NO791974L - Middel til anvendelse ved cellestoffgjenvinning og fremgangsmaate til cellestoffgjenvinning - Google Patents

Middel til anvendelse ved cellestoffgjenvinning og fremgangsmaate til cellestoffgjenvinning

Info

Publication number: NO791974L
Authority: NO; Norway
Prior art keywords: weight; agent according; keto; organic; anthraquinone
Prior art date: 1978-06-21

Application number

NO791974A

Other languages

English (en)

Norwegian (no)

Inventor

Dieter Bauer

Paul Schiller

Volker Hassmann

Konrad Nonn

Karlheinz Wolf

Original Assignee

Bayer Ag

Priority date (The priority date 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 date listed.)

1978-06-21

Filing date

1979-06-13

Publication date

1979-12-27

1979-06-13 Application filed by Bayer Ag filed Critical Bayer Ag

1979-12-27 Publication of NO791974L publication Critical patent/NO791974L/no

Links

238000000034 method Methods 0.000 title claims description 39
239000000126 substance Substances 0.000 title description 21
239000000463 material Substances 0.000 title description 6
238000004064 recycling Methods 0.000 title 2
239000003795 chemical substances by application Substances 0.000 claims abstract description 66
239000000203 mixture Substances 0.000 claims abstract description 30
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 22
239000004094 surface-active agent Substances 0.000 claims abstract description 16
125000000468 ketone group Chemical group 0.000 claims abstract description 5
229930194542 Keto Natural products 0.000 claims abstract description 4
239000006185 dispersion Substances 0.000 claims description 58
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 49
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 45
239000001913 cellulose Substances 0.000 claims description 36
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 34
238000004519 manufacturing process Methods 0.000 claims description 31
229940076442 9,10-anthraquinone Drugs 0.000 claims description 30
RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 claims description 29
150000001875 compounds Chemical class 0.000 claims description 27
125000004122 cyclic group Chemical group 0.000 claims description 17
239000007859 condensation product Substances 0.000 claims description 16
239000012978 lignocellulosic material Substances 0.000 claims description 16
239000002245 particle Substances 0.000 claims description 15
238000001035 drying Methods 0.000 claims description 9
-1 aromatic sulfonic acids Chemical class 0.000 claims description 8
238000009835 boiling Methods 0.000 claims description 8
239000003945 anionic surfactant Substances 0.000 claims description 7
239000003960 organic solvent Substances 0.000 claims description 7
239000003755 preservative agent Substances 0.000 claims description 6
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230000000087 stabilizing effect Effects 0.000 claims description 2
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229920001131 Pulp (paper) Polymers 0.000 abstract description 3
150000001923 cyclic compounds Chemical class 0.000 abstract 1
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230000029087 digestion Effects 0.000 description 24
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238000009826 distribution Methods 0.000 description 10
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 9
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238000003756 stirring Methods 0.000 description 7
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 6
FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
229920005610 lignin Polymers 0.000 description 6
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 6
238000002156 mixing Methods 0.000 description 6
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238000010422 painting Methods 0.000 description 6
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JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 5
239000002002 slurry Substances 0.000 description 5
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239000002253 acid Substances 0.000 description 4
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229940021013 electrolyte solution Drugs 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
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230000002378 acidificating effect Effects 0.000 description 3
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150000001298 alcohols Chemical class 0.000 description 3
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239000007788 liquid Substances 0.000 description 3
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HCJLVWUMMKIQIM-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorophenolate Chemical compound [Na+].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HCJLVWUMMKIQIM-UHFFFAOYSA-M 0.000 description 3
YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 2
CQGDBBBZCJYDRY-UHFFFAOYSA-N 1-methoxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2OC CQGDBBBZCJYDRY-UHFFFAOYSA-N 0.000 description 2
FDLFMPKQBNPIER-UHFFFAOYSA-N 1-methyl-3-(3-methylphenoxy)benzene Chemical compound CC1=CC=CC(OC=2C=C(C)C=CC=2)=C1 FDLFMPKQBNPIER-UHFFFAOYSA-N 0.000 description 2
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
NJWGQARXZDRHCD-UHFFFAOYSA-N 2-methylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3C(=O)C2=C1 NJWGQARXZDRHCD-UHFFFAOYSA-N 0.000 description 2
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
PCFMUWBCZZUMRX-UHFFFAOYSA-N 9,10-Dihydroxyanthracene Chemical compound C1=CC=C2C(O)=C(C=CC=C3)C3=C(O)C2=C1 PCFMUWBCZZUMRX-UHFFFAOYSA-N 0.000 description 2
150000004058 9,10-anthraquinones Chemical class 0.000 description 2
241000609240 Ambelania acida Species 0.000 description 2
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229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000009533 lab test Methods 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
238000005259 measurement Methods 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000003973 paint Substances 0.000 description 1
239000000123 paper Substances 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
150000004714 phosphonium salts Chemical class 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
239000001205 polyphosphate Substances 0.000 description 1
235000011176 polyphosphates Nutrition 0.000 description 1
150000007519 polyprotic acids Polymers 0.000 description 1
229920001021 polysulfide Polymers 0.000 description 1
230000008092 positive effect Effects 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
238000005086 pumping Methods 0.000 description 1
230000003134 recirculating effect Effects 0.000 description 1
239000013049 sediment Substances 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
239000006163 transport media Substances 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C3/00—Pulping cellulose-containing materials
- D21C3/22—Other features of pulping processes
- D21C3/222—Use of compounds accelerating the pulping processes

