CN106168004B - A kind of preparation method of medical packing paper Cypres - Google Patents

A kind of preparation method of medical packing paper Cypres Download PDF

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CN106168004B
CN106168004B CN201610746866.6A CN201610746866A CN106168004B CN 106168004 B CN106168004 B CN 106168004B CN 201610746866 A CN201610746866 A CN 201610746866A CN 106168004 B CN106168004 B CN 106168004B
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paper
sizing agent
supernatant
fermentation
parts
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CN106168004A (en
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潘勤霞
韩德娟
王之红
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Haimen Biwei Intellectual Property Service Co ltd
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H21/00Non-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
    • D21H21/14Non-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 characterised by function or properties in or on the paper
    • D21H21/16Sizing or water-repelling agents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65BMACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
    • B65B47/00Apparatus or devices for forming pockets or receptacles in or from sheets, blanks, or webs, comprising essentially a die into which the material is pressed or a folding die through which the material is moved
    • B65B47/02Apparatus or devices for forming pockets or receptacles in or from sheets, blanks, or webs, comprising essentially a die into which the material is pressed or a folding die through which the material is moved with means for heating the material prior to forming
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65BMACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
    • B65B51/00Devices for, or methods of, sealing or securing package folds or closures; Devices for gathering or twisting wrappers, or necks of bags
    • B65B51/10Applying or generating heat or pressure or combinations thereof
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20Bacteria; Culture media therefor
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/20Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/34Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising cellulose or derivatives thereof

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Abstract

本发明涉及一种医用包装纸表面施胶剂的制备方法,属于表面施胶剂制备技术领域。本发明首先将黄单胞杆菌培养、发酵后获得含有黄原胶的上清液,再将新鲜牛骨与沼气液一起发酵,收集发酵液并脱色、除杂后得到滤液,再将氧化锌等进行粉碎后过筛,得到混合粉末,最后将含有黄原胶的上清液、滤液等与助剂搅拌得到医用包装纸表面施胶剂。本发明制备的施胶剂解决了灭菌过程中表面施胶剂容隐粘附在包装物上的问题,使用本发明的施胶剂制备的纸袋,纸张与薄膜的热强度高,密封性好,剥离时纸张与薄膜能够完全分离,不会造成纸袋破损或纸张纤维粘出的问题,经表面施胶剂施胶的医用包装纸具有一定的透气度、耐水性、良好的表面强度和纸塑结合力。The invention relates to a method for preparing a surface sizing agent for medical packaging paper, and belongs to the technical field of surface sizing agent preparation. In the present invention, the supernatant liquid containing xanthan gum is firstly obtained by culturing and fermenting Xanthomonas bacteria, then fermenting fresh bovine bone and biogas liquid together, collecting the fermented liquid, decolorizing and removing impurities to obtain the filtrate, and then adding zinc oxide, etc. After pulverizing and sieving, mixed powder is obtained, and finally the supernatant, filtrate, etc. containing xanthan gum are stirred with auxiliary agents to obtain a surface sizing agent for medical packaging paper. The sizing agent prepared by the invention solves the problem that the surface sizing agent is implicitly adhered to the packaging during the sterilization process, and the paper bag prepared by using the sizing agent of the invention has high thermal strength of paper and film and good airtightness , the paper and the film can be completely separated when peeling off, and will not cause damage to the paper bag or sticking out of the paper fiber. The medical packaging paper sized by the surface sizing agent has a certain degree of air permeability, water resistance, good surface strength and paper-plastic Binding force.

Description

一种医用包装纸表面施胶剂的制备方法A kind of preparation method of medical packaging paper surface sizing agent

技术领域technical field

本发明涉及一种医用包装纸表面施胶剂的制备方法,属于表面施胶剂制备技术领域。The invention relates to a method for preparing a surface sizing agent for medical packaging paper, and belongs to the technical field of surface sizing agent preparation.

