JPH0234972B2 - FUIBURITSU DONOSEIZOHOHO - Google Patents
FUIBURITSU DONOSEIZOHOHOInfo
- Publication number
- JPH0234972B2 JPH0234972B2 JP27465184A JP27465184A JPH0234972B2 JP H0234972 B2 JPH0234972 B2 JP H0234972B2 JP 27465184 A JP27465184 A JP 27465184A JP 27465184 A JP27465184 A JP 27465184A JP H0234972 B2 JPH0234972 B2 JP H0234972B2
- Authority
- JP
- Japan
- Prior art keywords
- precipitant
- polymer
- fibrid
- gas
- precipitation
- 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.)
- Expired - Lifetime
Links
- 229920000642 polymer Polymers 0.000 claims description 37
- 238000001556 precipitation Methods 0.000 claims description 29
- 239000000243 solution Substances 0.000 claims description 26
- 239000002904 solvent Substances 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 10
- 238000010008 shearing Methods 0.000 claims description 8
- 239000004760 aramid Substances 0.000 claims description 6
- 229920003235 aromatic polyamide Polymers 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 150000001408 amides Chemical class 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 230000001376 precipitating effect Effects 0.000 claims description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 14
- 239000007789 gas Substances 0.000 description 14
- 230000000704 physical effect Effects 0.000 description 12
- -1 precipitant Substances 0.000 description 9
- 239000004952 Polyamide Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 229920002647 polyamide Polymers 0.000 description 8
- 238000010586 diagram Methods 0.000 description 4
- 238000010292 electrical insulation Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920001059 synthetic polymer Polymers 0.000 description 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920006017 homo-polyamide Polymers 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 229910001867 inorganic solvent Inorganic materials 0.000 description 2
- 239000003049 inorganic solvent Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 2
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- XFDUHJPVQKIXHO-UHFFFAOYSA-N 3-aminobenzoic acid Chemical compound NC1=CC=CC(C(O)=O)=C1 XFDUHJPVQKIXHO-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 1
- JCQPONUUPNAEGZ-UHFFFAOYSA-N 4-aminobenzoyl chloride Chemical compound NC1=CC=C(C(Cl)=O)C=C1 JCQPONUUPNAEGZ-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 102000009123 Fibrin Human genes 0.000 description 1
- 108010073385 Fibrin Proteins 0.000 description 1
- BWGVNKXGVNDBDI-UHFFFAOYSA-N Fibrin monomer Chemical compound CNC(=O)CNC(=O)CN BWGVNKXGVNDBDI-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- 238000012695 Interfacial polymerization Methods 0.000 description 1
- GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 229960003375 aminomethylbenzoic acid Drugs 0.000 description 1
- QCTBMLYLENLHLA-UHFFFAOYSA-N aminomethylbenzoic acid Chemical compound NCC1=CC=C(C(O)=O)C=C1 QCTBMLYLENLHLA-UHFFFAOYSA-N 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 229950003499 fibrin Drugs 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- QZUPTXGVPYNUIT-UHFFFAOYSA-N isophthalamide Chemical compound NC(=O)C1=CC=CC(C(N)=O)=C1 QZUPTXGVPYNUIT-UHFFFAOYSA-N 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000003791 organic solvent mixture Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- CMDGQTVYVAKDNA-UHFFFAOYSA-N propane-1,2,3-triol;hydrate Chemical compound O.OCC(O)CO CMDGQTVYVAKDNA-UHFFFAOYSA-N 0.000 description 1
- 239000012783 reinforcing fiber Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Paper (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Artificial Filaments (AREA)
Description
【発明の詳細な説明】
産業上の利用分野
本発明は合成重合体からなるフイブリツドの製
造方法に関する。更に詳しくは、合成重合体の溶
液を、該重合体の非溶剤であり且つ該溶液中の溶
媒とは親和性を有する沈澱剤中に導入し、該溶液
に剪断作用を加えつつ重合体を沈澱させることに
よりフイブリツドを製造する方法の改良に関す
る。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method for producing fibrids made of synthetic polymers. More specifically, a solution of a synthetic polymer is introduced into a precipitant that is a non-solvent for the polymer and has an affinity for the solvent in the solution, and the polymer is precipitated while applying a shearing action to the solution. The present invention relates to improvements in the method of manufacturing fibrids by.
