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WO1998029208A1 - Procede pour preparer des particules enrobees d'une couche de verre soluble et articles contenant des particules ainsi enrobees - Google Patents

Procede pour preparer des particules enrobees d'une couche de verre soluble et articles contenant des particules ainsi enrobees Download PDF

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Publication number
WO1998029208A1
WO1998029208A1 PCT/DK1997/000575 DK9700575W WO9829208A1 WO 1998029208 A1 WO1998029208 A1 WO 1998029208A1 DK 9700575 W DK9700575 W DK 9700575W WO 9829208 A1 WO9829208 A1 WO 9829208A1
Authority
WO
WIPO (PCT)
Prior art keywords
particles
water
water glass
covered
mould
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
PCT/DK1997/000575
Other languages
English (en)
Inventor
Ole Huusmann
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.)
DTI Industri
Original Assignee
DTI Industri
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
Priority to SK806-99A priority Critical patent/SK80699A3/sk
Priority to NZ336304A priority patent/NZ336304A/en
Priority to AU53103/98A priority patent/AU726238B2/en
Priority to EEP199900251A priority patent/EE9900251A/xx
Priority to EP97949992A priority patent/EP0948419A1/fr
Priority to CA002274687A priority patent/CA2274687A1/fr
Application filed by DTI Industri filed Critical DTI Industri
Priority to IL13039097A priority patent/IL130390A/en
Priority to US09/331,295 priority patent/US6248284B1/en
Publication of WO1998029208A1 publication Critical patent/WO1998029208A1/fr
Priority to NO993032A priority patent/NO993032L/no
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22C—FOUNDRY MOULDING
    • B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22C—FOUNDRY MOULDING
    • B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
    • B22C1/18—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of inorganic agents
    • B22C1/186—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of inorganic agents contaming ammonium or metal silicates, silica sols
    • B22C1/188—Alkali metal silicates

