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NOX AND SOX EMISSION 
CONTROL
ABSTRACT 
 Ship’s SOX emissions forms 60% of total SOX 
Emissions. 
 We are polluting our environment by our 
choice of fuel. 
 Emission control in the angle of MARPOL 
and the technologies for reduction are taken 
into account.
POLLUTANTS 
 Air pollutants can also be of primary or secondary 
nature. 
 Primary is emitted directly to atmosphere. 
 Secondary is formed by reactions between primary 
pollutants. 
 The major pollutants are 
1. Oxides of nitrogen 
2. Oxides of sulphur 
3. Particulate matter
CHEMISTRY OF FORMATION 
 N2+O2 2NO 
 2NO+O2 2NO2 
 S+O2 SO2 
 SO2+NO2 NO+SO3 
 2NO+O2 2NO2 
 NO2+SUNLIGHT NO+O 
 O+O2 O3
HAZARDS 
 Corrosion 
 Climate change 
 Photochemical smog 
 SO2 irritates the eyes, nose and lungs 
 SO2 causes acid rain 
 NO2 causes pulmonary edema
MARPOL LEGISLATION 
 Annex VI- Regulations for the prevention of 
air pollution from ships 
 Came to force on 19th May 2005 
 For every ship with 400 gross tonnage and 
above and for fixed and floating drilling rig 
 Certificate- “International air pollution 
prevention certificate” 
 Validity- period not exceeding five years
MAJOR REGULATIONS 
 There are 19 Regulations but the following 
Regulations impact Vessel operation : 
 Regulation 12 – Ozone Depleting Substances 
 Regulation 13 – NOx emissions 
 Regulation 14 – Sulphur Oxide emissions 
 Regulation 15 – VOC emissions 
 Regulation 16 – Shipboard Incinerators 
 Regulation 18 – Fuel Oil Quality control
 Emission standards are referred to a Tier I, 
II,III 
 Tier I came into force on 19th May 2005. 
 The revised Annex VI enters into force on 1st 
July 2010. 
 Tier II,III are more stringent than Tier I . 
 Tier II standards are expected to be met by 
combustion process optimization. 
 Tier III standards are expected to require 
dedicated NOx emission control technologies.
REGULATION 13 
 Deals with control of NOX emissions. 
 All engines with power more than 130KW and 
built on or after 1/1/2000 
 Doesn’t apply to engines used in emergency. 
 Emissions must be limited to, 
 17.0 g/kWh when n <130 rpm; 
 45.0 x n-0.2 g/kWh when n is 130 or more but 
less than 2000 rpm; 
 9.8 g/kWh when n is 2000 rpm or more
SOX CONTROL 
 Sulphur content of fuel shall not exceed 4.5%. 
 SOX emission ECA include Baltic and North sea 
area. 
 Sulphur content shall not exceed 1.5% in ECA. 
 Total emission must be less than 6 g SOX/kWh 
in ECA
FUEL OIL QUALITY 
 Fuel oil shall be free from inorganic acid. 
 Bunker delivery note must be maintained. 
 Bunker delivery note must kept for 3 years. 
 Fuel oil sulphur content must never exceed 
4.5%. 
 Parties of 1997 protocol must maintain a 
register of local suppliers of fuel oil.
EMISSION MEASUREMENT 
 For Attaining Interim Certificate of 
Compliance. 
 Engines combined into engine groups by 
manufacturer 
 Engine from this group selected for emission 
testing
EXHAUST GAS MONITORING 
TECHNIQUES 
Exhaust Gas 
Monitoring 
Equipments 
EExxttrraaccttiivvee 
SSyysstteemmss NNoonn--EExxttrraaccttiivvee 
SSyysstteemmss 
UUVV AAnnaallyysseerrss Chemi-luminescence 
IInnffrraarreedd 
AAnnaallyysseerrss 
UUllttrraa--VViioolleett 
AAnnaallyysseerrss
Extractive Systems 
 Permanently installed 
 Requires additional equipment to process the 
exhaust gas sample. 
 Advantages 
 Able to be remotely located in a controlled environment 
 Easier to operate, calibrate and maintain. 
 Can be set up to monitor exhaust gas emissions from more 
than one engine. 
 Disadvantage 
 High Cost
NON-EXTRACTIVE SYSTEMS 
 Predominately use infrared or ultra-violet 
techniques. 
 Measure the exhaust gas emissions without 
extracting the exhaust gas from the uptake 
system. 
 Advantages 
 More portable 
 Provides more rapid responses. 
 Disadvantages 
 Difficult to calibrate.
CHEMILUMINESCENCE 
 HCD (Heated Chemiluminescence Detector). 
 Accepted standard for laboratory and test cell 
measurement of NOx. 
 Was the only available NOx detector available 
during the development of the IMO Technical 
code. 
 Needs to have a continuous supply of clean 
dry air else damage to the analyser 
components will result. 
 NO determination with detection limits down 
to 1 ppb.
ULTRA-VIOLET ANALYSERS 
 Particularly useful for measuring SO2 . 
 Used in extractive and non-extractive systems. 
 Not suitable for the measurement of NOx.
REDUCING SOX EMISSIONS 
 2 Possibilities :- 
 Burning fuels with lower sulphur content 
 Treating the engine exhaust gases 
 At Present limits on sulphur content of marine 
fuel 
 Globally – 4.5% 
 SECA – 1% from 1st july,2010 
 SOX emission control areas (SECA) 
 North Sea, English Channel and the Baltic Sea.
