Solvent vapor degreasing
is a parts cleaning process that has been used in many applications for some years.
Virtually every communications or electronics system and aircraft flying today
has components that have been vapor degreased. Also, surgical tools and medical
implants often are cleaned using solvent vapor degreasing. In fact, solvent vapor
degreasing is almost limitless in its possible uses. There are five reasons for
its widespread use:
1.The halogenated solvents
used are non-flammable and will not burn or explode.
2.Solvent soluble oils,
greases and other materials are removed effectively and economically.
3.Solvent
vapor degreasing requires a minimum amount of labor, energy and floor space.
4.The self-distilling nature of the equipment allows cleaning to be done with
pure, distilled solvent.
5.The cleaning solvents can be recovered from the
soils and recycled.
Solvents
Solvents are effective cleaners because of their ability to dissolve grease and
oil. Therefore, they remove contaminants more easily than other cleaning methods.
Two solvents widely used
in the past for vapor degreasing were 1,1,1-trichloroethane and CFC 113. According
to the Montreal Protocol, these solvents have been phased out due to their reported
damaging of upper atmosphere ozone levels.
In the SNAP (Significant
New Alternatives Policy) program, EPA lists acceptable alternatives to 1,1,1-trichloroethane
and CFC 113. The most common alternatives used today are trichloroethylene, methylene
chloride and perchloroethylene. These solvents, however, are listed as hazardous
air pollutants under the 1992 Clean Air Act.
Much effort has been devoted
to find and develop new solvents, and a few are available for vapor degreaser
use (see Table I). This table shows whether the solvent is a VOC implicated in
smog and related air pollution or if the solvent is an ozone depletor. Solvent
power is an important consideration when choosing a solvent as well. While Table
I is based on published data and believed correct, the latest data should be obtained
when considering solvents.
Choosing the appropriate
solvent is very complex and depends on a number of factors. It is best to consult
with solvent and equipment manufacturers before making a decision. State and federal
regulations will have a significant effect too.
The
Process
Vapor
degreasing is a relatively simple process. A heat source raises the liquid solvent
to its boiling point. When the solvent boils, it produces hot, heavy vapors that
rise to an established vapor line. At this point, the vapors are condensed on
cold circumferential condenser coils, and the vapors rise no higher. Because the
solvent vapors are heavier than air, they push the air above the vapor line. Parts
at ambient temperature are then introduced into the solvent vapor, and the solvent
vapor condenses on the parts surface. The liquid solvent produced as a result
of this condensation dissolves the greases and oils on the part and flushes them
away. As the parts are cleaned, more vapors are produced in the boiling sump to
replace those that were condensed.
To clean parts only by
pure vapor condensation from the vapor zone, enough vapors must condense into
liquid on the parts to remove the contaminants. This makes the solvents
boiling point an important consideration. As the solvents boiling point
increases, more solvent will condense on a part (see Table II).
Vapor
Degreasing Equipment
A diagram of a basic vapor degreaser can be seen in Figure 1 (see previous section
to read how the degreaser works).
Sometimes it is necessary
to enhance the cleaning capability of the degreaser. In these cases, a spray feature
is added to the degreaser. The addition of a condensate spray system allows flushing
and cleaning of many complex-shaped parts that vapor condensation alone could
not clean. Spraying must be done with care, below the vapor line and never deflected
into the freeboard air. Heat input into this degreaser must be adequate to produce
condensate for the production load and spray volume required.
