Tuesday, January 19, 2016

LADLE FURNACE

     almost 10 years ago, when my career started, i had a tough time operating Ladle Furnaces (LF). problem was, not that study materials were not available, but there were no easy-to-understand, made-simple guidelines available.

     every theoretical book talked about secondary metallurgy, some discussed about thermodynamics and kinetics in depths. but....what i was missing was, a set of guidelines for beginners like me.....i may call it- LF for dummies. none such was available. and...even after so many years, i could not find any book that bridges the gap between theory and practice in secondary metallurgy units-a gap between colleges and shopfloors. beginners need a kick-starter.

     though not many....,there would be certainly a few like me, who would be happy to find a set of hints that would help operating LFs. recently when my boss asked me for a write-up on that i spent almost 2 hours writing that. later i thought i shall bring it to blog-post, as i could not recently find time to write articles of general interests....and also to keep blog alive. so.....an article that is purely technical....

     here it goes....

STAGES of LF treatment in sequential order:

1. Complete homogenization and ceiling temperature.
2. Slag-killing and desulphurization.
3. Chemistry trimming.
4. Calcium treatment.
5. Settling time/soft rinsing.

Points to note during these stages:

1. As soon as the ladle arrives in LF station, arcing for 2 to 3 minutes shall be done to DISSOLVE tapping-addition-lumps floating on top of the bath. Purging (~4-5bar & 30-40NM3/hr) shall be controlled in such a way to concentrate temperature accumulation on top of melt to dissolve those lumps. Care must be taken not to permit arc-flare which would damage slag-lining.

2. Once lumps are dissolved, hi-purging (>10bar & >100 NM3/hr) is started for homogenizing. Then sample, temperature and slag-sample are taken.

3. Sample is sent to lab for initial analysis. Arcing is restarted to soak the ladle. If it’s a circulation ladle, then temperature is raised around 10-20 degrees above LIFTING temperature, depending upon the remaining time in caster. Shorter the remaining time, lesser the ceiling temperature.

4. Slag-sample shall be dipped in water and cooled. Most likely, it would appear black (FeO) & shiny (Silica). Green-tinged-white (Alumina+CaO) & powdery (CaO) slag should be finally achieved to ensure complete Oxygen killing and basicity in the range of 2.8 to 3.2 (facilitates desulpharisation and inclusion retention. This basicity ensures right fluidity).

5. Aluminum is added (in the form of pellets & cubes. Have more surfacearea-to-volume ratio for better kinetics) that stays afloat on top of the bath, over the slag to reduce black-FeO (FeO+Al=> Fe+Alumina). reaction-collision-rate is much accelerated by full rate purging. (Can be added during arcing also, while purging is kept moderate). On addition of lime in right quantity, desulpharisation takes place in parallel and slag becomes white. (Lime-CaO+Al => Ca-ion+alumina) (Ca-ion+FeS => CaS +Fe)

6. Adding CaO balances Silica, changes shiny slag into powdery slag, (increasing basicity=CaO/Silica) giving better sulphur partitioning.

7. In situ, slag fluidity has to be VISUALLY OBSERVED with full argon purging rate, through the sampling door. It should be mushy (soupy), neither too viscous nor watery.

8. Care must be taken not to add excess CaO that produces thick, dry slag, which impedes both desulphurization and inclusion-retention capacity. Insufficient CaO produces thin (more fluidic) slag that gets easily saturated with lesser S (lesser S partitioning, less (%s)/[%s]) & has poor inclusion absorption.

9. Further, this controlled slag ensures buried arc, better heat transfer and thermal yield and reduced arc-flare (which damages slag-lining, leading to ladle-throughs). Arcing at this stage produces humming sound against blasting, burst sounds produced during dry/open arcing & flaring. It shall also be noted, that too-silent arcing may indicate foamy-oxidising-carryover slag that completely buries the arcing sound.

