Dr Sujesh kumar N
1
FILM
PROCESSING
Film
Photochemistry and Latent
image
Basic principles of processing
Manual processing
Automatic processor
Abnormal densities & Processing
artefacts
2
FILM
X-ray film-
photographic
film with
radiosensitive
emulsion
coated on a
transparent
base. 3
4
BASE
1.Cellulose nitrate
2.Triacetate
3.Polyester
EMULSION
1.Gelatin
2.Silver halide
3.Anti frothing
agents
4.Anti foggants
5.Wetting agents
6.Fungicides
SILVER HALIDES
Radiosensitive
Contains silver
and halide ions
arranged in a
crystal lattice.
Xray film*90-
99%AgBr,1-
10%AgI
5
SENSITIVITY SPECK
Chemical sensitisation-
sensitivity of Ag halide is
increased by addition of
allylthiourea which reacts
with it to form AgS.
AgS located on the surface
of the crystal –SENSITIVITY
SPECK
6
 When light falls
on xray film
photons are
absorbed by
the crystal.
 Release of an
electron from
Bromine ion
7
 This electron is captured and
fixed at the low energy electron
trap or Sensitivity speck.
 The now –ve spec attracts a +ve
Ag ion and forms a Ag atom.
 The process repeats forming a
clump of Ag atoms at the speck.
 No noticeable difference to the
appearance of the crystal
8
 This tiny collection of silver atoms has a
critical effect on the chemical behavior of the
silver halide crystal.
 It renders the crystal much more vulnerable
than unexposed crystals to attack by the
reducing agent in photographic developer.
 The sensitivity speck now acts as a
development centre in exposed crystals,
enabling them to be reduced completely to
silver during the development process.
9
 The existence on a film of numbers of silver
halide crystals possessing development
centres is said to constitute a latent image.
 Invisible image formed as a result of
exposure to radn,and which may later be
made visible by photographic devlpt.
10
The emulsion of X ray films must
be chemically processed to
render visible and permanent
the information recorded in the
latent image.
Complex chemical reaxns whose
activity and efficiency is
governed by factors like temp,
pH of the chemical environment.
11
Development
Rinsing
Fixing
Washing
Drying
12
 First stage in processing.
 Converts invisible latent
image to visible form.
 Amplifies L.I by millions.
 The basic reaxn is
REDUCTION ie addn of
electrons.
 Starts at the L.I centre.
13
PRINCIPLE
The chemical redn of Ag
halides in an exposed
sample is much more
faster than that of an
unexposed sample.
14
CHARGE BARRIERS
For development to be effective it’s
action should be selective on the
exposed Ag halides.
Both exposed and unexposed Ag
halides are surrounded by –ve
barrier of Br ions.
 Excess KBr added during
manufacture.
15
This charge
barrier
protects Ag
halides from
the attack of
electrons in
the developing
soln.
16
 Exposed Ag halide
crystals have a
weakness in this
charge barrier d/t
presence of neutral Ag
atoms collected at the
sensitivity speck.
 This allows the
developer electrons to
easily penetrate such
crystals.
17
Thus the Ag atoms in the
latent image acts as a
catalyst for the reduction
reaxn during developing.
18
CONSTITUENTS
 Reducing agents
 Solvent- Water Wetting agents
 Accelerators Antifoaming agents
 Restrainers Sequestrating agents
 Preservative Fungicides
 Hardners
 Buffers
19
A) DEVELOPER
 Reducing agents- supply electrons for
conversion of silver halides to metallic silver.
 Phenidone, Metol, Hydroquinone – used in
different combns.
 MOA: Developer + Ag ions  ox.developer +
Ag atoms + (H)ions
 Black metallic Ag thus formed is deposited at
the L.I centres.
 Microscopic L.I is enlarged to a visible pattern.
20
METOL
Quick onset of action.
Once initiated process
continues more slowly.
Poor selectivity (fogging).
Becomes weak soon- highly
susceptible to Br ion
concentration.
21
PHENIDONE
Quick acting.
Poor selectivity.
Produce chemical fog if used
alone.
Less susceptible to Br ion
concentration.
22
HYDROQUINONE
 Slow onset of action.
