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Patent 2131784 Summary

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Claims and Abstract availability

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(12) Patent Application: (11) CA 2131784
(54) English Title: PARTICLE ANALYSIS AND SORTING
(54) French Title: ANALYSE DE PARTICULES ET TRI
Status: Deemed Abandoned and Beyond the Period of Reinstatement - Pending Response to Notice of Disregarded Communication
Bibliographic Data
(51) International Patent Classification (IPC):
  • G01N 23/222 (2006.01)
(72) Inventors :
  • TAPPER, ULF ANDERS STAFFAN (South Africa)
  • GUZEK, JACEK (South Africa)
(73) Owners :
  • DE BEERS INDUSTRIAL DIAMOND DIVISION (PROPRIETARY) LIMITED
(71) Applicants :
  • DE BEERS INDUSTRIAL DIAMOND DIVISION (PROPRIETARY) LIMITED (South Africa)
(74) Agent: GOWLING WLG (CANADA) LLP
(74) Associate agent:
(45) Issued:
(22) Filed Date: 1994-09-09
(41) Open to Public Inspection: 1995-03-10
Examination requested: 2001-04-05
Availability of licence: N/A
Dedicated to the Public: N/A
(25) Language of filing: English

Patent Cooperation Treaty (PCT): No

(30) Application Priority Data:
Application No. Country/Territory Date
93/6657 (South Africa) 1993-09-09

Abstracts

English Abstract


ABSTRACT
The invention relates to a method and apparatus for analysing samples
for the presence of a particular element or isotope. In the method a
pulsed neutron beam is directed at the sample. The beam is at an energy
level chosen for the neutrons to interact with the element or isotope and
produce a detectable gamma spectrum. A gamma detector detects the
neutron-induced gamma spectrum. The detector is time-gated in such a
manner that neutron-induced gamma radiation is detected while
neutrons scattered by the sample are at least substantially excluded.
Analysis of the spectrum enables a determination to be made as to
whether a spectral peak characteristic of the particular element or
isotope is present. The invention also provides apparatus for carrying out
the method.


Claims

Note: Claims are shown in the official language in which they were submitted.


- 12 -
THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1.
A method of analysing a sample for the presence therein of a particular
element or isotope, the method comprising the steps of:
- directing at the sample a pulsed neutron beam at an energy level
chosen for the neutrons to interact with the element or isotope
and produce a detectable table gamma spectrum.
- detecting the neutron-induced gamma spectrum by means of
gamma detection apparatus which is time-gated in such a manner
that neutron-induced gamma radiation is detected while neutrons
scattered by the sample are at least substantially excluded, and
- determining whether a spectral peak characteristic of the
particular element or isotope is present in the gamma spectrum.
2.
A method according to claim 1 wherein the neutron beam is mono-
energetic or with a well-defined energy level.
3.
A method according to claim 1 wherein the neutron-induced gamma
spectrum is detected by a gamma detector which is shielded from the
pulsed neutron beam.

- 13 -
4.
A method according to claim 1 wherein the pulsed neutron beam is
produced by accelerating a pulsed particle beam and directing at a
deuterium gas target.
5.
A method according to claim 4 wherein the neutron beam is pulsed in
nanosecond bursts.
6.
A method according to claim 4 when used to detect the presence in a
sample of carbon-12.
7.
A method according to claim 6 when used to detect the presence of
diamond in a kimberlite sample.
8.
A method according to claim 7 wherein the neutron beam has an energy
level in the range 4MeV to 10MeV.

- 14 -
9.
A method according to claim 8 wherein the neutron beam has an energy
level in the range 6MeV to 8MeV.
10.
A method according to claim 9 wherein the neutron beam has an energy
level of about 6,3MeV.
11.
A method according to any one of claim 1 when used to detect carbon
and/or oxygen in steel samples.
12.
A method of sorting particles comprising the steps of:
- analysing each particle for the presence therein of a particular
element or isotope, the analysis comprising the steps of:
- directing at each particle a pulsed neutron beam at an
energy level chosen for the neutrous to interact with the
element or isotope and produce a detectable gamma
spectrum,