Landscapes

Paper (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)
Compositions Of Macromolecular Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Micro-Organisms Or Cultivation Processes Thereof (AREA)
Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Confectionery (AREA)

NO791974A 1978-06-21 1979-06-13 Middel til anvendelse ved cellestoffgjenvinning og fremgangsmaate til cellestoffgjenvinning NO791974L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782827111 DE2827111A1 (de)	1978-06-21	1978-06-21	Mittel zur verwendung bei der zellstoffgewinnung

Publications (1)

Publication Number	Publication Date
NO791974L true NO791974L (no)	1979-12-27

Family

ID=6042304

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO791974A NO791974L (no)	1978-06-21	1979-06-13	Middel til anvendelse ved cellestoffgjenvinning og fremgangsmaate til cellestoffgjenvinning

Country Status (16)

Country	Link
EP (1)	EP0006201B1 (de)
JP (1)	JPS556585A (de)
AT (1)	ATE3449T1 (de)
AU (1)	AU537690B2 (de)
BR (1)	BR7903896A (de)
CA (1)	CA1140706A (de)
DE (2)	DE2827111A1 (de)
ES (1)	ES481720A1 (de)
FI (1)	FI66442C (de)
IN (1)	IN151933B (de)
NO (1)	NO791974L (de)
NZ (1)	NZ190753A (de)
PH (1)	PH15789A (de)
PT (1)	PT69751A (de)
TR (1)	TR20455A (de)
ZA (1)	ZA793064B (de)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2925545A1 (de) *	1979-06-25	1981-01-29	Bayer Ag	Verfahren zur herstellung eines mittels, das organische, cyclische, keto- und/oder hydrogruppen enthaltende verbindungen und tenside enthaelt, sowie verfahren zur zellstoffgewinnung unter verwendung dieses mittels
US4295928A (en) *	1980-08-07	1981-10-20	Nalco Chemical Company	Phenolic compounds as viscosity preservatives during hypochlorite pulp bleaching
JPS57177080A (en) *	1981-04-24	1982-10-30	Kawasaki Kasei Chem Ltd	Preparation of composition for digestion assistant
JPS6197492A (ja) *	1984-10-18	1986-05-15	川崎化成工業株式会社	高濃度パルプ蒸解助剤水溶液
CA1321449C (en) *	1988-03-02	1993-08-24	Cheng-I Chen	Process for producing kraft pulp for paper
DE3905311C2 (de) *	1989-02-21	1994-09-29	Bayer Ag	Verfahren zur Herstellung von Anthrachinon/Tensid-Gemischen und Verwendung dieser Gemische
AU626407B2 (en) *	1989-05-19	1992-07-30	Betz International, Inc.	Process for producing kraft pulp for paper
CA2111921A1 (en) *	1992-12-21	1994-06-22	Kenji Kumagai	Formulated composition of pulp digesting assistant agent
WO1995029288A1 (fr) *	1994-04-26	1995-11-02	Harima Chemicals, Inc.	Adjuvant pour lessivage des pulpes
US6346536B1 (en)	1997-09-03	2002-02-12	Guilford Pharmaceuticals Inc.	Poly(ADP-ribose) polymerase inhibitors and method for treating neural or cardiovascular tissue damage using the same
MY182109A (en)	2014-07-10	2021-01-18	Leaf Sciences Pty Ltd	Methods for hydrolysing lignocellulosic material
CN106661834B (zh) *	2014-07-10	2020-09-15	利芙科学私人有限公司	用于处理木质纤维素材料的方法
JP7165323B2 (ja) *	2018-07-04	2022-11-04	株式会社片山化学工業研究所	パルプ蒸解助剤、及びそれを用いた化学パルプの製造方法
US20240175205A1 (en) *	2022-11-29	2024-05-30	Solenis Technologies, L.P.	Method for digesting lignocellulosic material

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2049567A (en) *	1934-06-05	1936-08-04	Du Pont	Manufacture of paper pulp
FR950573A (fr) *	1947-07-09	1949-09-30		Application de mouillants à la fabrication des pâtes à papier
SE384883B (sv) *	1974-09-06	1976-05-24	Kopparfors Ab	Sett att oka cellulosautbytet vid sulfitkokning av ved
FI783563A (fi) *	1977-12-01	1979-06-02	Sandoz Ag	Foerbaettringar i och angaoende organiska foereningar
DE2816473A1 (de) *	1978-04-15	1979-10-25	Bayer Ag	Dispersion zur verwendung bei der zellstoffgewinnung

