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ASTM-D2892 2005

$58.50

D2892-05 Standard Test Method for Distillation of Crude Petroleum (15-Theoretical Plate Column)

Published By Publication Date Number of Pages
ASTM 2005 32
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1.1 This test method covers the procedure for the distillation of stabilized crude petroleum (see Note 0) to a final cut temperature of 400C Atmospheric Equivalent Temperature (AET). This test method employs a fractionating column having an efficiency of 14 to 18 theoretical plates operated at a reflux ratio of 5:1. Performance criteria for the necessary equipment is specified. Some typical examples of acceptable apparatus are presented in schematic form. This test method offers a compromise between efficiency and time in order to facilitate the comparison of distillation data between laboratories.

Note 0

Defined as having a Reid vapor pressure less than 82.7 kPa (12 psi).

1.2 This test method details procedures for the production of a liquefied gas, distillate fractions, and residuum of standardized quality on which analytical data can be obtained, and the determination of yields of the above fractions by both mass and volume. From the preceding information, a graph of temperature versus mass % distilled can be produced. This distillation curve corresponds to a laboratory technique, which is defined at 15/5 (15 theoretical plate column, 5:1 reflux ratio) or TBP (true boiling point).

1.3 This test method can also be applied to any petroleum mixture except liquefied petroleum gases, very light naphthas, and fractions having initial boiling points above 400C.

1.4 This test method contains the following annexes and appendixes:

1.4.1 Test Method for the Determination of the Efficiency of a Distillation Column,

1.4.2 Test Method for the Determination of the Dynamic Holdup of a Distillation Column,

1.4.3 Test Method for the Determination of the Heat Loss in a Distillation Column (Static Conditions),

1.4.4 Test Method for the Verification of Temperature Sensor Location,

1.4.5 Test Method for Determination of the Temperature Response Time,

1.4.6 Practice for the Calibration of Sensors,

1.4.7 Test Method for the Verification of Reflux Dividing Valves,

1.4.8 Practice for Conversion of Observed Vapor Temperature to Atmospheric Equivalent Temperature (AET),

1.4.9 Test Method for Dehydration of a Sample of Wet Crude Oil, and

1.4.10 Practice for Performance Check.

1.5 &si-value;

This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see Section .

1.6 This test method is for determining the efficiency of a distillation column, under total reflux conditions using the test mixture n -heptane/methylcyclohexane at atmospheric pressure.

1.7 The efficiency is not measured under vacuum conditions because there is no satisfactory test mixture that has a constant relative volatility with pressure.

1.8 This test method is for determining the dynamic holdup of a distillation column using a test mixture of stearic acid in n -heptane.

1.9 This test method is for determining the heat loss of a distillation column under static conditions when a temperature differential exists between the inner and outer walls of a distillation column.

1.10 This test method is for determining whether the temperature sensor is in the proper position for optimum performance.

1.11 This test method is for the determination of temperature response time based upon the rate of cooling of the sensor under prescribed conditions.

1.12 This test method is for determining whether a liquid reflux dividing valve produces the prescribed reflux ratio.

1.13 This practice is for conversion of the actual distillation temperature obtained at sub-ambient pressure to AET corresponding to the equivalent boiling point at atmospheric pressure, 101.3 kPa (760 mm Hg), by means of equations derived by Maxwell and Bonnell.

1.14 This practice is for dehydrating a sample of wet crude oil prior to fractional distillation.

1.15 This practice covers a procedure for calculating column performance from GC boiling point distributions on fractions and residues, obtained by distilling an average (30 to 40 API-gravity) crude oil under actual Test Method D 2892 distillation conditions.

Note 2

There are no theoretical reasons to limit the API-gravity range from 30 to 40. However, the use of a crude oil in the quoted range will, more or less, ensure that sufficient product is available to assess performance, both at the upper and lower end of the temperature scale. The use of heavier crudes may not yield sufficient quantities at the low end, while the reverse is true for lighter crudes.

1.16 The assessment of column performance can be made at any cut point where samples of two adjacent fractions or a residue can be analyzed by gas chromatography. Either fresh or stored samples can be analyzed, as long as they have been protected from loss by evaporation. Recommendations are given for the number and spacing of cut points to be analyzed for performance.

1.17 A precise mathematical method for the calculation of distillation efficiency of multi-component mixtures is described and is recommended. For convenience sake, a simple graphical solution based on the same method is also included.

