Odd Schedules

Schedules appear on the internet which do not seem to have a logical sequence in the firing schedule.  Some have multiple soaks at intervals up to 540°C.  Others have kind of dance toward the top temperature – slow, quick, slow.  Some initially cool at a given rate and then slow to about half that initial rate.

Multiple soaks

These schedules have been referred to as catch-up schedules.  They tend to look something like this:

200°C to 150°C for 20 minutes

250°C to 300°C for 20 minutes

300°C to 590°C for 20 minutes

50°C   to 677°C for 30 minutes

330°C to 804°C for 10 minutes

AFAP   to 482°C for 60 minutes

60°C   to 370°C for  0 minutes

Off

The justification for the first two soaks is given as allowing the glass to catch up to the air temperature.  It would be much safer for the glass to have a moderate steady advance in temperature rather than risking the heat shocking of the glass.  You could achieve the same work in the same amount of time by altering the rate of advance to a single one of 198°C to 590°C.  This achieves the same temperature in the same amount of time, but has less risk of heat shock, as there is a steady input of heat.  

Secondly, if the glass can survive the initial rate of heat up without breaking, there is no need to soak at an arbitrary temperature.  The first relevant point where a change in temperature makes sense is above the softening point, which for most fusing glasses is about 540°C. The equivalent softening point for float glass is about 700°C

Slow, quick, slow

This kind of schedule alters rates up and down with little justification as far as I can see.  This is an example:

139°C  to 560°C  for 30 minutes

222°C  to 621°C  for 30 minutes

139°C  to 786°C  for 15 minutes

9999 to  515°C  for 120 minutes  

60°C   to 427°C  for 10 minutes

115°C  to 350°C  for 10  minutes

The question for me is why the slow down to top temperature. There is a lot of heat work being put into the glass, so that the higher top temperature may not be required.  The slower rate from 621°C does allow a form of a bubble squeeze to occur, but is not the traditional one.  A 139°C rate from 621°C to 677°C with a soak would be faster than usual, but may be acceptable.  I would prefer 50°C per hour with a 30-minute soak at the end.  Then advancing at 300°C per hour to top temperature.  The anneal soak and cool of this schedule are acceptable, even though different than I would do it.

Erratic Slumping Schedule

The fusing schedule above was followed by this slumping schedule:

83°C to 148°C  15 minutes

167°C to 590°C  10 minutes

83°C to 720°C  10 minutes

222°C to 410°C  120 minutes

83°C to 427°C  10 minutes

This schedule seems to have a catch-up phase in that it goes at half speed for the first 148°C and then doubles the speed to 590°C (a little above the brittle phase of the glass).  It then slows the rate and continues that to a very high slump temperature.  It is, of course, necessary to have a slower rate of advance in the slumping than the fusing, as the piece is now thicker. Slowing the rate of advance as much as in this should be able to achieve the slump at around 620°C (100°C) less than the target temperature used by the schedule. 

Once the top temperature soak is finished, a very slow cool to the annealing soak is used in this schedule.  This is not ideal as it invites devitrification to form.  The kiln and its contents should be allowed to cool as quickly as possible to the temperature equalisation soak at the annealing point.

The schedule then uses an annealing soak temperature 100°C below that used for the fusing. This does not make sense. The annealing soak should be at the same temperature for both firings.  The length of the soak is not in question, but the early turn off the kiln at 427°C is questionable. The anneal cool of the fused piece extended down to 350°C.  The anneal cool on slumping should be almost the same as the fuse.  Almost all anneal cools extend to 370°C at least.

Anneal Cools

Some anneal cools have erratic rather than progressive cooling.  In this example the early part of the schedule is eliminated:

……………..

AFAP to 482°C 120 minutes

110°C to 427°C 0 minutes

55°C to 370°C 0 minutes

200°C to 100°C 0 minutes

off

Here the schedule is faster in the most critical part of the anneal cool than in the next, cooler part.  This will not provide as good an anneal as if the first two segments after the equalisation soak were reversed.  Start slowly in the anneal cool and then you can speed up (approximately twice the previous segment rate) on each of the following segments.

