Magnetic recording media having a branched thermoplastic polyurethane binder containing a polysiloxane component in the main chain

Abstract
Magnetic recording media consist of a nonmagnetic substrate and at least one magnetizable layer which is firmly applied thereon and is based on a polyurethane binder which may be crosslinked with polyisocyanate, not less than 50% by weight of the binder consisting of a low molecular weight branched polyureaurethane having OH-containing urea groups at the chain ends, and the sliding properties of the said binder being improved and its coefficient of friction reduced by incorporation of siloxane groups.
Description

The present invention relates to magnetic recording media, consisting of a nonmagnetic substrate and at least one magnetizable layer which is firmly applied thereon and is based on a polyurethane binder which may be crosslinked with a polyisocyanate, not less than 50% by weight of a binder consisting of a low molecular weight branched polyureaurethane having OH-containing urea groups at the chain ends and the sliding properties being improved and friction reduced by the incorporation of siloxane groups.
In modern audio and video recording and playback apparatuses, magnetic recording media have to meet many different requirements. In addition to the high requirements for the recording and playback properties of audio tapes, video tapes and computer tapes, which are constantly being improved, there is a demand for constant improvement especially with regard to the mechanical properties of the recording media. Magnetic layers must be very flexible and have high resilience and high tensile strength. In addition, in order to avoid drops in output level, there is an increasing need to reduce the coefficients of friction and increase the abrasion resistance and resistance to wear.
The recording and playback properties of the magnetic recording systems can be improved, for example, by increasing the pigment volume concentration or by using magnetic material which is more finely divided. However, such measures have a permanent effect on the mechanical stability of the magnetic layer.
The patent literature describes many polyurethanes or polyurethane elastomers which are suitable for the production of magnetic recording media, for example DE-B 11 06 959, DE-B 25 00 921 or 24 42 763, DE-B 27 53 694 or DE-A 32 27 164.
When these conventional binder systems are used, depending on the formation of the layer very high frictional forces and frequently also the stick-slip effect or squeal phenomena occur in the recording or playback of signals by means of magnetic recording media which are guided in contact with the head and also moved over guide rollers, guide pins or other guidance elements. Stick-slip denotes irregular tape transport, where the tape alternately stops and travels forward. Squeal is irregular tape transport where, although the speed of the tape is not constant, the tape does not come to a stop. The resulting abrasion affects both the life and the operational reliability.
The properties of magnetic recording media during continuous operation are thus greatly affected by the surface friction (sliding friction) of the magnetic layer. Hence, very low surface friction is desirable, without the recording or playback of signals being adversely affected.
It is therefore usual to add lubricants to the layer compositions of the magnetic recording media. Suitable lubricants for this purpose are a large number of different lubricants, such as polydimethylsiloxanes, liquid paraffins, waxes, saturated and unsaturated fatty acids, fatty esters, fatty amides, salts of fatty acids and solid lubricants, such as molybdenum sulfide, graphite, polytetrafluoroethylene powder and polytrichlorofluoroethylene powder. It has also been reported that, compared with the solid lubricants, liquid or pasty lubricants have the advantage that the surface to be lubricated is covered by a homogeneous thin surface film of these lubricants; the amount of lubricant added must be kept very small since otherwise the surface readily becomes tacky. However, these liquid lubricants frequently cannot be used as the sole lubricant and are therefore combined with solid or pasty lubricants. When liquid lubricants are used exclusively neither sticking nor blocking of the tapes can be permanently avoided in many fields of use, in particular during prolonged operation and under unfavorable climatic conditions.
For example, reducing the surface friction by adding silicone oil, as described in, for example, DE-B 877 213, leads to exudation of the lubricant and hence to sticking or blocking of individual magnetic layers, especially in the environmental test at 40.degree. C. and 80% relative humidity.
When lubricants in the form of finely divided, insoluble hydrophobic solids or waxy substances are added, the lubricating effect is not uniform; instead, shortly after production, the solid particles are located only in limited areas at the surface and in the interior of the magnetic layer. These hydrophobic lubricants coat the generally hydrophilic magnetic material poorly if at all and are readily exuded, particularly under unfavorable climatic conditions, such as high temperature and high atmospheric humidity. This results in deposits on all parts which come into contact with the tape, in particular on the head, causing drops in output level.
The application of polymeric siloxane-containing compounds, as described in DE-B 23 64 879, results in satisfactory behavior under high temperature and humidity conditions, but there is a danger here that the oligomeric components will be collected by the read head, these deposits on the read head causing a deterioration in the recording and playback properties.
Independently of this, it was found that the known high molecular weight polyurethane elastomers, as binders or in binder combinations, can no longer meet the increasing quality requirements with regard to layer adhesion if both temperature and atmospheric humidity are increased, for example to 30-60.degree. C. at 80-100% relative humidity.
