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Diss Factsheets
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EC number: 266-340-9 | CAS number: 66402-68-4 This category encompasses the various chemical substances manufactured in the production of ceramics. For purposes of this category, a ceramic is defined as a crystalline or partially crystalline, inorganic, non-metallic, usually opaque substance consisting principally of combinations of inorganic oxides of aluminum, calcium, chromium, iron, magnesium, silicon, titanium, or zirconium which conventionally is formed first by fusion or sintering at very high temperatures, then by cooling, generally resulting in a rigid, brittle monophase or multiphase structure. (Those ceramics which are produced by heating inorganic glass, thereby changing its physical structure from amorphous to crystalline but not its chemical identity are not included in this definition.) This category consists of chemical substances other than by-products or impurities which are formed during the production of various ceramics and concurrently incorporated into a ceramic mixture. Its composition may contain any one or a combination of these substances. Trace amounts of oxides and other substances may be present. The following representative elements are principally present as oxides but may also be present as borides, carbides, chlorides, fluorides, nitrides, silicides, or sulfides in multiple oxidation states, or in more complex compounds.@Aluminum@Lithium@Barium@Magnesium@Beryllium@Manganese@Boron@Phosphorus@Cadmium@Potassium@Calcium@Silicon@Carbon@Sodium@Cerium@Thorium@Cesium@Tin@Chromium@Titanium@Cobalt@Uranium@Copper@Yttrium@Hafnium@Zinc@Iron@Zirconium
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
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Sediment toxicity
Administrative data
Link to relevant study record(s)
Description of key information
Based on the justification of the three main components, it can be concluded:
Aluminium, aluminium powders and aluminium oxide are non hazardous (not classified for the environment). Aluminum (Al) is the most commonly occurring metallic element, comprising eight percent of the earth's crust (Press and Siever, 1974) and is therefore found in great abundance in both the terrestrial and sediment environments.
The equilibrium partitioning method is not applicable to calcium oxide, since its effect is caused by the hydroxyl ions (pH effect). The fate and behaviour of these ions is determined by the pH buffer capacity of the sediment rather than a partitioning coefficient (Kd).
Magnesium oxide (MgO) is exempted from registration according to EC 1907/2006 Annex V Section 10.
Key value for chemical safety assessment
Additional information
There are no studies available for “Reaction product of thermal process between 1000°C and 2000°C of mainly aluminium oxide and calcium oxide based raw materials with at least CaO+Al2O3+MgO >80% , in which aluminium oxide, magnesium oxide and calcium oxide in varying amounts are combined in various proportions into a multiphase crystalline matrix”. As this substance is an UVCB substance with aluminium oxide (AL2O3), calcium oxide (CaO) and magnesium oxide (MgO) as main constituents, justification based on these main components were taken into account by read across following a structural analogue approach.
Aluminium-compounds:
Aluminium, aluminium powders and aluminium oxide are non hazardous (not classified for the environment). Aluminum (Al) is the most commonly occurring metallic element, comprising eight percent of the earth's crust (Press and Siever, 1974) and is therefore found in great abundance in both the terrestrial and sediment environments. Concentrations of 3-8% (30,000-80,000 ppm) are not uncommon. The relative contributions of anthropogenic aluminium to the existing natural pools of aluminium in soils and sediments is very small, and therefore, not relevant either in terms of added amounts or in terms of toxicity. Based on these exposure considerations, additional sediment and/or soil testing is not warranted. More information about exposure based waiving for aluminium in soil and sediments can be found in attached document (White paper on exposure based waiving for Fe and Al in soils and sediments final 15-03-2010. pdf, see attachment).
Calcium-compounds:
In accordance with column 2 of REACH Annex VII there is no need to consider testing, since CSA indicates no need to investigate further effects on sediment organisms. Furthermore, the equilibrium partitioning method is not applicable to calcium oxide, since its effect is caused by the hydroxyl ions (pH effect). The fate and behaviour of these ions is determined by the pH buffer capacity of the sediment rather than a partitioning coefficient (Kd).
Because the sediment is expected to be more buffered than the water column, higher effect concentrations can be expected for sediment organisms. Furthermore, the substance will be present in its dissociated form in the natural aquatic environment. The ions will react with HCO3- to form water and carbonate ions which react with Ca2+ to form calcium carbonate. Calcium carbonate precipitates and deposits on the sediment. Calcium carbonate is a constituent of natural soils.
Magnesium oxide:
Magnesium oxide (MgO) is exempted from registration according to EC 1907/2006 Annex V Section 10.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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