FI90573C - A way to improve the retention or treatment of pulp fiber suspensions or wastewater in the paper, pulp or board industry - Google Patents
A way to improve the retention or treatment of pulp fiber suspensions or wastewater in the paper, pulp or board industry Download PDFInfo
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- FI90573C FI90573C FI875123A FI875123A FI90573C FI 90573 C FI90573 C FI 90573C FI 875123 A FI875123 A FI 875123A FI 875123 A FI875123 A FI 875123A FI 90573 C FI90573 C FI 90573C
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/54—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
- C02F1/56—Macromolecular compounds
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/06—Paper forming aids
- D21H21/10—Retention agents or drainage improvers
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/24—Polysaccharides
- D21H17/25—Cellulose
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/24—Polysaccharides
- D21H17/28—Starch
- D21H17/29—Starch cationic
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/47—Condensation polymers of aldehydes or ketones
- D21H17/48—Condensation polymers of aldehydes or ketones with phenols
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/53—Polyethers; Polyesters
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- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Paper (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Cleaning Implements For Floors, Carpets, Furniture, Walls, And The Like (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
1 905731 90573
Tapa parantaa paperi-, massa- tai kartonkiteollisuudessa sellukuitususpensioiden tai jatevesien retentiota tai puh-distusta 5 Kasiteltavana oleva keksinto koskee tapaa paran taa paperi-, massa- tai kartonkiteollisuudessa sellukuitususpensioiden tai jatevesien retentiota ja/tai puhdistus-ta kasittelemållå niita yhdistelmållå, joka muodostuu fe-noliformaldehydihartsista ja suurimolekyylisestå polyetee-10 nioksidista seka kationisesta tarkkolysjohdannaisesta tai kationisesta selluloosajohdannaisesta.The present invention relates to a method for improving the retention and / or purification of pulp fiber suspensions or effluents in the paper, pulp or paperboard industry by treating them by combining them. noliformaldehyde resin and high molecular weight polyethylene 10 oxide, as well as a cationic precision derivative or a cationic cellulose derivative.
Paperi-, massa- ja kartonkiteollisuudessa tunne-taan useita tapoja retention parantamiseksi sellukuitususpensioiden vedenpoiston yhteydessa lisååmållå erilai-15 sia polyelektrolyytteja kuten kationista polyamiinia, ka-tionista polyakryyliamidia ja kationista selluloosajoh-dannaista. Sellukuitususpensiot voivat sellukuitujen ohel-la sisåltaa myds vaihtelevia maariå epaorgaanisia tayte-aineita, esim. savea, dolomiittikalkkia ja kipsiå, epa-20 orgaanisia ja orgaanisia sideaineita, ligniinia ja hemi-selluloosia. Lisa&nalia polyelektrolyytteja helpotetaan massasuspension sisaltSmien tuotteiden flokkautumista ja tamS edistaS puolestaan retentiota. Lansi-saksalaisesta patenttijulkaisusta 2 549 089 tunnetaan myos retention 25 parantaminen sellukuitususpensioiden vedenpoiston yhteydessa kHyttamalla suurimolekyylisen polyeteenioksidin, fenoliformaldehydihartsin, vaihtoehtoisesti fenolirikki-hartsin, ja polyamidin yhdistelmaa.Several ways are known in the paper, pulp and board industry to improve retention in the dewatering of pulp fiber suspensions by the addition of various polyelectrolytes such as cationic polyamine, cationic polyacrylamide and cationic cellulose derivative. Pulp fiber suspensions may contain, in addition to pulp fibers, various amounts of inorganic fillers, e.g. clay, dolomite lime and gypsum, epa-20 organic and organic binders, lignin and hemicellulose. The addition of polyelectrolytes facilitates the flocculation of the products contained in the pulp suspension and in turn promotes retention. West German Patent 2,549,089 also discloses the improvement of retention in the dewatering of pulp fiber suspensions by the use of a combination of high molecular weight polyethylene oxide, phenol-formaldehyde resin, alternatively phenol-sulfur resin, and polyamide.
