LABORATORY CATALOGUE for milk analysis - Funke-Dr.N.Gerber
Transcript of LABORATORY CATALOGUE for milk analysis - Funke-Dr.N.Gerber
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LABORATORY
CATALOGUE
for milk analysis
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We look forward to working with you!
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A detailed description by graduate chemist Alfred Toepel
Determination of fat content in cream, ice cream, cheese, butter, milk powder, etc.
The butyrometer – an overview of the entire product spectrum
Implements and utensils used in the determination of fat content
Some important points about the acquisition and operation of a Gerber centrifuge K. Schaefer, graduate engineer, reports
Anna Politis, graduate engineer, reports
Filter papers, Sedilab, Aspilac, etc.
Butter melting beaker, testing spoon, spatula, aluminium foil, crystalline quartz sand, Bunsen burner, separating funnel, thin layer chromatography, etc.
One of the main focuses of Funke - Dr. N. Gerber Labortechnik GmbHK. Schaefer, graduate engineer, W. Spindler, graduate physician
CONTENTS
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ColonyStar bacteria counter, autoclaves, incubators, magnetic stirrers, photometers, microscopes, water distillation apparatuses, water baths
Dr. Ulrich Leist, DRRR GmbH, reports
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TRADITIONPROGRESSCONTINUITY
Partners in dairy farming since 1904
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PRODUCTS:
Founded: 1904Managing director: Graduate engineer Konrad SchaeferAuthorised signatory:
graduate economist Georg Hoernle
„Gerber method of determining
fat content“
Funke-Dr.N.Gerber Labortechnik GmbHRingstraße 4212105 BerlinTelephone: (+49-30) 702 006-0Fax: (+49-30) 702 006-66E-mail: [email protected]: www.funke-gerber.de
ACTIVITES:
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Accessories for BagMixer 400
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BUTYROMETRIC DETERMINATION
OF FAT CONTENT ACCORDING
TO GERBER’S METHODby graduate chemist Alfred Toepel
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PRINCIPLES OF THE METHOD
APPLICATION
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CHEMICALS NEEDED
colourless or only slightly discoloured and free from any substances which might influence the outcome
•
The required density corresponds to 90 to 91 % by mass. Stronger or weaker concentrations are to be avoided. At 65°C, more highly concentrated sulphuric acid attacks the amyl alcohol, producing olefins through dehydration which influence the result. Weaker concentrations reduce the oxidization effect. Destruction of the fat globule coating is incomplete which can lead to the formation of lumps.
An isomer mixture of 2-methylbutane-1-ol and 3-methylbutance-1-ol
The isomers of amyl alcohol have different boiling points: 2-methylbutane-1-ol at 128°C and 3-methylbutane-1-ol at 132°C.
Of the 8 known isomers of amyl alcohol, only this mixture is suitable for the Gerber method.
Contamination with other isomers of amyl alcohol, particularly with the tertiary amyl alcohol 2-methylbutane-2-ol, produces false results. The obtained fat content result is too high.
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Boiling boundary: 98 % (by volume) has to distil at between 128°C and 132°C at 1 bar. The amyl alcohol must not contain any substances which could influence the result.A substitute for amyl alcohol can be used provided that it will bring about the same test results as would be achieved with amyl alcohol.
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PREPARATION OF THE TEST SPECIMEN
Milk fat is lighter than water and creams if it is left standing. A fat-rich layer accumu-lates on the surface. Stirring and careful shaking restore the original distribution.
Foam breaks the fat globule coating. The milk may begin to turn into butter when stirred and uniform distribution of fat is no longer possible.
The fat liquefies at 35-40° and the distribution process is speeded up.
The volumeters are calibrated at 20°C. Any variations in temperature will influence the volume. Air pockets reduce the density and hence the mass of milk measured.
REQUIRED EQUIPMENT
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CONDUCTING A TEST = WORK PROCEDURES
When the Gerber method was first introduced, 11.0 ml of milk were used.
