Water Freezes Because God Wants It To
- Martin Milner
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- missy
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aw - heck - fly - we used to have chemical engineers baking cookies here!
And you know, depending on your definition of "chemical" - ALL food products are chemicals, since they are made up of carbon, hydrogen, oxygen, and other assorted elements, put together in unique ways to make the unique food.
Missy
And you know, depending on your definition of "chemical" - ALL food products are chemicals, since they are made up of carbon, hydrogen, oxygen, and other assorted elements, put together in unique ways to make the unique food.
Missy
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Ingredients:missy wrote:we used to have chemical engineers baking cookies here!
1. 532.35 cm3 gluten
2. 4.9 cm3 NaHCO3
3. 4.9 cm3 refined halite
4. 236.6 cm3 partially hydrogenated tallow triglyceride
5. 177.45 cm3 crystalline C12H22O11
6. 177.45 cm3 unrefined C12H22O11
7. 4.9 cm3 methyl ether of protocatechuic aldehyde
8. Two calcium carbonate-encapsulated avian albumen-coated protein
9. 473.2 cm3 theobroma cacao
10. 236.6 cm3 de-encapsulated legume meats (sieve size #10)
To a 2-L jacketed round reactor vessel (reactor #1) with an overall heat-transfer coefficient of about 100 Btu/F-ft2-hr add one, two, and three with constant agitation.
In a second 2-L reactor vessel with a radial flow impeller operating at 100 rpm add four, five, six, and seven until the mixture is homogeneous.
To reactor #2 add eight followed by three equal portions of the homogeneous mixture in reactor #1. Additionally, add nine and ten slowly with constant agitation. Care must be taken at this point in the reaction to control any temperature rise that may be the result of an exothermic reaction.
Using a screw extrude attached to a #4 nodulizer place the mixture piece-meal on a 316SS sheet (300 x 600 mm). Heat in a 460K oven for a period of time that is in agreement with Frank & Johnston's first order rate expression (see JACOS, 21, 55), or until golden brown.
Once the reaction is complete, place the sheet on a 25 deg. C heat-transfer table allowing the product to come to equilibrium.
- missy
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avanutria - you forgot this part:
Maillard Reaction
Maillard reaction is a type of non-enzymatic browning which involves the reaction of simple sugars (carbonyl groups) and amino acids (free amino groups). They begin to occur at lower temperatures and at higher dilutions than caramelization.
Chemistry of the reaction
An outline of the Maillard reaction is given in Figure 1. Maillard reactions have three basic phases. The initial reaction is the condensation of the carbonyl group of a reducing sugar (aldose) with a free amino group of a protein or an amino acid, which loses a molecule of water to form N-substituted glycosylamine (Step A). This is unstable and undergoes the "Amadori rearrangement" to form "1-amino-1-deoxy-2-ketoses" (known as "ketosamines") (step B). The ketosamine products of the Amadori rearrangement can then react three ways in the second phase. One is simply further dehydration (loss of two water molecules) into reductones & dehydro reductones (step C). These are essentially "caramel" products and in their reduced state are powerful antioxidants. A second is the production of short chain hydrolytic fission products such as diacetyl, acetol, pyruvaldehyde, etc (step D). These then undergo "Strecker degradation" with amino acids to aldehydes (step E) and by condensation to aldols, or they may react in the absence of amino compounds, to give aldols and high molecular weight, nitrogen-free polymers (step F). A third path is the Schiff's base/furfural path. This involves the loss of 3 water molecules (step C), then a reaction with amino acids and water. All these products react further with amino acids in the third phase to form the brown nitrogenous polymers and copolymers called melanoidins (step G). These can be off flavours (bitter), off aromas (burnt, onion, solvent, rancid, sweaty, cabbage) or positive aromas (malty, bread crust-like, caramel, coffee, roasted). Step H in Figure 1 illustrates a direct route to fission products from N-substituted glycosylamines, without the formation of an ARP (Amadori rearrangement product)..
Temperature and time
Studies of model systems showed that an increase in temperature and/or time of heating resulted in increases in colour development, the carbon-to-nitrogen ratio and the degree of unsaturation and the chemical aromaticity.
Composition of the system
Pentose sugars (e.g. ribose) react more readily than hexoses (e.g. glucose) which, in turn, are more reactive than disaccharides (e.g. lactose).
Of all the amino acids, lysine results in the most colour in the Maillard reaction, due to its Î -amino group; cysteine results in the least colour. Therefore, foods containing proteins that are rich in lysine residues (e.g. milk proteins) are likely to brown readily. The sugar-to-amino-compound ratio also influence the amount of colour produced. For example, a glucose-glycine model system containing 65% water and stored at 65oC showed a rapid increase in colour formation as the glucose-to-glycine ratio was decreased (e.g. from 10:1 or 2:1 to 1:1 or 1:5). In foods, attempts to prevent the reaction should be directed towards removing one of the reactants: the amino compounds (for carbohydrate-rich foods) or the reducing sugars for protein-rich foods.
