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ESD Dissipative Sleeving

  1. Permanent Static Dissipative
  2. Insensitive to environment
  3. Special design for cleanroom application

STOCK AVAILABILITY (SLEEVING FOR WIRES & ETC)

 Inner Diameter (mm)  Outer Diameter (mm)  Standard Roll (Meter)  Part No.
 3 3.8 100 ESD 030 / 038 
 6 6.8 100 ESD 060 / 068
 10 10.8 100 ESD 100 / 108
 15 15.9 100 ESD 150 / 159
 28 29 5m ESD 280 / 290
 31 33 5m ESD 310 / 320
 40.5 43 5m ESD 405 / 430
 Surface Resistivity 8 * 10 to power of 8 
 Decay time at centre of tube 0.5 to 1.2 seconds
 Decay time at end of tube 0.8 to 1.3 second
 Float voltage observed 0V to 3 V
 Peel off voltage observed 0V to 3V
 The Sleeving are free from silicon  

OUTGASSING – Three samples of Bluish Sleeving were used and placed in an outgassing vessel at 85 Degree C. It was then flushed continually for three hours at 50ml/min with grade 5 nitrogen. A carbotrap ‘B’ / carbotrap ‘C’ tube were then used to trap the outgassing constituents after which analyzing using GC/MS with ATD.

FTIR / SILICONE OIL / HYDROCARBONS – The presence of silicone oil and hydrocarbons were extracted in solvent soluble residue from one piece of 15.5 “ of ESD Bluish Sleeving. Both the inner and outer surfaces, a total of 121cm square, were rinsed with 10ml of hexane and isopropanol by mixing a portion of 1 : 1 (v/v) of the solvent solution. A clean 30ml glass beaker was used to collect the rinsate. The solvent solution was evaporated to dryness. Thereafter, FTIR / HATR was used to analyze for the presence of silicone oil and hydrocarbons on any residue rinsed from the sample.

IONIC CONTAMINATION – A ESD Bluish Sleeving sample were divided into three sections to test for ionic contamination. Three pre-clean glass beaker containing 10ml of de-ionized water was given one section of the sleeving sample each and then capped off to prevent evaporation. The glass beakers were then placed in an 80 Degree C oven. The water extract was then analyzed using ion chromatography. A hand measured apparent surface area of 10.2cm square was used to calculate the results. 

OUTGASSING - Below are the data obtained from using the following chemical

 COMPOUND INDENTIFICATION 

 Section 1 Sample 

 Section 2 Sample 

 Section 3 Sample 

 Average 
 BHT 13 ug/g 12 ug/g 13 ug/g 13 ug/g
 KETONES 25 ug/g 27 ug/g 23 ug/g 25 ug/g
 SILOXANE 0 ug/g 1 ug/g 0 ug/g 1 ug/g
 HYDROCARBON, OTHERS 16 ug/g 15 ug/g 19 ug/g 17 ug/g
 TOTAL 54 ug/g 55 ug/g 55 ug/g 56 ug/g


FTIR / SILICONE OIL / HYDROCARBONS

- Below shown was obtain from the analyzed result on one section of the Sleeving.

 

 Section 1 Sample 

 Limits
 SILICONE OIL 9 As per customer's specification 
 HYDROCARBONS  158 As per customer's specification


Note:
Result for both the silicone oil and hydrocarbons are in nanograms/cm square surface area.


IONIC CONTAMINTAION
 - The result tested as follows

 SAMPLE

 Section1 Sample (ug/cm square) 

 Section 2 Sample (ug/cm square)  Section 3 Sample (ug/cm square)  Average  Limits
 AMMONIUM0.0170.0180.0150.017 As per customer's specification 
 BROMIDE0.0070.0080.0040.006
 CALCIUM0.0220.0200.0200.021
 CHLORIDE0.0100.0090.0110.010
 FLUORIDE0.0300.0310.0300.030
 MAGNESIUM0.0010.0010.0010.001
 NITRATE0.0030.0030.0040.003
 NITRITE0.0000.0000.0000.000
 PHOSPHATE0.0780.0800.0700.076
 POTASSIUM0.0100.0100.0110.011
 SODIUM0.1540.1520.1470.151
 SULFATE0.0000.0040.0010.002

 TOTAL SUM
 OF 
ANIONS 

0.3320.3360.3140.327


ROHS FOR SPIRAL COIL
 - On analysis, the following result were obtain:

 Test Parameter Digestion / Extraction Method Analysis Method  Result, ppm (w/w) 
 Mercury (Hg) AC/RoHS/0010 Ver1.1/05 Wet Acid Digestion (Microwave) CVAASND
 Lead (Pb) AC/RoHS/0007 Ver1.0/05 Dry AshingICP-AESND
 Cadmium (Cd) AC/RoHS/0007 Ver1.1/05 Wet Acid Digestion (Microwave)ICP-AESND
 Hexavalent Chromium (Cr 6+) Ac/RoHS/0011 Ver1.0/05 EPA 3060A / 7196A (Modified)ND
 Polybrominated Biphenyls (PBB) AC/RoHS/0012 Ver1.1/05 (Microwave)GC-MSND
 Plybrominated Diphenyl Ethers (PBDEs)  AC/RoHS/0012 Ver1.1/05 (Microwave)GC-MSND
  1. Sample was prepared as in AC/ROHS/0006 Ver1.0/05 and all the methods listed above are reference to the IEC 111/24/CD/Ed.1- Procedure for determination of levels of regulated Substances in Electrotechnical Products.
  2. CVAAS = Cold Vapour Atomic Absorption  Spectrometry
    ICP – AES = Inductively- Coupled Plasma – Atomic Emission Spectrometry
    GC-MS = Gas Chromatography – Mass Spectrometry 
  3. The Method detection limits(MDL) for Lead, Cadmium, Polybrominated Biphenyls and Polybrominated Diphenyl Ethers = 1 ppm each
  4. The Method detection limits(MDL) for Hexavalent Chromium = 2ppm
  5. The Method detection limits(MDL) for Mercury = 0.5ppm
  6. “ND” = Not detected (Less than or equal to 5ppm)
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