JPS6410521B2 - - Google Patents
Info
- Publication number
- JPS6410521B2 JPS6410521B2 JP16663980A JP16663980A JPS6410521B2 JP S6410521 B2 JPS6410521 B2 JP S6410521B2 JP 16663980 A JP16663980 A JP 16663980A JP 16663980 A JP16663980 A JP 16663980A JP S6410521 B2 JPS6410521 B2 JP S6410521B2
- Authority
- JP
- Japan
- Prior art keywords
- cellulose
- amount
- cellulose derivative
- acetic acid
- dmso
- 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
Links
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 59
- 229920002678 cellulose Polymers 0.000 claims description 58
- 239000001913 cellulose Substances 0.000 claims description 58
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 57
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 13
- 239000001632 sodium acetate Substances 0.000 claims description 13
- 235000017281 sodium acetate Nutrition 0.000 claims description 13
- 238000010521 absorption reaction Methods 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- -1 methylenedioxy chain Chemical group 0.000 claims description 6
- 125000003132 pyranosyl group Chemical group 0.000 claims description 6
- 229930040373 Paraformaldehyde Natural products 0.000 claims description 4
- 229920002866 paraformaldehyde Polymers 0.000 claims description 4
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
- BPGDAMSIGCZZLK-UHFFFAOYSA-N acetyloxymethyl acetate Chemical compound CC(=O)OCOC(C)=O BPGDAMSIGCZZLK-UHFFFAOYSA-N 0.000 claims description 3
- 230000001747 exhibiting effect Effects 0.000 claims description 2
- 239000002798 polar solvent Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 description 17
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 10
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 10
- 238000006116 polymerization reaction Methods 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 238000000862 absorption spectrum Methods 0.000 description 9
- 239000012046 mixed solvent Substances 0.000 description 9
- 239000000376 reactant Substances 0.000 description 9
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 229920002301 cellulose acetate Polymers 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 229910015900 BF3 Inorganic materials 0.000 description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229940113088 dimethylacetamide Drugs 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 229920000875 Dissolving pulp Polymers 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000007809 chemical reaction catalyst Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 description 1
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012345 acetylating agent Substances 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- IHPHPGLJYCDONF-UHFFFAOYSA-N n-propylacetamide Chemical compound CCCNC(C)=O IHPHPGLJYCDONF-UHFFFAOYSA-N 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Polysaccharides And Polysaccharide Derivatives (AREA)
Description
本発明は、メチロール化セルロースにメチレン
ジアセテートまたはエチレンジアセテートを作用
させて得られる新規なセルロース誘導体に関す
る。
従来、セルロースの繊維、フイルムなどの成形
品を工業的に得る方法としては、セルロースを銅
アンモニア液に溶解するか、またはザンテート化
して溶液となし、これを、酸を用いて凝固、再生
することによつて行なわれている。しかし、これ
らの工業的方法は大量の水消費、重金属の回収の
必要性、エネルギー多消費など多くの改善を要す
る点を含んでいる。
近年、かかる欠点を解消するために、工程のク
ローズド化を目的として、セルロースを新しい有
機溶媒に溶解し、得られたドープを直接紡糸・成
形する方法が提案されている。近年注目を集めて