| TABLE
ISolvent Properties |
| Property |
Trichloro-ethylene |
Methylene Chloride |
Perchloro-ethylene |
N Propyl Bromide |
AKA 225 |
HFE 7100 |
HFC 4310 |
Water |
| Boiling Point (F) |
188 |
104 |
250 |
156 |
129 |
140 |
129 |
212 |
| Weight (lb/gal) |
12.10 |
11.00 |
13.48 |
11.13 |
12.9 |
13.0 |
12.95 |
8.3 |
| Kauri Butanol Value
(solvent power) |
130 |
136 |
90 |
129 |
31 |
|
|
|
| Heat of Vaporization
(Btu/lb) |
103 |
142 |
90 |
106 |
62 |
54 |
56 |
1000 |
| Heat of Vaporization
(Btu/lb) |
1246 |
1560 |
1200 |
1180 |
800 |
675 |
730 |
8300 |
| Vapor Density (Air
= 1.0) |
4.45 |
3.30 |
5.22 |
|
|
|
|
|
| Specific Heat |
0.225 |
0.280 |
0.205 |
|
|
|
|
|
| Surface Tension (dynes/cm) |
31.6 |
28.2 |
32.3 |
25.9 |
16.2 |
|
14 |
72.8 |
| SNAP Approval |
yes |
yes |
yes |
no |
until 2005 |
yes |
yes |
n/a |
| VOC |
yes |
no |
no |
yes |
no |
no? |
no? |
n/a |
| HAP |
yes |
yes |
yes |
|
no |
|
|
n/a |
| Upper Ozone Depleter |
no |
no |
no |
|
yes |
|
|
n/a |
| TABLE
IIWeight of Solvent Condensed on a 40 lb Steel Load |
| Solvent |
Boiling Point |
Part Entering at 70F |
| Perchlorethylene |
250F |
8.8 lb |
| Trichlorethylene |
188F |
5 lb |
| Methylene Chloride |
104F |
1 lb |
Spray degreasers are similar
to standard vapor degreasers except for the spraying system, which consists of
solvent pump, filter canister and spray wand and/or a fixed spray header. The
system also has a condensate tank where clean distillate is collected and stored
for spray use.
Effectively sprayed or
where an accumulation of parts in a basket obstructs the spray from impinging
all the parts, liquid immersion de-greasing is desirable (see Figure 2). In an
immersion degreaser, parts are lowered into the boil sump, or sump No.1, for 15-60
sec then transferred beneath the vapor line to the condensate sump, or sump No.
2, for another 15-60 sec. The load is then held in the vapor zone until the solvent
has completely drained off the part.
The cleaning quality of
immersion degreasers depends on a number of factors, including the manner in which
the load is handled. The most important factor though is the cleanliness of sump
No. 2, which directly affects the cleanliness of the finished work. Sump No. 2
is kept clean by the internal distillation of the degreaser. Solvent boils from
sump No. 1, condenses on the condensing coil, travels through the water separator
and into sump No. 2. Sump No. 2 then overflows to sump No. 1.
If no work is processed
through it, sump No. 2 becomes full of pure condensed solvent. However, the soil
being removed in sump No. 1 contaminated that sump. Some of this contaminated
solvent is carried into sump No. 2.
One way to improve the
cleanliness of an immersion degreaser is to add a third sump (see Figure 3). The
distilled clean solvent circulation is counter current to the workflow. Results
are similar to the great advantage counter current rinsing provides in an electroplating
process.
For example, 1 gal of oil
is deposited into the degreaser per hour. At the same time, we have heaters providing
enough vapor generation from sump No. 1 to put 50 gal of condensate into sump
No. 3. This amount of flow also occurs from sump No. 3 to sump No. 2 to No. 1.
If we introduce 1 gal of oil into sump No. 1 along with the 50 gal of solvent
overflow, sump No. 1 will have an oil concentration at equllibrium of about 2%.
If we assume that the workload carries over about the same volume, or 1 gal of
2% oil and solvent into sump No. 2, sump No. 3 becomes contaminated to a level
of about 0.04% oil (400 ppm). By the same reasoning, sump No. 3s oil level
content is reduced to approximately 8 ppm. This is virtually the equal of new
solvent as to cleanliness and better than DI water.
If we add a still of 50
gph capacity to take dirty solvent from sump No. 1 and return clean solvent to
sump No. 3 we would have
Clean pure solvent to sump
No. 3 = 100 gph
Oil to sump No. 1 = 1 gph
Oil concentration in sump No.
1 = 1%
Oil concentration in sump No. 2 = 0.001%
Oil concentration in sump
No. 3 = 0.00001%
While this purity will
not be totally realized in such an operation, it is proven in production machines
that extremely high cleanliness is easily and consistently achievable.
Vacuum degreasers have
been in use for about 35 years. With these systems, the workload is placed in
a vacuum chamber. The chamber is evacuated and then solvent is introduced to clean
the parts. The solvent is then removed and the chamber evacuated again, with solvent
vapors recovered by refrigeration. Final solvent residues are generally recovered
by carbon adsorption. Air is then reintroduced into the chamber so it can be opened
and the parts removed. The smaller the diameter and volume of the vacuum chamber,
the more practical these systems become.
