Breaks after the Piece is Cool

People sometimes fire a piece only to have it break after it is cool.  They decide to re-fire with additional decoration to conceal the break.  But it breaks again a day after it has cooled.  Their questions centre around thermal shock and annealing. They used the same CoE from different suppliers, so it must be one of these elements that caused the breakage.

Thermal Shock

This is an effect of a too rapid heat changes.  Its can occur on the way up in temperature or on the way down.  If it occurred on the way up to a fuse, the edges will be rounded.  If it occurred on the way up to a slump the edges may be sharp still, but the pieces will not fit together because the slump occurred before the slump.  It the break occurs on the way down the pieces will be sharp.  The break will be visible when you open the kiln.  More information is here.

If the break occurs after the piece is cool, it is not thermal shock.

Annealing

Another possible cause of delayed breakage is inadequate annealing.  Most guidelines on annealing assume a flat uniform thickness.  The popularity of tack fused elements, means these are inadequate guides on the annealing soak and annealing cool.  Tack fused items generally need double the temperature equalisation soak and half the annealing cool rate. This post gives information on how the annealing needs modification on tack fused items. 

The annealing break usually crosses through the applied pieces and typically has a hook at each end of the break.  If the piece has significant differences in thicknesses, the break may follow the edge of the thicker pieces for some distance before it crosses it toward an edge. This kind of break makes it difficult to tell from an incompatibility break.

Compatibility

The user indicated all the glass was of the same CoE.  

This is not necessarily helpful. 

Coefficient of Linear Expansion (CoE) is usually measured between 20°C and 300°C. The amount of expansion over this temperature range is measured and averaged. The result is expressed as a fraction of a metre per degree Celsius. CoE90 means that the glass will expand 9 one-thousandths of a millimetre for each degree Celsius.  If this were to hold true for higher temperatures, the movement at 800C would be 7.2mm in length over the starting size.  However, the CoE rises with temperature in glass and is variable in different glasses, so this does not tell us how much the expansion at the annealing point will be.  It is the annealing point expansion rate that is more important.  More information is here.

• Compatibility is much more than the rate of expansion of glass at any given temperature.  
• It involves the balance of the forces caused by viscosity and expansion rates around the annealing point.

Viscosity is probably the most important force in creating compatible glasses. There is information on viscosity here.  To make a range of compatible glass the forces of expansion and viscosity need to be balanced.  Each manufacturer will do this in subtly different ways.  Therefore, not all glass that is claimed by one manufacturer to compatible with another’s will be so. 

All is not lost.  It does not need to be left to chance.

Testing glass from different sources is required, as you can see from the above comments.  It is possible to test the compatibility of glass from different sources in your own kiln.  The test is based on the principle that glass compatible with a base sheet will be compatible with other glasses that are also compatible with that same base sheet.  There are several methods to do this testing, but this is the one I use, based on Shar Moorman’s methods.  

If you are buying by CoE you must test what you buy against what you have.

If you are investing considerable effort and expense in a piece which will use glass from different sources or manufacturers, and which is simply labelled CoE90, or CoE96, you need to use these tests before you start putting the glass together.  The more you deviate from one manufacturer’s glass in a piece, the more testing is vital. 

In the past, people found ways of combining glass that was not necessarily compatible, by different layering, various volume relationships, etc.  But the advent of manufacturers’ developing compatible lines of glass eliminated the need to do all that testing and experimenting.  While the fused glass market was small, there were only a few companies producing fusing glass.  When the market increased, the commercial environment led to others developing glass said to be compatible with one or other of the main producers of fusing compatible glass.

An incompatibility break may occur in the kiln, or it may occur days, months or years later.  Typically, the break or crack will be around the incompatible glass.  The break or crack may follow one edge of the incompatible glass before it jumps to an edge.  The greater the incompatibility, the more likely it is to break apart.  Smaller levels of incompatibility lead to fractures around the incompatible glass pieces, but not complete breaks.

If the break occurs some length of time after the piece is cool, it can be an annealing or a compatibility problem.  They are difficult to distinguish apart sometimes.  There is more information about the diagnosis of the causes of cracks and breaks here.

The discussion above shows that even with the best intentions, different manufacturers will have differences that may be small, but can be large enough to destroy your project.  This means that unless you are willing to do the testing, you should stick with one manufacturer of fusing compatible glass. 

Do not get sucked into the belief that CoE tells you much of importance about compatibility.