However, the disadvantage of using the high molecular weight binders is the high solvent requirement, the long dispersing time and also the required two-phase dispersing process. Furthermore, in these binder systems, the particular properties of the magnetic materials are unsatisfactory.
Another method was proposed in JP-A 61-42745. Here, two protective layers are applied to the magnetic layer to improve the coefficients of friction and the abrasion resistance, the outer layer consisting of a silicone-modified polyurethane acrylate. However, the production of such a layer structure is very expensive.
Moreover, the use of a polyurea resin which has siloxane compounds in the molecule as a binder has already been described (JP-A 61-84717). This binder is used in an uncrosslinked form. To obtain the desired properties, a very high Si content of from 5 to 50% by weight is necessary. Incorporation of more than 10 equivalent percent of the silicon component leads to binders having reduced strength and lower adhesive strength. A straight-chain polyurethaneurea resin which has siloxane units in the polymer chain is disclosed in JP-A 62-62428. To obtain the desired properties, however, external lubricants in an amount of from 0.2 to 20 parts by weight per 100 parts of binder are additionally required.
It is an object of the present invention to provide magnetic recording media, consisting of a non-magnetic substrate and at least one magnetizable layer which is firmly applied thereon and is based on magnetic material finely dispersed in a polymer binder which has greatly improved sliding friction and contains further conventional additives, the said recording media having both improved resistance to wear and reduced coefficients of friction, even under unfavorable climatic conditions, but nevertheless not exhibiting disadvantageous blocking during operation of the recording media or exudation of lubricants.
We have found that this object is achieved by a magnetic recording medium, consisting of a nonmagnetic substrate and at least one magnetic layer which is applied firmly thereon and is based on a magnetic material finely dispersed in a binder consisting of not less than 50% by weight of a thermoplastic polyurethane, if the thermoplastic polyurethane used is a siloxane-containing, iso-cyanate-free, branched polyurethane which is soluble in tetrahydrofuran, has OH-containing urea groups at the chain ends and a molecular weight of from 4,000 to 30,000 and is prepared from
A) 1 mole of a polyol having a molecular weight of from 400 to 4,000,
B) from 0.3 to 9 moles of a diol of 2 to 18 carbon atoms,
C) from 0.01 to 1 mole of a triol of 3 to 18 carbon atoms,
D) from 0.001 to 0.4 mole of an organofunctional polysiloxane compound having two terminal groups reactive to isocyanates and a molecular weight of from 300 to 4,000,
E) from 1.25 to 13 moles of a diisocyanate of 6 to 30 carbon atoms, the NCO: OH ratio in the sum of the components A, B, C. and D being 1.05:1.0-1.4:1.0, and
F) from 0.05 to 4 moles of an OH-containing primary or secondary amine which is reactive to isocyanates.
To obtain special properties, it is advantageous if the polymer has an OH number of from 30 to 160, preferably from 40 to 80. The molecular weight is from 4,000 to 30,000, corresponding to a K value (1% strength in dimethylformamide) of from 20 to 45. In synthesizing this polymer, it has proven advantageous if some, preferably more than 80%, in particular more than 90%, of the terminal OH groups consist of one of the following radicals: ##STR1## where R is --(CH.sub.2).sub.n --, R' is --H, --CH.sub.3, --(CH.sub.2).sub.m --CH.sub.3, n is from 2 to 10 and m is from 1 to 10.
Polymers having this composition have better adhesive strength than those without these terminal groups. Consequently, it is also possible to increase the content of terminal OH groups with the result that, in the crosslinking with polyisocyanate, the degree of crosslinking can be varied within wide limits, meeting the requirements for the magnetic layer. The urea groups, which increase the dispersibility compared with the conventional magnetic materials, are also advantageous.
Polyurethanes used according to the invention as binders in the magnetic layers have in general a hardness of from 20 to 130 s according to DIN 53,157. Furthermore, they have a modulus of elasticity (according to DIN 53,457) of from 50 to 2500 Nmm.sup.-2, an elongation at break of greater than 70% (DIN 53,455) and a tensile strength of from 25 to 70 Nmm.sup.-2 (DIN 53,455). The softening point is from 80.degree. to 180.degree. C. A pendulum hardness (DIN 53,157) of from 25 to 125 s, a modulus of elasticity of from 55 to 2000 Nmm.sup.-2 and an elongation at break of from 80 to 500% and a tensile strength of from 25 to 50 Nmm.sup.-2 are particularly advantageous.