TECHNIQUES FOR 
REDUCING SOX EMISSIONS 
 3 possibilities to reduce SO2 emissions from 
combustion processes: 
1) REMOVAL OF SULPHUR BEFORE COMBUSTION 
2) REMOVAL OF SULPHUR DURING COMBUSTION 
3) REMOVAL OF SOX AFTER COMBUSTION ( I.E. 
FLUE GAS DESULPHURISATION )
REMOVAL OF SULPHUR 
BEFORE COMBUSTION 
 Process used : Hydrotreating or Hydrodesulphurisation 
 Treatment of the oil with hydrogen gas obtained e.g. during 
catalytic reforming. 
 Sulphur compounds are reduced by conversion to hydrogen 
sulphide (H2S) in the presence of a catalyst. 
 H2S washed from the product gas stream by an amine wash 
 H2S is recovered in highly concentrated form 
 Converted to elemental sulphur via the Claus-Process 
 Feedstock is mixed with hydrogen-rich make-up and recycled 
gas and reacted at temperatures of 300 - 380 °C.
 Removal of sulphur from heavier oils such as marine fuel oil 
often requires pressures of up to 200 bar. 
 Catalysts employed : cobalt, molybdenum or nickel finely 
distributed on alumina extrudates.
CLAUS PROCESS 
 Most significant Gas desulphurizing process 
 Recovers elemental sulphur from gaseous 
hydrogen sulphide 
 The overall main reaction equation is: 
2 H2S + O2 → S2 + 2 H2O
REMOVAL OF SULPHUR 
DURING COMBUSTION 
 Experimental Stage 
 The combustible compound is mixed with an 
admixture of water soluble and water insoluble 
sulphur sorbent. 
 Such admixtures, remarkably, produces a 
reduction in the SOX level far greater than 
would be expected based on the activity of 
each sorbent alone.
REMOVAL OF SOX AFTER 
COMBUSTION 
TTHHEE 
SSEEAAWWAATTEERR 
SSCCRRUUBBBBEERR 
SSPPRRAAYY 
DDRRYY 
SSYYSSTTEEMM 
WWEELLLLMMAANN--LLOORRDD 
PPRROOCCEESSSS 
LLIIMMEESSTTOONNEE 
//GGYYPPSSUUMM 
SSYYSSTTEEMM 
FFLLUUEE 
GGAASS 
DDEESSUULLPPHHUURRIISSAATTIIOONN 
((FFGGDD))
LIMESTONE/GYPSUM 
SYSTEM 
 Most widely used process 
 Principle 
 Suspension of crushed limestone in water is 
sprayed into the flue gases. 
 SO2 reacts with calcium ions to form calcium 
sulphite slurry 
 Aeration of the slurry with compressed air 
oxidizes calcium sulphite to calcium sulphate 
 After removal of the water, the calcium 
sulphate can be disposed off
 Advantage : 
 SO2 reduction around 90 % 
 Disadvantages : 
 limestone has to be stored onboard 
 large quantities of gypsum waste is produced
SPRAY DRY SYSTEM 
 A slurry of slaked lime is used as an alkaline 
sorbent 
 The slurry is injected into the flue gases in a 
fine spray. 
 The flue gases are simultaneously cooled by 
the evaporation of water 
 The SO2 present reacts with the drying sorbent 
to form a solid reaction product, with no 
wastewater.
WELLMAN-LORD PROCESS 
 Hot flue gases are passed through a pre-scrubber 
 Ash, hydrogen chloride, hydrogen fluoride and SO3 are 
removed. 
 the gases are then cooled and fed into an absorption tower 
 SO2 reacts with a saturated sodium sulphite solution to form 
sodium bisulphite. 
 The sodium bisulphate is regenerated after a drying step to 
sodium sulphite again. 
 The released and clean SO2 - may then be liquefied or 
converted to elemental sulphur or sulphuric acid. 
 The sorbent is regenerated during the combustion process and 
is continuously recycled, but the products (sulphur 
compounds) have to be stored.
TTHHEE SSEEAAWWAATTEERR SCRUBBER 
 Krystallon Sea-Water Scrubber 
 Removes 90-95 % of SO2 
 In addition removes 80 % of the particulates 
and 10-20% of hydrocarbons. 
 Advantages 
♦ no limestone has to be stored on board, 
♦ no waste (gypsum) is produced, which has to 
be deposited on land, 
♦ the seawater already contains substantial 
amounts of sulphate and nitrate 
♦reduction of engine noise and a reduction of 
the diesel smell..
FFeeaattuurreess 
 Uses Cyclone Technology 
 The system needs only a little extra space 
 Aeration of the effluent is necessary 
 high degree of recirculation
WWoorrkkiinngg 
 Water in contact with hot exhaust gas 
 Exhaust gas is channelled through a concentric 
duct into a shallow water tank. 
 Mixing baffles break up large gas flow into 
smaller bubbles 
 SOx in exhaust gas is dissolves in seawater 
 Larger particles (greater than 2.5 micron) 
captured in the water. 
 Fine particles (smaller than 2.5 micron) may 
pass through without capture.
 Pumped through a set of large cyclones 
 Designed to separate some of the heavy 
particles, as well as light particles in a two-stage 
system. 
 Fed to a settling tank for collection of soot and 
oil. 
 Runs with no ongoing maintenance 
 Cleaned recirculated water is maintained at 
extremely low concentrations of hydrocarbons, 
making it safe for discharge to sea.
