![]() Method for preparing biocarrier for fixing biomass charcoal by using thermoplastic resin
专利摘要:
The invention, belonging to the field of biological treatment of pollutants and functional materials, presents a method for the preparation of biofilm carrier with biochar fixed by thermoplastic resin. Extrusion grade polyethylene/polypropylene particles are used as the basic material. One or some combination of plant biochar, straw biochar, rice husk biochar, shell biochar, excess sludge and animal waste biochar are used as the functional material. The biofilm carrier with biochar fixed by thermoplastic resin is prepared by the screw extrusion process, which is a simple, flexible and controllable method, and possesses strong adaptability. The reactor with these biofilm carriers has high removal efficiency of refractory organic pollutants. 公开号:EP3695955A1 申请号:EP17932137.7 申请日:2017-11-17 公开日:2020-08-19 发明作者:Xie QUAN;Yanjun MAO;Shuo Chen;Hongtao Yu;Yaobin ZHANG 申请人:Dalian University of Technology; IPC主号:B29B7-00
专利说明:
[0001] The present invention related to a method for the preparation of biofilm carrier with biochar fixed by thermoplastic resin, is applied to the biological treatment of environmental pollutants, and is particularly suitable for the biological wastewater treatment, and belongs to the field of biological treatment of pollutants and functional materials. Background [0002] Domestic sewage and industrial wastewater are the main pollution sources of water in China. Compared with domestic sewage, the discharge of industrial wastewater and the types of pollutants in the wastewater are increasing, and the components are more complex, including a variety of refractory organic pollutants. Refractory organic pollutants are those that can hardly be degraded by microorganisms, or require a very long time for degradation. They are easily accumulated in natural media such as water bodies and soils. The refractory organic wastewater involve a wide range of industries, mainly chemical, light industry, printing and dyeing, pharmaceutical, pesticide and coal chemical wastewater. These wastewater mainly contain refractory organic components such as phenols, halogenated compounds, monocyclic aromatic compounds, polycyclic aromatic hydrocarbons, polychlorinated biphenyls, pesticides, herbicides and dyes, and their harm to the environment has been widely recognized in the world. The control of refractory organic pollutants is an important issue in the field of water pollution prevention and control. Recent studies have shown that the addition of artificial redox mediators can accelerate the extracellular electron transfer rate of microorganisms, thereby enhancing the biodegradability of refractory organic pollutants and shortening the degradation time. Therefore, the redox mediators have been paid more and more attention because of its good application potential. [0003] The redox mediator can transfer electrons through its own redox capacity, which mainly involved in microbial extracellular electron transfer process to accelerate the electron transport rate. Hence the degradation rate of pollutants could be significantly improved. At present, the commonly used redox mediators mainly include some quinone, phenazine, phthalocyanine and so on. These compounds have π-π conjugated systems and have active sites for the gain/loss of electrons, such as carbonyl (C = O). However, these compounds are soluble, and it is necessary to add these compounds from time to time during the biological water treatment process, which will result in an increase of operation cost, and secondary pollution also. Carbonaceous materials such as graphene, carbon nanotubes, biochar, etc., are redox mediators with high reusability that have been studied in recent years. Biochar, also known as black carbon, is a kind of insoluble, stable, highly aromatic, carbon-rich solid residue produced by high temperature pyrolysis (carbonization) of biomass under low or no oxygen (usually < 700 °C). The raw material cost of biochar preparation is low, the source is plentiful, such as the wood, the fruit shell, the straw, the sludge, the animal excrement and so on. Related research results show that the surface of the biochar is rich in oxygen containing functional groups (such as carbonyl, hydroxyl, etc.). In the process of bioremediation of pollutants, biochar can receive electrons which derived from the biodegradation of pollutants. After that, the reduced biochar can transfer the electrons to receptors. During the whole biodegradation process, biochar acted as redox mediators and can improve the biodegradation efficiency. However, if the biochar is directly used as the redox mediator, the problem of loss will also exist, so there will also be problems such as increasing investment cost and causing secondary pollution to the environment. Based on this, the purpose of the present invention is to fix the biochar functional materials on the thermoplastic resin and develop a new biological carrier for fixing the biochar functional materials with the thermoplastic resin. Summary [0004] The present