More selective to exposed Ag
halides.
Gives good contrast.
23
M-Q COMBINATION
Metol & Hydroquinone produce a
photographic density which is
greater than the sum of the effects
they produce when used separately -
Superadditivity.
HQ reacts with some of the oxidized
metol and regenerates it thus
prolonging its action.
24
P-Q developer
 Commonly used combn.
 High selectivity and therefore low chemical fog.
 Adequate activity,adequate contrast
characteristics and also fast acting.
 Synergestic or Super additive effect.
 10-15 times more effective than M-Q developer.
 HQ regenerates some of the oxidised phenidone-
prolongs working life of the soln.
 Cheaper.
 Available as liquid concentrate.
 Less incidence of contact dermatitis &
staining of body parts. 25
CHEMICAL FOG
The developer is also capable of
reducing the unexposed Ag halides if
the film spends too much time in it.
Fog is the development of unexposed
Ag halides that donot contain the
latent image.
Thus time is the most important factor in
this process.
26
Development should be
DISCONTINUED when the
differential between
EXPOSED DEVELOPED
GRAINS and UNEXPOSED
UNDEVELOPED GRAINS is
MAXIMUM.
27
 Optimal pH range of developers- 9.8-11.4
 Alkalinity established by addn of strong
alkalis like K carbonate, KOH,NaOH, Na
carbonate.
 This alkali is known as an accelerator, since its
effect is to accelerate the developing process.
 Too high pH- Over active.
 Too low pH- Sluggish reaxn.
28
B) ACCELERATORS
C) RESTRAINERS
Increase selectivity of
developers.
By increasing the charge barriers
around the unexposed grains.
Minimize formation of fog- also
known as ANTI FOGGANTS.
KBr, Benzotriazole.
29
D) PRESERVATIVES
Pottassium sulphite.
To decrease atmospheric
oxdn of developer.
To increase regeneration of
phenidone by HQ.
30
E) HARDNERS
Mainly in automatic processors.
Prevent mechanical damage from
rollers.
Decrease the amount of water
absorbed by gelatin- easy drying.
Allows use of higher temperatures
during processing.
Glutaraldehyde
31
F) WETTING AGENTS
 These are detergent based compounds that
decrease the surface tension of b/w the developer
& the emulsion.
 Allows easy penetration of the chemicals
G) SEQUESTRATING AGENTS
These are chemicals which prevent
the precipitation of insoluble
mineral salts,which tend to occur in
‘hard water’ areas - EDTA
32
Developer replenisher- With continuous use
developer becomes weak and it has to be
replenished with replenisher.
Starter solution
33
 Initially when the tank is filled with new
developer, it will be over active d/t high pH and low
KBr.
 First few films will be over developed-FOG
 Prevented by starter solution- ACID RESTRAINER
 When added to developer it decreases pH to
working value and provides KBr restrainer
 Mostly used in automatic processor.
FACTORS AFFECTING DEVELOPMENT
1. Constitution of the developing
soln.
2. Developer temperature.
3. Development time.
34
 Constitution of the developing solution like the
choice and concentration of the developing agent,
also pH of the developer solution.
 Developer activity increases with temperature
 Manufactureres of developers for manual
processing recommend a temp. of about 20 degree
C for optimum results.
 Development time again depends on the
constitution of the developer solution and
developer temp. Also the type of film emulsion
and the agitation of developer solution.
35
2. RINSING
Stage between Developing and
Fixing.
This stage is not present in
automatic processor.
Objective- Prevent film materials
from carrying active developer
chemicals into the fixer.
36
TYPES
1. Plain water rinse- dilutes
developer.
2. Acid stop bath- inhibits further
development.
 PLAIN RINSE
1. Static bath/Dip rinse
2. Spray rinse
3. Running rinse
37
3. FIXING
A film thus taken out of the developer
contains the complete radiological
image.
The unexposed, undeveloped Ag halide
remains in the film as a light sensitive
material.
This if left there will have an obscuring
effect, impending the transmission of
light giving the image an opalescent,
milky appearance.
38
DURING FIXING THE
UNEXPOSED INSOLUBLE Ag
halides ARE CONVERTED TO
SOLUBLE COMPOUNDS
AND REMOVED.
