Cause analysis and solutions for ESP corrosion

Kiln back-end electrostatic precipitator (ESP) of an Egypt cement plant experienced severe corrosion within one year of operation. Based on the chemical composition of samples, calculation of the acid dew point and XRD analysis of rust powder, ESP corrosion reasons were found, including the high chloride content in raw meal, high water vapor content, the severe air leaking. Solutions were proposed.

1 Introduction

A cement plant, one of EPC projects by Tianjin Cement Industry Design & Research Institute (TCDRI) Co. Ltd., is situated in Egypt directly on the Mediterranean Sea. The climate is moist and the day-night temperature difference is big. The nominal capacity of this production line is 5500 t of clinker per day. The production line firing natural gas is a 5-stage precalciner kiln, equipped with a TTF calciner (TCDRI Tri-spouted Furnace).

Severe corrosion occurred on the pole wire, pole plate, shell (Fig. 1) of the kiln back-end electrostatic precipitator (ESP) within one year after...

1 Introduction

A cement plant, one of EPC projects by Tianjin Cement Industry Design & Research Institute (TCDRI) Co. Ltd., is situated in Egypt directly on the Mediterranean Sea. The climate is moist and the day-night temperature difference is big. The nominal capacity of this production line is 5500 t of clinker per day. The production line firing natural gas is a 5-stage precalciner kiln, equipped with a TTF calciner (TCDRI Tri-spouted Furnace).

Severe corrosion occurred on the pole wire, pole plate, shell (Fig. 1) of the kiln back-end electrostatic precipitator (ESP) within one year after commissioning. The ESP dust collection efficiency reduced significantly, which affected the normal operation. During the kiln shutdown, internal surfaces of ducts from ID fan to ESP fan, conditioning tower, ESP, bucket elevator and air slide seemed wet and muddy due to water absorption by material particles. Liquid gathered from the ESP had a PH value of 6.

2 Iron rust and ESP corrosion

When impure iron is in contact with water, oxygen, and other strong oxidants or acids, it rusts. The rusting of iron is an electrochemical process. The rate of corrosion is affected by water and accelerated by electrolytes. The key reaction is the reduction of oxygen:
O2 + 4 e + 2 H2O → 4 OH

Because it forms hydroxide ions, this process is strongly affected by the presence of acid. Indeed, the corrosion of most metals by oxygen is accelerated at low pH. Providing the electrons for the above reaction is the oxidation of iron that may be described as follows:

Fe → Fe2+ + 2 e

The Fe(OH)2 formed is insoluble and is readily oxidized to form Fe(OH)3, which ordinarily dehydrates. The final product (when dry) has the reddish-brown flaky character. This kind of corrosion is normally called oxygen-consuming corrosion.

Generally, the reasons for ESP corrosion include caustic gas, high moisture content, high air leakage rate, uneven gas velocity, ineffective heat preservation for the shell and so on. However, which factor is the culprit for the ESP collapse of this plant within extremely short time?

3 Cause analysis

3.1 Material analysis
SO3 content and Cl content of raw meal were in the range of 0.35 %~0.61 % and 0.196 %~0.263 %, among which the Cl content was well above the ordinary cement plants. The chemical composition of materials is shown in ­Table 1. Ash from conditioning tower and ESP had a high content of chlorine. Iron oxides were the main component of the rust powder scraped from the ESP plate, which was high in SO3 content (0.47 %) and extremely high in Cl content (1.698 %).

Studies show that pyrite and organic sulfur in raw materials are oxidized to form SO2 at temperatures between 400 °C and 600 °C, preferably in cyclone Stage II or Stage III. Also, combustible chlorine appears in gas mostly in the form of HCl in the temperature range 300 °C ~ 600 °C. To evaluate the gas composition, raw meal was calcined at 600 °C. The results and assumed conditions are displayed in Table 2.

After the above-mentioned low-temperature calcination, the SO3 content of raw meal decreased from 0.35 % to 0.31 % and the Cl content decreased from 0.207 % to 0.148 % (the mass loss had been considered). The previous studies [1] show that the cyclones at the lower temperature end are much less efficient in removing SO2 with CaCO3, due to the combined effects of low temperature and the small amount of CaO or Ca(OH)2. Thus ignoring the SO2 and HCl removal from the upper preheater stages, SO2 and HCl concentration from C1 flue gas was 340 mg/Nm3 (119 ppm) and 645 mg/Nm3 (396 ppm), respectively.

