Classifications

• • 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
  • D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
  • D01F6/605—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides from aromatic polyamides
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J41/00—Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
  • B01J41/04—Processes using organic exchangers
  • B01J41/07—Processes using organic exchangers in the weakly basic form

Definitions

• isophthaloyl chloride (IC1) is condensed with m-phenylene diamine (MPD) in dimethylacetamide (DMAc) as solvent.
• Hydrogen chloride (HCl) is a by-product.
• the HCl is ordinarily neutralized with lime since it is highly corrosive.
• the salt which forms, calcium chloride, must ultimately be removed and disposed of. Presence of the salt in the solution limits the solubility of the MPD-I and hinders removal of the solvent during the spinning process. This all works against obtaining high solids MPD-I solutions which are desirable for spinning processes.
• the present invention provides a process for preparing poly(m-phenylene isophthalamide) filaments comprising: a) reacting m-phenylene diamine with isophthaloyl chloride in an amide solvent to produce poly(m-phenylene isophthalamide) in an HCl-containing amide solution; b) passing the polymer solution through a bed of ion exchange resin in base form to remove HCl and collecting an amide solution of the polymer as effluent; c) removing amide solvent from the effluent as necessary to attain suitable viscosity and concentration of the solution for spinning; and d) spinning the solution to form filaments.
• a substantially HCl-free, clear spinning solution consisting of at least 18% by weight of poly(m-phenylene isophthalamide) in dimethylacetamide.
• MPD-I is made by reacting MPD with ICl in an amide solvent such as DMAc.
• amide solvent such as DMAc.
• minor amounts, generally less than 10%, of p-phenylene diamine and/or terephthaloyl chloride may be included in the reaction mixture to form copoly ers with slightly different solubility, melting point, etc. provided their presence does not adversely interfere with the normal preparation of polymer and manufacture of filaments.
• Other amide solvents such as dimethylformamide (DMF) and N-methylpyrrolidone (NMP) may also be useful. Suitable conditions for reacting the diamine and diacyl chloride are well-known to those skilled in the art.
• the reaction produces a solution of MPD-I in the amide solvent.
• HCl formed as an undesirable byproduct.
• the HCl has been neutralized with lime to minimize corrosion.
• the high concentration of calcium chloride produced by the neutralization limits the solubility of the polymer and hinders removal of the solvent during the spinning process.
• HCl is removed by passing the as-produced solution of the polymerization through a bed of basic ion exchange resin. It may be desirable to first add more amide solvent to the solution to reduce viscosity before contact with the ion exchange resin, so that it can pass through the ion exchange column more efficiently.
• Useful ion exchange resins for this purpose are commercially available. They react with strong mineral acids to form amine salts of the acid. Preferably the resin is weakly basic.
• One such resin having tertiary amine functional groups is Amberlyst® A-21 available from Rohm and Haas Company of Philadelphia, Pennsylvania.
• the concentration and viscosity of the HCl-free effluent from the ion exchanger is normally adjusted as desired for preparing a spin dope.
• the extruded filaments pass directly into an aqueous quench coagulation bath and the solvent depleted filaments are extraction-drawn as before.
• the solution resulting from the polymerization may be divided and a major portion thereof processed as described above to remove HCl and the remainder combined with the HCl-free solution.
• the combined solution can be neutralized with lime and a spin dope prepared by adjusting solvent content to attain suitable viscosity and concentration for spinning. Since the combined solution contains a relatively small amount of HCl, most having been removed upon passage through the ion exchange resin column, only a small amount of lime will be needed to effect neutralization. Similarly, the small amount of calcium chloride which is formed will interfere less with solvent removal in the spinning process and will present less. of a disposal problem.
• Still another procedure that is useful employs the polymer-forming reactants in less than equivalent proportions. For example, a stoichiometric excess of diamine will produce low molecular weight polymer having an excess of amine ends. Because of the low molecular weight of the polymer, the solution viscosity will be low and it can be passed through the ion exchange column very efficiently. The effluent can then be combined with additional ICl to form high molecular weight polymer in a solution that contains less HCl than it would have, had equivalent quantities of MPD and ICl been used initially. The solution containing a reduced amount of HCl can then be processed as described above.
• a jacketed flask, with an inlet port on the top and an outlet port on the bottom, which is approximately 10.2 cm in diameter and 30 cm in height is filled to a height of 21 cm with weakly basic A-21 ion exchange resin.
• the resin is conditioned by pumping the following solutions through ion exchange resin: two bed volumes of 1.5 N aqueous sodium hydroxide followed by a water wash until the effluent is neutral, and then two bed volumes of 2 N HCl, followed by water rinsing until the effluent is neutral.
• the resin in the column is treated with two bed volumes of 1.5 N aqueous sodium hydroxide and rinsed with water until the column effluent is neutral. Water is removed from the column by rinsing the resin with 5 bed volumes of anhydrous DMAc.
• SUBSTITUTE SHEET (RULE 26 ⁇ ICl with MPD in DMAc. This flask serves as the reservoir for the acid polymer.
• the jacketed flask containing polymer and the jacketed flask containing the resin are heated using a circulation water bath of 70"C.
• the polymer solution is stirred and pumped into the top port of the resin containing flask at a rate of approximately 14 g/min.
• the eluent of the flask containing resin is collected at the outlet port of the flask and tested periodically for polymer (by sampling and testing for polymer via precipitation) . Once polymer is detected, the effluent is collected in a separate container. Polymer is collected until very little polymer is detected in the effluent.
• the collected material is a solution of poly(m-phenylene isophthalamide) in DMAc. Some dilution of the polymer with DMAc occurs so that the final solids content of the acid free polymer solution is approximately 5% MPD-I in DMAc.
• Polymer effluent from Example 1 is concentrated via vacuum distillation of DMAc as follows:
• a salt-free solution consisting of 24% MPD-I in DMAc was extruded through a 50 hole, 5 mil per hole, spinneret submerged in a coagulation medium.
• the coagulating medium consisted of DMAc/CaCl 2 /Water in a
• the coagulation medium was contained in an 8' long bath.
• the jet velocity of the spinning solution through the spinneret was 13.6 FPM (ft/min) , with a wind-up speed of 40 FPM.

