EP3015188A1 - Moulding sand and a method of curing of moulding sand - Google Patents

Moulding sand and a method of curing of moulding sand Download PDF

Info

Publication number
EP3015188A1
EP3015188A1 EP14196636.6A EP14196636A EP3015188A1 EP 3015188 A1 EP3015188 A1 EP 3015188A1 EP 14196636 A EP14196636 A EP 14196636A EP 3015188 A1 EP3015188 A1 EP 3015188A1
Authority
EP
European Patent Office
Prior art keywords
sand
starch
moulding
cms
binder
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
Application number
EP14196636.6A
Other languages
German (de)
French (fr)
Other versions
EP3015188B1 (en
Inventor
Beata Grabowska
Karolina Kaczmarska
Dariusz Drozynski
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.)
Akademia Gomiczo Hutnicza
Original Assignee
Akademia Gomiczo Hutnicza
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 Akademia Gomiczo Hutnicza filed Critical Akademia Gomiczo Hutnicza
Publication of EP3015188A1 publication Critical patent/EP3015188A1/en
Application granted granted Critical
Publication of EP3015188B1 publication Critical patent/EP3015188B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions 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
    • B22C1/20Compositions 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 organic agents
    • B22C1/26Compositions 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 organic agents of carbohydrates; of distillation residues therefrom
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions 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
    • B22C1/18Compositions 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
    • B22C1/186Compositions 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