Rationale

This critique of the schedules above is not to batter anyone.  It is to make clear that there needs to be a conscious rationale for each of the segments in relation to the others.  If you take a schedule from a source, it is a good idea to see if there is a reason for each segment and how it relates to the next. 

·        The scheduling must take account of the nature of the glass.  Glass is a poor conductor of heat and needs steady moderate input of heat.

·        Glass is brittle until approximately 55°C above the annealing temperature when you can accelerate the rate of advance.

·        Time is required to allow air out from between the layers of glass. This usually done in the range of 620°C to 675°C and is known as the bubble squeeze.

·        You need to go relatively quickly through the devitrification range of temperatures – approximately 700°C to 760°C - both up and down.

·        Glass needs a temperature equalisation soak at the annealing point (or nearby) related to its thickness.

·        The rate of cooling needs to be progressive.  The first 55°C below the annealing soak is the most important.

·        Cooling rates must be related to thickness.

·        The second cooling rate can be up to double the initial one.

·        The final cooling rate can be double the previous one.

·        The rate of firing will affect the required top temperature.

Factory Installed Firing Schedules

Factory installed schedules are a quick starting point for the novice kilnformer.  

Many kiln manufacturers install schedules in the controllers of entry level kilns.  Some install them in larger kilns too.  They will work for for gaining basic experience of kiln operations.

However, these schedules are not universal.  Each maker programmes schedules according to their understanding of a mid-range firing schedule for various processes. 

An example of some installed programmes from Scutt

This means that when referring to an installed programme on your controller, you need to give the full schedule so others can understand.

Why?

Not only because a tack fuse schedule may be to a different temperature, but also a "fast" schedule as programmed into one kiln might be quite different to one in another.

This matters, because how fast you get to the top temperature affects what temperature you need to use. You will probably experience the difference in final effect between a fast and a slow fuse to the same temperature.  If you haven’t seen it yet, try both schedules on the same layup of glass.

You will see that a fast rate of advance to a tack fuse will give a much more angular appearance, while a slow rate of advance will give a much more rounded appearance.  This is the effect of heat work, which is essentially the effect of the combination of temperature and time.

The longer it takes the glass to reach a given temperature, the greater the heat work.  Longer times to the top allow the use of lower temperatures. 

The consequence of accounting for heat work is that a simple top temperature cannot be given.  It is not just that kilns are different, but that the amount of heat work put into the glass will change the top temperature required for a given look.

The Purpose of Flux

The primary purpose of flux is to prevent oxidation of the base and filler materials in the short time between cleaning and soldering. Tin-lead solder, for example, attaches very well to copper, but poorly to the various oxides of copper that form quickly at soldering temperatures. This applies to lead and brass too.

Flux is a substance that is nearly inert at room temperature, but it becomes strongly reducing at elevated temperatures, preventing the formation of metal oxides. Secondarily, flux acts as a wetting agent in soldering processes for lead, copper and brass.

Without flux the solder does not firmly attach to the lead or copper foil and often forms sharp peaks.


See also
Flux, an introduction
Fluxes, a description
The Purpose of flux
The action of fluxes

Soldering fluxes

The Action of Fluxes

All common untreated metals and metal alloys (including solders) are subject to an environmental attack in which their bare surfaces become covered with a non-metallic film, commonly referred to as tarnish. This tarnish layer consists of oxides, sulfides, carbonates, or other corrosion products and is an effective insulating barrier that will prevent any direct contact with the clean metal surface which lies beneath. When metal parts are joined together by soldering, a metallic continuity is established as a result of the interface between the solder and the surfaces of the two metals. As long as the tarnish layer remains, the solder and metal interface cannot take place, because without being able to make direct contact it is impossible to effectively wet the metals surface with solder.

The surface tarnishes that form on metal are generally not soluble in (and cannot be removed by) most conventional cleaning solvents. They must, therefore be acted upon chemically [or mechanically] in order to be removed. The required chemical reaction is most often accomplished by the use of soldering fluxes. These soldering fluxes will displace the atmospheric gas layer on the metal’s surface and upon heating will chemically react to remove the tarnish layer from the fluxed metals and maintain the clean metal surface throughout the soldering process.