- detecting the neutron-induced gamma spectrum by means
of gamma detection apparatus which is time-gated in such
a manner that neutron-induced gamma radiation is
detected while neutrons scattered by the sample are at
least substantially excluded, and
- determining whether a spectral peak characteristic of the
particular element or isotope is present in the gamma
spectrum; and
- separating from other particles those particles for which the
detected gamma spectrum is indicative of the presence of a
particular element or isotope.
13.
Apparatus for analysing a sample for the presence therein of a particular
element or isotope, the apparatus comprising:
- a neutron source for directing at the sample a pulsed neutron
beam at an energy level chosen for the neutrons to interact with
the element or isotope and produce a detectable gamma
spectrum,
- detection means for detecting the neutron-induced gamma
spectrum, the detection means being time-gated in such a manner
that neutron-induced gamma radiation is detected while neutrons
scattered by the sample are at least substantially excluded, and

- 16 -
- means for determining whether a spectral peak characteristic of
the particular element or isotope is present in the detected
gamma spectrum.
14.
Apparatus according to claim 13 wherein the neutron source is adapted
to produce a neutron beam which is mono-energetic or with a well-
defined energy level.
15.
Apparatus according to claim 14 wherein the neutron-induced gamma
spectrum is detected by a gamma detector shielded from the pulsed
neutron beam.
16.
Apparatus according to claim 15 wherein the detection means comprises
a germanium gamma detector.
17.
Apparatus according to claim 13 wherein the neutron source comprises
means for accelerating a pulsed particle beam and directing it at a
deuterium gas target.

- 17 -
18.
Apparatus according to claim 17 wherein the neutron source is adapted
to produce a neutron beam pulsed in nanosecond bursts.
19.
Apparatus according to claim 17 when used to detect the presence in a
sample of carbon.
20.
Apparatus according to claim 19 when used to detect the presence of
diamond in a kimberlite sample.
21.
Apparatus according to claim 20 wherein the neutron source is adapted
to produce a neutron beam having an energy level in the range 4MeV
to 10MeV.
22.
Apparatus according to claim 21 wherein the neutron source adapted
to produce a neutron beam having an energy level in the range 6MeV
to 8MeV.

- 18 -
23.
Apparatus according to claim 22 wherein the neutron source is adapted
to produce a neutron beam having an energy level of about 6,3MeV.
24.
A method according to claim 13 when used to detect carom and/or
oxygen in steel samples.
25.
A particle sorting apparatus comprising:
- apparatus for analysing each particle for the presence therein of
a particular element or isotope, the analysing apparatus
comprising:
- a neutron source for directing at each particle a pulsed
neutron beam at an energy level chosen for the neutrons
to interact with the element or isotope and produce a
detectable gamma spectrum,
- detection means for detecting the neutron-induced gamma
spectrum, the detection means beam time-gate such a
manner that neutron-induced gamma radiation is detected
while neutrons scattered by the sample are at least
substantially excluded, and

- 19 -
- means for determining whether a spectral peak
characteristic of the particular element or isotope is
present in the detected gamma spectrum; and
- means for separating from other particles those particles for
which the detected gamma spectrum is indicative of the presence
of a particular element or isotope.

Description

Note: Descriptions are shown in the official language in which they were submitted.


U8~U~ 5Ull &81}~û gp~lJR ~ FlSHLR '~lUli~
~ r~
- 2 -
~ ~V~ON
TE~IS ilIve3~tioll r~l~tes to parucle an~lysis ~d sor~g
~el;~on acdqation allalysis is a well~ wn technique ill whi~h, typical~,
a s~nple ~Jf a ~ew ~niIligrams m~cs is subjected ro a hi,l~b flux or intensity
of ~ermal or low ener~- neu~ons fro~n a nuclca~ T~to}. Ihc
radioac~ve sample is ~en ~ansportcd to a mc:as~ement station where
a ga~una emiss~o~ ~cLl~ is collected. Each ~vate~ ~sotope m the
sample gr~es one or more peilks in ~e spectrum, fi:om whi~ ~he
elcmelltal concentr~tions present ~ lhe sample can ~e determ~ed
By way of ex~le, US pat~nt ~,340,443 to Clayton et al di~closes a
tec~ e fo~ dete~n~n~ng tbe g~ld conterlt a~ allrif.erous ro~ic sampl~s.
In the ~anique, the 5~ le is bon.bardcd w~1;h nentrons a~d there~er
the i~tensiy of tbe cmit ed gamma spectrum at an eIler~y level of
279keV is delermi~d to give a me~sure of the gold concen~ n in the
: :
.,
.r i.~ ,g~ ~ggg~g~ V~g ~ r-~