従来技術
合成重合体から「フイブリツド」とよばれるパ
ルプ状粒子を製造することは古くから知られてお
り、例えば、特公昭35−11851号公報、特公昭37
−5732号公報等には、沈澱剤を高速で撹拌し、こ
れに重合体溶液を導入して剪断作用(及び叩解作
用)を加えつつ重合体を沈澱させることにより、
フイブリツドを製造する方法が開示されている。Prior Art It has been known for a long time to produce pulp-like particles called "fibrids" from synthetic polymers.
-5732 publication etc., by stirring a precipitant at high speed, introducing a polymer solution into the precipitant, and precipitating the polymer while applying shearing action (and beating action),
A method of manufacturing a fibrid is disclosed.
また、かかる方法に従つてフイブリツドを製造
するに当り効率的に沈澱を行わせる装置として、
特公昭40−9044号公報や特開昭52−151621号公報
に記載の装置等が知られているが、これらの沈澱
装置でも剪断作用を与える手段として高速回転体
を用いており、該回転体により重合体溶液、沈澱
剤、沈澱物の混合系を強力に撹拌混合する必要が
あるため、フイブリツド製造に要する動力は非常
に大となる。 In addition, as an apparatus for efficiently performing precipitation when producing fibrids according to such a method,
Devices such as those described in Japanese Patent Publication No. 40-9044 and Japanese Patent Application Laid-Open No. 52-151621 are known, but these precipitation devices also use high-speed rotating bodies as means for applying shearing action, and the rotating bodies Because of this, it is necessary to vigorously stir and mix the mixture system of the polymer solution, precipitant, and precipitate, and therefore the power required to produce the fibrid is extremely large.
さらに、前述の方法並びに装置において、絶対
剪断速度と沈澱を生ずるため要する時間とによつ
てフイブリツドやそれを用いて抄造した紙状物の
物性が微妙に変化することが知られており、良好
なフイブリツドを得るにはこれらを適切な条件に
コントロールする必要があるが、実際にはこれら
の条件を常に適切な範囲に維持することは難し
く、また、これらの条件をいかに調整しても得ら
れるフイブリツドの大きさや品質のバラツキが小
さいものを製造することが難しい。さらに、この
ようにして製造したフイブリツドは、これを用い
て抄造した紙状シートの物性、とりわけ電気絶縁
性が必ずしも十分でないという問題もある。 Furthermore, in the above-mentioned method and apparatus, it is known that the physical properties of the fibrid and the paper-like material made using the same change slightly depending on the absolute shear rate and the time required to cause precipitation. In order to obtain fibrids, it is necessary to control these conditions to appropriate conditions, but in reality it is difficult to always maintain these conditions within an appropriate range, and no matter how you adjust these conditions, the fibrids that can be obtained It is difficult to manufacture products with small variations in size and quality. Furthermore, the fibrid produced in this manner has a problem in that the physical properties of the paper-like sheet made using the fibrid, particularly the electrical insulation properties, are not necessarily sufficient.
発明の目的
本発明の目的は、前述の如き従来のフイブリツ
ド製造方法における諸問題を解決し、フイブリツ
ド製造時における消費動力を大幅に低減するとと
もに、得られたフイブリツドの大きさが揃つてお
り、これを用いて抄造したとき良好な物性の紙状
シートを形成し得るようなフイブリツドを容易に
製造する方法を提供することにある。Purpose of the Invention The purpose of the present invention is to solve the various problems in the conventional fibrid manufacturing method as described above, to significantly reduce the power consumption during fibrin manufacturing, and to make the obtained fibrs uniform in size. It is an object of the present invention to provide a method for easily producing a fibrid which can form a paper-like sheet with good physical properties when paper-formed using the fibrid.
