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Volume 10, Issue 03, March 2019, pp. 1210–1216, Article ID: IJMET_10_03_123
Available online at http://www.iaeme.com/ijmet/issues.asp?JType=IJMET&VType=10&IType=3
ISSN Print: 0976-6340 and ISSN Online: 0976-6359
ABSTRACT
The process of anodizing aluminium alloys in an ozone-containing electrolyte when
a flat cathode is replaced with a needle shape was studied. The microstructure of the
oxide layer and the density distribution of the phases in the volume of the film in two
positions of the cathode — stationary and during its rotation — were investigated. The
mechanical properties of the surface layer were determined.
Key words: anodizing, needle-shaped cathode, ozonation, pore microgeometry, phase
distribution, surface hardness, activation.
Cite this Article: N. F. Kolenchin, The Influence of the Cathode Shape on the Phase
Composition and Structure During Oxidation, International Journal of Mechanical
Engineering and Technology 10(3), 2019, pp. 1210–1216.
http://www.iaeme.com/IJMET/issues.asp?JType=IJMET&VType=10&IType=3
1. INTRODUCTION
The search for ways to activate the interelectrode gap during oxidation is one of the promising
areas in the technology of hardening the surface layer of aluminium alloys. For most
researchers, the range of factorial variability is determined by the boundaries of the electrolytic
cell and, as a rule, is associated with changes in the chemical composition of the electrolyte and
the conditions of energy excitation. The performance is estimated by the degree of activity of
the main participants of the process - aluminium and oxygen under the conditions of the
necessary and sufficient influence of the working environment.
Non-traditional is the technology of external activation of oxygen and its transfer into the
interelectrode space. This is achieved through the introduction of ozone into the electrolyte [1].
Being the strongest oxidizer, ozone itself or atomic oxygen formed during its decomposition
acts, contributing to the intensification of the process, changing the structure and phase
composition of the oxide. Questions of the effectiveness of oxide formation in the ozonized
electrolyte are the motive for finding ways to activation, including changing the shape of the
cathode.
With traditional anodizing, a flat-shaped cathode is used [2,3]. This ensures a uniform
distribution of the electric field strength in the electrolytic cell. To change the density of
discharges on the surface of the anode, the amperage or voltage of forming increases.
Study of the influence of the cathode shape on the near-anode space is prompted by the
results of processes of the same nature in which a pointed cathode was used. According to the
authors of [4], the scientific and practical aspects of electrochemical processes in process gases
between the needle-shaped cathode and the liquid anode, when the pores of the oxide layer are
filled with steam, confirm the identity of the processes for anodizing aluminium and its alloys.
During plasma-electrolytic anodizing [5], passing a pulsed current of high density, a thin
cathode is placed over the surface of the electrolyte, and the anode is immersed to a depth of 1
mm. At the time of the breakdown, a vapour-gas funnel with oxygen donors is formed. The rate
of oxidation increases and the phase composition of alumina changes.
Studying the effect of electrode geometry on the distribution of electric fields in a discharge
of a high-current low-inductance vacuum spark type [6], when the cathode was the pointed tip
and the anode was the plane, it was found that the field strength is maximum at the anode
surface at a distance of approximately 1/4 of the radius from the centre, Figure 1.
The anodizing process was carried out in a bath tank (1), made of corrosion-resistant steel
12Kh18N10T with a capacity of 20 litres. Air was injected into the supply system by a SO-45A
grade compressor (2), passing through an air absorption dryer (3) HLS-R012-HL0030 entered
an ozoniser (4) "OZON-5PV1" with a power capacity not more than 150 W and a maximum
productivity of 16g/m3. Ozone-resistant PVC hoses and glass tubes were used as a pipeline for
transporting the ozone-air mixture. The ozone content in the air was determined using Medozon
254/5 with a measurement range from 0 to 150 mg/l. The ozone content in the liquid was
measured by Medozon-254/5Zh with a range of measured concentrations from 0.1 to 25 mg/l.
Adjustment of the flow rate of the gas-air mixture was carried out using a rotameter (5) Emis
Meta 210-R-008V-G. As a current source (7), a VSA-5K selenium rectifier was used which
allows adjusting the current in the range from 0 to 20 A at voltages up to 90 V. Contact with
the cathode was carried out using a sliding contact (9). The current strength was monitored with
a high-precision desktop digital multi-meter MS8050. Cooling and mixing were carried out in
a storage tank (12) with the help of a refrigeration unit (8) VS 0.7-3 and a bubbler (6). The
electrolyte with dissolved ozone was fed into the electrolytic bath by a pump (13).
