A kind of determination method of biomass in activated sludge embedding gel
A technology of activated sludge and determination method, which is applied in the field of determination of biomass in embedded gel, can solve the problems such as difficult determination of embedded particle biomass, and achieve repeatability, high sensitivity and high repeatability of measurement results Effect
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Embodiment 1
[0030] Utilize the present invention to measure the biomass in the anammox embedding particle, the specific process is as follows:
[0031] Take a certain volume of anaerobic ammonium oxidation sludge with stable treatment effect, according to MLVSS (in mg): 10, 30, 50, 70, 90, 110, 130, 150. Rinse with 50ml of PBS and pour into the first in a triangular beaker. Another 20ml volume of anammox embedding particles was taken, washed with 50ml PBS after crushing, and then poured into the second conical beaker. Add 1ml of lysate to the first conical beaker and the first conical beaker respectively (according to every 10 7 The ratio of each cell to 1ml of cell lysate), and the protein samples in the anammox sludge and embedded particle samples were extracted respectively by ultrasonic waves. Working conditions: ultrasonic (11kHz, 10s×84 cycles, interval 1min, ice bath), oscillation (5×30s, interval 1min, ice bath). Centrifuge the treated suspension at 4°C and 14,000 rpm for 30 mi...
Embodiment 2
[0036] Using the present invention to measure the biomass in the denitrification embedding particles, the specific process is as follows:
[0037] Take a certain volume of denitrification sludge with stable treatment effect, according to MLVSS (in mg): 10, 30, 50, 70, 90, 110, 130, 150. Rinse them with 50ml of PBS and pour them into a triangular beaker . Another 20ml volume of denitrification embedding particles was taken, washed with 50ml PBS after crushing, and then poured into a triangular beaker. Add 1ml of lysate to the first conical beaker and the first conical beaker respectively (according to every 10 7 The ratio of each cell to 1ml of cell lysate), and the protein samples in the denitrification sludge and embedded particle samples were extracted respectively by ultrasonic waves. Working conditions: ultrasonic (11kHz, 10s×84 cycles, interval 1min, ice bath), oscillation (5×30s, interval 1min, ice bath). Centrifuge the treated suspension at 4°C and 14,000 rpm for 30 ...
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