いる、N−メチルモルホリンN−オキシド系をは
じめ、ジメチルスルホキシド(以下、DMSOと
略記する)/パラホルムアルデヒド(以下、
PFAと略記する)系に於いても、実際の応用に
際し、溶媒は二成分以上を併用することが必要で
あり、従つて、溶媒を回収して再利用する方法が
煩雑になる等、作業性と溶媒回収性に致命的欠点
があることが判明している。これらの欠点に加え
て、特にDMSO/PFA系を用いる場合には、セ
ルロース成形品の製造過程および溶媒回収工程で
DMSOの熱分解と言う問題を生じ易い。
他方、セルロース誘導体は、特定溶媒との組合
せで液晶を形成し、これから得られる成形品は、
機械的特性の大幅な改良が期待されている。
本発明者等は、上記した様な従来技術の欠点や
新たな可能性について総合的に検討した結果、単
独溶媒に可溶で、しかも特定溶媒との組合せによ
り光学的異方性を与える新規なセルロース誘導体
を見い出し本発明に到達した。すなわち、本発明
の目的は、単独溶媒に可溶なため回収が容易であ
り、しかも、成形性の優れたドープを与える新規
なセルロース誘導体を提供するにある。
本発明に係る新規なセルロース誘導体は、セル
ロースをメチロール化セルロースの形態で
DMSO/PFA混合溶媒に溶解し、しかる後、メ
チレンジアセテート(以下、MDAと略記する)
またはエチレンジアセテート(以下、EDAと略
記する)と反応せしめることによつて得られ、一
つの高分子鎖中の数平均ピラノーズ環数が100以
上で、且つ、ピラノーズ環中にメチレンジオキシ
連鎖を有し、その末端が結合酢酸量に換算して
8.4〜42%の割合でアセチル基で置換され、溶液
状態で260nm〜280nmに紫外吸収をもつことを特
徴とする。
これまで、セルロースをDMSO/PFA混合溶
媒に溶解し、これに反応剤を作用して新規な誘導
体を得ようとする試みは、いく例か知られてい
る。セルロースのヒドロキシエチル化もその一例
である。また、上記セルロース溶液系に、酢酸、
無水酢酸、酢酸クロリドを作用して新規物質を得
る試みもアール・ビー・セイモア(ジヤーナル・
オブ・ポリマー・サイエンス、11、(1978))等に
よつて報告されている。彼等の指摘によると、一
般にセルロースを不均一系でアセチル化し得る反
応剤の内、無水酢酸だけが、DMSO/PFA混合
溶媒に溶解したセルロースと反応し、得られる誘
導体の特徴として340nm付近に紫外吸収を示すと
している。更に、彼等は、DMSOやPFAの存在
が、セルロースに対する各反応剤に対し、それぞ
れに個有の影響を及ぼし、従来、不均一系で知ら
れていた各種反応剤とセルロースとの反応からは
予測され得ない誘導体を与えることも示唆してい
る。
本発明者等もDMSO/PFA混合溶媒に溶解し
たセルロースとアセチル化剤との反応について検
討を重ねた結果、アール・ビー・セイモア等の指
摘に反してMDAまたはEDAを反応剤としてセル
ロースと反応せしめた結果、驚くべきことに、溶
液状態で260nm〜280nmに紫外吸収をもつ新規な
セルロース誘導体を合成することに成功したので
ある。
本発明に使用されるセルロース原料は、綿、木
材等の天然セルロース(リグニン等の不純物を含
んでよい。)であつても、また、再生セルロース
であつてもよい。リグニン等の不純分を含む天然
セルロースは、これをDMSO/PFA混合溶媒で
溶解する時、不純部分は不溶性のため容易に別
できる。原料の重合度(この明細書において、
「重合度」とは、一つの高分子鎖中の数平均ピラ
ノーズ環数を指す。)は目的に応じて調整でき、
通常少なくとも100以上有れば充分である。また、
生成物の機械的特性の向上を計るために重合度
1000以上のものも使用できる。
セルロースをDMSO/PFA混合溶媒に溶解す
る場合、溶液中のセルロース濃度は、その重合度
にも依るが、2〜10重量%とすることが好まし
い。加えるパラホルムアルデヒドの量は溶解すべ
きセルロースのグルコース残基当り3〜5モルで
充分である。溶解温度は70℃〜90℃が望ましい。
過激な加熱は、DMSOの分解を惹起し、工業化
に於いての致命的欠点となるので避けるべきであ
る。一度溶解したセルロース溶液から過剰のパラ
ホルムアルデヒドを除去することも場合によつて
は、後の反応工程や溶媒回収工程で有利となる。
反応剤として使用するMDA、EDAの量は、得
るべき最終生成物の性質、特に置換度によつて適
宜選択できる。例えば、結合酢酸量8.4〜30%に
おいて、水やジメチルホルムアミド、ジメチルア
セトアミド(以下、DMACと略記する)、ホルム
アミド(以下、FAと略記する)等の極性溶媒に
可溶な誘導体を得たい場合には、セルロースのグ
ルコース残基当り3〜40モルの反応剤が必要であ
る。より高い結合酢酸量のものを得たい場合に
は、40モル以上の反応剤を加えればよい。一般
に、MDA、EDAはともに、DMSO/PFA混合
溶媒に溶解したセルロースの非溶媒となるため、
過剰に使用するとセルロースの沈殿をひき起こす
ので好ましくない。例えば、3重量%のセルロー
ス溶液に対して許容できるMDAの量は、溶媒
DMSOの2倍の体積までである。ちなみにこの
場合、MDAの量は、セルロースに対して約90モ
ルである。この場合、他の反応条件を変動して
も、得られる誘導体の最大結合酢酸量は42%前後
である。
一方、MDAまたはEDAとの反応において、触
媒の選択は重要であり、触媒としては酢酸ソーダ
が最適である。その他の触媒、例レばピリジン、
塩化アルミニウム、三弗化ほう素エーテル錯体な
どを用いた場合、および触媒を使用しない場合
は、全く反応しないか、または殆んど反応を促進
する効果がない。加えるべき酢酸ソーダ触媒の量
は、数ppm〜数千ppmの間で適宜選択できる。こ
こで重要な点は、触媒量の相異によつて、得られ
る生成物の同一溶媒に対する溶解域が結合酢酸量
に依存して変動することである。例えば、水に対
する溶解域を比較した場合、酢酸ソーダ使用量が
100ppmであるとき、水溶性を示す結合酢酸量の
下限が8.4%であるのに対し、酢酸ソーダ使用量
を250ppmとするとき、水溶性を示す結合酢酸量
の下限は18%である。この理由は明らかではない
が、酢酸ソーダによるホルムアルデヒドのセルロ
ースに対する反応性が変化することも一因と考え
られる。しかしながら、いずれの場合にも、得ら
れた生成物の水溶液は、264nm付近に紫外吸収を
示し、アール・ビー・セイモア等の得た物質とは
明らかに異なるものである。本発明にて得られる
セルロース誘導体は、ピラノーズ環中にメチレン
ジオキシ連鎖を有し、その末端にアセチル基が置
換している。なお、反応温度は90〜100℃が好ま
しい。
本発明のセルロース誘導体の置換度は、一義的
に決定できないため、結合酢酸量で代用する。結
合酢酸量とは、一定重量の生成物を苛性ソーダに
て処理した際、遊離してくる酢酸(酢酸ソーダと
して遊離)量の元のセルロース誘導体量に対する
重量%である。本明細書に於ける結合酢酸量は
ASTMD−68Tに準じて得た値である。
本発明のセルロース誘導体は、その結合酢酸量
にもよるが、概して、水、ジメチルホルムアミ
ド、ホルムアミド、N−メチルホルムアミド、N
−プロピルアセトアミド等のアミド系溶媒、
DMSOその他のスルホキシド系溶媒や、ピリジ
ン、ギ酸、アセトン、水/アセトン混合溶媒等に
容易に溶解する。これらから得られるドープは、
成形用ドープとして利用できる。例えば、水を溶
媒に用いて得られる溶液を乾式紡糸すれば、無公
