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CS205972B1 - Method of preparation of the netted powder holocellulose - Google Patents

Method of preparation of the netted powder holocellulose Download PDF

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Publication number
CS205972B1
CS205972B1 CS349579A CS349579A CS205972B1 CS 205972 B1 CS205972 B1 CS 205972B1 CS 349579 A CS349579 A CS 349579A CS 349579 A CS349579 A CS 349579A CS 205972 B1 CS205972 B1 CS 205972B1
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CS
Czechoslovakia
Prior art keywords
holocellulose
preparation
sodium hydroxide
sawdust
isopropyl alcohol
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Application number
CS349579A
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Czech (cs)
Slovak (sk)
Inventor
Anna Ebringerova
Jan Pastyr
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Anna Ebringerova
Jan Pastyr
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Application filed by Anna Ebringerova, Jan Pastyr filed Critical Anna Ebringerova
Priority to CS349579A priority Critical patent/CS205972B1/en
Publication of CS205972B1 publication Critical patent/CS205972B1/en

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Description

Vynález aa týká sieťovanie nového východiskového materiálu - holocelulozy dřevených pilin - na přípravu polysacharidových iónomeničov.The invention aa relates to the cross-linking of a novel starting material - wood sawdust holocellulose - for the preparation of polysaccharide ion exchangers.

Doteraz aú známe spdsoby sieťovanie rdznyeh polysacharidových materiálov: mikrokryštalickej celulózy (Čs. pat. 136062), škrobu (Can. pat. 960652), pektínov (Ča. pat. 140713), amylózy (B. Pfannemuller, lú. Sperlich, Makromol. Chem. 1978, str. 1965), hemiceluloz (čs. pat. 161464, NSR-Offen. 1 924000) a polobuničín (NSR pat. 1 696233).There are known methods of cross-linking various polysaccharide materials: microcrystalline cellulose (US Pat. 136062), starch (Can. Pat. 960652), pectins (US Pat. 140713), amylose (B. Pfannemuller, Lu Sperlich, Makromol. Chem. 1978, p. 1965), hemicellulose (U.S. Pat. No. 161464, NSR-Offen. 1924000), and semi-cellulose (U.S. Pat. No. 1,662,333).

Východisková holocelulóza sa mdže pripraviť rdznymi postupmi delignifikácie dřevených pilin, ktoré sú sprevádzané len miernou degradáciou a atratami polysacharidových zložiek celulózy a hemiceluloz (Timell T. B.: Adv. Carbohydr. Chem. 19, 296 - 1964).The starting holocellulose can be prepared by various procedures for the delignification of wood sawdust, which are accompanied only by slight degradation and atrophy of the polysaccharide components of cellulose and hemicellulose (Timell, T. B., Adv. Carbohydr. Chem. 19, 296-1964).

Podstata vynálezu spočívá v tom, že holocelulóza vytriedených dřevných pilin aa po alkalizácii v emulzii 25 až 30 % hydroxidu sodného a izopropylalkoholu pri teplote 20 až 25 °C po 1 hodině odfiltruje alebo odstředí na váhu 200 až 250 % jej pdvodnej navážky. Alkalická holocelulóza sa preneaie do nádoby s možnosťou miešania a ohrievania a sieťuje přidáním 0,5 až 1 mólu sieťovadla, 8 výhodou epichlórhydrínu, pri teplote 50 až 60 °C po dobu 1 až 2 hodin. Po premytí eieťovaného produktu vodou do neutrálnej reakoie a vytěsnění vody etanolom alebo acetónom sa voTne vysuší pri teplote miestnosti. Získá sa váhový prírastok 20 až 30 %, pričom sieťovaný produkt má rozpustnost v zriedených alkáliách do 5 %·SUMMARY OF THE INVENTION The holocellulose of sorted wood sawdust aa after alkalinization in an emulsion of 25-30% sodium hydroxide and isopropyl alcohol at 20-25 ° C after 1 hour filtered or centrifuged to a weight of 200-250% of its initial weight. The alkaline holocellulose is transferred to a mixing and heating vessel and crosslinked by adding 0.5 to 1 mole of crosslinker, preferably epichlorohydrin, at a temperature of 50 to 60 ° C for 1 to 2 hours. After washing the crosslinked product with water until neutral and displacing the water with ethanol or acetone, it is freely dried at room temperature. A weight gain of 20 to 30% is obtained, wherein the crosslinked product has a solubility in diluted alkali of up to 5% ·