発明の構成
本発明者らは、前述の目的を達成すべく研究を
重ねた結果、重合体溶液と沈澱剤とを接触させて
沈澱させる系に一定量の気体を混在せしめること
によつて、フイブリツド製造時の消費動力が著し
く減少し、しかも得られるフイブリツドはバラツ
キの小さいものとなり、これを用いて抄造したシ
ートの物性も改善されることを見い出し、本発明
に到達したものである。Composition of the Invention As a result of repeated research to achieve the above-mentioned object, the present inventors have discovered that fibrils can be produced by mixing a certain amount of gas into a system in which a polymer solution and a precipitant are brought into contact with each other and precipitated. The present invention was achieved based on the discovery that power consumption during production is significantly reduced, the resulting fibrils have less variation, and the physical properties of sheets made using the same are improved.
すなわち、本発明は、重合体溶液を沈澱剤中に
導入し、該溶液に剪断作用を加えつつ重合体を沈
澱させることによりフイブリツドを製造する方法
において、沈澱系を気体と液体との混合相にする
ことを特徴とする方法である。 That is, the present invention provides a method for producing fibrids by introducing a polymer solution into a precipitant and precipitating the polymer while applying a shearing action to the solution, in which the precipitation system is changed to a mixed phase of gas and liquid. This method is characterized by:
本発明において使用する重合体は、適当な溶媒
に溶解し得る繊維形成性重合体であればどのよう
な重合体でもよいが、耐熱性が良好でありかつ良
好なフイブリツドを形成し易い芳香族ポリアミド
が特に好適である。かかる好適な芳香族ポリアミ
ドとしては、例えば次のものがあげられる。 The polymer used in the present invention may be any fiber-forming polymer that can be dissolved in an appropriate solvent, but aromatic polyamides that have good heat resistance and can easily form good fibrils are preferred. is particularly suitable. Examples of such suitable aromatic polyamides include the following.
(a) 芳香族環を有するジカルボン酸の好適には酸
ハライド等の高活性誘導体と芳香族環を有する
ジアミンとの縮合ポリアミド;例えば、ジカル
ボン酸として、イソフタル酸、テレフタル酸等
の一種又は二種以上と、ジアミンとしてメタフ
エニレンジアミン、パラフエニレンジアミン、
3,4′−又は4,4′−ジアミノジフエニルエー
テル、3,4′−又は4,4′−ジアミノジフエニ
ルメタン、キシリレンジアミン、N−メチルパ
ラフエニレンジアミン等の一種又は二種以上を
用い、両者を実質的に等モルで反応させて縮合
させたホモポリアミド又はコポリアミド;かか
る縮合ポリアミドのうち最も好適なものとして
はポリメタフエニレンイソフタルアミド又はメ
タフエニレンイソフタルアミドとメタフエニレ
ンテレフタルアミドとの共重合体があげられ
る。(a) A condensation polyamide of a dicarboxylic acid having an aromatic ring, preferably a highly active derivative such as an acid halide, and a diamine having an aromatic ring; For example, as the dicarboxylic acid, one or two kinds of isophthalic acid, terephthalic acid, etc. In addition to the above, diamines include metaphenylenediamine, paraphenylenediamine,
One or more of 3,4'- or 4,4'-diaminodiphenyl ether, 3,4'- or 4,4'-diaminodiphenylmethane, xylylene diamine, N-methyl paraphenylene diamine, etc. A homopolyamide or copolyamide obtained by reacting and condensing both in substantially equimolar amounts; Among such condensed polyamides, the most preferable one is polymetaphenylene isophthalamide or metaphenylene isophthalamide and metaphenylene. Examples include copolymers with terephthalamide.
(b) 芳香族環を有するアミノカルボン酸を好適に
は活性化して縮合したポリアミド;例えば、ア
ミノカルボン酸として、パラ又はメタ−アミノ
安息香酸、パラアミノメチル安息香酸等を使用
したホモポリアミド又は二種以上のアミノカル
ボン酸の共縮合により得たコポリアミド;かか
る縮合ポリアミドのうち好適なものとしてはポ
リ(パラアミノ安息香酸)があげられる。(b) A polyamide obtained by activating and condensing an aminocarboxylic acid having an aromatic ring; for example, a homopolyamide using para- or meta-aminobenzoic acid, para-aminomethylbenzoic acid, etc. as the aminocarboxylic acid, or two types thereof Copolyamide obtained by co-condensation of the above aminocarboxylic acids; preferred among such condensed polyamides is poly(para-aminobenzoic acid).