害でかつ溶媒回収を要しない繊維の製造が可能で
ある。また、例えば、ホルムアミドに溶解すれ
ば、ポリマー濃度約30重量%で光学的異方性を示
すドープを形成でき、このドープより機械的特性
の優れた成形品を得ることができる。
本発明に係るセルロース誘導体の第1の特徴
は、セルロースをDMSO/PFA混合溶媒に溶解
し、これをMDA、EDAと反応させて得られたも
のであり、出発セルロースとして重合度の高いも
のを用いれば、それに応じて高重合度のものとな
る。従つて、このセルロース誘導体を原料として
成形すれば機械特性の優れた成形品が得られる。
本発明のセルロース誘導体の第2の特徴は、メチ
レンジオキシ連鎖を分子中に含んでいるため、酸
等を添加して熱処理することによつて簡単に成形
品の性質を変化させ得ることである。本発明のセ
ルロース誘導体の第3の特徴は、低結合酢酸量
域、例えば、8.4〜27%において強力な界面活性
を有し、エマルジヨン安定化剤等の分野に展開が
可能になること等である。
以下、実施例について本発明を説明する。
実施例 1
2種のセルロース(重合度=300および1000)
をそれぞれ60℃で7時間真空乾燥し、3g採取し、
DMSO100ml、PFA3gと混合し、80℃の温度下で
撹拌し、5時間で均一なセルロース溶液を得た。
次いで、余剰のPFAを80℃にて系外に排気した。
この溶液に3.75mgの酢酸ソーダを添加して溶解
し、次いで15mlのMDAを加え、90℃で10時間反
応させた後、500mlのメタノール中に沈殿させて
ポリマー成分を回収し、乾燥した。得られた合成
物は水に可溶であり、UVで264〜268nmに特異
な吸収を示した。結合酢酸量は22.0%であつた。
この生成物はまた有機溶媒に例えば、ギ酸、ホル
ムアミド、ジメチルスルホキシド、ジメチルアセ
トアミド、N−メチルピロリドン、γ−ブチロラ
クタム等に溶解した。
MDAの使用量を種々変えて、上述の方法を繰
返した。得られたセルロース誘導体の水溶性の範
囲を下記表−1に結合酢酸量で示した。
The present invention relates to a novel cellulose derivative obtained by reacting methylolated cellulose with methylene diacetate or ethylene diacetate. Traditionally, the industrial method for producing molded products such as cellulose fibers and films involves dissolving cellulose in a cupric ammonia solution or xanthating it to form a solution, which is then coagulated and regenerated using an acid. It is carried out by. However, these industrial methods include many points that require improvement, such as large amounts of water consumption, the need to recover heavy metals, and high energy consumption. In recent years, in order to eliminate such drawbacks, a method has been proposed in which cellulose is dissolved in a new organic solvent and the resulting dope is directly spun and shaped, with the aim of closing the process. In addition to N-methylmorpholine N-oxide, which has attracted attention in recent years, dimethyl sulfoxide (hereinafter abbreviated as DMSO)/paraformaldehyde (hereinafter abbreviated as DMSO)
In the case of PFA (abbreviated as PFA) system, it is necessary to use two or more solvents in combination in actual application, which makes the method of recovering and reusing the solvent complicated, etc. It has been found that there is a fatal drawback in solvent recovery. In addition to these drawbacks, especially when using the DMSO/PFA system, there are
It is easy to cause the problem of thermal decomposition of DMSO. On the other hand, cellulose derivatives form liquid crystals in combination with specific solvents, and the molded products obtained from them are
Significant improvements in mechanical properties are expected. As a result of comprehensively examining the shortcomings of the prior art and new possibilities as described above, the present inventors have developed a new method that is soluble in a single solvent and that provides optical anisotropy when combined with a specific solvent. The present invention was achieved by discovering a cellulose derivative. That is, an object of the present invention is to provide a novel cellulose derivative which is easy to recover because it is soluble in a single solvent and which provides a dope with excellent moldability. The novel cellulose derivative according to the present invention comprises cellulose in the form of methylolated cellulose.