背景技术Background technique

随着我国与国际包装的逐渐接轨,对医用产品的包装要求日趋变高,同时考虑到对环境保护的要求,国际上推崇纸塑复合、以纸代塑包装形式。而医用纸袋就是一种满足现代医用包装要求的产品,它一般采用和塑料薄膜复合制成,具有密封可靠、热封易撕的特点。该产品适用于手套、纱布、棉球、棉棒、口罩、导管、手术器材、牙科器材、注射器等医疗器械包装,在国外已得到较普遍使用,国内的需求量也越来越大。医用消毒包装纸袋的制造是通过制袋机的高温高压使原料的施胶层与薄膜粘合,从而使其达到很好的密闭性,经过表面施胶的纸需要具有一定的透气度,以满足灭菌消毒时灭菌因子的进入,灭菌过程中表面施胶剂决不能粘附在包装物上破坏包装物卫生,在使用时要求纸张具有良好的表面强度及热封合强度,从而在医用包装纸袋剥离时保证适宜的粘合力以及剥离界面的绝对干净。针对医用纸袋的这些特点就需要选用特殊的热熔型表面施胶剂,从而使产品满足密封性好、不粘医疗器械、热封强度适宜、且剥离时纸张与薄膜不能相互粘连的性能要求。目前的医用包装袋一般采用在医用纸的一侧围绕边缘涂一圈胶黏剂,然后覆盖薄膜,热压粘合、裁切,从而形成纸袋,热压时预留一边以便放入包装物,封口只需要将开口一端在热合封边机上密封即可,使用时只要在纸袋开启端从两层纸粘合处剥离即可打开。With the gradual integration of our country and international packaging, the packaging requirements for medical products are becoming higher and higher. At the same time, considering the requirements for environmental protection, paper-plastic composite and paper-plastic packaging are highly recommended internationally. The medical paper bag is a product that meets the requirements of modern medical packaging. It is generally made of a composite with plastic film, and has the characteristics of reliable sealing, heat sealing and easy tearing. This product is suitable for the packaging of gloves, gauze, cotton balls, cotton swabs, masks, catheters, surgical equipment, dental equipment, syringes and other medical equipment. It has been widely used abroad, and the domestic demand is also increasing. The manufacture of medical sterilization packaging paper bags is to bond the sizing layer of the raw material with the film through the high temperature and high pressure of the bag making machine, so that it can achieve a good airtightness. The paper after surface sizing needs to have a certain degree of air permeability to meet The entry of sterilizing factors during sterilization, the surface sizing agent must not adhere to the packaging during the sterilization process to destroy the hygiene of the packaging, and the paper is required to have good surface strength and heat sealing strength during use, so that it can be used in medical When peeling the wrapping paper bag, ensure proper adhesive force and absolutely clean peeling interface. According to these characteristics of medical paper bags, special hot-melt surface sizing agents need to be selected, so that the products can meet the performance requirements of good sealing performance, non-sticking of medical devices, suitable heat-sealing strength, and non-sticking of paper and film when peeling off. The current medical packaging bags are generally coated with a circle of adhesive around the edge on one side of the medical paper, then covered with a film, heat-pressed, bonded, and cut to form a paper bag. When heat-pressing, one side is reserved for packaging. To seal the bag, you only need to seal one end of the opening on a heat-sealing edge banding machine. When in use, you only need to peel off the opening end of the paper bag from the joint of the two layers of paper to open it.

目前,用于医用包装纸表面施胶剂普遍存在灭菌过程中表面施胶剂容易粘附在包装物上破坏包装物卫生,纸张与薄膜的热封强度不够,造成纸袋密封不牢固,并且剥离时纸张与薄膜不能完全分离,造成纸袋破损或纸张纤维粘出。At present, the surface sizing agent used in medical packaging paper is common. During the sterilization process, the surface sizing agent is easy to adhere to the packaging and damage the hygiene of the packaging. The heat seal strength between the paper and the film is not strong enough, causing the paper bag to be sealed weakly and peel off. When the paper and the film cannot be completely separated, the paper bag is damaged or the paper fiber sticks out.

