US2710404A - Anti-static sound-recording medium and method of making the same - Google Patents
Anti-static sound-recording medium and method of making the same Download PDFInfo
- Publication number
- US2710404A US2710404A US303836A US30383652A US2710404A US 2710404 A US2710404 A US 2710404A US 303836 A US303836 A US 303836A US 30383652 A US30383652 A US 30383652A US 2710404 A US2710404 A US 2710404A
- Authority
- US
- United States
- Prior art keywords
- sound
- wax
- recording
- static
- recording medium
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title description 7
- RZCHTMXTKQHYDT-UHFFFAOYSA-N N-Lactoyl ethanolamine Chemical compound CC(O)C(=O)NCCO RZCHTMXTKQHYDT-UHFFFAOYSA-N 0.000 claims description 5
- 239000001993 wax Substances 0.000 description 33
- 239000000203 mixture Substances 0.000 description 15
- NEQXUPRFDXNNTA-UHFFFAOYSA-N 2-hydroxyethylazanium;2-hydroxypropanoate Chemical compound [NH3+]CCO.CC(O)C([O-])=O NEQXUPRFDXNNTA-UHFFFAOYSA-N 0.000 description 13
- 239000002216 antistatic agent Substances 0.000 description 10
- SXQFCVDSOLSHOQ-UHFFFAOYSA-N lactamide Chemical compound CC(O)C(N)=O SXQFCVDSOLSHOQ-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000344 soap Substances 0.000 description 5
- 230000003068 static effect Effects 0.000 description 5
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- CKQVRZJOMJRTOY-UHFFFAOYSA-N octadecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O CKQVRZJOMJRTOY-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 240000005125 Myrtus communis Species 0.000 description 1
- 235000013418 Myrtus communis Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/15—Antistatic agents not otherwise provided for
- Y10S260/19—Non-high polymeric antistatic agents/n
Definitions
- This invention relates to a novel group of anti-static agents adapted to be incorporated in a sound-recording medium to reduce the tendency of static electrical charges to accumulate on the surfaces of such a medium, and more particularly to sound-recording media incorporating such anti-static agents and a method of making such media.
- the anti-static agents of the present invention are particularly useful for reducing the accumulation of static charges on the well-known Wax recording cylinders, and will be illustratively described in that environent.
- sound-recording wax will be used hereafter to designate the material of which such cylinders are made, although as is well known sound-recording waxes are ordinarily largely composed of metallic soaps, higher fatty acids, or both, and may contain no wax at all in a strict chemical sense.
- the removal of the chips from the surface of the cylinder is desirable for a variety of reasons.
- the cylinders are usually kept in cylindrical containers having an interior lining made of a fibrous fabric, and if the chips are not completely removed from the cylinder surface, they may be transferred to the interior of the container.
- the sound record may be scratched or otherwise deformed as the cylinder is inserted into or withdrawn from the container. If the chips are not removed by contact with the interior of the container, they may interfere with transcription of the sound record.
- the adhering chips are generally untidy since,
- the objects of the present invention may be achieved .in general by providing a sound-recording wax containing a relatively small quantity of N-Z-hydroxyethyl lactamide.
- a sound-recording wax containing a relatively small quantity of N-Z-hydroxyethyl lactamide I have found that the tendency of static electrical charges to collect on the surface of a sound-recording wax containing a small proportion of N-2-hydroxyethyl lactamide, is materially reduced, and that when this compound is incorporated in the Wax nearly all .of the chips formed by the action of a sound-responsive stylus thereon fall off as soon as they are formed.
- the quantity of lactamide incorporated in the sound-recording wax may vary from 2% to 10% by weight, although in most cases preferred results are obtained by using about 4% by weight of the lactamide.
- the present anti-static agent is preferably added to the wax while the wax is in molten condition and prior to the time that it is cast into a cylinder.
- N-2-hydroxyethyl lactamide may be added to the molten Wax as such, I prefer rather to add to the wax monoethanolamine lactate which, during the process of manufacturing the wax cylinder, is converted into the lactamide.
- the present invention comprises incorporating in a sound-recording wax a compound selected from the group consisting of monoethanolamine lactate and N-Z-hydroxyethyl lactamide. So far as I am aware, N-2- hydroxyethyl lactamide and monoethanolamine lactate are both new compounds.
- the crude reaction product is transferred to a vacuum still and distilled under reduced pressure.
- the fraction boiling at about 367 F. at 43 mm. is segregated as monoethanolamine lactate. It is a viscous, light yellow-colored liquid, insoluble in benzene and kerosene and soluble in water, acetone, and denatured ethyl alcohol, S. D. #1. Its specific conductivity, although not comparable with that of a metal, is substantially higher than the conductivity of other chemically related materials.
