EP0148869A1 - Keramisches Material - Google Patents

Keramisches Material

Info

Publication number
EP0148869A1
EP0148869A1 EP84902431A EP84902431A EP0148869A1 EP 0148869 A1 EP0148869 A1 EP 0148869A1 EP 84902431 A EP84902431 A EP 84902431A EP 84902431 A EP84902431 A EP 84902431A EP 0148869 A1 EP0148869 A1 EP 0148869A1
Authority
EP
European Patent Office
Prior art keywords
component
fine
alkali metal
coarse
metal compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP84902431A
Other languages
English (en)
French (fr)
Other versions
EP0148869A4 (de
Inventor
Gordon Wallace Collett
Henry Wynands
Bruce Gordon Small
Kathleen Marjorie Day
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monier Ltd
Original Assignee
Monier Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Monier Ltd filed Critical Monier Ltd
Publication of EP0148869A1 publication Critical patent/EP0148869A1/de
Publication of EP0148869A4 publication Critical patent/EP0148869A4/de
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B30/00Compositions for artificial stone, not containing binders
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/001Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing unburned clay
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/24Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing alkyl, ammonium or metal silicates; containing silica sols
    • C04B28/26Silicates of the alkali metals
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/91Use of waste materials as fillers for mortars or concrete

Definitions

  • the fly ash and slag components are mixed, usually with a binder such as bentonite or sodium silicate which provides green strength, formed into shape and fired at elevated temperatures, generally in the region of 1100°C.
  • a binder such as bentonite or sodium silicate which provides green strength
  • the fly-ash or, in the case of Smith 4,120,735, the incinerator residue
  • the particle size distribution of the coarse component will also effect the properties and composition of the green and fired product. For example, where the coarse component is relatively deficient in smaller particles, a greater proportion of fine component will be required to achieve a given bulk density.
  • the alkali metal compound typically sodium silicate
  • the alkali metal compound will normally be added in aqueous solution, and the quantity of additional water, which may also be required to achieve correct plasticity, will be determined by experiment.
  • the total initial water content of the unfired mixture will depend on the process by which the article is to be formed, whether by extruding or pressing, for example.
  • the green product is, of course, dried before firing, to minimize the quantity of free water.
  • the blast furnace slag had a maximum particle size of 3 mm and the following approximate composition:
  • the sodium silicate solution was that with a silica-soda weight ratio of the order of 2.25 and a density of the order of 1.56 with a solid content of approximately 46%.
  • the proportion of fly-ash was determined by adding fly-ash to a sample of slag until maximum bulk density was achieved, so that the proportions employed represent the maximum packing of the two ingredients for the particle size range of the two components.
  • the ingredients were mixed for three minutes in a planetary mixer and tiles were formed on pallets in a conventional concrete tile making machine. The tiles were then dried for two hours at approximately 90°C. Immediately after the tiles left the drier, a low temperature acid resistant ceramic glaze was applied by spray applicator.
  • the glazed tiles were stripped from the pallets and fired over a period of three hours, the maximum temperature being approximately 820°C, and the tiles being gradually reduced from this temperature to a kiln exit temperature of approximately 130°C.
  • Pieces of sample tile were tested for water absorption by being stood on end in approximately 1 cm of water for 24 hours, then totally immersed in water for a further 24 hours, and then boiled in water for 45 minutes.
  • the following table shows the water absorption ( % ) measured after each of these treatments, respectively designated as A, B and C:
  • the quality of glaze on the fired tile was excellent, with a strong bond and very little gas bubble formation.
  • Sodium silicate solution 15 In order to examine the physical behaviour of the tile during a firing cycle, a bar of this material was taken through a cycle of heating to 1000°C in a dilatometer followed by cooling, and the same sample was subsequently subjected to a further heating and cooling cycle in the dilatometer.
  • Fig. 1 illustrates the dilatometer curve produced in the first "firing" of the sample, while Fig. 2 shows the curve obtained in the second cycle.
  • Figs. 1 and 2 the percent change in length is plotted against temperature in °C.
  • the dilatometer was operated on a normal cycle with a rate of temperature change of 3°C per minute, the sample being in an air atmosphere.
  • Fig. 1 The major effects revealed in Fig. 1 occur between 600°C and 850°C.
  • the bar Prior to 620°C, the bar expands linearly with rising temperature. In the region of 620-630°C softening of the material commences, and the dilatometer records a sharp contraction through the temperature zone of 700- 800°C where the material is in a pyroplastic state, while beyond approximately 850°C linear expansion is resumed, although the expansion of the sample recorded in this region is assumed to be in fact bloating, as the slag particles soften sufficiently to release entrapped gases.
  • the curve of Fig. 2 shows the material behaving quite linearly throughout the temperature range, with no contraction occurring in the region of 600-800°C.
  • the linear behaviour of the sample in Fig. 2 indicates that the reaction occurring in the unfired sample in the 600- 800°C region is not repeated, and was completed in the course of the first dilatometer cycle.
  • Fig. 3 shows the dilatometer curve of a tile sample previously fired over a 4-hour cycle to 860°C. In this curve the scale of the vertical axis is magnified for the purpose of clarity. The sample shows the characteristic form of Fig. 1, but the contraction which occurs in the pyroplastic zone is only of the order of 0.3%, compared with 2% in the unfired specimen of Fig. 1.
  • the coefficient of thermal' expansion revealed by the dilatometer curves is of the order of 10 x 10 , and is comparable with those of terracotta tiles or common bricks.
  • fly-ash and blast furnace slag are employed, it is believed that a reaction occurs at the surface of the fly-ash particles which essentially involves the dissolution of Al 2 0 3 to form a sodium aluminosilicate. At the interface with the slag particles, it is believed that a similar reaction takes place, accompanied by the formation of a lime soda alumina silica glass.
  • tile composition employing a substitute for the fly-ash as the fine component material was prepared from a mixture of slag, manganese mud and sodium silicate solution in the following proportions:
  • An attractive alternative to blast furnace slag for the purpose of the coarse component in products according to the present invention is fine-grained mafic rock such as basalt.
  • Such a material contains no significant quantities of free silica, and therefore does not exhibit a quartz inversion. It has a low coefficient of thermal expansion and is capable of short firing times.
  • Mafic rocks also contain no hydrated water, and the green product is therefore not subject to drying shrinkage, which cannot be tolerated in the production of tiles on pallets.
  • Basalt furthermore contains suitable quantities of metal oxides to enable a surface reaction with the sodium silicate.
  • Basalt-based tiles have been produced with strengths approximating those of the slag-based tiles (3000 Newtons) but with superior characteristics in greater acid insolubility, and in the shorter firing cycle which is possible due to the fact that the tiles can be raised to the maximum firing temperature and cooled from this temperature more quickly without the cracking which would occur when using blast furnace slag.
  • Example V
  • O PI raised to approximately 700°C, and the contraction of the material through the pyroplastic region is more gradual.
  • the slag will no doubt contribute silica to the reaction with the caustic soda, and fly-ash may also act as a source of silica.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
EP19840902431 1983-06-17 1984-06-15 Keramisches Material. Ceased EP0148869A4 (de)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
AU9863/83 1983-06-17
AUPF986383 1983-06-17
AU1093/83 1983-08-29
AUPG109383 1983-08-29