OPERATIONAL CONCERNS 
AROUND THE CHANGE TO 
LOW SULPHUR FUELS 
 REDUCED FUEL VISCOSITY 
 FUEL ACIDITY 
 IGNITION AND COMBUSTION QUALITY 
 FUEL LUBRICITY
REDUCED FUEL VISCOSITY 
 MGO and MDO fuels have a lower inherent 
viscosity than heavy fuel oil which can : 
 Effect Diesel Engines 
 Effect Steam Boilers
Effect On Diesel Engines 
 Changes in fuel atomisation 
 Adversely affects power output and engine 
starting performance. 
 Solution Recommended : Use fuel coolers to 
control fuel viscosity
Effect On Steam Boilers 
 Affects fuel flow setting (for a given pressure) 
at the burners 
 Can lead to “Over Firing” 
 Increased risk of flame failures and flame 
impingement on boiler tube plates. 
 Solution Recommended : 
 Change the nozzle 
 Or the air/fuel ratio settings
FFUUEELL AACCIIDDIITTYY 
 Does not present a problem for steam boilers 
 But has a significant effect on diesel engines 
 Engine lube oils are formulated with alkaline 
additives to neutralise the acidic, sulphur, by-products 
of combustion. 
 IF amount of sulphur in the fuel is reduced, THE 
amount of alkaline additives should be reduced. 
 Too much alkalinity causes build-up of deposits that 
will affect the lubricating film 
 Solution Recommended : Oil with a lower Base 
Number (BN).
IIGGNNIITTIIOONN AANNDD 
CCOOMMBBUUSSTTIIOONN QQUUAALLIITTYY 
 Effect On Diesel Engines 
 Effect On Steam Boilers
Effect On Diesel Engines 
 Poor combustion and ignition may lead to 
increased fouling of the engine 
 Fouling is so excessive that moving parts such 
as exhaust valves are inhibited by the soot, 
leading to broken/bent valves 
 Excessive fouling of the scavenge air receiver 
combined with late ignition or prolonged 
combustion may lead to a buildup of soot 
deposit and the risk of fire.
Effect On Steam Boilers 
 Leads to starting failures and more frequent 
flame failures 
 May lead to increased soot formation and 
consequent fouling of the boiler and exhaust 
system. 
 Solution Recomended: Follow detailed advice 
given by manufactures on procedures to follow 
when switching fuel qualities.
FFUUEELL LLUUBBRRIICCIITTYY 
 Ultra Low Sulphur Diesel (ULSD) contains 
<15ppm sulphur. 
 Inherent lubricity of such diesel is reduced 
which in turn increases wear on fuel pumps 
and injectors. 
 Solution : Lubricity additives are commonly 
added at source to such fuels to reduce these 
problems
EENNGGIINNEE EEXXHHAAUUSSTT DDEEPPEENNDDSS 
UUPPOONN 
 ENGINE TYPE ( i.e LOW,MEDIUM AND 
HIGH SPEED) 
 ENGINE SETTING ( i.e LOAD,SPEED AND 
FUEL INJECTION TIMING) 
 FUEL USED
FFAACCTTOORRSS AAFFFFEECCTTIINNGG 
NNOOxx FFOORRMMAATTIIOONNSS 
 SPEED OF ENGINE 
 MAXIMUM TEMPERATURE 
INSIDE CYLINDER 
 COMPRESSION RATIO/PEAK 
PRESSURE 
 AMOUNT OF SCAVENGE AIR
NNOOxx RREEDDUUCCTTIIOONN 
TTEECCHHNNIIQQUUEESS 
PRE-TREATMENT 
INTERNAL 
MEASURE 
(PRIMARY 
METHODS) 
AFTER 
TREATMENT 
(SECONDARY 
METHODS)
NNOOxx RREEDDUUCCTTIIOONN 
TTEECCHHNNIIQQUUEESS 
PRE-TREATMENT 
INTERNAL 
MEASURE 
(PRIMARY 
METHODS) 
AFTER 
TREATMENT 
(SECONDARY 
METHODS)
AALLTTEERRNNAATTIIVVEE FFUUEELLSS 
 METHANOL 
 LIQUIFIED PETROLEUM GAS
MMEETTHHAANNOOLL 
 50% REDUCTION 
 NO SULPHUR 
 BAD IGNITION QUALITY 
 CORROSIVE 
 EXPENSIVE FUEL
LLIIQQUUIIFFIIEEDD PPEETTRROOLLEEUUMM GGAASS 
 BUTANE(C4H10)+PROPANE(C3H8) 
 LOW ENERGY DENSITY SO MORE FUEL 
CONSUMPTION 
 NON-CORROSIVE 
 NON-TOXIC
WWAATTEERR AADDDDIITTIIOONN TTOO FFUUEELL 
 UNDER RESEARCH WITH 30% OF 
WATER IN FUEL 
 30% REDUCTION IN NOx EMISSION 
 EFFECT ON ENGINE COMPONENTS IS 