Chemical reactions
The chemical reaction that is required will usually be one of two basic types. It can be a reaction where the tarnish and flux combine forming a third compound that is soluble in either the flux or its carrier.

An example of this type of reaction takes place between water-white rosin and copper oxides. Water-white rosin, when used as a flux is usually in an isopropyl alcohol carrier and consists mainly of abietic acid and other isomeric diterpene acids that are soluble in several organic solvents. When applied to an oxidized copper surface and heated, the copper oxides will combine with the abietic acid forming a copper abiet (which mixes easily with the un-reacted rosin) leaving a clean metallic surface for solder wetting. The hot molten solder displaces the rosin flux and the copper abiet, which can then be removed by conventional cleaning methods.

Another type of reaction is one that causes the tarnish film, or oxidized layer to return to its original metallic state restoring the metals clean surface.

An example of this type of reaction takes place when soldering under a blanket of heated hydrogen. At elevated temperatures (the temperature that is required for the intended reaction to take place is unique to each type of base metal) the hydrogen removes the oxides from the surface, forming water and restoring the metallic surface, which the solder will then wet. There are several other variations and combinations that are based on these two types of reactions.

Acids commonly in fluxes

Flux as a temporary protective coating
Once the desired chemical reaction has taken place (lifting or dissolving the tarnish layer) the fluxing agent must provide a protective coating on the cleaned metal surface until it is displaced by the molten solder. This is due to the elevated temperatures required for soldering causing the increased likelihood that the metal’s surface may rapidly re-oxidize if not properly coated. Any compound that can be used to create one of the required types of chemical reactions, under the operating conditions necessary for soldering, might be considered for use as a fluxing material. However, most organic and inorganic compounds will not hold up under the high temperature conditions that are required for proper soldering. That is why one of the more important considerations is a compound's thermal stability, or its ability to withstand the high temperatures that are required for soldering without burning, breaking down, or evaporating.

When evaluating all of the requirements necessary for a compound to be considered as a fluxing agent, it is important to consider the various soldering methods, techniques and processes available and the wide range of materials and temperatures they may require. A certain flux may perform well on a specific surface using one method of soldering and yet not be at all suitable for that same surface using a different soldering method. When in doubt it never hurts to check with the flux, or solder manufacturer for recommendations.

Courtesy of American Beauty Tools


See also:
Flux, an introduction
Fluxes, a description
The Purpose of flux
The action of fluxes
Soldering fluxes

Flux

Flux is a material that provides a “wetting” action between the metal (lead or copper in our case) and the solder.


There are various types of flux. Some are of more use in some circumstances than others. Among them are:

Tallow
This normally comes in a candle-like stick. It is made from rendered animal fat. Although this may put some vegetarians off, it is one of the best fluxes for leaded glass work and will work for copper foil, but is not generally preferred.  It is relatively natural, does not contain chemicals, and does not require re-application if left for a while. Over generous application does not produce any problems during the soldering. It just leaves more solidified tallow to clean after soldering. The cleaning normally requires a mild abrasive such as a brass or fibreglass brush to get the cooled tallow off the piece.

 




Oleic acid and other safety fluxes
Many of the safety fluxes are made of oleic acid (sometimes called stearin oil). These fluxes do not produce chemical fumes in the soldering process. They are easy to clean up with detergents and warm water. Safety fluxes require re-application if left to dry, as they are only effective while wet. Putting too much on leads to boiling off the liquid, making holes in the solder joint or line.

An example only.  There are many water soluble paste fluxes available

Chemical Paste fluxes
These fluxes come in a variety of compositions. You need to be careful about choosing, as some are very difficult to clean off the glass or solder line or joint. They do produce chemical fumes, so a fume mask is advisable while using this kind of flux. The paste does not require re-application if left, so the whole piece can be fluxed at once.

