By Authority Of

THE UNITED STATES OF AMERICA

Legally Binding Document

By the Authority Vested By Part 5 of the United States Code 552(a) and
Part 1 of the Code of Regulations 51 the attached document has been duly
INCORPORATED BY REFERENCE and shall be considered legally
binding upon all citizens and residents of the United States of America.
HEED THIS NOTICE: Criminal penalties may apply for noncompliance.

e
Document Name: ASTM D1945: Standard Test Method for Analysis of
Natural Gas By Gas Chromatography

CFR Section(s):

40 CFR 60.45(f)(5)(i)

Standards Body:

American Society for Testing and Materials

Official Incorporator:
THE EXECUTIVE DIRECTOR

OFFICE OF THE FEDERAL REGISTER

WASHINGTON, D.C.

~~l~

Designation: D 1945 - 96

Standard Test Method for

Analysis of Natural Gas by Gas Chromatography 1

This standard is issued under the fixed designation D 1945; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (,) indicates an editorial change since the last revision or reapproval.

. j

for calculating. physical properties of the sample, such as

heating value and relative density, or for monitoring the
concentrations of one or more of the components in a
mixture.

1. Scope
1.1 This test method covers the deterniination of the
chemical composition of natural gases and similar gaseous
mixtures within the range of composition shown in Table 1.
This test method may be abbreviated for the analysis of lean
natural gases containingnegligible amounts of hexanes and
higher hydrocarbons; .or for the determination of one or
more components, as required.
.
1.2 The values stated in SI units are to be regarded as the
standard. The values given in parentheses are for information only.
1.3 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 oj regulatory limitations prior to use.
2. Referenced Documents

2.1 ASTM Standards:

.
D 2597 Test Method for Analysis of Demethanized Hy. drocarbon Liquid Mixtures Containing Nitrogen atiq.
Carbon Dioxide by Gas Chromatography2.
..
D 3588 Practice for Calculating Heat Value,. Compressibility Factor, and Relative Density (Specific Gravity) of
. Gaseous Fuels3
' .
.
E 260 Practice for PackedColurnn Gas Chromatography'4
3; Summary of Test Method
3.1- Components in a representative sample are physically
separated by gas chromatography (GC) and compared to
calibration data obtained under identical operating conditions from a reference standard mIxture of known composition. The numerous heavy-end components of a sample can
be grouped into irregular peaks by reversing the direction of
the carrier gas through the column at such time as to group..
the heavy ends either as Cs and heavier, C6 and heavier, or
C7 and heavier. The composItion of the sample is calculated
by comparing either the peak heights, or the peak areas, or
both, with the corresponding values obtained with the
reference standard.
4. Significance and Use
4.1 This test method is of significance for providing data
1 This test method is under the jurisdiction of ASTM Committ~e D-3 o~ "
Gaseous Fuels and is the direct responsibility of Subcommittee D 03.07 on
Analysis of Chemical Composition of Gaseous Fuels.
Current edition approved Nov. 10, 1996. Published January 1997. Originally
published as D 1945 - 62 T. Last previous edition D 1945 - 91.
2 Annual Book ofASTM Standards, Vol 05.02.
3 Annual Book ofASTM Standards, Vol 05.05.
4 Annual Book of ASTM Standards, Vol. 14.02.

5. Apparatus
5.1 Detector-The detector shall be a thermal-conductivity type, or its equivalent in sensitivity and stability. The
thermal conductivity detector must be sufficiently sensitive
to produce a signal of at least 0.5 m V for 1 mol % n-butane;
in a 0.25-mL sample.
5.2 Recording Instruments-Either strip-chart recorders
or electronic integrators, or both, are used to display the
separated components. Although a strip-chart recorder is not
required when using electronic integration, it is highly
desirable for evaluation of instrument performance.
.
". 5.2.1 The recorder shall be a strip-chart recorder wjth a
full-range scale 'of 5'mV or less (1 ~V preferred). The widtll
of the chart shall be not hiss than 150 mm. A ma:ximum pen
response time of 28,(1 s preferred) and a minimum chart
speed orIO mm/minshall be required. Faster speeds up to
100 mm/min are desiJ:able if the chromatQgram is to be
interpreted using manual methods to obtain areas.
.
5.2.2 Electronic or Computing In{egrators-,roof of separation and response equival~nt to that for a recorder is
required for displays other than by.~hart recorder. Baseline
tracking with tang~nt skim p~ak" detectio~ is reqO?Ini~nd,ed. .
5.3 Attenuator-Ifthe chromatogra~ IS t9 bemterp~eted
using manual methods,an attenuator mustb~ u~ed With the
detector output signfl.l to main~ain'in&ximunipea~s iwithin
the recorder chart range. The atten).lator must by,accurate tq
within 0.5 % between the attenuator range steps.""
5.4 Sample Inlet System:
5.4.1 The sample inlet system shall be constructed of
materials that are inert and nonadsorptive with respect to the
components in the sample. The preferred material of construction is stainless steel. Copper, brass, and other copperbearing alloys are unacceptable. The sample inlet system
from the cylinder valve to the GC column inlet must be
niaintainedat a temperature constant to 1C.
5.4.2 Provision musibe made to introduce into the carrier
gas ahead of the analyzing column a gas-phase sample that
, has been entrapped in a fixed volume loop or tubular
'section. The fixed loop or section shall be so constructed that
the total volume, incl\lding d~ad space, shall not normally
exceed 0.5 mL at 1 atm. If increased aC9uracy of the hexanes
and heavier portions of the analysis is required, a larger
sample size may be used (see Test Method D 2597). The
sample volume must be reproducible such that successive
runs agree within 1 % on each component. A flowing sample
,inlet system. is acceptable. as long as viscosity effects are

'51

~t D 1945
TABLE 1

constant to 1 % throughout the analysis of the sample and

the reference standard. The purity of the carrier gas may be
improved. by flowing the carrier gas through selective fllters
prior to its entry into the chromatograph.
5.S Columns:
5.S.1 The columns shall be constructed of materials that
are inert and nonadsorptive with respect to the components
in the sample. The preferred material of construction is
stainless steel. Copper and copper-bearing alloys are unacceptable.
5.S.2 An adsorption-type column and a partition-type
column may be used to make the analysis.

Natural Gas Components and Range of

Composition Covered
Mol %

Component

0.01 to 10
0.01 to 10
0.01 to 20
0.01 to 100
0.01 to 20
0.01 to 100
0.01 to 100
0.3 to 30
0.01 to 100
0.01 to 10
0.01 to 10
0.01 to 2
0.01 to 2
0.01 to 2
0.01 to 2
0.01 to 1

Helium
Hydrogen
Oxygen
Nitrogen
Carbon dioxide
Methane
Ethane
Hydrogen sulfide
Propane
isobutane
n-Butane
neoPentane
isoPentane
n-Pentane
Hexane isomers
Heptanes plus

NOTE

2-See Practice E 260.

5.S.2.1 Adsorption Column-This column m,ust completely separate oxygen, nitrogen, and methane. A 13X
molecular sieve S0/100 mesh is recommended for direct
injection. A SA column can be used if a pre-cut column is
present to remove interfering hydrocarbons. If a recorder is
used, the recorder pen must return to the baseline between
each successive peak. The resolution (R) must be 1.5 or
greater as calculated in the following equation:
x -x

accounted tor.
NOTE I-The sample size limitation of 0.5 mL or smaller is selected
relative to linearity of detector response, and efficiency of column
separation. Larger samples may be used to determine low-quantity
components in order to increase measurement accuracy.