发明内容Contents of the invention

本发明所要解决的技术问题:针对目前医用包装纸表面施胶剂普遍存在灭菌过程中表面施胶剂容易粘附在包装物上破坏包装物卫生,纸张与薄膜的热封强度不够,造成纸袋密封不牢固,并且剥离时纸张与薄膜不能完全分离,造成纸袋破损或纸张纤维粘出的问题,提供了一种医用包装纸表面施胶剂的制备方法,本发明首先将黄单胞杆菌进行培养、发酵后获得含有黄原胶的上清液,然后再将新鲜牛骨进行清洗后,与过滤后的沼气液一起发酵,然后收集发酵液并用活性炭进行脱色、除杂后得到滤液,再将氧化锌等进行粉碎后过筛,得到混合粉末,最后将含有黄原胶的上清液、滤液等与助剂一同高速搅拌得到医用包装纸表面施胶剂。本发明制备的施胶剂解决了灭菌过程中表面施胶剂容隐粘附在包装物上的问题,使用本发明的施胶剂制备的纸袋,纸张与薄膜的热强度高,密封性好,剥离时纸张与薄膜能够完全分离,不会造成纸袋破损或纸张纤维粘出的问题,经表面施胶剂施胶的医用包装纸具有一定的透气度、耐水性、良好的表面强度和纸塑结合力。The technical problem to be solved by the present invention: in view of the ubiquity of the surface sizing agent on the medical packaging paper at present, the surface sizing agent is easy to adhere to the packaging during the sterilization process and destroys the hygiene of the packaging, and the heat sealing strength of the paper and the film is not enough, causing the paper bag The seal is not firm, and the paper and the film cannot be completely separated when peeling off, resulting in the problem of paper bag damage or paper fiber sticking out. A method for preparing a surface sizing agent for medical packaging paper is provided. The invention firstly cultivates Xanthomonas 1. Obtain the supernatant containing xanthan gum after fermentation, then clean the fresh bovine bone, and ferment it with the filtered biogas liquid, then collect the fermentation liquid and use activated carbon to decolorize and remove impurities to obtain the filtrate, and then oxidize Zinc, etc. are crushed and sieved to obtain a mixed powder. Finally, the supernatant, filtrate, etc. containing xanthan gum are stirred at high speed with auxiliary agents to obtain a surface sizing agent for medical packaging paper. The sizing agent prepared by the invention solves the problem that the surface sizing agent is implicitly adhered to the packaging during the sterilization process, and the paper bag prepared by using the sizing agent of the invention has high thermal strength of paper and film and good airtightness , the paper and the film can be completely separated when peeling off, and will not cause damage to the paper bag or sticking out of the paper fiber. The medical packaging paper sized by the surface sizing agent has a certain degree of air permeability, water resistance, good surface strength and paper-plastic Binding force.

为解决上述技术问题,本发明采用的技术方案是:In order to solve the problems of the technologies described above, the technical solution adopted in the present invention is:

(1)称取20~30g淀粉、3~5g硝酸钠、2~4g磷酸二氢钾、0.4~0.6g硫酸镁、6~8g柠檬酸和800~1000mL去离子水,搅拌后置于灭菌罐中,在100~110℃灭菌5~10min,得到培养基,按接种量8~10%将黄单胞杆菌接种到培养基中,随后转移至培养箱中,在30~40℃、120~130r/min下培养2~3天,然后置于离心机中,在1200~1300r/min下离心20~30min,收集上清液,即黄单胞杆菌菌液;(1) Weigh 20-30g starch, 3-5g sodium nitrate, 2-4g potassium dihydrogen phosphate, 0.4-0.6g magnesium sulfate, 6-8g citric acid and 800-1000mL deionized water, stir and place in a sterile In the tank, sterilize at 100-110°C for 5-10 minutes to obtain a culture medium, inoculate Xanthomonas bacilli into the culture medium according to the inoculum size of 8-10%, and then transfer it to an incubator, at 30-40°C, 120 Cultivate at ~130r/min for 2~3 days, then place it in a centrifuge, centrifuge at 1200~1300r/min for 20~30min, collect the supernatant, that is, the Xanthomonas bacteria liquid;

