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CRYSTIC COMPOSITES HANDBOOK Composites Handbook

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    Composites Handbook

  • Performance Resins in Composites

  • 50 years of reliability, experience and innovation.The Crystic family of resins is at the heart of our success. In 1946 Scott Bader were the first UK company to manufacture unsaturated polyester resins in Europe. In 1953 the Crystic range of polyesters was introduced and its revolutionary applications have meant that Crystic has been the byword for superior technological achievement ever since.

  • CONTENTSIntroductionPlastics Thenatureofreinforcedplastics

    MaterialsResins Unsaturatedpolyesters-DCPDpolyesters-Epoxies- Vinylesters-Phenolics-HybridsReinforcements Glassfibre-Carbonfibre-Polyaramidfibre-Glass combinations-Hybridcombinations SpecialitymaterialsCatalysts MEKPs-CHPs-AAPs-BPOs-TBPOs&TBPBsAccelerators Cobalts-AminesFillers Calciumcarbonate-Talc-Metalpowders-Silica- Microspheres-Aluminatri-hydratePigments PolyesterpigmentpastesReleaseAgents Polyvinylalcohol-Wax-Semi-permanents-Wax/semi- permanenthybrids-Releasefilm-InternalreleasesystemsCorematerials 2-componentpolyurethanefoam-Polyurethanefoamsheet -PVCfoam-Polyetheramidefoam-Styreneacryilonitrile foam-Balsawood-Honeycombcores-Non-wovencoresAdhesives Polyesters-Epoxies-Acrylics(methacrylates)- Polyurethanes-Urethaneacrylates(Crestomer)Mouldmakingmaterials Flexiblematerials-Plaster&clay-CompositesAncillaryproducts Polishingcompounds

    ProcessesOpenmouldprocessesGelcoating-Laminating-Handlay-up-Spraylay-up- Sprayequipment-Roller/saturatorlay-up-Heatassisted curing-Mouldrelease-Postcuring-Trimming& finishingClosedmouldprocessesVacuuminfusion(VI)-Vacuumassistedresintransfer/ (VacFlo)-Resintransfermoulding(RTM)-Cold/warm pressmouldingHotmouldprocesses Wetmoulding-Mouldingcompounds-Doughmoulding compound(DMC)-Bulkmouldingcompound(BMC)- Sheetmouldingcompound(SMC)-Lowpressure mouldingcompound(LPMC)Continuousprocesses Pultrusion-Filamentwinding-Pulwinding-Centrifugal moulding-Machinemadesheeting

    Properties

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  • GeneralconceptsMechanicalproperties Castresins-Glassreinforcedlaminates-Polyaramidandcarbon reinforcedlaminates-Sandwichconstruction-Thermalandelectrical propertiesFireperformance Firetests-LowfirehazardCrysticresinsEnvironmentalproperties Weatherandwaterresistance-Chemicalresistance

    Applications Un-reinforcedpolyesterresin-Bodyfiller-Buttoncasting- Embeddingandpotting-Decorativecasting-Flooring-Polyester concrete-Polyestermarbleandonyx-SolidsurfacesReinforced polyesterresin-Chemicalcontainment-Marine-Matched performancemarinesystems-Landtransport-Building&construction

    Quality Control Materialstorage-Stockcontrol-Workshopconditions-Reinforcementpreparation-Compoundingandmixingofresins-Mouldpreparationandmoulding-Trimmingandfinishing-Mouldcare-Resinusage-Thecuringreaction-Geltime-Hardeningrate-Maturingtime-Hotcuring-Coldcuring-Factorsaffectinggeltime-Effectofadditivesonresinproperties-Commonfaults-Repair-Repairinggelcoatscratches-Fillingdentsandcracks-Repairinglaminatedamage-Inspection-Resintoglassratios-Degreeofcure-Controlofvariables

    Mould MakingTheimportanceoftoolingCompositemouldtools PlugproductionMouldmakingmaterials Gelcoat-Laminatingresin-ReinforcementsWorkshopconditionsMouldconstructionschedule

    Health Safety andthe Environment Storage-Use-Styrenereduction

    Appendix 1 BibliographyandAddresses

    Appendix 2 SIUnits

    Index

    Scott Bader Product Range

    Scott Bader Regional Centres

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  • ListofTables page

    1 Comparative properties of cast un-reinforced resins and fibres 452 Typical properties of glass reinforced composites compared with steel and aluminium alloy 473 Comparative properties of glass, polyaramid and carbon reinforced polyester laminates 474 Percentage retention of tensile properties at various temperatures. CSM reinforced isophthalic polyester resin with an HDT of 116C 505 Minimum properties of reinforced laminate plies 506 Comparative thermal properties 527 Typical thermal and electrical properties of cast polyester resin 528 Classification for external fire exposure roof test 549 Classification for surface spread of flame of products 5510 Classification for NFP-92501 Epiradiateur test 5711 Low fire hazard Crystic resins 5812 Low fire hazard Crystic gelcoat/resin systems 5913 Strength retention of FRP composite after immersion in distilled water at 20C 6114 Cold curing catalysts 6715 Effect of catalyst on the hardening rate of a typical orthophthalic polyester resin 6816 Catalyst and accelerator equivalents 6917 Materials for RTM tooling 76

    ListofPlatespage

    1 Performance resins in composites frontispiece2 50 years of reliability, experience and innovation frontispiece3 Reinforcements and core materials 984 Ernest Bader Technical Centre 995 Closed Mould technology 1006 Continuous process 1017 Solid surface technology 1028 Crystic Stonecast applications 1039 Underground in-situ pipe lining 10410 Composite chemical tank 10511 Luxury composite motor cruiser 10612 Composite luxury yacht 10713 Composite super yacht and pilot boat 10814 Luxury composite motor cruiser 10915 Composite super yacht 11016 Composite sailing dinghy 11117 Sponsored composite racing cars 11218 Eurostar - High speed passenger train 113 19 Composites executive motor home 11420 Common faults in composites

  • ListofFigures

    page

    1 Derivation of compounds used in the manufacture of a typical polyester resin 102 Specific tensile strength - steel, aluminium and GFRP 403 Specific tensile modulus - steel, aluminium and GFRP 404 Comparative material and fabrication costs for component manufacture 415 Effect of glass content on the tensile strength of random glass reinforced polyester laminates 466 Effect of glass content and orientation on the tensile strength of random glass reinforced polyester laminates 467 Effect of glass content and orientation on the tensile strength of glass reinforced polyester laminates 468 The effect of CSM skin construction (at R:F = 2.3:1) and core thickness on flexural rigidity for balanced double skinned sandwich laminates 499 The effect of WR (glass) skin construction (at R:F = 1:1) and core thickness on flexural rigidity for balanced double skinned sandwich laminates 4910 Predicted effect of fibre type and content on tensile strength using property data from Table 5 5111 Predicted effect of fibre type and content on tensile modulus using property data from Table 5 5112 Effect of weathering on the light transmission of GFRP sheeting at various resin contents 6113 Effect of weathering on the gloss retention of low fire hazard GFRP laminates with gelcoat 6114 Effect of weathering on the gloss retention of GFRP laminates with various surfaces (orthophthalic resin/glass mat: 70% resin content) 6115 Typical exotherm of polyester resin 6616 Equivalent post curing times and temperatures 6617 Hot curing of a typical polyester resin using 2% benzoyl peroxide catalyst 6618 Effect of ambient temperature on the geltime of a typical polyester resin 6719 Effect of addition of plasticising resin 6920 Laminate repair method 7321 Construction of reinforcing ribs 7922 Construction of flange for split moulds 80

  • COMPOSITESHANDBOOK

    PrefaceTheglobalnatureoftodaysreinforcedplasticsindustrycreatesademandfromallovertheworld,forbasicbackgroundinformation.ThissixteentheditionoftheCompositesHandbookprovidesanintroductiontoreinforcedplasticintermsofbasicchemistry,resins,reinforcementsandapplicationtechniques.Italsoencompassesthemajoradvancesinmaterialandprocesstechnologieswhichhaveoccurredsincethefirsteditionwaspublishedin1953.

    Theuniquenessofreinforcedplasticliesinthefactthatthematerialofconstructionandtheendproductareproducedsimultaneously,soqualitycontrolisahighlysignificantpartoftheprocess.

    Thegeneralguidance,adviceandtechnicaldatacontainedinthishandbookisintendedtohelpdesigners,mouldersandend-userstorealisethefullpotentialofthisuniquematerialasatrulystructuralengineeringplastic.

    December2005ScottBaderCompanyLtd.

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    Allinformationisgiveningoodfaithbutwithoutwarranty.Wecannotacceptresponsibilityorliabilityforanydamage,lossorpatentinfringementresultingfromtheuseofthisinformation.

    Copyright(c)2005ScottBaderCompanyLimited

  • IntroductionPlasticsThetermplasticisusedtodescribethemouldedformofasynthetic(i.e.man-made)resin.Theseresinsarecomposedoflarge,chain-likemoleculesknownaspolymers,whichalsooccurnaturallyas,forexample,cellulose,proteinandrubber.Mostsyntheticresinsaremadefromchemicalsderivedfromoilanditistheseman-madepolymerswhichareusedtoproducewhatarecommonlyknownasplastics.

    Plasticsintheirvariousformshaveexistedsincethelate19thcentury,butmostofthematerialsreferredtoasplasticstodayhavebeendevelopedduringthepast50years.

    Alargevarietyofplasticsisnowavailableandtheyexistinvariousphysicalforms.Theycanbebulksolidmaterials,rigidorflexiblefoams,orintheformofsheetorfilm.Mostfallintooneoftwocategories;thermoplasticorthermoset.Thermoplasticscanbeformedandre-formedbytheuseofheat(eg.polyethylene,PVC,etc.).Thermosets,ontheotherhand,hardenbyachemicalreaction,generatingheatwhentheyareformedandcannotbemeltedorre-formed(eg.unsaturatedpolyesters,epoxies,vinylestersetc.).

    The Nature of Reinforced PlasticsReinforcedPlasticisthegenerictermusedtodescribespecificplasticmaterialsreinforcedwithhighstrengthfibres.Sincetheirdevelopment,thesematerialshavebeencommonlyknownbynamessuchasFibreglassandGRP(GlassReinforcedPlastic).ThoughGRPisstillthemostusedterm,thedevelopmentandutilisationoffibresotherthanglassmakesFRP(FibreReinforcedPlastic)amoreaccurateandcomprehensivedescription.Withinthereinforcedplasticsindustryitself,Compositeisthetermfelttobestdescribethislight,durableandastonishinglytoughconstructionalmaterial.

    Compositescanbefabricatedintoawidespectrumofproducts,fromthepurelydecorativetocomplex,engineeredstructures.Theymaybetranslucent,opaqueorcoloured,thickorthin,flatorshapedandthereisvirtuallynolimitonsize.Compositescanbefoundinmostareasofdailylife,intheformofroofsheeting,tanks,pipes,vehiclebodies,buildings,boats,etc.

    Toproduceacompositeitem,twobasiccomponentsarerequired,thesebeingasyntheticresinandastrongfibre.Theresin,whichcouldbeapolyester,epoxyorvinylester,isnormallysuppliedasaviscousliquid,whichsetstoahardsolidwhensuitablyactivated.Thefibremaybeglass,carbon,polyaramid,oracombinationofsomeorallofthese.Whatmakescompositesuniqueisthefactthatthematerialofconstructionandtheendproductareproducedsimultaneously.Usingasuitablemould,layersoffibreareimpregnatedwithactivatedresinuntiltherequiredthicknessisachieved.Whencomplete,themouldingisremovedandthemouldcanthenbere-usedtoproducemore,identicalitems.

    Thishandbookdescribesindetailthematerials,techniquesandapplicationsofcompositemanufacture,andpresentssolutionstoanyproblemsthatmayarise.

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  • MATERIALS

    Resins

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  • Severalresintypesareemployedinthemanufactureofcompositeproducts.Alloftheseresinsarethermosetsbuttheydifferintheirchemicalmake-up,thusexhibitingdiverseproperties.Thismeansthatmanufacturerscanchooseresinswhichenablethemtotailortheirproductstomeetspecificrequirements.ThishandbookisconcernedmainlywithCrysticpolyesterresins,butothertypessuchasvinylester,epoxy,DCPD,phenolicandalsohybridsystemsaredescribedinthissection.