39
FUNCTIONS OF FIXER
To stop further development.
To clear the image by removing
undeveloped Ag halides.
To fix the image, ie to make it
chemically and radiologicaly
stable and storable.
To harden the emulsion.
40
CONSTITUENTS
Solvent
Fixing agent
Acid
Hardner
Buffer
Preservative/Stabilizer
Anti-sludging agents
41
A. SOLVENT
Water
Carrying medium for active
constituents.
Hard water is undesirable.
42
B. FIXING AGENTS
A chemical which combines with
insoluble Ag halides in the emulsion to
form soluble compounds which can
diffuse out and be washed off.
MUST NOT affect the developed
metallic Ag.
Na thiosulphate, Ammonium
thiosulphate.
43
Na THIOSULPHATE
Commonly known as hypo
Reaction with Ag halide gives
Argentothiosulphate and Na halide.
These are soluble and
diffuses out into the fixing
bath.
44
AMMONIUM thiosulphate
More rapid action.
Forms highly soluble
compounds.
Washed off very quickly.
Used mainly in automatic
processors.
45
Disadvantage
Compounds formed are less
stable.
Improper washing after fixing
leads to quicker staining and
deterioration of the image.
46
C. ACID
 Acidic pH to stop developer action and to provide
suitable environment for hardner.
 Ideal pH = 4-4.5
 Weak acids like acetic acid is used.
 Insufficient acidity – inadequate hardening.
 Too acidic – thiosulphate breaks down and ppt
insoluble sulphur – Sulphurisation.
47
D. HARDNERS
Limits water uptake by the
emulsion.
Essential in automatic processors.
Decrease drying time and prevents
physical damage by rollers.
Allows use of higher temperatures.
Al chloride, Al sulphate,
Chrome alum, Potash alum.
48
E. BUFFER
 For precise control of pH, to
prevent sulphurisation , to
ensure neutralization of
developer, to provide optimal
hardening.
 Sodium acetate
49
F. PRESERVATIVE
Retards decomposition of
thiosulphate.
Delays onset of sulphurisation.
Eg: Na sulphite, Na acetate
Na and K metabisulphates- acts
as acid stabilizers with some
buffering action.
50
G. Anti-sludging agents
Aluminium salts used as hardners
have a tendency to produce
insoluble Al compounds which
may ppt out of the solution to form
a sludge.
This adheres to the film and sides
of the fixing tank.
BORIC ACID
51
FACTORS AFFECTING FIXING RATE
1. CONSTITUTION OF FIXING
SOLUTION
2. FIXER TEMPERATURE
3. FIXING TIME
52
1. FIXER CONSTITUTION
Fixer type- Ammonium thiosulphate-
rapid
Concentration of fixing agent
Hardners- slows fixing
Increasing Ag thiosulphates- retards
fixing
Soluble halides- slows down
pH of fixer
53
2. FIXER TEMPERATURE
Fixing is faster at higher
temperatures as the emulsion
softens.
A big difference in the
temperatures of fixer and
developer results in emulsion
damage, d/t rapid swelling of
gelatin- RETICULATION
54
3. FIXING TIME
 Higher the fixer activity, the shorter is the
required fixing time.
 Type of emulsion- AgBr faster
 Emulsion thickness- thin- rapid
 Direct exposure films-thick-more processing time
 Agitation accelerates fixing by speeding up the
removal of byproducts from the film surface and
replacement with fresh fixer.
55
Fixer replenisher– With continuous
use fixer becomes weak and needs
to be replenished with the
replenisher. Available as liquid
concentrates.
56
4. WASHING
 When the film leaves the fixing
tank it carries in its emulsion a
layer comprising of
1. Argento-thiosulphates
2. Residual fixers
3. Remaining salts- NaBr, NH4Br
57
These compounds if left on the film will
destroy the image.
Ag thioSO4- decompose to AgS-
Yellow brown discoloration.
Residual fixers + Ag in the image –
AgS- Yellow brown discoloration.
Residual salts crystallize on the
surface making it difficult to view.
58
 All these compounds being water
soluble can be removed by washing-
the process being simple diffusion.
