EP3938570A1 - A method for bleaching cotton fabrics - Google Patents
A method for bleaching cotton fabricsInfo
- Publication number
- EP3938570A1 EP3938570A1 EP19920252.4A EP19920252A EP3938570A1 EP 3938570 A1 EP3938570 A1 EP 3938570A1 EP 19920252 A EP19920252 A EP 19920252A EP 3938570 A1 EP3938570 A1 EP 3938570A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- bleaching
- cotton
- weight
- hot
- hydrogen peroxide
- 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.)
- Pending
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
- D06L4/12—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen combined with specific additives
Definitions
- the present invention relates to a method for bleaching raw cotton or cotton fabrics.
- the present invention particularly relates to a hot bleaching method for bleaching raw cotton or cotton fabrics by using peroxide.
- finishing is the process of cleaning the cotton for the dyeing process, after the cotton is processed as fiber, fabric or yarn. This process is based on removal of all of the dirts from fiber except cellulose.
- Bleaching process is substantially important for removing oil, dirt and brown pigments existing in the nature of cotton and for obtaining a floor which has uniform characteristics before dyeing. There is no need for bleaching to be very good for dyeing except light and brilliant colors. However, it is important that the hydrophility (water absorption) is good, there remains no bleaching wastes (hydrogen peroxide, etc.) thereon and dyeing shall be realized with a light acidic bath. On the other hand, a good bleaching process is needed for dyeing of light colored fabrics.
- Bleaching activators create peracid by reacting with perhydroxyl anion which occurs as a result of deterioration of hydrogen peroxide in the presence of alkali and hydrogen peroxide during the bleaching process.
- Peracids provide more effective bleaching when compared with the bleaching process realized by only hydrogen peroxide at low temperature.
- hydrogen peroxide bleaching realized by using bleaching activators a better whiteness level and higher polymerization degree are obtained at low temperature and in short time when compared with traditional peroxide bleaching.
- TAED tetra-acetyl- ethylene-diamine
- NOBS nano-benzoiloxy-benzene sulphonate
- a liquid detergent comprising anhydrous bleaching activator together with surfactants.
- the liquid matrix comprises TAED as the activator.
- the amount of TAED is low and it can be stored in a stable manner only when it has high viscosity.
- the document with number KR201301 13245 relates to an environment-friendly cotton fiber bleaching method, using an enzyme, which does not give harm to humans.
- the cotton fiber is cleaned and bleached in a bath comprising cellulase, stabilizer, Na2CC>3, triacetine, hydrogen peroxide, water, bleaching agent and catalase.
- the present invention relates to a method for bleaching raw cotton or cotton fabrics, for meeting the above mentioned requirements and for eliminating the above mentioned disadvantages and for bringing new advantages to the related technical field.
- the primary object of the present invention is to obtain a hot bleaching method realized at lowered temperatures.
- An object of the present invention is to obtain a bleaching method realized at lowered pH values and where neutralization process is not needed by means of addition of acid afterwards.
- Another object of the present invention is to obtain a bleaching method which requires rinsing steps with reduced number.
- Another object of the present invention is to obtain a bleaching method where water consumption is reduced.
- Another object of the present invention is to obtain a bleaching method where the waste water load is reduced.
- Another object of the present invention is to obtain an environment-friendly bleaching method.
- Another object of the present invention is to obtain a bleaching method which eliminates problems like weight loss, decrease in break and tear strength in fabric.
- a similar object of the present invention is to obtain a bleaching method which decreases energy and time loss.
- the present invention describes a method for hot or cold bleaching of raw cotton or cotton fabrics in the presence of hydrogen peroxide, said method comprises the step of adding at least one glycol derived compound, which is in mixture form with X-COCH 3 dissolved in water, to the bleaching bath comprising hydrogen peroxide and caustic and which is in contact with raw cotton or cotton fabric, and X group in said X-COCH 3 structure is selected from at least one O-acetylated acetyl donor selected from salicylic acid (C 6 H 4 (OH)COOH), Acetic acid (CH 3 COOH), Diacetin (CH 3 COOCH 2 ) 2 CHOH), Cellulose ((C 6 H 10 O 5 )n), Glicose (C 6 H 12 O 6 ), Sucrose (C 1 2 H 22 O 1 1 ).