    PolyestersCrysticresinsareunsaturatedpolyesters.Therawmaterialsusedforthemanufactureofunsaturatedpolyesterresinsareoilbased(seeFigure1)andtoproduceapolyesterofthistype,threebasicchemicalcomponentsaregenerallyrequired:-A:saturatedacid(e.g.phthalicanhydride)B:unsaturatedacid(e.g.maleicanhydride)C:dihydricalcohol(e.g.propyleneglycol)

    Withtheapplicationofheat,thesechemicalscombinetoformaresinwhichisaviscousliquidwhenhot,butabrittlesolidwhencold.ThetermpolyesterisderivedfromthelinkbetweenAorBwithC,whichistermedanesterlink.Whilstitisstillhot,theresinisdissolvedinamonomerwhichisusuallystyrenethoughotherscanbe,andare,used.Themonomerperformsthevitalfunctionofenablingtheresintocurefromaliquidtoasolid,bycrosslinkingthemolecularchainsofthepolyester.Noby-productsareevolvedduringthisprocess,whichmeanstheresinscanbemouldedwithouttheuseofpressure.Theyarethereforeknownascontactorlowpressuremouldingresins.Themolecularchainsofthepolyestercanberepresentedasfollows:ACBCACBCACBC

    WiththeadditionofstyreneSandinthepresenceofacatalystandaccelerator,thestyrenecross-linksthechainstoformahighlycomplexthreedimensionalnetworkasfollows:

    ACBCACBCACBC

    SSS

    ACBCACBCACBC

    Atthisstage,thepolyesterresinissaidtobecured.Itisnowachemicallyresistantand(usually)hardsolid.Thecross-linking,orcuring,processiscalledpolymerisationandisanon-reversiblechemicalreaction.

    Oncecured,theresinwillcontinuetomature,duringwhichtimethemouldingwillacquireitsfullproperties.Thisprocess,whichcantakeseveralweekstocompleteatroomtemperature,canbeacceleratedbypostcuringthemouldingatelevatedtemperatures(seeQualityControlsection).

    Polyesterresinswithdifferingcharacteristicsandpropertiesareproducedbymanipulatingthetypesandamountsofrawmaterialsusedintheirmanufacture(seePropertiessection).

    DCPD Polyesters

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  • TheuseofDCPD(Dicyclopentadiene)inunsaturatedpolyesterresinmanufacturewasfirstintroducedintheUnitedStatesinthelate1970s.Sincethattime,itscommercialusehasdevelopedandresinscontainingDCPDarenowproducedworldwide.

    TherearetwobasicmethodsofproducingDCPDpolyesters,asfollows:-

    Dow Hydrolysis MethodThismethodinvolvesaninitialreactionusingthreecomponents:-A:MaleicAnhydrideB:WaterC:DCPDThesethreecomponentsarereactedtogetheratatemperaturelowerthan130C,toproducewhatisknownasanacidfunctionalisedendcap.Afurtherreactionisthencarriedout,usingtheacidendcapandotherstandardpolyesterrawmaterials.Duringthisreaction,theacidendcapattachestothemolecularchainsofthepolymer,thusrestrictingtheirlengthandtherebyreducingtheviscosityofthefinalproduct.Thismeansthatlessstyreneisneededtoachievearesinwithausableviscosity.Upto30%weightforweightDCPDcanbeaddedtoapolyester(onsolidresin)usingthismethod.

    Diels - Alder Reaction MethodThismethodallowsupto70%weightforweightDCPDtobeused(onsolidresin)inthemanufactureofapolyester.Itinvolvesconvertingdicyclopentadiene(DCPD)tocyclopentadiene(CPD)atatemperaturegreaterthan130C.TheCPDisthengraftedontotheresinbackbonebyreactionwithasiteofunsaturation.Thiscanbeachievedbyanearlyreactionwithmaleicanhydrideoratalaterstageofthepolymerisationprocess.

    Thesetwoprocessesaresimilarinthatbothreactionsoccurinbothsystemsbutindifferentratios.Thedegreeofeachreactiontypeiscontrolledbytemperatureandwatercontentinthefirststage.TheadvantagesofincorporatingDCPDintopolyesterresinsarelowerstyrenecontent,combinedwithgoodproperties.ThemaindisadvantageisthefactthatDCPDsolidifiesatroomtemperaturesoheatedstorageandhandlingfacilitiesarerequired.

    Epoxy ResinsEpoxyresinshavebeencommerciallyavailablesincetheearly1950sandarenowusedinawiderangeofindustriesandapplications.

    Epoxiesareclassifiedintheplasticsindustryasthermosettingresinsandtheyachievethethermosetstatebymeansofanadditionreactionwithasuitablecuringagent.Thecuringagentusedwilldeterminewhethertheepoxycuresatambientorelevatedtemperaturesandalsoinfluencephysicalpropertiessuchastoughnessandflexibility.Therearetwobasictypesofepoxyresin,thesebeing:

    i)BisphenolA-DiglycidylEtherii)EpoxyPhenolNovolac

    Epoxyphenolnovolacresinshavethehighercross-linkdensityofthetwotypesandareusedinhighperformanceapplicationssuchaspre-pregsfortheelectricalindustryandalsoinsomehighperformancelaminatingapplications. Lowviscosity,lowmolecularweightBisphenolAepoxiesaretheonesmostwidelyusedinthecompositesindustry.Theyareavailableas2packsystemswhichcanbecuredatroomtemperatureusingasuitablecuringagent,thevarioustypesofwhichareasfollows:-

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  • i)Amines(di-functional)Cureiseffectedbytwoepoxygroupsreactingwithoneprimaryamineandthesearemostwidelyusedforstandardroomtemperatureapplications.Astherearehealthimplicationswithfreeamines,thesesystemsareoftensuppliedasamineadducts.

    ii)Polyamides iii)AnhydridesThesecuringagentsreactonlywithheatandneedtemperaturesbetween120Cand140Ctobeeffective.Theyareusedinhightemperatureapplicationssuchasfilled,sanitarywaresystems.

    Epoxyresinsarehighlychemicalandcorrosionresistant.Theyhavegoodphysicalpropertiesandtheirlowshrinkcharacteristicsmeantheycanbeusedwheredimensionalaccuracyisofprimeimportance.Epoxiesexhibitexcellentadhesiontoawidevarietyofsubstratesincludingconcrete,glass,wood,ceramicsandmanyplastics.

    Thiscombinationofpropertiesmakesepoxyresinsuitableforuseinmanyapplicationswithinthecompositesindustry.Theseincludeadhesives,construction/repair,casting,laminatingandflooring.

    Thereare,however,healthissuesassociatedwithresinsensitisationandcostcansometimesbeaprohibitingfactor.

    Vinyl Ester ResinsVinylestersarethermosetresinswhichincorporateandbuildontheexcellentphysicalpropertiesofepoxysystems.Theyareusedinsimilarapplicationstopolyesterresins,particularlywherehigherperformanceisrequired.

    Therearetwobasictypesofvinylesterresin,asfollows:-

    i)BisphenolA-diglycidylethertype(BADGE)ThistypeofvinylesterisproducedbyreactingaBADGEsystemepoxywithmethacrylicacid.Theresultantresinisthendilutedinstyrenetoproducearesinwithasolidscontentofatleast50%.

    BADGEvinylestersareusedmainlyinhighperformanceapplicationssuchaschemicaltanksandpipes,thoughtheiruseinthemarineindustryisbecomingmorewidespread.

    ii)Epoxyphenolnovolactype(EPN)ThisformofvinylesterisareactionproductofEPNandmethacrylicacid,dilutedwithstyrenetoasolidscontentof30%to36%.

    EPNbasedvinylestershaveahighercross-linkdensitythanBADGEsystemswhichmakesthemsuitableformoredemandingapplications,mainlyinthechemicalplantindustry.

    Vinylesterresinshaveamolecularstructurewhichallowsthemtoreactmorecompletelythanpolyesters.Thisisduetothefactthatinvinylesterscross-linkingisterminal(ie.attheendsofthemolecularchain)ratherthanthroughoutthechainaswithunsaturatedpolyesters.

    Becauseofthisuniquestructure,vinylesterresinscanbeusedtoproducetoughlaminateswhicharehighlyresistanttowaterandaggressivechemicals.Theyalsoexhibitamorerapidcuredevelopmentwhichresultsinareductioninprint-throughonthelaminatesurface.Optimumperformanceisonlyachieved,however,bypostcuringlaminatesatveryhightemperatures(atleast100C).Laminatescuredatroomtemperaturewillhavesimilarphysicalpropertiestothosemadeusingahighperformancepolyesterresin.

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  • Phenolic ResinsPhenolicresinsarepolycondensatesofphenolsandaldehydes,orketonesandwerefirstdiscoveredinthelate19thcentury.Theuseofphenolicresinsinthecompositesindustryisrelativelysmall,thoughgrowingandthemostcommontypeusedisanaqueousresolephenolformaldehydesystem,whichcuresinthepresenceofanacidcatalyst.Phenolicsarebestsuitedtoapplicationsrequiringhighlevelsoffireretardancy,coupledwithlowsmokeemissionandlowtoxicity.

    Duetothenatureoftheresinandcatalystsystems,effectivehealthandsafetyproceduresandefficientventilation/extractionsystemsareveryimportantwhenusingphenolicresins.Crosscontaminationofpolyesterresinsshouldalsobeavoidedinordertopreventinhibitionoftheircure.

    Hybrid ResinsHybridresinsareproducedbyblendingorreactingtogetherresinsofdifferingtypes,inordertoimpartthebestpropertiesofeachtothenewendproduct.

    OnesuchseriesofresinsistheCrestomer rangewhichconsistsofurethaneacrylateresinsdissolvedinstyrenemonomer.Theurethanecomponentisfullyreactedintothemolecularbackbone.Thiscontributesadhesivepropertiesandflexibilitywithoutfreeisocyanatehazard,whilsttheacrylateunsaturationandstyrenemonomerimparttough,hard,thermosetcharacteristics.Thenovelstructureoftheseresinsmeanstheyarecompatiblewithandhandleaswellas,polyesterresinsandcanbecuredusingconventionalperoxidecuringagents.

    Urethaneacrylatesareusedasbaseresinsforformulatedrangesofadhesivesandhighperformancelaminatingsystems,andasadditionstounsaturatedpolyesterresins,toenhancetheperformanceofcompoundsandlaminates.

    Crestomer resinsandadhesivesexhibitexcellentadhesiontomanysubstrates,fibresandcuredlaminates.Theyaretough,resilientandflexible,withchemicalresistancepropertiessuperiortothoseofaconventionalflexiblepolyester.Thefillertoleranceofthematerialsishighandtheyarecompatiblewithpolyesterpigmentsandthixotropicadditives.

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  • 10

    Figure1-Derivationofcompoundsusedinthemanufactureofatypicalpolyesterresin.

    PETROLEUM

    MALEIC ANHYDRIDE

    MONOMERIC STYRENEUNSATURATED POLYESTER BASE

    UNSATURATED POLYESTER RESIN

    PHTHALIC ANHYDRIDE GLYCOLS

    BENZENEXYLENE

    ETHYLENE

    PROPYLENE

  • ReinforcementsTherearethreemaintypesofreinforcementusedinthecompositesindustrytoday;glassfibre,carbonfibreandpolyaramidfibre.

    Glass FibreThecommercialavailabilityoffine,consistentglassfibres,coupledwiththedevelopmentoflowpressurepolyesterresinsmarkedthebirthofthefibrereinforcedcompositesindustryoverfiftyyearsago.

    Glassisanidealreinforcingfibreforplastics.Itisoneofthestrongestofmaterials(theultimatetensilestrengthofafreshlydrawnsinglefilamentof9-15micronsdiameterisabout3.5GPa).Itsconstituentsarereadilyavailable,itisnon-combustibleandalsochemicallyresistant.Glassfibreisproducedbydrawingandrapidlycoolingmoltenglassandisavailableinavarietyoftypesandformats.Itsfinalformatwilldependonhowthedrawnglassisfurtherprocessed.

    Inthecompositesindustrytoday,E(Electrical)andC(Chemical)arethepredominantgradesofglassused.ThethreemostcommonEglassformatsare:i)Uni-directional(allfibresinonedirection)e.g.continuousrovings(UD)

    ii)Bi-directional(fibresat90toeachother)e.g.wovenroving(WR)

    iii)Random(fibresrandomlydistributed)e.g.choppedstrandmat(CSM)

    ThepredominantformatsforCglassareassurfacingtissues,whicharewidelyusedaschemicalbarriersandforaestheticpurposes.

    Developmentsinglassfibretechnologymeanthatglassreinforcementsarenowavailableinawidevarietyofstylesandformats,suitedtodiverseapplicationsinmanyindustrialsectors.

    Carbon FibreCarbonfibrereinforcementshavebeenavailabletothecompositesindustrysincethe1960swhenhighstrength,highmodulusfibreswerefirstdevelopedattheRoyalAircraftEstablishmentinFarnborough.

    Carbonfibresareproducedbycarbonisingafibreprecursoratatemperaturebetween1000Cand3500C.Themostcommonlyusedprecursorispolyacrylonitrile(PAN).Fibresbasedonother,cheaperprecursorsarecommerciallyavailablebuttheirpropertiestendtobeinferiortothoseofPANbasedfibres.Propertiessuchasdensityandelasticmodulusaredeterminedbythedegreeofcarbonisationemployedandcarbonfibrereinforcementsarenowavailabletomeetawiderangeofstrengthandstiffnessrequirements.

    Compositesmadeusinghighmodulus,uni-directionalcarbonfibrecanexceedthemodulusofsteel.Bi-directionalmaterialsaremorecommonlyused,however,toproducecompositestructurescapableofmeetingthestringentdemandsofhighperformanceapplicationssuchasthoseintheaerospaceindustry.