invention is directed to the problem of slow treatment rate of refractory organic matter in water due to the limitation of electron transfer rate in biological water treatment technology. The present invention aims to provide a method the preparation of biofilm carrier with biochar fixed by thermoplastic resin. [0005] Technical solution of the present invention:A method for the preparation of biofilm carrier with biochar fixed by thermoplastic resin, comprising the following steps:(1) Biochar functional materials is ground to powder, and dried to constant weight under ≤ 80 °C; (2) Biochar functional materials powder, which is pretreated according to step (1), is blended into thermoplastic resin particles, and stirred evenly. The mass percentage of biochar powder to thermoplastic resin particles is 20%-50%; (3) The solid mixture obtained from step (2) is melt extruded into strips by a screw extruder, and mechanically cut to obtain a granular blend. The processing temperature of each section of the screw extruder is 130-190 °C to ensure that the thermoplastic resin is fully mixed with biochar functional materials powder in the molten state. (4) The granular blend prepared in step (3) and the thermoplastic resin particles are mechanically stirred evenly, and then are added to the screw extruder for co-mixing and extrusion. Then the carrier pipes of different shapes are obtained according to the design of mould. The ratio of biochar mass to the total mass of thermoplastic resin particles in granular blends is less than 20%. (5) The carrier pipes prepared in step (4) are cut mechanically and the biological carriers are obtained according to the required size. [0006] The biochar functional materials mentioned are one or more combinations of grass biochar, straw biochar, rice husk biochar, nut shell biochar, sludge biomass biochar and animal excrement biochar. [0007] The thermoplastic resin particles are extruded grade polyethylene particles or extruded grade polypropylene particles. [0008] The screw extruder is heated in four sections, and the temperature range and effects of each section heating are as follows: (1) The temperature is 120-140 °C, and the thermoplastic resin reaches the semi-molten state, which is conducive to the continuity of solid transport. (2) The temperature is 130-160 °C, which accelerates the transformation of the thermoplastic resin from the semi-molten state to the molten state, and is conducive to the homogeneous mixing of the blends in the heating section. (3) The temperature is 140-170 °C, which can make the blend in a solid-liquid mixing state, so that the melting thermoplastic resin and solid biochar functional materials are fully mixed, which is conducive to the uniform distribution of biochar functional materials and thermoplastic resin in the molten state. (4) The temperature is 115-145 °C to ensure the quantitative and constant pressure outflow of the blends, and to ensure the stability and continuity of extrusion and the subsequent smooth shaping. [0009] Advantages of the Invention: the preparation method of the biofilm carriers for fixing biochar by thermoplastic resin is described in the invention, which is a simple, flexible and controllable method, and possesses strong adaptability, and it can be produced on a large scale. The biofilm carriers have an efficient removal efficiency of refractory organic pollutants. Detail description [0010] The specific implementation of the present invention will be described in detail below in conjunction with the technical solution. Example 1: [0011] The preparation of the biofilm carrier with straw biochar fixed by thermoplastic resin: (1) The straw biochar is ground to powder, and dried into constant weight at 60 °C; (2) Biochar powder, which is pretreated according to step (1), is blended into thermoplastic resin particles, and stirred evenly; (3) The solid mixture obtained from step (2) is melt extruded into strips by a screw extruder. The processing temperature of each section of the screw extruder is 175 °C. The mass percentage of straw biochar powder to thermoplastic resin particles is 30%; (4) The granular blend prepared in step (3) and the thermoplastic resin particles are mechanically stirred evenly, and then added to the screw extruder for co-mixing and extrusion, the carrier pipes of different shapes are obtained, according to the design of mould. The ratio of biochar functional materials mass to the total mass of thermoplastic resin particles in granular blends is less than 4%; (5) The carrier pipes prepared in step (4) are cut mechanically and the biological carriers are obtained according to the required size. [0012] The biofilm carriers are applied to the aerobic biodegradation experiment of phenol wastewater (the dissolved oxygen was controlled at 2.0-3.0 mg/L), and its effect on the biodegradation performance of microorganisms in water is investigated. In the experiment, the dosage of carriers is 30% of the effective volume of the reactor, and the hydraulic retention time is 8 hours. The experimental results show that: (1) in the absence of microorganisms, the