Indium Corporation
From One Engineer to Another®

Strategies in Light Trade Show

Thursday, January 19, 2012 by Eric Bastow [Eric Bastow]
Indium Compounds
Indium Corporation is hosting a
booth (#809) and will be highlighting a series of products and solutions related to all aspects of LED and lighting manufacturing and assembly at Strategies in Light, Santa Clara, CA, February 7-9, 2012





The show is a who's who in the global lighting industry. Along with the exhibition, there is a full line up of workshops and tutorials encompassing the latest in LED and lighting technology.





Gold Solder Alloys ApplicationsIndium Corporation is proud to be a part of the Strategies in Light trade show.  Please stop by and see us. Technically orientated staff will be available to discuss your application, as well as: 



Indium Compounds


Gallium Compounds

Indium HeatSpringThermal Interface Materials


Gold Alloy Assembly Materials

NanoFoilUnique Bonding Materials and Techniques


Indium-Copper Intermetallics in Soldering

Friday, January 13, 2012 by Eric Bastow [Eric Bastow]
Indium ShotIndium and indium-containing alloys see wide use in a multitude of soldering applications. Indium has many attractive properties such as remaining ductile at cryogenic temperatures, compatibility with thick gold metallizations, and excellent thermal cycling performance.....to name just a few.

However, indium and indium-containing alloys may not be appropriate for every application. One such possible inappropriate scenario is the use of indium and alloys of indium against copper or copper-containing alloys, such as brass and bronze. This is because, even in the solid state, indium will diffuse into the copper material over time. The rate of diffusion is a function of temperature. The indium and copper react and form intermetallics. This intermetallic layer is much harder and stiffer than the parent indium and copper materials. This intermetallic layer can be subject to fracture. Depending on the application and the exact nature of the materials being used, this may or may not be a problem. It is recommended that one investigate the long term implications of this interaction. Given that the phenomenon is a function of time, it is important to understand that the effects of the interdiffusion, may not be readily evident. It make take several months or years for any effects to manifest. Accelerated life testing is suggested.

It should be noted that there are several applications where indium is used against copper successfully and reliably, everyday, the world over. This post is not meant to generate panic, but rather to empower the end user to make the best decision for their application.

Copper Wire

One way to by-pass the whole issue is to plate the copper with a layer of nickel. Literature suggests a minimum thickness of 50 microns of nickel. Nickel is known to act as an effective diffusion barrier, preventing the indium from ever coming in contact with the copper.

For more information on this phenomenon, please read a work titled "Effects of Interdiffusion on the Properties of Indium-Plated Contacts" by R.W. Barnard Ph.D. of Bell Telephone Laboratories, August 1974.

Let me know if I can help you with this issue.

Eric

Tombstoning: The Death of a PCBA

Wednesday, November 30, 2011 by Eric Bastow [Eric Bastow]
Tombstoning DiodeTombstoning (also known as the Manhattan effect, drawbridge effect, or Stonehenge effect) is described (in the simplest, and most common, sense) as occurring when one end of a passive device, such as a resistor or capacitor, rises up out of the solder and breaks contact with the circuit. But it is not limited to passive devices. Other surface mount devices can tombstone as well (see the tombstoning diode image - top). Tombstoning is a "fatal" defect because it produces an open circuit.

Tombstoning has, once again, become a central issue - primarily due to two main issues:
  • Tombstoningthe transition to Pb-Free (higher reflow temperatures, and related flux issues)
  • miniaturization (0201s and 01005s)
Tombstoning is almost always the result of uneven wetting forces on the terminations of the component. When one end "wets" before the other, the (now unbalanced) wetting force of the solder "pulls" the component, rotating it, causing it to stand on end.

Various factors contribute to tombstoning. The one that we (as a solder paste supplier) typically encounter  is uneven heating of the PCB assembly - which causes one paste deposit to melt and wet before the other - per component (as described above). Trying to achieve a higher reflow temperature, as required with the new mainstream Pb-Free alloys, can exacerbate the greater thermal gradient across the PCB (and from one end of a component to the other).

Reflow ProfileThermal gradients are usually easily remedied with minor adjustments to the reflow profile:
  • The reflow oven operator can slow down the ramp rate. A slower ramp rate allows for more uniform warming of the PCBA.
  • Another technique is to employ a "soak" just below the melting temperature (solidus) of the alloy. For example, for a SAC305 profile (217°C solidus), one may implement a "soak" at 205 to 210°C for 30 to 120 seconds. This allows for the cooler parts of the PCBA to "catch up" to the warmer parts. After thermal equilibrium has been achieved, one can spike the temperature up to the appropriate peak temperature (i.e. 245°C). This technique (depicted in the reflow profile shown at the right) allows for all of the solder paste deposits to melt and wet the component terminations at roughly the same time; thereby, mitigating tombstoning.