    Polyaramid FibresPolyaramid(AromaticEtherAmide),fibreswerediscoveredbyDuPontin1965.Theyareorganic,man-madefibres,whichhaveauniqueblendofproperties.Polyaramidfibresareflameresistant,chemicalandcorrosionresistantandhaveexcellentelectrical

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  • properties.Theirlightweight(density1.4-1.45)combinedwiththeirstrengthandmoduluscharacteristicsresultinspecificstrengthandspecificmodulusproperties,whicharesuperiortoallglassfibresandsomecarbonfibres.

    Therearetwomaingradesofpolyaramidfibre,onewithanelasticmodulussimilartothatofglassfibreandonewithanelasticmodulusdoublethatofglassfibre.Thelowermodulusmaterialisusedinballisticapplications,bothasdryfibreandasacomposite,whilstthehighermodulusmaterialistheonemostwidelyusedinthecompositesindustrytoday.

    Polyaramidfibresareusedtoproducecompositeswhicharelight-weightandincrediblystrong,withexcellentimpactproperties.Someofthem,however,exhibitlowcompressionstrengthwhichshouldbetakenintoconsiderationwherestructuresarelikelytobesubjectedtoflexureorcompressionloading.

    Glass Combination MaterialsManyglassfibrereinforcementsarenowavailableascombinationsofstylesandtypes,forinstancewovenrovingstitchedtoachoppedglassdeposit.Theseproductshavebeendevelopedtoamalgamatetheimprovedmechanicalpropertiesofawovenfabricwiththeeaseandspeedofapplicationofachoppedmatortissue.

    Non-wovencombinationmaterialsmadefromEglassarealsoavailable.Theseproducts,whicharecrimpfree,consistoflayersofreinforcementheldtogetherbyalightstitching.Theyaredesignedtomaximisedirectionalstrengthpropertiesandareavailableinbi-axial,tri-axialorquadri-axialformats,somewithachoppedglassbackingforeaseofuse.

    Hybrid Combination MaterialsReinforcementswhichcontainmorethanonefibretype,areknownashybrids.Themostcommonofthesearepolyaramid/glassandpolyaramid/carboncombinations,thoughcarbon/glasscombinationsarealsoavailable.Theuseofdifferentfibresinonereinforcementresultsinafabricwhichexhibitsalltheadvantagesofeachconstituentfibre,withnoneofthedisadvantages.Forinstance,theuseofapolyaramid/glassreinforcementwillproduceacompositewiththeimpactresistanceofpolyaramidfibresandthecompressivestrengthofglassfibres.

    Speciality MaterialsDevelopmentsinclosedmouldprocessessuchasRTMhaveresultedintheintroductionofspecialisedreinforcingmaterialswhichaddresstheneedforimprovedquality,speedandeaseofproduction.Thesematerialsareavailableinvariousforms,fromcontinuousfilamentmatstosophisticatedpre-formednet-shapes.Theuseofstitchedproductsisincreasingandastitchedmatspecificallydevelopedtooptimisethespeedandefficiencyofclosedmouldprocessesisnowavailable.Itconsistsofchoppedglassfibresstitchedtoeachsideofanon-wovensyntheticcoreandallowsalaminatethicknessupto6mmtobeachievedperlayerofmaterial.Theuniquestructureofthisproductmeansitispre-formablewhencold,easytotailorandpermitsexcellentresinflowthroughthemould.Todayscompositesindustryhasaccesstoaninfinitevarietyofreinforcementtypesandstyles.Thisenablesspecifiersanddesignerstocreatecompositestructurescapableofmeetingthemostdemandingofapplications.

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  • CureSystemsInordertoproduceamouldingorlaminateusingapolyesterresin,theresinmustbecured.Thisisachievedeitherbytheuseofacatalystandheating,oratroomtemperaturebyusingacatalystandanaccelerator.MostCrysticresinsaresuppliedpre-accelerated,incorporatinganacceleratorsystemdesignedtogivethemostsuitablecurecharacteristicsforthefabricator.Theseresinsneedonlytheadditionofacatalysttostartthecuringreactionatroomtemperature.Certainresinscannotbepre-accelerated,however,duetotheircurecharacteristicsandtheserequiretheadditionofbothanacceleratorandacatalysttoinitiatecure.

    N.B.Catalystsandacceleratorsmustneverbemixeddirectlytogethersincetheycanreactwithexplosiveviolence.

    Thosecatalystandacceleratorsystemsmostcommonlyusedinthecompositesindustryaredescribedinthissection.

    Catalysts Organicperoxidesarenormallyusedascatalystsinthecompositesindustry.Sincethesematerialsareunstableintheirpureform,theyaremixedwithaninertcompoundbeforebeingsuppliedcommercially.Thisprocessisknownasphlegmatisationandiscarriedoutduringmanufacture.Phlegmatisersareusuallyliquids(e.g.phthalates)orinertfillers(e.g.chalk)butothermediaaresometimesused.

    Thetypesofcatalystmostcommonlyused,particularlyinconjunctionwithpolyesterresins,areMethylEthylKetonePeroxide(MEKP),CyclohexanonePeroxide(CHP),AcetylAcetonePeroxide(AAP)andBenzoylPeroxide(BPO).

    MEKP CatalystsLiquiddispersionsofmethylethylketoneperoxidearemostwidelyusedincontactmouldingapplications(handlayorspray).Variousstandardgradesareavailable,differingonlyintheirreactivity*andactivity.

    *Reactivityandactivitymustnotbeconfused.Lowreactivitycatalystssimplyextendgeltime,whereaslowactivitycatalystscanresultinundercureifincorrectlyemployed.

    CHP CatalystsCyclohexanoneperoxidecatalystsareavailableaspowders,pastesandliquidsandareusedincontactmouldingapplicationswhereamoregradualcureisrequired.Inpasteform,CHPcatalystcanbemadeavailableintubes.

    AAP CatalystAcetylacetoneperoxidecatalystsareusedwherefastcuretimesarerequired.ThemainuseforAAPcatalystsisinapplicationswherefastmouldturn-roundisrequired,forexampleRTMandcoldpressmoulding.

    BPO CatalystMostbenzoylperoxidecatalystsaresuppliedaspowders,thoughpasteversionsandpourablesuspensionsarealsoavailable.Benzoylperoxidesaredesignedtocureatelevatedtemperatures(above80C),andtheyonlycureatroomtemperaturewhenusedinconjunctionwithatertiaryamineaccelerator.

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  • TBPO and TBPB CatalystsTertiarybutylperoctoateandtertiarybutylperbenzoatearecatalysttypescommonlyusedinheatcuringprocessessuchaspultrusionandhotpressmoulding.Theycanbeusedsingly,orincombinationwitheachother,toadjusttime/temperaturecurvestosuitspecificmouldingrequirements.

    Thecatalystsdescribedabovearethestandardmaterialsmostcommonlyusedinthecompositesindustry.Asthecompositesindustryhasdeveloped,curetechnologyhasalsoadvancedandcatalystsarenowavailableinawiderangeoftypes,withpropertiestailoredtosuitthemanyapplicationsandprocessescurrentlyinuse.

    AcceleratorsManychemicalcompoundswillactasacceleratorsforpolyesterresins,makingitpossibleforcatalysedresintocureatroomtemperature.Themostimportantofthesearethosebasedoncobaltsoapsoraromatictertiaryamines.

    Cobalt AcceleratorsCobaltacceleratorsconsistofvariousconcentrationsofcobaltsoap,usuallydissolvedinstyrene.Thestandardstrengthsusedare0.4%,1.0%and6.0%thoughotherconcentrationsareavailable.

    Amine AcceleratorsAmineacceleratorsarenormallyusedinconjunctionwithBenzoylPeroxidecatalysttoachieverapidcureatroomtemperature.Theyareusuallysuppliedassolutionsdissolvedinstyrene,phthalateorwhitespirit.

    Itisessentialtochoosethecorrectcuresystemandtousethecorrectlevel.Ifmanufacturersformulationsareusedunderrecommendedconditions,thecuredresinwillachieveitsmaximumstrength,durability,chemicalresistanceandstability,ensuringthatthefinalmouldingwillattainoptimumproperties.

    FillersWhenmineralfillerswerefirstintroducedtothecompositesindustryitwasasameansofreducingcost.Atthattime,excessivelyhighloadingswereusedandthisresultedinaseriousdeteriorationinthemechanicalstrengthandchemicalresistanceofmouldingsproduced.

    Today,theeffectsoffillersarebetterunderstoodandtheyareusedtoenhanceandimprovecertainpropertiesofaresin.Filledresinsexhibitlowerexothermandshrinkagecharacteristicsthanunfilledsystems,andtheytendtobestiffer,thoughmorebrittle.Thelevelofcostreductionachievablebytheuseoffillersisnolongerasignificantfactor.

    Therangeoffillersavailableisnowwideandvariedandsomeofthosemostcommonlyusedaredescribedoverleaf.

    14

  • Calcium Carbonate Surfacetreatedcalciumcarbonatefillers,particularlycrystallinetypes,arewidelyused,especiallywherelowerexothermtemperaturesandlowershrinkagearedesirable(e.g.castingormouldmakingapplications).

    TalcMagnesitictalcsareusedtoincreasebulkandreduceexothermtemperature,usuallyincastingapplications.

    Metal PowdersFinemetalpowderscanbeaddedtocatalysedpolyesterresintoproducerealisticmetalliccastings.Aluminium,brass,bronzeandcopperpowdersareallreadilyavailable.

    SilicaHydrophilicfumedsilicaisusedtoimpartthixotropytopolyesterresins.Ahighshearmixerisrequiredtoensureadequatedispersion.

    MicrospheresHollowmicrospheresareavailableinglassandthermoplasticform.GlassmicrospheresareproducedfromEglass,whilstpolypropyleneisthemostcommonrawmaterialforthethermoplasticspheres.Microspherestrapairinasphericalshell,sowhenincorporatedintoaresinmix,theyincreasevolume,reduceweightandreduceshrinkage.Polyesterputties,andculturedmarblearetwoapplicationswheremicrospheresareusedtoenhancethepropertiesofthefinishedproduct.

    Alumina trihydrateAluminatrihydrateisaflameretardantfillerusedtoimprovethefireresistanceofpolyesterresins.ATHisnon-toxic,supressessmokeproductionandimpedesburning.Althoughitsprimaryuseisasafireretardant,thetranslucentnatureofATHmakesitidealforuseincastingandsyntheticmarbleoronyxproduction.Specificgradesareavailablefortheseapplications.

    15

  • PigmentsMostpolyestergelcoatsandresinscanbesuppliedpre-pigmented,butpigmentpastesareavailabletoenablethefabricatortocolourtohisownrequirements.

    Crysticpolyesterpigmentpastesarespeciallyformulatedforuseinpolyestergelcoatsandresinsandconsistoffinepigmentpowdersdispersedinamediumwhichcross-linksintothebaseresinduringcuring.Recommendedadditionlevelsarebetween8%and10%forgelcoatsand4%to5%forbackingresins.

    Toensurecolourreproducibility,itisimportantthatallsub-assembliesofmulti-componentmouldingsaremanufacturedusingthesamemixofpigmentedmaterial.

    ReleaseAgentsReleaseagentsareanintegralpartofthecompositemouldingprocessandarevitaltothesuccessfulproductionofhighqualityFRPcomponents.Thechoiceofreleaseagentwillbeinfluencedbyvariousfactorssuchasmouldsizeandcomplexity,mouldingnumbers,surfacefinishrequirements,etc.Selectingtherightoneisveryimportantinensuringqualityandconsistencyinthefinishedproduct.

    Themostcommontypesofreleaseagentaredescribedinthissection.

    Polyvinyl AlcoholPolyvinylalcoholisavailableinconcentratedform,orasasolutioninwaterorsolvent.Itcanbesuppliedcolouredorcolourlessandappliedbycloth,spongeorspray.

    Polyvinylalcohol-basedreleaseagentsarenormallyusedforsmallmouldingswithasimpleshape,orasasecondaryreleaseagentandaresuitableforuseonmetalandFRPcompositemoulds.

    Careshouldbetakenwhenusingpolyvinylalcohol-basedreleaseagentinverticalsections.Becauseitislowinviscosityitwilldraindownandaccumulateincornerswhereitmaytakealongtimetodry.Ifamouldingislaidupbeforeanysuchareasaredry,itwillalmostcertainlystick,causingdamagetothemould.

    WaxWaxwasfirstusedasareleaseagentinthecompositesindustryinthe1950s.Carnaubawax-basedproductsarethemostsuitableforusewithcompositematerialsandthesearewidelyemployed,particularlyincontactmouldingapplications.

    Siliconemodifiedproductscanbeusedbutcarehastobeexercisedassiliconecaninterferewiththereleaseinterfacemakingseparationdifficult.Anysilicone-basedreleaseagentsshouldbethoroughlytestedbeforeuse.

