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Welding Metallurgy & Weld Ability of Metals

Apr 06, 2018

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    WELDING METALLURGY

    AND

    WELDABILITY OF METALS

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    IT IS ESTIMATED THAT THERE ARE MORE THAN

    40,000 METALLIC ALLOYS CURRENTLYIN USE.

    THIS LARGE NUMBER OF METALLIC ALLOYS

    OFTEN MAKE IT DIFFICULT:

    - TO IDENTIFY THE PARTICULAR TYPE ON HAND,

    AND,

    - TO IDENTIFY THE WELDING TASKS THAT ARE

    FIT FOR PURPOSE IN ALL KINDS OF SERVICE.

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    CRITERIA IN INITIAL SCREENING OF METALLIC

    ALLOYS AND THEIR WELDABILITY:

    PERFORMANCE REQUIREMENTS:

    - WHAT IS IT?

    - WHAT DOES IT DO?- HOW DOES IT DO IT?

    WELDABILITY REQUIREMENTS

    RELIABILITY REQUIREMENTS

    RESISTANCE TO SERVICE CONDITIONS

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    GENERAL CLASSIFICATION OF METALLIC

    ALLOYS:

    FERROUS IRON-BASED

    NON-FERROUS NON-IRON-BASED

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    FERROUS METALLIC ALLOYS:

    STEELS ACCOUNT FOR OVER 60%OF THE METALLIC ALLOYS USED

    IN THE INDUSTRY

    CAST IRONS

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    NON-FERROUS METALLIC ALLOYS FOR

    MAJOR INDUSTRIAL APPLICATIONS:

    NICKEL ALLOYS

    TITANIUM ALLOYS

    COPPER ALLOYS

    ALUMINUM ALLOYS

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    3 BASIC TYPES OF PLAIN CARBON STEELS:

    LOW-CARBON STEELS ( MILD STEELS )

    < 0.2% C

    MEDIUM-CARBON STEELS

    ~ 0.5% C

    HIGH-CARBON STEELS

    ~ 0.8% C

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    PREPARING AMETALLOGRAPHIC SPECIMEN

    FOR MICROSTRUCTURE ANALYSIS

    CUT A SECTION OF THE METALLIC ALLOYS FORMICROSTRUCTURE ANALYSIS.

    GRIND THE SPECIMEN IN SUCCESSIVELY FINERSILICON CARBIDE ABRASIVE GRITS OF 120 / 320 /600 / 1200.

    POLISH THE FINELY GROUND SPECIMEN ONNAPPED POLISHING CLOTHS IN, FIRST,COLLOIDAL CHROMIUM OXIDE SUSPENSION,THEN, IN COLLOIDAL ALUMINUM OXIDESUSPENSION.

    DIP THE BUFFED SPECIMEN IN A 3% NITRICACID SOLUTION.

    THE SPECIMEN IS NOW READY TO BE VIEWEDUNDER A METALLOGRAPHIC MICROSCOPE.

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    THE ETCHED SPECIMEN CAN NOW BE VIEWEDUNDER AN OPTICAL METALLOGRAPHIC MICROSCOPE

    CAPABLE OF UP TO 1000X MAGNIFICATION.

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    A MORE SOPHISTICATEDSCANNING ELECTRON METALLOGRAPHIC MICROSCOPE

    CAPABLE OF UP TO 10,000X MAGNIFICATION.

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    A TYPICAL MICROSTRUCTURE OF A LOW-PLAIN-CARBON

    STEEL SHOWING GRANULAR FERRITES ( ).BECAUSE OF THE VERY LOW CARBON CONTENT, ALL THE

    CARBON IS DISSOLVED AND FINELY DISPERSED IN THEIRON MATRIX.

    THE GRANULAR FERRITES STRUCTURES ARE

    VERY SOFT, LOW-STRENGTH AND DUCTILE.THE GRANULAR FERRITES IN A LOW-PLAIN-CARBON

    STEEL DO NOT TRANSFORM TO A DIFFERENT STRUCTUREEVEN AFTER CYCLIC HEATING AND COOLING -

    TRANSLATING TO VERY GOOD WELDABILITY OF THE LOW-PLAIN-CARBON STEEL STRUCTURE

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    IMPACT STRESSES

    IMPACT STRESSES

    TENSILE /COMPRESSIVESTRESSES

    THE GRANULAR FERRITES, WHEN SUBJECTEDTO IMPACT STRESSES, JUST FLATTEN,

    AND WHEN SUBJECTED TO TENSILE AND

    COMPRESSIVE STRESSES, JUST ELONGATE.

    THE FERRITE GRAINS ACT AS SLIP PLANES, GIVING THEMICROSTRUCTURE A CERTAIN AMOUNT OF DUCTILITY.

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    ANY EXCESS CARBON IN A MEDIUM-PLAIN-CARBON STEEL,

    WHICH CAN NOT BE DISSOLVED IN THE IRON MATRIX,COMBINES WITH IRON TO FORM HARD AND BRITTLE IRONCARBIDES ( CEMENTITES ) WHICH APPEAR AS PEARLITES.

    THE MICROSTRUCTURE CONTAINS FREE GRANULARFERRITES AND LAMELLAR PEARLITES.

    PEARLITES CONTAIN PARALLEL LAYERS OF FERRITEGRAINS AND CEMENTITE. THE PARALLEL LAYERS ACT ASSLIP PLANES, GIVING THESE METALLIC ALLOYS A CERTAIN

    AMOUNT OF DUCTILITY.

    ON THE OTHER HAND, THESE METALLIC ALLOYS START

    BECOMING HARD AND BRITTLE BECAUSE CARBIDESBEGIN TO FORM.

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    THE PLAIN-HIGH-CARBON STEEL CONSISTS OFFULLY PEARLITE MICROSTRUCTURES.

    THE MICROSTRUCTURE IS CALLED PEARLITE

    BECAUSE IT LOOKS LIKE MOTHER OF PEARLS

    AS SEEN UNDER THE MICROSCOPE.

    PEARLITES ARE LAMELLAR OR LAYERED ALTERNATEPLATELETS STRUCTURES OF FERRITE ( WHITE STREAKS )

    AND CEMENTITE ( DARK STREAKS )

    THE PLATELETS STRUCTURES ACT AS SLIP PLANES,INDUCING A CERTAIN AMOUNT OF DUCTILITY. THE

    PRESENCE OF CARBIDES, OF AROUND 35% IN THE OVER-ALL STRUCTURE, PROMOTES HARDENABILITY, STRENGTH

    AND RIGIDITY.

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    IN ORDER TO FULLY APPRECIATE THE EFFECTS OFWELDING HEAT TO PLAIN CARBON STEELS,

    WE WILL ATTEMPT TO EXPLAIN THE BASICS OFHEAT TREATMENT.

    HEAT TREATMENT IS THE CONTROLLED HEATING ANDCOOLING OF METALS TO ALTER THEIR PROPERTIES

    SUCH AS HARDNESS AND STRENGTH WITHOUTCHANGING THE PRODUCT SHAPE.

