UST896044I4 - Defensive publication - Google Patents
Defensive publication Download PDFInfo
- Publication number
- UST896044I4 UST896044I4 US896044DH UST896044I4 US T896044 I4 UST896044 I4 US T896044I4 US 896044D H US896044D H US 896044DH US T896044 I4 UST896044 I4 US T896044I4
- Authority
- US
- United States
- Prior art keywords
- benzo
- pyrylium
- perchlorate
- aryl
- butylamino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01T—MEASUREMENT OF NUCLEAR OR X-RADIATION
- G01T1/00—Measuring X-radiation, gamma radiation, corpuscular radiation, or cosmic radiation
- G01T1/16—Measuring radiation intensity
- G01T1/20—Measuring radiation intensity with scintillation detectors
- G01T1/203—Measuring radiation intensity with scintillation detectors the detector being made of plastics
Definitions
- This invention relates to solid scintillators which are 2-aryl-4-sec-amino-benzo [b]pyrylium salts or 2-aryl-4-secaminobenzo[b]thiapyrylium salts.
- the solid scintillators which may be employed according to the invention can be represented by the structural formula:
- X is a sulfur or oxygen atom
- Z is an anionic function as exemplified by perchlorate, halides, fluoroborate, sulfonate and the like
- R is an alkyl or aryl group; each of R can be a hydrogen atom, an alkyl group or an alkoxy group; and R and R each can be a hydrogen atom or when taken together are attached to adjacent carbon atoms and represent the atoms necessary to form a fused cyclic aromatic moiety such as benzo or naphtho and substituted fused aromatic rings.
- the preferred compounds are 4-butylamino-2- (4-methoxyphenyl benzo [b] pyrylium perchlorate, 4-butylamino-2-(4-methoxyphenyl) benzo[b]pyrylium fiuoroborate and (4-benzylamino)-2- pheny1benzo[b]pyrylium perchlorate.
- the solid scintillators are advantageously employed in the continuous monitoring of beta-radiation in e'filuents, particularly in conjunction with liquid column chromatography.
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- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Physics & Mathematics (AREA)
- High Energy & Nuclear Physics (AREA)
- Molecular Biology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Measurement Of Radiation (AREA)
Abstract
THIS INVENTION RELATES TO SOLID SCINTILLATORS WHICH ARE 2-ARYL-4-SEC-AMINO-BENZO(B)PYRYLIUM SALTS OR 2-ARYL-4-SECAMINOBENZO(B)THIAPYRYLIUM SALTS. THE SOLID SCINTILLATORS WHICH MAY BE EMPLOYED ACCORDING TO THE INVENTION CAN BE REPRESENTED BY THE STRUCTURAL FORMULA:
WHEREIN X IS A SULFUR OR OXYGEN ATOM; Z IS AN ANIONIC FUNCTION AS EXEMPLIFIED BY PERCHLORATE, HALIDES, FLUOROBORATE, SULFONATE AND THE LIKE; R IS AN ALKYL OR ARYL GROUP; EACH OF R1 CAN BE A HYDROGEN ATOM, AN ALKYL GROUP OR AN ALKOXY GROUP; AND R2 AND R3 EACH CAN BE A HYDROGEN ATOM OR WHEN TAKEN TOGETHER ARE ATTACHED TO ADJACENT CARBON ATOMS AND REPRESENT THE ATOMS NECESSARY TO FORM A FUSED CYCLIC AROMATIC MOIETY SUCH AS BENZO OR NAPHTHO AND SUBSTITUTED FUSED AROMATIC RINGS. THE PREFERRED COMPOUNDS ARE 4-BUTYLAMINO-2-(4-METHOXYPHENYL)BENZO(B) PYRYLIUM PERCHLORATE, 4-BUTYLAMINO-2-(4-METHOXYPHENYL) BENZO(B)PYRYLIUM FLUOROBORATE AND (4-BENZYLAMINO)-2PHENYLBENZO(B)PYRYLIUM PERCHLORATE. THE SOLID SCINTILLATORS ARE ADVANTAGEOUSLY EMPLOYED IN THE CONTINUOUS MONITORING OF BETA-RADIATION IN EFFLUENTS, PARTICULARLY IN CONJUNCTION WITH LIQUID COLUMN CHROMATOGRAPHY.