    Waxreleaseagentsareavailableinseveralformsbutthosemostcommonlyusedarepastesorliquids.Amongtheadvantagesofwaxreleaseagentsaretheireaseofuse,convenienceandeconomy.Waxesareusedmostlyinlowvolumecontactmouldingapplications,astheneedforregularre-applicationcanbetimeconsuming.Thereisalsothepotentialforproblems,createdbywaxbuild-upandtransfer.

    Semi-permanent Systems

    16

  • Whenappliedtoreleaseagents,thetermsemi-permanentusuallyreferstothoseproductswhichfunctionbydepositingamicro-thinfilmonthesurfaceofthemould.Theyusuallyconsistofapolymericresininacarriersolventandonceappliedtoamouldsurfacethesolventevaporatesleavingaresininterface.

    Semi-permanentreleaseagentsallowmultiplereleasesfrommoulds,makingthemidealforhighvolumeproductionprocessessuchasresintransfermoulding(RTM).Thereisnobuild-uportransferofreleaseagent,sotheneedforcleaningofmouldsand/ormouldingsisreducedtoaminimum.Itisvitalwhenusingtheseuniquereleasesystemsthatthemouldsurfaceisperfectlycleantoensuregoodfilmformationandpropercureofthereleasecoating.

    Wax / Semi-permanent HybridsThesematerialsnormallyconsistofawaxamalgamatedwithasemi-permanentreleaseagent.Theycombinetheeaseofuseofawaxwiththemulti-releasecharacteristicsofasemi-permanentsystem.

    Aswithsemi-permanentreleaseagents,wax/semi-permanenthybridsrequiremouldsurfacestobeperfectlycleanbeforeuseiftheyaretobeeffective.

    Release FilmCellophaneorpolyesterfilmisusedasareleasemedium.Itisnotsuitableforcomplexshapesbutisanidealsystemforuseinthemanufactureofcompositesheetingordecorativeflatpanels.

    Internal Release AgentsInternalreleaseagentsareusedmainlyinhighvolume,mechanisedprocessessuchaspultrusion,RTMandSMC/DMChotpressmoulding.Asuitableproductisdissolvedintheresinmixandduringprocessingitmigratestothesurfaceandformsabarrierbetweentheresinandthemould.

    CoreMaterialsLowdensitycorematerialsareusedinthemanufactureofFRPcompositecomponentstoincreasestiffnesswithoutincreasingweight.Theycanbeemployedinspecificareasofastructurewhereextrastiffnessisrequired(e.g.boathullribs),orthroughouttheareaofalaminatetoproducewhatisknownasasandwichpanel.

    Therearetwocategoriesofcorematerial;structuralandnon-structuralandsomeofthemorecommonlyusedtypesaredescribedinthissection.

    Two-Component Polyurethane FoamThetwocomponentsofthismaterialaremixed1:1byvolumetoproducearigidpolyurethanefoam.Thefoamexpandsrapidlytoapproximately25timesitsoriginalvolumeandisusedinbuoyancyandgeneralgap-fillingapplications.

    Polyurethane Foam SheetSheetsofrigid,closedcellpolyurethanefoamcanbeusedasacoreinsandwichconstruction,orformakingformers.Itisnormallyusedinnon-structuralapplications,thoughstructuralgradesareavailableforuseinfastproductionprocesses.Groovedpolyurethanefoamsheetisalsoavailable.Thisisusedasanon-structuralcoreinapplicationswhereconformitytocurvedsurfacesisrequired.

    17

  • PVC Foam Closedcell,linearandcross-linkedPVCfoamsareusedasstructuralcoresinmarine,transport,buildingandmanyotherapplications.Theyaretough,rigidmaterialsandtheirhighstrengthandstiffnesstoweightratiomakesthemidealfortheproductionoflightweightsandwichpanels.

    Theyareavailableasplainsheets,perforatedsheetsandalsoasscrimcloths(squaresoffoambondedtoaglassfibrescrim).

    Polyetherimide FoamPolyetherimidefoamsareusedwhereresistancetofireisimportant.Theydonotburn,producenegligibleamountsoftoxicgasandsmokeandmaintaintheirpropertiesattemperaturesupto180C.

    Styrene Acrylonitrile FoamThismaterialcombineshighstrengthandstiffnesswithlowwaterabsorptionandlowcreepvalues,makingitidealforuseinoffshorebuoyancyapplications.

    Balsa WoodEnd-grainbalsawoodhasbeenusedasacorematerialformanyyears.Classifiedasahardwood,balsahasaveryhighstrengthtoweightratioandcanbeusedinstructuralornon-structuralapplications.

    Asanon-synthetic(ie.natural)product,balsacanbeinconsistentindensityandunlessitiskilndried,itsmoisturecontentcancauseproblems.Itisalsogenerallymoredensethanmostfoamcorematerials.

    Honeycomb CoresHoneycombcoresaremanufacturedfromavarietyofplasticandmetalmaterialsandareusedtoproducecompositestructureswithextremelyhighstrengthtoweightratios.

    Twocommontypesofhoneycombcorearealuminiumandphenoliccoated,polyaramidfibrepaperswhicharebothusedextensivelyintheproductionofcomponentsfortheaerospaceindustry.

    Non-Woven Core MaterialsNon-wovencoresarechemicallybondedmaterialsimpregnatedwithmicro-spheres.Thesematerialsproducelaminateswithhighstiffnesstoweightratiosandhighimpactandshearresistance.

    Theyareeasytouse,withexcellentdrapabilityandconformabilityandarecompatiblewithmostunsaturatedpolyesterresinsystems.

    Asecondaryadvantageofthesematerialsisthepreventionofprint-through,whichisachievedduetoimprovedresindistributionandlackofshrinkageinthecorematerial.

    Adhesives

    18

  • Thedevelopementofadhesivematerialsspecificallydesignedforapplicationsinthecompositesindustryhasresultedinamarkedincreaseintheiruse.Adhesivesarenowavailabletofulfilmostrequirements,fromrelativelysimplebondingfunctionsthroughtotechnicallydemandingstructuralapplications.

    Therearefourmainadhesivetechnologiesemployedintodayscompositesindustry.Allofthesearedescribedinthissection,togetherwithScottBadersuniqueCrestomerrangeofadhesives.

    Polyester ResinsCrysticpolyesterresinsareusedtoproducebondingpasteswhichareviscous,filledcompoundsdesignedfortheassemblyandbondingofFRPmouldings.Theyareusedinmainlynon-structuralorsemi-structuralapplicationssuchasinternalframes,ribs,hulltodeckassembliesandcarcomponents,togivemoderatelyhighshearstrengthswithouttheneedformechanicalfixings.

    Epoxy ResinsEpoxyresinsareusedtoproducestructuraladhesivessuitableformanyapplications.Epoxybasedadhesiveswillbondawiderangeofsubstratesincludingcomposites,metals,ceramicsandrubber.Theycanbeformulatedtoimpartheatandchemicalresistanceandtoexhibitgapfillingandotherrequiredproperties.Adhesivesbasedonepoxyresinsarecapableofachievingveryhighshearstrengthsandareusedextensivelyinstructuralbondingapplicationsintheaircraftindustry.

    Acrylic (Methacrylate) ResinsAdhesivesbasedonmethacrylatesaretough,resilientmaterialswithhighshear,peelandimpactstrengths.Theycanbeformulatedtobondtomanysubstratesandtooperateoveranextensivetemperaturerange.Veryshortcuretimesareachievablewiththisclassofadhesive,thusallowingfastturn-roundtimes.

    Polyurethane ResinsMostpolyurethanebasedadhesivesaremoisturecuringmaterials.Theyareextremelyflexibleandadheretoawidevarietyofsubstrates.Acombinationofhighpeelstrengthandmoderateshearstrengthmakestheseadhesivessuitableforuseinvariedapplicationsfromsealingtostructuralbonding.

    Crestomer (Urethane Acrylate) ResinsTheadhesivepropertiesofCrestomermaterialsareduetothenovelstructureofthebaseurethaneacrylateresin.Theurethanecomponentisfullyreactedintothemolecularbackbone,contributingadhesivepropertiesandflexibilitywithoutisocyanatehazard.Theacrylateunsaturationandstyrenemonomerimparttough,hardthermosetcharacteristics.Crestomeradhesivesthereforeexhibitexcellentadhesiontosubstratessuchasfoamandbalsacorematerials,curedcompositesandmetals.TheCrestomerrangeistailoredforspecialistadhesiveandconstructionrequirementssuchasstructuralandsemi-structuralbonding,filleting,corebondingandgapfilling.

    RecentdevelopmentsinCrestomertechnologymeanthisuniqueadhesivesystemisnowavailableincartridgeform,withvariouscureoptions,thusextendingevenfurtheritsareasofapplication.

    MouldMakingMaterialsandAncillaryProductsManymouldmakingmethodsareemployedwithinthecompositesindustry,dependingonthenatureofthefinishedproduct,andeachmethodrequiresitsownsupplementarymaterials.Thediversenature

    19

  • ofproducts,processesandmanufacturingmethodscreatesaneedforanextensiverangeofancillarymaterials.

    Thissectiondealswitharangeofancillaryitemsavailabletomaximisethemanufactureandqualityofcompositeproducts.

    Flexible Mould Making Materials Thesecompoundsarewidelyusedinthedecorativecastingindustryandtherearethreemaintypesavailable:i) LatexRubber:-Thisiscommonlyused,indippingform,toproducesmallresincastingssuchas chesspieces.

    ii) Vinyl-basedSyntheticRubber:-Vinyl-basedsyntheticrubbersareavailableinsolidformandare meltedinapurposedesignedmeltingpot.Thegradeuseddependsontherequirementsofthe finishedproduct,withadurablegradeforlimitedproductionrunsandaflexiblegradeforcomplex originals.Mouldscanbecutupandmelteddownforre-use.

    iii) ColdCureSiliconeRubber:-Thismaterialisusedtoproducedurable,highdefinitionmoulds withexcellentreproductionoffinedetail.Itisatwopartsystemcomprisingabaseandacatalyst andisidealforlongerproductionruns.Thixotropicadditivesareavailabletoconvertthematerial fromapourableliquidtoabutter-onform,ifrequired.

    Plaster and Clay MaterialsHighstrengthmouldplastersareusedtoproducerigidmouldsforlimitedproductionruns.Itisimportantthatplastermouldsaresealedandhavesuitablereleaseagentsapplied,beforeuse.

    Highstrengthclays,whichcanbeovenhardened,arecommonlyusedtoproducedetailedformers,whilstgeneralpurposemodellingclaysareusedfortemporaryfillingandfilletingapplications.

    Waxisalsowidelyused,insheetandfilletform,inmouldproduction.

    Composite Mould Making MaterialsContactmouldingisthemostcommonlyusedmethodofcompositeproductionandthemouldsusedinthisprocessarenormallythemselvesproducedfromcompositematerials.Aseparatesectionhas,therefore,beendevotedtothesubjectofmaterialsandprocessesforcompositemouldmanufacture(seeMouldMakingSection).

    Polishing Compounds and Associated ProductsTheappearanceofafibrereinforcedcompositeproductcanbegreatlyenhancedbypolishingthesurfaceafterreleasefromthemould.

    Polishingcompoundsandtheirassociatedproductsdesignedspecificallyforusewithcompositesarenowwidelyavailable.Theseincludecompoundsforhandandmachineapplication,polishingclothsandbonnetsandfinishingglazes.

    20

  • PROCESSES

    OpenMouldProcessesThedevelopment,inthe1950s,ofresinswhichcuredinthepresenceofairledtotheintroductionofcontactmouldingprocesses,whichstilldominatemanyareasofthecompositesindustry.

    21

  • Contactmouldingisaparticularlyadaptablemethodofmanufacturingcompositecomponentsofallshapes,sizesandcomplexityforrelativelylittlecapitalinvestment.Onlyonemouldisneededandthiscanbemaleorfemale,dependingonwhichfaceofthemouldingneedstobesmooth.

    Therearethreemaintechniquesusedincontactmoulding,thesebeinghandlay-up,spraylay-upandrollersaturator.Whichevertechniqueisemployedtoproduceacontactmouldedpart,theconstructionofthemouldplaysavitalroleindeterminingthequalityofthefinishedcomponent.Forthisreason,acompletesectionisdevotedtomaterialsandproceduresformouldmaking,laterinthishandbook.

    GelcoatingThedurabilityofacompositemouldingisverydependentonthequalityofitsexposedsurface.Protectionofthesurfaceisachievedbyprovidingaresinrichlayer,whichnormallytakestheformofagelcoat.Specialcaremustbetakenintheformulationandapplicationofthegelcoat,asitisaveryimportantpartofthelaminateandisalsothemostvulnerablepart.

    Thoroughmixingofthegelcoatisextremelyimportant,particularlywhenaddingcatalyst,asinadequatecatalystdispersionwillresultinunevencureofthegelcoat,whichmayimpairitsphysicalproperties.Poormixingofpigmentwillresultinsurfaceimperfectionswhichwilldetractfromtheappearanceofthemoulding,soitisrecommendedthatpre-pigmentedgelcoatsareusedwhereverpossible.Theuseoflowshearmechanicalstirrershelpstominimiseanypotentialmixingproblems.

