Technology · Acid-gas and NOx control
Flue-gas treatment: DeSOx and DeNOx systems
Flue-gas treatment adds acid-gas and NOx control to the particulate train: dry sorbent injection at 1.5–2.5 stoichiometry, spray-dry or wet flue gas desulfurization removing 90–98 % of SO₂, and SNCR (30–60 % NOx reduction at 850–1,050 °C) or SCR (80–95 %). Arrow Energy engineers these as integrated systems on its ESP and bag-filter line.
01 — Scope and position
What flue-gas treatment covers — and where Arrow Energy stands
Acid-gas and NOx control engineered onto the particulate train, stated honestly as a development line.
Flue-gas treatment (FGT) is the set of systems that remove acid gases — chiefly SO₂, plus HCl and SO₃ — and nitrogen oxides from combustion gas: DeSOx by alkaline reagent, DeNOx by selective reduction with ammonia or urea. Unlike particulate collection, which is one unit operation, FGT is a chain: reagent preparation and injection, a reaction zone, and a particulate collector that must now also capture the spent sorbent. The particulate train and the FGT system are therefore one design problem, not two purchases.
A plain statement of position: flue-gas treatment is Arrow Energy Co., Ltd.'s development line. We offer it as engineering capability and system integration — process selection, reagent-injection design, reaction-zone engineering and resizing of the downstream collector — built on the company's established gas-cleaning technology: electrostatic precipitators, the proprietary Electrocyclone and bag filters. It is not presented as an installed FGD fleet, and we will not imply one. Where a project needs a full wet FGD absorber island, we scope and integrate it with partners and state that scope explicitly in the offer. Guaranteed emission figures are stated per project after the technical assessment, on a defined basis — mg/Nm³, reference O₂, dry or wet, load range.
The pages on the wet scrubber, electrostatic precipitator and bag filter cover the individual vessels; this page covers how the chemistry is chosen and what it does to the rest of the train.
02 — DeSOx routes
Flue gas desulfurization: dry sorbent injection, spray-dry, wet
Three routes, ranked by removal fraction, water use and what they dump on the particulate collector.
Dry sorbent injection (DSI) is the simplest retrofit: powdered reagent is blown into the duct upstream of the particulate collector, reacts in flight and in the collector, and leaves with the ash. Two reagents dominate. Hydrated lime, Ca(OH)₂, is cheap and widely available but reacts on its outer surface only, so practical designs run stoichiometric ratios of 1.5–2.5 mol of reagent per mol of SO₂ removed, with utilization falling as the target removal rises. Sodium bicarbonate, NaHCO₃, behaves differently: at 140–160 °C it calcines in flight to sodium carbonate, releasing CO₂ and water vapour and leaving a porous, high-surface-area particle — the reason bicarbonate stays reactive at lower stoichiometry. That activation window is precisely the operating band of most bag filters and ESPs on biomass boilers, which is why bicarbonate DSI pairs so naturally with an existing collector. The trade-off is reagent price and a soluble sodium ash that changes the ash-disposal route.
Semi-dry / spray-dry absorption (SDA) atomizes lime slurry into a reactor vessel where the droplets absorb SO₂ while evaporating to dryness, cooling the gas toward (but not to) saturation. Removal sits between DSI and wet FGD, water consumption is a fraction of a wet system's, there is no liquid effluent, and the product is a dry lime/sulfite mix collected downstream — almost always in a bag filter, because the filter cake gives a second pass at unreacted lime.
Wet FGD — limestone or caustic scrubbing in a tray or spray tower — is the high-removal end: 90–98 % SO₂ removal at near-stoichiometric reagent use, with limestone yielding gypsum. It brings the full water circuit described on the wet scrubber page: saturated gas, purge treatment, chloride metallurgy, visible plume.
| Parameter | DSI (lime) | DSI (NaHCO₃) | Spray-dry (SDA) | Wet FGD |
|---|---|---|---|---|
| SO₂ removal, typical design band | 40–70 % | 70–90 % | 80–95 % | 90–98 % |
| Stoichiometric ratio | 1.5–2.5 | 1.1–1.5 | 1.2–1.8 | ≈1.0–1.1 |
| Working temperature | 130–350 °C | 140–160 °C activation | outlet 15–30 °C above saturation | saturated, 50–70 °C |
| Water demand | None | None | Moderate, fully evaporated | Highest; liquid purge |
| By-product | Dry Ca sulfite/sulfate in ash | Dry soluble Na salts in ash | Dry lime/sulfite mix | Gypsum or Na-salt effluent |
| Effect on particulate train | Adds sorbent load; resistivity shift on ESP | Adds sorbent load; best with bag filter | Dedicated collector after reactor | Downstream of collector; demister carryover |
| Retrofit intrusion | Lowest — silo, blower, lances | Low — plus milling | Reactor vessel + collector | Absorber island + water plant |
Ranges in this table are indicative design envelopes for route screening, not offer figures; removal on a specific fuel and collector is established in the project technical assessment.
