EP0473430A2 - PEEK hot press felts and fabrics - Google Patents
PEEK hot press felts and fabrics Download PDFInfo
- Publication number
- EP0473430A2 EP0473430A2 EP91307912A EP91307912A EP0473430A2 EP 0473430 A2 EP0473430 A2 EP 0473430A2 EP 91307912 A EP91307912 A EP 91307912A EP 91307912 A EP91307912 A EP 91307912A EP 0473430 A2 EP0473430 A2 EP 0473430A2
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- European Patent Office
- Prior art keywords
- fabric
- polyetherketone
- peek
- fibre
- crystallinity
- 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.)
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Classifications
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/66—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyethers
- D01F6/665—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyethers from polyetherketones, e.g. PEEK
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21F—PAPER-MAKING MACHINES; METHODS OF PRODUCING PAPER THEREON
- D21F7/00—Other details of machines for making continuous webs of paper
- D21F7/08—Felts
- D21F7/083—Multi-layer felts
Definitions
- This invention relates to fibres and fabric for use in press felts to be employed in a high temperature environment.
- Typical fibres are materials from the generic classes of polyaramids, polybenzimidazoles, polyetherimides, polysulfones, polyphenylene sulfide, and polyarylates. While all these materials have high temperature use capabilities, most do not possess adequate physical properties to be useful for press fabric applications. Many materials such as polysulfones and polyetherimides are non-crystalline materials which tend to deform under load at temperatures above their glass transition and suffer irreversible deformation upon repeated passage through a press nip. Other materials such as the polyaramids, polybenzimidazoles and polyarylates are semi-crystalline polymers, but are, in general, highly aromatic rigid materials which suffer brittle fracture in a press nip after a relatively few compression cycles.
- polyetherketones while being semi-crystalline and highly aromatic do not show brittle fracture at ambient or at elevated temperatures, when produced to have a specific fibre morphology.
- a fabric for a paper making machine which fabric comprises a woven substrate carrying batt fibre on a surface thereof characterised in that at least one of the batt fibre and the substrate comprises a polyetherketone.
- the present invention also includes a method of manufacturing paper which method comprises forming a furnish of paper making constituents, introducing said furnish as a layer to a dewatering station to dewater said furnish to produce a cohesive sheet and thereafter pressing at an elevated temperature wherein the paper is transported by continuous fabrics and characterised in that the pressing and drying of the sheet in at least part of the process in conducted at a temperature in excess of 100°C and further characterised in that the fabric in at least said part of the process comprises a woven, knitted, braided or nonwoven substrate carrying batt fibre on a surface thereof and where at least one of said batt fibre and said substrate comprises a polyetherketone.
- the polyetherketone may be a fabric wherein the polyetherketone is selected from one or more of polyetherketone (PEK), polyetheretherketone (PEEK), polyetherketoneketone (PEKK) and polyetheretherketoneketone (PEEKK).
- PEK polyetherketone
- PEEK polyetheretherketone
- PEKK polyetherketoneketone
- PEEKK polyetheretherketoneketone
- the polyetherketone may include an effective proportion of an anti-oxidant therefor.
- Fibres used in the invention may be made from commercially available polyetherketones such as those commercially available under the trade name "VICTREX PEK” or “VICTREX PEEK” both of which are currently commerically available from ICI Limited and are intended principally as injection molding materials, but they can be extruded into fine fibre or monofilament.
- polyetherketones maintain a relatively cooler fabric surface temperature after passage through a heated press environment than other materials evaluated and may at the same time provide an enhanced sheet release characteristic.
- higher fabric temperatures near the sticking point of lignin
- cooler press fabric surfaces promote ease of sheet release.
- the polymer molecular weight is high and it has been found that the optimum properties in both the maintenance of molecular weight during extrusion and subsequent use is obtained if a proportion of anti-oxidant is compounded with the resin prior to extrusion.
- Typical antioxidants suitable for use in the present invention are phenolic antioxidants and/or those based on ⁇ -tocopherol.
- the fibre morphology for PEEK fibres for the Impulse Drying process requires a moderately drawn fibre with moderate orientation and crystallinity, and should not be at the extremes of low or high orientation and crystallinity, thus providing superior mechanical properties for Impulse Drying. Fibres with either low or high orientation and cystallinity result in more rapid and undesirable mechanical failure, such as flattening and fibrillation.
