Cleaning and Evaluating Drawdown Rods

Question: We use your wire-wound draw down bars here, and have a couple of questions on their care, and how to evaluate their condition. First, please let us know the recommended care and cleaning instructions. Would blasting with baking soda be safe and effective? Second, what is the best way to determine their overall condition?

Answer: Thanks for the question. The most important factor in keeping Mayer rods clean is to use an appropriate solvent immediately after every use. For non-aggressive, low viscosity fluids, simply wiping with a solvent-wetted soft, lint-free cloth may be all that is needed. In other cases, solvent immersion in an ultrasonic cleaning tank, along with brisk scrubbing with a very fine bristle brass brush, may be required. Please keep in mind that this abrasive method may cause burrs on the wire, which will affect subsequent coating performance.

It is important that the final rinse or wipe be done with a liquid such as water or high purity isopropyl alcohol, which will not leave a residue on the surface.

Once cleaned, it is imperative that metering rods be thoroughly dried before re-use, or the residual solvent may interact with the wet film coating when next used. Please note that compressed air – a fast, non-contact drying technique – generally contains trace amounts of oil, and should not be employed.

I don’t necessarily recommend blasting them with baking soda – or any other media – as even with stainless steel there is a potential for some degree of etching, which one would expect would be most pronounced at the “high” spots on the wire winding. This would reduce the area between the windings, with a concommitant reduction of coating thickness. However, if other methods have proven unsatisfactory, I suppose it would be worth a try, especially if the coating formulation is acidic. I would certainly want to check the resulting wet film thickness and finish after trying this! Other than those potential effects, the worst that is likely to happen is that the wire loses its weld or simply breaks and unwinds. If you try this, start with the largest wire sizes first.

As to evaluation of the rod’s condition, precise measurement of the wet film thickness applied would be most important . Evaluating the surface finish quality of the dried (or cured) coating would also be important. If you have a good microscope, that would be an effective inspection tool in this case.

Finally, as the cost of replacement rods is relatively modest, if there is any doubt about quality, it is probably best to simply replace the rods, rather than putting too much time and effort into trying to maintain them forever.

Test Marker Results Seem Inconclusive

Question: I used your test markers to test some film extruded from a masterbatch we are developing, and the results seemed inconclusive. It was hard to tell if the ink was beading or maintaining its integrity. Any comments?

Answer: If the test marker results seem inconclusive, it sounds like the surface energy of the film varies from spot to spot. There are several possible reasons for this.

First, if there are spots of contamination on the surface (fingerprints, transfer of contaminants from a process roll, contact of the sample with a foreign object, etc.), the contaminated spots will definitely have a lower surface energy, which would cause the swath of test ink you applied to show inconsistency in wetting vs. beading.

In the case of a polymer blend, or a polymer modified with multiple additives, it is possible that the blend is not being adequately dispersed in the extruder barrel, causing the various components of the formulation to segregate in the melt. In this case, concentrations of lower surface energy additives – or of lower surface energy polymers in a blend – will naturally bloom to the surface, creating “puddles” of low energy scattered across the film. Blends that include additives or modifiers with incompatible solubility coefficients could have the same problem: Even if they blend in the extruder barrel, they may disassociate before setting in the final film structure.

If the film is surface treated, it is possible that the treatment itself is contributing to the variation in dyne level. This case usually manifests in patterns that can be traced back to the mechanics and geometry of the treater.

To properly investigate any of these causes, it would be best to perform the dyne test using the drawdown method, which allows you to evaluate a relatively large area of film surface all in one pass. Patterns of variation will appear, which will be a valuable clue in determining the root cause of the problem. Also, by testing over a variety of dyne levels, you may be able to determine what might be called surface energy topography: just as an example, you may find that some randomly dispersed areas are testing at only about 32 dynes/cm, whereas the majority of the surface holds at 38. That might suggest blooming of low surface energy partials at those locations. And, in the case of film which has not been surface treated, it may provide a clue to which constituent is not being properly dispersed.