Which SO₂ control fits an existing biomass plant?
Start from the removal fraction the limit actually requires. If 40–90 % removal closes the gap, DSI — lime at 1.5–2.5 stoichiometry or bicarbonate activating at 140–160 °C — retrofits onto the existing collector with a silo and injection lances. Only limits demanding more than ~90 % force a spray-dry or wet absorber and its vessel, water and by-product systems.
On low-sulfur biomass such as bagasse the SO₂ burden is often modest and DSI or SDA closes the compliance gap at a fraction of wet-FGD cost; on high-sulfur or mixed-fuel duties the arithmetic moves toward wet systems. The screening calculation — inlet SO₂, required outlet, reagent and disposal cost per tonne removed — is short, and we run it before proposing hardware.
03 — DeNOx
SNCR versus SCR: temperature window against catalyst risk
SNCR is cheap and coarse; SCR is deep and fragile on biomass. The fuel decides.
SNCR (selective non-catalytic reduction) injects urea solution or ammonia into the furnace where the gas passes through 850–1,050 °C. In that window the reagent reduces NO to N₂ without a catalyst; below it the reaction stalls and unreacted ammonia slips through, above it the reagent oxidizes and can generate NOx. Achievable reduction is 30–60 %, set less by chemistry than by mixing: the injection lances must cover the furnace cross-section at the plane where the window sits, and that plane moves with load and fouling. Practical SNCR on a bagasse boiler therefore means multiple injection levels selected automatically from furnace-exit-temperature measurement, droplet sizing matched to penetration depth, and ammonia-slip control — holding slip to low single-digit ppmv by zone selection and feedback trim, because slip is both a stack emission and, with any SO₃ present, a source of sticky ammonium salts on downstream surfaces.
SCR (selective catalytic reduction) performs the same reaction over a vanadia–titania catalyst at 180–420 °C depending on placement, reaching 80–95 % reduction with near-complete reagent utilization. The risks concentrate in the catalyst. It oxidizes a fraction of SO₂ to SO₃, and SO₃ plus ammonia slip forms ammonium bisulfate (ABS) — a sticky, acidic salt that condenses in catalyst pores and on air-preheater surfaces, blinding both. On biomass the exposure is worse: potassium and sodium in the fly ash are direct chemical poisons to vanadia catalysts, and high-dust placement on a fuel like bagasse or rice husk, with its abrasive high-silica ash, erodes and deactivates catalyst layers quickly. Biomass SCR is therefore usually placed low-dust — after the ESP or bag filter — which in turn may require reheat, an energy cost that belongs in the comparison.
| Factor | SNCR | SCR |
|---|---|---|
| NOx reduction | 30–60 % | 80–95 % |
| Operating window | 850–1,050 °C furnace gas | 180–420 °C at catalyst |
| Reagent utilization | Low–moderate; slip-limited | High; slip typically lower |
| Capital intrusion | Lances, pumps, tanks | Reactor, catalyst layers, possible reheat |
| Biomass-specific risks | Window wanders with load and fouling | Alkali poisoning; ABS fouling of catalyst and air preheater; ash erosion |
| Fits when | Limit needs a moderate cut | Limit needs a deep cut and catalyst life is protected |
Does SNCR or SCR make sense on a bagasse boiler?
SNCR first. Bagasse units usually face moderate NOx limits, and a well-mixed multi-level SNCR system delivers its 30–60 % cut with no catalyst to poison. SCR's 80–95 % is available but must be engineered around potassium-laden ash and ammonium-bisulfate fouling — normally low-dust placement after the collector, with the reheat penalty counted honestly.
04 — Train integration
What DeSOx and DeNOx do to the particulate train
Every kilogram of sorbent injected is a kilogram the collector must catch.
DSI and SDA convert a gas-phase problem into a particulate problem: the sorbent and its reaction products leave the process through the ESP or bag filter. The collector must be sized — or verified — for the combined burden of fly ash plus sorbent at the design stoichiometry, and the effect is not marginal: at ratios of 1.5–2.5 the injected mass can be several times the mass of SO₂ removed. On an electrostatic precipitator the added load raises the required collecting area for the same outlet concentration, and the sorbent shifts ash resistivity — sodium salts generally helpfully, calcium-rich mixes sometimes the other way — so a retrofit assessment reruns the SCA and power calculations rather than assuming the margin exists. On a bag filter the news is better: the sorbent-laden filter cake acts as a fixed-bed reactor, giving unreacted sorbent a second contact with the gas, which is why the same removal typically needs a lower stoichiometric ratio in front of a bag filter than in front of an ESP. The costs are higher cleaning frequency, higher pressure-drop baseline and a hotter ash-handling duty for soluble sodium salts.