R(I,2) =

5.4.3 An optional manifold arrangement for entering

vacuum samples is shown in Fig. 1.
5.5 Column Temperature Control:
5.5.1 Isothermal-When isothermal operation is utilized,
maintain the analyzer columns at a temperature constant to
0.3e during the course oftlie sample run and corresponding
reference run.
5.5.2 Temperature Programming-Temperature programming may be used, as feasible. The oven temperature shall
not exceed the recommended temperature limit for the
materials in the column.
5.6 Detector Temperature Control-Maintain the detector
temperature at a temperature constant to 0.3C during the
course of the sample run and the corresponding referency
run. The detector temperature shall be equal to or greater
than the maximum column temperature.
5.7 Carrier Gas Controls-The instrument shall be equipped with suitable facilities to provide a flow of carrier gas
through the imalyzer arid detector at a flow rate that is

_2_ _1 X

Y2

2,

+ YI

where Xl' X2 are the retention times and Yl> Y2 are the peak
widths. Figure 2 illustrates the calculation for resolution.
Figure 3 is a chromatogram obtained with an adsorption
column.
5.S.2.2 Partition Column-This column must separate
ethane through pentanes, and carbon dioxide. If a recorder is
used, the recorder pen must return to the base line between
each peak for propane and succeeding peaks, and to base line
within 2 % of full-scale deflection for components eluted
ahead of propane, with measurements being at the attenuation of the peak. Separation of carbon dioxide must be
sufficient so that a 0.25-mL sample containing O.l-mol %
carbon dioxide will produce a clearly measurable response.
The resolution (R) must be 1.5 or greater as calculated in,the
above equation. The separation should be completed within
40 min, including reve.r:sal of flow after n-pentane to yield a
group response for hexane~ and heavier components. Figures

TO
TO
MERCURY
TRAP

CARRIER
""::::::~ __TO
GAS ~
COLUMN
VENT
GAS CHROMATOGRAPH
SAMPLE VALVE
MANOMETER
SAMPLE
CYLINDER

FIG. 1

(1)

Suggested Manifold Arrangement for Entering Vacuum Samples

52

~t D 1945
~--------------X2-------------~----~

....J
<[

z
(.!)
(J)

o
RETENTION
FIG. 2

Calculation for Resolution

4, 5, and 6 are examples of chromatograms obtained on

some of the suitable partition columns.
5.8.3 General-Other column packing materials th~t pro- ,
vide satisfactory separation of components of intere~t may be ...
utilized (see Fig. 7). In multi-column applications, it is
preferred to use front-end backflush of the heavy ends.
NOTE 3-The chromatograms in Figs. 3 through 8 are only illustrations of typical separations. The operating. conditions, including columns, are also typical and are subject to optimization by competent
personneL"'

5.9 Drier-Unless water is known not to interfere in the

analysis, a drier must be provided in the sample entering
system, ahead of the sample valve. The .drier must remove

moisture without removing selective components to be

determined in the analysis.
NOTE

4-See Annex A2.2 for preparation of a suitable drier.

5.10 Valves':"'-Valvesor sample splitters, or both, are

required to permit switching, backflushing, or for simultaneous analysis.
.", . '
. 5.11 Manometer-May be either U-tube type or well type
equipped with an accurately graduated and easily read scale
covering the range 0 to 900 mm (36 in.) of mercury or larger.
, The U-tube type is useful,since it permits filling the sample
loop with up to two atmospheres of sample pressure, thus
extending the range of all components. The well type
inherently offers better precision and is preferred when
calibrating with pure components. Samples with up to one

COLUMN: 2 meter ,Type 13X molecular

Sieve, 80-100' mesh
SAMPLE SIZE:

0.25 mL.

CARRIER GAS: . He Hum @ 30 .. mL. /min.

',6

0,

Minutes
'FIG. 3

Separation Column for Oxygen, Nitrogen, and Methane (See Annex A2)

53

~m~ D 1945
COLUMN-25% BMEE on Chromosorb P,
7 meters @ 25C
CARRIER GAS: Helium @ 40 mL./min.
SAMPLE SIZE: 0.25 mL.

co

0\
0
~.

I.Q

co

.
:s:
0

~I.Q

~r-...
c..:>

c..:>

18

16

14 12

Minutes
FIG. 4

Chromatogram of Natural Gas (SMEE Column) (See Annex A2)

COLUMN.:

Chromoorb PAW, 200/500". lam

I=il

HI=il

CARRIER GAS: Helium @ 40 mL./min.

SAMPLE SIZE: ' 0.25 mL.

I=il

<t:

p.,
0

~ z
H
I=il
p.,

I=il

CI)

IIH

:s:

Cl

~~

I=il

>x..

~~

Cl)H

25

~
~
~

r:Q
I

I=il
CI)

t><~

I=il

::r::

I=il

p.,
0

.~

p.,

J:I::

~~
H
:x:
0

Cl

<t:

r:Q

r:Q

CI)

c..:>

po

>x..

30

z )

I=il~

20

15

10

Minutes
FIG. 5

Chromatogram of Natural Gas (Silicone 200/500 Column) (See Annex A2)

6. Preparation of Apparatus

atmosphere of pressure can be entered. With either type

manometer the mm scale can be read more accurately than
the inch scale. Caution should be used handling mercury
because of its toxic nature. Avoid contact with the skin as
much as possible. Wash thoroughly after contact.
5.12 Vacuum Pump-Must have the capability of producing a vacuum of 1 mm of mercury absolute or less.

6.1 Linearity Check-In order to establish linearity of

response for the thermal conductivity detector, it is necessary
to complete the following procedure:
6.1.1 The major component of interest (methane for
natural gas) is charged to the chromatograph by way of the
fixed-size sample loop at partial pressure increments of 13
54

dt

D 1945

DIDP-3meter +DMS-6meter
, @350C.

COLUMN:

H
rz:l

II

CARRIER GAS: Helium @ 75 mL./min.

SAMPLE SIZE: 0.5 mLo

.. I=Q

rz:l

~H

~
H

:z;

rz:l
p..,

rz:l
p..,
0

Z
I

(J)

:z;

t.(J

~::r::

\.

18 . 16

p..,
0
p::<
p..,

I=Q

I=Q
I

H,

r:;

r:;

(J)

:z;

20

14-

12

10

6 -

8p::<
f-i

~
C,)

rz:l

rz:l

Minutes
FIG. 6

Chromatogram of Natural Gas (See Annex A2)

,"jl

COLm-1N 1: '3 meters x 3mm 152 Squalane

Chromosorb PAW. 80-100 mesh.
:I

> 2 meter's :x 3mm porapak N

__ " ,80:--100 mesil .

COLUMN '2:

COLUMN ,3:

,,-,'

2 meters x 3mm Molecular Sieve

SMA, 80-100 'm"esh.