Even by using the simple method of applying the test fluids with cotton swabs, some patterns are easily recognizable. For example, spreading 38 dyne/cm test fluid over and around a fingerprint on a 44 dyne/cm surface will show the print as clearly as a forensics lab photo.

Dyne Testing at Elevated Temperatures and/or Humidity Levels

Question: I know that ideally dyne testing should be done under standard laboratory conditions, but as we test in our shop, which is not air conditioned, that is not possible for us – we sometimes reach temperatures as high as 40° Celsius, at high humidity. How do we deal with this?

Answer: Ideally, we do recommend testing at about 20° to 25° Celsius, with humidity in the range of 40% to 60% RH, Some variation from these conditions is not likely to affect results meaningfully, as the surface tension of liquids and the surface energy of solids are similarly affected by temperature changes, as shown in the following table. But with more seriously elevated temperatures, caution should be employed.

Material Surface Tension(a) Change per °C
2-ethoxyethanol 28.8 -0.13
40 dyne/cm test fluid 40.0 -0.14
Formamide 57.0 -0.15
Water 72.7 -0.21
Nylon 6-6 42.2 -0.065
PC 44.0 -0.060
PE 31.6 -0.057
PET 39.0 -0.065
PMMA 37.5 -0.076
PP 30.5 -0.058
PS 34.0 -0.072
PTFE 19.4 -0.058

Surface tension, and change per degree Celsius are shown in dynes/cm (equivalent to mJ/m2).

(a) Critical surface tension in dynes/cm at 20° to 25° C, generally determined by the Zisman method (regression of the cosine of the contact angle), or by the wetting tension method, using solutions of 2-ethoxyethanol and formamide per ASTM Std. D-2578. A more complete list of polymers is available here, and a more complete list of liquids is available here.

The largest numeric effect would be seen when testing at very high treat levels, where the test solutions are formulated from formamide and water. In the most extreme case – polyethylene treated to be water-wettable at 72 dynes/cm – the net drift works out to 0.153 dyne/cm per degree Celsius. This translates to an effect on test results of roughly -3 dynes/cm at 40° C, as the substrate surface energy would be reduced by only 1.14 dynes/cm, whereas the test solution (100% reagent grade water) would be reduced by 4.2 dynes/cm. It can be argued that even in this extreme case, an error of 3 dynes/cm at a treat level of around 70 dynes/cm would not be critical in most instances. But even at a more typical treat level of 40 dynes/cm, the net drift is still 0.083 dyne/cm per degree Celsius, resulting in an effect of about 1.7 dynes/cm, which could be significant.

So much for the hard data. Please note that this analysis assumes that both the test solution and the substrate have been stabilized at the elevated ambient temperature. If this is not ensured, then one component or the other will obviously be affected more by the temperature change, and test results could deviate from those that would be obtained under laboratory conditions in a less predictable fashion.

However, elevated temperatures pose their own problems. Surface tension test fluids will tend to degrade faster at elevated temperatures, and, while open, bottles will be far more prone to preferential evaporation of 2-ethoxyethanol, which has a higher evaporation rate. When testing with ACCU DYNE TESTTM Marker Pens, the test fluid may pass somewhat more readily through the spring-loaded valve tip – this can have an effect due to a tendency towards gravitational wetting when an excess of test fluid is applied. Also, the rate of evaporation of the test fluids once applied to the surface will increase, so the two second timeframe on which the test is based could come into question. Finally, solubility parameters are affected by temperature as well, so the chemical affinity of the fluids to the surface may be changed.

With regard to the substrate, the rate of crosslinking may be affected, which could have an impact on the surface energy when tested vs. its level over time. Finally, elevated temperature (as well as humidity) levels will tend to accelerate treat loss of the substrate. The mobility of surface-blooming additives will be enhanced, and transfer of the treatment from the treated to untreated side of a film once it is wound will also be more pronounced. This will not only drop the dyne level, but can also lead to blocking of the film when it is paid off from the roll during further processing operations. The latter effects are perhaps the best arguments for limiting product exposure to extreme environments to whatever extent is possible.

