Aluminum Foil with Cryogenic Insulation Paper

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Loading Port:
Shanghai
Payment Terms:
TT OR LC
Min Order Qty:
1 m²
Supply Capability:
100000 m²/month

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Product Description:

Description: 

The fire retardation glass fiber Cryogenic & Insulation paper is made of  superfine glass fiber with special processing. This is usually used with aluminium foil and used for transport containers which store liquid helium, liquid hydrogen, liquid nitrogen,LNG etc. 

 

The superfine glass fiber Cryogenic & Insulation paper's diameter between 0.1-0.6μm and fiber glass filament (diameter between 3-5 μm).  According to a certain proportion, the paper is produced under the wet & vacuum forming process to make the paper have the space lattice structure. All the glass fiber is inorganic material, so it has outstanding flame retardant properties. Specifically engineered for use at big temperature range (approaching -273—500) and also the paper is really stable in the low temperature condition.

 

 

Cryogenic Insulation Paper Features:

 

The main way of heat conduction is by radiation heat exchange in the low and vacuum condition. In order to reduce the radiation heat exchange to meet the good heat insulation effect, by using aluminum foil for reflecting screen and superfine glass fiber insulation paper for spacer, then the multilayer combination of aluminum foil reflective screen and cryogenic & insulation material can build up the efficient thermal barrier against heat transfer in insulated vacuum storage containers. This material can be freely winding, and help the user to reduce the waste of manpower and material waste.

 

 

Cryogenic Insulation Paper Application:

Cryogenic liquid (liquid helium, liquid hydrogen, LNG, liquid oxygen, liquid nitrogen, liquid argon, etc.)

 

Cryogenic Insulation Paper Specifications

1.light weight 
2.good uniformity 
3.low thermal conductivity


Technical data:

Aluminum Foil with Cryogenic Insulation Paper


FAQs:

Q1  What’s the transport method?

A1  FCL delivery goods with wooden pallet; If LCL delivery, must with wooden case; Sometimes need open top, flat rack or bulk cargo.

Q2  What’s the required payment term?

A2  Generally 30% TT as the prepayment, 70% TT before delivery. If need, 100% Irrevocable Letter of Credit or negotiation.

Q3  Which country are our products exported to?

A3  Apart from entire Chinese market, the US, Russia, Japan, Korea, Australia and some Southeast Asian Nations.

 

Aluminum Foil with Cryogenic Insulation Paper

Aluminum Foil with Cryogenic Insulation Paper


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The biggest advantage of using reverse osmosis water purifier is that the water filter is very clean, than the outside to sell the mineral water but also clean a lot, the biggest drawback is the small amount of water can not be used as family life to water, and the higher cost.
Q:Will the degree of zero is ultra-low temperature, cold storage is a special equipment?
Pressure pipe, refers to the use of a certain pressure, for the delivery of gas or liquid tubular equipment, the scope of the provisions of the maximum working pressure greater than or equal to 0.1MPa (gauge pressure), the media for the gas, liquefied gas, steam or flammable, explosive , Toxic, corrosive, the highest operating temperature is higher than or equal to the standard boiling point of the liquid, and the nominal diameter greater than or equal to 50mm pipe. Nominal diameter less than 150mm, and its maximum working pressure of less than 1.6MPa (gauge pressure) of the non-toxic, non-flammable, non-corrosive gas pipeline and equipment, except for the body of the pipeline. Among them, the oil and gas pipeline safety supervision and management should also be in accordance with the "Safety Production Law", "Oil and Natural Gas Pipeline Protection Law" and other laws and regulations.
Q:Medical low temperature refrigerator offer is how much
③ capacity: the greater the capacity, the higher the price.
Q:What aspects of low temperature plasma equipment can be used?
The surface cleaning of the material is activated Welding, painting, printing, sealing, foaming, coating and silicification before surface activation. Gas cracking and efficient sterilization Accelerated chemical reactions ---- You Pu Lai plasma professional engaged in plasma research and development
Q:Is the medical large equipment configuration permit canceled?
Therefore, this is not only a large public hospital concerned about the important licensing power, and even some of the vigorous development of private hospitals are also concerned about this issue. In 2009, the former Ministry of Health on Beijing, Shanghai, the top three hospitals without permission to purchase surgical robots made a rare public criticism, once in the industry caused too much discussion. In addition, the health sector searched a number of provincial health and family planning departments and found that they are currently retained "non-administrative license" is generally about 10, B large medical equipment configuration permit are in the publicity. And to the municipal health and family planning departments on the website, because the information is not clear, the health sector can not understand the approximate number of non-administrative licensing projects. Suzhou Municipal Health Bureau website announced two non-administrative licensing matters - "AIDS screening screening laboratory set up audit" and "issued nursery health insurance certificate." The former is set up according to the National Measures for the Administration of HIV / AIDS, which is based on a document set up by the local health department in 2003 as one of the basis for the accreditation of the educational administrative departments for examination and approval.
Q:Henan Kaifeng in 2015 for the examination of medical equipment, when the job certificate to receive
2015 national medical equipment business ability assessment certificate issued by the work has begun, please pass the assessment of the candidates to the provincial cities, straight pipe County Health Bureau (Medical Association) to receive, the provincial units of the candidates to the unit to receive the competent authorities.
Q:How to do medical equipment grounding in the operating room
If the building design has been equipped with equipotential design, then the operating room medical equipment ground connected to the potentiometer on it.
Q:What is the medical cleaning device? What should I consider? Solution
1, single ion exchange editing Process: raw water → raw water pressurized pump → multi-media filter → activated carbon filter → water softener → precision filter → a reverse osmosis equipment → intermediate water tank → intermediate water pump → ion exchange → purified water tank → pure water pump → UV sterilization Device → microporous filter → water point Although this process has a small initial cost and a small footprint, it is necessary to carry out ion regeneration frequently in the later stage of operation. In addition to the large amount of acid and alkali cost, it is harmful to the environment. 2, reverse osmosis and ion exchange combination editing Process: raw water → raw water pressurized pump → multi-media filter → activated carbon filter → water softener → precision filter → first level reverse osmosis → PH adjustment → intermediate tank → second reverse osmosis (reverse osmosis membrane surface with Charge) → purified water tank → pure water pump → UV disinfection → microporous filter → water point This process uses a combination of reverse osmosis and ion exchange, although it is higher than the single ion exchange equipment, but the relative ion regeneration cycle is longer; therefore, the cost of acid and alkali consumption is less than the simple ion exchange process; But there are still shortcomings of environmental pollution.
Q:What are the requirements for the use of medical grade equipment for 100,000 clean rooms? 25
You are the manufacturers? Manufacturers how R & D out of it? If you are buying equipment, then buy a device to achieve their own requirements on the line?
Q:Where can I apply for medical electrical equipment training?
hereinafter referred to as IVD) shall comply with this directive to complete the conformity assessment procedures, affixed with the CE mark, to be listed in the EU.

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