a ~ S ~ a a Sl~l~OR & F' ' Si~ER _ __ _~
.. i ~J i. ~' i3 ~
- 3 -
It is ~mown ~ gamma rays call ~ ernitted prompt3y by carbo4 nuclei
irrddia~d wi~h ~eutror~s either ~hen ~he neutron~ a~e captured in the
~bo~ dei or when hi~ ener~y, typic~l~y greater thall 4~5MeV,
neutrons are i:~ela~cally scattered at the nuclci In this re~ard, ~outh
A~ica~l patem ~/6868 dis~loses the use of hi~h ene~y neutron
bomba~dmenl ~o~ the co4rinuous on-llrle evaluation of the q~ty of
b~ c coal samples. ~he paten~ discloses the use o~ compo~, te sau~ ion
detectors, ie. detector:~ ~ade up of a phlrAli~y of s~ llators t~ detect
primary a~d related secondary events. However because thc typc of
analys~s disclosed in the patent operates at a low lcvcl of sensitiv~ty~
application ~s probably l~mited ~o evaluation o~ ~al samples w~ere ~ere
3 Is a m~b carbon contellt, typi~:al1y greater tban 505~. It is believed tha~
it would be un~itable for a~ly~is of, say, diarnol~d content i~
l~n~erli~ ores l~e~u;lse of the low G3~00n~dlamond coIItent of t~e
san~le.
. ..
Added to ~s~ a problem encountered ~ll thc prior art techniques is that
of isolat~ng ~e ch3~acteristic ~cc~um of a paI ticular element or i~otope
~om the back~round ~lo~se~ at least part of whi~h is produced by
nehtrons scattered by ~e sall~le und~r ~ ;is.
=~_ ' .
Acco~g to a ~r~t aspect of the înve~tion ~here is pravided a me~hod
of aDalysin~ a samyle for the pr~sence therein of a particlllar element
or isotope, the method comprising the steps o
.
: ~:
::
,
:
.
..

ll~,'O~ P~ SPi:)~Ji~ ~ ~ ISilLk
~ A ~
-- 4 --
- d~re~ting a~ ~:he s~mple a pulsed neu~on beam ~t an energy level
c~osen for the neutro~s to interact wit~ the element or 3sotope
a;ud produc~ a detectabie gamma spectrum,
- detec~ng t~e neu~ro~a-induced gam~a spectmm by n~eallS of
gam~nR detection appara~s wl,ich is ~ne~tcd in such a m~er
that neu~on-inducca gamn~a radiation is detected wh~e nentrolls
scattered by the sa~ple are al leasc substaDtia~ly exe]udcd~ and
- determint~ whether a spectr~l pea~c cbaracteristic of the
particular elemellt or isotope is prese~t in thc g~mm~ spectrum.
A~ord~g to a seeo~d a~ect of thc i~ven~o l, there is p~ovided
appa~tus for ana~ a sample ~or the presence therein of a par~
ele-n~r~ or ~sorope, the ap~a.~dt~s compnsmg
- a neutron solLr~e for direc~ at the sample a pulsed neutron
be~ at ~n ener~ level c~osen for the ncutrons to i4leract wi~
t~e e~r~er~t or ~otope ~d produce a detectable ga~ma
- dete:c~on ~ne~ or de~ecting ^.be neul:ron-indnced g~mma
spec~ the detecti~m ~eans being t~me-gated in s~lch a r~nner
~ eutroll-mduced ~mrn~ ~ad~ation is detected while neU~o~s
sc:attered by the sa~plc are al lcast subsrantially excl~ded~ aud
.~

