US20030075291A1 - Method for the production of insulation plates and binding agent mixture for same - Google Patents

Method for the production of insulation plates and binding agent mixture for same Download PDF

Info

Publication number
US20030075291A1
US20030075291A1 US10/231,410 US23141002A US2003075291A1 US 20030075291 A1 US20030075291 A1 US 20030075291A1 US 23141002 A US23141002 A US 23141002A US 2003075291 A1 US2003075291 A1 US 2003075291A1
Authority
US
United States
Prior art keywords
additive
resin mixture
fatty acid
acid amides
novolak
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.)
Abandoned
Application number
US10/231,410
Inventor
Josef Suren
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.)
Hexion Specialty Chemicals AG
Original Assignee
Individual
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 Individual filed Critical Individual
Assigned to BAKELITE AG reassignment BAKELITE AG ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SUREN, JOSEF
Publication of US20030075291A1 publication Critical patent/US20030075291A1/en
Priority to US11/254,980 priority Critical patent/US20060037726A1/en
Assigned to JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT reassignment JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT SECURITY AGREEMENT Assignors: HEXION SPECIALTY CHEMICALS, INC.
Assigned to WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT reassignment WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: HEXION SPECIALTY CHEMICALS, INC.
Abandoned legal-status Critical Current

Links

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
    • B22C1/20Compositions 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
    • B22C1/22Compositions 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 resins or rosins
    • 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
    • B22C1/24Compositions 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 oily or fatty substances; of distillation residues therefrom
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/04Reinforcing macromolecular compounds with loose or coherent fibrous material
    • C08J5/10Reinforcing macromolecular compounds with loose or coherent fibrous material characterised by the additives used in the polymer mixture
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/20Carboxylic acid amides
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F27FURNACES; KILNS; OVENS; RETORTS
    • F27DDETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
    • F27D1/00Casings; Linings; Walls; Roofs
    • F27D1/0003Linings or walls
    • F27D1/0006Linings or walls formed from bricks or layers with a particular composition or specific characteristics
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2361/00Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
    • C08J2361/04Condensation polymers of aldehydes or ketones with phenols only
    • C08J2361/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols

Definitions

  • the invention relates to a method for the production of refractory insulation plates comprised of mineral fillers, cellulose-containing products and a thermosetting binding agent.
  • Such plates are employed, inter alia, as mold covering plates or as so-called tundish plates in continuous casting processes. They are produced by heating and curing a mixture preformed into the corresponding plate form, which is produced by removing water from an aqueous pulp comprised of cellulose-containing products, mineral fillers and a thermosetting binding agent. For this purpose, the pulp is poured onto a fine screen and the water is extracted under vacuum, but this process step is highly time-consuming and a need exists to shorten it.
  • the conventionally employed thermosetting binding agent is a mixture of a novolak and a curing agent, wherein a relatively highly condensed product must be used having an average molecular weight of 800 to 900 and a flow distance of approximately 20 to 30 mm as the novolak.
  • a relatively highly condensed product having an average molecular weight of 800 to 900 and a flow distance of approximately 20 to 30 mm as the novolak.
  • novolaks only moderate strengths of the insulation plates are attained.
  • An improvement of the strength values results if novolaks with lower average molecular weights or greater flow distances are used.
  • these binding agents swell more strongly in the pulp and thereby, the water extraction times are drastically increased, so that the use of these resins is not suitable for reasons of economy.
  • the novel resin mixture of the invention is derived by pulverizing a solidified melt of a novolak and as an additive, at least one member selected from the group consisting of fatty acid amides and substituted fatty acid amides.
  • the improved method of the invention to produce insulation plates comprises forming a resin powder of a solidified melt of a novolak and at least one additive selected from the group consisting of fatty acid amides and substituted fatty amides, forming an aqueous pulp of said resin powder, cellulose containing products and mineral fillers, pouring the aqueous pulp onto a fine-mesh flat screen and extracting the water under vacuum to obtain a “green” filter cake plate and curing the plate at a temperature of at least 120° C., preferably 150° C.
  • aqueous pulp comprised of cellulose-containing products, mineral fillers and novolak, which additionally contain at least one product selected from the group consisting of fatty acid amides or substituted fatty acid amides
  • the water extraction times are significantly shortened.
  • the strength of the plates produced from these mixtures is not impaired by this addition.
  • these additives from the group of fatty acid amides or substituted fatty acid amides make it possible to use novolaks with lower average molecular weight, i.e. with greater flow distance, without the water extraction time being lengthened. Therefore, insulation plates are obtained whose strengths are 30% higher than those produced by prior art methods.
  • the fatty acid amides and the substituted fatty acid amides are solid or semisolid compounds of the formulae
  • R is optionally branched alkyl of 10 to 30 carbon atoms
  • R′ and R′′ are individually hydrogen or alkyl of 1 to 6 carbon atoms and n is an integer of 1 to 6.
  • Preferred compounds are oleamide, behenamide, stearamide and, more preferably, bisstearamide. These compounds are known from Chem. Ab. 129:55251 as parting compounds in epoxy resin or phenolic resin formulations.
  • Binding agents comprised of phenolic resin in combination with substituted and unsubstituted fatty acid amides are described as binding agents for sand in the production of molds in the field of casting [JP-A 60111734 (C.A. 103:182359) or JP-A 57209741 (C.A. 98:165573].
  • a study regarding the effect of additive substances onto the flow and curing behavior of phenolic resin molding compounds found that, with increasing content of mold release compounds, the flow behavior is improved, but also that with increasing quantity of, for example, ethylene bisstearyl amide, the full depth-curing rate is impaired. A person skilled in the art would thus expect that the strength of the resulting products is also decreased.
  • the products from the group of fatty acid amides or substituted fatty acid amides are added in amounts of 1 to 10 wt. %, preferably of 3 to 5 wt. %, relative to the amount of the resin of the thermosetting binding agent.
  • the addition preferably takes place to the novolak.
  • This powdered resin mixture can then be mixed with the curing agent for the novolak and, optionally, it can as well be mixed with further fillers and additives.
  • the binding agent mixture for carrying out the method of the invention is generated.
  • the preferred latent curing agent for the novolaks is hexamethylene tetramine, which is mixed into the novolak, or into the powdered resin mixture of novolak and the additive substance of fatty acid amides or substituted fatty acid amides, in amounts of 3 to 6 wt. % relative to the weight of the novolak.
  • novolaks are all condensation products of phenolic compounds and an aldehyde, particularly, formaldehyde, which can be produced in an acidic medium in a molar ratio of phenolic compound to aldehyde of 1:0.9 to 1:0.2, and having a melting point of 50 to 110° C.
  • mixtures of novolaks can be used which have a lower and a higher melting point.
  • the preferred novolaks have an average molecular weight of 500 to 800, preferably 600 to 750, or a flow distance in the range of 35 to 55 mm.
  • the amounts of the employed novolaks are in the range of 1 to 10 wt. % relative to the total dry mixture.
  • phenolic compounds are mono- or polynuclear phenols or mixture of the named compound classes and specifically mono- as well as polynuclear phenols.
  • examples of these are phenol itself, its alkyl-substituted homologues, such as o-, m- or p-cresol, xylols or higher alkylated phenols, as well as polyvalent phenols such as resorcinol or purocatechol, and polynuclear phenols such as naphthols, bisphenol A or bisphenol F.
  • Phenol or the phenolic compound or mixtures of phenolic compounds are reacted with aldehyde, preferably with formaldehyde or a compound splitting off formaldehyde to form the desired novolak.
  • the novolaks can be modified with conventional modification means, such as, epoxy resins, raw rubber, polyvinyl butyral and inorganic additive substances.
  • composition of the corresponding mixtures for the production of the insulation plates with respect to the composition of the individual components as well as also with respect to their quantities corresponds to those of the mixtures conventionally used and known for this purpose.
  • mineral fillers can be employed all fillers conventionally employed in the refractory industry. Preferred are silicon dioxide, magnesium and aluminum oxide, magnesite, bauxite or andalusite and their mixtures in any desired mixing ratios.
  • Examples of cellulose-containing products include, in principle, all small-particle, cellulose-containing raw materials, such as cellulose fibers, wood fibers, wood shavings, wood powder or mechanical wood pulp, but preferably shredded paper.
  • the individual components are mixed with one another in any sequence desired per se and mixed with water and processed in a manner known per se into pulp, which subsequently under shaping is poured onto a fine-mesh flat screen and water is extracted under vacuum therefrom.
  • the “green” plate obtained as filter cake is subsequently cured at temperatures above 120° C., preferably above 150° C.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Mold Materials And Core Materials (AREA)
  • Reinforced Plastic Materials (AREA)
  • Organic Insulating Materials (AREA)

