EP2323783A1 - Mit wasserglas beschichteter und/oder vermischter kern- oder formsand mit einem wassergehalt im bereich von > etwa 0,25 gew.-% bis etwa 0,9 gew.-% - Google Patents
Mit wasserglas beschichteter und/oder vermischter kern- oder formsand mit einem wassergehalt im bereich von > etwa 0,25 gew.-% bis etwa 0,9 gew.-%Info
- Publication number
- EP2323783A1 EP2323783A1 EP09778098A EP09778098A EP2323783A1 EP 2323783 A1 EP2323783 A1 EP 2323783A1 EP 09778098 A EP09778098 A EP 09778098A EP 09778098 A EP09778098 A EP 09778098A EP 2323783 A1 EP2323783 A1 EP 2323783A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- core
- sand
- molding
- casting
- molding sand
- 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.)
- Granted
Links
- 235000019353 potassium silicate Nutrition 0.000 title claims abstract description 68
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 title claims abstract description 66
- 239000004576 sand Substances 0.000 title claims abstract description 55
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 51
- 238000005266 casting Methods 0.000 claims abstract description 51
- 229910052751 metal Inorganic materials 0.000 claims abstract description 15
- 239000002184 metal Substances 0.000 claims abstract description 15
- 239000003110 molding sand Substances 0.000 claims description 69
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 57
- 238000000034 method Methods 0.000 claims description 38
- 238000000465 moulding Methods 0.000 claims description 34
- 238000004519 manufacturing process Methods 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 25
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 239000012778 molding material Substances 0.000 claims description 24
- 239000000654 additive Substances 0.000 claims description 17
- 239000002318 adhesion promoter Substances 0.000 claims description 12
- 238000002156 mixing Methods 0.000 claims description 11
- 238000011049 filling Methods 0.000 claims description 7
- 230000000996 additive effect Effects 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000006004 Quartz sand Substances 0.000 claims description 5
- 239000002274 desiccant Substances 0.000 claims description 5
- 238000003384 imaging method Methods 0.000 claims description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- 239000010450 olivine Substances 0.000 claims description 3
- 229910052609 olivine Inorganic materials 0.000 claims description 3
- 229910052845 zircon Inorganic materials 0.000 claims description 3
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000007822 coupling agent Substances 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 12
- 239000000155 melt Substances 0.000 abstract description 3
- 239000007767 bonding agent Substances 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000011230 binding agent Substances 0.000 description 16
- 239000007787 solid Substances 0.000 description 16
- 239000007864 aqueous solution Substances 0.000 description 13
- 239000002585 base Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 229920002545 silicone oil Polymers 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 7
- 229910021486 amorphous silicon dioxide Inorganic materials 0.000 description 7
- 229910002804 graphite Inorganic materials 0.000 description 7
- 239000010439 graphite Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000004594 Masterbatch (MB) Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 5
- 238000007711 solidification Methods 0.000 description 5
- 230000008023 solidification Effects 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical class [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000002671 adjuvant Substances 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 235000013980 iron oxide Nutrition 0.000 description 4
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 229910052582 BN Inorganic materials 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- -1 boronitrides Substances 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000003958 fumigation Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000006259 organic additive Substances 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 230000002123 temporal effect Effects 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000002920 hazardous waste Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 229910001338 liquidmetal Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
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
- 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
-
- 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
Definitions
- Water glass coated and / or mixed core or foundry sand having a water content in the range of> about 0.25% to about 0.9% by weight.
- the invention relates to a core or molding sand for the production of cores and
- Casting molds for casting molten metal which comprises a molding base material (for example quartz sand, chrome ore sand, zircon sand, olivine sand, synthetic sands), the
- the core or molding sand has a water content in the range of> about 0.25 wt .-% to about 0.9 wt .-%, based on the total weight of the core and
- Formsands has. Furthermore, the invention relates to a method for producing such a core or foundry sand as well as a method for producing a core or a casting mold with this core or molding sand and its use.
- Core or molding sands for the production of cores or other casting molds are known. Usually, these are first brought into the desired shape by a casting mold forming tool, such as a core tool, with the core or molding sand and then the core or molding sand is compacted and cured. After opening the tool, the desired molding, such as a casting core, can be removed. Using this casting core, metal melts, including aluminum alloy melts, can then be poured into the desired shape. After the molten metal has solidified, the casting core or the casting mold can be removed, for example by means of shaking. By shaking the previously solid and stable G thinkkern- / form disintegrates.
