Difference between revisions of "Mycelium Leather"

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Since an electronic CO<sub>2</sub> sensor costs 60 CHF I make an analog one. Henry's law states that the amount of a dissolved gas in water is proportional to the partial pressure in the air above the water. Furthermore, dissolved CO<sub>2</sub> lowers the ph of water. This means that by filling a small bowl with distilled water and measuring its pH we can guess the CO<sub>2</sub> concentration of the air. Since the math are complicated, we just assume a linear (or exponential) relation and calibrate with the known atmospheric concentration and gas mixtures with CO<sub>2</sub> made from baking soda and vinegar.  
 
Since an electronic CO<sub>2</sub> sensor costs 60 CHF I make an analog one. Henry's law states that the amount of a dissolved gas in water is proportional to the partial pressure in the air above the water. Furthermore, dissolved CO<sub>2</sub> lowers the ph of water. This means that by filling a small bowl with distilled water and measuring its pH we can guess the CO<sub>2</sub> concentration of the air. Since the math are complicated, we just assume a linear (or exponential) relation and calibrate with the known atmospheric concentration and gas mixtures with CO<sub>2</sub> made from baking soda and vinegar.  
  
'''''pH = a + b [CO<sub>2</sub>]'''''
+
'''''[CO<sub>2</sub>] = a(T) + b(T)*pH'''''
  
 
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Revision as of 17:56, 13 May 2023

The dutch company Ecovative grows Reishi mycelium into the air, separates it from the substrate and compresses it to make leather. I try to recreate this procedure.

Literature

Growth environment

To prevent fruiting, CO2 concentration is kept at 5-7% and the temperature at +-30° C. A mister maintains the humidity above 99%. The hyphae grow up to escape CO2 and get oxygen.

Airflow increases homogeneity by delivering humidity and/or minerals, by eliminating micro climates or by mechanical force.

Minerals in the mist increase growth speed by osmotic pressure.

A humid substrate means faster growth but lower density.

Growth substrates

From the patent "Increased homogeneity of mycological biopolymer grown into void space":

Corn stover 600 g
Poppy seeds 144 g
Maltodextrin 25 g
Calcium sulfate 8 g
Water 1600 g
Spawn 288 g

Procedure

After compression, the mycelium is left for 3 days to strengthen, then dried at 43° C followed by heat pressing if desired.

My own experiments

First test in a monotub

First I made grain spawn out of bird seeds. Then I sterilized a box with rubbing alcohol, lined the bottom with a clean plastic film and spread sterilized substrate made of 0.75l hardwood pellets, 0.2l wheat bran and 0.75l water onto the film. I distributed some grain spawn on top of it, closed the box and waited.

After one day, the mycelium already comes out of the grain spawn.
The mycelium has almost colonized the whole surface, but probably got crushed by water droplets

The mycelium colonized the surface and grew about 1.5 cm thick as in the pictures. After four days I sprayed water on it to keep it humid, but the droplets crushed the fluffy mycelium and it stopped growing.

My first try to do mycelium leather

I let it dry and peeled it off the substrate. It was fused with the chunks of grain spawn, so I didn't get one big tissue but many small pieces, the biggest one shown in the picture. Depending on how much it was crushed it feels like paper (but more fragile) or like a very soft, light and flexible tissue. It is very thin and rips apart easily.

What to improve

The grain spawn should be broken into smaller pieces using disposable gloves, and evenly mixed with the substrate. Using unpopped popcorn as grains may be a good idea since it doesn't stick together as much as bird seeds.

Experimenting with substrates in petri dishes

On the 2.5.2023 I filled petri dishes with Agar, malt extract, maizena, yeast extract and gypsum according to the following table.

Nutrient tests on petri dishes
Ingredient Substrate Malt Maizena Yeast Gypsum 8 days
1 Agar very bad
2 Agar 0.5 g good
3 Agar 0.05 g very bad
4 Agar 0.5 g 0.05 g bad
5 Agar 0.5 g 0.05 g 0.025g bad
6 Agar 0.5 g very bad
7 Agar 0.5 g 0.05 g very bad
8 Agar 0.5 g 0.025g bad
9
10 Pellets & Bran good
11 Pellets & Bran 0.5 g very good
12 Pellets & Bran 0.05 g very good
13 Pellets & Bran 0.025g very good

To accurately measure those values I dissolved the nutrients in water solutions and used a pipetter. However gypsum is not soluble so the quantities may be inaccurate, and Maizena clumped together, so I put clumps of it into the petri dishes.

Heated inoculation chamber

It would be nice to have a chamber that can heat sterilize itself and the substrate, and then keep the temperature constant at 25 or 30° C. I am buying the XH-W1209 thermostat: https://www.berrybase.ch/xh-w1209-digitales-thermostat/temperaturschalter-12v-frei-programmierbar

A very cheap CO2 meter

Since an electronic CO2 sensor costs 60 CHF I make an analog one. Henry's law states that the amount of a dissolved gas in water is proportional to the partial pressure in the air above the water. Furthermore, dissolved CO2 lowers the ph of water. This means that by filling a small bowl with distilled water and measuring its pH we can guess the CO2 concentration of the air. Since the math are complicated, we just assume a linear (or exponential) relation and calibrate with the known atmospheric concentration and gas mixtures with CO2 made from baking soda and vinegar.

[CO2] = a(T) + b(T)*pH

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