10. Once slag is killed (white slag), aluminium wire shall be fed into the bath (piercing through the top-slag layer) to kill metal oxygen(leftover &limited). Total aluminium added at this stage is the combination, necessary for killing left-over metal oxygen and elemental, dissolved aluminium required in the grade-chemistry. {Total (Al)} = {Dissolved Al} + {bath-oxygen killing Al}.

11. Once the slag is killed, it’s most likely that metal will have lesser free oxygen; because oxygen in slag & metal is in equilibrium. i.e,. if we kill metalbathoxygen from slag enters into metalbath. And if we kill slagoxygen from metalbath enters into slag as they are in equilibrium. So when killed-white slag is produced, metal-oxygen will be very less. So requires only little aluminium to kill it (giving lesser aluminium fading effects over longer holding times; more Al recovery %).

12. Trimming additions are done to meet grade-chemistry. Hi-rate purging ensures complete homogenization.

13. Amount of P reversion indicates the amount of converter-slag carryover.

14. Amount of Si and Mn reversion(without external addition) into metal indicates more reducing capacity of the killed-slag. (because additions done before slag-killing is lost to the slag; but when that slag is killed with better deoxidizer-Al,……after FeO reduction, these Silica and MnO are also reduced and return to metal as Si and Mn)

15. Ca-Fe/Ca-Si/Ca-Fe-Al cored wire is fed to form and modify inclusions (C12A7 & MnS) for better castability and rolling properties.

16. Calcium recovery is in the range of only 15-20% during ideal conditions, as it boils during addition. Excess slag depth, dry slag, more bath top distance from wire discharge point, slower (<220m/min) wire feedrate and non-uniform density of powder in the wirecore reduce recovery further (produce unpredictable Ca pickup). Vigorous boiling, splatters of slag &metal and excess turbulence in ladle are indications of Ca being picked into the bath.

17. Though Ca has high affinity towards oxygen (of alumina), it (>30/35ppm) also reacts with S to produce CaS, when S is available in sizeable (>0.01 wt%) quantity. This solid CaS inclusion can lead to choking, worse than non-Ca heats. This calls for inevitable desulphurization before Ca treatment.

18. It should be noted, both excess and insufficient Ca tend to form solid inclusions that choke SESs. Ca ppm should be proportionate (as to produce ~45%Cao- ~55%Alumina) to alumina in the bath to form liquid C12A7. All other ratios produce solid calcium aluminate, making it difficult to hit the minor Ca window that produces liquid calcium aluminate. Hence attempts should be made to attain ~20ppm of Ca by visual observation for cues during Ca feeding and sampling.

19. Just before lifting heat, settling time of 3-5 minutes should be given with soft rinsing (~3-5bar & 25-35 NM3/hr so as to assist floatation of micro inclusions that don’t have sufficient buoyancy to reach slagtop. Lesser pressure produces smaller bubbles that have more surface area to volume ratio, helping in smaller inclusion floatation. Formation of a small (~10-15cm) eye opening on slag top indicates the right argon flowrate.) Unless this step is religiously followed, be sure to have choking, making all the heat making efforts null and void. This helps in floating smaller solid inclusions through assisted buoyancy and coalescence of liquid inclusions into larger ones. Float maximum, keep rest as liquids.

20. Intermittent slag sampling & observation helps in tracking the progress of heat making. Change of slag appearance over time follows this sequence. Shiny, black (oxidizing) slag >>> dark brown >>> red brown >>> deep green >>> light green >>> greenish gray (very short duration) >>> greenish white & powdery (reducing).

21. Si killed heats are much much easier to kill and desulphurise, compared to only Al killed heats. overkilling of slag in only Al killed heats quickly and easily reduces silica from slag, leading to excess Si in the metal through Si reversion, in turn to offgrades.

