MEDIUM FOR IMPROVING THE HEAT TRANSFER IN STEAM GENERATING PLANTS

Abstract
The present invention relates to a medium in the form of an aqueous mixture for improving the heat transfer coefficient and use thereof in power plant technology, in particular in steam generating plants. The medium contains at least one film-forming amine (component a) with the general formula: R—(NH—(CH2)m)n—NH2/, where R is an aliphatic hydrocarbon radical with a chain length between 12 and 22 and m is an integral number between 1 and 8 and n is an integral number between 0 and 7, contained in amounts up to 15%.
Description

The present invention relates to a medium in the form of an aqueous mixture for improving the heat transfer coefficient and the use thereof in power plant technology, in particular in steam generating plants.


Water is always required for operating steam generating plants. Wherever water is used, either in the form of cooling water or as a medium for the heat transfer, the water must be treated with water conditioning agents. Process water for operating steam generating plants can always contain salts, mainly alkali and alkaline earth metal cations in the dissolved form, e.g. as hydrogen carbonate, which can then be deposited as coatings in the form of scale on the surfaces of the boilers and the tubes of the heat transfer systems, owing to the increased concentration in the evaporating water. As a result, the heat transfer in the systems is hindered considerably and overheating may occur. Added to this is the danger of corrosion of the tubes and the boiler materials.


For economic and safety reasons, the operators of said plants or systems are obligated to avoid and/or prevent these precipitations and corrosion by using a corresponding water conditioning concept, so as not to endanger the functions of the plants.


Owing to the complete removal of the mineral salts from the water, for example via ion exchangers or reverse osmosis, it is possible in an economically acceptable manner to prevent the scale forming caused by the precipitating out of non-soluble salts such as calcium carbonate.


A further method for avoiding corrosion is the alkalization of the water-steam circuit, e.g. through adding alkalizing conditioning agents which prevent iron from being dissolved out of the apparatus components at high temperatures by increasing the pH values. These agents can be inorganic compounds such as phosphates, but also organic conditioning agents.


The use of film-forming amines for inhibiting corrosion has been described multiple times in the prior art.


Thus, the EP 0 134 365 B1 discloses a medium for inhibiting corrosion in steam generating plants and for conditioning boiler feed water in power plants, wherein this medium is composed of a mixture of aliphatic polyamines with 12 to 22 C atoms in the aliphatic radical, of an alkalizing amine such as cyclohexylamine, and of an amine ethanol.


The EP 0 184 558 B1 describes a method for preventing the depositing of scale by adding a synergistically acting mixture of polymer salts, ethylenically unsaturated carbonic acids, and aliphatic polyamines to the water to be treated.


The EP 0 463 714 A1 describes a ternary composition of dihydroxyacetone, catalytic amounts of hydroquinone and volatile amines for eliminating oxygen from the feed water and to prevent corrosion. So-called “film-forming amines” can also be contained in this composition.


The EP 0774 017 B1 describes a corrosion inhibitor of a polysulfonic acid which additionally contains polyamines, in particular a dispersing agent in the form of oxyalkylated polyamines.


In addition to the corrosion and scale forming, the secure heat transfer during the boiling of water in steam generators is a very important problem that continues to be relevant. A particular problem is the possible start of the Burnout I effect or condition, meaning a changeover of the nucleate boiling to a film boiling as a result of an excessively high number of steam bubble forming centers, but also a Burnout III condition, meaning a boiling crisis resulting from the suppression of steam bubble forming centers which can be activated. A negative influence was expected from organic as well as inorganic conditioning agents. The problem of increasing the safety during the heat transfer has so far not been solved in a satisfactory manner, especially not with the aid of the medium known from the aforementioned prior art which did not deal with this problem.


Despite the fact that organic conditioning agents which also contain film-forming amines for fighting corrosion and to prevent the scale forming have long been known, the effect of amines in the steam cycle of improving the heat transfer was not suspected, even though experiments relating thereto were conducted in 2003 already.


According to the publication VBG Power Tech, 9/2003 entitled: “SIND AMINE EINE ALTERNATIVE ZU HERKOEMMLICHEN KON-DITIONIERUNGSMITTELN FUER WASSER-DAMPF-KREISLÄUFE?” [Do Amines Represent An Alternative To Traditional Conditioning Medium For Water-Steam-Cycles?] by Professor Steinbrecht, it was determined in a model apparatus that neither Na3PO4 nor the amines had too negatively an effect on the heat transfer, especially in the technical area of interest relating to heat flux densities <500 kW/m2, realized in large-scale water boilers. In this case, the medium examined are sold under the brand names of “Helamin” and “Odacon” and are organic amines and/or contain organic amines.