Definitions

  • the present invention relates to a process for preparing particles covered with a layer of water glass and a process for preparing articles comprising such covered particles. Furthermore, the invention concerns such particles and articles obtainable by these pro-lapses.
  • moulds and cores of various materials are used.
  • the present invention is directed to such cases where the main ingredient of the material in the moulds and cores is constituted by solid particles such as sand.
  • binders can be of either organic or inorganic nature .
  • Organic binders are usually phenol-based and to a large extent preferred by iron and metal foundries.
  • phenol-based binders are detrimental to the environment as during the casting, the heating of phenol-based binders entails pyrolysis whereby CO and polyaromatic hydrocarbons
  • Water glass as a binder was used to adhere sand in foundries for the first time about 1920.
  • sand is mixed with an aqueous solution of water glass, and this mixture is subsequently filled into a mould to be cured by evaporation of the water.
  • This process was essentially improved about 1950 by the development of the C0 2 process in which the CC gas is led through the wet mixture of sand and water glass in order to cure the binder.
  • Cores and moulds obtained by the COumble process are relatively porous and their strength is weak.
  • the curing is effected by supplying an organic ester to the wet mixture of sand and water glass before filling it into a mould.
  • the present invention relates to a process for preparing particles covered with a layer of water glass, which process is characterized by the steps of
  • water glass in the present description and claims is to be understood as sodium or potassium silicates.
  • the ratio SiOfact/IV O is designated the weight module.
  • a water glass with a low weight module is easily soluble in water and strongly basic because a high content of the basic component M mac0.
  • a water glass possessing a high weight module has a smaller basic character, and a smaller water solubility.
  • the use of water glass with a weight module between 0.5 and 4, especially betwen 1.8 and 3.5, is preferred.
  • M Na is preferred.
  • the particles to be covered with a layer of water glass can be any material to which water glass can adhere .
  • Examples of such materials are metallic materials and ceramics.
  • Examples of usable metallic materials are aluminium, copper, iron, tungsten, chrome, vanadium and manganese.
  • Examples of ceramics are SiO ⁇ (quartz sand), Ti0 2 , Zr0 2 , Al 2 0 3 , CaO and MgO.
  • the size and the size distribution of the particles are not corresponding to the production of the covered particles according to the invention.
  • particles For use in mould and core boxes, it is in general preferred to use particles with a size of from 0.05 mm to 2.0 mm, especially 0.10 to 0.60 mm.
  • the selected particles can have a broad or narrow particle size distribution or the particle mass can be composed by socalled double sieved particles (double sieved sand) in which there are two peaks on the grain size curve.
  • the quantity of water in the mixture in step (a) depends on several factors, such as the specific surface, porosity and the electrostatic nature of the particles, but is preferably at least 0.1 % by weight, calculated on the weight of particles to be covered.
  • a quantity of typical 1-3 % by weight is chosen to ensure a sufficient humidification of the particles.
  • the quantity of water does preferably not surpass 5 % by weight as supplying water in surplus of this quantity will not contribute further to the humidification of the surface of the particles to be covered.
  • the quantity of water glass in the mixture comprising particles to be covered, water, and water glass depends on factors such as the desired thickness of the layer and the specific surface of the particles to be covered. According to the invention, 0.1-5 % by weight water glass can be used, calculated on the basis of the weight of the particles. It is in general preferred to use 1-3 % by weight.
  • step (a) The mixture in step (a) is obtained preferably by the steps of
  • step (a2) the water glass is preferably supplied to the mixture in solid state, it being preferred to use particles of water glass prepared by spray drying .
  • the stirring is preferably effected with such an intensity that the mixture is heated and such that the water evaporates.
  • heat can be provided from an external source and/or evaporation can be effected in vacuum in order to increase the evaporation velocity.
  • the used particles can be preheated prior to the mixture with water and water glass. This is especially advantageous if the used water glass is sparingly soluble, i.e. has a weight module from 3.0 to 4.0 wherein it is preferred to heat the particles to a temperature of up till 100 °C, preferably 80-90°C, before the particles are mixed with water and water glass.
  • the stirring may be continued until all the water is evaporated and the dry particles covered with a layer of water glass are provided, but the humidified and nonsticky particles can be taken out at a previous time with a view to immediate subsequent further processing.
  • such particles covered with water glass have outstanding flowing properties, both in a dry form and a slightly wet, but nonsticky, form. These flowing properties are supposedly obtained both as a consequence of the layer of water glass being smooth and hard and as a consequence of the covered particles, during drying, exercising an influence on each other such that the produced covered particles have a more rounded form in relation to the uncovered particles.
  • the particles obtainable by the proces indicated above can, according to the invention, be further processed to an article by a process characterized by the steps of (c) providing particles covered with water glass in a mould, (d) ensuring the presence of water for activation of water glass in the particle mass, and
  • mould in the present description and claims indicates among other, mould boxes and core boxes for preparing moulds for use with iron and metal casting or injection moulding of plastics and cores for use with iron and metal casting, respectively.
  • models are to be understood as casts wanted to obtain an article with an outer negative surface corresponding to that of the positive model.
  • the particles covered with water glass can be procured in the mould in an arbitrarily chosen way.
  • the particles is filled in bulk into a mould whereupon the mould is slightly vibrated in order to fill all cavities and to obtain a tight and uniform packing. By such a vibration the smaller particles will move towards the surface of the particle mass and thus increase the density of the surface of the article.
  • a suitable pressure e.g. with a plumb to promote a tighter packing of the particles.
  • the particles covered with water glas are obtained in the mould by blowing the particles borne by an airflow into the mould.
  • the carrier airflow escapes through valves in the mould and the particles will be packed in the mould under influence of the pressure of the airflow.
  • the particles covered with water glass can be provided in the mould by extrusion of the particles into the mould by a process designated "impact moulding".
  • impact moulding By this process, the particles are bumped into the mould under influence of a major pressure which can be effected e.g. by suddenly released compressed air.
