GB2160398A - Electrothermal atomiser - Google Patents

Abstract

An electrothermal atomiser comprises a tubular member (1) having a dosing aperture (7) situated midway between its ends and two pairs of graphite contact members (2, 4; 3, 5). Two gas entry blocks (30, 35) are urged against the contact members (4, 5) so that a closed volume comprising the interior of the tubular member (1), apertures (15) in the contact members (4, 5) and chambers (31, 36) in the gas entry blocks (30, 35) is formed. Inlets (32, 37) for the flow of protective gas are provided in the gas entry blocks (30, 35) and in addition bleed holes (33, 38) are provided to allow escape of a portion of the protective gas as an addition to the flow through the dosing aperture (7) in the tubular member (1). The provision of the bleed holes (33, 38) enables an increased measured chemical sensitivity to be achieved when the atomiser forms part of an atomic absorption spectrophotometer. By placing the bleed holes (33, 38) opposite the inlets (32, 37) a flow of gas across the quartz windows (34, 39) is produced which reduces the deposition of vapourised sample products on the quartz windows. <IMAGE>

Description

SPECIFICATION Electrothermal atomiser The invention relates to an electrothermal atomiser for atomic spectroscopy comprising a tubular body of electrically conductive material having a dosing aperture situated substantially mid way between its ends, first means for applying an electrical potential between the ends of the tubular body, and second means for providing a flow of protective gas through the tubular body, said second means comprising first and second enclosed chambers, each having a protective gas supply inlet, which chambers open into each end of the tubular body.

Such an atomiser is disclosed in U.K. Patent No.

1461807 and shown in Figure 1 of the complete specification. It can be seen that when the gas flow is stopped, which is the normal state during atomisation, a fixed volume is formed which is closed except for the dosing aperture. This volume is filled with protective gas until it has escaped through the dosing aperture since there is no other outlet. There are advantages in causing the protective gas to flow into the ends of the tubular body and out of the dosing aperture since the central portion of the tube is at a higher temperature than the ends and the gas flow prevents or reduces the condensation of sample products on the cooler portions of the tubular body. However, a loss of sensitivity has been observed with such an atomiser.

It is an object of the invention to enable the provision of an electrothermal atomiser as set forth in the opening paragraph having an improved sensitivity.

The invention provides an electrothermal atomiser as set forth in the opening paragraph characterised in that each chamber is provided with a bleed hole through which a proportion of the protective gas may escape.

It has been found that with a given construction of electrothermal atomiserthe provision of chambers having bleed holes of the same diameter as that of the dosing aperture has doubled the sensitivity compared with that of the same atomiserwithout the bleed holes. It is believed that the reason for the reduced sensitivity when the bleed holes are not present is that as the tubular body is rapidly heated to a very high temperature (2-3000'C) the gas contained within the tubular body, and to a lesser extent that within the chambers, rapidly expands and since the dosing aperture is the only means of escape it is forced through that aperture taking with it a large proportion of the sample. Consequently by providing bleed holes in the chambers an alternative escape path for the gases is provided remote from the sample deposition area.

Provided that a sufficient flow of protective gas can be supplied it may be advantageous to increase the diameter of the bleed holes particularly if a slot is provided in the tubular body for insertion of a sampling probe. The diameter of the bleed holes is limited by the requirement for a sufficient flow of protective gas into the tubular body. It is also desirable that a proportion of the protective gas is allowed to escape through the dosing aperture andl or probe slot so that smoke and particulate matter produced during the ashing phase can be scavenged from the inside of the tubular body.

An electrothermal atomiser in which the chambers are provided with quartz windows aligned with the longitudinal axis of the tubular body may have the protective gas inlet and bleed hole formed in opposite sides of the chamber so that a flow of protective gas sweeps across the quartz window. This reduces the tendency for vapourised sample products to settle on the quartz windows cutting down the radiation able to pass through them.

The tubular body may be substantially enclosed within a graphite containment zone, an optical pyrometer being focused on the tubular body by means of a lens and a further protective gas inlet being provided for causing a flow of protective gas over the outside of the tubular body, the further protective gas inlet being arranged to cause the protective gas flow over the lens in such a manner as to minimise deposition of sample products on the lens. This enables longer periods to elapse before cleaning of the lens becomes necessary.

