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ElectroRedes 98-1
Safety in the Design of Electric
Distribution Networks
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choose the most convenient solution 98
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WHAT
ARE THE MAIN DETERIORATION MECHANISMS FOR CONDUCTORS OF OVERHEAD ELECTRIC
NETWORKS?
SUMMARY
The
preceding publication, titled "What criteria are involved in the
selection of material for conductors?", contains basic information
that will be further developed in this article. Without entering into
the well-known Engineering Design, it summarizes the essence of the benefits
offered by overhead electric conductors, examining the elements and mechanisms
of atmospheric corrosion on copper and aluminum, as well as the normal
forms of wear, permitting a qualitative appreciation of these materials.
1.
Introduction
2. Main advantages inherent to electric
conductors for overhead networks
3. How the enviroment attacks the material
of the conductors and accesories
4. Which mechanisms of corrosion
cause the deterioration of overhead conductors
5. Prevention of corrosion and measures
to offset it
6. Conclusions
1.
INTRODUCTION
Natural
wear of metals in general is manifested as the relatively quick dissolution
or loss of material, due to the local or general establishment of chemical
mutations that have intrinsic electric manifestations. This electro-chemical
process is known as corrosion. The phenomenon occurs independently of
the kind of usage, form or designated use, which, although it certainly
depends on the aggressiveness of the environment itself, also occurs with
the spontaneous tendency of metals to return to the combined state they
initially had as minerals. La publicación precedente bajo el título de
"¿ Qué Parámetros del Entorno Participan en la Elección del Material
de los Conductores ?" contiene, en parte la información de base para
el desarrollo del presente artículo. Este, sin abordar el Diseño de Ingeniería
que es ampliamente conocido, resume la esencia de las prestaciones que
están llamadas a cubrir los conductores eléctricos aéreos, examinando
los elementos y los mecanismos del ataque corrosivo atmosférico sobre
los metales Cobre y Aluminio, y las formas usuales del deterioro, permitiendo
la apreciación cualitativa de dichos materiales.
2.
WHAT ARE THE MAIN ADVANTAGES INHERENT TO ELECTRIC CONDUCTORS FOR OVERHEAD
NETWORKS?
The
requirements to which electric conductors of Overhead Networks are submitted,
are related to the transport requirements for Electric Energy, to the
initial and exceptional mechanical conditions of the installation, and
to the conditions imposed by the aggressiveness of the environment and
the surroundings. These demands, which prevail over the projected useful
lifetime of the infrastructure, establish the advantages that must be
offered efficiently, which depends in great measure on the properties
of the basic metals.
2.1
Primary Electrical Advantages
The electric and thermal conductivity with minimal energy loss and
minimal reduction in tension, are the main qualities that must be covered.
Specifically regarding copper and aluminum, between 16 and 95 mm2 caliber,
it is apparent that for similar sections, copper has 28% greater transport
capacity, with 77% greater thermal conductivity, which favors the transfer
of heat. On the other hand, given the same load current and line length,
aluminum has 60% more loss than copper, and for similar sections, load
current and length of line, aluminum has a 45 to 55% greater loss in tension
than copper. The technology of alloys for these metals only achieves slight
variations in these results.
2.2
Primary Mechanical Advantages
The resistance to traction with minimal linear expansion and minimal
permanent elongation, particularly under every day stress and other exceptional
greater demands that may occur during the service, all constitute the
primary qualities that must be covered. In this case, copper has more
than twice the mechanical resistance to traction stress. In addition,
given increases in temperature that occur periodically during the service,
it shows a comfortable Linear Expansion coefficient that is 30% less than
that of aluminum, a metal that due to its reduced Elasticity (55% less
than copper) allows greater loosening with permanent deformation. However,
it does have the advantage of having 70% lower specific weight than copper.
2.3
Primary Environmental Advantages
Resistance and durability against erosion derived from thermal cycles
and daily radiation, and against the abrasion caused by solid particles
carried by the wind, and the permanent establishment of various electro-chemical
processes originating from contamination and humidity, are all the primary
qualities that must be covered by overhead conductors. Regarding these
natural demands, the metals generate a protective coating of oxidation,
whose mechanical and electrical performance is related to its intrinsic
vulnerability. In his case, copper patina has the qualities of great strength
and compactness, as well as an excellent Electric Resistance that is not
prone to corrosion.