- X group in said X-COCH 3 structure is selected from at least one O-acetylated acetyl donor selected from salicylic acid (C 6 H 4 (OH)COOH
- X group in said X-COCH 3 structure is diacetin ((CH 3 COOCH 2 ) 2 CHOH) or salicylic acid (C 6 H 4 (OH)COOH).
- said glycol derived compound is selected from ethylene glycol, polyethylene glycol derivatives and glycerol esters.
- said glycol derived compound is propane-1 ,2,3 triol.
- the bleaching bath moreover comprises peroxide stabilizer.
- the bleaching bath moreover comprises wetting agent.
- the hot bleaching process is realized between 60 and 80°C.
- the hot bleaching process is realized at 75°C.
- the hot bleaching process is realized between 30 and 90 minutes.
- the hot bleaching process is realized between 30 and 60 minutes.
- the hot bleaching bath comprises caustic between 0.1% and 1% by weight, hydrogen peroxide between 0.1% and 1 % by weight and O-acetylated acetyl donor (-O-COCH 3 ) between 0.1% and 1 % by weight.
- the cold bleaching process is realized at room temperature and the cold bleaching bath comprises caustic between 5% and 10% by weight, peroxide between 6% and 10% by weight and O-acetylated acetyl donor between 0.5% and 2% by weight.
- the molar proportion of glycol derived compound to O-acetylated acetyl donor or donors is between 1 :1 and 1 :10.
- the present invention moreover describes a method for hot or cold bleaching of raw cotton or cotton fabrics in the presence of hydrogen peroxide, wherein the following steps are provided: heating a bleaching bath, comprising hydrogen peroxide between 0.1 % and 1% by weight, caustic between 0.1 % and 1% by weight, stabilizer and wetting agent and which is in contact with the raw cotton or cotton fabric to be bleached, to 75°C, afterwards adding O- acetylated diacetin or salicylic acid dissolved in water in mixture form with propane-1 ,2,3 triol to the bleaching bath, and subjecting raw cotton or cotton fabric to bleaching process for 30- 60 minutes at 75°C.
- the present invention moreover describes the usage of acetyl donor, selected from at least one O-acetylated salicylic acid (C 6 H (OH)COOH), Acetic acid (CH 3 COOH), Diacetin (CH 3 COOCH 2 ) 2 CHOH), Cellulose ((C 6 H 10 O 5 )n), Glicose (C 6 H 12 O 6 ), Sucrose (C 1 2 H 22 O 1 1 ) dissolved in water in mixture form with at least one glycol derivative, as a peroxide activator for hot or cold bleaching of raw cotton or cotton fabrics.
- acetyl donor selected from at least one O-acetylated salicylic acid (C 6 H (OH)COOH), Acetic acid (CH 3 COOH), Diacetin (CH 3 COOCH 2 ) 2 CHOH), Cellulose ((C 6 H 10 O 5 )n), Glicose (C 6 H 12 O 6 ), Sucrose (C 1 2 H 22 O 1 1 ) dissolved in water in mixture
- said usage is for hot bleaching of raw cotton or cotton fabrics.
- said glycol derived compound is selected from ethylene glycol, polyethylene glycol derivatives and glycerol esters.
- said glycol derived compound is propane-1 ,2,3 triol.
- the molar proportion of glycol derived compound to O-acetylated acetyl donor or donors is between 1 :1 and 1 :10.
- a method for bleaching raw cotton or cotton fabrics by using peroxide.
- at least one bleaching bath is used where raw cotton or cotton fabrics are bleached.
- Said bleaching bath comprises hydrogen peroxide.
- Hydrogen peroxide forms active oxygen and oxidizes the color components inside the fiber and decomposes them and thus, hydrogen peroxide makes them colorless.
