WO2005012540A1 - Enzymatic depolymerisation of carboxymethylcellulose in hydroalcoholic solutions - Google Patents
Enzymatic depolymerisation of carboxymethylcellulose in hydroalcoholic solutions Download PDFInfo
- Publication number
- WO2005012540A1 WO2005012540A1 PCT/EP2004/051491 EP2004051491W WO2005012540A1 WO 2005012540 A1 WO2005012540 A1 WO 2005012540A1 EP 2004051491 W EP2004051491 W EP 2004051491W WO 2005012540 A1 WO2005012540 A1 WO 2005012540A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- carboxymethylcellulose
- preparation
- aqueous solution
- cellulase
- carboxymetylcellulose
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/20—Post-etherification treatments of chemical or physical type, e.g. mixed etherification in two steps, including purification
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/14—Preparation of compounds containing saccharide radicals produced by the action of a carbohydrase (EC 3.2.x), e.g. by alpha-amylase, e.g. by cellulase, hemicellulase
Definitions
- This invention refers to the procedure for the preparation of aqueous concentrated solutions of low viscosity carboxymethylcellulose by enzymatic depolymerisation of medium viscosity carboxymethylcellulose in the form of dispersed powder in a hydro-alcoholic heterogeneous medium, and to such aqueous concentrated solutions.
- the aqueous solutions of carboxymethylcellulose obtained with the procedure of the invention have low viscosity, can be easily handled with the conventional industrial pumping devices, have high content of carboxymethylcellulose, are stable and ready-to-use.
- Background Art [0003] Low viscosity carboxymethylcellulose is employed in various industrial fields, where excellent filming properties and/or adhesion are required and highly concentrated carboxymethylcellulose solutions are needed.
- the rheological properties of carboxymethylcellulose are strongly influenced by its molecular weight; the degree of polymerisation of carboxymethylcellulose (DP) is an index of molecular weight and is therefore directly related to the rheological behaviour of carboxymethylcellulose solutions, thus to viscosity.
- High DPs which are characteristic of high viscosity carboxymethylcellulose preparations, are obtained using as starting material the so called cellulose linters (cotton cellulose); medium DPs, typical of medium viscosity carboxymethylcelluloses, are obtained using wood cellulose as starting material.
- low or very low viscosity and low DP carboxymethylcellulose are obtained by depolymerising medium or high viscosity carboxymethylcellulose.
- low viscosity carboxymethylcellulose we mean carboxymethylcellulose whose aqueous solutions at 20-40 % by weight (wt%) have Broo field viscosity from 2000 to 5000 mPa*s, at 20°C and 20 rpm; with the expression “medium viscosity carboxymethylcellulose” we mean carboxymethylcellulose whose aqueous solutions at 4 wt% have Brookfield viscosity from 20 to 1000 mPa*s, at 20°C and 20 rpm.
- the process according to the invention can be accomplished by means of normal industrial reactors; it avoids the need for the elimination of large quantities of water (with considerable saving in operating time and energy) and it preserves the product from excessive thermal stress.
- the obtained dispersion is heated at a temperature of 35-55 °C, 0.5 to 10 pbw (each 100 pbw of carboxymethylcellulose) of a cellulase preparation are added, and the mixture is stirred at this temperature for 60-200 minutes;
- the cellulase preparation is deactivated by alkalinising at a pH from 11 to 13 and heating at 60-70°C for 20-120 minutes;
- the final carboxymethylcellulose concentration is adjusted by adding water.
- a catalase an enzyme which dismutates hydrogen peroxide into oxygen and water
- the carboxymethylcellulose normally used for the realisation of the present invention has a DS (Degree of substitution) comprised between 0.5 and 1.0, preferably between 0.6 and 0.8; preferably its Brookfield viscosity, at 4 wt%, 20 rpm and 20 °C, is from 20 to 500 mP*s.
- DS Degree of substitution
- the alcohols which can be used for the realisation of the invention are those completely miscible with water in all proportions: particularly preferred are ethanol and isopropanol.