  • the water glass By the presence of water in the particle mass and by supplying energy from a source, the water glass will be activated such that a coherent article is formed.
  • water must be provided for activation of the water glass in the particle mass.
  • This water can be e.g. crystallization water, be supplied as aqueous vapour, or the used particles can comprise a minor quantity of water before filling the mould, e.g. from 0.1 to 0.7 % by weight water, preferably about 0.3 % by weight.
  • the energy source for the curing can be e.g. a source for microwaves or high-frequency waves, warm air, convection heat or vapour.
  • vapour is led through the particles covered with water glass and provided in a mould in order to activate the water glass layer.
  • Compressed air is then supplied at a tem- perature of 160-200°C to effect a further heating of the covered particles and a beginning evaporation of the water.
  • the temperature is lowered to 80-160°C to remove the water from the produced article.
  • the humidity should be essentially uniformly distributed in all areas of the mould without the water glass being rinsed off the particles.
  • a variant of this embodiment uses particles covered with water glass which are humidified with up to 0.7 % by weight water instead of vapour for humidification the covered particles.
  • the pressure of the compressed air and the duration of the various temperature periods vary depending on the quantity of water used for humidification, the size of the article, the quantity of used water glass, etc., and such periods can be defined by the person skilled in the art by routine tests.
  • a typical distribution of the duration of the different temperature periods when produc- ing an article of 10 kg where the particles are quartz sand with an average grain size of 0.30 mm covered with a water glass quantity of 0.8 % by weight (module 2.0) and humidified with a water quantity of 1 % by weight, is the following for an air pressure of 700 kPa : 10 seconds air pressure at a temperature of 160-200°C, 30 seconds at a temperature of 80-160°C, and 20 seconds at room temperature.
  • the particles covered with water glass are cured by microwaves or high-frequency waves.
  • the water required for activation of the water glass can be present as crystallization water in the water glass layer, can be supplied by using humidified particles with a water content of 0.1 to 0.7 % or can be provided by supplying water vapour . As to the latter, it appeared to be possible to obtain curing of an article by placing a mould containing particles covered with water glass in a microwave oven where the charging opening faces a humidified blotting paper.
  • a third preferred embodiment is to use moulds which are provided with heat by convection, e.g. by placing the moulds in an oven, by placing the moulds on a heating plate or by using a mould with a heating jacket .
  • the used particles are preferably quartz sand. If the produced articles is a core and this core must be removed after the metal casting process, it is preferred to use water glass with a low module, i.e. up to module 3.0 as the core will then be easily rinsed away by water after the casting.
  • the produced article is to be used as mould tools, it is expedient to use particles of metal. If a poorer solubility of the mould tools in water is desired, a sparingly soluble water glass is preferably used, i.e. a water glass with a module of 3.0-3.5.
  • the mould tools may e.g. be used for plastic injection moulding, optionally after a surface treatment hereof.
  • quartz sand with an average grain size of 0.26 mm was weighed and placed in a cylindrical plastic container with a diameter of 200 mm and a height of 190 mm.
  • the plastic container was provided with a stirrer comprising a central axis from which four wings extend. The length of the wings is 95 mm. The stirrer was started and adjusted to a rotational speed of 450 revolutions per minute.
  • the stirring was continued for about 60 minutes which can be divided into three periods.
  • Period 1 0-30 minutes after supplying water glass, the mixture is heated by the mechanical energy supplied from the stirrer, and water is allowed freely to evaporate;
  • Period 2 30-45 minutes after supplying the water glass, the evaporation of the water is so advanced that the water glass begins to be sticky, and a tendency to formation of loosely coherent agglomerates can be observed.
  • the sticki- ness of the mixture decreases as the quantity of water in the mixture falls below the lowest binding level and the agglomerates are broken by the stirring.
  • the water content of the mixture is about 0.7 % by weight at the end of this period;
  • Period 3 45-60 minutes after supplying the water glass, the remaining free quantity of water evaporates whereupon quartz sand covered with water glass is obtained.
  • the temperature of the obtained product is about 60°C.
  • the obtained product is in a microscope observed to have an even and smooth cover of water glass which is presumed to be the reason for the observed free flowing property.
  • the product may used after the end of period 2 direct in the further processing.
  • quartz sand with an average grain size of 0.26 mm was heated to a temperature of about 90 °C and placed in the container described in example 1 and provided with the stirrer which is also described in said example whereupon the stirrer is started and adjusted to a rotational speed of 450 revolutions per minute.
  • 90 ml water is supplied to the sand and stirred for 15-30 seconds whereupon 60 g water glass with a weight module of 3.0 is supplied. The water glass is dissolved practically immediately.
  • Quartz sand covered with water glass produced according to example 1 was loosely filled into a mould with a volume of about 4 liters (corresponding to a sand weight of about 2200 g) , whereupon the mould with the covered sand was vibrated with a free surface in 3 minutes with 2900 vibrations per minute.
  • the dimension of the surface was 250 mm x 280 mm.
  • the surface of the covered sand was levelled with a blade, and a plumb of aluminium covering the entire surface and with a weight of 5.0 kg was placed on the surface. Subsequently, the vibrations went on for further 2 minutes and the plumb was then removed.
  • a water absorbent fibre fabric was placed over the surface of the sand and the fibre fabric was wetted with 40 g water.
  • the plumb was placed on the fibre fabric and a heating plate positioned on the plumb. The evaporated water was ensured not to escape to an essential extent, but essentially to be distributed in the sand.
  • the plumb was heated to 175°C whereby the water in the fibre fabric evaporated, and humidified and activated the water glass layer.
  • the temperature of the mould at the end of the heating is about 90°C.
  • the heating plate, plumb and fibre cloth are then removed.
  • the mould was heated to 150°C within 30 minutes and this temperature was maintained for yet an hour.
  • the mould containing the produced article is then allowed voluntarily to cool to room temperature.
  • Iron powder covered with water glass, produced according to example 2 was processed to an article by using the same method as indicated in example 5.
  • the obtained article was not conductive which indicates the completeness of the water glass cover around the iron powder .