- the orientation and the crystallinity lie within 30% to 75%, preferably 40% to 70% of the range between the low and high extremes of each of these properties.
- the crystallinity of the polyetherketone is within the range of 50 to 65% of the extremes of crystallinity for that particular polyetherketone employed.
- the polyetherketone may be a PEEK fibre and may have a shrink force at 150°C not greater than 0.20 gpd.
- polyetherketones may be employed which have at least one yield point below 3.0 gpd.
- Figure 1 is a photomicrograph of a sample PEEK-h of Example II.
- Figure 2 is a photomicrograph of a sample PEEK-a of Example II.
- Figure 3 is a plot of shrink force against temperatures for samples of Example II.
- Figure 4 is a plot of applied stress against % elongation for samples of Example II.
- a polyetheretherketone resin commercially available from ICI under the name Victrex PEEK 380G and hereinafter referred to as PEEK-a was extruded and drawn into approximately 17 denier per filament multifilament yarn in a standard melt extrusion spinning operation.
- the fibre produced had moderate orientation and moderate crystallinity.
- the fibre was crimped and cut into three inch staple. Fibre properties obtained were 3.1 g/den tenacity, 31% elongation to break and 26 g/den initial modulus. This fibre was carded into a web and needled onto the top surface of a pre-made press fabric. The press fabric was run on a pilot machine press section to assess fibre performance.
- PEEK-a was a crimped fibre of 15dtex in 80mm staple length manufactured by Hoechst Aktiengesellschaft. Both PEEK-a and PEEK-h were of equivalent molecular weight but different in fibre morphology.
- a layer of each PEEK fibre was needled onto the surface of the pilot press fabric in separate areas.
- the fabric was run on a pilot press machine at the following wet pressing conditions:
- Figure 1 is a photomicrograph of PEEK-h; it can be seen that the fibres have undergone extensive flattening and fibrillation, as a result the dewatering ability of this sample is severely impaired.
- Figure 2 the sample of PEEK-a shown in Figure 2 after 106compressions, is in a much superior condition; although the fibres have undergone some flattening, the integrity of the fibres remains and the dewatering characteristics of the structure remain intact.
- Shrink force data further corroborates higher orientation and crystallinity in PEEK-h fibre.
- the shrink force values thoughout the test are consistently greater for PEEK-h fibre than for PEEK-a fibre.
- Shrink force data at 80°C and 150°C are shown.
- the 80°C represents the water temperature used with current wet pressing technology while the 150°C temperature represents a typical Impulse Drying temperature.
- Figure 3 is a plot of shrink force measured in grammes per denier (gpd) as ordinate against temperature in °C as abscissa. The less oriented nature of the sample PEEK-a can be discerned clearly which compared with PEEK-h by the lower shrink force curve.
- a needled nonwoven fabric was prepared by needling together successive card web layers of the same PEEK fibre as described in Example I. Each batt of approximately 120 gm/m2 weight was crosslapped at a 90° angle prior to needling. The total fabric product consisted of eight batt layers and was approximately 1000 gm/m2 in weight.
- An identical fabric was prepared from commercial polyamide 6,6 fibre typical of that used for commercial paper machine clothing fabrics. Each fabric was used in an experiment to dewater a 25% solids paper sheet in an Impulse Drying apparatus similar to that described by Lavery, H.P. in CPAA Annual Meeting preprints, 73B: 121-126 (Jan 29, 1987).
- the PEEK sample successfully removed water from the paper to high levels of dryness without suffering apparent physical damage.
- the polyamide sample in the same test fused to an impermeable mass during the initial impact. The temperature of the falling plate was maintained at 300°C, peak pressure was 600 psi and equivalent nip residence time was 4.5 ms.
- PEEK-i A sample of another PEEK fibre, spun from a commercially available resin, was evaluated on a pilot Impulse Drying machine.
- This PEEK fibre designated PEEK-i is produced by ICI under the trade name ZYEX with a 13.3 dtex and 80 mm fibre length, and was spun to a similar fibre morphology as PEEK-a (moderate orientation and crystallinity).