U~ 5 '~`~ `lY~ SP~ `lSilE~ JU
,~ ~ ;J i i (~ 'J
- 5 -
- me~s for ~eterm~g whether a spe~ral pea~ charae~er ~c of
the pa;~cu~ar- clemer~ or isotope is presem irl tbe gamm~
spec~um.
T~e neu~on ~e~ îs prefer~bly mo~o-energetic or at lea~t ~as a well-
de~ned ener~y ]~vcl. C~ne ~pplic~tioll oi tbe n:~ethod a~d apparanls of
~Pe inveD~on is ~n the a~ysis of l~m~erli~e samples for the pr~sence of
car~o~ dlc~ti~re of a d~ 0nà mclusio~ e sa~ple. ~ this case,
the neu~on beam m~y have arl en~rgy level i~L the range 4Me~ to
lO~e.V, preferably 6MeV to ~Me~ mo~ pre~erably about 6,3MeV.
The nlet~od ~d appar~n~s of the ~ention ~y fo~ par~ of a p~icle
so~ ,ystem i~ wh~ch par~cles are allalysed or~-linc; and partic~e~, for
wh~ch the ga~:~la spc~ i:~lcludes a spec~ral pealc characteris~c of the
partlc~l~r ~leme~t or isotope are se.parated f~on:~ othe~ pa~ticles.
BRIEF I~CRII~WZNGS
l~e i~Ven~aOL will now be descn~ed in mo~ detail~ by wa~ of exa~ple
o~ly, wi~ refere}lce tO t~e accoTnpallyrng drawings"sl which~
Fl~re 1 L~a~atically illustrates the princi~ ; o~ ~}e
. in~e~ltion;
ESg~e 2 di~g~Dmalicallyi ustratesclecllonic~mpos~en~y
used in the im~le~e~ on oft~e inven~or~ d
,

O~ 16 :16 ~u l l ~ 8 .SPOOR B~ FISHER 4~' U~
. ~ J.i. i '; -~
- G -
s 3a and 3b
show gamma spec~a obtamed fo.r a kim~erlite
samp~e with a 175% cari~on content b~ ~ss.
~PECIFI~ DE~scR~ o?~
Re~elIill~, ~o Figure 1, a neutron ~n 10 is dile~ed ~om a source 12
onto a ~imberlite sample 14 whicb is to bc analy~cd for thc presen~e of
di~smond l~e neutron b--~m is produced by ~ccelera4ll~ a pulsed
particle beam and d~rec~n~ it at a deuterium gas target, thereby causing
deuteron~ienterorL reaf~tions irl the ta~OeL This gives rise to a pulsed
neutron beanL Tbe particle bea~n m~y, for InsT~ce, be accelera~ed usi~g
a r~ uency quadrupole (RFQ) accelera~or
`: :
~ plas;tice, it i~ desilable for the neutron be~L LO be pulsed in
}~ d ~ a~d ~or ~e n~utro~ls to b~ fast, mon{~energe~c
~eutroDs with a hi~;h energy level ~ypically in the r~nge 4MeY lo lOMeV
and mosl prefe~bly in tbe range 6MeV to 8MeY A gas targe~, such a~
the deuten~u ~s ta~get meIltioned above, is co~s~dered preferable to
a sol~d tar~et in the produc~ion of a neutron bcam w~th these
char~Lcteristics~ The use o~ a de~lteron~euteron reac~on in a gas wget
provides a mon~nerg~c neutron beam tha~ can be m~t~hed to gLve a
high level of se~ y for ~e cha~acteris~c peak of t}~e ele~ent or
~sotope of interest. Irl the presenr case, where rhe Isotop~ o~ int~resr i~
~oll-12, rese~cb by tbe i~velltors indicates t~at tbe appropriate
eut~on be~n ener~ level is ~bout ~,3Me~.
: ~
.
, . .. ,. .... ~

