Газовый высококачественный генератор азота PSA N2 газовый раствор для фармацевтической перерабатывающей промышленности с бесплатным послесервисным
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Product Description
CAN GAS CAPN /CAPN HP series PSA Nitrogen Gas Generator
CANGAS PSA( pressure swing adsorption) on-site nitrogen generator -product gas technical indicators:
Nitrogen flow rate:5-8000Nm3/h
Nitrogen purity: ≥97%~99.999%
Nitrogen dew point:-20~-80℃
Nitrogen outlet pressure: 0.2~1.0Mpa (adjustable)
CANGAS PSA nitrogen production equipment is divided into: 95%,97%, 98%, 99%, 99.5%, 99.9%, 99.99%, 99.995%, 99.999%,99.9995%
according to nitrogen purity, for your choice.
Nitrogen Generator type: PSA N2 generator , Membrane nitrogen generator , Skid mounted type ,small box type ,container type, trailer type, truck type .
CANGAS PSA( pressure swing adsorption) on-site nitrogen generator -product gas technical indicators:
Nitrogen flow rate:5-8000Nm3/h
Nitrogen purity: ≥97%~99.999%
Nitrogen dew point:-20~-80℃
Nitrogen outlet pressure: 0.2~1.0Mpa (adjustable)
CANGAS PSA nitrogen production equipment is divided into: 95%,97%, 98%, 99%, 99.5%, 99.9%, 99.99%, 99.995%, 99.999%,99.9995%
according to nitrogen purity, for your choice.
Nitrogen Generator type: PSA N2 generator , Membrane nitrogen generator , Skid mounted type ,small box type ,container type, trailer type, truck type .
Pharmaceutical Manufacturers Rely on Nitrogen
Pharmaceutical Processing is the process of drug manufacturing and can be broken down into a range of unit operations, such as blending, granulation, milling, coating, tablet pressing, filling, and others. The Pharmaceutical manufacturing process has precise requirements and manufacturing guidelines for quality. As a result, pharmaceutical manufacturing equipment must comply with good manufacturing practices.
Pharmaceutical processing
Pharmaceutical process development is from research and development, laboratory formulation to commercial production of pharmaceuticals.
While health is a crucially important social and economic asset, both infectious and non-communicable diseases pose a significant threat to the well-being and prosperity of populations. In the pharmaceutical product development process, quality is essential –cutting-edge research, excellent processes, and perfect products make pharmaceutical companies stand out. New diseases require new cures; increased competition requires faster, leaner processes in all operations.
manufacturing of pharmaceutical processing
The pharmaceutical manufacturing process is typically made up of a combination of specific unit processes chosen according to the physical and chemical characteristics of the active pharmaceutical ingredient.
Dry granulation: Compaction of a low-density powder to a granule. The roller compaction process consists of screw feed,
compaction, and milling systems.
Powder blending: A wide range of excipients may be blended to create the final blend used to manufacture the solid dosage form in the pharmaceutical industry. The uniqueness of each drug formulation assures that no two blending processes can ever be identical.
High shear and wet granulation: Commonly used processes for densification, to improve flowability, content uniformity, or
wettability or to improve dispensing qualities.
Fluid bed granulation: Top spray, bottom spray (Wurster), and rotary (tangential spray) are commonly used in the food and
pharmaceutical industries.
Hot-melt extrusion: Utilized in pharmaceutical processing to deliver drugs with poor solubility and bioavailability. Of particular interest is the use of HME to disperse active pharmaceutical ingredients (APIs) in a matrix at the molecular level, thus forming solid solutions.
Drying: Understanding and controlling the moisture content of powders is critical to many pharmaceutical processes. Fluid bed or laminar flow drying conditions impact powder and granules’ physical and chemical characteristics.
Pharmaceutical milling: The process of using rotary cutters in pharmaceutical equipment machinery to remove materials from a workpiece by feeding in at an angle with the axis of the tool.
Compression of powder or granules into tablets: An efficient process for producing a solid dose medication.
Tablet coating equipment: Options include batch process coating pan, off-press continuous coating, or continuous processing.
Pharmaceutical encapsulation: The containment of a solid or liquid dose of a drug in a softshell or hard pre-formed capsule.
Micronization: The process of reducing the particle sizes of pharmaceutical products under very high pressures, shear, turbulence, acceleration, and impact, to make them more stable and clinically effective.
Pharmaceutical processing
Pharmaceutical process development is from research and development, laboratory formulation to commercial production of pharmaceuticals.
While health is a crucially important social and economic asset, both infectious and non-communicable diseases pose a significant threat to the well-being and prosperity of populations. In the pharmaceutical product development process, quality is essential –cutting-edge research, excellent processes, and perfect products make pharmaceutical companies stand out. New diseases require new cures; increased competition requires faster, leaner processes in all operations.
manufacturing of pharmaceutical processing
The pharmaceutical manufacturing process is typically made up of a combination of specific unit processes chosen according to the physical and chemical characteristics of the active pharmaceutical ingredient.
Dry granulation: Compaction of a low-density powder to a granule. The roller compaction process consists of screw feed,
compaction, and milling systems.
Powder blending: A wide range of excipients may be blended to create the final blend used to manufacture the solid dosage form in the pharmaceutical industry. The uniqueness of each drug formulation assures that no two blending processes can ever be identical.