22. CaO-lime addition for desulfurisation shall be done in smaller quantities in multiple batches. doing so helps in increasing the S partitioning gradually while providing better reaction collisions as the slag is thinner and more fluidic at the beginning. the quotes, "GOOD STEEL MAKING is only GOOD SLAG MAKING"....."take care of the slag, and that will take care of the metal.." all make real sense.

it would be relevant to add, that these observations were made during the operations of SMS-DEMAG supplied twin station LFs with single-swivel gantry. average heat size was 185 T, and those LFs supplied only Al killed steel ladles to thin slab casters that run at an average speed of 5.8mtr/min during 2007 in india. peak speed touched was 7 mtr/min.i.e., that speed was targeted and maintained throughout the heat size of 185T.

abt grades....mostly CG04** cold rolled galvanised sheets, but mettle-testing grades were PP70**- petroleum pipe line grades and LPG grades...every element on higher side. (i was rarely a success in this grade ;-) ). attempts on IF steels with extra-LC are unforgettable.

other specifications about those casters are LCR-liquid core reduction enabled. that was done from 65mm thickness to 55mm thickness, and was done in multiple stages, rather than achieving it in a single shot. slab widths varied from 950mm to as high as 1550 mm. but most of the production was done in 1250mm sized slabs.

certainly, i am grateful to rbv.ramana sir, ss.upadhyay sir, sridharan unni chakkungal sir, zakir sir, giyas, birendar, babban prasad, bakshi and ispat industries as they PATIENTLY helped me learn all these. hints about specific approach to treat VD/VOD heats shall be added later.

happy to engage in any healthy, value-adding discussions. have a great time.

PERITECTIC Rn_Tn

      a few months back we started to take trial castings of peritectic grade steels. more than generally expected breakouts, we had start of casting failures due to tundish inner-working lining temperature losses in large tundishes (~ 30T working capacity) with relatively smaller dia nozzle openings (~12mm overlapping round ports) and smaller billets (150mm * 150mm ).


      some 5 years back, while working in bloom (250 *250 & 320 *250) casters, we had to face the menace of breakouts that are an inherent threats in casters where the mould levels were controlled manually.

      the approach for breakouts analysis was sooooo unsystematic, we became fed up with the entire workculture. esp, when breakdowns are blamed on us, we wanted to have a better understanding of casting PERITECTIC grade steel. that naturally led to the very basic of physical metallurgy, iron-iron carbide equilibrium phase diagram, more focussed on the top-left of it. that is the peritectic region was given full attention. and to understand that portion better, i drew up this pic in ms-paint.

       to my understanding, peritectic reactions involve 2 different reactants( solid-A + liquid ::::: delta ferrite +liquid steel) giving a product (solid-B ::::: austenite). and `transform'ation involves the conversion of delta-ferrite into austenite without reacting with liquid steel. tried my best to make the image self-explanatory.... here it is....



that was a time, when i had almost no knowledge of computers and image formats. i saved this pic in lossy " .JPG " format rather than lossless " .gif / .png " formats; lead to a compromise in quality. and thanks to my friend-bap=B.ArunPrasad for gifting me the first PC.      

CONTINUOUS CASTING MOULD SIMPLIFIED

DESULPHURISATION

There are certain grades which have a strict limitation on max-Si permitted, typically 0.03% (wt), so it’s necessary to avoid silicon reversion from slag (that happens when we “OVER” kill slag[FeO] with Al).

            Normally de-O precedes de-S. Once SUFFICIENT de-O is achieved, de-S should be initiated WITHOUT delay & deep de-O should be avoided. In order to de-O, we add Al in ONLY-Al killed grades. Once added, this aluminium reduces FeO(unstable, weak oxide) first. THEN…., it looks for other oxides to reduce, when this heavily-reducing atmosphere is maintained UNBALANCED. Once free oxygen and FeO are killed, now Al looks at silica and MnO, and starts reducing them- unless CaO (lime) is added to raise the basicity.

Once lime is added, reaction-collisions (Al + SiO=>Al2O3+ Siˇ) decrease, leading to lesser Si reversion. aluminium is now surrounded by more CaO molecules than SiO2 molecules, so Al now attacks CaO and develops Ca-ions. These Ca-ions attack FeS and START de-S reaction. So instead of [Al + SiO=>Al2O3+Siˇ), [Al + CaO => Ca+ + Al2O] reaction dominates, enabling better de-S.

So when it comes to Al-killed grade, we need to control slag very carefully. De-O of only FeO & MnO should be permitted. De-O of silica should NOT be allowed to happen.