NOT KNOWN 
 DECREASE MAXIMUM TEMPERATURE 
INSIDE CYLINDER 
 HIGH SPECIFIC HEAT
NNOOxx RREEDDUUCCTTIIOONN 
TTEECCHHNNIIQQUUEESS 
PRE-TREATMENT 
INTERNAL 
MEASURE 
(PRIMARY 
METHODS) 
AFTER 
TREATMENT 
(SECONDARY 
METHODS)
MMOODDIIFFIICCAATTIIOONNSS IINN 
CCOOMMBBUUSSTTIIOONN PPRROOCCEESSSS 
 INJECTION TIMING RETARDATION 
 INCREASE IN INJECTION PRESSURE 
 OPTIMIZATION OF INDUCTION SWIRL 
 MODIFICATION OF INJECTOR 
SPECIFICATION 
 CHANGE IN NUMBER OF INJECTORS
IINNJJEECCTTIIOONN TTIIMMIINNGG 
RREETTAARRDDAATTIIOONN 
 REDUCE MAXIMUM COMBUSTION 
TEMPERATURE & PRESSURE 
 REDUCTION UPTO 30% OF NOx 
EMISSION 
 INCREASE IN SFC BY 5% 
 MORE EFFECTIVE FOR MEDIUM/HIGH 
SPEED ENGINES
IINNCCRREEAASSEE IINN IINNJJEECCTTIIOONN 
PPRREESSSSUURREE 
 COMBINED WITH OTHER TECHNIQUES 
 PROVIDES BETTER ATOMIZATION
OOPPTTIIMMIIZZAATTIIOONN OOFF 
IINNDDUUCCTTIIOONN SSWWIIRRLL 
 COMBINED WITH OTHER NOx 
REDUCTION TECHNIQUES 
 HELPS IN GOOD COMBUSTION 
 NO ADDITIONAL COST
IINNJJEECCTTOORR SSPPEECCIIFFIICCAATTIIOONNSS 
 INJECTION PRESSURE 
 NUMBER AND ANGLE OF HOLES 
 SIZE OF HOLES
CCHHAANNGGEE IINN NNUUMMBBEERR OOFF 
IINNJJEECCTTOORR 
 COMBUSTION PROCESS CAN BE 
CONTROLLED BETTER 
 REDUCE MAXIMUM COMBUSTION 
TEMPERATURE 
 ADDITIONAL COST OF FUEL INJECTOR 
AND PIPING 
 INCREASE IN MAINTENANCE COST 
 30% REDUCTION IS ACHIEVABLE
SSCCAAVVEENNGGEE//CCHHAARRGGEE AAIIRR 
CCOOOOLLIINNGG 
 14% REDUCTION IS POSSIBLE BY 
LOWERING CHARGE AIR TEMP. FROM 
40oC to 25oC 
 REDUCE COMBUSTION TEMPERATURE 
 SUITABLE FOR MEDIUM AND HIGH 
SPEED ENGINES 
 COOLING AIR TOO MUCH COULD LEND 
TO COMBUSTION PROBLEMS
WWAATTEERR IINNJJEECCTTIIOONN 
 DURING COMBUSTION THROUGH 
SPECIAL INJECTOR 
 REDUCES THE BULK TEMPERATURE OF 
COMBUSTION 
 40% REDUCTION IN NOx EMISSION IS 
ACHIEVED
WWAATTEERR IINNJJEECCTTIIOONN 
LLIIMMIITTAATTIIOONNSS 
 NEED OF SEPARATE PUMP FOR FUEL 
AND WATER 
 COST FACTOR 
 CORROSION
NNOOxx RREEDDUUCCTTIIOONN 
TTEECCHHNNIIQQUUEESS 
PRE-TREATMENT 
INTERNAL 
MEASURE 
(PRIMARY 
METHODS) 
AFTER 
TREATMENT 
(SECONDARY 
METHODS)
WWHHAATT IISS SSCCRR?? 
SELECTIVE CATALYST REDUCTION IS 
THE PROCESS OF REDUCING NOx 
COMPOUNDS WITH AMMONIA INTO 
NITROGEN AND WATER VAPOURS IN 
PRESENCE OF CATALYST.
SSCCRR SSYYSSTTEEMM CCOOMMPPOONNEENNTTSS 
 REDUCTANT STORAGE TANK 
 PUMP 
 VAPORIZER (NOT IN CASE OF 
ANHYDROUS AMMONIA) 
 MIXER 
 INJECTION NOZZELS 
 CATALYST CHAMBER
WWOORRKKIINNGG OOFF SSCCRR SSYYSSTTEEMM 
 AFTER TREATMENT TECHNIQUE 
 REDUCTANT(AMMONIA) IS INJECTED 
AND MIXED INTO EXHAUST 
 PASS THIS MIXTURE THROUGH 
CATALYST CHAMBER 
 TEMPERATURE OF CATALYST 
CHAMBER SHOULD BE 450K-720K
RREEAACCTTIIOONNSS IINNVVOOLLVVEEDD
RREEDDUUCCTTAANNTTSS UUSSEEDD 
 ANHYDROUS AMMONIA 
 AQUEOUS AMMONIA 
 UREA
CCAATTAALLYYSSTT UUSSEEDD 
 BASE METAL OXIDES SUCH AS 
(VANADIUM AND TUNGSTEN) 
 TITANIUM OXIDE 
 ZEOLITE (HIGH TEMPERATURE 
DURABILITY)
EEXXHHAAUUSSTT GGAASS 
RREECCIIRRCCUULLAATTIIOONN 
 REDUCES LOCAL COMBUSTION 
TEMPERATURE. 
 HIGH SPECIFIC HEAT OF EXHAUST GAS 
AND WATER VAPOUR. 
 DECREASES OXYGEN 
CONCENTRATION.
BBUUBBBBLLEE BBAATTHH SSCCRRUUBBBBEERR
EMISSION TRADE 
 Credit based system 
 This system was proposed by the swedish ship 
owners association. 
 Large combustion installations are capped by 
their maximum annual emissions. 
 Installation that emits less than its allocated 
credits can trade the difference in the 
emissions market.
HOW IT WORKS? 
 Emission reductions become a tradable 
commodity, which can be bought and sold like 
any other product in the market. 