- the pH of the dispersion from step a. is adjusted to 5-7 by adding acetic acid or NaOH.
- cellulase that can be used in the process of the invention are the commercially available preparation of cellulase containing natural cellulase complexes having endoglucanase activity (EG-I, EG-II, EGIII), exoglucanase activity (CBH-I and CBH-II) and ⁇ - glucosidase activity, or, preferably, preparation of cellulase without CBH-I but EG-I and EG-II enriched, or having a single EG-III activity expressed by a cloned gene; by way of example we cite the products Indiage ® Super L and Indiage ® MAXL, commercialised by Genencor; Ecostone ® L/900 from AB Enzymes; Denimax ® 991 L, Denimax ® 601 L, Denimax ® 399 and Denimax ® Acid XCL from Novozymes, Rocksoft ® ACE from Dyadic International.
- the utilisable microbial sources (strains) of the preparation of cellulase are several, such as: Trichoderma, Streptomyces, Aspergillus, Humicola, Mycelophthora, Chrisosporium, Melanocarpus ecc.
- alcohol removal is performed by distillation under vacuum at a temperature of 40-45'C for periods that can vary from 4 to 12 hours.
- aqueous solutions containing from 25 to 40 wt% of carboxymethylcellulose, obtained by enzymatic depolymerisation in hydro- alcoholic heterogeneous phase from medium viscosity carboxymethylcellulose, and having Brookfield viscosity from 2000 to 5000 mPa * s, are stable and are a fundamental aspect of the present invention.
- stable aqueous solutions we mean aqueous solutions whose Brookfield viscosity at 20°C and 20 rpm, expressed in mPa*s, does not vary of more than by 10% when measured after three months at room temperature.
- aqueous solutions of the invention has colour characteristics which render them suitable for direct use, without the need for whitening treatments, but can be further whitened, when specific application requirements are present.
- Carbocel ® MM3 150 (carboxymethylcellulose having DS 0.6-0.8, Brookfield viscosity 200-500 mPa*s, at 4 wt%, from Lamberti SpA) are dispersed under stirring in 80 Kg of a mixture water/isopropanol (containing 41 wt% of isopropanol).
- the mixture is cooled to 50°C, 20 Kg of a 30 wt% aqueous solution of hydrogen peroxide are added, heated to 60°C and stirred for 20 minutes.
- 1000 g of Terminox ® 50 Ultra (catalase from Novozymes, DK) are added and the mixture is stirred for 10 minutes more.
- the solution is cooled to 30°C and 2.5 Kg of Carbosan CD40 (biocide from Lamberti SpA) are added.
- Example 3 An aqueous solution of carboxymethylcellulose having a dry content of 25 wt%, Brookfield viscosity, at 20 rpm and 20°C, of 4400 mPa*s, and pH 8 is obtained; the viscosity of the solution is stable (varying less than 10% In three months).
- Example 3 In a 80001 reactor 1450 Kg of Carbocel ® MM3 (carboxymethylcellulose having DS 0.6-0.8, Brookfield viscosity 200-500 mPa*s, at 4 wt%, from Lamberti SpA) are dispersed under stirring in 5720 Kg of a mixture water/ethanol (containing 49 wt% of ethanol).
- the dispersion is stirred for 145 minutes; a mixture of water and ethanol is removed by distillation under vacuum at 40-43°C over a period of 5.5 hours until the residual concentration of alcohol is 0.5 wt% (determined by Gas Chromatography); 80 Kg of 50 wt% NaOH are added and the mixture is stirred at 67°C for 60 minutes.
- the mixture is cooled to 60°C, 38.7 Kg of a 30 wt% aqueous solution of hydrogen peroxide are added, heated to 65 C C and stirred for 30 minutes.
- Terminox ® 50 Ultra (a catalase from Novozymes, DK) are added and the mixture is stirred for 20 minutes more.