- the monoethanolamine lactate as thus formed may be incorporated in a conventional sound-recording wax, for example, the wax formula disclosed at page 35 of The Reproduction of Sound by Henry Seymour (1918), in the following manner: A suitably healed vessel is charged with 3,333 lbs. of S. Stearine (commercial stearic acid) and the S. Stearine is melted. To the molten S. Stearine a solution of 208 lbs. of 98% caustic soda in 525 lbs. of water is slowly added. As the caustic soda solution is added, neutralization of the S. Stearine occurs and the mixture is heated to such an extent as to remove all water from the resulting soap mixture.
- S. Stearine commercial stearic acid
- red lead is added to the mixture in the reaction vessel.
- the addition of the red lead may be effected by removing a small quantity of the molten soap mixture from the heated vessel and mixing the red lead in powder form therewith, after which the mixture of red lead and soap is added to and mixed with the main body of material in the vessel.
- the molten mixture is cast into cylinders in the usual manner, and the cylinders machined to form the desired sound-recording surface.
- Cylinders made in accordance with the foregoing procedure are strikingly superior to conventional cylinders in respect to the extent to which chips fall off the surfaces thereof when they are cut by a sound-responsive stylus. Moreover, tests have shown that the electrical conductivity of the wax is appreciably increased by incorporation of the present anti-static agent therein.
- the monoethanolamine lactate of the foregoing procedure may be replaced by N2-hydroxyethyl lactamide, which may be prepared as follows: A suitable reaction vessel is charged with 106 lbs, of 85% lactic acid and 67 lbs. of monoethanolamine (about 10% excess amine) added thereto slowly with stirring. After addition of the acid is completed, the reaction mixture is heated to 275 to 280 F. and maintained at this temperature for about 2 hours. At the end of this period, 41 lbs. of the product is removed by distillation. The remaining material is crude N-Z-hydroxyethyl lactamide which, either in the crude state or after refining, can be added to the molten wax in the manner previously described for the lactate.
- a sound-recording medium having anti-static properties comprising a sound-recording wax containing from 2% to 10% by weight of N-Z-hydroxyethyl lactamide.
- a sound-recording medium having anti-static prop erties comprising a sound-recording wax containing about 4% by weight of N-Z-hydroxyethyl lactamide.
- the method of making a sound-recording medium having anti-static properties which comprises preparing a melt of a sound-recording wax, mixing with said molten wax between 2% and 10% by weight of monoethanolamine lactate, heating the resulting mixture to convert said lactate to a corresponding lactamide, and cooling and casting said mixture to form a solid sound-recording medium.
- the method of making a sound-recording medium having anti-static properties which comprises heating a mixture of fatty acid, caustic alkali, and paraffin wax to form a molten mass, adding to said molten mass from about 2% to 10% by weight of monoethanolamine lactate, heating the resulting mixture to convert said lactate to a corresponding lactamide, and cooling and casting the resulting mixture to form a solid soundrecording medium.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
United States Patent ANTI-STATIC SOUND-RECORDING MEDIUM AND METHOD OF MAKING THE SAME Richard G. Rowe, Redding Ridge, Conn., assignor to Dictaphone Corporation, Bridgeport, Conn., a corporation of New York No Drawing. Original application May 11, 1950, Serial No. 161,476. Divided and this application August 11, 1952, Serial No. 303,836
4 Claims. (Cl, 106-37) This invention relates to a novel group of anti-static agents adapted to be incorporated in a sound-recording medium to reduce the tendency of static electrical charges to accumulate on the surfaces of such a medium, and more particularly to sound-recording media incorporating such anti-static agents and a method of making such media. The anti-static agents of the present invention are particularly useful for reducing the accumulation of static charges on the well-known Wax recording cylinders, and will be illustratively described in that environent. The phrase sound-recording wax will be used hereafter to designate the material of which such cylinders are made, although as is well known sound-recording waxes are ordinarily largely composed of metallic soaps, higher fatty acids, or both, and may contain no wax at all in a strict chemical sense.
The present application is a division of my pending application Serial No. 161,476 filed May 11, 1950, now abandoned. The claims of the present case are directed to sound recording media incorporating anti-static agents such as those claimed in myco-pending case, and to methods of making such media.
For many years sound-recording wax cylinders have been used for a variety of sound-recording purposes. As ordinarily used, such cylinders are mounted on a horizontal rotating mandrel .of a dictating machine, and a laterally movable sound-responsive stylus cooperates with the rotating cylinder to cut a helical sound track in the surface thereof. As an incident of this cutting action, short, curly fibers of the wax material are removed from the surface of the cylinder, which fibers are sometimes referred to as chips, and a container or chip collector is usually provided beneath the cylinder to collect those chips that fall off the cylinder. It is, of course, desirable that all of the chips fall off the cylinder as soon as they have been formed so that they may be collected and disposed of in an orderly manner, but unfortunately there is a tendency under normal circumstances for the majority of the chips formed to continue to adhere to the cylinder surface. Although the reasons for the adherence of the chips to the surface of the cylinder are not completely understood, my investigations indicate that the principal reason for this undesired adherence of the chips is the accumulation of a static electrical charge on the surface of the cylinder.