3.
HOW THE ENVIRONMENT ATTACKS THE MATERIAL OF THE CONDUCTORS AND ACCESSORIES?
The
interaction of the environment and surroundings, made up basically of
external radiation and the variation of seasonal meteorological and atmospheric
conditions, as well as the ground morphology and its topographical characteristics,
and the presence of contamination sources, all directly affect exposed
materials and cause their deterioration (aging). This translates into
loss of weight and a reduction in the scope of qualities.
3.1
Attack by Erosion
The weathering of metals refers mainly to their permanent exposure
to Cosmic Radiation and radiation derived from sunlight, particularly
the ultraviolet range. These phenomena are related to daily thermal variations
and the action of air currents. Given this incidence of factors of deterioration,
metals in general have a high superficial resistance thanks to the Patina
layer, the protective oxidation that metals spontaneously and immediately
form, which lessens the attack and makes any consequences insignificant
and very slow to appear in the long run.
3.2
Attack by Abrasion
The natural process of abrasion suffered by conductors and their accessories,
presupposes the existence of a moving element (the wind), and a projectile
element (light and heavy solid particles) that are lifted, transported
and projected against the metallic surface. They either slowly wear down
the protective layer of oxidation (with moderate winds) that simultaneously
reconstitutes itself on the next lower level, or else they break it (with
gusts of wind), which may cause localized processes of deep deterioration.
In this case, the performance of the metals (aside from their physical
qualities) and of the protective layer of oxidation, depends on the presence
of predominant winds and unstable or desert ground and other electro-chemical
conditions created by the environment. Save exceptional cases, having
only natural abrasion will cause minimal wearing, but may be a catalyst
for other kinds of wear.
3.3
Electro-chemical Attack
Atmospheric corrosion is basically an electro-chemical reaction to
the Electrode Potential between a metal or a metallic alloy and the surrounding
environment, creating localized deterioration. Chemically, the metallic
atoms of the affected or ANODIC areas (where oxidation or acidification
occurs) are transformed into Ions (Mn+), and give up their Electrons (ne-)
to a non-metal that could be (H+) or (O2), through the healthy or CATHODIC
areas (where reduction or alkalinization occurs). The circuit closes through
the ohmic resistance of the Electrolyte (on the metal surface).
-
ANODIC process: Dissolution of the metal and production of electrons.
M ---> MN+ + ne-
- CATHODIC process: Preservation of the metal and consumption of
electrons.
Mn+ + ne- ---> nM
- Hydrolisis: Complementary reaction of unstable metallic ions in
water.
M2 + H2O ---> M (OH) + H+
4.
WHICH MECHANISMS OF CORROSION CAUSE THE DETERIORATION OF OVERHEAD CONDUCTORS?
The
process of corrosion is established by the presence of the intrinsic potentials
of the metals (Electrode Potential), which may be measured in relation
to hydrogen (Standard), giving for copper (+0.340 volts) and for aluminum
(-1.700 volts), values that correspond to the scale of Reaction to Reduction,
according to which aluminum is apparently the most susceptible to dissolution
or corrosion.
a.
Formation of Electrolytes and the Protective Barrier.
The conductor surface that is covered irregularly by contamination,
suffers the daily phenomenon of natural environmental dampening, which
is very efficient in reduced thicknesses (at 80% Hr, from 30 um to 150
um), or else the phenomenon of condensation at greater thicknesses that
could become dew with run-off, which could limit the process of the attack.
Under these conditions, electrolytes form with different concentrations
and dilutions. Through the covering, oxygen from the air enters and molecular
hydrogen from the reaction exits, and the products of corrosion are also
transported. The protective barrier is identical for all metals, and is
a fine film of oxidation with specific characteristics that in each case
determines the kinetics of the deterioration, under the influence of other
factors such as temperature, the mechanical demands, and basically the
kind of contamination.
b.
Participation of Electric Current
When the conductors are energized, during the anodic cycle the process
of corrosion is added the emphasis on the formation of an alkaline
medium in the electrolyte as a product of the concentration of (OH)- in
the fault; or else, during the negative alternation or cathodic cycle,
the acidification from the greater concentration of hydrogen as ions (H)+.
Both phenomena affect the dissolution of the protective barrier, leaving
the metal unprotected.