    Gelcoatcanbeappliedbybrushorspray,thoughdevelopmentsingelcoattechnologyandsprayequipmenthavecombinedtomarkedlyincreasetheuseofsprayapplicationmethods.Whicheverapplicationmethodischosen,itisimportanttouseagelcoatfromtheCrysticrange,speciallyformulatedwiththecorrectrheologyforthatmethod.Thevarioustypesofsprayequipmentavailablearedescribedlaterinthissection.Foroptimumperformance,itisimportanttocontrolthegelcoatthicknessto0.4mm-0.5mmandasaguide,450g-600g/m2ofgelcoatmixturewillgivetherequiredthickness.Ifthegelcoatistoothinitmaynotcurefullyandthepatternofthereinforcingfibremayshowthroughfromthebackinglaminate.Thingelcoatsarealsopronetosolventattackfromtheresinusedinthebackinglaminateandthiscanresultingelcoatwrinkling.Ifthegelcoatistoothick,itmaycrackorcrazeandwillbemoresensitivetoimpactdamage,particularlyfromthereversesideofthelaminate.Agelcoatofuneventhicknesswillcureatdifferentratesoveritssurface.Thiscausesstressestobesetupintheresinwhichmayleadtocrazingor,inthecaseofpigmentedgelcoats,apatchyappearanceandwatermarking.

    Full,evencureisvitalifagelcoatistoachieveoptimumperformance,soitisimportantthatcureconditionsandsystemsarecontrolled.Workshopandmaterialtemperaturesshouldbemaintainedataminimumof18CandamediumreactivityMEKPcatalystshouldalwaysbeused,ata2%additionlevel.Indeepmouldsthecureofagelcoatcanbeinhibitedbytheaccumulationofevaporatedstyrenefumes.Extractionofthesefumesis,therefore,necessarytoensureevengelationofthegelcoat.

    Oncethegelcoathascuredsufficiently,thenextstepinthecontactmouldingprocessistoapplythebackinglaminate.Asimpletesttoassessthestateofcureofthegelcoatistogentlytouchthesurfacewithacleanfinger.Ifthesurfacefeelsslightlytacky,butthefingerremainsclean,thenthegelcoatisreadyforlaminating,whichshouldcommencewithinfivehours.

    LaminatingHand Lay-UpChoppedstrandglassfibrematisthereinforcementmostcommonlyusedincontactmoulding,thoughthe

    22

  • useofwovenandvariouscombinationmaterialshasgrownconsiderablyovertheyears.Thepreparationofreinforcementpacks,specificallytailoredtothemouldbeingused,savestimeandreduceswastage.

    Theamountofresinrequiredforalaminatecanbecalculatedbyweighingthereinforcementtobeused.Forchoppedstrandmattheresintoglassratioshouldbebetween2.3:1and1.8:1(30%to35%glasscontent).Resintoglassratiosofapproximately1to1(50%glasscontent)arenormalforwovenroving,whilstthoseachievablewithcombinationreinforcementswillvarydependingontheconstructionoftheparticularfabricused.Oncethegelcoathascuredsufficiently,aliberalcoatofresinisappliedasevenlyaspossible.Thefirstlayerofglassisthenpressedfirmlyintoplaceandconsolidatedusingabrushorroller.Thisactionwillenabletheresintoimpregnatetheglassmatanddissolvethebinderwhichholdsthefibrestogether.Thereinforcementwillthenconformreadilytothecontoursofthemould.Oncethefirstlayerofmatisfullyimpregnated,furtherresincanbeadded,ifnecessary,beforeapplyingsubsequentlayersofreinforcement.Itisimportantthatthefirstlayerisasfreeofairbubblesaspossible,asanyairtrappedimmediatelybehindthegelcoatcouldleadtoblistering,shouldthemouldingbeexposedtoheatorwaterduringitsworkinglife.

    Impregnationofthereinforcementcanbecarriedoutusingabrush,oramohairorpolyesterroller.Ifabrushisused,itshouldbeworkedwithastipplingaction,asanysidewaysbrushingmotionwilldisplacethefibresanddestroytheirrandomnature.Theuseofrollersisadvantageouswhenworkingonlargemouldsandtheyareavailablewithlongorshortpile.Longpilerollerspickupmoreresinthanshortpileones,butcareneedstobetakentoaccuratelycontrolresintoglassratios.Consolidationofthelaminateismoreeffectiveifcarriedoutusingarollerandseveraltypeshavebeendevelopedforthepurpose.Metalpaddle,discorfinrollersareavailable,andofthese,thinfintypeshaveprovedparticularlyeffectiveinremovingairbubblestrappedintheresin.

    Subsequentlayersofresinandreinforcementareapplieduntiltherequiredthicknesshasbeenachieved,ensuringthateachlayeristhoroughlyimpregnatedandproperlyconsolidated.Itisrecommendedthatnomorethanfourlayersofresinandreinforcementareappliedatanyonetime,topreventthebuildupofexcessiveexotherm.Highexothermtemperaturescanleadtogelcoatcracking,pre-release,distortionorscorchingofthelaminate.Wherethicklaminatesarerequired,eachseriesoffourlayersshouldbeallowedtoexotherm,thencool,beforesubsequentlayersareapplied,thoughlengthydelaysshouldbeavoided\unlessaresinwithalonggreenstageisused.Greenstageisthetermusedtodescribetheperiodbetweengelationandcureoftheresin,duringwhichtimeitisinasoft,rubberystate.Inthiscondition,thelaminatecanbeeasilytrimmedtothedimensionsofthemouldandtrimedgescanbebuiltintothemouldtofacilitatethisoperation.

    Shouldamouldingneedtobestrengthened,thiscanbeachievedbyincorporatingreinforcingribsintothelaminate.Thestageatwhichtheribsareputintopositionwilldependontheshape,thicknessandenduseofthemoulding,thoughasageneralguide,itisbesttolocatethemimmediatelybeforethelastlayerofreinforcementisapplied.Theribformersshouldbecoveredwithreinforcingmatandthoroughlyimpregnatedwithresin.Thefinallayerofreinforcementcanthenbeappliedoverthewholeareaofthemouldingtogiveauniformappearancetothebacksurface.

    Metalinsertsaresometimesnecessary,aslocatingorfixingpoints,etc.andthesecanbeputintoplaceduringthelaminatingoperation.Ifaninsertislikelytobesubjectedtoaheavyload,thethicknessofthemouldingshouldbetaperedawayfromtheinsert,inordertospreadtheload.Insertsshouldbepositionedasneartothemiddleofthelaminateaspossibleandthecontactareabetweenlaminateandinsertshouldbeaslargeaspracticable.Todayscompositesmanufacturersbenefitfromtheavailabilityofawiderangeofmetalfastenersandinsertsspeciallydevelopedfortheindustry.ThedevelopmentofadhesivesystemsintheCrestomerrangemeansthatmetalinsertscannowbebondeddirectlyintolaminates,thusreducingproductiontimes.

    23

  • Wherepiecesofreinforcementrequirejoiningtocoverthesurfaceofamould,buttorlapjointscanbeused.Buttjointsshouldbemadewithcaresothatnospaceisleftbetweenthetwoedgesandlapjointsshouldnotoverlapbymorethan25mm(unlessrequiredforstiffening).Joinsinchoppedstrandmatcanbemadelessconspicuousbyspreadingtheexcessmatoneithersidebyrotatingabrushinsmallcirclesalongthelineofthejoin.

    Thebacksurfaceofamouldingcanberathercoarseinappearance,particularlyifchoppedstrandmatisthereinforcementused.Thiscanbeimprovedinoneoftwoways;eitherbyincorporatingasurfacetissueasthefinallayerofthelaminatetogiveasmoother,resinrichsurface,orbycoatingthesurface,onceithascured,withaformulatedflowcoatsuchasthatintheCrysticrange.Theuseofaflowcoatgivestheaddedadvantagethatitcanbepigmentedifrequired.

    Spray Lay-upThistechniqueinvolvestheuseofaspraygunforthesimultaneousdepositionofchoppedglassandcatalysedresinontothesurfaceofamould.

    Achopperunitattachedtothespraygunchopsglassrovingsintospecifiedlengths(usuallybetween20mmand50mm),andthechoppedstrandsarethendirectedtowardsastreamofcatalysedresinasitexitsthespraygun.ThoseresinsintheCrysticrangewhicharedesignedforsprayapplicationaregenerallylowinviscosity,sotheyrapidlywetoutthechoppedstrands.Thisensurestheyaremoreeasilyatomisedintothedesiredspraypattern.Therapidwet-outachievedbyspraydepositionallowsfasterandeasierconsolidationthanwouldbeachievedwithhandlaymethods,butthoroughrollingofthelaminateisstillnecessarytoensurecompleteairremoval.Theefficiencyofthecatalystdispersionintheresincanalsobecheckedatthisstage.Ifusingresinswhichincorporateacolourchangemechanismoncatalystaddition,orcatalystswhichcontaincoloureddyes,theuniformityofcatalystdispersioncanbeeasilymonitored.

    Manycommercialsprayingsystemsarenowavailablebutduetotheirhigheroutputandconvenience,pumpedsystemsaremorecommonthantheolderpressurepotequipment,particularlyfortheproductionoflargermouldings.

    SprayEquipmentPumped SystemsTherearethreeprincipalpumpedsystems,asfollows:-

    24

  • 1) Airless AtomisationCompressedairisusedtooperatepumpswhichtransferresinorgelcoatfromtheiroriginalcontainerstothespraygun.Catalystisthenintroducedeitherwithinthegun(internalmix)orimmediatelyafteritleavesthegun(externalmix).Thegelcoatorresinisforcedthroughasmallspraytipathighpressureinordertoatomisethematerialandproduceafan.Compressedairisnotuseddirectlytoatomisethematerial,hencethetermairlessatomisation.Thepressureonthegelcoatcanvarybetween57bar(800psi)and214bar(3000psi),dependingonthetypeofequipmentused.Catalystismeteredintotheresinstreambyeitheracatalystpumplinkedtotheresinpump,orfromacatalystpressuretank.

    2) Air Assisted AirlessThissystemisavariantoftheairlesssystemwhichcombinesconventionalairatomisationandairlesstechniquestoallowtheuseofloweratomisingpressures(typically28.5barto57baror400psito800psi).Thegelcoatispumpedatrelativelylowpressureandatomisingairisintroducedthroughamodifiedspraytipinordertorefinethespraypatternandeliminatefingering,etc.Thelowerpumppressuresusedinthissystemcanreduceoutputcomparedtoastandardairlesssystem,butporosityintheappliedgelcoatfilmtendstobelowerandstyreneemissionsarereduced.

    3) HVLP SystemsHighvolume,lowpressurespraygunshavebeenusedforsometimeinthepaintindustrybutarerelativelynewforgelcoatapplication.Thesesystemsutilisehighvolumesofairatlowpressure(typically0.7baror10psiorless),inordertoatomisegelcoatswithminimalstyreneemission.

    Othertypesofsprayequipmentcommonlyusedaregravityfed,siphonandpressurepotsystems.

    Gravity Fed SystemsInthismethod,acontainerholdingcatalysed,acceleratedmaterialisattachedtoanindustrialspraygunfittedwithasuitablenozzle.Thecontainerisheldabovethegunandflowsintoitundergravity.Becauseoftheirthixotropicnature,gelcoatsappliedusingthismethodtendtofeatureacoarse,orangepeeleffectontheirbacksurfaceandoutputisratherslow.Theequipmentrequireslittlecleaningandmaintenance,however,socanbeusefulforapplyinggelcoattosmallmoulds,particularlyiffrequentcolourchangesarerequired.

    Siphon GunsTheuseofspraygunswhichoperatebythesiphonsystemisnormallyrestrictedtotheapplicationofgelcoatinminorrepairwork.Thisisduetothefactthatoutputisratherslowbecauseofthethixotropicnatureofthematerial.

    Pressure Pot SystemsInthissystem,materialisheldinapressurevessel.Itisforcedtothespraygunatlowpressure(typically2.1barto3.5baror30psito50psi),whereitisatomisedbyaseparateairstream.Atomisationcantakeplacewithinthegun,butitismorecommonlyexternaltothegunasthematerialexitsthespraytip.

    25

  • Atomisingpressuresgenerallyrangefrom3.5barto5.0bar(50psito70psi).

    Pressurepotsystemsproducesmoother,moreuniformfilmsatafasterratethangravityfedorsiphonsystems,butaresignificantlyslowerandlessconvenientthanpumpedsystems,particularlywherelargemouldsareinvolved.Forexample,wherethecatalystisaddedtothegelcoatinthepressurepot(hotpotsystems),productionrunsarelimitedbytheworkinglifeofthematerial,asitisessentialtospraythemouldandcleantheequipmentwithinthistime.However,thesesystemsarerelativelysimpletooperateandmaintainandcanbeusefulforsmalltomediumsizedmouldswhereregularcolourchangesarerequired.

