June 2011 Archives

#084 Anodizing Layer Types and Characteristics

| No Comments | No TrackBacks

There are wide variety of anodize layer types with varying characteristics for aluminum and aluminum alloys.
The factors that determine the surface layers depend on the base metal. The mechanism of anodized layer forming differs from the electro-plating where anodized layers are created by the base metal being electrolytically dissolved to form oxidized layers. The thicker the layer becomes, more base metal is dissolved. Additionally, the base metal properties dictate how easily the oxidized layers can be formed.
There are many types of aluminum alloys with various compositions depending on their purposes, and they can be divided into heat treated alloys and non heat treated alloys. From a machining perspective, there are plates, bars, rods that are rolled, and cast, and die-cast mateials.
Various levels of anodizing difficulties based on different alloys exist and a number of schemes have been developed for the difficult alloys. Generally practiced anodizing processes are shown on [Table 1] below.

[Table 1] Types of Anodize Processes

Table

There are virtually infinite number of industrial anodizing processes combinations as the [Table 1] suggests, based on bath types, power supply waveforms, process speeds, and application purposes.
Currently, the most common electrolyte type is the sulfuric acid bath. The reason for the popularity is that the formed layer is colorless, and the power supply voltage and power consumption required for the electrolysis is low and economical for colored parts production. For specialized colors and wear resistance requirements, oxalic acid bath layers and oxalic acid added sulfuric acid bath are used.
Of the various electrolytes, the chromic acid bath is used almost only in the aerospace industry. As for the classification based on power supply waveforms, AC, AC superimposed, and pulse methods are used when the orthodox continuous DC does not yield satisfactory results.
Process speed classification in turn is a classification based on electrical current density. Large applied currents will form hard oxide layers by preventing the formed layer from dissolving into the electrolytes.
Various anodizing types discussed so far are in commercial use based on application requirements. Various aluminum materials will be discussed in the next volume.

#083 Anodizing

| No Comments | No TrackBacks

Previously, electro and electroless plating were discussed. Anodizing process for light metals will be discussed from this volume.

Anodizing is a surface treatment process of creating an oxidized surface layer by an electrolysis process where the subject part is made and anode (+ pole) in an electrolyte solution. Processed aluminum and its alloy parts are called by well know name of "Alumite".
The anodizing process using various electrolytes such as sulfuric acid, oxalic acid, chromic acid, or organic acid, as well as different temperatures and power source electrical waveforms will produce surface layers of different properties.
The oxygen produced at the anode produces porous layer with good electrical isolation characteristics, corrosion resistance, and wear resistant properties. The layer porosity is utilized for coloring as well as various functions added, and used for products such as reflector plates, household pots and pans, construction materials, automotive components, machinery/optical/communications, and computer components.
In addition to aluminum, anodizing is used on magnesium, titanium, and tantalum, but are not for the same purpose as the processes on aluminum but for electrical components such as capacitors utilizing the nature of the surface oxidation layers.

The layers created by the anodizing process can be classified into two categories. One is the former Porous Layer Type represented by the "Alumite Process", and other is the Barrier Type used for capacitors. The layer properties for these two are completely different. In our discussion, the Porous Layer Type" will be explained for our purpose of Surface Treatment subject.

image

#082 Corrosion Protection Measures - Corrosion Resistant Linings

| No Comments | No TrackBacks

A lining process is where corrosion resistant materials are adhered to the inside of steel plating vessels and material transfer pipes in order to protect from corrosions. The thickness of the linings are normally several millimeters as opposed to 100 to several hundred micro-meters of painting, and the linings offer superior chemical stability and mechanical strengths compared to those of paints.

Surface treatment processes such as plating, etc. use various tubs such as plating tubs, de-greasing tubs, electrolytic tubs, neutralizing tubs, and washing tubs with strong acids, alkali, and highly oxidizing solutions. The tubs are made of steel to support the weights of these chemical solutions and subject materials. These tubs are lined with corrosion resistant linings to prevent the tub structures from corrosions and contamination of the contents.

[Table 1] shows currently used corrosion resistant lining material in frequent use. The linings are selected based on chemical resistance applicability.
In addition to the corrosion resistant characteristics, specific gravity and thermal conductivity are of significant importance. Low specific gravity equates to light weight for easier handling during the lining installation processes which also reduces overall costs. Lower thermal conductivity of the linings as compared to that of steel (48.3w/m-k) means the process liquid temperatures are maintained better.

[Table 1] Corrosion Resistance Comparisons of Lining Materials
MaterialCorrosion Resistant FRPVinyl ChlorideNeoprene RubberPolypropylene
Physical PropertiesSpecific Gravity 1)1.4-1.81.451.640.91
Tensile Strength 2)85-18050-6020-3525-380
Thermal Conductivity 3)0.25580.15120.11630.0930
Corrosion ResistanceFormic Acid
50% or Less

40℃or Less
Chloroacetic Acid
60℃ or Less
Dilute Sulfuric Acid
60℃ or Less
Concentrated Sulfuric Acid
90% or Less

60℃ or Less

Norm. Temp.

50% or Less
Hydrochloric Acid
60℃ or Less
Phosphate
60℃ or Less
Chromic Acid
30% or Less

60℃ or Less

3%70℃ or Less
Hydrofluoric Acid
10% or Less

25% or Less
Caustic Soda
50% or Less

60℃ or Less

50% or Less
Ammonia Water
30% or Less
Sodium Hypochlorite

Note 1) g/cm3、Note 2) Mpa/mm2、Note 3) w/m・k、Good Corrosion Resistance、Poor Corrosion Resistance

#081 Corrosion Protection Measures - Corrosion Resistant Paints

| No Comments | No TrackBacks

Simply using the previously discussed corrosion resistant metals for structural materials in order to protect from corrosions will quickly become very expensive. Paints are used to protect from electrolytic and chemical corrosions by physically isolating the subject metals by surface coating with organic materials such as plastics.

Painting is applied on the subject metals by spraying, brushing, and roller coating. Subsequently, strong paint coats are formed by chemical polymerization of the ingredients. Some paints require 120 degrees C or higher temperature heating for the curing processes but natural curing paints are used for large structures such as steel beams, etc.

[Table 1] shows the general characteristics of corrosion resistant paints used in chemical plants and plating facilities.

[Table 1] General Characteristics of Paints
Resin
Type
Main
Appli
cation
Water Resist
ance
Acid Resist
ance
Alkali Resist
ance
Sulfur Dioxide Resist
ance
Solvent Resist
ance
Heat Resist
ance
Wea
ther Resist
ance
Alkyd
Resin
Steel Beams, Plates, General
Vinyl
Chloride
Steel, Concrete
AcrylicBuilding Exterior, Concrete
PhenolSteel Beams, Chemical Plants
Chlori
nated Rubber
Zinc
Plated Surfaces, Bridges, Steel Towers
Epoxy
Ester
Chemical Plants, Steel
Epoxy +
Amin
Chemical Plants, Steel
Tar +
Epoxy +
Amin
Water Proofing, Subme
rged Objects
×
Poly
iso
cyanate
Steel,
Pro
tection
of
Light Metals
Thermo-plastic AcrylicInterior Alu
minum, Steel Parts
Nitro
cellulose
Wood, Steel×
SiliconFor heat resist
ance
×
Note : Excellent, Good, OK, Not Applicable

月別 Archives

Pages

Powered by Movable Type 6.0.3

About this Archive

This page is an archive of entries from June 2011 listed from newest to oldest.

May 2011 is the previous archive.

July 2011 is the next archive.

Find recent content on the main index or look in the archives to find all content.