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• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Textile Engineering (AREA)
• Organic Chemistry (AREA)
• Artificial Filaments (AREA)
• Polyamides (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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• 1993
  • 1993-03-29 US US08/039,564 patent/US5340519A/en not_active Expired - Lifetime
• 1994
  • 1994-03-28 JP JP52216894A patent/JP3299757B2/ja not_active Expired - Fee Related
  • 1994-03-28 CA CA002159181A patent/CA2159181C/en not_active Expired - Fee Related
  • 1994-03-28 SG SG1996008242A patent/SG43318A1/en unknown
  • 1994-03-28 DE DE69428591T patent/DE69428591T2/de not_active Expired - Fee Related
  • 1994-03-28 EP EP94912845A patent/EP0692038B1/en not_active Expired - Lifetime
  • 1994-03-28 RU RU95118153A patent/RU2114940C1/ru active
  • 1994-03-28 AU AU65233/94A patent/AU677053B2/en not_active Ceased
  • 1994-03-28 UA UA95094342A patent/UA35613C2/uk unknown
  • 1994-03-28 BR BR9406502A patent/BR9406502A/pt not_active IP Right Cessation
  • 1994-03-28 ES ES94912845T patent/ES2164101T3/es not_active Expired - Lifetime
  • 1994-03-28 WO PCT/US1994/003145 patent/WO1994023099A1/en not_active Ceased
  • 1994-04-06 TW TW083102981A patent/TW272998B/zh active

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Non-Patent Citations (2)

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