US3412044A - Diamine soap as dispersant in magnetic tape formulations - Google Patents

Diamine soap as dispersant in magnetic tape formulations Download PDF

Info

Publication number
US3412044A
US3412044A US461170A US46117065A US3412044A US 3412044 A US3412044 A US 3412044A US 461170 A US461170 A US 461170A US 46117065 A US46117065 A US 46117065A US 3412044 A US3412044 A US 3412044A
Authority
US
United States
Prior art keywords
soap
diamine
dispersant
magnetic tape
magnetic
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 - Lifetime
Application number
US461170A
Inventor
Graubart Lawrence
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.)
Ampex Corp
Original Assignee
Ampex Corp
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 Ampex Corp filed Critical Ampex Corp
Priority to US461170A priority Critical patent/US3412044A/en
Priority to DEA52561A priority patent/DE1285004B/en
Priority to BE681701D priority patent/BE681701A/xx
Priority to GB24004/66A priority patent/GB1079609A/en
Priority to FR63665A priority patent/FR1481679A/en
Priority to NL6607670A priority patent/NL6607670A/xx
Application granted granted Critical
Publication of US3412044A publication Critical patent/US3412044A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material
    • G11B5/68Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent
    • G11B5/70Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer
    • G11B5/7013Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by the dispersing agent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes
    • C08L75/06Polyurethanes from polyesters
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material

Definitions

  • This invention relates to magnetic recording tapes and, more particularly, relates to magnetic recording tapes wherein a novel fatty acid soap of a long chain diamine is used as a dispersing agent informing a dispersion of the magnetic iron oxide utilized in making the recording tape.
  • the dispersant mixture contains at least 50% of the diamine soap in order to secure effective results.
  • the novel dispersant was employed in conjunction with a polyurethane resin system.
  • the particular polyurethane employed is sold under the trade name of Estane 5701 by B. F. Goodrich.
  • This particular polyurethane was made by reacting p-p'- diphenylmethane diisocyanate, adipic acid and butanediol- 1,4 in such proportions that all of the isocyanate groups have reacted to give a substantially unreactive polymer having the following characteristics:
  • This polyurethane resin can be used either alone or in combination with other resins such as a vinyl chloridevinyl acetate copolymer.
  • the particular copolymer selected is one sold under the trade name VAGH by Union Carbide and Chemical Corporation.
  • This particular vinyl chloride-vinyl acetate copolymer contains approximately: 91% vinyl chloride; 3% vinyl acetate; 6% vinyl alcohol.
  • This copolymer has an intrinsic viscosity in cyclohexanone at 20 C. of 0.57 c.p.s. and a specific gravity of 1.39.
  • a novel fatty acid soap of a long chain diamine is employed to replace all or part of the licithin which is normally used in pre paring dispersions of magnetic iron oxides.
  • One particularly suitable fatty acid soap is sold under the trade name Troykyd 98C, and this is a soap made by reacting stoichiometric amounts of a saturated fatty acid having from 12 to 18 carbon atoms and a diamine having from 12 to 18 carbon atoms in each chain.
  • Troykyd 98C has a molecular weight of about 490. As the following examples show, this can be effectively combined with lecithin for use as a dispersant or it can be used along as a dispersant.
  • Components 1 to 5 are dispersed in a pebble-mill using appropriate amounts of methylethyl ketone, methylisobutyl ketone and toluol for 48 hours. At the end of this grinding period a solution of the binder in similar solvents is added and grinding is continued for 24 hours. This mixture is then coated on a plastic base and dried.
  • Example 3 The dispersion and coating of this example is the same as Example 1.
  • the improvement consisting essentially of employing as a dispersing agent a diamine soap having a molecular weight of about 490; said soap being made from a fatty acid having 12 to 18 carbon atoms and a diamine having from 12. to 18 carbon atoms in each chain.
  • the dispersant comprises a mixture of the long chain fatty acid-diamine soap and lecithin, wherein the amine soap constitutes at least one half of the dispersant.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Magnetic Record Carriers (AREA)