Revised 30.12.24

Effects of Annealing at the Top End of the Range

It is possible to begin your annealing at any point in the annealing range.

The annealing point is the temperature at which the glass most quickly relieves the stress within.  This occurs at the glass transition point. 

The  annealing range is between the softening point and the strain point of the glass.  No annealing can be achieved above the softening point, nor below the strain point.  This range, for practical purposes can be taken to be 55°C above and below the published annealing point.  For thick slabs, Bullseye has chosen to start the anneal 34°C below the published annealing point of 516°C.

High Annealing Point

A high annealing temperature, even up to 571°C, the approximate strain point of the glass could have been chosen, but this is impractical.  The effect of this is a greater slow cool range and so an extended anneal cool.  The reasons are as follows:  

• The anneal cool range is greater as the first rate of cool needs to be maintained to the strain point.
• The anneal cool has to extend to at least just below the strain point.
• The highest practical annealing temperature is determined by the viscosity of the glass.  Any soaks above that temperature are ineffective in production of soundly annealed glass.
• The purpose is to get all the glass at the same temperature in preparation for  cooling.  It is more difficult to maintain the small differentials in temperature achieved by the annealing soak over a large range of temperature.

Low Annealing Point

Starting the anneal cool closer to the strain point requires a slightly longer soak to ensure the glass is all at the same temperature (+/- 2.5°C, often called the Delta T=5C) before the anneal cool begins.  Typically, this initial soak would be for an hour before the initial cool begins (for a 6mm/0.25" thick piece).

Effect of the Differences in Approach

The advantages and disadvantages centre around the need to:

• soak long enough to get all the glass to the same temperature, and to 
• cool slowly enough to maintain the delta T throughout the glass.

Example

If you think of an example of a piece of Bullseye glass 12mm/0.5" thick, it will show the differences in approach.

High temperature soak

A soak of 120 minutes at 571°C/1060°F (the highest possible start for an annealing soak) is still required to even the temperature.  To ensure the temperature differentials in the glass do not deviate from the Delta T, the cool needs to be at 18°C/32°F per hour down to 427°C/800°F.  It is possible then to increase the speed to 36°C/65°F per hour down to 370°C/700°F.  This gives you a total annealing cool of just over 11.5 hours.

Low temperature soak

Starting the anneal at 482°C still requires a two hour soak followed by a decrease in temperature of 18°C/32°F per hour to 427°C, and an increased rate of 36°C/65°F to 370°C/700°F.  This gives an anneal cool time of just over 6.6 hours.

The example shows how, although the annealing result may be the same, there is considerable time saved (and especially for thicker pieces) in using the lower part of the annealing range to begin the annealing.  It also will save some electricity.

However, an anneal of two hours at 516°C with a cool of 18°C/32°F per hour to 427°C/800°F and 36°C/65°F to 370°C/700°F will still give a perfectly adequate anneal for 12mm thick pieces even though it will take about 2 hours longer.

Revised 30.12.24

Glass Volume for a Frit Mould

There are several ways to determine the volume of a mould. 

Calculation of the weight of glass needed

Calculate the amount in the metric system of measures, as that gives much easier calculations. Cubic centimetres of volume times the specific gravity of glass (2.5) will give you the number of grams of glass required.

This works best on regular geometric forms.  Rectangles and parallelograms are easy to measure the length, width and depth in centimetres.  Multiply together and you obtain cubic centimetres.  That times the specific gravity – 2.5 – will give the number of grams to fill the mould.  The frit will of course be mounded above the levelled surface, because of the air spaces between the frit pieces.

Example of a small frit mould

Irregular shaped moulds

The moulds which are irregular in shape or depth are more difficult to calculate. 

You can determine the volume by starting with a measured amount of water.  Quickly fill the mould to the surface, so that no water is absorbed into the mould. Empty the water from the mould into the drain so it does not become soaked. The difference between the starting and finishing amount of water is the volume of glass required to fill the mould. 

You can use that volume in cubic centimetres times the specific gravity (2.5) to get the number of grams of glass required.

However, it is much easier to put the frit into the water until the measure shows the same amount as before the mould was filled. Then you only need pour off the water and allow glass and mould to dry.  No calculation required.

This post gives some alternatives.

Revised 30.12.24

Annealing Strategies

This is a power point presentation I gave a few weeks ago to a group.  It may be of interest to others.  There is no commentary.

