Simple method for quickly predicting whether water quality is biologically stable
A bio-stable and water-quality technology, applied in the preparation of test samples, material excitation analysis, fluorescence/phosphorescence, etc., can solve the problems of cumbersome measurement steps, and it takes a long time to determine the maximum growth value of bacteria, and achieves high promotion value. , the prediction method is simple and fast effect
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Embodiment 1
[0048] Method Description
[0049] Measuring instruments, utensils and materials
[0050] Constant temperature incubator; sterile operating table; alcohol lamp; ATP tester; 40ml carbon-free sampling bottle;
[0051] Test bacteria
[0052] The bacterium used in the embodiment is P17 (Pseudomonas fluorescense) and NOX (Spirillum sp.)
[0053] test preparation
[0054] 1. Preparation of 1000╳standard carbon solution (the carbon concentration of acetic acid is 1000mg / L)
[0055] NaAc:5.67g / L
[0056] 2. Preparation of 1000╳buffer solution
[0057]
[0058] 3. Preparation of 2╳standard carbon solution (the carbon concentration of acetic acid is 2000μg / L)
[0059] 1000╳standard carbon solution: 2ml / L
[0060] 1000╳Buffer solution: 1ml / L
[0061] 4. Cultivation of inoculated bacterial mother solution in the test
[0062] Inoculate P17 and NOX colonies into 2╳ standard carbon solution for constant temperature cultivation at 30°C for about one month, and store them in cold ...
Embodiment 2
[0074] Refer to Example 1 for method description, measuring instruments, utensils and materials, etc.
[0075] This assay method specifically comprises the steps:
[0076] (1) Preparation of the test bacterial liquid: a specific bacterial culture liquid is used as the test bacterial liquid. Specific bacteria refer to bacteria that are in the maintenance growth stage after being cultured at room temperature for 1 month; the type of bacteria is NOX (Spirillum sp.).
[0077] (2) Preparation of water samples: use ultrapure water (JC) as a control water sample, and prepare pure water (CS) (pure water does not contain bacteria, so no conversion is required).
[0078] (3) Preparation of the inoculated water sample: add the same amount (50 μl of bacteria solution / ml of water sample) of the bacterial test solution to the water sample to be tested.
[0079] (4) ATP fluorescence detection: at room temperature, test inoculated pure water (CS) and inoculated ultrapure water (JC), record ...
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