(2)依次称取30~40g淀粉、6~8g蛋白胨、2~4g硝酸钠和800~1000mL去离子水,搅拌均匀后转移至灭菌罐中,在100~110℃灭菌10~20min,得到发酵培养基,随后转移至发酵罐中,待发酵培养基温度降至30~40℃后,取200~300mL上述黄单胞杆菌菌液加入到发酵罐中,在30~40℃下发酵3~4天,待发酵结束升温至100~110℃,搅拌5~10min,随后收集发酵液,并置于离心机中,在6000~7000r/min下离心30~40min,收集上清液,备用;(2) Weigh 30-40g of starch, 6-8g of peptone, 2-4g of sodium nitrate and 800-1000mL of deionized water in sequence, stir evenly, transfer to a sterilization tank, and sterilize at 100-110°C for 10-20min. Obtain the fermentation medium, and then transfer it to the fermenter. After the temperature of the fermentation medium drops to 30-40°C, take 200-300mL of the above-mentioned Xanthomonas bacteria liquid and add it to the fermenter, and ferment at 30-40°C for 3 ~4 days, after the fermentation is completed, the temperature is raised to 100-110°C, stirred for 5-10 minutes, then the fermentation liquid is collected, placed in a centrifuge, centrifuged at 6000-7000r/min for 30-40 minutes, the supernatant is collected, and set aside;

(3)称取200~300g新鲜牛骨,用去离子水洗涤干净,随后放入发酵罐中,取沼气液过滤,收集滤液,取1~2L滤液加入到发酵罐中,控制温度在30~40℃,密闭发酵2~3天,发酵结束,升温至100~110℃,搅拌灭菌20~30min,将发酵后的牛骨取出,收集发酵液,并置于离心机中,在5000~6000r/min下离心30~40min,收集上清液,将上清液加入到烧杯中,再加入2~4g活性炭,静置1~2h,过滤,得到滤液,备用;(3) Weigh 200-300g of fresh beef bone, wash it with deionized water, then put it into a fermenter, filter the biogas liquid, collect the filtrate, take 1-2L of the filtrate and add it to the fermenter, and control the temperature at 30- 40°C, airtight fermentation for 2-3 days, when the fermentation is over, raise the temperature to 100-110°C, stir and sterilize for 20-30min, take out the fermented bovine bones, collect the fermentation liquid, and put it in a centrifuge at 5000-6000r Centrifuge for 30-40min at 1/min, collect the supernatant, add the supernatant to the beaker, add 2-4g of activated carbon, let stand for 1-2h, filter to obtain the filtrate, and set aside;

(4)称取3~5g氧化锌、2~4g羧甲基纤维素、6~8g碳酸钙加入到粉碎机中进行粉碎,过100~200目筛,得到混合粉末;(4) Weigh 3-5g of zinc oxide, 2-4g of carboxymethyl cellulose, and 6-8g of calcium carbonate into a pulverizer for pulverization, and pass through a 100-200 mesh sieve to obtain a mixed powder;

(5)按重量份数计,称取40~50份步骤(2)备用的上清液、20~30份步骤(3)备用的滤液、5~8份上述混合粉末、3~5份硬脂酸钠、1~3份十二烷基苯磺酸钠、1~3份二月桂酸二丁基锡加入到搅拌机中,在10000~12000r/min下搅拌2~3h,得到医用包装纸表面施胶剂。(5) In parts by weight, weigh 40 to 50 parts of supernatant from step (2), 20 to 30 parts of filtrate from step (3), 5 to 8 parts of the above mixed powder, 3 to 5 parts of hard Add sodium fatty acid, 1-3 parts of sodium dodecylbenzenesulfonate, and 1-3 parts of dibutyltin dilaurate into the mixer, and stir at 10000-12000r/min for 2-3 hours to obtain surface sizing of medical packaging paper agent.