Water activity
Figure 1 shows that water is produced during the Maillard reaction. Thus, as a consequence of the law of mass action, the reaction occurs less readily in foods with a high aw value. In addition, the reactants are diluted at high aw values while, at low aw, the mobility of reactants is limited, despite their presence at increased concentration. In practice, the Maillard reaction occurs most rapidly at intermediate aw values (0.5-0., and aw is of most significance to the reaction in dried and intermediate-moisture foods (IMFs), which have aw values in this range.
pH
Low pH values (£ 6) favour the formation of furfurals from Amadori rearrangement products, while the routes to reductones and fission products are preferred at a high pH (> 6). However, in practice, the effect of pH is not this clear cut, and reactions take place by all three pathways, with the pH of the system influencing the ratio of products formed. For sugar-glycine systems the descending order of color development at pH lower than 6 was xylose > fructose >glucose >lactose > maltose; at pH 6 the order was xylose > glucose > fructose > lactose > maltose. This suggested that in Maillard browning the rate of color development is not directly related to the structural stability of the sugars.
http://www.agsci.ubc.ca/courses/fnh/410/colour/3_82.htm
Missy
Maillard Reaction
Maillard reaction is a type of non-enzymatic browning which involves the reaction of simple sugars (carbonyl groups) and amino acids (free amino groups). They begin to occur at lower temperatures and at higher dilutions than caramelization.
Chemistry of the reaction
An outline of the Maillard reaction is given in Figure 1. Maillard reactions have three basic phases. The initial reaction is the condensation of the carbonyl group of a reducing sugar (aldose) with a free amino group of a protein or an amino acid, which loses a molecule of water to form N-substituted glycosylamine (Step A). This is unstable and undergoes the "Amadori rearrangement" to form "1-amino-1-deoxy-2-ketoses" (known as "ketosamines") (step B). The ketosamine products of the Amadori rearrangement can then react three ways in the second phase. One is simply further dehydration (loss of two water molecules) into reductones & dehydro reductones (step C). These are essentially "caramel" products and in their reduced state are powerful antioxidants. A second is the production of short chain hydrolytic fission products such as diacetyl, acetol, pyruvaldehyde, etc (step D). These then undergo "Strecker degradation" with amino acids to aldehydes (step E) and by condensation to aldols, or they may react in the absence of amino compounds, to give aldols and high molecular weight, nitrogen-free polymers (step F). A third path is the Schiff's base/furfural path. This involves the loss of 3 water molecules (step C), then a reaction with amino acids and water. All these products react further with amino acids in the third phase to form the brown nitrogenous polymers and copolymers called melanoidins (step G). These can be off flavours (bitter), off aromas (burnt, onion, solvent, rancid, sweaty, cabbage) or positive aromas (malty, bread crust-like, caramel, coffee, roasted). Step H in Figure 1 illustrates a direct route to fission products from N-substituted glycosylamines, without the formation of an ARP (Amadori rearrangement product)..
Temperature and time
Studies of model systems showed that an increase in temperature and/or time of heating resulted in increases in colour development, the carbon-to-nitrogen ratio and the degree of unsaturation and the chemical aromaticity.
Composition of the system
Pentose sugars (e.g. ribose) react more readily than hexoses (e.g. glucose) which, in turn, are more reactive than disaccharides (e.g. lactose).
Of all the amino acids, lysine results in the most colour in the Maillard reaction, due to its Î -amino group; cysteine results in the least colour. Therefore, foods containing proteins that are rich in lysine residues (e.g. milk proteins) are likely to brown readily. The sugar-to-amino-compound ratio also influence the amount of colour produced. For example, a glucose-glycine model system containing 65% water and stored at 65oC showed a rapid increase in colour formation as the glucose-to-glycine ratio was decreased (e.g. from 10:1 or 2:1 to 1:1 or 1:5). In foods, attempts to prevent the reaction should be directed towards removing one of the reactants: the amino compounds (for carbohydrate-rich foods) or the reducing sugars for protein-rich foods.
