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1. Giới thiệuPhân tích kích hoạt gamma Prompt (PGAA) là mộtphương pháp phát triển nhanh chóng trong phân tích nguyên tố(Molnar và cộng sự, 1993, Moln Ar và Lindstrom, 1998). Nólà không phá hủy và đòi hỏi một lượng nhỏChuẩn bị mẫu. PGAA có thể được thực hiện tối ưutrên một chùm neutron có hướng dẫn cung cấp tuyệt vời, thấpđiều kiện nền cho các thí nghiệm trong chùm. Trongmặc dù điều này, bản chất của kết quả phản ứng (n. g)một nhiễu quang phổ phức tạp, và một tích lũynền liên tục do Compton tán xạ trongmáy dò. Do đó phổ PGAA cho các mẫu thựcphức tạp hơn nhiều so với quang phổ của InstruPhân tích kích hoạt neutron thần kinh (Ehmann vàVance, 1991a, b) (INAA). Các detec được sử dụng rộng rãi nhấttion cho PGAA là một Compton bị đàn ápquang phổ (Belgya, 1996), làm giảm đáng kểkích thước của liên tục và các đỉnh núi thoát hiểm.Phát hiện coincident của tia gamma (g2g coincidence) là một kỹ thuật được thành lập trong lĩnh vực hạt nhânnghiên cứu cấu trúc (Wapstra, 1979). Cũng được biết rằngcác phương pháp trùng hợp ngẫu nhiên có thể làm giảm đáng kể giao thoaence, và do đó cũng là sự phức tạp của quang phổ. Cácích lợi của kỹ thuật trùng hợp g2g trong các nguyên tốphân tích (Ehmann và Vance, 1991) đã đượcđã chứng minh trong trường hợp INAA của một sốcác tác giả (Meyer, 1987, Meyer và cộng sự, 1993, Jakubek et al,1998; Koeberl và Huber, 2000). Họ tìm thấy nóđặc biệt hữu ích trong việc xác định Ir và Se về địa chấtmẫu ở mức ppb. Mục tiêu chính của họ là để cải thiệnđộ nhạy của phương pháp bằng cách ngăn chặnnền liên tục và giảm liên tục quang phổference.Phương pháp thông thường để thực hiện sự trùng hợp ngẫu nhiên g2glà yêu cầu một mối quan hệ ngẫu nhiên với một lựa chọn đầy đủđỉnh cao năng lượng; ở đây chúng ta gọi đây là đỉnhtrùng hợp ngẫu nhiênphương pháp. Hạn chế này làm giảm phổ tớitín hiệu của các photon gamma nằm trong một thácmối quan hệ với đỉnh cao đó. Nó làm giảm nềnđáng kể, tăng tỷ lệ đỉnh điểm lên nền.Tốc độ đếm số liệu đỉnh cũng giảm, vì nó là

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Improvement of the capabilities of PGAA by coincidence

techniques

P.P Ember*, T Belgya, G.L Moln !ar

Institute of Isotope and Surface Chemistry, Chemical Research Centre, Hungarian Academy of Sciences, POB 77, H-1525 Budapest,

Hungary Received 1 July 2001; received in revised form 16 August 2001; accepted 28 August 2001

Abstract

Applicability of the g2g regional coincidence method to prompt gamma activation analysis has been examined in a series of model experiments It is shown that the requirement of coincidence with a spectral range instead of a single peak greatly improves the signal to background ratio, yet preserves the linear relationship between concentration and analytical signal The method is especially suitable for trace analysis of solutions containing hydrogen, and of matrices containing boron or other strong single g-ray emitters r 2002 Elsevier Science Ltd All rights reserved

PACS: 25.40.Lw; 81.70.Jb; 82.80.Ej; 82.80.Jp

Keywords: (n,g); E n =cold; PGAA; coincidence; spectral interference

1 Introduction

Prompt gamma activation analysis (PGAA) is a

rapidly developing method in elemental analysis

(Moln!ar et al., 1993; Moln!ar and Lindstrom, 1998) It

is non-destructive and requires a minimal amount of

sample preparation PGAA can be optimally performed

on a guided neutron beam providing excellent,

low-background conditions for in-beam experiments In

spite of this, the nature of the (n; g) reaction results in

a complicated spectral interference, and a cumulated

background continuum due to Compton scattering in

the detector Thus the PGAA spectra for real samples

are much more complex than the spectra of

Instru-mental Neutron Activation Analysis (Ehmann and

Vance, 1991a, b) (INAA) The most widely used

detec-tion instrument for PGAA is a Compton suppressed

spectrometer (Belgya, 1996), which greatly reduces the

size of the continuum and of the escape peaks

Coincident detection of gamma rays (g2g coinci-dence) is a well-established technique in nuclear structure studies (Wapstra, 1979) It is well known that coincidence methods can substantially reduce interfer-ence, and hence also the complexity of spectra The usefulness of the g2g coincidence technique in elemental analysis (Ehmann and Vance, 1991) has already been demonstrated in the case of the INAA by several authors (Meyer, 1987; Meyer et al., 1993; Jakubek et al., 1998; Koeberl and Huber, 2000) They found it especially useful in determining Ir and Se in geological samples at a ppb level Their main goal was to improve the sensitivity of the method by suppressing the continuous background and reducing spectral inter-ference

