parsley leaves, blached for 30 sec, sprinkled with lemon juice, chopped to pieces of about 2-3 mm
  5. freeze dried parsley from Goutess (picture above, right)
  6. plain, dried parsley from my local store (picture above, front)

I used the same recipe as last time, but split the whipped sugar-gelatin-banana mixture into six different bowls before mixing with the parsley. I used approximately 0.6-0.8 g of fresh parsley for each of the entries 1-4. I tried to estimate the amount of dried parsley to use by eye, comparing with the amount of fresh leaves. The amount of dried parsley used was less than 0.1 g, so my balance was not of much help. The picture below might give you an idea.

parsley-six-bowls.jpg
Six different types of parsley were prepared immediately prior to mixing with the marshmallow base to minimize oxidation.

marshmallow-six-bowls.jpg
If the term ‘parallel cooking’ has not been invented yet, this might be good time to introduce it.

parchment-paper-marshmallow.jpg
I let the marhsmallows set between two sheets of greased parchment paper.

banana-parsley-marshmallow-tasting.jpg
Blind tasting of banana parsley marshmallows.

My wife helped me do a blind tasting to avoid any bias. The six marshmallow samples were each associated with a three digit code and presented on a plate to the taster. We both did two rounds each (A1/A2 and B1/B2) and the results are summarised in the table below. The scoring only describes the parsley flavour unless otherwise noted.

Parsley used A1 A2 B1 B2 Sum
Fresh parsley 5 5 5 5 20
Blanched parsley 4/* 1 2/* 2 9
Parlsey with lemon juice 0 1 5 5 11
Blanched parsley with lemon juice 1 0/* 2/- 0/- 3
Freeze dried parsley 4 2 2 2 10
Dried parsley 0/- 0/- 0 2 2

Legend:
5 fresh parsley, strong
4 fresh parsley, weak
2 grassy/hay-like parsley, weak
1 grassy/hay-like parsley, strong
0 neither fresh nor grassy, weak overall
- disagreeable
* banana dominates

I was quite surprised once I had decoded the score sheets. Fresh parsley cut into relatively large pieces gave a parsley flavour without any hints of grassy or hay-like off flavours! Blanching or treatment with lemon juice were both detrimental to the parsley flavour, and even more so when combined. The variation observed for could be a result of an uneven distribution of the parsley in the marshmallow (increased parsley flavour if you happen to chew a leaf). The freeze dried parsley didn’t do very well compared with fresh parsley, but outperformed the dried parsley from my local store which didn’t have much flavour at all. Both samples of dried parsley however were dominated by a grassy/hay-like flavour. I should add that the grassy/hay-like flavour in itself is not especially disagreeable, but it does not go very well together with the banana.

The result is interesting and perhaps a little counter intuitive. Generally one would say that a larger surface area (= finely chopped) would enhance the flavour release. This experiment however shows that this is not universally true, especially if the flavours can be oxidized. So next time you make banana parsley marshmallows remember that less chopping gives better parsley flavour.

Coffee cream foam

Tuesday, April 10th, 2007

coffee-cream-foam.jpg

Based on some googling of espuma and foam recipes (including Ferran Adria’s coffee espuma), I figured that the following should work:

2 dL coffee
2 sheets of gelatine
3 dL heavy cream
sugar/vanilla sugar

Soak gelatine in cold water. Strain. Dissolve gelatin sheets in the hot coffee and stir in sugar while heating. Cool. Add heavy cream. Filter through a fine meshed sift (just in case there should be any undissolved sugar, gelatin or particles) into a 0.5 L iSi gourmet whipper. Screw on top and charge with a cream charger. Shake 2-3 times and leave in fridge for a couple of hours. Hold whipper upside down, shake once to displace mixture towards the nozzle in case it is stuck and dispense. Texture is soft and silky. Tastes delicious!

Some more chemistry: The cream chargers contain dinitrogen oxide (N2O) which is less polar than carbon dioxide (CO2), and hence more soluble in fat (such as heavy cream for instance). Another reason why carbon dioxide is not used in this recipe is probably that when it dissolves, some carbonic acid is formed which could curdle milk based products if pH drops to much and also influence taste (but carbonated milk has actually been marketed!). The idea of using dinitrogen oxide for soda/beer has also been explored.