Pre-collection changes the arithmetic again. Taking 85–95 % of the coarse ash out in an Electrocyclone stage ahead of injection means the final collector handles mostly sorbent, keeps the reacted product stream separable from coarse ash — relevant when the ash is sold or the sodium salts must be landfilled separately — and protects the collector's margin. SNCR adds no solids, but its ammonia slip converts to ammonium salts on cooler surfaces; SCR adds ABS management on the air preheater. These interactions are exactly why we quote FGT as an integrated system with the collector, not as a bolt-on.
05 — Emission limits
Emission limits that drive FGT selection
The limit, its reference O₂ and its averaging period decide the technology — verify all three before screening.
FGT selection starts from the applicable limit read precisely: the numeric value, the reference oxygen level, dry or wet basis, and the averaging period. A limit quoted without its basis is not usable for design. The table below lists the regimes most relevant to Arrow Energy's markets; numeric limits are deliberately left as verification items rather than quoted from memory, because limit tables are revised and fuel- and capacity-class-dependent.
| Jurisdiction / instrument | Applies to | PM | SO₂ | NOx | Reference basis |
|---|---|---|---|---|---|
| Thailand — PCD / MoI notifications | Biomass power and industrial boilers by fuel and capacity class | CONFIRM: verify current limit | CONFIRM: verify current limit | CONFIRM: verify current limit | CONFIRM: reference O₂ per notification |
| EU — IED with LCP BAT-AEL ranges | Combustion plants ≥ 50 MWth; BAT-AELs by fuel and size band | CONFIRM: verify current BAT-AEL range | CONFIRM: verify current BAT-AEL range | CONFIRM: verify current BAT-AEL range | 6 % O₂ dry for solid biomass |
| India — CPCB / MoEFCC norms | Boilers and TPPs by capacity and vintage | CONFIRM: verify current limit | CONFIRM: verify current limit | CONFIRM: verify current limit | CONFIRM: reference O₂ per norm |
| Brazil — CONAMA 436/2011 | Existing combustion sources by fuel and capacity class | CONFIRM: verify current limit | CONFIRM: verify current limit | CONFIRM: verify current limit | CONFIRM: reference O₂ per fuel class |
Two practical notes. First, particulate limits are always evaluated together with the acid-gas system, because DSI raises the collector's inlet load — the compliance margin on PM can shrink at the moment SO₂ compliance is achieved. Second, continuous-monitoring requirements (CEMS) and averaging periods often decide between a technology that is excellent on average and one that is robust minute-to-minute; SNCR's load-following behaviour, for instance, must be assessed against short averaging windows. Comparable gas-cleaning installations are listed under project references.
What information is needed to size a DeSOx or DeNOx system?
Six items: fuel analysis including sulfur, chlorine and alkali content; gas flow and temperature profile through the train; measured inlet SO₂ and NOx at stated O₂; the applicable limit with reference basis and averaging period; the existing collector's design margins; and the ash-disposal route. With these, route screening and a budget stoichiometry take days, not months.
FAQ
Engineering questions, answered
What is flue gas desulfurization?
Flue gas desulfurization (FGD) removes SO2 from combustion gas with an alkaline reagent. Dry sorbent injection with hydrated lime or sodium bicarbonate gives moderate removal at 1.5–2.5 stoichiometric ratio; spray-dry absorbers do better with lime slurry; wet limestone or caustic scrubbing removes 90–98 % of inlet SO2.
What is the difference between SNCR and SCR?
SNCR injects urea or ammonia straight into furnace gas at 850–1,050 °C and removes 30–60 % of NOx with no catalyst. SCR reacts ammonia over a catalyst at lower temperature and removes 80–95 %, but costs more and risks ammonium-bisulfate fouling and alkali catalyst poisoning on biomass fuels.
Why use sodium bicarbonate instead of hydrated lime for dry sorbent injection?
Sodium bicarbonate decomposes at 140–160 °C into porous sodium carbonate, opening fresh reactive surface exactly in the temperature range where most bag filters and ESPs operate, so it works at lower stoichiometric ratios. Hydrated lime is cheaper per tonne but typically needs ratios toward 2.5 for comparable removal.
Does adding DeSOx affect the ESP or bag filter?
Yes. Injected sorbent and its reaction products add to the particulate load the collector must capture, so ESP collecting area or bag-filter cloth area must be sized for the extra burden. A bag filter often improves sorbent utilization because unreacted sorbent held in the filter cake keeps contacting the gas.
Does Arrow Energy supply complete FGD plants?
Arrow Energy offers flue-gas treatment as an engineering and system-integration line under development, built on its installed particulate technologies — ESP, Electrocyclone and bag filters. Scope, reagent selection and guaranteed figures are defined per project after a technical assessment, on a stated basis of mg/Nm3 at reference O2.
Related engineering pages
Send us your plant data
Fuel, boiler capacity, gas flow, current emission and the limit you must meet. An Arrow engineer replies with a technical assessment basis — not a brochure.