Wednesday, 29 December 2021

Mineral Wool Fibres


Refractory Fibres


The general name that includes refractory fibre is mineral wool. It is any fibrous material formed by spinning or drawing molten minerals and ceramics.  These are used as thermal insulation, filtering, soundproofing and as a hydroponic medium, in addition to high temperature insulation as in kilnforming and furnaces.

The initial manufacture of mineral wool was in Wales in the mid-19th century, but the process was so dangerous that it was abandoned. The first commercial production was in 1870’s Germany, manufactured by blowing air through a fall of molten slag metal.  At the end of the century an American developed a technique to turn molten rock into fibres, so initiating the rock wool industry.  The high temperature versions were developed during the second world war, but not commercially available until the 1950’s.

Current manufacturing involves a flow of molten minerals (at ca 1600°C) through which air is forced.  This creates fibres of amorphous structure that can be compressed together without binders.  More advanced production rapidly spins molten minerals similar to the production of candy floss, or cotton candy. This results in a mass of fine, intertwined fibres with a typical diameter of 2µm to 6µm (microns).


Credit: Knauf.com


High-Temperature Mineral Wool


High temperature mineral wools are rated for about 650°C to 1600°C and are made in similar ways to the lower temperature versions.  However, they are more expensive and so are used in refractory circumstances including kiln forming.

The three main types of HTIWs include:

Low Bio-persistent (LBP) Wool, including Alkaline Earth Silicate (AES) wools and others:

Alkaline earth silicate (AES) wool
       Calcium magnesium silicate wool
       Calcium silicate wool
       Magnesium silicate wool
Alkali metal silicate (AMS) wool
       Potassium alumino silicate wool

Alumino Silicate Wool (ASW), also known as Refractory Ceramic Fibres (RCF)
       Aluminium silicate wool
       Aluminium zirconium silicate wool

Polycrystalline Wool (PCW)
       Aluminium oxide wool
       Mullite wool

The main forms that kilnformers are interested in are blanket, paper and board.  The paper and board normally contain binders ranging from latex to cellulose. There are other forms: bulk fibres, modules or blocks formed ready for installation, vacuum formed shapes, cement mastics, textiles, yarns and ropes.


A brief description of these kinds of refractory mineral wools are:

Alkaline earth silicate wool (AES)

AES wool consists of amorphous glass fibres that are produced by melting a combination of calcium, magnesium oxides and silicone dioxide.  Products made from AES are generally used in equipment that continuously operates and in domestic appliances. AES wool has the advantage of being bio-soluble—it dissolves in bodily fluids within a few weeks and is quickly cleared from the lungs and so has been excluded from carcinogenic classifications. It is generally rated up to 1200°C.

Alumino silicate wool (ASW)

This is also known as refractory ceramic fibre (RCF), again consisting of amorphous fibres produced by melting minerals and blowing air across the flow.  In this case, a combination of aluminium oxide and silicon dioxide.  It has a low thermal conductivity, and good resistance to chemicals. Alumino silicate wool is generally used at temperatures from 600°C to 1300°C  for intermittent operation, making it good for kilnforming. 

This was classified in Europe as a carcinogen category 2 – “Substances that should be regarded as if they are carcinogenic to humans” under the Dangerous Substances Directive in 1997. This was translated under CLP Regulation into a carcinogen category 1B “Known or presumed human carcinogen; presumed to have carcinogenic potential for humans, classification is largely based on animal evidence”.

Some of the trade names used are:
  • Kaowool®, a high-temperature mineral wool made from kaolin. It was one of the first types of high-temperature mineral wool and continues to be used. It can withstand temperatures to 1250°C. 
  • Cerablanket®, is a spun blanket manufactured from a high purity blend of alumina-silica and is classified up to 1315°C.
  • Cerachem® and Cerachrome® provide chemical stability and strength and have acoustic as well as thermal insulation characteristics. They are classified to 1426°C.

There are bio-soluble fibres produced under trade names such as Superwool® with temperature ratings of 1300°C and 1450°C.  Superwool® fibres are exonerated from carcinogen classification within Europe and not classified as hazardous by IARC or under any national regulations throughout the world.

Polycrystalline wool (PCW)

Polycrystalline wool was commercialised in the 1970’s and consists of fibres that contain more than 70% aluminum oxide. It is produced by sol–gel method from aqueous spinning solutions. The water-soluble green fibres obtained as a precursor are crystallized by means of heat treatment. This is produced in small quantities for specialised applications.  Its characteristics are that the fibres are of regular defined dimensions, it is chemically and thermally stable, with low shrinkage and high tensile strength, all with less dust produced in handling.  It is a more expensive process than producing RCW papers and blankets.

The polycrystalline wool is generally used at temperatures above 1300°C.  One trade name is Denka Alcen with a temperature rating up to 1600°C. Denka blankets are more resistant to acid and alkaline solutions than conventional alumino-silicate fibre blankets and have good thermal insulation characteristics.

Other than kilnforming, applications are in the ceramics, metals, petrochemicals, aerospace and automotive industry sectors. Typical PCW applications include use as support mats in catalytic converters and diesel particulate filters to reduce exhaust emissions, and as insulation in industrial high temperature furnaces for energy conservation, particularly in high temperature and/or chemically aggressive environments.