That means…in Si-killed grades, slag can be maintained fluidic FOR PROLONGED DURATION, while in Al-killed grades longer durations of reducing atmosphere+fludic slag returns Si into metal. Hence CaO addition at the RIGHT time* in RIGHT quantity$ is very important. Excess fluidity is not permitted for longer duration.

RIGHT time*- because late addition, would have already resulted in Si reversion into metal.
RIGHT time*- because early addition, will impede de-O RATE.
RIGHT quantity$ - because too much, will reduce de-S RATE due to reduced reaction-collisions.
RIGHT quantity$ - because too less, will permit Si-reversion & will reduce de-S as slag becomes easily S-saturated.

We can NOT add lime in excess quantity (basicity should not go beyond 3.2). Excess lime will make slag very thick/dry/stiff, so de-S RATE will be heavily reduced due to reduced reaction-collisions.

             This thick/dry/stiff slag may lead to arc-flare as arc gets deflected, which may reduce ladle-lining-life, apart from reduced de-S rate.

            And, thin/fluidic slag will NOT bury the arc, leads to energy waste, arc flare may also happen. ULC/IF grades will pickup too much carbon from electrode. May lead to electrode spalling.

            So we have to walk a thin-line between too-thin slag and too-thick slag in only-Al-killed, de-S grades, where Si reversion is NOT permitted (Si < 0.03 wt%).

            In Si-killed grades de-S becomes easier, since Si-reversion is permitted; delayed CaO addition can be done in too many multiple batches of very small quantities.This permits slower thickening of slag, thereby expediting de-S through increased reaction-collisions of fluid slag molecules.

            Finally, one more point I shall add. It is not Al or Si that decides the basicity but the oxides of them. Both oxides are acidic slag formers, making slag more fluidic.


About amphoteric nature of alumina in basic-steel-making practices, I have no clear idea; though I may venture to say, aumina acts as an acidic slag in basic steel making conditions.

BAUXITE ADDITION

Bauxite/dross addition is sometimes done in steel making units. Limitations presented by bauxite shall be kept in mind while looking for the advantages.

There’s no question that alumina keeps secondary slag fluidic. But….the question is where it comes FROM !?

            Endogenous or exogenous!? That makes a very very big difference.

            To understand this, lets consider the reactions involved in secondary steel making conditions.

                                                            Al + CaO => Ca+ + Al2O3

            When this alumina is introduced from outside in the form of bauxite, simply it slows down the reaction in the FORWARD direction by establishing equilibirium. New/ fresh alumina formation rate will be reduced.

            Then what will happen?! Cageneration will also be reduced as alumina (product of this reaction) is made already present. Since Ca-ions generation is reduced, de-S rate will also get reduced.

            Instead, if aluminium is added into the heat, that will reduce CaO, FeO, MnO, free-O, to form alumina on the slag. This is ENDOGENOUS alumina, unlike the alumina (EXOGENOUS) introduced from outside into the slag. This alumina indeed keeps the slag fluidic, while creates conditions suitable for de-S too.


            Further, bauxite may introduce some FeO also, thereby reducing de-O rate a little. When deO is incomplete, de-S efforts will become incomplete/ inefficient.

            Happy steel making.



Monday, January 18, 2016

SECONDARY SLAG MAKING

   You...dont sell slag. so....slag has no economic value in itself. Its importance lies not in the cost at which, if at all, it sells, but…by the ROLEs it plays in steel making.
               Its importance is underestimated/ never gets understood by all. But it is important for those who just start into REAL secondary steelmaking process. That is, only during our formative years as secondary steel makers do we slowly….very slowly…. understand the crucial role of slag. that understanding is absolutely necessary for good performance of secondary steel making process metallurgists to make good heats CONSISTENTLY & ALWAYS.

               Slag must perform a couple of functions SUCCESSFULLY in steel making.

