BENEFIT
Permanent Static Dissipative
Insensitive to environment
Special design for cleanroom application
APPLICATION
To wrap cable or wire inside cleanroom
To coil pen inside cleanroom
Other
SPECIFITION
Decay time at end of tube |
0.8 to 1.3 seconds |
Decay time at centre of tube |
0.5 to 1.2 seconds |
Float voltage observed |
0V to 3V |
Peel Off Voltage Observed |
8 * 10 to the power of 8 |
PROCEDURE
OUTGASSING – Three samples of Spiral Coil 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 Spiral Coil. 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 Spiral Coil 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 spiral coil 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.
RESULTS
Below are the data obtained from using the following chemical
COMPOUND |
Section 1 Sample |
Section 2 Sample |
Section 3 Sample |
Average |
BHT |
12 ug/g |
12 ug/g |
13 ug/g |
12 ug/g |
KETONES |
28 ug/g |
28 ug/g |
21 ug/g |
26 ug/g |
SILOXANE |
1 ug/g |
0 ug/g |
0 ug/g |
1 ug/g |
HYDROCARBON, OTHERS |
19 ug/g |
15 ug/g |
14 ug/g |
16 ug/g |
TOTAL |
60 ug/g |
55 ug/g |
48 ug/g |
54 ug/g |
FTIR / SILICONE OIL / HYDROCARBONS
- Below shown was obtain from the analyzed result on one section of the Spiral Coil.
|
Section 1 Sample |
Limits |
SILICONE OIL |
10 |
As per customer's specification |
HYDROCARBONS |
160 |
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 |
Section 3 Sample |
Average |
Limits |
AMMONIUM |
0.015 |
0.014 |
0.020 |
0.016 |
As per customer's specification |
BROMIDE |
0.008 |
0.008 |
0.004 |
0.007 |
|
CALCIUM |
0.019 |
0.020 |
0.022 |
0.020 |
|
CHLORIDE |
0.008 |
0.010 |
0.014 |
0.010 |
|
FLUORIDE |
0.032 |
0.029 |
0.031 |
0.030 |
|
MAGNESIUM |
0.001 |
0.001 |
0.001 |
0.001 |
|
NITRATE |
0.003 |
0.004 |
0.004 |
0.003 |
|
NITRITE |
0.000 |
0.000 |
0.000 |
0.000 |
|
PHOSPHATE |
0.086 |
0.069 |
0.071 |
0.075 |
|
POTASSIUM |
0.010 |
0.012 |
0.011 |
0.011 |
|
SODIUM |
0.155 |
0.150 |
0.147 |
0.150 |
|
SULFATE |
0.000 |
0.005 |
0.000 |
0.001 |
|
TOTAL SUM OF ANIONS |
0.337 |
0.322 |
0.325 |
0.324 |
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) |
CVAAS |
ND |
Lead (Pb) |
AC/RoHS/0007 Ver1.0/05 Dry Ashing |
ICP-AES |
ND |
Cadmium (Cd) |
AC/RoHS/0007 Ver1.1/05 Wet Acid Digestion (Microwave) |
ICP-AES |
ND |
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-MS |
ND |
Plybrominated Diphenyl Ethers (PBDEs) |
AC/RoHS/0012 Ver1.1/05 (Microwave) |
GC-MS |
ND |
REMARKS
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.
CVAAS = Cold Vapour Atomic Absorption Spectrometry
ICP – AES = Inductively- Coupled Plasma – Atomic Emission Spectrometry
GC-MS = Gas Chromatography – Mass Spectrometry
The Method detection limits(MDL) for Lead, Cadmium, Polybrominated Biphenyls and Polybrominated Diphenyl Ethers = 1 ppm each
The Method detection limits(MDL) for Hexavalent Chromium = 2ppm
The Method detection limits(MDL) for Mercury = 0.5ppm
“ND” = Not detected (Less than or equal to 5ppm)