Inside:

Basic Principles of Headspace

Analysis
Instrumentation
System Optimization
(Troubleshooting)
Headspace Applications
Recommended Headspace Analysis
Products
Technical Guide
A Technical Guide
for Static Headspace
Analysis Using GC
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Table of Contents
Introduction................................. 2
Basic Principles of Headspace
Analysis ........................................ 3
Partition Coefficient
Phase Ratio
Combining K and
Derivatization/Reaction
Headspace
Headspace Sample Size
Instrumentation .......................... 6
Gas-Tight Syringe Injection
Balanced-Pressure System
Pressure-Loop System
System Optimization
(Troubleshooting) ........................ 8
Sample Preparation
Sample Vial
Sample Vial Heater and Mixer
Sampling
Transfer Line
Injection Port Interface
Headspace Applications ........... 11
Blood Alcohol Analysis
USP <467>
European Pharmacopoeia Tests
Recommended Headspace Analysis
Products ..................................... 15
Capillary Columns
Guard Columns
Press-Tight

Connectors
Analytical Reference Materials
GC Accessories
tatic headspace gas chromatography (GC) is a technique used for the concentra-
tion and analysis of volatile organic compounds. This technique is relatively S
Time and money are two of the many reasons why an analyst
would use static headspace analysis. Other reasons may include
ease of operation and the ability to assay a variety of sample
matrices.
simple and can provide sensitivity similar to dynamic purge and trap analysis. The
popularity of this technique has grown and has gained worldwide acceptance for
analyses of alcohols in blood and residual solvents in pharmaceutical products.
Other common applications include industrial analyses of monomers in polymers
and plastic, flavor compounds in beverages and food products, and fragrances in
perfumes and cosmetics.
Sample matrices like blood, plastic, and cosmetics contain high molecular weight,
non-volatile material that can remain in the GC system and result in poor analytical
performance. Many laboratory analysts use extensive sample preparation techniques
to extract and concentrate the compounds of interest from this unwanted non-
volatile material. These extraction and concentration techniques can become time
consuming and costly. Static headspace analysis avoids this time and cost by directly
sampling the volatile headspace from the container in which the sample is placed.
Because of the diversities in the industry and related products, this guide attempts to
cover only the basic principles of static headspace and demonstrate how to apply
them to achieve optimum chromatographic results. With an understanding of these
principles, various instrumentation will then be reviewed to help build upon this
knowledge and identify the benefits and potential problems associated with each
mode of sample transfer. Information from the Basic Principles and Instrumentation
sections of this guide can then be brought together and applied to the conditions and
methodology of common analyses. Like most applications, a variety of problems
may arise in which the System Optimization section will help to identify these
problems and offer techniques to help resolve them.
3
Figure 1
Phases of the headspace vial.
Equation 1
Partition Coefficient (K) = C
s
/C
g
Equation 2
Phase Ratio () = V
g
/V
s
C
s
=concentration of analyte in sample phase
C
g
=concentration of analyte in gas phase
V
s
=volume of sample phase
V
g
=volume of gas phase
Figure 2
K and are important variables in
headspace analysis.
Solvent K Value
cyclohexane 0.077
n-hexane 0.14
tetrachloroethylene 1.48
1,1,1-trichloromethane 1.65
o-xylene 2.44
toluene 2.82
benzene 2.90
dichloromethane 5.65
n-butyl acetate 31.4
ethyl acetate 62.4
methyl ethyl ketone 139.5
n-butanol 647
isopropanol 825
ethanol 1355
dioxane 1618
Table I
K Values of Common Solvents in Air-
Water Systems at 40C
Basic Principles of Headspace Analysis
Most consumer products and biological samples are composed of a wide variety of
compounds that differ in molecular weight, polarity, and volatility. For complex
samples like these, headspace sampling is the fastest and cleanest method for
analyzing volatile organic compounds. A headspace sample is normally prepared in
a vial containing the sample, the dilution solvent, a matrix modifier, and the
headspace (see Figure 1). Volatile components from complex sample mixtures can
be extracted from non-volatile sample components and isolated in the headspace or
vapor portion of a sample vial. An aliquot of the vapor in the headspace is delivered
to a GC system for separation of all of the volatile components.
In order to achieve the best performance when using headspace/GC, careful atten-
tion should be used in sample preparation and instrument setup. Key issues to
address when setting up headspace/GC systems include minimizing system dead
volume, maintaining inert sample flow paths, and achieving efficient sample
transfer. These issues, as well as other instrument setup-related topics, are addressed
later in the System Optimization section of this guide.
Samples must be prepared to maximize the concentration of the volatile components
in the headspace, and minimize unwanted contamination from other compounds in
the sample matrix. To help determine the concentration of an analyte in the
headspace, you will need to calculate the partition coefficient (K), which is defined
as the equilibrium distribution of an analyte between the sample phase and the gas
phase (Figure 2).
Partition Coefficient
Compounds that have low K values will tend to partition more readily into the gas
phase, and have relatively high responses and low limits of detection (Figure 3). An
example of this would be hexane in water: at 40C, hexane has a K value of 0.14 in
an air-water system. Compounds that have high K values will tend to partition less
readily into the gas phase and have relatively low response and high limits of
detection. An example of this would be ethanol in water: at 40C, ethanol has a K
value of 1355 in an air-water system. Partition coefficient values for other common
compounds are shown in Table I.
volatile
analytes
sample, dilution
solvent, and matrix
modifier
}
}
G
S
G=the gas phase (headspace).
The gas phase is commonly referred to as the headspace
and lies above the condensed sample phase.
S=the sample phase.
The sample phase contains the compound(s) of interest
and is usually in the form of a liquid or solid in combina-
tion with a dilution solvent or a matrix modifier.
Once the sample phase is introduced into the vial and the
vial is sealed, volatile components diffuse into the gas
phase until the headspace has reached a state of equilib-
rium as depicted by the arrows. The sample is then taken
from the headspace.
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(Ideal)
K
C
g
(Ideal)
Figure 3
Sensitivity is increased when K
is minimized.
K and
Figure 5
Lower K and result in higher C
g
and better sensitivity.
ammonium chloride
ammonium sulfate
sodium chloride
sodium citrate
sodium sulfate
potassium carbonate
Table II
Common salts used to decrease
matrix effects.
(Ideal)