A needle-shaped cathode (10), which is a cylindrical structure with a 40- mm outer diameter
and a 20-mm inner diameter, is made of thin, corrosion-resistant wire with a diameter of 0.1
mm. To ensure uniform contact with the anode plane, the working, end surface of the needle-
shaped cathode was sanded. The rotation speed was provided by an adjustable electric motor
(11). The distance between the electrodes varied in the interval of 0.1-0.5 mm.
Tests were conducted on the D16T alloy. The size of the anode was 60x40x3 mm. The study
of the structure of the samples was carried out using a JEOLJ5M-6150 scanning electron
microscope with an attachment module for X-ray spectral analysis and an Integra Aura atomic-
power probe microscope using the semi-contact method with scanning the sample previously
purified from organic pollutants with ethyl alcohol. Samples were scanned with a resolution of
1024 points per side. When scanning, the relief of the sample and the distribution of the
amplitude and phase of the probe oscillations over the scan area were recorded. The lateral
scanning resolution of the microscope is at least 3 nm, the height resolution is at least 0.5 nm.
Hardness was measured using an ultrasonic contact thickness gauge "Konstanta-K5". This
device allows measuring oxide coatings up to 2 mm thick, excluding preliminary sample
preparation. Hardness was determined by a multifunctional ultrasonic device "Konstanta-
K5U". Measurement limits were from 20 to 80 HRC, error was +/-2. The concentration of
transmitted ozone in the air mixture corresponded to 3 mg/l.
Figure 3 The oxide surface formed with a stationary cathode. Voltage of forming - 25V. Electrolyte - a 10%
solution of sulfuric acid cooled to 0 °C:
а - microgeometry of the flat part of the surface;
b - microgeometry of the surface in 3D
The crater-shaped surface is the result of the concentration of current density on the edges
of the cathode — the centre of elevated temperature and, accordingly, the zone of elevated
etching rates. The film was formed diametrically unevenly in thickness with a decrease in the
direction of the axis of the stationary electrode. Over 60 minutes, the average oxide thickness
turned out to be insignificant and amounted to 15 µm.
By imparting rotation to the cathode at a speed of 150 rpm, the electrolyte bubbling in the
contact zone was improved. The maximum convergence of two electrodes, with intensive
homogenization, provides an increase in current density at the tip, which contributes to the
dissolution of ozone in the interelectrode gap and, accordingly, increases the likelihood of its
participation in oxide formation. The results of measurements of the thickness and hardness of
the oxide layer over 30 minutes of the process are shown in Table 1. The oxide formed on the
inner surface of the sample has low hardness and thickness.
Figure 4 Geometry of the pores formed during the rotation of the cathode at a speed of 150 rpm with a
magnification: a-100 times; b-1000 times
The results of the electronic study of the oxide layer are presented in Figure 4. Stretched
pores in one vector variant are the result of stretching the discharge spot in the course of the
electrode rotation. The concentration of current density at the cathode tip during movement
creates an elongated temperature zone into which dissolved gases are drawn. The unreacted part
of ozone, in the form of large gas bubbles, is split into small fractions, increasing the solubility
and intensification of the anodic process. The vector of oxidation takes a two-dimensional
direction; one beam is directed perpendicular to the anodizing plane, and the other - towards
the rotation of the cathode, which causes some curvature of the pores. This is confirmed by the
results of studies of the formed structure in the mode of reflected electrons presented in Figure
5. The darker part of the image indicates the formation of phase structures with the highest
density of atoms. The distribution of dark areas occurs both along the filiform channels and in
the horizontal direction.
Figure 4 Geometry of the pores formed during the rotation of the cathode at a speed of 150 rpm with a
magnification: a-100 times; b-1000 times
4. CONCLUSIONS
1. The use of a needle-shaped cathode during oxidation in an ozone-containing medium
increases the potential of the electric field in the reaction zone and contributes to the dissolution
of unreacted ozone in the electrolyte as a result of grinding the macro-bubbles of the gas-air
mixture;
2. An increase in the temperature gradient and an increase in the concentration of the
oxidizing agent in the pore space intensifies the process of oxidation with an increase in the
hardness and thickness of the oxide by 10% in comparison to anodizing with a flat-shaped
anode;
3. The mobile version of the electrode changes the pore geometry in the direction of
movement of the pointed cathode with the formation of phase structures in two directions —
perpendicular to and along the anode surface.
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