Definitions

  • the present invention relates to moulding sand comprising a modified biopolymer and a method of curing thereof.
  • Moulding sands are used in the foundry industry for production of moulds and cores, which are then used to produce castings.
  • a typical process of producing a casting comprises filling a mould (prepared from a moulding sand) with a liquid material (such as metal alloy, gypsum, wax or plastic) in order to obtain a product having desired structure and properties. After the casting is solidified, the mould is subject to the process of striking, wherein the material of the mould is separated from the casting.
  • a liquid material such as metal alloy, gypsum, wax or plastic
  • the moulding sand is typically composed of a matrix, usually in the form of an inorganic, loose material, such as silica sand, and a binder for "connecting" the grains of the matrix; green sands additionally comprise water.
  • the main requirements for the moulding sands are the ability to be moulded while maintaining appropriate cohesion, as well as the strength of the bonds between sand grains - i.e. lack of tendency of the mould to be friable, both while waiting for filling, and during thermal and erosive impact on the mould of liquid material introduced into the mould.
  • moulds and cores made of moulding sand are highly influenced by the type of the binder applied.
  • One typical binder used for moulding sands is bentonite.
  • binders in the form of hydrocarbon resins wherein bonding process of the binder is carried out by a chemical reaction.
  • mixtures of synthetic polymers and biopolymers can be used as binders as well.
  • various types of additives can be introduced into moulding sands at the stage of their preparation, such as pulverised coal or sulphite lye, which are aimed at reducing mould friability and at reducing the tendency of casting defects to be formed, such as streaks, scars or dusting.
  • additives for moulding sands can be replaced by additives of natural origin, such as starch, cellulose or modifications thereof, including dextrins, carboxymethyl starch or carboxymethyl cellulose.
  • native starch can be used as an auxiliary substance which improves hardness and durability of moulding sands with bentonite, and reduces friability.
  • Native starch can also be introduced in the form of boiled starch, which helps to prevent casting defects associated with expansion.
  • a side effect of the presence of starch in the composition of the moulding sand is, however, deterioration in liquidity and in resistance of the sand to erosion and to penetration of metal into the mould.
  • Native starch is composed of glucose mers linked by ⁇ -1,4-glycosidic bonds in amylose, and by ⁇ -1,4- and ⁇ -1,6-glycosidic bonds in amylopectin.
  • Amylose forms viscous solutions at the temperature of 90°C
  • amylopectin forms hydrogel at the temperature of 70°C.
  • a disadvantage of native starch is its insolubility in cold water. Native starch begins to partially dissolve and swell at the temperature of about 70°C. In order to improve solubility of native starch in water, it is typically modified by introducing polar groups, such as hydroxyl groups.
  • the Polish Standard PN-87/A-74820 defines a modified starch as a natural starch in which one or more of its initial physical or chemical properties are changed by an appropriate treatment. Modification of starch aims at improving functional properties of starch or at giving it new characteristics.
  • Starch properties can be changed within a wide range by interacting with chemical agents, physical agents or enzymatically.
  • Products of chemical modification of starch by esterification, etherification and oxidation are widely used in the industry, including products with modified molar mass, gelatinisation temperature, solubility, viscosity, water binding capacity, temperature stability and resistance to acids and enzymes.
  • Products of starch modification such as, for example, etherified starch, i.e. comprising hydroxyethyl, hydroxypropyl or carboxymethyl groups, for example, carboxymethyl starch, can be used as binder components of moulding sands in the form of multicomponent mixtures.
  • Modified biopolymers including modified products of starch and cellulose, introduced into binders due to their natural origin (as renewable raw materials), relatively low price and biodegradability, do not have a negative impact on the natural environment.
  • WMSB water-soluble modified starch binder
  • the sand after drying (self-curing under ambient conditions) has a tensile strength at the level of 0.7-2.5 MPa, depending on the amount of WMSB in the sand.
  • the sand has a tendency to absorb moisture from the environment and is a gas generant (14.2 ml/g).
  • CMS carboxymethyl starch
  • sand consists of bentonite 0.5%, pulverised graphite 0.3%, phosphate 0.01%, water 12-15% and synthetic residues of fatty acids 1.0%. Curing of the sand is carried out by heating the mould for 1 h in the temperature of 160-180°C.
  • the sand is characterised by tensile strength after curing of 1.5-2.2 MPa, gas generation capacity at the level of 14-16 ml/g and coefficient of moisture absorption of 43-50%.
  • a publication " Synthesis and Application of Modified Starch as a Shell-Core Main Adhesive in a Foundry” (Xia Zhou, Jinzong Yang, Feng Qian,Guohui Qu, Journal of Applied Polymer Science, 116/5 (2010), pp. 2893-2900 , DOI 10.1002/app.31781) describes a method for obtaining sand for the preparation of shell cores with the participation of corn-based binder CMS having DS of 0.25-0.78.
  • the sand consists of matrix, CMS, bentonite, graphite powder, phosphates, surfactants and water in the ratio of 100:4.0:0.5:0.3:0.01:0.03:(14-20).
  • the shell cores are prepared in a core box having the temperature of 100-200°C.
  • 77- 84 describe a technology for preparing core sands of 4-12% of tapioca starch, 6-12% of water and 5% of locally occurring clay. Curing of the sand is carried out at the temperature of 180°C for 2 hours.
  • the maximum compressive strength of the sand (10% of water, 10% of starch) in wet state is 290 N/mm 2 , and that for the dried sand is, respectively, 4122 N/mm 2 .
  • compositions of moulding sands which contain biopolymers in the form of products of chemical modification of starch and cellulose.
  • a Japanese patent application JPS5731439 describes a binder for moulding sands which are obtained by esterification by adding, to the starch, chloroacetic acid and NaOH solution, and then cold water.
  • this publication does not relate to moulding sands as such and methods for their preparation and curing.
  • a Polish patent application PL285979 describes a moulding sand consisting of a matrix in the form of silica sand, carbon additive in the amount of 0-6% by weight, starch and cellulose formulations in the amount of 0.5-3.0% by weight, basaltic loam acting as a binder in the amount of 5-20% by weight and water.
  • a Polish patent application PL93595 describes an additive for moulding sands, based on silica sand, bentonite and water, reducing the tendency of the sand to friability.
  • the additive consists of formamyle in the amount of 40% by weight, flocculant in the amount of 30% by weight, glycol in the amount of 5% by weight and wood flour or harl flour in the amount of 25% by weight.
  • a Chineese patent application CN101898226 describes a use of carboxymethyl starch as an additive to the binder in the form of a multicomponent mixture for binding moulding sands.
  • the moulding sand consists of sand, modified starch, malt sugar, glycerine, sodium hydroxide, pulverised coal, iron oxide, starch, carboxymethyl cellulose and water. These components are of natural origin, which ensures lack of negative impact of the sand on the environment and its nontoxicity.
  • a Dutch patent application NL6913413 describes a moulding sand consisting of bentonite, water-soluble grafted polymer of acrylic acid on a base of carboxymethyl cellulose.
  • a Chinese patent application CN103521696 describes a composition of moulding sand, consisting of china clay, pulverised coal, aluminum powder, carboxymethyl cellulose, sodium hexametaphosphate, stearic acid, chlorinated paraffin, borax, boron oxide, boric acid and water.
  • the moulding sand is characterised by good gas permeability and cohesiveness.
  • a Polish patent application PL396105 describes a composition of moulding sand with a biodegradable polymeric binder, consisting of 100 parts by weight of refractory matrix and of 1-5 parts by weight of organic binder.
  • the organic binder applied consists of a mixture of aqueous solutions of poly(acrylic acid) or poly(sodium acrylate) in the amount of 30-70% by weight and of biopolymer from the group of polysaccharides in the form of modified starch or dextrin in the amount of 30-70% by weight.
  • compositions of moulding sands with biopolymers are characterised by multicomponent nature of the binder, which is associated with the need to meet specific performance and strength parameters by the moulding sand.
  • a multicomponent nature of the binder negatively affects also prolongation of preparation of the sand and its price.
  • the object of the invention is a moulding sand comprising water, a binder and a silica sand matrix, wherein it further comprises sodium salt of carboxymethyl starch (CMS-Na) having a degree of substitution (DS) in the range of 0.2 to 0.9, in the amount of 0.2 to 2.5 parts by weight per 100 parts by weight of the matrix.
  • CMS-Na carboxymethyl starch
  • DS degree of substitution
