U.S. patent application number 10/938282 was filed with the patent office on 2005-02-10 for method for solid-phase microextraction and analysis, and a collector for this method.
This patent application is currently assigned to Gerstel Systemtechnik GmbH & Co. KG. Invention is credited to Baltussen, Erik, David, Frank, Sandra, Patrick.
Application Number | 20050032237 10/938282 |
Document ID | / |
Family ID | 27219053 |
Filed Date | 2005-02-10 |
United States Patent
Application |
20050032237 |
Kind Code |
A1 |
Sandra, Patrick ; et
al. |
February 10, 2005 |
Method for solid-phase microextraction and analysis, and a
collector for this method
Abstract
The invention relates to a method for solid-phase
microextraction and analysis of substances in a carrier fluid, in
which a collector is brought into contact with the stirred fluid
containing the substances for a sufficient time and is then
subjected to a solid-phase extraction directed at at least one
substance adhering to the collector, and desorbed substances are
transported for analysis by means of a carrier gas, in which the
carrier fluid containing the substances is stirred in a receptacle
of a magnetic stirrer by means of a coated magnetic stirring
element as the collector, and/or the carrier fluid is made to move
intimately relative to the collector by means of ultrasound, and
then the stirring element is placed in a solid-phase extraction
device.
Inventors: |
Sandra, Patrick;
(Kortrijk-Marke, BE) ; Baltussen, Erik; (Den
Bosch, NL) ; David, Frank; (Brugge, BE) |
Correspondence
Address: |
TOWNSEND AND TOWNSEND AND CREW, LLP
TWO EMBARCADERO CENTER
EIGHTH FLOOR
SAN FRANCISCO
CA
94111-3834
US
|
Assignee: |
Gerstel Systemtechnik GmbH &
Co. KG
Mulheim
DE
|
Family ID: |
27219053 |
Appl. No.: |
10/938282 |
Filed: |
September 9, 2004 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10938282 |
Sep 9, 2004 |
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|
09967333 |
Sep 27, 2001 |
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6815216 |
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09967333 |
Sep 27, 2001 |
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09524682 |
Mar 14, 2000 |
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Current U.S.
Class: |
436/174 ;
422/400 |
Current CPC
Class: |
G01N 2030/009 20130101;
Y10T 436/255 20150115; Y10T 436/25 20150115; Y10T 436/25125
20150115; Y10T 436/156666 20150115; Y10T 436/25875 20150115; B01D
2015/389 20130101; B01D 2015/389 20130101; G01N 2030/121 20130101;
G01N 2030/009 20130101; G01N 2030/128 20130101; Y10T 436/25375
20150115; G01N 2030/062 20130101; G01N 2030/121 20130101; G01N
1/405 20130101; Y10T 436/2525 20150115; G01N 30/12 20130101; G01N
1/34 20130101 |
Class at
Publication: |
436/174 ;
422/099 |
International
Class: |
G01N 001/00 |
Foreign Application Data
Date |
Code |
Application Number |
Mar 26, 1999 |
DE |
19913809.5 |
Jul 14, 1999 |
DE |
19933017.4 |
Claims
1-51. (canceled)
52. A collector for the solid-phase microextraction and analysis of
substances to be examined, comprising a rod-like element sheathed
in a flexible tube of material selected from the group consisting
of a sorbent, an adsorbent and a combined sorbent and adsorbent,
and capable of being picked up by a discharging device selected
from the group consisting of a gripping device, suction device, and
a magnet, and removed.
53. The collector of claim 52, adapted to be insertable in a
thermal desorption apparatus of a gas chromatograph.
54. The collector of claim 52 wherein said material is a member
selected from the group consisting of polyethylene glycol,
silicone, polyimide, octadecyltrichlorosilane,
polymethylvinylchlorosilane, liquid-crystal polyacrylates, grafted
self-organized monomolecular layers and inorganic coating
materials.
55. The collector of claim 52 wherein said rod-like element is a
section of wire.