- the bleaching bath of the present invention moreover comprises peroxide stabilizer which supports decomposition of peroxide in a stepped manner during the bleaching process realized in hot medium and which supports formation of uniform/homogeneous whitening.
- peroxide stabilizers which are preferred according to the performances of controlling peroxide decomposition, there are alkali metal salts, phosphinic acids and salts thereof. Other suitable stabilizers can also be used.
- the bleaching bath moreover comprises caustic (sodium hydroxide).
- caustic sodium hydroxide
- Caustic cleans the impurities by saponifying the impurities and triggers decomposition of hydrogen peroxide into active oxygen.
- caustic sponifies the oil derived impurities existing in the structure of cotton and directly affects water absorption and whiteness characteristics.
- Potassium hydroxide can also be used for the same purpose instead of caustic.
- peroxide activator peroxide activator (X- COCH3) comprising at least one acetyl group is used as the peroxide activator.
- Peroxide activator enters into reaction with hydrogen peroxide in the bleaching bath and active oxygen occurs as a result of this reaction.
- the chemical structure of the peroxide activator (X-COCH3) comprising at least one acetyl group is shown by Formula I.
- acetyl group donor or donors are used as the peroxide activator.
- Said acetyl group donor or donors is/are selected from N-acetylated and O-acetylated acetyl donor molecules.
- N-acetylated acetyl donor or donors is/are selected from N,N,N'N'-tetra- acetyl-ethylene-diamine (TAED), N-acetyl glycine, N-acetyl-DL-metionine, N-acetyl-L-sistein and acetaminopheny (4-acetamidophenol).
- TAED N,N,N'N'-tetra- acetyl-ethylene-diamine
- N-acetyl glycine N-acetyl-DL-metionine
- N-acetyl-L-sistein N-acetaminopheny (4-acetamidophenol
- O-acetylated acetyl donor or donors is/are selected from sugar acetates like triacetine, penta-acetate-glicose and octa-acetate sucrose, acetate mannitole (acetate esters of sugars), acetic anhydride and acetyl salicylic acid.
- triacetine or acetyl salicylic acid is used as the O- acetylated acetyl donor.
- X one of the structures of salicylic acid (C 6 H (OH)COOH), Acetic acid (CH 3 COOH), N,N,N- triacetylethylenediamine (C 8 H 14 N 2 O 3 ), Diacetin (CH 3 COOCH 2 ) 2 CHOH), Glycine (C 2 H 5 NO 2 ), Cysteine (C 3 H7NO2S), Aminophenol (C 6 H7NO), Cellulose ((C 6 H 10 O 5 )n), Glicose (C 6 H12O 6 ), Sucrose (C 12 H 22 O 11 ), Methionine (C 5 H 11 NO 2 S) can be used.
- salicylic acid C 6 H (OH)COOH
- Acetic acid CH 3 COOH
- N,N,N- triacetylethylenediamine C 8 H 14 N 2 O 3
- Diacetin CH 3 COOCH 2 ) 2 CHOH
- Glycine C 2 H 5 NO 2
- Cysteine C 3 H7NO2S
- salicylic acid C 6 H 4 (OH)COOH
- Acetic acid CH 3 COOH
- Diacetin CH 3 COOCH 2 ) 2 CHOH
- Cellulose ((C 6 H 10 0 5 ) n )
- Glicose C 6 H12O 6
- Sucrose C 12 H 22 O 11
- X for the X-COCH3 acetyl donor, diacetin (CH 3 COOCH 2 ) 2 CHOH) is used since it provides peracetic acid concentration to be higher.
- salcylic acid C 6 H 4 (OH)COOH
- peroxide activator acetyl donor enters into reaction with hydrogen peroxide in the bleaching bath and peracetic acid is formed which has a stronger bleaching effect.
- Peracetic acid formation from hydrogen peroxide by means of N,N,N'N'-tetra-acetyl-ethylene-diamine (TAED), which is an N-acetylated acetyl donor, is realized according to the reaction schema given below.
