Application 1
CN201810861140.6 discloses an energy storage lead-acid battery life enhancing solution and a preparation method thereof. The energy storage lead-acid battery life enhancing solution comprises the following raw materials by weight: 10-16 parts of aluminum ethylphosphate, 16-27 parts of dithiothreitol, 6-14 parts of diallyl dimethyl ammonium chloride, 11-15 parts of sodium thioglycolate, 6-12 parts of chromium chloride, 5-10 parts of azelaic acid, and 45-60 parts of water. The energy storage lead-acid battery life enhancing solution of the present invention is composed of a combination of aluminum ethylphosphate, dithiothreitol, diallyl dimethyl ammonium chloride, sodium thioglycolate, chromium chloride, azelaic acid, and water. The battery prepared using the energy storage lead-acid battery life enhancing solution has advantages such as high cycle life, low capacity degradation rate, and strong charging acceptance ability, and has good social and economic value; The preparation method is simple and conducive to achieving industrial production.
Application 2
CN201310368942.0 reported an anaerobic enrichment culture medium and its preparation method, which includes peptone, yeast extract, brain heart extract broth, glucose, sodium thioglycolate, hemin, vitamin K1, anticoagulant, anaerobic indicator, and distilled water; According to its special ratio, a culture medium that can promote the proliferation of anaerobic bacteria can be prepared. This culture medium can be applied to the cultivation of anaerobic pathogens in clinical practice, which can improve the positive detection rate of anaerobic pathogens.
Application 3
CN202010912802.5 reported a culture medium for isolating and counting Clostridium butyricum, belonging to the field of microbial isolation and counting. This includes 15.0g of pancreatic casein peptone, 3.0g of beef extract powder, 1.0g of yeast extract powder, 5.0g of sodium chloride, 0.5g of L-cysteine hydrochloride, 0.5g of sodium thioglycolate, 10.0g of xylose, 0.04g of bromothymol blue, 15.0g of agar powder, 900ml of purified water, 0.25g of D-cycloserine, 0.012g of kanamycin sulfate, and 25ml of egg yolk. Compared with the existing technology, the beneficial effects of the present invention are: 1. By analyzing the unique physiological characteristics of Clostridium butyricum and making targeted formula combinations and adjustments, the culture medium of the present invention can clearly distinguish Clostridium butyricum from other bacteria in visual observation, thereby achieving the purpose of separating and counting Clostridium butyricum. 2. The effect is significant, directly effective, and cost-effective.