C
g
Figure 4
Sensitivity is increased when
is minimized.
C
g
K can be lowered by changing the
temperature at which the vial is equili-
brated or by changing the composition of
the sample matrix. In the case of ethanol,
K can be lowered from 1355 to 328 by
raising the temperature of the vial from
40C to 80C. It can be lowered even
further by introducing inorganic salt into
the aqueous sample matrix. High salt
concentrations in aqueous samples
decrease the solubility of polar organic
volatiles in the sample matrix and promote their transfer into the headspace,
resulting in lower K values. However, the magnitude of the salting-out effect on K is
not the same for all compounds. Compounds with K values that are already rela-
tively low will experience very little change in partition coefficient after adding a
salt to an aqueous sample matrix. Generally, volatile polar compounds in polar
matrices (aqueous samples) will experience the largest shifts in K and have higher
responses after the addition of salt to the sample matrix. Table II lists most of the
common salts used for salting-out procedures.
Phase Ratio
The phase ratio () is defined as the relative volume of the headspace compared to
volume of the sample in the sample vial (Figure 2). Lower values for (i.e., larger
sample size) will yield higher responses for volatile compounds (Figure 4). How-
ever, decreasing the value will not always yield the increase in response needed to
improve sensitivity. When is decreased by increasing the sample size, compounds
with high K values partition less into the headspace compared to compounds with
low K values, and yield correspondingly smaller changes in C
g
. Samples that contain
compounds with high K values need to be optimized to provide the lowest K value
before changes are made in the phase ratio.
Combining K and
Partition coefficients and phase ratios
work together to determine the final
concentration of volatile compounds in
the headspace of sample vials. The
concentration of volatile compounds in
the gas phase can be expressed as
C
g
=C
o
/(K+) (where C
g
is the concen-
tration of volatile analytes in the gas
phase and C
o
is the original concentra-
tion of volatile analytes in the sample).
Striving for the lowest values for both
K and will result in higher concentra-
tions of volatile analytes in the gas
phase and, therefore, better sensitivity
(Figure 5).
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Compound of Interest Derivatizing Reagent Resulting Derivative
fatty acids
methanol
esterification
with boron trifluoride
glycerol
acetic anhydride
acetylation
with sodium carbonate
For more information on derivatization, please refer to the Handbook of Analytical
Derivatization Reactions by Daniel R. Knapp or to the text at right.
Table III
Common reagents used to derivatize compounds of interest.
Common derivatization techniques used in reaction headspace/GC are esterification,
acetylation, silylation, and alkylation. Any of these derivatization techniques can be
performed using the sample vial as the reaction vessel (see Table III for a list of
commonly used reagents). Although derivatization may improve chromatographic
performance and volatility for some compounds, derivatization reactions may
introduce other problems into the analytical scheme. Derivatization reagents as well
as the by-products from derivatization reaction may be volatile and can partition into
the headspace along with derivatized compounds. These extra volatile compounds
may pose problems by eluting with similar retention times as the compounds of
interest, causing either partial or complete coelutions.
Derivatization reactions also are typically run at elevated temperatures. Pressures
inside the sample vial may exceed the pressure handling capabilities of the vial or
the septa. Specially designed septa are available that allow excess pressure to be
vented during derivatization reactions.
Headspace Sample Size
In addition to working with K, , and derivatization reactions, sensitivity also can be
improved by simply increasing the size of the headspace sample that is withdrawn
from the sample vial and transferred to the GC. Increasing the sample size also
means that the amount of time it takes to transfer the sample to the column will
increase in proportion to the column volumetric flow rate. Sample size can be
increased only to the point that increases in peak width, as a result of longer sample
transfer times, will not affect chromatographic separations. Larger sample sizes and
longer transfer times can be offset by using cryogenic cooling and sample refocus-
ing at the head of the column.
Derivatization/Reaction Headspace
Derivatization is another technique that can be used to increase sensitivity and
chromatographic performance for specific compounds. Compounds such as acids,
alcohols, and amines are difficult to analyze because of the presence of reactive
hydrogens. When attempting to analyze these types of compounds, they can react
with the surface of the injection port or the analytical column and result in tailing
peaks and low response. In addition, they may be highly soluble in the sample
phase, causing very poor partitioning into the headspace and low response.
Derivatization can improve their volatility, as well as reduce the potential for surface
adsorption once they enter the GC system.
For more information on headspace
anaysis, check out the textbook,
Static Headspace-Gas
Chromatography, Theory and Practice
by Bruno Kolb and Leslie S. Ettre.
Instrumentation
Gas-Tight Syringe Injection
Use of a gas-tight syringe autosampling system is one of three common techniques
(gas-tight syringe, balanced pressure, and pressure loop) used to transfer a
headspace sample. Most of the autosampling units can retrofit to a standard GC with
a split/splitless injection port, making them relatively simple to use and understand.
These systems do not require the use of special configurations or special instrumen-
tation other than the autosampler itself. The gas-tight syringe autosampler is
beneficial for use with diverse samples because of the variety of sampler configura-
tions and method options available.
The gas-tight syringe technique operates by initially thermostatting the sample in an
incubation oven at a given temperature and for a given time until it has reached a
state of equilibrium (Figure 6, Step 1). Once the sample has reached an equilibrium,
an aliquot is taken from the headspace using the gas-tight syringe (Figure 6, Step
2), and the aliquot is injected into the GC as if it were a liquid sample injection
(Figure 6, Step 3).
Several concerns exist regarding this technique. Because the sample is being trans-
ferred from a heated oven, the syringe also must be heated to ensure that the sample will
not recondense in the syringe. Many manufacturers have taken this into consideration
and their samplers now come with a heated syringe assembly. There also are reproduc-
ibility issues because of possible sample loss. As the sample is transferred from the vial
to the injection port, some of it may be lost because of the pressure differences between
the vial and atmospheric conditions. Beyond these concerns, the gas-tight syringe
technique is simple to use, can retrofit into a variety of GC systems, and is best suited
for diverse samples. Examples of manufacturers and models of the gas-tight syringe
units are: the ThermoQuest TRACE