The advantageous properties of the magnetic recording media having the composition according to the invention compared with those obtained using the conventional thermoplastic polyurethane elastomers are also clearly evident if a polyisocyanate is added before the dispersion is applied to the substrate. Many organic di-, tri- or polyisocyanates or isocyanate prepolymers having a molecular weight of not more than 10,000, preferably from 500 to 3,000, may be used for crosslinking. Polyisocyanates or isocyanate prepolymers which carry more than 2 NCO groups per molecule are preferred. Polyisocyanates based on toluylene diisocyanate, hexamethylene diisocyanate or isophorone diisocyanate, which are formed by polyaddition to di- or triols or by biuret and isocyanurate formation, have proven particularly suitable. An adduct oftoluylene diisocyanate with trimethylolpropane and diethylene glycol is particularly advantageous.
Depending on the requirements set for the recording material, the polyisocyanate component can be added in an amount corresponding to up to 70% less than the stoichiometric amount, preferably up to 50%, or in an excess of up to 100%, preferably up to 50%, based on the OH group of the polyurethane binder to be crosslinked.
For the preparation of the polyurethanes, a polydiol having a molecular weight of from 400 to 4,000, preferably from 700 to 2,500, is used as component A. The known polyesterols, polyetherols, polycarbonatediols and polycaprolactonediols are suitable for this purpose.
Polyesterols are advantageously predominantly linear polymers having terminal OH groups, preferably those having two terminal OH groups. The acid number of the polyesterols is less than 10, preferably less than 3. The polyesterols can be prepared in a simple manner by esterifying aliphatic or aromatic dicarboxylic acids of 4 to 15, preferably 4 to 8, carbon atoms with glycols, preferably those of 2 to 25 carbon atoms, or by polymerization of lactones of 3 to 20 carbon atoms. Examples of suitable dicarboxylic acids are glutaric acid, pimelic acid, suberic acid, sebacic acid, dodecanedioic acid and preferably adipic acid, succinic acid and phthalic acid. The dicarboxylic acids can be used individually or as mixtures. For the preparation of the polyesterols, it may be advantageous to use the corresponding acid derivatives, such as anhydrides or acyl chlorides, instead of the dicarboxylic acids. Suitable aromatic dicarboxylic acids are terephthalic acid, isophthalic acid or mixtures of these with other dicarboxylic acids, for example diphenic acid, sebacic acid, succinic acid and adipic acid. Examples of suitable glycols are diethylene glycol, 1,5-pentanediol, 1,10-decanediol and 2,2,4-trimethyl-1,5-pentanediol. 1,2-Ethanediol, 1,4-butanediol, 1,6-hexanediol and 2,2-dimethyl-1,3-propanediol, 1,4-dimethylolcyclohexane, 1,4-diethanolcyclohexane and ethoxylated/-propoxylated products of 2,2-bis-(4-hydroxyphenylene)propane (bisphenol A) are preferably used. Depending on the desired properties of the polyurethanes, the polyols can be used alone or as a mixture in various ratios. Examples of suitable lactones for the preparation of the polyesterols are .alpha.,.alpha.-dimethyl-.beta.-propiolactone, .gamma.-butyrolactone and preferably .epsilon.-caprolactone.
The polyetherols are essentially linear substances which have terminal hydroxyl groups, contain ether units and possess a molecular weight of about 600-4,000, preferably 1,000-2,000. Suitable polyetherols can readily be prepared by polymerization of cyclic ethers, such as tetrahydrofuran, or by reacting one or more alkylene oxides, where the alkylene radical is of 2 to 4 carbon atoms, with an initiator molecule which contains two bonded active hydrogen atoms in the alkylene radical. Examples of alkylene oxides are ethylene oxide, 1,2-propylene oxide, epichlorohydrin and 1,2- and 2,3-butylene oxide. The alkylene oxides can be used individually, alternately one after the other or as a mixture. Examples of suitable initiator molecules are water, glycols, such as ethylene glycol, propylene glycol, 1,4-butanediol and 1,6-hexanediol, amines, such as ethylenediamine, hexamethylenediamine and 4,4'-diaminodiphenylmethane, and amino alcohols, such as ethanolamine. Like the polyesterols, the polyetherols too can be used alone or in the form of mixtures. The polycarbonatediols and their preparation are described in US-A 4 131 731, the polycarbonatediols generally being based on 1,6-hexanediol.
Diols of 2 to 20, preferably 2 to 10, carbon atoms are used as building block B, for example 1,2-ethanediol, 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, 1,5-pentanediol, 1,10-decanediol, 2-methyl-1,3-propanediol 2-methyl-2-butyl-1,3-propanediol, 2,2-dimethyl-1,4-butanediol, 2-methyl-2-butyl-1,3-propanediol, neopentylglycol hydroxypivalate, diethylene glycol, triethylene glycol and methyldiethanolamine. The diols can be used individually or as mixtures. Diamines of 2 to 15 carbon atoms, such as ethylenediamine, 1,6-hexamethylenediamine, 4,9-dioxododecane-1,12-diamine or 4,4'-diaminodiphenylmethane, or amino alcohols, e.g. monoethanolamine, monoisopropanolamine or 2-amino-2-methylpentan-2-ol, can also be used, in minor amounts. It has proven advantageous to incorporate the resulting urea groups in the polymer chain. The urea groups at the chain end are of minor importance.