- the PEEK-i was part of a multi-candidate pilot fabric evaluation.
- press roll temperatures as high as 205°C were tried. At this temperature, PEEK-i sample had excellent temperature resistance and sheet handling ability with acceptable dewatering performance.
- Fibre U13 aromatic aliphatic polyamide resin which was spun into a fibre sample called Fibre U13 which is a fibre spun (at AIRESCO) from BASF Ultramid T resin Grade KR4351, and a metaphenylene isothalamid called BXC.
- PEEK-i, U13 and BXC were all high temperature materials, Fibres U13 and BXC had poor sheet handling properties. Fibres U13 and BXC surfaces were extremely tacky and did not release the paper sheet after passing through the heated press nip. PEEK-i had excellent sheet release properties.
- PEEK-i sample was evaluated on another Impulse Drying pilot paper machine which includes a heated long nip press.
- the PEEK-i fibre was prepared into a pilot size needled fabric and evaluated on the pilot machine at roll temperatures as high as 202°C, machine speeds as high as 2000 fpm and roll pressures as high as 6700 pl.
- the PEEK-i fabric had excellent sheet release properties and good dewatering performance.
- the surface temperature of the fabric which was measured throughout the trial remained relatively low. We believe maintenance of a low fabric surface temperature is critical for good sheet release.
- Other fibres evaluated on the same equipment which did not release the paper sheet were either extremely tacky or were measured to have a "hotter" fabric surface temperature.
- the post nip fabric surface temperature of PEEK-i was approximately 60°C; this was favourable when compared with another fabric candidate, having a sheet contacting surface of polytetrafluorethylene (PTFE) which experienced sheet release problems, and had a post nip fabric surface temperature of approximately 93°C.
- PTFE polytetrafluorethylene
Abstract
Description
- This invention relates to fibres and fabric for use in press felts to be employed in a high temperature environment.
- Recent proposals in paper making technology have disclosed that dewatering of a paper sheet in the press section of a paper making machine leads to a significantly higher dryness value if the press section is heated to temperatures above the boiling point of water. This process is commonly referred to as Impulse Drying. The best results, that is to say, the highest sheet dryness, are obtainable at press roll temperatures in excess of 150°C. It has been observed that the application of such Impulse Drying technology to conventional commercial paper making machines typically involving roll presses or shoe presses will lead to a more energy efficient process and improved paper properties. The difficulty with such proposals is that the fabrics normally employed to convey the paper sheet through the press and to assist in sheet dewatering, will not withstand the combination of high temperatures and mechanical pressures currently being proposed for Impulse Drying as indicated above.
- Commercial press fabrics are generally constructed of synthetic polyamide fibre; these materials have superior impact, abrasion and hydrolytic stability properties and give excellent life in commercial operations run at temperatures between ambient and about 80°C. At temperatures much above the foregoing, however, conventional polyamide fabrics fuse into a condensed mass which is not useful for dewatering a paper sheet.
- The advent of the new technology for high temperature dewatering requires a press fabric composed of fibres which do not deform or degrade when exposed to high temperature and mechanical pressure and thus maintain useful dewatering characteristics over the life of the press fabric.
- Many high temperature fibres have been developed in recent years for demanding applications in aerospace and industrial processes. Typical fibres are materials from the generic classes of polyaramids, polybenzimidazoles, polyetherimides, polysulfones, polyphenylene sulfide, and polyarylates. While all these materials have high temperature use capabilities, most do not possess adequate physical properties to be useful for press fabric applications. Many materials such as polysulfones and polyetherimides are non-crystalline materials which tend to deform under load at temperatures above their glass transition and suffer irreversible deformation upon repeated passage through a press nip. Other materials such as the polyaramids, polybenzimidazoles and polyarylates are semi-crystalline polymers, but are, in general, highly aromatic rigid materials which suffer brittle fracture in a press nip after a relatively few compression cycles.
- Surprisingly, we have found that polyetherketones, while being semi-crystalline and highly aromatic do not show brittle fracture at ambient or at elevated temperatures, when produced to have a specific fibre morphology.
