IE45421B1 - Proteinaceous foodstuff - Google Patents

Proteinaceous foodstuff

Info

Publication number
IE45421B1
IE45421B1 IE1189/77A IE118977A IE45421B1 IE 45421 B1 IE45421 B1 IE 45421B1 IE 1189/77 A IE1189/77 A IE 1189/77A IE 118977 A IE118977 A IE 118977A IE 45421 B1 IE45421 B1 IE 45421B1
Authority
IE
Ireland
Prior art keywords
protein
process according
slurry
mixture
alkali metal
Prior art date
Application number
IE1189/77A
Other versions
IE45421L (en
Original Assignee
Unilever Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Unilever Ltd filed Critical Unilever Ltd
Publication of IE45421L publication Critical patent/IE45421L/en
Publication of IE45421B1 publication Critical patent/IE45421B1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23JPROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
    • A23J1/00Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
    • A23J1/14Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from leguminous or other vegetable seeds; from press-cake or oil-bearing seeds
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L11/00Pulses, i.e. fruits of leguminous plants, for production of food; Products from legumes; Preparation or treatment thereof
    • A23L11/30Removing undesirable substances, e.g. bitter substances
    • A23L11/34Removing undesirable substances, e.g. bitter substances using chemical treatment, adsorption or absorption

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Biochemistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Botany (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Beans For Foods Or Fodder (AREA)

Abstract

A process for producing a foodstuff mainly consisting of highly functional vegetable protein substantially free of off-flavour components and pigments, which comprises subjecting vegetable protein containing material to alkaline conditions in the presence of an alkali metal halide and separating released pigments and off-flavour components from the protein by ultrafiltration or iso-electric precipitation.