Abstract

A method for the production of insulation plates from an aqueous pulp comprised of mineral fillers, cellulose-containing products and a binding agent based on a novolak wherein a pulp is used comprising an additive substance selected from the group consisting of fatty acid amides or substituted fatty acid amides, the plates obtained after curing are used, inter alia, as mold covering plates or as so-called tundish plates for application in continuous casting processes.

Description

  • The invention relates to a method for the production of refractory insulation plates comprised of mineral fillers, cellulose-containing products and a thermosetting binding agent. [0001]
  • STATE OF THE ART
  • Such plates are employed, inter alia, as mold covering plates or as so-called tundish plates in continuous casting processes. They are produced by heating and curing a mixture preformed into the corresponding plate form, which is produced by removing water from an aqueous pulp comprised of cellulose-containing products, mineral fillers and a thermosetting binding agent. For this purpose, the pulp is poured onto a fine screen and the water is extracted under vacuum, but this process step is highly time-consuming and a need exists to shorten it. [0002]
  • The conventionally employed thermosetting binding agent is a mixture of a novolak and a curing agent, wherein a relatively highly condensed product must be used having an average molecular weight of 800 to 900 and a flow distance of approximately 20 to 30 mm as the novolak. With these novolaks, however, only moderate strengths of the insulation plates are attained. An improvement of the strength values results if novolaks with lower average molecular weights or greater flow distances are used. However, these binding agents swell more strongly in the pulp and thereby, the water extraction times are drastically increased, so that the use of these resins is not suitable for reasons of economy.[0003]
  • OBJECTS OF THE INVENTION
  • It is an object of the invention to provide a method for the production of insulation plates, which, in principle, corresponds to the method conventionally used until now, but in which the water extraction times are shortened. [0004]
  • It is another object of the invention to provide a method with which insulation plates of high strength can be produced without the water extraction time being increased. [0005]
  • These and other objects and advantages of the invention will become obvious from the following detailed description. [0006]
  • THE INVENTION
  • The novel resin mixture of the invention is derived by pulverizing a solidified melt of a novolak and as an additive, at least one member selected from the group consisting of fatty acid amides and substituted fatty acid amides. [0007]
  • The improved method of the invention to produce insulation plates comprises forming a resin powder of a solidified melt of a novolak and at least one additive selected from the group consisting of fatty acid amides and substituted fatty amides, forming an aqueous pulp of said resin powder, cellulose containing products and mineral fillers, pouring the aqueous pulp onto a fine-mesh flat screen and extracting the water under vacuum to obtain a “green” filter cake plate and curing the plate at a temperature of at least 120° C., preferably 150° C. [0008]
  • By employing an aqueous pulp comprised of cellulose-containing products, mineral fillers and novolak, which additionally contain at least one product selected from the group consisting of fatty acid amides or substituted fatty acid amides, the water extraction times are significantly shortened. The strength of the plates produced from these mixtures is not impaired by this addition. It was further found that these additives from the group of fatty acid amides or substituted fatty acid amides make it possible to use novolaks with lower average molecular weight, i.e. with greater flow distance, without the water extraction time being lengthened. Therefore, insulation plates are obtained whose strengths are 30% higher than those produced by prior art methods. [0009]
  • The fatty acid amides and the substituted fatty acid amides are solid or semisolid compounds of the formulae [0010]
    Figure US20030075291A1-20030424-C00001
  • wherein R is optionally branched alkyl of 10 to 30 carbon atoms, R′ and R″ are individually hydrogen or alkyl of 1 to 6 carbon atoms and n is an integer of 1 to 6. Preferred compounds are oleamide, behenamide, stearamide and, more preferably, bisstearamide. These compounds are known from Chem. Ab. 129:55251 as parting compounds in epoxy resin or phenolic resin formulations. [0011]
