|Publication number||US3518059 A|
|Publication date||Jun 30, 1970|
|Filing date||May 31, 1967|
|Priority date||May 31, 1967|
|Publication number||US 3518059 A, US 3518059A, US-A-3518059, US3518059 A, US3518059A|
|Inventors||Levy Eugene J|
|Original Assignee||Hewlett Packard Co|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (48), Classifications (24)|
|External Links: USPTO, USPTO Assignment, Espacenet|
June 30, 1970 E. J. LEVY METHOD AND APPARATUS FOR DETERMINING CHEMICAL STRUCTURE Filed May 31, 1967 5 Sheets-Sheet 1 SAMPLE 2 r R m Em g 0 0 3 E1 E T 8 S H m g p t 1. 2 m T S amv wm w mo 2 ws M m From 86 \lllllllllllllll] I m n u w i m o EU W d v 1 T mw w 7 MC, h n T m T w mm N. T "W: m R m 5 4 o L1 IIIU IIIIII IL 0 m 1 E H T N T D n 4 m w s 1 1 w a 1 0 5 7 Q T 6 t N M E/ m O .7 m u E c a k 9 mu 4 5 0 nc 1 m S P lllll lllillL fzvmv n mu! 7! Hip Z OLECVLE COLUHN 60L .U'IURNEYS E. J. LEVY June 30, 1970 METHOD AND APPARATUS FOR DETERMINING CHEMICAL STRUCTURE Filed May 31, 1967 5 Sheets-Sheet 3 lllllllllll m 3N m o wsmwmu mmfiu 2 m mwsfi 5: 0 L J g m J M n m m m m y g QQN. H Y m9 E B 93 a g J QNEEQQQ NW! -MN F @N 53$ mmwwwggommu mwfiofizmu SEER fiN ESE QR \SNAQ QQQQRE NESEEQQ Q Q N .FHNI 1 I. w u k Qififim? MWW mww IIIIIIK Wm mgu wwwfiv D \i N 533 \E Q6 R rmfiw m L Q ATTQENEYS E. J. LEVY June 30, 1970 METHOD AND APPARATUS FOR DETERMINING CHEMICAL STRUCTURE Filed May 31, 1967 5 Sheets-$heet 25 w llllllllllllllllllll J RH mm m $8 mwwsw QESEEQQ n" W 38? o n W QMN MEQEMQ \\33 @Q n mmzi W%O.D QQQQ mqk w PQQNE EQWMNEQHW INVENTOR fcganelleg RENE ATTORNEYS June 30, 1970 M E. J. LEVY 3,518,059
METHOD AND APPARATUS FOR DETERMINING CHEMICAL STRUCTURE Filed May 31, 1967 5 Sheets-Sheet 4 CO -=*%X4 X2 QHg CO "2:: H 2 4 4 2% X2 c 60 w C H4 MINUTES 2 CH4 C0 X2 0 110 6 64 2 0 123 C H s fi g 3 6 C234 -fi 4 H S X2 6 C y R) INVENTOR ELgmw J Le /y A T TORNEYS June 30, 1970 Y 3,518,059
METHOD AND APPARATUS FOR DETERMINING CHEMICAL STRUCTURE Filed May 31, 1967 5 Sheets-Sheet 5 g l H H g rr l fl".
75100 150 200250 300 Z5100 150 200250300 RETENTION INDEX A INVENTOR EzganeJLey ATTORNEYS United States Patent 3,518,059 METHOD AND APPARATUS FOR DETERMINING CHEMICAL STRUCTURE Eugene J, Levy, Oxford, Pa., assignor to Hewlett- Packard Company, Palo Alto, Calif., a corp-oration of California Filed May 31, 1967, Ser. No. 646,443 Int. Cl. G01n 31/08 US. Cl. 23-232 5 Claims ABSTRACT OF THE DISCLOSURE A method of and apparatus for pyrolyzing chemical compounds and using their volatile and non-volatile thermolytic dissociation products to obtain partial cracking patterns which are directly relatable to the molecular This invention relates to a method for identifying the chemical nature of compounds and, more particularly, to a method and apparatus for pyrolyzing compounds and observing their volatile and non-volatile components as an aid in identifying the compounds.
In recent years, gas chromatography has proven to be an extremely useful and effective separating technique by which sample mixtures may be separated into their components. The relative quantity of each component may be readily determined with the aid of any one of many gas detectors. While quite satisfactory for quantitative analiyses, difliculties are encountered in identifying the separated components. To identify such components, resort usually is had to whatever auxiliary analytical tools are available. Optical or mass spectrometers have been used for such identifications, but usually these are quite costly. Infrared and ultraviolet spectrometers can also be used, but in many cases these give limited information. Additionally, the infrared spectroscopic method has the disadvantage of requiring relatively large quantities of the .sample for a definite identification.
It is, therefore, an object of this invention to facilitate the identification of substances using pyrolysis techniques.
Keulemans and Perry described an identification system using a pyrolysis tube and a gas chromatograph in a paper entitled Identification of Hydrocarbons by Thermal Cracking presented at the Fourth International Gas Chromatography Symposium, Hamburg, Germany, 1962. A reprint of the Kuelemans et al. paper was published in 1962 in London by 'Butterworth. As proposed by Keulemans et al., a sample is passed by menas of a carrier gas through a continuous flow system including a pyrolysis chamber and a gas chromatograph located dowstream of the pyrolysis tube. The most volatile, low molecular weight products are discarded and higher molecular weight products, which are gaseous under the conditions used, are separated by the gas chromatograph and individually detected and recorded as a chromatogram. By determining the relative quantities of the said larger decomposition products, distinctive and reproducible patterns, called cracking patterns, are obtained and the observed cracking pattern is closely related to the carbon skeleton of the parent organic molecule.
