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"Don't Do Different Things - Do Things Differently"



May 14, 2011

EMISSION STANDARDS - POWER PLANTS

The emission standards for thermal power plants in India are being enforced based on Environment (Protection) Act, 1986 of Government of India and it’s amendments from time to time.A summary of emission norms for coal and gas based thermal power plants is given below in Tables
Environmental standards for coal & gas based power plants
Capacity
Pollutant
Emission limit
Coal based thermal plants
Below 210 MW
Particulate matter(PM)
350 mg/Nm3
210 MW & above

150 mg/Nm3
500 MW & above

50 mg/Nm3
Gas based thermal plants
400 MW & above
NOX(V/V at 15% excess oxygen)
50 PPM for natural gas;
100 PPM for naphtha
Below 400 MW & up to 100 MW

75 PPM for natural gas;
100 PPM for naphtha
Below 100 MW

100 PPM -naphtha/natural gas



The norm for 500 MW and above coal based power plant being practiced is 40 to 50 mg/Nm and space is provided in the plant layout for super thermal power stations for installation of flue gas desulphurisation (FGD) system. But FGD is not installed, as it is not required for low sulphur Indian coals while considering SO X emission from individual chimney
 Stack height requirement for SO2 control
Power Generation Capacity
Stock Height (Metre)
Less than 200/210 MWe
H = 14 (Q)0.3 where Q is emission rate of SO 2 in kg/hr, H = Stack height in meters
200/210 MWe or
less than 500 MWe
200
500 MWe and above 275 (+ Space provision for FGD systems in future)
However the norms for SOx are even stricter for selection of sites for World Bank funded projects. For example, if SOx level is higher than 100 ? g/m 3, no project with further SOx emission can be set up; if SO X level is 100 ? g/m 3, it is called polluted area and maximum emission from a project should not exceed 100 t/day; and if SOx is less than 50 ? g/m 3, it is called unpolluted area, but the SOx emission from a project should not exceed 500 t/day. The stipulation for NOX emission is that its emission should not exceed 260 gram s of NOX per Giga Joule of heat input.
In view of the above, it may be seen that improved environment norms are linked to financing and are being enforced by international financial institutions and not by the policies/laws of land.

May 12, 2011

BOILER WATER TREATMENT,SCALES & CORROSION

In general there are two types of boilers, low pressure and high pressure:
 A) Low pressure boilers will be found heating water or steam to be circulated around a building for heating purposes via radiators. These systems are "closed circuit" types and require little or no "make" water to top them up. Mostly low pressure boilers operate below 10 psi.
B) High pressure boilers will be found in industry, generating steam for a variety of uses, locomotion via a steam engine, or for end use of steam in laundries, rubber product manufacturing, wood pulp products, food manufacture etc. These boilers operate at over 10 psi and all require constant "make up" water as some of the steam is used.
Boiler feed water ("BFW") may either be the same as the makeup water, or may consist of returned steam condensate, or (as in most cases) will be a mixture of both.
The relative amounts of makeup and condensate may vary. A typical figure is 5% makeup with 95% condensate, but this depends on how the steam plant is operated and how much of the steam is condensed and recovered for recirculation.
In order to be non-scaling, the BFW must be a softened or demineralised water . In order to be non-corrosive to the carbon-steel or low-alloy steel components from which boilers are usually constructed, the water must be thoroughly deaerated. This is partially achieved by thermomechanical means (use of deaeration heating tanks), while the last traces of dissolved oxygen are removed by chemical agents ("oxygen scavengers").