    WHEN A HIGH-PLAIN-CARBON STEEL IS HEATED TOAROUND 1,000C, ALL THE STRUCTURES FERRITES,

    CEMENTITES, PEARLITESTRANSFORM TO THE AUSTENITE PHASE ( ).

    IT IS IN THE DIFFERENT COOLING RATES, FROM THEAUSTENITE PHASE, THAT THE HIGH-PLAIN-CARBON STEELWILL TRANSFORM BACK TO DIFFERENT STRUCTURES TO

    ROOM TEMPERATURE, AND ALTER ITS PROPERTIES.

    THE DIFFERENT COOLING RATES ARE AS FOLLOWS:

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    FULL ANNEALING ( FURNACE-COOLING ) SOFTENINGVERY SLOW-COOLING RATES, ALLOWING ALL THECARBON TO GET DISSOLVED AND FINELY DIFFUSED INTHE IRON MATRIX. A FULLY FERRITIC MICROSTRUCTUREIS FORMED, WHICH IS VERY SOFT, LOW-STRENGTH AND

    DUCTILE.

    NORMALIZING ( AIR-COOLING ) TOUGHENINGQUICKER COOLING RATES THAN ANNEALING, FREEFERRITES AND PEARLITES ARE FORMED. START OFHARDENING OF THE MICROSTRUCTURE DUE TO

    FORMATION OF CARBIDES, BUT SOME DUCTILITY ISRETAINED DUE TO THE FREE FERRITES AND THEPLATELET STRUCTURES OF PEARLITE.

    OIL QUENCHING ( RAPID-COOLING ) HARDENINGMICROSTRUCTURE BECOMES VERY HARD AND BRITTLETHROUGH THE FORMATION OF MARTENSITES.

    WATER QUENCIHING ( DRASTIC RAPID COOLING )

    HARDENING

    COARSE, JAGGED, ROUGH AND DISORIENTEDMARTENSITES ARE FORMED, WHICH ARE EXTREMELYHARDER AND MORE BRITTLE, COMPARED TO

    MARTENSITES FORMED BY OIL QUENCHING.

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    MARTENSITES ARE FORMED BY RAPID COOLING,WHICH TRAPS THE CARBON ATOMS THAT DO NOTHAVE TIME TO DIFFUSE OUT OF THE IRON MATRIX,

    AND CHEMICALLY COMBINE WITH THE IRONTO FORM IRON CARBIDES. A TYPICALMICROSTRUCTURE OF MARTENSITES HAS

    ACICULAR, SHARP, NEEDLE-LIKE APPEARANCE.MARTENSITES ARE VERY HARD AND BRITTLE

    AND ARE USUALLY NOT WELDABLE.

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    UNTEMPERED MARTENSITES, WHILE VERY HARDAND STRONG, ARE TOO BRITTLE TO BE USEFUL

    FOR MOST INDUSTRIAL APPLICATIONS.

    AFTER WATER OR OIL QUENCING, THE STEELSARE TEMPERED, TO AROUND150C ~ 550C, TO IMPART

    TOUGNESS.

    AT THESE TEMPERATURES, THERE IS NO CHANGEIN THE MICROSTRUCTURES OF THE STEELS. WHAT

    HAPPENS IS THAT THE MARTENSITES ARE REFINED ANDRE-ORIENTED.

    AFTER WELDING, THE TERMS USED FOR

    THIS HEAT TREATMENT PROCESS ARESTRESS-RELIEVING, OR PWHT.

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    IN WELDING, THE EFFECT OF HEAT TREATMENT

    IS SOMETIMES INADVERTENTLY DONE.THE WELDING HEAT INPUT MAY RAISE THE

    TEMPERATURE OF THE PLAIN CARBON STEELSIN EXCESS OF 800C.

    THE HIGHER THE CARBON CONTENT,

    AND, THE FASTER THE COOLING RATE,RESULT IN THE FORMATION OF

    MORE CARBIDES. THIS WILL MAKETHE PLAIN CARBON STEELS

    MORE SUSCEPTIBLE TO CRACKINGDURING WELDING.

    IN WELDING, NECESSARY PRECAUTIONSSHOULD ALREADY BE TAKEN TO AVOID THESE

    FORMATION OF CARBIDES IN MEDIUM-AND HIGH-PLAIN-CARBON STEELS .

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    FROM THE VIEWPOINT OF WELDING, CARBIDES IN PLAIN-CARBON-STEELS ARE HARMFUL, BECAUSE OF THEIR

    CRACKING TENDENCIES.

    HOWEVER, THERE ARE ATTRIBUTES OF THESE CARBIDESWHICH ARE VERY BENEFICIAL TO MANY INDUSTRIAL

    APPLICATIONS.

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    LONG-SPAN BEAMS, SUPPORTING HEAVY LOADS ALONGTHEIR AXIS, MUST HAVE RIGIDITY, OTHERWISE THE

    BEAMS WILL SAG.

    CARBIDES IN PLAIN-CARBON STEELS GIVERIGIDITY TO THE BEAMS.

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    MANY INDUSTRIAL PARTS ARE MANUFACTUREDFROM HEAT-TREATED, HIGH-HARDNESS STEELS

    FOR METAL-TO-METAL WEAR RESISTANCE.

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    REALIZING THE STRONG INFLUENCE OF CARBON

    ON THE HARDNESS AND STRENGTH OFPLAIN-CARBON STEELS, AND THE CONSEQUENT

    BENEFICIAL EFFECTS, THE TENDENCY IS TO ADDMORE CARBON TO THE PLAIN-CARBON STEELS.

    HOWEVER, THERE IS A MAXIMUM LIMITON THE SOLUBILITY OF CARBON IN STEELS,

    BEYOND WHICH ANOTHER DIFFERENT

    MICROSTRUCTURES WILL BE FORMEDWHICH ARE CAST IRONS,

    TO INDUCE THE SAME EFFECT AS CARBON,ALLOYING ELEMENTS ARE ADDED INSTEAD, WITH EACH

    HAVING THEIR INDIVIDUAL CARBON EQUIVALENT.

    THESE ALLOYED CARBON STEELS LOW-ALLOYEDOR HIGH-ALLOYED OR TOOL STEELS

    VARY IN TERMS OF ALLOYING ELEMENTS,STRENGTH AND DURABILITY.

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    THE CARBON EQUIVALENT SCALES THE CONCENTRATIONOF EACH ALLOYING ELEMENT BY ITS ABILITY TO

    PROMOTE CARBIDE FORMATION.

    C.E. = %C + %Mn + %Ni + %Cr + %Cu + %Mo

    6 15 5 13 4

    THE ALLOYING ELEMENTS INTERACT WITHCARBON TO PRODUCE DESIRED COMBINATIONS

    OF HARDENABILITY, STRENGTH AND TOUGHNESS

    CARBON STRONG CARBIDE FORMERS.

    CHROMIUM NEXT TO CARBON AS STRONG CARBIDEFORMERS.

    MANGANESE / NICKEL / MOLYBDENUM / VANADIUMMILD CARBIDE FORMERS; IMPROVES TOUGHNESS ANDSTRENGTH.