In this connection, the model apparatus developed by Professor Steinbrecht appeared to be suitable to also examine the mixture, developed according to our invention, for its suitability and effect in steam boilers during the heat transfer.


Owing to the similar structure of the medium, the expectation was that the use of the new agent would not result in noticeable differences as compared to the known products.


However, the researchers were surprised to discover during the experiments that the use of the inventive agent, which is an aqueous mixture containing among other things several film-forming amines, resulted in a considerable improvement of the heat transfer, a result which could be quantified by measuring the heat transfer coefficient on the side of the water.


In the technical field of thermodynamics, the heat transfer coefficient or K-value is computed with the aid of the algorithm shown in FIG. 1.


The total value for the heat transfer coefficient is composed of different shares:


1) the heat transfer coefficient of combustion gas onto the tube (KFG);


2) the thermal conductivity of the tube (Ksteel) and


3) the heat transfer coefficient of the tube on the steam/water phase (Kmeas). See the following outline in this connection:


The inventors discovered a noticeable improvement of Kmeas on blank tubes—deltaL=0 (L is the thickness of the layer on the tube)—up to the thermally stationary condition of deltaL>0. Ksteel remained constant during the duration of the experiment. The tube and thus also the combustion gas (KFG) are heated electrically and can therefore also be viewed as constant.


It should be emphasized here that the measured effect of the improvement for Kmeas cannot be traced back to the known, indirect improvement as a result of preventing inorganic deposits of components in the water, e.g. calcium carbonate. This was ensured by using fully de-salinized water for the feed water.


The invention is specified in greater detail below with the aid of the claims:


1. A medium for improving the heat transfer coefficient in steam generating plants, wherein this medium contains at least one film-forming amine (component a) with the general formula:


a. R—(NH—(CH2)m)n—NH2, wherein R is an aliphatic hydrocarbon radical with a chain length ranging from 12 to 22, m is a whole number between 1 and 8 and n is a whole number between 0 and 7, in amounts of up to 15%.


2. The medium according to claim 1 for improving the heat transfer coefficient in steam generating plants, characterized in that it also contains one or more components b to d in addition to the film-forming amine:


b. One or more alkalizing amino alkanols with the formula ZO—Z′—NR′R″, wherein Z and Z′ represent a C1-C6 linear or branched alkyl group or hydrogen and can be identical or different and wherein R′ and R″ represent a C1-C4- alkyl group or hydrogen and can be identical or different, in amounts of up to 50%.


c. One or more dispersing agents, in an amount of up to 5 weight %, which are selected from compounds having the general structural formula,




embedded image


wherein R represents an aliphatic alkyl group with a chain length of C6 to C22, k represents a number between 2 and 3, and the parameters u, v, and w represent whole numbers, wherein the sum of v+w+(nu) ranges between 2 and 22 and/or a compound with the formula R3—C—O—((CH2)o—O—)p—Z′, wherein R3 represents an aliphatic alkyl group (saturated or unsaturated) with a chain length between C6 and C22, Z′ is defined as above, o is a whole number between 1 and 4 (boundaries included), p represents a whole number between 2 and 22 (boundaries included).


d. Water to supplement up to 100 weight %.


3. The medium according to claim 1, characterized in that the compound octadecenylpropane-1,3-diamine in amounts of 0.5 to 5 weight % is preferably used as the film-forming amine (component a).


4. The medium according to claim 1, characterized in that ammonia and/or cyclohexylamine and/or morpholine and/or diehtylaminoethanol and/or aminomethylpropanol are used as component b, preferably in amounts of up to 30%.


5. The medium according to claim 1, characterized in that the compound ethoxylated talcum-amine is used as component c in 15 to 20 EO units, preferably in amounts of 0.5 to 1 weight %.


6. The use of the medium according to claims 1 to 5, as a medium for improving the heat transfer in steam generating plants, characterized in that the concentration of the film-forming amine (component a) in the condensate ranges from 0.05 to 2 ppm and preferably from 0.1 to 1 ppm.







The model apparatus and/or the measuring equipment, shown schematically in FIG. 1 and specially designed for measuring the heat transfer, is not the subject matter of the invention.