本发明的应用方法:在医用纸的一侧边缘处涂抹一圈本发明制备的表面施胶剂,然后将薄膜覆盖到涂有施胶剂的医用纸上,然后在150~160℃、4~6kPa下热封3~5s,预留一边作为封口,形成纸袋,然后将包装物装入纸袋中,然后将开口一端进行热封即可,使用时只要在纸袋开启端从两层纸粘合处剥离即可打开。Application method of the present invention: apply a circle of the surface sizing agent prepared by the present invention on one side edge of the medical paper, then cover the film on the medical paper coated with the sizing agent, and then heat it at 150~160°C, 4~ Heat seal at 6kPa for 3 to 5 seconds, reserve one side as a seal to form a paper bag, then put the package into the paper bag, and then heat seal the open end. Peel to open.

本发明与其他方法相比,有益技术效果是:Compared with other methods, the present invention has beneficial technical effects as follows:

(1)本发明制备的施胶剂解决了灭菌过程中表面施胶剂容隐粘附在包装物上的问题,使用本发明的施胶剂制备的纸袋,纸张与薄膜的热强度高,密封性好,剥离时纸张与薄膜能够完全分离,不会造成纸袋破损或纸张纤维粘出的问题;(1) The sizing agent prepared by the present invention solves the problem that the surface sizing agent implicitly adheres to the packaging during the sterilization process. The paper bag prepared by using the sizing agent of the present invention has high thermal strength of paper and film, Good sealing performance, the paper and film can be completely separated when peeling off, and will not cause damage to the paper bag or sticking out of the paper fiber;

(2)经本发明的表面施胶剂施胶的医用包装纸具有一定的透气度、耐水性、良好的表面强度和纸塑结合力;(2) The medical packaging paper sized by the surface sizing agent of the present invention has certain air permeability, water resistance, good surface strength and paper-plastic bonding force;

(3)本发明主制备步骤简单,所需成本低。(3) The main preparation steps of the present invention are simple and the required cost is low.

