GB906424A - Improvements in or relating to tobacco smoke filter elements - Google Patents

Improvements in or relating to tobacco smoke filter elements

Info

Publication number
GB906424A
GB906424A GB39235/58A GB3923558A GB906424A GB 906424 A GB906424 A GB 906424A GB 39235/58 A GB39235/58 A GB 39235/58A GB 3923558 A GB3923558 A GB 3923558A GB 906424 A GB906424 A GB 906424A
Authority
GB
United Kingdom
Prior art keywords
filaments
waxy material
plasticizer
acids
booth
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.)
Expired
Application number
GB39235/58A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
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 Eastman Kodak Co filed Critical Eastman Kodak Co
Publication of GB906424A publication Critical patent/GB906424A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24DCIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
    • A24D3/00Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
    • A24D3/06Use of materials for tobacco smoke filters
    • A24D3/14Use of materials for tobacco smoke filters of organic materials as additive
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D39/00Filtering material for liquid or gaseous fluids
    • B01D39/14Other self-supporting filtering material ; Other filtering material
    • B01D39/16Other self-supporting filtering material ; Other filtering material of organic material, e.g. synthetic fibres
    • B01D39/18Other self-supporting filtering material ; Other filtering material of organic material, e.g. synthetic fibres the material being cellulose or derivatives thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cigarettes, Filters, And Manufacturing Of Filters (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Fats And Perfumes (AREA)