Kun vesi on poistettu sellukuitususpensiosta, saa-30 daan suuria maSria jåtevetta, joka hyvallakin retentiolla sisSltåa pienehkoja maaria hienokuitua, ns. nollakuitua, tayteaineita ja sideainetahteita seka ligniinista ja hemi-selluloosasta liuenneita aineosia. Jateveden puhdistuk-sessa pyritaan tunnetusti flokkaamaan epapuhtaudet lisåa-35 malla epaorgaanisia ja/tai orgaanisia polyelektrolyytteja 2 90B73 kuten alumiinisulfaattia, rautakloridia, polyakryyliami-dia, polyakrylaattia, polyeteeni-imiinia ja kationista tarkkelysjohdannaista.After the water has been removed from the pulp fiber suspension, large MaSria effluents are obtained, which, even with good retention, contain smaller Maaria fine fibers, so-called zero fiber, fillers and binder residues, as well as dissolved ingredients from lignin and hemicellulose. In wastewater treatment, it is known to flocculate impurities by adding inorganic and / or organic polyelectrolytes 2 90B73 such as aluminum sulfate, ferric chloride, polyacrylamide, polyacrylate, polyethyleneimine and a cationic starch derivative.
Kanadalaisesta patenttijulkaisusta CA 1 004 782 5 tunnetaan myos fenoliformaldehydin kaytto yhdistelmånå suurimolekyylisen polyeteenioksidin kanssa parantamaan retentiota sellukuitususpensioiden vedenpoiston yhteydes-sa. SekS sellukuitususpensioiden vedenpoiston etta jate-veden puhdistuksen yhteydessa polyeteenioksidiaddukti hel-10 pottaa fenoliformaldehydihartsin kanssa muodostuvien flok-kien agglomeroitumista, jolloin retentio ja puhdistus hel-pottuvat.Canadian patent CA 1 004 782 5 also discloses the use of phenol formaldehyde in combination with high molecular weight polyethylene oxide to improve retention in the dewatering of pulp fiber suspensions. In connection with the dewatering and waste water purification of SekS pulp fiber suspensions, the polyethylene oxide adduct facilitates the agglomeration of the Flocks formed with the phenol-formaldehyde resin, thereby facilitating retention and purification.
Vaikka suurimolekyylisen polyeteenioksidin ja feno-liformaldehydihartsin yhdistelma mahdollistaa hyvan reten-25 tion ja puhdistumisen, on osoittautunut, etta osa hieno-kuiduista ja kolloidisista hiukkasista ja liuenneesta aineksesta ei pidåty kuiturainaan tai ei saada poistetuk-si jåtevedestå ehdotetulla menettelylla. Siten on tarvet-ta saada kayttodn menettelyja, jotka parantavat edelleen 20 retentiota ja puhdistusta. Tallaisia ongelmia esiintyy mm. poistettaessa vesi uusiomassasta tai mekaanisesta mas-sasta saaduista kuitususpensioista tai puhdistettaessa naistå massoista tai kuorimoista syntyviå jåtevesiå. Siten on olemassa tarve saada kåyttoon menettelyja, joilla 25 retentio ja puhdistus paranevat entisestaankin.Although the combination of high molecular weight polyethylene oxide and phenol-liformaldehyde resin allows for good retention and purification, it has been found that some of the fine fibers and colloidal particles and solutes are not retained in the fibrous web or cannot be removed from the effluent by the proposed process. Thus, there is a need for procedures that further improve retention and purification. Such problems occur e.g. in the removal of water from fiber suspensions obtained from recycled pulp or mechanical pulp, or in the treatment of waste water from pulp or hulls. Thus, there is a need for procedures that further improve retention and purification.