As to RH, it is best to avoid excessive humidity, as it can cause higher variability in test results. Also, if there is any moisture on the surface, it will absorb into the test solution, changing its surface tension and invalidating the test. Nylons especially may be prone to this, as they absorb water vapor far mote readily than most other polymers.

Given the range of physicochemical effects which can have an impact on the accuracy of test results produced at elevated temperature and or humidity, if product end-use requirements are rigorous, such as in the automotive industry and for many medical applications, it would be prudent to set up an experimental study to correlate dyne testing results obtained in the shop vs. those obtained under laboratory conditions. You can randomly split your samples into two groups. On one set, test at the machine as usual. For the other set, remove to the laboratory, allow the material to stabilize under that environment, then perform the same dyne test (with a separate set of test fluids or test markers which are to be kept in the lab!). Results can be compared readily. If there is a meaningful difference, I would also suggest looking closely at which set of results best predicts end-use performance or adherence to customer specs. Considering all the factors discussed above, you might even find that the results from the elevated temperature testing are the better predictor of product suitability. I wouldn’t want to bet against it a priori, even though such an outcome does seem rather counter-intuitive.

Overtreatment of TPO

Question: We supply solvent-borne automotive coatings, and recommend that our customers flame treat their TPO components to 48 to 60 dynes/cm for best adhesion and durability. We have seen adhesion failures at higher dyne levels. Would you expect that? And, would your test markers be able to identify overtreatment?

Answer: First, you are correct that any polymer can be over-treated by either flame or corona. The mechanistic details of just what happens to the material’s surface layers are undoubtedly different for the two treating methods. But what basically occurs in either case is the surface layer gets etched and oxidized to the point where it may be water-wettable, but it has been so decimated by the aggressive treatment environment that it no longer anchors well to the bulk of the polymer. The paint adheres well to the surface layer, but the entire paint/surface layer will easily lift away from the bulk of the polymer.

Over-treatment will not cause a decrease in dyne testing results unless too much pressure or abrasive force is used during the test – this would have the same effect as mentioned above, with the untreated underlayer exposed at the surface. So, as long as a light application pressure is used, as directed in the instructions, ACCU DYNE TESTTM Marker Pens can definitely identify the excessive levels of surface treatment that you have found to cause defects.

The problems that arise from over-treated surfaces suggest that it should be standard practice to establish a realistic maximum treatment level, as measured by the dyne test, as well as a lower one. Your suggested range of 48 to 60 dynes/cm sounds reasonable, but I would think that for most applications you’d do fine with a surface energy of 44 dynes/cm or so for solvent-based paints. The presence and concentration of additives and pigments could affect this minimum, especially with thick parts, where there is a large polymer bulk compared to surface area. And, for waterborne or energy cured coatings, the required dyne level would increase substantially.

Finally, as this is a rigorous application (automotive finishing), I would recommend that your customer consider an experimentally designed study of treatment parameters and measured dyne levels vs. end-use quality and durability metrics. Tightening the window of optimal treatment level could prove commercially beneficial.

What Dyne Levels Should I Be Testing At?

Question: My ink requires a minimum of 40 dynes/cm, and my film supplier says they run their poly at 56 dynes/cm. Should I use a 40 as a threshold test, or does the marker dyne level need to match the material? What range should I be using?

Answer: If the poly were actually at 56 dynes/cm when you tested it, a test with a 40 dyne/cm test marker would probably wet out so well and have such an attraction to the treated surface that it would permanently mark the film. That would tell you that the surface was way higher than 40 dynes/cm – if it was actually only 40 dynes/cm, the test fluid would start to bead up within two seconds or so. But there’s a lot more to the story than that.