 Washing time in manual processing
-a minimum of 10 min.
 The film surface is ideally exposed to
continuous flow of uncontaminated water,
either by spray mechanism or rapidly flowing
fresh water bath.
59
5. DRYING
Final stage in processing.
To remove all the surface water and
most of the water retained in the
emulsion.
Some moisture must remain to prevent
it from becoming too brittle.
Ideally the film should retain 10-15% of
its own weight of water.
60
DRYING METHODS
The most common method of
drying employed in manual
processors is by air.
Hot air drying or infra red
drying are used in automatic
processors.
61
MANUAL PROCESSING UNIT
62
 The manual processor essentially
consists of a large master tank with
some smaller tanks & divisions.
1. A lidded tank for developer
2. A compartment for rinsing (tap
water)
3. A tank for fixer
4. A large compartment of water for
washing the fixed films.
63
A MANUAL
PROCESSING
UNIT
MANUAL PROCESSING
PROCEDURE
64
After exposure the cassette
containing the film is taken to the
dark room.
The film is unloaded under safe
lighting.
The film is placed in the processing
hanger of appropriate size.
The loaded hanger is immersed in
the developer solution and lightly
65
When adequate development has
occurred the hanger is transferred
into the rinse tank.
Next the film is suspended in the
fixer solution.
The last wet stage of processing is
washing.
The film is then dried in air & is
ready for viewing.
Duration of different stages in a manual
processor-
66
Development- 3-5min
Rinse- 10-20sec
Fixing- 5-10min
Washing- 10-15min
Drying- 20min
Total= 40-50min
 All automatic processors possess :-
 A system which mechanically transports
films through the processor.
 A system which provides for replenishment
& recirculation of the chemical solutions.
 A system concerned with water circulation.
 A system for temperature control.
 A system for drying films.
67
All factors which influence
the quality of the
radiograph can be kept with
in fine limits.
Processing time is much
less.
68
 A film which is introduced into the
automatic processor is moved
through the different chambers by
means of a system of rollers in 2
ways
1. Vertically
2. Horizontally
 Rollers are made of- Rubber/ Steel/
PVC
69
70
 Developer - 26 sec
 Fixer - 15 sec
 Wash - 15 sec
 Dryer - 24 sec
 Travel time - 10 sec
Total – 90 sec
71
ABNORMAL DENSITIES
 Films without sufficient density:
1. Too short development time.
2. Exhausted developer.
3. Too low developer tank temperature.
4. Too low developer pH.
 Films with too high density:
1. Too high developer temperature.
2. Starter solution missed – High pH.
3. Too long development time.
72
PROCESSING ARTEFACTS
FINGER MARKS
 Handling the film surface with the
fingers before it has been
processed.
 Moisture transferred to the film
surface from the skin modifies the
action of the chemicals.
 Hands previously contaminated
with chemicals or metals more
likely to cause markings. 73
PRESSURE MARKS
 Application of undue pressure/stress to
the emulsion before/during devlpt.
 Crimp marks – Crescent shaped marks
occur during handling if a film becomes
kinked or creased when it droops under
its own weight.
74
CHEMICAL STAINING
Fixer artefacts – White marks d/t
fixer droplets falling on the
undeveloped film.
 Inadequate fixing results in a milky
white, opalescent appearance.
 Inadequate washing leads to
yellow-brown staining, d/t unstable
sulphur compds. Develops slowly
over time.
75
Black Splashes
 The film has been splashed with
developer before the development.
This area develops faster than the
rest of the film making it darker.
 Due to splashes of water falling on
the film before development.
Water softens the emulsion  faster
development.
76
SURFACE DAMAGE
 Film emulsion is delicate & prone to
damage during processing.
 A badly adjusted transport system may
cause abrasions on the film surface.
Pi marks – Regularly placed marks
across the film - damage produced by
the rollers in the processor.
Reticulation/ Frilling - Detachment of
the emulsion from the base d/t adverse
processing conditions.
77
STATIC MARKS
 These are d/t the
static electrical
charges that
accumulate as a
result of friction.
 Such electrical
discharges trigger
chemical changes
which mimic an
exposure & lead to
the black static
marks.