Different flux chemistries, and types, can also impact tombstoning. It is often desirable to have a solder paste that wets well, even to old, oxidized components. One possible negative side effect of an excellent wetting solder paste is tombstoning. When the paste wets "aggressively" to the component terminations, causing a strong wetting force, even the slightest disparity (temperature, cleanliness, flux area, etc.) from one termination or pad to the other can cause the component to tombstone.

The wetting speed and force is also directly related to the rate at which the solder melts. It should be obvious that wetting only occurs when the solder is in a liquid state, not while solid. For this reason, solder alloys that are not eutectic (alloys that start to melt at one temperature but are not fully liquid until some higher temperature) can produce less tombstoning than a eutectic (clearly defined melting point) alloy, all other things being equal. Sn63 (63Sn 37Pb) is a eutectic alloy and makes a clean transition from a solid to a liquid at 183°C. Sn60 (60Sn 40Pb) is not eutectic and starts to melt at 183°C but is not fully liquid until 191°C. In the case of "non-eutectic" alloy like Sn60, between 183°C and 191°C, solid and liquid are coexisting. To this end, some solder paste manufacturers have developed alloys that melt gradually (are purposely not eutectic) to combat tombstoning.  

Wetted Passive ComponentThe pad design and lay-out can also affect tombstoning. Usually pads that are located mostly beyond the terminations or have large pad areas beyond the terminations can contribute to tombstoning. To the left is an image of a cross section of a soldered passive component. Notice how the solder fillet reaches to the top of the termination. Solder paste deposits that extend well beyond the component cause a lot of wetting force and leverage to be applied to the extreme ends and tops of the component. This wetting force, if not evenly applied to both terminations, can cause the component to tombstone.









Reduced Solder VolumeSimilar to the placement of the solder paste deposit (pad design), solder volume can also impact tombstoning. It is very simple. More solder equates to more wetting force and vice versa. To the right is an image that has an extremely reduced amount of paste volume (not recommended to this degree). If one could imagine that this component had indeed properly soldered to the pads, one could see how it would be nearly impossible for the component to tombstone. There is simply not enough solder to wet the entire end of the termination. Solder deposit volumes that restrict the solder from being able to wet up to the top of the component greatly reduce the wetting force and leverage that the solder can apply to the component. Depending on the class of workmanship that one is building to, it may not be practical to reduce the solder volume. The product class may require fully wetted terminations.



It is also critical that the solder paste deposit and component sit squarely on the pads. Any offset can affect the way the solder wets the terminations and can cause tombstoning.

Offset Solder Paste Deposit


Miniaturization, as characterized by smaller, lighter passive components, such as 0201s and 01005s, creates a struggle where tombstoning is concerned. Issues of solder paste deposit location (see image to the right), component placement, and solder paste volume are difficult to control given the overall minuscule scale of the scenario. Also, smaller components are inherently lighter and, therefore, easier to pull up on end.

Controlling tombstoning is a critical issue in SMT assembly. But, with understanding what causes tombstoning, one can control it.

CONTACT ME to discuss tombstoning:

Eric Bastow: Senior Technical Support Engineer

Phone: +1.315.853.4900
E-mail: ebastow@indium.com

Solder Paste Expiration / Shelf Life

Monday, November 21, 2011 by Eric Bastow [Eric Bastow]
Solder Paste Expiration Date / Shelf LifeSolder paste is comprised of powdered solder alloy suspended in a flux vehicle. There is a group of flux ingredients that is generically identified as "activators". It is the activators whose primary function is to remove oxides not only on the surfaces that are being soldered but any oxides that may be present on the solder powder, itself. These activators are generally "activated" by heat. The flux chemist knowingly selects activators that are relatively dormant at room temperature but become very active at soldering temperatures. Their level of activity is often directly related to temperature.

Given that the flux is in direct contact with the solder powder, this allows for the flux activators to interact with the solder powder even while the solder paste sits on the shelf. Those activators can begin to "react" with the powder, and, given enough time, can "clean" the powder surface to the point where the solder particles will actually "weld" together. So, now instead of the paste containing free-flowing powder, it contains clumps of welded together solder particles. Those clumps often increase the viscosity and can clog stencil apertures and dispensing needles. For these reasons, the paste manufacturer will require refrigerated storage of the paste in order to realize the optimum shelf life.


