EP0553493A1 - Coated bobbins, process for their fabrication and their use in the treatment of glass fibers - Google Patents

Coated bobbins, process for their fabrication and their use in the treatment of glass fibers Download PDF

Info

Publication number
EP0553493A1
EP0553493A1 EP92122078A EP92122078A EP0553493A1 EP 0553493 A1 EP0553493 A1 EP 0553493A1 EP 92122078 A EP92122078 A EP 92122078A EP 92122078 A EP92122078 A EP 92122078A EP 0553493 A1 EP0553493 A1 EP 0553493A1
Authority
EP
European Patent Office
Prior art keywords
sleeves
sleeves according
carbon atoms
sleeve
alkyl radical
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.)
Granted
Application number
EP92122078A
Other languages
German (de)
French (fr)
Other versions
EP0553493B1 (en
Inventor
Raymond Dr. Audenaert
Hubertus Eversheim
Sabine Dr. Schlitte
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.)
Bayer Antwerpen NV
Bayer AG
Original Assignee
Bayer Antwerpen NV
Bayer AG
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 Bayer Antwerpen NV, Bayer AG filed Critical Bayer Antwerpen NV
Publication of EP0553493A1 publication Critical patent/EP0553493A1/en
Application granted granted Critical
Publication of EP0553493B1 publication Critical patent/EP0553493B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/647Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65HHANDLING THIN OR FILAMENTARY MATERIAL, e.g. SHEETS, WEBS, CABLES
    • B65H75/00Storing webs, tapes, or filamentary material, e.g. on reels
    • B65H75/02Cores, formers, supports, or holders for coiled, wound, or folded material, e.g. reels, spindles, bobbins, cop tubes, cans, mandrels or chucks
    • B65H75/18Constructional details
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions

Definitions

  • the present invention relates to specially coated sleeves, a process for their production and their use in the production of glass fibers.
  • the glass fibers are usually wound onto so-called cores after they have been pulled out of the so-called bushing. These wound glass fibers are then dried together with the sleeve, the so-called cake. After the drying process, the sleeve is removed by pulling it out of the side of the cake. The wound glass fiber is then processed further.
  • the sleeves are made of reinforced or unreinforced paper or reinforced or unreinforced plastic and are uncoated or partially coated with polyurethanes.
  • the task was therefore to provide a process in which the above-mentioned glass waste no longer arises.
  • the invention relates to sleeves on which the glass fiber is wound during its manufacture and which are characterized in that they have been coated with silicone oils and / or resins.
  • the radicals R1, R2, R3 and R5 are preferably methyl groups.
  • the sleeves are preferably coated with silicone oils of the above general formula, in which R4 represents a dodecyl and / or tetradecyl radical.
  • the silicone oil or resin is suitably, i.e. e.g. applied to the sleeve by roller coating, dipping or spraying. If silicone resins are used, salts of tin, iron, titanium, lead or aluminum are added to these individually or as a mixture, so that the resins can crosslink with the sleeve. Titanium tetrabutylate and / or dibutyltin dilaurate are preferably used as catalysts.
  • the sleeves according to the invention are used in the winding of glass fibers.
  • the tubes used up to now were treated by the method according to the invention and were also used in the winding of various glass fibers.
  • the sleeves according to the invention could be pulled out of the cake with almost no loss of glass fibers.
  • the loss of glass fibers when using the sleeves according to the invention is thus considerably less than when using the known sleeves.
  • a methoxy-functional methyl-phenyl silicone resin with the following composition 36 mol% PhSiO 3/2 64 mol% Me2SiO and about 17 wt% methoxy groups catalyzed with 2000 ppm titanium tetrabutylate and 2000 ppm dibutyltin dilaurate is applied in an amount of 50 g / m2 to a commercially available sleeve. Then it is dried at 80 ° C and 30 minutes.
  • the glass fiber is wound onto this sleeve and the cake thus obtained is dried. Then the glass fiber is freed from the sleeve by pulling the sleeve out of the side of the cake. The sleeve can then be used again.
  • Table 1 The results are listed in Table 1.
  • the sleeve could be removed with little loss of fiber.
  • a methoxy functional methyl alkyl silicone resin having the following composition 18 mol% of Me (alk) SiO 2/2 (alk C12-C14 alkyl) 82 mol% MeSiO 3/2 and about 20% by weight methoxy groups catalyzed with 2000 ppm titanium tetrabutylate and 2000 ppm dibutyltin dilaurate is used as in Example 1.
  • the sleeve is used in accordance with Example 1.
  • the sleeve is then dried at 80 ° C for 30 minutes.
  • the glass fiber is wound onto this sleeve and the cake thus obtained is dried.

