DE1758977A1 - Foundry sand binders - Google Patents

Foundry sand binders

Info

Publication number
DE1758977A1
DE1758977A1 DE19681758977 DE1758977A DE1758977A1 DE 1758977 A1 DE1758977 A1 DE 1758977A1 DE 19681758977 DE19681758977 DE 19681758977 DE 1758977 A DE1758977 A DE 1758977A DE 1758977 A1 DE1758977 A1 DE 1758977A1
Authority
DE
Germany
Prior art keywords
foundry sand
binders
sand binders
found
mixtures
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
DE19681758977
Other languages
German (de)
Other versions
DE1758977C3 (en
DE1758977B2 (en
Inventor
Karl-Heinz Dipl-Chem Bruening
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.)
HUETTENS ALBERTUS CHEMISCHE WE
Original Assignee
HUETTENS ALBERTUS CHEMISCHE WE
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 HUETTENS ALBERTUS CHEMISCHE WE filed Critical HUETTENS ALBERTUS CHEMISCHE WE
Priority to DE19681758977 priority Critical patent/DE1758977C3/en
Priority claimed from DE19681758977 external-priority patent/DE1758977C3/en
Publication of DE1758977A1 publication Critical patent/DE1758977A1/en
Publication of DE1758977B2 publication Critical patent/DE1758977B2/en
Application granted granted Critical
Publication of DE1758977C3 publication Critical patent/DE1758977C3/en
Expired 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
    • B22C1/22Compositions 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
    • B22C1/2233Compositions 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 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • B22C1/2273Polyurethanes; Polyisocyanates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/54Polycondensates of aldehydes
    • C08G18/542Polycondensates of aldehydes with phenols

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Mold Materials And Core Materials (AREA)

Description

Gie#ereisand-Bindemittel Zusatz zu Patent...... (Anmeldung P 15 70 203. 1) Das Hauptpatent..... (Anmeldung P 15 70 203. 1) betrifft Bindemittel für die Herstellung von Formen und Kernen nach dem Hotbox-Verfahren, die unter Verwendung von Phenolen, Formaldehyd, Furfurylalkohol und geringen Mengen Harnstoff hergestellt waren und gekennzeichnet sind dadurch, da# eine überformalisierte konzentrierte Harnstofflösung unter Zugabe von k'urfurylalkohol, p-Formaldehyd und einem 2henol im alkalischen Medium in einem solchen Verhältnis zueinander kondensiert werden, daß im Endprodukt der Anteil an Furfurylalkohol bis zu 50s, vorzugsweise 10 bis 30%, das Molverhaltnis der phenolischen Komponente zum Gesamtformaldehydanteil im Bereich von 1 : 1,2 bis 1 : 1, 6 liegt und der Stickstoffgehalt im Endprodukt weniger als 3% beträgt.Casting sand binder additive to patent ...... (registration P 15 70 203. 1) The main patent ..... (Application P 15 70 203. 1) relates to binders for the production of molds and cores according to the hotbox process using made from phenols, formaldehyde, furfuryl alcohol and small amounts of urea goods and are characterized by the fact that # an over-formalized focused Urea solution with the addition of kurfuryl alcohol, p-formaldehyde and a phenol are condensed in an alkaline medium in such a ratio to each other, that in the end product the proportion of furfuryl alcohol up to 50s, preferably 10 to 30%, the molar ratio of the phenolic component to the total formaldehyde content in the The range is from 1: 1.2 to 1: 1.6 and the nitrogen content in the end product is less than 3%.

Eine besondere Ausführungsart dieser Bindemittel ist dadurch gegeben, daß die Kondensation im pH-Bereich 7, 2 bis 10, 0 mittels basisch reagierender Verbindungen der Elemente der 1. und 2 Gruppe des periodischen Systems, vorzugsweise der 2. Gruppe, und/oder organischen Aminen bzw. Aminoalkoholen bei einer Temperatur zwischen 50 und 110°C durchgefuhrt und dann das Reaktionswasser bis zum Erhalten einer Viskosität zwischen vorzugsweise 10 bis 70 P20o abdestilliert wird.A special embodiment of these binders is given by that the condensation in the pH range 7.2 to 10.0 by means of compounds with a basic reaction the elements of the 1st and 2nd group of the periodic table, preferably the 2nd group, and / or organic amines or amino alcohols at a temperature between 50 and 110 ° C and then the water of reaction until a viscosity is obtained between preferably 10 to 70 P20o is distilled off.