An improved method and system for obtaining these ice cracking patterns is described and. claimed in the US. Pat. No. 3,425,807, issued Feb. 4, 1969 entitled Pyrolysis Systems by Eugene J. Levy. To obtain better reproducibility of the cracking patterns, the pyrolysis pressure, temperature and residence time of the sample in the pyrolysis unit must be maintained within certain carefully controlled limits as pointed out by Levy. To overcome many of these deficiences and to facilitate the handling of relatively small samples, Levy describes an apparatus and a method for identifying a sample component by introducing the sample mixture into a first flow system, separating the components of the sample mixture in the first flow system, introducing one of the separated components into a second flow system, pyrolyzing such separated component in a second fiow system and introducing the pyrolysis products in a third flow system in order to separate and obtain a cracking pattern which is indicative of the sample component, the most volatile, low molecular weight products again being completely ignored as in the Keulemans et a1. teaching.
In the Levy system, valves interconnect the several flow systems to permit a discrete portion of the first flow system to be sampled and passed on for pyrolysis. In like manner, the pyrolysis products are taken from the second flow system and introduced into the third flow system for separation and detection. Information as to the relative quantities of pyrolysis products affords a means of identifying the parent molecule.
The Levy and other prior art systems make use only of the large (higher molecular weight) molecules in the pyrolyzate to obtain the thermal cracking pattern which is related to the carbon skeleton of the parent molecule of the individual sample being analyzed.
It is an object of this invention to utilize the small (lower molecular weight) molecules resulting from the thermal decomposition of samples as an additional means of identifying the parent compounds, especially in relation to the determination and identity of functional groups present in the original compounds.
Another object of this invention is to provide an improved method of applying pyrolysis to the identification of compounds present in a sample of material.
Another object of this invention is to provide an improved system for identifying substances by pyrolysis techniques.
In accordance with the illustrated method of this invention, a sample of a mixture of components is analyzed. The preferred method includes introducing the sample into a first chromatographic column, separating the sample into certain of its components in the first column, eluting one of the said components and pyrolyzing it to produce pyrolysis products including heavy (molecular weight) constituents as well as light (molecular weight) constituents, passing the pyrolysis products to a second chromatographic system, separating the light constituents of the pyrolysis products in the second column, detecting each of these constituents on elution from the second column, and measuring the retention times in the second column of said constituents, thereby relating the presence and relative quantities of these light constituents to the functional groups and structures present in the originally separated components.
One embodiment of the apparatus of this invention includes a sample injection means, a pyrolysis chamber, a chromatograph column capable of separating light pyrolyzate products, a sample loop, and first and second detectors. Also included is a valve means for alternatively passing the sample from the injection means through the pyrolysis chamber, sample loop, and first detector when the valve is in a first postion and from the sample loop where it is stored through the column and second detector when the valve is in a second position, whereby the pyrolysis products are separated by the column and detected by the second detector. A timer is employed to measure the the time required for the several pyrolysis products to pass through the separating column. This time 18 related to the chemical structure of the low molecular weight pyrolysis products and these determine the identity of the parent molecule.
The novel features that are considered characteristic of this invention are set forth with particularity in the appended claims. The invention itself, however, both as to its organization and method of operation, as well as additional objects and advantages thereof will best be understood from the following description when read 1n connection with the accompanying drawings, in which:
FIG. 1 is a block-flow schematic diagram illustrating a system capable of performing the method of this invention' FlG. 2 is a detailed part schematic and part block dia gram of a system suitable for performing the method of this invention by isolating the flow streams of the separating and pyrolyzing system.
FIG. 2A is a block-flow schematic diagram of the detail of the third chromatograph shown in FIG. 2;
FIG. 3 is a block-flow schematic diagram of an alternative embodiment of this invention that may be employed in connection with the system illustrated in FIG. 2;
FIG. 4 is a block-flow schematic diagram illustrating still another alternative embodiment that may be employed in connection with the system illustrated in FIG. 2 for performing the method of this invention;
FGIS. 5AH are a series of pyrograms in which the detector output signal amplitude as the ordinant is plotted against retention time as the abscissa to show the retention times and quantities of small molecules present in the products produced by pyrolyzing several different parent molecules; and
FIGS. 6A-H are a series of bar graph representations of the total area of each small molecule of the pyrolysis products plotted against relative retention time for each of the several different parent molecules.
According to the preferred method of this invention, a chemical sample to be identified is introduced successively into three separate flow systems or streams. The first and third flow systems are gas chromatographs, and the second, or intermediate, flow system is a pyrolysis chamber. Although preferred, the first gas chromatograph may be eliminated from the system to provide a more simple system of the type illustrated in FIG. 1. As used herein flow stream is intended to denote a complete integrated flow system which includes a suitable conduit for providing a confined path for gases and vapors between elements of the system.
In FIG. 1 there is seen a source of carrier gas 10 which may be any of the suitable carrier gases employed in gas chromatography and preferably should be inert. By the term inert is meant a gas that does not pyrolyze and is nonreactive with the sample undergoing the analysis at the respective temperatures that exist throughout the system. A suitable gas that serves this purpose is helium. The carrier gas source 10 is connected by means of a conduit 12 to a sampling system 14 of suitable design and thence to the remaining elements of the system. The sampling system 14 may be no more than a conventional injection port permitting the sample to be introduced, as by a suitable sampling syringe, through a septum 16. The output of the sampling system 14 is connected through successive conduits 12 to a pyrolysis chamber 20, a gas chrom-atograph separating column 24, and a detector 28 to a vent to atmosphere 30.
The pyrolysis chamber 20 may be a suitable non-reactive tube of appropriate diameter and length, as will be described in more detail in connection with FIG. 2, heated to obtain thermal decomposition of the sample components passed therethrough. The gas chromatograph column 24 may contain any suitable column material adapted to separate molecules of lighter molecular weight constituents, typically organic through C and small polar molecules such a water, H 8, NH S0 etc. A suitable column for this purpose, as will be described with more detail in connection with FIG. 2, may be one packed with a bed of an insoluble cross-linked, finely divided microporous, organic polymer such as a copolymer of divinyl benzene and ethyl vinyl benzene. A column packing of this type, sold under the trade name Porapak is available from Waters Associates, Inc., Framingham, Mass. Other suitable packing may be used such as a silicon oil column on a Teflon support.