    Airless,airassistedairlessandHVLPcatalystinjectionsystemsemployinginternalorexternalcatalystmixingmeanthatsprayequipmentisavailabletomeetthediverseneedsofindividualusers.Unitscapableofmultiplecolourgelcoatsprayingarealsoreadilyavailable.

    Althoughsprayingdoesnotsolvealltheproblemsinherentinhandlaycontactmoulding,itisnowwidelyusedthroughoutthecompositesindustry.Inthehandsofaskilledoperatormosttypesofsprayequipmentwillsignificantlyincreaseoutputcomparedwithhandapplication.

    Roller/Saturator Lay-upRoller/Saturatorequipmentisdesignedtosaturateglassreinforcementssuchaschoppedstrandmat,clothorwovenrovingswithactivatedresin.Theresinisheldinacontainerandpumpedasrequiredtoarollerhead.

    Itisrelativelyeasytocontroltheresintoglassratioofalaminateusingthismethodandsignificantlylessstyreneisreleasedintotheatmosphereduringlaminatingoperations.

    Theuseofaroller/saturatorisidealforlargemouldingssuchasbuildingpanelsandlargeradiusboathulls,etc.

    Themouldingmethodspreviouslydescribedinthissectionareallcoldcuringprocessessothelaminatesproducedcantakeseveralhourstomature.Itispossibletoacceleratethecuringprocessbyapplyingamoderateamountofheattothemoulding,takingcaretoraisethetemperatureslowlytoavoidstyreneevaporationorblistering.

    Forgelcoats,thetemperatureshouldberaisedto30-35Cmeasuredonthemouldand,oncethegelcoathasgelled,itmaybenecessarytoallowthemouldtocoolbeforeproceedingwiththebackinglaminate.Oncelaminatingiscomplete,thetemperaturecanberaisedagain,butitshouldnotexceed35Cbeforegelation.Aftergelation,thetemperaturecanbeincreasedgraduallyto60Candmaintainedforaboutonehour.Themouldingshouldthenbeallowedtocoolbacktoambienttemperaturebeforeremovalfromthemould.

    Mould ReleaseProvidedthemouldreleaseagenthasbeencorrectlyapplied,releaseshouldbeafairlysimpleoperation.Theedgeofthemouldingshouldbeeasedawayfromthemouldusingplasticwedgesdesignedforthispurposeandthenadirectpullwillusuallyeffectreleaseofthemoulding.Withmoredifficultshapestheuseofcompressedairbetweenthemouldandthemouldingwillassistreleaseandcompressedairpointscanbebuiltintothemouldduringitsconstruction.Boathullsandmouldingsofsimilarshapecanbeseparatedbyrunningwaterslowlybetweenthemouldingandthemould,providedawatersolublereleaseagenthasbeenused.Onlarge,thickmoulds,itmaybenecessarytostrikeafewcarefulblowswitharubbermalletontheoutsidesurfaceofthemould.Thisshould,howeverbealastresortasitcanresultincrackingofthemouldsurface.

    Ifasplitmouldhasbeenused,screworhydraulicjackscanbeemployedtoparttheseparatepieces.The

    26

  • mouldflangesmustbeheavilyreinforcedandseveraljacksused,toensurethatevenforceisappliedoverthelengthoftheflanges.

    Post CuringContactmouldedlaminatescantakeseveralweekstofullymatureatambienttemperaturebutthisperiodcanbereducedbypostcuringatelevatedtemperatures.Bestresultsareobtainedbyallowingthemouldingtostabilisefor24hoursatambienttemperatureandthenpostcuringforeither3hoursat80C,8hoursat60C,12hoursat50Cor16hoursat40C.Thesetimesandtemperaturesareforgeneralguidanceonlyandwheremouldingsaretobeusedforwaterorchemicalcontainment,differentconditionsmayapply.

    Trimming and FinishingProductiontimecanbesavedifmouldingsaretrimmedwhiletheresinisstillatthegreenstage.Thisoperationisbestcarriedoutusingasharptrimmingknifewhichisheldatrightanglestothelaminate,thoughscissorscanbeused.Ifsuitablyreinforced,theedgeofthemouldcanbeusedasatrimmingguide,butcareshouldbetakennottodistortordelaminatethemouldingatthisstage.

    Fullycuredcompositelaminatesaredifficulttocutormachineusingconventionalsteeltools.Waterjetandlaserjetcuttersarenowreadilyavailableforlargescalemachiningofcomposites,butforsmalleroperationsafullrangeofportablediamondorcarbidetippedcuttersanddrillsisavailable.Manyoftheseoperatebymeansofcompressedair,makingthemsafeforuseintheworkshop.Thehealthandsafetyaspectsofhandlingandmachiningcompositematerialsaredealtwithinaseparatesectionlaterinthishandbook.

    Oncealltrimmingoperationsarecomplete,anyreleaseagentshouldberemovedfromthesurfaceofthemouldingpriortobuffingandpolishing.Whereamouldingistobepainted,waxreleaseagentsshouldbeavoidedastheyaredifficulttoremovewithouttheuseofwetordryrubbingpaper.Mostpaintsystemscanbeusedwithcompositesbut,forstovingfinishes,itisrecommendedthatthemouldingispostcuredat80Cbeforeapplyingthepaint.Specialprimers,designedtoachieveexcellentadhesiontogelcoatedsurfaces,areavailableandtheiruseisrecommendedfordurability.SandablegelcoatsintheCrysticrangehavealsobeendevelopedspecificallytoenhancethepaintabilityofcompositemouldings.

    ClosedMouldProcessesFormanyyears,contactmouldinghasbeenthepredominantmethodofmanufacturingcompositecomponents.Whilstitisaparticularlyadaptableprocess,legislativeandcommercialpressuresaremakingitlesscosteffectiveasaproductionmethod.

    Manyclosedmouldprocesses,whichaddresstheenvironmentalandquality/consistencyissuesinherentinopenmouldmethods,arenowavailabletocompositemoulders.Thesecoverawiderangeofproductionandtechnicalneeds,fromrelativelylowvolume,lowcapitalcostthroughtohighlyautomated,largevolume,highinvestmentprocesses.

    Vacuum Infusion : VIThisprocesscanbeintroducedtoamouldingshopwithminimuminvestment.Existingopenmouldscanbeusedwithlittleornomodification,andtheprocessisadaptabletolargeorsmallcomponents.

    27

  • 28

    IntheVIprocess,dryreinforcementsareencapsulatedbetweenarigid,airtightmouldandaflexiblemembrane(vacuumfilmorbag)whichissealedaroundtheedgeofthemould.Thisformsacavitywhichisthenplacedundervacuumtocompactthereinforcement.

    Catalysedresinisintroducedintothecavityandthevacuumpullsitthroughthereinforcement.Oncethecomponentisfullyinfused,itisallowedtocure,afterwhichthebagandthecomponentareremovedfromthemould.

    ResinsforuseintheVIprocessneedtobelowinviscosityandmayalsorequirecontrolledexothermproperties,forlargersectionsorthickercomponents.

    ThereareseveralvariantsoftheVIprocess,themostsignificantofwhichisprobablytheSCRIMPsystemdevelopedbyWilliamSeemanintheUnitedStatesofAmerica.

    Vacuum Assisted Resin Transfer : VacFlo

    Vacuum Assisted Resin Transfer : VacFloVacFloisaresintransferprocessthatfeaturesmuchofthesimplicityofVIandmanyofthebenefitsofconventionalRTMwithoutincurringtheassociatedhighcostsofinjectionmachineryandsubstantialtooling.VacFloisoperatedbyapplyingagelcoattooneorbothmouldfacesasrequired,placingthereinforcementsandanycorematerialsinthelowertoolandclosingthemould.Avacuum(approx.1baror14psi)ispulledbetweenthedoublesealaroundtheperimeterofthemould,effectivelyclampingthetwohalvestogether.Asecondvacuum(approx.0.5baror7psi)isthenpulledinthecavityofthetoolusingacentrallyplacedvacuumport.Catalysedresinisintroducedviaaninjectionportattheedgeofthepart.Theresinmaybedrawninusingvacuumonly,orbyusingacombinationofvacuumandinjectionunderpressure.Astheresinentersthecavityitflowsaroundtheperimeterandthenintothecentreofthetool.Oncethemouldisfull,injectionisstoppedandthemouldisheldundervacuumuntiltheresinhasgelled.Whencured,thepartisde-moulded.

    TheVacFlosystemwillworkwithVIorRTMresins,sothemouldercanselectmaterialsfromtheCrysticrangetobestsuithisconditions.

    Resin Transfer Moulding : RTMDevelopmentsinmaterials,machineandtoolingtechnologieshaveenabledtheRTMprocesstobecomehighlyefficientforbothsmallandlargecomponentsandshortorlongproductionruns.

    ThebasicRTMprocessinvolvespre-loadingamouldcavitywithdry,continuousreinforcement,closingthecavityandinjectingacatalysedresin.Oncetheresinhaswet-outthereinforcementandhascured

    Vacuum InfusionGelcoat

    Reinforcement

    Core material (with holes punched through)

    Peripheral channel

    Mould

    Vacuum take-off point

  • sufficiently,thecavityisopenedandthepartremoved.RTMtoolscanbemanufacturedfromcompositesor,formaximumdurability,frommetals.Thetoolsmayoperateatroomtemperatureorincorporateaheatingsystemforoptimumproduction.

    TheRTMprocessisnowwidelyacceptedinthecompositesindustryasaneffectivemethodofmanufacturingpartsrangingfromaerospaceapplicationsthroughtolandtransport,marineandbuildingandconstruction.ForRTMitisvitalthatthegelandcurecharacteristicsofaresincanbetailoredtosuitparticularmouldcycletimes.

    Cold/Warm Press MouldingThistechniqueinvolvestheuseofapairofmatchedtoolswhicharemountedinapress.Thetoolsareoftenconstructedfromcompositesandareeitherusedatroomtemperature,ormodesttemperaturesupto60C.

    Tooperatetheprocess,agelcoatisappliedtotherequiredmouldface(normallythefemalehalf).

    Oncethegelcoatissufficientlycured,thereinforcementisputinplace.Finally,therequiredamountofcatalysedresinispouredintothemouldandthetoolsareclosed.

    Asthemouldhalvesarecompressedtogether,theresinisforcedtoflowthroughthecavityandwetoutthereinforcement.Byusingapinch-offaroundtheperimeterofthetool,itispossibletoallowairtoventwhilestillcreatingsufficientbackpressuretoensuretheresinfillsallareasofthecavity.

    Itispossibletousevacuumtodrawthemouldstogetherandactasthepress,inwhichcasenoexternal

    29

    Vacuum on

    Resin flow

    Resin inlet tube passing through vacuum bag

    VacFlo

    Peripheral channel. Used to clamp both mould halves together

    Upper mould half

    Vacuum (1 bar)

    Vacuum (0.5 bar)Resin Inlet port

    Flexible Seals

    Lower mould half

  • pressisnecessaryandthemouldscanbelightweightandsemi-rigid.

    ResinrequirementsforpressmouldingaresimilartothoseforRTM,thoughincertaincircumstancesthegeometryofthepartrequiresamorethixotropicproduct.Resins,reinforcementsandassociatedproductsintheCrysticrangearespecificallydesignedtoenablemoulderstooptimisewhicheverclosedmouldprocessischosen.

    Althoughclosedmouldtechniquesgenerallyrequiremorecapitalinvestmentthancontactmouldingmethods,theyhavemanyadvantages.Qualitycanbemorecloselycontrolledandcloserdimensional

    tolerancesachieved,leadingtomechanicalpropertieswhicharemoreconsistentandeasiertoaccuratelypredict.Oneofthegreatestbenefitsofclosedmouldsystems,however,istheirimpactontheenvironment,asstyreneemissionsduringmouldingcanbevirtuallyeliminatedbyusingtheseprocesses.

    HotMouldProcessesHotpressmouldingtechniquesareusedforhighvolumeproductionofcompositecomponents.Theprincipleoftheprocessisthatreinforcementandacontrolledquantityofcatalysedresinareenclosedandcuredbetweenheated,polished,matchedmetalmoulds.Ahydraulicpressisusedtobringthemouldstogetherunderpressureattemperaturesbetween100Cand170C.Cycletimes,whicharedependentontemperature,mouldingcomplexityandweight,aregenerallybetween2and4minutesbutcanbeaslowas30seconds.

    Thesameequipmentcanbeusedtoproducecomponentsbywetmouldingorbytheuseofmouldingcompoundsorpre-pregs.

    Wet MouldingDryreinforcementisplacedintothemouldandcatalysedresinpouredontoit.Theresiniscatalysedusingacuringagentwhichisactivatedbytheheatofthemouldbutisstableatambienttemperature.Thehydraulicpressurecreatedbytheclosureofthemouldforcestheresinthroughthereinforcementandintothepinchoffarea,thusensuringtotalwetoutofthereinforcingfibre.Pressureisreleasedoncecurehastakenplaceandthecomponentisthenremovedfromthemould.

