US3847164A - Method of making reconstituted tobacco having reduced nitrates - Google Patents

Method of making reconstituted tobacco having reduced nitrates Download PDF

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Publication number
US3847164A
US3847164A US00405383A US40538373A US3847164A US 3847164 A US3847164 A US 3847164A US 00405383 A US00405383 A US 00405383A US 40538373 A US40538373 A US 40538373A US 3847164 A US3847164 A US 3847164A
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Prior art keywords
tobacco
extract
resin
denitrated
midribs
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Expired - Lifetime
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US00405383A
Inventor
C Mattina
W Selke
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Kimberly Clark Corp
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Kimberly Clark Corp
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Application filed by Kimberly Clark Corp filed Critical Kimberly Clark Corp
Priority to US00405383A priority Critical patent/US3847164A/en
Priority to CA205,949A priority patent/CA1001039A/en
Priority to GB3391674A priority patent/GB1455349A/en
Priority to ZA00745020A priority patent/ZA745020B/en
Priority to IE1699/74A priority patent/IE40439B1/en
Priority to BR7211/74A priority patent/BR7407211D0/en
Priority to DE2441719A priority patent/DE2441719A1/en
Priority to ES429718A priority patent/ES429718A1/en
Priority to CH1238274A priority patent/CH590620A5/xx
Priority to BE149022A priority patent/BE820483A/en
Priority to JP49112689A priority patent/JPS5064500A/ja
Priority to FR7433963A priority patent/FR2247169B1/fr
Priority to DK530974A priority patent/DK530974A/da
Priority to SE7412765A priority patent/SE7412765L/xx
Priority to NL7413440A priority patent/NL7413440A/en
Application granted granted Critical
Publication of US3847164A publication Critical patent/US3847164A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/24Treatment of tobacco products or tobacco substitutes by extraction; Tobacco extracts
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/10Chemical features of tobacco products or tobacco substitutes
    • A24B15/12Chemical features of tobacco products or tobacco substitutes of reconstituted tobacco
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/30Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances

Definitions

  • Reconstituted tobacco as such is well known.
  • One way of producing reconstituted tobacco is to extract the soluble ingredients of natural tobacco, which preferably has been macerated or comminuted in preparation for extraction. The extraction is performed by use of water, and generally withdraws from 30 percent to 55 percent by weight of the starting material. An aqueous slurry is then formed containing the fibers, an by usual papermaking techniques, the slurry with or without additives is transformed into a selfsustaining web. The tobacco extract, which may be concentrated to a liquor, is then introduced into the web. The application of the extracted tobacco material may be achieved in any appropriate manner, as by spraying, saturating, or otherwise.
  • the extract is contacted with a resin which selectively removes ionic components.
  • the invention has particular value in connection with reconstituted tobacco made from appreciable proportions of burley tobacco midribs since these contain substantial amounts of potassium nitrate.
  • the invention is not limited to use with any specific type of tobacco.
  • the retardation llA8 resin bead consists of Dowex l, a cross-linked styrenedivinylbenzene polymer lattice having attached quaternary animonium groups, interwoven with polymerized acrylic acid. The structure follows:
  • a typical procedure according to the invention involves extracting tobacco with water and then concentrating the extract so that it has a dry solids content of between one and 40 percent, and preferably about 10 percent.
  • the concentrated extract is filtered or centifuged to remove suspended insoluble matter.
  • Any suitable technique such as those discussed in the aforementioned patent, may then be used to remove potassium nitrate using the resin described above.
  • the AG l1A8 resin may be arranged in a column and the aqueous tobacco extract passed through the column.
  • a series of mixed contactors in which the resin is stirred with the extract, could be employed.
  • a continuous contactor providing a moving bed of resin, as developed for continuous ion exchange, could also be employed.
  • the denitrated extract may then be concentrated and used as is, or it may be mixed with other extract liquors to achieve a desired blend.
  • natural tobacco may be blended in desired proportions before extraction and the extract obtained from the blend passed over the resin column to remove nitrates.
  • EXAMPLE I I EXAMPLE lll Burley tobacco midribs were extracted with water The procedure of Example 2 was followed except and the fibrous residue was formed into a paper-like hat the liquor had the following proportions: sheet by ordinary papermaking techniques.
  • the extract 5 50 percent burley midrib was concentrated, and passed through a column of AG l percent flue-cured midrib l 1A8 to effect removal of potassium nitrate from the 40 percent flud-cured dust The test results were as extract. The denitrated extract was then applied to the 0 follpws:
  • Nitric Oxide Methyl Nitrite Free Burn (Micrograms per (micrograms per Sample (minutes/4O mm) cigarette) cigarette) Control 5,5 650 360 Denitrated 6.6 85 25 sheet by means of a size press. As a control, reconsti- V tuted tobacco was made exactly as described above, ex-
  • Nitric Oxide Methyl Nitrite Free Burn (micrograms per (micrograms per Sample (minutes/40 mm) cigarette) cigarette) Control 6.2 300 i 215 Denitrated 7.7 25 15 This liquor was blended with tobacco liquors prepared The test results of these examples show that cigaconventionally from flue-cured tobacco midrib and rettes made with reconstituted tobacco containing exflue-cured tobacco dust to give a liquor with the followtract material which has been denitrated according to ing proportions: this invention burn more slowly than otherwise identi- 30 percent burley midrib cal cigarettes, and contain less of the compounds which 30 percent flue cured midrib otherwise occur due to the presence of potassium ni- 40 percent flue-cured dust trate in the tobacco.
  • the panel preferred the cigarette including the denitrated tobacco because the smoke was less acrid and more flavorful.
  • a method of making reconstituted tobacco comprising the steps of:
  • a method as defined in claim 1 wherein the natural tobacco which is extracted is a blend of different types of tobaccos, one of the types being burley tobacco midribs.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Manufacture Of Tobacco Products (AREA)
  • Manufacturing Of Cigar And Cigarette Tobacco (AREA)