Carbonated fruit the iSi way

Monday, April 9th, 2007

I blogged about carbonated strawberries some while ago. Those were made using dry ice which unfortunately is not always easy to get hold of. Last week however I bought a iSi Gourmet Whipper - one of those Ferran Adria uses to make foams/espumas. I plan to experiment with that as well, but the first thing I decided to prepare was carbonated fruit. In fact this is a safe way (the only?) to make carbonated fruit at home using a pressurized container.

isi-whipper.jpg

The instruction booklet which comes with the iSi Gourmet Whipper only mentions cream chargers (filled with N2O, dinitrogen oxide), whereas soda chargers (filled with CO2, carbon dioxide) are not mentioned (I guess the opposite is true for the iSi Siphons?). This is quite amazing actually! Luckily however the cream and soda chargers are exactly the same size and both hold 8 g of gas. So it should be possible to make carbonated fruit with any of the iSi whippers (cream, easy, gourmet, dessert, thermo) or siphons available.

Here’s how you proceed:

  1. Fill you iSi whipper (or siphon) with fruit, preferably fruit which has a cut, wet surface to allow the carbon dioxide to dissolve in the water/juice.
  2. Screw on top securly
  3. Charge with one soda charger (two if you have the 1 L whipper)
  4. Leave in fridge over night
  5. Release pressure with valve (Important!)
  6. Unscrew top and serve immediately!
  7. Enjoy!

carbonated-grapes.jpg
This is what carbonated grapes look like. As you see, I decided to cut the grapes in to halves.

carbonated-grapes-closeup.jpg
Notice how they sizzle!

A quick recap of the chemistry: cold water dissolves more CO2 than tempered water, that’s why we leave it in the fridge. Also, remember that it takes some time for the carbon dioxide to dissolve in water, therefore it’s better not to be in a hurry. A quick calculation of the pressures gives the following: Both gases have molecular weights of 44 g/mol, so 8 g of gas corresponds to 0.1818 moles or 4.1 L at 25 °C and 1 atm pressure. The volume of the chargers is 0.01 L which gives an initial pressure in the chargers of impressive 445 atm! With an approximate volume of 0.7 L this gives a pressure (in an empty whipper) of nearly 6 atm - the same as in a bottle of champagne. However once you add water, the equilibriums will change and the pressure in the head space will drop. Anyone who remembers how to calculate the head space pressure at equilibrium if the container is filled with 0.5 L of water and cooled to 4 °C?

I’ve done some googling and there is also some mention of making carbonated fruit with an iSi whipper over at Ideas in food.

(The word play in the title works better for those with a mother tongue where iSi would be pronounced just like “easy”!)

First experiments with sodium alginate

Friday, March 30th, 2007

Here’s some pictures and a video of my first experiments with sodium alginate and spherification. I used sodium alginate from the Texturas series and calcium chloride from a drug store. Needless to say, I’m very fascinated by the texture and the whole process. I have blogged about the chemistry behind previously.

Materials used:
2.0 g sodium alginate
200 g water (with low calcium content!)
50 g blueberry syrup

2.5 g calcium chloride
500 g water

Procedure:
2 g sodium alginate and 200 g water were mixed vigourously in blender. The mixture was then left to stand for some hours to get rid of the air bubbles. 50 g blueberry syrup was then added to the sodium alginate solution. A calcium chloride bath was prepared by dissolving 2.5 g calcium chloride in 500 g water. The sodium alginate/blueberry mixture was dripped into the calcium chloride bath using a plastic syringe with a steel cannula. After 1-3 min the pearls were removed and rinsed with water.