'
~

"
~
>:
~

.~

>:

~,

"
z'"

, '

gj

til

00

"

til

~
til

~:>

:j~ ~
:>

10

, " FIG.' 7

("

12

14

16

18

20

Chromatogram- of Natural Gas (Multi-Column Application) (See Annex A2)

min

kPa(lOO mm Hg) from 13 to 100kPa'(100 to 760

Hg)
or the prevailing atmospheric pressure. "
6. [2" The Integrated peak responses for the area generated
at each of the pressure increments are plotted ver~us their
partial pressure (see Fig. 9). '
6.1.3 The plotted results should yield a straight line. A
perfectly linear response would display a straight Hne at ~ 4~O

angle using the logarithmic values.

" "
6.1.4 Any curVed line indicates the fi~ed volume sample
~oop is too large. A smaller loop size should teplace the fixed
volume loop and 6.1.1 through 6.1.4 should be repeated (see
Fig. 9).
. ", "
'
6.1.5 The lip.earity over the range of interest must be
known for each component. It is usefuCtoconstritcta table

~m~D 1945
a

2 meter x 3mm mol. sieve 13x @ 50 C

Argon carrier @ 40 mL./min.
Detector @ 100n~.

Minutes
FIG. 8

Separation of Helium and Hydrogen

noting the response factor deviation in changing concentration. (See Table 2 and 3).
6.1.6 It should be noted that nitrogen, methane, and
ethane exhibit less than 1 % compressibility at atmospheric
pressure. Other natural gas components do exhibit a significant compressibility at pressures less than atmospheric.
6.1.7 Most components that have vapor pressures of less
than 100 kPa (l5 psia) cannot be used as a pure gas for a
linearity study because they will not exhibit sufficient vapor
pressure for a manometer reading to 100 kPa (760 mm Hg).
For these components, a mixture with nitrogen or methane
can be used to establish a partial pressure that can extend the
total pressure to 100 kPa (760 mm Hg). Using Table 4 for
vapor pressures at 38C (lOOF), calculate the maximum
pressure to which a given component can be blended with
nitrogen as follows:
B = (100 x V)/i
(2)
(3)
P = (i x M)/lOO

sample valve to place the sample onto the column. Record

the peak area of the pure component.
6.2.4 Repeat 6.2.3 for 26, 39, 52, 65, 78, and 91 kPa (200,
300, 400, 500, 600, and 700 mm Hg) on the manometer,
recording the peak area obtained for sample analysis at each
of these pressures.
6.2.5 Plot the area data (x axis) versus the partial pressures
(y axis) on a linear graph as shown in Fig. 9.
6.2.6 An alternative method is to obtain a blend of all the
components and charge the sample loop at partial pressure
over the range of interest. If a gas blender is available the
mixture can be diluted with methane thereby giving response
curves for all the components.
NOTE 5: Caution-If it is not possible to obtain information on the
linearity of the available gas chromatograph detector for all of the test
gas components, then as a minimum requirement the linearity data
must be obtained for any gas component that exceeds a concentration of
5 mol %. Chromatographs are not truly linear over wide concentration
ranges and linearity should be established over the range of interest.

where:
_
B = blend pressure, max, kPa (mm Hg),
V = vapor pressure, kPa (mm Hg),
i = mol %
P = partial pressure, kPa (mm Hg), and
M = manometer pressure, kPa (mm Hg).
6.2. Procedure for Linearity Check:
.
6.2.1 ConJ;lect the pu:re-component source to the sampleen,try system. Evaouate the sample-entry system and observe
the manometer fqr .Ie?;~s. (See Fig. 1 for a suggested manifold
arrangement.) The sample-entry system must be vacuum tight.
6.2.2 Carefully open the needle valve to admit the pure
componeni up to 13 kPa (100 mm Hg) of partial pressure.
6.2.3 Record the exact partial pressure and actuate the

7. Reference Standards
7.1 Moisture-free gas mixtures of known composition are
required for comparison with the test sample. They must
contain known percents of the components, except oxygen
(Note 6), that are to be determined in the unknown sample.
All components in the reference standard must be homogenous in the vapor state .at the time of use. the concentration
of a component in the reference standard gas should not be
less than one half nor more than twice the concentration of
the corresponding component in the test gas.
NOJ:E 6-Unless the reference standard is stored in a container that
has been tested and proved for inertness, to oxygen, it is preferable to
calibrate for bxygen by an alternative method.

56

~t D 1945
-

800

II
I

I
700

II
I

I;! !

I
i

i!

li"1

'II'
":11 I

I'Ii:I ", 'I

II

iill

I
I

, I

! '

I
I ! ' Ii
I,,
i!I i I IIII i I:!!
III i '"
i~ :
600
,
,
I ,
I
!~ :!
I
I
, ,I
I
iii
j
' ii l
I
:'j
!I
ii
i
I
iii! i I il I I .1: Ii! I :I I ~r !
'i ,
500
I!I I I
I: Ii; !II II, I !II 11II!.: .I!I : I 'Iii' I II
:i I
,!
I :! ! rr
,Iii";I: ii iI
!
II"IIII i' ;!i i I i I!!:
I
,I,I ,
400
,
'! I ;
Ul;fl'i : I' !,: ii ,I' iiii i;!' I, i
, i i iii i II i II! Ii ' : l,
f, i
I
'1 j!_lil"I"
, !!!:: II II" I, ;. Methane , I! Ii I
t

"

: !

.i.1

C>

J:

I:

E
E

:>

'"'"
0.

1\'

j"

!!!
.9l

1:

,
II

! II'.
. I!!

,I

i:

:>

'0

'"

.0

300

.,"

200

iii II
!!I! II

ii! II
!
I
i

111 i '!

I!

II

' ,I'
: ;'1

'1I

" III
i;:!
I, i

IiI

' i
I

Ii

Ii

,
100

'I !

o
10,000

FIG. 9
. TABLE 2

TABLE 3 :'.' i.i~~~;ity

SIB mole %/area

223119392
242610272
261785320
280494912
299145504
317987328
336489056
351120721

51
56
61
66.
71
76
81
85

2.2858e-07
2.3082e-07
. 2.3302e-07
2.3530e-07
2.3734e-07
2.3900e-07 .
2.4072e-07
2.4208e-07

Ev.aluati~n for Nitrog~~

SIB diff ;", (low mole %-:- high mole %)/low mole % '?< '100

SIB diff = (low inole % :- high mole %)/lriw mole % x 100

S mole %

11000
, 0'

Linearity of Detector Response

Linearity Evaluation of Methane

B area

90,000

70,000

5P,000
Area Count

30,QOO

SIB djff., % on low

value

SIB mole %/area

B area
5879836
29137066
57452364
84953192
111491232,
137268784 .
162852288
187232496

":'0.98
-0.95
-0.98
-0.87
-0.70
-0.72
-0.57

TABLE 4

7.2 Preparation-A reference sta11-dard may be prepared

by blending pure components. Diluted dry air is a suitable
standard for oxygen and ~it~ogen (see 8.5_1 )',5,6'

Component
Nitrogen
Methane .
Carbon dioxide
Ethane
Hydrogen sulfide
Propane
.
Isobutane
n-Butane
Isopentane
n-Pentane
n-Hexane
n-Heptane

8. Procedure
.
.
8.1 Instrument Preparation'-Place the proper column(s)
in operation as needed for the desired run (as described in
either 8.4, 8.5, or 8.6). Adjust the operating conditions and
5 A suitable reference standard is available from Phillips Petroleum Co., Borger,
TX"79007.
' : '
.
, 6 A, ten-component reference standard traceable to the National Institute of
Standards and Technology (NIST) is a~ailable from Institute of Gas Technology
(IGT), 3424 S. State St., Chicago, IL 60616'.