Water activity
Figure 1 shows that water is produced during the Maillard reaction. Thus, as a consequence of the law of mass action, the reaction occurs less readily in foods with a high aw value. In addition, the reactants are diluted at high aw values while, at low aw, the mobility of reactants is limited, despite their presence at increased concentration. In practice, the Maillard reaction occurs most rapidly at intermediate aw values (0.5-0., and aw is of most significance to the reaction in dried and intermediate-moisture foods (IMFs), which have aw values in this range.
pH
Low pH values (£ 6) favour the formation of furfurals from Amadori rearrangement products, while the routes to reductones and fission products are preferred at a high pH (> 6). However, in practice, the effect of pH is not this clear cut, and reactions take place by all three pathways, with the pH of the system influencing the ratio of products formed. For sugar-glycine systems the descending order of color development at pH lower than 6 was xylose > fructose >glucose >lactose > maltose; at pH 6 the order was xylose > glucose > fructose > lactose > maltose. This suggested that in Maillard browning the rate of color development is not directly related to the structural stability of the sugars.
http://www.agsci.ubc.ca/courses/fnh/410/colour/3_82.htm
Missy
- FJohnSharp
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I spent a week on this in grad schoolmissy wrote:avanutria - you forgot this part:
Maillard Reaction
Maillard reaction is a type of non-enzymatic browning which involves the reaction of simple sugars (carbonyl groups) and amino acids (free amino groups). They begin to occur at lower temperatures and at higher dilutions than caramelization.
Chemistry of the reaction ...
"Meon an phobail a thogail trid an chultur"
(The people’s spirit is raised through culture)
Suburban Symphony
(The people’s spirit is raised through culture)
Suburban Symphony
- Flyingcursor
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emmline wrote:Golly apples Fly! Did you miss that whole Lorna the Jungle Queen thread a while back? (Pre-divestiture)Flyingcursor wrote:... which leads me to believe Bloomfield is having a little fun. It's not Bloomfield's normal style.
I musta missed it. Sad.
I'm no longer trying a new posting paradigm
- chas
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I have no problem with intelligent design (aka guided evolution); in fact I have many colleagues who believe in it. I'm not sure it should be taught as science, though. On the other hand, I don't think evolution should be taught as though we know everything about it, nor that we understand how it works, nor that there aren't many points of debate.Walden wrote:The lampooning of the very idea of intelligent design (and boycotting of the Kansas government's hearing of the matter) is pretty hard evidence that the "establishment" is indeed very closed minded and egotistical on this matter. Yes, yes, "I work with it every day, and it is a daily fact of life" is a great argument. . .
But there are too many zealots out there. I've heard more than one "expert" say, "Evolution is the most tested theory in the history of science." That's a load of crap. There is almost irrefutable evidence for it, but it's something that really can't be tested as I understand the word test. What tests have been done? (Relativity is a theory that has been tested: experiments have been designed, the results have been predicted, and the results have agreed with the theory.) If it's such a good theory, and we know God has nothing to do with it, why are there such gaping holes in our understanding? How come evolutionary biologists can't agree on how it happens? Why haven't we been able to discover the missing link? I think people who claim to know everything there is about evolution and refuse to give the other side the time of day do a disservice to their field and its perception by the populace as a whole.
I think if these questions were brought up in the teaching of evolution, those in the intelligent design camp wouldn't have such issues with the way evolution is taught. I really don't think it would hurt our youth if they were told that some scientists believe that evolution is gradual, some think it happens in bursts, some think there's a "higher power" involved; the truth is we really don't know for sure. Heck, I didn't believe in atoms, and when I voiced my skepticism to my junior high science teacher, he thought it was a perfectly healthy attitude. And I work with them now, so it obvoiusly didn't hurt me to have a teacher who said it was valid not to believe in atoms till I convinced myself.
Charlie
Whorfin Woods
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- Nanohedron
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- Nanohedron
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Man...first 32F, now "Maillard Reactions". So browning isn't miraculous; just wait 'til your inevitable meeting with your Keebler elves. There will be a wailing and gnashing of teeth, I can tell you.FJohnSharp wrote:I spent a week on this in grad schoolmissy wrote:avanutria - you forgot this part:
Maillard Reaction
Maillard reaction is a type of non-enzymatic browning which involves the reaction of simple sugars (carbonyl groups) and amino acids (free amino groups). They begin to occur at lower temperatures and at higher dilutions than caramelization.
Chemistry of the reaction ...
- dfernandez77
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*raises hand*Cranberry wrote:I don't know a single person who disagrees that water freezes at 32º F.
Actually, altitude (atmospheric pressure) is a factor. It's simple...
Anyway, isn't where the world came from and where it will go irrelevant? I mean, here we are, and we can't change it - so why all the fuss?The result for the specific case of the change in the melting point of a substance is given by:
d T/T fusion = [DV fusion / DH fusion] x d P, where d T, and d P are the change in the temperature and pressure respectively, and DV fusion, DH fusion and Tfusion are the change in the enthalpy (the heat absorbed or given off), the change in volume, and the melting point of the substance at 1 atmosphere applied pressure, respectively. Note that DH fusion is always positive -- to melt a substance always requires input of heat energy; DV fusion is usually positive, but is negative for water. For solids and liquids d T/T fusion is very small.
Daniel
It's my opinion - highly regarded (and sometimes not) by me. Peace y'all.
It's my opinion - highly regarded (and sometimes not) by me. Peace y'all.