- a known process for the production of core or foundry sand is also called “croning process” according to its inventor, in which a fine-grained quartz sand is used as mold base, in which each sand grain is coated with a thermoplastic phenolic resin layer state solid at room temperature.
- the core or foundry sand now in an a molding cavity forming such as a the mold imaging tool, for example a Kemwerkmaschine introduced and heated to 250 0 C to 300 0 C, to melt the binder film and make it through to Polycondensation Binder bridges that are solid after completion of the polycondensation reaction and have thermosetting properties
- the finished core or the finished form can be removed from the tool
- the core or molding sand used in the croning process has the advantage over the other common core / mastering processes (eg cold box, hot box, furan Resin, water glass CC * method) that the curing reaction, in contrast to the aforementioned method not directly after mixing, but only after renewed heat supply (250 ° C-300 ° C) begins.
- the shelf life of the ready-mixed core or foundry sand is virtually unlimited when properly stored.
- the core or molding sand exhibits good flowability, good image accuracy, high dimensional accuracy, high edge sharpness and high surface quality.
- a disadvantage of the croning process is that the tool temperature for the production of the cores or the Fo ⁇ nmaschine from the core or molding sand must be extremely high, causing a high energy demand.
- the phenolic resin burns, releasing Harmful and polluting emissions (eg mono- and polycyclic aromatics).
- the disposal of the used core or molded parts after casting is an environmental problem, since they can be deposited only with high financial cost (hazardous waste landfill). Even a possible thermal regeneration is associated with extremely high costs and environmental pollution.
- a molding material with an inorganic, for example.
- Water glass-based binder The Fomignmdstoff is mixed with an aqueous solution of water glass and immediately ansch manend injected into a mold.
- ansch manend injected into a mold.
- For solidification of the core or molding sand to a molding heat can be supplied to solidify by dehydration, the core or molding sand (physical hardening).
- the core or molding sand will be gassed with CQ to chemically cure the molded article.
- a method for producing a molding for casting molds in which case a core or molding sand is used, which is produced on the basis of quartz-free sand and an inorganic binder produced by water glass.
- a mixture of a water glass binder and a molding material is mixed and this is filled directly into a mold.
- Kemformlingen for foundry technology in which case filled a mixture of an inorganic refractory molding sand and an inorganic binder based on water glass in a Kemkasten and then withdrawn to solidify the core, the water or CO 2 is fumigated.
- a waterglass-based binder system which can be used in these processes is described in DE 199 51 622. This consists of an aqueous alkali silicate solution, wherein it additionally contains a hygroscopic base. The solids content of the alkali metal silicate solutions used is described as 20 to 40%.
- EP 0 917 499 discloses a process for producing core moldings for the foundry industry, in which a mixture of an inorganic refractory molding sand and a waterglass-based inorganic binder is used under certain conditions to form the core.
- EP 0 917 499 describes a process for the production of a circulating core sand, consisting of residues of old skins of core moldings. This means that this sand has passed through the casting process at least once, i. the cores were poured off, gutted and then singled out.
- an aqueous alkali metal silicate solution is mixed with a molding material and then this moist mixture is introduced directly into a molding tool.
- a disadvantage of this method is that after mixing the molding base material and the aqueous alkali silicate solution obtained is not storage-stable or is only partially storable, as in a closed Fo ⁇ nstof ⁇ alterner. This means that the mixture must be prepared immediately before the production of the molding and then used immediately.
- the core or molding sand of FormgrundstofF and an aqueous alkali metal silicate solution is limited trickle and therefore additional measures must be taken to ensure that the core or molding sand fills all the cavities of a mold, such as by applying negative pressure or Shaking the mold.
- the core circulation sand described in EP 0 917 499 is also unsuitable for obtaining a storage stability combined with good properties in the production of a core molding, since the circulation core sand can not be used directly for the production of core moldings.
- the present invention is therefore based on the object to provide a core or molding sand available, which overcomes the disadvantages of the conventional Kem- or molding sand and in particular to provide a core or molding sand available, which is storage stable and immediately, without further Steps can be used to manufacture a molded article without health or environmental risks associated with its use. Furthermore, the core or molding sand should allow easy and safe filling into a mold.
- a core or molding sand for cores and casting molds for casting molten metal which comprises a molding material, which with
- Water glass is coated or mixed and has a water content in the range of> about 0.25
- the water content is understood to include the upper and lower values of the region (s).