1
'.5
10
. 15 :
20
25
30'
35

S/Bdiff., % on low,
. .value

.,1.7007e-,07, .
1.71609-07
1.7046e..07 '
1.7657e-07.1~

-0.89'
-1.43
-1.44
"-1.60 .
-1.53

,.- .

.1..7939e-07
1.8212e-07
1.8422e-07
. 1.8693e-07

'-1.15

':"1.48;'

Vapor Pressure at 38C (100F)A

'kPa absolute '. , .
>34 500
'>34 500
>5520
>5520
2 720
1 300
501
356
'141
'108
34.2
11.2

psia:
>5 000
>5 000'
>800
>800
39.5
189
'72.6
51.7
20.5
15.6
4.96
1.62

A The most recent d~ta for the vapor pressures listed are a:~ailable from the
Thermodynamics Research Center, Texas A&M University System, College'
, .
Station, TX 77843. '

57

~ffi~ 0.,1945
absol~te pressure. Close the valve to the vacuum source and
carefully meter the fuel-gas sample ftom the sample cylinder
'until the sample loop is' filled to the desired pressure, as
NOTE 7-Most modenichromatographs have valve ovens that can
indicated on the manometer (see Fig. 1). Inject the sample
be temperaturl? controlled. It is strongly recom111elJ.ded in ~he absl?nce of
into, the chromatograph. '
valve ovens to mount the gas sampling valve in,the chromatograph oven
and operate at the column temperature.
8A, Partition Column Runfor Ethane and Heavier Hydro, carbons and Carbon Dioxide -This run is made using either
8.1.2 After the ~nstrument has apparently stabilized; make
helium or hydrogen as the carrier gas; if othyr than a thermal
check runs on the reference standard to establish instrument
conductivity detector is used, select a suitable carrier gas for
repeatability. Two consecutive checks must agree within ,% ' that detector. Select a sample size in accordance with 8.1.
of the amount present of each component. Either the averag~
Enter the sample, and backflush heaVy components when
of the two consecutive checks, or the latest check agreeing
appropriate. Obtain a corresponding response on the referwithin 1 % of the previous check on each component may be
ence standard.
' ,
used as the reference standard for all subsequent runs until
8.4.1 Methane may also be determined on this column if
there is a change in instru;nient operating conditions. Daily
the column will separate the methane from nitrogen and
calibrations are recommended.
;
oxygen (such as with silicone 200/500 as shown in Fig. 5),
8.2 Sample Preparation-If desired, hydrogen sulfide may
and the sample size does not exceed 0.5 mL.
be removed by at least two meth.ods (see Annex A2.3).
8.5 Adsorption Column Run for Oxygen, Nitrogen, and
8.2.1 Preparation and Introduction of Sa1?lple-Samples
Methane-Make this run using helium or hydrogen as the
must be equilibrated in the l~boratory at 20-50F above the
carrier-gas. The sample size must not exceed 0.5 mL for the
source temperature of the field sampling: The higher the
determination of methane. Enter the samPle and obtain a retemperature the shorter the equilibration time (approxisponse through methane (Note 6). Likewise, obtain a remately two hours for small sample containers of 300 mL or
sponseon the reference standard fot nitrogen and methane.
less). This analysis method assumes field sampling methods
ObtliiB a response on dry air for nitrogen and oxygen, if dehave removed, entraind' liquids. If the hydrocarbon
sired. The air must be either entered at an accurately measdewpoint of the sample is,known to be lower than the lowest
ured reduced pressure, or from a helium-diluted mixture.
temperature to which the sample has been exposed, it is not
8.5.1 A mixture containing approximately 1 % of oxygen
necessary to heat the sample.
can be prepared by pressurizing a container of dry air at
8.2.2 Connections from: the sample container to the
atmospheric pressure to 2 MPa (20 atm) with pure helium.
should be made with stainless
sample inlet of the instrument
This pressure need not be measured precisely, as the concen,\1
steel or with short 1lbieces' of TFE-fluorocarbon. Copper,
tration of nitrogen 'jn the mixture' thus: prepared must be
vinyl, or rubber connections are not a,qceptable. Hea~ed lines
determined by cOl;,nparison to nitrogen in the reference
may be necessary for high hydrocarbon content samples.
standard. The percent nitrogen is multiplied by 0.268 to
8.3 Sample Introduction-The size of the sample introobtain the mole percent of oxygen, or by 0.280 to obtain the
duced to the chromatographic columns shall not exceed 0.5
mole percent total of oxygen and argon. Do not rely on
mL. (This small sample ,size is necessary to obtain a linear
oxygen standards that have been prepared for more than a
detector respbnse for m'ethane.) Sufficient accuracy can be
few days. It is permissible to use a response factor for oxygen
obtained for the deterlnination of all but the minor constitthat is relative to a stable constituent.
uents by the use of this sample size. When increased response
8.6 Adsorption Column Run for Helium and Hydrogenis requir6d for the determination of components present in
Make this run using either nitrogen or argon as the carrier
concentrations not exceeding 5 mol %, it is permissible to
gas. Enter a 1 to 5-mL~ample and record the response for
use sample and reference standard volumes not exceeding 5
helium, followed by hydrogen, which will be just ahead of
mL. (Avoid introduction ofliquids into the sample system.)
oxygen (Note 6). Obtain a corresponding response on a
8.3.1 Purging Method-Open the outlet valve' 'of the
reference standard containing suitable concentrations of
sample cylinder and purge the sample through the inlet
helium and hydrogen (see Fig. 8).
system and sample loop or tube. The amount of purging
required must be established and verified for each instru9. Calculation
ment. The sample loop pressure shQ],Ild be near atmospheric.
Close the cylinder valve and allow the pressure of the sample
9.1 The number of significant digits retaine~ for the
in the loop or tube to stabilize. Then immediately inject the
quantitative value of each component shall be such tl~at
contents, of the loop or tube into the chromatographic
accuracy is neither sacrificed or exaggerated. The expressed
column to avoid infiltration of contaminants.
numerical value of any component in the sample shouldinot
8.3.2 Water Displacemerlt~rfthe sample was obtained by
be presumed tq be ,more accu~ate than" tl1e corresponding
water displacement, then water displacement may be used to
certified value oIthat component jn the calibration standard.
purge and fill the sample loop or tube.
9.2 External Standard Method~
.
9.2.1 Pentanes ~nd Lighter Components-Measure the
NOTE 8: Caution-Some components, such as carbon dioxide, hydrogen sulfide, and hexanes and higher hydrocarbons, may be partially
height of each component peak for pentanes and lighter,
or completely removed by the water.
convert to the same attenuation for corresponding components in the sample and reference standard, and calculate'the
8.3.3 Evacuation Method-Evacuate the charging system,
concentration of each compon~ht in the sa.mp~e as follows:
induding the sample loop, and the sample line back to the
valve on the sample cylinder, to less than 0.1 kPa (1 mm Hg)
C=SX(A/B)
(4)

allow the chromatograph to stabilize.