Description

This invention relates to a process for the preparation of a proteinaceous foodstuff.
For the production of various food systems oil seed proteins are oftfen used in the form of flours, concentrates or isolates, whivh have been subjected to some treatment in order to remove undesirable components such as off-flavours, pigments, trypsin inhibitors and flatulence factors.
The products obtained after removal of the undesirable components are often denatured and not very useful especially in the case where a relatively high functionality is required There is thus a need for a process resulting in a product combining a high functionality with good organoleptic properties.
We have found a process enabling a facilitated release 15 of pigments and off-flavour components from plant material, particularly oil-bearing seeds and especially soy.
The process according to the invention comprises: a) forming an aqueous slurry or defatted vegetable protein-containing material; b) subjecting said vegetable protein-containing material to alkaline conditions at a pH from 9 to 12, in the presence of 0.2 M to 1 M of an alkalimetal halide to obtain a mixture in which pigments and off-flavour components are substantially - 3 completely released from the protein-containing material. c) separating the released pigments and off-flavour components from the protein-containing material.
The vegetable protein material is preferably originating from readily available oil-bearing seeds such as soybeans, cottonseed, sunflower, etc. Soybeans are however preferably used.
The starting vegetable protein material is defatted prior to use, using e.g. solvent extraction. Extraction with e.g. hexane gives excellent results. The aqueous slurry of the starting material is easily prepared by thoroughly mixing the defatted material with suitable amounts of water. The applied weight ratio of solids to liquid can vary within wide limits but preferably a weight ratio of solids to liquid from 1:5 to 1:30 is used.
The alkaline conditions can be obtained by using a base, preferably an alkali metal hydroxide such as sodiumor potassium-hydroxide, which can be added in solid form to the aqueous slurry or in the form of concentrated aqueous solution in a proportion sufficient to give a pH from 9 to 12 and preferably from 10 to 11.
The alkali metal halide is preferably a sodium- or potassium halide. Ideally sodium chloride is used.
The concentration of the alkali metal halide should range from 0.2 to 1 M, preferably from 0.35 to 0.70 M.
The treatment of the vegetable protein-containing material under alkaline conditions in the presence of the alkali metal halide can be performed after removal of aS42i insoluble material, mainly consisting of carbohydrates, or in the presence thereof.
We have found that an effective removal of off-flavour components and pigments is obtained if the treatment (step b) is carried out in the absence of the insoluble material (mainly consisting of carbohydrates), rather than in the presence thereof, in the case where the treatment of the starting material is followed by an ultra-filtration operation (step c) which is carried out in order to separate the released off-flavour components and pigments from the rest of the material. However in the ease where step (c) consists of an isoelectric precipitation it is more advantageous to perform the treatment (step b) in the presence of the insoluble material.
The alkali metal halide can be added either before or after adjusting the pH of the aqueous slurry of vegetable protein-containing material to the desired value which, as already stated, lies between 9 and 12.
In some instances it has been found advantageous to first raise the pH of the aqueous slurry to a pH value within the given range and then to add the alkali metal halide.
The treatment under alkaline conditions in the presence of the alkali halide is carried out for a sufficiently long time to achieve a sufficient dissociation of pigments and release of off-flavour components. A suitable method for assessing the released amount of off-flavour components is GL chromatography.
The duration of the treatment and the temperature should preferably be such that the treated protein remains substantially undenatured by which term is meant that the functionality of the protein (solubility, heat-setting properties, etc.) remains practically unchanged.
Usually a treatment of less than one hour and preferably from 1 to 15 minutes at a temperature ranging from 20 to 40°C will be adequate.
Anyhow the man skilled in the art will easily find the ideal conditions in each particular case.