Polymers lose treatment – especially when induced by corona treatment – over time and with downstream processing, so if a film tests at 56 dynes/cm at the end of your supplier’s extrusion line, you might find it to have a surface energy of as low as 44 dynes/cm a few weeks later, when you are ready to print it. (Please don’t take these treat loss numbers as gospel – they are for explanatory purposes only!) After a few months of storage in a hot and humid environment, it may well have dropped to below 40 dynes/cm. Slip agents are especially problematic when it comes to treatment loss over time, especially at elevated temperatures.

ACCU DYNE TESTTM Marker Pens measure surface energy by testing over a range of dyne levels, starting with a low enough level that you expect it will wet out for at least several seconds. In your case, I would recommend starting at 34 dynes/cm, and having the ability to test up to 56 dynes/cm, which is at the high end of what you are likely to ever see.

While your ink supplier probably is correct about 40 dynes/cm being the minimum acceptable treat level, it will still be instructive to test filmstock as it goes to press. Keeping records of dyne levels (and any comments testers may report) along with other process data may prove to be a valuable tool in troubleshooting at some point. Also, you may find that with higher substrate dyne levels you are able to increase press speed somewhat, and/or improve print quality. Quantifying these relationships can streamline your operation and ultimately reduce costs by enabling you to develop better specifications for your purchased rollstock.

TSCA Review

Question: I am conducting an environmental review on ACCU DYNE TEST Marker Pens, and the SDS does not have the information I need for approval. I need to verify that “all the components of the product are either listed or exempt from listing under the TSCA section 8(b) chemical inventory list.” Your SDS lists the TSCA inventory but references only the TSCA section 5(a) (significant new use) for one ingredient. Can you please provide the requested information?

Answer: All constituents of ACCU DYNE TESTTM Marker Pens and surface tension test fluids (both use the same formulations) are listed in the TSCA inventory. For full information on 2-ethoxyethanol (CAS 110-80-5), please see https://www.federalregister.gov/documents/2005/11/29/05-23421/2-ethoxyethanol-2-ethoxyethanol-acetate-2-methoxyethanol-and-2-methoxyethanol-acetate-significant.

Shelf Life of 72 Dyne/cm Surface Tension Test Fluids

Question: We purchase 4 ounce bottles of dyne solution at 72 dynes/cm. Can you tell me how you determine the expiration date? We don’t always use up the container before its shelf life is over.

Answer: Given that your purchase is of 72 dyne/cm surface tension test fluid, containing only reagent-grade water and Methyl Violet dye, this is an interesting question. The typical dyne solutions containing 2-ethoxyethanol and formamide (mixed per ASTM Std. D2578) definitely have a finite shelf life, as the constituents will react with one another over time, eventually changing their wettability regardless of whether they have been used or not. I do not believe it has ever been determined whether the dye acts as a catalyst, whether it is the cause, or whether the change happens with dye or without. At any rate, historically, suppliers of these test fluids have assigned a shelf life of approximately 3 to 4 months from date of manufacture. We are confident enough with our reagent grade materials to offer a shelf life of 5 months.

No data is available on the aging of water/Methyl Violet mixes. My best guess is that any degradation would be slower than with the binary mix dyne levels, but I am not willing to bet on that and change the expiration dates for this single constituent dyne level (the same can be said for 30 dyne/cm test fluid, which contains only 2-ethoxyethanol and Methyl violet dye, or 57 dyne/cm test fluid, which contains only formamide and Methyl violet dye).

A final concern pertaining to the stability of the 72 dyne/cm test fluid regards potential leaching of compounds from the packaging bottle (HDPE for narrow and wide mouth bottles; LDPE for dropper bottles) into the test fluid. A good deal of information on this phenomenon is available from the literature, but most of it pertains specifically to health effects, and most of the studies are not limited to additive-free polymer formulations. One review(1) presents a litany of mostly solvents and short-chain molecules that have been identified leaching from HDPE water pipes – if these do, in fact, leach from unmodified HDPE, they would generally reduce the surface tension of water over time. Another study(2) demonstrates changes in LDPE over time when exposed to pure water. It seems reasonable to assume that eventually there will be some effect on the test fluid due to polymer leaching.