(c) 前記(a)(b)を共縮合したポリアミド;かかる共
縮合ポリアミドの好適なものとしては、例えば
メタフエニレンジアミン、イソフタル酸クロラ
イド、パラアミノ安息香酸クロライド塩酸塩の
三成分を縮合したコポリアミドがあげられる。(c) A polyamide obtained by co-condensing the above (a) and (b); Preferred examples of such co-condensing polyamides include polyamides obtained by condensing three components: metaphenylene diamine, isophthalic acid chloride, and para-aminobenzoic acid chloride hydrochloride. Examples include polyamide.
前述の重合体には、必要に応じ雲母粒子やその
他の無機物質の微粒子を含有させてもよい。 The above-mentioned polymer may contain mica particles or other inorganic substance fine particles, if necessary.
本発明において重合体を溶解して溶液とするた
めの溶媒は、該重合体を溶解し得るものであれば
特に制限されず、無機溶媒、有機溶媒の何れでも
よい。 In the present invention, the solvent for dissolving the polymer to form a solution is not particularly limited as long as it can dissolve the polymer, and may be either an inorganic solvent or an organic solvent.
重合体が芳香族ポリアミドの場合は、硫酸、ク
ロル硫酸、フロル硫酸、フツ化水素等の無機溶媒
あるいは、N−メチル−2−ピロリドン、
NN′−ジメチルホルムアミド、NN′−ジメチル
アセトアミド、ジメチルスルホキシド、テトラメ
チル尿素等の有機溶媒が用いられるが、ポリメタ
フエニレンイソフタルアミド系重合体の場合は、
N−メチル−2−ピロリドン又はNN′−ジメチ
ルアセトアミドの如き極性アミド系溶媒が特に好
適である。 When the polymer is an aromatic polyamide, an inorganic solvent such as sulfuric acid, chlorosulfuric acid, fluorosulfuric acid, hydrogen fluoride, or N-methyl-2-pyrrolidone,
Organic solvents such as NN'-dimethylformamide, NN'-dimethylacetamide, dimethyl sulfoxide, and tetramethylurea are used, but in the case of polymetaphenylene isophthalamide-based polymers,
Polar amide solvents such as N-methyl-2-pyrrolidone or NN'-dimethylacetamide are particularly preferred.
溶液中の重合体濃度は、重合体の種類、重合体
の重合度等によつても異なるが、一般に2〜15重
量%が好ましい。 The concentration of the polymer in the solution varies depending on the type of polymer, the degree of polymerization of the polymer, etc., but is generally preferably 2 to 15% by weight.
一方、沈澱剤としては、重合体溶液中の溶媒と
は親和性があるが重合体に対しては非溶媒である
液体が用いられる。 On the other hand, as the precipitant, a liquid is used that has an affinity for the solvent in the polymer solution but is a non-solvent for the polymer.
溶媒として有機溶媒を使用した場合に使用でき
る沈澱剤としては、水単独あるいは水−有機溶媒
混合液、グリセリン、エチレングリコール、グリ
セリン−水混合液、エーテル等でもよい。これら
の沈澱剤中には塩化カルシウム、塩化リチウム、
塩化マグネシウム等の無機塩を含んでもよい。 When an organic solvent is used as the solvent, the precipitant that can be used may be water alone, a water-organic solvent mixture, glycerin, ethylene glycol, a glycerin-water mixture, ether, or the like. These precipitants include calcium chloride, lithium chloride,
It may also contain an inorganic salt such as magnesium chloride.
なかでも、ポリメタフエニレンイソフタルアミ
ド系の芳香族ポリアミドをアミド系溶媒に溶解し
た重合体溶液に対する沈澱剤としては、該アミド
系溶媒を50重量%以下、特に10〜40重量%の割合
で含む水溶液が最適である。 Among these, as a precipitant for a polymer solution in which a polymetaphenylene isophthalamide-based aromatic polyamide is dissolved in an amide-based solvent, a precipitant containing the amide-based solvent in an amount of 50% by weight or less, particularly 10 to 40% by weight is used. Aqueous solutions are best.
