Livestock carcass processing device using useful microorganisms
A corpse treatment and microbial technology, which is applied in the field of corpse treatment devices, can solve the problems of large volume, hard bones, and reduced efficiency of livestock corpse treatment, so as to achieve the effect of reducing efficiency
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experiment example 1
[0069] The corpse decomposition ability was confirmed by Experimental Example 1 as described below.
[0070] 1. Experimental method
[0071] As an example, in order to confirm the decomposing ability of the dead body prepared as above and using the effective microbial culture solution produced in the culture tank 210, the following steps were carried out: 300 ml of drinking water and 0.2% Chlorine dioxide (v / v) is injected into the air after 24 hours to disperse chlorine dioxide in the air.
[0072] Among them, as the solid matter, 20% by weight of humus, 20% by weight of humic acid, 20% by weight of fulvic acid, 20% by weight of charcoal, 10% by weight of rice bran, and a solution of H. The solid matter made of 10% by weight of the culture liquid is fermented at 23 to 35° C. for 90 to 240 hours, and dried to prepare a dormant solid matter with a water content of 14 to 17%.
[0073] Then, add the solid matter to the internal space 110 of the main body 100 and add it to 2 / 5 o...
experiment example 2
[0082] As described below, in Experimental Example 1, the thermophilic properties of the respective strains of the same species of effective microorganisms were confirmed.
[0083] 1. Experimental method
[0084] Bacillus kochii strain, Bacillus horikoshii strain, Bacillus amyloliquefaciens strain, Bacillus methylotrophicus strain, Bacillus subtilis strain Bacillus subterraneus (Bacillus subterraneus) strains, Bacillus firmus (Bacillus firmus) strains, and Bacillus infantis (Bacillus infantis) strains were used as objects, and were inoculated into 5ml of nutrient liquid medium (Nutrient Broth; NB) respectively. , and shaking culture at 35°C for 16 hours, the cultured strain culture solution was allowed to react at 25°C for 1 hour. After adding 1 ml of the culture solution reacted for 1 hour to two tubes, one of the two tubes to which 1 ml of the culture solution was added was allowed to react at 25°C for 3 hours, and the other tube was allowed to react at 90°C 3 hours.
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