An embodiment of the invention will now be described, by way of example, with reference to the accompanying drawings, in which: Figure 1 shows a front elevation of an electrochemical atomiser according to the invention, Figure 2 is a cross-sectional view on line A-A of Figure 1 with the upper graphite contact member pivotted upwardly away from the lower graphite contact member, Figure 3 is a cross-sectional view on line B-B of Figure 2 with the upper and lower graphite contact members clamped together, Figure 4 is a perspective view of the lower graphite contact member, Figure 5 is a perspective view of the upper graphite contact member, Figure 6 is an end elevation of the upper graphite contact member, and Figures 7 and 8 illustrate the interaction between the upper and lower graphite contact members and the graphite tubular member.

Figures 1,2 and 3 show an electrothermal atomiser according to the invention which comprises a graphite tube 1 which, in operation, is clamped at each end between upper 2,3 and lower 4, 5 graphite contact members which also provide an enclosure 6 to contain a protective gas atmosphere when the tube 1 is to be heated to high temperatures. The enclosure 6 is not completely sealed as access is required to the tube 1 for inserting a sample into the tube via a dosing aperture 7 and also possibly to a slot 8 for entry of a probe through the wall of the tube 1, which entry may be achieved as described in U.K. Patent Application No. 8305745 (PHB32962).

Figures 4, 5 and 6 show the form of the graphite contact members 2 and 4, the members 3 and 5 being of substantially the same form but of the opposite hand. The graphite member 4 shown in a perspective view in Figure 4 is substantially Lshaped, the horizontal limb 10 having an inclined upper surface 11 in which is formed a semi-circular groove 12. The groove 12 extends from the free end of the limb 10 towards the other limb 13 of the member 4 but stops short of the junction of the two limbs. Asemi-circulargroove 14which has a smaller radius than that of the groove 12 forms an extension of the groove 12 and extends to the other limb 13 of the member 4.The radius of the groove 14 is chosen to provide good electrical contact between the graphite member 4 and the end of the graphite tube 1, while the radius of the groove 12 is chosen to provide electrical isolation and to enable easy removal and replacement of the tube 1. The length of the groove 14 is chosen to provide the required contact surface area for efficient conduction of electrical current into the tube 1. An aperture 15 is formed in the limb 13 which aperture has a diameter substantially equal to the internal diameter ofthe tube 1 at the surface 15 ofthe limb 13 and extends through the limb 13 in the form of a truncated cone with a mimimum diameter at the surface 16. A further semi-circular groove 17 extends radially into the groove 12 adjacent to the free end of the limb 10.

A perspective view of the graphite contact member 2 is shown in Figure 5 and an end elevation is shown in Figure 6. The member 2 comprises a rectangular block having an inclined lower face 20 in which a semi-circular groove 21 is formed, the groove 21 having the same length and diameter as the groove 12 in the member 2. A further semicircular groove 22 having the same length and diameter as the groove 14 in the member 4 is formed between the end of the groove 12 and the hidden face of the member 2. An inverted L-shaped portion 23 extends from the upper surface 24 of the member 2. The groove 21 extends from an end which comprises two parallel faces 25, 26 separated by a step 27.

Returning to Figures 1 to 3, the graphite contact members 4 and 5 are mounted on copper electrodes 46 and 47 which are separated by a block 48 of electrically insulating material having an upstanding rib 49 to prevent the graphite members 4 and 5 making electrical contact with each other. A clearance gap between the rib 49 and the graphite members 46 and 47 normally exists when the tubular body 1 is inserted between the members 46 and 47 to ensure that sealing of the end of the body 1 onto the members 46 and 47 can occur. The upper surfaces of the copper electrodes 46 and 47 are a ground finish and are maintained in the same plane to the best tolerance obtainable commercially to ensure the best possible electrical contract.The graphite contact members 4 and 5 together with the members 2 and 3 cover the copper electrodes to protect them from corrosive products from the sample, provide a seating and good electrical contact between the graphite tube 1 and the electrodes 46 and 47, and provide a means for introducing protective gas into the interior of the graphite tube 1.

A first gas entry block 30 is lightly sealed against the graphite contact member4 and comprises a chamber 31 which is open to the aperture 15 in the graphite contact member 4 and which is provided with a gas inlet aperture 32, a bleed hole 33 and a quartz window 34. A second gas entry block 35 is lightly sealed against the graphite contact member 5 and comprises a chamber 36 which is open to the aperture 15 in the graphite contact member 5 and which is provided with a gas inlet aperture 37, a bleed hole 38 and a quartz window 39.