3.2 Acid dew point
As a broad generality, the flue gas from C1 is composed of nitrogen (N2), excess oxygen (O2), carbon dioxide (CO2) and water vapor (H2O). The flue gas may also contain small amounts of carbon monoxide (CO), nitrogen oxides (NOx) and sulfur oxides in the form of sulfur dioxide (SO2) and sulfur trioxide (SO3). The SO3 is present because a portion of the SO2 formed is further oxidized to SO3. The gas phase SO3 then combines with the water vapor to form gas phase sulfuric acid H2SO4. Particularly in this plant, C1 flue gas contains gaseous hydrochloric acid (HCl). Given a flue gas composition, the sulfuric acid dew point can be calculated according to the formula:
1000/T =1.7842 + 0.0269 log10 (pH2O) - 0.1029 log10 (pSO3) + 0.0329 log10 (pH2O) log10 (pSO3)
A cement plant consequentially has a high water vapor content in C1 flue gas, which is assumed to be 18 vol. % for this Egyptian plant. It is commonly assumed that about 1 to 5 % of the SO2 will be further oxidized into SO3, thus about 1 ppmv (parts per million per volume) to 6 ppmv SO3 exists in C1 flue gas. Multiplying the total gas pressure by the volume fraction, the partial pressure can be obtained. As an approximation, the sulfuric acid dew point of the C1 flue gas ranges from about 120 °C to about 130 °C.

During the operation, the flue gas from C1 maintained a low temperature of 280 °C. When the raw mill was off, the ESP inlet gas temperature was approximately 140 °C and the outlet gas temperature was only 85 °C. When the raw mill was on, the ESP inlet gas temperature was merely 100 °C to 120 °C.The water dew point and the acid dew point of hydrochloric acid of the flue gas are far below the flue gas temperature from ID fan to ESP fan. The liquid condensation on the equipment wall is ascribed to the presence of gaseous sulfuric acid, the acid dew point of which is much higher.

3.3 XRD analysis of rust powder scraped from the ESP plate
Figure 2 shows the XRD patterns for rust powder scraped from the ESP plate. The main phases are Fe2O3, FeOOH and CaCO3. Chloride and sulfate of iron are not detected, probably due to the low concentration below the analytical limits.

3.4 SEM of outer rust layer from corroded ESP plate
Figures 3a and 3b show the SEM micrograph of the ­ou­ter rust layer from a corroded ESP plate. Magnifications of Figure 3a is 10000x resp. 20000x at 3b. The flaky crystals observed from Figure 3a and rod-like crystals observed from Figure 3b are probably responsible for different crystal structure of FeOOH.

3.5 Corrosion analysis
Chloride ion plays an important role in the corrosion reaction rate by changing the structure of the passive film and increasing the dissolution of the film. Normally, a thin protective layer forms on the metal which discourages further corrosion. However, chloride ion will destroy the protective layer. The existence of the chloride ion leads to the increase of FeOOH in the rust layer. FeOOH is typically friable and easily crumbles off to continually expose fresh metal for reaction, thus accelerating the corrosion reaction. In addition, chloride ion has a high electron negativity and absorbs on the metal surface or the thin passive layer more easily than oxygen or hydroxide ions. In this case, the metal is dissolved and corrosion is enhanced.

It is induced that the present gaseous HCl in the ESP inlet gas leads to the high Cl content of 1.698 % for the rust powder scraped from ESP plate. Meanwhile, ash from ESP contains a high Cl content, as shown in Table 1.

To sum up, the high chloride content of 0.207 % in raw meal is responsible for the ESP corrosion in this plant. The reaction occurring on the ESP plate is the oxygen-consuming corrosion, while more importantly, chlorine favor the corrosion and cause the collapse within such a short time. Of course, the high water ­vapor content due to the combined effects of firing natural gas and the local moist climate is a necessity for the accelerated corrosion. It is worth mentioning that the large temperature difference of 55 °C between the ESP inlet and outlet gas indicates the severe air leaking, which is the main inducement for the corrosion.

4 Solutions

Although there are many reasons for the ESP corrosion, the direct reason is the existence of gaseous acid and  that the flue gas temperature is below the acid dew point. As a result, the gaseous acid condenses into liquid acid on the equipment wall and speeds up the corrosion reaction. Focusing on this cement plant, the following solutions are recommended.

Take all measures to guarantee the ESP seal and reduce the air leaking rate.

Enhance the heat preservation performance of the ESP shell.

Past experiences show that keeping the flue gas temperature 30 °C above the acid dew temperature is effective in retarding the corrosion. For this plant, the ESP inlet gas temperature should reach 150 °C or higher. It can be realized by adjusting the feeding point in the preheater tower.

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