The stated diols may furthermore be completely or partly replaced by water as building blocks B in the same manner.
Compounds of 3 to 18, preferably 3 to 6, carbon atoms are used as triols (building blocks C). Examples of corresponding triols are glycerol and trimethylolpropane. Low molecular weight reaction products of, for example, trimethylolpropane with ethylene oxide and/or propylene oxide are also suitable. The presence of triols in the polyaddition leads to branching of the end product, which has an advantageous effect on the mechanical properties of the polyurethane, unless local crosslinking occurs.
Components D are polysiloxanediols, polysiloxanedicarboxylic acids, .omega.-hydroxypolysiloxanecarboxylic acids or .omega.-hydroxypolysiloxaneamines. These products can be used individually or in combination. Because of the good handling properties and solubility in the relevant solvents, polysiloxanediols are preferred.
Such silicone oils having terminal hydroxyalkyl groups bonded to the silicon have, for example, the structure ##STR2## where R is a hydrocarbon radical of 1 to 20 carbon atoms, m is 1 and n is 2-133. Where R is CH.sub.3, for example, the Baysilon.RTM. grades from Bayer or Tego.RTM. OF-1010 or Tego.RTM. OF-1025 from Goldschmidt can be used.
For the formation of the siloxane-containing polyurethanes or NCO-containing intermediates, the building blocks stated under A, B, C and D are reacted with aliphatic, cycloaliphatic or aromatic diisocyanates of 6 to 30 carbon atoms (building block E). For example, compounds such as toluylene 2,4-diisocyanate, toluylene 2,6-diisocyanate, m-phenylene diisocyanate, 4-chlorophenylene 1,3-diisocyanate, naphthylene 1,5-diisocyanate, hexamethylene 1,6-diisocyanate, cyclohexylene 1,4-diisocyanate, tetrahyd-ronaphthylene 1,5-diisocyanate, diphenylmethane 4,4'-diisocyanate, dicyclohexylmethane 4,4'-diisocyanate or isophorone diisocyanate are suitable for this purpose. Siloxane-containing diisocyanates can also be used. These siloxane-containing isocyanates may account for up to 32 mol percent of the total molar amount of diisocyanate.
For the formation of the OH-containing polyurethaneurea elastomers, the NCO-containing intermediate obtained from A to E is reacted with amino alcohols (of 2 to 16 carbon atoms). These amino alcohols of 2 to 16, preferably 3 to 6, carbon atoms include monoethanolamine, methylisopropanolamine, ethylisopropanolamine, methylethanolamine, 3-aminopropanol, 1-ethylaminobutan-2-ol, 4-methyl-4-aminopentan-2-olandN-(2-hydroxyethyl)-aniline. Diolamines are particularly suitable since, as a result of their addition at the chain end, the OH number of the polymer is doubled. Diethanolamine and diisopropanolamine have proven particularly advantageous.
The ratio of components A to F to one another may be varied from 1.25 to 13 moles of diisocyanate per mole of polydiol when from 0.3 to 9, preferably from 0.5 to 5, moles of the diol of 2 to 18 carbon atoms and from 0.01 to 1, preferably from 0.15 to 0.5, mole of triol are used, the amount of the diol used partly depending on the molecular weight of the polydiol used. The amount of isocyanate used should be from 5 to 35% less than the stoichiometric amount, based on the amounts of NH-containing or hydroxyl-containing compounds, so that, at the end of the reaction, there is virtually no free, unconverted isocyanate but there are free, unconverted hydroxyl groups. For practical reasons and reasons relating to coating technology, however, it is frequently advantageous to use a diisocyanate excess of from 5 to 40%, preferably from 10 to 30%, based on the amount required for complete conversion of the reactants, in a preliminary reaction of components A, B, D and E, so that the ratio of the number of hydroxyl groups used to the number of isocyanate groups in this reaction stage is from about 1:1.05 to 1:1.4, preferably from about 1:1.1 to 1:1.30. In the second reaction stage, an amount of component F such that the NH content corresponds to the NCO content, i.e. from 0.05 to 4, preferably from 0.3 to 2.5, moles per mole of component A, is added, or the NCO prepolymer is added to the amino alcohol so that the amino groups react with the isocyanate. If, in the second reaction stage, slightly less than the stoichiometric amount of NH or NH.sub.2 groups relative to the NCO groups is available, some of the amino alcohol is incorporated in the molecule and, depending on the amino alcohol, results in a branching point. If an excess of NH groups is used, the amino alcohol is completely incorporated in the polymer only during the crosslinking reaction. Thus, by the choice, i.e. by variation of the terminal groups, it is possible to adapt the polymer to the particular requirements, such as the capability of film formation and of dispersion.