Credit: Alibaba.com


Kilnforming Refractory Papers

There are two fibre papers widely used in kilnforming: Papyros and Thinfire.  These are special cases of the RCF papers and deserve particular attention, although they are subsets of the previously described RCF wools.

Papyros
This is a fibre paper similar in thickness to cartridge paper.  It consists of  aluminium hydroxide, hydrated magnesium silicate (hazard classification: irritant), alumina borosilicate glass (hazard classification: irritant), wood pulp and resin (both binders).  None of the materials used in the composition of Papyros are classified as a possible carcinogenic substance.  It is recommended that eye, breathing and skin protection be used when handling the fired residue to reduce any irritation.  Washing after handling the dusts is recommended.


Thinfire
This fibre paper is also like cartridge paper in thickness and has a slightly finer texture than Papyros.  Its constituents are aluminium hydroxide, glass fibre, polyvinyl alcohol, cellulose, and polyamide resin.  Only the glass fibre is classified as an irritant.  The dust can be an irritant to eyes and skin.  If either are irritated, wash with large amounts of water. It is sensible to use breathing protection while handling the fired residue.


The materials used place both these fibre papers in the AES group of refractory fibres, which are biosoluble.  The use of hydrated magnesium silicate in Papyros gives an extremely small increased health risk over Thinfire.

Credit: cdc.com

Fibre Paper – Health and Safety

Mineral wool fibres and refractory ceramic fibres have been  classified as "possibly carcinogenic to humans" (Group 2B).  In contrast, the more commonly used vitreous fibre wools produced since 2000, including insulation glass wool, stone wool, and slag wool, are considered "not classifiable as to carcinogenicity in humans" (Group 3). The International Agency for Research on Cancer (IARC) elected not to make an overall evaluation of the newly developed fibres designed to be less bio-persistent such as the alkaline earth silicate (AES) or high-alumina, low-silica (ASW) wools. 


Bio-soluble fibres are produced that do not cause damage to the human cell. These newer materials have been tested for carcinogenicity and most are found to be non-carcinogenic.

Due to the mechanical effect of fibres, mineral wool products may cause temporary skin itching. To diminish this and to avoid unnecessary exposure to mineral wool dust, information on good practices is available on the packaging of mineral wool products with pictograms or sentences. Safe Use Instruction Sheets like safety data sheets are also available from each producer.

People can be exposed to mineral wool fibres in the workplace by breathing them in, skin contact, and eye contact. … The National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 5mg/m3 total exposure and 3 fibres per cm3 over an 8-hour workday [the highest existing standard].  The equivalent European standard is set by the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH).

AES, ASW and PCW have been registered before the first EC deadline of 1 December 2010 and can, therefore, be used on the European market.
ASW/RCF is classified as carcinogen category 1B.
AES is exempted from carcinogen classification based on short-term in vitro study result.
PCW wools are not classified; self-classification led to the conclusion that PCW are not hazardous.

Based on the total experience with humans and the findings of scientific research (animals, cells), it can be concluded that elongated dust particles of every type have in principle the potential to cause the development of tumours providing they are sufficiently long, thin and bio-persistent. According to scientific findings inorganic fibre dust particles with a length-to-diameter ratio exceeding 3:1, a length longer than 5μm (0.005 mm) and a diameter smaller than 3μm (WHO-Fibres) are considered health-critical.

High-temperature mineral wool is processed into products containing fibres with different diameters and lengths. During handling of high-temperature mineral wool products, fibrous dusts can be emitted. These can include fibres complying with the WHO definition.

There is concern about the silica content of refractory fibres.  The silica that is of concern is of a crystalline structure.  The method of production does not produce crystalline silica. The process used to create the fibres is:
Amorphous high-temperature mineral wool [fibres] (AES and ASW) are produced from a molten glass [or mineral] stream which is aerosolised by a jet of high-pressure air or by letting the stream impinge onto spinning wheels. The droplets are drawn into fibres; the mass of both fibres and remaining droplets cool very rapidly so that no crystalline phases may form.

The potential effects on health of the materials in refractory fibres have been tested and found to be non-hazardous.

In after-use high-temperature mineral wool crystalline silica crystals are embedded in a matrix composed of other crystals and glasses. Experimental results on the biological activity of after-use high-temperature mineral wool have not demonstrated any hazardous activity that could be related to any form of silica they may contain.

Thus, no crystalline silica is produced and the risk of silicosis from refractory fibres does not exist.  Certain sizes of any fibre present other risks.

Risks


Consideration of risks and therefore precautions, relate to three factors: Dimension, Durability and Dose.

Dimension

Fiber dimensions are critical, as only fibres of a certain size can reach the lungs…. Mineral fibres with a diameter greater than 3 microns are, in humans, “non respirable”. … Even below this respirability threshold only the finest fibres may be deposited into the gas exchange region of the lungs.

While respirability is determined by fiber diameter, fiber length is also important. Short fibres behave as if they are compact particles and can be cleared by the normal mechanisms which involve cells called macrophages. However long fibres [greater than 5 microns] frustrate this mechanism and, for some still unknown reason, are more biologically active.