By reducing the quantity of milk 10.75 ml, the determined fat content more
closely matches the results of the reference method. If the butyrometer
neck is wetted with milk, residues may cling to it.
A clear dividing line between the acid and the milk, without a brownish-
coloured edge, is the sign of good layering.
Due to the low density of amyl alcohol, the two liquids do not mix.
As a rule, the lower end of the stopper comes into contact with the liquid.
When the liquids are mixed, a consid-
erable amount of heat is given off. The
gas built up in this way can cause the
stopper to shoot out, or the butyrometer
to break.
The butyrometer tube is used as
a safety precaution. Instead of using a
butyrometer tube, the butyrometer can
be wrapped in a cloth.
Too lax shaking of the butyrometer or
holding it unnecessarily in a slanted
position inhibits quick mixing and
therefore the rapid oxidation of the en-
tire specimen, thus ruining the careful
work done layering the liquid.
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It is important to maintain an exact temperature so as to obtain accurate
results. Only a read-off at 65°C will ensure an exact result. If the
temperature is too low, the volume of the column is reduced and a fat
content reading that is too low will be indicated.
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RESULT AND DEGREE OF ACCURACY
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After the first centrifuging, the two values were read off at 3.55 % and 3.60 %.
After the second centrifuging, the two values were 3.60 % and 3.65 %. The homogenised milk fat content is stated to be 3.65 %.
Should the difference still be greater than 0.05 % after the two last repetitions, i.e. after the 3rd and 4th centrifuging, the results of this test are to be discarded.
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FOREWORD:
1.0 FIELD OF APPLICATION
2.0 VOLUMES
BUTYROMETRIC DETERMINATION OF THE
FAT CONTENT OF VARIOUS DAIRY PRODUCTS
The butyrometric determination of the fat content in milk has been and is being replaced at a progressive rate by other routine tests (with appliances such as LactoStar, for instance). However, milk products such as cheese, ice cream, etc. either cannot be tested with such appliances or can only be tested after elaborate specimen preparation. For these products, butyro-metric methods are a good alternative for routine analysis.
3.0 BRIEF DESCRIPTION OF THE BUTYROMETRIC DETERMINATION OF FAT CONTENT:
3.1 ... IN MILK (ACCORDING TO GERBER’S METHOD):
3.2 ... IN HOMOGENISED MILK
As above, except that the specimens are centrifuged three times, for 5 minutes each time. In between centrifugings, the butyrometers are heated in a 65°C water bath for 5 minutes (for more detail, see page 19).
3.3 ... IN SKIM MILK AND WHEY
Use of skim milk butyrometers with narrowed scales according to Sichler’s method.
3.4 ... IN CONDENSED MILK (UNSWEETENED)
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3.5 ... IN BUTTERMILK (MOHR AND BAUR’S MODIFICATION)
3.6 ... IN POWDERED MILK ACCORDING TO TEICHERT’S METHOD
Use of powdered milk butyrometer according to Teichert’s method.
3.7 ... IN CREAM ACC. TO ROEDER’S METH. (WEIGHING METH.)
Use of cream butyrometer according to Roeder’s method.
3.8 ... IN CREAM ACC. TO SCHULZ-KLEY’S METH. (WEIGHING METH.)
Use of cream butyrometer according to Schulz-Kley’s method.
3.9 ... IN CREAM ACC. TO KOEHLER’S METH. (MEASURING METH.)
Use of cream butyrometer according to Koehler’s method.
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3.10 ... IN CHEESE ACC. TO VAN GULIK’S METH. (WEIGHING METH.)
(see ISO 3433) Use of the cheese butyrometer according to Van Gulik’s method.
3.11 ... IN ICE CREAM ACC. TO KOEHLER’S METH. (MEASURING METH.)
Use of the ice cream butyrometer according to Koehler’s method.