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    STAINLESS STEELS THE BASE METAL COMPOSITIONSARE TYPICALLY THAT OF CARBON STEELS, WITH THEADDITION OF AT LEAST 11% CHROMIUM. THIS IS THEMINIMUM AMOUNT OF CHROMIUM NECESSARY TOFORM A STABLE, PASSIVE CHROMIUM OXIDE FILM. ITIS THIS FILM THAT IS THE BASIS FOR THE CORROSIONRESISTANCE OF ALL STAINLESS STEELS, THAT GIVESSTAINLESS STEELS THAT UNIQUE STAINLESS STEELLUSTER.

    THE BASIC CLASSIFICATIONS OF STAINLESS STEELS ARE:

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    THE BASIC CLASSIFICATIONS OF STAINLESS STEELS ARE:

    AUSTENITIC STAINLESS STEELS ( 300 SERIES ) WITH AMINIMUM OF 11% CHROMIUM AND 8% NICKEL, THE HIGHCHROMIUM AND NICKEL FREEZE THE AUSTENITE PHASEDOWN TO ROOM TEMPERATURE. THE NICKEL FURTHER

    ACTS AS AUSTENITE STABILIZER DURING THERMALCYCLIC CONDITIONS.

    THERMAL CYCLE CAUSED BY WELDING HAVE LITTLEINFLUENCE ON MECHANICAL PROPERTIES. THEADJACENT BASE MATERIAL TEMPERATURE, THOUGH,

    HAS TO BE CONTROLLED DOWN TO A MAXIMUNM OF250C TO PREVENT CARBIDE PRECIPITATION ALONGTHE GRAIN BOUNDARIES.

    PRE-HEAT AND PWHT ARE SELDOM REQUIRED.

    AUSTENITIC STAINLESS STEELS ARE TOUGH AND NON-

    MAGNETIC.

    THE TWO TYPES OF AUSTENITIC STAINLESS STEELSMOST COMMONLY USED ARE:

    304FOR GENERAL CORROSION RESISTANCE.

    316

    WITH THE ADDITION OF A MINIMUM OF 2.5%MOLYBDENUM; FOR SEVERE CORROSION RESISTANCE.

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    A TYPICAL MICROSTRUCTURE OF AN AUSTENITIC

    STAINLESS STEEL APPEARING AS AUSTENITE GRAINS, ( ) WHICH ARE SOFT, HIGHLY-DUCTILE, TOUGH

    AND NON-MAGNETIC.

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    THREE KINDS OF CRYSTAL STRUCTURE IN STEELS

    GRANULAR FERRITES ARE BODY-CENTERED CUBIC.

    GRANULAR AUSTENITES ARE FACE-CENTERED CUBIC,BEING MORE COMPACT, ARE TOUGHER.

    CEMENTITES AND MARTENSITES ARE HEXAGONAL

    CLOSE-PACKED, THOUGH MORE COMPACT, ARE LESSSTABLE.

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    DURING WELDING AUSTENITIC STAINLESS STEELS, WHENTHE TEMPERATURE REACHES 500C ON THE BASE

    METAL, CHROMIUM CARBIDES PRECIPITATEPREFERENTIALLY ALONG THE GRAIN BOUNDARIES

    OF THE AUSTENITE MICROCTRUCTURES, ALSO CALLEDSENSITIZATION. THIS DETERIORATION MAKES THE

    AUSTENITIC STAINLESS STEELS MORE SUSCEPTIBLE TOCORROSION ATTACKS, AND IS THE MOST COMMON

    REASON IN WELD FAILURES OF AUSTENITIC STAINLESSSTEELS

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    THE HEAT-TINT VISUAL APPEARANCE OF THE

    WELD AREA IS DUE TO CARBIDES PRECIPITATION,OR SENSITIZATION.

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    THE 400 SERIES STAINLESS STEELSTHESE ARE THESTRAIGHT-CHROMIUM, WITHOUT THE ADDITION OF A

    MINIMUM OF 8% NICKEL.THE TWO TYPES OF 400-SERIES STAINLESS STEELSARE:

    FERRITIC GRADES STAINLESS STEELSTHESESTAINLESS STEELS ARE FERRITIC AT ALL TEMPERATURES,

    WITH THE ADDITION TO BASIC 400-SERIES STAINLESSSTEELS OF FERRITE STABILIZERS HIGHER CHROMIUM,SILICON, MOLYBDENUM, COBALT, TITANIUM.

    FERRITIC STAINLESS STEELS ARE SOFT, DUCTILE ANDHIGHLY MAGNETIC.

    A TYPICAL APPLICATION FOR FERRITIC STAINLESSSTEELS ARE IN MAGNETIC TRAPS IN PIPELINES, WHICHFACILITATE TRAMP METAL SEPARATION FROM CORROSIVEFLUIDS.

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    MAGNETIC TRAPS MADE FROM WIRE MESHOF FERRITIC STAINLESS STEELS FACILTATE

    TRAMP METAL SEPARATION FROMCORROSIVE LIQUIDS.

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    MARTENSITIC GRADES STAINLESS STEELSTHESE ARE

    ESSENTIALLY 400-SERIES STAINLESS STEEL ALLOYS OFA HIGHER CHROMIUM AND CARBON CONTENTS THATPOSSESS A FULLY MARTENSITIC MICROSTRUCTURE INTHE HARDENED CONDITION.

    THE MARTENSITIC GRADES STAINLESS STEELS ARE

    HIGHLY MAGNETIC AND ARE HARDENABLE BY HEATTREATMENTS.

    A TYPICAL APPLICATION OF MARTENSITIC GRADESSTAINLESS STEELS ARE INDUSTRIAL KNIFE BLADES. THEMARTENSITE MICROSTRUCTURES AND EXCESS

    CARBIDES MAINTAIN CUTTING EDGES AND CORROSIONRESISTANCE.

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    KNIFE BLADES USED IN THE FOOD INDUSTRYARE SOME OF THE TYPICAL APPLICATIONS

    FOR MARTENSITIC GRADE STAINLESS STEELSREQUIRING HARDNESS ON CUTTING EDGES

    BE MAINTAINED AND SUPERIORCORROSION RESISTANCE IN SERVICE.

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    DUPLEX GRADES STAINLESS STEELS THEY GETTHEIR NAME BECAUSE THEY CONTAIN BOTH FERRITICAND AUSTENITIC MICROSTRUCTURE IN EQUAL AMOUNT.

    IN FULLY AUSTENITIC STAINLESS STEELS REQUIRINGEXTENSIVE AND HEAVY WELDING, PRECIPITATEDCARBIDES FORM ALONG THE GRAIN BOUNDARIES OF THEAUSTENITE MICROSTRUCTURES, THESE PRECIPITATEDCARBIDES ARE VERY PRONE TO CORROSIVE ATTACK,WHICH MAY RENDER THE PART IMPRACTICAL, SPECIALLY

    IN APPLICATIONS REQUIRING RESISTANCE TO VERYAGGRESSIVE MEDIA.