Publications (2)

Publication Number Publication Date
EP0148869A1 true EP0148869A1 (de) 1985-07-24
EP0148869A4 EP0148869A4 (de) 1985-11-07

Family

ID=25642669

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19840902431 Ceased EP0148869A4 (de) 1983-06-17 1984-06-15 Keramisches Material.

Country Status (4)

Country Link
EP (1) EP0148869A4 (de)
ES (1) ES8604044A1 (de)
IT (1) IT1199142B (de)
WO (1) WO1985000035A1 (de)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0199941B2 (de) * 1985-04-06 1995-05-03 Ht Troplast Ag Anorganische Formmasse mit Gehalten einer steinbildenden Komponente
EP0203899A1 (de) * 1985-05-07 1986-12-03 Lundström, Claes Methode zur Herstellung einer wasserglashaltigen Formmasse
NL185916C (nl) * 1988-02-11 1991-12-16 Hendrikus Veldhoen Werkwijze voor het vervaardigen van een gevormd, keramisch bouwmateriaal.
BE1005303A3 (nl) * 1991-09-04 1993-06-22 Isomo Nv Werkwijze voor het vervaardigen van een isolerend element en aldus vervaardigd element.
WO2004085334A1 (en) * 2003-03-26 2004-10-07 Jajanya Datta Panda A composition for the manufacture of silica insulating refractory brick
ITTV20070054A1 (it) * 2007-03-28 2008-09-29 Luca Toncelli Procedimento per la fabbricazione di lastre in materiale ceramico
ES2385570B1 (es) * 2010-12-31 2013-06-17 María Lidón Bou Cortes Método de fabricación de un producto cerámico a partir de cenizas volantes como materia prima.
RU2502701C1 (ru) * 2012-04-17 2013-12-27 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Самарский государственный аэрокосмический университет имени академика С.П. Королева (национальный исследовательский университет)" (СГАУ) Керамическая масса для изготовления керамического кирпича
RU2494992C1 (ru) * 2012-04-20 2013-10-10 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Петербургский государственный университет путей сообщения" Керамическая масса для изготовления керамического кирпича
CN107922270A (zh) * 2015-05-31 2018-04-17 贝西姆私人有限公司 绝热材料

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE703321A (de) * 1966-09-01 1968-02-29

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3137657A (en) * 1962-04-11 1964-06-16 John F Quirk Ceramic product comprising sintered beryllia and bentonite and method
JPS5118967B1 (de) * 1970-10-27 1976-06-14
GB1392227A (en) * 1971-06-29 1975-04-30 Carborundum Co Refractory bodies and method of making same
GB1402757A (en) * 1972-04-21 1975-08-13 Kroyer K K K Constructional material
GB1434737A (en) * 1972-08-08 1976-05-05 Magnesium Elektron Ltd Bonding of inorganic particles
GB1496683A (en) * 1974-05-03 1977-12-30 Ici Ltd Manufacture of calcium sulphate alphahemihydrate
AT349965B (de) * 1975-10-03 1979-05-10 Veitscher Magnesitwerke Ag Verfahren zur herstellung von gebrannten feuerfesten steinen

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE703321A (de) * 1966-09-01 1968-02-29

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO8500035A1 *

Also Published As

Publication number Publication date
WO1985000035A1 (en) 1985-01-03
IT8448413A0 (it) 1984-06-18
EP0148869A4 (de) 1985-11-07
ES8604044A1 (es) 1986-01-16
ES533902A0 (es) 1986-01-16
IT1199142B (it) 1988-12-30

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Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19850215

AK Designated contracting states

Designated state(s): DE FR GB

17Q First examination report despatched

Effective date: 19870310

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 19881121

RIN1 Information on inventor provided before grant (corrected)

Inventor name: DAY, KATHLEEN, MARJORIE

Inventor name: COLLETT, GORDON, WALLACE

Inventor name: WYNANDS, HENRY

Inventor name: SMALL, BRUCE, GORDON