DE1545040A1 - Blade cover for razor blades and process for producing the coating substance and for applying it to the razor blades - Google Patents
Blade cover for razor blades and process for producing the coating substance and for applying it to the razor bladesInfo
- Publication number
- DE1545040A1 DE1545040A1 DE19641545040 DE1545040A DE1545040A1 DE 1545040 A1 DE1545040 A1 DE 1545040A1 DE 19641545040 DE19641545040 DE 19641545040 DE 1545040 A DE1545040 A DE 1545040A DE 1545040 A1 DE1545040 A1 DE 1545040A1
- Authority
- DE
- Germany
- Prior art keywords
- razor blades
- blades
- temperatures
- blade cover
- groups
- 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.)
- Pending
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B26—HAND CUTTING TOOLS; CUTTING; SEVERING
- B26B—HAND-HELD CUTTING TOOLS NOT OTHERWISE PROVIDED FOR
- B26B21/00—Razors of the open or knife type; Safety razors or other shaving implements of the planing type; Hair-trimming devices involving a razor-blade; Equipment therefor
- B26B21/54—Razor-blades
- B26B21/58—Razor-blades characterised by the material
- B26B21/60—Razor-blades characterised by the material by the coating material
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Forests & Forestry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Paints Or Removers (AREA)
Description
T ο η d e ο -Werk Adolf N ο s s in Solingen-Auf derHöhe .Tο η d e ο -Werk Adolf Nο s s in Solingen-Auf the height .
Schneidenüberzug„für Rasierklingen und Verfahren zur Herstellung der Überzugssubstanζ sowie zu deren Aufbringung auf die Rasierklingen.Blade cover "for razor blades and processes for Manufacture of the coating substance and its application on the razor blades.
Die Erfindung bezieht sich auf einen Schneidenüberzug für Sicherheitsrasierklingen zur Verbesserung deren Rasiereigenschaften, bzw. Rasierklingen mit einem Schneidenüberzug zu diesem Zweck, sowie ein Verfahren zur Herstellung der Überzugssubstanz und zu deren Aufbringen auf die Rasierklingen.The invention relates to a cutting edge cover for safety razor blades for improvement their shaving properties or razor blades with a cutting edge coating for this purpose, as well as a process for preparing the coating substance and for applying it to the razor blades.
Es sind bereits Substanzen bekannt,Substances are already known
welche auf Rasierklingen aufgebracht, ein angenehmeres Rasieren zulassen. Solche Substanzen sind beispielsweise Polytetrafluoräthylen und vernetzte Polysiloxane. In dieser Hinsicht wirksame Polytetrafluorathylene können jedoch nur auf rostfreie Chromstahlklingen durch aufwendige und teure Verfahren, bei hohen Temperaturen in Reinstickstoff- oder Argonatmosphäre aufgebracht werden. Dem gleichen Zweck dienende Polysiloxane müssen durch sorgfältig eingehaltene Temperaturen und Zeiten auf den Klingen vernetzt werden, was einen größeren apparativen Aufwand bedingt. Durch die verhältnismäßig hohe Temperaturbeanspruchung bei mit Polytetrafluoräthylen behandelten Klingen ist ein Härteabfall nicht zu vermeiden.which applied to razor blades, a more pleasant one Allow shaving. Such substances are, for example, polytetrafluoroethylene and crosslinked polysiloxanes. However, polytetrafluoroethylene effective in this regard can only pass through stainless chrome steel blades complex and expensive processes, applied at high temperatures in pure nitrogen or argon atmosphere will. Polysiloxanes serving the same purpose must be carefully maintained at temperatures and Times on the blades are networked, which requires a greater amount of equipment. By the proportionate high temperature stress on blades treated with polytetrafluoroethylene is a A drop in hardness cannot be avoided.