More detailed procedure with pictures and video:
I had to obtain a scale with a 0.1 g accuracy to weigh out 2.0 g of sodium alginate (my first experiments using a normal kitchen scale failed). The model I got cost about $100 and is inteded for school laboratories. Amazon provides several scales with this accuracy.

alginate-1.jpg

I used a blender to dissolve sodium alginate in water. This incorporates a lot of air in the mixture which we don’t want. It could possibly be avoided by using an immersion blender/mixer. However, I just left the alginate solution on the bench and after 3-4 hours the air bubbles had all escaped from the solution.

alginate-2.jpg

Plastic syringes and cannulas can be obtained from your local drug store or pharmacist. I found it was easier to produce evenly sized drops with a sharp cannula (CAREFULL!) than with just the plastic tip of the syringe. This of course depends on the viscosity of the solution. By thickening (with xanthan for instance) you can produce larger drops.

alginate-6.jpg

After 1-3 min the spheres were removed from the calcium chloride solution and rinsed with clean water. I dried the spheres carefully using a kitchen towel or paper.

alginate-7.jpg

alginate-3.jpg

Definitely looks like caviar when presented on a spoon like this!

alginate-4.jpg

Larger spheres were made by filling a small measuring spoon with the alginate mixture (I used a syringe for this so the outsides of the spoon would not be covered with alginate solution) and carefully emptied it into the calcium chloride bath. It takes some trial and error to achieve good results.

alginate-5.jpg

The spheres are suprisingly robust and can be handled without rupturing.

alginate-8.jpg

If cut with a knife, the spheres rupture and the liquid contents flows out.

alginate-9.jpg

The small spheres didn’t taste much, so I could have added more blueberry syrup. The large spheres however had a nice taste. The surprise element when they rupture in your mouth is very nice!

Practical molecular gastronomy, part 4

Saturday, March 17th, 2007


(Photo by vintage_patrisha at flickr.com)

4. Learn how to control the texture of food

Taste and flavour normally get more attention when food is discussed, but the texture of food is equally important and our tongue is very sensitive, not only to taste and temperature, but also to the texture of food. The texture of food determines it’s mouthfeel and it is related to many physical properties of the food. Wikipedia lists the following aspects of mouthfeel (click to see the full description of each aspect) which can be useful when analyzing food:

Adhesiveness, Bounce/Springiness, Chewiness, Coarseness, Cohesiveness, Denseness, Dryness, Fracturability, Graininess, Gumminess, Hardness, Heaviness, Moisture absorption, Moisture release, Mouthcoating, Roughness, Slipperiness, Smoothness, Uniformity, Uniformity of chew, Uniformity of bite, Viscosity, Wetness

I will barely scratch the surface of how texture can be controlled by highlighting a couple of topics and point you to further resources. Hopefully it will spark your interest and give some new ideas for you to play with in the kitchen. Those interested in a comprehensive review of food texture are referred to the CRC handbooks on food texture (volume 1: semi-solid foods, volume 2: solid foods).

What determines the texture of food?
Put very simple, it’s the relative amounts of air, liquid and solids that determines the texture of food. This is complicated by the fact that liquids have different viscosities. Furthermore the air, liquid and solid ratio is not necessarily constant. A liquid can solidify or evaporate, solids can melt or dissolve, and air bubbles can escape during cooking or storage. An elegant but quite abstract way of describing the complicated mixtures of air, liquids and solids found in food, is to use the CDS formalism (CDS = complex disperse systems), introduced by Hervé This.


(Photo by Subspace at flickr.com)

How can texture be controlled and changed?
Texture can be controlled by temperature, pH, air/liquid/solid ratio, osmosis, hydrocolloids and emulsifiers - to mention a few. Here’s some examples:

  • Heating induces a change in the structure of proteins referred to as coagulation or denaturation. Typical examples are the boiling of eggs and the cooking of meat. When proteins denature they contract and become firmer. There are several helpful tables relating the doneness of different meats to temperature.
  • At around 70 °C (160 °F) collagen, the connective tissue in meat, turns into gelatin. As a result the meat becomes more tender, which is desireable in stews and other slow cooked meats.
  • Heat causes air/gas to expand and water to evaporate to give a foamy/airy texture. For example, experiments have shown that it is mainly the evaporation of water that causes a soufflé to rise.
  • Heat will cause certain hydrocolloids to solidify (for exaple methyl cellulose) whereas it will cause others to melt (such as gelatin).
  • Brining meat can greatly improve it’s texture and juicyness. This is done by immersing the meat in a 3-6% salt solution from anyhere between a few hours to two days before cooking.
  • Frozen water in the form of tiny ice crystals are important for the smooth texture of sorbets and ice cream. Ice cream that has been partly melted and frozen again will grow larger ice crystals that impart a coarser texture to the ice cream.
  • Acidic solutions (low pH) can cause proteins to denature. This allows fish to be cooked without the use of any heat. An example is the use of lime juice in ceviche.
  • Emulsifiers, thickeners and gelling agents have almost become synonymous with molecular gastronomy for many. They can greatly alter the texture of foods and typically only a very small amount is required. Where gelatin was the only gelling agent videly available to cooks in Europe and America only a decade ago, this has changed with the advent of many internet suppliers of speciality ingredients.
  • Cooking under vacuum can create new and exciting textures. First of all it’s a way of removing excess water without having to raise the temperature all the way up to 100 °C. When the water is removed, this will create pockets of air in the food, and when the pressure is released, the liquid surrounding the food that is prepared will rush in and fill these pockets. There is a commercially available vacuum cooker, but a DIY version can be made from a pressure cooker and a vacuum pump.

  • (Photo by Trinity at flickr.com)

  • Green leaf vegetables such as lettuce loose water upon storage. As the pressure inside the cells drops, the leaf becomes softer. By immersing the leaves in cold water for 15-30 min, thanks to osmosis, water will enter into the cells again. As the pressure increases, the leaves become crisper.
  • Air bubbles can greatly modify textures, and foams really are ubiquitious (which becomes obvious if you read the book “Universal foam - from cappuccino to the cosmos”). Ferran Adria’s espumas have become very popular, as has his recent invention, the Espesso. Air bubbles are also very important for the texture of ice cream, in fact ice cream is nearly 50% air (just consider the fact that ice cream is sold by volume, not by weight!).
  • A very recent addition to the modern kitchen pantry is the enzyme transglutaminase. The enzyme acts like a meat glue and Chadzilla has nice blog post on his transglutaminase experiments.
  • There are also enzymatic counterparts of transglutaminase available: proteolytic enzymes also known as proteases. You can find them in pineapple (bromelain/bromelin), papaya (papain), figs (ficin) and kiwi (actinidin) - and they are capable of degrading proteins and muscle tissue. Despite this, they have only found limited use in marinades, as their action can be difficult to control (as Nicholas Kurti experienced, look for the “But the crackling is superb” link).
  • When mixing flour and water, glutenin and gliadin react to form gluten which gives bread it’s elasticity and plasticity. Addition of 1-2% salt to bread tightens the gluten network and increases the volume of the finished loaf. Similarly, addition of 1% oil to the dough (after the first kneading) can further increase the volume. Larger amounts of fat added before kneading will interfere with the formation of long gluten strands, hence the name shortening.
  • The no-knead bread that recently hoovered around in the blogosphere challenges the conventional wisdom that bread needs kneading to get a good texture.
  • Once bread is baked, the staling process starts. Staling does not necessarily involve loss of water from the bread and is caused by crystallisation (or retrogradation) of starch. In this process water molecules are trapped. The process proceeds fastest at 14 °C, but is halted below -5 °C. This is the reason why bread should be stored at room temperature. The staling process can be slowed down by addition of an emulsifier such as lecithin which is abundant in egg yolk.
  • A way of turning high fat foods and oils into powders is by the use of tapioca maltodextrin. Hungry in Hogtown has shown how Nutella can be turned into a powder.
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    Check out my previous blogpost for an overview of the tips for practical molecular gastronomy. The collection of books (favorite, molecular gastronomy, aroma/taste, reference/technique, food chemistry) and links (webresources, people/chefs/blogs, institutions, articles, audio/video) at khymos.org might also be of interest.