Nyt on osoittautunut, etta retentiota ja puhdistusta voidaan parantaa, jos kuitususpensioon tai jateve-teen lisåtcian formaldehydihartsin ja suurimolekyylisen polyeteenioksidin lisåksi kationista tårkkelysjohdannais-30 ta tai kationista selluloosajohdannaista. On osoittautunut, etta kationisen tarkkelysjohdannaisen lasnaolo parantaa nollakuitujen ja flokkautuneen aineksen, joita on tai muodostuu kasittelyn aikana, "siepattavuutta". Kun vesi poistetaan kuitususpensiosta, nollakuidut, sideainehiuk-35 kaset, flokit ym.sitoutuvat enenevassa maarin sellukuitu- 3 90573 rainaan, mikå merkitsee suurempaa saantoa, nopeampaa ve-denpoistoa ja puhtaampaa jåtevetta. Jåteveden puhdistuk-sessa on voitu havaita, etta keksintoå sovellettaessa nol-lakuidut, sideainehiukkaset, tåyteaineet, pigraentit, lig-^ niini ja hemiselluloosa agglomeroituvat huomattavasti suu-remmassa måårin kuin ennen flokeiksi. Flokit ovat hyvin pysyvia ja ne on helppo poistaa sediraentoinnin, vaahdotuk-sen tai sentrifugoinnin jålkeen.It has now been found that retention and purification can be improved if a cationic starch derivative or a cationic cellulose derivative is added to the fiber suspension or water in addition to formaldehyde resin and high molecular weight polyethylene oxide. It has been shown that the presence of a cationic starch derivative improves the "traceability" of zero fibers and flocculated material present or formed during processing. When water is removed from the fiber suspension, zero fibers, binder particles, flocs, etc. increasingly bind to the web of pulp fibers, which means higher yields, faster dewatering, and cleaner wastewater. In wastewater treatment, it has been found that in the application of the invention, the zero fibers, binder particles, fillers, pigments, lignin and hemicellulose agglomerate to a much greater extent than before into flocs. The flocs are very stable and easy to remove after sedimentation, flotation or centrifugation.
Keksinnon mukaisessa tavassa kåyttokelpoisen suu-j^q rimolekyylisen polyeteenioksidin molekyylipainon on olta- va yli 500 000 ja mieluiten yli 2 000 000. Mitaan kriittis-ta ylarajaa ei ole voitu havaita ja siten on hyvia tulok-sia saavutettu polyeteenioksidilla, jonka molekyylipaino on 12 000 000. Huomattavasti suurempien molekyylipainojen saavuttaminen on osoittautunut vaikeaksi valmistuksessa tapahtuvan ketjunlyhenemisen vuoksi. Keksinndn mukainen polyeteenioksidi rakentuu suurimmaksi osaksi oksieteeni-ryhmista, mutta siina voi olla pienehko maara muita ryh-miS/ esim. oksipropeeniryhmia. Muiden kuin oksieteeniryh-2Q mien mSaraa rajoittaa ehto, etta polyeteenioksidin on oltava vesiliukoinen.In the process according to the invention, the molecular weight of the oral polyethylene oxide usable must be more than 500,000 and preferably more than 2,000,000. No critical upper limit has been observed and thus good results have been obtained with polyethylene oxide having a molecular weight of 12,000. 000. Achieving significantly higher molecular weights has proven difficult due to chain shortening in manufacturing. The polyethylene oxide according to the invention is mostly composed of oxyethylene groups, but there may be a small number of other groups / e.g. oxypropylene groups. The mSara of non-oxyethylene groups is limited by the condition that the polyethylene oxide must be water-soluble.
Keksinnon mukainen fenoliformaldehydihartsi on suh-teellisen vesiliukoinen, joskin voidaan kayttaa hartseja, joiden liukoisuus on rajallinen neutraaleissa tai emaksi-25 sissS pH-arvoissa. Hartsi saostuu yleensa happamissa pH-arvoissa.The phenol-formaldehyde resin of the invention is relatively water-soluble, although resins with limited solubility at neutral or mother-to-mother pH values may be used. The resin usually precipitates at acidic pH values.