Abstract

Natural tobacco is extracted with water to produce a soluble extract and an insoluble fibrous residue. The extract is passed over an ion retardation resin to remove potassium nitrate from the extract. The resin is a rigid styrene-divinylbenzene crosslinked polymer lattice having attached quaternary ammonium groups, interwoven with a flexible linear acrylic acid polymer. Thereafter, the denitrated extract is recombined with the fibrous tobacco residue.

Description

United States Patent 1 Mattina et a1.
ill] 3,847,164
[ 51 Nov. 12, 1974 METHOD OF MAKING RECONSTITUTED TOBACCO HAVING REDUCED NITRATES [75] Inventors: Charles F. Mattina, Lenox; William A. Selke, Stockbridge, both of Mass.
[73] Assignee: Kimberly-Clark Corporation,
Neenah, Wis.
22 Filed: Oct. 11, 1973 211 Appl. No.: 405,383
[52] US. Cl. 131/143, 131/17 R [51] Int. Cl. A24b 03/14, A24b 15/02 [58] Field of Search 131/143, 140, 144,15,
[56] References Cited UNITED STATES PATENTS 3,616,801 ll/197l Hind 131/143 Primary ExaminerMelvin D. Rein Attorney, Agent, or FirmBreitenfcld & Levine ABSTRACT 4 Claims, N0 Drawings This invention relates to reconstituted tobacco, and more particularly to a method of making reconstituted tobacco from which a substantial proportion of the nitrate has been removed.
Reconstituted tobacco as such is well known. One way of producing reconstituted tobacco is to extract the soluble ingredients of natural tobacco, which preferably has been macerated or comminuted in preparation for extraction. The extraction is performed by use of water, and generally withdraws from 30 percent to 55 percent by weight of the starting material. An aqueous slurry is then formed containing the fibers, an by usual papermaking techniques, the slurry with or without additives is transformed into a selfsustaining web. The tobacco extract, which may be concentrated to a liquor, is then introduced into the web. The application of the extracted tobacco material may be achieved in any appropriate manner, as by spraying, saturating, or otherwise.
According to the present invention, after the extraction step but before the tobacco extract is recombined with the fibrous web, the extract is contacted with a resin which selectively removes ionic components. The invention has particular value in connection with reconstituted tobacco made from appreciable proportions of burley tobacco midribs since these contain substantial amounts of potassium nitrate. However, the invention is not limited to use with any specific type of tobacco.
Removal of potassium nitrate from tobacco is desirable for several reasons. First, the burn rate of tobacco products is decelerated when the nitrate is eliminated. Secondly, the generation of several components in the smoke, among them oxides of nitrogen, methyl nitrate, and acetonitrile, is reducd. Somev of these compounds have been suggested to be undesirable constituents in the smoke from the health standpoint. Furthermore, when potassium nitrate is burned, it produces an acrid smoke reminiscent of burned gunpowder.
in general, the idea of removing inorganic constituents from aqueous tobacco extracts is now new. In fact, removal of alkali metal salts from such extracts by passing the extract through an ion exchange resin is described in U.S. Pat. No. 3,616,801. However, the ion exchange resins referred to in that patent present certain problems. It has been found that although the resins described in the above-identified patent are effective in removing metallic ions from tobacco extract material, they remove almost all the desirable constituents of the extract as well. Furthermore, elution of the desirable tobacco components from the resins can be effected only with great difficulty. In addition, the anion exchange resins mentioned in that patent become fouled very rapidly and require cleaning steps to restore them to a usable condition after a single cycle of use.
All of these problems are overcome by the present invention. It has been found that by contacting aqueous tobacco extract with a particular resin, termed an ion retardation resin, the ionic material and specifically potassium nitrate, is selectively retarded while nonionic constituents of the extract pass through unaffected.
An example of the resin usable in this invention is manufactured by Dow Chemical Company of Midland,
Mich., and identified as AG HA8. This resin is dc scribed in'Dow Chemical Company Technical Bulletin "lon Retardation dated Nov. I957. This type of resin is made by polymerizing an anionic (or cationic) monomer inside a "cage" of cationic (or anionic) exchange resin. Specifically, the retardation llA8 resin bead consists of Dowex l, a cross-linked styrenedivinylbenzene polymer lattice having attached quaternary animonium groups, interwoven with polymerized acrylic acid. The structure follows:
on, CHzI IRa---O o 0 -oHi1 IR3-----0 o o The quaternary ammonium groups are strongly basic anion exchange groups, and the carboxyl groups are weakly acidic cation exchange groups. Thus AG 1 1A8 absorbs both anions and cations in equivalent amounts. However, organic molecules are not absorbed by the resin. As a result, the original extract material which passes through the resin is desalted, while losing little or no essential tobacco constituents and after the denitrated extract is removed, the inorganic salts can be eluted from the resin simply by rinsing it with water. There is very little degradation of the valuable organic constituents of the tobacco extract during desalting with AG 1 1A8 since the resin is neutral, in contrast to the acidic and basic natures of conventional resins, such as those described in Pat. No. 3,616,80l.