Thus an optical path is provided from the quartz window 34 via the chamber 31, aperture 15 in a graphite contact member 4, the interior of the graphite tubular member 1, aperture 15 in graphite contact member 5, and chamber 36 to the quartz window 39. Further when the protective gas flow is stopped a volume is formed which has outlets via the bleed holes 33 and 38 and via the central dosing aperture 7 in the tubular member 1. The aperture 7 is that normally provided for inserting a sample to be atomised into the tubular member 1. If the sample is to be introduced into the tubular member 1 on a probe there may also be a further aperture (in the form of a longitudinally extending slot 8) in the tubular member 1.

The assembly of the gas entry blocks 30,35, graphite contact members 4,5 and graphite tubular member is located between a stop 41 mounted on the electrode 46 and a leaf spring 42 mounted on the electrode 47. The electrodes 46 and 47 and insulating block 48 are bolted together to form a rigid assembly.

As can be seen from Figure 2 which is a crosssection on line A-A of Figure 1 the upper graphite contact members 2,3 are carried by copper bars 50, 51 whose other ends are pivotted on a shaft 52 mounted on end members, one of which is shown referenced 53. The upper graphite contact member 3 is shown in its raised position in Figure 2, in which position the graphite tubular member 1 is accessibie for removal or replacement. The insulating block 48 carries a temperature sensing arrangement for measuring the temperature of the tubular member 60 in which a lens 61 is mounted, the lens 61 focusing radiation emitted by the tubular member 1 onto the end of an optical fiber 62. The other end of the optical 62 illuminates an optical pyrometer to measure the temperature of the tubular member 1.

The tubular member 60 is mounted with a further tubular member 63 in the insulating block 48 the furthertubular member 63 being open at both ends and having an aperture 64 in its wall, the aperture 64 communicating with a passageway 65 in the insulating block 48. A plate 66 of ceramic material is inset into the block 48 under the graphite contact members 4 and 5 so that the material of the insulating block 48 is shielded from the high temperatures reached by the tubular member 1. The ceramic plate 66 has an aperture 67 which is aligned with the grooves 17 in the graphite contact members 4, 5 to enable radiation from the tubular member 1 to pass to the lens 61.Protective gas is fed via the passageway 65 and aperture 64 to an annular chamber 68 formed between the tubular members 60 and 63 and subsequently over the lens 61 and through the aperture 67 along a channel formed by the grooves 17 in the graphite contact members 4 and 5 and round the outside of the graphite tubular member 1.

In operation a sample is deposited into the tubular member 1 through the dosing aperture 7. The temperature of the tubular member 1 is then raised to dry the sample and possibly raised still further to ash the sample depending on the composition of the sample. The drying and ashing stages may be carried out with either a flow of air or of protective gas through inlet apertures 32 and 37 and passageway 65 depending on the nature of the sample. In all cases before the temperature of the tubular body 1 is raised to the atomisation temperature a flow of protective gas is produced so that the tubular body contains and is surrounded by a protective gas. It is usual to stop the gas flow to the interior of the tubular body 1 during the atomisation phase. It has been found that if the bleed holes 33 and 38 are not present in the atomiser shown the measured chemical sensitivity is reduced.It is believed that the explanation for this phenomenon is that when the temperature of the tubular member 1 is rapidly increased the gas contained in the volume formed by the chambers 31,36, apertures 15 and the tubular body 1 expands and is forced out of the dosing aperture 7 carrying with it part of the sample. By providing an alternative escape path for the expanding gases by means of the bleed holes 33 and 38 the escape of the expanding protective gas through the dosing aperture may be substantially reduced with a corresponding reduction in the loss of sample. With the bleed holes having a diameter substantially equal to that of the dosing aperture a doubling of sensitivity has been achieved. Clearly as the diameter of the bleed holes is increased so the proportion of the gases escaping through the dosing aperture is decreased.However, there is a limit to the diameter of the bleed holes since it must be possible to fill the interior of the tubular body 1, and it is also desirable to have some scavenging action to carry away components produced during the ashing phase.