Description

United States Patent Oifice 3,412,044 Patented Nov. 19, 1968 3,412,044 DIAMINE SOAP AS DISPERSANT IN MAGNETIC TAPE FORMULATIONS Lawrence Graubart, Daly City, Calif., assignor to Ampex Corporation, Redwood City, Calif., a corporation of California No Drawing. Filed June 3, 1965, Ser. No. 461,170 2 Claims. (Cl. 252-6256) ABSTRACT OF THE DISCLOSURE In making magnetic tapes and the like it is necessary to first form a dispersion of the magnetic particles in an organic solvent. The invention relates to the use of along chain fatty acid diamine soap as the dispersing agent. This can be used alone or in admixture with lecithin.
This invention relates to magnetic recording tapes and, more particularly, relates to magnetic recording tapes wherein a novel fatty acid soap of a long chain diamine is used as a dispersing agent informing a dispersion of the magnetic iron oxide utilized in making the recording tape.
In the manufacture of magnetic recording media wherein a dispersion of magnetic particles is held in a resinous binder on a substrate it is the universal practice to first prepare a dispersion of a magnetic iron oxide in an organic solvent and a surfactant. These materials are ordinarily ground together as in a ball mill for many hours or days with the other nonresin components of the binder such as carbon black, silicone oil, fungicides and the like in order to secure the best possible dispersion. The magnetic iron oxide tends to form clumps resulting in a tape having a low output and nonuniform response characteristics necessitating the long grinding time. To a large measure, it is the degree of dispersion which determines the ultimate quality of the tape. After the dispersion is produced, it is mixed with a solution of the resinous binder to produce the composition which is used as a coating. This mixture is then applied to a tape base and the solvent evaporated to produce the final recording medium.
In preparing the dispersion, it is universal practice to incorporate a surfactant or wetting agent in the mixture to reduce surface tension and permit the binder constituent to penetrate between particles of the magnetic iron oxide to aid in breaking up the particles and to prevent agglomeration of the particles. The commonly used agent for this purpose is lecithin which is not fully effective as a surfactant but which is the best material for this purpose heretofore found. It has now been found that if a fatty acid soap of a long chain diamine is incor porated in the dispersion, a superior dispersion is produced resulting in a tape having a high, uniform output. The diamine soap may be used to entirely replace the lecithin or can be used in conjunction with it. Ordinarily, the dispersant mixture contains at least 50% of the diamine soap in order to secure effective results.
In the following nonlimiting examples illustrating preferred embodiments of the invention, the novel dispersant was employed in conjunction with a polyurethane resin system. The particular polyurethane employed is sold under the trade name of Estane 5701 by B. F. Goodrich. This particular polyurethane was made by reacting p-p'- diphenylmethane diisocyanate, adipic acid and butanediol- 1,4 in such proportions that all of the isocyanate groups have reacted to give a substantially unreactive polymer having the following characteristics:
This polyurethane resin can be used either alone or in combination with other resins such as a vinyl chloridevinyl acetate copolymer. The particular copolymer selected is one sold under the trade name VAGH by Union Carbide and Chemical Corporation. This particular vinyl chloride-vinyl acetate copolymer contains approximately: 91% vinyl chloride; 3% vinyl acetate; 6% vinyl alcohol.
This copolymer has an intrinsic viscosity in cyclohexanone at 20 C. of 0.57 c.p.s. and a specific gravity of 1.39.
However, it should be understood that the employment of these particular resin mixtures is for illustration purposes only, and that the crux of the present invention is the employment of a novel dispersing system for dispersing a magnetic iron oxide in an organic solvent which is then added to a solution of the selected resin. Thus, the novel dispersing system of the present invention could be used with any resin system.
In accordance with the present invention, a novel fatty acid soap of a long chain diamine is employed to replace all or part of the licithin which is normally used in pre paring dispersions of magnetic iron oxides. One particularly suitable fatty acid soap is sold under the trade name Troykyd 98C, and this is a soap made by reacting stoichiometric amounts of a saturated fatty acid having from 12 to 18 carbon atoms and a diamine having from 12 to 18 carbon atoms in each chain. Troykyd 98C has a molecular weight of about 490. As the following examples show, this can be effectively combined with lecithin for use as a dispersant or it can be used along as a dispersant.
The following nonlimiting examples illustrate preferred embodiments of the invention:
EXAMPLE I Percent solids volume 1. Magnetic oxide 42.0 2. Conductive carbon black 7.9 3. Lecithin 2.4 4. Troykyd 98C 5.4 5. Additives 1 4.9 6. Binder (20% VAGH-% Estane 5701) 37.4
1 Silicone oil, fungicides.
Components 1 to 5 are dispersed in a pebble-mill using appropriate amounts of methylethyl ketone, methylisobutyl ketone and toluol for 48 hours. At the end of this grinding period a solution of the binder in similar solvents is added and grinding is continued for 24 hours. This mixture is then coated on a plastic base and dried.
EXAMPLE II Percent solids volume 1. Magnetic oxide 41.6 2. Conductive carbon black 7.8 3. Lecithin 4.0 4. Troykyd 98C 4.0 5. Additives 1 5.2 6. Binder (30% VAGH-70% Estane 5701) 37.4
1 Silicone oil, fungicides.
3 The dispersion and coating of this example is the same as Example 1.
EXAMPLE III Percent solids volume 1. Magnetic oxide 43.8 2. Conductive carbon black 7.8 3. Troykyd 98C 9.1 4. Additives 1 2.6 5. Binder (Estane 5701) 36.7
1 Silicone oil, fungicides.
oxide in an organic solvent as a preliminary step in manufacturing a magnetic recording tape or the like, the improvement consisting essentially of employing as a dispersing agent a diamine soap having a molecular weight of about 490; said soap being made from a fatty acid having 12 to 18 carbon atoms and a diamine having from 12. to 18 carbon atoms in each chain.
2. The process of claim 1 wherein the dispersant comprises a mixture of the long chain fatty acid-diamine soap and lecithin, wherein the amine soap constitutes at least one half of the dispersant.
References Cited UNITED STATES PATENTS 9/1964 Wagner et a1. 25262.54 7/1966 Falk 252-6254
US461170A 1965-06-03 1965-06-03 Diamine soap as dispersant in magnetic tape formulations Expired - Lifetime US3412044A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US461170A US3412044A (en) 1965-06-03 1965-06-03 Diamine soap as dispersant in magnetic tape formulations
DEA52561A DE1285004B (en) 1965-06-03 1966-05-18 Process for the production of a magnetizable recording medium
BE681701D BE681701A (en) 1965-06-03 1966-05-27
GB24004/66A GB1079609A (en) 1965-06-03 1966-05-27 Improvements in or relating to magnetic iron oxide dispersions suitable for magnetic recording media
FR63665A FR1481679A (en) 1965-06-03 1966-06-01 An improved dispersing agent for the preparation of a dispersion of a magnetic iron oxide in an organic solvent
NL6607670A NL6607670A (en) 1965-06-03 1966-06-02