Es wurde nun eine neue Substanzklasse gefunden, welche sich auf Klingen jeder Art bei Raumtemperatur aufbringen läßt und den Klingen eine ausgezeichnete Raslersanftheit über längere Zelt verleiht. Hierbei ist es nicht notwendig, die SubstanzA new class of substances has now been found which can be found on blades of all types at room temperature can be applied and gives the blades an excellent rasp gentleness over a longer period of time. It is not necessary to use the substance
009830/0014009830/0014
15A504Q15A504Q
zur Fixierung auf der Klinge zu vernetzen. In bestimmten Fällen können auch erhöhte Temperaturen bis 2000C angewandt werden. Im Gegensatz zu den Fluorcarbonpolymeren können die Substanzen vor allen Dingen auch auf normale Kohlenstoffklingen aufgebracht werden.to be networked for fixation on the blade. In certain cases, elevated temperatures of up to 200 ° C. can also be used. In contrast to the fluorocarbon polymers, the substances can also be applied to normal carbon blades.
Die erfindungsgemäßen Substanzen sind Polydiorganosiloxane, welche einen wechselnden Gehalt an Acetylaoetonatgruppen in den Seitenketten haben und folgende allgemeine Struktur aufweisen:The substances according to the invention are polydiorganosiloxanes, which have a varying content of acetylaoetonate groups in the side chains and have the following general structure:
-ξ--ξ-
η Zη Z
-O--O-
-O-O
CH3-CT TJ-(B,CH 3 -CT TJ- (B,
(D(D
= gleich oder verschieden Alkyl, Aralkyl, Aryl, vorzugsweise Methyl und/oder Phenyl,= identical or different alkyl, aralkyl, Aryl, preferably methyl and / or phenyl,
= unverzweigter oder verzweigter zweifunktioneller Kohlenwasserstoffrest, vorzugsweise -CH2CH2-, -(CHg)5-, -CH2,CH(CH,). CHiCH,).CH2-, -CH2.CH(CH3)-, -(= unbranched or branched two-functional hydrocarbon radical, preferably -CH 2 CH 2 -, - (CHg) 5 -, -CH 2 , CH (CH,). CHiCH,). CH 2 -, -CH 2 .CH (CH 3 ) -, - (
= 0 bis 500, ' = 1 bis 10 000= 0 to 500, '= 1 to 10,000
Je nach dem Gehalt an Aoetylaoetonalgruppen der Art von Z und R sind.die Produkte zähe Kautschuke oder hoohviskose Öle· Diese sind in zahlreiohen organischen Lösungsmitteln leicht löslich und können in Lösung auf kalte oder waJRlfle Rasierklingen aufgesprüht werden.Depending on the content of aoetylaoetonal groups of the type Z and R. The products are viscous rubbers or high-viscosity oils Easily soluble in organic solvents and in solution can be sprayed onto cold or hot razor blades will.
Vorzugsweise werden der Lösung zusätzlich Silikonöle und Braffinöle verschiedener Viskositäten oder Oktomethylceolotetrasiloxan u.a. in Gehalten von 5 bis 300 # bezogen auf festes Produkt zugesetzt. Der Überzug kann bei Raumtemperatur getrocknet oder gegebenenfalls je naoh Zusammensetzung bei Temperaturen bis einige Sekunden bis Stunden erhitzt werden. 'Preferably silicone oils and braffin oils of various viscosities are added to the solution or Oktomethylceolotetrasiloxan inter alia in contents of 5 to 300 # based on solid product added. Of the Coating can be dried at room temperature or optionally, depending on the composition, at temperatures up to heated for a few seconds to hours. '
009830/0014 8AD original009830/0014 8AD original
15450Α015450Α0