  • CMS-Na is a binder in the amount of 1.5 to 2.5 parts by weight per 100 parts by weight of the matrix.
  • the moulding sand is a bentonite-bound sand and CMS-Na is an additive in the amount of 0.2 to 2.0 parts by weight per 100 parts by weight of matrix.
  • the moulding sand comprises a binder in the form of activated bentonite comprising montmorillonite in the amount of 70% to 90% by weight.
  • Another object of the present invention is a method of curing a moulding sand as described above by evaporating water from the sand by subjecting the moulding sand to electromagnetic waves of microwave frequency in the range of 2 GHz to 3 GHz.
  • the moulding sand according to the invention comprises a single-component binder, a matrix and a solvent or it may contain a normally used binding material, such as an activated bentonite.
  • One of the sand components is a biodegradable sodium salt of carboxymethyl starch (CMS-Na), wherein depending on the amount of CMS-Na introduced into the moulding sand, it may serve only as an additive to the sand, improving certain utility properties, or it may serve as an additive and a binder.
  • CMS-Na carboxymethyl starch
  • silica sand is used, preferably acidic
  • the solvent is constituted by water capable of solvating CMS-Na, which is generally available, does not influence the environment negatively, and has a low price.
  • CMS-Na for the moulding sand according to the invention can be obtained in any known manner, for example by etherification of starch, for example potato starch, and then by neutralization of the etherification product by means of an aqueous solution of sodium hydroxide (NaOH), preferably having the concentration of: 2-10%, and more preferably having the concentration of 5%.
  • NaOH sodium hydroxide
  • Fig. 1 shows a reaction scheme for obtaining CMS-Na from starch by etherification of native starch slurry in ethyl alcohol by means of sodium salt of monochloroacetic acid in the presence of NaOH (Williamson synthesis). Products having different properties can be obtained, depending on the conditions for conducting modification. Changes that take place in the starch molecule are determined based on the degree of substitution (DS) which defines the average number of carboxymethyl groups (-CH 2 -COOH) or sodium carboxymethyl groups (-CH 2 -COONa) attributable to a single link of starch in each glucopyranose ring. Viscosity, water solubility and durability of CMS-Na increase proportionally to the degree of substitution (DS).
  • DS degree of substitution
  • CMS-Na is introduced in a loose form into the matrix, optionally with another loose material, such as for example activated bentonite, and all the components are stirred.
  • the time of stirring may be adapted depending on the needs, for example, depending on the efficiency of the stirrer applied.
  • the stirring time is 1 to 2 minutes, and more preferably the stirring time is 1 minute.
  • a polar solvent e.g. water
  • the stirring time of the loose components with water is 1 to 2 minutes, and more preferably the stirring time of the loose components with water is 2 minutes. Addition of the solvent ensures wetting of matrix grains, which provides appropriate adhesion of the binder-matrix system.
  • CMS-Na introduced into the sand as an additive in minor amounts, i.e. in the range of 0.2 to 2, and more preferably in the amount of 0.5 parts by weight per 100 parts by weight of the matrix, results in reduction of friability of the moulding sand. Further, it appeared that CMS-Na serves as a carrier of lustrous carbon in the moulding sand, and therefore it can be used as a bio-substitute for pulverised coal and hydrocarbon resins, which allows for achieving a simple composition of the moulding sand and ensures elimination of components from the sand, which could negatively affect the natural environment.
  • CMS-Na can also serve as a binder, when introduced into the moulding sand in the amount of 1.5 to 2.5 parts by weight per 100 parts by weight of the matrix - it exhibits the ability to bind the moulding sand permanently.
  • CMS-Na carboxymethyl starch
  • CMC carboxymethyl cellulose
  • CMS carboxymethyl starch
  • the degree of substitution (DS) has an impact on the binding properties of CMS-Na, wherein the best binding properties are achieved with the degree of substitution (DS) in the range of 0.2 to 0.9, and preferably 0.6 to 0.8.
  • DS degree of substitution
  • solubility of CMS-Na in polar solvents the higher DS (i.e. the greater share of side polar groups within a polymer chain - starch), the higher the solubility of CMS-Na in polar solvents. Therefore, an increase in solubility of CMS-Na improves the binding properties of this substance.
  • the moulding sand can be cured physically - by evaporating part of the water contained in the sand.
  • the evaporation can be performed by supplying energy in a thermal way, i.e. by heating the moulding sand until it solidifies.
  • the moulding sand can be annealed through thermal drying in the temperature of 80 to 150°C, and preferably in the temperature of 100°C.
  • the sand with CMS-Na binder can be subjected to electromagnetic radiation having a microwave frequency, preferably in the range of 2 to 3 GHz, and more preferably 2.45 GHz and with the power of 600 W to 1200 W, preferably 800 W. Radiation exposure time is selected depending on the amount and/or the weight of the sand.
  • the composition of the moulding sand which contains CMS-Na as an additive various types of typically used binding materials can be used, such as for example activated bentonite having montmorillonite content of 70 to 90%.
  • the moulding sand can be composed of 100 parts by weight of mineral matrix, 5-8 parts by weight of bentonite, 0.5-2 parts by weight of CMS-Na and 1.5-4 parts by weight of water.
  • the moulding sand according to the invention is its simple composition; the sand can be composed of only three components: CMS-Na binder, mineral matrix and solvent; introduction of CMS-Na as a binder allowed obtaining the effect of better binding of the matrix, and therefore obtaining moulds and cores having better functional parameters.
  • the simple composition of the moulding sand according to the invention is also related to the multifunctionality of CMS-Na in the sand.
  • This substance can simultaneously serve in the moulding sand as a binder and as an additive, providing reduction in friability of the bentonite-bound sand and allowing elimination from the system of substances such as pulverised coal or hydrocarbon resins, which significantly simplifies the composition of the sand.
  • CMS-Na binder such as degree of substitution (DS) or viscosity
  • starch modification provides additionally the possibility of producing, depending on the needs, the moulding sand with desired properties, such as bending strength or friability.
  • CMS-Na is a biodegradable polymer, and products of CMS-Na decomposition are substances which occur naturally in the environment and are harmless.
  • the moulding sand with CMS-Na according to the invention is characterised by allowing easy striking of the products out of the mould and by a high quality of the castings produced.
  • the moulding sand according to the invention is further characterised by good recoverability.
  • CMS-Na binder can be retrieved from the sand after a technological process.
  • CMS-Na bound sand is characterised by insignificant harmfulness to the environment and workers (the used sand can be utilised in the industry).
  • CMS-Na bound sand An important advantage of the CMS-Na bound sand is the possibility of its preparation with acidic matrices.
  • CMS-Na bound sand may be an alternative for the sands used in foundry industry due to the physicochemical characteristics of its components, and technological, ecological and economic aspects.
  • the starch component of CMS-Na sand can be produced from cheap raw materials, such as for example potato starch, or from vegetable waste containing starch (e.g. potato processing waste).
  • Modification of potato starch with the moisture content of up to 14.0% was conducted in a glass reactor equipped with a mechanical stirrer, a thermocouple and capillaries supplying nitrogen to the reaction system.
  • the starch was etherified in a mixture of isopropanol (IPOH) and water in a single-step process.
  • Monochloroacetic acid (MCA) was dissolved in IPOH in the reactor, and then was introduced in aqueous solution of NaOH.
  • the molar ratio of NaOH/(S)MCA was 2.25:1.
  • After stirring for 90 min and homogenisation of the mixture a fine fraction of NaOH was introduced into the reactor.
  • the reaction was conducted for the period of about 150 - 180 min in the temperature of 50°C.
  • the product obtained was filtered off and neutralised with acetic acid, then it was washed several times with methanol solution, once with pure methanol, and then it was left on a heated surface to be dried in the air.
  • CMS-Na The above example of the synthesis of CMS-Na should only be considered as illustrative, while CMS-Na to be used in further examples can be also obtained by other known methods.
  • the moulded pieces were subjected to curing under the influence of microwave radiation with power of 800W and frequency of 2.45 GHz for 120s, an then properties of the cured sand were examined.
  • the sand with the following properties was obtained:
  • the moulded pieces were subjected to curing under the influence of microwave radiation with power of 800W and frequency of 2.45 GHz for 120s, an then properties of the cured sand were examined.
  • the sand with the following properties was obtained:

Abstract

A moulding sand comprising water, a binder and a silica sand matrix, characterised in that it further comprises sodium salt of carboxymethyl starch (CMS-Na) having a degree of substitution (DS) in the range of 0.2 to 0.9, in the amount of 0.2 to 2.5 parts by weight per 100 parts by weight of the matrix.

Description

    TECHNICAL FIELD
  • The present invention relates to moulding sand comprising a modified biopolymer and a method of curing thereof.
  • BACKGROUND
  • Moulding sands are used in the foundry industry for production of moulds and cores, which are then used to produce castings.
  • A typical process of producing a casting comprises filling a mould (prepared from a moulding sand) with a liquid material (such as metal alloy, gypsum, wax or plastic) in order to obtain a product having desired structure and properties. After the casting is solidified, the mould is subject to the process of striking, wherein the material of the mould is separated from the casting.
  • The moulding sand is typically composed of a matrix, usually in the form of an inorganic, loose material, such as silica sand, and a binder for "connecting" the grains of the matrix; green sands additionally comprise water.
  • The main requirements for the moulding sands are the ability to be moulded while maintaining appropriate cohesion, as well as the strength of the bonds between sand grains - i.e. lack of tendency of the mould to be friable, both while waiting for filling, and during thermal and erosive impact on the mould of liquid material introduced into the mould.
  • The functional properties of moulds and cores made of moulding sand are highly influenced by the type of the binder applied. One typical binder used for moulding sands is bentonite. There are also known binders in the form of hydrocarbon resins, wherein bonding process of the binder is carried out by a chemical reaction. Further, mixtures of synthetic polymers and biopolymers can be used as binders as well.
  • In order to improve the functional properties of casting moulds and cores, various types of additives can be introduced into moulding sands at the stage of their preparation, such as pulverised coal or sulphite lye, which are aimed at reducing mould friability and at reducing the tendency of casting defects to be formed, such as streaks, scars or dusting.
  • In order to reduce the negative impact on the environment, some of the synthetic additives for moulding sands can be replaced by additives of natural origin, such as starch, cellulose or modifications thereof, including dextrins, carboxymethyl starch or carboxymethyl cellulose.
  • For example, native starch can be used as an auxiliary substance which improves hardness and durability of moulding sands with bentonite, and reduces friability. Native starch can also be introduced in the form of boiled starch, which helps to prevent casting defects associated with expansion. A side effect of the presence of starch in the composition of the moulding sand is, however, deterioration in liquidity and in resistance of the sand to erosion and to penetration of metal into the mould.
  • Native starch is composed of glucose mers linked by α-1,4-glycosidic bonds in amylose, and by α-1,4- and α-1,6-glycosidic bonds in amylopectin. In terms of its chemical composition, native starch is not homogeneous and is composed of amylose (20-25%, (C6H10O5)n with n=5000) and amylopectin (75-80%, (C6H10O5)n with n=50000). Amylose forms viscous solutions at the temperature of 90°C, and amylopectin forms hydrogel at the temperature of 70°C. A disadvantage of native starch is its insolubility in cold water. Native starch begins to partially dissolve and swell at the temperature of about 70°C. In order to improve solubility of native starch in water, it is typically modified by introducing polar groups, such as hydroxyl groups.
  • The Polish Standard PN-87/A-74820 defines a modified starch as a natural starch in which one or more of its initial physical or chemical properties are changed by an appropriate treatment. Modification of starch aims at improving functional properties of starch or at giving it new characteristics.
  • Starch properties can be changed within a wide range by interacting with chemical agents, physical agents or enzymatically. Products of chemical modification of starch by esterification, etherification and oxidation are widely used in the industry, including products with modified molar mass, gelatinisation temperature, solubility, viscosity, water binding capacity, temperature stability and resistance to acids and enzymes.
  • Products of starch modification, such as, for example, etherified starch, i.e. comprising hydroxyethyl, hydroxypropyl or carboxymethyl groups, for example, carboxymethyl starch, can be used as binder components of moulding sands in the form of multicomponent mixtures.
  • Modified biopolymers, including modified products of starch and cellulose, introduced into binders due to their natural origin (as renewable raw materials), relatively low price and biodegradability, do not have a negative impact on the natural environment.
  • There are known numerous examples of using starch and its etherified derivatives in the technology of moulding sands.
  • For example, a publication "Preparation and experiments for a novel kind of foundry core binder made from modified potato starch" (Wenbin Yu, Hong He, Nanpu Cheng, Bingtai Gan, Xuelian Li, Materials and Design 30 (2009) pp.210-213), discloses water-soluble modified starch binder (WMSB) is described, which consists of 28-30% of potato starch, 1% of formaldehyde, 0.1% of phosphoric acid, 2% of polyvinyl alcohol, 1% of urea and water. The binder is introduced into the sands with bentonite (2-3%) in the amount of 4-7%. The sand after drying (self-curing under ambient conditions) has a tensile strength at the level of 0.7-2.5 MPa, depending on the amount of WMSB in the sand. The sand has a tendency to absorb moisture from the environment and is a gas generant (14.2 ml/g).
  • A publication "Study on synthesis and properties of modified starch binder for foundry" (Xia Zhou, Jinzong Yang, Guohui Qu, Journal of Materials Processing Technology 183 (2007) pp. 407-411) describes a technology for synthesising carboxymethyl starch (CMS) with a degree of substitution DS of 0.25-0.78, and for preparing sands with a starch binder based on carboxymethyl starch having DS of 0.3-0.5. The sand consists of bentonite 0.5%, pulverised graphite 0.3%, phosphate 0.01%, water 12-15% and synthetic residues of fatty acids 1.0%. Curing of the sand is carried out by heating the mould for 1 h in the temperature of 160-180°C. The sand is characterised by tensile strength after curing of 1.5-2.2 MPa, gas generation capacity at the level of 14-16 ml/g and coefficient of moisture absorption of 43-50%.
  • A publication "Synthesis and Application of Modified Starch as a Shell-Core Main Adhesive in a Foundry" (Xia Zhou, Jinzong Yang, Feng Qian,Guohui Qu, Journal of Applied Polymer Science, 116/5 (2010), pp. 2893-2900, DOI 10.1002/app.31781) describes a method for obtaining sand for the preparation of shell cores with the participation of corn-based binder CMS having DS of 0.25-0.78. The sand consists of matrix, CMS, bentonite, graphite powder, phosphates, surfactants and water in the ratio of 100:4.0:0.5:0.3:0.01:0.03:(14-20). The shell cores are prepared in a core box having the temperature of 100-200°C.
  • Publications "The high-temperature resistant mechanism of α-starch composite binder for foundry" ( Xia Zhou, Jinzong Yang, Depeng Su, Guohui Qu, Journal of Materials Processing Technology 209 (2009) pp. 5394-5398), " Hygroscopicity-resistant mechanism of an α -starch based composite binder for dry sand molds and cores" (Xia Zhou , Jiyang Zhou , Guohui QU, China foundry, (2) 2005, pp. 97-101) and "Adhesive Bonding and Self-Curing Characteristics of α-Starch Based Composite Binder for Green Sand Mould/Core" (Xia Zhou ,Jinzong Yang ,Guohui QU., J. Mater. Sci. Technol., (20/05)2004,) pp. 617-621) describe a binder consisting of α-starch, kaolin, sodium silicate, dextrin, phosphate and water in the respective proportions of: 2.5-4.0%, 1.5-3.0%, 0.55%, 0.35%, 0.04% and 2.5-3.5%. Curing is carried out by annealing at the temperature of 160-200°C for 1 h. This sand is resistant to absorption of moisture from the environment and to high temperatures, bending strength of the sand at about 1000°C is maintained at the level of about 0.4 MPa.
  • A publication "The Use of Yarn Flour (Starch) as Binder for Sand Mould Production in Nigeria", (T. Shehu and R.S. Bhatti, World Applied Sciences Journal (16/6) 2012, pp. 858-862) describes a technology for producing sands with the use of starch of yarns as an independent binder introduced into the sand in the amount of 25-30% (water content in the sand of 6-7%). The obtained maximum strength of the dried sands under ambient conditions is 309 KN/m2.
  • A publication "Synergistic effects of starch and rubber-latex as core binders for foundry sand cores production" (A. Oyetunji , S.O. Seidu , Acta Technica Corvininesis - Bulletin of Engineering; (5/4) 2012, pp. 103) describes a binder in the form of mixture of tapioca starch and latex rubber (at the ratio of 1:2). The suggested share of the binder in the sand is 2-9 % in relation to the matrix. The sand is dried under ambient conditions for 3 days. Compressive strength of the sand produced in wet and cured states is respectively 72 N and 65 N. This sand is an alternative to sands with bentonite.
  • Publications "Evaluating the Baked Compressive Strength of Produced Sand Cores Using Cassava Starch as Binder for the Casting of Aluminium Alloy T-Joint Pipe" (Opaluwa A. I and Oyetunji A., Journal of Emerging Trends in Engineering and Applied Sciences (JETEAS) (3/1), pp. 25-32) and "Littlestudy on the shear strength of foundry sand cores using clay and cassava starch as binder" (Oyetunji A., Seidu S.O. and Opaluwa A. I., DAFFODIL INTERNATIONAL UNIVERSITY JOURNAL OF SCIENCE AND TECHNOLOGY, (8/2) 2013, pp. 77- 84) describe a technology for preparing core sands of 4-12% of tapioca starch, 6-12% of water and 5% of locally occurring clay. Curing of the sand is carried out at the temperature of 180°C for 2 hours. The maximum compressive strength of the sand (10% of water, 10% of starch) in wet state is 290 N/mm2, and that for the dried sand is, respectively, 4122 N/mm2.
  • There are also known compositions of moulding sands which contain biopolymers in the form of products of chemical modification of starch and cellulose.
  • A Japanese patent application JPS5731439 describes a binder for moulding sands which are obtained by esterification by adding, to the starch, chloroacetic acid and NaOH solution, and then cold water. However, this publication does not relate to moulding sands as such and methods for their preparation and curing.