The advantage to vacuum
degreasers is that they have very low solvent emissions. However, there are many
factors against their use, especially their high cost, low production of one to
two loads per hour and complex operation.
Parts can be cleaned using
a sealed chamber degreaser, which contains air. Solvent is introduced as suited
to clean the parts, and excessive solvent is drained off. The air in the chamber
is circulated through a carbon adsorption system or refrigeration system until
the solvent level is low enough for the chamber to be opened and the work removed.
For vacuum and sealed-chamber
systems, perchloroethylene has been the preferred solvent because it is most effectively
recovered with carbon adsorption or refrigeration.
In the past, open top degreasers
were commonly exposed to undesirable air movement, resulting in excessive solvent
losses. Therefore, automatic handling of the loads through the degreaser is very
desirable. This permits total enclosure of the degreasers and insures a proper
cleaning cycle.
Such degreasers eliminate
solvent losses caused by air movement. Also, human errors in work handling are
eliminated in an automatic system. In cleaning applications where production is
significant, the enclosed automated system can provide sufficient solvent and
labor savings to economically justify the cost. In addition, it improves worker
safety by removing the operator or other personnel from the operation.
Part
Handling
Good cleaning and efficient
solvent use requires proper work handling:
1. Parts must be handled
so they fill and drain readily.
2. Sufficient time in sumps must be provided
to remove soils and to heat the load.
3. Parts transfers must always be below
the vapor line.
4. It is desirable to minimize the amount of extraneous material
that goes along with the work through the vapor solvent sumps. Chains, conveyors,
baskets and racks all increase solvent loss.
Solvent
Losses
Vapor
degreasing can be a highly efficient method of cleaning, using a fraction of the
energy of other processes with no water pollution. However, one must use the right
equipment to minimize the amount of solvent loss from the cleaning process. There
are four main causes of solvent loss: dragout; air movement; diffusion; and convection.
Dragout and air movement represent 80-90% of solvent losses while diffusion and
convection make up the balance.
Dragout. Dragout
of solvents on parts has been a major cause of solvent loss in most degreaser
operations in the past. All parts from an ordinary degreaser carry out liquid
solvent. This could not be prevented in the past, but new technology can eliminate
it.
Additional heat is required
to provide the heat of vaporization to remove liquid solvent residue from the
part. That heat is not available from a solvent vapor at a boiling point that
is the same temperature as the part and remaining liquid solvent. By super heating
the vapor, the heat necessary to vaporize all liquid on the part is now available.
The part will come out perfectly dry with no liquid solvent present. This applies
to conveyorized and in-line degreasers as well as spray or dip systems.
Air Movement. It
has been long recognized that drafts around and above degreasers have a significant
effect on increasing solvent losses. Open windows, doors, air intakes, fans and
heaters are typical sources of air movement and corresponding solvent losses.
What was not realized was how small an amount of air movement can impact the amount
of solvent loss.
Solvent losses are extremely
low from air movement of 0-30 fpm across the degreaser while losses increase rapidly
at higher rates of air movement. The EPA selected 50 fpm, a breeze of 0.57 mph,
as a low rate of air movement. This is virtually a dead calm and is not detectable
to a person. Therefore, if air movement is detectable, it is too much. Simple
instruments are available to measure air movement.
Diffusion. Diffusion
is the process by which two gasses tend to mix with each other by the motion of
their molecules. It is the movement of solvent molecules through air without air
movement. Diffusion results in a mixing that occurs regardless of the relative
densities of the gasses. Diffusion is greater with low boiling solvents. Diffusion
is a minor cause of solvent loss from a vapor degreaser.
Convection. Convection
is air movement caused by heated air rising in the freeboard area because of its
contact with hot parts, hot vapor or equipment surfaces. Convection losses are
higher with high boiling solvents.
Tests shows that convection
losses are typically larger than diffusion losses and are more difficult to control.
However, the use of vapor line covers is most effective. Such covers close just
above the primary condensing coil, effectively reducing diffusion and convection
losses. Using fixed sprays mounted and operated below a closed vapor line cover
can eliminate the use of an operator and a manual spray lance. This helps provide
maximum efficiency.
Proper consideration
and evaluation of all the factors presented here can result in a
highly efficient and economical vapor degreaser. Also, because of
the low energy use of vapor degreasing when compared to other cleaning
processes, it may become the choice to reduce global warming.