Durability

Durability in this context describes the ability of a material to persist in the body and so is more accurately called “bio-persistence”. …  Fibres can dissolve or they may break into shorter pieces which can then be removed to the airways or through the lymphatic system. The rate of removal of different fibres is typically measured … and expressed as their “half-life” – that is the time it takes to reduce the number of fibres in the lungs by 50%.

Dose

The [dose] is the result of [dimension and durability] and is often referred to as “lung burden”.  With chronic exposures the lung burden is the result of … [continued exposure] and … bio-persistence. If the exposure is high enough and clearance slow then a sufficiently large dose will accumulate for adverse health effects to result.


The scientific knowledge about fiber toxicity allows comparison of fibres in terms of their toxicological potency and has also driven several initiatives to reduce potential risks in the workplace.  This has led to development of manufacturing processes for thicker fibres, although this is limited by the lesser thermal efficiency of thick fibres.  Thicker fibres are also more likely to cause skin irritation.  A lot of effort has been put into the development of bio-soluble fibres such as the AES wools which are increasingly available.

Recent research has shown a gradation of increasing bio-persistence is in the order of – least to greater –
AES (Calcium Silicate);
AES (Magnesium Silicate);
PCW;
RCF. 
This same research shows that fibres longer than 20 microns cannot be easily cleared from the lungs.  Breathing protection must filter out all particles larger than 20 microns. 

The WHO research shows that lung health effects can be produced by particles down to 3 microns. This means that filters used must be able to eliminate particles larger than 3 microns to provide effective protection against high exposure.

 

Handling practices

Sensible precautions when handling refractory fibre papers are eye, breathing and skin protection.  This can be safety goggles, dust mask (see filter size above), and long gloves and long sleeves.  Higher levels of protection can be used, but are not indicated as necessary by the research and classifications of health and safety organisations in the western world.

During clean-up the fibres should be dampened before any brushing of the residue, or vacuumed with HEPA filters to reduce the movement of fibres into the air.  You should also wash exposed skin after handling any of the dust.  Clothes should also be cleaned and washed frequently. 

Do not smoke, eat or drink in areas where the fibre dust is present.


More detailed information is available in the e-book: Low Temperature Kilnforming.

The understanding of the composition and manufacture of refractory fibre papers and blankets should help assess the small risks of using these materials, and the precautions that should be taken in handling both the un-fired and fired forms.

 


Monday, 27 December 2021

Using Calcium Phosphate to Heal Bone Defects

 

Using Calcium Phosphate to Heal Bone Defects

Posted  on 

Bone defects arising as a consequence of trauma or disease typically require surgical intervention to promote healing. The defect must be filled to provide a framework to support and encourage the growth of new, living bone.

The gold standard for filling bone defects is autologous bone, but the additional morbidity involved for the patient in harvesting bone for grafting has led to a growing preference for alternative methods. The need for further surgery to acquire the bone is eliminated by using donated bone, but such allografts carry the risk of an immune response preventing the graft from being accepted.

Biomaterials ebook cover

Learn more about calcium phosphate and other materials in our ebook, The Physician’s Guide to Synthetic Bone Grafting Biomaterials. Written by Mo-Sci CTO, Dr. Steve Jung.

Access the Guide »

Consequently, the use of synthetic bone graft materials is steadily gaining popularity.1 A variety of bone graft substitutes have been used in the search to find an alternative to bone that provides a rapid and strong repair. These include demineralized bone matrix, calcium phosphates, collagen- and hydroxyapatite-based substitutes, and bone morphogenetic proteins. This article will focus on calcium phosphate ceramics and bioactive glasses.

Calcium Phosphates for Synthetic Bone Grafts

Calcium phosphate ceramics closely resemble the mineral components naturally present in bone tissue, and so represent an attractive option for a synthetic bone filling material. Their biocompatibility and ready availability have led to calcium phosphate ceramics being widely used as an alternative to autografts and allografts.

Calcium phosphates have proven to result in good cell attachment when used as bone substitutes and tissue engineering scaffolds. They are also known to provide predictable outcomes and lower morbidity for the patient whilst being cost effective compared with traditional bone grafts.2,3

Initially, calcium phosphate ceramics lacked sufficient porosity to allow immediate bone ingrowth and rapid integration into the bone tissue. However, variations in the parameters used during the preparation of calcium phosphates has led to the production of products with more favorable chemical and physical characteristics, such as specific surface areas and porosity.

Careful selection of the precise combination of properties has enabled development of bone filling materials that improve the adhesion, proliferation and differentiation of cells, thereby allowing improved osteoconductivity.4

Bioactive Glasses

Bioactive glass is a particularly favorable form of synthetic bonegraft as it is osteoconductive, bioactive and antimicrobial. In addition, minerals, such as calcium, are released from the bioactive glass providing key substrates for the production of new bone.

Bioactive glass induces specific biological activity when implanted in the body that causes an amorphous calcium phosphate layer to develop on its surface. Over a few hours, this layer incorporates blood proteins and collagen and crystallizes into hydroxycarbonate apatite, which makes it very similar to natural bone mineral. Bioactive glass thus bonds readily to the recipient bone.