As a rule water-washable solder pastes often include activators that are more aggressive than the activators found in no-clean and RMA type solder pastes. This is because water-washable flux residues are designed to be washed off. So, there is no concern about the flux causing corrosion over the life of the product. On the other hand, a no-clean flux generally has milder activators, because the flux residue may remain on the device indefinitely; where corrosion would be detrimental to the performance and life of the device. As a result, no-clean type solder pastes typically have a longer shelf life and are more tolerant to higher storage temperatures than water-soluble/washable solder pastes.

A solder paste typically has a shelf life of 6 months when refrigerated. One may ask what happens if the paste has been refrigerated for 2 months, then thawed to room temperature, remains at room temperature for 12 hours and is then re-refrigerated....Will it still have a 6 month shelf life? That is a very difficult question to answer. The same situation could arise with a perishable food item that requires refrigeration, such as milk. Lets say that one buys a container of milk at the store and it has an expiration date that is 5 days away. After having it home, properly refrigerated, for 2 days, one of the kids leaves the milk on the counter for 3 hours before anybody notices it and puts it back in the refrigerator. Can one expect the milk to stay good for the remaining 3 days? What about if it is left out of the refrigerator for 1 hour? or 5 hours? You can see how difficult the questions become to answer. What is the impact if a solder paste is exposed to elevated temperatures when it is 3 days old or 3 weeks old or 3 months old or with 3 days left to expiration????? The answer is not fully known. It is impossible for the solder paste manufacturer to study every possible scenario for its impact on the shelf life of the paste.

The best and only sure approach is to refrigerate solder paste immediately upon receipt and only thaw when needed, in amounts that will be completely consumed. Avoid thawing and re-refrigerating pastes as much as possible, in order to take advantage of the full shelf life.

The particle (mesh) size of the solder powder can also impact shelf life. As the powder size decreases, the surface area per volume or mass of powder drastically increases. More powder surface area means more area for the flux to react with, and more surface area for welding to occur. Therefore, a type 3 solder paste that has a shelf life of 6 months may not provide a full 6 months of shelf life with a type 6 solder powder, all other things being equal.

For the most part, solder paste manufacturers are conservative in assigning shelf life. It is highly unlikely that a properly stored solder paste's performance is going to collapse 1 day after the expiration date. In fact, depending on the paste, it may still be good for months beyond the expiration date.

How does one know if their solder paste is still usable? This can be determined rather easily. As mentioned earlier, one artifact of a degrading paste is a rise in viscosity. So one can perform a simple printing or dispensing test to see if it still performs adequately in that regard. Another aspect that often suffers is coalescence. As the flux degrades it looses its ability to adequately remove oxides on the solder powder. In order to gauge the degradation, it is best to put a small amount of paste on a non-wettable substrate, like a piece of ceramic. Reflow the paste and see how well it coalesces. If coalescence is good, the solder paste will reflow into a ball, surrounded by a flux pool that is relatively free of uncoalesced solder particles. If the paste has significantly degraded, the paste will not coalesce well and there will be a significant amount of uncoalesced solder particles in the flux pool.

Please see this IPC test method for determining the coalescent properties of a solder paste.

Intermetallics In Soldering

Friday, November 11, 2011 by Eric Bastow [Eric Bastow]
Intermetallics are a necessary evil in the metal-to-metal bonding world, which definitely includes soldering. There are two basic ways that metal will "chemically" bond to another metal: 1) solid solution 2) intermetallic. We will focus just on intermetallics for the moment as that is the most pertinent to the soldering world.

Many people confuse or interchange "wetting" for intermetallic formation (bonding). Wetting is just wetting. Just because a solder "wets" to a surface does not mean that an intermetallic "bond" has been formed. For example, and I have done this myself, 55.5Bi 44.5Pb can be melted onto a piece of copper. The molten BiPb will flow and "wet" to the surface of the copper. However, upon solidification (cooling) of the alloy, the BiPb can be peeled off. Why?... because no intermetallic was formed between the BiPb and the copper surface.