HS2000 and HS850 (Figure 7) Headspace

Autosamplers and the Leap Technologies CTC COMBI PAL Sampler.
Balanced-Pressure System
Figure 7
Gas-tight syringe autosampler
TRACE HS850
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Figure 6: Gas syringe system
Step 1
Sample reaches
equilibrium
Step 3
Sample is injected
Step 2
Sample is extracted from
headspace
Another common technique is the balanced-pressure system, which is capable of
generating results with a high degree of repeatability. It uses a seamless injection
directly from the vial into the carrier gas stream without additional moving parts other
than a valve and a needle. The balanced-pressure system, like other techniques, uses
an incubation oven to thermostat the vial so the sample reaches equilibrium (Figure 8,
Step 1). During these initial steps, a needle is inserted into the vial and then is
pressurized with a carrier gas (Figure 8, Step 2). After the vial is pressurized and
equilibrium has been reached, the valve is switched for a specific amount of time to
redirect the sample into the transfer line and onto the column (Figure 8, Step 3).
Figure 8: Balanced-pressure system
Because this technique uses a theoretical amount of time to inject the sample, the
absolute volume of the sample is unknown. However, this technique is highly repro-
ducible because the number of moving parts are minimized, which decreases the
chance for compound adsorption and loss via leaks. An example of a balanced-
pressure system is the HS 40XL manufactured by Perkin-Elmer (Figure 9).
Pressure-Loop System
The last common injection technique discussed in this guide is the pressure-loop
system. Unlike balanced-pressure, the pressure-loop system uses a known amount of
sample. This technique typically uses a six-port valve, and initially thermostats and
pressurizes the vial as in the previously described techniques (Figure 10,
Step 1). After pressurization, the valve is turned and the loop is filled with the
sample (Figure 10, Step 2). After the loop has been filled, the valve is turned again to
redirect the gas flow and flush the sample into the transfer line leading to the analyti-
cal column (Figure 10, Step 3).
Figure 9
Balanced-pressure autosampler
Perkin-Elmer HS 40XL
The pressure-loop system has several advantages and disadvantages. One of the
advantages of this system is that the loop can be thermostatted to high temperatures,
which helps to lessen adsorption of higher molecular weight and sensitive com-
pounds. The fixed volume of the sample loop also helps to improve run-to-run
reproducibility. A disadvantage of a pressure-loop system is that it may cause ghost
peaks because of sample carryover from a previous analysis.
1
Several makes and
models of pressure-loop systems include the OI Model 4632 (Figure 11), Varian
Genesis, Tekmar 7000HT, and the HP 7694E.
Step 1
Sample reaches
equilibrium
Step 3
Sample is extracted and
injected
Step 2
Pressurization of injection
Figure 10: Pressure-loop system
Step 1
Sample reaches
equilibrium/pressurization
Step 3
Sample is injected
Step 2
Sample is extracted from
headspace
7
Figure 11
Pressure-loop system
OI Model 4632
outlet
inlet/outlet
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Always use pre-cleaned vials for
sample preparation and storage.
Sample Vial
Sample vials should be selected to match the type and size of the sample being
analyzed. Always use pre-cleaned vials for sample preparation and storage. Vials
that are not properly cleaned prior to packaging or that absorb contaminants during
shipping can produce unknown chromatographic peaks, or ghost peaks. Ghost
peaks that are the result of vial contamination can be identified by running method
blanks and zero standards during the system calibration sequence.
The septa used to seal the headspace vials also can be a source for contaminants,
which can bleed into the headspace of the vial during equilibration. These contami-
nants can appear as single peaks or multiple peak patterns. Some septa are available
with a PTFE face to eliminate bleed from the rubber portion of the septa. These
septa should not be re-used. Once the PTFE face has been punctured by a syringe,
contaminants from the rubber portion of the septa can migrate into the headspace
and show up as unidentified peaks. Again, the use of method blanks can help to
determine the source of contaminants.
System Optimization (Troubleshooting)
Chromatographic performance in Headspace/GC is greatly influenced by how the
sample is introduced into the analytical column. Variables that affect sample
preparation and transfer of the sample from the headspace unit to the analytical
column must be optimized to obtain reproducible and efficient separations. Key
issues to address when setting up headspace/GC systems include minimizing system
dead volume, maintaining inert sample flow paths, and achieving efficient sample
transfer. This section will explain how to optimize areas that are critical in address-
ing these issues and providing good chromatographic performance.
Sample Preparation
Samples for headspace/GC must be prepared in such a manner as to maximize the
concentration of the volatile sample components in the headspace while minimizing
unwanted contamination from other compounds in the sample matrix. Sample
matrices such as biological samples, plastics, and cosmetics can contain high
molecular weight, volatile material that can be transferred to the GC system. Water
from the sample matrix also can cause problems by recondensing in the transfer line.
Incomplete or inefficient transfer of high molecular weight compounds or water
vapor from sample matrices can produce adsorptive areas in the transfer line or
injection port that can lead to split peaks, tailing peaks, or irreproducible responses
or retention times. To minimize matrix problems and prevent water condensation
from aqueous samples, use a higher transfer line temperature (~125C150C).
High-concentration samples need to be prepared appropriately to obtain optimal
chromatography. High-concentration samples can produce ghost peaks in subse-
quent analyses due to carryover of sample from previous injections. Sample
carryover can be minimized by using higher transfer line and injection port tempera-
tures, but some samples may need to be diluted and re-analyzed to obtain reliable
results. Additionally, we recommend injecting standards and samples in order from
low to high concentrations to help minimize carryover. When sample carryover or
ghost peaks are evident, you may need to bake-out the column at its maximum
operating temperature and elevate the transfer line temperature in order to remove
all of the residual sample. If high-concentration samples are anticipated in a
sequence of samples, running a blank after the suspected samples will reduce
carryover contamination of following ones. It is good lab practice to handle stan-
dards and method blanks the same way samples are handled to make any vial or
sample preparation problems easier to identify.
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Sample Vial Heater and Mixer
Once the sample is placed inside a clean, non-contaminating vial and the vial is
sealed, volatile compounds from the sample will partition into the headspace until a
state of equilibrium is reached. The rate at which volatile compounds partition out of
the sample matrix and into the headspace, as well as the equilibrium concentration
of volatile compounds in the headspace depends on several parameters (see also
Introduction of this guide).
Temperature, time, and mixing can be
used to improve the transfer of volatile
analytes from the sample into the
headspace of the vial. Adjusting the
temperature of the sample will change
the solubility of the analyte in the
sample matrix and can be used to drive
the equilibrium in favor of the gas
phase. Sufficient time must be built into
the sample cycle in order to achieve a
constant state of equilibrium. Some sample matrices require longer equilibration
times due to physical characteristics like high viscosity. Shaking or vibrating the vial
during heating can assist in achieving equilibrium more quickly by exposing more
sample surface area for the transfer of volatile analytes to the headspace.
Sampling
There are several techniques used to transfer samples from the vial to the
GC. When using a gas-tight syringe for sampling, heat the syringe to a
temperature comparable to the sample vial temperature. This minimizes
pressure differences and condensation problems. To prevent carryover from
inside the syringe, flush the syringe after each injection. Because gas-tight
syringe samplers inject through the GC injection port septum, ensure the
septum is well maintained to decrease the possibility of a leak.
For balanced-pressure sampling instruments, analysts should consider the
inertness and efficiency of the components that make up the sample pathway
inside the autosampler. If sensitive compounds are being analyzed, an inert
pathway should be used to decrease possible adsorption. Materials such as
stainless steel, nickel, Silcosteel