  • Binding agents comprised of phenolic resin in combination with substituted and unsubstituted fatty acid amides are described as binding agents for sand in the production of molds in the field of casting [JP-A 60111734 (C.A. 103:182359) or JP-A 57209741 (C.A. 98:165573]. A study regarding the effect of additive substances onto the flow and curing behavior of phenolic resin molding compounds (C.A. 104:34743) found that, with increasing content of mold release compounds, the flow behavior is improved, but also that with increasing quantity of, for example, ethylene bisstearyl amide, the full depth-curing rate is impaired. A person skilled in the art would thus expect that the strength of the resulting products is also decreased. [0012]
  • In the method of the invention, the products from the group of fatty acid amides or substituted fatty acid amides are added in amounts of 1 to 10 wt. %, preferably of 3 to 5 wt. %, relative to the amount of the resin of the thermosetting binding agent. The addition preferably takes place to the novolak. [0013]
  • It was found that the strength of the insulation plates is improved and that the water extraction times are significantly shortened if the additive substances from the group of fatty acid amides or substituted fatty acid amides are not only mixed with the powdered resin, but rather if they are melted together with this resin and the resulting mixture is pulverized after solidification. Consequently, a new powdered resin mixture is obtained, produced by melting a thermosetting resin with an additive substance selected from the group consisting of fatty acid amides or substituted fatty acid amides and pulverization of the solidified melt. [0014]
  • This powdered resin mixture can then be mixed with the curing agent for the novolak and, optionally, it can as well be mixed with further fillers and additives. Thus, the binding agent mixture for carrying out the method of the invention is generated. The preferred latent curing agent for the novolaks is hexamethylene tetramine, which is mixed into the novolak, or into the powdered resin mixture of novolak and the additive substance of fatty acid amides or substituted fatty acid amides, in amounts of 3 to 6 wt. % relative to the weight of the novolak. [0015]
  • Examples of novolaks are all condensation products of phenolic compounds and an aldehyde, particularly, formaldehyde, which can be produced in an acidic medium in a molar ratio of phenolic compound to aldehyde of 1:0.9 to 1:0.2, and having a melting point of 50 to 110° C. In order to work carefully, mixtures of novolaks can be used which have a lower and a higher melting point. The preferred novolaks have an average molecular weight of 500 to 800, preferably 600 to 750, or a flow distance in the range of 35 to 55 mm. The amounts of the employed novolaks are in the range of 1 to 10 wt. % relative to the total dry mixture. [0016]
  • Examples of phenolic compounds are mono- or polynuclear phenols or mixture of the named compound classes and specifically mono- as well as polynuclear phenols. Examples of these are phenol itself, its alkyl-substituted homologues, such as o-, m- or p-cresol, xylols or higher alkylated phenols, as well as polyvalent phenols such as resorcinol or purocatechol, and polynuclear phenols such as naphthols, bisphenol A or bisphenol F. [0017]
  • Phenol or the phenolic compound or mixtures of phenolic compounds are reacted with aldehyde, preferably with formaldehyde or a compound splitting off formaldehyde to form the desired novolak. The novolaks can be modified with conventional modification means, such as, epoxy resins, raw rubber, polyvinyl butyral and inorganic additive substances. [0018]
  • The composition of the corresponding mixtures for the production of the insulation plates with respect to the composition of the individual components as well as also with respect to their quantities corresponds to those of the mixtures conventionally used and known for this purpose. As mineral fillers can be employed all fillers conventionally employed in the refractory industry. Preferred are silicon dioxide, magnesium and aluminum oxide, magnesite, bauxite or andalusite and their mixtures in any desired mixing ratios. [0019]
  • Examples of cellulose-containing products include, in principle, all small-particle, cellulose-containing raw materials, such as cellulose fibers, wood fibers, wood shavings, wood powder or mechanical wood pulp, but preferably shredded paper. [0020]
  • The individual components are mixed with one another in any sequence desired per se and mixed with water and processed in a manner known per se into pulp, which subsequently under shaping is poured onto a fine-mesh flat screen and water is extracted under vacuum therefrom. The “green” plate obtained as filter cake is subsequently cured at temperatures above 120° C., preferably above 150° C. [0021]
  • Various modifications of the compositions and process of the invention may be made without departing from the spirit or scope thereof and it should be understood that the invention is intended to be limited only as defined in the appended claims. [0022]