具体实施方式detailed description

首先称取20~30g淀粉、3~5g硝酸钠、2~4g磷酸二氢钾、0.4~0.6g硫酸镁、6~8g柠檬酸和800~1000mL去离子水,搅拌后置于灭菌罐中,在100~110℃灭菌5~10min,得到培养基,按接种量8~10%将黄单胞杆菌接种到培养基中,随后转移至培养箱中,在30~40℃、120~130r/min下培养2~3天,然后置于离心机中,在1200~1300r/min下离心20~30min,收集上清液,即黄单胞杆菌菌液;然后依次称取30~40g淀粉、6~8g蛋白胨、2~4g硝酸钠和800~1000mL去离子水,搅拌均匀后转移至灭菌罐中,在100~110℃灭菌10~20min,得到发酵培养基,随后转移至发酵罐中,待发酵培养基温度降至30~40℃后,取200~300mL上述黄单胞杆菌菌液加入到发酵罐中,在30~40℃下发酵3~4天,待发酵结束升温至100~110℃,搅拌5~10min,随后收集发酵液,并置于离心机中,在6000~7000r/min下离心30~40min,收集上清液,备用;再称取200~300g新鲜牛骨,用去离子水洗涤干净,随后放入发酵罐中,取沼气液过滤,收集滤液,取1~2L滤液加入到发酵罐中,控制温度在30~40℃,密闭发酵2~3天,发酵结束,升温至100~110℃,搅拌灭菌20~30min,将发酵后的牛骨取出,收集发酵液,并置于离心机中,在5000~6000r/min下离心30~40min,收集上清液,将上清液加入到烧杯中,再加入2~4g活性炭,静置1~2h,过滤,得到滤液,备用;称取3~5g氧化锌、2~4g羧甲基纤维素、6~8g碳酸钙加入到粉碎机中进行粉碎,过100~200目筛,得到混合粉末;最后按重量份数计,称取40~50份备用的上清液、20~30份备用的滤液、5~8份上述混合粉末、3~5份硬脂酸钠、1~3份十二烷基苯磺酸钠、1~3份二月桂酸二丁基锡加入到搅拌机中,在10000~12000r/min下搅拌2~3h,得到医用包装纸表面施胶剂。First weigh 20-30g starch, 3-5g sodium nitrate, 2-4g potassium dihydrogen phosphate, 0.4-0.6g magnesium sulfate, 6-8g citric acid and 800-1000mL deionized water, stir and place in a sterilized tank , sterilized at 100-110°C for 5-10 minutes to obtain a culture medium, inoculated Xanthomonas bacilli into the culture medium according to the inoculum size of 8-10%, and then transferred to an incubator, at 30-40°C, 120-130r Cultivate at 1200-1300r/min for 2-3 days, then put it in a centrifuge, centrifuge at 1200-1300r/min for 20-30min, collect the supernatant, that is, Xanthomonas bacteria liquid; then weigh 30-40g starch, 6-8g of peptone, 2-4g of sodium nitrate and 800-1000mL of deionized water, stirred evenly and then transferred to a sterilization tank, sterilized at 100-110°C for 10-20min to obtain a fermentation medium, and then transferred to a fermentation tank After the temperature of the fermentation medium drops to 30-40°C, take 200-300mL of the above-mentioned Xanthomonas bacteria liquid and add it to the fermenter, and ferment at 30-40°C for 3-4 days, and after the fermentation is completed, the temperature is raised to 100-100°C. Stir at 110°C for 5-10 minutes, then collect the fermented liquid, put it in a centrifuge, centrifuge at 6000-7000r/min for 30-40 minutes, collect the supernatant, and set aside; then weigh 200-300g of fresh beef bone, and use Wash it with deionized water, then put it into a fermenter, filter the biogas liquid, collect the filtrate, take 1-2L of filtrate and add it to the fermenter, control the temperature at 30-40°C, and ferment in an airtight manner for 2-3 days, and the fermentation is over. Raise the temperature to 100-110°C, stir and sterilize for 20-30 minutes, take out the fermented bovine bone, collect the fermentation broth, put it in a centrifuge, centrifuge at 5000-6000r/min for 30-40min, collect the supernatant, Add the supernatant to the beaker, then add 2-4g of activated carbon, let it stand for 1-2 hours, filter to obtain the filtrate, and set aside; weigh 3-5g of zinc oxide, 2-4g of carboxymethyl cellulose, 6-8g of carbonic acid Calcium is added into a pulverizer for pulverization, and passed through a 100-200 mesh sieve to obtain a mixed powder; finally, in parts by weight, 40-50 parts of the spare supernatant, 20-30 parts of the spare filtrate, 5-8 Add the above mixed powder, 3-5 parts of sodium stearate, 1-3 parts of sodium dodecylbenzenesulfonate, and 1-3 parts of dibutyltin dilaurate into the mixer, and stir at 10000-12000r/min for 2 ~3h to obtain the surface sizing agent for medical packaging paper.