  • A Polish patent application PL285979 describes a moulding sand consisting of a matrix in the form of silica sand, carbon additive in the amount of 0-6% by weight, starch and cellulose formulations in the amount of 0.5-3.0% by weight, basaltic loam acting as a binder in the amount of 5-20% by weight and water.
  • A Polish patent application PL93595 describes an additive for moulding sands, based on silica sand, bentonite and water, reducing the tendency of the sand to friability. The additive consists of formamyle in the amount of 40% by weight, flocculant in the amount of 30% by weight, glycol in the amount of 5% by weight and wood flour or harl flour in the amount of 25% by weight.
  • A Chineese patent application CN101898226 describes a use of carboxymethyl starch as an additive to the binder in the form of a multicomponent mixture for binding moulding sands. The moulding sand consists of sand, modified starch, malt sugar, glycerine, sodium hydroxide, pulverised coal, iron oxide, starch, carboxymethyl cellulose and water. These components are of natural origin, which ensures lack of negative impact of the sand on the environment and its nontoxicity.
  • A Dutch patent application NL6913413 describes a moulding sand consisting of bentonite, water-soluble grafted polymer of acrylic acid on a base of carboxymethyl cellulose.
  • A Chinese patent application CN103521696 describes a composition of moulding sand, consisting of china clay, pulverised coal, aluminum powder, carboxymethyl cellulose, sodium hexametaphosphate, stearic acid, chlorinated paraffin, borax, boron oxide, boric acid and water. The moulding sand is characterised by good gas permeability and cohesiveness.
  • A Polish patent application PL396105 describes a composition of moulding sand with a biodegradable polymeric binder, consisting of 100 parts by weight of refractory matrix and of 1-5 parts by weight of organic binder. The organic binder applied consists of a mixture of aqueous solutions of poly(acrylic acid) or poly(sodium acrylate) in the amount of 30-70% by weight and of biopolymer from the group of polysaccharides in the form of modified starch or dextrin in the amount of 30-70% by weight.
  • It follows from the above-mentioned publications, that the known compositions of moulding sands with biopolymers are characterised by multicomponent nature of the binder, which is associated with the need to meet specific performance and strength parameters by the moulding sand. A multicomponent nature of the binder negatively affects also prolongation of preparation of the sand and its price.
  • It would, therefore, be advisable to develop a composition of moulding sand which would not contain multiple components and would contain primarily substances which are non-toxic and neutral to the environment. It would also be advisable for such a composition to exhibit good performance and durability parameters.
  • SUMMARY
  • The object of the invention is a moulding sand comprising water, a binder and a silica sand matrix, wherein it further comprises sodium salt of carboxymethyl starch (CMS-Na) having a degree of substitution (DS) in the range of 0.2 to 0.9, in the amount of 0.2 to 2.5 parts by weight per 100 parts by weight of the matrix.
  • Preferably, CMS-Na is a binder in the amount of 1.5 to 2.5 parts by weight per 100 parts by weight of the matrix.
  • Preferably, the moulding sand is a bentonite-bound sand and CMS-Na is an additive in the amount of 0.2 to 2.0 parts by weight per 100 parts by weight of matrix.
  • Preferably, the moulding sand comprises a binder in the form of activated bentonite comprising montmorillonite in the amount of 70% to 90% by weight.
  • Another object of the present invention is a method of curing a moulding sand as described above by evaporating water from the sand by subjecting the moulding sand to electromagnetic waves of microwave frequency in the range of 2 GHz to 3 GHz.
  • DETAILED DESCRIPTION
  • The moulding sand according to the invention comprises a single-component binder, a matrix and a solvent or it may contain a normally used binding material, such as an activated bentonite. One of the sand components is a biodegradable sodium salt of carboxymethyl starch (CMS-Na), wherein depending on the amount of CMS-Na introduced into the moulding sand, it may serve only as an additive to the sand, improving certain utility properties, or it may serve as an additive and a binder. As the matrix, silica sand is used, preferably acidic, and the solvent is constituted by water capable of solvating CMS-Na, which is generally available, does not influence the environment negatively, and has a low price.
  • CMS-Na for the moulding sand according to the invention can be obtained in any known manner, for example by etherification of starch, for example potato starch, and then by neutralization of the etherification product by means of an aqueous solution of sodium hydroxide (NaOH), preferably having the concentration of: 2-10%, and more preferably having the concentration of 5%.
  • Fig. 1 shows a reaction scheme for obtaining CMS-Na from starch by etherification of native starch slurry in ethyl alcohol by means of sodium salt of monochloroacetic acid in the presence of NaOH (Williamson synthesis). Products having different properties can be obtained, depending on the conditions for conducting modification. Changes that take place in the starch molecule are determined based on the degree of substitution (DS) which defines the average number of carboxymethyl groups (-CH2-COOH) or sodium carboxymethyl groups (-CH2-COONa) attributable to a single link of starch in each glucopyranose ring. Viscosity, water solubility and durability of CMS-Na increase proportionally to the degree of substitution (DS).
  • In order to produce the moulding sand according to the invention, CMS-Na is introduced in a loose form into the matrix, optionally with another loose material, such as for example activated bentonite, and all the components are stirred. The time of stirring may be adapted depending on the needs, for example, depending on the efficiency of the stirrer applied. Preferably, the stirring time is 1 to 2 minutes, and more preferably the stirring time is 1 minute. After the loose components have been mixed, a polar solvent (e.g. water) is introduced into the mixture, and the components are stirred until the mass becomes consistent. Preferably, the stirring time of the loose components with water is 1 to 2 minutes, and more preferably the stirring time of the loose components with water is 2 minutes. Addition of the solvent ensures wetting of matrix grains, which provides appropriate adhesion of the binder-matrix system.
  • Research conducted for moulding sands with CMS-Na having various compositions has shown that CMS-Na introduced into the sand as an additive in minor amounts, i.e. in the range of 0.2 to 2, and more preferably in the amount of 0.5 parts by weight per 100 parts by weight of the matrix, results in reduction of friability of the moulding sand. Further, it appeared that CMS-Na serves as a carrier of lustrous carbon in the moulding sand, and therefore it can be used as a bio-substitute for pulverised coal and hydrocarbon resins, which allows for achieving a simple composition of the moulding sand and ensures elimination of components from the sand, which could negatively affect the natural environment.
  • In turn, CMS-Na can also serve as a binder, when introduced into the moulding sand in the amount of 1.5 to 2.5 parts by weight per 100 parts by weight of the matrix - it exhibits the ability to bind the moulding sand permanently.
  • Research has shown unexpectedly that the binding properties of sodium salt of carboxymethyl starch (CMS-Na) are better than the binding properties of other known binding biopolymers, such as carboxymethyl cellulose (CMC) and carboxymethyl starch (CMS), which allows the use of CMS-Na as the main "binding agent" of the moulding sand - without the need to introduce auxiliary binding substances or to use binding mixtures having complex compositions.
  • Further research has shown that the degree of substitution (DS) has an impact on the binding properties of CMS-Na, wherein the best binding properties are achieved with the degree of substitution (DS) in the range of 0.2 to 0.9, and preferably 0.6 to 0.8. This is caused by the impact of DS on solubility of CMS-Na in polar solvents: the higher DS (i.e. the greater share of side polar groups within a polymer chain - starch), the higher the solubility of CMS-Na in polar solvents. Therefore, an increase in solubility of CMS-Na improves the binding properties of this substance.
  • It further appeared that the type of matrix applied has an impact on the increase in binding properties of CMS-Na. Research results have shown that the best binding properties of CMS-Na are achieved with acidic matrix materials, including for example silica sand.
  • For example, addition of 1.5-2.5 parts by weight of binder CMS-Na and 3-5 parts by weight of water to 100 parts by weight of silica sand, very good functional parameters of sand and very good durability parameters of moulds and cores are achieved.
  • In case CMS-Na serves as a binder, the moulding sand can be cured physically - by evaporating part of the water contained in the sand. The evaporation can be performed by supplying energy in a thermal way, i.e. by heating the moulding sand until it solidifies. For example, the moulding sand can be annealed through thermal drying in the temperature of 80 to 150°C, and preferably in the temperature of 100°C.
  • Optionally, with a view to solidification, the sand with CMS-Na binder can be subjected to electromagnetic radiation having a microwave frequency, preferably in the range of 2 to 3 GHz, and more preferably 2.45 GHz and with the power of 600 W to 1200 W, preferably 800 W. Radiation exposure time is selected depending on the amount and/or the weight of the sand.
  • For the composition of the moulding sand which contains CMS-Na as an additive, various types of typically used binding materials can be used, such as for example activated bentonite having montmorillonite content of 70 to 90%. For example, the moulding sand can be composed of 100 parts by weight of mineral matrix, 5-8 parts by weight of bentonite, 0.5-2 parts by weight of CMS-Na and 1.5-4 parts by weight of water.
  • One of the advantages of the moulding sand according to the invention is its simple composition; the sand can be composed of only three components: CMS-Na binder, mineral matrix and solvent; introduction of CMS-Na as a binder allowed obtaining the effect of better binding of the matrix, and therefore obtaining moulds and cores having better functional parameters.
  • The simple composition of the moulding sand according to the invention is also related to the multifunctionality of CMS-Na in the sand. This substance can simultaneously serve in the moulding sand as a binder and as an additive, providing reduction in friability of the bentonite-bound sand and allowing elimination from the system of substances such as pulverised coal or hydrocarbon resins, which significantly simplifies the composition of the sand.