Separation of the undesirable components such as offflavour components and pigments from the rest of the material can be achieved by using conventional techniques. Preferably isoelectric precipitation or ultrafiltration is applied. When starting from e.g. an aqueous slurry of defatted soy flakes or soyaieal isoelectric precipitation of the protein is carried out at a pH from 4.5 to 5.5, preferably at a pH from 4.5 to 4.8.
Dilution of the aqueous slurry prior to isoelectric precipitation is sometimes required to facilitate the separation of the insoluble carbohydrate and to effectively perform the isoelectric precipitation, especially if relatively high concentrations of the alkali metal halide have been used.
Depending on whether the desired end-product is a protein concentrate having a protein concentration of about 70% or a protein isolate having a protein concentration of about 90%, the isoelectric precipitation is performed in the 'presence or in the absence of insoluble material mainly consisting of carbohydrates.
A preferred embodiment of the process according to the invention involves; 4S4 31 ΙΟ i) forming an aqueous slurry of defatted soymeal; ii) Subjecting said slurry to alkaline conditions at a pH from 9 to 12 in the presence of 0.2 M to 1 M of an alkali metal halide to obtain a mixture in which pigments and off-flavour-components are substaptially completely released; iii) diluting said mixture with water to obtain a mixture in which the molarity of the alkali metal halide is less than 0.2 M; iv) precipitating the protein at a pH ranging from 4.5 to 5.5; v) separating the insoluble material consisting of carbohydrates and protein from the liquid, to obtain a soyprotein concentrate.
Another preferred embodiment of the process according to the invention involves: i) forming an aqueous slurry of defatted soymeal; ii) subjecting said slurry to alkaline conditions at a pH from 9 to 12 in the presence of 0.2 M to 1 M 20 of an alkali metal halide to obtain a mixture in which pigments and off-flavour components are substantially completely released; iii) diluting said mixture with water to obtain a mixture in which the molarity of the alkali metal halide is less than 0.2 M; iv) separating the insoluble material, mainly consisting of carbohydrates from the mixture to obtain a clarified protein solution; v) precipitating the protein at a pH ranging from 4.5 to 5.Ξ from the solution to obtain a protein isolate.
According to the invention the undesirable off-flavour components and pigments can be separated from the rest of the material by using ultra-filtration. Ultra-filtration can be carried out preferably from lowering the pH of the vegetable protein containing mixture from the alkaline value to a value from 6-8, by using conventional membranes having a molecular weight cut-off limit of not less than 1000 daltons and preferably not less than 5000 daltons. Depending on which end-product is envisaged (protein concentrate or protein isolate), the ultrafiltration can be carried out in the presence or in the absence of the insoluble carbohydrate.
A particularly preferred embodiment of the process according to the invention for the preparation of a soyprotein isolate involves: i) forming an aqueous slurry of defatted soymeal? ii) removing insoluble material, mainly consisting of carbohydrates, from said slurry to obtain a clarified solution; iii) subjecting said clarified solution to alkaline conditions at a pH ranging from 9 to 12 in the presence of 0.2 M to 1 M of an alkali metal halide, to obtain a mixture in which pigments and off-flavour components are substantially completely released; iv) lowering the pH of the mixture to a value ranging - 8 from 6 to 8; and v) ultra-filtering said mixture on a membrane having a molecular weight cut-off limit of not less than 1000 daltons, to obtain a soyprotein isolate.
Another particularly preferred embodiment of the process according to the invention for the preparation of a soyprotein isolate involves: i) forming an aqueous slurry of defatted soymeal; ii) subjecting said slurry to alkaline conditions at a pH ranging from 9 to 12, in the presence of 0.2 M to 1 M of an alkali metal halide, to achieve a substantially complete release of pigments and off-flavour components; iii) lowering the pH of the slurry to a value ranging from 6 to 8; iv) removing insoluble material mainly consisting of carbohydrates from said slurry to obtain a clarified solution; v) ultra-filtering said clarified solution on a 20 membrane having a molecular weight cut-off limit of not less than 1000 daltons, to obtain a soy protein-isolate.
A particularly preferred embodiment of the process according to the invention for the preparation of a soy25 protein concentrate involves: 1) forming an aqueous slurry of defatted soymeal; ii) subjecting said slurry to alkaline conditions at a pH ranging from 9 to 12, in the presence of 0.2 M 4B421 - 9 to 1 M of alkali metal halide; iii) lowering the pH of the slurry to a value ranging from 6 to 8; iv) ultra-filtering the slurry on a membrane having a molecular weight cut-off limit of not less than 1000 daltons, to obtain a protein concentrate.