- a method for producing a core or molding sand according to the invention is provided and a method for producing a core and a
- the waterglass used according to the invention preferably has a dynamic viscosity of> 10 2 Pa * s, more preferably> 10 2 " 5 Pa * s, in particular of> 10 3 Pa * s.
- Waterglass with a dynamic viscosity of> 10 2 Pa * s is solid This means that the core or foundry sand according to the invention is coated or mixed in particular with solid water glass.
- the core and foundry sand according to the invention has a water content in the range of> about 0.25 wt .-% to about 0.9 wt .-%, based on the total weight of the core and foundry sand, preferably from about> about 0.3 Wt .-% to about 0.9 wt .-%, in particular from> about 0.3 wt .-% to about 0.9 wt .-%, based on the total weight of Kem- and molding sand.
- the water content of the core and molding sand is less than about 0.25 wt .-%, based on the total weight of the core and molding sand, then no core and molding sand is obtained, which can be used immediately, in particular no core and molding sand which would be useful in the inventive method of making a core and mold described below. If the water content is above about 0.9 wt .-%, then no storage-stable core or molding sand is obtained. Of the Water content is determined according to the VDG leaflet "Testing of clay-bound molded materials Determination of water content" P 32, Section 4.1., April 1997.
- coated means that the individual particles of the molding material are substantially uniformly coated by a waterglass coating, but the term is not to be understood as meaning that each individual particle of the molding material is separate from one another must be coated with a water glass coating, but also includes embodiments in which particles are only partially coated or even several particles are coated together by a water glass coating.
- mixed means that the water glass is firmly mixed (homogenized) with the molding base material.
- the core or molding sand according to the invention is characterized in that it is dry and free-flowing.
- the determination of the flowability is carried out, for example, with measuring funnels or special pourability testing devices, such as from the company Karg Industrietechnik, wherein the trickle time at a given mass or volume is measured as a comparison indicator and given in seconds.
- the core and foundry sand according to the invention preferably has a flowability of ⁇ about 4 s, more preferably ⁇ about 3.5 s, measured at a sample amount of 35Og in a measuring funnel with an inner diameter at the upper, wide edge of 90 mm and a funnel height of a total of 95 mm and a length of 32 mm and an inner diameter of the spout of 15 mm at room temperature of about 20 0 C.
- the waterglass coated or blended with the mold base comprises additional additives selected from the group consisting of adhesion modifiers, flow improvers, casting surface improvers, and release agents.
- the additive is preferably selected from the group consisting of caustic soda, amorphous SiO 2, graphite, silicone oil emulsion, stearates, various oils, surfactants, aluminum oxides, iron oxides, talc, boron nitrides, magnesium oxide and various metal oxides.
- the adhesion promoter is preferably selected from sodium hydroxide solution, hygroscopic bases and / or surfactants.
- the flow improvers used are preferably additives selected from the group consisting of amorphous SiO 2, graphite, silicone oil, silicone oil emulsion, stearates, various oils and surfactants.
- As the improving agent for the casting surface there are preferably additives selected from the group consisting of amorphous SiO 2 , graphite, aluminum oxides, iron oxides. Talc, boronitrides, magnesium oxide and various metal oxides used.
- the release agents used are preferably additives selected from the group consisting of silicone oil, silicone oil emulsion, aluminum oxides, iron oxides, talc, graphite and boron nitride.
- the drying agent and / or flow aid used is preferably dry, amorphous SiO 2.
- the molding material used is preferably a refractory mineral or synthetic sand, in particular quartz sand, zircon sand, chrome ore sand, almost spherical sand, olivine sand or mixtures thereof.
- the molding material preferably has a mean particle size of about 0.08 mm to 0.6 mm, in particular from 0.08 mm to 0.5 mm.
- further adjuvants can be added to the coated core or foundry sand according to the invention, such as flow aids, drying agents, flow improvers, improvers for the casting surface and / or release agents.
- the other auxiliaries are preferably selected from the group consisting of dry amorphous SiO 2 , aluminum oxides, iron oxides, talc, graphite and boron nitrides. The properties of the other adjuvants are as described above with respect to their addition to the waterglass coating.
- a total amount of additives (without water glass) of up to 4 wt .-%, in particular up to 3 wt .-%, based on the total weight of the core or foundry sand added.
- the molding sand according to the invention preferably does not comprise any organic additives or additives.
- the core or foundry sand according to the invention is preferably produced in a process comprising the following steps: a) a molding base material according to the invention is provided, b) an aqueous solution of waterglass and / or dry waterglass powder is added and c) the core or molding sand is formed mixed, dried and mixed.