Acid fluxes
Acid fluxes such as the kind that is in the core of plumbers solder are intended to clean the joint at the same time as acting as the wetting agent. These are not recommended for stained glass work as they can affect the glass surfaces, especially irridised glass. They do produce fumes that require the user to have on a fume mask while soldering. The ease of cleaning relates to the particular composition of the flux, so testing samples is required before application.

See also:
Flux, an introduction
Fluxes, a description
The Purpose of flux
The action of fluxes
Soldering fluxes

Flux, an Introduction

Flux is a key contributor to most soldering applications. It is a compound that is used to lift tarnish films from a metals surface, keep the surface clean during the soldering process, and aid in the wetting and spreading action of the solder. There are many different types and brands of flux available on the market; check with the manufacturer or reseller of your flux to ensure that it is appropriate for your application, taking into consideration both the solder being used and the two metals involved in the process. Although there are many types of flux available, each will include two basic parts, chemicals and solvents.

an example of paste flux

The chemical part includes the active portion, while the solvent is the carrying agent. The flux does not become a part of the soldered joint, but retains the captured oxides and lies inert on the joints finished surface until properly removed. It is usually the solvent that determines the cleaning method required to remove the remaining residue after the soldering is completed. 

It should be noted that while flux is used to remove the tarnish film from a metal's surface, it will not (and should not be expected to) remove paint, grease, varnish, dirt or other types of inert matter. A thorough cleaning of the metal's surface is necessary to remove these types of contaminates. This will greatly improve the fluxing efficiency and also aid in the soldering methods and techniques being used.

Courtesy of American Beauty Tools


See also:
Flux, an introduction
Fluxes, a description
The Purpose of flux
The action of fluxes
Soldering fluxes

Snugging the Came to the Glass

It is important to have the came fit snugly to the glass (assuming the glass to be the right size and shape). If it does not, the panel is likely to grow beyond the intended dimensions.

To ensure the came is tucked snugly against the glass, you use a fid of firm material (wood or plastic, for example) to press against the heart of the lead. You can press directly toward the glass, or make multiple passes along the length of the came to ensure the heart is touching the glass all along its length.

You should avoid steel tools, because you may cut the lead, and if the blade is long you will not find it easy to fit along all of the curves.

Fitting the Glass to the Cartoon

Often you find that the next piece of glass does not fit properly. Possibly it rocks a bit in the came’s channel. Possibly it is simply just a little too big.  Wait! Don't adjust the piece just yet. It may not be the problem.

The first thing to do is to take the too-large piece of glass out and remove the came it fits into, to ensure the previous piece of glass is not too large. The glass should not overlap the cut line. If you have drawn your cut lines to 1.2mm (1/16”) you should see only the faintest line of paper between the glass and the dark cut line. 

If the glass seems too large, check that it is firmly in the channel of the previous came, as sometimes the glass catches on the edge of the came and does not go into the channel.

If that piece seems too large, the next check is to determine whether the apparently too large piece of glass really fits the cartoon cut lines. Place the glass inside the cut lines. You should see a faint line of paper between the glass and the cut line.

When you are sure both pieces of glass are the correct size, put the came back between them and check again. If the glass is still too large, check the length of the came. Make sure the came butting onto the came separating the glass is not too long. This is a common reason for lead panels to grow beyond their initial dimensions.

If the glass is the correct size and the butting cames are correct, replace the came. Put the too large piece of glass into the came and position it so it has the best fit to the next cut line. 

Do not be tempted to start reducing the glass at the visible portion.  After all, you cut it to the right size. It may be that the fit under the came is not very good.

To check use a felt tipped pen (Sharpie) to run along the edge of the came, marking the too-large piece of glass. Take it out and check on where the line is farthest from the edge of the glass. That is where you need to reduce the piece.

The nail points to the area that needs adjustment

When you have reduced the "high" spots on the glass so it fits under the came evenly along its length, you can begin to adjust the outer edge, if necessary.

Leading Tight Curves

Sometimes it can be difficult to get the lead came to conform to the curves of the glass, especially on compound curves.  This is a method to make the leading more accurate.