- An aqueous solution of carboxymethylcellulose having a dry content of 36.4 wt%, Brookfield viscosity, at 20 rpm and 20°C, of 4400 mPa*s, and pH 7.8 is obtained; the viscosity of the solution is stable (varying less than 10% in three months).
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04766221A EP1649035A1 (en) | 2003-07-17 | 2004-07-14 | Enzymatic depolymerisation of carboxymethylcellulose in hydroalcoholic solutions |
US10/564,741 US20060281154A1 (en) | 2003-07-17 | 2004-07-14 | Enzymatic depolymerisation of carboxymethylcellulose in hydroalcoholic solutions |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT000025A ITVA20030025A1 (en) | 2003-07-17 | 2003-07-17 | ENZYMATIC DEPOLYMERIZATION OF CARBOSSIMETHYL CELLULOSE AND RELATED PRODUCTS. |
ITVA2003A000025 | 2003-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005012540A1 true WO2005012540A1 (en) | 2005-02-10 |
Family
ID=34113448
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2004/051491 WO2005012540A1 (en) | 2003-07-17 | 2004-07-14 | Enzymatic depolymerisation of carboxymethylcellulose in hydroalcoholic solutions |
Country Status (4)
Country | Link |
---|---|
US (1) | US20060281154A1 (en) |
EP (1) | EP1649035A1 (en) |
IT (1) | ITVA20030025A1 (en) |
WO (1) | WO2005012540A1 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ITVA20100045A1 (en) * | 2010-05-25 | 2011-11-26 | Lamberti Spa | METHOD FOR SEALING PODS |
US8560760B2 (en) | 2007-01-31 | 2013-10-15 | Microsoft Corporation | Extending flash drive lifespan |
WO2015144596A1 (en) | 2014-03-24 | 2015-10-01 | Lamberti Spa | Moisturizing agents |
US9535625B2 (en) | 2007-03-06 | 2017-01-03 | Bohdan Raciborski | Selectively utilizing a plurality of disparate solid state storage locations |
WO2018060262A1 (en) | 2016-09-28 | 2018-04-05 | Cp Kelco Oy | Detergent compositions comprising ultra-low molecular weight polysaccharides |
IT201900012597A1 (en) | 2019-07-22 | 2021-01-22 | Lamberti Spa | COMPOSITIONS OF PLASTER |
IT202000021232A1 (en) | 2020-09-08 | 2022-03-08 | Lamberti Spa | METHOD FOR IMPROVING THE PERFORMANCE OF SYSTEMIC ACTIVE SUBSTANCES AND MICROBIAL INOCULANTS |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112608388B (en) * | 2020-12-28 | 2022-11-22 | 浙江圣兆药物科技股份有限公司 | Refining method of sodium carboxymethylcellulose for injection |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63243181A (en) * | 1987-03-30 | 1988-10-11 | Pentel Kk | Ink for ball point pen |
EP0382577A1 (en) * | 1989-02-10 | 1990-08-16 | Alko Group Ltd. | Enzymatic cellulose derivative hydrolysate |
EP0465992A1 (en) * | 1990-07-02 | 1992-01-15 | Aqualon Company | High solids low viscosity polysaccharide composition |
GB2281073A (en) * | 1993-07-26 | 1995-02-22 | Courtaulds Plc | Hydrolysis of polysaccharides |
EP0708113A1 (en) * | 1994-09-26 | 1996-04-24 | Hoechst Aktiengesellschaft | Process for preparing low molecular weight cellulose ethers |
-
2003
- 2003-07-17 IT IT000025A patent/ITVA20030025A1/en unknown
-
2004
- 2004-07-14 US US10/564,741 patent/US20060281154A1/en not_active Abandoned
- 2004-07-14 EP EP04766221A patent/EP1649035A1/en not_active Withdrawn
