Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.


  1. Advanced Patent Search
Publication numberUS3332316 A
Publication typeGrant
Publication dateJul 25, 1967
Filing dateApr 16, 1964
Priority dateJan 25, 1962
Publication numberUS 3332316 A, US 3332316A, US-A-3332316, US3332316 A, US3332316A
InventorsRaymond A Saunders
Original AssigneeRaymond A Saunders
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Variable space liquid microcell
US 3332316 A
Previous page
Next page
Description  (OCR text may contain errors)

1967 R. A. SAUNDERS 3,332,316


PATH LENGTH INDICATED HERE PATH LENGTH INDICATED HERE ATTORNEY United States Patent 1 Claim. or. 88-14) The invention described herein may be manufactured and used by or for the Government of the United States of America for governmental purposes without the payment of any royalties, thereon or therefor.

This application is a division of application Ser. No. 168,852, filed Jan. 25, 1962, now Patent No. 3,194,111, for Variable Space Infrared Liquid Microcell.

The present invention relates to spectroscopy in general, and more particularly, to spectroscopy of very small samples.

To obtain spectra of very small liquid samples having all absorption bands in the desired transmission range, it has been necessary up to the present time for the spectroscopist to prepare a plurality of separate fixedthickness cells before proceeding with the spectral analysis.

In processing the separate cells there has been considerable loss of the sample occuring with many filling or emptying operations. The procedure of using cells of fixed thickness requires also that there be two openings into the sample space, with filling of the sample space accomplished either by capillarity or by forcing or drawing the liquid into the cells through one of the openings by applying pressure or suction at the other. The fixed-thickness cells are made by grinding and polishing suitable alkali-halide crystalline material to produce window surfaces that are reasonably flat, parallel and transparent. Openings must be drilled through or into these windows, and the composite operation is difi'icult, expensive, and slow in completion, especially where very small, thin and fragile windows are required for the microcells.

The present invention is directed toward a liquid microcell which avoids the many disadvantages of fixed thickness cells and provides a microcell of variable space which permits the spectroscopist to obtain spectra of very small liquid samples of the order of 0.1 to microliters at any desired optical pathlength. Only one sampling operation is required with the cell of the present invention.

Accordingly, it is an object of the present invention to provide a cell for containing microliquid samples in which many optical pathlengths are provided in a single cell.

It is another object of the present invention to provide a microcell for containing liquid samples which may be filled through one filling operation and with only one opening therein.

It is a further object of the present invention to provide a microcell for liquid samples which may accommodate conveniently samples of the order of 0.1 to 10 microliters.

It is a still further object of the present invention to provide a microcell for the spectroscopic analysis of small liquid samples in which no optical finishing is required of the cells.

It is a still fur-ther object of the present invention to provide microcells for liquid samples which are inexpensive to manufacture and easy and simple to assemble.

It is a further object of the present invention to provide microcells for containing liquid samples which are filled through a single opening by syringe-like action.

Other objects and many of the attendant advantages of this invention will be readily appreciated as the same 3,332,316 Patented July 25, 1967 becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings wherein:

FIG. 1 illustrates a first embodiment of the invention.

FIG. 2 illustrates a second embodiment of the present invention.

FIG. 3 illustrates a third embodiment of the invention.

FIG. 4 illustrates a fourth embodiment of the invention.

The present invention permits a spectroscopist to obtain spectra of very small liquid samples at any desired optical path with but only one cell and a single cell-filling operation The spectroscopist can select the pathlength or pathlengths to give the optimum spectrum for the purpose desired.

FIGS. 1 and 2 are sectional views of variable space microcells, FIG. 1 showing a cell having a cylindrical sample space 26, which is formed by pressed potassium bromide windows 27 and 28, solid structural members 31 and 32, and hollow cylinder 33 preferably made of Teflon. Filling tube 30 is inserted in a hole drilled in member 31, while exterior members 34 and 35 complete the components, In FIG. 2, members 31 and 32 have been cut away in the areas indicated at 40 and 41 so that windows 27 and 28 and cylinder 33 alone form sample space 26.