Abstract

The invention relates to specially coated bobbins, a process for their fabrication and their use in the production of glass fibres.

Description

Die vorliegende Erfindung betrifft speziell beschichtete Hülsen, ein Verfahren zu ihrer Herstellung sowie ihre Verwendung bei der Herstellung von Glasfasern.The present invention relates to specially coated sleeves, a process for their production and their use in the production of glass fibers.

Bei der Herstellung von Glasfasern werden die Glasfasern normalerweise, nachdem sie aus dem sogenannten Bushing gezogen worden sind, auf sogenannte Hülsen aufgewickelt. Diese aufgewickelten Glasfasern werden anschließend gemeinsam mit der Hülse, dem sogenannten Cake, getrocknet. Nach dem Trocknungsprozeß wird die Hülse entfernt, indem sie seitlich aus dem sogenannten Cake herausgezogen wird. Die gewickelte Glasfaser wird anschließend weiter verarbeitet. Die Hülsen bestehen aus verstärktem oder unverstärktem Papier bzw. aus verstärktem oder unverstärktem Kunststoff und sind unbeschichtet oder teilweise mit Polyurethanen beschichtet.In the manufacture of glass fibers, the glass fibers are usually wound onto so-called cores after they have been pulled out of the so-called bushing. These wound glass fibers are then dried together with the sleeve, the so-called cake. After the drying process, the sleeve is removed by pulling it out of the side of the cake. The wound glass fiber is then processed further. The sleeves are made of reinforced or unreinforced paper or reinforced or unreinforced plastic and are uncoated or partially coated with polyurethanes.

Bei dem seitlichen Herausziehen der Hülse aus dem Cake wurde bisher immer ein Teil der aufgewickelten Glasfaser mit herausgezogen, der dann der weiteren Verarbeitung nicht mehr zur Verfügung stand und als Abfall die Ausbeute abgewickelter Glasfaser stark vermindern konnte.When pulling the sleeve out of the cake laterally, part of the wound glass fiber has always been used pulled out, which was then no longer available for further processing and could significantly reduce the yield of unwound glass fiber as waste.

Aufgabe war es daher ein Verfahren zur Verfügung zu stellen, bei dem der oben bezeichnete Glasabfall nicht mehr anfällt.The task was therefore to provide a process in which the above-mentioned glass waste no longer arises.

Diese Aufgabe konnte durch das erfindungsgemäße Verfahren sowie durch die zur Verfügungstellung der neuen erfindungsgemäßen Hülsen gelöst werden.This problem could be solved by the method according to the invention and by the provision of the new sleeves according to the invention.

Gegenstand der Erfindung sind Hülsen, auf die die Glasfaser bei ihrer Herstellung aufgewickelt wird und die sich dadurch auszeichnen, daß sie mit Siliconölen und/oder -harzen beschichtet worden sind.The invention relates to sleeves on which the glass fiber is wound during its manufacture and which are characterized in that they have been coated with silicone oils and / or resins.