    DUPLEX GRADES STAINLESS STEELS WERE FORMULATEDFOR FABRICATIONS OF STAINLESS STEELS REQUIRINGEXTENSIVE AND HEAVY WELDING WORK. THE FERRITIC

    STRUCTURES IN THE MATRIX REDUCE CARBIDESPRECIPITATION.

    TYPICAL USES OF DUPLEX GRADES STAINLESS STEELSARE FOR HEAT EXCHANGERS, CHEMICAL TANKS,REFINERIES, PRESURE VESSELS AND OFFSHOREAPPLICATIONS.

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    TYPICAL MICROSTRUCTURES OF DUPLEX GRADESSTAINLESS STEELS, WHICH ARE A MIX OF 50 / 50

    FERRITES AND AUSTENITES MICROSTRUCTURES.THE DARK AREAS ARE FERRITE MICROSTRUCTURES

    AND THE WHITE AREAS ARE AUSTENITESMICROSTRUCTURES.

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    FABRICATION OF A FRACTIONATION TOWER OF DUPLEX

    GRADES STAINLESS STEELS. EVEN IN VERY EXTENSIVEAND HEAVY WELDING, THE PART IS NOT PRONE TO

    CARBIDES PRECIPITATION BECAUSE OF THE PRESENCEOF THE FERRITIC MICROSTRUCTURES IN THE MATRIX.

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    BECAUSE OF THE HEAT INPUT DURING WELDING OFDUPLEX GRADES STAINLESS STEELS, THE

    BALANCE OF THE FERRITES AND AUSTENITESMICROSTRUCTURES MAY BE ALTERED.

    IF THE FERRITES ARE TOO LOW BECAUSE OFTRANSFORMATION, CARBIDES PRECIPITATIONMAY TAKE PLACE.

    ALTERNATIVELY, IF THE FERRITES BECOME HIGH,THE STAINLESS STEELS ARE PRONE TO CORROSIONBECAUSE OF THE DEPLETION OF THE AUSTENITICMICROSTRUCTURES.

    THE FERRITE DETECTOR IS USED TO DETERMINETHE FERRITE NUMBER ( FN ) OF DUPLEX GRADESSTAINLESS STEELS. THE VOLUME PERCENTAGEOF FERRITES CAN BE ESTIMATED AS ABOUT 70%OF THE FN.

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    THE FERRITE DETECTOR IS A NON-DESTRUCTIVEINSPECTION INSTRUMENT BASED ON THE MUTUAL

    ATTRACTION OF A PERMANENT BAR MAGNET TO A KNOWNSTANDARD AND AN UNKNOWN MATERIAL.

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    IRON-IRON CARBIDE

    PHASE DIAGRAM

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    THE IRON-IRON CARBIDE PHASE DIAGRAM ISESSENTIALLY A MAP OF THE PHASES THAT EXISTIN IRON AT VARIOUS CARBON CONTENTS ANDTEMPERATURES UNDER EQUILIBRIUM CONDITIONS.

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    AUSTENITIC MANGANESE STEELS THESE TYPICALLYCONTAIN 1.2% C AND A MINIMUM OF 12% MANGANESE.

    A UNIQUE COMBINATION OF PROPERTIES IS ACHIEVEDIN THAT IT IMPARTS HIGH TOUGHNESS AND DUCTILITY

    WITH HIGH WORK-HARDENING CAPACITY AND, GOODRESISTANCE TO WEAR.

    TOOL STEELS MAY HAVE HIGH-WEAR AND ABRASIONRESISTANCE, BUT IN SOME INDUSTRIAL APPLICATIONS,MAY NOT BE ABLE TO WITHSTAND THE HIGH-IMPACT

    LOADS BECAUSE OF THEIR CRACKING TENDENCIES.AUSTENITIC MANGANESE STEELS ARE PRIMARILY USEDIN EARTHMOVING, MINING, CEMENT PLANTS, QUARRYING,OIL WEL DRILLING, RAILROADING, DREDGING.

    IN THE AS-CAST CONDITION, AUSTENITIC MANGANESE

    STEELS ARE RELATIVELY SOFT. THEY CAN BE MACHINEDTO SHAPES IN THIS CONDITION. ONCE THESE ARE USEDAND SUBJECTED TO CONSTANT IMPACT LOADS, THEYWORK-HARDENED ( OR, COLD-HARDENED ), ACHIEVINGHIGH-HARDNESS TOGETHER WITH THEIR HIGH-IMPACTPROPERTIES.

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    THE RAIL WHEELS AND THE RAIL TRACKSARE MANUFACTURED FROM AUSTENITIC

    MANGANESE STEELS, REQUIRING METAL-TO-METAL WEARRESISTANCE AND HIGH-IMPACT LOADS..

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    AUSTENITIC MANGANESE STEELS ARE USEDEXTENSIVELY IN EARTH-MOVING EQUIPMENT FOR

    BUCKETS, SHOVELS, TEETH, WHEREVERY SEVERE WEAR AND IMPACT LOADS

    ARE ENCOUNTERED.

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    IN ROCK-CRUSHING MACHINERIES FOR MINING ANDCEMENT PLANTS, AUSTENITIC MANGANESE STEELS AREEXTENSIVELY USED FOR HANDLING AND PROCESSINGEARTHEN MATERIALS SUCH AS CRUSHERS, GRINDING

    MILLS. MANGANESE STEELS PROVIDE TOUGH, RUGGED,HIGH-WEAR RESISTANCE AND HARSH IMPACT

    PROPERTIES FOR THE RUGGED APPLICATIONS.

    THERMIT RAILROAD WELDING THIS IS A PROCESS OFIGNITING A FORMULATED PYROTECHNIC POWDER MIX OF

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    IGNITING A FORMULATED PYROTECHNIC POWDER MIX OFEXOTHERMIC, HIGH-ENERGY ALUMINO-THERMIC METALALLOYS, PRODUCING A SUPER-HEATED LIQUID METALTHAT IS POURED BETWEEN THE RAILTRACKS END-JOINTS,TO FORM A WELDED JOINT.

    THE CHEMICAL REACTION IS AS FOLLOWS:

    8Al + 3Fe3O4 + FeMn ( Mn Alloys ) + Mg ( IGNITER )

    = 9Fe + 4Al2O3 + HEAT

    TYPICALLY THE ENDS OF THE RAILS ARE CLEANED,ALIGNED FLAT, AND SPACED APART, AROUND 2 INCHES. AGRAPHITE MOLD IS CLAMPED AROUND THE RAIL ENDS.THE RAILS ENDS ARE PREHEATED TO AROUND 500C.THE POWDER MIX IS IGNITED IN THE REFRACTORYCRUCIBLE AND ALLOWED TO REACT TO COMPLETION.

    THE REACTION CRUCIBLE IS THEN TAPPED AT THEBOTTOM ( LEAVING THE ALUMINUM OXIDE IN THECRUCIBLE ), THE MOLTEN STEEL FLOWS INTO THE MOLD,FUSING WITH THE RAIL ENDS, AND FORMING THE WELD.AFTER COOLING, THE MOLD IS REMOVED AND THE WELDIS CLEANED AND GRINDED TO PRODUCE A SMOOTHJOINT.