Keksinnon mukaisesti kåytettavana kationisena tark-kelysjohdannaisena on edullisesti peruna-, maissi- tai vehnåtårkkelys, joka on substituoitu kvartaarisilla amitio-3Q niumryhmillå. Substituutioaste on edullisesti 0,01-0,1.The cationic observation derivative used according to the invention is preferably potato, corn or wheat starch substituted by quaternary amethio-3Q sodium groups. The degree of substitution is preferably 0.01 to 0.1.
Kationisesta selluloosajohdannaisesta tulee modifioimalla vesiliukoinen. Kationisen selluloosajohdannaisen on oltava vesiliukoinen ja se voi edella mainittujen kationisten ryhmien lisaksi sisMltaå myos alempi-alkyyliryhmia kuten 35 metyyli- tai etyyliryhmia seka alempi-hydroksialkyyliryhmia 4 90573 kuten hydroksietyyli-, hydroksipropyyli- ja hydroksibutyy-liryhmia. Selluloosajohdannaisen kationisten ryhmien, edullisesti kvartaaristen ammoniumryhmien sopiva substi-tuutioaste on 0,01-0,5 anhydroglukoosiyksikkoa kohti ja 5 molekyylipaino noin 10 000 - noin 1 000 000.The cationic cellulose derivative becomes water-soluble by modification. The cationic cellulose derivative must be water-soluble and may contain, in addition to the above-mentioned cationic groups, lower alkyl groups such as 35 methyl or ethyl groups as well as lower hydroxyalkyl groups 4,90573 such as hydroxyethyl, hydroxypropyl and hydroxybutyl groups. A suitable degree of substitution of the cationic groups of the cellulose derivative, preferably the quaternary ammonium groups, is 0.01 to 0.5 per anhydroglucose unit and the molecular weight is from about 10,000 to about 1,000,000.
Fenoliformaldehydihartsin, polyeteenioksidin ja ka-tionisen tarkkelysjohdannaisen tai kationisen selluloosa-johdannaisen måaråt eivat ole kriittisiå. LisaysmaSra so-vitetaan edullisesti nollakuitujen, tåyteaineiden, side-X0 aineiden, pigmenttien, ligniinin ja hemiselluloosan maaran ja tyypin mukaan. Fenoliformaldehydihartsimaårå on norraaa-listi yli 1, edullisesti yli 5 ppm, polyeteenioksidin maa-rå on yli 0,1 ppm, edullisesti yli 1 ppm ja kationisen tSrkkelysjohdannaisen mååra yli 1, edullisesti yli 5 ppm 15 jatevedesta laskettuna. Sopivat yiarajat ovat vastaavasti noin 100, 20 ja 200 ppm jatevedesta laskettuna. Reten-tiolle edulliset lisaysmaarat ovat 0,01-0,5 paino-% feno-liformaldehydihartsia, 0,001-0,1 paino-% polyeteenioksi-dia ja 0,01-1,0 paino-% kationista tarkkelysjohdannaista 20 tai kationista selluloosajohdannaista suspension sisåltå-mista aineksista laskettuna. Fenoliformaldehydin ja polyeteenioksidin suhde on edullisesti 1:5 - 50:1 ja kationisen tarkkelysjohdannaisen tai kationisen selluloosajohdannaisen ja polyeteenioksidin suhde on txlull isesti 1:5 -25 100:1 riippumatta siita, kaytetaanko komponentteja veden- puhdistukseen vaiko retentioon.The amounts of phenol formaldehyde resin, polyethylene oxide and cationic starch derivative or cationic cellulose derivative are not critical. LisaysmaSra is preferably adapted to the amount and type of zero fibers, fillers, binders, binders, lignin and hemicellulose. The amount of phenol formaldehyde resin is normally more than 1, preferably more than 5 ppm, the amount of polyethylene oxide is more than 0.1 ppm, preferably more than 1 ppm and the amount of cationic starch derivative is more than 1, preferably more than 5 ppm based on the effluent. Suitable yia limits are about 100, 20 and 200 ppm of effluent, respectively. Additional additives preferred for retention are 0.01-0.5% by weight of phenol-liformaldehyde resin, 0.001-0.1% by weight of polyethylene oxide and 0.01-1.0% by weight of cationic starch derivative 20 or cationic cellulose derivative in suspension. calculated on its own. The ratio of phenol formaldehyde to polyethylene oxide is preferably 1: 5 to 50: 1 and the ratio of cationic starch derivative or cationic cellulose derivative to polyethylene oxide is preferably 1: 5 to 25,100: 1, regardless of whether the components are used for water purification or retention.