The detector 28 preferably is a non-destructive type detector such as the Well-known thermal conductivity detector in which changes in the resistance of a resistance element occur in accordance with the thermal conductivity of a mixture of carrier gas and sample components. The detectors resistance element is placed in a bridge circuit to provide an electrical output signal. The electrical output signal from the detector 28 is amplified and may be applied to a suitable indicator such as an industrial charttype recorder. The retention time of each separated component is measured. These retention times depend upon the chemical structure of the light constituents, i.e., small molecules or low boilers, eluted from the column. Knowledge as to the identity of these low boilers aids in the determination of the identity of the original molecule introduced at the septum 16.
The retention time may be obtained either manually from the chart record or automatically by connecting the detector output signal to a slope detector 32 and timer 33. The slope detector 32 is a device for electronically differentiating an electrical signal to determine the rate of change of its amplitude. When the electrical signal is represented graphically, as by a recorder, the rate of change may be seen as the slope of a particular curve or wave form. One such electronic differentiating device may be constructed by connecting a capacitor and resistor in series. Depending upon the input wave form, the output from the differentiating circuit will be an electrical signal which is either zero, positive, or negative going. The magnitude of this electrical signal depends upon the rate of the change. A pip or peak in the detector output wave form, is produced by the detectors denoting the presence of a particular eluted component. This amplitude varying signal from the slope detector 32 may be passed through a suitable threshold circuit such as a Schmidt trigger, which in turn actuates the timer 33. The timer 33, initially manually actuated when the sample is introduced into the system, measures the elapsed time, from the time of the sample introduction until each of the sample components are detected by the detector. Another type of slope detector may utilize a voltage-to-frequency converter in which the rate of frequency variations are a measure of the slope.
As a result of the remarkable and varied capacity of carbon for combining with itself and other elements, many different types of organic compounds are possible. Many of these types of classes are characterized by particular groups of elements known as functional groups. The method of this invention is based on the discovery that if a molecule containing a functional group is pyrolyzed under the proper conditions, as taught by the said Levy patent, the molecule will dissociate into smaller molecules which include certain low boiling or light (molecular weight) constituen directly relatable to the functional groups. These so c led proper conditions are those which minimize secondary recombination reactions during pyrolysis, i.e., pyrolysis is not complete.
A few of the principal classes of organic compounds and their principal low molecular weight dissociation products are shown in the following Table I:
TABLE I Pattern Type Compound Principal products A..- Hydrocarbon OH3(CH2)5CH3 CH H C H CaHa B.. AlCOhO], 2 CH3(CH2)5CH2OH C0; CH C211 02H H20; C3H5 Aldehyde C a( 2)n 4; 2 4; 2 0; 1 0
i D Ketone CHaCHzAXCHzhCHa C0; CH C211 C2110; 03110 There may be seen by reference to FIGS. SA-H typical 15 amounts of each differ very substantially as can be chromatograms of low molecular weight pyrolysis, hereinafter referred to as pyrograms, illustrating retention times of many of the possible small molecules resulting from the thermal dissociation of larger molecules listed in Table -I. The pattern letters A through H correspond to compounds A to H in Table I and in each pyrogram each peak is identified as to the compound to which it corresponds. The identity of each peak is established from a knowledge of typical retention times of the several compounds.
It may be noted from FIGS. SA-H that the pyrogram resulting from the pyrolysis of each different substance A to H is a unique (no two are the same) pyrogram which is a fingerprint or indicator denoting the existence of a particular compound in the sample under analysis. The uniqueness of these pyrograms is characterized not only by the presence or absence of particular decomposition products as noted in Table I, but several peaks of the pyrograms of the particular decomposition products for that compound. For example, an aldehyde,
and having the indicated formula, includes the principal reactions CO; CH C H C H C =H Again, the decomposition of a mercaptan, as exemplified by the compound CH (CH CH SH, producesthe principal reaction products CH C H C H H 8; C H Even though the aldehyde C and ketone give the same products, the
seen, to give distinctive patterns.
To illustrate the uniqueness of this identification technique, the areas under each of the pyrograms A through H in FIG. 5 were computed and converted to a percentage of the total peak areas in each pyrogram. These percentages were then plotted in bar graph form as the ordinant against relative retention times, as determined by the wellknown Kovats formula, for the abscissa. As may be seen in FIGS. 6A-H, each compound is easily distinguished from the other ones. This means that the identification of a particular functional group is possible if the pyrogram pattern of its small molecule dissociation products is known.
For example, if a particular analysis produced a pyrogram which when converted to the bar graph form re sulted in an identification pattern similar to pattern D it is immediately known that the compound is ethyl pentyl ketone.
Experimental pyrograms were obtained from many dilferent compounds. Each of the compounds listed, including the various alcohols, aldehydes, ketones, etc. were first initially pyrolyzed and their thermal dissociation products passed through the column 24 (FIG. 1) to be separated in time. As the dissociation products were eluted for each compound, they were detected by the detector 28 and recorded. Their relative peak areas and retention times (Kovats index) were then computed and the results of the computations set forth in Table 11 below:
TABLE II,--COMPOSITION OF SMALL MOLECULES Retention index Pyr. tem Type (compound) C 080 CH 10O C 02123 02H 165 0211 200 NH 207 11 0214 H S218 C H 283 8 Hydrocarbon (Ag:
0 3(CH2)B H; 49 26 654. 5 CH (CHz) 50113 48 25 655. 0 CH CH2CH(CHs) (CHmCHa. 26 42 655.0 Alcohol (B):
CH (CH; )3CH2OH 5 46 20 657.0 OH3(GH2)6CH2OH 7 41 23 656.0 Aldehyde (C):
OH (CH2)QCHO 25 14 37 17 657. 0 OHKOH MCHO 2 14 34 657. 0
II CH (CH2)zC(CH2) CH3. 18 17 39 5 21 657.0
II CHQCHZC (CHmCHs. 12 41 11 16 656.5
lO CH (CH;) (CH2)aCH3 17 14 34 s 27 656.5
f) CH CH WH hCH 23 16 39 1O 12 656. 0
' Ester (E):
O CHaHi-O-(CfiflgCH: 4 11 6 33 3 13 29 656. 5
(I) CH J0(CH OH 5 10 6 35 4 15 656.5
TABLE II.Continued Retention Index Pyr.
temp Type (compound) 0080 0114100 002123 C2H4165 02116200 NH3207 H20214 B28218 631-16283 Amino (F):
3( 2)sCHzNHg These particular compounds were pyrolyzed under the temperature conditions indicated in the far right column. The retention index for each of these dissociation products is listed at the head of each column. If desired, typical pyrogram or other retention time and peak area information for many different chemicals may be stored in computer storage for subsequent retrieval and automatic identification of the compound pyrolyzed. Alternatively such information may be accumulated and stored in tabular form for comparison and identification purposes if desired. In these cases the reference pyrograms or cracking patterns are obtained by individually pyrolyzing a variety of chemicals under controlled conditions, Each pyrolyzed chemical has its pyrolysis products passed through a chromatographic column for separation and detection. The detector output signal is recorded to obtain the control pyrogram for each chemical.