- According to the present invention, therefore, there is provided a fabric for a paper making machine, which fabric comprises a woven substrate carrying batt fibre on a surface thereof characterised in that at least one of the batt fibre and the substrate comprises a polyetherketone.
- The present invention also includes a method of manufacturing paper which method comprises forming a furnish of paper making constituents, introducing said furnish as a layer to a dewatering station to dewater said furnish to produce a cohesive sheet and thereafter pressing at an elevated temperature wherein the paper is transported by continuous fabrics and characterised in that the pressing and drying of the sheet in at least part of the process in conducted at a temperature in excess of 100°C and further characterised in that the fabric in at least said part of the process comprises a woven, knitted, braided or nonwoven substrate carrying batt fibre on a surface thereof and where at least one of said batt fibre and said substrate comprises a polyetherketone.
- In a particular embodiment of the present invention, the polyetherketone may be a fabric wherein the polyetherketone is selected from one or more of polyetherketone (PEK), polyetheretherketone (PEEK), polyetherketoneketone (PEKK) and polyetheretherketoneketone (PEEKK).
- In another aspect of the present invention, the polyetherketone may include an effective proportion of an anti-oxidant therefor. Fibres used in the invention may be made from commercially available polyetherketones such as those commercially available under the trade name "VICTREX PEK" or "VICTREX PEEK" both of which are currently commerically available from ICI Limited and are intended principally as injection molding materials, but they can be extruded into fine fibre or monofilament.
- In another aspect of the invention, polyetherketones maintain a relatively cooler fabric surface temperature after passage through a heated press environment than other materials evaluated and may at the same time provide an enhanced sheet release characteristic. At higher fabric temperatures (near the sticking point of lignin) there is a tendency for the paper sheet to stick to the press fabric, causing difficulties with sheet release. In general, cooler press fabric surfaces promote ease of sheet release.
- For press fabric use, it is preferred that the polymer molecular weight is high and it has been found that the optimum properties in both the maintenance of molecular weight during extrusion and subsequent use is obtained if a proportion of anti-oxidant is compounded with the resin prior to extrusion. Typical antioxidants suitable for use in the present invention are phenolic antioxidants and/or those based on α-tocopherol.
- In a further aspect of the invention, it has been found that the fibre morphology for PEEK fibres for the Impulse Drying process requires a moderately drawn fibre with moderate orientation and crystallinity, and should not be at the extremes of low or high orientation and crystallinity, thus providing superior mechanical properties for Impulse Drying. Fibres with either low or high orientation and cystallinity result in more rapid and undesirable mechanical failure, such as flattening and fibrillation. In a preferred aspect of the invention, the orientation and the crystallinity lie within 30% to 75%, preferably 40% to 70% of the range between the low and high extremes of each of these properties.
- In another aspect of the present invention, the crystallinity of the polyetherketone is within the range of 50 to 65% of the extremes of crystallinity for that particular polyetherketone employed.
- In another aspect of the invention, the polyetherketone may be a PEEK fibre and may have a shrink force at 150°C not greater than 0.20 gpd.
- In another aspect of the present invention, polyetherketones may be employed which have at least one yield point below 3.0 gpd.
- Following is a description by way of example only and with reference to the accompanying drawings of methods of carrying the invention into effect.
- In the drawings:-
- Figure 1 is a photomicrograph of a sample PEEK-h of Example II.
- Figure 2 is a photomicrograph of a sample PEEK-a of Example II.
- Figure 3 is a plot of shrink force against temperatures for samples of Example II.
- Figure 4 is a plot of applied stress against % elongation for samples of Example II.
- A polyetheretherketone resin commercially available from ICI under the name Victrex PEEK 380G and hereinafter referred to as PEEK-a was extruded and drawn into approximately 17 denier per filament multifilament yarn in a standard melt extrusion spinning operation. The fibre produced had moderate orientation and moderate crystallinity. The fibre was crimped and cut into three inch staple. Fibre properties obtained were 3.1 g/den tenacity, 31% elongation to break and 26 g/den initial modulus. This fibre was carded into a web and needled onto the top surface of a pre-made press fabric. The press fabric was run on a pilot machine press section to assess fibre performance. As a comparison, card web samples of conventional polyamide fibres normally used in PMC applications and samples of representative high temperature fibres such as PBI polybenzimidazole, Ryton polyphenylene sulfide, Nomex polyamide and Kevlar polyaramide were needled onto the same pilot fabric. The fabric was run at the following conditions:
- Samples of each fibre were removed after 10⁵, 2x10⁵, 3x10⁵, 4x10⁵, 5x10⁵, 7.5x10⁵, and 10⁶ compression cycles. The PEEK fibre was found to perform equivalent to the best commercial polyamide fibre while the other high temperature fibres were significantly damaged (flattened and fibrillated) and judged to be no longer functional after 2x10⁵ and 3x10⁵ cycles.