 

Rehearsing Special Cuts

For difficult cuts you can increase your confidence by rehearsing the score with a feather light movement of the cutter on the glass along the score line. Make any adjustments shown to be necessary by this rehearsal before beginning the score.

It is important to remember the basic scoring tips as they become even more important with difficult cuts:

• Keep an even/constant speed during the scoring.
• Keep a consistent pressure - less than 3kg/ 7 lbs is all the pressure required.
• Make sure the cutter is vertical – eye the cutter from top to wheel to cut line.
• Stand behind the direction of the cut line.
• Use your body to turn, do not use the wrist or arm.

Start with the most difficult score first. Any break-outs or mistakes will not waste much work or glass.

Break out each score as you make it. You can store up trouble by making multiple scores before starting to break. The score lines can run across the main piece when breaking off the scored glass. Any inaccuracies will also be magnified by making all the scores before breaking.

More information is given in these blog posts:

Diagnosis of cutting

Scoring Glass

Testing Scoring Pressure

Opalescent Glass

Revised 30.12.24

Slumping a Form Flat

There are a variety of reasons that you might want to make a formed piece flat again for another kind of slump or drape.  There are a variety of things to think about when preparing to make a shaped piece flat.  I am going to assume there are no large bubbles in the piece and there are posts on Large bubbles and Bubble at bottom  including the causes.

There are five groups of things to consider when contemplating flattening an already formed shape.

Shape/form

• Shallow forms with no angles have the fewest difficulties.  Take it out of the mould, put it on the prepared shelf and fire to the slump temperature.  Observe when it is flat and proceed to the annealing.
• Forms with angles or multiple curves are a little more difficult.  If the piece has stretched in some areas to conform to the mould, you will have some distortion in the pattern and possibly some thinner areas.  It should be easy to flatten pieces on a prepared shelf with the same schedule, but a slightly higher top temperature than in the previous slump.
• Forms where the sides have pulled in will become flat, but continue to have curved sides.
• Deep forms are possibly the most difficult.  The glass may have stretched, giving thin areas.  It may be that the process of flattening the glass will cause a rippled effect as the perimeter of the piece is a smaller size than the original footprint.  These deep forms are the least likely to flatten successfully.

Orientation

• Which way up? Upside down or right side up?  Shallow forms are easiest to flatten by placing them right side up on a prepared shelf.  For deep or highly formed pieces, it may be best to put it upside down to allow the now higher parts to push the perimeter out if it is necessary.

Thickness

• Thick glass will flatten more quickly than thin glass when using slower ramp rates, so you need to keep a watch on the progress of the work to avoid excess marking of the surface of the glass.
• Very thin pieces are likely to develop wrinkles as they flatten.  Even if they do not, there will be thick and thin areas which might cause difficulty in subsequent slumping.
• Tack fused pieces are likely to tend to flatten at different places and times due to the differences in thickness and therefore weight. This makes observation of the flattening process more important.

Temperatures

• In all these processes, you should use the lowest practical temperature to flatten.  This means that you will need to peek at intervals to see when it is flat.
• Your starting point for the top temperature to use will be about the same as  the original slump, normally.  The amount of time may need to be extended significantly. The reason for this is to avoid as much marking on the finished side as possible.
• Shallow forms and thick pieces will flatten more quickly than others, so a lower temperature can be used.  You will still need to observe the progress of the flattening.
•  Angled shapes and deep forms will need more heat and time than the shallower ones. 
• Thin pieces may require more time than thick pieces.
• Tack fused pieces need more attention and slow rates of advance to compensate for the differences in thicknesses.

Separators

• Kiln washed shelves are usually adequate for flattening.
• Thinfire or Papyros are needed when flattening upside down to ease any sliding necessary.
• Powdered kiln wash or aluminium hydrate can be dusted over the kiln washed shelf when it is felt the form will need to slide on the shelf while flattening.

It may be that after all this, you feel it is not worth it to flatten.  It certainly is worth the effort, if only to learn about the characteristics of the form and its behaviour in reversing the slump or drape.

Devitrification

What is it? When does it happen? Why does it happen? These are frequent questions.

Dr. Jane Cook states that devitrification is not a category (noun), but a verb that describes a process. Glass wants to go toward devitrification; a movement toward crystallisation.*

Mild devitrification is the beginning of crystallisation on the surface of the glass. It can look like a dirty film over the whole piece or dirty patches. At its worst, the corners begin to turn up or a crackling can appear on a granular surface.  This is distinct from the effects from an unstable glass or the crizzling as in a ceramic glaze. Devitrification can occur within the glass, but normally is a surface effect as oxygen is required.