Furthermore, the properties of bioactive glass, such as particle size and rate of reabsorption, can be tailored by adjusting the exact composition to meet the requirements of a specific repair procedure.4,5

Bioactive Glasses Encourage Bone Repair

Bioactive glass has been successfully used in a range of tissue engineering procedures.3 With its versatility, achieved through the tailoring of properties, its intrinsic strength and biocompatibility, bioactive glass presents many of the features needed in a synthetic bone substitute.

Bioactive glass bone filler composites have also been loaded with drugs, proteins and growth factors to facilitate repair by delivering the therapeutic agents directly into the defect region.7

It has been shown that damaged bone regained its original strength more quickly when repaired using a composite bone filler material that included bioactive glass compared with bone repair using composite alone. Furthermore, when bioactive glass is added to the bone substitute, the efficacy achieved is comparable to that obtain with the gold standard—autologous bone grafting. A bioactive glass synthetic bone substitute was recently shown to be effective in the repair of cavitary bone defects in patients with chronic osteomyelitis.8

Bioactive glass has also shown great promise in a variety of other orthopedic applications including spinal fusion and the coating of implants and the strengthening of bone at the site of joint replacements, plates, or screws. Bioactive glass coatings on orthopedic implants did not induce any adverse effects or inflammatory response in the surrounding tissue.9 Furthermore, bioactive glass coatings accelerated cell attachment, spreading, proliferation, differentiation, and mineralization of the extracellular matrix and promoted rapid bone growth. Spine fusion performed in rabbits using a mineralized collagen bone substitute with and without added bioactive glass demonstrated that the addition of bioactive glass led to earlier fusion of the bone. In addition, the addition of bioactive glass achieved a repair very similar to that seen with autograft in terms of the amount and quality of the new bone.10

Mo-Sci produce implant grade bioactive glass in a variety of forms suitable for a range of bone repair applications, and can tailor its composition to meet specific requirements.5 The composition and form of the bioactive glass can be adjusted to match the intrinsic conditions of the patient and the rate and pattern of bone formation required.4

References and Further Reading

  1. Kinaci A, et al. Trends in Bone Graft Use in the United States. Orthopedics 2014;37(9):e783 e788.
  2. Saffar JL, et al. Bone formation in tricalcium phosphate-filled periodontal intrabony lesions. Histological observations in humans. J Periodontol 1990;61(4):209–216.
  3. Barrère F, et al. Bone regeneration: Molecular and cellular interactions with calcium phosphate ceramics. Int. J. Nanomed. 2006, 1, 317–332.
  4. Lobo SE, et al. Biphasic Calcium Phosphate Ceramics for Bone Regeneration and Tissue .Engineering Applications. Materials 2010;3:815-826.
  5. Mo Sci Corporation website. http://www.mo-sci.com/en/products
  6. Jia W, et al. Bioactive Glass for Large Bone Repair. Adv Health Mater. 2015;4(18):2842 2848.
  7. Schumacher M, et al. Calcium phosphate bone cement/mesoporous bioactive glass composites for controlled growth factor delivery. Biomater. Sci. 2017;5:578 588.
  8. Ferrando A, et al. Treatment of Cavitary Bone Defects in Chronic Osteomyelitis: Biogactive glass S53P4 vs. Calcium Sulphate Antibiotic Beads. Bone Jt Infect. 2017;2(4):194 201.
  9. Mehdikhani-Nahrkhalaji M, et al. Biodegradable nanocomposite coatings accelerate bone healing: In vivo evaluation. Dent Res J (Isfahan). 2015;12(1):89 99.
  10. Pugely AJ, et al. Influence of 45S5 Bioactive Glass in A Standard Calcium Phosphate Collagen Bone Graft Substitute on the Posterolateral Fusion of Rabbit Spine. Iowa Orthop J. 2017; 37: 193–198.

Sunday, 26 December 2021

Annealing

I have just come across this item which is scientific, but not highly technical. It may help understanding some of the difficulties of annealing


Glass 101: Annealing

The process of annealing glass relieves internal stresses, which could otherwise leave it susceptible to cracking or shattering in response to minor mechanical or thermal shock. This makes annealing a vital step in the production of strong, stable, and heat-resistant glass.

Why Anneal?

From a physical perspective, glass is a highly unusual material. Most solid materials are highly ‘ordered’ with their constituent molecules or atoms arranged in regular, repeating patterns called crystal lattices. But the molecules in glass obey a different set of rules: they are, by definition, disordered. In fact, the arrangement of molecules inside solid glass resembles that of a liquid, except that they are fixed in place and don’t move around. We say that glass is an amorphous solid.

Crystalline solids and amorphous solids (i.e., glasses) respond to heat in very different ways. When crystalline solids are heated, they undergo a spontaneous phase transition at their melting temperature. Take water, for example: at -1 °C it’s an ordered, crystalline solid (ice), at 1 °C it’s a completely disordered liquid. But when glass is heated, it doesn’t undergo a phase transition per se. Instead, it very gradually tends toward a more liquid state. This smooth decrease in viscosity as temperature increases is due to the glass transition (transformation), and it’s one of the defining features of glasses.2 The glass transition temperature can be practically considered as the temperature where the liquid converts to a solid on cooling or conversely of which the solid begins to behave as a viscoelastic solid on heating.

