• High-speed Co2 Flying Laser Marking Machine CNBM System 1
High-speed Co2 Flying Laser Marking Machine CNBM

High-speed Co2 Flying Laser Marking Machine CNBM

Ref Price:
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Loading Port:
Tianjin
Payment Terms:
TT OR LC
Min Order Qty:
1 set
Supply Capability:
30 set/month

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Detailed Product Description:


Equip with with the production line and automatic marking application .

Application & Materials:

 
Flying marking machine is my company special designing for the electronics, pharmaceutical, tobacco, leather, packaging, foods and other industries laser marking application .it can mark all the nonmetal materials very well.

 

This type laser flying marking machine  can equip our own production line or equip with your production line to reach at high speed flying marking application .

 

Co2 Laser:

 

Our CO2 Laser Series equiped the importing RF CO2 Laser,High-Speed Resonace Mirror System .The speed is quicker and the performance is stable.This series Laser Equipments have widely won user’s trust depend on it’s superior performance and reliable quality.

 

 

Matching Type :

BMC10A

BMC30A

BMC50A

BMC100A

Technology

Parameter

Output Power

10W

30W

50W

100W

Wavelength

 10.64μm

Repeat frequency

 ≤≤50KHz

Marking scope

110mm×110mm 

Marking speed

≤7000mm/s

Min.line width

0.015mm

Characters type

English letters, numbers and  punctuations

Max .Production line speed

70m/ min

Coding lines

≤8 lines

Input power

0.6KW

1.5KW

2.2KW

4KW

Electrical source

220V / Single-Phrase Circuit / 50Hz

3A

8A

11A

20A


 

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1) the Avery,Mcleod and Mccarty experiment. 2)the Hershey and Chase experiment. _ Hershey and Chase conducted their experiments on the T2 phage, a virus whose structure had recently been shown by electron microscopy.In their first set of experiments, Hershey and Chase labeled the DNA of phages with radioactive Phosphorus-32 (the element phosphorus is present in DNA but not present in any of the 20 amino acids from which proteins are made). They allowed the phages to infect E. coli.were able to observe the transfer of P32 labeled phage DNA into the cytoplasm of the bacterium.n their second set of experiments, they labeled the phages with radioactive Sulfur-35 (Sulfur is present in the amino acids cysteine and methionine, but not in DNA). Following infection of E. coli they then sheared the viral protein shells off of infected cells using a high-speed blender and separated the cells and viral coats by using a centrifuge. After separation, the radioactive S35 tracer was observed in the protein shells, but not in the infected bacteria, supporting the hypothesis that the genetic material which infects the bacteria was DNA and not protein hope it helps.:)
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Processing technology is divided into cold processing and processing of cold processing, including the car, pliers, planing, milling, grinding, etc. Hot processing is divided into casting and forging inside and can be divided into forging and stamping forging free forging (including upsetting,
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