- Two samples of commercially available PEEK resins were prepared into staple fibre and ultimately carded batts for evaluation on a pilot press fabric (as described in Example 1). One of the fibre samples was PEEK-a described in Example 1, the other fibre sample which was designated PEEK-h was a crimped fibre of 15dtex in 80mm staple length manufactured by Hoechst Aktiengesellschaft. Both PEEK-a and PEEK-h were of equivalent molecular weight but different in fibre morphology. The PEEK-h fibre had a higher level of orientation and crystallinity, as indicated by DSC, DMA and Shrink Force studies.
- A layer of each PEEK fibre was needled onto the surface of the pilot press fabric in separate areas. The fabric was run on a pilot press machine at the following wet pressing conditions:
- Machine speed:
- 1000 m/min
- Linear Pressure:
- 100kN/m
- Fabric Tension:
- 3 kN/m
- Suction Vacuum:
- 40 kPa
- Water spray Temp:
- 64-72°C
- Total No. of Compressions:
- 1,000,000
- The results of the pilot fabric trial is shown in Figures 1 and 2 of the accompanying drawings. Figure 1 is a photomicrograph of PEEK-h; it can be seen that the fibres have undergone extensive flattening and fibrillation, as a result the dewatering ability of this sample is severely impaired. In contradistinction, the sample of PEEK-a shown in Figure 2 after 10⁶compressions, is in a much superior condition; although the fibres have undergone some flattening, the integrity of the fibres remains and the dewatering characteristics of the structure remain intact. Thus, while the PEEK-h fibre flattened and fibrillated to an unacceptably high level, a performance ranking which was assigned to each fibre is listed below: it should be noted that on a scale from 1 to 5, a lower numerical value indicates better performance and a ranking difference of 0.5 is considered significant.
- PEEK-a
- Ranking - 3.3
- PEEK-h
- Ranking - 4.8
- Results of the analytical study are shown in the table below. DSC lst heating cycle data shows that both endotherm melt temperature and endotherm peak area are higher for PEEK-h indicating higher crystallinity. DMA results show Tan delta max temperature of PEEK-h is higher at a lower value than PEEK-a, indicating a higher level of orientation. E′ value (storage modulus) is also higher above Tg for PEEK-h fibre than for PEEK-a fibre, which also supports higher orientation in PEEK-h fibre. The E′ values for both fibres have been reported at two temperatures. The temperatures selected correspond to the Tan Delta Max temperature for each fibre: 182°C and 193°C. Shrink force data further corroborates higher orientation and crystallinity in PEEK-h fibre. The shrink force values thoughout the test are consistently greater for PEEK-h fibre than for PEEK-a fibre. Shrink force data at 80°C and 150°C are shown. The 80°C represents the water temperature used with current wet pressing technology while the 150°C temperature represents a typical Impulse Drying temperature.
- Reference to Figures 3 and 4 of the accompanying drawings, illustrates the difference in morphology between the samples PEEK-a and PEEK-h. Figure 3 is a plot of shrink force measured in grammes per denier (gpd) as ordinate against temperature in °C as abscissa. The less oriented nature of the sample PEEK-a can be discerned clearly which compared with PEEK-h by the lower shrink force curve.
- The less oriented nature of the PEEK-a sample can be seen from Figure 4 which is a plot of specific stress as an applied force in gpd as ordinate against % Elongation as abscissa. The curve for the more crystalline PEEK-h is smooth, whereas that for the sample PEEK-a shows a number of distinct yield points as shown by sudden and abrupt changes in slope on the curve, see for example at A and B.