Description
CROSS REFERENCE TO RELATED APPLICATION
[0001] This application is a continuation-in-part of co-pending
application Ser. No. 09/524,682, filed Mar. 14, 2000, the contents
of which are incorporated herein in their entirety.
BACKGROUND OF THE INVENTION
[0002] 1. Field of the Invention
[0003] The invention relates to a method for solid-phase
microextraction and analysis of substances originating for example
from a carrier fluid and to a collector for use within this method.
The invention also relates to a collector, which serves as a
passive collector in a gaseous, for example loaded environment
containing substances to be analyzed and a method for solid-phase
microextraction and analysis of these substances.
[0004] 2. Description of the Related Art
[0005] A method of this type is known from Boyd-Boland et al.,
Environ. Sci. Technol. Vol. 28, No. 13, 1994, 569A-574A and from EP
0,523,092 B1, in which a special syringe is used, which has a fiber
which can be telescoped through the syringe needle. The fiber,
which is expediently coated, is brought into contact with the
carrier fluid which contains the substances to be examined and at
the same time is being stirred, after which the fiber is retracted
and the syringe needle is introduced into a feeding device of an
analyzer, followed by desorption of adhering substances using a
carrier gas. The fiber has only a very limited absorption capacity
for substances which are to be examined and, moreover, is only
dipped into the stirred carrier fluid, so that consequently the
sensitivity of the analysis itself leaves something to be desired
if the coated fiber is vibrated. In addition, it is known from DE
196 19 790 C2 to have the microfiber functioning as a collector
rotate about its own axis by means of an electric motor with a
rotational speed of one's choice.
SUMMARY OF THE INVENTION
[0006] An object of the invention is to provide a method for
solid-phase microextraction and analysis of substances to be
analyzed and originating for example from a carrier fluid, which
provides a significantly improved sensitivity.
[0007] Another object of the invention is to provide a collector
for solid-phase microextraction and analysis of substances to be
analyzed and originating for example from a carrier fluid.
[0008] A further object of invention is to provide a collector
which may be used within the method for solid-phase microextraction
and analysis of substances.
[0009] A still other object of the invention is to provide a
collector as a passive collector for solid-phase microextraction
and analysis of substances for example pollutants to be analyzed
and originating for example from an environment.
[0010] A still other object of the invention is to provide a method
for solid-phase microextraction and analysis of substances to be
analyzed and originate from an environment, for example
pollutants.
[0011] A subject of the invention is a method for solid-phase
microextraction and analysis of substances in a carrier liquid, in
which a collector is brought into contact with the stirred liquid
containing the substances for a sufficient time and is then
subjected to a solid-phase extraction directed at at least one
substance adhering to the collector, and desorbed substances are
transported for analysis by means of a carrier gas, wherein the
carrier liquid containing the substances is stirred in a receptacle
of a magnetic stirrer by means of a coated magnetic stirring
element as collector, and/or the carrier liquid is made to move
intimately relative to the collector by means of ultrasound, and
afterwards the stirring element is arranged in a solid-phase
extraction device.
[0012] Another subject of the invention is a collector for the
solid-phase microextraction and analysis of substances to be
examined, in particular for use in a thermal desorption apparatus
of a gas chromatograph, comprising a carrier made from magnetic
material, which is suitable as a stirring element for a magnetic
stirrer and is provided with a sorbent and/or adsorbent coating for
the substances to be examined.
[0013] A still other subject of the invention is a coated magnetic
collector, which serves as a passive collector in a gaseous, for
example loaded, environment containing substances to be
analyzed.
[0014] A still other subject of the invention is a method for the
solid-phase microextraction and analysis of substances in an
environment, in which a collector is exposed to the environment for
a sufficient time as a passive collector and then the collector is
positioned in a solid-phase extraction device, desorbed substances
being transported for analysis by means of a carrier gas.
[0015] The use of a stirring element which is actuated by a
magnetic stirrer and/or an ultrasonic agitator increases the
accuracy of analysis very considerably, and moreover it is possible
to use large-volume receptacles, for example liter receptacles, for
the fluid containing the substances to be examined.