フイブリツドの製造に際しては、沈澱剤を高速
で撹拌し、この沈澱剤中に導入した重合体溶液か
ら脱溶媒すると同時に強い剪断作用を与えるよう
な沈澱装置を用いることが必要である。かかる沈
澱装置としては、特開昭52−151621号公報記載の
如き特定形状のステーターとタービン翼型のロー
ターとを組合せた連続沈澱装置が特に好ましい。 When producing fibrids, it is necessary to use a precipitation device that stirs the precipitant at high speed, removes the solvent from the polymer solution introduced into the precipitant, and at the same time applies a strong shearing action. As such a precipitation device, a continuous precipitation device in which a stator of a specific shape and a turbine blade-shaped rotor are combined as described in JP-A-52-151621 is particularly preferred.
本発明では、前述の如く重合体溶液に沈澱剤を
作用させてフイブリツドを製造するに際し、沈澱
系を気体と液体との混合相(気−液混合相)とす
る。ここで用いる気体としては空気が経済的であ
るが、炭酸ガス等の他の気体でもよい。 In the present invention, when producing a fibrid by applying a precipitant to a polymer solution as described above, the precipitation system is a mixed phase of gas and liquid (vapor-liquid mixed phase). Air is economical as the gas used here, but other gases such as carbon dioxide may also be used.
沈澱系を気−液混合相とするには、予め沈澱剤
に気体を混合又は溶解したのち沈澱装置に導入し
てもよく、また、沈澱剤、重合体溶液と同時に気
体を沈澱装置に導入してもよい。また、導入の方
法は、圧縮ガスで導入してもよく、また、沈澱装
置を工夫して沈澱系に外部から気体(空気)を吸
引するようにしてもよく、更には沈澱剤中に気体
を溶解しておき沈澱時に気体が発生するようにし
てもよい。要は、沈澱系において液体と気体とが
混在すればよく、その手段や方法は任意である。 In order to make the precipitation system into a gas-liquid mixed phase, the gas may be mixed or dissolved in the precipitant in advance and then introduced into the precipitation apparatus, or the gas may be introduced into the precipitation apparatus at the same time as the precipitant and polymer solution. It's okay. In addition, the introduction method may be to use compressed gas, or the precipitation device may be devised to draw gas (air) into the precipitation system from the outside, or even gas may be introduced into the precipitation system. It is also possible to dissolve it and generate gas during precipitation. The point is that liquid and gas need only be mixed in the precipitation system, and any means or method can be used.
導入される気体の量は、沈澱剤に対し5〜100
量%程度がよく、10〜50容量%の範囲内が特に好
ましい。 The amount of gas introduced is 5 to 100% relative to the precipitant.
The amount is preferably about % by volume, and particularly preferably within the range of 10 to 50% by volume.
この際、特公昭40−9044号公報や特開昭52−
151621号公報に記載の如き型式の沈澱装置では、
ローターを例えば5000rpm以上のような高速で回
転させ、きわめて大きな剪断作用が加えられてい
る沈澱系中の気体を混在させるのが効果的であ
り、低速回転の場合には効果が小さい。 At this time, Japanese Patent Publication No. 40-9044 and JP-A-52-
In a precipitation device of the type described in Publication No. 151621,
It is effective to rotate the rotor at a high speed, such as 5000 rpm or higher, to mix in the gas in the precipitation system, which is subjected to a very large shearing action, and is less effective when the rotor is rotated at a low speed.
発明の効果
前述の如き本発明によれば、剪断作用を有する
系において重合体溶液を沈澱剤中に気体を導入分
散させることによりフイブリツドを製造する際、
沈澱時の所要動力が大幅に低下し、かつ大きさや
品質の揃つた良好なフイブリツドが得られ、該フ
イブリツドを用いて抄造した紙状シートの物性も
良好となる。Effects of the Invention According to the present invention as described above, when producing a fibrid by introducing and dispersing a polymer solution into a precipitant in a system having a shearing action,
The power required during precipitation is significantly reduced, good fibrids of uniform size and quality are obtained, and the physical properties of paper-like sheets made using the fibrs are also good.
