Saturday, September 1, 2012

BGAS Practical Questions Banana Gauge


Practical Assessment 
From the picture shown answer for all questions.
 

1) - What is the name of this equipment?
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2) - What is the purpose of use this equipment?
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3) - On which substrate we can use this equipment?                                                                                                 
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4) - Can we used for measuring DFT of paint which applied on top of Non Ferrous substrate?
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5) - If the painting system containing MIO, and the substrate is Ferrous, this equipment can use or not?
     And why?
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6) - This equipment working in which principles?
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Thursday, August 30, 2012

BGAS Painting Study Material Chapter 2 continuation

Other properties of an abrasive have an effect on the resulting substrate also, these being.
A. Size of the particles
B. Hardness of the material
C. Density of the material
D. Shape of the particle
E. Velocity of abrasive
F. Angle of impingement
G. Time & distance

For example steel has a density of approximately 7.6 gm/cc and copper slag, approximately 4.2 gm/ccIf one particle of each material, of identical size, hit a steel substrate, then it would be logical to say that the steel would impinge further into the substrate, resulting in a deeper trough.

A spherical particle would not impinge as deeply because the large smooth surface area would use its energy up in preening or work hardening the surface rather than cutting into it. So a shot blasted surface is different in appearance and texture to that of grit blasted surface.

Sizing of abrasives
G Prefix = Grit (amorphous, points and cutting edges, irregular profile)
S Prefix = Shot (spherical, smoother profile)

The G or S notation is followed by a number, which denotes the particle size.
G-24 or S-330BS 2451 the 24 means nominally 24 thousandths of an inch.
SAE (society automotive engineer) USING THE J 444 SIEVE SYSTEM.it represents 1/24" = approximately 40 thou.
 
New BS ref. 7079 pt PARTICLE SIZE DISTRIBUTION Uses a different method again, in metric units. G140 would mean a nominal particle size of 1.4mm

Adhesion and Profile
A commonly used definition of Adhesion is: - The force required separating two surfaces in touch.

A newly rolled plate, perfectly smooth, 1m x 1m has an apparent surface area of 1m2 and an actual area of 1m2.  Abrasive blasting roughens the surface and increases the actual area, (the apparent area is still 1m2), thus increasing the adhesion.

Two theories of adhesion are:
1. Molecular Interference
Because the surface is rough and uneven the paint wets, and locks into the profile, Analogy Velcro Physical.
2. Molecular Attraction
Negatively charged particles attracted to positive areas, and vice versa Analogy Magnet (sometimes called Ionic Bonding) Chemical.

continue............

Wednesday, August 29, 2012

BGAS Painting Study Material Chapter 2 continuation

In the context of this course we are considering the following: -
a) Sand
It is not permitted to use sand.  SI 1657 states that any mineral used as an abrasive must release less than 1% free silica on impact.  (Silica causes preumonicosis or silicosis).  COSHH REGS does not allow the use of sand containing silica for dry blasting.  Sand itself is perfectly safe, but shattering on impact releases silica which can be inhaled. The amount of copper in the structure is extremely minute.

b) Copper Slag
Copper Slag
1. Minerals melted with the copper,
2. Liquefies and forms a protective cover over the molten copper to prevent reaction with the atmosphere. 
3. When the copper metal is run off the slag is rapidly cooled in cold running water
4. The material is supplied in grit form (random, sharp Edges, amorphous (no definite shape) and is very brittle), shatters into smaller pieces on impact, and should be used only once and then discarded and so classed as expendable.

Garnet
c) Garnet
A natural mineral classed as being “of a diamond type Hardness” can be either expendable or recyclable. Cleansing units are available to extract contamination so that the material can be reused, usually up to three times.  Doesn’t shatter on impact but does suffer some Wear” Supplied in Grit form. 

d) Metallic Grit
Metallic Grit
Steel and Iron are both metallic.  Steel grit being the Softer of the two to round off on impact and loses its sharp edges.  Angular Chilled Iron chips off small slivers on impact to produce sharp cutting surfaces on its next cycle.  Metallic abrasives are recyclable because the particles reduce in size slowly. Hence it can be re-used many times and still perform a useful function in a '‘working mix’. A working mix is an accepted ratio of large and small particles, where the large particles cut the profile and the smaller particles clean out the troughs.