A typical procedure according to the invention involves extracting tobacco with water and then concentrating the extract so that it has a dry solids content of between one and 40 percent, and preferably about 10 percent. The concentrated extract is filtered or centifuged to remove suspended insoluble matter. Any suitable technique, such as those discussed in the aforementioned patent, may then be used to remove potassium nitrate using the resin described above. For example, the AG l1A8 resin may be arranged in a column and the aqueous tobacco extract passed through the column. Alternatively, a series of mixed contactors, in which the resin is stirred with the extract, could be employed. A continuous contactor, providing a moving bed of resin, as developed for continuous ion exchange, could also be employed. The denitrated extract may then be concentrated and used as is, or it may be mixed with other extract liquors to achieve a desired blend. Alternatively, natural tobacco may be blended in desired proportions before extraction and the extract obtained from the blend passed over the resin column to remove nitrates.
The following examples illustrate some of the features of the present invention:
EXAMPLE I I EXAMPLE lll Burley tobacco midribs were extracted with water The procedure of Example 2 was followed except and the fibrous residue was formed into a paper-like hat the liquor had the following proportions: sheet by ordinary papermaking techniques. The extract 5 50 percent burley midrib was concentrated, and passed through a column of AG l percent flue-cured midrib l 1A8 to effect removal of potassium nitrate from the 40 percent flud-cured dust The test results were as extract. The denitrated extract was then applied to the 0 follpws:
Nitric Oxide Methyl Nitrite Free Burn (Micrograms per (micrograms per Sample (minutes/4O mm) cigarette) cigarette) Control 5,5 650 360 Denitrated 6.6 85 25 sheet by means of a size press. As a control, reconsti- V tuted tobacco was made exactly as described above, ex-
' h lflip; the extract was not passed throug the resin co 30 percent burley mdnb Both sheets were then shredded and made into ciga- S f g rettes The cigarettes were allowed to burn freely and c. E l-Ps; F H5 V the time it took for a 40 mm length of each cigarette was prepared and extracted with water. The extract A tobacco blend consisting of:
to burn was noted. In addition, the smoke produced by was passed through an AG 1 1A8 resin column and conthe cigarettes was analyzed by gas chromotography centrated. Reconstituted tobacco was made with this techniques to determine the amount of nitric oxide and liquor and tobacco fibers in the same proportions as set forth above. The tobacco was shredded and fashioned into cigarettes. Control cigarettes were prepared from methyl nitrite in the smoke of each cigarette. The results of this testing are as follows:
Nitric Oxide Methyl Nitrite Free Bum (micrograms per (micrograms per Sample (minutes/40 mm) cigarette) cigarette) Control 3.0 800 650 Der-titrated 9.5 100 EXAMPLE [I 3 5 reconstituted tobacco made exactly as described above Denitrated extract liquor was prepared from burley except that the liquor was not denitrated. The test retobacco midribs in the manner described in Example I. salts were as follows:
Nitric Oxide Methyl Nitrite Free Burn (micrograms per (micrograms per Sample (minutes/40 mm) cigarette) cigarette) Control 6.2 300 i 215 Denitrated 7.7 25 15 This liquor was blended with tobacco liquors prepared The test results of these examples show that cigaconventionally from flue-cured tobacco midrib and rettes made with reconstituted tobacco containing exflue-cured tobacco dust to give a liquor with the followtract material which has been denitrated according to ing proportions: this invention burn more slowly than otherwise identi- 30 percent burley midrib cal cigarettes, and contain less of the compounds which 30 percent flue cured midrib otherwise occur due to the presence of potassium ni- 40 percent flue-cured dust trate in the tobacco. ,Reconstituted tobacco was made with this liquor and For flavor testing, cigarettes were prepared by blendtobacco fibers in the same proportions set forth above. ing shredded leaf tobacco with each of the four deni- The material was shredded and fashioned into cigatrated reconstituted tobaccos, and each of the four rettes. Control cigarettes were prepared from reconsti-' control reconstituted tobaccos, prepared in Examples tuted tobacco of the same proportions but without re- IlV above, the reconstituted tobaccos also having moving the nitrate from the burley midrib liquor. The been shredded. In each case, the blend had a ratio of tests described in Example I were conducted with the 70:30, leaf tobacco to reconstituted tobacco. The cigafollowing results. cites were smoked by a panel of experts and evaluated Nitric Oxide Methyl Nitrite Free Burn (Micrograms per (Micrograms per Sample (minutes/4O mm) cigarette) cigarette) Control 6.2 300 215 Denitrated 7.2 2O
for flavor. In each case, the panel preferred the cigarette including the denitrated tobacco because the smoke was less acrid and more flavorful.
The invention has been shown and described in preferred form only, and by way of example, and many variations may be made in the invention which will still be comprised within its spirit. It is understood. therefore, that the invention is not limited to any specific form or embodiment except insofar as such limitations are included in the appended claims.
What is claimed is:
l. A method of making reconstituted tobacco, comprising the steps of:
a. extracting natural tobacco with water to produce a tobacco extract and a fibrous residue.
b. contacting the tobacco extract with an ion retardation resin to remove potassium nitrate from the extract, said resin comprising a cross-linked styrenedivinylbenezene polymer lattice having attached quaternary ammonium groups, interwoven with polymerized acrylic acid,
c. forming the fibrous residue into a paper-like sheet and d. recombining the denitrated extract with the fibrous tobacco sheet.
2. A method as defined in claim 1 wherein the natural tobacco includes burley tobacco midribs.
3. A method as defined in claim 1 wherein the extract which is contacted with the resin and thereby denitrated is obtained entirely from burley tobacco midribs. and the denitrated extract is blended with extracts of other types of tobacco prior to recombination with the tobacco sheet.
4. A method as defined in claim 1 wherein the natural tobacco which is extracted is a blend of different types of tobaccos, one of the types being burley tobacco midribs.