and PTFE coatings, or KEL-F

parts can
be used to minimize sample adsorption and peak tailing. Transfer line internal
diameter should be as narrow as possible to help maintain narrow sample band
widths and symmetrical peak shapes (see the following optimization of transfer lines
for more information). Analysts also should ensure that balanced-pressure instru-
ments are leak-free and operate with the least amount of dead volume in the sample
flow path. This will help obtain optimal peak shape and sensitivity.
When using pressure-loop sampling instruments, the same concerns apply as with
gas-tight syringe and balanced-pressure systems. Inert sample pathways and low
dead volume systems will yield the best chromatographic performance. In pressure-
loop systems, a gas sampling valve with a sample loop is used to transfer the sample
from the headspace unit to the GC. Adequate purging of the sample valve and loop
will guard against sample carryover. If low response or broad peaks are observed, it
may be necessary to increase the sample vial pressure to ensure that the sample loop
is being completely filled with headspace sample. If there are extraneous peaks
present due to carryover of matrix contaminants, increase the sample valve tempera-
ture to prevent sample carryover, condensation, and contamination.
Shaking or vibrating the
vial during heating can
assist in achieving
equilibrium.
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Transfer Line
After the headspace sample is withdrawn from the vial, it ready to be transferred to
the GC. In balanced-pressure and pressure-loop systems a short piece of tubing
called a transfer line is used to transfer the sample from the autosampler to the GC.
Transfer line material must be chosen that suits the sample analytes. Many different
materials can be used as transfer line tubing, including stainless steel, nickel, fused
silica, and Silcosteel

- or Siltek

-coated tubing. Stainless steel provides a strong,

flexible tubing material, but can be adsorptive towards more active analytes such as
alcohols, diols, and amines. Nickel and Silcosteel

tubing are highly inert towards

active compounds and provide ruggedness similar to stainless steel. Fused silica and
Siltek

tubing are extremely inert

towards active compounds, however
they are not as rugged as nickel or
Silcosteel

tubing.
The internal diameter of the
transfer line should be chosen
depending on the internal
diameter of the analytical
column, the column flow rate,
and the flow rate delivered
from the autosampler. To elimi-
nate tubing dead volume, use the smallest diameter tubing possible. For
example, compound residence time in a 1.0mm ID transfer line is 3.6 times greater
than in the same length of 0.53mm ID tubing. Reducing the residence time of the
headspace sample in the transfer line helps to minimize band broadening. Therefore,
the flow rate should be set as high as possible to quickly move the sample cloud
through the tubing and minimize any dead volume effects.
Transfer line temperature should be set depending on the analytes of interest and the
sample matrix. Typical transfer line temperatures range from 80C to 125

C. To
minimize matrix problems and prevent water condensation from aqueous samples,
use a higher transfer line temperature (~125C to 150

C).
Injection Port Interface
The quality of the connection of the transfer line to the analytical column greatly
affects sample bandwidth. In most cases, the transfer line has a smaller internal
diameter than the injection port liner, and the vaporized headspace sample carrying
the compounds of interest will be diluted into a larger volume of carrier gas when
the sample elutes from the transfer line into the inlet liner. This can lead to broader
peaks, tailing peaks, lower sensitivity, and loss of resolution. Because headspace
samples are already in a gaseous state (vapor cloud) when they enter the injection
port, there is no need to use a large buffer volume in the liner to allow for sample
expansion as when analyzing liquid samples. Using injection port liners that have
smaller internal diameters and lower buffer volumes will help maintain a narrow
bandwidth as samples move from the end of the transfer line to the head of the
analytical column. 1.0mm ID deactivated injection port liners are recommended for
most headspace applications to achieve the lowest injection port dead volume.
If band-broadening due to excess dead volume in the system is still a problem, peak
shape may be improved by refocusing sample analytes at the analytical column head.
Highly volatile compounds can be trapped at the column head and refocused into a
narrow bandwidth by reducing the initial oven temperature below the boiling point of
compounds of interest. After the sample is completely transferred to the column, the
oven temperature can be increased to move the compounds through the column.
Use an inert transfer
line when optimizing
pressure-loop systems.
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Rtx

-BAC1: 30m, 0.32mm ID, 1.8m (cat.# 18003) Rtx

-BAC2: 30m, 0.32mm ID, 1.2m (cat.# 18002)

Dual-column analysis using a two-hole ferrule. 1.0mL headspace sample of a blood alcohol mix.
Oven temp.: 40C isothermal; Inj. temp.: 200C; Carrier gas: He; Sample equilibration temp.: 70C; Sample equilibration time: 15 min.;
Vial pressure: 30psi; Vial pressurization time: 0.15 min.; Vial sampling time: 0.01 min.; Transfer line: 0.32mm ID FS Hydroguard

tubing;
Transfer line temp.: 200C; Injection port sleeve: 2mm ID; Split flow: 20mL/min.
Conc.
w/v
1. methanol 0.1%
2. acetaldehyde 0.2%
3. ethanol 0.2%
4. isopropanol 0.1%
5. acetone 0.01%
6. n-propanol 0.1%
Quantitation Technique for Blood
Alcohol Analysis (Internal Standard)
The internal standard technique uses one or
more designated compounds at known
concentrations spiked into the sample. The
response of the compounds of interest are
then compared to the results of the internal
standard. There are several advantages to
this technique. Multiple injections of the
standard are not necessary for concentra-
tion calculations; small changes in injection
volumes or detector response over time can
be determined.
Headspace Applications
Figure 12
Achieve baseline resolution of all blood alcohol components in less than 3 minutes using the
Rtx

-BAC1 and Rtx

-BAC2 columns and a Perkin-Elmer HS 40 headspace autosampler.

6
5
4
3
2
1
min. 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4 2.6 2.8 3.0 min. 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4 2.6 2.8 3.0
6
5
4
3
2
1
A balanced pressure sampling unit was used to transport the sample to the GC. This
type of sampling works better with columns that require higher head pressure
(smaller ID) to improve flow efficiencies. 0.32mm ID analytical columns were
chosen for this application because of their higher operating pressure. Optimal
column performance during headspace analysis depends on GC/headspace system
set up. Band broadening can occur if there is excess dead volume in the sample flow
path between the sample valve and the head of the column. Low volume inlet liners
or interfaces in the injection port should be used to reduce the amount of excess
volume at the exit end of the transfer line. A 2mm ID liner was used in this analysis
to reduce dead volume and maintain narrow peak widths. High carrier gas flow rates
through the transfer line also can be used to maintain narrow sample bandwidths and
speed up sample transfer to the column head. A flow of 40mL-per-minute was used
to optimize the analysis on the Perkin-Elmer HS 40 system.
Simulated blood alcohol samples were prepared and analyzed using a modification
of a procedure published by Christmore et al.
2
n-Propanol was used as the internal
standard and was prepared at a concentration of 0.03g/dL in 1.0M ammonium
sulfate as a diluent. Five milliliters of diluent were added to 1mL of sample in a
20mL headspace vial (Figure 12).
Blood Alcohol Analysis
Analysis time and resolution are two critical factors when developing a GC assay for
ethanol. Analysis time for each sample should be as short as possible while still
maintaining baseline resolution for all analytes. Isothermal analysis is the method of
choice because it eliminates the cool-down period between temperature-programmed
runs. Overall analysis time can be reduced in isothermal analysis by raising the oven
temperature or by increasing carrier gas flow rate. However, in attempting to shorten
the analysis time, either by increasing the flow rate or raising the temperature, many
traditional capillary column stationary phases fail to provide adequate resolution of
all the components commonly tested during blood alcohol analysis. Current advances
have aided in the design of two novel capillary column stationary phases to meet all of
these requirementsthe Rtx