e) Metallic Shot
Metallic Shot
Shot is spherical and doesn’t shatter (otherwise it would form grit).  When supplied the particles are virtually uniform in size and shape, (not a working mix) But like the grit they wear down slowly in size. The particles are worn down eventually to finings, and are drawn out of the system during cleansing.

f) Metallic Shot and Grit Mixed;
A mix of shot and grit results in a more uniform profile. 
1. The grit cuts the profile
2. The shot, being unable to enter the troughs produced, controls the peak height and so greatly reduces the number of ‘rogue peaks.’
Metallic Grit & Shot Mix

A rogue peak; is one, which is well proud of the acceptable profile range, and if painted over due to contraction of the paint, will leave bare metal in contact with the atmosphere, thus allowing corrosion to occur.  When rogue peaks are in concentrated area the effect is of a rash, hence rust rashing or rust spotting.

A typical mix ratio of Shot to Grit as used in a pipe coating mill would be 70 – 80 % shot to 20-30% grit.

Tuesday, August 28, 2012

CSWIP 3.1 Free Downloadable Question & Answers


Sl #
File Name
Download Link
1
CSWIP 3.1 Quiz 1
2
CSWIP 3.1 Quiz 2
3
CSWIP 3.1 Quiz 3
4
CSWIP 3.1 Quiz 4
5
CSWIP 3.1 Quiz Answer 1 ~ 4

We will add more questions and answers regularly

Monday, August 27, 2012

BGAS Painting Study Material Chapter 2

SURFACE PREPARATION METHODS & STANDARDS
If paint is applied over the corrosion reactions, and other contaminants,  
1. The poor adhesion of the coating and thus the coatings life would be far from satisfactory. 
2. A good surface preparation grade (degree of cleanliness) along with a suitable surface profile can give 10 years life from a typical four-coat paint system.  The same system applied over a substrate with little or no profile and contaminant remaining might give four to six years, or even less.
Surface Preparation
Involves removing these contaminants, and in some instances increasing the area available for adhesion by roughening up the substrate.
Therefore two factors need to be considered when inspecting a surface preparation.
1.         Degree of cleanliness
2.        Surface Profile (degree of roughness)
Surfaces can be prepared for paint application in several different ways; each one varies in cost, efficiency, ease and suitability.

a)      Dry Abrasive Blast Cleaning
b)      Water Blasting
c)      Hand and Power Tool Cleaning
d)      Flame Cleaning
e)      Pickling
f)      Vapour Degreasing
g)      Weathering

Dry abrasive blast cleaning
A. Dry abrasive blast cleaning involves compressing air and forcing it along a hose and out of a small aperture (gap) called a nozzle.

B. A pressure of 100 psi results in the air speed exiting the nozzle at approximately 450 mph.

C. Abrasive particles are mixed in with the air and travel at the same speed; they will carry a lot of work energy.  This energy is used in chipping away mill scale and other detritus from the substrate.  And shattering into small pieces and with others all the energy is used in impinging into the steel surface, roughening the surface and increasing the surface area to increase adhesion properties.
Because all standards refer to the amount of contamination remaining on the surface, (The longer the time spent on this operation, the higher the degree of cleanliness.)

Abrasives
Abrasives come in many forms and can be classified in several different ways, as shown below.

None metallic (Mineral) Expendable
Metallic (Recyclable)
Agricultural by-product
Copper Slag
 Nickel Slag
 Boiler Slag
 Glass Bead
 Aquamarine
 Garnet
 Sand
ACI (Angular Chilled Iron)
Steel Grit
Steel Shot
Grit and Shot Mix
Garnet
Walnut Shell
Coconut Shell
Eggshell
Corn Cob Husk
Peach Husk


continue......

API 510 Free Downloadable Question Bank

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Sunday, August 26, 2012

BGAS Painting Study Material Chapter 1 Corrosion

Corrosion can be generally defined as;” Degradation of a metal (material) by chemical or Electro-chemical means. It is obvious that two mechanisms are involved, Firstly an Electrical Circuit and secondly a Chemical Reaction.