Es hat sich nun überraschenderweise herausgestellt, daß die oben beschriebenen Bindemittel ihre Vorzüge, namlich Gasporenfreiheit der mit ihnen eratellten Abgüsse und gute Oberflächenbeschaffenheit der mit ihnen erstellten Kerne und AbgUsee nicht nut bei Härtung nach dem Hotbox-Verfahren entfalten, sondern unter gewissen Bedingungen auch kalthärtbare Formstoffmischungen ergeben.It has now surprisingly been found that the above-described Binders have their advantages, namely the absence of gas pores in the casts made with them and good surface quality of the cores and AbgUsee created with them are not unfold only when hardening according to the hotbox process, but under certain conditions cold-curable molding mixtures also result.

Gem§ß der deutschen Patentechrift 880 467 ist es bekannt, Formstoffmischungen aus Sand, Polyester mit noch reaktionsfähigen Hydroxyl-, Sulfhydryl-oder Aminogruppen und Di-oder Polyisocyanate herzustellen, die bei niedrigen Temperaturen bereits aushärten.According to German patent specification 880 467, it is known to use molding material mixtures made of sand, polyester with still reactive hydroxyl, sulfhydryl or amino groups and to produce di- or polyisocyanates that are already at low temperatures Harden.

Es wurde gefunden, daß die gemäß der Anmeldung P 15 70 203. 1 hergestellten modifizierten Phenolresole mit einem Di-oder Polyisocyanat zusammen als Bizidersystem in einur Formstoffmischung bei Raumtemperatur arstttrrende Mischungen etgeben.It has been found that those produced according to application P 15 70 203.1 modified phenol resols with a di- or polyisocyanate together as a bicider system In a molding mixture at room temperature, give mixtures that are ready for use.

Es wurde weiter gefunden, da# sowohl die Lebenszeit umso kürzer und die Aushärtegeschwindigkeit um so größer sind, je mehr der Furfurylalkoholgehalt innerhalb der in der Anmeldung P 15 70 203. 1 angeführten Grenzen von 10-50% sich dem oberen Grenzwert nähert. Des weiteren wurde gefunden, da# die bekannten, die Urethanbildung aus Isocyanaten und polyhydroxylgruppenhalti#en Verbindungen regelnden Katalysatoren (vgl. Ind. Eng. Chem. 51 (1959) S. 1299) die Erhärtung der erfindungsgemäßen fhenolharz-Hombination zu regeln gestatten.It was further found that # both the lifetime and the shorter the more the furfuryl alcohol content, the greater the curing speed within the limits of 10-50% listed in application P 15 70 203.1 approaches the upper limit. It was also found that # the known, the Regulating urethane formation from isocyanates and compounds containing polyhydroxyl groups Catalysts (cf. Ind. Eng. Chem. 51 (1959) p. 1299) the hardening of the invention to regulate phenolic resin combination.

Beispielsweise härten Sandmischungen bestehend aus 100 Gew. Teilen Quarzsand H 32 0, 8 " " Harz A der Anmeldung F 15 70 203. 1 1,2 " " Diphenlmethandiisocyanat(techn.) inherhalb einer Stunde zu transportstabilen Formkörpern, uie ausgezeichnete Oberflächeneigenschaften gußseitig erg Diese Härtungsreaktion wird auf eine Zeit von einigen bekunden verkürzt und die kernseitig festzustellenten Festigkeitseigenschaften noch erheblich verbessert, wenn als Katalysator die in der Zeitschrift Ind, Eng. Chem. erwähnten vorwiegend alkalischen Stoffe, wie z. B. tertiäre Amine, verwendet werden. Weitere Verbesserung der Festikeitswerte ist durch den bekannten Zusatz von Silanderivaten, z.B. laut der Anmeldeschrift A 58 063 VIa/31b1 möglich.For example, sand mixtures consisting of 100 parts by weight harden Quartz sand H 32 0.8 "" Resin A of application F 15 70 203. 1 1.2 "" Diphenlmethane diisocyanate (techn.) within an hour to transport-stable moldings, uie excellent surface properties On the cast side, this hardening reaction is shortened for a few years and the strength properties to be determined on the core are significantly improved, if the catalyst in the journal Ind, Eng. Chem. Mentioned mainly alkaline substances, such as B. tertiary amines can be used. Further improvement the strength values are due to the well-known addition of silane derivatives, e.g. loud the registration form A 58 063 VIa / 31b1 possible.