Oxygen scavengers include both volatile products (e.g., hydrazine, or other organic products like carbohydrazine, hydroquinone, diethylhydroxyethanol, methylethylketoxime, etc.) and non-volatile salts (normally: sodium sulphite, Na2SO3, or a derivative thereof). The latter salts often contain catalysing compounds to increase of rate of reaction with dissolved oxygen (e.g., cobaltous chloride).
Oxygen Scavengers:
While the oxygen scavenging salts tend to react rapidly with oxygen, even at lower temperatures, their reaction products result in increased levels of total dissolved solids in the boiler feedwater.
To minimize this disadvantage, the salt should be fed to the storage tank of the deaerating heater and care should be taken that no precipitates are introduced into the boiler feed.
As rule of thumb, one typically feeds 10 parts of sodium sulphite per part of oxygen (to compensate for reaction with atmospheric oxygen and for impurities in the sodium sulphate).
Volatile oxygen scavengers are normally employed for higher pressure systems (e.g., above 1000 psig). These materials may react directly with oxygen and or directly with carbon steel boiler surfaces to form gamma iron oxide or magnetite. The formation of such "oxygen-impervious" oxide films precludes excessive corrosion.
Except for the common hydrazine (N2H4), most other volatile organic oxygen scavengers are sold under some proprietary name. The use of hydrazine in boiler feedwater is very common and very well documented. Because hydrazine typically does not react with oxygen at a rapid rate at lower temperatures, it may not be the preferred oxygen scavenger for low temperature boiler feedwater systems. In addition, hydrazine is seriously toxic and great care should be taken in its handling. Food production sites should consider seriously the potential consequences of using highly poisonous chemicals.
Scaling:
As water is heated and converted into steam, contaminants brought into a boiler with makeup water are left behind. The boiler functions as a distillation unit, taking pure water out as steam, and leaving behind concentrated minerals and other contaminants in the boiler. Scale forms as a result of the precipitation of normally soluble solids that become insoluble as temperature increases. Some examples of boiler scale are calcium carbonate, calcium sulphate, and calcium silicate.
Corrosion
Corrosion is a general term that indicates the conversion of a metal into a soluble compound. 
In the case of boiler metal, corrosion is the conversion of steel into rust. In a boiler, two types of corrosion are prevalent:
1.)     Oxygen pitting corrosion, seen on the tubes and in the preboiler section.
2.)      Low pH corrosion, seen in the condensate return system.
Corrosion of either type can lead to failure of critical parts of the boiler system, deposition of corrosion products in critical heat exchange areas, and overall efficiency loss.
Carryover:
Carryover is caused by either priming or foaming. Priming is the sudden violent eruption of boiler water, which is carried along with steam out of the boiler, usually caused by mechanical conditions. Priming can cause deposits in and around the main steam header valve in a short period of time. Foaming causes carryover by forming a stable froth on the boiler water, which is then carried out with the steam. Over a period of time, deposits due to foaming can completely plug a steam or condensate line.
Typical Boiler Failures and Causes:
Oxygen Pitting:
The time when a boiler system is most vulnerable to oxygen pitting is during idle periods. In order to prevent oxygen pitting during these times it is important to utilize proper storage techniques. Please see our technical tip on this subject at Dry Storage of Boilers and Wet Storage of Boilers.
 When a boiler is in operation, oxygen pitting is most likely to occur in feedwater heaters or economizer tubes, since this is this is where the water is first heated above the deaerator temperature. Maintaining a properly operating deaerator with sufficient oxygen scavenger is the best method of prevention.
 If oxygen pitting is noticed, it is important to note if it is “old” or active pitting. Active oxygen pits can be distinguished by the red-brown tubercle which, when removed, exposes black iron oxide within the pit.
Short-Term Overheating: 
This type of failure is usually indicated by a "thin-lipped" burst of the boiler tube. These failures occur when water circulation in the tube is interrupted, and the flue gas temperatures cause a rapid overheating of the metal to a point where the metal becomes highly plastic and a violent burst occurs. Typical causes of short-term overheating are circulation problems caused by poor operation (sudden increase in steam demand or low water level) or design, and tube blockage. Tube blockage normally occurs from deposition in the tube or supply header.
Long-Term Overheating:
 This type of failure is usually indicated by a "thick-lipped" burst of the boiler tube. Long-term overheating can result from excessive deposition, flame impingement, mild flow restrictions, or poor water or flue gas circulation patterns. Probably the most common of these is excessive deposition, which prevents proper heat transfer and excessive metal temperatures. This prolonged overheating of the tube causes metal degradation to the point that in can no longer handle the operating pressure and a "thick-lipped" failure occurs. 
Caustic Gouging:
 Caustic gouging occurs when NaOH concentrates under porous boiler water deposits. An example of such deposition would be iron, which tends to be porous. Essentially, what occurs is that boiler water is present in the deposit. As steam escapes, the NaOH concentration increases dramatically, dissolving the protective magnetite and boiler tube metal.
 In addition to the gouging of the boiler tubes you may also notice a white substance (sodium carbonate) outlining the edges of the original deposit.
 There are other failure mechanisms such as caustic and hydrogen embrittlement, stress corrosion cracking and steam blanketing. In this tip we have dealt with those we feel are the most prevalent. If you believe that you have a failure that does not fit into one of the categories we discussed please feel free to contact our staff. Finally, for a complete analysis and understanding of a failure, a sample should be sent to an independent metallurgical lab.