1978
- 1978-06-21 DE DE19782827111 patent/DE2827111A1/de not_active Withdrawn
1979
- 1979-05-21 IN IN355/DEL/79A patent/IN151933B/en unknown
- 1979-06-11 PT PT69751A patent/PT69751A/pt unknown
- 1979-06-11 AT AT79101858T patent/ATE3449T1/de not_active IP Right Cessation
- 1979-06-11 DE DE7979101858T patent/DE2965428D1/de not_active Expired
- 1979-06-11 EP EP79101858A patent/EP0006201B1/de not_active Expired
- 1979-06-13 NO NO791974A patent/NO791974L/no unknown
- 1979-06-18 NZ NZ190753A patent/NZ190753A/xx unknown
- 1979-06-19 JP JP7637479A patent/JPS556585A/ja active Pending
- 1979-06-19 TR TR20455A patent/TR20455A/xx unknown
- 1979-06-19 CA CA000330073A patent/CA1140706A/en not_active Expired
- 1979-06-19 PH PH22668A patent/PH15789A/en unknown
- 1979-06-19 FI FI791949A patent/FI66442C/fi not_active IP Right Cessation
- 1979-06-20 ZA ZA793064A patent/ZA793064B/xx unknown
- 1979-06-20 ES ES481720A patent/ES481720A1/es not_active Expired
- 1979-06-20 AU AU48210/79A patent/AU537690B2/en not_active Ceased
- 1979-06-20 BR BR7903896A patent/BR7903896A/pt unknown

Also Published As

Publication number	Publication date
FI66442B (fi)	1984-06-29
EP0006201B1 (de)	1983-05-18
PH15789A (en)	1983-03-25
AU537690B2 (en)	1984-07-05
EP0006201A1 (de)	1980-01-09
FI66442C (fi)	1984-10-10
ZA793064B (en)	1980-08-27
BR7903896A (pt)	1980-02-20
PT69751A (en)	1979-07-01
JPS556585A (en)	1980-01-18
DE2827111A1 (de)	1980-01-10
NZ190753A (en)	1981-07-13
CA1140706A (en)	1983-02-08
ES481720A1 (es)	1980-02-16
DE2965428D1 (en)	1983-07-07
AU4821079A (en)	1980-01-03
TR20455A (tr)	1981-07-14
FI791949A (fi)	1979-12-22
IN151933B (de)	1983-09-03
ATE3449T1 (de)	1983-06-15

Publication	Publication Date	Title
NO791974L (no)	1979-12-27	Middel til anvendelse ved cellestoffgjenvinning og fremgangsmaate til cellestoffgjenvinning
US3841887A (en)	1974-10-15	Dyestuff compositions containing lignin surfactants carboxy substituted
US4308203A (en)	1981-12-29	Sulfonated lignin dispersants and dyestuffs
KR101319163B1 (ko)	2013-10-16	진남색 및 흑색 혼합물, 이들의 제조 방법, 및 히드록시기함유 물질의 염색을 위한 이들의 용도
NO154313B (no)	1986-05-20	Fremgangsmaate for dispergering av talk.
US3672817A (en)	1972-06-27	Alkylene chlorohydrin,oxide or carbonate modified sulfonated lignins in a disperse or vat dye cake
CN102587180B (zh)	2014-02-19	一种烷基磺酸盐蒸煮助剂
NO801730L (no)	1980-12-29	Fremgangsmaate til fremstilling av et middel som inneholder organiske, cykliske, keto- og/eller hydroksygruppeholdige forbindelser og tensider samt fremgangsmaate til cellulosefremstilling under anvendelse av dette middel
JPH0657804B2 (ja)	1994-08-03	冷水分散性染料粒子
US4351640A (en)	1982-09-28	Dye powder formulation
US2613218A (en)	1952-10-07	Vacuum neutralization of detergents
CN109750525A (zh)	2019-05-14	一种纳米级液体分散染料及其制备方法
NO803624L (no)	1981-06-18	Dispersjoner av dinitroantrakinoner fremgangsmaate til deres fremstilling og deres anvendelse
KR830002040B1 (ko)	1983-10-07	펄프제조용 약제
JPS6411669B2 (de)	1989-02-27
US20020121347A1 (en)	2002-09-05	Chemical composition and process
CN105585858A (zh)	2016-05-18	一种改性沥青组合物颗粒及其制备方法
DE2646273A1 (de)	1978-04-20	Verfahren zur herstellung von feinkristallinen aufhellern der bis- triazinylamino-stilbenreihe in der beta-kristallform
CA1136808A (en)	1982-12-07	Dispersion for use in pulp production
US4588412A (en)	1986-05-13	Solid formulations of dyes which are sparingly soluble or insoluble in water
MXPA96001982A (es)	2002-05-23	Preparaciones colorantes para textiles.
US4359321A (en)	1982-11-16	Dye compositions and method of using same
US2685494A (en)	1954-08-03	Dispersible vat dye powder
US2678256A (en)	1954-05-11	Dispersible dyestuff powders
CN1092631C (zh)	2002-10-16	易分散蒽醌及其生产和使用方法