The thermoplastic, resilient OH-containing polyurethanes having this composition are prepared in solution by the two-stage process, in the presence or absence of catalysts and other assistants and/or additives. It is not possible to prepare these products by the solvent-free batch process. Since partial or complete formation of gel particles takes place owing to the presence of the triol and the reaction of amine with NCO groups in the polyaddition in the absence of a solvent, the reaction is carried out in a solvent. In general, the danger of local over-crosslinking, as occurs in polyaddition in the absence of a solvent, is avoided in the case of solution polyaddition.
In the 2-stage process, two different procedures are possible, depending on the reaction conditions (amount of solvent, heat of reaction).
Procedure 1: The diisocyanate is initially taken with a little solvent, after which building blocks A, B, C, D and, where relevant, the catalyst and the assistants and additives in solvents are added at from 20.degree. to 90.degree. C., preferably from 30.degree. to 70.degree. C., in the course of from 0.2 to 5 hours. The components are reacted until the desired NCO content is obtained, after which the stopping agent (component F) is added in the second stage.
Procedure 2: In this process, all starting components A to E are dissolved in some of the solvent to give solutions having a solids content of from 15 to 50% by weight. Thereafter, the stirred solutions are heated to 20.degree.-90.degree. C., preferably 30.degree.-70.degree. C., if necessary after the addition of a catalyst. The components are then reacted until the desired NCO content is obtained, after which the stopping agent is added in the second stage.
In the 2-stage process, NCO is used in excess relative to building blocks A to D in the first stage. In both procedures, it is possible to begin the reaction in some of the solvent and to add the remaining solvent during or after the reaction.
Preferred solvents for the preparation of the polyurethanes are cyclic ethers, such as tetrahydrofuran and dioxane, and cyclic ketones, such as cyclohexanone. Depending on the field of use, the polyurethanes can of course also be dissolved in other strongly polar solvents, such as dimethylformamide, N-methylpyrrolidone, dimethylsulfoxide or ethyleneglycol acetate. It is also possible to mix the stated solvents with aromatics, such as toluene or xylene, and esters, such as ethyl or butyl acetate.
Examples of suitable catalysts for the preparation of the polyurethanes and for the crosslinking reaction are tertiary amines, such as triethylamine, triethylenediamine, N-methylpyridine and N-methylmorpholine, metal salts, such as tin dioctoate, lead octoate and zinc stearate, and organic metal compounds, such as dibutyltin dilaurate or titaniumtetrabutylate. The suitable amount of catalyst is dependent on the activity of the relevant catalyst. In general, it has proven advantageous to use from 0.005 to 0.3, preferably from 0.01 to 0.1, part by weight per 100 parts by weight of polyurethane.
The polyurethanes used according to the invention can be employed as sole binders for the production of magnetic layers; however, when magnetic recording media according to the invention are used for special purposes, it is advantageous to add a second binder component in amounts of from 5 to 50, preferably from 10 to 40, parts by weight, based on the resulting total amount of binder. The physically drying binders present in the binder mixture are known. These include a polyvinylformal binder which was prepared by hydrolysis of a polymer of a vinyl ester and subsequent reaction of the vinyl alcohol polymer with formaldehyde. The polyvinylformals advantageously contain not less than 65, in particular not less than 80, % by weight of vinylformal groups. Suitable polyvinylformals contain from 5 to 13% by weight of vinyl alcohol groups and from 80 to 88% by weight of vinylformal groups and have a specific gravity of about 1.2 and a viscosity of from 50 to 120 mPa.s measured at 20.degree. C. using a solution of 5 g of polyvinylformal in 100 ml of 1:1 phenol/toluene. In addition to the polyvinylformal, vinyl chloride/diol mono- or di(meth)acrylate copolymers, which can be prepared, for example, in a known manner by solution copolymerization or suspension copolymerization of vinyl chloride and the diol monomethacrylate or monoacrylate, are also suitable. The diol mono- or diacrylate or -methacrylate used for this purpose is an esterification product of acrylic acid or methacrylic acid with the corresponding molar amount of an aliphatic diol of 2 to 4 carbon atoms, such as ethylene glycol, 1,4-butanediol or, preferably, propanediol, the propanediol preferably consisting of 1,3-propanediol and from 0 to 50% by weight of 1,2-propanediol. The copolymers advantageously have a vinyl chloride content of from 50 to 95% by weight and a diol acrylate or methacrylate content of from 5 to 50% by weight. Particularly suitable copolymers preferably contain from 70 to 90% by weight of vinyl chloride and from 10 to 30% by weight of diol monoacrylate or diol monomethacrylate. A 15% strength solution of particularly suitable copolymers, such as the vinyl chloride/propanediol monoacrylate copolymers, in a mixture of equal parts by volume of tetrahydrofuran and dioxane has a viscosity of about 30 mPa.s at 25.degree. C. The K value according to H. Fikentscher (Cellulosechemie 13 (1932), page 58 et seq.) of the particularly suitable products is from 30 to 50, preferably about 40.