Realizing the Experiment:

A specially designed test arrangement, used for examining the heat transfer during the container boiling, allowed the experimental determination of the heat transfer coefficient k and the characterization of surface effects since the boiling behavior of the experimental heating surfaces is decisively influenced by their (micro) geometric features (thickness, porosity/roughness).


The measurement was designed to determine the pressure-dependent and time-dependent characteristic boiling curves of conditioned boiler systems in dependence on the impressed heat flux density q on the experimental scale. It was furthermore the goal of these experiments to demonstrate the quite surprising suitability of the medium according to the invention as compared to the medium used according to the prior art.


The test arrangement for simulating the conditions near the boiler consists of two hermetically separated, identical pressure vessels, thus making it possible to simultaneously carry out the testing of two different water treatments.


A tube heating surface, installed in the apparatus so as to be submerged below the exposed water surface, generates saturated steam with the appropriate state of saturation. This replaceable, cold-drawn precision steel tube with dimensions of (6×1) mm, which is inserted process-tight, is heated directly with resistance heating via a high-power transformer and the power supply lines. FIG. 1 schematically shows the total experimental configuration.


Pre-treatment of the Tubes

To ensure the highest possible reproducibility of the individual experiment, the tube samples are chemically cleaned and activated following the soldering into the power supply. This operation takes place using a clean pickling or scouring solution which removes surface oxidation products as well as impurities, acquired by the precision tubes through contact during the production, storage or transport of these tubes. The treatment is realized as follows:


1. removal of organic impurities with acetone;


2. activation of the tube surface with a pickling or scouring solution (25% HCl, 5% HNO3, VE (demineralized) water) by submerging it for an interval of 6 minutes;


3. flushing with tap water (1-2 minutes);


4. neutralizing with 10% soda solution and submerging;


5. flushing with VE water (1-2 minutes);


6. flushing with isopropanol and subsequent drying at 105° C. in the drying cabinet (for 20 minutes).


The dried boiling tube is then photographed and is inserted in the hot condition—electrically insulated against the test vessel—into this vessel. The electrical lines are installed, the sensor for the tube inside temperature (insulated with a ceramic tube) is positioned in such a way that it is located geometrically in the center of the tube and the container is filled with the conditioned water (approx. 4.2 1).


Test Program

The test program comprises the following points during the long-term treatment at a saturation pressure of ps=15bar and recurring determination of the heat transfer coefficient at different pressure stages (2, 15bar).



1. Reference treatment of blank metal tubes with sodium phosphate up to the steady-state for the oxide layer, demonstrated with measuring technology.


2. Treatment of blank metal sample bodies with inventive medium (EGM) up to the steady-state.


3. Change in the treatment from sodium phosphate to EGM, continued treatment with the organic product up to the demonstrated steady-state for the heat flux coefficient.


The initial conditioning for the reference treatment with sodium phosphate and the subsequent operations with the inventive medium (EGM) are summarized in the following Table 1.


The EGM material contains the following components for this experiment:


a. 2 weight % of oleyl propylene diamine


b. 7 weight % of cyclohexylamine


c. 18 weight % of monoethanolamine


d. 0.5 weight % of non-ionized tenside


e. residual water to 100%.


The inventive medium, however, is not restricted to this composition which only represents an exemplary variant.









TABLE 1







properties of boiler water at the start of the water treatment.













pH value of
pH value of



conditioning
concentration
boiler water
condensate
conductance in


medium
in ppm
(25° C.)
(25° C.) c
mS/cm





Na3PO4
15-25
10.0-10.5
7-7.5
100-140


inventive
0.5-1.0
>8
>9
60-80


medium









Guaranteeing the Operating Conditions

To guarantee the conditions in the boiler as listed in Table 1, the concentration of applied boiler additives is determined regularly, so as to meter in additional additives and/or to dilute a concentration that is too high.


With an inorganic operation, the pH value of the boiler water is viewed as control variable which should be in the range of 10.0≦pH≦10.5. Since the pH value in the batch operation is determined discontinuously, the adaptation to the desired value is also discontinuous. In the process, a volume of approx. 1 liter boiler water is removed following the sample taking (approx. 50 ml) if the value drops below the lower pH limit, which is then replaced with a correspondingly conditioned equivalent and is subsequently degased several times. Should the pH value be sufficient, no further measures are taken, so that as little influence as possible is exerted on the oxide layer formation.


The substitution of a small volume of water ensures that the test tube body remains permanently submerged below the exposed water level. Since the batch operation entails a concentration of steam components that are not volatile during the treatment period and which are only conditionally removed during the aforementioned water substitution, this results in part in higher phosphate contents (up to 50 ppm) and electrical conductivities (up to 180 mS/cm) at the end of the operational period of up to r=1000h.


