Method for preparing nano metal sulfides
A nano-metal and sulfide technology, applied in fermentation and other directions, can solve the problems of high temperature and impure products, and achieve the effects of uniform distribution, easy particle size control, and uniform reaction process.
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Embodiment 1
[0039] Configure the medium according to the following components: sodium acetate 1500mg; CaCl 2 .2H 2 O 80mg; MgSO 4 .7H 2 O 150mg; EDTA 20mg; Yeast extract 1200mg; K 2 HPO 4 1000mg; (NH 4 ) 2 SO 4 1500mg; KH 2 PO 4 800mg; FeSO 4 .7H 2 O 10mg; trace element solution 3ml; deionized water 1500ml. The pH of the medium was 7.
[0040] Wherein the trace element solution is composed of: H 3 BO 3 240 mg; Na 2 MoO 4 .2H 2 O 70mg; CuSO 4 7 mg; MnSO 4 .4H 2 O 200mg; ZnSO 4 .7H 2 O 24mg; deionized water 1650ml.
[0041] Inoculate 1 / 20 portion of Rhodobacter sphaeroides into the sterilized culture medium, and cultivate it for 20 days under light of 2500 lux, room temperature, and anaerobic conditions, as the inoculum;
[0042] The cultured Rhodobacter sphaericus was centrifuged at 6000rpm for 10min, the precipitate was washed with normal saline and centrifuged twice. Then mix the obtained 10% concentrated bacteria with 10% polyvinyl alcohol solution cooled to ...
Embodiment 2
[0046] Using Rhodopseudomonas palustris, adding 0.20mol / L of Pb(AC) a 10ml, transformation culture time 36h, other conditions and steps are identical with embodiment 1, the product nano-lead sulfide average particle diameter that obtains is 25nm, productive rate 90%, black powder, x-ray analysis result is cubic structure, and purity is high.
Embodiment 3
[0048] Rhodopseudomonas palustris (Rhodopseudomonas palustris) and spherical red bacillus (Rhodobactersphaeroides) were mixed and immobilized by 1:1, and the transformation culture time was 40h. Other conditions and steps were the same as in Example 1. 23nm, 89% yield, black powder, X-ray analysis shows cubic structure, high purity.
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