u& ~ 16 ~~ U~ JUK ~ IU~
The incident llentrons pene~ e the k~berlite sal3~ple 14 and iIlteract
with ~he nuclei of ca.-bon atoms in a~y diamona p~ides I the sarnple.
A hi~h pL~rity ~ermanium gamma delec~or 18, shielde~ ~om receivillg
dire~ r~ ion from the soulce 12 by ~ neutron shield æ. receiq~
~amma radiation 20 emitted by ~he sample 14 and forms a spec~n~n
~om ~he radiation rece*ed wit~Jin a predetermiued time arltelval. The
~pe~um, ~lusb~ated ~iagrarnmatically at 24 in Fi~ure 1, is aDalysed by
a cor~u~ (not shown) which compa~s it with standar~ data to
det~ine whether the spe~unl Is ~ndicat~ve of the presence of carbon-
12, in turn irldi~ive of diamo~ld, in the saulple.
If one or more diamond parucles are present i" the kimb~rlite sample,
a chalacteristic pealc w~l be obser~,ed in the dete~ed gs~Tnma spec~
at the a~propriate energy level eor carbo~-~ Le 4,43MeV The spectral
pea}; ~ supernnposed on a p,ellera~ bac3;g~owld attr~ ulable at least
partially to aeu~ron~ ffered by t~e s~mple 14 whieh reach and interact
with th~ g~nma dete~tor 18. The background spectrum detected ~3y -the
dete~tor 18 may he such as to immerse t:he charactens~c carbon-12 pe~c
i~di~ve of diamon~
'rO reduce the effe~: of backgroLmd radiation in the detected spec~um.
relia~oe ~s p~aced u:pon the differeDt speed~ at ~vhich ~eu~o~ and
gamn:~a ra~a~ion travel from ~he sample to ~he detector. Ga~nma
r~on ~ravels at the speed of li~ht ~om the sample to the delector
w~e neutron~ scar[ered by ~he sa~ple ~owards the detector travel
somewhat slower. For e~amplc, thc timc dclay ovcr a distauce of lm for
~mm~ r~dia~o~ and ~eutro~s at an crler~y of 6,~M~V is a~ut 30
r~ds. i.e. 30 x 10-9s.

I!~ U~1 1~ I 1; :1; '~(I I I S~ uh o. t I .S H~. K 1~1 1.11I) '
8 _ ,
i.
In accorda~ce ~ith ~h~ Inve~ltio~ Xin, use o~ fast ele~tror.ie
pro~essing apparatr~ te gam~ta deLee~ioll sy~ter~ me-~ted ~o ~at
the detector is cnabled du~ the ti,~e peri~d that ne~ron-induc~d
gamma rays re~cb. the detector, alid the~ disable~d by tht time the
~ca~tered neu~ons amve. In ~his way, ba~kground noise at~uta~le to
stray nwtrons sc~tered by the san~le 14 can ~e elin~a~e~, or at least
redu ;eL Fgure 12 dia~atically ~ 3strate~ tbe electro~c
compo~e~y used lo achieve the rlece~v time~ting,
Refer}ing to Fig~ a portion 30 of ~he sign31 produced by the
~e~u~ dctcctor 18 ~s direc~ed via a sig~l amplifier 34 to a lin~3~r
gate ~retc~er 48. 'rhe remaindcr 38 of the signal is dLrected ~om ~c
detector 18 to a ~imin~ filter a~plifier 40 which in tun~ feeds the signal
tG a ~t frdction delay u~i. 4~ '~he unit 4, applies a time delay 44
tO the s~ l wherea~er the ~ignal is fed to a t~e to pulse hei~t
corsvert~ 4~.
A~ the same timet a beal:n pick~of~ signal 50 is ini~ated by a beam pi~-
off uni~ 5Z which ~irects the 9gllZ.1 to a tirning fi~ter a~npl~fier 54. The
ampl~fier ~4 feeds the signal to th~ ~me to pulse height converter 46. I~
~sse~e, ~e be~m p~ ff ~gnal Sta}lS a ciock which controls a ~me
ate. The cor~verted signal controls lhe l~ear ~d~e stretche~ 4~, openinO
~he ~me gaIc for admission of an amplified spe~,~osoopv si ,nal 37 fro~
the am~fier 34 to a mul~ch~el analyser 36.
Thus p~lses from the amplifier 34 will oDly be registeI~ed by the
~ltichan~el analyser i~ ~hey ~ppear inside ~e relevant, predetermined
timo pe ~od,
... _ _ ______ ...... , .. ,_.. ,,,, ... _ ~
.' ~-
.