WHEREIN X IS A SULFUR OR OXYGEN ATOM; Z IS AN ANIONIC FUNCTION AS EXEMPLIFIED BY PERCHLORATE, HALIDES, FLUOROBORATE, SULFONATE AND THE LIKE; R IS AN ALKYL OR ARYL GROUP; EACH OF R1 CAN BE A HYDROGEN ATOM, AN ALKYL GROUP OR AN ALKOXY GROUP; AND R2 AND R3 EACH CAN BE A HYDROGEN ATOM OR WHEN TAKEN TOGETHER ARE ATTACHED TO ADJACENT CARBON ATOMS AND REPRESENT THE ATOMS NECESSARY TO FORM A FUSED CYCLIC AROMATIC MOIETY SUCH AS BENZO OR NAPHTHO AND SUBSTITUTED FUSED AROMATIC RINGS. THE PREFERRED COMPOUNDS ARE 4-BUTYLAMINO-2-(4-METHOXYPHENYL)BENZO(B) PYRYLIUM PERCHLORATE, 4-BUTYLAMINO-2-(4-METHOXYPHENYL) BENZO(B)PYRYLIUM FLUOROBORATE AND (4-BENZYLAMINO)-2PHENYLBENZO(B)PYRYLIUM PERCHLORATE. THE SOLID SCINTILLATORS ARE ADVANTAGEOUSLY EMPLOYED IN THE CONTINUOUS MONITORING OF BETA-RADIATION IN EFFLUENTS, PARTICULARLY IN CONJUNCTION WITH LIQUID COLUMN CHROMATOGRAPHY.
Description
DEFENSIVE PULICATION UNITED STATES PATENT OFFICE Published at the request of the applicant or owner in accordance with the Notice of Dec. 16, 1969, 869 O.G. 687. The abstracts of Defensive Publication applications are identified by distinctly numbered series and are arranged chronologically. The heading of each abstract indicates the number of pages of specification, including claims and sheets of drawings contained in the application as originally filed. The files of these applications are available to the public-for inspection and reproduction may be purchased for 30 cents a sheet.
Defensive Publication applications have not been examined as to the merits of alleged invention. The Patent Oifice makes no assertion as to the novelty of the disclosed subject matter;
PUBLISHED MARCH 21, 1972 T896,044 SOLID SCINTILLATORS Lorenzo Federico Costa, Frank Grum, and James Albert Van Allan, all Eastman Kodak Co., Kodak Park Division, Rochester, NY. 14650 Filed Mar. 4, 1971, Ser. No. 121,135 Int. Cl. G01t N20 US. Cl. 250-715 R No Drawing. 15 Pages Specification This invention relates to solid scintillators which are 2-aryl-4-sec-amino-benzo [b]pyrylium salts or 2-aryl-4-secaminobenzo[b]thiapyrylium salts. The solid scintillators which may be employed according to the invention can be represented by the structural formula:
wherein X is a sulfur or oxygen atom; Z is an anionic function as exemplified by perchlorate, halides, fluoroborate, sulfonate and the like; R is an alkyl or aryl group; each of R can be a hydrogen atom, an alkyl group or an alkoxy group; and R and R each can be a hydrogen atom or when taken together are attached to adjacent carbon atoms and represent the atoms necessary to form a fused cyclic aromatic moiety such as benzo or naphtho and substituted fused aromatic rings. The preferred compounds are 4-butylamino-2- (4-methoxyphenyl benzo [b] pyrylium perchlorate, 4-butylamino-2-(4-methoxyphenyl) benzo[b]pyrylium fiuoroborate and (4-benzylamino)-2- pheny1benzo[b]pyrylium perchlorate.
The solid scintillators are advantageously employed in the continuous monitoring of beta-radiation in e'filuents, particularly in conjunction with liquid column chromatography.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12113571A | 1971-03-04 | 1971-03-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
UST896044I4 true UST896044I4 (en) | 1972-03-21 |
Family
ID=22394784
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US896044D Pending UST896044I4 (en) | 1971-03-04 | 1971-03-04 | Defensive publication |
Country Status (1)
Country | Link |
---|---|
US (1) | UST896044I4 (en) |
-
1971
- 1971-03-04 US US896044D patent/UST896044I4/en active Pending
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