Bevorzugt werden dabei Siliconöle der folgenden Formel eingesetzt

Figure imgb0001

wobei in der allgemeinen Formel
x = 0 bis 500,
y = 5 bis 500,
z = 5 bis 500,

R¹, R², R³ und R⁵
unabhängig voneinander für einen gesättigten und/oder ungesättigten, gegebenenfalls auch verzweigten Alkylrest mit 1 bis 4 C-Atomen,
R⁴
für einen Alkylrest mit 6 bis 18 C-Atomen steht,
R⁶
für einen gesättigten oder ungesättigten, gegebenenfalls auch verzweigten Alkylrest mit 1 bis 4 C-Atomen oder für H steht und
wobei von der Anzahl der an Si gebundenen Reste jeweils mindestens 3 % R⁴ und H sind.Silicone oils of the following formula are preferably used
Figure imgb0001

being in the general formula
x = 0 to 500,
y = 5 to 500,
z = 5 to 500,
R¹, R², R³ and R⁵
independently of one another for a saturated and / or unsaturated, optionally also branched alkyl radical having 1 to 4 carbon atoms,
R⁴
represents an alkyl radical having 6 to 18 carbon atoms,
R⁶
represents a saturated or unsaturated, optionally also branched alkyl radical having 1 to 4 carbon atoms or represents H and
wherein of the number of radicals bound to Si are at least 3% R⁴ and H.

Vorzugsweise stehen die Reste R¹, R², R³ und R⁵ für Methylgruppen.The radicals R¹, R², R³ and R⁵ are preferably methyl groups.

Die Hülsen, die mit Siliconölen beschichtet sind, bei denen
x = 0 bis 100,
y = 5 bis 100,
z = 5 bis 100
sind, wobei x + y + z = 25 bis 300 ist
und von der Anzahl der an Si gebundenen Reste mindestens 3 % R⁴ und mindestens 10 % H sind,
sind besonders bevorzugt.
The sleeves that are coated with silicone oils in which
x = 0 to 100,
y = 5 to 100,
z = 5 to 100
where x + y + z = 25 to 300
and of the number of radicals bonded to Si are at least 3% R⁴ and at least 10% H,
are particularly preferred.

Siliconöle der obengenannten allgemeinen Formel mit
x = 0,
y = 5 bis 50,
z = 5 bis 60,
wobei y + z größer 25 ist und von der Anzahl der an Si gebundenen Reste mindestens 10 % R⁴ und mindestens 30 % H sind,
werden vorzugsweise eingesetzt.
Silicone oils with the above general formula
x = 0,
y = 5 to 50,
z = 5 to 60,
where y + z is greater than 25 and the number of radicals bonded to Si is at least 10% R⁴ and at least 30% H,
are preferably used.

Die Hülsen sind bevorzugt mit Siliconölen der obengenannten allgemeinen Formel beschichtet, in denen R⁴ für einen Dodecyl- und/oder Tetradecylrest steht.The sleeves are preferably coated with silicone oils of the above general formula, in which R⁴ represents a dodecyl and / or tetradecyl radical.

Die erfindungsgemäßen Hülsen weisen bevorzugt eine Schicht aus Siliconharzen auf, die folgender Formel genügen



        R¹aSi(OH)b(OR²)cO(4-a-b-c)/2



wobei
a = 1,0 bis 2,0
b + c = 0,1 bis 1,7

ein linearer oder verzweigter Alkylrest mit 1 bis 18 C-Atomen oder ein Phenylrest bedeutet und
einen linearen oder verzweigten Alkylrest mit 1 bis 4 C-Atomen darstellt.
The sleeves according to the invention preferably have a layer of silicone resins which satisfy the following formula



R1 a Si (OH) b (OR2) c O (4-abc) / 2



in which
a = 1.0 to 2.0
b + c = 0.1 to 1.7
is a linear or branched alkyl radical having 1 to 18 carbon atoms or a phenyl radical and
represents a linear or branched alkyl radical having 1 to 4 carbon atoms.

Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung der erfindungsgemäßen Hülsen, welches dadurch gekennzeichnet ist, daß

  • a) das Siliconöl oder das Siliconharz in Mengen zwischen 5 und 100 g/m² , vorzugsweise zwischen 10 und 70 g/m² auf die Hülse appliziert wird, wobei bei der Verwendung von Siliconharz diesen vorher ein üblicher Katalysator in Mengen von 100 bis 5000 ppm zugesetzt wird, und
  • b) die so behandelte Hülse unter Luftzutritt im Ofen bei Temperaturen zwischen 60° und 120°C über einen Zeitraum von 15 Minuten bis 2 Stunden getrocknet wird.
Another object of the invention is a method for producing the sleeves according to the invention, which is characterized in that
  • a) the silicone oil or the silicone resin is applied to the sleeve in amounts between 5 and 100 g / m², preferably between 10 and 70 g / m², with the use of silicone resin previously adding a conventional catalyst in amounts of 100 to 5000 ppm will, and
  • b) the sleeve thus treated is dried in the oven at temperatures between 60 ° and 120 ° C. over a period of 15 minutes to 2 hours.