- A needled nonwoven fabric was prepared by needling together successive card web layers of the same PEEK fibre as described in Example I. Each batt of approximately 120 gm/m² weight was crosslapped at a 90° angle prior to needling. The total fabric product consisted of eight batt layers and was approximately 1000 gm/m² in weight. An identical fabric was prepared from commercial polyamide 6,6 fibre typical of that used for commercial paper machine clothing fabrics. Each fabric was used in an experiment to dewater a 25% solids paper sheet in an Impulse Drying apparatus similar to that described by Lavery, H.P. in CPAA Annual Meeting preprints, 73B: 121-126 (Jan 29, 1987). The PEEK sample successfully removed water from the paper to high levels of dryness without suffering apparent physical damage. The polyamide sample in the same test fused to an impermeable mass during the initial impact. The temperature of the falling plate was maintained at 300°C, peak pressure was 600 psi and equivalent nip residence time was 4.5 ms.
- A sample of another PEEK fibre, spun from a commercially available resin, was evaluated on a pilot Impulse Drying machine. This PEEK fibre designated PEEK-i, is produced by ICI under the trade name ZYEX with a 13.3 dtex and 80 mm fibre length, and was spun to a similar fibre morphology as PEEK-a (moderate orientation and crystallinity). The PEEK-i was part of a multi-candidate pilot fabric evaluation. During the Impulse Drying trial, press roll temperatures as high as 205°C were tried. At this temperature, PEEK-i sample had excellent temperature resistance and sheet handling ability with acceptable dewatering performance. For comparison, two other high temperature fibres were evaluated: aromatic aliphatic polyamide resin which was spun into a fibre sample called Fibre U13 which is a fibre spun (at AIRESCO) from BASF Ultramid T resin Grade KR4351, and a metaphenylene isothalamid called BXC. Although fibres PEEK-i, U13 and BXC were all high temperature materials, Fibres U13 and BXC had poor sheet handling properties. Fibres U13 and BXC surfaces were extremely tacky and did not release the paper sheet after passing through the heated press nip. PEEK-i had excellent sheet release properties.
- PEEK-i sample was evaluated on another Impulse Drying pilot paper machine which includes a heated long nip press. The PEEK-i fibre was prepared into a pilot size needled fabric and evaluated on the pilot machine at roll temperatures as high as 202°C, machine speeds as high as 2000 fpm and roll pressures as high as 6700 pl. During this trial the PEEK-i fabric had excellent sheet release properties and good dewatering performance. The surface temperature of the fabric which was measured throughout the trial remained relatively low. We believe maintenance of a low fabric surface temperature is critical for good sheet release. Other fibres evaluated on the same equipment which did not release the paper sheet were either extremely tacky or were measured to have a "hotter" fabric surface temperature. The post nip fabric surface temperature of PEEK-i was approximately 60°C; this was favourable when compared with another fabric candidate, having a sheet contacting surface of polytetrafluorethylene (PTFE) which experienced sheet release problems, and had a post nip fabric surface temperature of approximately 93°C.
Claims (15)
- A fabric for a paper making machine which fabric comprises a woven, knitted, braided or nonwoven substrate carrying batt fibre on the surface thereof characterised in that at least one of the batt fibre and the substrate comprises a polyetherketone.
- A fabric as claimed in claim 1 wherein the polyetherketone is selected from one or more of polyetherketone (PEK), polyetheretherketone (PEEK), polyetherketoneketone (PEKK) and polyetheretherketoneketone (PEEKK).
- A fabric as claimed in claim 1 or claim 2 characterised in that the polyetherketone includes an effective proportion of antioxidant.
- A fabric as claimed in claim 3 characterised in that the antioxidant is selected from phenolic antioxidants and/or α-tocopheral.
- A fabric as claimed in any preceding claim characterised in that the polyetherketone has a high polymer molecular weight.
- A fabric as claimed in any preceding claim wherein the fabric fibres contain polyetherketone having moderate orientation and crystallinity within the range 30% to 75% at the extremes of low and high orientation and low and high crystallinity.
- A fabric as claimed in claim 6 wherein the moderate orientation and crystallinity lie within the range of 40% to 70% of the extremes of low and high orientation and of low and high crystallinity.