Er ist demnach nicht vernetzt. Es wird angenommen, daß die Acetylacetonalgruppen das Haften auf der Stahloberfläche bewirken. Der Überzug kann nach dem Trocknen gegebenenfalls mit Silikonölen verschiedener Viskositäten, so mit Ootamethylcyelotetrasiloxan oder mit Paraffinölen, übersprüht werden. Er ist über eine Vielzahl von Rasuren wirksam und hydrolytisch unempfindlich. Demzufolge wird der Überzug nach dem Eintauchen der Klingen, insbesondere in heißes Wasser, nicht durch Hydrolyse und unerwünschte Weitervernetzung stark nachteilig verändert. Eine solche Veränderung hätte einen Rückgang des günstigen Rasiervermögens bei einer zweiten Rasur oder sogar ein vollständiges Verschwinden der verbesserten Eigenschaften zur Folge. Ebenso würde die Wirkung auf der nichtbeniutzten anderen Seite durch das Eintauchen in Wasser wesentlich verschlechtert werden. Ein Vorteil des neuen Überzuges ist es auch, daß er gegen ein Abstreifen der Klinge mit einem Tuch unempfindlich ist. Der neue Überzug der Klingen verändert sich auch bei längerem lagern bei höheren Temperaturen nicht weiter.It is therefore not networked. It is believed that the acetylacetonal groups cause it to adhere to the steel surface. The coating can optionally after drying with silicone oils of different viscosities, e.g. with ootamethylcyelotetrasiloxane or with paraffin oils, be sprayed over. It is effective over a large number of shaves and is hydrolytically insensitive. As a result after immersion of the blades, especially in hot water, the coating does not become through hydrolysis and undesired further cross-linking changed significantly disadvantageously. Such a change would have a decrease in favorable Shaving ability on a second shave or even a complete disappearance of the improved properties result. Likewise, the effect on the unused other side would be due to immersion in Water can be significantly worsened. It is also an advantage of the new coating that it prevents stripping the blade is insensitive to a cloth. The new coating of the blades also changes at Do not store any longer at higher temperatures.
Da die Überzugssubstanzea keine Vernetzung einzugehen braucht, um auf der Klinge festzuwerden, sondern von Natur aus ein fester, linearpolymerer Stoff ist, ist es auch nicht notwendig, auf einen bestimmten Vernetzungsgrad mit den sich hieraus ergebenden Schattenseiten für das Einbrennen zu achten.Since the coating substance does not need to be crosslinked in order to become fixed on the blade, but is by nature a solid, linear polymeric substance, it is also not necessary to pay attention to a certain degree of crosslinking with the resulting downsides for the burn-in.
Die erfindungsgemäßen Substanzen werden durch Addition von Alkenylacetylaoeton der allgemeinen Formel: The substances according to the invention are obtained by adding alkenyl acetylaoetone of the general formula:
R2 CH^R 2 CH ^
1 r pC « 0 ■" Wasserstoff1 r pC «0 ■" hydrogen
an reguläre oder statistische Polydiorganosiloxane, welche einen wechselnden Oehalt an Si-H-Qruppen tragen, hergestellt. Die reguläre Sl-H-Gruppen enthaltendento regular or random polydiorganosiloxanes, which carry a changing content of Si-H groups, manufactured. Containing the regular Sl-H groups
0 0 9830/OOU n.D ORIGINAL0 0 9830 / OOU n . D ORIGINAL
Polydlorganosiloxane, der allgemeinen Formel: "Y R1 \ R-, Polydlorganosiloxane, of the general formula: "YR 1 \ R-,
I i1 \ ι5 (2). I i 1 \ ι 5 ( 2 ).
(H1, R2, Ry η und χ wie in Formel (l)(H 1 , R 2 , Ry η and χ as in formula (l)
- Si - 0 - Si - 0 -- Si - 0 - Si - 0 -
In H χ In H χ
werden durch Polykondensation voncC.60 - Polydiorganosiloxandiolen mit einem Organodichlorsilan der allgemeinen Formel R/^\SiHCLp in Gegenwart eines HCl-Acceptors erhalten.are made by polycondensation ofcC.60 - polydiorganosiloxanediols with an organodichlorosilane of the general formula R / ^ \ SiHCLp in the presence of an HCl acceptor obtain.