The conventional method for doing g2g coincidence

is to require a coincidence relation with a selected full-energy peak; here we call this the peak-coincidence method This constraint reduces the spectrum to the signals of those gamma photons which are in a cascade relation with that peak It lowers the background substantially, increasing the peak to background ratio The peak count rate is also reduced, since it is

*Corresponding author Fax:+36-1-392-2222/3153.

E-mail address: ember@alpha0.iki.kfki.hu (P.P Ember).

0969-8043/02/$ - see front matter r 2002 Elsevier Science Ltd All rights reserved.

PII: S 0 9 6 9 - 8 0 4 3 ( 0 1 ) 0 0 1 5 3 - 1

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proportional to the product of two full-energy peak

efficiencies A significant disadvantage is that this

method is extremely time consuming due to the low

coincidence count rate

Instead of using the peak-coincidence method, we

propose to define a coincidence relation not with a single

peak, but with a selected part of the spectrum containing

several peaks and a part of their Compton continuum to

increase the coincidence efficiency; here we call this the

g2g regional coincidence method (Ember et al., 2001)

In PGAA, a frequent problem is the presence of a few

strong g-rays emitted by the matrix Their Compton

continuum may mask the lower energy transitions of

trace elements Two of the most ‘‘problematic’’ elements

are hydrogen and boron Hydrogen is dominant in

biological samples and solutions Boron is used in heat

resistant glasses, and is also part of the neutron shielding

around the neutron guide Sometimes reactive samples

arrive, and they must be irradiated in sealed borated

glass containers, greatly increasing the background

Both elements have a monoenergetic g-spectrum with

no coincident cascades, so they may appear in

coin-cidence spectra only due to random coincoin-cidence

Recently, the possibility to eliminate the hydrogen

prompt g-ray background while increasing the signal/

noise ratio in PGAA was demonstrated (Gardner et al.,

2000) in a qualitative way

Here we compare the g2g regional coincidence

method for PGAA with the traditional singles mode

and Compton suppressed spectroscopies, demonstrating

the simplification of spectra and the increase of peak to

background ratio We also show that the coincidence

intensity is linearly related to the concentration, so the

method is quantitative and is suitable for

non-destruc-tive elemental analysis

2 Experimental work

In the measurements reported here we have studied

five different samples in three different experimental

arrangements using the same HPGe detector, at the

Budapest Research Reactor guided neutron PGAA

facility The detector had an energy resolution of

1.8 keV, and a relative efficiency of 25% Each of the

samples were measured for 13,700 s with the three

setups The neutron beam was collimated to

approxi-mately 2 cm  2 cm with an essentially constant

incom-ing neutron flux of 2  106cm 2s 1

The first arrangement is our standard setup with

Compton suppression4 In this geometry the HPGe

detector is surrounded by a BGO annulus which rejects

the unwanted Compton events, and also serves as an

active shield against background and scattered g-rays

approaching the detector The BGO shield is protected

by a massive lead passive shielding, to decrease the

number of g-rays that would hit the large volume of BGO and thereby overload the system Due to this requirement 23.5 cm is the minimum distance of the front surface of the HPGe detector from the sample The second setup is the singles mode, when the HPGe detector with no BGO annulus is placed 2 cm from the sample, thus maximising the solid angle while still maintaining some passive shielding For accumulation

of spectra in these two cases we have used a CANBERRA 8713 ADC and an S100 MCA card, with

16 K channels conversion gain

The third arrangement is a coincidence setup with two HPGe detectors Its overall performance is determined

by three factors These are the geometry, the settings of the timing electronics, and the data reduction procedure

We digitised the g-ray energy signals in 16 K channels, and the time signals in 4 K, and accumulated the events

in list mode The coincidence analysis was carried out off line This enabled us to determine the best gate conditions to improve the sensitivity The details of the electronics and the software will be described elsewhere (Ember et al., 2001)

2.1 Test samples

For the demonstration experiments we prepared a series of test samples with different concentrations The ingredients were chosen to simulate some of the difficult situations for PGAA These difficulties are usually associated with very complex spectral interference, extremely large capture cross section of a component,

or just a large amount of the matrix in the total sample

We have chosen a solution of CoCl2 and H3BO3 This sample contained two of the most problematic matrix elements for PGAA: hydrogen and boron As noted above, the main problem with this sample is the high Compton background due to the g-rays of boron and hydrogen All the intense cobalt lines and some of the low-energy chlorine peaks are situated on this back-ground Moreover, the back-scattering of hydrogen also interferes with the most intense peak of cobalt at