    Simple temperature calculations

    Thursday, March 8th, 2007

    Although I recommend the use of a thermometer, sometimes it’s convenient to know how you can also manage without. If you mix water at two different (but known) temperatures, you can easily calculate the temperature after mixing. Just multiply the temperature of each part with the relative amount. For example, if you have 3 dL at 100 °C and 7 dL at 10 °C (which happens to be the approximate temperature of my tap water), this gives (3 dL x 100 °C + 7 dL x 10 °C) / 10 dL = 37 °C which is just perfect for dissolving fresh yeast when making bread.

    You can also do it the other way around. Let’s say you have boiling water and you know that your tap water is approximately 10 °C. If you want water at approximately 37 °C, you can do as follows:

    temperature-calculation.jpg

    Start by writing what you have to the left (100 °C and 10 °C) and what you want in the middle (37 °C). Subtract: (100-37) = 63 and (37-10) = 27. And voilá - you need 27 parts water at 100 °C and 63 parts at 10 °C (and 27:63 simplifies to 3:7 which is what we found above). Now of course if you really wanted water at 37 °C, you would simply put your finger in to see if it’s at body temperature…

    Are there any practical applications of this? Yes - a simple, but elegant way to prepare fish would be to drop a fish of known weight and temperature (fridge @ 4 °C or freezer @ -18 °C) into water that has been brought to boil. Cover pot and turn off heat. The amount of water would be calculated based on the desired temperature of the fish. We are assuming here that there is no heat loss to the surroundings, which of course isn’t quite true. How fast pot of water will cool depends on how much water you use and on the pot. This can be corrected for, and luckily someone has already done it. More on this in my post on how to cook fish in cooling water.

    We can apply the temperature calculation from above to figure out roughly what the temperature will with this cooking method. 800 g of fish from the fridge (4 °C) and 2,4 L of boiling water gives a temperature of (0,8 x 4 °C + 2,4 x 100 °C) / 3,2 = 76 °C. The cooling curves for a pot with 2,5 L of water suggest a temperature loss of 15-20 °C in 30 min which would bring us down to 55-60 °C which - considering that no thermometer is used - is quite good.

    Cooking fish in cooling water

    Thursday, March 8th, 2007

    I have previously written about how you can cook a perfect steak with a simple DIY sous vide technique. Of course low temperature cooking applies equally well to fish with the only difference that the temperature can be turned down even lower.

    A slightly different approach for cooking fish was presented by Haqvin Gyllensköld in the Swedish book “Koka, steka, blanda” from 1977, which I became aware of through Östen Dahlgren’s book “Laga mat - hur man gör och varför”. In stead of keeping the fish at a constant temperature (which requires quite some attention unless you have a thermostated waterbath), in this method, as the hot water cools, the temperature of the fish increases until they’re at the same temperature.

    This is how you do it:

    1. Weigh the fish
    2. Boil the triple amount of water
    3. Add some salt to the water (15 g / L)
    4. Put the fish in the water and remove the pot from the stove
    5. Check the graph below for how long the fish should be left in the cooling water
    6. Serve!

    cooking-fish-in-cooling-water.jpg

    Need help on fish names in different languages? Yeah, me too!

    Staying warm: Cast iron vs. stainless steel

    Thursday, March 1st, 2007

    Cookware made from cast iron has a reputation for keeping food warm for a long time. Is that really true? Best way to find out is by an experiment. I decided to compare a cast iron pot with one of stainless steel. These are the pots I used:

    cast-iron-stainless-steel.jpg

    For the first experiment I filled them each with 2,5 L of water, put the lids on and brought both to the boil and let them boil for a minute so the pot itself would be warm throughout. Then both were placed on cork plates and left to cool. The temperature probe was carefully inserted under the lid in order to reduce the heat loss, and removed once the temperature had stabilized. For the second experiment 5 L of water were used. The measured temperatures are shown in the graph.

    cooling-curve.jpg

    Contrary to what I had expected, the stainless steel pot keeps water warmer! After approximately 1,5 hours there is a 10 °C difference between the two. As expected, when using 5 L of water, it stays warm longer. Physical data for the two pots are given in the following table:

    Cast iron Stainless steel
    Volume 6 L 6 L
    Diameter 27,9 cm 25,0 cm
    Height 11,5 cm 14,5 cm
    Surface area
    (top+sides)
    1619 cm2 1629 cm2
    Surface area
    in contact with 5 L water
    1301 cm2 1286 cm2
    Weight 6,1 kg 2,3 kg
    Wall thickness ~4 mm <1 mm
    Heat capacity of pan 2,8 kJ/K 1,2 kJ/K
    Thermal conductivity 80 Wm-1K-1 16 Wm-1K-1
    Thermal diffusivity 22 x 10-6 m2/s 4.3 x 10-6 m2/s
    Emissivity 0.95 0.07

    The heat capacity of the cast iron pot is more than double that of the stainless steel pot. But this is negligible compared to the heat capacity of water: 10.5 kJ/K (2,5 L) and 20,9 kJ/K (5,0 L). Also, there is only a small difference in their surface area which cannot explain the large difference in temperature loss observed.

    This leaves me with two eplanations:

  • Cast iron is better heat conductor and has a higer thermal diffusivity
  • Cast iron (being nearly black) has a much higher emissivity than a polished stainless steel surface. The reason for this is that absorption and reflection of radiation are related.
  • My guess is that the difference in emissivity is more important (but please correct me if I’m wrong). With an infrared thermometer, one should therefore be able to measure a difference between pots of cast iron and polished stainless steel (even though they’re at the same temperature!) due to the difference in emissivity. Any one who can do the experiment and report back?

    Conclusion: There are many good reasons to use cast iron, but keeping food warm is not one of them!

    Practical molecular gastronomy, part 3

    Monday, February 26th, 2007

    Get a basic understanding of heat transfer, heat capacity and heat conductance.

    Since a lot of cooking involves temperature manipulations, it’s a good idea to get a basic understandning of how heat is transferred and how well it is stored in different materials. “Heat” in this context does not imply high temperature since it also applies to the understanding of freezing/thawing.

    ceramic-stove-top.jpg
    Closeup of ceramic stove top

    Heat transfer

    Conduction: flow of heat through an object or between two objects in contact. Metals are typically good conducters whereas air is a poor heat conductor.

    Convection: heat transfer occurs because particles are moved from a warm region to a colder one. One can say that convection is a combination of conduction and mixing. For example, convection occurs when heating water since its density varies with temperature - warm water is lighter than cold water and will float. This video illustrates convection currents in water as a crystal of potassium permanganate dissolves (this salt is not edible).

    Radiation: in the kitchen we encounter two types of heat transfer by radiation corresponding to two different parts of the electromagnetic spectrum. The heat we feel from hot burning charcoal, a stove top or the sun are all a result of infrared radiation. The other type is microwave radiation. Heat transfer by radiation does not require a material for the heat to pass through (as a consequence, a blowing wind will not have any significant effect when grilling). Microwaves easily penetrate plastic, glass and wood, but not metal. Infrared radiation is blocked by opaque materials.

    Heat capacity and heat conductance

    Heat capacity: the heat requried to raise the temperature of the material. Water has a very high heat capacity, metals (shown in red) generally a low heat capacity.

    Heat conductance: how well heat flows through the material. Some metals (shown in red in the graph) are excellent heat conductors (silver, copper, aluminum), others less so (iron and stainless steel). All other materials (shown in blue) are generellay poor heat conductors.

    The heat capacity (or to be precise, the specific heat capacity - which means heat capacity per weight unit) and the heat conductance of materials encountered in the kitchen are plotted in the the graph below:

    heat-capacity-conductance.jpg
    (for the technically interested, the plot units are Wm-1K-1 for the heat conductance and Jg-1K-1 for the specific heat capacity)

    For a more extensive treatment of heat transfer, heat capacity and heat conductance (+ more on cooking methods and materials) in a gastronomical setting, I recommend the Gourmet Engineering Lecture Notes for a very interesting course given at Tufts University in Medford, MA, USA. Cooking for Engineers also has a nice post on heat transfer and browning of foods and one on common materials of cookware (with comprehensive comparisons of different materials used).

