WO2009009707A1 - Processus de décapage de solvant infrarouge - Google Patents

Processus de décapage de solvant infrarouge Download PDF

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Publication number
WO2009009707A1
WO2009009707A1 PCT/US2008/069717 US2008069717W WO2009009707A1 WO 2009009707 A1 WO2009009707 A1 WO 2009009707A1 US 2008069717 W US2008069717 W US 2008069717W WO 2009009707 A1 WO2009009707 A1 WO 2009009707A1
Authority
WO
WIPO (PCT)
Prior art keywords
solvent
nonwoven web
infrared
web
stripping
Prior art date
Application number
PCT/US2008/069717
Other languages
English (en)
Inventor
Christel Berta Laxton
B. Lynne Wiseman
Christopher William Newton
Simon Frisk
Original Assignee
E.I. Du Pont De Nemours And Company
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 E.I. Du Pont De Nemours And Company filed Critical E.I. Du Pont De Nemours And Company
Priority to JP2010516256A priority Critical patent/JP5377479B2/ja
Priority to CN2008800238991A priority patent/CN101809397B/zh
Priority to EP08781650.0A priority patent/EP2174084B1/fr
Publication of WO2009009707A1 publication Critical patent/WO2009009707A1/fr

Links

Classifications

    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F26—DRYING
    • F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
    • F26B3/00—Drying solid materials or objects by processes involving the application of heat
    • F26B3/28—Drying solid materials or objects by processes involving the application of heat by radiation, e.g. from the sun
    • F26B3/30—Drying solid materials or objects by processes involving the application of heat by radiation, e.g. from the sun from infrared-emitting elements
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F26—DRYING
    • F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
    • F26B13/00—Machines and apparatus for drying fabrics, fibres, yarns, or other materials in long lengths, with progressive movement
    • F26B13/10—Arrangements for feeding, heating or supporting materials; Controlling movement, tension or position of materials
    • F26B13/101—Supporting materials without tension, e.g. on or between foraminous belts
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F26—DRYING
    • F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
    • F26B13/00—Machines and apparatus for drying fabrics, fibres, yarns, or other materials in long lengths, with progressive movement
    • F26B13/24—Arrangements of devices using drying processes not involving heating
    • F26B13/30—Arrangements of devices using drying processes not involving heating for applying suction