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    THERMIT RAIL WELDING CRUCIBLE AND MOLD.

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    A GRAPHITE MOLD IS CLAMPED AROUND THE RAIL ENDS.

    THE RAILS ENDS ARE PREHEATED TO AROUND 500C.

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    THE POWDER MIX IS IGNITED IN THE REFRACTORYCRUCIBLE AND ALLOWED TO REACT TO COMPLETION. THE

    REACTION CRUCIBLE IS THEN TAPPED AT THE BOTTOM (LEAVING THE ALUMINUM OXIDE IN THE CRUCIBLE ), THE

    MOLTEN STEEL FLOWS INTO THE MOLD, FUSING WITH THE

    RAIL ENDS, AND FORMING THE WELD.

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    IN WELDING MANGANESE STEELS, THE BASE METALSHOULD NOT REACH MORE THAN 250C. TO DO THIS,SKIP / INTERMITTENT WELDING IS DONE. THE WELD

    AREA ITSELF IS SHOWERED WITH WATER AFTER PAUSINGEVERY AFTER LAYER.

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    IN HARDFACING STEELS, BUFFER LAYERSSHOULD NOT BE MORE THAN 45RC. THE 45RCHARDFACING ELECTRODES CAN BE WELDED

    MULTI-PASS. THE 60RC HARDFACING ELECTRODESCAN BE WELDED ONLY AT SINGLE-PASS LAYER.

    WELDING THE 60RC HARDFACING ELECTRODE MULTI-PASS WILL CAUSE CRACKING AND / OR SPALLING OF THE

    WELDS.

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    IN HARDFACING STEEL PARTS SUBJECTED TO METAL-TO-METAL CONTACT WEAR, ONE PART

    SHOULD HAVE A 10RC LOWER HARDNESS THANTHE OTHER PART.

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    IN THE TRANSITION FROM STEELS TO CAST IRONS,AT AROUND 2% CARBON, WHITE CAST IRONS

    ARE FORMED, IN WHICH THE CARBON IS PRESENTFULLY AS CARBIDES, OR CEMENTITES.

    THE WHITE CAST IRONS MICROSTRUCTURESARE VERY HARD, SUITABLE FOR APPLICATIONS

    REQUIRING METAL-TO-METAL CONTACT

    HIGH-WEAR, RESISTANCE. THEY CAN ONLYBE CASTED, THEY CAN NOT BE MACHINED,WROUGHT ( FORGED, ROLLED, EXTRUDED ),HEAT-TREATED NOR SUBJECTED TO IMPACT.

    THEY ARE USED IN SERVICE FROM THEIRAS-CAST CONDITION AS THEY CAN NOT BE

    SUBJECTED TO ANY FURTHER PROCESSING

    WHITE CAST IRONS ARE NAMED AFTERTHEIR WHITE FRACTURED SURFACE DUE

    TO THE CARBIDES.

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    WHITE CAST IRONS MICROSTRUCTURES SHOWINGNEARLY COMPLETE CARBON SOLUTION IN A MATRIX

    OF MASSIVE, ACICULAR, NEEDLE-LIKE CEMENTITES,WHICH ARE VERY HARD AND BRITTLE..

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    A TYPICAL EXAMPLE OF THE INDUSTRIAL APPLICATIONOF WHITE CAST IRON IS IN THE MIXER BLADES

    OF SAND MULLERS.

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    GRAY CAST IRONS AT 3.0-4.0% CARBON CONTENTS, THE

    CARBON REACHES A SUPERSATURATED CONDITIONWHERE THE EXCESS CARBON CAN NO LONGER DIFFUSE

    INTO THE IRON MATRIX, NOR COMBINE WITH THE IRON.THE SUPERSATURATED EXCESS CARBON WILL JUSTFLOAT AS FREE CARBON, IN THE FORM OF GRAPHITEFLAKES IN A MATRIX OF FERRITES AND PEARLITES.

    THE GRAPHITE FLAKES ACT AS STRESS RAISERS

    WHICH MAY INITIATE FRACTURE WHEN THEGRAY CAST IRONS ARE SUBJECTED TO MODERATE

    IMPACT. WHEN SLIGHTLY HEATED, DURINGEXPANSION AND CONTRACTION, THE

    GRAPHITE FLAKES ACT AS CRACK-PROPAGATORS.

    WITHOUT THE GRAPHITE FLAKES, THE MATRIX ISJUST LIKE PLAIN-CARBON STEELS, WHICH CAN HAVEA TENSILE STRENGTH OF UP TO 70,000 PSI. THE

    GRAPHITE FLAKES IN GRAY CAST IRONS FORM VOIDS ANDARE POROUS, REDUCING THE STRENGTH

    DOWN TO AROUND 25,000 PSI.

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    MOST COMMERCIAL GRADES OF GRAY CAST IRONSCONTAIN 3.0-4.0% CARBON. THE SUPERSATURATEDCARBON WHICH CAN NOT DIFFUSE NOR REACT WITH

    THE IRON ANYMORE, APPEARS AS FREE GRAPHITESIN A TYPICALLY STEEL MATRIX OF FERRITES ANDPEARLITES.

    IN MANY ENGINEERING MATERIALS WITH

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    IN MANY ENGINEERING MATERIALS, WITHINTRICATE DESIGNS OF COMPLICATED SHAPES ANDSIZES OF THICK AND THIN SECTIONS, WHERE THETENSILE STRENGTH OF 25,000 PSI IS SUFFICIENT

    ENOUGH FOR THE APPLICATION,GRAY CAST IRONS ARE HIGHLY BENEFICIAL.

    THE MICROSTRUCTURE OF GRAY CAST IRONSALLOW MASSIVE CASTINGS TO BE FORMED, FOR

    EXAMPLE A 10-TON OPEN GEAR.

    THE GRAPHITE FLAKES ACTS AS CHIP BREAKERS,

    MAKING THE GRAY CAST IRONS HIGHLY MACHINABLE.THEY TEND TO DAMPEN MECHANICAL VIBRATIONS,

    HELPING THE MACHINERIES RUN SMOOTHLY.GRAY CAST IRONS ALSO HAVE

    GOOD CORROSION RESISTANCE.

    TYPICAL EXAMPLES OF PARTS MANUFACTUREDFROM CAST IRONS ARE CYLINDER BLOCKS, HEADS

    AND GEARBOXES.

    GRAY CAST IRONS ARE NAMED AFTER THEIR GRAYFRACTURED SURFACE DUE TO THE GRAPHITE FLAKES.

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    A SPIRAL MOLD TESTS THE MEASURE OF FLUIDITY OF AMELT. THE HIGH CARBON CONTENT OF GRAY CAST IRON

    MAKES THE MELT HIGHLY FLUID TO FORM INTRICATETHICK AND THIN SECTIONS.

    PLAIN-CARBON STEELS EASILY SOLIDIFY IN THESPIRAL PASSAGE. HENCE, CAST STEELS ARE LIMITED

    TO MASSIVE, SIMPLE, UNCORED DESIGNS.