229 keV

All samples (S0, S1, S2, S3, S4) contained boron and hydrogen with approximately the same concentration Samples S0 and S2 had similar CoCl2mass concentra-tions, they differed only in the total mass; S0 contained

1 ml, the other four samples contained approximately 2.5 ml of solution, all in sealed Teflon containers The exact concentrations are shown in Table 1 in mass percent for each sample The last row of the table gives the sample mass in mg

In the coincidence measurement with S0, the detectors were placed at 2 cm from the sample This was the closest geometry we could achieve, thus it was used for comparison with the two conventional methods The other four samples were accurately positioned in a target

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chamber to assure the reproducibility of measurement

geometry Since this geometric precision for these four

measurements were adequate for the determination of

the count rate as a function of concentration (calibration

curve) Due to the size of the target chamber the closest

possible position for the detectors was 4.5 cm from the

sample

2.2 Experimental arrangement forg2g coincidence

As shown in Fig 1, two detectors were used for the

coincidence setup HPGe-I was mentioned above The

second detector (HPGe-II) had an energy resolution of

1.8 keV, and a relative efficiency of 15% They were

placed opposite each other and perpendicular to the neutron beam A 2 mm layer of6LiF loaded polyethy-lene protected both detectors from scattered neutrons A

1 mm thick lead plate was used to cut down the number

of X-rays, back-scattered and other low-energy gamma photons, which would only increase the dead time of the electronics The geometrical setup for the experiments with a target chamber was very similar In that case, a thin-windowed aluminium chamber was situated be-tween the detectors, surrounding the sample Lead bricks were placed around the sample and the detectors for biological and detector shielding, as shown in Fig 1 The detector signals were processed using standard electronics We will publish the details later (Ember

Table 1

Composition of the solutions, and total masses of the samples

Sample concentration (m%)

Fig 1 Experimental g2g coincidence setup with no target chamber.

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et al., 2001) The range of the time-to-amplitude

converter (TAC) was set to 200 ns, and the coincidence

resolving time was around 11.5 ns full width at half

maximum (see Fig 2)

2.3 Correction procedures

2.3.1 Random coincidence correction

Fig 2 shows a time peak with all collected events

summed up (full projection) The events of the hatched

area are considered as true coincidence events, although

there are random coincidence events among them The areas ‘‘Bkg1’’ and ‘‘Bkg2’’ selected for background, cover the same number of channels, but they consist only of random coincidence events They can be used to estimate the number of random coincidence events in the energy spectra

In this particular case, the above mentioned correc-tion does not improve the signal/noise ratio significantly Furthermore, if the coincidence experiment is performed using hardware gates instead of software gates, this correction is difficult to obtain Thus we did not apply this correction in our off-line analysis

2.3.2 Neutron flux correction The hydrogen peaks from the spectra collected

in singles mode with the second detector shown in Fig 1, were used as a neutron flux monitor The peak areas in the coincidence spectra were multiplied by the ratio of the corresponding hydrogen peak, setting the correction to unity for S1 We applied this correction only to samples S1–S4, used for obtaining the calibra-tion curve

3 Results and discussion

The spectra of sample S0, accumulated in the three different setups, are shown in Fig 3 The HPGe-I detector was at 23.5 cm from the sample in the

Fig 2 Typical time spectrum.

Fig 3 Spectra of sample S0 Thick line: ungated singles/9, medium-thick line: Compton suppressed, thin line: coincidence SE and DE denote single escape and double escape peaks, respectively.

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Compton-suppressed case but only at 2 cm in the other

two cases For easier comparison of the shapes of the

three spectra, the counts of the ungated singles spectrum

were divided by 9; thus the height of the hydrogen peak

became the same as in the Compton-suppressed

spectrum The third spectrum in the figure is a

coincidence spectrum, created by defining a coincidence

relation with every event having an energy higher than

2230 keV (just above the hydrogen peak) This region

mainly contains signals from primary and secondary

capture g-rays from the elements of interest Comparing

the singles and the Compton-suppressed spectra, we can

make the following observations

The Compton suppression reduces the hydrogen

single-escape peak to full-energy peak ratio by a factor

of 10, and reduces the double-escape peak to

unidentifi-able Due to the longer distance from the sample, the

hydrogen peak is lowered by a factor of 9 Furthermore,

the continuous Compton background is lowered by a

factor ofB100 at g-ray energies between 1 and 2 MeV However, the boron peak and its Compton background still dominate the low-energy part of the spectrum Peaks below the boron peak can hardly be seen on this background The Compton background due to boron is reduced only by a factor of 20–40, showing that the Compton suppression is very energy dependent