Claims (16)

What I claim is:
1. A resin mixture formed by pulverizing a solidified melt of a novolak and at least one additive selected from the group consisting of fatty acid amides and substituted fatty acid amides.
2. A resin mixture of claim 1 wherein the amount of the additive is 1 to 10% by weight based on the novolak.
3. A resin mixture of claim 1 wherein the additive is selected from the group consisting of oleamide, behenamide, stearamide, and bisstearamide.
4. A resin mixture of claim 2 wherein the additive is bisstearamide.
5. A resin mixture of claim 1 also containing a curing agent.
6. A resin mixture of claim 5 wherein the curing agent is hexamethylene tetramine.
7. A resin mixture of claim 1 wherein the additive has the formula
Figure US20030075291A1-20030424-C00002
wherein R is alkyl of 10 to 30 carbon atoms, R′ and R″ are individually hydrogen or alkyl of 1 to 6 carbon atoms and n is an integer from 1 to 6.
8. A resin mixture of claim 1 also containing filler.
9. A process for the production of insulation plates comprising forming an aqueous pulp comprised of cellulose containing products, mineral fillers and a novolak binding agent, probing the aqueous pump onto a fine-mesh screen, extracting the water from the pulp under vacuum to obtain a “green” filter cake plate and curing the plate at a temperature of at least 120° C., the improvement comprising adding to the pulp at least one additive selected from the group consisting of fatty acid amides and substituted fatty acid amides.
10. The process of claim 9 wherein the resin mixture of claim 1 is used.
11. The process of claim 9 wherein the additive has the formula
Figure US20030075291A1-20030424-C00003
wherein R is alkyl of 10 to 30 carbon atoms, R′ and R″ are individually hydrogen or alkyl of 1 to 6 carbon atoms and n is an integer from 1 to 6.
12. The process of claim 9 wherein the additive is selected from the group consisting of oleamide, behenamide, stearamide, and bisstearamide.
13. The process of claim 9 wherein the additive is bisstearamide.
14. The process of claim 9 wherein the novolak has an average molecular weight of 500 to 800.
15. The process of claim 9 wherein the novolak has an average molecular weight of 600 to 750.
16. An insulation plate formed by the process of claim 9.
US10/231,410 2001-09-11 2002-08-29 Method for the production of insulation plates and binding agent mixture for same Abandoned US20030075291A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/254,980 US20060037726A1 (en) 2001-09-11 2005-10-20 Method for the production of insulation plates and binding agent mixture for same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10144717.5 2001-09-11
DE10144717A DE10144717A1 (en) 2001-09-11 2001-09-11 Process for the production of insulation boards and binder mixture therefor

