Email:
info@huakegroup.in
H
U
A
K
E
HUAKE EN II Vaporized Hydrogen Peroxide Generator
1. **Thorough Disinfection**: Achieves a kill rate of >6 logs against persistent microorganisms such as Bacillus subtilis.
2. **Safe and Environmentally Friendly**: Decomposition products are water and oxygen, with no risk of chemical residue.
3. **Flexible Deployment**: Modular design enables rapid switching between mobile and fixed installation scenarios for diverse applications.
Product Categories:
HUAKE EN II Vaporized Hydrogen Peroxide Generator
Keywords:
- Product Description
-
Performance advantages:
1. **Thorough Disinfection**: Achieves a kill rate of >6 log against persistent microorganisms such as Bacillus subtilis.
2. **Safe and Environmentally Friendly**: The decomposition products are water and oxygen, with no risk of chemical residues.
3. **Flexible Deployment**: The modular design enables rapid switching between mobile and fixed deployment scenarios.
4. **Smart Control**: Built-in closed-loop concentration feedback system ensures the sterilization process is repeatable and verifiable.Hydrogen peroxide vaporizers have a wide range of applications, particularly in environments that require highly clean and sterile conditions. The following are the primary uses of hydrogen peroxide vaporizers:
1. Pharmaceutical Industry 2. Biotechnology 3. Medical Device Manufacturing 4. Hospital Environmental Disinfection 5. Aerospace 6. Food Industry 7. Electronics Industry 8. Conservation of Cultural Relics and ArtworksTechnical Analysis:
---**Core Technological Advantages**
- **Low-Temperature Flash System**: Employs multi-stage temperature-controlled flash modules to achieve complete vaporization of liquid hydrogen peroxide (vaporization rate > 99.9%), thereby preventing residual liquid droplets.
- **Dynamic Saturation Control**: Utilizing pressure-humidity coupling regulation technology, this system precisely maintains the stable suspended state of vaporized hydrogen peroxide (VHP) without any condensation throughout the entire process.**Intelligent Control System**
- **Process Monitoring Dimension**:
▶ Environmental parameters: Chamber temperature (accuracy ±1℃), relative humidity (accuracy ±3% RH)
▶ Sterilization parameters: VHP concentration (adjustable from 50 to 1000 ppm), steam saturation (≥95%)
- **Dynamically adjustable parameters**:
▶ Flash evaporation temperature (precisely controlled between 80-140℃)
▶ Circulating air velocity (continuously adjustable from 0.3 to 1.2 m/s)
▶ Drug infusion rate (linear control from 0.5 to 5 mL/min)
▶ Sterilization time (freely adjustable from 1 to 240 minutes)**Safe Operation Assurance**
- **Triple Protection Mechanism**:
1. Real-time monitoring of VHP concentration and emergency shutdown in case of exceeding the threshold.
2. Saturation closed-loop control prevents condensation on equipment.
3. The catalytic degradation module ensures residual levels are below 1 ppm (compliant with OSHA standards).
- **Integrated Design**: Integrates the VHP generator with the catalytic degradation unit, enabling fully automated sterilization-degradation processes.**Application Performance**
- Suitable for scenarios such as biosafety laboratories and pharmaceutical cleanrooms.
- Achieve a 6-log inactivation rate for Bacillus subtilis, with a sterilization compliance rate exceeding 99.99%.
- Supports pre-storing parameter combinations to meet the verification requirements of ISO 14937 standard.
Technical Analysis of the Four-Stage Sterilization Process:
**1. Intelligent Startup Phase**
- **System Self-Check Program**:
▶ Automatically verifies sensor accuracy (temperature/humidity/pressure)
▶ Basic environmental prediction: Temperature must be ≥25℃ and relative humidity must be ≥50% RH.
▶ Dynamic dehumidification mechanism: The molecular sieve dehumidification module is activated when humidity exceeds 65%.**2. Dynamic Equilibrium Stage**
- **Precise VHP Regulation**:
▶ The flash evaporation unit is started, generating a hydrogen peroxide aerosol with a particle size of less than 3 μm.
▶ Multi-directional circulation system operation, with spatial concentration deviation controlled within ≤ ±10%.
▶ Compliance Determination: Automatically switch to the next stage once the set concentration (400–800 ppm) or saturation level (≥95%) is reached.**3. Quantitative Sterilization Stage**
- **Process Monitoring System**:
▶ Real-time tracking of CT values (concentration × time), with an accuracy of ±5%.
▶ The electronic batch record system automatically stores sterilization curve data.
▶ Stage termination criteria: Both the preset CT value (≥2000 ppm·min) and the sterilization duration are met simultaneously.**4. Safe Degradation Stage**
- **Fourth-level catalytic decomposition**:
▶ Platinum catalytic bed decomposition efficiency > 99.5%
▶ Residual monitoring: The exhaust concentration is continuously measured below 1 ppm for three consecutive times (compliant with OSHA standards).
▶ System reset: Automatically restores positive environmental pressure and generates an electronically signed sterilization compliance report.**Process Control Characteristics**
- Stage switching: Fully automatic, condition-triggered stage transitions that require no manual intervention.
- Exception Handling: Built-in 25 fault diagnosis codes, supports breakpoint resume functionality.
- Compliance verification: Meeting the stringent requirements of ISO 14937 standard for sterilization process control.
Related Products
Product Information
Contact Us
Service Hotline
Location
No. 28, Dongke Road, Dongcheng Science and Technology Park, Dongcheng District, Dongguan City
QR code
Scan, recognize, and follow