Das Siliconöl bzw. -harz wird in geeigneter Weise, d.h. z.B. durch Walzenlackierung, Tauchen oder Spritzauftrag, auf die Hülse appliziert. Werden Siliconharze verwendet, wird diesen als Katalysatoren Salze von Zinn, Eisen, Titan, Blei oder Aluminium einzeln oder im Gemisch zugesetzt, damit die Harze mit der Hülse vernetzen können. Bevorzugt werden als Katalysatoren Titantetrabutylat und/oder Dibutylzinndilaurat verwendet.The silicone oil or resin is suitably, i.e. e.g. applied to the sleeve by roller coating, dipping or spraying. If silicone resins are used, salts of tin, iron, titanium, lead or aluminum are added to these individually or as a mixture, so that the resins can crosslink with the sleeve. Titanium tetrabutylate and / or dibutyltin dilaurate are preferably used as catalysts.

Die erfindungsgemäßen Hülsen werden bei der Aufwicklung von Glasfasern verwendet.The sleeves according to the invention are used in the winding of glass fibers.

Die Erfindung soll anhand nachfolgender Beispiele näher erläutert werden.The invention is illustrated by the following examples.

Bei der Verwendung der bisherigen Hülsen bei der Aufwicklung verschiedener Glasfasern wurde beim Herausziehen der Hülse aus dem sogenannten Cake die aufgewickelte Glasfaser zu einem großen Teil mit herausgezogen (siehe Tabelle 1). Diese mit der Hülse herausgezogene Glasfaser geht dem weiteren Prozeß bzw. der weiteren Verarbeitung verloren und mindert daher in erheblichem Maße die Ausbeute.When using the previous sleeves when winding various glass fibers was when pulling out The core of the so-called cake is largely pulled out of the wound glass fiber (see Table 1). This glass fiber drawn out with the sleeve is lost to the further process or further processing and therefore considerably reduces the yield.

Die bisher verwendeten Hülsen wurden nach dem erfindungsgemäßen Verfahren behandelt und ebenfalls bei der Aufwicklung verschiedener Glasfasern eingesetzt. Wie der Tabelle 1 zu entnehmen ist, konnten die erfindungsgemäßen Hülsen fast ohne Verlust an Glasfasern aus dem sogenannten Cake herausgezogen werden. Damit ist der Verlust an Glasfasern bei der Verwendung der erfindungsgemäßen Hülsen erheblich geringer als bei der Verwendung der bekannten Hülsen.The tubes used up to now were treated by the method according to the invention and were also used in the winding of various glass fibers. As can be seen from Table 1, the sleeves according to the invention could be pulled out of the cake with almost no loss of glass fibers. The loss of glass fibers when using the sleeves according to the invention is thus considerably less than when using the known sleeves.

Beispiel 1example 1

Ein methoxyfunktionelles Methyl-Phenyl-Siliconharz folgender Zusammensetzung
36 Mol-% PhSiO3/2
64 Mol-% Me₂SiO
und ca. 17 Gew.-% Methoxygruppen
katalysiert mit 2000 ppm Titantetrabutylat und 2000 ppm Dibutylzinndilaurat
wird in einer Menge von 50 g/m² auf eine kommerziell erhältliche Hülse aufgetragen. Danach wird bei 80°C und 30 Minuten getrocknet.
A methoxy-functional methyl-phenyl silicone resin with the following composition
36 mol% PhSiO 3/2
64 mol% Me₂SiO
and about 17 wt% methoxy groups
catalyzed with 2000 ppm titanium tetrabutylate and 2000 ppm dibutyltin dilaurate
is applied in an amount of 50 g / m² to a commercially available sleeve. Then it is dried at 80 ° C and 30 minutes.