    Wherethewetmouldingtechniqueisused,itispossibletopre-formglassreinforcementbeforeputtingitintothepress.Choppedrovingsaresuckedorblownontoafinemeshshapedtotherightcontours.Whenthedesiredthicknessofreinforcementisachieved,thepre-formissprayedwithbindertoholdthestrandstogether,thenovenheatedfor2-3minutesatatemperatureof150C.Thepre-formisthenreadyforthe

    30

    RTMMould seals (one or two can be used)

    Upper tool

    Supporting structure

    Supportingstructureclamped together

    Supporting structure

    Lower tool

    Cavity containing reinforcement

    Resininjection

    port

  • press.

    Moulding CompoundsTodayscompositesindustryemployshotpresstechniquesmainlytoproducecomponentsfrompolyestermouldingcompoundssuppliedtothemoulderinreadytouseform.

    Dough Moulding Compound (DMC)ThisisadoughlikemixturenormallybasedonpolyesterresinandEglassfibres.GeneralpurposeDMCsusecalciumcarbonateasthefiller,thoughotherfillersmaybeusedtoobtainspecificpropertiesrequiredinthemoulding.Thereinforcingfibrelengthisnormallybetween3mmand12mmandthefibrecontentofafinishedmouldingwouldbebetween15%and20%.

    Bulk Moulding Compound (BMC)BMCissimilarinappearancetoDMCbutisformulatedtoproducemouldingsofimprovedqualityandfinish.Isophthalicresinsareusedastheseexhibitbetterhotstrengthandstabilityandlowprofileadditivesmaybeincorporatedtoimprovesurfacefinish.

    N.B.Whenmouldingcompoundswerefirstdeveloped,themaindifferencebetweenBMCandDMCwasthatBMCcontainedachemicalthickener(e.g.MgO),whereasDMCwasunthickened.Today,mostmouldingcompoundsareunthickenedandthetwotermsareinterchangeable.ThetermDMCisusedextensivelyintheUKandUSA,withBMCbeingusedexclusivelyinmostofEurope.

    Sheet Moulding Compound (SMC)SMCconsistsofEglassreinforcementimpregnatedwithcatalysedpolyesterresincontainingvariousfillers.Itissuppliedinsheetformsandwichedbetweentwopolyethyleneorpolyamidefilms.

    TomouldSMC,sufficientpiecesofthesheetmaterialarecuttobetween40%and80%ofthesurfaceareaofthemouldinordertomakeupthedesiredweightofthefinishedmoulding.Thepiecesarestrippedoftheirprotectivefilmandplacedinthemouldwheretheapplicationofheatandpressurewillcausethecompoundtoflowthroughoutthetoolcavity.Thishomogeneousflowoccursevenwhenthemouldhasdeepdrawareasorsectionalchangesandgivesaconstantresin:glassratiothroughoutthemoulding.Thisallowscomplexpartsincludingthosewithribs,bossesandchangesinsectiontobemanufactured.SMCproducesmouldingswithexcellentdimensionalstability,highmechanicalproperties,goodchemicalresistanceandelectricalinsulation.MinimalshrinkgradesofSMCareavailable,andthesecanbeusedtoachieveasuperiorsurfacefinishforpostpainting.SMCisthereforesuitablefortheproductionofautomotivebodyparts,electricalhousings,chemicaltraysetc.

    Low Pressure Moulding Compound (Crystic Impreg) CrysticImpregissimilartoSMCbutusesanovel,patentedtechnologytophysicallythickenthecompoundduringmanufacture,ratherthantheconventionalmethodofchemicalthickeningusingareactivefiller.

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  • CrysticImpregcanbemouldedusingmuchlowerpressuresthanSMC.Foroptimumresults,themouldingprocessrequiresapressureof5-25barandatemperatureofbetween110Cand150C,whichwillgiveacycletimeof2-10minutesdependingonpartsizeandcomplexity.

    CrysticImpregLPMCcanbemouldedwithgreatconsistencyimmediatelyaftermanufacture,usingrelativelylowcapitalcostpressesandutilisingtoolsproducedfromawiderangeofmaterials.Itsuniquechemicalmake-upallowsmanydifferentgradestobepreparedforuseinvariousapplicationsincludingtheautomotiveindustry.Thismeansthatfeaturessuchasshrinkcontrol,fireresistance,improvedtoughnessandwaterresistancecanbeincorporated,thustailoringthematerialtosuitenduserrequirements.

    ContinuousProcessesContinuousprocessesareusedtoproducecompositecomponentssuchassheetingandpipes,whicharesuitedtolong,uninterruptedproductionruns.Severalcontinuousprocessesaredescribedinthissection.

    PultrusionThepultrusionprocessisusedtoproducecompositesofuniformcross-sectionwithexceptionallongitudinalstrengthandrigidity.Theprocesswasfirstusedinthe1950stoproducesimpleitemssuchasrodstock.Sincethen,developmentsinprocessandmaterialtechnologymeanthathighlycomplexprofilesofconsiderabledimensionscannowbemanufacturedusingthismethod.Expressedsimply,theprocessinvolvesdrawingreinforcements,impregnatedwithactivatedresinthroughaformingguide,whichpre-shapesthematerial.Usingcontinuousrovings,whichareusuallythepredominantreinforcementpresent,thematerialispulledthroughaheateddie,whichactivatesthecatalyst,thuscuringtheresin.Thecuredprofilethenpassesaflyingsawattachmentandisautomaticallycuttotherequiredlength.Thereinforcementiswettedouteitherbytheuseofaresinbath,orbyresininjectionatthefrontofthedie.Theresinbathsystemisstillthemostcommon,thoughresininjectionisgaininginpopularityandismoreenvironmentallyfriendlyasitdrasticallyreducesstyreneemissions.

    Thecuringsystemusedinthepultrusionprocessusuallyconsistsofacombinationofperoxides.Ahighlyreactiveperoxide,knownasakicker,isusedforinitialcure,incombinationwithmediumorlowreactivityperoxidestoachieveamoregradualthroughcure.Thisdualsystemensuresthatprofilesachieveoptimalcure,withlowresidualstyrenecontents.

    Thecuredprofileispulledthroughthedieusingeitherreciprocatingpullersoracontinuouscaterpillartracksystem.Thereinforcementmostcommonlyusedinthepultrusionprocessisglass,thoughcarbonandpolyaramidfibrescanalsobeusedsuccessfully.Resinsystemsforpultrusionincludepolyesters,vinylesters,epoxiesandmethacrylatedresins,withpolyestersbeingthemostcommon.

    PultrusionresinsintheCrysticrangearedesignedtoachievethebalanceofpropertiesnecessarytooptimisetheprocess.

    Filament WindingThefilamentwindingprocessisbasedonasimplebasicprinciple.Itconsistsofimpregnatingreinforcingfibreswithactivatedresin,thenwindingthemontoarotatingmandrel.Successivelayersofreinforcementarebuiltuponthemandreluntiltherequiredthicknessisachieved.Thereinforcementcanbewoundlongitudinally,circumferentially,helically,orinacombinationoftwoormoreofthese.Thepropertiesrequiredfromthefinishedarticlewilloftendeterminetheangleofwind.

    32

  • Themandrel,thoughnormallyofsteel,maybemadefromavarietyofmaterials,andpressurised,flexiblemandrelsareoftenutilisedinthemanufactureofcertaintypesofcylindricalvessels.InthecaseofcompositecomponentsusingPVC,polypropylene,etc.asaliningmaterial,theprefabricatedlinertakestheplaceofthemandrel.

    Continuousrovingsaregenerallyusedinthisprocessthoughotherformsofreinforcementsuchaswoventapescanbeincorporated.Glass,carbonandpolyaramidfibrescanallbeusedsuccessfully.Glassandthermoplasticveilsareoftenincludedwhereresinrichcorrosionbarriersarerequired.

    Polyester,vinylesterandepoxyresinsareallsuitableforuseinthefilamentwindingprocess,resinchoicebeingdependentontherequirementsofaspecificapplication.

    Filamentwindingisanidealprocessforthefabricationofcylindricalcompositeproductsandiswidelyusedfortheproductionoflargetanks,processvessels,ductingandpipescapableofmeetingstringentperformancerequirements.

    PullwindingPullwindingisaprocesswhichcombinespultrusionwithfilamentwindingandisusedtoproducethinwall,hollowcompositeprofileswhichexhibithighstrengthproperties.

    Reinforcements,impregnatedwithactivatedresin,arewoundontoamandrel,whichisthenpulledthroughaheateddie.Asinconventionalfilamentwinding,thereinforcement,whichisnormallyaroving,canbewoundinoneormoreofseveraldirections.

    Thoseresinsandreinforcementssuitableforfilamentwindingandpultrusioncanalsobeusedinpullwinding.

    Centrifugal MouldingThisprocessisusedtomouldtubes,pipesandcylinderswithamaximumdiameterof5metres.Choppedrovingorglassmatislaidinsideahollowmandrelandimpregnatedwithactivated,normallypolyester,resin.Themandrelisthenheatedandrotateduntiltheresincures.Thisprocesscreatescentrifugalforce,whichactstoconsolidatethelaminate.Un-reinforcedcastresinsheetcanalsobeproducedusingthecentrifugalmouldingmethod.

    ResinsfromtheCrysticrange,whichweredevelopedforuseinthefilamentwindingprocess,arealsosuitableforcentrifugalmoulding.

    Machine Made SheetingMostofthecompositecorrugatedsheetingmanufacturedtodayisproducedusingmachines.Thereareseveralpatentedmachineprocesses,allofwhicharesimilarinprinciple.

    Acontinuouslengthofreleasefilm,usuallypolyester,travelsalongamovingconveyorandglassfibreisfedontoit.Activatedpolyesterresinisthenmeteredontotheglassandafurtherlayerofreleasefilmaddedtocompleteaglass/resinsandwich.

    Thesandwichpassesunderaseriesofrollerswhichconsolidatethelaminate,controlitsthicknessandexpelanyair.Thelaminateisthenpassedintoaheatedformingareaonthemachineandcorrugatedbymeansofdiesorrollers.Heatcanbeappliedinthisareabymeansofanenclosedoven,orbyaseriesofheatlampssuspendedabovethesurface.Oncethelaminateisformedandcured,itistrimmedtothe

    33

  • correctwidthandthencuttothedesiredlength,usuallybymeansofanautomaticsaw.

    Eglassisalwaysusedinthemachinemanufactureoftransparentcompositesheeting,eitherinmatformorasrandomlydepositedchoppedrovings.ThisisbecausetherefractiveindexofEglasscanbematchedbyspecialisedpolyesterresinstoproducesheetingofhighclarity.

    Someoftodaysautomatedsheetingmanufactureutilisesultraviolet(UV)lighttocurethelaminate,soCrysticresinswithspeciallydesignedcuringmechanismshavebeendevelopedtomeetthisneed.

    ResinsintheCrysticrangeareavailabletoenablethemachineproductionofcompositesheetingwitharangeofpropertiesincludinglowfirehazard,goodweatheringandhighclarity.

    APPLICATIONS

    34

  • Un-reinforcedPolyesterResinThishandbookismostlyconcernedwiththeapplicationofpolyesterresinsinthefibrereinforcedcompositesindustry.However,polyesterresinsarealsowidelyusedinun-reinforcedapplications,someofwhicharedescribedinthissection.

    Body FillerPolyesterbasedcompoundsareusedextensivelyforthecosmeticrepairofvehiclebodies,torectifydamagedcompositemouldingsandformanyotherrepair/refurbishmentapplicationswhererapidcompletionisimportant.Thesecompoundsarealsoideallysuitedtotheproductionofformulatedwoodfillersandplasterfillers.

    CrysticStopperisaformulatedmaterialwhichconsistsofaliquidresinbaseandafillerpowder.Whenthesearemixedtogetherintherecommendedproportionstheyformapaste,whichcuresatroomtemperature.Thepasteiseasytoapplywithgoodtrowellingpropertiesandrapidcurecharacteristics.Itprovidesahard,rigidfilling,whichcanbemechanicallysandedwithoutclogging.Thismaterialisideallysuitedtothedo-it-yourselfmarket.

    Crysticresinsforformulatorstocompoundintobodyfillersaredesignedtoachievetheidealcombinationofstoragestabilitywithoptimumcuringproperties.Thepropertiesrequiredfromtheformulatedcompoundareachievedbyvaryingthecombinationandtypeoffillerused.Thiscanbeacomplexprocess,aspurity,softness,particlesizeandsizedistributionofthefillerwillallaffecttheperformanceof

    35

  • thefinalsystem.

    Flexibilityinthecuredcompoundisimportanttoensuregoodadhesionandtoimpartoptimumfinishingandsandingcharacteristics.Thelevelofflexibilityislargelydeterminedbytheresinconstituentofthecompoundandcanbetailoredbyincorporatingoneormoreresinsofdifferentflexibilityintotheformulation.Advancesinresinformulationandproductiontechniqueshaveenabledbodyfillertechnologytoprogresstomeetthedemandsofthistechnicallyorientedapplication.