78
THANK YOU…
79

FILM PROCESSING.ppt

  • 1.
    Dr Sujesh kumarN 1 FILM PROCESSING
  • 2.
    Film Photochemistry and Latent image Basicprinciples of processing Manual processing Automatic processor Abnormal densities & Processing artefacts 2
  • 3.
  • 4.
    4 BASE 1.Cellulose nitrate 2.Triacetate 3.Polyester EMULSION 1.Gelatin 2.Silver halide 3.Antifrothing agents 4.Anti foggants 5.Wetting agents 6.Fungicides
  • 5.
    SILVER HALIDES Radiosensitive Contains silver andhalide ions arranged in a crystal lattice. Xray film*90- 99%AgBr,1- 10%AgI 5
  • 6.
    SENSITIVITY SPECK Chemical sensitisation- sensitivityof Ag halide is increased by addition of allylthiourea which reacts with it to form AgS. AgS located on the surface of the crystal –SENSITIVITY SPECK 6
  • 7.
     When lightfalls on xray film photons are absorbed by the crystal.  Release of an electron from Bromine ion 7
  • 8.
     This electronis captured and fixed at the low energy electron trap or Sensitivity speck.  The now –ve spec attracts a +ve Ag ion and forms a Ag atom.  The process repeats forming a clump of Ag atoms at the speck.  No noticeable difference to the appearance of the crystal 8
  • 9.
     This tinycollection of silver atoms has a critical effect on the chemical behavior of the silver halide crystal.  It renders the crystal much more vulnerable than unexposed crystals to attack by the reducing agent in photographic developer.  The sensitivity speck now acts as a development centre in exposed crystals, enabling them to be reduced completely to silver during the development process. 9
  • 10.
     The existenceon a film of numbers of silver halide crystals possessing development centres is said to constitute a latent image.  Invisible image formed as a result of exposure to radn,and which may later be made visible by photographic devlpt. 10
  • 11.
    The emulsion ofX ray films must be chemically processed to render visible and permanent the information recorded in the latent image. Complex chemical reaxns whose activity and efficiency is governed by factors like temp, pH of the chemical environment. 11
  • 12.
  • 13.
     First stagein processing.  Converts invisible latent image to visible form.  Amplifies L.I by millions.  The basic reaxn is REDUCTION ie addn of electrons.  Starts at the L.I centre. 13
  • 14.
    PRINCIPLE The chemical rednof Ag halides in an exposed sample is much more faster than that of an unexposed sample. 14
  • 15.
    CHARGE BARRIERS For developmentto be effective it’s action should be selective on the exposed Ag halides. Both exposed and unexposed Ag halides are surrounded by –ve barrier of Br ions.  Excess KBr added during manufacture. 15
  • 16.
    This charge barrier protects Ag halidesfrom the attack of electrons in the developing soln. 16
  • 17.
     Exposed Aghalide crystals have a weakness in this charge barrier d/t presence of neutral Ag atoms collected at the sensitivity speck.  This allows the developer electrons to easily penetrate such crystals. 17
  • 18.
    Thus the Agatoms in the latent image acts as a catalyst for the reduction reaxn during developing. 18
  • 19.
    CONSTITUENTS  Reducing agents Solvent- Water Wetting agents  Accelerators Antifoaming agents  Restrainers Sequestrating agents  Preservative Fungicides  Hardners  Buffers 19
  • 20.
    A) DEVELOPER  Reducingagents- supply electrons for conversion of silver halides to metallic silver.  Phenidone, Metol, Hydroquinone – used in different combns.  MOA: Developer + Ag ions  ox.developer + Ag atoms + (H)ions  Black metallic Ag thus formed is deposited at the L.I centres.  Microscopic L.I is enlarged to a visible pattern. 20
  • 21.
    METOL Quick onset ofaction. Once initiated process continues more slowly. Poor selectivity (fogging). Becomes weak soon- highly susceptible to Br ion concentration. 21
  • 22.
    PHENIDONE Quick acting. Poor selectivity. Producechemical fog if used alone. Less susceptible to Br ion concentration. 22
  • 23.
    HYDROQUINONE  Slow onsetof action. More selective to exposed Ag halides. Gives good contrast. 23
  • 24.