Intermetallic LayerIn order for an intermetallic to form, some amount of the surface metallization must dissolve into the molten solder. For this reason, Sn (tin) has long been a critical component of solder alloys. Molten Sn (tin) is an excellent solvent of many other metals. And, conveniently for us, those "many other metals" include elements like copper, gold, silver and, to a lesser degree, nickel. The rates at which these other metals dissolve into molten tin (solder) will differ. Gold dissolves readily into solder; whereas nickel does so slowly. So, because the rate of dissolution is different for each metal, the rate of intermetallic formation is also different. I have dealt with companies that have a long history of soldering to copper, and, for whatever reason, they are forced to switch to an ENIG (Electroless Nickel / Immersion Gold ) surface. (It is important to note that the gold layer is very thin and only applied to protect the nickel from oxidation. This gold layer readily dissolves completely into the molten solder and the "bond" is actually made to the nickel surface). When they make the change they sometimes encounter a number of issues such as incomplete wetting, poor bond strength, etc. and do not know why. They are not aware that the same reflow profile (time and temperature) that yielded a good (intermetallic) bond to copper is not sufficient to get the same intermetallic bond to nickel. Once they adjust their profile (more time and/or higher temperature) to allow for sufficient intermetallic formation , they are able to achieve acceptable solder joints. Keep in mind that dissolution, the phenomenon of a solid dissolving into a liquid, is effected by both time and temperature. Generally speaking, more time and more temperature allows for more dissolution and, hence, more intermetallic formation.

As mentioned in my opening line, intermetallics are a necessary evil. Why "evil"? Because they tend to be the most brittle part of the solder joint. Some intermetallics are more brittle than others. (This should be taken into consideration when choosing a solder alloy for a particular metallization).  For example, intermetallics that form between Sn and Au are often extremely brittle.  Being brittle, they can be subject to fracture, etc. This is a case where more is not always better. Yes, you need an intermetallic to get a "bond". Too thin of an intermetallic layer can be bad; but too thick of an intermetallic layer can be just as bad, if not worse. Believe it or not, the solder may not adhere well to its own intermetallic layer. Intermetallics are generally crystalline and chemically-stable structures....they do not really react with anything else once they have formed. If you have ever looked at a fractured solder joint, you may have noticed that the fracture likely took place right at the interface between the intermetallic layer and the bulk solder.

One other possible outcome of an excessively thick intermetallic layer is "voiding" at the interface. Why? Well, we first need to look at the reaction products. There are two basic types of reaction products that form the intermetallic layer between Sn and Cu. They are Cu3Sn and Cu6Sn5. In the fKirkendall Voidingirst case there are 3 Cu atoms to every Sn atom and in the second case 6 Cu atoms to every 5 Sn atoms. In both cases the Cu is being consumed faster than the Sn atoms. Because of this disparity in the reaction, in an exaggerated scenario, little holes or vacancies ("voids") can form in the copper surface.

Intermetallic formation is not only limited to the solder process. Metal atoms can diffuse even in the solid state. And that movement can cause the metal atoms to interact, react, and form intermetallics or cause the existing intermetallic layer to thicken. "Ageing" experiments are often performed to measure how much the intermetallic layer will change and what effect it will have on the mechanical nature of the joint.

It is well beyond the scope or purpose of this blog post to provide an exhaustive discussion of intermetallics. Whole books could be written on the topic. So, I am far from doing justice to the topic of intermetallics. I can only hope to shed a little light on the subject.

Comments or questions are very welcome.

Is my unused indium sulfamate plating bath worth anything?

Thursday, August 25, 2011 by Eric Bastow [Eric Bastow]
Indium Hydroxide PowderIf you are left with an indium sulfamate plating bath or solution that you no longer use or need, you may have wondered what to do with it.

It may be surprising to know that the indium plating bath solution has a potential monetary value. Its value is derived from the indium metal still in solution. The plating solution, as supplied from the manufacturer, has approximately 30 grams of dissolved indium metal per liter. And, with normal plating bath use, the indium content of the bath can rise to twice the original amount (~60 grams per liter). So, in the example case of a 5 gallon tank, one could possibly have 1,200 grams of dissolved indium metal.

So.... How does one extract this hidden wealth?

The indium sulfamate plating solution has a low pH (acidic). This is needed to keep the indium in solution. If the pH of the bath rises, the indium will precipitate out in the form of indium hydroxide. Indium hydroxide is not soluble (in water). The bath will turn a milky white as the indium hydroxide is formed.
 
One can force the indium to precipitate out by adding NaOH (sodium hydroxide) to the bath to raise the pH. Raising the pH to 7 (neutral) is recommended because it will make disposal of the rest of the bath easier and safer. In a static bath (no stirring or agitation) the indium hydroxide will eventaully settle out to the bottom of Indium Metal Shotthe tank. The solution on the top can be siphoned off. And then the indium hydroxide can be dried - leaving a white powder.