このことは、気−液混合相では系の見掛粘度が
低下して系を高速で撹拌するための所要動力が低
下し、沈澱に要する時間が変るため、得られるフ
イブリツドの形状、大きさが変化して、フイブリ
ツドの大きさや品質のバラツキが減少し、また、
該フイブリツドを用いて抄造した紙状シートの物
性も向上するものと考えられる。 This means that in the gas-liquid mixed phase, the apparent viscosity of the system decreases, the power required to stir the system at high speed decreases, and the time required for precipitation changes, so the shape and size of the fibrids obtained will change. changes, reducing variations in fibrid size and quality, and
It is believed that the physical properties of paper-like sheets made using the fibrid are also improved.
したがつて、本発明により製造したフイブリツ
ドは、補強用繊維特に耐熱性の芳香族ポリアミド
繊維と混抄することにより強伸度、耐熱性、電気
絶縁性等の諸物性にすぐれた紙状シートとなる。 Therefore, the fibrids produced according to the present invention can be mixed with reinforcing fibers, particularly heat-resistant aromatic polyamide fibers, to form paper-like sheets with excellent physical properties such as strength and elongation, heat resistance, and electrical insulation properties. .
実施例
次に本発明の実施例及び比較例を詳述する。な
お、これらの例はいずれもポリメタフエニレンイ
ソフタルアミドのフイブリツドに関するものであ
るが、本発明はこれに限定されるものでないこと
は勿論である。Examples Next, examples and comparative examples of the present invention will be described in detail. Although these examples all relate to fibrils of polymetaphenylene isophthalamide, it goes without saying that the present invention is not limited thereto.
実施例 1
特公昭47−10863号公報に記載の界面重合法に
よりポリメタフエニレンイソフタルアミドを製造
した。このポリマーはN−メチル−2−ピロリド
ンに溶解して測定した固有粘度(I.V.)が1.35で
あり、ポリマー中に無機塩を全く含まないもので
あつた。このポリマーをN−メチル−2−ピロリ
ドンにポリマー濃度12.5重量%となるように溶解
し沈澱用のポリマー溶液とした。Example 1 Polymetaphenylene isophthalamide was produced by the interfacial polymerization method described in Japanese Patent Publication No. 47-10863. This polymer had an intrinsic viscosity (IV) of 1.35 when dissolved in N-methyl-2-pyrrolidone and was found to contain no inorganic salt at all. This polymer was dissolved in N-methyl-2-pyrrolidone to a polymer concentration of 12.5% by weight to obtain a polymer solution for precipitation.
一方、N−メチル−2−ピロリドンを濃度30重
量%となるように水に加えて水溶液をつくり、沈
澱剤とした。 On the other hand, N-methyl-2-pyrrolidone was added to water at a concentration of 30% by weight to prepare an aqueous solution, which was used as a precipitant.
このポリマー溶液及び沈澱剤を用い、特開昭52
−151621号公報に記載の沈澱装置(但し直径15mm
のもの)を用いて、同公報に記載の方法によりフ
イブリツドを製造した。 Using this polymer solution and precipitant,
- Precipitation device described in Publication No. 151621 (however, the diameter is 15 mm)
A fibrid was produced using the method described in the same publication.
この際、沈澱装置へ、ポリマー溶液60容量部に
対し上記N−メチル−2−ピロリドン水溶液を
1800容量部の割合で供給し、ローターの回転数を
10000rpmとしてフイブリツドを試作した。一方、
上記N−メチル−2−ピロリドン水溶液1800容量
部に対し200〜450容量部の割合で空気を混合して
供給し、同様の実験を行つた。 At this time, the above N-methyl-2-pyrrolidone aqueous solution was added to the precipitation apparatus for 60 parts by volume of the polymer solution.
Supply at a rate of 1800 parts by volume, and increase the number of rotations of the rotor.