carrier adsorption experiment of phenol in water is carried out, and the results show that the removal rate of phenol through the carrier adsorption is less than 3%. (2) in the presence of microorganisms, compared with the high-density polyethylene carrier without fixed biochar, the removal of phenol in the reactor fixed with high-density polyethylene (HDPE) is nearly 10% higher than that of the high-density polyethylene carrier without fixed biochar. Example 2: [0013] The preparation of the biofilm carrier with straw biochar fixed by thermoplastic resin:(1) The rice husk biochar is ground to powder, and dried into constant weight at 60 °C; (2) Biochar powder, which is pretreated according to step 1, is blended into thermoplastic resin particles, and stirred evenly; (3) The solid mixture obtained from step (2) is melt extruded by a screw extruder. The processing temperature of each section of the screw extruder is 185 °C to ensure that the basic material is fully mixed with biochar functional materials in the molten state, and can be shaped into particles, the mass percentage of rice husk biochar to thermoplastic resin is 50%. (4) The granular blend prepared in step (3) and the thermoplastic resin particles are mechanically stirred evenly, and then added to the screw extruder for co-mixing and extrusion, the carrier pipes of different shapes are obtained, according to the design of mould. The ratio of biochar functional materials mass to the total mass of thermoplastic resin particles in granular blends is less than 8%;(5) The carrier pipes prepared in step (4) are cut mechanically and the biological carriers are obtained according to the required size. The preparation methods of carbonylation modified graphene oxide (GO) as the biofilm carrier of functional materials are as follows: (1) preparation of carbonylation modified GO functional materials: the pH is adjusted to 10 with ammonia. The dispersion hydrothermally reacts at 90 °C for 6 hours, and then is cooled down and dried at 60 °C. The solid particles obtained are referred as N-GO. The 0.2 g solid particles N-GO are added to the water (20 mL), and uniformly dispersed by ultrasonication, and then 1.2 g potassium dichromate is added into the dispersion under the condition of the addition of acid (H2SO4 5 mL) and ice water bath. After being fully stirred for 3 hours and dried, the solid particles are obtained. They are carbonylation modified graphene oxide, and called as Q-GO. (2) the non-dissolved redox mediator material is ultrasonically dispersed in the water, and mixed with the basic material added with the mass ratio of the mediator material to the basic material being 1:100, and then soaked for 2 hours, stirred every half an hour to make the redox mediator fully contact with the basic material in the water, and the resulting solid mixture is dried at 80 °C. The biofilm carriers are prepared by extrusion, cooling, traction, incision and shaping. [0014] The modified (modified by biochar, carbonylation modification of graphene oxide, respectively) and unmodified (HDPE) carriers are used to treat phenol wastewater in the condition of aerobic or anaerobic. The effects of different carriers on the biodegradation performance of microorganisms in water with different phenol concentrations in the influent are investigated. In the experiment, the dosage of carriers is 30% of the effective volume of the reactor. [0015] The experimental results are shown in table 1. It can be seen from the table that under the conditions of aerobic and anaerobic with different phenol concentrations in the influent, the biodegradation performance of phenol in the reactor with modified carrier is better than that of the reactor with unmodified carrier. However, among the reactors with modified carriers, the biochar modified carriers have slightly better biodegradation performance than the reactors with modified carriers modified by carbonylation modification of graphene oxide. In addition, compared with the preparation method of carbonylation modified graphene oxide as functional material, the preparation method of bio-carrier fixed by thermoplastic resin is simpler, easier to operate, more timesaving and conducive to ensuring the continuity of the production process. Furthermore, compared with carbonylation modified graphene oxide as the functional materials, the biochar as the functional materials are more widely sourced, cheaper and more conducive to the realization of large-scale production and application. Tab. 1 Effect of modified carriers on biodegradability of phenol Phenol conc. (mg/L) Removal efficiency (%) PE Q-GO Biochar Aerobic 200 94.2 98.9 99.3 HRT 8 h 400 93.9 98.8 99.0 DO 2.0-3.0 600 92.9 98.6 98.7 mg/L 800 89.7 98 98.7 Anaerobic 200 89.3 93.5 96.7 HRT 12 h 400 66.4 90.1 93.6 DO <0.1 600 66.1 89 91.1 mg/L 800 65.4 87.8 89.3 Note: PE represents the reactor with unmodified biological carriers,Q-GO represents the reactor with the biological carriers modified by carbonylation modified graphene oxide, andBiochar represents the reactor with the biological carriers modified by biochar functional materials.