Claims (4)

1. A METHOD OF MAKING RECONSTITUTED TOBACCO, COMPRISING THE STEPS OF: A. EXTRACTING NATURAL TOBACCO WITH WATER TO PRODUCE A TOBACCO EXTRACT AND A FIBROUS RESIDUE. B. CONTACTING THE TOBACCO EXTRACT WITH AN ION RETARDATION RESIN TO REMOVE POTASSIUM NITRATE FROM THE EXTRACT, SAID RESIN COMPRISING A CROSS-LINKED STYRENE-DIVINYLBENEZENE POLYMER LATTICE HAVING ATTACHED QUATERNARY AMMONIUM GROUPS, INTERWOVEN WITH POLYMERIZED ACRYLIC ACID, C. FORMING THE FIBROUS RESIDUE INTO A PAPER-LIKE SHEET, AND D. RECOMBINING THE DENITRATED EXTRACT WITH THE FIBROUS TOBACCO SHEET.
2. A method as defined in claim 1 wherein the natural tobacco includes burley tobacco midribs.
3. A method as defined in claim 1 wherein the extract which is contacted with the resin and thereby denitrated is obtained entirely from burley tobacco midribs, and the denitrated extract is blended with extracts of other types of tobacco prior to recombination with the tobacco sheet.
4. A method as defined in claim 1 wherein the natural tobacco which is extracted is a blend of different types of tobaccos, one of the types being burley tobacco midribs.
US00405383A 1973-10-11 1973-10-11 Method of making reconstituted tobacco having reduced nitrates Expired - Lifetime US3847164A (en)