- a mixer is preferably initially filled with the molding base material, which ensures the homogenization of the core or molding sand with the binder components and optionally the additives.
- preference is given to using wing mixers, oscillating mixers, intensive mixers, vortex mixers or vertical rolling gears.
- an aqueous solution of water glass and / or dry / solid water glass and optionally further additives may then be added. If an aqueous solution is used, it preferably has a dynamic viscosity of up to 10 2 Pa * s.
- aqueous solution encompasses both viscous, viscous and pasty waterglasses.
- a dry / solid waterglass When a dry / solid waterglass is added, it preferably has a dynamic viscosity of more than 10 2 Pa * s.
- the waterglass used is an alkali silicate solution of the general composition xSiCh "yM ⁇ O * nHjO, where M is selected from Li * , K * or Na ⁇ and x: y is preferably about 1: 1 to 4: 1, especially about 2: 1 to 3.5: I is from 5 (where the ratio x: y as a module of the water glass, ie, the ratio SIOO: M 2 O is ).
- the index n determines the amount of HiO in the solution.
- an aqueous solution of alkali silicate having a solid content of not more than about 60% by weight based on the entire solution is preferably used.
- a primer may preferably be added in an amount of up to about 0.5% by weight, preferably about 0.1 to about 0.2% by weight, based on the weight of the masterbatch.
- the adhesion promoter is preferably an aqueous solution of sodium hydroxide solution, in particular about 10 to about 50%, particularly preferably a 30% strength sodium hydroxide solution.
- the adhesion promoter is added to the molding material in step b) before the addition of the aqueous solution of water glass.
- the aqueous solution of water glass is then added to the addition of the adhesion promoter.
- a layer structure comprising at least two layers is achieved, in which the first, inner layer is formed by the adhesion promoter and the second layer by the water glass becomes. It is also possible that further layers are applied. These may be applied below the adhesion promoter layer, between the adhesion promoter layer and the water glass layer and / or on the water glass layer. In the course of manufacture, such a layer structure can be controlled by the order of addition of the layer-forming materials during the mixing process.
- the aforementioned additives and / or auxiliaries are used.
- the formation of a separate adhesion promoter layer and a layer of water glass located thereon leads to a more stable coating of the core or molding sand with water glass, which, inter alia, relieves the mechanical stresses during the production process, in particular by the wing mixers, vibratory mixers, Intensive mixer, vortex mixer or vertical bunker can better resist.
- a flow improver or casting surface improver is preferably added in amounts up to about 3% by weight based on the weight of the masterbatch.
- Particularly preferred is first an aqueous suspension of amorphous SiO. preferably in an amount of up to about 3% by weight, in particular about 0.6 to about 1.0% by weight, based on the weight of the masterbatch, and then preferably an aqueous suspension of amorphous SiO 2 and graphite, preferably in one Amount of up to about 3 wt .-%, in particular about 0.6 to about 1.0 wt .-%, based on the weight of the mold base, added thereto.
- the aqueous suspension is preferably about 10 to about 80%, in particular about 30 to about 60% pure.
- a flow improver and / or release agent is preferably added in an amount of up to about 1% by weight, in particular up to about 0.8% by weight, based on the weight of the molding base material Silicone oil and / or a silicone oil emulsion.
- step b) is carried out by first an adhesion promoter, preferably sodium hydroxide solution, then the binder, namely the optionally aqueous solution of waterglass, then a flow improver and / or improver for the casting surface, particularly preferably an aqueous suspension of amorphous SiCh and then adding amorphous StO 2 and graphite followed by the addition of a flow improver and / or release agent, particularly silicone oil or a silicone oil emulsion.
- an adhesion promoter preferably sodium hydroxide solution
- the binder namely the optionally aqueous solution of waterglass
- a flow improver and / or improver for the casting surface particularly preferably an aqueous suspension of amorphous SiCh and then adding amorphous StO 2 and graphite followed by the addition of a flow improver and / or release agent, particularly silicone oil or a silicone oil emulsion.
- dry / solid water glass or a mixture of aqueous and dry / solid water glass can already be added in step b), whereby it is not necessary in the case of the addition of dry / solid water glass to dry the mixture.
- the mixing of the production of the most uniform mixture is used.
- step c) the core or molding sand is then dried.
- the friction energy introduced into the mixture by the mixer is preferably used.