Glass is worked and formed at very high temperatures, where its viscosity is low. When it is allowed to cool rapidly (supercool), the glass becomes stiffer and stiffer as the disordered molecules simply become more fixed in their positions. As this happens, internal stresses can become trapped in the solidifying glass. The result is extremely brittle glass that can shatter easily.

The process of annealing enables the elimination of internal stresses, producing strong and durable glass suitable for widespread application.

What is Annealing?

Essentially, annealing is the process of cooling glass in a controlled manner to reduce internal stresses in the finished glass.1 Annealing commonly occurs at one of two points in the glass production process:

  1. In many manufacturing processes (such as the float glass process), high-temperature glass is cooled gradually after it reaches its glass transition temperature. This is known as straight annealing.
  2. In some glass forming processes, for example, glass blowing, glass cools spontaneously after forming. In these cases, annealing is performed by reheating the glass to its glass transition temperature and then allowing it to cool in a controlled, gradual way. This process is sometimes called reannealing to distinguish it from straight annealing.

Whether a glass is straight annealed or reannealed, the fundamentals remain the same: within a certain temperature range known as the annealing temperature (close to the glass transition temperature), glass is soft enough that internal stresses can relax through microscopic molecular shifts, but stiff enough that it doesn’t deform under gravity.

Lowering the temperature of glass from its annealing temperature very slowly means that there is sufficient time for heat to distribute itself evenly, and molecules have sufficient time to find their most stable positions within the cooling glass.3 Once the glass passes the so-called strain point, at which point microscopic flow effectively stops and molecules are fixed in place, the glass can be cooled more rapidly to room temperature. Gradually cooling the glass in this manner prevents the formation of stresses and ensures there are no “weak points” in the finished glass.

Properties of Annealed Glass

Residual stresses in un-annealed glass mean that it can generally be expected to crack or shatter during handling (or even spontaneously). Annealed glass is much stronger and more durable than un-annealed glass, rendering it suitable for cutting and drilling processes; and subsequent use in standard applications such as windows and structural elements.

Achieving a uniform stress distribution within the glass also renders it capable of resisting thermal shock. This means that annealing plays an important role in the production of labware and bottles used in food processing, for example.

Annealing plays a special role in optical glasses. Optical applications require especially low spatial variations in refractive index, which can only be achieved by a highly uniform structural state.

The residual stresses that can be tolerated in optical glass are many orders of magnitude lower than that of ordinary glassware, so optical glass must be “fine-annealed” over much longer time periods. For example, ordinary glassware can generally be annealed in hours; but optical annealing may last for weeks or even months to allow a much greater minimization of stresses. Fine-annealed glasses exhibit consistent and well-characterized refractive indices and can be ground and polished without introducing undesirable birefringence in the glass.

Custom Glass Solutions

At Mo-Sci, we are experts in all stages of glass production, from forming and annealing right through to milling, surface treatments, and glass analysis. We produce highly specialized custom glasses for unique applications in healthcare and industry. Get in touch with us to find out more about our custom glass development services or to request a quote.

References and Further Reading

  1. Narayanaswamy, O. S. Annealing of Glass. in Glass Science and Technology vol. 3 275–318 (Elsevier, 1986).
  2. Dyre, J. C. Colloquium : The glass transition and elastic models of glass-forming liquids. Rev. Mod. Phys. 78, 953–972 (2006).
  3. Vogel, W. Glass Chemistry. (Springer Science & Business Media, 2012).
Link: https://mo-sci.com/glass-101-glass-annealing/



By the way, I hope you all have had a happy Christmas!

Wednesday, 22 December 2021

Glass Separators


Glass separators tend to be in three forms – powdered, liquid or fibre. These are applied to shelves, moulds and other surfaces that might come into contact with the hot glass.

What do they do?

Glass separators keep the glass from sticking to the shelves, kiln furniture and other supports during the higher temperature parts of the firing.  Glass as used for kilnforming reaches its softening point somewhere around 580°C. The glass will begin to stick to all surfaces as it gets warmer.  The separators are stable at high temperatures and do not stick to the glass or the materials used to separate the glass from its supports.


What are they?

       Liquid and powder separators are most often called kiln wash - or batt wash in the ceramics field.  Normally they are supplied in powder form that is mixed with water for painting onto shelves and moulds. 
They normally have a high content of alumina hydrate, some kaolin (also known as china clay) and sometimes a little silica, plus often a colouring agent that burns away on the first firing to indicate fired and unfired shelves.
       A high temperature lubricant, boron nitride, has come into use for kilnforming and has slightly different characteristics than the alumina hydrate-based kiln washes.

Sheet and blanket forms of glass separators are also widely used.  They have the general name of refractory mineral wool. They are often made from alkaline earth silicate (AES) wool, Alumino silicate wool (ASW) and Polycrystalline wool (PCW).  These have different temperature ranges and levels of health risk. The thin sheets are mainly used for covering shelves and other kiln furniture.  The blanket, which starts at about 12mm, is used mainly for insulation purposes.

Thin papers, similar in thickness to cartridge paper have been developed to give a finer texture than mineral wool separators.  These currently have the trade names Papyros and Thinfire, each with their own slightly different characteristics.