 Each ship will be allocated points depending 
on its yearly emissions in tons. 
 Trading can be made anonymously through an 
emissions market.
CONCLUSION 
 Emission control is a necessity to make 
shipping transport viable. 
 CSR and Green marketing are the new buzz 
words. 
 One time investment and high returns. 
 Decrease in peak temperature can limit NOX 
emission. 
 Limit SOX by removing sulphur prior 
combustion.
REFERENCES 
 Reduction of NOx and SOx in an emission a snapshot of 
prospects and benefits for ships in the northern European 
SECA area. 
 www.imo.org 
 MARPOL consolidated edition 2006 
 Exhaust emissions from ship engines - significance, 
regulations, control technologies by Laurie Goldsworthy 
 www.dieselnet.com
TTHHAANNKK YYOOUU

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Nox and sox emission control

  • 1. NOX AND SOX EMISSION CONTROL
  • 2. ABSTRACT  Ship’s SOX emissions forms 60% of total SOX Emissions.  We are polluting our environment by our choice of fuel.  Emission control in the angle of MARPOL and the technologies for reduction are taken into account.
  • 3. POLLUTANTS  Air pollutants can also be of primary or secondary nature.  Primary is emitted directly to atmosphere.  Secondary is formed by reactions between primary pollutants.  The major pollutants are 1. Oxides of nitrogen 2. Oxides of sulphur 3. Particulate matter
  • 4. CHEMISTRY OF FORMATION  N2+O2 2NO  2NO+O2 2NO2  S+O2 SO2  SO2+NO2 NO+SO3  2NO+O2 2NO2  NO2+SUNLIGHT NO+O  O+O2 O3
  • 5. HAZARDS  Corrosion  Climate change  Photochemical smog  SO2 irritates the eyes, nose and lungs  SO2 causes acid rain  NO2 causes pulmonary edema
  • 6. MARPOL LEGISLATION  Annex VI- Regulations for the prevention of air pollution from ships  Came to force on 19th May 2005  For every ship with 400 gross tonnage and above and for fixed and floating drilling rig  Certificate- “International air pollution prevention certificate”  Validity- period not exceeding five years
  • 7. MAJOR REGULATIONS  There are 19 Regulations but the following Regulations impact Vessel operation :  Regulation 12 – Ozone Depleting Substances  Regulation 13 – NOx emissions  Regulation 14 – Sulphur Oxide emissions  Regulation 15 – VOC emissions  Regulation 16 – Shipboard Incinerators  Regulation 18 – Fuel Oil Quality control
  • 8.  Emission standards are referred to a Tier I, II,III  Tier I came into force on 19th May 2005.  The revised Annex VI enters into force on 1st July 2010.  Tier II,III are more stringent than Tier I .  Tier II standards are expected to be met by combustion process optimization.  Tier III standards are expected to require dedicated NOx emission control technologies.
  • 9. REGULATION 13  Deals with control of NOX emissions.  All engines with power more than 130KW and built on or after 1/1/2000  Doesn’t apply to engines used in emergency.  Emissions must be limited to,  17.0 g/kWh when n <130 rpm;  45.0 x n-0.2 g/kWh when n is 130 or more but less than 2000 rpm;  9.8 g/kWh when n is 2000 rpm or more
  • 10.
  • 11.
  • 12. SOX CONTROL  Sulphur content of fuel shall not exceed 4.5%.  SOX emission ECA include Baltic and North sea area.  Sulphur content shall not exceed 1.5% in ECA.  Total emission must be less than 6 g SOX/kWh in ECA
  • 13.
  • 14.
  • 15. FUEL OIL QUALITY  Fuel oil shall be free from inorganic acid.  Bunker delivery note must be maintained.  Bunker delivery note must kept for 3 years.  Fuel oil sulphur content must never exceed 4.5%.  Parties of 1997 protocol must maintain a register of local suppliers of fuel oil.
  • 16. EMISSION MEASUREMENT  For Attaining Interim Certificate of Compliance.  Engines combined into engine groups by manufacturer  Engine from this group selected for emission testing
  • 17. EXHAUST GAS MONITORING TECHNIQUES Exhaust Gas Monitoring Equipments EExxttrraaccttiivvee SSyysstteemmss NNoonn--EExxttrraaccttiivvee SSyysstteemmss UUVV AAnnaallyysseerrss Chemi-luminescence IInnffrraarreedd AAnnaallyysseerrss UUllttrraa--VViioolleett AAnnaallyysseerrss
  • 18. Extractive Systems  Permanently installed  Requires additional equipment to process the exhaust gas sample.  Advantages  Able to be remotely located in a controlled environment  Easier to operate, calibrate and maintain.  Can be set up to monitor exhaust gas emissions from more than one engine.  Disadvantage  High Cost
  • 19. NON-EXTRACTIVE SYSTEMS  Predominately use infrared or ultra-violet techniques.  Measure the exhaust gas emissions without extracting the exhaust gas from the uptake system.  Advantages  More portable  Provides more rapid responses.  Disadvantages  Difficult to calibrate.
  • 20. CHEMILUMINESCENCE  HCD (Heated Chemiluminescence Detector).  Accepted standard for laboratory and test cell measurement of NOx.  Was the only available NOx detector available during the development of the IMO Technical code.  Needs to have a continuous supply of clean dry air else damage to the analyser components will result.  NO determination with detection limits down to 1 ppb.
  • 21. ULTRA-VIOLET ANALYSERS  Particularly useful for measuring SO2 .  Used in extractive and non-extractive systems.  Not suitable for the measurement of NOx.