- Such reactions are realized by means of attacking of the acetyl group in basic pH to the carbonyl carbon atom in a nucleophilic manner.
- N-acetylated or O-acetylated groups have electrophilic chemical characteristics and therefore, they are prone to nucleophilic attack.
- amide or ester bond is broken and acetyl group is formed from the donor molecule.
- bleaching method X-COCH3, which is dissolved in water, is added to a bleaching bath, comprising hydrogen peroxide, caustic and preferably peroxide stabilizer, as peroxide activator.
- X-COCH3 is added to the bleaching bath by mixing with a glycol derived compound which will support the solubility in water.
- X-COCH3 is mixed with one or more compounds selected from the compounds like preferably ethylene glycol, polyethylene glycol derivatives and glycerol esters and is added to the bleaching bath.
- cleaning function is also provided.
- said compounds also have effects like water absorption and whiteness performance.
- the molar proportion of the glycol derived compound to the acetyl donor is between 1 :1 and 1 :10.
- glycol derived compounds there are compounds like ethylene glycol, polyethylene glycol derivatives and glycerol esters. At least one of said glycol derived compounds is added to the bleaching bath by mixing one or more selected from the subject matter N-acetylated and/or O-acetylated acetyl donor dissolved in water. There is also the cleaning function besides the function of supporting solubility of glycol derived compounds. Thus, said compounds also have favorable effects on water absorption and whiteness performance.
- the bleaching process is preferably realized between 60°C and 80°C.
- the mixture of at least one of said glycol derived compounds and the subject matter N-acetylated and/or O-acetylated acetyl donor or donors dissolved in water is added to the bleaching bath at temperatures between 60°C and 80°C which is the process temperature.
- the solubility of the subject matter acetyl donor inside hydrogen peroxide is substantially high.
- peracetic acid is formed in situ and the formed peracetic acid can be used in a more effective manner in the system.
- the obtained peracetic acid is decomposed as a result of the effect of temperature and bleaching is realized.
- the mixture comprising at least one of the glycol derived compounds and the subject matter N-acetylated and/or O-acetylated acetyl donor or donors dissolved in water, is added to the bleaching bath comprising hydrogen peroxide, caustic and preferably peroxide stabilizer, peracetic acid formation is realized in a stable manner and in sufficient amount.
- peracetic formation in the bleaching bath is repeatable.
- the molar proportion of the subject matter glycol derived compound to the N- acetylated and/or O-acetylated acetyl donor or donors is between 1 :1 and 1 :10.
- propane-1 ,2,3 triol is used as the glycol derivative.
- the subject matter bleaching method is suitable for hot bleaching of raw cotton or cotton fabrics. Accordingly, in the subject matter hot bleaching method, the bleaching process is preferably realized at temperatures between 60 and 80°C. The hot bleaching process is preferably realized between 30 and 90 minutes.
- the hot bleaching bath preferably comprises caustic between 0.1% and 1% by weight.
- the hot bleaching bath preferably comprises hydrogen peroxide between 0.1% and 1 % by weight.
- the hot bleaching bath preferably comprises the subject matter N-acetylated and/or O-acetylated acetyl donor between 0.1% and 1 % by weight.
- the hot bleaching bath preferably comprises stabilizer between 15% and 80% by weight.
- the subject matter bleaching method moreover can be adapted in order to be applied in cold bleaching of raw cotton or cotton fabrics.
- the fabric is impregnated in the bleaching bath prepared in medium temperature, and after the impregnated fabric is compressed at a specific pressure, it is wrapped onto the ducks and the contact thereof to the air is broken and it is rotated for between 12 and 24 hours and waited.
- caustic, peroxide, ion holder, wetting agent and stabilizer are used.
- acetyl donor mixture dissolved in water, is added to the bleaching bath.
- the acetyl donor is mixed with a glycol derived compound which will support the solubility in water and is added to the bleaching bath.
- the beginning pH is near 1 1 ; however, pH decreases gradually due to peracetic formation.
- the cold bleaching bath preferably caustic between 5% and 10% by weight, peroxide between 6% and 10% by weight and peroxide activator between 0.5% and 2% by weight.