-BAC1 and the Rtx

-BAC2 columns.
12
N
e
w
Quantitation Technique for USP <467>
(External Standard)
This technique uses a separate sample
(standard) that has the compounds of interest
at known concentrations in the same matrix.
This technique is advantageous if various
samples are being analyzed, and all
compounds of interest can be assayed using
a single set external standards.
These conditions (PE Auto SYS GC and HS 40 headspace autosampler), combined
with unique columns (Rtx

-BAC1 and Rtx

-BAC2), provided excellent accuracy

and precision in the analysis of blood alcohol with complete resolution in less than 3
minutes. Calibration curves were constructed using concentrations ranging from
0.01% to 0.5% ethanol. Correlation coefficients above 0.999 were easily obtained
for all compounds. Response factor repeatability was less than +1% standard
deviation while analyzing six samples at a concentration of 0.2% ethanol. Based on
our experimentation, a system detection limit of 0.001% ethanol should be achiev-
able while maintaining a minimum signal-to-noise ratio of 10. For more informa-
tion on this analysis request, request cat.# 59548.
USP <467>
A new test for the gas chromatographic (GC) analysis of Organic Volatile Impurities
(OVI) in pharmaceutical products was published in the Third Supplement to the US
Pharmacopoeia (USP) XXII-NF XVII, which became effective November 15, 1990.
Since its original appearance in the USP, this
testing protocol has undergone many revisions
and additions.
1-6
The most recent of which was
published as USP 24, effective January 1, 2000.
7
The biggest change was to the limit test concen-
trations, which now match the European Pharma-
copoeia (EP) concentrations and the ICH
guidelines for the five USP <467>-regulated
solvents.
8, 9
USP issued an in-process revision
announcing that the limit test for
benzene is not required unless a specific
limit for benzene is included in the
individual drug monograph.
10
The
revision was needed because Methods I
and V were unable to detect benzene at
2ppm. Currently, Method IV is the only
method that detects benzene at 2ppm. It
is anticipated that USP will make more
revisions to benzene detection limits
during 2000.
USP also has clarified that a 5m phenyl-
methyl guard column is not needed for
the Method IV, headspace analysis.
10
Figure 13 shows an analysis using
Method IV at the revised concentrations, the method-specified sample preparation
procedure, a G43 analytical column, and no guard column.
USP made changes in 1997 to overcome the difficulties resulting from unregulated
solvents coeluting with regulated solvents, and thereby causing over-representation
of their concentrations using GC/flame ionization detection (FID) methods.
11
GC/
mass spectrometry (MS) or a second, validated column having a different stationary
phase may be used to confirm the presence of the coeluting unregulated solvent and
report the correct concentration of regulated solvent. For more information on this
analysis request, request cat.# 59577A.
benzene 2ppm
chloroform 60ppm
1,4-dioxane 380ppm
methylene chloride 600ppm
trichloroethene 80ppm
Limit Test Concentrations
for USP <467>
Method IV - Static Headspace
6% cyanopropylphenyl/94%
dimethylpolysiloxane (G43)
30m, 0.53mm ID, 3.0m
(Rtx

-G43 column, cat.# 16085-126)

Method for Coated Tablets -
Static Headspace
0.2% polyethylene glycol, MW 1500 (G39)
on graphitized carbon (S7)
(0.2% Carbowax

1500 on 80/100
CarboBlack

C packed column, cat. # 80122)

Table IV
Organic Volatile Impurities (OVI)
methods and corresponding
chromatographic systems.
13
www.restek.com
1. methylene chloride 600ppm
2. chloroform 60ppm
3. benzene 2ppm
4. trichloroethylene 80ppm
5. 1,4-dioxane 380ppm
Sample Preparation: 100L of cat.# 36007 in 5mL distilled water, 1 gram
sodium sulfate in a 20mL headspace vial.
30m, 0.53mm ID, 3.0m Rtx

-G43 (cat.# 16085)

Oven temp.: 40C (hold 20 min.) to 240C @ 35C/min. (hold 20 min.);
Inj. temp: 140C, 1mm split sleeve (cat.# 20916);
Det. temp.: 260C;
FID sensitivity: 1.25 x 10
-11
AFS;
Carrier gas: helium, 3.5psi constant pressure, 35cm/sec. set @ 40C; Split
ratio: 2:1; ThermoQuest HS 2000 Headspace Autosampler Vial 80C, 60
min. shaker on.
Figure 13
The Rtx

-G43 column provides the resolution and detection limits needed for USP 24
th
edition <467> revised limit
test concentrations in USP Method IV.
4
1
2
3 5
2 3 4 5 6 7 8
min.
Stock Solvent Methylene Chloride Chloroform Benzene 1,1,1-Trichlorethylene 1,4-Dioxane
1 6 . 8 1 5 7 . 6 1 2 5 . 4 1 4 6 . 0 1 9 1 . 0 1 r e t a W
Water w/ Sample 8.29 9.25 11.3 13.38 15.26
3 4 . 4 1 1 0 . 8 8 1 . 8 9 5 . 8 7 3 . 7 O S M D
DMSO w/ Sample 7.25 7.54 8.8 8.67 7.37
Table V
Percent RSD for stock solutions in water vs. DMSO
Comments in the September/October 1992 Pharmacopoeial Forum
3
propose the use
of dimethyl sulfoxide as the solvent for stock standard, but this has not been
approved as of the date of this publication.
In regards to this proposal, an investigation was conducted to determine if there
were significant changes in results if dimethyl sulfoxide was used as the diluent for
stock standard. Similar RSDs can be obtained when stock solutions are diluted in
dimethyl sulfoxide as opposed to solutions made with water (Table V).
14
www.restek.com
European Pharmacopoeia Tests
The International Conference on Harmonization (ICH) has proposed a set of guide-
lines for residue solvent testing in pharmaceutical formulation and the European
Pharmacopoeia (EP) was the first to revise their regulations.
7,8
However, these
guidelines are challenging, containing over 60 compounds of regulatory interest to
manufacturers of active substances, excipients, and medicinal products. The EP
methods also allow testing limits based on either a concentration limit in a product,
or calculated from the maximum daily dosage of the product and the permissible
daily exposure limit of the solvent. These technical challenges affect the sampling
method and capillary column needed to ensure precise and accurate results.
The recommended primary capillary column for EP residual solvent testing is the
Rtx