Abstract

Tobacco smoke filtering element manufacture includes the steps of spreading out a plurality of filaments, melting a wax or waxy material having a melting point above 35 DEG C. and spraying it on the filaments in a particle size of less than 30 microns (e.g. down to 0.5 micron) to form nodes and ridges thereon. The filaments may comprise a tow of at least 10,000 continuous crimped cellulose acetate filaments of from less than 3 to 16 individual denier and 20,000 to 100,000 total denier and the waxy material be a high-molecular-weight compound which is sprayed incorporated in a non-toxic plasticizer so as to constitute 25% to 80% of the spray formulation and comprises a fatty acid ester, fatty acid or fatty alcohol, miscible with the plasticizer at above 50 DEG C., the sprayed filaments being compacted into a bundle which is wrapped and cut into lengths which are stored at above 20 DEG C. for at least 20 minutes to set rigid. The waxy material is melted and dissolved in heated plasticizer, being insoluble therein below 35 DEG C. Alternatively, unheated plasticizer may be sprayed on in one booth and melted waxy material in a following booth. Exemplary plasticizers are triacetin, glycerol di-acetate, glycerol di- and tri-propionates, di(methoxyethyl) phthalate, ethyl phthalyl methyl glycollate, triethyl citrate and mixtures thereof. From 10% to 30% of filament weight of the wax or waxy material may be used. Exemplary fatty acid esters are glycerol monstearate, diethylene glycol stearate, ethylene glycol monostearate, polyethylene glycol monostearate, the triglyceride of 12-hydroxy stearic acid, the acetylated monoglyceride from hydrogenated lard, propylene glycol monostearate, and esters of polypropylene glycol; a mixture of glycol monostearate and hydrogenated acetylated monoglyceride may be used. Exemplary fatty acids are saturated acids of formula CnH2nO2, where n is from 10 to 24, e.g. lauric, myristic, palmitic and stearic acids, and unsaturated acids of formula CnH2n-2XO2, where n is from 10 to 24 and x from 1 to 5, e.g. erucic, elaidic, elaeostearic and angelic acids; such acids containing substituent groups (e.g. hydroxyl, carbonyl, chloro) may also be used. Exemplary fatty alcohols are stearyl alcohol (octadecanol) and cetyl alcohol (hexadecanol), with or without substituent groupings as above. Waxes which may be used are carnauba, paraffin, spermaceti, montan and polyolefin waxes, beeswax, "Acrawax" (Registered Trade Mark) and castorwax (hydrogenated castor oil). They may be applied alone or with, before or after plasticizer. Quantitive process examples and completed filter test results are given. The spray booth for the wax or waxy material is so heated and jacketed that any droplets not attaching to the filaments are maintained fluid and can be recycled. Cooling devices may be mounted adjacent the booth filament exit, the adjacent filament-forwarding rolls having blades which scrape solid depositions therefrom for re-melting.ALSO:Tobacco smoke filtering element manufacture includes the steps of spreading out a plurality of filaments, melting a wax or waxy material having a melting point above 35 DEG C. and spraying it on the filaments in a particle size of less than 30 microns (e.g. down to 0.5 micron) to form nodes and ridges thereon. The filaments may comprise a tow of at least 10,000 continuous crimped cellulose acetate filaments of from less than 3 to 16 individual denier and 20,000 to 100,000 total denier and the waxy material be as highmolecular-weight compound which is sprayed incorporated in a non-toxic plasticizer so as to constitute 25% to 80% of the spray formulation, and comprises a fatty acid ester, fatty acid or fatty alcohol, miscible with the plasticizer at above 50 DEG C., the sprayed filaments being compacted into a bundle which is wrapped and cut into lengths which are stored at above 20 DEG C. for at least 20 minutes to set rigid. The waxy material is melted and dissolved in heated plasticizer, being insoluble therein below 35 DEG C. Alternatively, unheated plasticizer may be sprayed on in one booth and melted waxy material in a following booth. Exemplary plasticizers are triacetin, glycerol di-acetate, glycerol di- and tri-propionates, di-(methoxy-ethyl) phthalate, ethyl phthalyl methyl glycollate, triethyl citrate and mixtures thereof. From 10% to 30% of filament weight of the wax or waxy material may be used. Exemplary fatty acid esters are glycerol monostearate, diethylene glycol stearate, ethylene glycol monostearate, polyethylene glycol monostearate, the triglyceride of 12-hydroxy stearic acid, the acetylated monoglyceride from hydrogenated lard, propylene glycol monostearate, and esters of polypropylene glycol; a mixture of glycol monostearate and hydrogenated acetylated monoglyceride may be used. Exemplary fatty acids are saturated acids of formula CnH2nO2, where n is from 10 to 24, e.g. lauric, myristic, palmitic and stearic acids, and unsaturated acids of formula CnH2n-2xO2, where n is from 10 to 24 and x from 1 to 5, e.g. erucic, elaidic, elaceostearic and angelic acids; such acids containing substituent groupings (e.g. hydroxyl, carbonyl, chloro) may also be used. Exemplary fatty alcohols are stearyl alcohol (octadeconal) and cetyl alcohol (hexadeconal), with or without substituent groupings as above. Waxes which may be used are carnauba, paraffin, spermaceti, montan and polyolefin waxes, beeswax, "Acrawax" (Registered Trade Mark) and castorwax (hydrogenated castor oil). They may be applied alone or with, before or after plasticizer. Quantitative process examples and completed filter test results are given. The spray booth for the wax or waxy material is so heated and jacketed that any droplets not attaching to the filaments are maintained fluid and can be recycled. Cooling devices may be mounted adjacent the booth filament exit, the adjacent filament-forwarding rolls having blades which scrape solid depositions therefrom for re-melting.
GB39235/58A 1957-12-09 1958-12-05 Improvements in or relating to tobacco smoke filter elements Expired GB906424A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US701310A US3026226A (en) 1957-12-09 1957-12-09 Process of manufacturing filters

Publications (1)

Publication Number Publication Date
GB906424A true GB906424A (en) 1962-09-19

Family

ID=24816853

Family Applications (1)

Application Number Title Priority Date Filing Date
GB39235/58A Expired GB906424A (en) 1957-12-09 1958-12-05 Improvements in or relating to tobacco smoke filter elements

Country Status (7)

Country Link
US (1) US3026226A (en)
CH (1) CH391550A (en)
DE (1) DE1079521B (en)
ES (1) ES245619A1 (en)
FR (1) FR1217814A (en)
GB (1) GB906424A (en)
MY (1) MY6400010A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999059436A1 (en) * 1998-05-20 1999-11-25 Rhodia Acetow Gmbh Method for producing hardened filter rods in the cigarette industry
WO2001066228A1 (en) * 2000-03-07 2001-09-13 Clariant Gmbh Agent and method for removing pollutants from gases
WO2001066229A1 (en) * 2000-03-07 2001-09-13 Rudolf Gutmann Filter for an air or gas purification device