  • The ability to control the properties of CMS-Na binder, such as degree of substitution (DS) or viscosity, already at the stage of its production (starch modification) provides additionally the possibility of producing, depending on the needs, the moulding sand with desired properties, such as bending strength or friability.
  • Further, the moulding sand according to the invention does not negatively affect the environment. CMS-Na is a biodegradable polymer, and products of CMS-Na decomposition are substances which occur naturally in the environment and are harmless.
  • The moulding sand with CMS-Na according to the invention is characterised by allowing easy striking of the products out of the mould and by a high quality of the castings produced.
  • The moulding sand according to the invention is further characterised by good recoverability. CMS-Na binder can be retrieved from the sand after a technological process.
  • The CMS-Na bound sand is characterised by insignificant harmfulness to the environment and workers (the used sand can be utilised in the industry).
  • An important advantage of the CMS-Na bound sand is the possibility of its preparation with acidic matrices.
  • The CMS-Na bound sand may be an alternative for the sands used in foundry industry due to the physicochemical characteristics of its components, and technological, ecological and economic aspects. Further, the starch component of CMS-Na sand can be produced from cheap raw materials, such as for example potato starch, or from vegetable waste containing starch (e.g. potato processing waste).
  • EXAMPLE I Synthesis of CMS-Na:
  • Modification of potato starch with the moisture content of up to 14.0% was conducted in a glass reactor equipped with a mechanical stirrer, a thermocouple and capillaries supplying nitrogen to the reaction system. The starch was etherified in a mixture of isopropanol (IPOH) and water in a single-step process. Monochloroacetic acid (MCA) was dissolved in IPOH in the reactor, and then was introduced in aqueous solution of NaOH. The molar ratio of NaOH/(S)MCA was 2.25:1. After stirring for 90 min and homogenisation of the mixture, a fine fraction of NaOH was introduced into the reactor. The reaction was conducted for the period of about 150 - 180 min in the temperature of 50°C. The product obtained was filtered off and neutralised with acetic acid, then it was washed several times with methanol solution, once with pure methanol, and then it was left on a heated surface to be dried in the air.
  • The above example of the synthesis of CMS-Na should only be considered as illustrative, while CMS-Na to be used in further examples can be also obtained by other known methods.
  • EXAMPLE II Preparation and curing of the sand with starch binder:
  • 1.5 parts by weight of non-crosslinked CMS-Na in a loose form having DS=0.87 (properties for 5% solution: pH=12 and viscosity is 4500 mPa·s) and 100 parts by weight of acidic silica sand having an average grain size in the range of 0.16-0.32 mm, were introduced into a roll mixer and the components were stirred for 1 min. Next, 3 parts by weight of water were added to the mixer and the sand was stirred for another 2 min, and then the liquidity of the sand was measured. The process of sand preparation was performed under ambient conditions - humidity of the air: 35% and the temperature of: 23°C.
  • From the moulding sand produced, two longitudinal moulded pieces, each weighing 150g, and four octal moulded pieces, each weighing 75g, were prepared.
  • The moulded pieces were subjected to curing under the influence of microwave radiation with power of 800W and frequency of 2.45 GHz for 120s, an then properties of the cured sand were examined.
    The sand with the following properties was obtained:
    • Tensile strength R m u
      Figure imgb0001
      in the cured state after storage time:
      • 1 h: 1.4(± 0.1) MPa
      • 24 h: 1.4 (± 0.1) MPa
    • Bending strength R g u
      Figure imgb0002
      in the cured state after storage time:
      • 1 h : 2.4 (± 0.1) MPa
      • 24 h : 2.0 (± 0.1) MPa
    • Sand permeability in the cured state after storage time:
      • 1 h: 218 (± 2) 10-8 m2/Pa·s
      • 24 h: 268 (± 3) 10-8 m2/Pa·s
    • Abrasion resistance of sand in the cured state after storage time:
      • 1 h: 1.92 (± 0.13) %
      • 24 h: 1.63 (± 0.11) %
    • Dietert liquidity of sand in the uncured state
    • 95 ((± 0.23) %
    EXAMPLE III Preparation and curing of the sand with starch binder:
  • 2.5 parts by weight of non-crosslinked CMS-Na in a loose form having DS=0.2 (properties for 5% solution: pH=11.3 and viscosity = 22000 mPa·s) and 100 parts by weight of acidic silica sand having an average grain size in the range of 0.16-0.32 mm, were introduced into a roll mixer and the components were stirred for 1 min. Then, 5 parts by weight of water were added to the mixer and the sand was stirred for another 2 min, and then liquidity of the sand was measured. The process of sand preparation was performed under ambient conditions - humidity of the air: 35% and the temperature of: 23°C.
  • From the moulding sand produced, two longitudinal moulded pieces, each weighing 150g, and four octal moulded pieces, each weighing 75g, were prepared.
  • The moulded pieces were subjected to curing under the influence of microwave radiation with power of 800W and frequency of 2.45 GHz for 120s, an then properties of the cured sand were examined.
    The sand with the following properties was obtained:
    • Tensile strength R m u
      Figure imgb0003
      in the cured state after storage time:
      • 1 h: 1.3 (± 0.1) MPa
      • 24 h: 1.2 (± 0.1) MPa
    • Bending strength R g u
      Figure imgb0004
      in the cured state after storage time:
      • 1 h: 2.4 (± 0.1) MPa
      • 24 h: 2.0 (± 0.1) MPa
    • Sand permeability in the cured state after storage time:
      • 1 h: 210 (± 3) 10-8 m2/Pa·s
      • 24 h: 222 (± 2) 10-8 m2/Pa·s
    • Abrasion resistance of sand in the cured state after storage time:
      • 1 h: 1.26 (± 0.15) %
      • 24 h: 1.5 (± 0.10) %
    • Dietert liquidity of sand in the uncured state
    • 89 ((± 0.2) %
    EXAMPLE IV Preparation and curing of the sand with starch binder:
  • 2.5 parts by weight of non-crosslinked CMS-Na in a loose form having DS=0.2 (properties for 5% solution: pH=11.3 and viscosity = 22000 mPa·s) and 100 parts by weight of acidic silica sand having an average grain size in the range of 0.16-0.32 mm, were introduced into a roll mixer and the compontents were stirred for 1 min. Then, 5 parts by weight of water were added to the mixer and the sand was stirred for another 2 min, and then liquidity of the sand was measured. The process of sand preparation was performed under ambient conditions - humidity of the air: 42% and the temperature of: 22°C.
  • From the moulding sand produced, two longitudinal moulded pieces, each weighing 150g, and four octal moulded pieces, each weighing 75g, were prepared. The moulded pieces were cured by thermal annealing in the temperature of 100°C for 30 min, and then their properties were examined.
    The sand with the following properties was obtained:
    • Tensile strength R m u
      Figure imgb0005
      in the cured state after storage time:
      • 1 h: 1.2 (± 0.06) MPa
      • 24 h: 1.2 (± 0.04) MPa
    • Bending strength R g u
      Figure imgb0006
      in the cured state after storage time:
      • 1 h: 2.6 (± 0.1) MPa
      • 24 h: 2.2 (± 0.1) MPa
    • Sand permeability in the cured state after storage time:
      • 1 h: 172 (± 2) 10-8 m2/Pa·s
      • 24 h: 192 (± 2) 10-8 m2/Pa·s
    • Abrasion resistance of sand in the cured state after storage time:
      • 1 h: 11.9 (± 0.2) %
      • 24 h: 14.9 (± 0.2) %
    • Dietert liquidity of sand in the uncured state
    • 91.2 (± 0.5) %
    EXAMPLE V Preparation of bentonite-bound green sand moulding with a starch additive:
  • 6 parts by weight of activated bentonite containing montmorillonite in the amount of 70-90%, 100 parts by weight of acidic silica sand having an average grain size in the range of 0.16-0.32 mm and 0.5 parts by weight of non-crosslinked CMS-Na in a loose form having DS=0.87 (property of 5% solution having pH of 10.2 and viscosity of 4500 mPa·s) were introduced into a roll mixer, the entirety was stirred for 1 min, then water was added to achieve moisture content at the level of 1.5 to 4% (optimal operating moisture content is 2.54%), and then the entirety was stirred for 2 min. The process of sand preparation was performed under ambient conditions - humidity of the air: 54% and the temperature of: 19.7°C. Then, certain parameters of the sand were measured.
    The sand with the following properties was obtained:
    • Compressive strength of green sand R c w = 0.1 MPa
      Figure imgb0007
    • Shear strength of green sand R t w = 0.03 MPa
      Figure imgb0008
    • Tensile strength of green sand R m w = 0.02 MPa
      Figure imgb0009
    • Permeability Pw= 300 x108 m2/Pa·s
    • Dietert flowability PD= 72%
    • Free flowability PS= 25%
    • Friability S = 10.3%
    • Compatibility Z = 52.0%
    • Properties for optimal operating moisture content of the sand being 2.54% determined on the basis of an indicator of moulding properties Wf = 75%.
    EXAMPLE VI Preparation of bentonite-bound green sand moulding with a starch additive:
  • 6 parts by weight of activated bentonite containing montmorillonite in the amount of 70-90%, 100 parts by weight of acidic silica sand having an average grain size in the range of 0.16-0.32 mm and 0.5 parts by weight of non-crosslinked CMS-Na in a loose form having DS=0.2 (property of 5% solution having pH of 11.4 and viscosity of 22000 mPa·s) were introduced into a roll mixer, the entirety was stirred for 1 min, then water was added to achieve moisture content at the level of 1.5 to 4% (optimal operating moisture content is 2.10%), and then the entirety was stirred for 2 min. The process of sand preparation was performed under ambient conditions - humidity of the air: 47.0% and the temperature of: 26.1°C. Then, certain parameters of the sand were measured.
    The sand with the following properties was obtained:
    • Compressive strength of green sand R c w = 0.09 MPa
      Figure imgb0010
    • Shear strength of green sand R t w = 0.02 MPa
      Figure imgb0011
    • Tensile strength of green sand R m w = 0.02 MPa
      Figure imgb0012
    • Permeability Pw= 300 x108 m2/Pa·s
    • Dietert flowability PD= 76.8 %
    • Free flowability PS= 17.0 %
    • Friability S = 13.5 %
    • Compatibility Z = 55.0 %
    • Properties for optimum operating moisture content of the sand being 2.10% determined on the basis of an indicator of moulding properties Wf = 75%.