Definitions

  • a process for stripping solvent from solvent-laden fibers in a solution-spun fiber web is disclosed.
  • the process of solution spinning involves dissolving a desired polymer into a suitable solvent, and spinning fibers from the polymer/solvent solution.
  • the solvent is an organic solvent which has undesirable properties in use of the so-formed fabric, such as adverse health effects, undesired odor and the like.
  • Solution spinning processes are frequently used to manufacture fibers and nonwoven fabrics, and in some cases have the advantage of high throughputs, such that the fibers or fabrics can be made in large, commercially viable quantities.
  • U.S. Published Patent Application No. 2002/0092423 discloses a solution spinning process for forming a nonwoven polymer web, in particular an electrospinning process, wherein polymeric microfibers or nanofibers are produced from a polymer solution exiting an electrically- charged rotating emitter and directed toward a grounded collector grid. The solvent is evaporated from the fibers "in flight" between the emitter and the collector grid.
  • the invention is a process for stripping chemically bonded spinning solvent from a solution-spun nonwoven web comprising the steps of providing a nonwoven web comprising solvent- laden polymeric fibers having average fiber diameters of less than about 1 micrometer, and transporting the nonwoven web through at least one infrared solvent stripping station wherein infrared radiation irradiates the nonwoven web in the absence of a solvent stripping fluid impinging on the nonwoven web in order to reduce the solvent concentration of the fibers to less than about 10,000 ppmw.
  • Fig. 1 is a schematic of a prior art electroblowing apparatus for preparing a nanofiber web according to the invention.
  • Fig. 2 is a schematic of an infrared solvent stripping station according to the present invention.
  • Fig. 3 is a schematic of a fluid/vacuum solvent stripping station according to the present invention.
  • the present invention relates to solvent-spun webs and fabrics for a variety of customer end-use applications, such as filtration media, energy storage separators, protective apparei and the like, including at least one nanofiber layer, and a process for removing excess spinning solvent from the solution-spun nanofiber webs or fabrics.
  • customer end-use applications such as filtration media, energy storage separators, protective apparei and the like
  • nanofiber layer including at least one nanofiber layer
  • a process for removing excess spinning solvent from the solution-spun nanofiber webs or fabrics There is a need for fibrous products made from a wide variety of polymers to suit various customer end-use needs.
  • Many polymeric fibers and webs can be formed from melt spinning processes, such as spun bonding and melt blowing.
  • melt spinning is limited to spinning fibers from polymers which are melt processable, i.e. those which can be softened or melted and flow at elevated temperatures.
  • solution spinning processes such as wet spinning, dry spinning, flash spinning, electrospinning and electroblowing, involve dissolving a desired polymer into a suitable solvent, and spinning fibers from the polymer/solvent solution.
  • the solvent is an organic solvent which has undesirable properties in use of the so-formed fabric, such as adverse health effects, undesired odor and the like.
  • the fabric is spun and wound into a large roll in an essentially continuous operation, such that even if the solvent were amenable to evaporation upon sitting, only the solvent entrained in the fabric on the outside of the roll is effectively evaporated, since the underlying fabric within the roll is not exposed to the atmosphere.
  • the fabric were to be provided sufficient time in the unrolled state to permit the spinning solvent to evaporate, an exceedingly long area would be necessary to provide room for the unrolled fabric, and recovery of the evaporated solvent would be difficult and expensive. It would be desirable to strip the unwanted solvent from the fibers or fabric during the production process, prior to shipping to the customer.
  • Solvent removal is often complicated by the fact that any particular polymer/solvent spinning system is chosen based upon a strong affinity of the solvent for the polymer, in order to effect complete dissolution of the polymer in the solvent during the spinning operation.
  • the fiber polymer is swollen by the solvent; i.e. the solvent molecules are absorbed and dispersed within the polymeric fibers.
  • the solvent chemically bonds to the polymer molecules making up the fiber, such as by hydrogen bonding, Van der Waals forces, or even ionically via salt formation.
  • solution spun fibers have diameters less than about 1 micrometer (nanofibers) to optimize the diffusion de-volatilization mechanism of solvent removal.
  • nanofibers refers to fibers having diameters varying from a few tens of nanometers up to several hundred nanometers, but generally less than about one micrometer, even less than about 0.8 micrometer, and even less than about 0.5 micrometer.
  • the solution spun fabrics and webs to be subjected to the process of the present invention include at least one layer of polymeric nanofibers.
  • the nanofibers have average fiber diameters of less than about 1 ⁇ m, preferably between about 0.1 ⁇ m and about 1 ⁇ m, and high enough basis weights to satisfy a variety of commercial end-uses, such as for air/liquid filtration media, energy storage separators, protective apparel and the like.
  • the process for making commercial quantities and basis weights of nanofiber layer(s) is disclosed in International Publication Number WO2003/080905 (U.S. Serial No. 10/822,325), which is hereby incorporated by reference.
  • FIG 1 is a schematic diagram of an electroblowing apparatus useful for carrying out the process of the present invention using electroblowing (or "electro-blown spinning") as described in International Publication Number WO2003/080905.