[0016] Further objects, advantages and embodiments of the invention
are evident from the following description.
[0017] The invention is explained in more detail below with
reference to exemplary embodiments of the invention, which are
illustrated in the attached drawings, of a device for carrying out
the method and of passive collectors.
BRIEF DESCRIPTION OF THE DRAWINGS
[0018] FIG. 1 is a diagrammatic view of a device for carrying out
the method for solid-phase microextraction and analysis of
substances which are in a carrier fluid.
[0019] FIGS. 2 to 4 show various embodiments of passive collectors,
in section.
[0020] FIG. 5 shows a comparison of two equilibrium curves relating
to the prior art and the invention.
[0021] FIG. 6 is a diagrammatic view of a further device for
carrying out the method for solid-phase microextraction and
analysis of substances which are in a carrier fluid.
[0022] FIG. 7 is a diagrammatic view of a headspace receptacle.
[0023] FIG. 8 diagrammatically depicts a device for carrying out
the method for solid-phase microextraction and analysis of
substances which are in a carrier liquid.
[0024] FIGS. 9 to 11 show various embodiments of collectors for
solid-phase microextraction and analysis of substances which are in
a carrier liquid, in section.
[0025] FIG. 12 shows a comparison of the yield with regard to a
method belonging to the prior art (SPME method) and the present
method (headspace sorptive extraction method: HSSE method).
[0026] FIG. 13 shows a GC spectrum of substances which are in a
carrier liquid using the present method.
[0027] FIG. 14 shows a gas chromatography spectrum (GC spectrum)
for substances which are in a carrier liquid using the SPME
method.
DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS
[0028] In accordance with FIG. 1, a magnetic stirrer 1 is provided,
which comprises a receptacle. 3 which is positioned on a base 2 and
is in the form of a beaker and may expediently be closed at its top
side by a septum 4. Before it is closed by the septum 4, the
receptacle 3 receives a carrier fluid containing substances which
are to be analyzed. The receptacle 3 may have been filled and
closed in advance at a sampling point. The carrier fluid may be
water and/or an organic solvent or a mixture thereof or liquefied
gas.
[0029] The base 2 comprises an electric motor 5, the shaft of which
bears a magnet 6 eccentrically. In the receptacle 3, there is a
stirring ball 7 made from ferromagnetic material, such as iron or
steel, which is advantageously glass- or plastic-sheathed and has a
diameter in the range of a few millimeters. The plastic sheathing
7a used may, for example, be polytetrafluoroethylene or another
fluorinated hydrocarbon polymer. The stirring ball 7 is preferably
covered with an active phase 7b for sorption/adsorption of
substances contained in the carrier fluid. This may be a coating
selected from the group comprising polyethylene glycol, silicone,
polyimide, octadecyltrichlorosilane, polymethylvinylchlorosilan- e,
liquid-crystal polyacrylates, grafted self-organized monomolecular
layers and inorganic coating materials.
[0030] The stirring ball 7 can be stirred for a sufficient time
during which it comes into intensive contact with the carrier fluid
and therefore with the substances contained therein and sorbs
and/or adsorbs the latter, so that it serves as a collector. After
the end of stirring, the stirring ball 7 is picked up and
introduced in a solid-phase extraction device, preferably a
desorption device 8. The latter advantageously comprises a
desorption tube 9 with a diameter section whose diameter is
slightly greater than that of the stirring ball 7, followed, via a
frustoconical section, by a diameter section whose diameter is
smaller than that of the stirring ball 7. The desorption device 8
is part of an analyzer 10, for example of a gas chromatograph,
connected to a carrier gas port 11, so that carrier gas flows
through the desorption tube 9 passing the stirring ball 7,
desorbing substances adhering thereto, and can supply these
substances for analysis. The desorption device 8 preferably
comprises a heating device 12, in order to carry out a thermal
desorption.