Auf diese Hülse wird die Glasfaser aufgewickelt und der so erhaltene Cake getrocknet. Anschließend wird die Glasfaser von der Hülse befreit, indem die Hülse seitlich aus dem Cake herausgezogen wird. Die Hülse kann anschließend wieder verwendet werden. Die Ergebnisse sind in Tabelle 1 aufgelistet.The glass fiber is wound onto this sleeve and the cake thus obtained is dried. Then the glass fiber is freed from the sleeve by pulling the sleeve out of the side of the cake. The sleeve can then be used again. The results are listed in Table 1.

Die Hülse konnte mit einem nur geringen Verlust an Glasfaser entfernt werden.The sleeve could be removed with little loss of fiber.

Beispiel 2Example 2

Ein methoxyfunktionelles Methyl-Alkyl-Siliconharz folgender Zusammensetzung
18 Mol-% Me(Alk)SiO2/2 (Alk = C₁₂-C₁₄-Alkyl)
82 Mol-% MeSiO3/2
und ca. 20 Gew.-% Methoxygruppen
katalysiert mit 2000 ppm Titantetrabutylat und 2000 ppm Dibutylzinndilaurat
wird wie in Beispiel 1 eingesetzt.
A methoxy functional methyl alkyl silicone resin having the following composition
18 mol% of Me (alk) SiO 2/2 (alk = C₁₂-C₁₄ alkyl)
82 mol% MeSiO 3/2
and about 20% by weight methoxy groups
catalyzed with 2000 ppm titanium tetrabutylate and 2000 ppm dibutyltin dilaurate
is used as in Example 1.

Die Hülse wird entsprechend Beispiel 1 eingesetzt.The sleeve is used in accordance with Example 1.

Beim Entfernen der Hülse aus dem Cake ging fast keine Glasfaser verloren.When the sleeve was removed from the cake, almost no fiber was lost.

Beispiel 3Example 3

Ein teilalkyliertes Si-H-funktionelles Siliconöl der Zusammensetzung
R¹, R², R³, R⁵, R⁶ = CH₃
R⁴ = C₁₂ bis C₁₄-Alkyl und x = 0, y = 10, z = 20
wird in einer Menge von 50 g/m² auf eine kommerziell erhältliche Hülse aufgetragen.
A partially alkylated Si-H functional silicone oil of the composition
R¹, R², R³, R⁵, R⁶ = CH₃
R⁴ = C₁₂ to C₁₄ alkyl and x = 0, y = 10, z = 20
is applied in an amount of 50 g / m² to a commercially available sleeve.

Die Hülse wird danach bei 80°C 30 Minuten lang getrocknet.The sleeve is then dried at 80 ° C for 30 minutes.

Auf diese Hülse wird die Glasfaser aufgewickelt und der so erhaltene Cake getrocknet.The glass fiber is wound onto this sleeve and the cake thus obtained is dried.

Beim Trennen der Hülse vom Cake ging fast keine Glasfaser verloren.

Figure imgb0002
When the sleeve was separated from the cake, almost no fiber was lost.
Figure imgb0002

Claims (9)