    Examples related to food preparation and handling

  • Convection ovens utilize fans to circulate hot air allowing reduced cooking times and temperatures. Because of efficient convection, two or more trays can be baked simultaneously.
  • In a steam oven water is introduced to increase the humidity (this can also be done by spraying water into the hot oven). Heat transfer is more efficient due to 1) the higher heat capacity of humid air and 2) the energy released when steam condenses onto the surface (it’s the energy it took to boil the water in the first place). For bread, the condesed water prevents the surface from drying out which facilitates the exapansion of the loaf. Furthermore, the hot surface causes starch to gelatinize and subsequently dry into a delicate crust.
  • Water will cool faster than the same volume of a thickened soup because of less resistance to the convection currents in water. The amount of convection decreases in the following order: water > chicken soup > creamy soup > thick onion soup > porridge. In the latter heat is transferred by conduction only from the interior to the exterior (where heat transfer proceeds mainly by radiation and conduction). This will also affect cooling times, which is of importance with regard to microbial safety (food should be cooled rapidly past the window from 30-60 °C where microorganism thrive).
  • For rapid defrosting, place the frozen food in cold water or on a metal object - this will allow an efficient transport of heat to the frozen food. Defrosting in a microwave is not easy because most of the water molecules are locked in rigid structure and even microwaves cannot make them move (they only melt by conduction of heat from melted neighbouring areas).
  • To freeze icecream or a parfait, use a metal container as this will allow a faster dissipation of the heat in the freezer.
  • When whipping cream, it’s essential to keep the temperature low (otherwise the fat will melt). Use a thick glas bowl and cool it in the freezer before whipping.
  • When cooking meat in a pan or on a grill, notice how the surface browns relatively fast compared to the time it takes for the interioir of the meat to heat up. Heat transfer to the surface by radiation or conduction is very efficient compared to conduction of heat through meat itself. Therefore it’s advisable to fry/grill the meat at high temperature first to get a nice browning, then let the meat rest for 5-10 min to allow for heat conduction to the interioir (cover with aluminum foil to reduce radiative heat loss), followed by a second frying/grilling at lower temperature until desired doneness.
  • In an oven, the heating caused by radiation can be increased by moving food closer to the walls or reduced by wrapping the food with reflective aluminum foil. For example, to caramellize sugar on a creme brulee if you don’t have gas burner, place them as high as possible in the oven, preferably using a grill element. Turkey legs stick out and easily get overdone - wrapping them with aluminum foil reduces heat radiation from the oven walls.
  • For a bain marie, always use a metal bowl as this gives you better temperature control. When making egg based sauces such as hollandaise or bernaise, use a thin metal bowl this allows rapid heating and cooling (if temperature gets to high, the metal bowl allows quick cooling which might save the sauce).
  • A pizza baking stone has a higher heat capacity than a metal plate/sheet - this ensures proper rising and gives a crispy crust.
  • Ever burnt your tongue on a pizza? Tomatoes (mostly water) retain heat far better than the crust (many air bubles, low heat capacity) and cheese topping (cools fast due to radiation from surface).
  • The vacuum in a thermos does not conduct heat by conduction or convection, only by radiation. The latter is minimized (in thermoses of glas) by a silver or aluminmum coating, creating a reflective mirror.
  • From the graph it doesn’t seem like cork is a particularly good insulator. This is because the heat conductance is plotted per weight unit. For a porous material such as cork, the effective heat conductance is much lower than for the same volume of other materials.
  • Lastly, just to illustrate how complex heat transfer and convection sometimes can be, take a look at the Mpemba effect: Believe it or not, under certain conditions, hot water freezes faster than cold water!
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    Check out my previous blogpost for an overview of the tips for practical molecular gastronomy. The collection of books (favorite, molecular gastronomy, aroma/taste, reference/technique, food chemistry) and links (webresources, people/chefs/blogs, institutions, articles, audio/video) at khymos.org might also be of interest.