Dissolve in DMSO/PFA mixed solvent, then methylene diacetate (hereinafter abbreviated as MDA)
Or obtained by reacting with ethylene diacetate (hereinafter abbreviated as EDA), the number average number of pyranose rings in one polymer chain is 100 or more, and a methylenedioxy chain is present in the pyranose ring. The terminus is converted into the amount of bound acetic acid.
It is characterized by being substituted with acetyl groups at a ratio of 8.4 to 42% and having ultraviolet absorption in the range of 260 nm to 280 nm in a solution state. Up to now, several attempts have been made to dissolve cellulose in a DMSO/PFA mixed solvent and react with a reactant to obtain new derivatives. Hydroxyethylation of cellulose is one example. In addition, acetic acid,
Attempts to obtain new substances using acetic anhydride and acetic chloride were also made by R.B. Seymour (Journal).
of Polymer Science, 11 , (1978)). According to their point, among the reagents that can generally acetylate cellulose in a heterogeneous system, only acetic anhydride reacts with cellulose dissolved in a DMSO/PFA mixed solvent, and the resulting derivative is characterized by an ultraviolet wavelength around 340 nm. It is said to indicate absorption. Furthermore, they found that the presence of DMSO and PFA had a unique effect on each reactant for cellulose, and that the reactions between various reactants and cellulose, which were previously known to be heterogeneous, were It has also been suggested that it gives derivatives that could not be predicted. The present inventors also conducted repeated studies on the reaction between cellulose dissolved in a DMSO/PFA mixed solvent and an acetylating agent, and found that, contrary to the suggestions of R.B. Seymour et al., MDA or EDA was used as a reactant to react with cellulose. As a result, they surprisingly succeeded in synthesizing a new cellulose derivative that has ultraviolet absorption in the wavelength range of 260 nm to 280 nm in a solution state. The cellulose raw material used in the present invention may be natural cellulose such as cotton or wood (which may contain impurities such as lignin), or may be regenerated cellulose. Natural cellulose containing impurities such as lignin can be easily separated when dissolved in a DMSO/PFA mixed solvent because the impurities are insoluble. The degree of polymerization of the raw material (in this specification,
"Degree of polymerization" refers to the number average number of pyranose rings in one polymer chain. ) can be adjusted according to the purpose,
Usually, it is sufficient to have at least 100. Also,
The degree of polymerization is determined to improve the mechanical properties of the product.
You can also use more than 1000. When cellulose is dissolved in a DMSO/PFA mixed solvent, the concentration of cellulose in the solution is preferably 2 to 10% by weight, although it depends on its degree of polymerization. A sufficient amount of paraformaldehyde to be added is 3 to 5 moles per glucose residue of cellulose to be dissolved. The melting temperature is preferably 70°C to 90°C.