Differences in the surface of glass promotes precipitation of the crystal formation of silica molecules.  This fact means that two defences against the formation of crystals are smooth and clean surfaces. There are other factors at play also.  The composition of the glass has an effect on the probability of devitrification.  Opaque glass, lime, opalising agents, and certain colouring agents can create microcrystalline areas to "seed" the devitrification process.  One part of the composition of glass that resists devitrification is the inclusion of boron in the composition of the glass, acting as a flux.

Visible devitrification generally occurs in the range of approximately 720°C – 830°C/1330F - 1525F, depending to some extent on the type of glass.  This means that the project needs to be cooled as quickly as possible from the working (or top) temperature to the annealing point, which is, of course significantly below this range.

There is evidence to show that devitrification can occur on the heat up by spending too long in this devitrification range, and that it will be retained in the cooling. Normally this is not a problem as the practice in kilnforming is for a quick advance on the heat up through this range, causing movement in the glass and so working against any crystallisation.  The quick advance does not (and should not for a variety of reasons) need to be as fast as possible.  A rate of 300°C per hour will be sufficient, as time is required for devitrification to develop.

Medical research into using a glass matrix to grow bone has shown that devitrification begins around 650C/1200F, but only becomes visible after 700C/1290F.  This has implications for multiple slumps.  Devitrification is cumulative, so the devitrification that may have begun on the flat piece will be added to in the slumping process and may become visible.  For me this has appeared as a haze on the edge of the slumped piece.  Avoidance of this effect is by thorough cleaning of the piece before placing it in the mould.

The devitrification seen in typical studio practice results more often from inadequately cleaned glass than from excessive time at a particular temperature, up or down, through the devitrification range.  It is often seen as a result of grinding edges to fit.  Even though the ground edge is cleaned, it may still be rough enough to promote devitrification.  The edge must be prepared for fusing by grinding to at least 400 grit (600 is better).  Alternatively, use a fine coating of clear powder to give a new surface to the whole piece.

Dr. Cook suggests three approaches to devitrification:*
Resistance through:
 - Schedules
 - Flux
Dealing with it:
 - Cold work
 - Acids
Embrace it:
 - Allow it
 - Use it

Other sources of information:
Temperature range for devitrification
Homemade devitrification solution

Visible devitrification
Frit to fill gaps
Low Temperature Kilnforming at Etsy and Bullseye

* From a lecture given by Dr. Jane Cook at the 2017 BECON

[entry revised 28.12.24]

Cleaning Materials and Solutions

You need to clean glass that is going into the kiln to avoid devitrification on the surfaces.  This can be a greater or lesser problem for different individuals.  It is probably related to the studio practice and the amount of oils in or on fingers.

The first things to consider in cleaning glass for kilnforming are what you are trying to eliminate from the glass, the chemical nature of glass, and how to avoid putting further contaminants on the glass.

Cleaning is to remove surface deposits

The sensitivity of glass to minor contamination is shown by the fact that the small amount of oil from your finger tips can provide sources of devitrification.  This means the glass needs to be really clean and free from any deposits.  You need to remove oils and dusts and anything you may have added during assembly to leave nucleation points for devitrification. This includes any minerals in the water used to clean the glass.

Avoid soaking in acids

Glass is an alkaline (or basic) material.  This means that acids can affect the surface of the glass – at the microscopic level – enough to provide those nucleation points for devitrification to develop.  An odd thing about the way vinegar attacks glass is that the more dilute it is, the more etching it does of the glass.  This has to do with the greater amount of oxygen to transfer from the vinegar water to the glass, leaving microscopic etching as the minerals encased in silica are released from the glass surface.  This is visible as mild dulling in the shine of the surface.

If acids are used to clean the glass, rinse immediately in an alkaline solution such as baking soda.  You need then to get rid of the chemical reaction products formed by the neutralisation of the acid.  This should be done by immediately rinsing with running clear water. Follow this with a polish dry using unprinted paper towels.

Cleaning with spirits

My recommendation is to avoid spirits, especially those with additives such as rubbing alcohol. The amount of oil that is to be removed from the glass is small, so application of large amounts of spirits is not necessary.  It is reported that some aggressive spirits may affect the surface of the glass by combining with the minerals or the silica of the glass – this is not proven. If you do use spirits make sure they are thoroughly cleaned off and polished dry.  It is all too easy to leave residues.