    M-Q COMBINATION Metol &Hydroquinone produce a photographic density which is greater than the sum of the effects they produce when used separately - Superadditivity. HQ reacts with some of the oxidized metol and regenerates it thus prolonging its action. 24
  • 25.
    P-Q developer  Commonlyused combn.  High selectivity and therefore low chemical fog.  Adequate activity,adequate contrast characteristics and also fast acting.  Synergestic or Super additive effect.  10-15 times more effective than M-Q developer.  HQ regenerates some of the oxidised phenidone- prolongs working life of the soln.  Cheaper.  Available as liquid concentrate.  Less incidence of contact dermatitis & staining of body parts. 25
  • 26.
    CHEMICAL FOG The developeris also capable of reducing the unexposed Ag halides if the film spends too much time in it. Fog is the development of unexposed Ag halides that donot contain the latent image. Thus time is the most important factor in this process. 26
  • 27.
    Development should be DISCONTINUEDwhen the differential between EXPOSED DEVELOPED GRAINS and UNEXPOSED UNDEVELOPED GRAINS is MAXIMUM. 27
  • 28.
     Optimal pHrange of developers- 9.8-11.4  Alkalinity established by addn of strong alkalis like K carbonate, KOH,NaOH, Na carbonate.  This alkali is known as an accelerator, since its effect is to accelerate the developing process.  Too high pH- Over active.  Too low pH- Sluggish reaxn. 28 B) ACCELERATORS
  • 29.
    C) RESTRAINERS Increase selectivityof developers. By increasing the charge barriers around the unexposed grains. Minimize formation of fog- also known as ANTI FOGGANTS. KBr, Benzotriazole. 29
  • 30.
    D) PRESERVATIVES Pottassium sulphite. Todecrease atmospheric oxdn of developer. To increase regeneration of phenidone by HQ. 30
  • 31.
    E) HARDNERS Mainly inautomatic processors. Prevent mechanical damage from rollers. Decrease the amount of water absorbed by gelatin- easy drying. Allows use of higher temperatures during processing. Glutaraldehyde 31
  • 32.
    F) WETTING AGENTS These are detergent based compounds that decrease the surface tension of b/w the developer & the emulsion.  Allows easy penetration of the chemicals G) SEQUESTRATING AGENTS These are chemicals which prevent the precipitation of insoluble mineral salts,which tend to occur in ‘hard water’ areas - EDTA 32
  • 33.
    Developer replenisher- Withcontinuous use developer becomes weak and it has to be replenished with replenisher. Starter solution 33  Initially when the tank is filled with new developer, it will be over active d/t high pH and low KBr.  First few films will be over developed-FOG  Prevented by starter solution- ACID RESTRAINER  When added to developer it decreases pH to working value and provides KBr restrainer  Mostly used in automatic processor.
  • 34.
    FACTORS AFFECTING DEVELOPMENT 1.Constitution of the developing soln. 2. Developer temperature. 3. Development time. 34
  • 35.
     Constitution ofthe developing solution like the choice and concentration of the developing agent, also pH of the developer solution.  Developer activity increases with temperature  Manufactureres of developers for manual processing recommend a temp. of about 20 degree C for optimum results.  Development time again depends on the constitution of the developer solution and developer temp. Also the type of film emulsion and the agitation of developer solution. 35
  • 36.
    2. RINSING Stage betweenDeveloping and Fixing. This stage is not present in automatic processor. Objective- Prevent film materials from carrying active developer chemicals into the fixer. 36
  • 37.
    TYPES 1. Plain waterrinse- dilutes developer. 2. Acid stop bath- inhibits further development.  PLAIN RINSE 1. Static bath/Dip rinse 2. Spray rinse 3. Running rinse 37
  • 38.
    3. FIXING A filmthus taken out of the developer contains the complete radiological image. The unexposed, undeveloped Ag halide remains in the film as a light sensitive material. This if left there will have an obscuring effect, impending the transmission of light giving the image an opalescent, milky appearance. 38
  • 39.
    DURING FIXING THE UNEXPOSEDINSOLUBLE Ag halides ARE CONVERTED TO SOLUBLE COMPOUNDS AND REMOVED. 39
  • 40.