The products obtained according to the invention can be used as an extender replacing part of the protein originally present in several food systems and particularly in those where good functional and organoleptic performance is required, like dairy desserts, simulated meat, or fish etc.
The following Examples illustrate the invention. Example I Production of a soyprotein concentrate by ultra-filtration One part by weight of defatty soybean meal was mixed with 10 parts by weight of water to form an aqueous slurry. Solid sodium chloride was added to the aqueous slurry in a proportion sufficient to obtain 0.6 M dissolved NaCl.
The pH of the mixture was raised to 10.0 using sodium hydroxide. After 10 minutes the pH was lowered to 6.5 by adding hydrochloric acid. The mixture was concentrated twofold in a conventional tubular module ultra-filtration plant at S5°C using a membrane cast from a solution of cellulose acetate in dimethylsulphoxide, of a molecular weight cut-off limit of more than 5,000 daltons. The inlet pressure was 90 psig. and the outlet pressure 40 psig.
The concentrated slurry was diluted with an equal volume of water and then reconcentrated by ultra-filtration *5421 ίο in order to remove the sodium chloride, water soluble sugars, and other low-molecular weight impurities. This washing step vzas repeated until at least 90% of the lowmolecular weight impurities had been removed. The concent5 rate obtained was spray-dried to yield a white powder containing about 70% of protein and 30% of insoluble carbohydrate.
Example IX Production of a soyprotein isolate by ultrafiltration The procedure of Example I vzas followed except that the insoluble material (mainly consisting of carbohydrates) present in the acidified mixture (pH 6,5) vzas centrifuged off and the clarified solution vzas ultra-filtered to yield a protein isolate having a protein concentration of about 90%.
Example III Production of a soyprotein isolate by ultrafiltration The general procedure of Example II was followed except that the insoluble material was removed from the aqueous slurry before the addition of salt and sodium hydroxide.
Example IV Production of a soyprotein concentrate by isoelectric precipitation One part by weight of defatted soybean meal was mixed with 10 parts by weight of vzater. · Sodium chloride was dissolved in the aqueous extract to give a concentration of 0.25 molar and the pH of the mixture was adjusted to 10.0 by adding sodium hydroxide. After 10 minutes the mixture vzas diluted vzith 2¾ volumes of water and the pH adjusted 54 31 - 11 to 4.8 by adding hydrochloric acid. The insoluble material consisting of precipitated protein and insoluble carbohydrate, was centrifuged off and spray-dried.
Example V Production of soyprotein isolate by isoelectric precipitation The general procedure of Example IV was followed except that the pH was first lowered from 10.0 to 6.5, and the insoluble material, mainly consisting of carbohydrate, was removed by centrifugation before performing the iso10 electric precipitation of the protein at pH 4.8.
The precipitated protein was washed once with water and spray-dried to yield a white bland protein pcwder with a protein concentration of about 90%.
Example VI Preparation of a proteinaceous ingredient for meat or fish analogues A fibrous ingredient useful for producing extended meat or fish products or full analogues was prepared starting from an isolate prepared according to Example II.
Following the procedure outlined in U.S. Patent 3,987,213 drops of 0.05 ml of an aqueous solution containing about 25% soyprotein were added to a laminar flow of water of 94°C. to coagulate the protein added. The product was collected and used for the production of 1) a seafood analogue and 2) a beef analogue.
Production of a seafood analogue 100 g. of the coagulated soyprotein were mixed with 200 ml. of a flavouring composition, pH 5.8-6.2 consisting of 3% natural seafood extracts, 1.5% seafood flavours, 0.1% salt and 95.4% water. The liquid was subsequently drained and the drained material was mixed with a dressing made of 94.9% mayonnaise, 5% tomato ketchup and 0.1% lemon juice.
Production of beef analogue A mould was filled with collected soyprotein coagul« 2 ates and the material was compressed at 550 kN/m between paper towelling to avoid a glossy surface on the final material.
The compressed sheet of material having a thickness 10 of 3 - 5 mm ms soaked for a few minutes in a favour/ texturising bath. The sheet was drained and then heat-set in steam for 10 minutes.
When cooked in gravy and vegetables the analogue looked and could be chewed and swallowed like a slice of beef.