DEOXIDATION:
               A good slag promotes good de-O.
               In general, secondary slag is reducing in nature. Necessary to remove oxygen from liquid steel, which will have lower solubility as the steel solidifies. Unless sufficiently removed, it will lead to poor quality castings through blowhole formations.
               This de-O is done using deoxidisers like C, Si, Mn, Al., in different combinations. Oxygen, from steel, forms corresponding oxides and various compound oxides too, mostly in the form of inclusions.
               Other than oxides, there will be sulphides, nitrides too. Almost all of these inclusions should be removed from steel as much as possible. Here’s where the term CLEAN STEEL figures in. loosely used in steel making contexts, it seems to mean different qualities to different people.
               Unless good amount of inclusions is reduced in steel bath, castability is hampered.
               Unless the liquid steel is cast smoothly in the caster and rolled neatly in the mills, it’s not good steel. Castability becomes an issue in high speed/quality casting.

DESULPHURISATION:
               A good slag promotes de-S.
               De-S follows, de-O. de-S is necessary to have good grade of steel, through better mechanical properties. MnS/ FeS layers formation along the grain boundaries will be reduced during casting/rolling. This gives better mechanical properties.
               Good slag has good amount of free Ca-ions to remove S from FeS. And this Ca is expected to come from lime, rather than from Ca-cored wires. Having sufficient Ca-ions needs controlled slag.
               One must bear in mind that, being surface active elements, O and S vie with each other to combine with Ca, in the most reactive zone of the steel bath- that is slag-metal interface. So a good steel making needs a very good control over this slag-metal interface/reaction zone.

SINK:
               A good slag acts as a sink to the inclusions.
               Slag must be prepared in such a way to accommodate the upcoming inclusions from bath. It should act as a buffer for inclusions. To act as a buffer, it needs to be tailor-made to have perfect combination of various oxides that impart the right viscosity.
               As many may know, thicker slag is tooooo viscous to permit the upcoming inclusions to enter into it, while thinner slag is tooooo fluidic to RETAIN inclusions within itself. Any amount of purging post calcium treatment would not produce good results.
Purging would only be able to float inclusions to the top layers of the steel, but not into the thicker slag-phase. In thinner slag, inclusions would be floated into the thinner-slag-phase but would be drawn/forced back into the steel-phase again as inclusions do not get trapped in the thinner-slag-phase.
If this function of slag fails, then, be ready to get choked suddenly in between the casting sequences, throwing the shop floor into dizzy logistics.
curiously, synthetic slag acts only as this sink, NOT as a desulphurising medium.

BURIED-ARCING:
               A good slag buries the arc, thereby reducing arc flare. Reduced arc flare would lead to reduced refractory damages, giving better ladle life (esp, in slag lining area).
               Buried arc further conserves energy by reducing radiation losses. Much of the heat produced by arc is trapped by slag and gets directed into the heat-bath.

ELECTRODE SPALLING:
               A good slag reduces electrode spalling by reducing harsh, direct arc being established between the hard-steel surface and the electrode tip. This open arc seems to generate a lot of vibrations that may or may not reach the resonance frequencies of the electrodes. Slag contains gases, esp CO/CO2, entrapped; that acts like a cushion to accommodate the vibrations that accompany arcing.
               Thicker, dry slag deflects the arc away.
               Thinner, wet slag may not bury the arc sufficiently and, may permit direct arcing too.

CARBON PICKUP:
               A good slag reduces carbon pickup into the metal from electrode. This may be attributed to thermionic emissions, mechanical erosion of electrode into the metal due to physically uncovered, direct arcing.
               This will become more visible during ULC grades making.

HYDROGEN/NITROGEN PICKUP:
               A good slag reduces hydrogen and nitrogen pickup by providing a good barrier between atmosphere and the steel-bath-top. Thinner slag permits pickup. So it has to be paid attention.
               In some applications, permitted N and H levels will have a limited threshold values.

OTHERs:
               A good slag permits easier deslagging as it does not cling hard to the ladle inner linings, due to optimal fluidity.
               A good slag permits easier penetration of Al/Ca-cored wires to pierce through into the metal-bath.
               A good slag is less reactive towards the ladle refractory linings. You will have better ladle lives.
               A good slag permits easier carbon pickups during pet-coke or coke breeze additions. You can make Hi-C grades easier in LF units.
               It’s true that good steel making is only a good slag making.