Safety

As with all refractory materials, safety precautions are needed.  In the kilnforming world the risks are not those of the industrial environment because the quantities are less, and the time of exposure is much less.  Still, breathing protection should be used. Eye protection is advisable, as the particles are hard and can scratch the eye surface.  Long sleeves and gloves are advisable when handling refractory fibres.
 

Kiln Wash

This blog concentrates on liquid and powdered separators. It draws on information from the ceramics and kilnforming communities.

Basic Kiln Wash Materials
A lot of the kilnforming knowledge of glass separators comes from the ceramics field. A brief look at the development of kiln wash by ceramicists is instructive to kilnforming. 

In order to make a good kiln wash you need to select materials that have very high melting points and that, when combined, do not create a eutectic that causes melting. Knowing a bit about the properties of materials and the principles of kiln wash allows you to choose the ingredients that make the best wash for your specific situation and avoid costly problems. 
(John Britt www.johnbrittpottery.com ceramicartsnetwork.org › firing-techniques)

The basic materials started as:
EPK Kaolin (which includes alumina)      50%
Silica                                                50%

EPK Kaolin is a high quality, water washed kaolin which is white, has unusually good forming characteristics and high green strength. In mixtures, EPK offers excellent suspension capabilities.  The source of alumina in kiln wash was often kaolin, but now is most often alumina hydrate or alumina oxide.

Silicon dioxide has a melting point of 1710°C and aluminium oxide has a melting point of 2050°C.  A mixture of these two materials will not melt, and will protect the kiln shelves at high temperatures.

This is a good kiln wash for low and mid-range electric firings [for ceramics]. The only problem is that it contains silica, which is a glass-former. So, if a lot of glaze drips onto the shelf, it can melt the silica in the kiln wash and form a glaze on the shelf. Also, when you scrape your shelves to clean them, you create a lot of silica dust, which is a known carcinogen. So, using silica in your kiln wash is not … the best choice.

Another drawback of this recipe is that, if it is used in salt or soda firings, it will most certainly create a glaze on the shelf. This is because silica, as noted above, is a glass-former. When sodium oxide, which is a strong flux, is introduced atmospherically, it can easily melt the silica in the kiln wash into a glass. This is why silica should not be used in a kiln wash recipe for wood, salt or soda kilns. 
(John Britt www.johnbrittpottery.com ceramicartsnetwork.org › firing-techniques)


For glaze firings a kiln wash with more separator and less glass former is better:

Alumina hydrate            50%
EPK kaolin                    50%


Kaolin has a melting point of 1770°C and alumina oxide has a melting point of 2050°C, so it will not melt, even in a … firing [of 1250°C to 1350°C]. These ingredients are called refractory because they are resistant to high temperatures. … This recipe can be used at all temperatures and in all kiln atmospheres. 
(John Britt www.johnbrittpottery.com ceramicartsnetwork.org › firing-techniques)


Kiln washes with kaolin, especially if applied thickly, can flake off the shelf after repeated firing.  The cause of this is the shrinking of the drying kaolin - which is a clay – similar to dried out lake beds. Adding at least half the kaolin as calcined EPK kaolin reduces this shrinkage. Calcining involves drying the kaolin at about 1000°C for some time.  This reduces the physical property of shrinkage, but retains the chemical and refractory properties of a glass separator intact.

This gives a kiln wash consisting of:
Alumina hydrate            50%
Calcined EPK kaolin        25%
EPK kaolin                    25%

You can add more calcined kaolin – up to 35% – if you want. You need to keep enough un-calcined kaolin in the recipe to suspend the other materials so that the suspended materials can be applied smoothly.  One difficulty of increasing the kaolin content of the kiln wash is that it tends to stick to the glass - especially opalescent - on a second firing.

It is, of course, possible to do away with the kaolin entirely.  You can mix alumina hydrate with water into a full milk consistency and apply that to the shelf or other kiln furniture.  It is difficult to maintain the alumina hydrate in suspension, though. After the firing you can brush the dried separator from the shelf into a container for re-use.  You do need to ensure that the powder to be reused is free of contaminants.  It is also important to find very fine grades of the alumina hydrate to minimise the texture on the base of the glass.  Most ceramic grades are coarser than wanted for kiln forming.  You can put the powder in a rock tumbler to make what you find finer than as purchased.

There are many variations on these basic kiln wash recipes. To illustrate the wide variety, some potters just dust alumina hydrate on their shelves to protect them, while some wood firing potters use 100% silica and wall paper paste to make a very thick (1/2-inch) coating that protects their shelves from excessive ash deposits. Still others, who have the new advanced nitride-bonded silicon carbide shelves, don’t even use kiln wash at all because the glaze drips shiver off when the shelves cool. Other potters, who are very neat and don’t share their space with others, may not even use kiln wash so that they can flip the shelves after every firing to prevent warping.

Kiln wash is such a ubiquitous material in the ceramics studio that we take it for granted. … There are many recipes to choose from and many solutions to common problems if we just take the time to learn about the materials we use. 
(John Britt www.johnbrittpottery.com ceramicartsnetwork.org › firing-techniques)

Variants on the traditional glass separators


There are variations in the use of alumina hydrate and kaolin, but there are also other glass separators available, although they tend to be expensive.