Kolmea keksinnon mukaista komponenttia voidaan li-sata mielivaltaisessa jarjestyksessa. Kationinen tarkkelys johdannainen ja kationinen selluloosajohdannainen voi-30 daan esim. lisata ensin, ja sitten fenoliformaldehydi- hartsi ja polyeteenioksidi mainitussa jarjestyksessa. Voidaan myos toimia siten, etta ensin lisataån fenoliform-aldehydihartsi ja sitten polyeteenioksidin ja kationisen tarkkelysjohdannaisen tai kationisen selluloosajohdannai-35 sen muodostama seos.The three components of the invention may be added in arbitrary order. The cationic starch derivative and the cationic cellulose derivative may be added, for example, first, and then the phenol formaldehyde resin and the polyethylene oxide in said order. It is also possible to act first by first adding a phenol formaldehyde resin and then a mixture of polyethylene oxide and a cationic starch derivative or a cationic cellulose derivative.
5 905735,90573
Seuraavat toteutusesimerkit selventavat keksintoå ja niiden tehtåvånå ei ole rajoittaa keksinnon piiria.The following embodiments illustrate the invention and are not intended to limit the scope of the invention.
Esimerkki 1Example 1
Lasiastiaan kaadettiin 800 ml jatevetta, joka muo-5 dostui CTMP-valmistuksessa ja kartonginvalmistuksessa syn-tyneiden jatevesien seoksesta. Jateveden pH oli 6,5 ja kuiva-ainepitoisuus 2,5 g per litra. Jatevettå sekoitet-tiin nopeudella 500 kierr/min ja lisattiin polyelektro-lyytti. Kun oli sekoitettu yksi minuutti, lisattiin feno-10 liformaldehydihartsi ja yhden lisaminuutin kuluttua lisattiin suurimolekyylinen eteenioksidiaddukti samalla se-koittaen nopeudella 500 kierr/min. Kun viimeisesta lisayk-sestd oli kulunut 10 sekuntia, sekoitusnopeus pienennet-tiin arvoon 100 kierr/min ja kun oli viela kulunut 50 se-15 kuntia, sekoitus lopetettiin. Jatevedessa muodostuneet flokit saivat sitten laskeutua ja sitten kirkkaasta faa-sista otettiin nMytteita ja sameus mitattiin nefelometri-sesti. Lisatyt kemikaalit, niiden maarat ja saavutettu selkeytys ilmenevat taulukosta 1.800 ml of effluent formed from a mixture of effluents from CTMP and board production was poured into a glass vessel. The pH of the wastewater was 6.5 and the dry matter content was 2.5 g per liter. The effluent was stirred at 500 rpm and polyelectrolyte was added. After stirring for one minute, pheno-10 liformaldehyde resin was added, and after one additional minute, a high molecular weight ethylene oxide adduct was added while stirring at 500 rpm. After 10 seconds from the last additional unit, the stirring speed was reduced to 100 rpm and after another 50 to 15 cycles, the stirring was stopped. The flocs formed in the wastewater were then allowed to settle and then nMytes were taken from the clear phase and turbidity was measured nephelometrically. The chemicals added, their amounts and the clarification achieved are shown in Table 1.