The removal of the chips from the surface of the cylinder is desirable for a variety of reasons. The cylinders are usually kept in cylindrical containers having an interior lining made of a fibrous fabric, and if the chips are not completely removed from the cylinder surface, they may be transferred to the interior of the container. Continued use of a container that has been contaminated with chips may cause the sound record to be scratched or otherwise deformed as the cylinder is inserted into or withdrawn from the container. If the chips are not removed by contact with the interior of the container, they may interfere with transcription of the sound record. Moreover, the adhering chips are generally untidy since,
if they do not fall into the chip collector of the dictating machine for disposal in a controlled manner, they have a tendency to fly off in the atmosphere and adhere to clothing, carpets and the like.
It is accordingly an object of the present invention to provide a wax sound-recording medium in cylindrical or other form that is of such a character that chips cut from the surface thereof by a sound-responsive stylus do not tend to adhere to the surface of the medium. It is another object of the invention to provide an improved anti-static agent adapted to be incorporated in a soundrecording wax to reduce the tendency of static electrical charges to accumulate on the surface of the sound record. It is a further object of the invention to provide a soundrecording wax incorporating such an anti-static agent. It is still another object of the invention to provide a method of making such an anti-static agent and a method of incorporating it efiectively into a sound-recording medium. Other objects of the invention will be in part obvious and in part pointed out hereafter.
The objects of the present invention may be achieved .in general by providing a sound-recording wax containing a relatively small quantity of N-Z-hydroxyethyl lactamide. I have found that the tendency of static electrical charges to collect on the surface of a sound-recording wax containing a small proportion of N-2-hydroxyethyl lactamide, is materially reduced, and that when this compound is incorporated in the Wax nearly all .of the chips formed by the action of a sound-responsive stylus thereon fall off as soon as they are formed. The quantity of lactamide incorporated in the sound-recording wax may vary from 2% to 10% by weight, although in most cases preferred results are obtained by using about 4% by weight of the lactamide.
The present anti-static agent is preferably added to the wax while the wax is in molten condition and prior to the time that it is cast into a cylinder. Although N-2-hydroxyethyl lactamidemay be added to the molten Wax as such, I prefer rather to add to the wax monoethanolamine lactate which, during the process of manufacturing the wax cylinder, is converted into the lactamide. Thus, in one aspect, the present invention comprises incorporating in a sound-recording wax a compound selected from the group consisting of monoethanolamine lactate and N-Z-hydroxyethyl lactamide. So far as I am aware, N-2- hydroxyethyl lactamide and monoethanolamine lactate are both new compounds.
In order to point out more fully the nature of the present invention, the following illustrative procedures are given for making the monoethanolamine lactate and N- 2-hydroxyethyl lactamide, and also for incorporating them in a sound-recording wax to produce a sound-recording medium having anti-static properties: A heated stainless steel vessel equipped with a motor driven agitator and condenser is charged with lbs. of 85% lactic acid. Using gentle agitation, 61 lbs. of monoethanolamine is added slowly to the acid. The resulting mixture is heated at F. for one hour, after which the temperature is raised to the boiling point and about 15 lbs. of the material distilled olf. The material remaining in the vessel is crude monoethanolamine lactate.
The crude reaction product is transferred to a vacuum still and distilled under reduced pressure. The fraction boiling at about 367 F. at 43 mm. is segregated as monoethanolamine lactate. It is a viscous, light yellow-colored liquid, insoluble in benzene and kerosene and soluble in water, acetone, and denatured ethyl alcohol, S. D. #1. Its specific conductivity, although not comparable with that of a metal, is substantially higher than the conductivity of other chemically related materials.
The monoethanolamine lactate as thus formed may be incorporated in a conventional sound-recording wax, for example, the wax formula disclosed at page 35 of The Reproduction of Sound by Henry Seymour (1918), in the following manner: A suitably healed vessel is charged with 3,333 lbs. of S. Stearine (commercial stearic acid) and the S. Stearine is melted. To the molten S. Stearine a solution of 208 lbs. of 98% caustic soda in 525 lbs. of water is slowly added. As the caustic soda solution is added, neutralization of the S. Stearine occurs and the mixture is heated to such an extent as to remove all water from the resulting soap mixture.
After completion of this neutralization step, 178 lbs, of red lead is added to the mixture in the reaction vessel. The addition of the red lead may be effected by removing a small quantity of the molten soap mixture from the heated vessel and mixing the red lead in powder form therewith, after which the mixture of red lead and soap is added to and mixed with the main body of material in the vessel.