An example is zirconium. It is a glass separator with refractory properties, as in its zirconium oxide form it melts 2700°C.  In its zirconium silicate form it has a melting point of 2550°C.  These are available under a number of trade names. This can be added to the kiln wash mix in the knowledge that it will be stable throughout the firing.

But you must be careful in the amount you use, as zirconium silicate is used as an opacifier in glass and glazes.  Also, zirconium oxide is one of the hardest substances in the world.

Boron Nitride

Another very popular glass separator is boron nitride.  It has two forms. 
One is cubic boron nitride, a cubic structure similar to diamonds.

     

  
In the cubic form of boron nitride, alternately linked boron and nitrogen atoms form a tetrahedral bond network, exactly like carbon atoms do in diamond.  Cubic boron nitride is extremely hard and will even scratch diamond. It is the second hardest material known, second only to diamond.  Cubic boron nitride has very high thermal conductivity, excellent wear resistance and good chemical inertness, all very useful properties for a material subjected to extreme conditions. Because of its hardness, chemical inertness, high melting temperature (2973°C) cubic boron nitride is used as an abrasive and wear-resistant coating. Cubic boron nitride (CBN) is used for cutting tools and abrasive components for shaping/polishing with low carbon ferrous metals.  (http://www.docbrown.info/page03/nanochem06.htm)



Hexagonal Boron Nitride

The second form, useful in kilnforming is the hexagonal form of boron nitride.  It forms white plates of hexagons one layer thick like graphite.  These plates have weak bonds and so slide easily against one another.


https://www.substech.com/dokuwiki/doku.php?id=boron_nitride_as_solid_lubricant


It is a good insulator and chemically very inert.  It is stable to about 2700°C.

Hexagonal boron nitride (HBN) is used as a lubricant, since the weakly held layers can slide over each other.  Because of its 'soft' and 'slippery' crystalline nature, and its high temperature stability, HBN is used in lubricants in very hot mechanical working environments.  

The slippery nature and high temperature stability characteristics make this material an excellent coating for moulds and other situations where the glass moves against its supports.

The coating of the moulds needs frequent re-coating because the layers slide from the mould. Boron nitride works very well on solid impermeable surfaces as it adheres easily to smooth surfaces. It can be used on porous surfaces, but does seal those surfaces, meaning that these surfaces cannot be returned to that porous state without significant abrasion.

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The next blog  has notes on refractory mineral wools as separators and health and safety in use.

Wednesday, 15 December 2021

Zinc Health and Safety

So much is said about the toxicity of zinc, I thought to look up some facts.

As there is significant concern about health issues, it is useful to look in detail at the health and safety issues around the use of zinc at elevated temperatures.  Zinc is absorbed into the body by inhalation of fumes and consumption of zinc containing materials.






Toxicity


Although zinc is an essential requirement for good health, excess zinc can be harmful. Excessive absorption of zinc suppresses copper and iron absorption … [which results in the symptoms of zinc intoxication].  Stomach acid contains hydrochloric acid, in which metallic zinc dissolves readily to give corrosive zinc chloride. … The U.S. Food and Drug Administration states that zinc damages nerve receptors in the nose, causing [loss of smell].

Evidence shows that people taking 100–300mg of zinc daily may suffer induced copper deficiency. … Levels of 100–300mg may interfere with the utilization of copper and iron or adversely affect cholesterol. … A condition called the zinc shakes or "zinc chills" can be induced by inhalation of zinc fumes while brazing or welding galvanized materials. 

Poisoning

Consumption of zinc can result in death, but requires large amounts (over 1 kg in one case).  Smaller amounts result in lethargy and gross lack of coordination of muscle movements or apparent intoxication. https://en.wikipedia.org/wiki/Zinc

Research and W.H.O. Information

The Essential Toxin: Impact of Zinc on Human Health, by Laura M. PlumLothar Rink, and Hajo Haase*
Compared to several other metal ions with similar chemical properties, zinc is relatively harmless. Only exposure to high doses has toxic effects, making acute zinc intoxication a rare event. In addition to acute intoxication, long-term, high-dose zinc supplementation interferes with the uptake of copper. Hence, many of its toxic effects are in fact due to copper deficiency. While systemic [balance] and efficient regulatory mechanisms on the cellular level generally prevent the uptake of [cell destructive] doses of [environmental] zinc, … zinc [within the body] plays a significant role in cytotoxic [death of individual cells] events in single cells. … One organ where zinc is prominently involved in cell death is the brain, and cytotoxicity in consequence of [inadequate blood supply] or trauma involves the accumulation of free zinc.

Rather than being a toxic metal ion, zinc is an essential trace element. Whereas intoxication by excessive exposure is rare, zinc deficiency is widespread and has a detrimental impact on growth, neuronal development, and immunity, and in severe cases its consequences are lethal. Zinc deficiency caused by malnutrition and foods with low bioavailability, aging, certain diseases, or deregulated homeostasis [equilibrium] is a far more common risk to human health than intoxication.