3.12 ... IN ICE CREAM ACC. TO ROEDER’S METH. (WEIGHING METH.)
Use of ice cream butyrometer according to Roeder’s method.
3.13 ... IN BUTTER ACC. TO ROEDER’S METH. (WEIGHING METH.)
Use of butter butyrometer according to Roeder’s method.
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3.14 ... IN MAYONNAISE ACC. TO ROEDER’S METH. (WEIGHING METH.)
Use of butter butyrometer according to Roeder’s method.
3.15 BUTYROMETRIC DETERMINATION OF THE FAT CONTENT OFMEAT AND SAUSAGE ACC. TO GERBER’S METHOD (VAN GULIK)
According to the recommended methodology of “Pohja and Associates“.
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BUTYROMETER
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LactoStar
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THE NEW GENERATION OF INSTRUMENTS
Chemical milk analysis device with fully automatic cleaning and rinsing system and zero point calibration for the fast and accurate testing of milk
* The reproducibility equals +0.02 % in the 0% to 8 % fat range. In the higher ranges of 8 % to 40 % fat, the reproducibility equals 0.2 %
ENTER
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LactoStar
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3511 *
3516 *
3563 *
(articles marked with * are included in the 3510 scope of delivery)
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3510-023
3510-023 A
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LactoFlash
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Inexpensive chemical analysis device for the fast and accurate determination of fat and SNF content
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ENTER
LactoFlash
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3563
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7157
3530-023
3530-023 A
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REFERENCE MATERIAL
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<
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SuperVario-N
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MULTIPURPOSE CENTRIFUGE FOR THE DAIRY LABORATORY
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K. Schaefer, graduate engineer, reports
QUIET OPERATION
TYPE 1: Centrifuge with flat-lying butyrometers
TYPE 2: Centrifuge with angular rotor
TYPE 3: Centrifuge with swing-out butyrometer holders
UNBALANCE
INTERLOCKING LID
HEATING
SET-UP
ROUTINE OPERATION/MAINTENANCE
MILK LABORATORY CENTRIFUGES
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RPM
whereby:
R = effective horizontal radius in mm;
N = revolutions per minute [min-1].
SYNOPTICAL TABLE OF THE DEPENDENCE OF G-FORCE AND RPM
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KJELDAHL’S NITROGEN DETERMINATION METHOD
KJELDAHL’S NITROGEN DETERMINATION METHODAnna Politis, graduate engineer of nutrition technology and of biotechnology, reports
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1
The addition of potassium sulphate serves to increase the boiling tempera-ture of the sulphuric acid and the addition of copper sulphate serves as anoxidation catalyst. They are also available as Kjeldahl tabs (art. no. 4230/4231).If the process is executed with tabs, then 5± 0.1 g of milk are mixed with20 ml of sulphuric acid and 2 Kjeldahl tabs and left to sit for 5 min. Then the temperature program can be carried out.
During the heating of the sample, foam is not allowed to climb higher then 4 - 5 cm below the flask opening.
The sulphuric acid is added in such a way that any copper sulphate solution, potassium sulphate or milk which may have adhered to the flask neck is flushed down. If the flask is sealed airtight, it can also be stored for later digestion.
To determine the specific digestion time, it is advisable to execute preliminary tests with samples high in protein and fat.
Substantial crystallisation is a sign of too little sulphuric acid and can lead to low protein values. It is therefore advisable to reduce the loss of sulphuric acid by minimising the amount sucked.
Before the hot digestion flasks can be taken from the digestion block, it must be ensured that no condensed fluid has collected in the extraction apparatus. If it has, the suction volume must be increased and the condensed liquid removed.
The undiluted digestion should not be stored in the flask for a longperiod of time (overnight) for any reason. There is a risk that the sample will solidify and it is difficult to bring it into solution form again. After the sample is cooled down and dilluted with 70 ml of water, there is no problem to keep it overnight.