Die Addition der Alkenjrlacetylacetone an die Si-H-Gruppe erfolgt durch Zugabe katalytischer Mengen radikalbildender "Verbindungen wie,Benzoylperoxyd und Azodiisobuttersäurenitril, oder durch Bestrahlen mit UV-Licht, vorzugsweise jedoch durch Erwärmen in Gegenwart katalytischer Mengen Hexaplationochlorwasserstoffsäure oder Platin-Kohle. Die Addition erfolgt vorzugsweise in inerten organischen Lösungsmitteln. Die Addukte werden dabei in praktisch quantitativer Ausbeute erhalten. Sie werden durch Erhitzen auf l40° C im Vakuum bei 0,5 Torr von flüchtigen Bestandteilen getrennt.The addition of the Alkenjrlacetylacetone the Si-H group is created by adding catalytic amounts of radical-forming compounds such as benzoyl peroxide and azodiisobutyronitrile, or by irradiation with UV light, but preferably by heating in Presence of catalytic amounts of hexaplationochloric acid or platinum charcoal. The addition is preferably carried out in inert organic solvents. the Adducts are obtained in practically quantitative yield. They are made by heating to 140 ° C in the Separated volatiles under vacuum at 0.5 torr.
Die Produkte werden vorzugsweise in Methylisobutylketon, Aceton, TriChloräthylen oder Tetra-Chlorkohlenstoff gelöst und in dieser Lösung auf entfettete Klingen aufgesprüht oder durch Tauchen aufgebracht .The products are preferably in methyl isobutyl ketone, Acetone, trichlorethylene or tetra-chlorocarbon dissolved and sprayed in this solution onto degreased blades or applied by dipping .
Claims (1)
η = 0 bis 500 und
χ = 1 - 10 000 bedeuten.Z is a two-functional branched or unbranched hydrocarbon radical,
η = 0 to 500 and
χ = 1 - 10,000.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DET0027341 | 1964-11-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1545040A1 true DE1545040A1 (en) | 1970-07-23 |
Family
ID=7553417
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19641545040 Pending DE1545040A1 (en) | 1964-11-02 | 1964-11-02 | Blade cover for razor blades and process for producing the coating substance and for applying it to the razor blades |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE1545040A1 (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2602776A1 (en) * | 1986-08-12 | 1988-02-19 | Rhone Poulenc Chimie | BETA-CETOESTER-FUNCTIONAL DIORGANOPOLYSILOXANE USEFUL AS STABILIZING VINYL POLYCHLORIDE-BASED POLYMERS |
WO1999006471A1 (en) * | 1997-08-01 | 1999-02-11 | Ppg Industries Ohio, Inc. | Acetoacetate functional polysiloxanes |
US5916992A (en) * | 1997-08-01 | 1999-06-29 | Ppg Industries Ohio, Inc. | Polysiloxane polyols |
US5939491A (en) * | 1997-08-01 | 1999-08-17 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
US6225434B1 (en) | 1997-08-01 | 2001-05-01 | Ppg Industries Ohio, Inc. | Film-forming compositions having improved scratch resistance |
US6387519B1 (en) | 1999-07-30 | 2002-05-14 | Ppg Industries Ohio, Inc. | Cured coatings having improved scratch resistance, coated substrates and methods thereto |
US6593417B1 (en) | 1999-07-30 | 2003-07-15 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
US6610777B1 (en) | 1999-07-30 | 2003-08-26 | Ppg Industries Ohio, Inc. | Flexible coating compositions having improved scratch resistance, coated substrates and methods related thereto |
US6623791B2 (en) | 1999-07-30 | 2003-09-23 | Ppg Industries Ohio, Inc. | Coating compositions having improved adhesion, coated substrates and methods related thereto |
US6635341B1 (en) | 2000-07-31 | 2003-10-21 | Ppg Industries Ohio, Inc. | Coating compositions comprising silyl blocked components, coating, coated substrates and methods related thereto |
US6657001B1 (en) | 1999-07-30 | 2003-12-02 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