               To put it exactly…… if you donot know how to PRACTICALLY make a good slag, then it’s an unfortunate fact that,….you DO NOT KNOW steel making.

Happy steel making!

arduino - 1

i "too" started playing with this micro-controller board, implying there are toooooooooo many players out there, many masters and few novices(meeeee!).

automation attracted me towards this, later i thought of working on a small prototype to measure mould oscillation mechanism( jargon of steel making, more precisely continuous casting field).

what i thought was to measure the acceleration generated by the mould as it moves/oscillates UP & DOWN throughout production process. any deviation unidentified during oscillation has the potential to cost dearly. but unfortunately in my previous workspot, we didnot have any means to measure these deviations, if any.

so i thought, "something is better than nothing"; i decided to make use of arduino coupled with an accelerometer, measuring the dynamic acceleration generated by the oscillating mould.

then again i had to be very careful about, "nothing is better than non-sense". so i HAD TO start working on someway to get those readings MAKE SENSE. this called for coding in PROCESSING language( im yet to START writing original code). that will help me display real-time graph.

point of focus of this article is....the EASE with which arduino coding can be done. here...is the screen shot of MY OWN original-tamilised code. ;-)



that's it. code is complete!

adxl335 is the accelerometer i use. it measures acceleration in x, y & z axes; feeds them to arduino's (induino-clone) 3 analog INPUT pins(A0, A1 & A2). internal 10bit-ADC converts that analog(voltage zero-to-3.3V) signal into digital(zero-to-1023) values.

those digital values are sent to my PC through USB(through usb to serial communication) connection.

those values are received by my PC as tab-separated-values (for easy storing as notepad friendly *.tsv files).

any serial monitor software can read those values in real-time. great thing is arduino-IDE has an inbuilt serial monitor, making the job very convenient.

when i attach this accelerometer to oscillating mould( oscillates in sinusoidal curve form), that accelerometer measures the dynamic acceleration and reports it to arduino; arduino then passes that converted info to PC.

if i these readings are graphically represented, then it will show a smooth sinusoidal curve( representing mould's smooth oscillation). if any abnormal jerk is observed, it is shown as unusual spike in the graph. this will give me an opportunity to get some useful info about oscillation mechanisms of my previous work unit( this doesnot have any means, till now).

not to deviate much from the context, these FEW LINES of code GET the INFO displayed on any serial-monitor.JUST a few lines! arduino is sooooooooooo simple!!!!!!!!

graphing THAT is a separate work on processing software.

prototype - mould oscillation checker

a simple prototype, meant for multiple uses with necessary minor modifications.
applied here for measuring deviations in mould oscillation.

results..... here.



******************************************************************************

here is the schematic of the setup created with the help of fritzing.



******************************************************************************

this is the actual arrangement.






accelerometer ADXL335 is kept on the left top side, connected to arduino-uno caged on the right side. there are 5 leads in ADXL335; 3 signal lines for measuring acceleration in 3-axes, and 2 powerlines.

but since, i wanted to measure only the vertical up-down motion, i had left 2 lines(black+blue) unconnected.

arduino is kept in transparent case on the right is connected to usb port thro' A-to-B connector. this feeds serial info to the PC emulating a virtual COM port (COM#5 in my PC).

arduino's 10bit ADC feeds data to PC's serial port in digital values ranging from 0 to 1023. but this wont make sense if just read digitally; graphing would be easier for tracking changes and abnormalities in the stream of values.

resorted to PROCESSING language for graphing. code in PDE is given on top, that includes the resulting graph window.

this can further be elaborated to measure abnormalities in 3-D. further can be extended into a real product from prototype. if controls are implemented thro' GUI, this setup can be applied to other applications like, slag-detection in ladle-to-tundish shroud, Calcium recovery in ladle furnace treatments.

or for anything that needs to be observed for abnormal vibrations.