8.1.1 For hexanes and higher, h~at the sample loop.

58

~m~ 0 1945
where:
C = component concentration in the sample, mol %,
A = peak height of component in the sample, mm,
B = peak height of component in the standard, mm, and
S = component concentration in the reference standard,
mol %.
9.2.1.1 If air has been run at reduced pressure for oxygen
or nitrogen calibration, or both, correct the equation for
pressure as follows:
C = S x (A/B) x (Pa/Pb )

(5)

where:

Pa = pressure at which air is run, and '

,
Pb = true barometric pressure during the run, with both
pressures being expressed in the same units.
9.2.1.2 Use composition values of 78.1 % nitrogen and
21.9 % oxygen for dry air, because argon elutes with oxygen
on a molecular sieves column under the normal conditions
of this test method.
9.2.2 Hexanes and Heavier Components-Measure the
areas of the hexanes portion and the heptanes and heavier
portion of the reverse-flow peak (see Annex AI, Fig. ALl,
and Appendix X3.6). Also measure the areas of both pentane
peaks on the sample chromatogram, and adjust all measured
areas to the same attenuation basis.
9.2.3 Calculate corrected areas of the reverse flow peaks as
follows:
(6)
Corrected C6 area = 72/86 x measured C6 area
CorreCted C7 and heavier area
,
= 72/A x measured C7 and heavier area ,(7)
where A
fraction.

= average molecular weight ofthe

.

9.2.4.1 If the mole percent of iCs + nCs has been

determined by a separate run with a smaller sized sample,
this value need not be redetermined.
9.2.5 The entire reverse flow area may be calculated in
this manner as C6 and heavier, or as C s and heavier should
the carrier gas reversal be made after n-butane. The measured area should be corrected by using the average molecular weights of the entire reverse-flow components for the
value of A. The mole percent and area of the iC s and nCs
reverse flow peak of an identically sized sample of reference
standard (free of C6 and heavier) shall then be used for
calculating the final mole percent value.
9.2.6 Normalize the mole percent values by multiplying
each value by 100 and dividing by the sum of the original
values. The sum of the original values should not differ from
100.0 % by more than 1.0 %.
9.2.7 See sample calculations in Appendix X2.

10. Precision
10.1 Precision-The precision of this test method, as
determined by the statistical examination of the
interlaboratory test results, for gas samples of pipeline
quality 38 MJ/m 3 (1000 Btu/SCF) is as follows:
, 10.Ll Repeatab ility-The difference between two successive results obtained by the same operator with the same
,apparatus under constant operating conditions on identical
test materials should be considered suspect if they, ,differ by
more than the following a:mounts:
Component, 'mol %

Repeatability

oto'O.1 .

0.01
0.04
0.07
0.08
0.10

0.1 to 1.0
1.0 to 5.0
5.0 to 10
Over 10

C7 and he~vier
,

10.1.2 Reproducibility-The difference between two results obtained by different operators in different laboratories
on identical test materials should be considered suspect if
they differ by more than the following amounts:

NOTE 9-The value of 98 is usually sufficiently accurate for use as

the C? and heavier fraction average molecular weight; the small amount
of C8 and heavier present is usually offset by the lighter methyl
cyc!opentane and cydohexane that occur in this fraction. A more
accurate value for the ni.blecular weight ofT?' and heavier can be
obtained as described in Annex AU.

Component; mol %

Reproducibility

oto 0.1

0.02
0.07
0.10 .
,0.12
0.15

0.1 to 1.0
1.0 to 5.0
. 5.0 to 10.:
, Over 10

two

9.2.4 Calculate the concentration of the

fractions in
the s~mple as follows:
"
:NJ;ol % C6 = (coqected C6 area)
'. " . '.' ."
x (mol % iC 5 + nC5 )/(iC5 + nC5 area). (8)
Mol % C7 + == (corrected C7 area)'
x (mol % iC5 + nC5 )/(iC5 + nC 5 area). (9)

,.. ,.
J',
11. Keywords
, n.l gas analysis; gas chromatography; natural gas com':'
position
.'
,
'

ANNEXES
(Mandatory Information)
At. SUPPLEMENTARY PROCEDURES

A1.l Anlllysis (or only Pf(>pam; and Heavier ,Components. ';

Al.L! This determination can be made in 10 to IS-min
run time: by using column conditions to separate propane,
isobutane" n-butane, isopent~ne, n-pentane, hexanes and
heptanes,and heavier, but disregarding separation on ethane
and lighter...
A1.1.2 Use a 5-m bis-(2(2-methoxyethoxy)ethyl)ether
(BMEE) 'column at about 30C, or a suitable length of