When leading tight inside curves, bend the came into a tighter curve than is needed for the glass. Then roll it into the glass. Finally, run your fid or stopping knife along the heart of the came to ensure it is firmly against the glass. All this helps the came to fit snugly into the curve.

Gravity

One of the fundamental elements in kiln forming is gravity. When glass is hot it moves according to the effects of gravity and you have to remember that gravity has a big effect on all your firings.

The effects mainly cause:

• Uneven thickness on shelves that are not level.
• Uneven slumps into moulds which are not level or the glass is not levelled.
• Uneven forming due to varying viscosities. Gravity acts on the softest parts of the glass first.
• Faster or slower forming due to span width. With greater span, gravity pulls the glass into the mould more quickly than with a small span.
• Gravity acts on things of greater thickness more quickly than those of lighter weight. So a thick piece will form more quickly than the same sized thin piece.
• Surface tension (affected by viscosity and heat) is affected by gravity also. The glass will attempt to draw up or spread out to about 7 mm if there is enough heat, time, and low viscosity.
• The effect of gravity causes upper pieces to thin lower ones, as it presses down while the glass is plastic. This has the effect of making the colour of the lower piece less strong.

More information on each of these effects can be found throughout this blog.

Cutting Opalescent Glass

People often find cutting opalescent glass more difficult than transparent. My observation is that people exert too much pressure in scoring opalescent glass by listening for the creaking/scratching sound. 

Not all glass is made the same, even by the same manufacturer.  But all the same rules apply in scoring opalescent as transparent glass.  However, they sound different.

No more pressure should be put on opalescent glass than transparent.  Only about two kilograms (5 to 7 pounds) of pressure is required to score glass sufficiently to create the weakness that we exploit when running the score.

If you concentrate on keeping the pressure on both types of glass the same, you will hear different things.  On transparent glass you normally hear a creaking or light scratching sound and you do not get a whiteness along the score line.  If you hear same sound on opalescent glass, too much pressure is being applied. 

The same pressure (2 kilograms) on opalescent glass gives only a rumble of sound. No creaking or scratching is heard.  You can test this by placing a piece of glass on kitchen scales. Zero the scales with the transparent glass on it and score. Note the pressure you used.  Now zero the scales with a piece of opalescent glass on it. Ensure you score to the same pressure as on the transparent glass by looking at the readout on the scales.

Just as excessive pressure on transparent glass leads to erratic breaking of the glass, so it does on opalescent glass.  You will need some practice to stop listening for a sound and begin to feel the pressure you are applying to the glass. Once you do apply the same pressure to opalescent as to transparent glass, your success in scoring and breaking opalescent glass will increase greatly.

Scoring and breaking opalescent glass successfully is the same for both transparent and opalescent glass.  Use moderate pressure and don’t listen for the sound.

Feel the pressure. Ignore the sound.

Annealing Range for Unknown Glass

It is possible to anneal unknown glass with some degree of certainty by using what is known as the slump point test.  This will not be as accurate as a factory determined test, so you do have to extend the range over which you do the annealing.  

The annealing of glass with unknown characteristics is possible in two ways - shotgun and calculated.  The examples here are for 6mm thick glass.  The soak and cooling times need to be extended for thicker glass.  

Both the shotgun and calculated approaches exemplified here assume glass of 6mm thickness.  For thicker glass the soak time needs to be extended and the anneal cool rate slowed more than indicated above.  Using the Bullseye chart for annealing thick slabs will give you an indication of the relationship of thickness to speed.

1)  One is the traditional shotgun approach – pick an arbitrary, but slightly high temperature, and soak for a minimal amount of time there. Then go very slowly through the next 55°C.  This may be as slow as 25°C per hour, followed by a doubling of that rate for the next 55°C. Then double again to 300°C or less.

2)  By using the slump point test and the calculations, you will be sure of the annealing point/temperature equalisation point within 10°C.  The approach here would be to soak for half an hour at the calculated temperature, followed by a slow drop of 50°C per hour to 55°C below annealing soak and then at 100°C/hr to 110°C below your chosen temperature equalisation point. The final cooling could be at 200°C to room temperature.