With the atomiser described access to the tubular graphite member 1 is facilitated by the horizontal split between the graphite contact members 2 and 4 and 3 and 5 since when the upper members 2 and 3 are pivotted upwardly the graphite tubular member 1 is retained between the faces 16 of the lower members 4 and 5 in the grooves 14. The tubular member 1 may then be easily removed and replaced and the orientation ofthe dosing aperture 7 and probe entry aperture, if provided, adjusted. The light pressure on the ends of the tubular member 1 caused by the leaf spring 42 may be mechanically relieved before removal of the tubular member if desired. This arrangement also has the advantage that the graphite contact members 4 and 5 may be easily removable since when the members 2 and 3 are pivotted upwardly no pressure is applied to the contact members 4 and 5.In practice the members 4 and 5 may be loosely fitted on the electrodes 46 and 47, for example by means of spring clips, the clamping force produced by the lowering of the upper graphite contact members 2 and 3 being sufficient to produce a good electrical connection.

Figures 7 and 8 illustrate how electrical contact between the ends of the tubular member 1 and the graphite contact members 2 and 4 and 3 and 5 is obtained. Each end of the tubular member 1 is located between respective upper and lower graphite contact members 2,4 and 3,5. The upper and lower graphite members are clamped together with a force which is sufficient to flex the ends of the tubular body 1 so that its external surface conforms to the internal surface of the grooves 14 and 22 in the graphite contact members. This is illustrated in Figures 7 and 8 where the cross-section of the tubular member 1 is shown before and after application of clamping force, respectively.It can be seen from Figure 8 that after application of the clamping force the area of the tubular member 1 in contact with the graphite contact members has been substantially increased thus giving a better electrical connection. The tubular member 1 is normally made from graphite as this material has the necessary chemical and physical properties but the use of other materials, for example the refractory metals, is possible in some circumstances. Typical dimensions for the tubular member 1 when made from electrographite are 5 mm bore with 600 pm wall thickness. When made totally from pyrolytic graphite the wall thickness may be reduced to about 300 pm. These dimensions are purely exemplary and may be changed, for example when using probe sampling.It has been found convenient to make the external diameter of the tubular member 1 and the diameter of the grooves 14 and 22 such that a tubular member at the high end of the manufacturing tolerance has a diameter equal to the diameter of a groove 14, 22 at the low end of its manufacturing tolerance. A clamping force of from 4 to 5 Kg between the graphite contact members at each end, i.e. a total clamping force of 8 to 10 Kg on the tubular member, has been found to produce a good electrical connection for tubular members having the dimensions given herein when the contact area extends over a 2 mm length of the tube.

In order to produce a desired clamping force between the graphite contact members 2 and 4 and 3 and 5 a mechanism which either pulls down the copper bars 50, 51 from underneath or pushes down the copper bars from on top is required. The design of such mechanisms is well known to those skilled in the art.

Claims (7)

1. An electrochemical atomiser for atomic spectroscopy comprising a tubular body of electrically conductive material having a dosing aperture situated substantially midway between its ends, first means for applying an electrical potential between the ends of the tubular body, and second means for providing a flow of protective gas through the tubular body, said second means comprising first and second enclosed chambers, each having a protective gas supply inlet, which chambers open into each end of the tubular body characterised in that each chamber is provided with a bleed hole through which a proportion of the protective gas may escape.

2. An electrothermal atomiser as claimed in Claim 1, characterised in that the diameter of the bleed holes is substantially equal to that of the dosing aperture.

3. An electrothermal atomiser as claimed in Claim 1, characterised in that the diameter of the bleed holes is greater than that of the dosing aperture.

4. An electrothermal atomiser as claimed in Claim 3, characterised in that a slot is formed in the wall of the tubular body to enable a probe to be inserted into the interior of the tubular body.

5. An electrothermal atomiser as claimed in any preceding claim in which the chambers are provided with quartz windows aligned with the longitudinal axis of the tubular body and the protective gas inlet and bleed hole are formed in opposite sides of the chamber so that a flow of protective gas sweeps across the quartz windows.

6. An electrochemical atomiser as claimed in any preceding claim in which the tubular body is substantially enclosed within a graphite containment zone, an optical pyrometer is focused on the tubular body by means of a lens, and a further protective gas inlet is provided for causing a flow of protective gas over the outside of the tubular body, the further protective gas inlet being arranged to cause the protective gas to flow over the lens in such a manner as to minimise the deposition of sample products on the lens.

7. An electrothermal atomiser for atomic spectroscopy substantially as described herein with reference to the accompanying drawings.