Phenoxy resins whose constitution can be described by the repeating formula ##STR3## where n is roughly 100, can also advantageously be used. These are polymers such as those known under the trade names Epikote.RTM. from Shell Chemical Co. or epoxy resin PKHH.RTM. from Union Carbide Corporation.
Cellulose ester binders are also suitable for use in the binder mixture defined. These are esterification products of cellulose with nitric acid or with carboxylic acids of 1 to 4 carbon atoms, e.g. cellulose acetate, cellulose triacetate, cellulose acetopropionate and cellulose acetobutyrate.
Further processing of the binder mixture with magnetic materials and assistants to give the novel magnetic recording media is carried out in a conventional manner.
Suitable anisotropic magnetic materials are the conventional pigments, which substantially influence the properties of the resulting magnetic layers, for example gamma-iron(III) oxide, finely divided magnetite, undoped or doped ferromagnetic chromium dioxide, cobalt-modified gamma-iron(III) oxide, barium ferrites or ferromagnetic metal particles. Acicular cobalt-modified or unmodified gamma-iron(III) oxide and ferromagnetic chromium dioxide and metal pigments are preferred. The particle size is in general from 0.2 to 2 .mu.m, preferably from 0.3 to 0.8 .mu.m.
The magnetic layers may also contain known additives, such as dispersants and also further lubricants in minor amounts which are small compared with the prior art, as well as fillers, which are admixed during dispersing of the magnetic pigments or during production of the magnetic layer.
The ratio of magnetic material to binder in the novel recording materials is from 1 to 10, in particular from 3 to 6, parts by weight of magnetic material to one part by weight of the binder mixture. Of particular advantage is the fact that, owing to the excellent pigment-binding capacity of the special polyurethanes, high concentrations of magnetic material in the magnetic layers are possible without the mechanical and resilient properties being adversely affected or the use characteristics suffering markedly.
The nonmagnetic and non-magnetizable substrates used may be the conventional rigid or flexible substrate materials, in particular films of linear polyesters, such as polyethylene terephthalate, in general having thicknesses of from 4 to 200 .mu.m, in particular from 6 to 36 .mu.m. Recently, the use of magnetic layers on paper substrates for electronic computing and accounting machines has also become important; the novel coating materials can advantageously be used for this purpose too.
The novel magnetic recording media can be produced in a known manner. Advantageously, the magnetic pigment dispersion prepared in a dispersing apparatus, for example a tubular ball mill or stirred ball mill, from the magnetic material and a solution of the binder, with the addition of dispersants and other additives, is filtered, after the polyisocyanate crosslinking agent has, if necessary, been mixed in, and is applied to the nonmagnetic substrate by means of the conventional coating apparatus, for example a knife coater. As a rule, magnetic orientation is effected before the liquid coating mixture is dried on the substrate; the latter procedure is advantageously carried out in from 10 to 200 s at from 50.degree. to 90.degree. C. The magnetic layers can be calendered and compacted on conventional apparatuses by passage between heated and polished rollers, if necessary with the use of pressure and temperatures of from 25.degree. to 100.degree. C., preferably from 60.degree. to 80.degree. C. In the case of crosslinking binders, it has proven very advantageous to carry out calendering before crosslinking is complete, since the OH polymers in the uncrosslinked state are very thermoplastic without being tacky. The thickness of the magnetic layer is in general from 0.5 to 20 .mu.m, preferably from 1 to 10 .mu.m. In the case of the production of magnetic tapes, the coated films are slit in the longitudinal direction into the usual widths, generally specified in inches.
Without additional lubricants or with a greatly reduced amount of added lubricant, the novel magnetic recording media exhibit lower sliding friction compared with magnetic recording media which have been obtained using prior art polyurethanes or polyurethane mixtures. Their surface hardness, which is nevertheless great, and the high modulus of elasticity, which decrease by less than 50% even at 50.degree. C., are further advantageous properties of the novel recording media. Moreover, all requirements set are fulfilled in the durability test and especially in the environmental test (at 40.degree. C. and 80% relative humidity).





In the Examples and Comparative Experiments which follow, parts and percentages are by weight, unless stated otherwise. Parts by volume bear the same relation to parts by weight as that of the liter to the kilogram.