[0031] The stirring ball 7 can be removed from the receptacle 3
automatically by means of a discharging device 13 which penetrates
the septum 4 and may be designed in the form of a gripping device,
suction device or also as a magnet, and can be positioned in the
desorption tube 9, which can then be placed automatically in the
desorption device 8, so that the entire solid-phase microextraction
and analysis can be performed automatically. For this purpose, an
appropriate receptacle 3 for a plurality of samples can be arranged
on a turntable which can rotate in steps and beneath which, in one
position, the base 2 of the magnetic stirrer 1 is arranged.
[0032] In order to achieve reproducible measurements, stirring
times of approximately 45 to 60 minutes are generally required.
[0033] As an alternative to a stirring element in the form of a
stirring ball, it is also possible to use an element in the form of
a stirring rod 14. This may have a coated rod-like carrier 15 made
from ferromagnetic or paramagnetic material; in the latter case, it
should have a minimum length of approximately 2 cm, while shorter
lengths are also possible if ferromagnetic material is used. For
example, it may be a rod-like carrier 15 which is rounded at the
ends and is entirely coated with the active phase 15b (FIG. 3) or
also a carrier comprising a section of wire which is surrounded by
a cylindrical sheath 16 made from material of the active phase
which is in the form of a flexible tube (FIG. 4). By way of
example, the rod-like carrier 15 may have a diameter of
approximately 3 to 6 mm.
[0034] It is also possible to achieve improved analysis if the
carrier fluid which contains the substances and is situated in a
receptacle containing a collector, which is preferably a stirring
ball 7, is alternatively or additionally set in motion by means of
ultrasound. FIG. 6 shows one embodiment of such an ultrasonic
stirring device as a resonator unit 17 in which one or more
ultrasonic generators (vibrators) 19, which are shielded by means
of insulating plate 18, arc incorporated at the bottom and/or on
the sides of a housing 20. A metal wall 21 which is mounted in
front of the ultrasonic generator 19 and has a wall thickness of
d=n*.lambda./2 (.lambda.=acoustic wavelength) transmits the
vibrations to a coupling liquid 22 in the resonator unit 17,
preferably water, which is set in motion. The receptacle containing
the substances to be analyzed is introduced into the resonator unit
17.
[0035] In this case, the receptacle 3 is also advantageously one of
a magnetic stirrer, in which case stirring is carried out by means
of the coated magnetic stirring ball 7 as collector, so that the
ultrasound is applied in addition to the magnetic stirring.
[0036] In general, thermal, liquid or desorption by means of
supercritical gases is possible.
[0037] As an alternative to being introduced into a thermal
desorption device 8, the stirring element can be arranged in a
headspace receptacle 23 (FIG. 7), the diameter of which is only
slightly greater than the diameter of the stirring ball 7, by means
of the discharging device 13. The headspace receptacle 23 is then
closed by means of a septum 24 and a sealing ring 25, using a
closure instrument, and is introduced into a headspace head 26. In
the latter, the headspace receptacle 23 is preheated by means of a
heating device 27 and there is a build-up of pressure, during which
an equilibrium for the volatile substances to be examined with the
gas phase 28 above the stirring ball 7 is established. These
substances can be removed by means of a syringe which penetrates
the septum 24 and can be fed to the separation column of, for
example, a gas chromatograph.
[0038] As an alternative to being desorbed in a thermal desorption
device 8, the stirring element may also be introduced into an
extraction device containing an organic liquid, the organic liquid
used exhibiting a high level of interaction with the substances to
be examined and absorbing the latter--if necessary during a
stirring movement of the stirring element with respect to this
liquid, after which the liquid which is enriched with the
substances to be examined is taken up by means of a syringe and
taken to a feeding device of, for example, a gas chromatograph, in
order to be fed for analysis, for example using a
gas-chromatography separation column, by means of a carrier
gas.