Electrical Circuit
In corrosion circuit the current is always D.C. (Direct Current). For corrosion circuit to exist three things are needed: AnodeCathode and Electrolyte.
1. An Anode
Is a positively charged area?  (It becomes positively charged because the atoms release two     electrons), the iron atom has 26 of each, 26 protons and 26 electrons, in its passive state
When the two electrons are released the atom still has its 26 protons, but now only 24     electrons(In this state the atom is now an ion, positively charged by two units and written as Fe++(An ion is a charged particle, and can be positive or negative, a single atom or a group of atoms, known as a molecule.)
This losing of electrons can be shown as: - FeFe+++2e (The Fe++ is called a positive iron ion). 
2. A Cathode
Is a negatively charged area (where there are more electrons than needed in its   passive state).   At the cathode the electrons enter into the electrolyte to pass back to the anode.
3. An Electrolyte
Is a substance, which will conduct a current and be broken down by it, (dissociate into ions). Water, Acids, alkalis and salts in solution are very efficient electrolytes.
As the electrons pass into the electrolyte it is dissociated or (separated) into positive and negative ions, as shown by the formula: -2eH2O2H++2OĦ.
The couple electrons back with the Hydrogen ions to form two full Hydrogen atoms, which join together to form Hydrogen gas.  The hydroxyl ions return to the anode through the electrolyte carrying the electrons.
Corrosion Triangle
Osmotic or Hygroscopic Blisters
MATERIAL
KNOWN POTENTIAL AV. VALUES
Graphite
+ 0.25 v
Silver
- 0.1 v
Nickel 200
- 0.15 v
Copper
- 0.35 v
Mill Scale
- 0.4 v
Mild Steel
- 0.7 v
Aluminium Alloys
- 0.9 v
Zinc
- 1.0 v
Magnesium
- 1.6 v

The Chemical Reaction
Only the chemical reaction, (the formation of corrosion products), occurs at the Anode.The positive iron ions, Fe++, receive the returning hydroxyl ions and ironically bond together to form iron hydroxide, which is hydrous iron oxide, rust, and is shown by the formula: Fe++ + 2OĦ Fe (OH)2
Corrosion only occurs at the Anode, never at the Cathode.
The corrosion triangle shows the three elements needed for corrosion to occur, Anode, Cathode and Electrolyte. If any one of these three is removed from the triangle, corrosion cannot occur. The one most commonly eliminated is the electrolyte.  Placing a barrier between the electrolyte and the anodic and cathodic areas, in the form of a coating or paint system does this. If electrolyte is not in direct contact with anode and cathode, there can be no circuit, and so no corrosion.

Certain factors can increase the reaction rate, listed below are some of these.
1. Temperature.
Steel, is thermodynamically unstable metal.
The hotter steel is faster in corrosion than the other cooler one.
2. Hygroscopic Salts
(Hygroscopic-tending to observe)
A hygroscopic salt is one, which will attract water and dissolve in it.
When salts are present on a substrate (top of the surface) and a coating is applied over them, water will be drawn through the film and the resulting solution builds up a pressure under the film.
Eventually the film is forced up to form blisters.
These blisters are called osmotic or hygroscopic blisters, and are defined as ‘pinhead sized water filled blisters’.
Sulphates and Chlorides are the two most common salts, chlorides predominant in marine environments, and sulphates in industrial areas and sometimes agricultural.
3. Aerobic conditions
(Presence of oxygen) By introducing oxygen into the cathodic reaction the number of Hydroxyl ions doubles.
This means that double the number of iron ions will be passivated and therefore double the corrosion rate.  Shown by:  2H2O + O2 + 4e  4OH-
4. Presence of some types of bacteria
On the metal surface, for example Sulphur Reducing Bacteria, better known as (SRB), or MEMs, Metal Eating Microbes.
5. Acids and alkalis
6. Bi-metallic contact.(corrosion) Otherwise known as Bi-Metallic Corrosion.

Metals can be listed in order of nobility. A noble metal is one, which will not corrode.  In descending order, the further down the list the metal is, the more reactive it is, and so, the more anodic it is, the metal loses its electrons to become reactive ions. The degree of activity can be expressed as potential, in volts. The list can be called Galvanic ListElectro Motive forces series or the Electro-Chemical series.


Mill scale
Is immediately above steel on the galvanic list.
This means that mill scale is Cathodic to steel, and if left on the surface of steel will accelerate the corrosion of the steel substrate.
Mill scale is formed during the rolling operation of steel sections e.g. RSC, RSA, RSJ.
The oxides of iron form very quickly at temperatures in excess of 580°C
The first oxide formed is FeO, iron oxide, the next is Fe3O4 and last of all Fe2O3. Common names in order are Wustite, Magnetite and Haematite.
These oxides are compressed during the rolling operation to produce blue mill scale.
The thickness of mill scale varies from 25 to 100 um(Microns)
When it has been removed by any surface preparation method, it can never re-cur.

Will continue…