High shear and wet granulation: Commonly used processes for densification, to improve flowability, content uniformity, or
wettability or to improve dispensing qualities.
Fluid bed granulation: Top spray, bottom spray (Wurster), and rotary (tangential spray) are commonly used in the food and
pharmaceutical industries.
Hot-melt extrusion: Utilized in pharmaceutical processing to deliver drugs with poor solubility and bioavailability. Of particular interest is the use of HME to disperse active pharmaceutical ingredients (APIs) in a matrix at the molecular level, thus forming solid solutions.
Drying: Understanding and controlling the moisture content of powders is critical to many pharmaceutical processes. Fluid bed or laminar flow drying conditions impact powder and granules’ physical and chemical characteristics.
Pharmaceutical milling: The process of using rotary cutters in pharmaceutical equipment machinery to remove materials from a workpiece by feeding in at an angle with the axis of the tool.
Compression of powder or granules into tablets: An efficient process for producing a solid dose medication.
Tablet coating equipment: Options include batch process coating pan, off-press continuous coating, or continuous processing.
Pharmaceutical encapsulation: The containment of a solid or liquid dose of a drug in a softshell or hard pre-formed capsule.
Micronization: The process of reducing the particle sizes of pharmaceutical products under very high pressures, shear, turbulence, acceleration, and impact, to make them more stable and clinically effective.
Working Principle
How to select nitrogen generator
Tell CAN GAS purity/ pressure/ flow rate needed in your application, our professional sales team will help you .
Host model | Extended model | Purity（%） | 99.999 | 99.995 | 99.99 | 99.9 | 99.5 | |||||||
CAPN HP-20 | CAPN HP-20 | Capacity（Nm³/h） | 11.2 | 17.6 | 20 | 32 | / | |||||||
Size（mm） | 1500×1500×1700 | |||||||||||||
Weight（KG） | 1000 | |||||||||||||
CAPN HP-20C | Size（mm） | 1600×1550×1750 | ||||||||||||
Weight（KG） | 1050 | |||||||||||||
CAPN HP-30 | CAPN HP-30 | Capacity（Nm³/h） | 18.2 | 28.6 | 30 | 50 | / | |||||||
Size（mm） | 1700×1500×2100 | |||||||||||||
Weight（KG） | 1320 | |||||||||||||
CAPN HP-30C | Size（mm） | 1800×1600×2150 | ||||||||||||
Weight（KG） | 1400 | |||||||||||||
CAPN HP-35 | CAPN HP-35 | Capacity（Nm³/h） | 19.6 | 19.6 | 35 | 56 | 64.4 | |||||||
Size（mm） | 1600×1450×1950 | |||||||||||||
Weight（KG） | 1400 | |||||||||||||
CAPN HP-35C | Size（mm） | 1700×1550×2000 | ||||||||||||
Weight（KG） | 1450 | |||||||||||||
The above table shows some models of nitrogen generators, others can be customizable. | ||||||||||||||
Company Profile
We have the largest professional production base of PSA oxygen generators，PSA nitrogen generator,membrane nitrogen
generator,medical on-site oxygen generator etc air seperation system in China since 1998, covers an area of 28,000m2.
1. One of the most experienced manufacturer of air separation Unit(ASU) in China CAN GAS is one of the first air separation technology developing companies in China, dedicated to researching and developing more suitable onsite medical gas solutions for hospitals.
2. Most professional oxygen generator manufacturer in China
(1)Since establishment, R&D and production of ASU is our professional field.
(2)The only company own High-tech enterprise and new tech product/service certificate for medical PSA oxygen generator.
(3)The most patent certificate for medical oxygen generator and software copyright.
(4)Unique company covering business sectors, medical, commercial and artificial environment.
(5)Trusted by customers and distributors
generator,medical on-site oxygen generator etc air seperation system in China since 1998, covers an area of 28,000m2.
1. One of the most experienced manufacturer of air separation Unit(ASU) in China CAN GAS is one of the first air separation technology developing companies in China, dedicated to researching and developing more suitable onsite medical gas solutions for hospitals.
2. Most professional oxygen generator manufacturer in China
(1)Since establishment, R&D and production of ASU is our professional field.
(2)The only company own High-tech enterprise and new tech product/service certificate for medical PSA oxygen generator.
(3)The most patent certificate for medical oxygen generator and software copyright.
(4)Unique company covering business sectors, medical, commercial and artificial environment.
(5)Trusted by customers and distributors
Certifications
References
Service
After service and Warranty:
Warranty: PERIOD of warranty is 18 months after shipment or 12 months after commissioning, whichever occurs first. It is responsible for CANGAS to analysis, answer breakdowns for users all through the working life of CANGAS oxygen generator. Engineer can be sent on-site for free after-service service if necessary. Please refer to Warranty terms for more information.
Installation & Commissioning & Training: CANGAS service engineer is available to instruct the installation and start up of this plant (6 days at job site with service fee or remotely).If job site service is needed the buyer should prepare flights, accommodation, food and local transportation for CANGAS service engineer.
Installation & Commissioning & Training: CANGAS service engineer is available to instruct the installation and start up of this plant (6 days at job site with service fee or remotely).If job site service is needed the buyer should prepare flights, accommodation, food and local transportation for CANGAS service engineer.
Application
Customer Photos
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