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    THE CYLINDER BLOCKS, HEADS, ETC., OF GENERATOR

    SETS ARE MADE OF GRAY CAST IRONS

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    TURBINE HOUSINGS ARE MADE OF GRAY CAST IRONS.

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    THE CYLINDER BLOCKS, HEADS,TRANSMISSION HOUSINGS, GEARBOX CASES,

    EXHAUST MANIFOLDS, ETC., OF MOTOR ENGINESARE MADE OF GRAY CAST IRONS.

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    IN WELDING GRAY CAST IRONS, THERE IS A TEARINGEFFECT ON THE BASE METAL AS IT EXPANDS ANDCONTRACTS, SINCE THE STRENGTH OF THE BASE

    METAL IS LOWER THAN THE WELD METAL. THIS CANBE COUNTER-ACTED BY PEENING THE BASE METAL,

    TO PUSH BACK THE TEARING FORCE.

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    WHEN WELDING GRAY CAST IRONS, THE HEATGENERATES GASES FROM THE MOISTURE, OILS,

    CHEMICALS ABSORBED BY THE GRAPHITE FLAKES.THE GRAPHITE FLAKES THEMSELVES OXIDIZE TO

    FORM GASES. THESE GASES RISE AND FLOAT AT THESURFACE, FORMING A GAS FILM WHICH CAN NOT BEPENETRATED BY THE WELDING ARC.

    THE SURFACE IS SEARED BY RUNNING AN

    OXY-ACETYLENE FLAME AT THE SURFACEAND BRUSHING THE CARBON SOOT FORMED

    BY THE GAS FILM.

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    IF THE GRAPHITE FLAKES IN GRAY CAST IRONS WEREROUNDED INSTEAD FLAKE-LIKE SHAPES, THEY ACT AS

    CRACK-STOPPERS AND INCREASE THE STRENGTHSIMILAR TO CARBON STEELS OF 70,000 PSI.

    ROUNDED EXCESS CARBON IS PRODUCED EITHER

    BY MALLEABILIZING HEAT TREATMENTS ORINOCULATION OF THE WHITE CAST IRON MELT

    WITH EITHER MAGNESIUM OR CESIUM,

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    MALLEABLE CAST IRONS ARE MADE BY HIGH-TEMPERATURE HEAT TREAMENTS OF WHITE

    CAST IRON CASTINGS. AT THE MALLEABILZINGTEMPERATURE OF 950C, THE CEMENTITESDECOMPOSE AND THE CARBON LIBERATED

    FORMS ROUNDED GRAPHITES.

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    THE INOCULANTS MAGNESIUM OR CESIUM ARE HIGHLY

    VOLATILE. THEY GO FROM SOLID TO GAS IN CONTACTWITH THE MELT. THIS PHENOMENA NODULARIZES THE

    EXCESS CARBON, FORMING NODULAR, OR SPHEROIDAL,OR DUCTILE CAST IRONS.

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    A TYPICAL MICROSTRUCTURE OF MALLEABLECAST IRONS FORMED BY MALLEABILIZING HEAT

    TREATMENTS OF WHITE CAST IRONS ORDUCTILE CAST IRONS ( ALSO CALLED NODULAR

    OR SPHEROIDAL CAST IRONS ) FORMED BYINOCULATION OF GRAY CAT IRONS WITHMAGNESIUM OR CESIUM. THE EXCESS CARBONIS ROUNDED, INCREASUING THE STRENGTH UPTO 70,000 PSI AND IMPROVING WELDABILITY OF

    THE MICROSTRUCTURE.

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    PIPE FITTINGS ARE MADE OF MALLEABLE CAST IRONS.

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    CRANKSHAFTS ARE MADE OF DUCTILE CAST IRONS.

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    THERMAL SPRAY WELDINGIS WIDELY USED, WHEREMELTED MATERIALS ARE SPRAYED ONTO THE SURFACEOF PARTS, THE COATINGS PROVIDING WEAR, IMPACT,

    TEMPERATURE OR CORROSION RESISTANCE.

    THERMAL SPRAYING CAN PROVIDETHIN ( AROUND I MM ) TO THICK EVEN COATINGS( OF SEVERAL MM ), OVER LARGE AREAS AT HIGH

    DEPOSITION RATES.

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    REBUILDING THE WORN-OUT SURFACE OF A NOZZLESEGMENT COMBUSTOR COMPONENT IN A GAS TURBINE

    USING THE HOT METAL SRAY FUSION PROCESS WITHCOBALT-BASED VACUUM-BRAZED METAL ALLOYS.

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    SPRAYING MAGNESIUM-ZIRCONATE THERMAL BARRIERCOATING ON THE INSIDE SURFACE OF A TRANSITIONPIECE COMBUSTOR COMPONENT IN A GAS TURBINE

    USING THE POWDER FLAME SPRAY PROCESS.

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    REBUILDING THE WORN-OUT SHAFTING OF THEHELICAL PINION GEAR OF THE ROLLING MILLS

    GEAR BOX USING THE COLD EXOTHERMIC METAL SPRAYPROCESS WITH NICKEL-CHROMIUM NICKEL ALLOYS.

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    REBUILDING THE SHAFTING BUSHING SURFACEOF THE SCREW CONVEYOR USING THE COLDEXOTHERMIC METAL SPRAY PROCESS WITH

    ALUMINUM-BRONZE METAL ALLOYS.

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    COATING A SINK ROLL USED IN A STEEL MILL PLANT WITH

    ZIRCONIA OR TUNGSTEN CARBIDE POWDERSON A HIGH-VELOCITY-OXYGEN-FUEL SPRAY GUN.

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    SPRAY COATING FOR EROSION AND CORROSIONPROTECTION OF BOILER TUBES IN POWER GENERATION

    PLANTS.

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    HIGH-VELOCITY-AIR-FUEL SPRAY COATING PROCESSON A TURBINE BLADE.

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    WE HAVE A HYPOTHETICAL SITUATION

    JOINING 2MM PLATES OF ALUMINUM ALLOYS

    AND STAINLESS STEEL.

    ARE THESE WELDABLE ?

    YES USING THE FRICTION STIR WELDING TECHNIQUE.

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    WE HAVE A HYPOTHETICAL SITUATION

    CLAD-WELDING BOTH SURFACES OF TWO DIFFERENTPLATES THICKNESSES OF ALUMINUM ALLOYS

    AND STAINLESS STEEL.

    ARE THESE WELDABLE ?

    YES USING THE EXPLOSION WELDING TECHNIQUE.

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    EXPLOSION WELDING USES THE ENERGYOF A CONTROLLED EXPLOSIVE DETONATION

    TO CREATE A METALLURGICAL WELDBETWEEN METALS.

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    EXPLOSION WELDING PROCESS IS USED FOR THEMETALLURGICAL JOINING OF DISSIMILAR METALS.

    THIS PROCESS IS USED MOST COMMONLY TO CLAD

    A THICKER PLATE ( BACKER ) WITH A THINNERLAYER OF CORROSION RESISTANT MATERIAL

    ( ALLOY CLADDER STAINLESS STEEL,NICKEL ALLOY, TITANIUM OR ZIRCONIUM ).