- a wing mixer which has a rotational speed of 160 rpm and it is preferably mixed for a long time.
- the water content of the waterglass with which the masterbatch is coated or mixed by mixing and dehydration is adjusted to a level in the range of from about 0.25% to about 0.9% by weight.
- a core or molding sand is obtained, which is provided with a solid coating of water glass.
- the molding material which is obtained by the process according to the invention is thus coated with water glass, at the same time a free-flowing core or molding sand is obtained, which is also storage stable.
- the drying can be carried out with any device as long as it is ensured that the water content of the water glass coating of the molding base material is maintained.
- An external heating, hot air, radiant heating, vacuum, or negative pressure or a heating jacket can preferably also be used for this purpose.
- each adjuvant will contain an amount of up to about 2% by weight, based on the weight of the masterbatch.
- At least one further additive selected from the group consisting of adhesion promoters, flow improvers, casting surface improvers and release agents may be added to the masterbatch before step c).
- at least one further adjuvant selected from the group consisting of flow aids, drying agents, flow improvers, casting surface improvers and release agents may preferably be added to the core or molding sand after step c).
- the core or molding sand thus obtained can then be screened for the deposition of agglomerates.
- the resulting core or foundry sand according to the invention can then be used directly to produce a core or a molded part.
- the core or foundry sand according to the invention can also be stored loose or packed and can be stored almost indefinitely because of its consistency.
- the core or foundry sand according to the invention can be prepared separately from a method for producing the molded part and stored, packaged or transported, which means a considerable work and time savings for the foundries and the manufacturer of core and moldings.
- the core and foundry sand according to the invention preferably does not comprise any organic additives or additives, so that no environmentally harmful substances are formed when it is used.
- the core or foundry sand according to the invention is then advantageously used in a method for producing a casting mold or a core or core molding for casting molten metal.
- a core or molding sand according to the invention is provided for the core production a) and b) a core tool or tool is filled with the core or molding sand according to the invention.
- the filling can eg be carried out by trickling, blowing and / or shooting with a carrier medium such as compressed air, hot air or steam.
- the core or molding sand is then compressed in the core tool.
- the core or molding sand in the tool is brought into contact with at least one hardening agent, preferably water, water-containing liquids and / or chemical hardening agents such as CO 2 .
- at least one hardening agent preferably water, water-containing liquids and / or chemical hardening agents such as CO 2 .
- steam is used for this purpose.
- the water vapor is preferably introduced into the tool.
- the water vapor can be introduced into the molding material, for example, by means of a gassing plate via the injections and / or through the steam connection to the tool vents.
- a water vapor-air mixture is used, which preferably contains an amount of water to about 6 wt .-% based on the mold base, in particular 3-4 wt .-%.
- the pressure is preferably up to about 10 bar, in particular about 0.5 to about 1.5 bar.
- the core or molding sand according to the invention is thus brought into a core tool or molding tool, preferably by firing or pouring, and then preferably compacted.
- the compaction is preferably carried out by shaking and pressing.
- the core or molding sand in the tool is preferably brought into contact with an aqueous solution or water.
- step b the contacting with water, in particular water vapor, can preferably be carried out during step b), for example, in a temporal relationship with the filling, in particular the shooting of the core or molding sand, or after its filling in a separate step c).
- step b the waterglass coating of the core or foundry sand according to the invention is dissolved and softened.
- softening the waterglass coating binder bridges form between the particles of the core or foundry sand.
- the core is solidified, in particular by removing the water or by chemical means. This can preferably be achieved in that in
- a heat transfer medium such as in the form of hot air or a water vapor-air mixture, which is passed through the core.
- the water can be removed by a
- Vacuum is applied to the tool. By removing the water, the water glass solidifies and it is a stable, solid molding obtained. It is thus a substantially physical process without the need for additional chemical reactions.
- the curing agent CO be used and the solidification is thus carried out essentially chemically.
- both methods for solidification can be carried out either simultaneously or also successively. After hardening or solidifying (drying) the molding, the tool can be opened and the finished molding, for example. A core removed.
- the core within the core tool can only be preconsolidated, for example pre-dried, until the core has sufficient strength to be removed from the core tool. Thereafter, the preconsolidated core may be further solidified outside the core tool, in particular, the predried core may be finish dried in, for example, a microwave, an oven, or a drying chamber.
- the tool for forming the core or molding during all steps b) to c) to a temperature of from room temperature or about 20 0 C to about 200 0 C, more preferably about 70 0 C to about 160 0 C, heated in particular about 70 to about 120 0 C.