[0039] Due to the use of a stirring element in a magnetic stirrer
or, alternatively or additionally, in an ultrasonic agitator and
its intensive contact with the carrier fluid containing the
substances to be examined, it is possible to achieve a sensitivity
of analysis which is orders of magnitude, for example about 1000
times, butter than the use of the known fiber. FIG. 5 shows a
diagram comparing the yield (plotted on the ordinate) of absorbed
substances for a known fiber coated with active phase (curve A) and
a stirring rod which is sheathed by active phase and has been
stirred by means of the magnetic stirrer according to the invention
(curve B) at mass equilibrium, the concentration quotient (K(o/w))
of a substance in octanol and water being plotted on the abscissa.
This coefficient (for normal temperature) can be found in the
literature for a wide range of substances. For example, if this
concentration quotient is 100, it can be seen from the diagram
shown in FIG. 5 that in this case the coated fiber provides a yield
of approximately 1% and the invention provides a yield of
approximately 50%. At a concentration quotient of below 100, the
coated fiber cannot generally carry out any reliable measurement,
while the sheathed stirring element generally still allows absolute
reliable measurements. Generally, the covered stirring element
improves the measurement accuracy considerably, i.e. by powers of
10, and widens the measurement range considerably, in that the
sensitivity of analysis is improved approximately by a factor of
1000. With the sheathed stirring element, there is generally no
need for the sensitivity of analysis to be improved by heating the
liquid containing the substances to be examined, as is necessary in
many cases for a coated fiber and also causes measurement
errors.
[0040] Moreover, a stirring element of this type may be arranged as
a passive collector in a gaseous, for example loaded, environment
containing substances to be examined or may be carried by a person
working in the environment, in which case the passive collector is
exposed to the environment for a sufficient time and afterwards the
substances which it has sorbed and/or adsorbed are subjected to
extraction, after which desorbed substances are transported for
analysis by means of a carrier gas via a feeding device, for
example in-order to monitor personal exposure to pollutants.
[0041] In the heatable headspace extraction apparatus 100
illustrated in FIG. 8, there is a headspace vessel 102, which is
expediently closed off at the top by a headspace vessel cap 103 and
by means of a septum 104, the headspace vessel 102, before it is
closed off, receiving a carrier liquid 105 containing substances
which are to be investigated and may be in a polar form, of medium
polarity or, if appropriate, may even be polar. The carrier liquid
may be water and/or an inorganic solvent or solvent mixture or
liquefied gas.
[0042] The headspace extraction apparatus 100 includes a heating
apparatus 106, which can be used to heat the contents of the
headspace vessel 102. An equilibrium of the volatile compounds is
established between the carrier liquid 105 and a gas phase 107
above it. When heated, additional pressure is built up inside the
headspace vessel 102. In the gas phase 107 above the carrier liquid
105 there is a collector 108 which comprises an inert support l 09,
for example a rod-like glass tube (closed off from the outside at
least during the headspace extraction), and a hose 10 which has
been pushed on, at least partially surrounds the glass tube and
comprises hydrophobic material as active phase. The hose 10 is used
for the sorption of substances which are situated in the gas phase
107, are derived from the carrier liquid 105 and are to be
investigated, the analysis of which can then be carried out
substantially without water. The material of the hose 110
comprises, as active sorption phase, by way of example substances
selected from the group consisting of polydimethylsiloxane,
polyethylene glycol, silicone, polyimide,
polymethylvinylchlorosilane, octadecyltrichlorosilane,
liquid-crystal polyacrylates, grafted self-organized monomolecular
layers and inorganic coating materials, or consists of these
materials.
[0043] The collector 108 is exposed to the gas phase 107, above the
carrier liquid 105, for a sufficient time, and therefore exposed to
the substances which are to be investigated, of which there is then
an increased level in the hose 110 of the collector 108, which has
a sorptive action on the substances. On account of the considerable
thickness of the hose 110, the substances which are to be
investigated can accumulate in the hose 110 until virtually
complete saturation, since the equilibrium of the generally
volatile substances which is established between the carrier liquid
105 and the gas phase 107 can be shifted towards the gas phase on
account of permanent sorption of these substances in the active
phase of the collector 108.