2a) An additional tweak to the slump point test calculations is to use the Bullseye concept behind their recommendations for thick slabs.  Using their concept, you reduce the calculated annealing point by 30°C from the calculated annealing point to do the temperature equalisation soak at the lower end of the annealing range.  Having calculated the annealing point, you reduce that temperature by 30°C and soak for  a longer time of 60 minutes and at a slower rate as noted in the chart.

In using the chart for unknown glass you substitute the calculated temperatures, but continue to use the rates and times indicated.  An example:

• You have calculated that the annealing point is approximately 535°C.
• Subtract 30°C from that to get a equalisation temperature of 505°C.
• Assume the piece is uniformly 12mm thick or 6mm tack fused (when you want to use rates for  twice the actual thickness to account for the difficulties in tack fusing). 
• For a 12mm thick piece your soak time at 505°C will be two hours.
• The cooling rate for the first 55°C is given as 55°C per hour according to the chart. Therefore the first cooling segment will be 55°C from 505°C to 450°C.  The second will be 99°C per hour from 450°C to 395°C.  The third rate will be 330°C per hour from 395°C to room temperature.

You can see that the times and rates are taken as given by the chart (as determined by the thickness of your piece), but the temperature set points are determined by the calculations for the glass you have tested.

When determining what temperature you should use to anneal a glass about which you are uncertain of its characteristics, you can use one of two basic approaches.  Pick an arbitrary temperature and soak for some time there and then proceed slowly in 55°C segments to about 370°C.  A second more certain method is to use the slump point test to determine the annealing point and then apply the Bullseye chart for thick slabs for the soak times and cooling rates.

Further information is available in the ebook Low Temperature Kiln Forming.

Heat Work

“Heat work” is a term applied to help understand how the glass reacts to various ways of applying of heat to the glass. In its simple form, it is the amount of heat the glass has absorbed during the kiln forming heat up process.

There is an relationship between how heat is applied and the temperature required to achieve the wanted result.  Heat can be put into the glass quickly, but to achieve the desired result, it will need a relatively higher temperature. If you put the heat into the glass more slowly, it will require a relatively lower temperature.

For example, you may be able to achieve your desired result at 814C with a 400C/hr rise and 10min soak. But you may also be able to achieve the same result by using 790C with a 250C/hr rise and 10min soak. The same amount of heat has gone into the glass, as evidenced by the same result, but with different kinds of schedules. This can be important with thick glass, or with slumps where you want the minimum of mould marks. Of course, you can also achieve the same results with the fast rise with a longer soak at the lower temperature, e.g. a 400C/hr to 790C with a 30 min soak.

In short, this means that heat work is a combination of time and temperature.  The same effect can be achieved in two ways: 
- fast rates of advance and high temperatures
- slow rates of advance and low temperatures.

You obtain greater control over the processes when firing at slower rates with lower temperatures.  There is less marking of the back of the piece.  There is less sticking of the separators to the back and so less cleanup.  There is less needling with the lower temperature.  

The adage “slow and low” comes from this concept of heat work. The best results come from lower temperature processing, rather than fast processing of the kiln forming.

Use of Sal Ammoniac block

A block of sal ammoniac is an excellent aid to keeping your soldering iron tip (or bit) clean and able to hold a small blob of solder.

A description of what sal ammoniac is and the safety precautions in its use are here. 

You should place the block in such a way that it cannot slide around as you rub your iron over it.

Place your hot soldering iron tip on the block until it begins to smoke. Then move your iron slowly back and forth along the block.  Initially, the block will be black from the contaminants coming from the soldering iron bit.  As you rub the bit along the block, it will begin to clear. As it does, you can add a touch of solder and turn the bit over to check whether there are still any black spots on the face of the bit. 

If there are still black spots, return to rubbing on the block for a time.  If these spots are persistent, you can use a brass wire brush to help clean the contaminants off.  Then add a touch of solder and return to rubbing along the block.  Repeat this check until the whole bit is bright and holding a small blob of solder.