'J11 t~ J'd S~'IJi~K ~ I!LK 4~iU11
- ~ ? ,! ~ .
~ ~ ~ .J .L
_ g _
Exper~menta~ion by the inventor~ indicates that the time~at~ng
techr~q~e de~nrbed above bas the e~ect of Sllpp:le55illg the baekgrouDd
radiation or naise l~is is i~ s~ated by a oompa~r~so~ of Figuresi 3a a~d
3b i~ wbi~h logarithmie count ~cquen~y is plot~ed on the ver~ic~ ax:is
ag~irst ~h~el valu~s represen~alive of energy level o~ tbe ho~i70ntal
a~is. Figure 3a ~lustrates a gamma spectrum in which no time-gating bas
been employeLi Tbe 4,43MeV peak 60, inidicatIve of the priesence in the
l~mberlite sa~ple of i~rbon-~2 and hence d~nond, ~s m~sked to a large
d~ree in the b~:kgrol}~d r.oise. Figure 3b illus~rates a corresponrling
gamma sipec~ obt~ ed usirl~ timc~ated detec~on a~paranLs as
d~bed. In t s case, a clear spec~l peak 62 is discermble a~ the
cha~ac1el~sbc 4,43MeV ~r~y level of carbon-12, ~lear1y showing the
suppfession of back~ouIId r~oise that is attri~table to ~me-v,a~g.
Ref~ g again to F~re 1 it wil1 be lloted that the gamma delector 18
i~ positio~ at a }eversc a~gle relative to the incident nelltron 1~ 10.
It is belie~ed ~at ~is geomel!y wflI give nse to an optima! si~nal to
~ois~ ratio. The sha~e and alTan~ement o~ the neutroll shield .Z2
Figure 1 are slso considered ~o be impo~an~ fearures, in that the shield
shotlld prevent a~y direct passage of the neutron beam 10 ~om abe
~ource 12 to the detector 18.
At t~e s~me time, as ~uy neutrons as posslb1e ~hat ale scattered l~y the
sam~le 14 shonld be divert~ away from the detector rather d~an
towards the de~ecr~r. For ~ese reasons, the shield 2~ h~s the illus~ted
~iangllar cross section and the apex 80 ~d3ereof does llot extend
fc~wardly i~o the field of v~ew of the dct~tor where it might d~vert
neutrons u~wards the detector.
.'

I)~ U~ U 5~'0(11~ & I:lS~ '4'1UI.
.
~, ` j `,i,~,'l
Spe~G mention has ~een ~ads of analys~ng a kim:~r~i~e sample ~or the
pres~nce of carbon-12 and hence of diamon~ Hnwever it will be
appr~d tha~ prirlc~ples nf t:he ~vention have ~ar wider
a~?plicatio~ Fo~ iu~oe ~e ~echn~qlle of the inven~on could, ie is
believed, be used w~2h good e~fect i~ the detection of ~bon and/o~
Q~;ygen în steel samples
I~ sho~ld a~o ~e noted that while the abo~e descr~p~io~ is directed to
the arlalysis of a single, stauc sample, the pIi~ciples of ~he ~hlvention are
~:q~lly aypl~cable to on-hne analys~s with a sue Lm of partîcles pa~si~
seq~lentially throu~h a detectio~L and analysis station. The ~veIItioIL
could for instanee be en~ployed in a p~r~cle sorting system in which,
once a pa~licle has bee~ detected tha~ includes a desirabl~ elem~llt or
iSOtOpe, suc~ p3rticl~ is automatic~lly ej~cted from Lhe particle strea~
T~is could ~e achieved usillg ~onventional ejec~on equLpm~nI such as
gas blast or other ejectors to remove desir.Lble par~icles from the ~n
s~eam ~r colle~on a~t ~ r~ other particles which are bar~en iIL
term~ their conterlt of the des~red element or isotope.
Irl tbe case of ~nberlite arlalysis a m~jor advantag~ of detecting a
diamorld mclusior~ 3g ~e technique of the il~ve~ioII is that ~arren
l~nberlite particles caII immediately be rejected without the rlecessît y for
filrther p~oces~ng. Only p~dcles for whic~ a l?os~iti~ e ~nialysis iS
obmi!od ilr~ scI~d for 511~tOqu~=t pToCCssiD~.
. .....
: ,:
: -
:........ . : ':. ,: r, . :,- ' ':::: :: :: .: .. ,.. ::::,:: '` .: :: ::'i :,:,.. '': , ' '