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    IN PREPARATION, THE BACKER AND THE

    ALLOY CLADDER MATING SURFACES ARE GROUND.

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    THE PREPARED BACKER AND THE ALLOY CLADDER

    ARE THEN FIXTURED PARALLEL AT A PRECISE SPACING.

    A MEASURED QUANTITY OF A SPECIFICALLYFORMULATED EXPLOSIVE IS PLACED ON THECLADDING METAL SURFACE.

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    THE EXPLOSIVE IS THEN DETONATED AND THEDETONATION FRONT TRAVELS UNIFORMLY ACROSS

    THE SURFACE FROM INITIATION. THE CLADDING METALBENEATH THE DETONATING EXPLOSIVE IS PROPELLED TO

    COLLIDE WITH THE BASE METAL AT A SPECIFIC IMPACTVELOCITY AND ANGLE. THE MATING SURFACES COLLIDE

    UNDER PRESSURE. THE EXTREME PRESSUREPRODUCES A CONTINUOUS METALLURGICAL WELD.

    ALTHOUGH THE EXPLOSION CLADDING GENERATESINTENSE HEAT, THERE IS INSUFFICIENT TIME FOR

    THE HEAT TO CONDUCT INTO THE METALS AND

    NO BULK HEATING OCCURS.

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    THE EXPLOSION WELDING CLADDED-PLATESARE THEN FLATTENED AND CUT.

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    TESTING AND INSPECTION

    ULTRASONIC

    EXAMINATION OF BOND

    PHISICAL MEASUREMENT

    CERTIFICATIONS

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    A TYPICAL MICROSTRUCTURE OF THE ZONEOF AN EXPLOSION WELDED JOINT BETWEEN

    PLAIN-LOW-CARBON STEEL AND STAINLESS STEEL.

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    AS-EXPLOSION CLAD FLAT PLATE CONSISTINGOF 20MM THICK STAINLESS STELL CLAD ON

    200MM THICK CARBON STEEL.

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    EXPLOSION-CLAD 6MM THICK TITANIUM PLATETO 45MM THICK CARBON STEEL PLATE

    FOR BOILER TUBE SHEET BLANKS,AFTER POST EXPLOSION WELDING FLATTENING.

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    FINISHED VESSEL FABRICATED FROMEXPLOSION CLAD PLATE.

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    A 5 METER DIAMETER DOME OF 5MM THICK TYPE 410STAINLESS STEEL ON 80MM THICK TYPE A387 STAINLESS

    STEEL FORMED FROM EXPLOSION CLAD PLATE.

    GALVANIC CORROSION SERIESCORRODED END (ANODIC OR LEAST NOBLE)

    MAGNESIUMMAGNESIUM ALLOYS

    ZINC ALUMINUM

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    ZINC ALUMINUM

    ALUMINUM 28CADMIUM ALUMINUM 17ST

    STEEL OR IRONCAST IRON

    CHROMIUM-IRON (ACTIVE STAINLESS TYPE 410)NICKEL-RESIST CAST IRON

    18-8 CHROMIUM-NICKEL IRON (ACTIVE STAINLESS TYPE 304)18-8-3 CHROMIUM-NICKEL-MOLYBDENUM IRON (ACTIVE STAINLESS TYPE 316)

    LEAD-TIN SOLDERSLEADTIN

    NICKEL (ACTIVE)INCONEL-NICKEL-CHROMIUM ALLOY (ACTIVE)

    HASTELLOY ALLOY C (ACTIVE)BRASSESCOPPER

    BRONZESCOPPER-NICKEL ALLOYSMONEL-COPPER ALLOYS

    SILVER SOLDERSNICKEL (PASSIVE)

    INCONEL-NICKEL-CHROMIUM ALLOYS (PASSIVE)CHROMIUM-IRON (PASSIVE STAINLESS TYPE 410)TITANIUM

    18-8 CHROMIUM-NICKEL-IRON (PASSIVE STAINLESS TYPE 304)18-8 CHROMIUM-NICKEL-MOLYBDENUM-IRON (PASSIVE STAINLESS TYPE 316)

    HASTELLOY C (PASSIVE)SILVER

    GRAPHITEGOLD PLATINUM

    PROTECTED END (CATHODIC OR MOST NOBLE)

    GALVANIC CORROSION AN ELECTRICAL POTENTIAL,OR VOLTAGE, DIFFERENCE WILL EXIST BETWEEN

    TWO DIFFERENT METALS THAT ARE IN ELECTRICAL

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    CONTACT AND IMMERSED IN A CORROSIVE SOLUTION.THIS POTENTIAL DIFFERENCE CAUSES CURRENT TO

    FLOW AND THE LESS NOBLE, OR MORE ANODIC. METALSUFFERS INCREASED CORROSION RATE. THE SEVERITY

    OF ATTACK DEPENDS UPON THE RELATIVE VOLTAGEDIFFERENCE BETWEEN THE METALS, THE RELATIVEEXPOSED AREAS OF EACH, AND THE PARTICULAR

    CORROSIVE ENVIRONMENT.

    IN WELDING, THE SELECTION OF THE DISSIMILARMETALS TO BE JOINED, AND THE FILLER METALSTO BE USED, MUST TAKE INTO CONSIDERATION

    THE PHENOMENA OF GALVANIC CORROSION.

    A CLEAR EXAMPLE WHERE GALVANIC CORROSION

    FINDS USEFUL APPLICATION IS IN CATHODICPROTECTION. A SACRIFICIAL METAL IS ATTACHEDTO THE METAL TO BE PROTECTED.

    CATHODIC PROTECTION SYSTEMS ARE MOST COMMONLYUSED TO PROTECT STEEL, FUEL PIPELINES, OFFSHORE

    OIL PLATFORMS AND ONSHORE OIL WELL CASINGS.

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    THE SACRIFICIAL ALUMINUM ANODE IS USEDTO PROTECT THE STEEL STRUCTURE AT AN

    OFFSHORE OIL PLATFORM.

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    THE CHEAPEST, MOST ECONOMICAL, FASTEST,RELIABLE AND NON-DESTRUCTIVE METAL IDENTIFICATION

    IS BY CHEMICAL REAGENT REACTION TEST,

    WHICH ARE SHOWN ON THE FOLLOWING DIAGRAMS.

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    THE ATOMIC ABSORPTION SPECTROMETER TECHNIQUETYPICALLY USES A FLAME TO ATOMIZE THE METAL

    SAMPLE. A BEAM OF LIGHT PASSES THROUGH THISFLAME, ABSORBING A SET OF QUANTITY OF ENERGY

    ( LIGHT OF A GIVEN WAVELENGTH ). EACH WAVELENGTHIN THE SERIES IS SPECIFIC TO ONLY ONE

    PARTICULAR ELEMENT.

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    A PORTABLE NON-DESTRUCTIVE FIELDATOMIC ABSORPTION SPECTROMETER.