Hülsen für die Aufwicklung von Glasfasern bei deren Herstellung, dadurch gekennzeichnet, daß diese Hülsen mit Siliconölen und/oder Harzen beschichtet sind.Sleeves for winding glass fibers during their manufacture, characterized in that these sleeves are coated with silicone oils and / or resins. Hülsen gemäß Anspruch 1, dadurch gekennzeichnet, daß die Siliconöle der folgenden Formel genügen
Figure imgb0003
wobei in der allgemeinen Formel
x = 0 bis 500,
y = 5 bis 500,
z = 5 bis 500, R¹, R², R³ und R⁵   unabhängig voneinander für einen gesättigten und/oder ungesättigten, gegebenenfalls auch verzweigten Alkylrest mit 1 bis 4 C-Atomen, R⁴   für einen Alkylrest mit 6 bis 18 C-Atomen steht, R⁶   für einen gesättigten oder ungesättigten, gegebenenfalls auch verzweigten Alkylrest mit 1 bis 4 C-Atomen oder für H steht und wobei von der Anzahl der an Si gebundenen Reste jeweils mindestens 3 % R⁴ und H sind.
Sleeves according to claim 1, characterized in that the silicone oils satisfy the following formula
Figure imgb0003
being in the general formula
x = 0 to 500,
y = 5 to 500,
z = 5 to 500, R¹, R², R³ and R⁵ independently of one another for a saturated and / or unsaturated, optionally also branched alkyl radical having 1 to 4 carbon atoms, R⁴ represents an alkyl radical with 6 to 18 carbon atoms, R⁶ represents a saturated or unsaturated, optionally also branched alkyl radical having 1 to 4 carbon atoms or H and wherein of the number of radicals bound to Si are at least 3% R⁴ and H.
Hülsen gemäß Anspruch 2, dadurch gekennzeichnet, daß die Reste R¹, R², R³ und R⁵ für Methylgruppen stehen.Sleeves according to claim 2, characterized in that the radicals R¹, R², R³ and R⁵ stand for methyl groups. Hülsen gemäß Anspruch 2, dadurch gekennzeichnet, daß
x = 0 bis 100,
y = 5 bis 100,
z = 5 bis 100
wobei x + y + z = 25 bis 300
und von der Anzahl der an Si gebundenen Reste mindestens 3 % R⁴ und mindestens 10 % H sind.
Sleeves according to claim 2, characterized in that
x = 0 to 100,
y = 5 to 100,
z = 5 to 100
where x + y + z = 25 to 300
and of the number of radicals bonded to Si are at least 3% R⁴ and at least 10% H.
Hülsen gemäß Anspruch 2, dadurch gekennzeichnet, daß
x = 0,
y = 5 bis 50,
z = 5 bis 60,
wobei y + z größer 25 ist und von der Anzahl der an Si gebundenen Reste mindestens 10 % R⁴ und mindestens 30 % H sind.
Sleeves according to claim 2, characterized in that
x = 0,
y = 5 to 50,
z = 5 to 60,
where y + z is greater than 25 and of the number of radicals bound to Si are at least 10% R⁴ and at least 30% H.
Hülsen gemäß Anspruch 2, dadurch gekennzeichnet, daß R⁴ für einen Dodecyl- und/oder Tetradecylrest steht.Sleeves according to claim 2, characterized in that R⁴ represents a dodecyl and / or tetradecyl radical. Hülsen gemäß Anspruch 1, dadurch gekennzeichnet, daß die Siliconharze folgende Formel aufweisen



        R¹aSi(OH)b(OR²)cO(4-a-b-c)/2



wobei
a = 1,0 bis 2,0
b + c = 0,1 bis 1,7 R¹   ein linearer oder verzweigter Alkylrest mit 1 bis 18 C-Atomen oder ein Phenylrest bedeutet und R²   einen linearen oder verzweigten Alkylrest mit 1 bis 4 C-Atomen darstellt,
Sleeves according to claim 1, characterized in that the silicone resins have the following formula



R1 a Si (OH) b (OR2) c O (4-abc) / 2



in which
a = 1.0 to 2.0
b + c = 0.1 to 1.7 R¹ is a linear or branched alkyl radical having 1 to 18 carbon atoms or a phenyl radical and R² represents a linear or branched alkyl radical having 1 to 4 carbon atoms,
Verfahren zur Herstellung der Hülsen nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, daß a) das Siliconöl oder das Siliconharz in Mengen zwischen 5 und 100 g/m², vorzugsweise 10 und 70 g/m² auf die Hülse appliziert wird, wobei bei der Verwendung von Siliconharz diesem vorher ein üblicher Katalysator in Mengen von 100 bis 5000 ppm zugesetzt wird, b) die so behandelte Hülse unter Luftzutritt im Ofen bei Temperaturen zwischen 60° und 120°C über einen Zeitraum von 15 Minuten bis 2 Stunden getrocknet wird. Process for the production of the sleeves according to one of Claims 1 to 7, characterized in that a) the silicone oil or the silicone resin is applied to the sleeve in amounts between 5 and 100 g / m², preferably 10 and 70 g / m², wherein if silicone resin is used, a conventional catalyst is added beforehand in amounts of 100 to 5000 ppm, b) the sleeve thus treated is dried in the oven at temperatures between 60 ° and 120 ° C. over a period of 15 minutes to 2 hours. Verwendung der Hülsen nach einem der Ansprüche 1 bis 7 bei der Aufwicklung von Glasfasern.Use of the sleeves according to one of claims 1 to 7 in the winding of glass fibers.
EP92122078A 1992-01-10 1992-12-28 Coated bobbins, process for their fabrication and their use in the processing of glass fibers Expired - Lifetime EP0553493B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4200445A DE4200445A1 (en) 1992-01-10 1992-01-10 COATED CASES, A METHOD FOR THE PRODUCTION THEREOF AND THEIR USE IN THE PROCESSING OF FIBERGLASS
DE4200445 1992-01-10

