Sterile Glove Box
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Sterile Glove Box

1.Type:
1)Acrylic Type A glove box: No sample transfer window, must be take it out from the door.
2)Acrylic Type B glove box:There is a sample transfer window, which can protect the gas environment inside the box from being damaged by the outside world.
3)Acrylic Type B glove box:The air in the box can be extracted through the vacuum pump, and then through the high purity dry inert gas into the box, and reach the lower water oxygen content in the box
2.Customization:
1)Single, double, multiple people and other different station boxes.
2)Different shapes, different structures, different applications, different thickness customization options.
3)Doors of different sizes can be opened on any side of the box to facilitate the entry and exit of equipment and accessories.
4)For other optional configurations, contact sales personnel.
***Price List for whole above, inquire us to get
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Description

Technical Parameters

The sterile glove box, also known as a glovebox, is a crucial piece of equipment in various industries, particularly in biological research, pharmaceutical manufacturing, and sterile processing environments. It serves as an enclosed, controlled atmosphere chamber that allows operators to manipulate materials within a sterile or controlled environment without direct exposure to the external contaminants.

The core feature is its pair of rubber or plastic gloves attached to ports on the front panel. These gloves enable researchers or technicians to work inside the box while maintaining a sterile barrier. The interior of the glove box is typically sterilized using methods such as HEPA filtration, UV light, or chemical sterilization to ensure a contamination-free workspace.Moreover, they come with advanced controls for monitoring and maintaining critical parameters like temperature, humidity, and oxygen levels, depending on the specific application needs. This precision is vital for preserving the integrity of sensitive samples and maintaining optimal conditions for cell cultures, microbial studies, or the handling of sterile medical devices.

As the core equipment for aseptic operation, the technological development of this device has directly promoted the progress in fields such as biomedicine, semiconductors, and new energy. In the future, with the popularization of intelligent and modular technologies, as well as the growth of cross-disciplinary demands, sterile glove boxes will evolve towards higher cleanliness and greater flexibility. For enterprises, choosing suppliers with customization capabilities and in line with international standards will be the key to enhancing R&D efficiency and product competitiveness.

 

Specifications

 

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Glovebox Specifications | Shaanxi Achieve chem-tech

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Glovebox Specifications | Shaanxi Achieve chem-tech

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Glovebox Specifications | Shaanxi Achieve chem-tech

 

applications

 

nuclear energy industry

 

The nuclear energy industry relies heavily on radioactive materials, which are substances that emit ionizing radiation. These materials are integral to both the generation of nuclear power and various medical, industrial, and research applications.

Radioactive elements, such as uranium and plutonium, are commonly used as fuel in nuclear reactors. Uranium-235, for instance, undergoes fission when bombarded with neutrons, releasing energy that is harnessed to produce electricity. Plutonium-239, another fissile material, can also be used in reactors and has been employed in nuclear weapons.

Besides fuel, radioactive isotopes play crucial roles in nuclear medicine, imaging, and treatment. Radioisotopes like iodine-131 and cobalt-60 are used in diagnosing and treating cancers, while tritium, a beta emitter, is employed in self-luminous signs and watches.

However, handling radioactive materials necessitates stringent safety measures due to their potential hazards. Exposure to high levels of radiation can lead to acute radiation syndrome and increase the risk of cancer. Therefore, nuclear facilities are designed to contain radiation and minimize worker exposure through shielding, distance, and time constraints.

 

In the nuclear energy industry, the sterile glove box is used to handle radioactive materials safely and effectively. The following are some specific application cases:

Radioactive Waste Management

During the storage and disposal of radioactive waste, it provides a controlled environment to prevent the leakage of radioactive particles. Operators can safely handle and package radioactive waste within the glove box, reducing the risk of contamination and exposure.

Fuel Assembly Handling

In nuclear reactors, fuel assemblies contain uranium or plutonium, which are highly radioactive. It allows operators to handle fuel assemblies during maintenance, inspection, and replacement operations without direct exposure to radiation.

Radioactive Material Synthesis & Research

Research and development of new radioactive materials often require a controlled environment to prevent contamination and ensure safety. It provides such an environment, allowing researchers to perform experiments and synthesize new materials without risk of exposure to radiation.

 

What is it?