Výhodou navrhovaného spdsobu přípravy sieťovanej holocelulozy dřevených pilin je, že:The advantage of the proposed method for the preparation of cross-linked holocellulose wood sawdust is that:

205 972205 972

i.i.

205 972205 972

- nevyžaduje výrobu buničiny, resp. mikrokryštalickej celulózy,- does not require pulp production, resp. microcrystalline cellulose,

- v porovnaní s vláknitými polobuničinami má korpuskulárny charakter, pretože si zachová tvar pilin, ktorých velkost aa mOže meniť vhodným preeitkovaním dřevených pilin,- it has a corpuscular character in comparison to filamentous solids, as it retains the shape of sawdust, the size of which can and can be varied by suitable sawdust of wood sawdust,

- ekonomicky využívá drevnú surovinu, pretože okrem celulózovej zložky sa zosietuje aj hemucelulózy, ktoré predstavujú přibližné 1/3 drevnej hmoty a při výrobě buničiny tvoria rozpustný odpad,- economically utilizes wood raw material because, in addition to the cellulosic component, hemucelluloses, which account for approximately 1/3 of the wood mass and form soluble waste in the pulp production, are cross-linked,

- ako surovinu je možné použit piliny rdznych dřevin, připadne ich zmesi,- sawdust of various woods or mixtures thereof may be used as raw material,

- sietovaný produkt je stély v určitom rozmedzí pH, čo umožňuje jeho použitie ako východiskového materiálu pre přípravu iónomeničov,- the crosslinked product is stele within a certain pH range, allowing its use as a starting material for the preparation of ion exchangers,

- emulziu hydroxidu sodného v izopropylalkohole je možné po úpravě alkality znova použit pre alkalizéciu.- the sodium hydroxide emulsion in isopropyl alcohol can be reused for alkalization after alkalinity treatment.

Příklad 1 kg vzduchosuchej holocelulózy vytriedených bukových pilin (velkost častíc 0,1 až 3 mm a obsah ligninu do 5 %). sa za mieéania vsype do emulzie 10 1 izopropylalkoholu a 1,0 1 30 % hydroxidu sodného. Zmes sa nechá za miešania alkalizovať pri teplote miestnosti 1 hodinu. Potom sa alkalizovaňá holocelulóza odfiltruje alebo odstředí ne váhu 2 až 2,5 kg a prenesie do nádoby s možnosťou miešania a ohrievania. Po přidaní 0,24 1 epichlorhydrínu aa při 60 °C nechá reagovat 1 hodinu. Po reakcii sa produkt premyje vodou do neutrálnej reakcie, etanolom alebo acetónom a vysuší volné na vzduchu. Získá sa 1,1 kg sieťovanej holocelulózy e rozpuetnostou v 5 % hydroxide sodnom - 5 %·Example 1 kg of air-dry holocellulose of sorted beech sawdust (particle size 0.1 to 3 mm and lignin content up to 5%). The mixture is stirred into an emulsion of 10 l of isopropyl alcohol and 1.0 l of 30% sodium hydroxide with stirring. The mixture was allowed to basify with stirring at room temperature for 1 hour. Thereafter, the alkalized holocellulose is filtered or centrifuged to a weight of 2 to 2.5 kg and transferred to a mixing and heating vessel. After addition of 0.24 L of epichlorohydrin and at 60 ° C, it is allowed to react for 1 hour. After the reaction, the product is washed with water until neutral, with ethanol or acetone and dried in the air. 1.1 kg of cross-linked holocellulose are obtained with a solubility in 5% sodium hydroxide - 5% ·