another partition column that will separate propane through

n-pentane in about 5 min. Enter a 1 to 5-mL sample into the
column 'al1d reverse the carrier gas. flow aftern-pentane is
separated. Obtain a corresponding chromatogram on the
reference standard, whichc,an be accomplished in about 5min ru;Q. time, as there.is no need to reverse the. flow on the
reference standard. Make calculations in the same manner as
f~)J;'thecomplete analysismetho,d.
' .'
'
59

~~~ D 1945

+~

~:x:

E-i

rx:!

~
~
E-i

rx:!
~E-i

~I
:j2

rx:!
~

~:x:

~~
:X::X:

:::c:
~

:::C::::C:
0...:1
...:1:::C:

~E-i

tr.l

~E-i

t;~

OE-i/

P-<

20

rx:!

rx:!rx:!

~-~
~~

rx:!E-i

~~
~~

E-i

~I

NN

E-i

~(")
I

("))

!:l

~------

10 U

I--~!I Imin. I
FIG. A1.1

8
~!l/min.

2
1 rl /min.

0
I

Composition of Hexanes and Heavier Fraction

A 1.1.3 A determination of propane, isobutane, n-butane,

and pentanes and heavier can be made in about 5-min run
time by reversing the carrier-gas flow after n-butane. How~
ever, it is necessary to know the average molecular weight of
the pentanes and heavier components.

and the sum of the determined components.

A1.3 Special Analysis to Determine Hexanes and Heavier
Components
Al.3.1 A short partition column Can be used advantageously to separate heavy-end components and obtain a
more detailed breakdown on composition of the reverse-flow
fractions. This information provides quality data, and a basis
for calculating physical properties such as molecular -weight
on these fractions.
A1.3.2 Figure ALl is a chromatogram that shows components that are separated by a 2-m BMEE column in 20 min.
To make this determination, enter a 5-mL sample into the
short column and reverse the carrier gas after the separation
of n-heptane. Measure areas of all peaks' eluted after
n-pentane. Correct each peak area to the mol basis by
dividing each peak area by the molecular weight of the
component. A value of 120 may be used for the molecular
weight of the octanes and heavier reverse-flow peak. Calculate the mole percent of the hexanes and heavier components
by adding the corrected areas and dividing to make the total
100 %.

A1.2 Single-run Analysis for Ethane and Heavier Components

A 1.2.1 In many cases, a single partition run using a sample
size in the order of 1 to 5 mL will be adequate for determining all components except methane, which cannot be
determined accurately using this size sample with peak
height measurements, because of its high concentration.
A 1.2.2 Enter a 1 to5-mL sample into the partition column
and reverse the carrier gas flow after n-pentane is separated.
Obtain a corresponding chromatogram of the reference
standard. Measure the peak heights of ethane through
n-pentane and the areas of the pentane peaks of the standard.
Make calculations on ethane and heavier components in the
same manner as for the complete analysis method. Methane
and lighter may be expressed as the difference between 100

A2. PREPARATION OF COLUMNS AND DRIER

ahead of the sample container during sampling, or ahead of
the drying tube when entering the sample into the chromatograph. This procedure also removes carbon dioxide, and
the results obtained will be on the acid-gas free basis.
A2.3.2 Hydrogen sulfide may also be removed by connecting a tube of pumice ,that has ,been impregnated with
cupric sulfate in the line upstream of both the chromatograph and drying tube; This procedure will 'remove small
amounts of hydrogen sulfide while having but minimal effect
on the-carbon dioxide in the sample.
A2.4 Column Arrangement-For analyses in' which

A2.1 Preparation of Columns-See Practice E 260.

A2.2 Preparation of Drier-Fill a 10-mm diameter by
100-mm length glass tube with granular phosphorus pentoxide or magnesium perchlorate, observing all proper safety
precautions. Mount as required to dry the sample. Replace
the drying agent after about one half of the material -has
become spent.
A2.3 Removal of Hydrogen 'Sulfide:
A2.3.1 For samples containing more than abotrt 300 ppm
by mass hydrogen sulfide, remove the hydrogen sulfide by
connecting a tube of sodium hydrate absorbent (Ascarite)
60

~m~ D 1945

LONG PARTITION
COLUMN
SHORT PARTITION
COLUMN

(For Spplementary Use Only)

ABSORPTION COLUMN
CARRIER GAS FROM
SAMPLING VALVE TO COLUMN

CARRIER GAS
FROM COLUMN
TO DETECTOR
FIG. A2.1

Column Arrangement

column lengths, by using them either singly or in series. The

connection between VI and V2 in Fig. A2.1 should be as
short as possible (20 mm is practical) to minimize dead space
between the columns: when used in series. If al190lumns ::ire
chosen to operate at the same temperature, then stabilization
time between changing columns will be minimized.

hexanes and heavier components are to be determined, Fig.

A2.1 shows an arrangement whereby columns can be quickly
and easily changed by the turn of a selector valve. Two
columns are necessary to determine all of the components
covered in this test method. However, short and long
partition columns provide the flexibility of three partition

APPENDIXES
(Nonmandatory Information)
Xl. REFERENCE STANDARD MIXTURE
Cylinder,20-L
Pressure Cylinders, two 100-mL(A and B)
Balance, 2000-g capacity, sensitivity of 10 mg. ,
Pure Components, .methane through l'l-pentane, and carbon
dioxide. The pure components should be 99+ % Pllre.
Methane should be in a l-L cylinder at 10 MPa (lOO-atm)
pressure. Run a chromatogram of each component to check
on its given compositiori.
X1.1.2.2 Evacuate the 20-L cylinder for several hours.
Evacuate lOO-mL Cylinder A, and obtain its true weight.
Connect Cylinder A to a cylinder of pure n-pentane with a
metal connection Of calculated length to contain approximately the amount bf n-pentane to be added. Flush the
connection with the n"pentane by loosening the fittirig at the
valve on Cylinder A. Tighten the fitting. Close the n-pentane
cylinder valve and open Cylinder A valve to admit' the
n-pentane from the connection and then close the valve on
Cylinder A. Disconnect and weigh Cylinder A to obtain the
weight of n-pentane added.
X1.1.2.3 Similarly, add isopentane, n-butane, isobutane,
propane, ethane, and' carbon dioxide, in 'that order, as
desired, in the reference standard. Weigh Cylinder A after
each addition to obtain;the weight of the component added.
Connect Cylinder A. to theevacuated20-L cylinder with as

XLI Preparation
X 1.1.1 Gas mixtures of the following typical compositions
will suffice for use as reference standards for most analytical
requirements (Note X1.l):
Lean gas, mol
Comp'onent
Helium
Hydrogen
Nitrogen
Methane (maximum)
Ethane .
Carbon dioxide
Propane
Isobutane
n-Butane

neopentane
Isopentane ,
n-pentane
Hexanes +

Rich gas, mol

%'

1.0
,"3,0 .
4.0
85
6.0
, 1.0
4.0
2.0
2.0
0.5

0.5
0.5
0.5
74
10
. 1;0
7.0
3.0
3.0
1.0

0 . 5
. 0.5
0.1

'

.1.Q

1.0
0.2

NOTE Xl.f-If the mixture is stored under pressure, take care to

ensure that the partial pressure of any component does not exceed its
vapor pressure at the temperature and pressure a~ whicp the sample is
stored and used. The Leap mixture has a cricondentherm at 60F and
the Rkh mixture has a cricondentherm at 100F.

X 1.1.2 A useful method for preparation of a reference

standard by weight is as follows: 5
Xl. 1.2.1, Obtain the following equipment and material:
61

~t D 1945
I BUTANE

...5<51
9994.Ht

158911

R
E

6.11488

46693"1

314649

159383

8.158

8.458

8.388

a.688

8.158

8.988 1.888

Mole %
FIG. X1.1
TABLE X1.1

Cylinder B to. obtain the weight of the mixture that was not
transferred to the 20~L cylinder.
,
Xl.1.2.5 Weigh a l-L cylinder containing pure methane
at about 1O-MPa (lOO-atm) pressure. Transfer the methane
to the 20-L cylinder until the pressure equalizes. Weigh the
l-L cylinder to determine the weight of methane transferred.
Xl.L2.6 Thoroughly mix the contents of the 20-L cylinder by heating at the bottom by a convenient means such
as hot water or a heat lamp, and leaving the cylinder in a
vertical position for at least 6 h.
Xl.1.2.7 Use the weights and purities of all components
added to calculate the weight composition of the mixture.
Convert the weight percent to mole percent.

Least Square Calculation for Slope of iso-Butane

area

mole %

XV.

y2

1
0.9
0.75
0.6
0.45
0.3
0.15

984515
810369
569187.75
366892.8
209716.65
94394.7
23895.45

9.693e+11
8.107e+11
5.670e+11
3.73ge+11
2.172e+11
9.900e+10
2.538e+10

4.15

3058971.35

3.071452e+12

};Xy/};y2

9.9594e-07

984515
900410
758917
611488
466037
314649
159303
sum

Example of Deriving a Relative Molar Response Factor

4195319
slope

short a clean, small-diameter connector as possible. Open the

valve on the 20-L cylinder, then open the valve on Cylinder
A. This will result in the transfer of nearly all of the contents
of Cylinder A into the 20-L cyli1,lder. Close the cylinder
valves, disconnect, and weigh Cylinder A to determine the
weight of mixture that was not transferr~d to the 20-L
cylinder.
Xl.1.2.4 Evacuate and weigh 100-mL Cylinder B. Then
fill Cylinder B with 'helium and hydrogen respectively to the
pressures required to provide the desired cop-centrations of
these components in the final blend. (Helium and hydrogen
are prepared, al,ld measured separately from the other components to prevent their pressures, while in the 100-mL
cylinder, from causing condensation of the higher hydrocarbons.) Weigh .Cylinder B after eaeh addition to obtain the
weight of the component added. Connect Cylinder B to the
20-L cylinder with as short a clean, small-diameter connector
as possible.' Open;the valve on the 20-L cylinder, then open
the valve on CyliD.der B, which will result in the transfer of
nearly all of. the contents of Cylinder B into the 20-L
cylinder. Close the cylinder valves, disconnect, and weigh

Xl.2 Calibration with Pure Components

X1.2.1 Use helium carrier gas to admit a sample volume
of 0.25 to 0.5 mL into the adsorption column, providing
methane at 50 kPa (375 mm Hg) and nitrogen at 10 kPa (75