  • 22. REDUCING SOX EMISSIONS  2 Possibilities :-  Burning fuels with lower sulphur content  Treating the engine exhaust gases  At Present limits on sulphur content of marine fuel  Globally – 4.5%  SECA – 1% from 1st july,2010  SOX emission control areas (SECA)  North Sea, English Channel and the Baltic Sea.
  • 23.
  • 24. TECHNIQUES FOR REDUCING SOX EMISSIONS  3 possibilities to reduce SO2 emissions from combustion processes: 1) REMOVAL OF SULPHUR BEFORE COMBUSTION 2) REMOVAL OF SULPHUR DURING COMBUSTION 3) REMOVAL OF SOX AFTER COMBUSTION ( I.E. FLUE GAS DESULPHURISATION )
  • 25. REMOVAL OF SULPHUR BEFORE COMBUSTION  Process used : Hydrotreating or Hydrodesulphurisation  Treatment of the oil with hydrogen gas obtained e.g. during catalytic reforming.  Sulphur compounds are reduced by conversion to hydrogen sulphide (H2S) in the presence of a catalyst.  H2S washed from the product gas stream by an amine wash  H2S is recovered in highly concentrated form  Converted to elemental sulphur via the Claus-Process  Feedstock is mixed with hydrogen-rich make-up and recycled gas and reacted at temperatures of 300 - 380 °C.
  • 26.  Removal of sulphur from heavier oils such as marine fuel oil often requires pressures of up to 200 bar.  Catalysts employed : cobalt, molybdenum or nickel finely distributed on alumina extrudates.
  • 27. CLAUS PROCESS  Most significant Gas desulphurizing process  Recovers elemental sulphur from gaseous hydrogen sulphide  The overall main reaction equation is: 2 H2S + O2 → S2 + 2 H2O
  • 28.
  • 29. REMOVAL OF SULPHUR DURING COMBUSTION  Experimental Stage  The combustible compound is mixed with an admixture of water soluble and water insoluble sulphur sorbent.  Such admixtures, remarkably, produces a reduction in the SOX level far greater than would be expected based on the activity of each sorbent alone.
  • 30. REMOVAL OF SOX AFTER COMBUSTION TTHHEE SSEEAAWWAATTEERR SSCCRRUUBBBBEERR SSPPRRAAYY DDRRYY SSYYSSTTEEMM WWEELLLLMMAANN--LLOORRDD PPRROOCCEESSSS LLIIMMEESSTTOONNEE //GGYYPPSSUUMM SSYYSSTTEEMM FFLLUUEE GGAASS DDEESSUULLPPHHUURRIISSAATTIIOONN ((FFGGDD))
  • 31. LIMESTONE/GYPSUM SYSTEM  Most widely used process  Principle  Suspension of crushed limestone in water is sprayed into the flue gases.  SO2 reacts with calcium ions to form calcium sulphite slurry  Aeration of the slurry with compressed air oxidizes calcium sulphite to calcium sulphate  After removal of the water, the calcium sulphate can be disposed off
  • 32.
  • 33.  Advantage :  SO2 reduction around 90 %  Disadvantages :  limestone has to be stored onboard  large quantities of gypsum waste is produced
  • 34. SPRAY DRY SYSTEM  A slurry of slaked lime is used as an alkaline sorbent  The slurry is injected into the flue gases in a fine spray.  The flue gases are simultaneously cooled by the evaporation of water  The SO2 present reacts with the drying sorbent to form a solid reaction product, with no wastewater.
  • 35. WELLMAN-LORD PROCESS  Hot flue gases are passed through a pre-scrubber  Ash, hydrogen chloride, hydrogen fluoride and SO3 are removed.  the gases are then cooled and fed into an absorption tower  SO2 reacts with a saturated sodium sulphite solution to form sodium bisulphite.  The sodium bisulphate is regenerated after a drying step to sodium sulphite again.  The released and clean SO2 - may then be liquefied or converted to elemental sulphur or sulphuric acid.  The sorbent is regenerated during the combustion process and is continuously recycled, but the products (sulphur compounds) have to be stored.
  • 36. TTHHEE SSEEAAWWAATTEERR SCRUBBER  Krystallon Sea-Water Scrubber  Removes 90-95 % of SO2  In addition removes 80 % of the particulates and 10-20% of hydrocarbons.  Advantages ♦ no limestone has to be stored on board, ♦ no waste (gypsum) is produced, which has to be deposited on land, ♦ the seawater already contains substantial amounts of sulphate and nitrate ♦reduction of engine noise and a reduction of the diesel smell..
  • 37. FFeeaattuurreess  Uses Cyclone Technology  The system needs only a little extra space  Aeration of the effluent is necessary  high degree of recirculation
  • 38. WWoorrkkiinngg  Water in contact with hot exhaust gas  Exhaust gas is channelled through a concentric duct into a shallow water tank.  Mixing baffles break up large gas flow into smaller bubbles  SOx in exhaust gas is dissolves in seawater  Larger particles (greater than 2.5 micron) captured in the water.  Fine particles (smaller than 2.5 micron) may pass through without capture.
  • 39.  Pumped through a set of large cyclones  Designed to separate some of the heavy particles, as well as light particles in a two-stage system.  Fed to a settling tank for collection of soot and oil.  Runs with no ongoing maintenance  Cleaned recirculated water is maintained at extremely low concentrations of hydrocarbons, making it safe for discharge to sea.
  • 40.