-1301. The Rtx

-1301 column shows excellent resolution of most EP Class 1 and

Class 2 compounds at the regulation limit concentration (Figure 14). Restek also
offers Stabilwax

columns, the recommended confirmational column for European

Pharmacopoeia residual solvent testing. For more information on this analysis
request, request cat.# 59107.
min. 2 4 6 8 10 12 14 16 18 20 22 24 26 28 30 32 34
1
2
3
4
5
6
7
8
9,10
11
12
13,14
15
16
17
18
19
20
21
22,23
24,25
26
27
28
30m x .53mm ID x 3.0mm Rtx

-1301 w/5m phenyl methyl Integra-Guard

guard column
(cat.# 16085-126). Oven temp.: 40C (hold 20 min.) to 240C @ 10C/min. (hold 20 min.);
Inj./det. temp.: 200C/250C; FID sensitivity: 1.1 x 10
-11
AFS;
Carrier gas: H
2
@ 35cm/sec.; Split ratio: 2:1.
Figure 14
The Rtx

-1301 column shows

excellent resolution of most
European Pharmacopoeia Class 1
and 2 compounds at the regulation
limit concentration.
Quantitation Techniques for European
Pharmacopoeia
(External Standard)
This technique uses a separate sample
(standard) that has the compounds of
interest at known concentrations in the
same matrix. This technique is advanta-
geous if various samples are being
analyzed, and all compounds of interest
can be assayed using a single set
external standards.
(Standard Addition)
The standard addition technique uses
known amounts of the compounds of
interest and adds it to the existing sample.
The original concentration of the
compounds of interest are then calculated
using linear regression.
1. methanol
2. 1,1-dichloroethene
3. acetonitrile
4. methylene chloride (dichloromethane)
5. hexane (C6)
6. cis-1,2-dichloroethene
7. nitromethane
8. chloroform
9. cyclohexane
10. 1,1,1-trichloroethane
11. carbon tetrachloride
12. benzene
13. 1,2-dimethoxyethane
14. 1,2-dichloroethane
15. trichloroethylene (1,1,2-trichlorethene)
16. methylcyclohexane
17. 1,4-dioxane
18. pyridine
19. toluene
20. 2-hexanone
21. chlorobenzene
22. DMF
23. ethylbenzene
24. m-xylene
25. p-xylene
26. o-xylene
27. N,N-dimethylacetamide
28. 1,2,3,4-tetrahydronaphthalene
Headspace injection of 28 Class 1
and Class 2 residual solvents for
pharmaceutical processing. Prepared at
the regulatory limit concentration.
Samples shaken and heated at 80C
for 15 minutes, 1mL headspace injection.
Peak List for Figure 15
Guide References
These references are not available from Restek.
1. M.S. Bergren and D.W. Foust, Comments on USP
General Chapter, Organic Volatile Impurities <467>, and
Associated Monograph Proposals, Pharmacopoeial
Forum, May/June 1991, Vol. 17, No. 3, pp. 1963-1968.
2. J.A. Krasowski, H. Dinh, T.J. OHanlon, R.F. Lindauer,
Comments on Organic Volatile Impurities, Method I,
<467>, Pharmacopoeial Forum, May/June 1991, Vol. 17,
No. 3, pp. 1969-1972.
3. Pharmacopoeial Forum, March/April 1991, Vol. 17, No. 2,
p. 1653.
4. Fifth Supplement, USP-NF, Organic Volatile Impurities
<467>, Nov. 15, 1991, pp. 2706-2708.
5. Organic Volatile Impurities <467>, Pharmacopoeial
Forum, May-June 1993, Vol. 19, No. 3, pp. 5335-5337.
6. Pharmacopoeial Forum, September/October 1992, Vol. 18,
No. 5, p. 4028.
7. USP 24/NF 19, <467> Organic Volatile Impurities, (1877-
1878).
8. ICH Harmonized Tripartite Guideline, Impurities: Guideline
for Residual Solvents, The Fourth International Conference
on Harmonization, July 17, 1997.
9. European Pharmacopoeia, Supplement 1999, pp. 14-15, 208.
10. Pharmacopoeial Forum, November - December 1999, Vol. 25,
Number 6, (9223 - 9224).
11. Sixth Supplement, USP-NF, Organic Volatile Impurities
<467>, May 15, 1997, pp. 3766-3768.
15
www.restek.com
Rtx

-BAC1 Capillary Columns Rtx

-BAC2 Capillary Columns

Rtx

-G27 Integra-Guard

Column Rtx

-G43 Integra-Guard

Column
Stabilwax

Capillary Columns
Rtx

-1301 Capillary Columns

ID (mm) df (m) 30-Meter
0.32 1.80 18003
0.53 3.00 18001
ID (mm) df (m) 30-Meter
0.32 1.20 18002
0.53 2.00 18000
Rtx

-5 Capillary Columns
ID (mm) df (m) 30-Meter
0.53 5.00 10279-126
ID (mm) df (m) 30-Meter
0.53 3.00 16085-126
ID (mm) df (m) 30-Meter
0.32 3.00 10284
0.53 5.00 10279
ID (mm) df (m) 30-Meter
0.32 1.50 16069
0.53 3.00 16085
ID (mm) df (m) 30-Meter
0.32 0.25 10624
0.53 0.50 10640
0.53 1.00 10655
s n m u l o C d r a u G s n m u l o C y r a l l i p a C
Fused Silica Guard Columns
ID (mm) OD (mm) 5-Meter
0.32 0.45
+
0.04 10044
0.53 0.69
+
0.05 10045
Integra-Guard

Guard Columns
ID (mm) OD (mm) Length Suffix
0.32 0.45
+
0.04 5m -125
0.32 0.45
+
0.04 10m -128
0.53 0.69
+
0.05 5m -126
0.53 0.69
+
0.05 10m -129
Universal Angled Press-Tight

Connectors
Ideal for connecting guard columns to
analytical columns.
Designed at an angle approximating the
radius of a capillary column.
Reduces strain on column-end
connections.
5-pk. 25-pk. 100-pk.
20446 20447 20448
Universal Y Press-Tight