Claims (5)

  1. A moulding sand comprising water, a binder and a silica sand matrix, characterised in that it further comprises sodium salt of carboxymethyl starch (CMS-Na) having a degree of substitution (DS) in the range of 0.2 to 0.9, in the amount of 0.2 to 2.5 parts by weight per 100 parts by weight of the matrix.
  2. The moulding sand according to claim 1, characterised in that CMS-Na is a binder in the amount of 1.5 to 2.5 parts by weight per 100 parts by weight of the matrix.
  3. The moulding sand according to claim 1, characterised in that the moulding sand is a bentonite-bound sand and CMS-Na is an additive in the amount of 0.2 to 2.0 parts by weight per 100 parts by weight of matrix.
  4. The moulding sand according to claim 3, characterised in that it comprises a binder in the form of activated bentonite comprising montmorillonite in the amount of 70% to 90% by weight.
  5. A method of curing a moulding sand according to any of claims 1-4 by evaporating water from the sand by subjecting the moulding sand to electromagnetic waves of microwave frequency in the range of 2 GHz to 3 GHz.
EP14196636.6A 2014-10-30 2014-12-05 Moulding sand and a method of curing of moulding sand Active EP3015188B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL409935A PL233870B1 (en) 2014-10-30 2014-10-30 Moulding sand and method for moulding sand curing

Publications (2)

Publication Number Publication Date
EP3015188A1 true EP3015188A1 (en) 2016-05-04
EP3015188B1 EP3015188B1 (en) 2020-03-04

Family

ID=52003683

Family Applications (1)

Application Number Title Priority Date Filing Date
EP14196636.6A Active EP3015188B1 (en) 2014-10-30 2014-12-05 Moulding sand and a method of curing of moulding sand

Country Status (2)

Country Link
EP (1) EP3015188B1 (en)
PL (1) PL233870B1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108723285A (en) * 2018-07-11 2018-11-02 佛山陵朝新材料有限公司 A kind of preparation method of high green compression strength moulding sand binder material
CN112317679A (en) * 2020-11-07 2021-02-05 郑州远东耐火材料有限公司 Novel modified resin adhesive special for sand mold of fused brick and preparation method thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2838406A (en) * 1954-10-06 1958-06-10 Mo Och Domsjoe Ab Methods of preparing sand cores and other sand mould parts for metal casting
NL6913413A (en) 1968-09-04 1970-03-06
US3645937A (en) * 1968-09-04 1972-02-29 Int Minerals & Chem Corp Foundry sand compositions containing graft copolymers of acrylic acid with water-soluble polyhydroxy polymeric compounds
PL93595B1 (en) 1974-08-30 1977-06-30
JPS5731439A (en) 1980-08-04 1982-02-19 Sintokogio Ltd Binder for molding sand
PL285979A1 (en) 1990-07-06 1992-01-13 Inst Odlewnictwa Moulding sand mix
CN101898226A (en) 2010-08-16 2010-12-01 新蔡县东邦铸造有限责任公司 Casting sand mixing auxiliary material
PL396105A1 (en) 2011-08-29 2013-03-04 Akademia Górniczo-Hutnicza im. Stanislawa Staszica Moulding or core substance bonded by biodegradable polymer binder
CN103521696A (en) 2013-10-16 2014-01-22 合肥市田源精铸有限公司 Molding sand for pressure plate casting and preparation method of molding sand