mm Hg) absolute pressure. Run a sample of the stanqard
mixture at 70 kPa (525 mm Hg) pressure, and obtain peaks
'
for methane and nitrogen.
NOTE X1.2-Each run made throughout this procedure should be
repeated to ensure that peak heights are reproducible after correction for
pressure differences to within 1 mm or 1 % of the mean value. All peaks
should be recorded at an instrument attenuation that gives the maximum measurable peak height.
'

Xl.2.2 Change the carrier gas to argon or nitrogen and,

after the, base line has stabilized, enter a sample of pure
helium at 7 kPa (50 mm Hg) absolute pressure,. recording the
peak at an attenuation that allows maximum peak height.
Run a sample of the mixture at 70 kPa (525 mm: Hg)
absolute pressure, and obtain the helium peak.
x 1.2.3 Switch to the partition column with' helium carrier
gas, and run the gas mixture at 70 kPa (525 mm Hg) absolute
62

~m~,D 1945
TABLE X1.2. Calculation of Response Factors Using Relative Molar Response Values
Compo

Nitrogen
Methane
Ethane
Propane
Carbon Dioxide
iso-Butane
n-Butane
neopentane
iso-Pentane
n-Pentane
Hexanes +

Response of

Mole % in
Reference
Standard

Response Factor
From Reference
Standard
S/B,K

5.08
82.15
8.75
4.02

2685885
36642384
6328524
3552767

1.8914E-6
2.2419E-6
1.3826E-6
1.1315E-6

Referenc~.

Standard

Relative MolarA
Response from
SlopedKJ
RMR J

Response Factor
of Referenced
Components
(RMRJ)x(KJ)

1.11607c2
0.7295803
0.6931003
0.68271 03
0.6387403
0.60041 03
0.5476203

1.5429E-6
9.9594E-7
9.1142E-7
8.9776E-7
8.3994E-7
7.8953E-7
7.2012E-7

A The Relative Molar Response is a constant that is calculated by dividing the slope of the referenced component by the component that is present in the reference
standard. For example:

RMR'c4 = (slopeic4 )/(Kca)

== 9.9594E-7

1.1315E-6 = 0.72958

pressure. Then admit samples of pure ethane and propane at

lO kPa (75 mm Hg) absolute pressure, and butanes,
pentanes, and carbon dioxide at 5 kPa (38 mm Hg) absolute
pressure.
X1.2.4 Run the gas mixture at 70 kPa, (525 mm Hg)
absolute pressure.
X1.2.5 Calculate the composition of the prepared gas
mixture as follows:
XI.2.5.l Correct peak heights of all pure components and
the respective components in the blend to the same attenuation (Note Xl.2).
X1.2.5.2 Calculate the concentration of each component
as follows:

30 %, and 15 %, of absolute pressure. For 100 kPa (760 mm

Hg) the pressures used are 90 kPa (684 mm Hg), 75 kPa (570
mm Hg), 60 kPa (456 mm Hg), 45 Kpa (342 mm Hg), 30
kPa (228 mm Hg), 15 kPa (114 mm Hg).
X1.3.4 Plot the area or height (attenuated at the same
height as the reference component) versus concentration and
calculate the slope of the line, by the least squares method.
Given the equation of the line as Y= ao + a1X yvhere Y
represents the area or height points and Xthe concentration
points. The line is assumed to intersect through the origin
and ao = O. The slope a1 can be calculated by:

where:
C
component concentration, mol%,
A = peak height of component in blend,
B = peak height of pure component,
:
Pa = pressure at which blend is run, kPa (mm Hg),
Ph = pressure at which component is run, kPa (nim Hg),
and
Vf = volume fraction of pure component.

X1.3.5 Ratio the s.lopes of the referenced components (i)

to the slopes of the reference compomints (r) present in the
daily calibration standard. This gives the Relative Molar
Response factor (RMRi) for component (i). The reference
component must be present in the same instrumentru
sequence (except Hexanes+) as the referenced components.
For instance, propane can be the reference component for
the butanes andpentanes if propane separated on the same
column in the same sequence as the butanes and pentanes.
Ethane can be the reference component for carbon dioxide if
it elutes in the same sequence as carbon dioxide. The
hexanes + peak can be referenced toptopime or calculated as
mentioned in the body of the standard.
Xl.3.6 For daily calibration a four component standard is
used containing nitrogen, methane,' ethane, and propane.
The fewer components eliminates dew point problems,
reactivity, is more accurate and can be blended at a higher
pressure. The referenced components' response factors are
calculated from the current reference factor and the Relative
Molar Response factor. Following is a description of the
basic calculations, an example of deriving a Relative Molar
Response factor (Fig; X 1.1), and a table showing how
response factors are calculated (Table X1.2).
Mole %

2;XY

(XU)

al = (2;y)2,

is

NOTE X 1.3....,.. ~= 1.000 if the calibration component' is free of

impurities.
'

X1.2.5.3 Normalize values to JOO.O %.

X1.3 Calibration using Relative Molar Response Values

X1.3.l Relative response ratios can be derived from
linearity data and used for calculating response factors. This
eliminates the need for amulti-component standard for daily
ciuibration. The test method can be used on any gas chromatograph using a thermal conductivity: or thermistor de~
tector... , .
'.
X1.3.2 Obtain a blend that brackets the expected concentration the instrument will be analyzing. The major componept (methane) is used as.the.balance gas and.may fall below
the expected concentration. This component is present in the
daily calibration .standard al)d linearity is' assured Jrom
prev~ous tests.
X1.33 Inject the sample at reduced pressures using the
apparatus in Fig. 1 Or using a mechanical gas .blender.' Obtain
repeatalJle peak areas or height at 90'%, 75 %, 60 %, 45 %,

Response Factor (R) = - - - ,

Area

.
RelatIve Molar Response (RMRJ
:
"

R iC4 = RMRic4
63

Mole %(i)/Area(i)
, %"
Mole o(r)/Area(r)
X

Rc3

(Xl.2)

(X 1.3)

(X 1.4)

~~ 01945
these operating conditions, all of the components will be
affected equally and the calculated response factors will shift
accordingly. See Table X1.1 and Figs. X1.1 and X1.2.

X1.3.7 Periodic checks of the RMR relationship is recommended. The relationship is independent of temperature,
sample size, and carrier gas flow rate. If changes occur in

X2. SAMPLE CALCULATIONS (SEE SECTION 9)

TABLE X2.1
Component
Helium
Hydrogen
Oxygen
Nitrogen
Methane
Ethane
Carbon dioxide
Propane

Isobutane
n-Butane
neopentane
Isopentane
n-Pentane
Hexanes +D

Sample Calculations

Mol % in
Reference
Standard,8

Response of Reference
Standard, B

Response
Factor, SIB

Response for Sample,A

Percent

C = (8 x A)IB

0.50
0.74
0.27
4.89
70.27
9.07
0.98
6.65
2.88
2.87
0.59
0.87
0.86

41.1
90.2
35.5
77.8
76.4
96.5
57.5
55.2
73.2
60.3
10.4
96.0
86.8

0.0122
0.0082
0.0076
0.0629
0.9198
0.0940
0.0170
0.1205
0.0393
0.0476
0.0567
0.0091
0.0099

12.6
1.5
2.1
75.6
90.4
79.0
21.2
20.6
11.0
15.0
0.1
24.0
20.5

0.154
0.012
0.Q16
4.755
83.150
7.426
0.360
2.482
0.432
0.714
0.006
0.218
0.203
0.166 0
100.094 %

72.1B

Normalized, %

0.15
0.0'1
0.02
4.75
83.07
7.42
0.36
2.48
0.43
0.71
0.Q1
0.22
0.20
0.17
100.00 %

A The response for a constituent in the sample has been corrected to the same attenuation as for that constituent in the reference standard.
B Corrected Ce resporse = (original response of 92.1) x (72/92) = 72.1.
o Mol % Ce+ = (0.2Hl + 0.203) x (72.1)/(96.0 + 86.8) = 0.166.
% iC s
% nCs
Areas iC + nCs
D Average molecular weiglJt of Ce+ = 92.

X3. PRECAUTIONS FOR AVOIDING COMMON CAUSES OF ERRORS

both, are to be taken, qse completely dry sample cylinders,
connections, and lines,' as moisture will selectively absorb
appreciable amounts of the acid gases. If hydrogen is present,
use aluminum, stainless steel, or other materials inert to
hydrogen sulfide for the cylinder, valves, lines, and connections.
.

X3.1 Hexane and Heavier Content Change

X3.1.1 The amounts of heavy-end components in natural
gas are easily changed during handling and entering of samples to give seriously erroneous low or high values. Concentration of these components has been observed to occur in a
number of cases because of collection of heavier components
in the sample loop,during purging of the system. The surface
effect of small diameter tubing acts as a separating column
and must not be used in the sampling and entering system
when components heavier than pentanes are to be determined. An accumulation of oily fllm in the sampling system
greatly aggravates this problem. Also, the richer the gas, the
worse the problem. Periodically, check C6 and heavier repeatability of the apparatus by making several check runs on the
same sampl~. It is helpful to retain a sample containing some
hexanes and h~avier for periodic checking. When enlargement.of the htfa'(Y end pe~ks is noted, thoroughly clean the
sampling valve and loop with acetone. This trouble has been
experienced with ~ome inlet systems even when clean and
with the specified sample loop size. This contamination can
be minfmized by ~uch techniques as purging with inert gas,
heating the sample loop, using a vacuum system, or other
such effective means.

X3.3 Sample Dew Point

X3.3.1 Nonrepresentative samples frequently occur because of condensation of liquid. Maintain all samples above
the hydrocarbon dew point. If cooled below this, heat lOoC
or more above the dew point for several hours before using.
If the dew point is unknown, heat above the sampling
temperature.
X3.4 Sample Inlet System
X3.4.1 Do not use rubber or plastic that may preferentially
adsorb sample components. Keep the system short and the
drier small to minimize the purging required.
X3.5 Sample Size Repeatability
X3.5.1 Varying back pressures' 0n the sample loop may
impair sample size repeatability.
X3.S.2 Make it a practice to make all reverse flow
determinations in the same carrier gas flow direction. All
single-peak determinations and corresponding reference runs
will then be made in the same carrier gas flow direction.
X3.S..3 Be sure that the inlet drier is in good condition.

X3.2 Acid Gas Content Change

X3.2.1 The carbon dioxide and hydrogen sulfide contents
of gas are easily altered during sampling and handling. If
samples containing carbon dioxide or hydrogen sulfide, or
64