The microcells of FIGS. 1 and 2 provide variable pathlengths through movement apart or together of members 34 and 35. The cell components are prepared by first pressing into openings 42 and 43 of inner members 31 and 32 potassium bromide crystals or other suitable crystals. Suificient pressure is applied to form a liquid tight seal between the crystals and the walls of openings 42 and 43, and also to form plane and parallel surfaces across the openings. Inner members 31 and 32 and outer members 34 and 35 are constructed to fit together in a press fit along surfaces 45, and tubular member 33 is constructed to fit similarly between the mating members 31 through 34 and 32 through 35. With components assembled as shown in FIGS. 1 and 2, and with windows 27 and 28 adjoining one another, a liquid introduced in filling tube 30 will be drawn into sample space 26 upon movement apart of the halves of the cell. Such movement apart provides a variable pathlength without permitting escape of fluid since the halves slide along tubular member 33 a distance limited only by the length of the tubular member. In FIG. 2, filling tube 30 passes through a portion of window 27. It will be appreciated that window 27 may be drilled or otherwise cored to accommodate filling tube 30 entirely therewithin where desired, for example, where it is necessary to avoid contact between the sample and cell members 34 and 35. Also, windows 27 and 28 in FIG. 2 may only partially fill their respective openings within the concept of this invention.

A die may be used to shape the windows, thereby providing means for rapidly forming any desired number of variable space cells. Structural members 34 and 35 are identical, as are members 31 and 32, thus requiring but three componentsincluding tube 33-for completion of each cell. The die used to shape the windows may be constructed of any of a variety of materials having sufiicient rigidity to withstand the forces involved without deforming. Positioning means should be included in a die to hold member 31 or 32 a desired distance from the plane forming the windows inner surface so that a desired thickness at 40 or 41 may be obtained. Such details in the die are conventional and therefore will not be enlarged further herein. 7

The cells illustrated in FIGS. 3 and 4 are alternate embodiments of this invention and differ from those of FIGS. 1 and 2 generally in the absence of tube 33. In FIG. 3 sleeve 50 forms the circular periphery of sample space 26 and windows 27 and 28 the planar sides. Win- 3 dow 28 is pressed within one end of sleeve 50 forming a fluid tight seal therewith, while window 27 is shaped to form a press fit within the end opposite to that of window 28. Ring 51 is attached or pressed onto window 27 to provide means both for holding and moving window 27 axially along the radiation path and for determining exteriorly the thickness of sample space 26, it being noted that members 50 and 51 contact one another at Zero thickness of the sample space. Sleeve 50 may extend axially any desired distance to form the maximum thickness of sample space desired, with window 27, of course, extended a comparable distance. Sleeve 50 may be made of a variety of materials having the rigidity necessary as Well as being nonreactive with the fluid to be examined. In FIG. 4 sleeve 54 accommodates tubular member 55 in a press fit with windows 28 and 27 enclosing the ends,

respectively, in fluid tight seals. Tabs 57 and 58 are attached to tube 55 and sleeve 54, respectively, to provide external means for determining the pathlength of sample space 26. Filling tube 30 is shown extending partly through sleeve 54 and partly through window 28, however, the filling tube may be placed in a number of positions, a determining factor being that the tube obscure as little as possible of the radiation path. The composition of sleeve 54 and tubular member 55 may be any of a number of materials having desired rigidity and nonreactiveness with the fluid or fluids to be examined. In FIG. 4 the pathlength is varied by simply sliding tubular member 55 within sleeve 54.

In each of FIGS. 3 and 4 window 28 is stationary while window 27 is movable to form the pathlength desired. These windows are formed in an appropriate testing and die assembly, or by similar means, by applying sufficient pressure to a predetermined quantity of either finely divided powder or to a single crystal of potassium bromide or NaCl or similarly formed crystalline structure. Since the windows are pressure formed in a component of the device, they require no optical finishing of any kind and are thus substantially less expensive to manufacture than conventional windows for such cells. In the embodiments of FIGS. 1 through 4 the filling of the sample space is accomplished by moving the windows apart from an initial position where they are in contact with one another. Subsequent movement apart will draw fluid into the sample space as well as increase pathlength; movement together after an initial separation will provide decreasing pathlength as well as extrusion of fluid through filling tube 30.