Connectors
Split sample flow onto two columns.
Split a single column flow into two
different detectors.
Perform confirmational analysis with a
single injection.
each 3-pk.
20405 20406
Universal Press-Tight

Connectors
Ideal for connecting guard columns to
analytical columns.
Repair broken columns.
Connect column outlets to transfer lines.
5-pk. 25-pk. 100-pk.
20400 20401 20402
Universal Angled Y
Press-Tight

Connectors
Alleviates column-end connection strain.
Inlet and outlet ends conform to the
column radius.
Perform confirmational analysis with a
single injection.
each 3-pk.
20403 20404
Universal Angled Siltek

-Deactivated
Press-Tight

Connectors
Siltek

deactivation for inert pathways

to maintain sample integrity.
Ideal for connecting guard columns to
analytical columns.
Designed at an angle approximating the
radius of a capillary column.
5-pk. 25-pk. 100-pk.
20482 20483 20484
Recommended Static Headspace Analysis Products:
Press-Tight

Connectors
16
www.restek.com
European Pharmacopoeia/ICH Reference Material Mixes
Analytical Reference Materials
USP <467> Calibration Mix #2
L m / g 0 0 1 e n e z n e b
0 5 m r o f o r o l h c
1,4-dioxane 100
methylene chloride 500
trichloroethene 100
Prepared in methanol, 1mL/ampul
Ea.: cat.# 36002 10-pk.: cat.# 36102
USP <467> Calibration Mix #3
L m / g 0 0 1 e n e z n e b
0 5 m r o f o r o l h c
1,4-dioxane 100
methylene chloride 500
trichloroethene 100
Prepared in DMSO, 1mL/ampul
Ea.: cat.# 36004 10-pk.: cat.# 36104
USP <467> Calibration Mix #4
L m / g 2 e n e z n e b
0 6 m r o f o r o l h c
1,4-dioxane 380
methylene chloride 600
trichloroethene 80
Prepared in methanol, 1mL/ampul
Ea.: cat.# 36006 10-pk.: cat.# 36106
USP <467> Calibration Mix #5
L m / g 2 e n e z n e b
0 6 m r o f o r o l h c
1,4-dioxane 380
methylene chloride 600
trichloroethene 80
Prepared in DMSO, 1mL/ampul
Ea.: cat.# 36007 10-pk.: cat.# 36107
Class 1 Mix
L m / g 2 e n e z n e b
carbon tetrachloride 4
1,2-dichloroethane 5
1,1-dichloroethene 8
1,1,1-trichloroethane 1500
Prepared in water:dimethylsulfoxide 90:10, 1mL/
ampul
Each 5-pk. 10-pk.
36228 36228-510 36328
Class 2 Mix A
chlorobenzene 360g/mL
cyclohexane 3880
cis-1,2-dichloroethene 1870
dichloromethane 600
ethylbenzene 369
0 9 2 e n a x e h
methylcyclohexane 1180
N,N-dimethylformamide 880
0 9 8 e n e u l o t
1,1,2-trichloroethene 80
m 2 0 3 1 e n e l y x -
o 5 9 1 e n e l y x -
p 4 0 3 e n e l y x -
Prepared in water:dimethylsulfoxide 90:10, 1mL/
ampul
Each 5-pk. 10-pk.
36229 36229-510 36329
Class 2 Mix B
L m / g 0 1 4 e l i r t i n o t e c a
0 6 m r o f o r o l h c
1,2-dimethyoxyethane 100
N,N-dimethylacetamide 1090
1,4-dioxane 380
1,2,3,4-tetrahydronaphthalene (tetraline) 100
0 5 e n o n a x e h - 2
0 0 0 3 l o n a h t e m
nitromethane 50
0 0 2 e n i d i r y p
Prepared in water:dimethylsulfoxide 90:10, 1mL/
ampul
Each 5-pk. 10-pk.
36230 36230-510 36330
Class 2 Mix C
2-ethoxyethanol 160g/mL
ethylene glycol 620
0 2 2 e d i m a m r o f
2-methoxyethanol 50
N-methylpyrrolidone 4840
0 6 1 e n a l o f l u s
Prepared in water, 1mL/ampul
Each 5-pk. 10-pk.
36231 36231-510 36331
USP <467> Reference Material Mixes
17
www.restek.com
GC Accessories
. k p - 0 0 0 1 . k p - 0 0 1 n o i t p i r c s e D
6mL Clear Vial 21166 21167
10mL Clear Vial, Flat Bottom 24683 24684
10mL Clear Vial, Rounded Bottom 21164 21165
20mL Clear Vial, Flat Bottom 24685 24686
20mL Clear Vial, Rounded Bottom 21162 21163
27mL Clear Vial 21160 21161
. k p - 0 0 0 1 . k p - 0 0 1 n o i t p i r c s e D
Silver Seal w/ PTFE/Gray Butyl Rubber 21761 21762
Silver Seal w/ PTFE/Silicone 21763 21764
Pressure Release, Silver Seal w/ PTFE/
Gray Butyl Rubber Septa <125 6 6 7 1 2 5 6 7 1 2 C
Pressure Release, Silver Seal w/ PTFE/
Silicone Septa >125 8 6 7 1 2 7 6 7 1 2 C
Headspace Autosampler Vials
20mm Aluminum Seals w/Septa, Assembled
The crimper is adjustable for optimized sealing performance. It also is comfortable enough
for pro- longed use. For chromatographers who need to save, transfer, or dispose of their
samples, we provide a decapper that allows the user to remove a crimp-top cap safely and
easily. If you havent used an aluminum seal decapper, order one today!
Aluminum Seal Crimper and Decapper
r e p p a c e D r e p m i r C e z i S
6 3 7 1 2 5 3 7 1 2 m m 8
1 7 1 1 2 0 7 1 1 2 m m 1 1
0 4 7 1 2 9 3 7 1 2 m m 3 1
8 3 7 1 2 7 3 7 1 2 m m 0 2
Septum Diameter 25-pk. 50-pk. 100-pk.
9.5mm (
3
/8") 20359 20360 20361
0 8 3 0 2 9 7 3 0 2 8 7 3 0 2 m m 0 1
11mm (
7
/16") 20363 20364 20365
12.5mm (
1
/2") 20367 20368 20369
6 8 3 0 2 5 8 3 0 2 4 8 3 0 2 m m 7 1
Shimadzu Plug 20372 20373 20374
Thermolite