A preferred system for performing the method of this invention and thereby identifying small as well as large molecules is illustrated in FIG. 2. This simultaneous analysis of the large molecules provides much useful information as described in the said Levy application. By separating and detecting the large molecules contained in the pyrolysis products and noting their relative amounts, information relative to the carbon skeleton of the parent molecule may be Obtained. Ratios of the quantities of the pyrolysis products to each other and to the total quantity of pyrolysis products, has been found to be uniquely indicative of the identity of the pyrolyzed sample components. This relationship is described in a paper entitled Mechanism of Some Chain Reactions by R. 0. Rice and H. F. Herzfeld in the Journal of American Chemical Society, vol. 56, page 284, published in 1934.
In FIG. 2, a suitable source of carrier gas is connected to a first gas chromatograph 32 having a nondestructive efiiuent detector 42, such as a thermal conductivity detector. In the alternative, an efiiuent splitter and a destructive detector such as a flame detector of conventional type may be employed. The gas chromatograph 32 is conventional and typically includes an injec tion port 44, a separating column 46, and the detector 42. The sample mixture may be injected through a sample inlet or septum 16 in the injection port of known type. The rate of flow through the chromatograph 32 may be regulated by a suitable flow controller (not shown). The output of the detector 42 is connected to the first port 48 of a two-way, four port switching valve 34. The switching valve 34 is illustrated in its first, or sampling, position by the solid lines and its second, or non-sampling, position by the dotted lines. (The first and second positions of all two-way valves illustrated in the drawings are denoted by solid and dotted lines.) All conduits or gas fiow connections illustrated in the drawings comprise any suitable tubing, such as stainless steel or other tubing as desired.
The second port 50 of the switching valve 34 is connected to a vent to atmosphere or other exhaust. The third port 52 of the valve 34 is connected to a flow controller 54 which regulates the carrier gas flow rate from the carrier gas source 10 via a conduit 19. The sampling system 14 including a sample inlet 16, if desired, may be included in the conduit 19 between the second flow controller 54 and the valve 34. The fourth and final port 56 of the valve is connected through a conduit to a delay coil or loop 58 which may be nothing more than an unobstructed coil of stainless steel tubing having a desired volume. Such volume imparts a time delay to the componentsv transit time through the system. The switching valve 34, as well as the delay loop 58, are enclosed within a sampling oven denoted by the dashed line enclosure 60. The sampling oven 60 may be adjusted to maintain such temperature as is necessary to prevent condensation of the eluted sample component. The length and diameter of the delay loop 58 should be selected to provide sufficient volume for containing the entire amount of any given eluted sample component from the gas chromatograph 10 in vapor or gaseous form. The delay loop may be omitted if the sample is to be introduced directly through the sampling system 14.
From the delay loop 58, the second flow stream is directed by a suitable conduit through an open quartz, gold, or other non-reactive, high temperature pyrolysis tube 72 enclosed within a pyrolysis oven 74 and thence through one side of a pyrolyzate detector 76. This pyrolyzate detector 76 preferably is a non-destructive detector such as a thermal conductivity detector having an analytical and reference side or cell. The detector 76 preferably is enclosed in a separate detector oven 80, as is customary in gas chromatography, to facilitate precise control of the detectors temperature.
From the pyrolyzated detector 76, the second flow stream, containing the now pyrolyzed sample components, is directed through an efliuent splitter 78 which preferably provides a 1:1 split ratio. The two split flow streams are directed respectively to a second gas chromatograph, denoted by the dashed enclosure 24, and if desired to a third chromatograph, shown in FIG. 2A to simultaneously detect large molecules as taught by Levy. The third chromatgraph 116 is substantially identical to the second, except for the backflush valve, contained in the second chromatograph, but its column is selected to separate larger molecules rather than small. Carrier gas for the third chromatograph 116 comprises the third separate flow stream or system and is derived from a flow controller 112 connected to the carrier gas source 10. Returning now to the second chromatograph 24, from the efiiuent splitter, the split second flow stream is connected to the first port 82 of a two-position, six-port switching valve 81 which selectively interconnects the gas streams directed to and from different adjacent pairs of its six ports 82,84, 86, 88, and 92 together. Although a rotary valve is illustrated diagrammatically, a linear motion valve or other known type may be employed if desired.
In the first position of the switching valve 81, as illustrated by the solid lines, the second flow stream on entering the first port 82 passes out of the second port 84 to a sample loop 87. This sample loop 87 may be, for example, an open or unobstructed stainless steel tubing wound in the form of a helix. The sample loop 87 must be of sufiicient volume or capacity to contain at one time all of the pyrolysis products resulting from pyrolysis of the sample in their vapor or gaseous form. From the sample loop 87, the second fluid stream passes back through the fifth port 90 of the six-port switching valve 81, thence out of the sixth port 92 and out to vent or atmosphere.
In its second switching position, denoted by the dotted lines, the switching valve 81 interconnects those pairs of ports 84-86, 88-90, 82-92 necessary to introduce the sample contained in gaseous or vapor form in the sample loop 87 into a fourth separate flow system or stream.