  • This prior art electroblowing method comprises feeding a solution of a polymer in a solvent from mixing chamber 100, through a spinning beam 102, to a spinning nozzle 104 to which a high voltage is applied, while compressed gas is directed toward the polymer solution in a blowing gas stream 106 as it exits the nozzle to form nanofibers, and collecting the nanofibers into a web on a grounded collector 110 under vacuum created by vacuum chamber 114 and blower 112.
  • the moving collection apparatus is preferably a moving collection belt positioned within the electrostatic field between the spinning beam 102 and the collector 110. After being collected, the nanofiber layer is directed to and wound onto a wind-up roll on the downstream side of the spinning beam.
  • the nanofiber web can be deposited onto any of a variety of porous scrim materials arranged on the moving collection belt 110, such as spunbonded nonwovens, meltblown nonwovens, needle punched nonwovens, woven fabrics, knit fabrics, apertured films, paper and combinations thereof.
  • a single nanofiber layer having a basis weight of between about 2 g/m 2 and about 100 g/m 2 , even between about 10 g/m 2 and about 90 g/m 2 , and even between about 20 g/m 2 and about 70 g/m 2 , as measured on a dry basis, i.e., after the residual solvent has evaporated or been removed, can be made by depositing nanofibers from a single spinning beam in a single pass of the moving collection apparatus.
  • significant quantities of residual spinning solvent especially those solvents with strong affinities for the fiber polymers, can remain in the nanofiber webs so-formed.
  • the infrared solvent stripping process and apparatus of the present invention which is disposed downstream of the collection belt 110 of the prior art apparatus (Fig. 1), acts to effect reduction or elimination of unwanted residual solvent from solution spinning processes in a continuous manner, prior to wind-up of the fabric or web.
  • the infrared solvent stripping process and apparatus of the present invention can be used "off-line" or in a separate process after the as-spun nanofiber web has been collected.
  • the infrared solvent stripping apparatus comprises an optional continuous moving belt 14 for supporting the solvent spun nanofiber web and its optional supporting scrim 10 and directing it through one or more infrared solvent stripping stations 11 , each of which comprise an infrared radiation source 12.
  • the infrared solvent stripping stations 11 can be positioned on either or both sides of the plane of the solvent spun nanofiber web.
  • Fig. 2 shows two infrared solvent stripping stations 11 on opposite sides of the plane of the solvent spun nanofiber web.
  • the infrared (IR) radiation source can be either a medium wavelength (1.5-5.6 microns) or a short wavelength (0.72-1.5 microns) source, and can be varied in intensity to heat the solvent-laden nanofiber webs to temperatures up to just below the decomposition temperature of the web polymer.
  • suitable web temperatures can vary from about 120 °C to as high as about 340 °C, without decomposition of the web polymer, depending upon the residence time of web exposure to the IR source.
  • Polymer/solvent combinations which can benefit from the present invention are those in which the polymer exhibits a strong affinity for the solvent, particularly those in which chemical bonding occurs between the polymer and the solvent, such as hydrogen bonding and the like.
  • Some combinations of polymer/solvent which are difficult to separate are polyamide/formic acid and polyvinyl alcohol/water.
  • a fluid/vacuum solvent stripping station as disclosed in U.S. Patent Application Serial Number 11/640625, can also be used.
  • a fluid/vacuum solvent stripping process and apparatus can be disposed downstream of the collection belt 110 of the prior art apparatus (Fig. 1 ) and disposed either before or after the infrared solvent stripping apparatus, which can further act to effect reduction or elimination of unwanted residual solvent from solution spinning processes in a continuous manner, prior to wind-up of the fabric or web.
  • the fluid/vacuum solvent stripping apparatus comprises an optional continuous moving belt 14 for supporting the solvent spun nanofiber web and its optional supporting scrim 10 and directing it through one or more solvent stripping stations 20, each of which comprise a fresh solvent stripping fluid heating apparatus 16, disposed on one side of the moving belt 14, and a vacuum apparatus 18, disposed on the opposite side of moving belt 14.
  • a spent solvent stripping fluid collector (not shown) is disposed downstream of the vacuum apparatus to scrub the excess spinning solvent from the spent stripping fluid for recycling or disposal.
  • the temperature, vacuum pressure and even the fresh solvent stripping fluid itself can be individually controlled within each solvent stripping station.
  • the examples below were prepared from a polymer solution having a concentration of 24 wt% of nylon 6,6 polymer, Zytel® FE3218 (available from E. I. du Pont de Nemours and Company, Wilmington, Delaware) dissolved in formic acid solvent at 99% purity (available from Kemira Oyj, Helsinki, Finland) that was electroblown to form a nonwoven web containing some residual solvent.
  • the residual formic acid content in the nonwoven sheets of nylon was determined using standard wet chemistry techniques and ion chromatography analysis. In a typical determination, a sample of known mass was placed in caustic solution. An aliquot of the resulting solution was analyzed by ion chromatography and the area under the peak corresponding to neutralized formic acid (formate anion) was proportional to the quantity of formic acid in the sample. Comparative Example A
  • Comparative Example A was prepared as set forth above and was transported into a fluid/vacuum solvent stripping station on a moving porous screen.
  • a solvent stripping fluid of air at a temperature of 120°C was impinged onto the nonwoven web from one side while a vacuum was applied to the other side of the nonwoven web.
  • the vacuum was measured at approximately 180 mm H 2 O.
  • the air pressure and the vacuum were coupled to yield a near constant atmospheric pressure in the solvent stripping station.
  • the nonwoven web remained in the solvent stripping station for 4.3 seconds.