Extreme heating should be avoided as it causes decomposition of DMSO, which is a fatal drawback in industrialization. In some cases, it may be advantageous to remove excess paraformaldehyde from the cellulose solution once dissolved in subsequent reaction steps or solvent recovery steps. The amounts of MDA and EDA used as reactants can be appropriately selected depending on the properties of the final product to be obtained, especially the degree of substitution. For example, when you want to obtain a derivative that is soluble in polar solvents such as water, dimethylformamide, dimethylacetamide (hereinafter abbreviated as DMAC), and formamide (hereinafter abbreviated as FA) when the amount of bound acetic acid is 8.4 to 30%. requires 3 to 40 moles of reactant per glucose residue of cellulose. If it is desired to obtain a product with a higher amount of bound acetic acid, 40 moles or more of the reactant may be added. In general, both MDA and EDA serve as non-solvents for cellulose dissolved in a DMSO/PFA mixed solvent, so
Excessive use causes cellulose precipitation, which is not preferable. For example, the amount of MDA acceptable for a 3% by weight cellulose solution is
Up to twice the volume of DMSO. Incidentally, in this case, the amount of MDA is approximately 90 moles relative to cellulose. In this case, even if other reaction conditions are varied, the maximum amount of acetic acid bound in the resulting derivative is around 42%. On the other hand, in the reaction with MDA or EDA, the selection of catalyst is important, and sodium acetate is the most suitable catalyst. Other catalysts, such as pyridine,
When aluminum chloride, boron trifluoride ether complex, etc. are used, or when no catalyst is used, no reaction occurs or there is almost no effect of promoting the reaction. The amount of the sodium acetate catalyst to be added can be appropriately selected from several ppm to several thousand ppm. The important point here is that due to differences in the amount of catalyst, the solubility range of the resulting product in the same solvent varies depending on the amount of bound acetic acid. For example, when comparing the solubility range in water, the amount of sodium acetate used is
When the amount is 100 ppm, the lower limit of the amount of bound acetic acid that shows water solubility is 8.4%, whereas when the amount of sodium acetate used is 250 ppm, the lower limit of the amount of bound acetic acid that shows water solubility is 18%. The reason for this is not clear, but it is thought that one factor is that sodium acetate changes the reactivity of formaldehyde to cellulose. However, in any case, the aqueous solution of the product obtained exhibits ultraviolet absorption around 264 nm, and is clearly different from the material obtained by R.B. Seymour et al. The cellulose derivative obtained in the present invention has a methylenedioxy chain in the pyranose ring, and an acetyl group is substituted at the end of the methylene dioxy chain. Note that the reaction temperature is preferably 90 to 100°C. Since the degree of substitution of the cellulose derivative of the present invention cannot be uniquely determined, the amount of bound acetic acid is used as a substitute. The amount of bound acetic acid is the weight % of the amount of acetic acid (liberated as sodium acetate) liberated when a given weight of the product is treated with caustic soda relative to the amount of the original cellulose derivative. The amount of bound acetic acid in this specification is
This is a value obtained according to ASTMD-68T. The cellulose derivative of the present invention generally contains water, dimethylformamide, formamide, N-methylformamide, and N-methylformamide, although it depends on the amount of bound acetic acid.
- Amide solvents such as propylacetamide,
Easily soluble in DMSO and other sulfoxide solvents, pyridine, formic acid, acetone, water/acetone mixed solvents, etc. The dope obtained from these is
Can be used as a molding dope. For example, by dry spinning a solution obtained using water as a solvent, it is possible to produce fibers that are pollution-free and do not require solvent recovery. For example, when dissolved in formamide, a dope exhibiting optical anisotropy at a polymer concentration of about 30% by weight can be formed, and a molded article with excellent mechanical properties can be obtained from this dope. The first feature of the cellulose derivative according to the present invention is that it is obtained by dissolving cellulose in a DMSO/PFA mixed solvent and reacting this with MDA and EDA, and a cellulose with a high degree of polymerization is used as the starting cellulose. If so, the degree of polymerization will be correspondingly high. Therefore, by molding this cellulose derivative as a raw material, a molded article with excellent mechanical properties can be obtained.
The second feature of the cellulose derivative of the present invention is that since it contains a methylenedioxy chain in its molecule, the properties of the molded product can be easily changed by adding an acid or the like and heat treating it. . The third feature of the cellulose derivative of the present invention is that it has strong surface activity in a low bound acetic acid content range, for example, 8.4 to 27%, and can be applied to fields such as emulsion stabilizers. . Hereinafter, the present invention will be explained with reference to examples. Example 1 Two types of cellulose (degree of polymerization = 300 and 1000)
Each was vacuum dried at 60℃ for 7 hours, and 3g was collected.
The mixture was mixed with 100 ml of DMSO and 3 g of PFA, and stirred at a temperature of 80°C to obtain a homogeneous cellulose solution in 5 hours.
Then, excess PFA was exhausted out of the system at 80°C.
To this solution, 3.75 mg of sodium acetate was added and dissolved, and then 15 ml of MDA was added and reacted at 90° C. for 10 hours. The polymer component was recovered by precipitation in 500 ml of methanol and dried. The resulting compound was soluble in water and exhibited specific absorption in the UV wavelength range of 264-268 nm. The amount of bound acetic acid was 22.0%.