Conclusions
Zinc is an essential trace element, and the human body has efficient mechanisms, both on systemic and cellular levels, to maintain [balance] over a broad exposure range. Consequently, zinc has a rather low toxicity, and a severe impact on human health by intoxication with zinc is a relatively rare event.

Nevertheless, on the cellular level zinc impacts survival and may be a crucial regulator of [the death of cells occurring as a normal and controlled part of an organism's growth or development]  as well as neuronal death following brain injury. Although these effects seem to be unresponsive to nutritional supplementation with zinc, future research may allow influencing these processes via substances that alter zinc [balance] instead of directly giving zinc.

Whereas there are only anecdotal reports of severe zinc intoxication, zinc deficiency is a condition with broad occurrence and potentially profound impact. Here, the application of “negative zinc”, i.e., substances or conditions that deplete the body of zinc, constitute a major health risk. The impact ranges from mild zinc deficiency, which can aggravate infections by impairing the immune defence, up to severe cases, in which the symptoms are obvious and cause reduced life expectancy.  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872358/

Zinc came
Credit: leadandlight.co.uk


World Health Organisation Document

10.2.2 Occupational exposure

Occupational exposure to dusts and fumes of zinc and zinc compounds can occur in a variety of settings in which zinc is produced, or in which zinc and zinc-containing materials are used. Typical airborne exposures observed include 0.19–0.29 mg/m3 during the smelting of zinc-containing iron scrap, 0.90–6.2 mg/m3 at non-ferrous foundries and 0.076–0.101 mg/m3 in hot-dip galvanizing facilities. Far higher exposures are possible during particular job activities, such as welding of zinc-coated steels in the absence of appropriate respiratory protection and/or fume extraction engineering controls.

Occupational exposure to high levels of zinc oxide and/or nonferrous metals is associated with metal-fume fever. [a condition in which the sufferer has influenza type symptoms - a raised temperature, chills, aches and pains, nausea and dizziness. It is caused by exposure to the fume of certain metals - commonly zinc].  This is usually a short-term, self-limiting syndrome…. Induction of metal-fume fever is most common with ultra-fine particles capable of deep lung penetration under conditions of exposure. Studies on volunteers conducted under short-term exposure conditions (77–153 mg/m3 for 15–30 min) have detected pulmonary inflammation responses (including [inflammation] induction) which are consistent with manifestations of metal-fume fever and support an immunological [cause] for this acute reversible syndrome.

Evaluation

Based on the available information, it is not possible to define a no-effect level for pulmonary inflammation from exposure to zinc oxide fume.

10.2.4 Risks of zinc excess

Toxic effects in humans are most obvious from accidental or occupational inhalation exposure to high concentrations of zinc compounds, such as from smoke bombs, or metal-fume fever. Modern occupational health and safety measures can significantly reduce potential exposure. Intentional or accidental ingestion of large amounts of zinc leads to gastrointestinal effects, such as abdominal pain, vomiting and diarrhoea.

In the case of long-term intakes of large amounts of zinc at pharmacological doses (150–2000 mg/day), the effects (sideroblastic anaemia [inability to make haemoglobin], leukopenia [low white cell quantities] and hypochromic microcytic anaemia [iron deficiency]) are reversible upon discontinuation of zinc therapy and/or repletion of copper status, and are largely attributed to zinc-induced copper deficiency.

High levels of zinc may disrupt the [balance] of other essential elements. For example, in adults, subtle effects of zinc on copper utilization may occur at doses of zinc near the recommended level of intake of 15 mg/day and up to about 50 mg/day. Copper requirements may be increased, and copper utilization may be impaired with changes in clinical chemistry parameters, but these effects are not consistent and depend largely upon the dietary intake of copper. Distortion of lipoprotein metabolism and concentrations associated with large doses of zinc are inferred to be a result of impaired copper utilization. In groups with adequate copper intake, no adverse effects, with the exception of reduced copper retention, have been seen at daily zinc intakes of [less than] 50 mg/day. There is no convincing evidence that excess zinc plays a [casual] role in human carcinogenesis. The weight of evidence supports the conclusion that zinc is not genotoxic [damaging of genetic information in cells] or teratogenic [affecting the development of embryos]. At high concentrations zinc can be cytotoxic [toxic to cells].   https://www.who.int/ipcs/publications/ehc/221_Zinc_Part_3.pdf?ua=1

zinc sheet 
Credit: Belmont Metals


Use and Risks of Zinc in Kilnforming


Zinc melts at 420°C and boils at 907°C, so any fumes will be emitted only around and above the full fusing temperature of glass.

The main problem in kilnforming is that the metal melts at such a low temperature that it is not useful for containing the glass.

There is anecdotal evidence to indicate that firing zinc contaminates the kiln, leading to subsequent devitrification issues.  This can be cleared by firing bentonite at high temperature in the kiln to absorb the zinc.

It is not a high-risk metal, even if it were to vaporise (above 900°C).

Research papers show zinc poisoning to be extremely rare. It is usually associated with taking too large daily doses of zinc as a dietary supplement, or swallowing USA pennies - made largely of zinc - which dissolves in stomach acid and creates large problems for the digestive system.  Where zinc intoxication occurs, it is largely reversible.

Conclusion

The idea that zinc will poison you in kilnforming conditions is simply not correct.