- the water can then be withdrawn, for example, by the tool being heated to said temperatures.
- the water may additionally or alternatively be withdrawn using hot air and / or warm carrier gas and / or by applying a negative pressure / vacuum.
- the duration of contact with water may be carried out, for example, for about 5 minutes to about 3 hours.
- the core or mold of the present invention preferably has a flexural strength of at least about 300 N / cm 2 , more preferably at least about 400 N / cm 2, and most preferably at least about 450 N / cm 2 .
- the flexural strength of the core is tested in accordance with the VDG leaflet P 72 "Binder Testing, Testing of Cold-curing Resin-Bonded Wet Forming Materials with Addition of Hardening" dated October 1999.
- Such a manufactured core according to the invention can then be used to produce a casting mold for casting molten metal.
- Kemwerkmaschine can be introduced.
- the process of the invention can be carried out by purely physical steps for solidification of the molded part, wherein no environmentally harmful substances are formed become. This is advantageous because when pouring the liquid metal no elaborate extraction systems must be kept in the foundry and the employees are exposed to no hazardous gases such as phenolic compounds. The recycling and disposal of the used inorganic core or foundry sand are easily possible.
- significantly lower temperatures can be used for solidification, which leads to considerable energy savings.
- it has been found to be advantageous that when using the inorganically bonded cores in chill casting condensation products in the mold are significantly reduced. This results in a lower cleaning costs of the mold after casting and thus a higher mold availability, whereby an increase in productivity can be achieved.
- molded parts can be produced, which have a good imaging accuracy and high edge sharpness.
- the invention relates to a core tool or molding tool for producing a core molding or a casting mold.
- the core tool is provided according to conventional core tools suitable for making a casting mold, wherein at least one port suitable for introducing a curing agent such as water vapor or a chemical curing agent is provided.
- a curing agent such as water vapor or a chemical curing agent
- further openings may be provided in the core tool from which the curing agent, such as the water vapor or chemical curing agent, may again escape.
- the core tool comprises a suitable mold for producing the desired Keraformlings or casting mold and at least one connection for introducing or shooting the core and molding sand, and at least one connection for the introduction of a curing agent, such as water vapor or a chemical curing agent.
- the terminals may also be provided together in one terminal, i. a connector which is suitable both for injecting the core and molding sand and the curing agent, such as water and / or the chemical curing agent.
- the connection may also be a gassing plate, at the same time the injections and / or a separate steam connection to the tool vents.
- the core tool is preferably designed in two parts in order to simply remove the core filler or the casting mold after production.
- Binder 3.0% by weight of water glass ⁇ modulus 2.5; 48% solids
- the required heat energy was completely introduced by the resulting friction energy.
- the mixing time could be through the use of another
- the agglomerates were separated using a sieve with a mesh size of
- the core or foundry sand produced according to Example 1 has the same good flowability as a Croning produced and is superior to the other conventional Kemsanden.
- Mold temperature 8O 0 C
- Application of molding sand pouring
- Amount of water in steam-air mixture 13mL Duration: 30s
- the determination of the flowability was carried out at a sample size of 350 g in a measuring funnel with an inner diameter at its upper, wide edge of 90 mm and funnel height of 95 mm in total and 32 mm in length and 15 mm in inner diameter of the outflow tube at room temperature of about 20 0 C measured.
- the water glass coated FormstofT after the manufacturing process still has a water content or moisture content (based on the molding material weight) of 0.38%.
- the circulating core sand (thermally and mechanically loaded) only has a moisture content of 0.18%.
- test bars were prepared from both foam mixtures and the flexural strength was measured.