- A fabric as claimed in claim 6 wherein the crystallinity lies within the range of 50% to 65% of the extremes of low and high crystallinity.
- A fabric as claimed in any one of claims 1 to 8 wherein the polyetherketone is a PEEK fibre having a shrink force at 150°C of not more than 0.2 gpd.
- A fabric as claimed in any preceding claim characterised in that the polyetherketone has a tensile stress property having one or more yield points below 3.0 gpd.
- A fabric as claimed in any preceding claim wherein the sheet contacting surface comprises a polyetherketone which in use on a press exhibits a post-nip surface temperature of at least 15 centigrade degrees below that of a comparable fabric having a sheet contacting surface of poly-tetrafluorethylene when the latter is run under identical press conditions.
- A method of manufacturing paper which method comprises forming a furnish of paper making constituents, introducing said furnish as a layer to a dewatering station to dewater said furnish to produce a cohesive sheet and thereafter pressing at an elevated temperature wherein the paper is transported by continuous fabrics and characterised in that the pressing and drying of the sheet in at least part of the process in conducted at a temperature in excess of 150°C and further characterised in that the fabric in at least said part of the process comprises a woven, knitted, braided or nonwoven substrate carrying batt fibre on a surface thereof and where at least one of said batt fibre and said substrate comprises a polyetherketone.
- A method as claimed in claim 12 wherein the said fabric is in a wet pressing section of the dewatering station.
- A method as claimed in claim 12 or claim 13 wherein said fabric is used in a dry section of the process.
- A method as claimed in any one of claims 12 to 14 wherein the fabric is the fabric claimed in any one of preceding claims 1 to 11.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB909018987A GB9018987D0 (en) | 1990-08-31 | 1990-08-31 | Peek hot press felts and fabrics |
GB9018987 | 1990-08-31 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0473430A2 true EP0473430A2 (en) | 1992-03-04 |
EP0473430A3 EP0473430A3 (en) | 1993-01-20 |
EP0473430B1 EP0473430B1 (en) | 1996-03-20 |
Family
ID=10681414
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP91307912A Revoked EP0473430B1 (en) | 1990-08-31 | 1991-08-29 | PEEK hot press felts and fabrics |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP0473430B1 (en) |
JP (1) | JP3005345B2 (en) |
AT (1) | ATE135756T1 (en) |
AU (1) | AU651841B2 (en) |
BR (1) | BR9103768A (en) |
CA (1) | CA2049585C (en) |
DE (1) | DE69118054T2 (en) |
ES (1) | ES2085968T3 (en) |
FI (1) | FI914102A (en) |
GB (1) | GB9018987D0 (en) |
MX (1) | MX9100888A (en) |
NO (1) | NO913376L (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0529506A1 (en) * | 1991-08-23 | 1993-03-03 | Ems-Inventa Ag | Paper-machine felt and method of making the same |
GB2309712A (en) * | 1996-02-05 | 1997-08-06 | Shell Int Research | Papermachine clothing woven from aliphatic polyketone fibres |
US6207276B1 (en) | 1998-11-26 | 2001-03-27 | Ems-Chemie Ag | Sheath-core bicomponent fiber and its applications |
US7014733B2 (en) | 2002-05-14 | 2006-03-21 | Stowe Woodward L.L.C. | Belt for shoe press and shoe calender and method for forming same |
WO2010107976A1 (en) | 2009-03-20 | 2010-09-23 | Arkema Inc. | Polyetherketoneketone nonwoven mats |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2391749B1 (en) * | 2009-02-02 | 2018-03-28 | Arkema Inc. | High performance fibers |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0077901A2 (en) * | 1981-10-28 | 1983-05-04 | Albany International Corp. | Hydrolysis resistant fabric for paper making and like uses |