 



May 10, 2011

RANKINE CYCLE -PRINCIPLE

A Rankine cycle describes a model of steam-operated heat engine most commonly found in power generation plants. Common heat sources for power plants using the Rankine cycle are the combustion of coal, natural gas and oil, and nuclear fission.
The Rankine cycle is sometimes referred to as a practical Carnot cycle because, when an efficient turbine is used, the TS diagram begins to resemble the Carnot cycle. The main difference is that heat addition (in the boiler) and rejection (in the condenser) are isobaric in the Rankine cycle and isothermal in the theoretical Carnot cycle. A pump is used to pressurize the working fluid received from the condenser as a liquid instead of as a gas. All of the energy in pumping the working fluid through the complete cycle is lost, as is all of the energy of vaporization of the working fluid, in the boiler. This energy is lost to the cycle in that first, no condensation takes place in the turbine; all of the vaporization energy is rejected from the cycle through the condenser. But pumping the working fluid through the cycle as a liquid requires a very small fraction of the energy needed to transport it as compared to compressing the working fluid as a gas in a compressor (as in the Carnot cycle).
The efficiency of a Rankine cycle is usually limited by the working fluid. Without the pressure reaching super critical levels for the working fluid, the temperature range the cycle can operate over is quite small: turbine entry temperatures are typically 565°C (the creep limit of stainless steel) and condenser temperatures are around 30°C. This gives a theoretical Carnot efficiency of about 63% compared with an actual efficiency of 42% for a modern coal-fired power station. This low turbine entry temperature (compared with a gas turbine) is why the Rankine cycle is often used as a bottoming cycle in combined-cycle gas turbine power stations.
The working fluid in a Rankine cycle follows a closed loop and is reused constantly. The water vapor with entrained droplets often seen billowing from power stations is generated by the cooling systems (not from the closed-loop Rankine power cycle) and represents the waste energy heat (pumping and vaporization) that could not be converted to useful work in the turbine. Note that cooling towers operate using the latent heat of vaporization of the cooling fluid. The white billowing clouds that form in cooling tower operation are the result of water droplets that are entrained in the cooling tower airflow; they are not, as commonly thought, steam. While many substances could be used in the Rankine cycle, water is usually the fluid of choice due to its favorable properties, such as nontoxic and un reactive chemistry, abundance, and low cost, as well as its thermodynamic properties.


There are four processes in the Rankine cycle. These states are identified by numbers (in brown) in the diagram below. 
Process 1-2: The working fluid is pumped from low to high pressure, as the fluid is a liquid at this stage the pump requires little input energy.  
Process 2-3: The high pressure liquid enters a boiler where it is heated at constant pressure by an external heat source to become a dry saturated vapor. The input energy required can be easily calculated using mollier diagram or h-s chart or enthalpy-entropy chart also known as steam tables.   
Process 3-4: The dry saturated vapor expands through a turbine, generating power. This decreases the temperature and pressure of the vapor, and some condensation may occur. The output in this process can be easily calculated using the Enthalpy-entropy chart or the steam tables.  
Process 4-1: The wet vapor then enters a condenser where it is condensed at a constant temperature to become a saturated liquid.



    Apr 30, 2011

    RANKINE CYCLE

    Rankine Cycle:
        Saturated or superheated steam enters the turbine at state 1, where it expands isentropically to the exir pressure at state 2. The steam is then condensed at constant pressure and temperature to a saturated liquid, state3. The heat removed from the steam in the condenser is typically transferred to the cooling water. The saturated liquid then flows through the pump which increase the pressure to the boiler pressure (state 4), where the water is first heated to the saturation temperature, boiled and typically superheated to state 1. Then whole cycle is repeated.