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2838406A (en) * 1954-10-06 1958-06-10 Mo Och Domsjoe Ab Methods of preparing sand cores and other sand mould parts for metal casting
NL6913413A (en) 1968-09-04 1970-03-06
US3645937A (en) * 1968-09-04 1972-02-29 Int Minerals & Chem Corp Foundry sand compositions containing graft copolymers of acrylic acid with water-soluble polyhydroxy polymeric compounds
PL93595B1 (en) 1974-08-30 1977-06-30
JPS5731439A (en) 1980-08-04 1982-02-19 Sintokogio Ltd Binder for molding sand
PL285979A1 (en) 1990-07-06 1992-01-13 Inst Odlewnictwa Moulding sand mix
CN101898226A (en) 2010-08-16 2010-12-01 新蔡县东邦铸造有限责任公司 Casting sand mixing auxiliary material
PL396105A1 (en) 2011-08-29 2013-03-04 Akademia Górniczo-Hutnicza im. Stanislawa Staszica Moulding or core substance bonded by biodegradable polymer binder
CN103521696A (en) 2013-10-16 2014-01-22 合肥市田源精铸有限公司 Molding sand for pressure plate casting and preparation method of molding sand

Non-Patent Citations (12)

* Cited by examiner, † Cited by third party
Title
A. OYETUNJI; S.O. SEIDU: "Synergistic effects of starch and rubber-latex as core binders for foundry sand cores production", ACTA TECHNICA CORVININESIS - BULLETIN OF ENGINEERING, 2012, pages 103
OPALUWA A. I; OYETUNJI A.: "Evaluating the Baked Compressive Strength of Produced Sand Cores Using Cassava Starch as Binder for the Casting of Aluminium Alloy T-Joint Pipe", JOURNAL OF EMERGING TRENDS IN ENGINEERING AND APPLIED SCIENCES (JETEAS, pages 25 - 32
OYETUNJI A.; SEIDU S.O.; OPALUWA A. I.: "Littlestudy on the shear strength of foundry sand cores using clay and cassava starch as binder", DAFFODIL INTERNATIONAL UNIVERSITY JOURNAL OF SCIENCE AND TECHNOLOGY, 2013, pages 77 - 84
T. SHEHU; R.S. BHATTI: "The Use of Yam Flour (Starch) as Binder for Sand Mould Production in Nigeria", WORLD APPLIED SCIENCES JOURNAL, 2012, pages 858 - 862
WENBIN YU; HONG HE; NANPU CHENG; BINGTAI GAN; XUELIAN LI: "Preparation and experiments for a novel kind of foundry core binder made from modified potato starch", MATERIALS AND DESIGN, vol. 30, 2009, pages 210 - 213
XIA ZHOU ET AL: "Synthesis and application of modified starch as a shell-core main adhesive in a foundry", JOURNAL OF APPLIED POLYMER SCIENCE, 1 January 2010 (2010-01-01), US, pages NA - NA, XP055237635, ISSN: 0021-8995, DOI: 10.1002/app.31781 *
XIA ZHOU; JINZONG YANG; DEPENG SU; GUOHUI QU: "The high-temperature resistant mechanism of a-starch composite binder for foundry", JOURNAL OF MATERIALS PROCESSING TECHNOLOGY, vol. 209, 2009, pages 5394 - 5398
XIA ZHOU; JINZONG YANG; FENG QIAN; GUOHUI QU: "Synthesis and Application of Modified Starch as a Shell-Core Main Adhesive in a Foundry", JOURNAL OF APPLIED POLYMER SCIENCE, vol. 116/5, 2010, pages 2893 - 2900
XIA ZHOU; JINZONG YANG; GUOHUI QU.: "Adhesive Bonding and Self-Curing Characteristics of a-Starch Based Composite Binder for Green Sand Mould/Core", J. MATER. SCI. TECHNOL., 2004, pages 617 - 621
XIA ZHOU; JINZONG YANG; GUOHUI QU: "Study on synthesis and properties of modified starch binder for foundry", JOURNAL OF MATERIALS PROCESSING TECHNOLOGY, vol. 183, 2007, pages 407 - 411
XIA ZHOU; JIYANG ZHOU; GUOHUI QU, CHINA FOUNDRY, 2005, pages 97 - 101
ZHOU X ET AL: "Study on synthesis and properties of modified starch binder for foundry", JOURNAL OF MATERIALS PROCESSING TECHNOLOGY, ELSEVIER, NL, vol. 183, no. 2-3, 23 March 2007 (2007-03-23), pages 407 - 411, XP022760951, ISSN: 0924-0136, [retrieved on 20070208], DOI: 10.1016/J.JMATPROTEC.2006.11.001 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108723285A (en) * 2018-07-11 2018-11-02 佛山陵朝新材料有限公司 A kind of preparation method of high green compression strength moulding sand binder material
CN112317679A (en) * 2020-11-07 2021-02-05 郑州远东耐火材料有限公司 Novel modified resin adhesive special for sand mold of fused brick and preparation method thereof

Also Published As

Publication number Publication date
PL409935A1 (en) 2015-08-31
PL233870B1 (en) 2019-12-31
EP3015188B1 (en) 2020-03-04

Similar Documents

Publication Publication Date Title
US6379446B1 (en) Methods for dispersing fibers within aqueous compositions
US5618341A (en) Methods for uniformly dispersing fibers within starch-based compositions
US4096326A (en) Dihydroxypropyl cellulose
JP5902697B2 (en) Novel cellulose ethers and their use
CN101015712B (en) Process for preparation of polycaprolactone-chitosan network/hydroxyapatite porous compound support frame material
EP3015188B1 (en) Moulding sand and a method of curing of moulding sand
JP4484426B2 (en) Delayed dissolution cellulose ethers and their preparation
JPH02212374A (en) Preparation of inorganic fiber composition
Nasir et al. Recent review on synthesis, evaluation, and SWOT analysis of nanostructured cellulose in construction applications
CA3054977C (en) Polysaccharide compositions and particulate materials coated therewith
Rachtanapun et al. Study of carboxymethyl cellulose from papaya peels as binder in ceramics
Kaczmarska et al. Modified polysaccharides as alternative binders for foundry industry
CN107321909A (en) A kind of strong wearability full-mold casting coating and preparation method thereof
CN108841390B (en) Cationic fenugreek gum-humic acid sand-fixing agent and preparation method thereof
CN111393080B (en) High-performance cementing material and preparation method thereof
JP2007084680A (en) Easily water-soluble polymer and method for producing the same
CN110776612A (en) Furan resin and preparation method thereof
JP4869632B2 (en) Water-soluble polymer compound and method for producing the same
CN106046924A (en) Preparation method of wear-resisting UV-curing printing ink composition
US20030145763A1 (en) Flocculant or binder composition, slurry containing the flocculant or binder composition, method for making ceramics using the slurry, and ceramic products made therefrom
KR20150058099A (en) Process for obtaining carboxymethyl cellulose from agro-industrial residues and carboxymethyl cellulose and use thereof
CN101116896A (en) Water-based cast iron resin sand coating with low gas-forming property and high air permeability
US4400502A (en) Readily dispersible anionic, water-soluble cellulose derivatives and a method for their preparation
JPH0143761B2 (en)
MXPA02010035A (en) Method for the production of easily wetted, water soluble, powdered at least alkylated non ionic cellulose ethers.

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: 20141209

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

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

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20170629

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

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

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20190917

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

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

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1239803

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200315

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602014061799

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200604

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20200304

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200605

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200604

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200704

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200729

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1239803

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200304

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602014061799

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

26N No opposition filed

Effective date: 20201207

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20201205

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20201231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201205

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201205

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201231

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201231

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201205

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20211227

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200304

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201231

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602014061799

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230701