 

The nuclear energy industry represents a pivotal sector in the global energy landscape, harnessing the power of atomic nuclei to produce electricity on a massive scale. It leverages nuclear fission-where heavy atomic nuclei split into lighter ones, releasing vast amounts of energy-or, in the future, nuclear fusion, which combines light nuclei into heavier ones with even greater energy yield.

 

The industry boasts advanced technology and rigorous safety protocols to ensure the safe and efficient operation of nuclear reactors. These reactors, found in nuclear power plants, convert the heat generated by nuclear reactions into steam, which then powers turbines to create electricity. This process emits virtually no greenhouse gases, positioning nuclear energy as a key player in the fight against climate change.

 

Despite its clean energy output, the nuclear industry faces challenges, including the management of radioactive waste, which requires careful storage and disposal to protect human health and the environment. Additionally, the high costs of constructing and decommissioning nuclear facilities, as well as concerns over nuclear proliferation and safety incidents, continue to shape public perception and regulatory frameworks.

 

Yet, advancements in reactor design, such as smaller modular reactors and advanced fuel cycles, offer promising avenues for improving economic viability, safety, and waste management. The nuclear energy industry remains committed to innovating and refining its practices to harness the immense potential of atomic energy responsibly and sustainably.

 

Sterile Glove Box Applications | Shaanxi Achieve chem-tech

Sterile Glove Box Applications | Shaanxi Achieve chem-tech

 

Pharmaceutical Industry

 

In the pharmaceutical industry, the sterile glove box is used to handle sterile and sensitive materials, ensuring the quality and safety of drugs. Here are some specific applications:

Sterile Drug Manufacturing

In the production of sterile drugs, such as injectable solutions or vaccines, it provides a controlled environment to prevent contamination. Operators can safely perform manufacturing operations within the glove box, ensuring the sterility of the final product.

Cell Culture and Tissue Engineering

In cell culture and tissue engineering applications, it provides a controlled environment to prevent contamination by microorganisms. This allows researchers to culture cells and tissues safely, ensuring the success of experiments and the quality of research results.

Drug Packaging and Sterilization

It can be used for the packaging and sterilization of drugs. By providing a sterile environment, the glove box ensures that drugs are not contaminated during packaging and sterilization processes.

 

what is Sterile drugs

 

Sterile drugs represent a crucial class of pharmaceuticals that are meticulously manufactured to ensure the absence of viable microorganisms throughout their entire shelf life. These medications are vital for treating patients who are immunocompromised, undergoing surgeries, or require intravenous infusions, as contamination could lead to severe infections and life-threatening complications.

 

The production of sterile drugs involves several rigorous steps, including the use of sterile raw materials, aseptic processing techniques, and hermetic packaging to maintain sterility. Manufacturers employ advanced technologies such as isolators, closed-system transfers, and automated filling lines to minimize human intervention and the risk of contamination.

 

Before reaching patients, sterile drugs undergo extensive quality control testing, including sterility testing, endotoxin testing, and pyrogen testing, to confirm their safety and purity. This comprehensive approach ensures that patients receive medications that are free from microorganisms, toxins, and other contaminants.

 

Furthermore, sterile drugs often require specific storage conditions, such as controlled temperatures and humidity, to maintain their sterility and efficacy. Proper handling and administration of these drugs are also crucial to prevent contamination and ensure patient safety.

 

In summary, sterile drugs are essential for treating vulnerable patients and require meticulous manufacturing, testing, and handling processes to ensure their safety and effectiveness.

 

Accuracy of filtration system

 

The accuracy of the filtration system of the sterile glove box is one of the key factors to ensure the sterile environment of the box and the accuracy of the experiment. The filtration system creates a highly clean working environment inside the glove box by removing particles, bacteria, viruses and other contaminants from the air. In this equipment, the accuracy of the filtration system is crucial, which directly determines the degree of external contamination that the glove box can resist. The following is a detailed description of the accuracy of its filtration system:

The importance of the accuracy of the filtration system

 

Aseptic glove boxes are widely used in biological science, pharmaceutical research and development, materials science and other fields, which have high requirements for the cleanliness of experimental environments. As an important part of the glove box, the accuracy of the filtration system directly determines whether the glove box can effectively prevent external particles and microorganisms from entering the box, so as to protect the experimental sample from contamination.