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2
The water distiller must be set up on a stable laboratory bench with an even, horizontal support which is located near a cold wa-ter supply and a drain. The water pressure must be at least 0.5 bar.
Before starting the operation, all hoses must be connected and the coolant en-gaged. The storage tank must be correctly positioned and the fluid level checked. The water vapour discharge hose must be in-troduced into the digestion flask. The water distiller is equipped with a safety gate.
During the first distillation, the water va-pour comes into contact with cold pipes and glass parts. This leads to increased build-up of condensation which can in turnlead to excessive sample dilution andliquid volume in the digestion vessel.A trial run is therefore essential. The dis-charge of water vapour with a temperature of approx. 106°C creates loud noises. This is no cause for alarm.
The distillation is conducted until a distil-lation volume of 150 ml is obtained.
About 2 minutes before the end of the dis-tillation, the Erlenmeyer flask is lowered in such a way that the end of the discharge pipe is no longer submerged in the acid solution. The pipe must be flushed with water. This water is collected in the Erlen-meyer flask.
KJELDAHL’S NITROGEN DETERMINATION METHOD
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3
The mixture of methyl red and bromcresol green (see 2.5, 2.6) serves as the indicator. The indicator is responsible for the colour change and signals the end of the titration.
The neutral background improves the accuracy and reproducibility of the results. This means that the titrations are always carried out under optical conditions that are as similar to each other as possible.
Kjeldahl’s digestion method is not specific to amino acids and proteins and includes all organically bonded nitrogen. Other non-protein compounds are also are digested and collected (NPN: non-protein nitrogen). However, the pro-portion of these compounds is very small and is disregarded in the calculation.
If the non-protein containing nitrogen should also be es-tablished, then method must be executed in accordance with DIN EN ISO 8968-4. If only the protein nitrogen should be determined, then the milk proteins must first be sepa-rated. 5±0.1 ml of milk diluted with 5±0.1 ml of water is washed in stages with in total 60 ml of 15 % (w/v) trichlo-roacetic acid in accordance with DIN EN ISO 8968-5, the proteins are precipitated and finally filtered out into a hard paper filter. The filtrate contains the components of the non-protein nitrogen and the filtered-out precipitate con-tains the protein nitrogen. The filter with the precipitate is put into a digestion vessel and Kjeldahl’s nitrogen deter-mination method is carried out as described above. The protein content is calculated by multiplying by a factor of 6.38.
The value 6.38 is specific to milk and dairy products and was established because milk proteins have a nitrogen content of 15.65 % (100:15.65 = 6.38).
The blind trial is important for the calculation of the nitrogen content of the sample.
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Caution! The addition of hydrogen peroxide causes an intense reaction.
The blind trial is executed with 2 ml of water and 0.25 g of sucrose. The effectiveness of the decomposition is tested with 0.08 g of tryptophan or 0.06 g of lysine hydrochloride.
KJELDAHL’S NITROGEN DETERMINATION METHOD
In order to monitor the effectiveness of the de-composition, 0.18 g of tryptophan or 0.16 g or lysine hydrochloride and 0.67 g of sucrose are used. 98 % of the nitrogen content must be re-covered. If that is not the case, either the decom-position temperature or time is insufficient or the sample is charred.
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pH VALUE MEASUREMENTAnna Politis, graduate engineer of nutrition technology and of biotechnology, reports
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To clean off fat or oil deposits, the membrane must be degreased with cotton which has been soaked in acetone or soap solution.
If protein has settled on the diaphragm, the electrode is soaked in HCI/Pepsin solution for approx. 1-2 hours.
In case of a silver sulphide contamination, the electrode is to be set in a thiocarbamide solution and left to soak.
To remove inorganic films, the electrode is dipped into 0.1 M HCl or 0.1 M NaOH. With40-50°C solutions, cleaning is more effective.
After every cleaning procedure, the electrode is to be set in a 3M KCl solution about a quarter of an hour a new conditioning and subsequently calibrated once again.