    FUNCTIONS OF FIXER Tostop further development. To clear the image by removing undeveloped Ag halides. To fix the image, ie to make it chemically and radiologicaly stable and storable. To harden the emulsion. 40
  • 41.
  • 42.
    A. SOLVENT Water Carrying mediumfor active constituents. Hard water is undesirable. 42
  • 43.
    B. FIXING AGENTS Achemical which combines with insoluble Ag halides in the emulsion to form soluble compounds which can diffuse out and be washed off. MUST NOT affect the developed metallic Ag. Na thiosulphate, Ammonium thiosulphate. 43
  • 44.
    Na THIOSULPHATE Commonly knownas hypo Reaction with Ag halide gives Argentothiosulphate and Na halide. These are soluble and diffuses out into the fixing bath. 44
  • 45.
    AMMONIUM thiosulphate More rapidaction. Forms highly soluble compounds. Washed off very quickly. Used mainly in automatic processors. 45
  • 46.
    Disadvantage Compounds formed areless stable. Improper washing after fixing leads to quicker staining and deterioration of the image. 46
  • 47.
    C. ACID  AcidicpH to stop developer action and to provide suitable environment for hardner.  Ideal pH = 4-4.5  Weak acids like acetic acid is used.  Insufficient acidity – inadequate hardening.  Too acidic – thiosulphate breaks down and ppt insoluble sulphur – Sulphurisation. 47
  • 48.
    D. HARDNERS Limits wateruptake by the emulsion. Essential in automatic processors. Decrease drying time and prevents physical damage by rollers. Allows use of higher temperatures. Al chloride, Al sulphate, Chrome alum, Potash alum. 48
  • 49.
    E. BUFFER  Forprecise control of pH, to prevent sulphurisation , to ensure neutralization of developer, to provide optimal hardening.  Sodium acetate 49
  • 50.
    F. PRESERVATIVE Retards decompositionof thiosulphate. Delays onset of sulphurisation. Eg: Na sulphite, Na acetate Na and K metabisulphates- acts as acid stabilizers with some buffering action. 50
  • 51.
    G. Anti-sludging agents Aluminiumsalts used as hardners have a tendency to produce insoluble Al compounds which may ppt out of the solution to form a sludge. This adheres to the film and sides of the fixing tank. BORIC ACID 51
  • 52.
    FACTORS AFFECTING FIXINGRATE 1. CONSTITUTION OF FIXING SOLUTION 2. FIXER TEMPERATURE 3. FIXING TIME 52
  • 53.
    1. FIXER CONSTITUTION Fixertype- Ammonium thiosulphate- rapid Concentration of fixing agent Hardners- slows fixing Increasing Ag thiosulphates- retards fixing Soluble halides- slows down pH of fixer 53
  • 54.
    2. FIXER TEMPERATURE Fixingis faster at higher temperatures as the emulsion softens. A big difference in the temperatures of fixer and developer results in emulsion damage, d/t rapid swelling of gelatin- RETICULATION 54
  • 55.
    3. FIXING TIME Higher the fixer activity, the shorter is the required fixing time.  Type of emulsion- AgBr faster  Emulsion thickness- thin- rapid  Direct exposure films-thick-more processing time  Agitation accelerates fixing by speeding up the removal of byproducts from the film surface and replacement with fresh fixer. 55
  • 56.
    Fixer replenisher– Withcontinuous use fixer becomes weak and needs to be replenished with the replenisher. Available as liquid concentrates. 56
  • 57.
    4. WASHING  Whenthe film leaves the fixing tank it carries in its emulsion a layer comprising of 1. Argento-thiosulphates 2. Residual fixers 3. Remaining salts- NaBr, NH4Br 57
  • 58.
    These compounds ifleft on the film will destroy the image. Ag thioSO4- decompose to AgS- Yellow brown discoloration. Residual fixers + Ag in the image – AgS- Yellow brown discoloration. Residual salts crystallize on the surface making it difficult to view. 58
  • 59.