The indium hydroxide powder can then be shipped to an indium reclaimer. The reclaimer will convert the indium hydroxide back into indium metal which has market value. The value of indium metal can be tracked through such entities as the Metal Bulletin.



Note: Please consult local environmental regulations to insure proper disposal of the indium sulfamate plating solution.

Contact me with any questions.

Eric Bastow

Why doesn't my 80Au 20Sn solder look any thing like gold?

Wednesday, August 24, 2011 by Eric Bastow [Eric Bastow]
80Au 20Sn solder frames compared to the appearance of stainless steel tweezersIf you have ever handled a piece of 80Au 20Sn solder alloy, one of the things that you might have noticed is that it does not look anything like gold (yellow lustrous metal). In fact, it does not look all that different than tin or any other tin based alloy.

And, yes, before we continue....it is the same gold (Au) used in jewelry, etc.

To the AuSn newbie, the first shipment of 80Au 20Sn solder may cause a little bit of alarm. "Did they send me the wrong alloy? This doesn't look like it has any gold in it!!!"

To the human mind, when one thinks of something that is comprised of 80% of a material, one naturally assumes that material will dominate the properties of the composite material. And, normally, that would be a valid assumption. However, in the case of a solder alloy, the composition is almost always reported in terms of percent by weight. So, in the case of 80Au 20Sn, the alloy is 80% by weight gold and 20% by weight tin. The "issue" lies in the fact that gold is more than twice as dense as tin; 19.3 g/cc versus 7.3 g/cc. 

So, let's think about this.............

If we have 100 grams of 80Au 20Sn alloy, you have an alloy comprised of 80 grams of gold and 20 grams of tin. But, it terms of volume of gold and tin, you have 4.15 cc of gold and 2.74 cc of tin. So, by volume, the alloy is 60% gold and 40% tin. The 40% (by volume) of tin in the alloy is enough to "dilute" the gold and greatly diminish any "yellowing" that one would expect the gold to impart to the appearance of the alloy. 


If anyone has ever attempted to accurately photograph a shiny metallic surface, one can appreciate the difficulty in so doing. So, the photo shows some 80Au 20Sn solder preform in comparison to a pair of stainless steel tweezers. Visually there is very little, if any difference in appearance.

 

Humidity and Solder Paste Do Not Mix

Tuesday, May 31, 2011 by Eric Bastow [Eric Bastow]
Condensation on side of cold solder paste jarUnbeknowst to me, the refrigerator where I store my solder paste and fluxes that I use for SIR (Surface Insulation Resistance) testing was being moved. One of my colleagues showed up at my desk with 2 jars that he had just removed from the refrigerator. In the time it took him to walk 50 feet, a significant amount of moisture had condensed on the outside of the jars. They were simply wet...as if somebody had just dunked them in a tank of water.

 
The incident impressed upon me the importance of allowing the paste/flux temperature to rise to room temperature before opening their containers. If I had Condensation on bottom of cold paste jarremoved the lids of either of the containers when they were handed to me (still cool), moisture would have quickly condensed on the surface of the paste/flux. As a rule, solder pastes and solder flux (tacky flux), be they no-clean (rosin/resin based) or water washable, do not react well to moisture. Moisture-contaminated paste or flux may:
  • exhibit reduced viscosity
  • spatter during reflow
  • produce excessive oxidation of the solder joint
CONCLUSION: Always allow your solder pastes and fluxes to equilibrate to room temperature before opening their containers. Often, this means planning ahead - sometimes removing them the night before you plan to use them. This is especially important as the northern hemisphere heads into the summer months.

Plating of Indium using an Indium Sulfamate Plating Bath

Monday, April 25, 2011 by Eric Bastow [Eric Bastow]
The following videos show a live demonstration of the set-up and operation of the indium sulfamate plating bath. The workpiece in this demonstration is a strip of NanoFoil®. (NanoFoil® has traditionally been available with a tin plating as a bonding medium. We are looking at expanding this to using an indium plated coating as the bonding medium.)

This first video is a shot of the general set-up. You will notice that the workpiece (NanoFoil® strip) is suspended from a copper bar in the center of the container. The workpiece is connected to the negative (-) terminal on the rectifier via the blue colored wire. (The copper rod is just used as a support. It is not connected electrically.) The indium anodes (connected to the positive (+) terminal on the rectifier via the orange colored wires) are taped to the inside of the bucket. There is one on each side of the NanoFoil® strip to insure that both sides of the strip are evenly plated.