A fibrid was prototyped with a speed of 10,000 rpm. on the other hand,
A similar experiment was conducted by mixing and supplying 200 to 450 parts by volume of air to 1800 parts by volume of the above N-methyl-2-pyrrolidone aqueous solution.
これらの実験における結果を第1図〜第3図に
示す。第1図は、沈澱装置における電動機の負荷
のデータを示すが、同図より明らかな如く、沈澱
剤中に空気を混合(導入しない場合は沈澱装置に
おける電動機の負荷が200A近くなるのに対し空
気を混合することによりこれが100A付近にまで
低下し、所要動力の大幅な節減が達成される。 The results of these experiments are shown in FIGS. 1-3. Figure 1 shows data on the load on the electric motor in the precipitation equipment. By mixing these, this can be reduced to around 100A, resulting in a significant reduction in power requirements.
また、第2図はフイブリツドの粘度分布の状態
を示すが、沈澱剤中に空気を混合したものは、24
メツシユ以上の大きな粒子の含有量が少なく、ま
た80メツシユ以下の小さな粒子の含有量も少なく
て、生成フイブリツド粒子における粒度のバラツ
キが小さいことが判る。 Also, Figure 2 shows the state of the viscosity distribution of fibrids.
It can be seen that the content of particles larger than 80 meshes is small, and the content of small particles smaller than 80 meshes is also small, indicating that the variation in particle size in the produced fibrillated particles is small.
第3図は、このフイブリツド60重量部と繊度2
デニール、カツト長4mmのポリメタフエニレンイ
ソフタルアミド繊維(登録商標「コーネツクス」)
40重量部とを混合抄紙し、圧力200Kg/cm2、温度
300℃で加圧加熱し、紙状シートとしたものの物
性を示すが、空気を混合して製造したフイブリツ
ドを用いて抄造したものは、いずれも電気絶縁性
(絶縁破壊電圧B.V.Dで示す)、強伸度等の諸物性
にすぐれていることを示している。 Figure 3 shows 60 parts by weight of this fibrid and a fineness of 2.
Polymetaphenylene isophthalamide fiber with denier and cut length of 4 mm (registered trademark "Konex")
40 parts by weight was mixed to make paper at a pressure of 200Kg/cm 2 and a temperature of
This shows the physical properties of a paper-like sheet made by heating under pressure at 300℃, but the paper made using a fibrid made by mixing air has electrical insulation properties (as indicated by dielectric breakdown voltage BVD) and strength. This shows that it has excellent physical properties such as elongation.
実施例 2
実施例1と同じポリマー溶液、沈澱剤を用い、
特開昭52−151621号公報記載の装置にポリマー溶
液60重量部、沈澱剤1800容量部及び空気180〜432
容量部を別々に導入した。なお、空気は前記装置
のポリマー溶液入口となつている位置から軸に向
つて180゜ずれた位置から導入した。Example 2 Using the same polymer solution and precipitant as in Example 1,
60 parts by weight of polymer solution, 1800 parts by volume of precipitant, and 180 to 432 parts by volume of air were added to the apparatus described in JP-A-52-151621.
Capacity parts were introduced separately. Note that air was introduced from a position deviated by 180° toward the axis from the position serving as the polymer solution inlet of the apparatus.
これらの実験の結果を第4図〜第6図に示す。
第4図は沈澱装置の所要動力を示し、第5図は得
られたフイブリツドの叩解度(水度)と150メ
ツシユ以下の小さな粒度のフイブリツドの含有割
合を示している。また、第6図は、このフイブリ
ツドを用いて実施例1と同様にポリメタフエニレ
ンイソフタルアミド繊維と混合抄紙した紙状シー
トの物性を示す。 The results of these experiments are shown in FIGS. 4-6.
FIG. 4 shows the power required for the precipitation apparatus, and FIG. 5 shows the freeness (water content) of the obtained fibrids and the content of fibrids with a small particle size of 150 mesh or less. Furthermore, FIG. 6 shows the physical properties of a paper-like sheet made by using this fibrid and mixing it with polymetaphenylene isophthalamide fiber in the same manner as in Example 1.