[0044] After the sorption or a predetermined time has ended, the
collector 108 is picked up and is placed in a solid-phase
microextraction apparatus, preferably a desorption apparatus 111.
The latter expediently comprises a small desorption tube 112 with a
diameter section whose diameter is slightly greater than that of
the collector 108 and which is adjoined, via a frustoconical
section, by a diameter section whose diameter is less than that of
the collector 108. The desorption apparatus 111 is connected, as
part of an analysis unit 113, for example a gas chromatograph, to a
carrier gas connection 114, so that carrier gas can flow through
the desorption tube 112 past the collector 108, so that substances
adhering thereto are desorbed and can pass these substances for
analysis. The desorption apparatus 111 preferably comprises a
heating device 115, in order to be able to carry out thermal
desorption.
[0045] The entire method for carrying out the solid-phase
microextraction and analysis of substances in a carrier liquid can
be fully automated, by the collector 108 being automatically
removed from the headspace vessel 102 with the headspace vessel cap
103 and the septum 104 by means of a transfer member 116, which may
be designed in the form of a gripper, sucker or as a magnet, and
transferred into the desorption tube 112. The desorption tube 112
is then likewise automatically placed in the desorption apparatus
111, so that the entire solid-phase microextraction and analysis
can be performed automatically.
[0046] For this purpose, for a plurality of samples corresponding
headspace vessels 102 may be arranged on a turntable which can be
rotated in steps and next to which, in one position, the headspace
extraction apparatus 100 and in a further position the transfer
member 116 are arranged.
[0047] To enable reproducible measurements to be carried out,
sorption times of a few minutes up to 60 min are generally
required, depending on the volatility of the substances to be
investigated and therefore any heating operations which may
additionally be required.
[0048] In the embodiment of the collector 108 illustrated in FIG.
9, the inert support 109 is in the form of a rod and is at least
partially surrounded by the hose 110 which has a sorptive
action.
[0049] However, the collector 108 may also be provided with a
ferromagnetic or paramagnetic support 109 which is surrounded by an
inert casing of, for example, glass in which case the hose 110 at
least partially surrounds the inert casing 117, as illustrated in
the embodiment shown in FIG. 10. The collector 108 may then be
detachably secured to a separate magnetic or magnetizable holder
(not shown). However, any other type of detachable holder using a
plug connection, a screwed connection, or any other suitable
connection for detachably securing it to the collector 108 is
possible, for example if a magnetic support 109 is not used.
[0050] The inert support 109 preferably has a minimum internal
diameter of 0.8 mm, in particular has an internal diameter of 1.0
to 1.3 mm, since this minimum internal diameter is expedient in
order to provide sufficient hose material for sorption.
[0051] In the embodiments of the collector 108 with a ferromagnetic
or paramagnetic support 109, it is preferable to use a transfer
member 116 with a magnetic action.
[0052] In the further embodiment illustrated in FIG. 11, the
collector 108 is formed integrally with the headspace vessel cap
103. This unit can be fitted onto the desorption tube 112 so as to
close off the latter in a sealed manner, by means of the transfer
member 116. The hose 110 virtually completely surrounds the inert
support 109.
[0053] Depending on the nature of the substances to be
investigated, the hose 110 should have a length of preferably 5 to
60 mm, in order to provide sufficient sorption material.
EXAMPLE AND COMPARATIVE EXAMPLE
[0054] The following examples demonstrate the advantages of the
present HSSE method over the known SPME method.