  • the nonwoven web was not subjected to the solvent stripping process of the present invention.
  • the final solvent level was 1820 ppm measured prior to preparing Comparative Example B and Example 1.
  • Comparative Example B was prepared in the same manner as Comparative Example A except it was additionally transported through an infrared solvent stripping station with solvent stripping fluid impinging on the nonwoven web, according to the process of U.S. Patent Application Serial Number 11/640,625.
  • This stripping station consisted of a stainless steel belt, a windup station, an infrared heater, a stationary vacuum source located beneath the belt below the infrared heater and two sources of heated air, one impinging normal to the nonwoven web before the infrared heater and one impinging normal to the nonwoven web after the infrared heater.
  • the infrared heater was a Radiant Energy heater, a 3 phase shortwave heater, rated at 12 kW at 240 volts, and was set at a level high enough to heat the web to 180 °C. Hot air at a temperature of 100°C was swept above the web. A vacuum source was located on the opposite side of the nonwoven web from the infrared heaters with a vacuum of 114.3 mm H 2 O. The web was fed through the dryer at a speed 1.016 meters per minute, corresponding to a total residence time of approximately 15 seconds. The sheet temperature in the oven was measured to be on average 153°C. The final solvent level was 1431 ppm.
  • Example 1 Example 1
  • Example 1 was prepared in the same manner as Comparative Example A except it was additionally transported through an infrared solvent stripping station without solvent stripping fluid impinging on the nonwoven web.
  • the stripping station consisted of a stainless steel belt, a windup station and an infrared heater.
  • the infrared heater was a Radiant Energy heater, a 3 phase shortwave heater, rated at 12 kW at 240 volts, and was set at a level high enough to heat the web to 180 °C. No impingement fluid was utilized on either side of the web.
  • the web was fed below the heater at a rate of 1.016 meters per minute, resulting in a residence time of 15 seconds.
  • the final solvent level was 696 ppm.
  • Comparative Example A shows the effect of a fluid/vacuum solvent stripping station with solvent stripping fluid impinging on the nonwoven web, which removed residual solvent to levels suitable for some commercial uses.
  • Comparative Example B shows the effect of an infrared based solvent stripping with solvent stripping fluid impingement on the nonwoven web, which removed additional residual solvent.
  • Example 1 shows the effect of an infrared based solvent stripping without solvent stripping fluid impingement on the nonwoven web, which removed additional residual solvent to an extremely low residual solvent level in the nonwoven web.
  • Comparative Example C was prepared as set forth as in the Examples section above and was transported into a fluid/vacuum solvent stripping station on a moving porous screen.
  • a solvent stripping fluid of air at a temperature of 65°C was impinged onto the nonwoven web from one side while a vacuum was applied to the other side of the nonwoven web.
  • the vacuum was measured at approximately 100 mm H 2 O.
  • the air pressure and the vacuum were coupled to yield a near constant atmospheric pressure in the solvent stripping station.
  • the nonwoven web remained in the solvent stripping station for 20 seconds.
  • the nonwoven web was not subjected to the solvent stripping process of the present invention.
  • the final solvent level was 7501 ppm.
  • Comparative Examples D. E and F Comparative Examples D, E and F were prepared in the same manner as Comparative Example C except they were additionally transported through an infrared solvent stripping zone with solvent stripping fluid impinging on the nonwoven web. This additional step consisted in transporting the web through a floatation dryer.
  • the dryer consists of three sections composed of two banks of infrared heaters each, both above and below the web.
  • the infrared heaters used were Radplane Series 80 Heaters rated at 31 A kW, 480 volts, 1 phase, medium wavelength available from GlenRo. Hot air at a temperature of 49°C, 107°C and 205°C, for Comparative Examples D, E and F respectively, was swept above and below the web countercurrent to the web motion.
  • the web was fed through the dryer at a speed of 12.2 meters per minute, corresponding to a total residence time of approximately 12 seconds.
  • the final solvent levels were 2624 ppm, 596 ppm and 235 ppm, respectively.
  • Example 2 was prepared in the same manner as Comparative Example C except it was additionally transported through an infrared solvent stripping station without solvent stripping fluid impinging on the nonwoven web. This additional step consisted in transporting the web through a floatation dryer.
  • the dryer consists of three sections composed of two banks of infrared heaters each, both above and below the web.
  • the infrared heaters used were Radplane Series 80 Heaters rated at 31.4 kW, 480 volts, 1 phase, medium wavelength available from GlenRo.
  • hot air was not swept above and below the web countercurrent to the web motion.
  • the web was fed through the dryer at a speed of 12.2 meters per minute, corresponding to a total residence time of approximately 12 seconds.
  • Comparative Examples D, E and F show the effect of an infrared based solvent stripping with solvent stripping fluid impingement on the nonwoven web, which removed additional residual solvent. The amount of residual solvent removed is strongly dependent on the temperature of the solvent stripping fluid.
  • Example 2 shows the effect of an infrared based solvent stripping without solvent stripping fluid impingement on the nonwoven web, which removed additional residual solvent to an extremely low residual solvent level in the nonwoven web.
  • the residual solvent level in the material was almost as low as for Comparative Example F, but the possibility of having polymer degradation was significantly reduced when not using the hot stripping fluid.
  • Table 1 The data from Comparative Examples D, E and F and Example 2 are summarized in Table 1.