20 Tuloksista kay ilmi, etta keksinndn mukaisissa ko- keissa 2 ja 3 saavutettiin huomattavasti parempi selkeytys kuin kokeessa 1, joka on kanadalaisen patentin CA 1 004 782 mukainen. Kokeeseen 1 verrattuna muiden po-lyelektrolyyttien kuin kationisen tarkkelysjohdannaisen 25 lisaaminen ei parantanut tuloksia.From the results, Kay shows that experiments 2 and 3 of the invention achieved significantly better clarification than Experiment 1, which is in accordance with Canadian Patent CA 1,004,782. Compared to Experiment 1, the addition of polyelectrolytes other than the cationic starch derivative 25 did not improve the results.
Esimerkki 2Example 2
Jatevesi, joka saatiin valkaisemattoman kerayspape-rin pesusiistausvaiheesta, puhdistettiin 25°C:ssa samalla tavoin kuin esimerkissS 1. Jåteveden kuiva-ainepitoisuus 30 oli 2,5 g/1 ja pH-arvo 7. Lisatyt kemikaalit, niiden måå-rat ja tulokset ilmenevSt taulukosta 1.The effluent obtained from the bleaching step of unbleached ceramic paper was purified at 25 ° C in the same manner as in Example 1. The dry matter content 30 of the effluent was 2.5 g / l and the pH value 7. The added chemicals, their amounts and results are apparent. from Table 1.
Tuloksista kay ilmi, etta keksinnon mukaisen kationisen tdrkkelysjohdannaisen tai kationisen selluloosajoh-dannaisen lisaaminen aikaansaa huomattavasti paremman puh-35 distumisen kuin tavanomainen fenoliformaldehydihartsin ja suurimolekyylisen polyeteenioksidin yhdistelma. Mitaan pa- 6 90573 rantumista ei tapahtunut yhdistelmillå, jotka sisalsi-vat fenoliformaldehydihartsia ja suurimolekyylistå poly-eteenioksidia ja muita polyelektrolyytteja.From the results, Kay shows that the addition of the cationic spray derivative or cationic cellulose derivative according to the invention provides a significantly better purification than the conventional combination of phenol formaldehyde resin and high molecular weight polyethylene oxide. No improvement occurred with combinations containing phenol-formaldehyde resin and high molecular weight polyethylene oxide and other polyelectrolytes.
Esimerkki 3 5 Jatevesi, joka saatiin valkaistun kerayspaperin pesusiistausvaiheesta, puhdistettiin 25°C:ssa samalla tavoin kuin esimerkisså 1. Jåteveden kuiva-ainepitoisuus oli 4,4 g per litra ja pH-arvo 8. Lisåtyt kemikaalit, nii-den mSårat ja tulokset ilmenevat taulukosta 3. Tuloksista 10 kay ilmi, ettS keksinnSn mukaisissa kokeissa saavutettiin huomattavasta parempi puhdistuminen kuin kaytettåessa pelkkaa fenoliformaldehydihartsia tai suurimolekyylista polyeteenioksidia tai nåiden yhdistelmaa.Example 3 5 The effluent obtained from the bleaching step of bleached ceramic paper was purified at 25 ° C in the same manner as in Example 1. The effluent had a dry matter content of 4.4 g per liter and a pH of 8. The added chemicals, their mSarages and results are shown Table 3. It can be seen from the results that the experiments according to the invention achieved a significantly better purification than the use of phenol-formaldehyde resin alone or high molecular weight polyethylene oxide or a combination thereof.