You could run a study comparing results from fresh test fluids vs. those that are aged, though this could be a challenge, as any number of variables may affect the aging process (average storage temperature and RH, degree of temperature and humidity cycling, exposure to light, etc.). Realistically, the best strategy would be to purchase one or two ounce bottles, which will offer full usage before there are any problems related to aging.

References:

1) no author cited, https://plasticpipesleach.org/wp-content/uploads/2018/01/White-Paper_A-Review-of-Chemical-Substances-Shown-to-Leach-from-Common-Drinking-Water-Piping-Materials.

2) S. Massey, A. Adnot, A. Rjeb, and D. Roy, “Action of water in the degradation of low-density polyethylene studied by X-ray photoelectron spectroscopy,” eXPRESS Polymer Letters, 1, No.8 (2007) 506–511.

Dyne Testing of Materials to be Processed in a Dry Room

Question: We test plastics at incoming inspection that will later be processed in a dry room at <1% RH, and your test procedure sets limits of 30% to 70% RH. What impact would you expect this to have on the validity of the dyne readings?

Answer: The only effect that I know of regarding humidity is that unusually high levels tend to increase the variability of test results. I suspect this is due to condensate on the sample surface. If that is, in fact, the mechanism, then extremely low humidity should not significantly affect readings for most materials. There is one notable exception to this – the nylon family of polymers (polyamides), which are quite hydrophilic in the presence of water vapor. If your testing includes these materials, I would strongly recommend that you do a controlled study, as discussed below. There is little question that a significant change in adsorbed water vapor will have an impact on surface energy test results.

You should keep in mind that evaporation rate comes into play with the dyne test, as discussed here, and extremely low humidity levels may affect the rate of test fluid evaporation. The question is whether the constituents of the test fluids evaporate preferentially in a moisture-starved, compared to a moisture-rich, environment. One would intuitively assume so, but both 2-ethoxyethanol and formamide are miscible in water, so it is not out of the question that they would be drawn more readily to the gas phase in the presence of water vapor. Dyne levels 58 and higher contain water in their formulations, so there is no question that extremely low humidity would to some degree alter the evaporation effect on these formulations.

The evaporation of 2-ethoxyethanol and formamide under varying humidity conditions is an interesting question from the perspective of thermodynamic theory (and if any readers are experts on such matters, I would love to have some feedback on this!), but it probably does not amount to much in terms of real-world test results. The only warning I would have is to pay strict attention to the two second timeframe specified by the test, as that does relate to evaporation, as well as to de-wetting behavior.

In summary, the only way to be sure of the effect would be to test identical sets of samples at both 1% and 40% to 60% RH, and compare the results. In light of the comments pertaining to nylon noted above, if that is a polymer you are testing, I do suggest doing this comparison. But, even if you find a significant humidity effect, as long as the environment in the incoming inspection area is kept constant, results derived there should still provide good predictive information regarding the behavior of the material in the dry room.

Another consideration is that the time elapsed from testing at incoming inspection to introduction to the dry room, as well as the time elapsed from introduction to the dry room to when the materials are processed, should all be controlled as closely as possible. The surface characteristics of plastics – especially those that have been corona treated – change over time and under varying environmental conditions. So, controlling these variables will be important in making the most of the dyne testing results in the context of your overall quality program.

With these considerations in mind, the dyne level number you come up with may not exactly match the material’s surface energy at the time it is processed at low humidity, but it should still offer data which will be effective in helping predict its adhesion and wetting characteristics.

Reason for 2 Second Timeframe in Dyne Testing

Question: Why is two to three seconds the criterion of determination of a materials’ wetting level? Wouldn’t permanent wetting be a better criterion?

Answer: Actually, ASTM Std. D2578 and ISO 8296 both specify 2 seconds as the timeframe for evaluation, but we usually suggest 2 to 3 seconds, as most testers seem more comfortable when a brief range is specified, rather than a single instant in time. The timeframe is partly historical artifact, and partly due to the basis of the test, which derives from the behavior of retreating contact angles.