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/254,980 Continuation US20060037726A1 (en) 2001-09-11 2005-10-20 Method for the production of insulation plates and binding agent mixture for same

Publications (1)

Publication Number Publication Date
US20030075291A1 true US20030075291A1 (en) 2003-04-24

Family

ID=7698625

Family Applications (2)

Application Number Title Priority Date Filing Date
US10/231,410 Abandoned US20030075291A1 (en) 2001-09-11 2002-08-29 Method for the production of insulation plates and binding agent mixture for same
US11/254,980 Abandoned US20060037726A1 (en) 2001-09-11 2005-10-20 Method for the production of insulation plates and binding agent mixture for same

Family Applications After (1)

Application Number Title Priority Date Filing Date
US11/254,980 Abandoned US20060037726A1 (en) 2001-09-11 2005-10-20 Method for the production of insulation plates and binding agent mixture for same

Country Status (5)

Country Link
US (2) US20030075291A1 (en)
EP (1) EP1291096B1 (en)
AT (1) ATE497026T1 (en)
DE (2) DE10144717A1 (en)
ES (1) ES2355494T3 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4614700A (en) * 1984-11-15 1986-09-30 Konishiroku Photo Industry Co., Ltd. Image forming process with magnetic brush development
US5563190A (en) * 1994-08-04 1996-10-08 Sumitomo Bakelite Company Limited Phenolic resin molding material

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2909448A (en) * 1955-03-07 1959-10-20 Shell Dev Salts of polyamine polyepoxide adducts and their use as curing agents for polyepoxides
US3036950A (en) * 1959-06-22 1962-05-29 Burgess Cellulose Company Process for incorporating resins into paper
NL299783A (en) * 1963-10-25
CS151073B2 (en) * 1970-02-06 1973-09-17
JPS57209741A (en) * 1981-06-18 1982-12-23 Hitachi Chem Co Ltd Production of resin coated sand for casting
JPS60111734A (en) * 1983-11-24 1985-06-18 Arakawa Chem Ind Co Ltd Resin composition for shell molding sand
US4487797A (en) * 1983-12-01 1984-12-11 Ppg Industries, Inc. Glass fibers to reinforce polymeric materials
DE3705540A1 (en) * 1986-06-13 1987-12-17 Ruetgerswerke Ag HIGH TEMPERATURE RESISTANT MOLDS
DE3620065A1 (en) * 1986-06-14 1987-12-17 Basf Ag METHOD FOR PRODUCING PAPER, CARDBOARD AND CARDBOARD
US4980232A (en) * 1987-03-05 1990-12-25 Allied-Signal Inc. Short fibers composed of antisotropic polymers and composites of thermoplastic and/or thermoset resins and such fibers
US5104590A (en) * 1988-10-26 1992-04-14 Wright Medical, Inc. Fabrication of an intraocular lens
DE4015440C1 (en) * 1990-05-15 1991-11-07 Ruetgerswerke Ag, 6000 Frankfurt, De
ES2040679T3 (en) * 1991-11-07 1996-06-01 Bakelite Ag BINDER BASED ON LIGNINE AND ARTIFICIAL RESINS.
EP0741813B1 (en) * 1994-01-17 1998-03-25 Akzo Nobel N.V. Aromatic polyamide pulp and its production process
GB9501605D0 (en) * 1995-01-27 1995-03-15 Kobe Steel Europ Ltd Radiation-curable compositions
JPH10130462A (en) * 1996-10-29 1998-05-19 Sumitomo Bakelite Co Ltd Epoxy resin composition for sealing semiconductor
JPH11244991A (en) * 1998-02-26 1999-09-14 Gun Ei Chem Ind Co Ltd Manufacture of resin coated sand
AUPQ544900A0 (en) * 2000-02-04 2000-02-24 Commonwealth Scientific And Industrial Research Organisation Treatment of cellulosic material
US7144972B2 (en) * 2004-07-09 2006-12-05 E. I. Du Pont De Nemours And Company Copolyetherester compositions containing hydroxyalkanoic acids and shaped articles produced therefrom