[0055] An analysis using the HSSE method was carried out under the
following conditions: 40 ppb of a solvent mixture (C6-C13) were
added to 10 mL of an aqueous sample and the mixture was introduced
into a 250 mL Erlenmeyer flask, which was closed off by means of a
septum coated with aluminum foil, so that a gas phase formed above
the liquid. A glass rod which was encased by 50 mg of
polydimethylsiloxane (PDMS) as pushed-on hose 110, was held in the
gas phase as inert support 109; the hose 110 surrounded the inert
support 109 over a length of 5 cm and with a wall thickness of 0.2
mm. The enclosed glass rod was introduced into a thermal desorption
apparatus by means of a small thermal desorption tube and was
subjected to thermal desorption, during which the thermal
desorption tube, which had been heated to 40.degree. C., was heated
in splitless mode to 250.degree. C. with a heating rate of
60.degree. C./min, and the desorbed substances to be investigated
were then transferred to a cold charging system by means of carrier
gas and via a transfer line. In the cold charging system, in this
case a Tenax-filled quartz liner, the substances to be investigated
were received at -150.degree. C. and then released again using a
heating rate of 600.degree. C./min up to a final temperature of
250.degree. C. With a split ratio of 1:50, in order to obtain
signal peaks which are suitable for the quantity of sorbed
substances. The Tenax-filled quartz liner in the cold charging
system prevents the highly volatile components from breaking
through. The substances to be investigated were then transferred to
a GC column by means of a carrier gas; in this example, a GC column
which was 30 m long, had an internal diameter of 250 .mu.m and a
film thickness of 1 .mu.m was used. The GC column was heated by a
furnace which surrounds it and initially held the temperature at
30.degree. C. for 1 min and then raised it to 300.degree. C. with a
heating rate of 10.degree. C./min. The substances to be
investigated were analyzed using an MSD 5973 (mass-selective
detector) in scan mode in the range from 20-400 amu (atomic mass
units).
[0056] In the comparative example using the known SPME method, the
specimen was prepared in a similar manner and a fiber coated with
PDMS in a layer thickness of 100 .mu.m was held in the gas phase in
the closed Erlenmeyer flask. This layer thickness approximately
corresponds to a coating quantity of 0.5 mg of PDMS. The thermal
desorption and cold charging likewise took place in a similar
manner to the HSSE method, but the phase of heating up the cold
charge and the subsequent transfer to the GC column was only able
to take place in splitless mode, on account of the small quantities
of substance present, while the subsequent analysis was once again
carried out in a similar manner to the HSSE method.
[0057] FIG. 12 shows a comparative diagram illustrating the yield
(plotted on the ordinate) for the hose using the HSSE method of the
example and for the coated fiber of the SPME method of the
comparative example; the retention time of the substances
investigated is plotted on the abscissa. If the retention time is
approximately 10 min, it can be seen from the diagram shown in FIG.
12 that, in this case, the coated fiber of the SPME method gives a
yield of virtually 0%, while the HSSE method gives a yield of
approximately 6%. With retention times of less than 10 min, the
coated fiber of the SPME method generally does not allow a reliable
measurement to be carried out (cf. also FIG. 14), while the hose
generally allows reliable measurements (cf. also FIG. 13). Overall,
the comparative diagram of FIG. 12 demonstrates that, with the hose
of the HSSE method, the yield is improved considerably, i.e. by at
least one power of 10, and the measurement range is widened
considerably, since the analysis sensitivity is improved by
approximately a factor of 50.
[0058] FIG. 13 shows a GC spectrum using the HSSE method, in which
the intensities are plotted against the retention times; this
spectrum is obtained by means of the example described above and
constitutes the basis for the comparative diagram shown in FIG.
12.
[0059] FIG. 14 shows a GC spectrum using the SPME method, in which
the intensities are plotted against the retention times; this
spectrum is obtained by means of the comparative example described
above and constitutes the basis for the comparative diagram shown
in FIG. 12.
[0060] A comparison of FIG. 13 and FIG. 14 shows that overall the
HSSE method reveals a significantly improved sensitivity and lower
retention times with, at the same time, a considerably higher
intensity, which in this example, moreover, emerges particularly
clearly for substances with low molecular masses as well.
[0061] Although the foregoing has been a description of preferred
embodiments of the invention, it will be apparent to those skilled
in the art that numerous variations and modifications may be made
in the invention without departing from the scope as described
herein.
* * * * *