During the water treatment with the inventive medium, the concentration of the free film-forming amine (FA) in the condensate serves as benchmark, wherein respectively one sample is removed from the liquid and the condensate for determining it. A calibrated photometric test provides information on the amount of film-forming amine contained therein. If the actual value falls below the desired value window of 0.5 ppm≦[fA]≦1.0 ppm, an adjustment is made by adding formula via a N2 overpressure metering system. For higher volumes, a metering pump can be used, if applicable. Depending on the measured concentration in the boiler, up to 230 μl formula is subsequently metered in. A substitution of water identical to the one for the phosphate operation does not take place in this case.


Should an excess be detected, this also countered by substituting a water volume of 1 liter (VE).


The system loses water and/or especially water vapor and thus volatile steam components as a result of unavoidable leakages at the valve seats and tube connections. The make-up dose is thus configured such that following the adaptation, the upper limit value (approx. 1 ppm) of the film-forming amine is briefly reached in the condensate. The average of the aforementioned concentration range can be maintained at all times through regular monitoring.


Data Logging

Up to nine thermal flux densities are measured for each pressure stage in order to create a boiling characteristic.


Owing to the heat transfer into the boiler water, a certain non-stationarity of the operating point results for low and/or high thermal flux densities. That is to say, with high saturation pressures and correspondingly high heat losses and a small thermal flux density, the saturation temperature is subject to a negative trend. The reverse case applies for low saturation pressures and high thermal flux densities. This phenomenon is countered by using the auxiliary heating unit (only in the nucleate boiling range).


A further measure involves the “passing through” the actual operating point as a result of the cooling/heating of the system. A subsequent averaging of the measuring values (which have a maximum temperature deviation of 0.5° K for the desired saturation temperature) ensures the further processing of representative measuring values.


The aforementioned averaging and correction of the systematic measuring errors for the temperature and/or the current measurement takes place—in the same way as the determination of the heat transfer coefficient - using an electronic evaluation routine under Matlab®.









TABLE 2







(prior art)












Ps = 2 bar
ps = 15 bar













treatment
heat flux
heat transfer
heat flux
heat transfer



period
density in
coefficient
density in
coefficient


treatment
in h
W/m2
in W/m2 K)
W/m2
in W/m2 K)















Na3PO4
 0
40000
5419.0
40000
11634.6




50000
6418.3
50000
13401.4




60000
7370.2
60000
15042.3




70000
8284.4
70000
16585.6




80000
9167.4
80000
18049.8




80000
10024.1
80000
19448.3




100000
10858.1
100000
20790.8




200000
18368.9
200000
32254.8




300000
24983.3
300000
41702.3




400000
31075.3
400000
50040.0




500000
36806.3
500000
57638.9




600000
42265.0
600000
64696.8



300
40000
4141.9
40000
8039.5




50000
4905.6
50000
9260.4




60000
5633.2
60000
10394.3




70000
6331.9
70000
11460.7




80000
7006.8
80000
12472.5




90000
7661.6
90000
13438.9




100000
8299.0
100000
1436.6




200000
14039.7
200000
22288.2




300000
19095.1
300000
28816.5




400000
23751.4
400000
34577.9




500000
28131.6
500000
39828.8




600000
32303.8
600000
44705.8
















TABLE 3







invention










Ps = 2 bar
ps = 15 bar













treatment
heat flux
heat transfer
heat flux
heat transfer



period
density in
coefficient
density in
coefficient


treatment
in h
W/m2
in W/m2 K)
W/m2
in W/m2 K)















EGM
 0
40000
5254.0
40000
23994.3




50000
8575.0
50000
26754.4




60000
9830.9
60000
29243.7




70000
11035.3
70000
31528.3




80000
12197.2
80000
33651.1




90000
13323.2
90000
35641.8




100000
14418.3
100000
37522.2




200000
24243.4
200000
52623.7




300000
32855.6
300000
64136.9




400000
40763.9
400000
73803.0




500000
48186.8
500000
82293.1




600000
55244.7
600000
89950.0



300
40000
5913.8
40000
18695.8




50000
6990.7
50000
20846.5




60000
8014.6
60000
22786.2




70000
8996.5
70000
24566.3




80000
9943.8
80000
26220.3




90000
10861.7
90000
27771.4




100000
11754.5
100000
29236.6




200000
19764.4
200000
41003.4




300000
26785.5
300000
4997.3




400000
33232.7
400000
57506.0




500000
39284.3
500000
64121.2




600000
45038.1
600000
70087.4









Tables 2 and 3 show the results of the tests performed with the prior art products and the inventive product (EGM). It is immediately obvious that the heat transfer coefficient W/m2 is clearly improved and/or increased as compared to the product according to the prior art. That is to say, the higher the coefficient, the better the transfer of heat.