Indium Sulfamate Plating Set Up

The second video shows the indium sulfamate plating bath solution being poured into the plating container. It is important that the plating solution only touch the indium anodes and workpiece. Allowing the solution level to get high enough to touch other surfaces can contaminate the plating solution.

Pouring of Indium Sulfamate Plating Solution

The third video shows the indium plating in process. Notice the evolution (bubbling) of hydrogen gas at the cathode (workpiece).

Indium Plating in Progress

The fourth video shows the finished workpiece. It has been rinsed with deionized water. Given the fragility of the NanoFoil® it must be patted dry. The matte area on the strip is the area where the indium has been plated. The shiny portion is the un-plated NanoFoil®. The thickness of the indium plated deposit is a function of the plated area, current, and time.

Drying of Indium Plated NanoFoil Strips

This image shows two pieces of indium plated NanoFoil®. The piece on the left exhibits dendritic type growth of the indium plated deposit. This is typical of electro-plated deposits because the current density is highest at edges and corners. Indium is very soft and these dendrites are easily removed.

Indium Plated NanoFoil Strips (showing dendrites)

What is the best way to solder to Nitinol?

Monday, February 28, 2011 by Eric Bastow [Eric Bastow]
Nitinol (a nickel titanium alloy) has become a very important material, especially in the medical world. It is often necessary to "attach" Nitinol to another piece of Nitinol or some other material such as platinum or stainless steel. Common high temperature bonding methods, like welding, are not suitable for bonding to Nitinol because high temperatures can ruin Nitinol's shape memory characteristic. However, the temperatures associated with soldering, considerably lower than welding, do not threaten the properties of Nitinol.
Nitinol Tubing
While soldering may be the desired means of attaching to Nitinol, it does not come without its challenges. Nevertheless, with the right material set and equipment, soldering to Nitinol can a robust process.

One of the obstacles to soldering to Nitinol is the inherent titanium-oxide-rich top layer. In order for soldering to take place, the molten solder must have access to clean oxide-free metal. That means that the titanium-oxide-rich layer has to be removed. There are a couple of ways to remove the oxide layer; they can be used in concert with each other and can be repeated as necessary. If the size of the part allows, the oxide layer can be mechanically abraded off. It is also possible to "chemically" remove the oxide layer. That is typically accomplished with a flux. Traditional soldering fluxes are typically designed for relatively pristine surfaces such as cleaned copper. Such a flux would not be effective for soldering to Nitinol. But highly active fluxes, capable of removing the titanium-oxide rich layer, are available.

Nitinol Soldering ProductsFurthermore, an appropriate solder alloy must be used. Given that many Nitinol devices are medical in nature, it is intuitive that solders containing Pb (lead) and other toxic metals would not be appropriate. Two solder alloys have emerged as "standard" for soldering to Nitinol:
  • 96.5%Sn 3.5%Ag (221C)
  • 80%Au 20%Sn (280C).
Which alloy is used is often determined by the expected life of the device and whether or not it will see high temperature autoclaving. Many single-use (disposable) devices use SnAg; whereas long -term or multiple use devices (autoclaved) use AuSn.

ITO (Indium-Tin Oxide) Sputtering Target Reclaim/Recycling

Thursday, February 3, 2011 by Eric Bastow [Eric Bastow]

ITO is one of the materials that makes the magic of flat panel displays (monitors, TVs, etc.) possible. When sputtered on in a thin layer, it acts as a transparent conductive film. However, the process of sputtering is very inefficient in its use of ITO. And, with the explosion of flat panel display sales, large amounts of ITO end up as "waste".

It is important to understand the economics of ITO. The main precursor of ITO is indium (metal). Indium is a semiprecious metal and trades on the open market like gold and silver. It is subject to price fluctuations just like the other precious metals. So, there is an economic impetus to reclaim as much of the unused ITO as possible.

Indium (Metal)
As mentioned earlier, flat panel displays employ a sputtered ITO coating. The indium metal must first be converted to indium oxide and then blended with the appropriate amount of tin oxide. The result is a pale green powder.
ITO (Indium-Tin Oxide) Powder
In order for the ITO to be usable, it must first be compressed in to a sputtering target. Planar sputtering targets are the dominant form of sputtering target used for sputtering of ITO. The geometry of the ITO sputtering target is often a rectangle or disc. Compressing the powder causes it to take on a darker color.
ITO (Indium-Tin Oxide) Sputtering Target (Disc)
Inherent to the sputtering process is the uneven erosion of the sputtering target. The target material erodes in a "race track" pattern. These images of a spent nickel-vanadium sputtering target show the classic "race track" erosion pattern (valley).
Used Sputttering Target

Sputtering Target "Race Track" Erosion (Valley)
The remaining material is unusable in the sputtering process. In the case of an ITO sputtering target, the unused portion can represent a significant amount of indium. It makes sense to reclaim or recycle as much of the target as possible.