As the test fluid is applied to the surface, it is spread over a given area – usually about a square inch (about 6 or 7 square cm) either in a line or as a block. The results of the test are based on how (and if) the fluid film reticulates (shrinks) into individual beads, and this is obviously a process that takes a finite amount of time to achieve a balance.

I believe the 2 second timeframe was originally established to balance the effect of evaporation (the lower surface tension component of the test fluids evaporates more readily) and the effect of de-wetting per se. In other words, if you wait longer, evaporation will start to have more of an effect, which induces greater de-wetting. The idea is to evaluate at the time that surface forces per se are most important to the interaction of the test fluid and the substrate. When the test was first developed some 60 years ago, the 2 second timeframe was established as a way to standardize interpretation and meet this goal. Based solely on empirical evidence, it appears to be an effective specification, as no serious alternatives have been suggested.

Like most questions regarding surface energy testing, whereas the question may be simple, often the answers are not so much so!

Should Surface Tension Test Fluids Be Stored at Reduced Temperature to Achieve Maximum Shelf Life?

Question: If chemical reactions affect the accuracy of dyne fluids, wouldn’t it be a good idea to store them in a refrigerator?

Answer: There’s no question that storing dyne solutions at a reduced temperature will slow down any chemical reactions, but that is only one factor that affects their aging or performance. There are a number of things to consider, as I’ll get to below. But first, please keep in mind that 55 to 60 dynes/cm test fluids will freeze at about +3°C (39°F), and we strongly recommend that a change of state be avoided (more information on that topic is available here). Also, in many cases low temperature storage ends up being at relatively high humidity. This can be detrimental, as there may be some degree of water vapor transmission over time from the storage environment into the bottles of test fluid (or the barrels of test markers).

For end-users of ACCU DYNE TESTTM Marker Pens and surface tension test fluids, the most critical considerations are ensuring that the test supplies and material samples are both at ambient temperature when the test is performed, and avoiding repeated temperature cycling from refrigerated to ambient. Temperature (and humidity) cycling are used in accelerated aging studies, which is enough to be said regarding that.

We’ll consider three different scenarios, and discuss the benefits and risks of refrigerated test fluid storage for each.

Some shops need to keep supplies on hand, but only use them for specific short run jobs. In this case, there may be periods of weeks or even a few months when they are not used at all, followed by short periods of relatively intense usage. In this situation, as long as it is ensured that the test markers or dyne fluids are removed from refrigeration long enough in advance – 24 hours is a nice conditioning period – then storing them refrigerated would probably be a prudent idea, especially if there is not an alternate storage area with good environmental control.

By contrast, in many industries – film extrusion, printing and converting for example – dyne testing is an ongoing requirement. In this case, the only reason to refrigerate would be if large “master” bottles (8 ounces or larger) are used to periodically replenish small bottles used for testing, or if ACCU DYNE TESTTM Marker Pens are bought in multiple sets for release to manufacturing as required. Generally speaking, we do not recommend refrigeration of inventory under these conditions, as the chance of using test supplies before they are adequately conditioned, along with the possibility of freezing and exposure to high humidity, combine to create more risk than I would care to take with sensitive reagents.

The last example would be for distributors who purchase to hold inventory for resale. In this case, it is clear that ideally it would be best to store refrigerated in a humidity-controlled environment. The most serious consideration is to make sure that the time your inventory is out of cold storage to fill orders is minimized, so its temperature stays as constant as possible.

So – what’s the quick and easy answer? Of course there is none – this is dyne testing after all, and every situation has its own unique twists – but if I had to make a blanket recommendation, I would say just store your product well sealed under normally controlled laboratory conditions in its original packaging. If your test supplies must be kept in the shop at elevated temperature or humidity, consider increasing the frequency of replenishment. Other than that, don’t worry yourself overmuch about the finer details of thermodynamics.