Coffee review

Professional coffee roasting| Can Taguchi make mistakes? Glass conversion temperature and coffee bitterness

Published: 2024-11-03 Author: World Gafei
Last Updated: 2024/11/03, Professional barista communication, please pay attention to coffee workshop (Weixin Official Accounts cafe_style). Usually, the more serious people are, the easier it is to get into the mud and difficult to get out. The more hard they are, the deeper they sink. For coffee bitter cause of discussion, the mainstream of today's argument is attributed to chlorogenic acid, and domestic coffee works are not many, Mr. Taguchi's translation is a very important source of relevant knowledge, especially

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Usually, the more serious people are, the easier it is to get stuck in the mud, and the harder they are, the deeper they get. As for the discussion of the causes of the bitterness of coffee, the mainstream way of saying is to blame it on chlorogenic acid, but there are not many works on coffee in China. Mr. Taguchi's translation is a very important source of relevant knowledge, especially in the Coffee equation in which he cooperated with Danbu. Taguchi no longer only talks about Taguchi's point of view, but with the theoretical support of Danbu, that book can be said to be very practical and valuable. However, it is reasonable to say that the morphological transformation in the process of coffee roasting and heating, that is, the so-called transformation of glassy state and rubber state, is linked to the chemical reaction of chlorogenic acid, which in turn affects whether the flavor of coffee is bitter or not. Not to mention how to achieve it in practice.

I've been hanging around on @ atti @ bug since I had friends there last night. I think it's necessary to try to sort out the information I collected and my own thoughts again. I hope it will be of some help to you.

Taguchi uses a simple dichotomy to express the heating reaction of chlorogenic acid in Mena stage. First, decomposition (hydrolysis) with water will produce quinic acid (sour) and caffeic acid (bitter). Further heating of caffeic acid will turn into vinyl catechol polymer (bad bitterness). Second, it is dehydrated and condensed into chlorogenic acid lactone (good bitter taste). When the coffee is in a rubber state with high water content, it is easy to decompose chlorogenic acid with water, so Mr. Tian advocated that it should go through the rubber zone as soon as possible when baking, but did not say how to do it to achieve its goal, so the believers had to rely on their own skills.

The so-called glassy / rubber state of coffee refers to the physical change process of coffee beans from hard (glassy) to soft and elastic (rubber) > hard (glassy) due to changes in temperature and water content during coffee roasting and heating.

Source: www.probatburns.com

The above picture cites the study of Schenker and Geiger, where the solid black line sliding from top left to right represents the boundary between the glassy state and the rubber state of coffee beans at different core temperatures and moisture contents, known as glass transition temperature (Glass transition temperature). In stage (1), the core temperature of the bean is lower than the glass transition temperature, so most of the tissue of the bean is in the hard glassy state; in stage (2), the core temperature of the bean is higher than the glass transition temperature, so most of the tissue of the bean is in a soft and elastic rubber state, and at the same time, due to the pressure formed by internal water vapor and other gases, the bean at this stage has the highest expansion rate. In stage 3, the core temperature of the bean is lower than the glass transition temperature again, at this time the moisture content of the bean is very low, and most of the tissue is in the dry and hard glass state.

Since the diagram expresses the relationship between the core temperature and moisture content of beans in a two-dimensional way, without taking into account the baking time, the red line with the left arrow on the picture is trying to express the path of the transition of beans between the glassy state and the rubber state during baking. the larger the area framed by the red line and glass conversion temperature, the greater the proportion of beans in the rubber state during the baking process, which can be inferred from this. The higher the proportion of chlorogenic acid decomposed by adding water.

The picture above is very clear, but it may be misleading to mark the specific figures, and so are the illustrations in Taguchi's book, because their numbers are a long way from everyone's operational experience.

Let's take a look at the source of the literature they quoted.

Literature source

Fig 33 above is the literature source of the drawings in probatburns and Taguchi. Have you noticed that this is a research paper by an official Swiss research institute, which does not show the figures of temperature and moisture content, which means that this is a schematic diagram, not the result of experimental measurements, which proves that the figures marked on it are unreliable.

In Fig 33, there are two baking modes: LTLT (slow baking at low temperature) and HTST (fast baking at high temperature). We found that the area of rubber state occupied by HTST is larger than that of LTLT, implying that in HTST mode, the proportion of chlorogenic acid decomposing with water should be higher. But the total baking time of HTST (high temperature fast baking) is only 180s, which is much lower than the 720s of LTLT (slow baking at low temperature). Isn't it faster to pass through the rubber state? How can the proportion of decomposition reaction by adding water be relatively high?

Remember this picture?

In the picture on the left, high temperature and fast drying will retain more water, while in the picture on the right, low temperature and slow drying, then after half the process of about 360 seconds, the evapotranspiration ratio has reached the lower limit, indicating that the water content in the Mena stage is already quite low.

In contrast, the meaning of rapid passage through the rubber state does not seem to have a direct relationship with time, but rather with how much water can evaporate during the dehydration stage (before turning yellow).

Suppose Tian Lao's argument of chlorogenic acid decomposition and dehydration condensation is correct, do you know how to bake it? For example, if you plan to bake the beans at the end of 12 minutes, then set the firepower and throttle to the extent that you can dehydrate and turn yellow at 5, 30, 6, 00, and then stimulate the fire to increase the fragrance or adjust the firepower down to master the development of various fragrances. This is another story.

Then think again, if you want to bring more water into the Mena stage, how to bake it?

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