Polymer A
53.1 g of toluylene diisocyanate and 75 g of diphenylmethane diisocyanate, dissolved in 234 g of tetrahydrofuran are heated to 60.degree. C. and one drop of dibutyltin dilaurate is added. 250 g of an OH-containing polyester obtained from adipic acid and 1,4-butanediol and having a molecular weight of 1,000, 5.7 g of a polysiloxanediol (molecular weight about 1,132), 27.1 g of 1,6-hexanediol and 1.34 g of trimethylolpropane, dissolved in 200 g of tetrahydrofuran, are added in the course of about two hours. After one hour, a further drop of dibutyltin dilaurate is added. After an NCO content of 1.04% has been reached, the mixture is cooled to 45.degree. C. and 22.05 g of diethanolamine are then added. The resulting product has a solids content of 50%, an OH number of 54.2 and a K value of 27.
Polymer B
146.1 g of toluylene diisocyanate and 65 g of diphenylmethane diisocyanate, dissolved in 255 g of tetrahydrofuran are heated to 60.degree. C. and one drop of dibutyltin dilaurate is added. 200 g of an OH-containing polycarbonate having a molecular weight of about 2,000, 5.7 g of a polysiloxanediol (molecular weight about 1,132), 40.7 g of 1,6-hexanediol and 2.23 g of trimethylolpropane, dissolved in 300 g of tetrahydrofuran, are added in the course of about two hours. After an NCO content of 0.46% has been reached, the mixture is cooled to 45.degree. C. and 10.5 g of diethanolamine are then added. The resulting product has a solids content of 40%, an OH number of 30.3 and a K value of 34.
Polymer C
The procedure described for polymer A is followed, except that, instead of the polysiloxanediol, an equivalent amount of the polyesterdiol is used.
Polymer D
The procedure described for polymer B is followed, except that, instead of the polysiloxanediol, an equivalent amount of the polycarbonatediol is used.
EXAMPLE 1
102 kg of tetrahydrofuran, 31 kg of a 50% strength solution of the polyureaurethanes according to Example A, 100 kg of a ferromagnetic chromium dioxide having an Hc of 40 kA/m and a mean needle length of 0.5 .mu.m, 1.0 kg of zinc stearate and 1.0 kg of a commercial silicone oil were introduced into a steel ball mill having a capacity of 600 parts by volume and containing 600 kg of steel balls having a diameter of from 4 to 6 mm, and the batch was dispersed for 36 hours. The dispersion was then filtered under pressure, 0.039 part of a 75% strength solution of a triisocyanate obtained from 3 moles of toluylene diisocyanate and 1 mole of trimethylolpropane were added per part of dispersion while stirring and immediately thereafter the mixture was applied to a 15 .mu.m thick polyethylene terephthalate film. The coated film was passed through a magnetic field to orient the magnetic particles and then dried at from 50.degree. to 80.degree. C. and calendered by passage between heated rollers under pressure (60.degree. C., nip pressure 200 kg/cm).
The magnetic properties were measured in a magnetic field of 160 kA/m: the residual magnetization was 178 mT and the orientation of the magnetic particles, ie. the ratio of the residual induction in the playing direction to that in the crosswise direction, was 3.0. After slitting into 3.81 mm wide tapes, the mechanical properties were determined as follows:
Test 1
Coefficient of friction layer/steel, before/after continuous operation
The coefficients of friction are determined according to DIN 45,522, Sheet 1, and are measured for the unused tape and after the tape has been subjected to continuous use.
Test 2
Quasistatic friction
The coefficient of friction is determined by measuring the tensile force produced as a result of friction by the magnetic tape passing over a stationary measuring drum. The measuring drum is a steel drum having a surface roughness of about 0.15 .mu.m and a diameter of 70 mm. The piece of tape is 25 cm long and is passed over the drum under a tension of 20 cN at a speed of 1 mm/sec and at an angle of wrap of 180.degree. C. The tension at the load cell F is a measure of the coefficient of friction .mu., in accordance with ##EQU1## (Test conditions: 23.degree. C., 50% relative humidity).
Test 3
Dynamic friction
The coefficient of friction is determined as in Test 2, except that the magnetic tape is passed over a measuring drum rotating at a peripheral velocity of 9.5 cm/sec.
Test 4
Abrasion in continuous operation
This measurement is used to evaluate the abrasion properties of a tape. The abrasion in the form of a weight loss of a tape loop in mg is measured. The loop length is 95 cm, the tape speed 4 m/sec, the tape tension 35 cN and the running time 1 hour, at an ambient temperature of 23.degree. C. and a relative humidity of 50%.
The results are shown in the Table.
EXAMPLE 2
The procedure described in Example 1 was followed, except that, instead of polymer A, 38.8 kg of polymer B and only 60% of the crosslinking agent were used. The results are shown in the Table.