-
1964
- 1964-11-02 DE DE19641545040 patent/DE1545040A1/en active Pending
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2602776A1 (en) * | 1986-08-12 | 1988-02-19 | Rhone Poulenc Chimie | BETA-CETOESTER-FUNCTIONAL DIORGANOPOLYSILOXANE USEFUL AS STABILIZING VINYL POLYCHLORIDE-BASED POLYMERS |
EP0263038B1 (en) * | 1986-08-12 | 1990-09-19 | Rhone-Poulenc Chimie | Beta-ketoester containing diorganopolysiloxane, and its use as a stabilizer for polyvinyl chloride |
US6136928A (en) * | 1997-08-01 | 2000-10-24 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
US6040394A (en) * | 1997-08-01 | 2000-03-21 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
US6187863B1 (en) | 1997-08-01 | 2001-02-13 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
US5952443A (en) * | 1997-08-01 | 1999-09-14 | Ppg Industries Ohio, Inc. | Acetoacetate functional polysiloxanes |
US6225434B1 (en) | 1997-08-01 | 2001-05-01 | Ppg Industries Ohio, Inc. | Film-forming compositions having improved scratch resistance |
US6046296A (en) * | 1997-08-01 | 2000-04-04 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
US6048934A (en) * | 1997-08-01 | 2000-04-11 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
US6274672B1 (en) | 1997-08-01 | 2001-08-14 | Ppg Industries Ohio, Inc. | Powder coating compositions containing functional polysiloxanes |
US6103838A (en) * | 1997-08-01 | 2000-08-15 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
US6103824A (en) * | 1997-08-01 | 2000-08-15 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
WO1999006471A1 (en) * | 1997-08-01 | 1999-02-11 | Ppg Industries Ohio, Inc. | Acetoacetate functional polysiloxanes |
AU726988B2 (en) * | 1997-08-01 | 2000-11-30 | Ppg Industries Ohio, Inc. | Acetoacetate functional polysiloxanes |
US5939491A (en) * | 1997-08-01 | 1999-08-17 | Ppg Industries Ohio, Inc. | Curable compositions based on functional polysiloxanes |
US5916992A (en) * | 1997-08-01 | 1999-06-29 | Ppg Industries Ohio, Inc. | Polysiloxane polyols |
US6054535A (en) * | 1997-08-01 | 2000-04-25 | Ppg Industries Ohio, Inc. | Acetoacetate functional polysiloxanes |
US6541119B2 (en) | 1997-08-01 | 2003-04-01 | Ppg Industries Ohio, Inc. | Film-forming compositions having improved scratch resistance |
US6534188B2 (en) | 1997-08-01 | 2003-03-18 | Ppg Industries Ohio, Inc. | Film-forming compositions having improved scratch resistance |
US6387519B1 (en) | 1999-07-30 | 2002-05-14 | Ppg Industries Ohio, Inc. | Cured coatings having improved scratch resistance, coated substrates and methods thereto |
US6593417B1 (en) | 1999-07-30 | 2003-07-15 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
US6610777B1 (en) | 1999-07-30 | 2003-08-26 | Ppg Industries Ohio, Inc. | Flexible coating compositions having improved scratch resistance, coated substrates and methods related thereto |
US6623791B2 (en) | 1999-07-30 | 2003-09-23 | Ppg Industries Ohio, Inc. | Coating compositions having improved adhesion, coated substrates and methods related thereto |
US6657001B1 (en) | 1999-07-30 | 2003-12-02 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
US6759478B2 (en) | 1999-07-30 | 2004-07-06 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
US6803408B2 (en) | 1999-07-30 | 2004-10-12 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
US6635341B1 (en) | 2000-07-31 | 2003-10-21 | Ppg Industries Ohio, Inc. | Coating compositions comprising silyl blocked components, coating, coated substrates and methods related thereto |
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Legal Events
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OHB | Non-payment of the publication fee (examined application) |