权利要求:
Claims (8) [0001] A method for the preparation of biofilm carrier with biochar fixed by thermoplastic resin, comprising the following steps: (1) biochar functional materials is ground to powder, and dried to constant weight at ≤80°C; (2) biochar functional materials powder, which is pretreated according to step (1), is blended into thermoplastic resin particles, and stirred evenly; the mass percentage of biochar functional materials powder to thermoplastic resin particles is 20%-50%; (3) the solid mixture obtained from step (2) is melt extruded into strips by a screw extruder, and mechanically cut to obtain a granular blend; the processing temperature of each section of the screw extruder is 130-190 °C to ensure that the thermoplastic resin is fully mixed with biochar functional materials in the molten state; (4) the granular blend prepared in step (3) and the thermoplastic resin particles are mechanically stirred evenly, and then added to the screw extruder for co-mixing and extrusion, the carrier pipes of different shapes are obtained, according to the design of mould; the ratio of biochar functional materials mass to the total mass of thermoplastic resin particles in granular blends is less than 20%; (5) the carrier pipes prepared in step (4) are cut mechanically and the biological carriers are obtained according to the required size. [0002] The method for the preparation of biofilm carrier according to claim 1, wherein the biochar functional materials are one or more combinations of grass biochar, straw biochar, rice husk biochar, nut shell biochar, sludge biomass biochar and animal excrement biochar. [0003] The method for the preparation of biofilm carrier according to claim 1 or 2, wherein the thermoplastic resin particles are extruded grade polyethylene particles or extruded grade polypropylene particles. [0004] The method for the preparation of biofilm carrier according to claim 1 or 2, wherein the screw extruder is heated in four sections, and the temperature range and effects of each section heating are as follows: (1) the temperature is 120-140 °C, and the thermoplastic resin reaches the semi-molten state, which is conducive to the continuity of solid transport; (2) the temperature is 130-160 °C, which accelerates the transformation of the thermoplastic resin from the semi-molten state to the molten state, and is conducive to the homogeneous mixing of the blends in the heating section; (3) the temperature is 140-170 °C, which can make the blend in a solid-liquid mixing state, so that the melting thermoplastic resin and solid biochar functional materials are fully mixed, which is conducive to the uniform distribution of biochar functional materials and thermoplastic resin in the molten state; (4) the temperature is 115-145 °C to ensure the quantitative and constant pressure outflow of the blends, and to ensure the stability and continuity of extrusion and the subsequent smooth shaping. [0005] The method for the preparation of biofilm carrier according to claim 3, wherein the screw extruder is heated in four sections, and the temperature range and effects of each section heating are as follows: (1) the temperature is 120-140 °C, and the thermoplastic resin reaches the semi-molten state, which is conducive to the continuity of solid transport; (2) the temperature is 130-160 °C, which accelerates the transformation of the thermoplastic resin from the semi-molten state to the molten state, and is conducive to the homogeneous mixing of the blends in the heating section; (3) the temperature is 140-170 °C, which can make the blend in a solid-liquid mixing state, so that the melting thermoplastic resin and solid biochar functional materials are fully mixed, which is conducive to the uniform distribution of biochar functional materials and thermoplastic resin in the molten state; (4) the temperature is 115-145 °C to ensure the quantitative and constant pressure outflow of the blends, and to ensure the stability and continuity of extrusion and the subsequent smooth shaping. [0006] The method for the preparation of biofilm carrier according to claim 1, 2 or 5, wherein the surface of the biochar functional materials is rich in oxygen-containing functional groups, which have the function of redox mediator. [0007] The method for the preparation of biofilm carrier according to claim 3, wherein the surface of the biochar functional materials is rich in oxygen-containing functional groups, which have the function of redox mediator. [0008] The method for the preparation of biofilm carrier according to claim 4, wherein the surface of the biochar functional materials is rich in oxygen-containing functional groups, which have the function of redox mediator.