4.1
Corrosion of Copper Conductors
The derivatives of chlorine and sulfur contained in coastal contamination,
originate the oxidation of copper by forming a blackish film called "Patina".
It is very dense, has low solubility, high electric resistance and high
resistance to the chemical attack and to corrosion. Thanks to this, it
protects the underlying metal, gradually limiting the rate of penetration
of corrosion to about 4.0 um/year near the coast and 1.0 um/year in areas
with a clean atmosphere.
a.
Compounds that form the protective barrier
The formation of the stable compounds of the Patina is variable, as
a function of the contaminants (Cl Na, SO2, etc.) and the catalysts (CIH)
that originate it. The (CuO and the (Cu2O) are found in the interface
with the metal, to which the insoluble hydroxides (Cu(OH)) with different
origins are superimposed; the following might predominate according to
each case: - In contaminated coastal areas - Brochantites: CuSO4 3Cu(OH)2
old Patinas - Antlerites: CuSO4 2Cu(OH)2 recent Patinas
- In areas free of contamination - Malachites: CuCO3 Cu(OH)2, mainly
- Azurites: 2CuCO3 Cu(OH)2, occasionally
- In contaminated and rainy areas - Langites: CuSO4 3Cu(OH)2 2H2O - In
agriculturally contaminated areas - Basic Cu Nitrates: Cu(NO3)2
Cu(OH)2
b.
Performance of Copper Conductors
The stated characteristics give copper a high resistance to corrosion,
except in the presence of NH3 or NH4 that is contained mainly in agricultural
contamination. Despite this, mechanical vibrations, abrasion, erosion
and thermal variations may cause fissures and faults in the Patina. When
this happens, the metal is uncovered, corrosion may occur, and electrolytes
with low contents of (Cl) could enter, causing a dislocation of the passivity;
otherwise, this may occur due to the deficit of oxygen that makes these
areas Anodic, in exceptional cases in certain seacoast splash areas that
are usually rare, and even so the foreseeable deterioration occurs over
a long term.
4.2
Corrosion of Aluminum Conductors
The oxidation of aluminum is originated primarily by the (Cl.H) resulting
from coastal contamination, forming a transparent gray Alumina film with
varying thickness, composed of a thin, compact, hard, layer that has low
solubility and high electric resistance, and acts as the main protective
barrier of the metal. It is also composed of another thicker layer that
is permeable and acts as an interface with the environment, providing
limited further protection. As a whole, the penetration of coastal corrosion
is lessened to an average rate of 16 um/year on the coast, and 3 um/year
in the sierra.
a. Compounds that Form the Protective Barrier
The layer of protective oxide is also formed by soluble compounds
that are formed as a function of aging. the stable Alumina (Al2 O3) is
found in the interface of the metal, superimposed by Hydracilles (Al2
O23 H2O), and finally the covering of hydroxides (Al(OH)2 3H2O) that in
the presence of the chlorides in coastal contamination, dissolves into
acid or alkaline solutions. Said deposits form independently of the nature
of the area, in this case the degree of contamination alone constitutes
a catalyst. They are called:
- Bahomite : Al2 O3 H2O Rhomboidal
- Bayerite : Al2 O3 3H2O Monoclinic
- Hydracillite : Al2 O3 3H2O Monoclinic
- Hydroxides : Al(OH)3 3H2O
b. Performance of Aluminum Conductors and Alloys
According to the stated characteristics, because aluminum is a very
alkaline and amphoteric metal, it is highly vulnerable to the aggressions
of a saline environment, particularly in coastal areas with direct marine
contamination. However, generalized superficial corrosion does not constitute
the main problem. the main problem is the localized corrosion that can
be particularly strong in the microfissures and faults in the layer of
protective oxide, which mainly have mechanical causes associated with
thermal variations, abrasion or vibration, uncovering the metal and allowing
the entry of electrolytes that accelerate the corrosion either by the
concentration of (OH)- or of (H)+, and extend the anodic areas without
interruption.