Claims (23)

1. CLAIMS :1. A process for the preparation of a vegetable protein product which comprises: a) forming an aqueous slurry of defatted vegetable protein-containing material; b) subjecting said vegetable protein-containing material to alkaline conditions at a pH from 9 to 12» in the presence of 0.2 M to 1 M of an alkali metal halide to obtain a mixture in which pigments and off-flavour components are substantially completely released from the protein-containing material; c) separating the released pigments and off-flavour components from the protein-containing material.
2. A process according to claim 1, wherein the defatted vegetable protein-containing material originates from soy.
3. A process according to claim 2, wherein defatted soy meal is used.
4. A process according to claim 1, wherein the weight ratio of the solids to liquid in the slurry is from 1:5 to 1:30.
5. A process according to any one of claims 1 to 4, wherein alkaline conditions are obtained by adding an alkali metal hydroxide to the slurry.
6. A process according to any one of claims 1 to 5, wherein a pH varying from 10 to 11 is applied.
7. A process according to any one of claims 1 to 6, wherein sodium chloride is used. 14
8. A process according to claim 7, wherein sodium chloride is added to obtain a concentration ranging from 0.35 M to 0.70 M.
9. A process according to claim 1, wherein step (b) is performed in such a way that the protein functionality remains substantially unchanged.
10. A process according to claim 9, wherein step (b) is performed at a temperature ranging from 20°C to 40°C for a period of less than one hour.
11. A process according to claim 1, wherein step (c) consists in ultra-filtering the mixture obtained under (b).
12. A process according to claim 11, wherein the pH of the mixture obtained under (b) is lowered to a value ranging from 6 to 8 prior to ultra-filtration.
13. A process according to claim 1, which comprises i) forming an aqueous slurry of defatted soymeal; ii) removing insoluble material mainly consisting of carbohydrates, from said slurry to obtain a clarified solution,iii) subjecting said clarified solution to alkaline conditions at a pH ranging from 9 to 12 in the presence of 0.2 I·! to 1 I-l of an alkali metal halide, to obtain a mixture in which pigments and off-flavour components are substantially completely released; iv) lowering the pH of the mixture to a value ranging from 6 to 8; and 4S421 - 15 I v) ultra-filtering said mixture on a membrane having a molecular weight cut-off limit of not less than 1000 daltons, to obtain a soyprotein isolate. 5
14. A process according to claim 1, which comprises: 1) forming an aqueous slurry of defatted soymeal; ii) subjecting said slurry to alkaline conditions al a pH ranging from 9 to 12, in the presence of 0.2 M to 1 M of an alkali metal halide, to 10 achieve a substantially complete release of pigments and off-flavour components; iii) lowering the pH of the slurry to a value ranging from 6 to 8; iv) removing insoluble material mainly consisting of 15 carbohydrates from said slurry to obtain a clarified solution; v) ultra-filtering said clarified solution on a memorane having a molecular weight cut-off limit of not less than 1000 daltons, to obtain a soy20 protein-isolate.
15. A process according to claim 1, which comprises: i) forming an aqueous slurry of defatted soymeal; ii) subjecting said slurry to alkaline conditions at a pH ranging from 9 to 12, in the presence of 25 0.2 M to 1 M of an alkali metal halide; iii) lowering the pH of the slurry to a value ranging from 6 to 8; iv) ultra-filtering the slurry on a membrane having a molecular weight cut-off limit of not less than 1000 daltons, to obtain a protein concentrate.
16. A process according to any one of claims 11 - 15 which comprises using a membrane having a molecular weight cut-off limit above 5,000 daltons.
17. A process according to claim 1, in which step (c) consists in precipitating the protein at its iso-electric point and separating the precipitated protein from the supernatant.
18. A process according to claim 17, which comprises: i) forming an aqueous slurry of defatted soymeal; ii) subjecting said slurry to alltaline conditions at a pH from 9 to 12 in the presence of 0.2 M to 1 M of an alkali metal halide to obtain a mixture in which pigments and off-flavour components are substantially completely released; iii) diluting said mixture with water to obtain a mixture in which the molarity of the alkali metal halide is less than 0.2 M; iv) precipitating the protein at a pH ranging from 4.5 to 5.5; v) separating the insoluble material consisting of carbohydrates and protein from the liquid, to obtain a soyprotein-concentrate.
19. A process according to claim 17, which comprises: i) forming an aqueous slurry of defatted soy meal; 4&421 - 17 ii) subjecting said slurry to alkaline conditions at a pH from 9 to 12 in the presence of 0.2 M to 1 K of an alkali metal halide to obtain a mixture in which pigments and off-flavour components are substantially completely released; iii) diluting said mixture with water to obtain a mixture in which the molarity of the alkali metal halide is less than 0.2 M; iv) separating the insoluble material, mainly consisting of carbohydrates from the mixture to obtain a clarified protein solution; v) precipitating the protein at a pH ranging from 4.5 to 5.5 from, the solution to obtain a protein isolate.
20. A process for producing proteinaceous foodstuffs including meat or fish analogues which comprises replacing at least part of the protein originally present by a product prepared according to any one of the preceding claims.
21. Foodstuffs produced according to claim 20.
22. A process substantially as hereinbefore described with particular reference tc the examples 1-5.
23. Vegetable protein product whenever prepared according to a process described in any one of claims 1 to 19.
IE1189/77A 1976-06-11 1977-06-10 Proteinaceous foodstuff IE45421B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB24351/76A GB1580051A (en) 1976-06-11 1976-06-11 Proteinaceous foodstuff

Publications (2)