Carrier gas for the fourth flow system is derived from a third flow controller 94 connected to receive carrier gas from the carrier gas supply Carrier gas forming the fourth flow system passes through a conduit 21 and a surge coil 96, which along with the sample loop 87, switching valve 81, a backfiush valve 159 a small molecule separating column 100 and a detector 76 form the second chromatograph 24. The surge coil 96 aids in preheating the carrier gas in the fourth flow system. Its length and diameter or volume depend on the volume of the sample loop 87, as will be described. From the surge coil 96, the fourth flow stream continues by way of a suitable conduit, as described, through the fourth port 88 of the switching valve 81, thence out of the third port 86 to the first port 160 of a two position four port backfiush valve 159, out through port 162 to the column 100, and then in the third port 166, out the fourth port 161 to the remaining side (reference) of the detector 76. After desired low molecular weight components have been separated and detected and while the higher molecular weight components are still in column 100, the backfiush valve 159 is switched to the second or dotted line position. The same carrier gas flow will now backfiush high molecular Weight compounds from column 100 into detector 76 to clean out column 100 preparatory to making subsequent runs.
The second chromatograph 24 should have a carrier gas obtainable from a 50 to 100 pounds per square inch (p.s.i.) helium line, and desirably can be an isothermal,
single column gas chromatograph using a non-specific detector such as a thermal conductivity detector. Suitable chromatographs for use in the first and fourth flow streams are available from Hewlett-Packard Company of Palo Alto, Calif, and are designated Model 5750. In each case the chromatograph detectors 42 and 76 and sampling systems 14 and 44 may be enclosed in separate ovens to insure accurate temperature control. The chromatograph detector 42 as well as the pyrolyzate detector 76 may be connected to suitable indicating devices as chart type potentiometric recorders. These provide a visual record of the amplitude variations of the respective detector output signals as a function of time.
In accordance with this invention, the separating column 100 is packed with suitable packing to permit or facilitate the separation of the small molecules present in the pyrolysis or dissociation products. The packing in this case may be the same as that employed or described in connection with separating column 24 in FIG. 1. The column of the third chromatograph 116 is packed to separate large molecules. One such packing may be Diatoport S liquid phase having a stationary phase of Apiezon L, although Triton X-305 may be preferred for the more polar molecules, both of which are available commercially.
The output of the detector 76 is connected to an indicator-timer denoted by block 104. The indicator as described may be a recorder. The timer may be a conventional clock mechanism which is actuated by a mechanical linkage denoted by the dash-dot line 106. This linkage 106 is the same as that which is employed to actuate the valve 81 from a suitable knob 108. Thus when the valve 81 is switched to introduce the dissociation products contained in the sample loop 87 into the separating column 100, the timer is switched on. With the occurrence of each peak, a microswitch on the recorder, sensing the recorder pen displacement, may cause the timer to print out the time, or store the time in a register for later digital handling of the information. In the alternative, the time may be measured manually by the operator directly from the chart record. These retention times may then be related as previously described to the functional groups, and therefore are helpful in establishing the identity of the parent molecules present in the original sample.
In one embodiment of the invention that was constructed, the delay loop 58 was constructed of 7 stainless steel tubing having a length to provide a delay volume of 50 milliliters. The sample loop was of similar dimension. All connecting conduit or tubing employed was stainless steel and the flow rate in the second stream 19 through the pyrolysis tube 72 was adjusted by flow controller 54 to be 6 cc. per minute. The quartz pyrolysis tube was 45 centimeters in length and in diameter. The surge coil 96 was 15' of stainless steel tubing. The flow rate of the first flow stream was adjusted to be approximately 20 cc. per minute and a As" analytical column 46 packed with Apiezon L on Diatoport S was employed. The separating column 100 was similarly packed.
The third chromatograph 116 is shown in FIG. 2a. Carrier gas for the third chromatograph is derived from the second flow controller 112. This carrier gas, which comprises a third flow system, passes through the conduit 23, through the flow controller 112, thence through the conduit 114, surge coil 118, a six port, two way valve 140, a large molecule separating column 156 and a detector 158 to vent. These elements together with a sample loop 154 make up the third chromatograph 116. All of the elements are substantially identical in location and function to the elements of the second flow system and hence need not be described further. The surge coil 118 aids in preheating the carrier gas in the third flow system as was the case in FIG. 2. The output of the detector 158 is connected to an indicator-timer 160 which is actuated through the linkage 162 denoted by the dotted line by the knob 164. This is the same knob which turns the switching valve as was the case in FIG. 2.
The pyrolyzate from the splitter 78 through the first port 142 of the valve 140, out of the second port 144, through the sample loop 154 in a reverse direction, thence back through the fifth port and out of the sixth port 152 to vent. Since the system described is substantially identical to that of the second chromatograph 24, no further description is deemed necessary. The only difference between the two systems is the fact that the separating column 156 is suitably packed to separatel arge molecules rather than small. This eliminates the necessity of utilizing the backfiush valve 150 as is preferred in the small molecule separation using the system of FIG. 2.
With the use of the second and third chromatographs, the large as well as the small molecules appearing in the pyrolysis products may be simultaneously separated and their respective elution times measured and recorded. From this data a wealth of information as to the identity of the parent molecule is obtainable. If desired a single indicator-timer 160 may be used. In this instance the single knob 108 (FIG. 2) actuates both valves 140 (FIG. 2a) and 81 (FIG. 2).
In a typical analysis made in accordance with the method of this invention the first switching valve 34 (FIG. 2) is placed in its second position such that the eluent from analytical column 46 is passed to vent. Suitable flow rates for the second and fourth flow streams 19 and 21 are established as previously described, i.e., high for chromatographic separation and low for pyrolysis. The temperature of the several detector ovens 60, 74 and 80, as well as the several chromatograph ovens, not separately shown, are brought up to their desired optimum operating temperatures. Assume that a one microliter sample is injected into the injection port 16 of the first flow system by a microliter syringe.
When the first chromatograph detector 42 indicates, by an increase in amplitude of the detector output signal, that the desired sample component, whose identity is to be determined, is being eluted, the first switching valve 34 is switched either manually or automatically from the second position, as illustrated by the dotted lines, to the first position as illustrated by the solid lines. The carrier gas plus separated sample component eluted from the first flow stream are passed into the delay loop 58 and the carrier gas forming the second flow stream (conduit 19) is vented. Just before the sample component to be identified is completely eluted, as denoted by the amplitude of the detector 42 output signal returning to its reference or zero level, or a corresponding peak on a recorder tracing returning to baseline, the first switching valve 34 is returned to its second position. The regulated flow of the second flow stream, isolated from that of the first flow stream, directs the flow of the sample component stored in the delay loop 58 thru the pyrolysis tube 72.