When the red lead has been incorporated into the molten soap, 212.5 lbs. of monoethanolamine lactate, 950 lbs. of paraffin wax, and 119.5 lbs. of myrtle Wax are successively added to the mixture in the kettle, and heating of the mixture continued at about 375 F. for a period of about 24 hours. During this heating period the monoethanolamine lactate is converted into N-Z-hydroxyethyl lactamide.
At the end of the heating period the molten mixture is cast into cylinders in the usual manner, and the cylinders machined to form the desired sound-recording surface.
Cylinders made in accordance with the foregoing procedure are strikingly superior to conventional cylinders in respect to the extent to which chips fall off the surfaces thereof when they are cut by a sound-responsive stylus. Moreover, tests have shown that the electrical conductivity of the wax is appreciably increased by incorporation of the present anti-static agent therein.
As previously indicated, the monoethanolamine lactate of the foregoing procedure may be replaced by N2-hydroxyethyl lactamide, which may be prepared as follows: A suitable reaction vessel is charged with 106 lbs, of 85% lactic acid and 67 lbs. of monoethanolamine (about 10% excess amine) added thereto slowly with stirring. After addition of the acid is completed, the reaction mixture is heated to 275 to 280 F. and maintained at this temperature for about 2 hours. At the end of this period, 41 lbs. of the product is removed by distillation. The remaining material is crude N-Z-hydroxyethyl lactamide which, either in the crude state or after refining, can be added to the molten wax in the manner previously described for the lactate.
It is, of course, to be understood that the foregoing detailed procedure is illustrative only and that numerous changes may be made therein without departing from the scope of the invention. As indicated previously, the desired result may be achieved by adding either N-Z-hydroxyethyl lactamide or monoethanolamine lactate to the molten wax. However, there is some advantage in using the lactate since it is easier to make than the lactamide and is automatically converted into the lactamide in the course of the formulation of the sound-recording wax. Many different wax formulae have been previously proposed for sound-recording purposes and my experiments indicate that the present anti-static agent can be used in any of these known formulae to improve the anti-static properties of the resulting sound-recording wax.
Since many embodiments might be made of the present invention and since many changes might be made in the embodiment disclosed herein, it is to be understood that the foregoing description is to be interpreted as illustrative only and not in a limiting sense.
I claim:
1. A sound-recording medium having anti-static properties, said medium comprising a sound-recording wax containing from 2% to 10% by weight of N-Z-hydroxyethyl lactamide.
2. A sound-recording medium having anti-static prop erties, said medium comprising a sound-recording wax containing about 4% by weight of N-Z-hydroxyethyl lactamide.
3. The method of making a sound-recording medium having anti-static properties which comprises preparing a melt of a sound-recording wax, mixing with said molten wax between 2% and 10% by weight of monoethanolamine lactate, heating the resulting mixture to convert said lactate to a corresponding lactamide, and cooling and casting said mixture to form a solid sound-recording medium.
4. The method of making a sound-recording medium having anti-static properties which comprises heating a mixture of fatty acid, caustic alkali, and paraffin wax to form a molten mass, adding to said molten mass from about 2% to 10% by weight of monoethanolamine lactate, heating the resulting mixture to convert said lactate to a corresponding lactamide, and cooling and casting the resulting mixture to form a solid soundrecording medium.
No references cited.
Claims (1)
1. A SOUND-RECORDING MEDIUM HAVING ANTI-STATIC PROPERTIES, SAID MEDIUM COMPRISING A SOUND-RECORDING WAX CONTAINING FROM 2% TO 10% BY WEIGHT OF N-2-HYDROXYETHYL LACTAMIDE.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US303836A US2710404A (en) | 1950-05-11 | 1952-08-11 | Anti-static sound-recording medium and method of making the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16147650A | 1950-05-11 | 1950-05-11 | |
US303836A US2710404A (en) | 1950-05-11 | 1952-08-11 | Anti-static sound-recording medium and method of making the same |
Publications (1)
Publication Number | Publication Date |
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US2710404A true US2710404A (en) | 1955-06-07 |
Family
ID=26857862
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Application Number | Title | Priority Date | Filing Date |
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US303836A Expired - Lifetime US2710404A (en) | 1950-05-11 | 1952-08-11 | Anti-static sound-recording medium and method of making the same |
Country Status (1)
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US (1) | US2710404A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3025323A (en) * | 1957-01-18 | 1962-03-13 | Union Carbide Corp | Amide diols and their esters |
-
1952
- 1952-08-11 US US303836A patent/US2710404A/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
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None * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3025323A (en) * | 1957-01-18 | 1962-03-13 | Union Carbide Corp | Amide diols and their esters |
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