    NICKEL AND ITS ALLOYS THESE ARE NON-FERROUSMETALS WITH HIGH-STRENGTH AND TOUGHNESS,EXCELLENT CORROSION RESISTANCE, AND SUPERIOR

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    ELEVATED TEMPERATURE PROPERTIES.

    NICKEL ALLOYS ARE USED FOR A WIDE VARIETY OF

    APPLICATIONS, THE MAJORITY OF WHICH INVOLVECORROSION RESISTANCE AND / OR HEAT RESISTANCE:

    - AIRCRAFT GAS TURBINES- STEAM TURBINE POWER GENERATION PLANTS- NUCLEAR POWER SYSTEMS

    - CHEMICAL AND PETROCHEMICAL INDUSTRIESAMONG THE MOST COMMON NICKEL ALLOYS USED IN THEHEAVY INDUSTRIES ARE:

    - INCOLLOY- INCONEL

    - HASTELOY- HAYNES- NIMONIC- MONEL

    NICKEL ALLOYS ARE HIGHLY WELDABLE AND NO SPECIALPRECAUTION IS REQUIRED.

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    NICKEL ALLOYS ARE PRIMARILY USED INTURBINE POWER GENERATION PLANTS.

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    TITANIUM AND ITS ALLOYSTHE COMBINATION OFHIGH STRENGTH-TO-WEIGHT RATIO, EXCELLENT

    MECHANICAL PROPERTIES,AND CORROSIONRESISTANCE MAKES TITANIUM AND ITS ALLOYS

    THE BEST MATERIAL CHOICE FOR MANY CRITICAL

    APPLICATIONS SUCH AS STATIC AND ROTATINGGAS TURBINE ENGINE COMPONENTS, AIRPLANES,MISSILES AND ROCKET.

    TITANIUM AND ITS ALLOYS ARE HIGHLY OXIDIZABLE WHENWELDED. CARE MUST BE TAKEN TO CONTROL THE HEAT

    OF THE BASE METAL DOWN TO 250C. OTHERWISE,TARNISHING WILL DEVELOP.

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    MAIN ENGINE LE7A

    H2A ROCKET

    TITANIUM AND ITS ALLOYS AREUSED VERY EXTENSIVELY INTHE AEROSPACE INDUSTRY.

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    COPPER AND ITS ALLOYS THERE ARE AS MANYAS 400 DIFFERENT COPPER AND COPPER-ALLOY

    COMPOSITIONS. THE FOLLOWING ARE THE PRINCIPALALLOYING ELEMENTS OF THE MORE COMMON TYPES:

    PURE COPPER FOR ELECTRICAL APPLICATION

    BRASS ZINC

    PHOSPHOR BRONZES TIN

    ALUMINUM BRONZES ALUMINUM

    SILICON BRONZES SILICON

    COPPER NICKEL, NICKEL SILVERS NICKEL

    COPPER AND ITS ALLOYS HAVE VERY FAST HEATDISSIPATION RATE. THE WELD AREA REMAINSALWAYS COLD DURING WELDING, MAKINGEXCESSIVE PREHEAT NECESSARY.

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    ELECTRICAL ENERGY IS WASTED IN ANY SYSTEMBECAUSE A PORTION OF THE ELECTRICITY FLOWINGTHROUGH THE CONDUCTOR IS CONVERTED TO HEAT

    RATHER THAN BEING DELIVERED AS USABLE ELECTRICALENERGY.

    ELECTROLYTIC COPPER ( PURE COPPER ) EXHIBITSHIGH ELECTRICAL CONDUCTIVITY AND HIGH HEAT

    DISSPATION RATE, MAKING IT VERY IDEAL FORELECTRICAL COMPONENT PARTS, LIKE BUS BARS.

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    BECAUSE OF THEIR UNIQUE LUBRICITY PROPERTIES,ESPECIALLY WHERE HIGH TEMPERATURES ARE

    INVOLVED, IN REDUCING FRICTION AND PROLONGINGSERVICE LIFE, COPPER ALLOYS FIND VERY GOOD

    APPLICATION IN BUSHINGS, BEARINGS AND SLEEVES.

    THEY FIND EXTENSIVE USES IN OFFSHORE, STEEL MILLAND CONSTRUCTION EQUUIPMENT.

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    AN ECCENTRIC BUSHING MADE OF COPPER ALLOYS USEDIN STEEL MILLS.

    ALUMINUM AND ITS ALLOYS THEY HAVE A STRONGRESISTANCE TO CORROSION, AND IS RATHER

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    MALLEABLE. THEY ARE RELATIVELY LIGHT METAL.THEY ARE EASILY MACHINABLEAND CAN HAVE A WIDE

    VARIETY OF SURFACE FINISHES. THEY ALSO HAVE GOODELECTRICAL AND THERMAL CONDUCTIVITIES AND ISHIGHLY REFLECTIVE TO HEAT AND LIGHT.

    PURE ALUMINUM HAS VERY LOW STRENGTH. HOWEVER,WHEN ALLOYED, MAINLY, WITH SILICON, CAN ATTAINSTRENGTH COMPARABLE TO CARBON STEELS, WHICH

    GIVE THE ALUMINUM ALLOYS A VERY WIDE APPLICATION,ESPECIALLY IN THE AUTOMOTIVE INDUSTRY.

    ALUMINUM AND ITS ALLOYS ARE HIGHLY HYGROSCOPIC.THEY ABSORB MOISTURE VERY RAPIDLY. AS A RESULT,THEIR SURFACES ARE OXIDIZED, FORMING ALUMINUM

    OXIDES. ALUMINUM OXIDES ARE VERY HARD AND HAVE AVERY HIGH MELTING POINT. THIS CAUSES WELDABILITYPROBLEMS. THE BEST REMEDY IS TO GRIND THE OXIDESKIN BEFORE ATTEMPTING TO WELD ALUMINUM AND ITSALLOYS.

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    THE H.M.S. LAURIER LAPIERRE IS THE WORLDS FIRST

    ALUMINUM WARSHIP. THE CONCEPT OF AN ALUMINUM

    WARSHIP IS ECONOMICALLY SOUND. THEY WILL ONLYWEIGH 1/12 OF TRADITIONAL IRON AND STEEL WARSHIPS.THE COST OF FUEL IS ONLY 1/4 OF THE TRADITIONALSTEEL-HULLED SHIPS. THE LIGHTER ALUMINUMWARSHIPS WILL TRAVEL FASTER AND WITH GREATMANEUVERABILITY, MAKING THEM LESS SUSCEPTIBLE TO

    TARGET AND CAN EASILY INTERCEPT ENEMY VESSELS.

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    ALUMINUM WHEELS GIVE THE AUTOMOBILESA SPORTY DESIGN. ALUMNUM WHEELS ALSO

    IMPROVE AUTOMOBILE PERFORMANCE

    BECAUSE OF THEIR LIGHTWEIGHT ANDVERY GOOD HEAT DISSIPATION.

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    TYPICAL APPLICATIONS OF ALUMINUM ALLOYSIN THE AUTOMOTIVE INDUSTRY.

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