  • 41. OPERATIONAL CONCERNS AROUND THE CHANGE TO LOW SULPHUR FUELS  REDUCED FUEL VISCOSITY  FUEL ACIDITY  IGNITION AND COMBUSTION QUALITY  FUEL LUBRICITY
  • 42. REDUCED FUEL VISCOSITY  MGO and MDO fuels have a lower inherent viscosity than heavy fuel oil which can :  Effect Diesel Engines  Effect Steam Boilers
  • 43. Effect On Diesel Engines  Changes in fuel atomisation  Adversely affects power output and engine starting performance.  Solution Recommended : Use fuel coolers to control fuel viscosity
  • 44. Effect On Steam Boilers  Affects fuel flow setting (for a given pressure) at the burners  Can lead to “Over Firing”  Increased risk of flame failures and flame impingement on boiler tube plates.  Solution Recommended :  Change the nozzle  Or the air/fuel ratio settings
  • 45. FFUUEELL AACCIIDDIITTYY  Does not present a problem for steam boilers  But has a significant effect on diesel engines  Engine lube oils are formulated with alkaline additives to neutralise the acidic, sulphur, by-products of combustion.  IF amount of sulphur in the fuel is reduced, THE amount of alkaline additives should be reduced.  Too much alkalinity causes build-up of deposits that will affect the lubricating film  Solution Recommended : Oil with a lower Base Number (BN).
  • 46. IIGGNNIITTIIOONN AANNDD CCOOMMBBUUSSTTIIOONN QQUUAALLIITTYY  Effect On Diesel Engines  Effect On Steam Boilers
  • 47. Effect On Diesel Engines  Poor combustion and ignition may lead to increased fouling of the engine  Fouling is so excessive that moving parts such as exhaust valves are inhibited by the soot, leading to broken/bent valves  Excessive fouling of the scavenge air receiver combined with late ignition or prolonged combustion may lead to a buildup of soot deposit and the risk of fire.
  • 48. Effect On Steam Boilers  Leads to starting failures and more frequent flame failures  May lead to increased soot formation and consequent fouling of the boiler and exhaust system.  Solution Recomended: Follow detailed advice given by manufactures on procedures to follow when switching fuel qualities.
  • 49. FFUUEELL LLUUBBRRIICCIITTYY  Ultra Low Sulphur Diesel (ULSD) contains <15ppm sulphur.  Inherent lubricity of such diesel is reduced which in turn increases wear on fuel pumps and injectors.  Solution : Lubricity additives are commonly added at source to such fuels to reduce these problems
  • 50. EENNGGIINNEE EEXXHHAAUUSSTT DDEEPPEENNDDSS UUPPOONN  ENGINE TYPE ( i.e LOW,MEDIUM AND HIGH SPEED)  ENGINE SETTING ( i.e LOAD,SPEED AND FUEL INJECTION TIMING)  FUEL USED
  • 51. FFAACCTTOORRSS AAFFFFEECCTTIINNGG NNOOxx FFOORRMMAATTIIOONNSS  SPEED OF ENGINE  MAXIMUM TEMPERATURE INSIDE CYLINDER  COMPRESSION RATIO/PEAK PRESSURE  AMOUNT OF SCAVENGE AIR
  • 52. NNOOxx RREEDDUUCCTTIIOONN TTEECCHHNNIIQQUUEESS PRE-TREATMENT INTERNAL MEASURE (PRIMARY METHODS) AFTER TREATMENT (SECONDARY METHODS)
  • 53. NNOOxx RREEDDUUCCTTIIOONN TTEECCHHNNIIQQUUEESS PRE-TREATMENT INTERNAL MEASURE (PRIMARY METHODS) AFTER TREATMENT (SECONDARY METHODS)
  • 54. AALLTTEERRNNAATTIIVVEE FFUUEELLSS  METHANOL  LIQUIFIED PETROLEUM GAS
  • 55. MMEETTHHAANNOOLL  50% REDUCTION  NO SULPHUR  BAD IGNITION QUALITY  CORROSIVE  EXPENSIVE FUEL
  • 56. LLIIQQUUIIFFIIEEDD PPEETTRROOLLEEUUMM GGAASS  BUTANE(C4H10)+PROPANE(C3H8)  LOW ENERGY DENSITY SO MORE FUEL CONSUMPTION  NON-CORROSIVE  NON-TOXIC
  • 57. WWAATTEERR AADDDDIITTIIOONN TTOO FFUUEELL  UNDER RESEARCH WITH 30% OF WATER IN FUEL  30% REDUCTION IN NOx EMISSION  EFFECT ON ENGINE COMPONENTS IS NOT KNOWN  DECREASE MAXIMUM TEMPERATURE INSIDE CYLINDER  HIGH SPECIFIC HEAT
  • 58. NNOOxx RREEDDUUCCTTIIOONN TTEECCHHNNIIQQUUEESS PRE-TREATMENT INTERNAL MEASURE (PRIMARY METHODS) AFTER TREATMENT (SECONDARY METHODS)
  • 59. MMOODDIIFFIICCAATTIIOONNSS IINN CCOOMMBBUUSSTTIIOONN PPRROOCCEESSSS  INJECTION TIMING RETARDATION  INCREASE IN INJECTION PRESSURE  OPTIMIZATION OF INDUCTION SWIRL  MODIFICATION OF INJECTOR SPECIFICATION  CHANGE IN NUMBER OF INJECTORS