The target user will break up the remaining target in to chunks.
ITO (Indium-Tin Oxide) Sputtering Target Chunks
The chunk ITO is sent to a recycling/reclaim center where the chunk ITO is converted back in to indium metal. And the cycle starts all over again.
Indium (Metal)

Solar Ink???

Tuesday, November 17, 2009 by Eric Bastow [Eric Bastow]

Environmental initiatives coupled with the recent run-up when oil achieved $150 per barrell has put alternative energy back on the table. Solar energy was readily considered given its very "clean" and available nature. However, how can the average person, in their day to day life, take advantage of solar energy. Visions of roofs covered with (expensive and perhaps unattractive) solar panels and apparatus come to mind.
Well, an article in Photonics Media called "Painting the roof with solar ink" by Anne Fischer puts an interesting twist on capturing the suns rays for the sake of generating electricity. A company in the San Francisco Bay area, Innovalight, manufactures a solar ink comprised of silicon nanoparticles that can be suspended in a liquid. The "ink" can then be applied to flexible or rigid surfaces by means of "spray painting". Therefore, rendering virtually any surface that is exposed to the sun, a solar collector. Efficiency is said to be on the order of 18% currently. A company in China, JA Solar, has plans to commercialize this technology.
One of the founders of Innovalight, Brian Korgel, is trying to apply this approach to CIGS. Work done at the University of Texas has achieved 1% efficiency. The goal is 10% before going commercial and is anticpated to take 3 to 5 years

Solder Paste – Mixing and Metal Loading

Friday, September 25, 2009 by Eric Bastow [Eric Bastow]

Once the flux has been formulated and scaled up it then must be mixed with solder powder. The mixing procedure and equipment must be capable of providing a homogenous product batch after batch after batch. However, because certain aspects of the solder paste must perform in a certain manner an optimum viscosity must first be determined by finding the proper powdered solder to flux ratio, or the “metal load”. Metal load is expressed in percent by weight.

 

Particle size impacts viscosity. Therefore the metal loading must be adjusted accordingly. The appropriate particle size for a paste is determined by the aperture sizes for stencil printing and the gauge (inner diameter) of the needle for dispensing applications. (Simply put, smaller particles are needed to fit through smaller holes.)

 

Each flux vehicle, solder alloy and particle size will have its own unique optimum metal load. The metal load is also application dependant. The optimum metal load for stencil printing will be higher than the optimum metal load for dispensing.

 

It just so happens that the optimum metal load (for stencil printing), expressed by weight percent, often equates to about 50% metal and 50% flux by volume.

 

Example Solder Paste Metal Load:

 

Application

Particle Size

Metal Load

Stencil Printing

Type III

90%

Stencil Printing

Type IV

89.5%

Dispensing

Type III

85%

Dispensing

Type IV

84%*

*The dispensing metal load is often not as sensitive to particle size as stencil printing. It could very well be that a metal load of 85% with type III may also be appropriate with type IV powder as well. The amount of powder has already been reduced enough to offset compaction due to smaller particle size.

 

All solder pastes have a shelf life. As mentioned earlier the flux can begin to react with the solder powder when both are in direct contact with each other in the paste form. The flux itself, often containing organic ingredients, can degrade over time. At a point, the paste will no longer be usable. The best way to optimize the shelf life of a paste is to keep it refrigerated.

Solder Paste – Flux

Thursday, September 24, 2009 by Eric Bastow [Eric Bastow]

The second main ingredient in solder paste is the flux (vehicle). Flux is a very complex group of chemicals/materials that must be able to do a number of things, some of which must happen simultaneously (a partial list is below). This requires the knowledge of experienced chemists and material scientists.

 

1)     The flux must not react with the powdered solder while in storage (shelf life). This is aggravated by the wide variety of solder alloys available in paste form. Each alloy family typically requires it own unique flux formulation.

2)     The flux must effectively remove any surface oxides present on the solder powder itself and mating surfaces prior to and during the melting of the solder.

3)     It must effectively prevent re-oxidation of the solder powder and mating surfaces at the elevated temperatures associated with reflow soldering, especially when performed in an air environment (air is ~21% oxygen).