これらの図により、沈澱系中に空気を導入する
ことによつて、沈澱装置の所要動力が減少し、得
られたフイブリツドは小粒子のものの割合が低下
し、かつ叩解度(水度)が変つていないこと、
また、これから抄造した紙状シートは物性が良好
で、空気導入量の多いものは特に電気絶縁性にす
ぐれていることが明らかである。 These figures show that by introducing air into the precipitation system, the power required for the precipitation device is reduced, the proportion of small particles in the resulting fibrids is reduced, and the freeness (water content) is changed. Not having a good time,
It is also clear that the paper-like sheets made from this have good physical properties, and those with a large amount of air introduced have particularly excellent electrical insulation properties.
第1図〜第6図はそれぞれ本発明の効果を説明
するための線図であり、第1図と第4図は、それ
ぞれ沈澱剤への空気の混合量と沈澱装置における
電動機の負荷(電流)との関係を示す図、第2図
と第5図はそれぞれ沈澱剤への空気の混合量と得
られたフイブリツドの特性との関係を示す図、第
3図と第6図はそれぞれフイブリツド製造時の沈
澱剤への空気の混合量と該フイブリツドを用いて
抄紙した紙状シートの物性との関係を示す図であ
る。
Figures 1 to 6 are diagrams for explaining the effects of the present invention, and Figures 1 and 4 respectively show the amount of air mixed into the precipitant and the load (current ), Figures 2 and 5 are diagrams showing the relationship between the amount of air mixed into the precipitant and the characteristics of the fibrids obtained, and Figures 3 and 6 are diagrams showing the relationship between the amount of air mixed in the precipitant and the characteristics of the fibrids produced, respectively. FIG. 3 is a diagram showing the relationship between the amount of air mixed into the precipitant and the physical properties of a paper-like sheet made using the fibrid.
Claims (1)
作用を加えつつ重合体を沈澱させることによりフ
イブリツドを製造する方法において、沈澱系を気
体と液体との混合相にすることを特徴とするフイ
ブリツドの製造方法。 2 沈澱系における液体の沈澱剤と気体との混合
比率を、気体が液体の5〜100容量%となるよう
に調整する特許請求の範囲第1項記載のフイブリ
ツドの製造方法。 3 重合体溶液が芳香族ポリアミドのアミド系溶
媒溶液であり、沈澱剤が該アミド系溶媒の水溶液
であり、かつ気体が空気であることを特徴とする
特許請求の範囲第1項又は第2項記載のフイブリ
ツドの製造方法。[Claims] 1. A method for producing a fibrid by introducing a polymer solution into a precipitant and precipitating the polymer while applying a shearing action to the solution, in which the precipitation system is converted into a mixed phase of gas and liquid. A method for producing a fibrid, characterized by: 2. The method for producing a fibrid according to claim 1, wherein the mixing ratio of the liquid precipitant and gas in the precipitation system is adjusted so that the gas accounts for 5 to 100% by volume of the liquid. 3. Claims 1 or 2, wherein the polymer solution is an amide solvent solution of an aromatic polyamide, the precipitant is an aqueous solution of the amide solvent, and the gas is air. Method of manufacturing the described fibrids.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27465184A JPH0234972B2 (en) | 1984-12-28 | 1984-12-28 | FUIBURITSU DONOSEIZOHOHO |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27465184A JPH0234972B2 (en) | 1984-12-28 | 1984-12-28 | FUIBURITSU DONOSEIZOHOHO |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61157532A JPS61157532A (en) | 1986-07-17 |
JPH0234972B2 true JPH0234972B2 (en) | 1990-08-07 |
Family
ID=17544660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27465184A Expired - Lifetime JPH0234972B2 (en) | 1984-12-28 | 1984-12-28 | FUIBURITSU DONOSEIZOHOHO |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0234972B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103774268B (en) * | 2014-01-20 | 2016-05-11 | 江苏巨贤合成材料有限公司 | A kind of preparation method of polyamidoimide fibrid |
-
1984
- 1984-12-28 JP JP27465184A patent/JPH0234972B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS61157532A (en) | 1986-07-17 |
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