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US461170A US3412044A (en) 1965-06-03 1965-06-03 Diamine soap as dispersant in magnetic tape formulations

Publications (1)

Publication Number Publication Date
US3412044A true US3412044A (en) 1968-11-19

Family

ID=23831478

Family Applications (1)

Application Number Title Priority Date Filing Date
US461170A Expired - Lifetime US3412044A (en) 1965-06-03 1965-06-03 Diamine soap as dispersant in magnetic tape formulations

Country Status (5)

Country Link
US (1) US3412044A (en)
BE (1) BE681701A (en)
DE (1) DE1285004B (en)
GB (1) GB1079609A (en)
NL (1) NL6607670A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1431854A (en) * 1972-04-07 1976-04-14 Sony Corp Magnetic recording media and methods of making them
DE3128013C1 (en) * 1981-07-15 1982-11-11 Siemens Ag Control circuit for at least one light emitting diode

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3149996A (en) * 1960-11-16 1964-09-22 Basf Ag Magnetic record member
US3262812A (en) * 1964-03-26 1966-07-26 Gen Electric Magnetic recording tape with magnetic layer of oxide coated iron-cobalt alloy particles in a binder

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3149996A (en) * 1960-11-16 1964-09-22 Basf Ag Magnetic record member
US3262812A (en) * 1964-03-26 1966-07-26 Gen Electric Magnetic recording tape with magnetic layer of oxide coated iron-cobalt alloy particles in a binder

Also Published As

Publication number Publication date
BE681701A (en) 1966-10-31
DE1285004B (en) 1968-12-12
NL6607670A (en) 1966-12-05
GB1079609A (en) 1967-08-16

Similar Documents

Publication Publication Date Title
US3247017A (en) Magnetic recording tape for sound, image and pulse recording
US3650828A (en) Magnetic coating formulation for recording tape
US3320090A (en) Phenoxy-polyurethane magnetic tape binder
US3149995A (en) Magnetic recording element and method of preparation thereof
DE3152313T1 (en)
US4544601A (en) Magnetic recording medium
US4115290A (en) Magnetic recording medium
US4234438A (en) Magnetic recording medium
US3647539A (en) Magnetic recording tape and method for preparing the same
DE3023799A1 (en) MAGNETIC RECORDING MEDIUM
US3412044A (en) Diamine soap as dispersant in magnetic tape formulations
US3558353A (en) Magnetic recording medium
US4671995A (en) Magnetic recording medium comprising an undercoating made of a mixture of thermosetting polyurethane and polyester resins
US4579778A (en) Magnetic recording medium
US3681137A (en) Magnetic recording media
US4634627A (en) Magnetic recording medium comprising a surface-treated abrasive
DE3414926C2 (en) Magnetic recording medium
EP0150005B1 (en) Magnetic storage medium
US3404997A (en) Magnetic recording media
US4414288A (en) Magnetic recording medium
JPH0263251B2 (en)
US4404260A (en) Magnetic recording medium and method of manufacture
US4370383A (en) Magnetic recording medium
JPS5857815B2 (en) Jikiki Rokutai
EP0083011A2 (en) Process for producing magnetic recording mediums