Esimerkki 4 15 Massasuspensiolla, jonka sellukuitukonsentraatio oli 0,55 paino-% ja pH-arvo 7, suoritettiin retentiokokei-ta 35°C:ssa. Sellukuidun koostumus oli 60 % pesusiistat-tua massaa, 30 % sulfaattimassahylkya ja 10 % valkaistua sulfaattimassaa. Retentiokokeet suoritettiin Brittin mu-20 kaan. Ks TAPPI 56(10), 46(1973). Lisatyt kemikaalit, nii-den mSSrSt ja tulokset ilmenevat alla olevasta taulukosta. Tuloksista kay ilmi, etta tulokset keksinnon mukaisesti suoritetussa retentiossa olivat olennaisesti paremmat kuin vertailukokeissa.Example 4 Retention tests were performed on a pulp suspension having a pulp fiber concentration of 0.55% by weight and a pH of 7 at 35 ° C. The composition of the pulp fiber was 60% washed detergent pulp, 30% sulphate pulp scrap and 10% bleached sulphate pulp. Retention experiments were performed according to Britt-20. See TAPPI 56 (10), 46 (1973). The added chemicals, their mSSrSt and results are shown in the table below. From the results, Kay showed that the results in the retention according to the invention were substantially better than in the comparative experiments.
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Claims (7)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE8604975 | 1986-11-21 | ||
SE8604975A SE454507B (en) | 1986-11-21 | 1986-11-21 | PUT IN THE PAPER, MASS OR BOARD INDUSTRIES IMPROVE RETENTION OR CELLULOSA FIBER SUSPENSION RESP RESP |
Publications (4)
Publication Number | Publication Date |
---|---|
FI875123A0 FI875123A0 (en) | 1987-11-19 |
FI875123A FI875123A (en) | 1988-05-22 |
FI90573B FI90573B (en) | 1993-11-15 |
FI90573C true FI90573C (en) | 1994-02-25 |
Family
ID=20366355
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI875123A FI90573C (en) | 1986-11-21 | 1987-11-19 | A way to improve the retention or treatment of pulp fiber suspensions or wastewater in the paper, pulp or board industry |
Country Status (3)
Country | Link |
---|---|
FI (1) | FI90573C (en) |
NO (1) | NO166456C (en) |
SE (1) | SE454507B (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5230808A (en) * | 1991-06-17 | 1993-07-27 | Nalco Canada Inc. | Liquid suspension of polyethylene oxide for use in treating paper and pulp wastewater |
US5173208A (en) * | 1991-06-17 | 1992-12-22 | Nalco Canada Inc. | Liquid suspension of polyethylene oxide for use in treating paper and pulp wastewater |
US5178770A (en) * | 1991-07-12 | 1993-01-12 | Nalco Canada Inc. | Method of treating bctmp/ctmp wastewater |
WO1993015271A1 (en) * | 1992-01-29 | 1993-08-05 | Kemira Kemi Aktiebolag | Improved process for production of paper |
SE500783C2 (en) * | 1992-05-05 | 1994-09-05 | Eka Nobel Ab | Ways to clean wood resin-containing process or wastewater |
SE509777C2 (en) * | 1997-07-07 | 1999-03-08 | Kemira Kemi Ab | Methods to improve retention in dewatering a cellulose fiber suspension using an agent comprising a phenol formaldehyde resin and a polyethylene oxide |
GB9800497D0 (en) * | 1998-01-09 | 1998-03-04 | Allied Colloids Ltd | Dewatering of sludges |
-
1986
- 1986-11-21 SE SE8604975A patent/SE454507B/en not_active IP Right Cessation
-
1987
- 1987-11-19 NO NO874840A patent/NO166456C/en not_active IP Right Cessation
- 1987-11-19 FI FI875123A patent/FI90573C/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FI875123A0 (en) | 1987-11-19 |
FI875123A (en) | 1988-05-22 |
NO874840D0 (en) | 1987-11-19 |
NO874840L (en) | 1988-05-24 |
NO166456B (en) | 1991-04-15 |
FI90573B (en) | 1993-11-15 |
NO166456C (en) | 1991-07-24 |
SE8604975D0 (en) | 1986-11-21 |
SE454507B (en) | 1988-05-09 |
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Legal Events
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MM | Patent lapsed |
Owner name: BEROL KEMI AB |