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Microbiology (AREA)
  • Nonwoven Fabrics (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)

Abstract

Processus de décapage d'un solvant à application centrifuge lié chimiquement d'une bande non tissée filée à partir d'une solution comprenant les étapes consistant à prévoir une bande non tissée comprenant des fibres polymères chargées de solvant ayant des diamètres de fibres moyens inférieurs à environ 1 micromètre, et à acheminer la bande non tissée dans au moins un poste de décapage de solvant infrarouge dans lequel un rayonnement infrarouge irradie la bande non tissée en l'absence d'un fluide de décapage de solvant touchant la bande non tissée afin de réduire la concentration en solvant des fibres à moins d'environ 10000 ppm en poids.
PCT/US2008/069717 2007-07-11 2008-07-11 Processus de décapage de solvant infrarouge WO2009009707A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2010516256A JP5377479B2 (ja) 2007-07-11 2008-07-11 赤外溶剤ストリッピング法
CN2008800238991A CN101809397B (zh) 2007-07-11 2008-07-11 红外溶剂反萃取法
EP08781650.0A EP2174084B1 (fr) 2007-07-11 2008-07-11 Processus de décapage de solvant infrarouge

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US95904507P 2007-07-11 2007-07-11
US60/959,045 2007-07-11

Publications (1)