4)     The performance of the flux must be unaffected by a wide range of temperature and humidity conditions.

5)     If the flux is “no-clean”, the residue must be non-corrosive and non-conductive per J-STD-004.

6)     If the flux is RMA, the residue must be easily cleaned with commercially available chemicals.

7)     If the flux is water soluble/washable, the residue must clean thoroughly with heated and pressurized deionized water.

8)     In a stencil printing application the flux must adequately fill and release from the apertures of a wide variety of sizes, shapes and stencil types, not stick to the squeegee, not dry out too quickly on the stencil, retain a brick like shape both at room temperature and elevated reflow soldering temperatures (minimize slumping), provide sufficient tack to hold components in place, not spatter during soldering (boiling of flux solvents), not outgas excessively (voiding)  and provide effective wetting of the solder to a wide variety of board metallizations, component lead platings and package bumps.

9)     In dispensing applications, the paste must dispense smoothly and consistently through a variety of needles sizes either through manual application or a variety of dispensing equipment types and technologies without clogging (and do many of the things listed in item 8).

10) Provide a cosmetically appealing solder joint and flux residue (if “no-clean”).

Solder Paste – Powder

Wednesday, September 23, 2009 by Eric Bastow [Eric Bastow]

Once an alloy has been made it then needs to be fashioned into very small spherical particles, often referred to as solder powder. There are a number of different techniques for making solder powder, all of which require significant amounts of capital equipment and engineering expertise. The solder powder must then be sorted according to size, often referred to as “mesh size” or “type”. Here again a significant amount of equipment and labor is required. These sizes or types are defined in J-STD-006.

 

Type

Mesh

Particle Distribution (microns)

1

-100/+200

75 - 150

2

-200/+325

45 - 75

3

-325/+500

25 - 45

4

-400/+635

20 - 38

5

-500/N/A

15 - 25

6

N/A

5 - 15

 

 

The medium in which the powder is made must be inert to prevent oxidation. Similarly, powder must also be stored in an inert environment until its time of use.

Solder Paste – Alloys

Tuesday, September 22, 2009 by Eric Bastow [Eric Bastow]

Much to the surprise of the SnPb and SAC alloy consuming world, there are a number of alloys available in solder paste, each with their own unique melting points and soldering and mechanical properties. Below is a table containing some of the alloys possible in solder paste (not exhaustive).

 

Alloy Composition

Melting Temperature (Solidus/Liquidus)

46Bi 34Sn 20Pb

96C (Eutectic)

52In 48Sn

118C (Eutectic)

58Bi 42Sn

138C (Eutectic)

57Bi 42Sn 1Ag

139C/140C

97In 3 Ag

143C (Eutectic)

80In 15Pb 5Ag

149C/154C

100In

157 (Melting Point)

43Pb 43Sn 14Bi

144C/163C

70In 30Pb

165C/175C

62Sn 36Pb 2Ag

179C

60In 40Pb

173C/181C

63Sn 37Pb

183C (Eutectic)

50In 50Pb

184C/210C

Sn Ag Cu (SAC alloys)

217C/220C

96.5Sn 3.5Ag

221C (Eutectic)

95Sn 5Sb

235C/240C

80Au 20Sn

280C (Eutectic)

88Pb 10Sn 2Ag

267C/299C

92.5Pb 5Sn 2.5Ag

287C/296C

92.5Pb 5In 2.5Ag

300C/310C

95Pb 5Sn

308C/312C

 

None of these individual metals are found pure on the planet. They have to be mined, refined and then alloyed to the proper proportion with the other metals to create these solder alloys. Oftentimes a wet chemical technique is required after alloying to validate that the alloy meets the allowable tolerances and purities spelled out in J-STD-006 or a customer specific specification.


What Is Solder Paste?

Monday, September 21, 2009 by Eric Bastow [Eric Bastow]

For many in the electronics assembly world solder paste is often treated as a near commodity item. However, from within the walls of a solder paste manufacturer it becomes quite obvious that it is a highly engineered and intricate material.

 

The simplest answer to the question “What is solder paste?” is “It is a mixture of powdered solder alloy suspended in a flux (vehicle).” But the real answer is deeper than that very cursory response.

 

Later, we will discuss these topics in detail:

  • Alloy
  • Powder
  • Flux
  • Mixing and Metal Loading

 

That grey “sludge” that you use for soldering did not come out of a tar pit deep in a jungle somewhere. It is a sophisticated material that requires intelligent engineering and chemistry, equipment and proper handling at all levels of manufacture