The effect of the improvement in the heat transfer coefficient with EGM is also maintained if the tubes are initially treated as disclosed in the prior art (Na3PO4) until the thermal stationarity is reached and the EGM is subsequently used for the conditioning.












TABLE 4









Ps = 2 bar
ps = 15 bar













treatment
heat flux
heat transfer
heat flux
heat transfer


treatment
period
density in
coefficient
density in
coefficient


with
in h
W/m2
in W/m2 K)
W/m2
in W/m2 K)















EGM after
 0
40000
6187.0
40000
18995.4


Na3PO4

50000
7176.6
50000
1895.4




60000
8101.5
60000
20750.5




70000
8975.9
70000
22360.3




80000
9809.3
80000
23855.4




90000
10608.4
90000
25257.0




100000
11378.2
100000
26580.4




200000
18039.8
200000
37194.0




300000
23622.0
300000
45271.6




400000
28601.6
400000
52045.7




500000
33176.2
500000
57990.7




600000
37452.0
600000
63348.8



450
40000
5599.2
40000
14549.2




50000
6494.7
50000
16211.1




60000
7331.8
60000
17708.9




70000
8123.1
70000
19082.8




80000
8877.3
80000
20358.8




90000
9600.5
90000
21554.9




100000
10297.2
100000
22684.3




200000
16325.9
200000
31742.2




300000
21377.7
300000
38635.8




400000
25884.2
400000
44417.0




500000
30024.1
500000
49490.6




600000
33893.7
600000
54063.3








Claims
  • 1. A medium for improving the heat transfer coefficient in steam generating plants, said medium comprising at least one film-forming amine (component a) in amounts of up to 15% with the general formula: a. R—(NH—(CH2)m)n—NH2, wherein R is an aliphatic hydrocarbon radical with a chain length of between 12 and 22, m is a whole number between 1 and 8 and n is a whole number between 0 and 7.
  • 2. The medium according to claim 1 for improving the heat transfer coefficient in steam generating plants, characterized in that it contains one or several components b to d in addition to the film-forming amine: b. one or several alkalizing aminoalkanols with the formula ZO—Z′—NR′R″ in amounts of up to 50%, wherein Z and Z′ represent a C1-C6 straight-chain or branched alkyl group or hydrogen and can be identical or different, and wherein R′ and R″ represent a C1-C4 alkyl group or hydrogen and can be identical or different.c. one or several dispersing agents selected from compounds with the general structural formula
  • 3. The medium according to claim 1, characterized in that the compound octadecenyl propane-1,3-diamine in amounts of 0.5 to 5 weight % is used for the film-forming amine (component a).
  • 4. The medium according to claim 2, characterized in that ammonia and/or cyclohexylamine and/or morpholine and/or diethylaminoethanol and/or aminomethylpropanol is used for the component b.
  • 5. The medium according to claim 2, characterized in that 15 to 20 EO units of ethoxylated talcum amine are used for component c.
  • 6. A method for improving heat transfer in steam generating plants, comprising adding the medium according to the claim 1wherein the concentration of the film-forming amine (component a) in a condensate is 0.05 to 2 ppm, preferably 0.1 to 1 ppm.
  • 7. The medium according to claim 4, wherein component b is used in an amount up to 30%.
  • 8. The medium according to claim 5, where component c is used in an amount of 0.5 to 1 weight %.
  • 9. The method according to claim 6, wherein the medium further comprises one or several components b to d in addition to the film-forming amine: b. one or several alkalizing aminoalkanols with the formula ZO—Z′—NR′R″ in amounts of up to 50%, wherein Z and Z′ represent a C1-C6 straight-chain or branched alkyl group or hydrogen and can be identical or different, and wherein R′ and R″ represent a C1-C4 alkyl group or hydrogen and can be identical or different.c. one or several dispersing agents selected from compounds with the general structural formula
Priority Claims (1)
Number Date Country Kind
10 2010 020 717.9 May 2010 DE national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/EP2010/005364 9/1/2010 WO 00 1/30/2013