Overview
| weight | 380kg | source | 380V |
| temperature range | 18-30 | measuring range | 18-30 |
| Processing customization | yes | Sterilization method | high temperature |
| model | KLT-KT01 | volume | 1m3 ± 0.1m3 |
| Studio size | eight hundred and fifty × one thousand and eighty × 1100mm | Appearance size | one thousand four hundred and sixty × one thousand two hundred and twenty-five × 1820mm |
| temperature control | Cycle temperature control | Humidity range | ≤ ± 3% RH |
| humidity control | Refrigeration dehumidification and steam humidification | Sealing performance | Gas leakage less than 5% |
| brand | Kolut | ||
Product Details
According to the set pressure, gas flow and spray time, spray bacteria. Use a fan to stir while spray to stain bacteria. Spray to contaminate bacteria 5. At the same time, sample the control group and the test group aerosol cabinet (or room) before disinfection, as the positive control (i.e. the amount of contaminated bacteria) before the start of the test in the control group and before the disinfection treatment in the test group. The number of positive control bacteria in the air of the aerosol cabinet (or room) should reach 5x104 cfu/m3~5x 100 cfu/m3. During the simulated on-site test, a six stage sieve air impact sampler is used for sampling. When sampling, the six stage sieve air impact sampler is placed at a height of 1m in the center of the cabinet room (sampling method is carried out according to the sampler user manual). During laboratory testing, a liquid impact sampler is used for sampling, and the sampler is placed in the center of the cabinet.
At the same time, pre operation bacterial concentration sampling was conducted in the experimental group and control group aerosol chambers, with sampling time ranging from 1 minute to 5 minutes. The sampling head should be facing upwards during sampling. It is required that the number of positive control bacteria in the air of the aerosol chamber should be between 5.0X10 CFU/m2 and 5.0X105 CFU/m ', otherwise the test will be invalid.
Operate the tested prototype to the highest sterilization condition specified by the manufacturer (if not specified by the manufacturer, the highest wind speed and maximum air outlet state shall prevail). For air conditioner products, conduct testing based on the air supply status.
After the completion of spray bacteria infection, the aerosol chamber of the control group and the test group shall be sampled before disinfection at the same time, as the positive control (i.e. the amount of bacteria infection) before the start of the test of the control group and before the disinfection treatment of the test group. The number of positive control bacteria in the air of the aerosol room should reach 5X10 * CFU/m3~5X105CFU/m3 (the number of positive control bacteria in the control group should not be less than 5X10 * CFU/m3 at one time after the disinfection test).
When the ultraviolet air disinfector is activated for the predetermined first time (0.5 times the time specified in the product manual), samples are immediately taken from both the experimental group and the control group aerosol chambers simultaneously; Continue to apply until two predetermined disinfection times (as specified in the product manual), and sample the experimental group and control group aerosol chambers simultaneously again.