As flow through the pyrolysis tube 72 continues, the sample component is pyrolyzed and the pyrolyzate or dissociation or thermal decomposition products pass through the pyrolyzate detector 76, splitter 78, switching valve 81, sample loop 87 and vent. Variations in the amplitude of the pyrolyzate detector 76 output signal as a function of time are observed. Once the first output signal from detector 76 returns to its quiescent value or baseline, as is described more fully in the said Levy application, the six-port switching valve 81 is switched from its first to its second position, as illustrated by the dotted lines. The pyrolyzate has by now passed into the sample loop 87 flowing in one direction.
Upon switching the valve 81, carrier gas in the fourth flow stream (conduit 21), passing through the surge coil 96, flows through the sample loop 87 in the opposite direction and backflushes the pyrolyzate from the sample lOOp 87. Such backflushing generally compresses the pyrolyzate and returns it to a more compact, slug-type sample for passage through the backflush valve 98 and the analytical column 100 of the fourth flow stream (conduit 21). The surge coil 96 aids in the compression and integration of the pyrolyzate into the third flow stream. This third stream generally has a higher flow rate than the second flow stream and may be of different temperature and pressure. The surge coil 96, preferably having a volume exceeding that of the sample loop, reduces the effect of these disturbances. The extra volume provided by the surge coil 96 serves to damp out transitory flow rate fluctuations, which affect detector accuracy.
The flow through the pyrolysis tube 72 is relatively slow to insure good heat transfer to the compounds and at a low pressure so as to inhibit secondary reactions during pyrolysis. On the other hand, the flow rate in the fourth flow stream is at a relatively high flow rate. When the extra pressure of the third flow stream is applied through the sample loop 87 for the backflush operation, the surge coil 96 acts as a reservoir so as to more quickly, and with less flow disturbance, adjust the flow rate in the sample loop 87 to that desired. The dissociation products now are separated by the separating column 100 and detected by the reference side of the pyrolyzate detector 76. Backflushing of the separating column 100 may be performed as described. The operation of the third chromatograph of FIG. 2a is substantially the same and need not be separately described.
If desired, the separating column 100 may be packed with a packing capable of separating not only the small molecule decomposition products, but also the large molecules as well. In this single column operation either a single non-specific detector can be employed, or multiple detectors, one of which must be sensitive to the small molecules such as thermal conductivity detector and the second, which preferably should be a flame detector. The multiple detectors can either be in the series or in parallel. This permits the simultaneous use of small molecules for identification of the functional groups of the parent molecule, as well as the use of the larger molecules for the determination of the carbon skeleton of the parent 12 molecule in accordance with the Rice-Herzfeld theory. In this event the effluent splitter 78 and third chromatotgraph 116 may be omitted.
An alternative embodiment to the system and method just described is that illustrated in FIG. 3 in which the splitter 78 and third chromatograph 116' are eliminated and the efliuent from the surge coil 96 (FIG. 2), after passing through the six-port valve 81, and out the third port 86, is passed on to an efliuent splitter similar to effluent splitter 78. In this case, however, the split ratio may be 10:1 with 10 parts going through a small molecule separating column and the 1 part going through the large separating column. The large molecule separating column 154 may be packed as hereinbefore described. The small molecule separating column 152 may be packed with the Polypak material described hereinbefore. Silicon oil on a Teflon packing may be equally advantageously employed for the small molecule columns.
Separate programming ovens may be used for columns 152 and 154 respectively. The output of the small molecule column 152 is connected through a suitable nondestructive detector such as thermal conductivity (TC) detector 156, whereas the output from the large molecule separating column 154 is preferably connected through a flame ionization detector 158. The output of each detector 156 and 158 is passed to vent. The electrical output of the TC detector 156 is coupled to a suitable indicator and timer 104 (FIG. 2). The flame ionization detector electrical output may also be connected to an indicator such as a chart recorder. In this manner, the separation and analysis of the small as Well as the large molecules contained in decomposition products, is obtained simultaneously.
Still another alternative embodiment of the invention for obtaining a simultaneous analysis of both the small and large molecules pyrolysis products is illustrated in FIG. 4. In this embodiment, the pyrolyzate is passed from the surge coil 96 (FIG. 2) through the third valve port 86 (FIG. 2) to a second six-port, two position valve 180 (FIG. 4) which may be substantially identical in construction to the switching valve 81. The second port 174 of the valve is coupled through a suitable conduit to the small molecule separating column 152 and thence to the fifth-port 180, out the sixth port 182 to a TC detector 156 and thence to vent. The second position of the valve 170 is denoted by the dotted lines. Gas from the source 10 passes through the fourth port 178, out the third port and through the large molecule separating column 154 and detector 158 to vent.
The pyrolyzate from the sample loop 87 enters the small molecuule separating column 152, is separated into its respective components and detected by the detector 156. When the several small molecule products have been detected, and before the large molecules are given an opportunity to pass through the small molecule column 152, the switching valve 170 is switched to its second position. In this position, fiow is from the carrier gas source 10 into the fourth port 178, out the fifth port 180, and back through the small molecule column 152 in a reverse direction so as to backflush the column. This compresses the remaining large moleculesinto a compact slug and carries them into the second port 174, out of the third port 176 and through the large molecule column 154 which separates the large molecules of the pyrolyzate. These separated large molecules are detected by the detector 158 in the same manner as described.
It will be obvious that various modifications may be made in the apparatus and in the manner of operating it. It is intended to cover such modifications and changes as would occur to those skilled in the art, as far as the following claims permit and as far as consistent with the state of the prior art.