Publications (2)

Publication Number Publication Date
EP0553493A1 true EP0553493A1 (en) 1993-08-04
EP0553493B1 EP0553493B1 (en) 1997-02-19

Family

ID=6449309

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92122078A Expired - Lifetime EP0553493B1 (en) 1992-01-10 1992-12-28 Coated bobbins, process for their fabrication and their use in the processing of glass fibers

Country Status (3)

Country Link
EP (1) EP0553493B1 (en)
DE (2) DE4200445A1 (en)
ES (1) ES2097857T3 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995001929A1 (en) * 1993-07-05 1995-01-19 Mölnlycke AB A method of producing a coreless roll of fibre-based, web-like material
US5849357A (en) * 1993-07-05 1998-12-15 Sca Hygiene Products Ab Method of producing a coreless roll of fibre-based, web-like material
WO2005037722A1 (en) * 2003-10-15 2005-04-28 Sonoco Development, Inc. Glass forming tube, and glass cake and method incorporating same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1801325A1 (en) * 1967-10-09 1969-05-08 Midland Silicones Ltd Process for the treatment of inorganic and organic fibers
FR2291253A1 (en) * 1974-11-15 1976-06-11 Ici Ltd ORGANOPOLYSILOXANE COMPOSITIONS
DE2751803A1 (en) * 1976-12-03 1978-06-08 Goldschmidt Ag Th PROCESS FOR ABHAESIVE COATING OF FLAT MATERIALS
US4763785A (en) * 1987-10-09 1988-08-16 Basf Aktiengesellschaft Center-pull fiber package and method for producing the package
EP0356827A2 (en) * 1988-08-31 1990-03-07 Bayer Ag Lubricant based on polyorganosiloxane
WO1990010244A1 (en) * 1989-02-23 1990-09-07 Hughes Aircraft Company Fiber optic cannister with compliant baselayer

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1801325A1 (en) * 1967-10-09 1969-05-08 Midland Silicones Ltd Process for the treatment of inorganic and organic fibers
FR2291253A1 (en) * 1974-11-15 1976-06-11 Ici Ltd ORGANOPOLYSILOXANE COMPOSITIONS
DE2751803A1 (en) * 1976-12-03 1978-06-08 Goldschmidt Ag Th PROCESS FOR ABHAESIVE COATING OF FLAT MATERIALS
US4763785A (en) * 1987-10-09 1988-08-16 Basf Aktiengesellschaft Center-pull fiber package and method for producing the package
EP0356827A2 (en) * 1988-08-31 1990-03-07 Bayer Ag Lubricant based on polyorganosiloxane
WO1990010244A1 (en) * 1989-02-23 1990-09-07 Hughes Aircraft Company Fiber optic cannister with compliant baselayer

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
WPIL, FILE SUPPLIER, DERWENT PUBLICATIONS LTD. LONDON, GB.; AN=78-48316A & JP-A-53 058 034 (TEIJIN KK) 25-05-1978 *
WPIL, FILE SUPPLIER, DERWENT PUBLICATIONS LTD., LONDON, GB.; AN=91-112021 & JP-A-3 051 374 (KANEBO KK) 05-03-1991 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995001929A1 (en) * 1993-07-05 1995-01-19 Mölnlycke AB A method of producing a coreless roll of fibre-based, web-like material
US5849357A (en) * 1993-07-05 1998-12-15 Sca Hygiene Products Ab Method of producing a coreless roll of fibre-based, web-like material
WO2005037722A1 (en) * 2003-10-15 2005-04-28 Sonoco Development, Inc. Glass forming tube, and glass cake and method incorporating same
US7332203B2 (en) 2003-10-15 2008-02-19 Sonoco Development, Inc. Glass forming tube, and glass cake and method incorporating same