The invention thus provides a cell which permits a spectroscopist to obtain spectra which exhibit maximum absorption intensity for the sample quantity available and to reduce pathlength without expending sample fluid whereby pathlengths of lesser absorption intensity may be obtained. For example, with the taper cells of this invention a spectrum of liquid benzene can be obtained with all absorption bands within the useable transmission range. The cells will perform all desirable and necessary functions of conventional macro variable space cells and in addition can do this for spectral examination of very small samples, of the order of 0.1 to 25 microliters, at optical pathlengths of from zero to one mm. or greater.

Obviously many modifications and variations of the present invention are possible in the light of the above teachings. It is therefore to be understood that within the scope of the appended claim the invention may be practiced otherwise than as specifically described.

What is claimed is:

A variable space liquid microcell which permits a wide range of absorption intensity measurements while requiring a minimum quantity of fluid sample comprising:

first and second windows composed of a material transparent to radiation,

a first pair of concentrically spaced hollow cylindrical members joined together at one end thereof and supporting said first window at the other end thereof,

a tubular member fixedly positioned between said first pair of concentric members at said other end and extending beyond said first window,

a second pair of concentrically spaced hollow cylindrical members joined at one end thereof and supporting said second window at the other end thereof, said second pair of cylindrical members spaced for slidably receiving at said other end the portion of said tubular member extending beyond said first window, said first and second windows and said tubular member forming a fluid tight cavity which is enlarged or reduced by axial movement apart or together, respectively, of said first and second pairs of concentric cylindrical members, and

filling means for introducing sample fiuid into said cavity.

References Cited UNITED STATES PATENTS 2,690,695 10/1954 Coates 88--14 2,954,472 9/1960 Frenzel 25043.5 2,974,226 3/1961 Fisher 25O43.5 3,079,505 2/1963 Weir ct al. 8814 X 3,205,764 9/1965 Letter 88---l4 FOREIGN PATENTS 667,896 3/ 1952 Great Britain. 796,745 6/ 1958 Great Britain.

JEWELL H. PEDERSEN, Primary Examiner.

T. L. HUDSON, O. B. CHEW, Assistant Examiners.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2690695 *Jan 3, 1952Oct 5, 1954Perkin Elmer CorpVariable space absorption cell
US2954472 *Aug 19, 1957Sep 27, 1960Phillips Petroleum CoSample cell for radiation analyzer
US2974226 *Nov 1, 1957Mar 7, 1961Phillips Petroleum CoUltraviolet analyzer
US3079505 *Aug 26, 1960Feb 26, 1963Charles E WeirHigh-pressure optical cell
US3205764 *Sep 1, 1961Sep 14, 1965Bausch & LombAbsorption cell with removable windows
GB667896A * Title not available
GB796745A * Title not available
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3475102 *Jun 22, 1966Oct 28, 1969Smithkline CorpMeasuring assembly for spectrophotometric analyzing apparatus
US3518010 *Mar 3, 1967Jun 30, 1970Technicon CorpColorimeter
US3520517 *Oct 5, 1965Jul 14, 1970Ceskoslovenska Akademie VedThrough-flow measuring cell for photometers
US3524709 *May 24, 1966Aug 18, 1970Ceskoslovenska Akademie VedMeasuring cell for through-flow photometers
US4037109 *Nov 24, 1975Jul 19, 1977Horiba, Ltd.Sample cell
US7515259Mar 10, 2006Apr 7, 2009Dionex CorporationFlow cell for optical detector and method of forming same
US8162140Apr 6, 2007Apr 24, 20122 View, LlcSpecimen retention container
EP1102057A1 *Nov 17, 1999May 23, 2001EG & G Perkin Elmer Ltd.Sample holder for use in spectroscopic analysis
U.S. Classification356/246, 65/DIG.100, 250/343
International ClassificationG01N21/03
Cooperative ClassificationG01N21/0303, Y10S65/01
European ClassificationG01N21/03A