COMPARATIVE EXPERIMENT 1
The procedure described in Example 1 was followed, except that polymer C. was used instead of polymer A. The results are shown in the Table.
COMPARATIVE EXPERIMENT 2
The procedure described in Example 2 was followed, except that polymer D was used instead of polymer B. The results are shown in the Table.
TABLE______________________________________ Comparative Examples Experiments 1 2 1 2______________________________________Test 1 before continuous operation 0.25 0.33 0.48 0.50Test 1 after continuous operation 0.32 0.29 0.62 0.60Test 2 0.28 0.28 0.50 0.51Test 3 0.28 0.28 0.50 0.51Test 4 0.3 0.4 2.4 2.3______________________________________
Claims
  • 1. A magnetic recording medium, consisting of a non-magnetic substrate and at least one magnetic layer which is applied firmly thereon and is based on a magnetic material finely dispersed in a binder consisting of not less than 50% by weight of a thermoplastic polyurethane, wherein the thermoplastic polyurethane used is a siloxane-containing, isocyanate-free, branched polyurethane which is soluble in tetrahydrofuran, has OH-containing urea groups at the chain ends and a molecular weight of from 4,000 to 30,000 and is prepared from
  • A) 1 mole of a polyol having a molecular weight of from 400 to 4,000,
  • B) from 0.3 to 9 moles of a diol of 2 to 18 carbon atoms,
  • C) from 0.01 to 1 mole of a triol of 3 to 18 carbon atoms,
  • D) from 0.001 to 0.4 mole of an organofunctional polysiloxane compound having two terminal groups reactive to isocyanates and a molecular weight of from 300 to 4,000,
  • E) from 1.25 to 13 moles of a diisocyanate of 6 to 30 carbon atoms, the NCO:OH ratio in the sum of the components A, B, C. and D being 1.05:1.0-1.4:1.0, and
  • F) from 0.05 to 4 moles of an OH-containing primary or secondary amine which is reactive to isocyanates.
  • 2. A magnetic recording medium as claimed in claim 1, wherein component D is a polysiloxanediol.
  • 3. A magnetic recording medium as claimed in claim 1, wherein less than 5, preferably less than 3, percent by weight, based on the binder, of the polysiloxane component is incorporated in the binder.
  • 4. A magnetic recording medium as claimed in claim 1, wherein from 0.001 to 0.4 mole of component E is an organofunctional polysiloxane diisocyanate, with the proviso that the sum of the number of moles of this polysiloxane diisocyanate component and the number of moles of component D is not more than 0.4 mole and the ratio of NCO to OH in the sum of the components A, B, C and D is from 1.05:1.0 to 1.4:1.0.
  • 5. A magnetic recording medium as claimed in claim 1, wherein some or all of component B is replaced with diamines of 2 to 15 carbon atoms.
  • 6. A magnetic recording medium as claimed in claim 1, wherein some or all of component B is replaced by primary or secondary amino alcohols of 2 to 20 carbon atoms.
  • 7. A magnetic recording medium as claimed in claim 1, wherein some or all of component B is replaced with water.
  • 8. A magnetic recording medium as claimed in claim 1, wherein the thermoplastic, silicon-containing, isocyanate-free, branched polyurethane which is soluble in tetrahydrofuran and has OH-containing urea groups at the chain ends is crosslinked with an isocyanate of the group consisting of the di-, tri- and polyisocyanates and of the isocyanate prepolymers having a molecular weight of not more than 10,000.
  • 9. A magnetic recording medium as claimed in claim 1, wherein more than 80% of the terminal OH groups consist of an ##STR4## where R is --(CH.sub.2).sub.n --, R' is --H, --CH.sub.3 or --(CH.sub.2).sub.m --CH.sub.3, n is from 2 to 10 and m is from 1 to 10.
  • 10. A magnetic recording medium as claimed in claim 8, wherein the crosslinking polyisocyanate component is a polysiloxane isocyanate having two or more NCO groups.
  • 11. A magnetic recording medium as claimed in claim 8, which contains the stated polyurethane as the sole binder.
Priority Claims (1)
Number Date Country Kind
3929165 Sep 1989 DEX
US Referenced Citations (4)
Number Name Date Kind
2871218 Schollenberger Jan 1959
4005242 Kopke et al. Jan 1977
4775595 Hasegawa Apr 1987
4780365 Kakuishi et al. Oct 1988
Foreign Referenced Citations (1)
Number Date Country
61-260419 May 1985 JPX
Non-Patent Literature Citations (4)
Entry
Japanese Abs. 61/84 717.
Japanese Abs. 61/66 316.
Japanese Abs. 62/62 428.
Japanese Abs. 61/42 745 (corresponds to U.S. 4,780,365).