Also Published As

Publication number Publication date
DE59208054D1 (en) 1997-03-27
DE4200445A1 (en) 1993-07-15
EP0553493B1 (en) 1997-02-19
ES2097857T3 (en) 1997-04-16

Similar Documents

Publication Publication Date Title
DE3426087C1 (en) Organopolysiloxane mixtures modified with acrylic acid esters, their preparation and use as abhesive coating compositions
DE2802242C2 (en)
DE1494881A1 (en) Process for the production of a water-soluble epoxy resin-containing sizing composition for glass fibers
DE2436981A1 (en) COATED FIBERGLASS AND AQUATIC FINISHES FOR THESE
DE1010941B (en) Process for treating glass fibers
DE2534760A1 (en) RESIN-COATED FIBERGLASS AND METHOD FOR MANUFACTURING IT
DE2606777A1 (en) RIBBON OR FLAT CABLES
EP0027942B1 (en) Sizing composition for glass fibres, glass fibres sized therewith and process for their preparation, as well as glass fibre composites
DE1769961C3 (en) Antistatic size containing organosilicon compounds for coating glass fibers and glass fibers with antistatic properties
EP0297602A2 (en) Size for glass fibers, its preparation and its use
DE2948140C2 (en) Magnetic recording medium and method for producing such a magnetic recording medium
EP0553493A1 (en) Coated bobbins, process for their fabrication and their use in the treatment of glass fibers
DE2502965A1 (en) THICK-COATED GLASS FIBER MATERIALS, USED WITH IT, FIBER REINFORCED PLASTIC BODIES AND THEIR PRODUCTION
EP0137427A2 (en) Sizing composition for glass fibres
WO1994001482A1 (en) Polyester resin for the production of high-transparency, neutral-coloured articles
EP0058299B1 (en) Process for the preparation of heat-setting silicone resins, particularly applicable as electrically insulating resins
EP0311894A2 (en) Aqueous dispersions, process for their preparation and their application
DE2528995A1 (en) SIZING AGENT FOR GLASS FIBERS
DE1933969C3 (en) Thermoplastic molding compounds based on saturated polyester
EP0411407B1 (en) Coupling agent for the sizing of glass fibres
DE2854396C2 (en) Sizing agent for glass fibers
DE4431735A1 (en) Inorganically treated barium sulphate, useful as filler in polymers
DE1720974A1 (en) Process for the production of polyesters
DE2426656C3 (en) Aqueous size for coating glass fibers to reinforce thermoplastic polyesters
DE3139301A1 (en) Process for the preparation of dialkyl (3-chloro-n-propyl)malonates or alkyl (3-chloro-n-propyl)cyanoacetates

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE ES FR GB IT NL

17P Request for examination filed

Effective date: 19930816

17Q First examination report despatched

Effective date: 19941216

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE DE ES FR GB IT NL

GBT Gb: translation of ep patent filed (gb section 77(6)(a)/1977)

Effective date: 19970219

REF Corresponds to:

Ref document number: 59208054

Country of ref document: DE

Date of ref document: 19970327

ITF It: translation for a ep patent filed

Owner name: 0508;06MIFING. C. GREGORJ S.P.A.

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2097857

Country of ref document: ES

Kind code of ref document: T3

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20021031

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20021119

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20021217

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20021218

Year of fee payment: 11

Ref country code: BE

Payment date: 20021218

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20021224

Year of fee payment: 11

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20031228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20031229

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20031231

BERE Be: lapsed

Owner name: *BAYER ANTWERPEN N.V.

Effective date: 20031231

Owner name: *BAYER A.G.

Effective date: 20031231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040701

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040701

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20031228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040831

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20040701

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20031229

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20051228