A method and bacterial strain for in-situ restoration of arsenic-contaminated high-saline water using cyanobacteria
An in-situ remediation and saline-alkaline water technology, applied in the direction of microorganism-based methods, water pollutants, chemical instruments and methods, etc., can solve the problems of secondary release of arsenic, arsenic desorption, etc. The effect of high adaptability, convenience and cost
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Embodiment 1
[0021] The separation and identification of embodiment 1 cyanobacteria
[0022] 1. Separation of cyanobacteria: Separation of cyanobacteria from arsenic-contaminated water body soil, sediment, water and algae biofilm in saline-alkali areas.
[0023] (1) Cultivation: Weigh 5g (wet weight, no drying) of soil and sediment removed from impurities and add them to a 250mL Erlenmeyer flask, add 50ml of water samples from Xinjiang Kuitun 123 group alkali drainage canal (salinity 15‰, pH8 .24), then add 100mL of sterilized NaCl with a final concentration of 5‰ (5g / L) and a final concentration of 5mg / L NaAsO 2 and 36mg / L CaCl 2 2H 2 The BG11 liquid culture medium of O was cultivated under the conditions of temperature of 25°C, light intensity of 2000lux, and light / darkness of 12h / 12h. When algae grow in the culture solution, the culture solution is mixed with sterile water by 10 -1 、10 -2 、10 -3 , 10 -4 、10 -5 、10 -6 Concentration gradient dilution, use a coating bar to coat in...
Embodiment 2
[0040] (1) Preparation of cyanobacteria: Inoculate cyanobacteria CCTCC NO: M 2019135 into 500ml containing 36mg / L CaCl 2 2H 2 In the Erlenmeyer flask of the BG11 liquid culture medium of O, and be placed on 25 ℃, light intensity 2000lux, light / darkness are in 12 / 12 environment, cultivate to logarithmic growth phase, obtain culture fluid (cyanobacteria OD 685 =0.7), the culture solution was centrifuged at 5500rpm for 20min, and after the supernatant was removed, the bacterial cell precipitate was collected, which was the cyanobacterial cell. Take a small amount of thalline precipitation, fix the cells with 2.5% aqueous solution of pentanediol with a mass concentration, after dehydrating with ethanol, dry in a freeze dryer (-80°C, vacuum environment) for 48h, take it out, and observe the cyanobacteria thallus by SEM, as figure 1 .
[0041] (2) Restoration of simulated water samples polluted by high salinity and alkali arsenic: BG11 liquid culture medium added with 25g / L NaCl a...
Embodiment 3
[0045]The NaCl concentration is adjusted to 35g / L in embodiment 2, other is the same as embodiment 1, carries out repair and the inspection of stability, the result shows, through laboratory simulation arsenic polluted water experiment, be 35g / L in salt content, different arsenic pollution Level (10mg / L, 20mg / L, 40mg / L) of the water environment, using cyanobacteria CCTCC NO: M 2019135, after 14 days of in-situ restoration, the removal rate of arsenic reached 73.67%, 74.84%, 73.48% respectively . After the stability detection of arsenic pollution in the laboratory, in a 35g / L saline environment, using the simulated arsenic-contaminated water sample repaired by the described cyanobacteria, after evaporation and redissolving, different arsenic pollution levels (10mg / L, 20mg / L, 40mg / L) still maintained a good removal rate, respectively: 51.02%, 47.17%, 45.71%.
[0046] According to the method of the present invention, through laboratory simulation of high salinity arsenic contam...
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