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TITRATION APPARATUS
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>
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HEATING CABINETS UFB
HEATING CABINETS UNB
INCUBATORS INE
STERILISING OVENS SNB
REFRIDGERATED INCUBATORS WITH COMPRESSION COOLING ICP
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INHIBITOR DETECTION
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LACTODENSIMETER
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THERMOMETER/ACCESSORIES
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PSYCHROMETER
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INSERTION/IMMERSION SENSORS
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The German chemist Beckmann, known for the thermometer named after him, began using the freezing point of milk in as early as 1895 to detect if it had been adulterated with water. The American Hortvet worked intensively with this method in 1920 and im-proved some of its essential features. The first thermistor cyroscopes were brought to the market in the 1960s. However, they had to be operated entirely by hand. At the beginning of the 1970s, the first automatic thermistor cyroscopes became available. With this development it was possible to determine the freezing point automatically at the push of a button.
A decisive step in the improvement of thermistor cryo-scopy was displayed at the “FoodTec” tradeshow in 1984: Funke-Gerber introduced the first device with automatic calibration. This successful and intensive development work reached a new peak at the “Food-Tec” in 1988, where Funke-Gerber presented a fully automatic freezing point determination mechanism with a capacity of 220 samples per hour.
With the introduction of an indirect freezing point measurement device (e.g. LactoStar) for routine analysis, interest was focused primarily on reference devices which are able to determine freezing points in accordance with the applicable standards and regulations. These devices must satisfy the strictest requirements with regard to measuring accuracy. For this reason Funke-Gerber developed a program-mable cryoscope with a resolution of 0.1 m °C. This instrument has proven its accuracy and reliability incountless laboratories all over the world. The productrange has been expanded with a multi-sample device (CryoStarautomatic). Since January 2007, these instru-ments have been equipped with a graphic colour dis-play. This makes it possible to show the entire freezing curve, in particular the process of the plateau search, with a patented screen presentation.
FREEZING POINT DETERMINATION
K. Schaefer, graduate engineer, W. Spindler, graduate physician report
HISTORY
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THE FREEZING POINT:
MEASURING PRINCIPLE:
MEASURING PROCEDURE:
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POSSIBLE SOURCES OF ERROR IN THE MEASUREMENT PROCESS
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„CryoStar I (or. CryoStar automatic), Funke Gerber“
IDENTIFYING TECHNICAL DEFECTS
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IDENTIFYING OPERATIONAL ERRORS
MIX UP: A CALIBRATION INSTEAD OF B CALIBRATION
MIX UP: TAKING THEA SOLUTION INSTEADOF THE B SOLUTION
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SPECIAL APPLICATIONS/MEASUREMENT OF CREAM
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CryoStarautomatic CryoStar I
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THE MOST IMPORTANT FEATURES AT A GLANCE:
(recommended value: 2.2 ml)
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I
I
SHORT TIME HEATING DETECTION
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8502-001
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(also: bias for the amplitude of a systematic mistake)
THE USE OF REFERENCE MATERIAL IN THE LABORATORY
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<
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QUALITY FROM THE VERY BEGINNING
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CALIBRATION PROCEDURE
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THE Z-SCORE
s
mscorez
ix
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LABORATORY GLASSWARE
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8860
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8887
8886
8885
8884
8883
8882
8895
8894
8893
8892
8891
8890
8889
8888
8920
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8984
8983
8982
8981
8980
8994
8993
8992
8991
8990
8974
8973
8972
8971
8970
8985
8995
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9081
9090
9121
9080
9120
9050
9056
9054
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9233
9232
9231
9230
9190
9211
9201
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9365
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9364
9363
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9360
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9440
9470
9411
9410
9409
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9407
9405
9406
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9510
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9484
9498
9495
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9488
9487
9489
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ALPHABETICAL INDEX
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NOTICES
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NOTICES
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