In comparison, the coincidence method completely removes the hydrogen peak, its Compton edge, and both

of its escape peaks The boron peak and its Compton continuum are also reduced substantially, making the low-energy g-rays much more visible

In Fig 4, the low-energy parts (under 550 keV) of the same spectra are enlarged Table 2 shows the total peak areas and their average background counts (for one channel) in cps for the two most intense cobalt peaks (229, 277 keV) and two intense chlorine peaks (518,

1164 keV) measured in the three setups for sample S1 The table also shows the signal/noise ratio calculated by

Fig 4 Spectra of sample S0 Dashed line: ungated singles/9, thin line: Compton suppressed, thick line: coincidence.

Table 2

Signal-to-noise ratio (=total peak area/average background) for the three setups with sample S1 Total peak areas and average backgrounds/channel are also given

E (keV) Peak (cps) Bkg (cps/ch) S/N Peak (cps) Bkg (cps/ch) S/N Peak (cps) Bkg (cps/ch) S/N

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dividing the peak area with the average background As

can be seen, Compton suppression gives a 1.5–2 times

better peak-to-background ratio than the ungated

singles, while the global g2g coincidence method gives

a 25–40 times better value at low energies With the

present conditions the signal/noise ratio for the highest

energy (1164 keV) is best with the Compton suppression

Fig 4 also shows that, the cobalt peak at 158 keV can

be identified only in the coincidence spectrum, where as

the background peak at 198 keV has been eliminated

completely

Fig 5 shows the calibration curve for the two

most intense peaks of cobalt at 229 keV and 277 keV

(solid curves), and for a chlorine doublet at

1164 keV (dashed curve) for comparison Data from

samples S1–S4 were used As can be seen in the figure,

the count rates increase linearly with the concentration

The calibration curves for 277 and 1164 keV peaks

go (within the 1s uncertainty) through the origin,

but the 229 keV calibration curve is only within 3s of

the origin This is because, as described earlier, the

maximum of the hydrogen back-scatter peak is

just under the 229 keV Co peak Back-scattering gives

a true coincidence between the two detectors, and

the lead shielding layers could not eliminate it

completely Changing the geometric positions of the

detectors might help with this problem For instance,

placing the detectors perpendicular to each other

and the neutron beam) instead of opposite to each

other should reduce the number of back-scattered

events The more intense 277-keV peak, which is not

affected by this problem, is therefore more suitable for

analytical work

4 Conclusions

We propose the regional g2g coincidence method

to improve the conditions of prompt gamma activat-ion analysis It improves the peak to background ratio substantially, yet the obtained calibration curve is linear, which means that the method can be used for analytical purposes over a wide range of concentra-tions This wide, dynamic range is an important advantage in those cases where both the major constituents and the trace element are to be studied The efficiency of the coincidence method can also

be improved over the efficiency of the Compton-suppression method by improving the efficiency of the second detector, thus capturing more coincidence events A trivial possibility is to use several ‘‘second’’ detectors with a higher total efficiency, in order to keep the individual detector count rate within the capability

of the electronics

We believe, it is possible to create a very accurate elemental analysis method with our coincidence ar-rangement It is clear however, that absolute measure-ments are not easy with this method Thus, it is simpler

to perform relative experiments based on standardisa-tion Also, the energy gates should be set differently for every sample composition, but once the setting is determined, then it is possible to set the energy gates electronically, simplifying the analysis by skipping the offline processing

A newly invented digital coincidence counting unit was recently introduced for 4pb–g counting (Butcher

et al., 2000), useful e.g for determining isotope activity Its use could greatly simplify the proposed regional

Fig 5 Calibration curve for the 229 keV (thick line ), 277 keV (thin line) cobalt peaks, and 1164 keV (dashed line) chlorine peak.

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coincidence method, and will enable much higher event

rates, facilitating the use of more efficient detectors

Acknowledgements

We are thankful for the help of Jesse Weil and the

continuous interest of P!al T!et!enyi during our work

References

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Koeberl, Ch., Huber, H., 2000 Optimalization of the multi-parameter g–g coincidence spectrometry for the determina-tion of iridium geological materials J Radioanal Nucl Chem 244, 655–660.

Meyer, G.J., 1987 Multiparameter coincidence spectrometry applied to the instrumental activation analysis of rocks and minerals Radioanal Nucl Chem 114, 223–230.

Meyer, G., Piccot, S., Rocchia, R., Toutain, J.P.J., 1993 Simultaneous determination of Ir and Se in K-T boundary clays and volcanic sublimates Radioanal Nucl Chem 168, 125–131.

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