~10~ '1111 0'~ r~J~ O. r~ r~ JlJ
~ .
The :Inono~energe~c Or well~ei~ne~ energy level of th~ pulsed neutron
~e~m is prefe~ed since il enables the selectio~ of the app}opri~te
ener~ vel f~Jr ~e elemem ~~ estion, thereby iIr.proving the
se~sit~y of ihe sy~em. l~e pulsed na~ure of the ~ n results Lll t~e
ac~:lm~on of repeu~ive d~ta whic3~ reduce~ ious backgroulld
ef~eces
The pu~sing vL 1he beam may ~e achieved in a conven~onal ma~er
~ing a br~m iotrrrllpr~r rf }3!0~ rype.
. I
. .... .... ., ,_ ,._.. _........ ... .

Representative Drawing
A single figure which represents the drawing illustrating the invention.
Administrative Status

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Event History

Description Date
Inactive: IPC expired 2024-01-01
Application Not Reinstated by Deadline 2005-09-09
Time Limit for Reversal Expired 2005-09-09
Deemed Abandoned - Failure to Respond to Maintenance Fee Notice 2004-09-09
Letter Sent 2001-05-15
Inactive: Application prosecuted on TS as of Log entry date 2001-05-15
Inactive: Status info is complete as of Log entry date 2001-05-15
Request for Examination Requirements Determined Compliant 2001-04-05
All Requirements for Examination Determined Compliant 2001-04-05
Application Published (Open to Public Inspection) 1995-03-10

Abandonment History

Abandonment Date Reason Reinstatement Date
2004-09-09

Maintenance Fee

The last payment was received on 2003-06-18

Note : If the full payment has not been received on or before the date indicated, a further fee may be required which may be one of the following

  • the reinstatement fee;
  • the late payment fee; or
  • additional fee to reverse deemed expiry.

Patent fees are adjusted on the 1st of January every year. The amounts above are the current amounts if received by December 31 of the current year.
Please refer to the CIPO Patent Fees web page to see all current fee amounts.

Fee History

Fee Type Anniversary Year Due Date Paid Date
MF (application, 3rd anniv.) - standard 03 1997-09-09 1997-07-07
MF (application, 4th anniv.) - standard 04 1998-09-09 1998-06-17
MF (application, 5th anniv.) - standard 05 1999-09-09 1999-06-16
MF (application, 6th anniv.) - standard 06 2000-09-11 2000-07-06
Request for examination - standard 2001-04-05
MF (application, 7th anniv.) - standard 07 2001-09-10 2001-07-09
MF (application, 8th anniv.) - standard 08 2002-09-09 2002-06-20
MF (application, 9th anniv.) - standard 09 2003-09-09 2003-06-18
Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
DE BEERS INDUSTRIAL DIAMOND DIVISION (PROPRIETARY) LIMITED
Past Owners on Record
JACEK GUZEK
ULF ANDERS STAFFAN TAPPER
Past Owners that do not appear in the "Owners on Record" listing will appear in other documentation within the application.
Documents

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({010=All Documents, 020=As Filed, 030=As Open to Public Inspection, 040=At Issuance, 050=Examination, 060=Incoming Correspondence, 070=Miscellaneous, 080=Outgoing Correspondence, 090=Payment})


Document
Description 
Date
(yyyy-mm-dd) 
Number of pages   Size of Image (KB) 
Representative drawing 1998-05-27 1 10
Claims 1995-06-04 8 256
Drawings 1995-06-04 4 184
Abstract 1995-06-04 1 29
Description 1995-06-04 10 439
Abstract 2001-05-24 1 23
Claims 2001-05-24 8 177
Description 2001-05-24 10 363
Drawings 2001-05-24 4 81
Reminder - Request for Examination 2001-05-09 1 117
Acknowledgement of Request for Examination 2001-05-14 1 178
Courtesy - Abandonment Letter (Maintenance Fee) 2004-11-03 1 176
Correspondence 1994-11-23 24 713
Fees 2003-06-17 1 32
Fees 2001-07-08 1 30
Fees 2002-06-19 1 36
Fees 1997-07-06 1 34
Fees 1998-06-16 1 32
Fees 1999-06-15 1 29
Fees 2000-07-05 1 30
Fees 1996-06-18 1 49