This product was also dissolved in organic solvents such as formic acid, formamide, dimethylsulfoxide, dimethylacetamide, N-methylpyrrolidone, γ-butyrolactam, and the like. The above method was repeated using various amounts of MDA. The range of water solubility of the obtained cellulose derivative is shown in Table 1 below in terms of the amount of bound acetic acid.
【表】【table】
【表】
表中、無は不溶、有は溶解することを示す。No.
6の誘導体はアセトンおよびホルムアミドに溶解
した。
実施例 2
実施例1で得たセルロース溶液100mlに3.0mgの
酢酸ソーダを加えて溶解し、15mlのEDAを100℃
で12時間反応させた。この反応物を500mlのメタ
ノール中で沈殿させて、ポリマー成分を回収し
て、乾燥した。得られた合成物は水溶性を示し、
そのUVは268nmに吸収ピークを示した。そのIR
図は実施例1で得たものと殆ど同じであつた。ま
た、この誘導体はギ酸、ホルムアミド、ジメチル
スルホオキシド、ジメチルアセトアミド、γ−ブ
チラクトム、N−メチルピロリドン等の有機溶媒
にも可溶であつた。
実施例 3
実施例1で調製したセルロース溶液100mlに
MDAの反応触媒として、酢酸ソーダに代えて三
フツ化ホウ素エーテル錯塩、塩化アルミニウムお
よびピリジンを別々に使用した。
まず、三フツ化ホウ素エーテル錯塩を0.05mlか
ら0.5mlまでの範囲において添加量を種々変化さ
せて、MDAを15ml加えて室温にて3〜5時間反
応させた。500mlのメタノールで沈殿させて、ポ
リマー成分を回収し、生成物の溶解性を検討した
が、実施例1で示したような溶媒には溶解しなか
つた。また、そのIRスペクトルもエステル基特
有の吸収を示さなかつた。
塩化アルミニウムおよびピリジンも同様に
0.01gから0.1gまでの範囲において添加量を種々
変化させて、MDAを15ml加えて、室温下に3〜
5時間反応させた。結果は、三フツ化ホウ素エー
テル錯塩の場合と同様に、反応物は実施例1で示
したような溶媒には溶解しなかつた。
反応剤としてMDAに代えてEDAを使用した場
合も、反応触媒として有効であつたのは酢酸ソー
ダのみであつて、三フツ化ホウ素エーテル錯塩、
塩化アルミニウムおよびピリジンは触媒として有
効でなかつた。
実施例 4
実施例1で調製したセルロース溶液100mlに、
添加量を変えて(1.5mgと3.75mg)酢酸ソーダを
加て、MDA15mlに対する反応性の違いを検討し
た。酢酸ソーダ1.5mgを加えた場合は、実施例1
で示した水溶性範囲よりもさらに反応率の低い位
置、即ち、結合酢酸量の低い領域でも水溶性を示
した。この場合の結合酢酸量は8.4%であつた。
この内の1試料について、紫外(UV)吸収ス
ペクトル及び赤外(IR)吸収スペクトルを測定
したところ、UVでは、264mμに吸収を示した
(添附図1参照)。IRでは950cm-1などに市販のセ
ルロースアセテートとは異なつた吸収が出現した
(添附図2参照)。
図1の実線で表わした曲線が上記セルロース誘
導体のUV吸収スペクトルであり、点線で表わし
た曲線は市販のセルロースアセテートのUV吸収
スペクトルである。上記セルロース誘導体はハン
ドマークを示した領域(260〜270mμ)に新しい
吸収が認められるが、セルロースアセテートには
認められない。また、図2の下側の曲線が上記セ
ルロース誘導体のIR吸収スペクトルであり、上
側の曲線が市販セルロースアセテートのIR吸収
スペクトルである。上・下両IR吸収スペクトル
の大きな相異点はハンドマークを示した950cm-1
附近の吸収バンドにある。
実施例 5
実施例1に記載した方法で得たセルロース誘導
体2種(原料セルロースの重合度(DP)300及び
1000)を水に溶解し、それぞれ濃度28%および20
%のドープを得た。一昼夜真空下で脱泡し、ドー
プ粘度を測定したところそれぞれ5400ポイズおよ
び7500ポイズであつた。
上記ドープを孔数76の紡糸ノズル(各孔の直径
=0.08mm)から、170℃に制御した乾式筒に吐出
量3.0c.c./分で押し出し、乾式紡糸した。得られ
た繊維の物性を表−2にまとめて示す。[Table] In the table, nothing means insoluble, and presence means soluble. No.
The derivative of 6 was dissolved in acetone and formamide. Example 2 3.0 mg of sodium acetate was added to 100 ml of the cellulose solution obtained in Example 1 to dissolve it, and 15 ml of EDA was heated at 100°C.