What is claimed is:
1. A method for analyzing an unknown organic material compound while having on hand for reference a.
multitude of separate control cracking patterns obtained by individually pyrolyzing a variety of chemicals under controlled conditions and in each instance passing the pyrolysis products produced from a given chemical to a chromatographic column and obtaining control cracking patterns thereby for said given chemical, said method comprising the steps of:
passing a sample of the unknown to be analyzed to a pyrolyzing chamber, pyrolyzing the sample under substantially the same conditions as were used in obtaining said control cracking patterns to obtain pyrolysis products,
passing the pyrolysis products through a splitter for dividing the pyrolysis products in to two portions by volume, simultaneously separating the most vola tile, low molecular weight pyrolysis products contained in one of said portions and the less volatile, high molecular weight pyrolysis products contained in the other of said portions in first and second chromatographic columns respectively,- and obtaining thereby first and second partial cracking patterns for said sample, and
comparing said partial cracking patterns to said control cracking patterns for identification purposes, thereby determining the kind of said sample.
2. A method according to claim 1 which includes the additional step of detecting the effluents of said first and second chromatographic columns, thereby to obtain said partial cracking patterns.
3. A method according to claim 1 wherein before the first passing step there are included the additional steps of:
passing said sample through a chromatographic separating column, thereby successively eluting components of said sample, and
selecting predetermined ones of said eluted components to be passed through said pyrolyzing chamber.
4. Apparatus for analyzing an unknown organic material compound while having on hand for reference a multitude of separate control cracking patterns obtained by individually pyrolyzing a variety of chemicals under controlled conditions and in each instance passing the pyrolysis products produced from a given chemical to a chromatographic column and obtaining a control cracking pattern thereby for said given chemical, said apparatus comprising:
a pyrolysis chamber,
means for passing a sample of the unknown to be analyzed through said pyrolysis chamber, under said controlled conditions, thereby to obtain pyrolysis products of said sample,
splitting means having an input connected to the output of said pyrolysis chamber and first and second outputs for dividing the pyrolysis products into two portions by volume,
first and second chromatographic separating columns connected to simultaneously receive the pyrolysis products from said first and second outputs of said splitting means, respectively;
said first chromatographic column being capable of separating the most volatile, low molecular weight pyrolysis products of said sample to provide a first partial cracking pattern;
/ said second chromatographic column being capable of separating the less volatile, high molecular weight pyrolysis products of said sample to provide a second partial cracking pattern;
wherein said first and second partial cracking patterns for said pyrolysis products can be related to said control patterns for determining the kind of sample.
5. The apparatus according to claim 4 which also includes detector means coupled to the output of each of said first and second chromatograph columns for providing said cracking patterns.
References Cited UNITED STATES PATENTS 3,111,835 11/1963 Jenkins. 3,236,603 2/1966 Durrett 23232 X 3,285,701 11/1966 Robertson 23-232 3,403,978 10/1968 Favre 23-232 X 3,425,807 2/1969 Levy 23-232 OTHER REFERENCES CA. 60: 12643f, (1964).
G. P. Happ et al., Anal. Chem., 36(8), 1678-1679, (1964).
JOSEPH SCOVRONEK, Primary Examiner S. MARANTZ, Assistant Examiner US. Cl. X.R.
Patent No. 3 518,059 Dated June 30 1970 Inventor(s) Eugene J. Levy It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 6, Table II, under the headin "Pyr. temp. C." the fifth item "656.0" should read 65%.5
Column 7, Table II, under the group heading "Amine (F)" the last-named formula "CH (CH )CH NH should read Column 10, line 37, after "78" insert passes line 46, "separatel arge" should read separate large SIGNED AN amen (SEAL) Attest:
Edward MFletcher, It. m
o E. W Anestmg Officer oomiasioner of Patents FORM PO-105O (\0-69) USCOMM-DC 00370-P09 U S GOVIINHKNY IHINYNG OFFICE III, OJIG-3!l -IGOOI U
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3111835 *||Nov 30, 1959||Nov 26, 1963||Core Lab Inc||Hydrocarbon gas chromatography and apparatus|
|US3236603 *||Sep 28, 1962||Feb 22, 1966||Shell Oil Co||Multiple-column gas chromatographic apparatus|
|US3285701 *||Jan 18, 1963||Nov 15, 1966||Sinclair Research Inc||Process and apparatus for separating and analyzing a fluid mixture|
|US3403978 *||Dec 14, 1964||Oct 1, 1968||Phillips Petroleum Co||Analysis of fluids|
|US3425807 *||Apr 15, 1965||Feb 4, 1969||Hewlett Packard Co||Pyrolysis system|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3584674 *||May 22, 1969||Jun 15, 1971||Fisher Scientific Co||Sample concentration apparatus|
|US3753653 *||Mar 1, 1971||Aug 21, 1973||Brieva A||Method and apparatus for gaseous-phase chemical reaction analysis|
|US3879181 *||Mar 2, 1973||Apr 22, 1975||Showa Denko Kk||Gas chromatograph, specimen capsule for use therein and process for gas chromatography|
|US3880587 *||Apr 1, 1974||Apr 29, 1975||Shell Oil Co||Method and apparatus for total analysis of hydrocarbon samples|
|US3915645 *||Apr 24, 1973||Oct 28, 1975||Us Army||Chemical reaction transducers for use with flueric gas concentration sensing systems|
|US3953171 *||Apr 22, 1974||Apr 27, 1976||Institut Francais Du Petrole, Des Carburants Et Lubrifiants||Method and apparatus for rapidly evaluating the hydrocarbon production capacity of sediments, using small samples thereof|
|US4018562 *||Oct 24, 1975||Apr 19, 1977||Antek Instruments, Inc.||Chemiluminescent nitrogen detection apparatus and method|