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Glass Compositions (AREA)
  • Glanulating (AREA)
  • Mold Materials And Core Materials (AREA)
  • Surface Treatment Of Glass (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Procédé pour préparer des particules à écoulement libre enrobées d'une couche de verre soluble sodium, consistant (a) à réaliser un mélange contenant les particules à enrober, de l'eau et de 0,1 à 5 % en poids de verre soluble sodium, calculé sur la base du poids des particules, le verre soluble étant dissous dans ce mélange, et (b) à brasser mécaniquement ce mélange, avec éventuellement un apport de chaleur provenant d'une source de chaleur extérieure, et à permettre à l'eau de s'évaporer du mélange au moins jusqu'à ce que le mélange ne soit plus visqueux. L'invention porte en outre sur un procédé pour préparer un article présentant une surface finie.
PCT/DK1997/000575 1996-12-18 1997-12-17 Procede pour preparer des particules enrobees d'une couche de verre soluble et articles contenant des particules ainsi enrobees Ceased WO1998029208A1 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
NZ336304A NZ336304A (en) 1996-12-18 1997-12-17 Process for preparing particles covered with a layer of water glass and articles comprising such covered particles
AU53103/98A AU726238B2 (en) 1996-12-18 1997-12-17 Process for preparing particles covered with a layer of water glass and articles comprising of such covered particles
EEP199900251A EE9900251A (et) 1996-12-18 1997-12-17 Meetod vesiklaasi kihiga kaetud osakeste valmistamiseks ja selliselt kaetud osakesi sisaldavad tooted
EP97949992A EP0948419A1 (fr) 1996-12-18 1997-12-17 Procede pour preparer des particules enrobees d'une couche de verre soluble et articles contenant des particules ainsi enrobees
CA002274687A CA2274687A1 (fr) 1996-12-18 1997-12-17 Procede pour preparer des particules enrobees d'une couche de verre soluble et articles contenant des particules ainsi enrobees
SK806-99A SK80699A3 (en) 1996-12-18 1997-12-17 Process for preparing particles covered with a layer of water glass and articles comprising such covered particles
IL13039097A IL130390A (en) 1996-12-18 1997-12-17 Process for preparing particles covered with a layer of water glass and articles comprising such covered particles
US09/331,295 US6248284B1 (en) 1996-12-18 1997-12-17 Process for preparing particles covered with a layer of water glass and articles comprising such covered particles
NO993032A NO993032L (no) 1996-12-18 1999-06-18 FremgangsmÕte for Õ preparere partikler dekket med et lag av vannglass og gjenstander som omfatter slike dekkede partikler