The mixture was allowed to react for 12 hours. The reaction was precipitated in 500 ml of methanol to recover the polymer components and dried. The resulting compound exhibits water solubility;
Its UV showed an absorption peak at 268 nm. Its IR
The figure was almost the same as that obtained in Example 1. This derivative was also soluble in organic solvents such as formic acid, formamide, dimethyl sulfoxide, dimethyl acetamide, γ-butylactone, and N-methylpyrrolidone. Example 3 Add 100 ml of the cellulose solution prepared in Example 1 to
As reaction catalysts for MDA, boron trifluoride ether complex salt, aluminum chloride, and pyridine were used separately in place of sodium acetate. First, the amount of boron trifluoride ether complex salt added was varied in the range from 0.05 ml to 0.5 ml, 15 ml of MDA was added, and the mixture was reacted at room temperature for 3 to 5 hours. The polymer component was recovered by precipitation with 500 ml of methanol, and the solubility of the product was examined, but it was not soluble in the solvent shown in Example 1. Moreover, its IR spectrum did not show any absorption characteristic of ester groups. Similarly aluminum chloride and pyridine
Add 15 ml of MDA, varying the amount added in the range from 0.01 g to 0.1 g, and let it cool at room temperature for 3 to 30 minutes.
The reaction was allowed to proceed for 5 hours. The results showed that, similar to the case of the boron trifluoride ether complex salt, the reactant did not dissolve in the solvent shown in Example 1. Even when EDA was used instead of MDA as a reactant, only sodium acetate was effective as a reaction catalyst, and boron trifluoride ether complex salt,
Aluminum chloride and pyridine were not effective as catalysts. Example 4 To 100 ml of the cellulose solution prepared in Example 1,
Sodium acetate was added in different amounts (1.5 mg and 3.75 mg) to examine the difference in reactivity to 15 ml of MDA. Example 1 when adding 1.5 mg of sodium acetate
It showed water solubility even in a region where the reaction rate was lower than the water solubility range shown in , that is, a region where the amount of bound acetic acid was low. The amount of bound acetic acid in this case was 8.4%. When we measured the ultraviolet (UV) absorption spectrum and infrared (IR) absorption spectrum of one of these samples, it showed absorption at 264 mμ in the UV (see attached Figure 1). In IR, an absorption different from that of commercially available cellulose acetate appeared at 950 cm -1 (see attached Figure 2). The solid line curve in FIG. 1 is the UV absorption spectrum of the cellulose derivative, and the dotted line curve is the UV absorption spectrum of commercially available cellulose acetate. In the above cellulose derivative, new absorption is observed in the region (260 to 270 mμ) showing the handmark, but not in cellulose acetate. The lower curve in FIG. 2 is the IR absorption spectrum of the cellulose derivative, and the upper curve is the IR absorption spectrum of commercially available cellulose acetate. The large difference between the upper and lower IR absorption spectra is the hand mark at 950 cm -1
It's in the nearby absorption band. Example 5 Two types of cellulose derivatives obtained by the method described in Example 1 (polymerization degree (DP) of raw material cellulose: 300 and
1000) dissolved in water at concentrations of 28% and 20%, respectively.
% dope was obtained. The dope was degassed under vacuum for a day and night, and the dope viscosity was measured to be 5,400 poise and 7,500 poise, respectively. The above dope was extruded from a spinning nozzle with 76 holes (diameter of each hole = 0.08 mm) into a dry cylinder controlled at 170° C. at a discharge rate of 3.0 cc/min, and dry spun. The physical properties of the obtained fibers are summarized in Table 2.
【表】
白度は、日立測色計EPR−型を用い波長
400nmでキヤリブレーシヨンし、その反射率で示
した。表より明らかな如く、重合度の高い誘導体
を用いた方が得られる繊維の物性面より好ましい
ことが判る。
実施例 6
実施例1の表−1中に記載した誘導体(No.6、
DP=300)をホルムアミドに38重量%の濃度にな
るよう溶解したところ、微小の剪断力を負荷する
ことにより容易に偏光顕微鏡直交ニコル下で光学
異方性を示すドープを得ることが出きた。このド
ープを減圧下で一昼夜脱泡処理し、エクストルー
ダ(内径12mmφ)を用いて、0.07mmφ、50孔のノ
ズルから吐出量2.5c.c./分で吐出し、1.8cmのエア
ギヤツプを通してメタノール/水(=1/1、
V/V)系凝固浴中に糸条を走行させ、ドラムに
巻取つた。しかる後、一昼夜水に浸漬した後、自
然乾燥した。得られた繊維の性能を表−3に示
す。[Table] Whiteness is measured using Hitachi colorimeter EPR-type.