Publication Number Publication Date
WO2009009707A1 true WO2009009707A1 (fr) 2009-01-15

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Application Number Title Priority Date Filing Date
PCT/US2008/069717 WO2009009707A1 (fr) 2007-07-11 2008-07-11 Processus de décapage de solvant infrarouge

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EP (1) EP2174084B1 (fr)
JP (1) JP5377479B2 (fr)
KR (1) KR20100047257A (fr)
CN (1) CN101809397B (fr)
WO (1) WO2009009707A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107604536A (zh) * 2017-09-12 2018-01-19 曾林涛 一种蓬松弹性三维微纳米纤维材料的制备方法、装置以及由该方法制备的纤维材料及其应用

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107300315A (zh) * 2017-04-30 2017-10-27 田东昊润新材料科技有限公司 一种链排式恒温烘干机组
CN114808162B (zh) * 2022-04-28 2023-05-26 上海迅江科技有限公司 闪蒸纺丝/静电纺丝复合超细纳米纤维材料及其制备方法

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US4798007A (en) * 1987-05-28 1989-01-17 Eichenlaub John E Explosion-proof, pollution-free infrared dryer
WO2003080905A1 (fr) * 2002-03-26 2003-10-02 Nano Technics Co., Ltd. Dispositif de fabrication et procede de preparation de nanofibres par un processus de filage par « electro-soufflage »
US20040016143A1 (en) * 2002-07-29 2004-01-29 Cleary John C. Method and apparatus for heating nonwoven webs
US20050056956A1 (en) * 2003-09-16 2005-03-17 Biax Fiberfilm Corporation Process for forming micro-fiber cellulosic nonwoven webs from a cellulose solution by melt blown technology and the products made thereby
WO2005085730A2 (fr) * 2004-03-02 2005-09-15 Nv Bekaert Sa Installation de sechage infrarouge d'une bande en mouvement
WO2008060424A2 (fr) * 2006-11-09 2008-05-22 E. I. Du Pont De Nemours And Company Processus d'élimination de solvant
WO2008076412A1 (fr) * 2006-12-18 2008-06-26 E. I. Du Pont De Nemours And Company Procédé de nettoyage de solvant par infrarouge

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US4798007A (en) * 1987-05-28 1989-01-17 Eichenlaub John E Explosion-proof, pollution-free infrared dryer
WO2003080905A1 (fr) * 2002-03-26 2003-10-02 Nano Technics Co., Ltd. Dispositif de fabrication et procede de preparation de nanofibres par un processus de filage par « electro-soufflage »
US20040016143A1 (en) * 2002-07-29 2004-01-29 Cleary John C. Method and apparatus for heating nonwoven webs
US20050056956A1 (en) * 2003-09-16 2005-03-17 Biax Fiberfilm Corporation Process for forming micro-fiber cellulosic nonwoven webs from a cellulose solution by melt blown technology and the products made thereby
WO2005085730A2 (fr) * 2004-03-02 2005-09-15 Nv Bekaert Sa Installation de sechage infrarouge d'une bande en mouvement
WO2008060424A2 (fr) * 2006-11-09 2008-05-22 E. I. Du Pont De Nemours And Company Processus d'élimination de solvant
WO2008076412A1 (fr) * 2006-12-18 2008-06-26 E. I. Du Pont De Nemours And Company Procédé de nettoyage de solvant par infrarouge

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107604536A (zh) * 2017-09-12 2018-01-19 曾林涛 一种蓬松弹性三维微纳米纤维材料的制备方法、装置以及由该方法制备的纤维材料及其应用

Also Published As

Publication number Publication date
JP2010533248A (ja) 2010-10-21
CN101809397A (zh) 2010-08-18
CN101809397B (zh) 2013-11-13
EP2174084B1 (fr) 2014-03-19
KR20100047257A (ko) 2010-05-07
JP5377479B2 (ja) 2013-12-25
EP2174084A1 (fr) 2010-04-14

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