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3276931A (en) * 1956-12-27 1966-10-04 Johns Manville Apparatus and process for combining glass fibers with synthetic resin fibers
US3173427A (en) * 1962-02-05 1965-03-16 Eastman Kodak Co Tow with internally incorporated additive
US3246655A (en) * 1963-03-19 1966-04-19 Lorillard Co P Selective cigarette filters
US3818863A (en) * 1962-08-14 1974-06-25 Celanese Corp Centrifugal spray apparatus
BE637586A (en) * 1962-09-19
US3298380A (en) * 1962-12-14 1967-01-17 Burke Oliver W Jun Process for purification of tobacco smoke
US3190295A (en) * 1962-12-21 1965-06-22 Eastman Kodak Co Filter with combination plasticizer
US3229699A (en) * 1962-12-21 1966-01-18 Eastman Kodak Co Plasticized filter
US3311519A (en) * 1964-01-28 1967-03-28 Eastman Kodak Co Additive filter
DE1300854B (en) * 1965-05-14 1969-08-07 Reemtsma H F & Ph Filters for cigarettes
US3501361A (en) * 1965-09-22 1970-03-17 Eastman Kodak Co Method for producing cigarette filters
US3326221A (en) * 1966-07-19 1967-06-20 Celanese Corp Filter
US4752348A (en) * 1985-03-29 1988-06-21 Celanese Corporation Localized liquid additive applicator system for continuous cylindrical product
US4729390A (en) * 1985-07-31 1988-03-08 Eastman Kodak Company Tobacco smoke filtering material
DE4322966C2 (en) 1993-07-09 1995-10-26 Rhodia Ag Rhone Poulenc Cellulose acetate molded structures and their use as filter tow and tobacco smoke filter element
DE19536505A1 (en) * 1995-09-29 1997-04-10 Biotec Biolog Naturverpack Biodegradable filter material and process for its manufacture
CA2291326C (en) * 1999-01-23 2007-02-13 Kyung-Ju Choi Treated filter media
CA2464149A1 (en) * 2001-10-30 2003-05-08 Japan Tobacco Inc. Cigarette filter and filter-tipped cigarette
CN106723341B (en) * 2017-03-16 2020-04-14 云南巴菰生物科技有限公司 Fragrance sustained-release material composition, sustained-release perfume colloid and application thereof
KR20200098515A (en) 2017-12-21 2020-08-20 필립모리스 프로덕츠 에스.에이. Reduction of aerosol ammonia in heated aerosol-generating articles

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2602766A (en) * 1948-04-10 1952-07-08 Richard J Francis Reinforced plastic rods and methods of making same
BE528827A (en) * 1951-11-27
US2694661A (en) * 1952-02-12 1954-11-16 Parallel Plastics Co Process for forming adhesive-embedded fiber rods
US2774354A (en) * 1952-05-21 1956-12-18 Florman Irving Chlorophyl impregnated filter means for tobacco products
IT599386A (en) * 1952-12-05
US2805671A (en) * 1953-10-07 1957-09-10 Liggett & Myers Tobacco Co Aerosol filters
US2881771A (en) * 1954-12-20 1959-04-14 Eastman Kodak Co Cigarette filters
US2855633A (en) * 1955-06-13 1958-10-14 Chicopee Mfg Corp Process of treating fibers

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999059436A1 (en) * 1998-05-20 1999-11-25 Rhodia Acetow Gmbh Method for producing hardened filter rods in the cigarette industry
WO2001066228A1 (en) * 2000-03-07 2001-09-13 Clariant Gmbh Agent and method for removing pollutants from gases
WO2001066229A1 (en) * 2000-03-07 2001-09-13 Rudolf Gutmann Filter for an air or gas purification device

Also Published As

Publication number Publication date
ES245619A1 (en) 1959-06-16
MY6400010A (en) 1964-12-31
DE1079521B (en) 1960-04-07
US3026226A (en) 1962-03-20
CH391550A (en) 1965-04-30
FR1217814A (en) 1960-05-05

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