Septa
Crimper Decapper
s
18
www.restek.com
Inlet Liners for HP/Finnigan GCs
Liner ID/OD/length ea. 5-pk. 25-pk.
2mm Splitless
2.0 x 6.5 x 78.5 20712 20713 20714
Gooseneck Splitless (2mm)
2.0 x 6.5 x 78.5 20795 20796 20797
Recessed Gooseneck (2mm)
2.0 x 6.5 x 78.5 20980 20981 20982
1mm Split
1.0 x 6.3 x 78.5 20972 20973
Liner ID/OD/length ea. 5-pk. 25-pk.
1mm Split
1.0 x 6.3 x 72 20970 20971
2mm Splitless
2.0 x 6.3 x 74 20721 20722 20723
Open 0.5mm ID
0.5 x 5.0 x 54 20992 20993
Open 0.75mm ID
0.75 x 5.0 x 54 21714 21715 21716
Inlet Liners for Varian GCs
Liner ID/OD/length ea. 5-pk. 25-pk.
17A 1mm Split
1.0 x 5.0 x 94 20976 20977 20978
Inlet Liners for Shimadzu GCs
Inlet Liners for Perkin-Elmer GCs
Liner ID/OD/length ea. 5-pk. 25-pk.
2mm Splitless
2.0 x 5.5 x 79.5 20811 20812 20813
Inlet Liners for CE Instruments/ThermoQuest GCs
Liner ID/OD/length ea. 5-pk. 25-pk.
2mm Splitless
2.0 x 5.0 x 100 20730 20731 20732
Auto SYS Splitless w/Wool (2mm)
2.0 x 6.2 x 92.1 20829 20830 20831
Auto SYS XL Split/Splitless w/ wool
2.0 x 4.0 x 81.2 21717 21718
for 5000 and 6000 GCs
1mm Split
1.0 x 8.0 x 105 20916 20917
Liner ID/OD/length ea. 5-pk. 25-pk.
for TRACE and 8000 GCs
Fits Vespel

/
Ferrule Column Graphite Graphite
ID (mm) ID (mm) 50-pk. 50-pk.
0.4 0.25 20227 20229
0.5 0.32 20228 20231
0.8 0.53 20224 20230
Capillary Ferrules
(for
1
/16" compression-type fittings)
Fits Vespel

/
Ferrule Column Graphite Graphite
ID (mm) ID (mm) 5-pk. 5-pk.
0.4 0.25 20235 20241
0.5 0.32 20235 20242
0.8 0.53 20245 20246
Two-Hole Ferrules
(for
1
/16" compression-type fittings)
Fits
Ferrule Column Graphite Graphite
ID (mm) ID (mm) 2-pk. 10-pk.
0.4 0.180.25 20280 20281
0.5 0.32 20282 20283
0.8 0.50 & 0.53 20284 20285
Graphite Ferrules for
M4 Fittings
(for QCQ Fisons 8000 & TRACE 2000)
19
Restek has specially engineered a high-precision,
1
/16-inch fitting that uses standard size, two-hole
capillary ferrules. The fitting kit comes with everything needed for dual-column confirmational analysis
using 0.25 and 0.32mm ID capillary columns (two-hole ferrules must be ordered separately).
Capillary Inlet Adaptor Fitting Kit (for 0.25/0.32mm ID columns): cat.# 20633
Replacement Inlet Seal (1.2mm hole): cat.# 20390, (2-pk.); cat.# 20391, (10-pk.)
Hewlett-Packard
1
/16-Inch Capillary Inlet Adaptor Fitting Kit
Restek has specially engineered a high-precision,
1
/8-inch fitting that uses standard
1
/8-inch, two-hole capillary ferrules. The fitting kit comes with everything needed for installation.
1
/8-inch Capillary Inlet Adaptor Fitting Kit (for 0.53mm ID columns): cat.# 20645
Replacement Inlet Seal (
1
/16-inch hole): cat.# 20392, (2-pk.); cat.# 20393, (10-pk.)
Hewlett-Packard
1
/8-Inch Capillary Inlet Adaptor Fitting Kit
Includes a
1
/16-inch nut, a
1
/16-inch ferrule, a base nut and
1
/4-inch Vespel

/graphite ferrule, a
1
/16-inch
capillary nut, a 5-pack of low-bleed plug septa, and a special low-mass septum nut. Order appropriate
capillary ferrules separately.
Low-Volume Injector for Hewlett-Packard and Varian GCs
Description Kit
LVI for HP Split/Splitless GC inlets cat.# 21692
LVI for Varian Split/Splitless GC inlets cat.# 21693
Includes a
1
/16-inch nut, a
1
/16-inch ferrule, a base nut and
1
/4-inch Vespel

/graphite ferrule, a
1
/16-inch
capillary nut, a 5-pack of low-bleed plug septa, and a special low-mass septa nut. Order appropriate
capillary ferrules separately.
Low-Volume Injector for Hewlett-Packard 5890 Septum Packed Purge Port
Description Kit
LVI for HP 5890 Septum Packed Purge Port cat.# 21698
Calculates linear velocity based on column ID.
Measures N2, He, H2, 5% Ar/Me, and Air.
Measures split flow and mass flow.
Has pulse-free operation that will not interfere with EPCs.
Reads flow accurately from 5 to 500mL/min.
Description Each
Restek Veri-Flow 500 Electronic Flowmeter (110 volts) cat.# 21643
Restek Veri-Flow 500 Electronic Flowmeter (220 volts) cat.# 21645
Restek Veri-Flow 500 Electronic Flowmeter
The Leak Detective

responds in less than 2 seconds to trace leaks of gases with thermal conductivities
different than air. Helium or hydrogen can be detected at 3 x 10-4 cc/sec.* or at an absolute concentra-
tion as low as 200ppm. Leaks are indicated by an audible alarm, as well as by an LED readout. (Batteries
and AC adaptor included.)
*Caution: not designed for determining leaks of combustible gases.
Description Each
Restek Leak Detective

Electronic Leak Detector (110 volts) cat.# 21607

Restek Leak Detective

Electronic Leak Detector (220 volts) cat.# 21609

Restek Leak Detective

Electronic Leak Detector

Restek U.S. 110 Benner Circle Bellefonte, PA 16823 1-814-353-1300 1-800-356-1688 fax: 1-814-353-1309 www.restek.com
Restek France phone: +33 (0)1 60 78 32 10 fax: +33 (0)1 60 78 70 90 e-mail: [email protected]
Restek GmbH phone: +49 (0)6172 2797 0 fax: +49 (0)6172 2797 77 e-mail: [email protected]
Restek Ireland phone: +44 (0)2890 814576 fax: +44 (0)2890 814576 e-mail: [email protected]
Restek Japan phone: +81 (3)6459 0025 fax: +81 (3)6459 0025 e-mail: [email protected]
Thames Restek U.K. LTD phone: +44 (0)1494 563377 fax: +44 (0)1494 564990 e-mail: [email protected]
Lit. Cat.# 59895B
2000 Restek Corporation. All rights reserved.
Printed in the U.S.A.
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