|US4133640 *||Feb 16, 1978||Jan 9, 1979||Gulf Oil Corporation||Chromatographic analysis apparatus|
|US4159894 *||Feb 13, 1978||Jul 3, 1979||The Boeing Company||Method for determining formulation and chemical structure of materials by improved pyrolysis gas chromatography|
|US4224279 *||Jun 8, 1978||Sep 23, 1980||The United States Of America As Represented By The Secretary Of Commerce||Reactive gas generator|
|US4234315 *||Sep 29, 1978||Nov 18, 1980||Phillips Petroleum Company||Gas chromatographic analysis method and apparatus|
|US4257772 *||May 7, 1979||Mar 24, 1981||Carlo Erba Strumentazione S.P.A.||Method and apparatus for chemical analysis of specimens|
|US4344917 *||Dec 19, 1980||Aug 17, 1982||Phillips Petroleum Company||Sample inlet for analysis instrument and method of sample analysis|
|US4357836 *||Dec 19, 1980||Nov 9, 1982||Phillips Petroleum Company||Sample injection system for chemical analyzer and method of sample analysis|
|US4359891 *||Jan 5, 1981||Nov 23, 1982||The Dow Chemical Company||Repetitive chromatographic apparatus|
|US4467038 *||Nov 30, 1981||Aug 21, 1984||Phillips Petroleum Company||Predetector reservoir for chromatographic analysis instrument|
|US4588422 *||Dec 7, 1983||May 13, 1986||Elf France||Process and equipment for sampling a gaseous effluent and their application to chromatography|
|US4650499 *||Nov 27, 1985||Mar 17, 1987||Phillips Petroleum Company||Gas chromatographic apparatus and method|
|US4843016 *||Feb 26, 1987||Jun 27, 1989||Thermedics Inc.||Detection system and method|
|US4883504 *||May 20, 1988||Nov 28, 1989||Eberhard Gerstel||Gas chromatograph|
|US4944921 *||Mar 6, 1984||Jul 31, 1990||Maxwell Laboratories||Automated PCB analyzer system|
|US5092155 *||Jul 8, 1987||Mar 3, 1992||Thermedics Inc.||High speed detection of vapors of specific compounds|
|US5092218 *||Jul 8, 1987||Mar 3, 1992||Thermedics Inc.||Selective detection of explosives vapors|
|US5092219 *||Jul 8, 1987||Mar 3, 1992||Thermedics Inc.||Selective decomposition of nitrite esters and nitramines|
|US5108705 *||Oct 3, 1990||Apr 28, 1992||Thermedics Inc.||Vapor detection with high speed gas chromatography|
|US5240604 *||Nov 25, 1992||Aug 31, 1993||The Dow Chemical Company||Multidimensional chromatographic system|
|US5268302 *||Mar 22, 1993||Dec 7, 1993||Thermedics Inc.||Selective, high speed detection of vapors with analysis of multiple GC-separated portions|
|US5338514 *||Aug 25, 1993||Aug 16, 1994||The Dow Chemical Company||Vented capillary gas chromatography apparatus|
|US5376277 *||May 28, 1993||Dec 27, 1994||The Dow Chemical Company||Multidimensional chromatographic system|
|US5492555 *||Jun 9, 1994||Feb 20, 1996||Lovelace Biomedical & Environmental Research Institute, Inc.||Automated two-dimensional interface for capillary gas chromatography|
|US5498279 *||May 13, 1994||Mar 12, 1996||Chromatofast||High speed gas chromatography system for analysis of polar organic compounds|
|US6730228||Aug 28, 2002||May 4, 2004||Symyx Technologies, Inc.||Methods and apparatus for characterization of polymers using multi-dimensional liquid chromatography with regular second-dimension sampling|
|US6855258||Aug 28, 2002||Feb 15, 2005||Symyx Technologies, Inc.||Methods for characterization of polymers using multi-dimensional liquid chromatography with parallel second-dimension sampling|
|US6866786||Aug 28, 2002||Mar 15, 2005||Symyx Technologies, Inc.||Rapid characterization of polymers|
|US6968729 *||Feb 27, 2004||Nov 29, 2005||Uop Llc||Method and apparatus for expediting analysis of samples|
|US9228984 *||Sep 11, 2012||Jan 5, 2016||Hongliang Lu||Gas chromatography-mass spectrometry method and gas chromatography-mass spectrometry apparatus therefor having a capture and release device|
|US20030070988 *||Aug 28, 2002||Apr 17, 2003||Miroslav Petro||Rapid characterization of polymers|
|US20030080062 *||Aug 28, 2002||May 1, 2003||Miroslav Petro||Methods and apparatus for characterization of polymers using multi-dimensional liquid chromatography with regular second-dimension sampling|
|US20030089663 *||Aug 28, 2002||May 15, 2003||Miroslav Petro||Methods and apparatus for characterization of polymers using multi-dimensional liquid chromatography with parallel second-dimension sampling|
|US20050257600 *||Feb 27, 2004||Nov 24, 2005||Arne Karlsson||Method and apparatus for expediting analysis of samples|
|US20130126719 *||May 23, 2013||Hongliang Lu||Gas chromatography-mass spectrometry method and gas chromatography-mass spectrometry apparatus therefor having a capture and release device|
|CN103134878A *||Jun 27, 2012||Jun 5, 2013||福建中烟工业有限责任公司||Trapping and releasing method for improving gas chromatogram center cutting technique performance|
|DE2420146A1 *||Apr 25, 1974||Nov 21, 1974||Inst Francais Du Petrole||Verfahren und vorrichtung zur schnellen ermittlung des erdoelproduktionspotentials geologischer sedimente auf der basis geringer probennahmen|
|DE3809096A1 *||Mar 18, 1988||Sep 28, 1989||Hoesch Ag||Method and apparatus for determining the specific evaporation behaviour of organic substances in thermal treatments|
|EP0051778A2 *||Oct 23, 1981||May 19, 1982||CARLO ERBA STRUMENTAZIONE S.p.A.||A device for vaporization injection in a gas-chromatographic column|
|EP0160224A2 *||Apr 2, 1985||Nov 6, 1985||International Business Machines Corporation||Multi-purpose plural-oven gas chromatography system with shared controls|
|WO1984004394A1 *||Apr 29, 1983||Nov 8, 1984||Elf France||Method and apparatus for taking a sample from a gas effluent and application to chromatography|
|WO2007021265A1 *||Aug 12, 2005||Feb 22, 2007||Akporiaye Duncan E||Method and apparatus for expediting analysis of samples|
|U.S. Classification||436/158, 422/78, 436/139, 96/104, 73/23.41, 422/89, 96/103, 95/25, 422/93, 422/80, 95/86|
|International Classification||G01N30/00, G01N30/12, G01N31/00, G01N30/10, G01N30/46|
|Cooperative Classification||G01N30/10, G01N31/00, G01N2030/125, G01N30/12, G01N30/466|
|European Classification||G01N30/46E, G01N31/00, G01N30/12|