~~~ D 1945
fixed zero line as the base line, but use the actual observed
base line. On high sensitivity, this base line may drift slightly
without harm and it need not frequently be moved back to
zero. A strip chart recorder with an offset zero is desirable.
The area of reverse flow peak may be measured by planimeter or geometric construction. The reverse flow area, and
the pentanes peaks used for comparison should be measured
by the same method. That is, use either geometric construction or planimeter, but do not intermix. When a planimeter
is used, carefully make several tracings and use the average.
Check this average by a secol1d group of tracings.

Moisture on the column will enlarge the reverse flow peak.

X3.S.4 Be sure the column is clean by occasionally giving
it several hours sweep of carrier gas in reverse flow direction.
A level base line should be quickly attained in either flow
direction if the column is clean.
X3.S.S When the reverse flow valve is turned there is a
reversal of pressure conditions at the column ends that
upsets the carrier gas flow. This flow should quickly return to
the same flow rate and the base line level out. If it does not,
the cause may be a leak in the carrier gas system, faulty flow
regulator, or an unbalanced conditio Il of the column or
plumbing.

X3.8 Miscellaneous
X3.8.I Moisture in the carrier gas that would cause trouble
on the reverse flow may be safeguarded againstbycinstalling
a cartridge of molecular sieves ahead of the in~trument.
Usually 1 m of 6-mm tubing packed with 30 to 60-mesh
molecular sieves is adequate, if changed with eaqh cylinder of
carrier gas.
X3.8.2 Check the carrier gas flow system periodically for
leaks with soap or leale detectqr. solution. ,
X3.8.3 Use electrical contact cleaner 011 the a,ttenuator if
noisy contacts are indicated.
'"'
X3.8.4 Peaks with, square tops with omission" of small
peaks can be caused by a sluggish recorder. If this condition
cannot be remedied by adjustment of the gain, check the
electronics in the recorder.

X3.6 ,Reference Standard

X3.6.I Maintain the reference standard at + IS C or a
temperature that is above the hydrocarbon dew point. If the
reference standard should be exposed to lower temperatures,
heat at the bottom for several hours before removing a
sample. If in doubt' about the composition, check the
n-pentane and isopentane values with pure components by
the procedure prescribed in Annex AV
X3.7 Me~surements
)(3.7.1 The base line and tops of peaks shOllld be plainly
visible for making- peak height
use a
. measurements.,
. . ' Do
. not
'-

" The American Society for Testing and Mat~ria/s takes no position respecting-the validity of ariypatent rights asserted in conne;tion
'with any item mentioned in this standard, Users of this starjdard are expressly advised that determination of the validity of any such
'
,; patent rights; and the risk of infringement of such rights, are entirely their own responsibility.
This standard is subject to revision at any time by the responsible technical committee and must be reviewed, every five years and
if not revised, either reapproved or withdrawn. Your corryme(1ts are invited either for revision of this standard or for additional standards
and should be addressed to ASTM Headquarters. Your comments will receive careful consideration at a meeting of the responsible'
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views known'to the ASTM Committee on Standards, 1~O Barr Harbor Drive, West Conshohocken, PA 1942.8.
!

",

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j'.1

65