- Begasungsdauer water vapor: 60s drying by means of negative pressure
- the waterglass-coated molding material according to the invention had an average bending strength of 481 N / cm 2 , while the circulating core sand was not bindable and it could not be made cores.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09778098.5A EP2323783B1 (de) | 2008-09-05 | 2009-08-25 | Mit wasserglas beschichteter und/oder vermischter kern- oder formsand mit einem wassergehalt im bereich von > etwa 0,25 gew.-% bis etwa 0,9 gew.-% |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08015735A EP2163328A1 (de) | 2008-09-05 | 2008-09-05 | Mit Wasserglas beschichteter und/oder vermischter Kern- oder Formsand mit einem Wassergehalt im Bereich von >= etwa 0,25 Gew.-% bis etwa 0,9 Gew.-% |
EP09778098.5A EP2323783B1 (de) | 2008-09-05 | 2009-08-25 | Mit wasserglas beschichteter und/oder vermischter kern- oder formsand mit einem wassergehalt im bereich von > etwa 0,25 gew.-% bis etwa 0,9 gew.-% |
PCT/EP2009/006153 WO2010025861A1 (de) | 2008-09-05 | 2009-08-25 | Mit wasserglas beschichteter und/oder vermischter kern- oder formsand mit einem wassergehalt im bereich von≥etwa 0,25 gew.-% bis etwa 0,9 gew.-% |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2323783A1 true EP2323783A1 (de) | 2011-05-25 |
EP2323783B1 EP2323783B1 (de) | 2016-03-23 |
Family
ID=39869511
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08015735A Withdrawn EP2163328A1 (de) | 2008-09-05 | 2008-09-05 | Mit Wasserglas beschichteter und/oder vermischter Kern- oder Formsand mit einem Wassergehalt im Bereich von >= etwa 0,25 Gew.-% bis etwa 0,9 Gew.-% |
EP09778098.5A Active EP2323783B1 (de) | 2008-09-05 | 2009-08-25 | Mit wasserglas beschichteter und/oder vermischter kern- oder formsand mit einem wassergehalt im bereich von > etwa 0,25 gew.-% bis etwa 0,9 gew.-% |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08015735A Withdrawn EP2163328A1 (de) | 2008-09-05 | 2008-09-05 | Mit Wasserglas beschichteter und/oder vermischter Kern- oder Formsand mit einem Wassergehalt im Bereich von >= etwa 0,25 Gew.-% bis etwa 0,9 Gew.-% |
Country Status (7)
Country | Link |
---|---|
US (1) | US8627877B2 (de) |
EP (2) | EP2163328A1 (de) |
JP (1) | JP5418950B2 (de) |
KR (1) | KR20110053259A (de) |
BR (1) | BRPI0918525A2 (de) |
CA (1) | CA2737334C (de) |
WO (1) | WO2010025861A1 (de) |
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JP5933169B2 (ja) * | 2010-10-01 | 2016-06-08 | リグナイト株式会社 | 粘結剤コーテッド耐火物、鋳型、鋳型の製造方法 |
DE102011105688A1 (de) | 2011-06-22 | 2012-12-27 | Hüttenes-Albertus Chemische Werke GmbH | Verfahren zum schichtweisen Aufbau von Modellen |
DE102012103705A1 (de) * | 2012-04-26 | 2013-10-31 | Ask Chemicals Gmbh | Verfahren zur Herstellung von Formen und Kernen für den Metallguss sowie nach diesem Verfahren hergestellte Formen und Kerne |
DE102012104934A1 (de) * | 2012-06-06 | 2013-12-12 | Ask Chemicals Gmbh | Forstoffmischungen enthaltend Bariumsulfat |
DE102012020509A1 (de) * | 2012-10-19 | 2014-06-12 | Ask Chemicals Gmbh | Formstoffmischungen auf der Basis anorganischer Bindemittel und Verfahren zur Herstellung von Formen und Kerne für den Metallguss |
JP5986498B2 (ja) * | 2012-12-19 | 2016-09-06 | 旭有機材株式会社 | コーテッドサンドの製造方法及び鋳型の製造方法 |
JP6193884B2 (ja) * | 2012-12-19 | 2017-09-06 | 旭有機材株式会社 | コーテッドサンド及びその製造方法並びに鋳型の製造方法 |
DE102012113073A1 (de) * | 2012-12-22 | 2014-07-10 | Ask Chemicals Gmbh | Formstoffmischungen enthaltend Aluminiumoxide und/oder Aluminium/Silizium-Mischoxide in partikulärer Form |
DE102013106276A1 (de) * | 2013-06-17 | 2014-12-18 | Ask Chemicals Gmbh | Lithiumhaltige Formstoffmischungen auf der Basis eines anorganischen Bindemittels zur Herstellung von Formen und Kernen für den Metallguss |