Příklad 2 kg vzduchosuchej holocelulózy vytriedených smrekových pilin (velkost častíc 0,1 až 3 mm a obsah ligninu do 5 %) sa za miešania vsype do emulzie 12 1 izopropylalkoholu a 1,2 1 25 % hydroxidu sodného. Zmes sa nechá za miešania alkalizovať při teplote mieetnosti 1 hodinu. Potom sa alkalizovaňá holocelulóza odfiltruje alebo odstředí na váhu 2 až 2,5 kg a prenesie do nádoby a možnosťou miešania a ohrievania. Po přidaní 0,48 1 epichlorhydrínu sa pri 50 °C nechá reagovat 2 hodiny. Po reakcii sa produkt premyje vodou do neutrálnej reakcie, etanolom alebo acetónom a vysuší volné na vzduchu. Zlska sa 1,3 kg sieťovanej holocelulózy s rozpustnosťou v 5 % hydroxide sodnom - 3,5 %·Example 2 kg of air-dry holocellulose of sorted spruce sawdust (particle size 0.1 to 3 mm and lignin content up to 5%) is mixed with stirring into an emulsion of 12 l of isopropanol and 1.2 l of 25% sodium hydroxide. The mixture was allowed to basify with stirring at room temperature for 1 hour. Thereafter, the alkalized holocellulose is filtered or centrifuged to a weight of 2 to 2.5 kg and transferred to a container with the possibility of stirring and heating. After the addition of 0.48 L of epichlorohydrin, it is allowed to react at 50 ° C for 2 hours. After the reaction, the product is washed with water until neutral, with ethanol or acetone and dried in the air. 1.3 kg of cross-linked holocellulose are obtained with a solubility in 5% sodium hydroxide - 3.5% ·

Vynález má rozeiahle využitie na přípravu katexov a anexov na báze eieťovaných dřevených polysacharidov - holocelulózy, ktoré sú aplikovatelné v analytickej i preparačnej chro matografii.The invention has extensive application for the preparation of cation exchangers and anion exchangers based on crosslinked wood polysaccharides - holocellulose, which are applicable in analytical and preparative chromatography.

Claims (1)

PBBDMBT VYNÁLEZUPBBDMBT OF THE INVENTION Spdeob přípravy sieťovanej práškovej holocelulózy, vyznačujúci sa tým, že holoceluloza z vytriedených dřevených pilin sa po alkalizácii v emulzii hydroxidu sodného a izopropylalkoholu za použitia váhového poměru : holocelulóza - 25 až 30 % hydroxid sodný - izopropylalkohol, 1 : 1,5 až 1,8 : 10 až 12, pri teplote 20 až 25 °C po 1 hodině odfiltruje aleboA method for the preparation of cross-linked powdered holocellulose, characterized in that the sieved wood sawdust is after alkalization in an emulsion of sodium hydroxide and isopropyl alcohol using a weight ratio of: holocellulose - 25 to 30% sodium hydroxide - isopropyl alcohol, 1: 1.5 to 1.8 10 to 12, filtered at 20 to 25 ° C after 1 hour, or 20S 972 odstředí na váhu 200 až 250 % pCvodnej navážky a přidáním 0,5 až 1 molu aieťovadla, a výhodou epichlóřhydřínu, ea při teplote 50 až 60 °C po dobu 1 až 2 hodin sieťuje, potom sa sletovaný produkt premyje vodou, etanolom alebo acetónom a vysuší na vzduchu.20S 972 is centrifuged to 200-250% by weight of the aqueous weighing and crosslinked by adding 0.5 to 1 mole of a crosslinker, preferably epichlorohydrin, e at 50 to 60 ° C for 1 to 2 hours, then washing the fused product with water, ethanol or acetone and air dried.
CS349579A 1979-05-21 1979-05-21 Method of preparation of the netted powder holocellulose CS205972B1 (en)

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