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DK199601441A DK172825B1 (da) 1996-12-18 1996-12-18 Fremgangsmåde til fremstilling af partikler belagt med et lag af vandglas og af emner omfattende sådanne belagte partikler.
DK1441/96 1996-12-18

Publications (1)

Publication Number Publication Date
WO1998029208A1 true WO1998029208A1 (fr) 1998-07-09

Family

ID=8104869

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DK1997/000575 Ceased WO1998029208A1 (fr) 1996-12-18 1997-12-17 Procede pour preparer des particules enrobees d'une couche de verre soluble et articles contenant des particules ainsi enrobees

Country Status (13)

Country Link
US (1) US6248284B1 (fr)
EP (1) EP0948419A1 (fr)
AU (1) AU726238B2 (fr)
CA (1) CA2274687A1 (fr)
DK (1) DK172825B1 (fr)
EE (1) EE9900251A (fr)
HU (1) HUP9904720A3 (fr)
IL (1) IL130390A (fr)
NO (1) NO993032L (fr)
NZ (1) NZ336304A (fr)
PL (1) PL334341A1 (fr)
SK (1) SK80699A3 (fr)
WO (1) WO1998029208A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1832357A1 (fr) * 2006-03-10 2007-09-12 Minelco GmbH Forme ou pièce brute, mélange de matériaux de formage de fonderie et son procédé de fabrication
WO2008113765A1 (fr) * 2007-03-16 2008-09-25 Chemex Gmbh Particule à noyau et enveloppe destinée à être utilisée comme charge dans des matières pour masselottes
WO2010025861A1 (fr) * 2008-09-05 2010-03-11 Minelco Gmbh Sable à noyaux ou sable de fonderie mélangé à verre soluble et/ou enduit de verre soluble avec une teneur en eau de l'ordre d'environ 0,25 % en poids à environ 0,9 % en poids

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102005011644A1 (de) * 2005-03-14 2006-09-21 AS Lüngen GmbH & Co. KG Exotherme und isolierende Speisereinsätze mit hoher Gasdurchlässigkeit
CN104903023B (zh) * 2012-12-19 2017-06-16 旭有机材工业株式会社 覆膜砂及其制造方法以及铸型的制造方法

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1889007A (en) * 1931-02-26 1932-11-29 Benjamin F Wallace Sand core for casting metal and method of making same
US2947641A (en) * 1958-11-03 1960-08-02 Ford Motor Co Shell molding material and process
US3255024A (en) * 1959-05-11 1966-06-07 Morris Bean & Company Molding composition and method
US3508936A (en) * 1968-09-27 1970-04-28 Abram Moiseevich Lyass Method of making fluid self-hardening mixture,preferably for manufacturing foundry moulds and cores
US3804643A (en) * 1969-05-27 1974-04-16 Mitsubishi Heavy Ind Ltd Process for producing casting molds using a dry flowable blended sand
DE2856267A1 (de) * 1978-12-27 1980-07-17 Woellner Werke Bindemittel fuer formstoffe zur herstellung von giessereiformen und -kernen
US4331197A (en) * 1979-07-02 1982-05-25 Ford Motor Company Microwave core process
FI89565B (fi) * 1992-09-23 1993-07-15 Greencast Oy Form- och kaernsand samt foerfarande foer tillverkning av densamma
WO1995015229A1 (fr) * 1993-11-30 1995-06-08 Borden (Uk) Limited Liant de fonderie