DE102014004914A1 (de) * | 2013-08-26 | 2015-02-26 | Gebrüder Dorfner GmbH & Co. Kaolin- und Kristallquarzsand-Werke KG | Gießform oder einen Gießformkern aus beschichtetem Formsand für Metallguss |
EP3040136B1 (de) * | 2013-08-30 | 2021-04-07 | Asahi Yukizai Corporation | Formverfahren für laminierte form |
JP6141539B2 (ja) | 2013-10-19 | 2017-06-07 | ピーク ドイチュラント ゲゼルシャフト ミット ベシュレンクテル ハフツングPeak Deutschland GmbH | 鋳造品製造のためのロストコア又は成形品を製造する方法 |
DE102015111418A1 (de) * | 2015-07-14 | 2017-01-19 | Nemak, S.A.B. De C.V. | Verfahren zum Herstellen eines Gießkerns und Gießkern |
DE102016004183A1 (de) | 2016-04-11 | 2017-10-12 | ancorro GmbH | Bau- und Formmaterial aus Sand sowie deren verfahrenstechnische Umsetzung |
WO2018097179A1 (ja) * | 2016-11-22 | 2018-05-31 | 旭有機材株式会社 | コーテッドサンド及びその製造方法並びにこれを用いた鋳型の製造方法 |
DE102016123050A1 (de) * | 2016-11-29 | 2018-05-30 | HÜTTENES-ALBERTUS Chemische Werke Gesellschaft mit beschränkter Haftung | Verfahren zum Herstellen von Kernen oder Formen für den Metallguss |
JP2020520808A (ja) | 2017-05-23 | 2020-07-16 | エクスワン ゲーエムベーハー | 粒状材料およびバインダからなる成形部品の熱間強度を高めるための後処理プロセス、3d印刷装置、ならびに成形部品 |
US20210023609A1 (en) * | 2018-03-30 | 2021-01-28 | Imerys Usa, Inc. | Compositions comprising oxidized materials for sand casting and methods of preparation and use thereof |
JP2021074725A (ja) * | 2019-11-06 | 2021-05-20 | トヨタ自動車株式会社 | 鋳型用接着剤の製造方法、鋳型の製造方法、及び鋳型 |
JP7577296B2 (ja) | 2020-06-09 | 2024-11-05 | 富士化学株式会社 | 鋳物用砂型の製造方法 |
US11724306B1 (en) | 2020-06-26 | 2023-08-15 | Triad National Security, Llc | Coating composition embodiments for use in investment casting methods |
DE102021002770A1 (de) | 2021-05-28 | 2022-12-01 | Voxeljet Ag | 3d-druckverfahren und damit hergestelltes formteil unter verwendung von wasserglasbinder und ester |
DE102023204391A1 (de) | 2023-05-11 | 2024-11-14 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein | Verfahren und System zur Herstellung eines Gießwerkzeugs oder eines Gießwerkzeugteils |
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US6371194B1 (en) * | 1996-08-09 | 2002-04-16 | Vaw Aluminium Ag | Method for producing core preforms and recycling core sand for a foundry |
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US7073557B2 (en) * | 2004-02-18 | 2006-07-11 | Hormel Foods, Llc | Method of drying a sand mold using a vacuum |
-
2008
- 2008-09-05 EP EP08015735A patent/EP2163328A1/de not_active Withdrawn
-
2009
- 2009-08-25 US US13/062,619 patent/US8627877B2/en active Active
- 2009-08-25 JP JP2011525445A patent/JP5418950B2/ja active Active
- 2009-08-25 CA CA2737334A patent/CA2737334C/en not_active Expired - Fee Related
- 2009-08-25 BR BRPI0918525A patent/BRPI0918525A2/pt not_active IP Right Cessation
- 2009-08-25 EP EP09778098.5A patent/EP2323783B1/de active Active
- 2009-08-25 WO PCT/EP2009/006153 patent/WO2010025861A1/de active Application Filing
- 2009-08-25 KR KR1020117007468A patent/KR20110053259A/ko not_active Application Discontinuation
Non-Patent Citations (1)
Title |
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See references of WO2010025861A1 * |
Also Published As
Publication number | Publication date |
---|---|
JP2012501850A (ja) | 2012-01-26 |
US8627877B2 (en) | 2014-01-14 |
BRPI0918525A2 (pt) | 2015-12-01 |
KR20110053259A (ko) | 2011-05-19 |
EP2323783B1 (de) | 2016-03-23 |
CA2737334A1 (en) | 2010-03-11 |
EP2163328A1 (de) | 2010-03-17 |
WO2010025861A1 (de) | 2010-03-11 |
US20110226436A1 (en) | 2011-09-22 |
CA2737334C (en) | 2013-11-05 |
WO2010025861A9 (de) | 2011-04-21 |
JP5418950B2 (ja) | 2014-02-19 |
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