Calibration was performed at 400 nm and the reflectance was shown. As is clear from the table, the use of derivatives with a high degree of polymerization is more preferable in terms of the physical properties of the resulting fibers. Example 6 Derivatives listed in Table 1 of Example 1 (No. 6,
DP = 300) was dissolved in formamide to a concentration of 38% by weight, and by applying a minute shearing force, it was possible to easily obtain a dope that exhibited optical anisotropy under crossed Nicols under a polarizing microscope. This dope was defoamed under reduced pressure for a day and night, and then extruded using an extruder (inner diameter 12 mmφ) from a 0.07 mmφ, 50-hole nozzle at a discharge rate of 2.5 cc/min, and passed through a 1.8 cm air gap with methanol/water (=1 /1,
The yarn was run through a V/V) system coagulation bath and wound onto a drum. After that, it was soaked in water for a day and night, and then air-dried. Table 3 shows the performance of the obtained fibers.
【表】
この表から判るように、実施例5と同じ重合度
(300)の誘導体を用いても使用する溶媒を変える
ことにより物性の優れた繊維を得ることができ
る。このことは、特異性、即ち、光学的異方性を
示すドープを紡糸すれば配向性の高い、ひいて
は、引張強度および初期ヤング率の高い繊維を得
ることができることを意味している。[Table] As can be seen from this table, even if a derivative with the same degree of polymerization (300) as in Example 5 is used, fibers with excellent physical properties can be obtained by changing the solvent used. This means that by spinning a dope that exhibits specificity, that is, optical anisotropy, it is possible to obtain fibers with high orientation, and thus high tensile strength and initial Young's modulus.
第1図は、本発明方法によつて得られた新規セ
ルロース誘導体の紫外(UV)吸収スペクトルを
示す(実線)。比較のためセルロースアセテート
のUVスペクトルも載せている(点線)。第2図
は、本発明方法によつて得られた新規セルロース
誘導体(下側曲線)と市販セルロースアセテート
(上側曲線)の赤外(IR)吸収スペクトルを示
す。
FIG. 1 shows the ultraviolet (UV) absorption spectrum of the novel cellulose derivative obtained by the method of the present invention (solid line). For comparison, the UV spectrum of cellulose acetate is also shown (dotted line). FIG. 2 shows infrared (IR) absorption spectra of the novel cellulose derivative obtained by the method of the present invention (lower curve) and commercially available cellulose acetate (upper curve).
Claims (1)
ドに溶解したセルロースとメチレンジアセテート
またはエチレンジアセテートとの反応によつて得
られ、一つの高分子鎖中の数平均ピラノーズ環数
が100以上で、且つ、ピラノーズ環中にメチレン
ジオキシ連鎖を有し、その末端が結合酢酸量に換
算して8.4〜42%の割合でアセチル基で置換され、
溶液状態で260nm〜280nmに紫外吸収を示すこと
を特徴とするセルロース誘導体。 2 触媒として酢酸ソーダを使用することによつ
て得られる特許請求の範囲第1項記載のセルロー
ス誘導体。 3 本質的に水およびその他の極性溶媒に可溶で
ある特許請求の範囲第1項まは第2項記載のセル
ロース誘導体。[Claims] 1. Obtained by the reaction of cellulose dissolved in dimethyl sulfoxide/paraformaldehyde with methylene diacetate or ethylene diacetate, the number average number of pyranose rings in one polymer chain is 100 or more, In addition, it has a methylenedioxy chain in the pyranose ring, and the terminal thereof is substituted with an acetyl group at a rate of 8.4 to 42% in terms of the amount of bound acetic acid,
A cellulose derivative characterized by exhibiting ultraviolet absorption at 260 nm to 280 nm in a solution state. 2. The cellulose derivative according to claim 1, which is obtained by using sodium acetate as a catalyst. 3. The cellulose derivative according to claim 1 or 2, which is essentially soluble in water and other polar solvents.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16663980A JPS5792002A (en) | 1980-11-28 | 1980-11-28 | Novel cellulosic derivative |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16663980A JPS5792002A (en) | 1980-11-28 | 1980-11-28 | Novel cellulosic derivative |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5792002A JPS5792002A (en) | 1982-06-08 |
| JPS6410521B2 true JPS6410521B2 (en) | 1989-02-22 |
Family
ID=15835000
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16663980A Granted JPS5792002A (en) | 1980-11-28 | 1980-11-28 | Novel cellulosic derivative |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5792002A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5328603A (en) * | 1990-03-20 | 1994-07-12 | The Center For Innovative Technology | Lignocellulosic and cellulosic beads for use in affinity and immunoaffinity chromatography of high molecular weight proteins |
-
1980
- 1980-11-28 JP JP16663980A patent/JPS5792002A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5792002A (en) | 1982-06-08 |
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