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3802902A (en) 1972-03-17 1974-04-09 Ti Tech Int Inc Method of making molds
US4347890A (en) 1981-03-09 1982-09-07 Pq Corporation Method for binding particulate materials
WO1989005204A1 (fr) 1987-12-08 1989-06-15 Harri Sahari Procede de preparation de moules et de noyaux utilises dans le coulage des metaux

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1889007A (en) * 1931-02-26 1932-11-29 Benjamin F Wallace Sand core for casting metal and method of making same
US2947641A (en) * 1958-11-03 1960-08-02 Ford Motor Co Shell molding material and process
US3255024A (en) * 1959-05-11 1966-06-07 Morris Bean & Company Molding composition and method
US3508936A (en) * 1968-09-27 1970-04-28 Abram Moiseevich Lyass Method of making fluid self-hardening mixture,preferably for manufacturing foundry moulds and cores
US3804643A (en) * 1969-05-27 1974-04-16 Mitsubishi Heavy Ind Ltd Process for producing casting molds using a dry flowable blended sand
DE2856267A1 (de) * 1978-12-27 1980-07-17 Woellner Werke Bindemittel fuer formstoffe zur herstellung von giessereiformen und -kernen
US4331197A (en) * 1979-07-02 1982-05-25 Ford Motor Company Microwave core process
FI89565B (fi) * 1992-09-23 1993-07-15 Greencast Oy Form- och kaernsand samt foerfarande foer tillverkning av densamma
WO1995015229A1 (fr) * 1993-11-30 1995-06-08 Borden (Uk) Limited Liant de fonderie

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1832357A1 (fr) * 2006-03-10 2007-09-12 Minelco GmbH Forme ou pièce brute, mélange de matériaux de formage de fonderie et son procédé de fabrication
WO2007104469A1 (fr) * 2006-03-10 2007-09-20 Minelco Gmbh Moule ou ébauche, mélange de matériau de moulage pour fonderie et procédé de réalisation associé
WO2008113765A1 (fr) * 2007-03-16 2008-09-25 Chemex Gmbh Particule à noyau et enveloppe destinée à être utilisée comme charge dans des matières pour masselottes
KR101429144B1 (ko) 2007-03-16 2014-08-11 케멕스 게엠베하 피더 조성물에 대한 필러로서 사용하기 위한 코어-시스 입자
US9352385B2 (en) 2007-03-16 2016-05-31 Chemex Gmbh Core-sheath particle for use as a filler for feeder masses
WO2010025861A1 (fr) * 2008-09-05 2010-03-11 Minelco Gmbh Sable à noyaux ou sable de fonderie mélangé à verre soluble et/ou enduit de verre soluble avec une teneur en eau de l'ordre d'environ 0,25 % en poids à environ 0,9 % en poids
EP2163328A1 (fr) * 2008-09-05 2010-03-17 Minelco GmbH Sable de noyau ou de moule revêtu par et/ou mélangés avec des silicates de potassium ayant une teneur en eau comprise entre environ 0,25 poids -% jusqu'à environ 0,9 poids -%
US8627877B2 (en) 2008-09-05 2014-01-14 Minelco Gmbh Core or foundry sand coated and/or mixed with water glass with a water content in the range of ≧ approximately 0.25% by weight to approximately 0.9% by weight

Also Published As

Publication number Publication date
NO993032D0 (no) 1999-06-18
EP0948419A1 (fr) 1999-10-13
NZ336304A (en) 2000-02-28
PL334341A1 (en) 2000-02-28
DK172825B1 (da) 1999-08-02
CA2274687A1 (fr) 1998-07-09
AU5310398A (en) 1998-07-31
IL130390A0 (en) 2000-06-01
AU726238B2 (en) 2000-11-02
NO993032L (no) 1999-06-18
US6248284B1 (en) 2001-06-19
HUP9904720A2 (hu) 2000-05-28
HUP9904720A3 (en) 2001-02-28
IL130390A (en) 2002-03-10
DK144196A (da) 1998-06-19
EE9900251A (et) 1999-12-15
SK80699A3 (en) 1999-12-10

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