Repeat this process for the other side too.

Leave a small blob of solder on each side of the bit to protect the bit from oxidising.  This cleaning process should be done at the end of each soldering session if the bit is not clean.  But it does not substitute for the frequent wiping of the bit on a damp sponge to clean the bit as you work.  The sal ammoniac block is for cleaning persistent contaminants off the bit.

Pot Melt Temperature Effects

When firing a pot melt, you have to consider how high a temperature you wish to use.

Viscosity is reduced with higher temperatures so increasing the flow and reducing the length of soak, although there are often some undesirable opacifying effects.

The size of the hole is also relevant to the temp chosen. The smaller the hole, the higher the temperature will have to be to empty the pot in the same amount of time. Of course, you can just soak for longer at a lower temperature to achieve the desired object of emptying of the pot without changing the temperature.

Using the same principle, the larger the hole the lower the temperature required to empty the pot in a given amount of time.

The temperature used to empty the pot will need to be between 840C and 925C. The problem with temperatures in the 900C to 925C range is that the hot colours tend to change, e.g., red opal tends to turn dark and sometimes become brown. Some transparent glasses also opacify. There is also the possibility that some of the glasses will change their compatibility.

So the best results seem to come from temperatures in the 840 to 850C range with longer soaks than would be required at 925C - possibly 4 or more hours.

Also remember to give melts a longer than usual anneal as they will be thicker than 6mm at the centre - somtimes as much as twice the edge thickness.

Soldering old lead

This is normally only a requirement when repairing old windows. Usually either to join new lead to the old, or to repair breaks at the original solder joint.

You will need to clean the lead down to the bright metal at the joints. This is more than a rub with steel wool. You need a glazing nail to scratch through the oxidisation layer, the corner of your lead knife, or in cases of mild oxidisation, a brass wire brush might do. But not a steel one as that may scratch the glass and any painting.  

Do not clean the oxidisation off the lead elsewhere. That is a protective layer already formed which leads to the longevity of the came. It is best to leave oxidised lead alone rather than expose the metal to further oxidisation.

Getting to the bright metal where you want to solder the joint means the flux can act appropriately and help the solder form a secure joint.  Otherwise only a weak, cold joint is possible.

Note that you always need to use dust masks or other breathing protection.  You need to have the work area well ventilated and need to do a damp wipe down of surfaces to reduce the amount of lead oxide in the work space.

Using Cut Running Pliers Without Cushions

Using Cut Running Pliers Without Cushions

There are a wide variety of cut running pliers for different purposes.  A description of some of them is here.

This post is to describe maintenance and use of this kind of cut runner.

The plastic covers that come with these cut runners eventually wear out.  The replacements are hard to find. There are things you can do other than buying a new pair just for the shields.

You can dip the jaws in tool coating compounds such as Plastidip.  This does not last as long as the plastic, but is easy to re-do.

You can wrap the jaws in tape.  Electrical tape, duct tape or even self-adhesive elastic bandage will do the job. Again, not long lasting, but easy to replace.

Or

You can use the cut running pliers without any covering on the jaws.  “You can’t do that. You will crush the glass!” is the response I hear.  You can use them bare. I do, and so can you.

The key is in the adjusting screw.  It is there not just to tell you which is the top of the pliers; it has a function too.  That screw adjusts the opening of the jaws to the thickness of the glass. 

A simple way to ensure you have the correct opening is to put one corner of the jaw on the edge of the glass with the jaw opening less than the glass is thick. Then tighten the screw until you feel the handles of the pliers begin to open.  Then you have the right opening for the thickness of the glass. 

It ensures you cannot crush the glass, as the jaws will not close at the centre to be less than the glass thickness. 

You also have a more direct feel of the glass without the spongy connection of the plastic. You can sense the glass beginning to bend just before the score runs due to the gentle pressure of the jaws of the cut runners on either side of the score.

Whether you use the cut runners with or without cushions on the jaws, it is important to keep the adjustment screw lubricated so you can adjust the width of the jaw opening for different thicknesses of glass.