EP0287297A1 (en) * | 1987-04-15 | 1988-10-19 | Albany Research (Uk) Limited | Paper machine felts |
EP0372769A1 (en) * | 1988-11-28 | 1990-06-13 | Albany International Corp. | Paper machine felts |
Family Cites Families (3)
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JPS62231016A (en) * | 1986-03-28 | 1987-10-09 | Teijin Ltd | Production of poly (aryl ether ketone) yarn |
US4896702A (en) * | 1988-12-01 | 1990-01-30 | Niagara Lockport Industries Inc. | Seam construction for papermaking fabrics |
-
1990
- 1990-08-31 GB GB909018987A patent/GB9018987D0/en active Pending
-
1991
- 1991-08-21 CA CA002049585A patent/CA2049585C/en not_active Expired - Fee Related
- 1991-08-23 AU AU83400/91A patent/AU651841B2/en not_active Ceased
- 1991-08-28 NO NO91913376A patent/NO913376L/en unknown
- 1991-08-29 ES ES91307912T patent/ES2085968T3/en not_active Expired - Lifetime
- 1991-08-29 AT AT91307912T patent/ATE135756T1/en not_active IP Right Cessation
- 1991-08-29 EP EP91307912A patent/EP0473430B1/en not_active Revoked
- 1991-08-29 DE DE69118054T patent/DE69118054T2/en not_active Revoked
- 1991-08-30 BR BR919103768A patent/BR9103768A/en not_active IP Right Cessation
- 1991-08-30 MX MX9100888A patent/MX9100888A/en not_active IP Right Cessation
- 1991-08-30 FI FI914102A patent/FI914102A/en unknown
- 1991-08-30 JP JP3299996A patent/JP3005345B2/en not_active Expired - Lifetime
Patent Citations (3)
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EP0077901A2 (en) * | 1981-10-28 | 1983-05-04 | Albany International Corp. | Hydrolysis resistant fabric for paper making and like uses |
EP0287297A1 (en) * | 1987-04-15 | 1988-10-19 | Albany Research (Uk) Limited | Paper machine felts |
EP0372769A1 (en) * | 1988-11-28 | 1990-06-13 | Albany International Corp. | Paper machine felts |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0529506A1 (en) * | 1991-08-23 | 1993-03-03 | Ems-Inventa Ag | Paper-machine felt and method of making the same |
AU656792B2 (en) * | 1991-08-23 | 1995-02-16 | Ems-Inventa Ag | Paper machine felt and method for the manufacture thereof |
GB2309712A (en) * | 1996-02-05 | 1997-08-06 | Shell Int Research | Papermachine clothing woven from aliphatic polyketone fibres |
US6207276B1 (en) | 1998-11-26 | 2001-03-27 | Ems-Chemie Ag | Sheath-core bicomponent fiber and its applications |
US7014733B2 (en) | 2002-05-14 | 2006-03-21 | Stowe Woodward L.L.C. | Belt for shoe press and shoe calender and method for forming same |
WO2010107976A1 (en) | 2009-03-20 | 2010-09-23 | Arkema Inc. | Polyetherketoneketone nonwoven mats |
EP2408830A1 (en) * | 2009-03-20 | 2012-01-25 | Arkema, Inc. | Polyetherketoneketone nonwoven mats |
EP2408830A4 (en) * | 2009-03-20 | 2013-03-27 | Arkema Inc | Polyetherketoneketone nonwoven mats |
US9422654B2 (en) | 2009-03-20 | 2016-08-23 | Arkema Inc. | Polyetherketoneketone nonwoven mats |
Also Published As
Publication number | Publication date |
---|---|
NO913376L (en) | 1992-03-02 |
AU8340091A (en) | 1992-03-05 |
ES2085968T3 (en) | 1996-06-16 |
EP0473430B1 (en) | 1996-03-20 |
DE69118054D1 (en) | 1996-04-25 |
ATE135756T1 (en) | 1996-04-15 |
CA2049585C (en) | 1995-03-28 |
FI914102A (en) | 1992-03-01 |
JP3005345B2 (en) | 2000-01-31 |
CA2049585A1 (en) | 1992-03-01 |
AU651841B2 (en) | 1994-08-04 |
DE69118054T2 (en) | 1996-09-12 |
NO913376D0 (en) | 1991-08-28 |
BR9103768A (en) | 1992-05-19 |
MX9100888A (en) | 1992-04-01 |
JPH0673684A (en) | 1994-03-15 |
FI914102A0 (en) | 1991-08-30 |
EP0473430A3 (en) | 1993-01-20 |
GB9018987D0 (en) | 1990-10-17 |
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