Anaerobic Bacillus ha and its application in degrading nitrogen oxides
A technology of anaerobic bacillus and culture, applied in the application field of biological treatment of nitrogen oxides, can solve the problems of low regeneration rate, high cost, and no longer have the ability to complex and absorb NO, and achieve a strong heat resistance Effect
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Embodiment 1
[0030] Example 1: Separation, purification and identification of Anoxybacillus contaminans HA
[0031] 1. Separation and purification of Anoxybacillus contaminans HA
[0032] AnoxybacilluscontaminansHA is selected from the sludge of the BioDeNOx reactor of our research group. The specific steps are as follows:
[0033] Basic medium, the preparation method is as follows: glucose 2000mg·L -1 , KH 2 PO 4 500mg·L -1 , K 2 HPO 4 500mg·L -1 , MgSO 4 ·7H 2 O100mg·L -1 , CaCl 2 100mg·L -1 , CuSO 4 1mg·L -1 , FeSO 4 1mg·L -1 , MnSO 4 5mg·L -1 , Na 2 MoO 4 1mg·L -1 , ZnCl 2 2mg·L -1 , The solvent is water, pH 7.0, and sterilization at 121°C for 20 minutes.
[0034] Fe II (EDTA)-NO solution preparation method: use equimolar FeSO 4 ·(NH 4 ) 2 SO 4 ·6H 2 O and Na 2 EDTA is configured as Fe in oxygen-driven deionized water II (EDTA) solution, then use 1mmol / L NaOH aqueous solution to prepare Fe II (EDTA) Adjust the pH value of the solution to about 7.0, pour it into a 500mL absorption bottle, pass i...
Embodiment 2
[0048] Example 2 Anaerobic Bacillus HA fermentation broth
[0049] (1) Inclined surface cultivation
[0050] The anaerobic bacillus HA was inoculated into a slant medium, cultured at 55°C for 3 days to obtain a bacterial slant; the final concentration of the slant medium was composed of 2000 mg·L glucose -1 , NaNO 3 1000mg·L -1 , KH 2 PO 4 500mg·L -1 , K 2 HPO 4 500mg·L -1 , MgSO 4 ·7H 2 O100mg·L -1 , CaCl 2 100mg·L -1 , CuSO 4 1mg·L -1 , FeSO 4 1mg·L -1 , MnSO 4 5mg·L -1 , Na 2 MoO 4 1mg·L -1 , ZnCl 2 2mg·L -1 , The solvent is water, pH value is 7.0, agar 18g·L -1 .
[0051] (2) Seed cultivation
[0052] Pick a colony from the slant surface of the bacterial cell and inoculate it into a seed culture medium, culture at 55°C for 1 day to obtain a seed liquid; the final concentration of the seed culture medium is composed of 2000 mg·L glucose -1 , NaNO 3 200mg·L -1 , KH 2 PO 4 500mg·L -1 , K 2 HPO 4 500mg·L -1 , MgSO 4 ·7H 2 O100mg·L -1 , CaCl 2 100mg·L -1 , CuSO 4 1mg·L -1 , FeSO 4 1mg·L...
Embodiment 3
[0055] Example 3: Denitrification performance test of Anoxybacillus contaminans HA
[0056] 1. Investigate the reduction of Fe by anaerobic bacillus HA under different initial pH conditions II (EDTA)-NO performance
[0057] The experiments of reducing Fe(II)EDTA-NO by anaerobic bacillus HA at different initial pHs have found that the pH has high denitrification ability at pH 7.0. From the perspective of practical application, pH=7.0 is the best pH. When the degradation rate is the highest, the specific implementation steps are as follows:
[0058] Take Fe II (EDTA)-NO is the only nitrogen source (concentration 5mmo1·L -1 ), according to the volume concentration of 1% inoculum 600 0.4 bacteria-containing suspension (prepared by the method in Example 2) was inoculated into Fe with different pH values II (EDTA)-NO liquid selective medium (pH value respectively 5.0, 6.0, 7.0, 8.0, 9.0), 55℃, 160rpm shaking culture 24h, obtain the culture solution, adopt spectrophotometric method to measu...
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