Claims (1)

P a t e n t a n s p r u c h V r w l u i d u n g von gemä# Hauptpatent..... P a t e n t a n s p r u c h V r w l u i d u n g of according to # main patent ..... (@nmeldung P 15 70 203.1,modifizierten Phenolresolen in Verbinduag mi@ Di- oder Polyisocyanaten und äblichen die Urethanbildung regelnden Zusätzen zur Herstellung von kalth@rtenden Formstoffgemischen.(@nmeldung P 15 70 203.1, modified phenol resols in connection mi @ di- or polyisocyanates and the usual additives regulating urethane formation for the production of cold-curing molding material mixtures.
DE19681758977 1968-09-11 Use of binders for the production of cold-curing molding material mixtures Expired DE1758977C3 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE19681758977 DE1758977C3 (en) 1968-09-11 Use of binders for the production of cold-curing molding material mixtures

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19681758977 DE1758977C3 (en) 1968-09-11 Use of binders for the production of cold-curing molding material mixtures

Publications (3)

Publication Number Publication Date
DE1758977A1 true DE1758977A1 (en) 1971-04-08
DE1758977B2 DE1758977B2 (en) 1976-11-11
DE1758977C3 DE1758977C3 (en) 1977-07-28

Family

ID=

Also Published As

Publication number Publication date
DE1758977B2 (en) 1976-11-11

Similar Documents

Publication Publication Date Title
DE3750509T2 (en) PHENOL RESIN POLYISOCYANATE BINDER SYSTEMS CONTAINING ORGANOPHOSPHATES.
DE3888356T2 (en) MODIFIER FOR AQUEOUS BASIC SOLUTIONS OF PHENOLIC RESOLE RESINS.
DE102016123051A1 (en) Amino acid-containing molding material mixture for the production of moldings for the foundry industry
DE68922996T2 (en) FOUNDRY RESIN.
EP0006973B1 (en) Resin binders with storable alkyl substituted organo amino silanes as adhesive agents
EP0540837A1 (en) Lignin modified binder
DE102015107016A1 (en) Process for reducing free formaldehyde in benzyl ether resins
DE3020089C2 (en) Molding compounds for foundry cores and molds and their use
DE3139484A1 (en) BINDING COMPOSITION FOR FOUNDRY SAND AND CORE SAND
DE1252853B (en) Binder for foundry sands
DE2235668C3 (en) Catalyst for a foundry binder
EP0157023A2 (en) Binder on base of furfurylalcohol, method of producing and using same
EP0362486B1 (en) Moulding materials
DE1758977A1 (en) Foundry sand binders
DE1758977C3 (en) Use of binders for the production of cold-curing molding material mixtures
DE3339174C2 (en)
DE3639233A1 (en) COLD-HARDENING MOLD BINDING AGENT AND THE USE THEREOF
DE1570203C3 (en)
AT356894B (en) METHOD FOR PRODUCING MODIFIED FURFURYL ALCOHOL FORMALDEHYDE RESINS
DE2925733A1 (en) POLYURETHANE-BASED BINDERS AND THE PRODUCTION THEREOF
DE2511165C3 (en) Process for stabilizing core and molding sand binders based on synthetic resin
DE2520363C3 (en) Molding and core sand binders
DE2733866A1 (en) RESIN COMPOUND
DE1159597B (en) Core and foundry sand binders
DE2152116C3 (en) Molding material mixture of olivine sand and a cold-curing binder system

Legal Events

Date Code Title Description
C3 Grant after two publication steps (3rd publication)
E77 Valid patent as to the heymanns-index 1977
8340 Patent of addition ceased/non-payment of fee of main patent