    Button CastingPolyesterresinshave,formanyyears,beenusedtomanufacturebuttons.Therearethreemainmethodsofmanufacturedependingonthetypeofbuttonbeingproduced.

    Pearlbuttonsaregenerallymanufacturedfromresinpigmentedwithnaturalorsyntheticpearlessence.Thepigmentedresiniscastintosheets,normallybycentrifugalcastingmethods.Thebuttonsaretheneitherblankedfromthesheetsbeforetheyarefullycured,ortrepannedfromtotallycuredsheetsandfinallymachinedandpolished.

    Plainbuttonscanbemanufacturedfromrodstock.Resiniscastintotubesmadefromsuitablematerialssuchaspolyurethane.Thebuttonsarecutfromtheresultingrodstockattherequiredthickness,machinedandpolishedonthecutsurfaces.Variouseffects(e.g.tortoiseshell)canbeachievedbytheuseoftwoormorecolouredpigmentsaddedtotheresin.

    Large,decorativeortexturedbuttonsareusuallymouldedindividuallyinmulti-cavitysiliconerubbermouldsattachedtoamovingbelt.Resinispouredintothemoulds,thebeltisvibratedtoremoveairandthenpassesthroughanoventoheatcuretheresin.Littleornomachiningisrequiredwiththismethodofmanufacture.

    Embedding and PottingGlassclearpolyesterresinscanbeusedforembeddingobjectstoproducepaperweightsandotherdecorativeitems,orforpreservingmedicalandbotanicalspecimens.Theseresinscanalsobeusedveryeffectivelyintheproductionofcostumejewellery.

    TheexcellentdielectricpropertiesandcuringcharacteristicsofcertainCrysticresinsmakesthemidealforencapsulatingelectroniccomponents.Theserangefromsinglecapacitorstocompleteminiaturisedcircuits.

    Decorative CastingPolyesterresinsarewidelyusedinthemanufactureofdecorativearticlessuchasstatuettes,figurines,modelsandreplicas,etc.

    Expressedsimply,thecastingprocessinvolvesmixinganinertfillerpowderintoaresin,pouringthemixintoamouldandleavingittocure.

    Selfreleasing,flexiblemouldcompoundsaremostcommonlyusedforcastingpurposes.Thethreemaintypesofmouldingcompoundarelatexrubber,hotmeltvinylrubberandcoldcuresiliconerubber.

    Thechoiceoffillerpowderfordecorativecastingdependstoalargeextentonthefinalfinishrequired.

    36

  • Ifthecastingistobepigmentedorpostpainted,thenthefillerisneededonlytobulkouttheresinandcalciumcarbonateortalccanbeused.Aluminatrihydratewillproducecastingswithasemi-translucentfinishreminiscentofmarble,whilstmarbleflouritselfcanalsobeusedtoachievethisaffect.

    Powderedmetalsusedasfillersresultincastingswitharealisticmetalfinish.Bronze,copper,aluminiumandbrasspowdersareallavailableandtheycanalsobemixedtogethertocreatedifferentmetalliceffects.Forinstance,mixingaluminiumandasmallquantityofbrasswillproduceagoodsimulationofold,tarnishedsilver.Metalliccastingsmustbebuffedandpolishedafterremovalfromthemouldinordertoproducetherealisticmetalsheen.

    GeneralpurposeandspecialisedpolyesterresinsintheCrysticrangehavebeendevelopedtocaterforallaspectsofthedecorativecastingindustry.

    Polyurethaneresinsarealsousedfordecorativecasting,astheyproducestrong,durablecastingswithveryhighdefinitionandexcellentreproductionoffinedetail.Theyareeasytomixandmeasureandfinishedcastingscanbepaintedusingenamel,acrylic,andoilpaints.Polyurethanesarewidelyusedinthecommercialmanufactureofhighqualitymodelkits.

    FlooringSpeciallyformulatedCrysticpolyesterresinshave,formanyyears,beenusedtoproduceseamlessindustrialanddecorativeflooringsystems.Whenproperlylaidandcuredonsuitablypreparedsubstratestheyhaveoutstandingresistancetoawiderangeofchemicalenvironments.Polyesterfloorshaveanattractive,aestheticfinish,whichisdurable,hygienicandeasytocleanandmaintain.

    Polyesterflooringsystemsgenerallyconsistofthreecomponentresins,thesebeingaprimer,abasecoatandatopcoatorglaze.Theprimerisformulatedtoprovideadhesiontosuitablypreparedsubstrates,thebasecoatisaclearresinwhichcanbepigmentedandfilledandthetopcoatisaclearresinusedtosealtheflooringsystemandprovidetheaestheticfinish.

    Polyester ConcreteResinbasedconcretecanbeanattractive,lighterweightalternativetocementbasedconcretepre-castingsandnaturalslate.Developmentsinresintechnologycoupledwithextensivefieldexperience,hasenabledarangeofpreviouslycementbasedconcretestructurestobepre-castwithresinaggregatecompositions.Withsuitableresin,filler,aggregateandpigmentsarangeofpre-castings,includingcladdings,tilesandsimulatedslatescanbemanufacturedwithattractive,durablefinishes.

    Resinconcreteformulationsforpre-castingsarepreparedbymixinganactivatedpolyesterresinwithappropriatefillersandaggregatestosuitspecificapplications.Forexample,asyntheticslatecanbeproducedfrompolyesterresinsfilledwithslatepowderandotherfillers.Artificialstonecanbeproducedeitherbyreconstitutingnaturalgroundstoneorbyusingstandardfillerswithsuitablepigments.Polyestersystems,suchasCrysticresins,offergreaterversatilitythanotherpolymersbecausetheircurecharacteristicscanbeadjustedwithoutseriouslyaffectingthepropertiesofthefinishedproduct.Finishedpre-castings,properlycured,aredurablewhenexposedtonaturalweatheringandtheirpropertiescanbeoptimisedtomaximiseresistancetoparticularenvironments.Otherbenefitsofpolyesterpre-castingsincludeimprovedimpactandmechanicalproperties,finemouldreproduction,fastsettingandrapidpropertydevelopment.

    Polyester Marble and Onyx

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  • Simulatedmarbleandonyx,producedusingpolyesterresins,areusedtomanufacturebasins,vanityunits,profiledpanels,etc.Claddingpanelsforwalls,stairsandcolumnsarealsoattractivelyproducedinthesematerials.

    Simulatedmarbleismanufacturedbymixinganactivatedpolyesterresinwithasuitablegradeofpowderedfillersuchascalciumcarbonate(typically75%byweight).Smalladditionse.g.2%to5%byweight,oflightweightglassbubblesaresometimesaddedtoimprovethehotandcoldwatercycleresistanceofthematerial,therebyreducingthecalciumcarbonatecontent.

    Simulatedonyxisusuallylighterincolourandmoretranslucentthansimulatedmarble.Colourismorecriticalandformulationsarenormallybasedonaluminatrihydrate(typically67%byweight)orglazedfrits(typically75%byweight).

    Whenabasecolourisrequired,pigmentpastesaremixedintotheresin.Thevariegatedeffectisachievedbypartiallymixinginpigmentswhicharedispersedinanincompatiblemedium,andusingartisticjudgementtodevelopandreproducethedesiredmarbleoronyxeffect.Theapplicationofacleargelcoattothemouldbeforepouringinthefilledresinmixgivesanaddedin-depthlustretothefinishedarticle.

    Solid SurfacesFibrereinforcedunsaturatedpolyesterresinshavebeenusedinbuildingapplicationsformanyyears.Recentdevelopmentsingranite-effectsurfaceshavecreatednewpotentialfortheiruseindecorativefinishesforindustrialanddomesticapplications.

    Solidsurfacecastingsaremanufacturedusinghighquality,Iso-NPGpolyesterresinssuchasthoseintheCrysticrange,containingcoloured,unsaturatedorsaturatedpolyesterbasedchipsandanaluminatrihydratefiller.

    Resinbasedsolidsurfacematerialscanbemixedandmouldedusingvacuum,sodonotrequireagelcoattoachieveagoodsurfacefinish.Thismeansthatthesurfacecanbere-polished,whennecessary,torestoretheoriginalshowroomgloss.Solidsurfacecastingsareeasytomachineandcanberoutedtoenabledifferentcolourstobeinlaid,thusallowinganinfiniterangeofdecorativefinishes.Solidsurfacecastingsaretoughanddurableandexhibitexcellentwaterandheatresistance.Thesepropertiesmeantheyareideallysuitedforkitchensurfaces,sanitarywareandwashrooms.Theexcellentweatherandchemicalresistantqualitiesofthebaseresinusedinsolidsurfacetechnologycreatesthepotentialforitsuseinexternalcladdingapplications.

    Rock AnchorsRockanchorsareusedinmining,civilengineeringandbuilding/constructionapplications,toprovidestrongpointsforbolts/rebars.

    Resinsforrockanchorsneedtobalanceverylongstoragestabilitywiththeapparentlyconflictingrequirementofveryrapidcure.Arangeofgeltimescanbeobtained,varyingfromafewsecondstoseveralhours,dependingontheparticularcuresystemused.

    Themostimportantmechanicalpropertyrequiredfromarockanchoriscompressionstrength,thoughgoodadhesionisalsoimportant.

    Fillersforuseinrockanchorsarecrucialintermsoftheirpull-outpropertiesandstoragestability.Thosecommonlyusedvaryfromlargesilicapieces,whichliterallyfloatintheresin,tofinelyground

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  • limestone.Thetypeoffillerusedwilldependontheapplication.Fillerpurityisimportant,asthiscanaffectthepropertiesoftheanchor.Itisadvisabletoavoidfillerswithhighcontentsoftransitionmetalssuchasironandcobalt,asthesecanadverselyaffectstoragestability.

    Cartridgeorsausagepackagingiscommonlyusedforrockanchorsinthecivilengineeringandminingindustries.Theresinissealedinastyreneresistantplasticsuchasnylon,andaglasstubeorplasticfilmcontainingcatalystisincorporatedwithinthepackage.Theactionoffixingtheboltorrebarintoplacemixesthecatalyst,whichisdispensedatasetratio(commonly10:1).

    RockanchorresinsfromtheCrysticrangearetailoredtomeetthedemandingrequirementsofthisapplication.

    ChemicalContainmentCompositeshavebeenusedformanyyearstomanufactureproductsforresistanceto,andthesafecontainmentof,awiderangeofchemicals.

    ChemicalresistantFRPcompositesgenerallyconsistofhightensilestrengthglassfibreprotectedbyachemicallyresistantunsaturatedpolyesterresin.Figures2and3giveexamplesofthespecifictensilepropertiesachievablewithglassfibrereinforcedpolyesterlaminates,incomparisonwithsteelandaluminium.TheeaseofuseandversatilityofFRPfacilitatesthecost-effectivemanufactureofawiderangeofcomponents,usingavarietyofmanufacturingprocesses.TypicalmaterialandfabricationcostsareshowninFigure4.

    Compositestructuresoffermanybenefitsoveralternativematerials,inchemicalcontainmentapplications.Theyarelightweightsosimplifyhandlingandinstallation.Beingselfcoloured,theyneednore-paintingandareeasilycleanedusingahighpressurehose.Ifnecessary,compositestructurescanbemodifiedin-situ,withminimuminterruptionofnormaloperations.TheabilityofaresintoresistaparticularchemicalenvironmentisnormallyclassifiedintermsofitsMaximumOperatingTemperature.InthecaseofchemicalresistantCrysticresinbasedlaminates,these

    temperatureshavebeendeterminedfromanumberofsourcesincludingcasehistories,laboratorytestsandpracticalexperience.

    Providedthatthecompositestructureismanufacturedtohighstandardsandfullypostcured,manyyearssatisfactoryserviceisachievable.ChemicaltanksshouldalwaysbedesignedinaccordancewiththerequirementsofBritishStandard4994:1987,whichusestheKfactorofsafetyapproach.(AnewEuropeanStandard,prEN13121,iscurrentlybeingdevelopedandwilleventuallyreplaceBS4994:1987).

    Inacidenvironments,GRPcansufferprematuredegradationduetostresscorrosioncrackingoftheglassfibrereinforcement.Itisthereforeimportanttoensurethatthestructurallaminateisadequatelyprotectedbyasubstantialbarrierlayer.Thiscanconsistofathermoplasticliner,orseveralmillimetresthicknessofGRPmadeusingCglassorsyntheticsurfacetissueandahighlyresinrichEglasslaminate.Therecommendedbarrierlayershouldbebackedwithanappropriateresin,reinforcedwithanacidresistantglasssuchasECR(ExtraChemicalResistant)glass.

    PolyesterresinsfromtheCrysticrangeareusedtomanufactureawiderangeofproductsandcomponentsforthesafecontainmentofmostmaterialsfromacidstoalkalis,fuelstofoodstuffsandwatertowine.

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  • Pipesand PipeLining

    40

    E-GlassWR/UPAluminiumAlloy

    MPaSG

    Steel

    120

    160

    80

    40

    0

    Figure2-SpecificTensil