- the cold bleaching bath preferably caustic between 5% and 10% by weight, peroxide between 6% and 10% by weight, at least one subject matter N-acetylated and/or at least one subject matter O- acetylated acetyl donor between 0.5% and 2% by weight.
- the bleaching bath can also comprise a wetting agent.
- Said wetting agent comprises the mixture of anionic and non-ionic surfactants which facilitate removing of the saponified impurity from the surface.
- the wetting agent must be resistant to bath conditions (pH, temperature). There shall be no affinity of the wetting agent to the fibers.
- the preferred wetting agents there are the etoxylates and propoxylates of the oil alcohols and sodium salt of the sulphonic acid and sodium salt of the aromatic sulphonic acid.
- Other suitable wetting agents can also be used.
- the bleaching bath can comprise wetting agent between 12% and 50% by weight.
- the bleaching bath can also comprise ion holder.
- ion holder Another factor which leads to rapid decomposition of hydrogen peroxide is the catalyst effect of some metal ions. Iron, manganese, copper, cobalt and the oxides thereof increase the decomposition speed of hydrogen peroxide in an important manner. If there are metal ions in the bleaching medium, hydrogen peroxide molecules begin to decompose in a very rapid manner when compared with radical chain mechanism and meanwhile, they oxidize cellulose fibers and damage them.
- ion holder can also be added, which will form complex, together with stabilizers to the bleaching bath.
- acrylic acid polymers, phosphonic acid derivatives, phosphonic acid salts, various metal salts and the mixtures thereof are provided. Other suitable ion holders can also be used.
- the solution comprising caustic with proportion of 0.25% by weight, hydrogen peroxide with proportion of 0.3% by weight, oil alcohol etoxilate mixture as wetting agent having 12 and 14 carbon chains with proportion of 0.02% by weight and ethylene diamine tetra (methylene phosphonic acid) as stabilizer with proportion of 0.02% by weight, has been loaded to the bleaching bath, where bleaching will be realized, together with the cotton towel fabric, and the system has been heated to 75°C at speed of 5°C/minute. Afterwards, 0.5% triacetine solution in mixture form with the propane-1 ,2,3 triol has been added to the bleaching bath. The towel fabric is subjected to the process for 45 minutes at 75°C.
- the solution comprising caustic with proportion of 0.5% by weight, hydrogen peroxide with proportion of 0.7% by weight, oil alcohol etoxilate mixture as wetting agent having 12 and 14 carbon chains with proportion of 0.02% by weight and ethylene diamine tetra (methylene phosphonic acid) as stabilizer with proportion of 0.02% by weight, has been loaded to the bleaching bath, where bleaching will be realized, together with the cotton towel fabric, and the system has been heated to 75°C at speed of 5°C/minute. Afterwards, 1 .5% triacetine solution in mixture form with the propane-1 ,2,3 triol has been added to the bleaching bath. Towel fabric has been subjected to process for 45 minutes at 75°C.
- the solution comprising caustic with proportion of 0.3% by weight, hydrogen peroxide with proportion of 0.7% by weight, oil alcohol etoxilate mixture as wetting agent having 12 and 14 carbon chains with proportion of 0.02% by weight and ethylene diamine tetra (methylene phosphonic acid) as stabilizer with proportion of 0.02% by weight, has been loaded to the bleaching bath, where bleaching will be realized, together with towel fabric, and the system has been heated to 75°C at speed of 5°C/minute. Afterwards, 1% acetyl salcylic acid solution in mixture form with the propane-1 ,2,3 triol has been added to the bleaching bath. Towel fabric has been subjected to process for 45 minutes at 75°C.