What can I use to clean the glass?

The simplest cleaner is water.  A drop or two of dish washing liquid can provide a break to the surface tension, allowing the water to flow smoothly over the whole surface.  Then polish dry with clean unprinted paper towels.  Often this will not be sufficient to clean all the oils and chemicals from the glass and the best alternative is to use isopropyl alcohol neat or diluted 1:1 with water.

In many areas, the public water supply is hard – i.e., has an appreciable level of minerals.  Calcium and iron are two common minerals in any water supply. Some water supplies have other additives such as chlorine, fluorine and other purifiers. Chlorine and fluorine react strongly with glass, so air drying is not a good choice in drying glass in areas where there are these chemicals in the water supply.  Iron is another strong reactor with glass.  In high iron areas it may make it difficult to use water as the cleaning element.

It is suggested that distilled water can be used instead of the public water supply.  Yes, it can.  But it is expensive and not necessary.  Instead there are a few commercial cleaning agents that work well.  In North America Spartan glass cleaner is recommended.  In Europe Bohle glass cleaner is recommended.  I use isopropyl alcohol as my final rinse.  

After applying these glass cleaners, you still must polish to squeaky clean and dry.

Revised 28.12.24

Breaks in Slumping - diagnosis

Diagnosis of breaks during slumping processes is often difficult because the temperature is not high enough to be able to apply the usual rule of 

• sharp edges indicate breaks on the cool down; 
• rounded edges indicate breaks on the heat up.

www.warm-glass.co.uk

This not a universally applicable diagnosis.

At low slump temperatures, the edges will be sharp in both a break on heating up, and on the way down in temperature.

The best test to determine when the break occurs is to observe periodically during the heat up.  You will be able to see if the piece breaks before the top temperature.  If it is whole at top temperature, the break occurred on the way down.

If you have been unable to observe the progress of the firing, you will need to diagnose when the break occurred from the clues left.  The test here is not whether the edges are rounded or sharp, because at normal slumping temperatures, the break will be sharp in both cases. 

If the break occurred before the top temperature, the pieces will shape separately as the will be on different parts of the mould. Therefore, If the pieces no longer fit together, the break was on the rise. If they do fit exactly, the break was on the way down.  Place the pieces very carefully together to see if they form part of a continuous curve.  If they do, the break was on the cool down.  If they almost  match, or do not match at all, then the break was on the rise in temperature.

In general, when the break is on the cool down, there has been an overhang of the flat glass onto the mould which causes the break.  But the most common break of a slumping piece is caused by a too quick rise in temperature.  The distance the pieces are apart will give an indication of the force of the break.  The farther apart the pieces are, the slower the ramp should be - either up or down.

For a flat 6mm piece, the slump temperature rise should be less than twp thirds as quick as the rise for the fusing.  If you have a tack fused piece to be slumped you should reduce the rate of advance to at least half of that for a smooth, flat piece of 6mm.  Thicker glass with tack fused elements will need to be even slower.

Draping is another story.

Revised 28.12.24

Characteristics of Some Glasses

This information has been taken from various sources. Some manufacturers may change the composition of their glasses or the published information about them from time to time. Therefore, this information can only be used as a guide. If the information about strain, annealing, and softening points is important, contact the manufacturer for the most accurate information.

The temperature information is given in Celsius.

Strain point – the temperature below which no annealing can be done.

Annealing point – the temperature at which the equalisation soak should be done before the annealing cool.

Softening point – the temperature at which slumping can most quickly occur.

Armstrong – Now made by Kokomo

Typical Borosilicate – nominal CoE 32

Strain point – 510 - 535C / 951 - 996F

Annealing point – ca. 560C/1041F
Softening point - ca. 820C/1509F

Blackwood OZ Lead – nominal CoE 92

Annealing point - 440C/825F

Blenko – nominal CoE 110

Annealing point – 495C/924F

Bullseye – nominal CoE 90

Transparents

Strain point - 493C/920F

Annealing point - (532C)  Note that Bullseye has changed this to 482C/900F for thick items

Softening point - 677C/1252F

Opalescents

Strain point - 463C/866F

Annealing point – (501C)  Note that Bullseye has changed this to 482C900F for thick items

Softening point - 688C/1272F

Gold Bearing

Strain point - 438C/821F

Annealing point - (472)   Note that Bullseye has changed this to 482C/900F for thick items