1.18 Overall column performance is assessed in terms of column efficiency (minimum tray number) and in terms of the differential between the nominal cut point (AET) and the calculated effective cut point (ECP). Criteria are given for acceptance of column performance. Possible corrective action(s), if required, are also indicated.

PDF Catalog

PDF Pages PDF Title
1 Scope
Referenced Documents
2 Terminology
3 Summary of Test Method
Significance and Use
Apparatus
TABLE 1
4 FIG. 1
5 TABLE 2
6 FIG. 2
7 Verification of Apparatus Performance
Sampling
8 Preparation of Apparatus
Procedure
FIG. 3
10 FIG. 4
11 Calculation
Report
Precision and Bias
12 Keywords
A1. TEST METHOD FOR THE DETERMINATION OF THE EFFICIENCY OF A DISTILLATION COLUMN
A1.1 Scope
A1.2 Significance and Use
A1.3 Apparatus
A1.4 Reagents and Materials
A1.5 Preparation of Apparatus
A1.6 Procedure
13 A1.7 Calculation
A1.8 Precision and Bias
14 FIG. A1.1
FIG. A1.2
15 FIG. A1.3
FIG. A1.4
16 FIG. A1.5
FIG. A1.6
17 A2. TEST METHOD FOR THE DETERMINATION OF THE DYNAMIC HOLDUP OF A DISTILLATION COLUMN
A2.1 Scope
A2.2 Summary of Test Method
A2.3 Significance and Use
A2.4 Apparatus
A2.5 Reagents and Materials
A2.6 Preparation of Apparatus
A2.7 Procedure
FIG. A1.7
18 A2.8 Calculation
A2.9 Precision and Bias
A3. TEST METHOD FOR THE DETERMINATION OF THE HEAT LOSS IN A DISTILLATION COLUMN (STATIC CONDITIONS)
A3.1 Scope
A3.2 Summary of Test Method
A3.3 Significance and Use
A3.4 Apparatus
A3.5 Preparation of Apparatus
A3.6 Procedure
19 A3.7 Calculation
A3.8 Precision and Bias
A4. TEST METHOD FOR THE VERIFICATION OF TEMPERATURE SENSOR LOCATION
A4.1 Scope
A4.2 Summary of Test Method
A4.3 Significance and Use
A4.4 Procedure
A4.5 Precision and Bias
20 A5. TEST METHOD FOR DETERMINATION OF TEMPERATURE RESPONSE TIME
A5.1 Scope
A5.2 Significance and Use
A5.3 Procedure
A5.4 Precision and Bias
A6. PRACTICE FOR CALIBRATION OF SENSORS
A6.1 Principle
A6.2 Temperature Sensors
FIG. A6.1
21 A6.3 Vacuum Sensors
FIG. A6.2
22 A7. TEST METHOD FOR VERIFICATION OF REFLUX DIVIDING VALVES
A7.1 Scope
A7.2 Summary of Test Method
A7.3 Significance and Use
A7.4 Apparatus
FIG. A6.3
23 A7.5 Reagents and Materials
A7.6 Preparation of Apparatus
A7.7 Procedure
A7.8 Precision and Bias
A8. PRACTICE FOR CONVERSION OF OBSERVED VAPOR TEMPERATURE TO ATMOSPHERIC EQUIVALENT TEMPERATURE (AET)
A8.1 Scope
A8.2 Significance and Use
A8.3 Calculation
FIG. A7.1
24 FIG. A8.1
25 X1. PRACTICE FOR DEHYDRATION OF A SAMPLE OF WET CRUDE OIL
X1.1 Scope
X1.2 Summary of Test Methods
X1.3 Significance and Use
X1.4 Apparatus
FIG. A8.2
26 X1.5 Preparation of Apparatus
X1.6 Procedure
X1.7 Calculation
X1.8 Precision and Bias
X2. PRACTICE FOR PERFORMANCE CHECK
X2.1 Scope
X2.2 Significance and Use
27 X2.3 Summary of Practice
X2.4 Procedure
X2.5 Calculation
29 FIG. X2.1
TABLE X2.1
TABLE X2.2
30 X2.6 Frequency of Test and Data Interpretation
TABLE X2.3
TABLE X2.4
31 FIG. X2.2
TABLE X2.5
ASTM-D2892 2005
$58.50