  • 60. IINNJJEECCTTIIOONN TTIIMMIINNGG RREETTAARRDDAATTIIOONN  REDUCE MAXIMUM COMBUSTION TEMPERATURE & PRESSURE  REDUCTION UPTO 30% OF NOx EMISSION  INCREASE IN SFC BY 5%  MORE EFFECTIVE FOR MEDIUM/HIGH SPEED ENGINES
  • 61. IINNCCRREEAASSEE IINN IINNJJEECCTTIIOONN PPRREESSSSUURREE  COMBINED WITH OTHER TECHNIQUES  PROVIDES BETTER ATOMIZATION
  • 62. OOPPTTIIMMIIZZAATTIIOONN OOFF IINNDDUUCCTTIIOONN SSWWIIRRLL  COMBINED WITH OTHER NOx REDUCTION TECHNIQUES  HELPS IN GOOD COMBUSTION  NO ADDITIONAL COST
  • 63. IINNJJEECCTTOORR SSPPEECCIIFFIICCAATTIIOONNSS  INJECTION PRESSURE  NUMBER AND ANGLE OF HOLES  SIZE OF HOLES
  • 64. CCHHAANNGGEE IINN NNUUMMBBEERR OOFF IINNJJEECCTTOORR  COMBUSTION PROCESS CAN BE CONTROLLED BETTER  REDUCE MAXIMUM COMBUSTION TEMPERATURE  ADDITIONAL COST OF FUEL INJECTOR AND PIPING  INCREASE IN MAINTENANCE COST  30% REDUCTION IS ACHIEVABLE
  • 65. SSCCAAVVEENNGGEE//CCHHAARRGGEE AAIIRR CCOOOOLLIINNGG  14% REDUCTION IS POSSIBLE BY LOWERING CHARGE AIR TEMP. FROM 40oC to 25oC  REDUCE COMBUSTION TEMPERATURE  SUITABLE FOR MEDIUM AND HIGH SPEED ENGINES  COOLING AIR TOO MUCH COULD LEND TO COMBUSTION PROBLEMS
  • 66. WWAATTEERR IINNJJEECCTTIIOONN  DURING COMBUSTION THROUGH SPECIAL INJECTOR  REDUCES THE BULK TEMPERATURE OF COMBUSTION  40% REDUCTION IN NOx EMISSION IS ACHIEVED
  • 67.
  • 68. WWAATTEERR IINNJJEECCTTIIOONN LLIIMMIITTAATTIIOONNSS  NEED OF SEPARATE PUMP FOR FUEL AND WATER  COST FACTOR  CORROSION
  • 69. NNOOxx RREEDDUUCCTTIIOONN TTEECCHHNNIIQQUUEESS PRE-TREATMENT INTERNAL MEASURE (PRIMARY METHODS) AFTER TREATMENT (SECONDARY METHODS)
  • 70. WWHHAATT IISS SSCCRR?? SELECTIVE CATALYST REDUCTION IS THE PROCESS OF REDUCING NOx COMPOUNDS WITH AMMONIA INTO NITROGEN AND WATER VAPOURS IN PRESENCE OF CATALYST.
  • 71.
  • 72. SSCCRR SSYYSSTTEEMM CCOOMMPPOONNEENNTTSS  REDUCTANT STORAGE TANK  PUMP  VAPORIZER (NOT IN CASE OF ANHYDROUS AMMONIA)  MIXER  INJECTION NOZZELS  CATALYST CHAMBER
  • 73. WWOORRKKIINNGG OOFF SSCCRR SSYYSSTTEEMM  AFTER TREATMENT TECHNIQUE  REDUCTANT(AMMONIA) IS INJECTED AND MIXED INTO EXHAUST  PASS THIS MIXTURE THROUGH CATALYST CHAMBER  TEMPERATURE OF CATALYST CHAMBER SHOULD BE 450K-720K
  • 74.
  • 76. RREEDDUUCCTTAANNTTSS UUSSEEDD  ANHYDROUS AMMONIA  AQUEOUS AMMONIA  UREA
  • 77. CCAATTAALLYYSSTT UUSSEEDD  BASE METAL OXIDES SUCH AS (VANADIUM AND TUNGSTEN)  TITANIUM OXIDE  ZEOLITE (HIGH TEMPERATURE DURABILITY)
  • 78. EEXXHHAAUUSSTT GGAASS RREECCIIRRCCUULLAATTIIOONN  REDUCES LOCAL COMBUSTION TEMPERATURE.  HIGH SPECIFIC HEAT OF EXHAUST GAS AND WATER VAPOUR.  DECREASES OXYGEN CONCENTRATION.
  • 79.
  • 80.
  • 82.
  • 83. EMISSION TRADE  Credit based system  This system was proposed by the swedish ship owners association.  Large combustion installations are capped by their maximum annual emissions.  Installation that emits less than its allocated credits can trade the difference in the emissions market.
  • 84.
  • 85. HOW IT WORKS?  Emission reductions become a tradable commodity, which can be bought and sold like any other product in the market.  Each ship will be allocated points depending on its yearly emissions in tons.  Trading can be made anonymously through an emissions market.
  • 86. CONCLUSION  Emission control is a necessity to make shipping transport viable.  CSR and Green marketing are the new buzz words.  One time investment and high returns.  Decrease in peak temperature can limit NOX emission.  Limit SOX by removing sulphur prior combustion.
  • 87. REFERENCES  Reduction of NOx and SOx in an emission a snapshot of prospects and benefits for ships in the northern European SECA area.  www.imo.org  MARPOL consolidated edition 2006  Exhaust emissions from ship engines - significance, regulations, control technologies by Laurie Goldsworthy  www.dieselnet.com