Softening point - 638C/1182F

Chicago – nominal CoE 92

Desag  Note that this glass is no longer produced

Artista – nominal CoE 94

Strain point – 480 - 510C / 897 - 951F

Annealing point – 515 - 535C / 960 - 996F

Softening point – 705 – 735C / 1302 - 1356F

Fusing range – 805 – 835C / 1482 - 1537

Float Glass (Pilkington UK)

Optiwhite

Strain point – 525 - 530C / 978 - 987F

Annealing point – 559C/1039F

Softening point – 725C/1338F

Optifloat

Strain point – 525 - 530C / 978 - 987F

Annealing point – 548C/1019F

Softening point – 725C/1338F

Float Glass (typical for USA) nominal CoE 83

Strain point - 511C/953F

Annealing point - 548C/1019F

Softening point – 715C/1320F

Float Glass (typical for Australia) nominal CoE 84

Strain point - 505-525C / 942 - 978F 

Annealing point – 540 -560C / 1005 - 1041F

HiGlass “GIN” range – nominal CoE 90

Annealing point - 535C/996F

Gaffer colour rod – nominal CoE 88

Gaffer NZ Lead – nominal CoE 92

Annealing point - 440C/825F

HiGlass

Annealing point - 495C/924F

Kokomo – nominal CoE 92 - 94

Cathedrals

Strain point - 467C/873F

Annealing point - 507C/946F

Softening point - ca. 565C/ca.1050F

Opal Dense

Strain point - 445C/834F

Annealing point - 477C/891F

Softening point – ca. 565C/1050F

Opal Medium

Strain point - 455C/834F

Annealing point - 490C/915F

Softening point – ca.565C/1050F

Opal Medium Light

Strain point - 461C/863F

Annealing point - 499C/931F

Softening point – ca.565C/1050F

Opal Light

Strain point - 464C868F

Annealing point - 502C/937F

Softening point – ca.565C/1050F

Kugler 

Clear – nominal CoE 96 +/- 2  (94-98)

softening point: - 694C/1281F

Annealing point: - 508C/946F

Strain point: - 485C/904F

Colours - nominal CoE 96 +/- 4 (92-100)

Annealing point: - 500C/932F

Strain point: - 460C-500C/860 -879F

Typical lead glass – nominal CoE 91

Lenox Lead – nominal CoE 94

Annealing point – 440C/825F

Merry Go Round – nominal CoE 92

Moretti/Effetre – nominal CoE 104

Strain Point: 448C/839F

Annealing Range: 493C – 498C / 920F - 929F

Softening Point: 565C/1050F

Pemco Pb83 – nominal CoE 108

Annealing point – 415C/780F

Reichenbach - 

nominal CoE 96 +/-2 (94 -98)

Annealing range; - 470C-530F/878F-986F; Ave 510C/950F

nominal CoE 104  no further information at present.

Schott Borosilicate (8330) nominal CoE 32

Annealing point - 530C/987F

Schott “F2” Lead – nominal CoE 92

Annealing point - 440C/825F

Schott “H” & “R6” rods - nominal CoE 90

Annealing point – 530C/987F

Schott “W” colour rod – nominal CoE 98

St Just

MNA

Strain point - ca.450C/843F

Annealing point – ca. 532C/ca. 991F

Spectrum

System 96 – nominal CoE 96

Transparents

Strain point – 476C  +/- 6C  /  890F +/- 11F

Annealing point – 513 +/- 6C  /  956C +/- 11F

Softening point – 680 +/- 6C  /  1257F +/- 11F

Opalescents

Annealing point – 505 -515C  /  942 - 960F

Spruce Pine 87 – nominal CoE 96

Annealing point – 480C/897F

Uroboros system 96 – nominal CoE 96

Transparents

Strain point - 481C/899F

Annealing point - 517C/964F

Opalescents
Strain point - 457C/855F
Annealing point - 501C/935F

Uroboros - nominal CoE 90

Transparents

Strain point - 488C/911F

Annealing point - 525C/978F

Opalescents

Strain point - 468C/875F

Annealing point - 512C/955C

Wasser - nominal CoE 89

Annealing point – 490C/915F

Wissmach
Wissmach 90
Annealing point - 483C/900F
Softening point - 688C/1272F
Full Fuse - 777+

Wissmach 96
Annealing point - 483C/900F

Softening point - 688C/1272F

Full Fuse - 777+ / 1432+

•