Priority Applications (15)

Application Number Priority Date Filing Date Title
US00405383A US3847164A (en) 1973-10-11 1973-10-11 Method of making reconstituted tobacco having reduced nitrates
CA205,949A CA1001039A (en) 1973-10-11 1974-07-30 Method of making reconstituted tobacco having reduced nitrates
GB3391674A GB1455349A (en) 1973-10-11 1974-08-01 Method of making reconstituted tobacco having reduced nitrates
ZA00745020A ZA745020B (en) 1973-10-11 1974-08-06 Method of making reconstituted tobacco having reduced nitrites
IE1699/74A IE40439B1 (en) 1973-10-11 1974-08-13 Method of making reconstituted tobacco having reduced nitrate
BR7211/74A BR7407211D0 (en) 1973-10-11 1974-08-29 PROCESS FOR RECONSTITUTED TOBACCO PRODUCTION
DE2441719A DE2441719A1 (en) 1973-10-11 1974-08-30 PROCESS FOR THE PROCESSING OF TOBACCO
ES429718A ES429718A1 (en) 1973-10-11 1974-09-02 Method of making reconstituted tobacco having reduced nitrates
CH1238274A CH590620A5 (en) 1973-10-11 1974-09-11
BE149022A BE820483A (en) 1973-10-11 1974-09-27 PROCESS FOR THE MANUFACTURING OF RECONSTITUTED TOBACCO WITH LESS ENNITRATES
JP49112689A JPS5064500A (en) 1973-10-11 1974-09-30
FR7433963A FR2247169B1 (en) 1973-10-11 1974-10-09
DK530974A DK530974A (en) 1973-10-11 1974-10-10
SE7412765A SE7412765L (en) 1973-10-11 1974-10-10
NL7413440A NL7413440A (en) 1973-10-11 1974-10-11 PROCEDURE FOR THE PREPARATION OF RECONSTRUCTED BUCKET WITH LOW NITRATE CONTENT.

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JP (1) JPS5064500A (en)
BE (1) BE820483A (en)
BR (1) BR7407211D0 (en)
CA (1) CA1001039A (en)
CH (1) CH590620A5 (en)
DE (1) DE2441719A1 (en)
DK (1) DK530974A (en)
ES (1) ES429718A1 (en)
FR (1) FR2247169B1 (en)
GB (1) GB1455349A (en)
IE (1) IE40439B1 (en)
NL (1) NL7413440A (en)
SE (1) SE7412765L (en)
ZA (1) ZA745020B (en)

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US4131118A (en) * 1976-11-12 1978-12-26 Philip Morris Incorporated Method for removal of potassium nitrate from tobacco extracts
US4131117A (en) * 1976-12-21 1978-12-26 Philip Morris Incorporated Method for removal of potassium nitrate from tobacco extracts
WO1981002379A1 (en) * 1980-02-21 1981-09-03 Philip Morris Inc Tobacco treatment
EP0035052A1 (en) * 1980-03-05 1981-09-09 Philip Morris Incorporated Method of treating tobacco extracts employing electrodialysis
EP0035273A1 (en) * 1980-03-05 1981-09-09 Philip Morris Incorporated Method for selective denitration of tobacco
US4302308A (en) * 1980-03-05 1981-11-24 Philip Morris, Inc. Method for electrolytic denitration of tobacco
US4308877A (en) * 1978-03-06 1982-01-05 Kimberly-Clark Corporation Method of making reconstituted tobacco having reduced nitrates
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EP0081231A2 (en) * 1981-12-07 1983-06-15 Adam Dr. Müller Process for the production of aromatic substances from a tobacco extract
US4448208A (en) * 1981-01-21 1984-05-15 Philip Morris Incorporated Tobacco extractor
US4556073A (en) * 1978-06-15 1985-12-03 Brown & Williamson Tobacco Corporation Process for reduction of nitrate content of tobacco by microbial treatment
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ZA745020B (en) 1975-08-27
IE40439L (en) 1975-04-11
CH590620A5 (en) 1977-08-15
FR2247169B1 (en) 1978-06-09
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SE7412765L (en) 1975-04-14
GB1455349A (en) 1976-11-10
DE2441719A1 (en) 1975-04-17
BE820483A (en) 1975-01-16
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DK530974A (en) 1975-06-09
IE40439B1 (en) 1979-06-06
FR2247169A1 (en) 1975-05-09
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JPS5064500A (en) 1975-05-31

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