- 2004-07-14 WO PCT/EP2004/051491 patent/WO2005012540A1/en not_active Application Discontinuation
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63243181A (en) * | 1987-03-30 | 1988-10-11 | Pentel Kk | Ink for ball point pen |
EP0382577A1 (en) * | 1989-02-10 | 1990-08-16 | Alko Group Ltd. | Enzymatic cellulose derivative hydrolysate |
EP0465992A1 (en) * | 1990-07-02 | 1992-01-15 | Aqualon Company | High solids low viscosity polysaccharide composition |
GB2281073A (en) * | 1993-07-26 | 1995-02-22 | Courtaulds Plc | Hydrolysis of polysaccharides |
EP0708113A1 (en) * | 1994-09-26 | 1996-04-24 | Hoechst Aktiengesellschaft | Process for preparing low molecular weight cellulose ethers |
Non-Patent Citations (4)
Title |
---|
DATABASE BIOSIS [online] BIOSCIENCES INFORMATION SERVICE, PHILADELPHIA, PA, US; 1981, KLESOV A A ET AL: "STABILITY OF SOLUBLE AND IMMOBILIZED CELLULASES IN WATER ALCOHOL SYSTEMS", XP002306857, Database accession no. PREV198273053322 * |
DATABASE WPI Section Ch Week 198846, Derwent World Patents Index; Class A11, AN 1988-327895, XP002306858 * |
PRIKLADNAYA BIOKHIMIYA I MIKROBIOLOGIYA, vol. 17, no. 2, 1981, pages 216 - 224, ISSN: 0555-1099 * |
TJERNELD F ET AL: "ENZYMATIC CELLULOSE HYDROLYSIS IN ATTRITION BIOREACTOR COMBINED WITH AN AQUEOUS TWO-PHASE SYSTEM", BIOTECHNOLOGY AND BIOENGINEERING. INCLUDING: SYMPOSIUM BIOTECHNOLOGY IN ENERGY PRODUCTION AND CONSERVATION, JOHN WILEY & SONS. NEW YORK, US, vol. 37, no. 9, 15 April 1991 (1991-04-15), pages 876 - 882, XP000179051, ISSN: 0006-3592 * |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8560760B2 (en) | 2007-01-31 | 2013-10-15 | Microsoft Corporation | Extending flash drive lifespan |
US9535625B2 (en) | 2007-03-06 | 2017-01-03 | Bohdan Raciborski | Selectively utilizing a plurality of disparate solid state storage locations |
ITVA20100045A1 (en) * | 2010-05-25 | 2011-11-26 | Lamberti Spa | METHOD FOR SEALING PODS |
WO2011147721A1 (en) | 2010-05-25 | 2011-12-01 | Lamberti Spa | Pod sealing method |
RU2558438C2 (en) * | 2010-05-25 | 2015-08-10 | Ламберти Спа | Method of pod sealing |
WO2015144596A1 (en) | 2014-03-24 | 2015-10-01 | Lamberti Spa | Moisturizing agents |
US9464227B2 (en) | 2014-03-24 | 2016-10-11 | Lamberti Spa | Moisturizing agents |
WO2018060262A1 (en) | 2016-09-28 | 2018-04-05 | Cp Kelco Oy | Detergent compositions comprising ultra-low molecular weight polysaccharides |
IT201900012597A1 (en) | 2019-07-22 | 2021-01-22 | Lamberti Spa | COMPOSITIONS OF PLASTER |
WO2021013751A1 (en) | 2019-07-22 | 2021-01-28 | Lamberti Spa | Gypsum compositions |
IT202000021232A1 (en) | 2020-09-08 | 2022-03-08 | Lamberti Spa | METHOD FOR IMPROVING THE PERFORMANCE OF SYSTEMIC ACTIVE SUBSTANCES AND MICROBIAL INOCULANTS |
WO2022053325A1 (en) | 2020-09-08 | 2022-03-17 | Lamberti Spa | Method for improving the performances of systemic active substances and microbial inoculants |
Also Published As
Publication number | Publication date |
---|---|
ITVA20030025A1 (en) | 2005-01-18 |
EP1649035A1 (en) | 2006-04-26 |
US20060281154A1 (en) | 2006-12-14 |
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