     All thesecompounds being water soluble can be removed by washing- the process being simple diffusion.  Washing time in manual processing -a minimum of 10 min.  The film surface is ideally exposed to continuous flow of uncontaminated water, either by spray mechanism or rapidly flowing fresh water bath. 59
  • 60.
    5. DRYING Final stagein processing. To remove all the surface water and most of the water retained in the emulsion. Some moisture must remain to prevent it from becoming too brittle. Ideally the film should retain 10-15% of its own weight of water. 60
  • 61.
    DRYING METHODS The mostcommon method of drying employed in manual processors is by air. Hot air drying or infra red drying are used in automatic processors. 61
  • 62.
    MANUAL PROCESSING UNIT 62 The manual processor essentially consists of a large master tank with some smaller tanks & divisions. 1. A lidded tank for developer 2. A compartment for rinsing (tap water) 3. A tank for fixer 4. A large compartment of water for washing the fixed films.
  • 63.
  • 64.
    MANUAL PROCESSING PROCEDURE 64 After exposurethe cassette containing the film is taken to the dark room. The film is unloaded under safe lighting. The film is placed in the processing hanger of appropriate size. The loaded hanger is immersed in the developer solution and lightly
  • 65.
    65 When adequate developmenthas occurred the hanger is transferred into the rinse tank. Next the film is suspended in the fixer solution. The last wet stage of processing is washing. The film is then dried in air & is ready for viewing.
  • 66.
    Duration of differentstages in a manual processor- 66 Development- 3-5min Rinse- 10-20sec Fixing- 5-10min Washing- 10-15min Drying- 20min Total= 40-50min
  • 67.
     All automaticprocessors possess :-  A system which mechanically transports films through the processor.  A system which provides for replenishment & recirculation of the chemical solutions.  A system concerned with water circulation.  A system for temperature control.  A system for drying films. 67
  • 68.
    All factors whichinfluence the quality of the radiograph can be kept with in fine limits. Processing time is much less. 68
  • 69.
     A filmwhich is introduced into the automatic processor is moved through the different chambers by means of a system of rollers in 2 ways 1. Vertically 2. Horizontally  Rollers are made of- Rubber/ Steel/ PVC 69
  • 70.
  • 71.
     Developer -26 sec  Fixer - 15 sec  Wash - 15 sec  Dryer - 24 sec  Travel time - 10 sec Total – 90 sec 71
  • 72.
    ABNORMAL DENSITIES  Filmswithout sufficient density: 1. Too short development time. 2. Exhausted developer. 3. Too low developer tank temperature. 4. Too low developer pH.  Films with too high density: 1. Too high developer temperature. 2. Starter solution missed – High pH. 3. Too long development time. 72
  • 73.
    PROCESSING ARTEFACTS FINGER MARKS Handling the film surface with the fingers before it has been processed.  Moisture transferred to the film surface from the skin modifies the action of the chemicals.  Hands previously contaminated with chemicals or metals more likely to cause markings. 73
  • 74.
    PRESSURE MARKS  Applicationof undue pressure/stress to the emulsion before/during devlpt.  Crimp marks – Crescent shaped marks occur during handling if a film becomes kinked or creased when it droops under its own weight. 74
  • 75.
    CHEMICAL STAINING Fixer artefacts– White marks d/t fixer droplets falling on the undeveloped film.  Inadequate fixing results in a milky white, opalescent appearance.  Inadequate washing leads to yellow-brown staining, d/t unstable sulphur compds. Develops slowly over time. 75
  • 76.
    Black Splashes  Thefilm has been splashed with developer before the development. This area develops faster than the rest of the film making it darker.  Due to splashes of water falling on the film before development. Water softens the emulsion  faster development. 76
  • 77.
    SURFACE DAMAGE  Filmemulsion is delicate & prone to damage during processing.  A badly adjusted transport system may cause abrasions on the film surface. Pi marks – Regularly placed marks across the film - damage produced by the rollers in the processor. Reticulation/ Frilling - Detachment of the emulsion from the base d/t adverse processing conditions. 77
  • 78.
    STATIC MARKS  Theseare d/t the static electrical charges that accumulate as a result of friction.  Such electrical discharges trigger chemical changes which mimic an exposure & lead to the black static marks. 78
  • 79.