Publication Number Publication Date
IE45421L IE45421L (en) 1977-12-11
IE45421B1 true IE45421B1 (en) 1982-08-25

Family

ID=10210353

Family Applications (1)

Application Number Title Priority Date Filing Date
IE1189/77A IE45421B1 (en) 1976-06-11 1977-06-10 Proteinaceous foodstuff

Country Status (11)

Country Link
JP (1) JPS52154553A (en)
BE (1) BE855597A (en)
CA (1) CA1080026A (en)
DE (1) DE2726185A1 (en)
FR (1) FR2354055A1 (en)
GB (1) GB1580051A (en)
IE (1) IE45421B1 (en)
IT (1) IT1083508B (en)
LU (1) LU77524A1 (en)
NL (1) NL7706381A (en)
SE (1) SE7706793L (en)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4072670A (en) * 1976-10-26 1978-02-07 Mead Johnson & Company Low phytate isoelectric precipitated soy protein isolate
US4091120A (en) * 1976-11-15 1978-05-23 Mead Johnson & Company Liquid dietary product containing soy protein membrane isolate
JPS5457663U (en) * 1977-09-30 1979-04-20
US4420425A (en) * 1982-08-02 1983-12-13 The Texas A&M University System Method for processing protein from nonbinding oilseed by ultrafiltration and solubilization
JP3416312B2 (en) * 1994-12-26 2003-06-16 森永製菓株式会社 How to make soy protein
EP1343386A2 (en) 2000-11-21 2003-09-17 Cargill, Inc. Modified oilseed material
US6630195B1 (en) 2000-11-21 2003-10-07 Cargill, Incorporated Process for producing oilseed protein products
US7429399B2 (en) 2001-06-18 2008-09-30 Solae, Llc Modified oilseed material
US7094439B2 (en) 2000-11-30 2006-08-22 Kraft Foods Holdings, Inc. Method of deflavoring whey protein
US7037547B2 (en) 2000-11-30 2006-05-02 Kraft Foods Holdings, Inc. Method of deflavoring soy-derived materials for use in beverages
US6787173B2 (en) 2000-11-30 2004-09-07 Kraft Foods Holdings, Inc. Method of deflavoring soy-derived materials
US20050053705A1 (en) * 2003-09-04 2005-03-10 Kraft Foods Holdings, Inc. Soluble soy protein with superior functional properties
US7045163B2 (en) 2000-11-30 2006-05-16 Kraft Foods Holdings, Inc. Method of deflavoring soy-derived materials
US7108881B2 (en) 2000-11-30 2006-09-19 Kraft Foods Holdings, Inc. Method of preparation of high quality soy cultured products
US7582326B2 (en) 2003-10-29 2009-09-01 Kraft Foods Global Brands Llc Method of deflavoring whey protein using membrane electrodialysis
US7354616B2 (en) 2003-11-25 2008-04-08 Solae, Llc Modified oilseed material with a high gel strength
DE102007012439A1 (en) * 2007-03-15 2008-09-18 Emsland-Stärke GmbH Process for obtaining plant proteins and / or peptides, proteins and / or peptides produced therefrom and use thereof
IT1399500B1 (en) * 2010-04-13 2013-04-19 Stazione Sperimentale Per L Ind Delle Conserve Alimentari BIOPOLYMER FROM WASTE OF THE FOOD INDUSTRY.

Also Published As

Publication number Publication date
FR2354055B1 (en) 1983-07-29
NL7706381A (en) 1977-12-13
JPS52154553A (en) 1977-12-22
FR2354055A1 (en) 1978-01-06
IE45421L (en) 1977-12-11
BE855597A (en) 1977-12-12
JPS5612421B2 (en) 1981-03-20
DE2726185A1 (en) 1977-12-22
LU77524A1 (en) 1978-01-26
SE7706793L (en) 1977-12-12
CA1080026A (en) 1980-06-24
IT1083508B (en) 1985-05-21
GB1580051A (en) 1980-11-26

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