Specifically, the high precision of the filtration system enables:

 

Effective removal of particles in the air: The filtration system can intercept dust, dander and other particles in the air to prevent them from adhering to the surface of the experimental sample or instrument and affecting the experimental results.

 

Prevent the invasion of microorganisms: bacteria, viruses and other microorganisms are one of the main sources of experimental pollution. The high-precision filtration system can effectively prevent these microorganisms from entering the glove box and ensure the sterile environment in the box.

 

Prolong the storage time of experimental samples: In a sterile environment, the storage time of experimental samples can be greatly extended, reducing the risk of experimental failure or sample failure due to contamination.

Definition and measurement of filtration system accuracy

 

Filtration system accuracy refers to the diameter of the smallest particles that the filter can intercept, usually measured in micrometers (μm). The higher the filtration accuracy, the smaller the diameter of the particles that the filter can intercept, the better the filtration effect.

In this device, the filtration system typically achieves high efficiency filter (HEPA) accuracy, capable of intercepting particles of 0.3 microns and above. However, for certain experiments that require very high cleanliness, such as semiconductor material preparation, biological product production, etc., higher precision filters may be required, such as ultra-High efficiency filters (ULPA), whose filtration accuracy can reach 0.1 microns or less.

Factors affecting the accuracy of the filtration system

 

 
Type of filter material

The filter material is one of the key factors determining the accuracy of the filtration system. Common filter materials include glass fiber, polypropylene fiber, polytetrafluoroethylene (PTFE) and so on. Different materials have different filtration accuracy, chemical stability, corrosion resistance and other characteristics, and need to be selected according to the experimental needs.

 
Filter structure

The structure of the filter will also affect its filtration accuracy. For example, the pleated filter has a larger filtration area and higher filtration efficiency than the flat filter. In addition, the sealing performance of the filter will also affect its filtration accuracy, and poor sealing will cause outside air to bypass the filter into the box.

 
Cleanliness of the operating environment

Although the filtration system can intercept most of the particles and microorganisms, in extremely harsh operating environments, such as the presence of a large number of particles or microorganisms in the air, the burden of the filtration system will be greatly increased, which may affect its filtration accuracy and life.

 
 
Selection and application of filtration system accuracy

 

When selecting the accuracy of the filtration system of this equipment, the following factors need to be considered:

Sterile Glove Box | Shaanxi Achieve chem-tech

Experimental requirements

LDifferent experiments have different requirements for cleanliness. For experiments requiring a highly clean environment, such as biologics production, semiconductor material preparation, etc., a high-precision filtration system should be selected.

Sterile Glove Box | Shaanxi Achieve chem-tech

Cleanliness of the operating environment

The cleanliness of the operating environment will also affect the selection of the filtration system. If the operating environment itself is relatively clean, you can choose a slightly lower precision filtration system; On the contrary, you need to choose a higher precision filtration system.

Sterile Glove Box | Shaanxi Achieve chem-tech

Cost factor

Lorem ipsum dolor sit amet,consectetur adHigh-precision filtration systems are often more expensive and require more frequent replacement and maintenance. Therefore, when choosing a filtration system, it is necessary to consider the cost factor comprehensively.

In practical applications, the filtration system of aseptic glove boxes is usually modular in design, which is convenient for users to select and replace according to experimental requirements. For example, some glove box manufacturers offer a variety of filter specifications for users to choose from, including coarse filter, medium filter, high efficiency filter (HEPA) and ultra-high efficiency filter (ULPA). Users can choose the appropriate filter combination according to the experimental requirements to achieve the best filtering effect.

Maintenance and testing of filtration system accuracy

 

In order to ensure the accuracy and performance of the sterile glove box filtration system, regular maintenance and testing are required. Specific measures include:

Regular filter replacement

According to the experimental frequency and filter life, regular filter replacement is the key to ensure the accuracy of the filter system. In general, the replacement cycle of high efficiency filters (HEPA) ranges from 6 months to 1 year, depending on the experimental environment and use.

Check the sealing performance of the filter

The sealing performance of the filter directly affects its filtration accuracy. Therefore, when replacing the filter, it is necessary to check whether the sealing performance of the filter is good to ensure that there is no air leakage.

Filtration efficiency test

Use a professional testing instrument to test the filtration efficiency of the filter to ensure that it meets the experimental requirements. If the filtration efficiency is found to be reduced, the filter should be replaced or repaired in time.

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