4.3
Kinds of Corrosion that Affect Conductors
They are related to the different factors under which Electric Conductors
are installed and operated. Without going into details of kinetics or
morphology, we may mention the kinds of corrosion that commonly occur
along the Peruvian Coast, which have been corroborated by field experience,
particularly in certain cases exclusive to aluminum conductors.
a. Corrosion from galvanic connections
This is produced due to the difference in Electrode Potential when
there is contact between different metals. This case demonstrates the
deterioration between the conductor and the clamp that leads to the breakage;
it also occurs in microcells when there are impurities in the manufacture
of the conductor.
b. Corrosion from Differential Airing Pitting
It occurs within the limit, between threads and inside the gaps on
the surface, due to the tightness of the conductors, in deep places where
the electrolyte has a greater concentration of oxygen, forming Anodic
and Cathodic areas. The reduction of oxygen occurs in the lower areas
that receive less air, producing a greater acidity in the electrolyte,
accelerating the deep corrosive attack.
c. Corrosion under Mechanical Tension Fatigue
This requires a mechanical tension (EDS of the installed conductors)
to combine with other demands (wind, its own weight, cycles of contraction
and expansion). In addition, it requires an alloy and a corrosive medium.
If under these conditions there are structural dislocations within the
crystal network or slippage within the grain of the metal, or else when
there are gaps or transversal cracks in the wiredraw, a combined process
of mechanical and electro-chemical corrosion will begin.
d. Corrosion from Concentration Cells
It occurs in the grooves of the wiredraw or in surface imperfections.
Within each groove, the metal dissolves by acidification or alkalinization,
becoming a solution. The same occurs on the outer part of the grooves,
but quicker, creating a chemical imbalance between the metal and the electrolyte,
which creates a flow of current of corrosion that establishes the process.
e. Inter-grain Corrosion
When the metal has a matrix phase and complementary precipitate phases,
upon the failure of the thermal treatment of hardening by excessive artificial
aging, an excess aging occurs that is characterized by the migration of
the precipitates to the edges of the grain, pushing the corrosive process
to the exterior, and making the threads brittle.This is because the phenomenon
continues at room temperature. The residual tensions of its manufacture
also contribute to this kind of corrosion.
f. Biological Corrosion
This is a metabolic process provoked by certain kinds of algae, fungus
or lichens, as well as by single-cell bacteria that land on the surface
of the conductors and actively decompose the organic and mineral matter
from the contamination trapped in the gaps, fissures, cracks and interfaces
of the threads.They produce enzymes, ammonia and sulfur and carbon dioxide
compounds that modify the local pH and cause corrosion.
5.
PREVENTION OF CORROSION AND MEASURES TO OFFSET IT
a.
Prevention of Corrosion
The main goal of Engineering Design is to ensure the quality of service
based on a trustworthy, safe and economic operation of the infrastructure,
closely observing this performance for a minimum period equivalent to
its designated useful lifetime (25 to 30 years); according to which the
examination of the environment and surroundings will lead to the selection
of appropriate materials frequently based on a technical-economic
analysis that will lead to the rejection of the minimum initial investment
which in the long run will be counterproductive.
b. Ways to offset corrosion
There are ways to extend the inexorable period of conductor deterioration
by corrosion; these technical resources are effective when the conditions
of the location are only moderately aggressive, which depends on the content
of the soluble matter in the atmospheric contamination. However, it is
impossible to ensure the trustworthiness of the installations.
When a more severe level of corrosive aggressiveness is determined, artificial
methods to counter corrosion in the installed infrastructure become merely
palliative since the failures from collapse in conductors do not occur
from generalized corrosion but rather from localized corrosion, which
may happen at any point.
6.
CONCLUSIONS
a.
The most important attributes that electric conductors for Overhead Networks
must have are mainly related to their performance given environmental
and surrounding aggressiveness, in which case the correct selection of
materials is fundamental.
b. The most common mechanisms of corrosion attacks on Overhead Conductors,
all lead to the localized or specific deterioration of the threads, whereupon
collapse is imminent. In these situations, copper ensures long duration
because it is a cathodic (noble) metal, even in seaside (Splash Zone)
installations.
c. The only way to ensure a trustworthy service and safe and economic
operation in the long run for coastal Overhead Electric Networks, is to
use the right material for the conductors. The justification of a lower
priced but qualitatively inferior alternative is only an illusion.
This
publication was prepared by Justo Yanque M., a Mechanical-Electric Engineer
(UNI), M.Sc. App. (FPMS-Belgium), who is a Consultant specialist with
extensive technical experience in electro-mechanical projects.
For more information on this subject, and for bibliographical references,
please contact Procobre
Peru.
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