- the solution comprising caustic with proportion of 0.07% by weight, hydrogen peroxide with proportion of 0.1% by weight, oil alcohol etoxilate mixture as wetting agent having 12 and 14 carbon chains with proportion of 0.5% by weight and the solution, comprising N,N,N'N'-tetra- acetyl-ethylene-diamine (TAED), as activator with proportion of 8% by weight, has been loaded to the bleaching bath, where bleaching will be realized, together with towel fabric, and the system has been heated to 75°C at speed of 5°C/minute. Towel fabric has been subjected to process for 45 minutes at 75°C. While the pH was near 11 at the beginning, pH value has decreased to 5.5-6 at the end of the process. After the bleaching process, the towel fabric has been rinsed three times with boiling water and once with cool water and dried and conditioned. 61 berger whiteness value has been obtained.
- TAED N,N,N'N'-tetra- acetyl-ethylene-diamine
- the solution comprising caustic with proportion of 0.07% by weight, hydrogen peroxide with proportion of 0.1% by weight, oil alcohol etoxilate mixture as wetting agent having 12 and 14 carbon chains with proportion of 0.5% by weight and TAED as activator with proportion of 6% by weight, has been loaded to the bleaching bath, where bleaching will be realized, together with towel fabric, and the system has been heated to 75°C at speed of 5°C/minute.
- Towel fabric has been subjected to process for 45 minutes at 75°C. While the pH was near 11 at the beginning, pH value has decreased to 5.5-6 at the end of the process.
- the towel fabric has been rinsed three times with boiling water and once with cool water and dried and conditioned. 45 berger whiteness value has been obtained.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TR2019/03932A TR201903932A2 (en) | 2019-03-15 | 2019-03-15 | |
PCT/TR2019/051069 WO2020190230A1 (en) | 2019-03-15 | 2019-12-12 | A method for bleaching cotton fabrics |
Publications (2)
Publication Number | Publication Date |
---|---|
EP3938570A1 true EP3938570A1 (en) | 2022-01-19 |
EP3938570A4 EP3938570A4 (en) | 2023-06-07 |
Family
ID=67980078
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19920252.4A Pending EP3938570A4 (en) | 2019-03-15 | 2019-12-12 | A method for bleaching cotton fabrics |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP3938570A4 (en) |
TR (1) | TR201903932A2 (en) |
WO (1) | WO2020190230A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT202000027666A1 (en) * | 2020-11-18 | 2022-05-18 | Prochimica Novarese S P A | PROCESS FOR THE PURGE AND BLEACHING OF TEXTILE FIBERS THROUGH THE USE OF NATURAL ESTERS OF POLYGLYCEROL |
WO2023129089A1 (en) | 2021-12-31 | 2023-07-06 | Akar Teksti̇l Gida Ve Turi̇zm Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ | Method of effect creating for piece-dyed products |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3687803A (en) | 1970-11-09 | 1972-08-29 | American Cyanamid Co | Acid chloride activators for hydrogen peroxide bleaching |
DE4024531A1 (en) | 1990-08-02 | 1992-02-06 | Henkel Kgaa | LIQUID DETERGENT |
EP0584710A3 (en) * | 1992-08-22 | 1995-02-01 | Hoechst Ag | Method for the bleaching of textiles. |
IT1398126B1 (en) * | 2010-02-19 | 2013-02-07 | Myriel S R L | COMPOSITION AND PROCEDURE TO OBTAIN A PEROSXIACETIC ACID-BASED SOLUTION |
KR101321526B1 (en) | 2012-04-05 | 2013-10-28 | (재)한국섬유소재연구소 | Process Of Dyeing Cotton Textiles Using Enzyme |
BE1024009B9 (en) * | 2013-10-04 | 2017-11-30 | Christeyns N V | DEVICE FOR PREPARING AND USING BLEACH AND / OR DISINFECTION AGENT ON THE SPOT |
-
2019
- 2019-03-15 TR TR2019/03932A patent/TR201903932A2/tr unknown
- 2019-12-12 EP EP19920252.4A patent/EP3938570A4/en active Pending
- 2019-12-12 WO PCT/TR2019/051069 patent/WO2020190230A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
EP3938570A4 (en) | 2023-06-07 |
WO2020190230A1 (en) | 2020-09-24 |
TR201903932A2 (en) | 2019-04-22 |
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