CLEANING OF EQUIPMENT FOR OXYGEN SERVICE - AIGA
CLEANING OF EQUIPMENT FOR OXYGEN SERVICE - AIGA
CLEANING OF EQUIPMENT FOR OXYGEN SERVICE - AIGA
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The amount of contaminants in a sample can be determined in three ways.<br />
- weight of residue (laboratory test)<br />
- volume of residue (laboratory test)<br />
- light transmission (laboratory test for qualitative figures)<br />
26<br />
<strong>AIGA</strong> 012/04<br />
This method is accurate in determining low amounts of oil or grease residues with small tolerances.<br />
6.2.4.1 Weight of Residue<br />
A known quantity (MS) of a representative sample of unfiltered used solvent is contained in a small<br />
weighed beaker and is evaporated to dryness being careful not to overheat the residue and the<br />
weight (m2) of the residue established. In the same manner the weight (in, ) of residue from a similar<br />
quantity of clean unused solvent is determined.<br />
The difference in weight between the two residues and the quantity of representative sample used is<br />
related to the total quantity (Mv) of solvent used and can be taken to compute the amount of residual<br />
contaminant removed per square metre (mc) of surface area (A) cleaned.<br />
m<br />
c<br />
=<br />
m2<br />
− m ) mv<br />
/ m<br />
A<br />
( 1<br />
s<br />
m1 = weight of residue (clean solvent)<br />
m2 = weight of residue (used solvent)<br />
ms = weight of representative sample (used solvent)<br />
mv = total weight of solvent used<br />
A = surface area of component cleaned<br />
Mc = weight of contamination present per area cleaned.<br />
6.2.4.2 Volume of Residue<br />
A measured quantity of a sample of the unfiltered used solvent can be placed in an Imhoff cone and<br />
evaporated to dryness. The volume of residue can be measured directly and used to compute the<br />
volume contaminant extracted per square metre of surface area cleaned. Greater sensitivity can be<br />
achieved by successive evaporation of quantities of the same extracted solvent batch in the same<br />
Imhoff cone.<br />
6.2.4.3 Light Transmission<br />
A sample of the unfiltered used solvent is compared a reference sample of unused solvent by<br />
comparing light transmission through the two samples simultaneously. The difference in colour or light<br />
absorption of the solvents is a qualitative indication of the amount of contaminants dissolved. The<br />
quantity of any contaminant in a sample can be estimated by analysis techniques e.g. making use of<br />
V or infrared light.<br />
6.2.5 Water Break Test<br />
Drinking or distilled water is sprayed on a surface as horizontal as possible. If the amounts of oil or<br />
grease are very small an unbroken layer of water stays for some seconds. If higher amounts of oil or<br />
grease are on the surface the water quickly contracts and forms small beads or droplets between<br />
water free areas.<br />
6.2.6 Spectrometric, Chromatographic and other Special Methods<br />
The measuring instruments used for these methods are very different. For their use special operating<br />
instructions are necessary. By some of them low amounts of oil or grease contamination can be<br />
detected and measured. In some cases the tolerances are low.<br />
Another method is the Total Organic Carbon Analysis-TOC". The technique is based on oxidation of<br />
the samples in furnace in flowing oxygen. The COZ-concentration gives an accurate quantitative