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4614700A (en) * 1984-11-15 1986-09-30 Konishiroku Photo Industry Co., Ltd. Image forming process with magnetic brush development
US5563190A (en) * 1994-08-04 1996-10-08 Sumitomo Bakelite Company Limited Phenolic resin molding material

Also Published As

Publication number Publication date
EP1291096A3 (en) 2007-02-14
ATE497026T1 (en) 2011-02-15
EP1291096B1 (en) 2011-01-26
DE50214875D1 (en) 2011-03-10
US20060037726A1 (en) 2006-02-23
EP1291096A2 (en) 2003-03-12
ES2355494T3 (en) 2011-03-28
DE10144717A1 (en) 2003-03-27

Similar Documents

Publication Publication Date Title
KR940000959B1 (en) Process for preparing phenolic resin binders for foundry and refractory uses
US5288774A (en) Novel low-emission, cold-curing binding agents
CA1227504A (en) Method of manufacturing an injection molded refractory shape and composition thereof
AU602089B2 (en) Modifiers for aqueous basic solutions of phenolic resoles
WO1995009892A1 (en) Ester cured no-bake foundry binder system
US3878159A (en) Foundry binders on the basis of phenolic resins
KR20190090828A (en) Amino acid-containing molding material mixture for the manufacture of moldings for the casting industry
KR101444046B1 (en) Binder composition for mold making purposes
US20030075291A1 (en) Method for the production of insulation plates and binding agent mixture for same
CA2149115A1 (en) Ester cured no-bake foundry binder system
KR890015801A (en) Composition for Casting Mold Process Using Recycled Sand
JP3492134B2 (en) Binder composition for mold
US4478269A (en) Furan Resin coated aggregate
US20190255599A1 (en) Aqueous akaline binder composition for curing with carbon dioxide gas and use thereof, corresponding moulding mixture for a producing foundry shape, a corresponding foundry shape and a method for producing a foundry shape
US4055528A (en) Phenol-formaldehyde resin for foundry applications
US6326418B1 (en) Acid-curable, refractory particulate material composition for forming mold
JPH0947840A (en) Mold forming composition
JPS603027B2 (en) Binder for refractory materials and refractories
JP2005095932A (en) Phenolic resin composition for shell mold, and resin-coated sand
JP2000015389A (en) Binder composition for carbon dioxide curing
KR20190025686A (en) Aqueous alkaline binder compositions for curing with carbon dioxide gas and uses thereof, corresponding molding mixtures for producing casting molds, corresponding casting molds and production methods of casting molds
KR20090057726A (en) Binder composition of carbon dioxide gas hardening type and molding method thereof
JPH0778158B2 (en) Powdered phenolic resin composition for binder
JP2003164943A (en) Novolac type phenolic resin composition for shell mold and resin-coated sand
CS240942B1 (en) Bonding agent of foundry covering substances

Legal Events

Date Code Title Description
AS Assignment

Owner name: BAKELITE AG, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SUREN, JOSEF;REEL/FRAME:013256/0072

Effective date: 20020820

STCB Information on status: application discontinuation

Free format text: EXPRESSLY ABANDONED -- DURING EXAMINATION

AS Assignment

Owner name: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT,DELA

Free format text: SECURITY AGREEMENT;ASSIGNOR:HEXION SPECIALTY CHEMICALS, INC.;REEL/FRAME:018535/0701

Effective date: 20061103

Owner name: JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT,

Free format text: SECURITY AGREEMENT;ASSIGNOR:HEXION SPECIALTY CHEMICALS, INC.;REEL/FRAME:018535/0556

Effective date: 20061103

Owner name: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT, DEL

Free format text: SECURITY AGREEMENT;ASSIGNOR:HEXION SPECIALTY CHEMICALS, INC.;REEL/FRAME:018535/0701

Effective date: 20061103