类似技术:
公开号 | 公开日 | 专利标题 Sheets et al.2015|Beyond land application: Emerging technologies for the treatment and reuse of anaerobically digested agricultural and food waste Zhang et al.2015|Anaerobic co-digestion of food waste with MSW incineration plant fresh leachate: process performance and synergistic effects CN103121882B|2015-04-15|Biomass straw charcoal based organic fertilizer and production method thereof Fezzani et al.2010|Two-phase anaerobic co-digestion of olive mill wastes in semi-continuous digesters at mesophilic temperature Wu et al.2009|The effect of pH on anaerobic fermentation of primary sludge at room temperature Molinuevo et al.2009|Anammox for ammonia removal from pig manure effluents: effect of organic matter content on process performance Paterakis et al.2012|The effectiveness of anaerobic digestion in removing estrogens and nonylphenol ethoxylates CA2939565C|2018-05-01|System and method for anaerobic digestion of biomasses Singhal et al.2003|Biogas production from water hyacinth and channel grass used for phytoremediation of industrial effluents CN1147440C|2004-04-28|Treatment method of high concentration organic wastewater using biological culture equipment CN101306867B|2010-09-08|High-efficiency purifier of biological enzyme Wang et al.2017|Improvement of pig manure compost lignocellulose degradation, organic matter humification and compost quality with medical stone Kim et al.2009|Carbon source recovery from waste activated sludge by alkaline hydrolysis and gamma-ray irradiation for biological denitrification Parawira et al.2006|Comparative performance of a UASB reactor and an anaerobic packed-bed reactor when treating potato waste leachate Muñoz et al.2005|Combined carbon and nitrogen removal from acetonitrile using algal–bacterial bioreactors Wang et al.2017|Comparison of biochar, zeolite and their mixture amendment for aiding organic matter transformation and nitrogen conservation during pig manure composting Verma et al.2007|Biogas production from plant biomass used for phytoremediation of industrial wastes Rani et al.2004|Ensilage of pineapple processing waste for methane generation Mohan et al.2007|Enhancing biohydrogen production from chemical wastewater treatment in anaerobic sequencing batch biofilm reactor | by bioaugmenting with selectively enriched kanamycin resistant anaerobic mixed consortia Buzzini et al.2007|Evaluation of a upflow anaerobic sludge blanket reactor with partial recirculation of effluent used to treat wastewaters from pulp and paper plants Driessen et al.1994|Experience on anaerobic treatment of distillery effluent with the UASB process CN104478098B|2016-03-02|For the treatment of the microbial preparation of coal chemical industrial waste water Lu et al.2011|Influences of light and oxygen conditions on photosynthetic bacteria macromolecule degradation: different metabolic pathways CN104528955B|2016-08-24|A kind of microorganism formulation for repairing chemical fertilizer factory's sewage Kotsopoulos et al.2008|The impact of different natural zeolite concentrations on the methane production in thermophilic anaerobic digestion of pig waste
同族专利:
公开号 | 公开日 US20210129408A1|2021-05-06| EP3695955A4|2020-10-21| WO2019095306A1|2019-05-23|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题
法律状态:
2019-05-27| STAA| Information on the status of an ep patent application or granted ep patent|Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE | 2020-07-17| STAA| Information on the status of an ep patent application or granted ep patent|Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE | 2020-07-17| PUAI| Public reference made under article 153(3) epc to a published international application that has entered the european phase|Free format text: ORIGINAL CODE: 0009012 | 2020-08-19| 17P| Request for examination filed|Effective date: 20200514 | 2020-08-19| AX| Request for extension of the european patent|Extension state: BA ME | 2020-08-19| AK| Designated contracting states|Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR | 2020-10-21| A4| Supplementary search report drawn up and despatched|Effective date: 20200922 | 2020-10-21| RIC1| Information provided on ipc code assigned before grant|Ipc: B29B7/90 20060101ALI20200916BHEP Ipc: B29B7/00 20060101AFI20200916BHEP Ipc: B29B7/38 20060101ALN20200916BHEP Ipc: B29B9/06 20060101ALN20200916BHEP Ipc: B29C 48/00 20190101ALI20200916BHEP Ipc: B29C 69/00 20060101ALI20200916BHEP Ipc: B29B7/74 20060101ALI20200916BHEP Ipc: C02F3/28 20060101ALN20200916BHEP Ipc: B29B9/12 20060101ALI20200916BHEP Ipc: B29B 13/04 20060101ALI20200916BHEP Ipc: C02F3/02 20060101ALN20200916BHEP Ipc: C02F 101/34 20060101ALN20200916BHEP Ipc: C02F3/10 20060101ALI20200916BHEP Ipc: B29B7/82 20060101ALI20200916BHEP | 2021-02-24| DAX| Request for extension of the european patent (deleted)| 2021-02-24| DAV| Request for validation of the european patent (deleted)| 2021-05-07| REG| Reference to a national code|Ref country code: DE Ref legal event code: R079 Ref document number: 602017044097 Country of ref document: DE Free format text: PREVIOUS MAIN CLASS: B29C0069000000 Ipc: B29B0007000000 | 2021-06-01| GRAP| Despatch of communication of intention to grant a patent|Free format text: ORIGINAL CODE: EPIDOSNIGR1 | 2021-06-01| STAA| Information on the status of an ep patent application or granted ep patent|Free format text: STATUS: GRANT OF PATENT IS INTENDED | 2021-06-16| RIC1| Information provided on ipc code assigned before grant|Ipc: C02F 101/34 20060101ALN20210507BHEP Ipc: C02F3/28 20060101ALN20210507BHEP Ipc: C02F3/02 20060101ALN20210507BHEP Ipc: B29B9/06 20060101ALN20210507BHEP Ipc: B29B7/38 20060101ALN20210507BHEP Ipc: B29C 69/00 20060101ALI20210507BHEP Ipc: B29C 48/92 20190101ALI20210507BHEP Ipc: B29C 48/00 20190101ALI20210507BHEP Ipc: B29B 13/04 20060101ALI20210507BHEP Ipc: C02F3/10 20060101ALI20210507BHEP Ipc: B29B9/12 20060101ALI20210507BHEP Ipc: B29B7/90 20060101ALI20210507BHEP Ipc: B29B7/82 20060101ALI20210507BHEP Ipc: B29B7/74 20060101ALI20210507BHEP Ipc: B29B7/00 20060101AFI20210507BHEP | 2021-06-30| INTG| Intention to grant announced|Effective date: 20210602 | 2021-07-07| GRAS| Grant fee paid|Free format text: ORIGINAL CODE: EPIDOSNIGR3 | 2021-07-09| STAA| Information on the status of an ep patent application or granted ep patent|Free format text: STATUS: THE PATENT HAS BEEN GRANTED | 2021-07-09| GRAA| (expected) grant|Free format text: ORIGINAL CODE: 0009210 | 2021-08-11| AK| Designated contracting states|Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR | 2021-08-16| REG| Reference to a national code|Ref country code: CH Ref legal event code: EP | 2021-09-02| REG| Reference to a national code|Ref country code: DE Ref legal event code: R096 Ref document number: 602017044097 Country of ref document: DE | 2021-09-15| REG| Reference to a national code|Ref country code: IE Ref legal event code: FG4D Ref country code: AT Ref legal event code: REF Ref document number: 1418916 Country of ref document: AT Kind code of ref document: T Effective date: 20210915 | 2021-12-10| REG| Reference to a national code|Ref country code: LT Ref legal event code: MG9D | 2021-12-15| REG| Reference to a national code|Ref country code: NL Ref legal event code: MP Effective date: 20210811 | 2022-01-15| REG| Reference to a national code|Ref country code: AT Ref legal event code: MK05 Ref document number: 1418916 Country of ref document: AT Kind code of ref document: T Effective date: 20210811 | 2022-01-31| PG25| Lapsed in a contracting state [announced via postgrant information from national office to epo]|Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20211111 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20211213 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20211111 Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 Ref country code: RS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 | 2022-01-31| PGFP| Annual fee paid to national office [announced via postgrant information from national office to epo]|Ref country code: GB Payment date: 20211006 Year of fee payment: 5 Ref country code: FR Payment date: 20211119 Year of fee payment: 5 Ref country code: DE Payment date: 20211118 Year of fee payment: 5 | 2022-02-28| PG25| Lapsed in a contracting state [announced via postgrant information from national office to epo]|Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20210811 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20211112 |
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|