实例1Example 1

首先称取20g淀粉、3g硝酸钠、2g磷酸二氢钾、0.4g硫酸镁、6g柠檬酸和800mL去离子水,搅拌后置于灭菌罐中,在100℃灭菌5min,得到培养基,按接种量8%将黄单胞杆菌接种到培养基中,随后转移至培养箱中,在30℃、120r/min下培养2天,然后置于离心机中,在1200r/min下离心20min,收集上清液,即黄单胞杆菌菌液;然后依次称取30g淀粉、6g蛋白胨、2g硝酸钠和800mL去离子水,搅拌均匀后转移至灭菌罐中,在100℃灭菌10min,得到发酵培养基,随后转移至发酵罐中,待发酵培养基温度降至30℃后,取200mL上述黄单胞杆菌菌液加入到发酵罐中,在30℃下发酵3天,待发酵结束升温至100℃,搅拌5min,随后收集发酵液,并置于离心机中,在6000r/min下离心30min,收集上清液,备用;再称取200g新鲜牛骨,用去离子水洗涤干净,随后放入发酵罐中,取沼气液过滤,收集滤液,取1L滤液加入到发酵罐中,控制温度在30℃,密闭发酵2天,发酵结束,升温至100℃,搅拌灭菌20min,将发酵后的牛骨取出,收集发酵液,并置于离心机中,在5000r/min下离心30min,收集上清液,将上清液加入到烧杯中,再加入2g活性炭,静置1h,过滤,得到滤液,备用;称取3g氧化锌、2g羧甲基纤维素、6g碳酸钙加入到粉碎机中进行粉碎,过100目筛,得到混合粉末;最后按重量份数计,称取40份备用的上清液、20份备用的滤液、5份上述混合粉末、3份硬脂酸钠、1份十二烷基苯磺酸钠、1份二月桂酸二丁基锡加入到搅拌机中,在10000r/min下搅拌2h,得到医用包装纸表面施胶剂。First, weigh 20g of starch, 3g of sodium nitrate, 2g of potassium dihydrogen phosphate, 0.4g of magnesium sulfate, 6g of citric acid and 800mL of deionized water, stir and place in a sterilizing tank, and sterilize at 100°C for 5 minutes to obtain a culture medium. Xanthomonas was inoculated into the culture medium according to the inoculation amount of 8%, then transferred to the incubator, cultured at 30°C and 120r/min for 2 days, then placed in a centrifuge, and centrifuged at 1200r/min for 20min, Collect the supernatant, that is, the Xanthomonas bacteria liquid; then weigh 30g starch, 6g peptone, 2g sodium nitrate and 800mL deionized water in sequence, stir evenly, transfer to a sterilization tank, and sterilize at 100°C for 10min to obtain The fermentation medium was then transferred to a fermenter. After the temperature of the fermentation medium dropped to 30°C, 200 mL of the above-mentioned Xanthomonas bacteria liquid was added to the fermenter, and fermented at 30°C for 3 days. After the fermentation was completed, the temperature was raised to Stir at 100°C for 5 minutes, then collect the fermentation broth, put it in a centrifuge, and centrifuge it at 6000r/min for 30 minutes, collect the supernatant, and set aside; then weigh 200g of fresh bovine bone, wash it with deionized water, and then put it Put it into the fermenter, filter the biogas liquid, collect the filtrate, take 1L of filtrate and add it to the fermenter, control the temperature at 30°C, and ferment in a sealed container for 2 days. Take out the bovine bone, collect the fermentation liquid, put it in a centrifuge, centrifuge at 5000r/min for 30min, collect the supernatant, add the supernatant to a beaker, add 2g of activated carbon, let stand for 1h, filter to obtain the filtrate , standby; take 3g zinc oxide, 2g carboxymethyl cellulose, 6g calcium carbonate and join in the pulverizer to pulverize, pass through 100 mesh sieves, obtain mixed powder; Clear liquid, 20 parts of spare filtrate, 5 parts of the above-mentioned mixed powder, 3 parts of sodium stearate, 1 part of sodium dodecylbenzenesulfonate, and 1 part of dibutyltin dilaurate are added to the mixer, and the mixture is mixed at 10000r/min Stir for 2 hours to obtain the surface sizing agent for medical packaging paper.

在医用纸的一侧边缘处涂抹一圈本发明制备的表面施胶剂,然后将薄膜覆盖到涂有施胶剂的医用纸上,然后在150℃、4kPa下热封3s,预留一边作为封口,形成纸袋,然后将包装物装入纸袋中,然后将开口一端进行热封即可,使用时只要在纸袋开启端从两层纸粘合处剥离即可打开。Apply a circle of the surface sizing agent prepared by the present invention on one edge of the medical paper, then cover the film on the medical paper coated with the sizing agent, then heat seal at 150°C and 4kPa for 3s, and reserve one side as Seal it to form a paper bag, then put the packaging into the paper bag, and then heat seal the opening end. When in use, just peel off the opening end of the paper bag from the adhesive part of the two layers of paper to open it.

实例2Example 2

首先称取30g淀粉、5g硝酸钠、4g磷酸二氢钾、0.6g硫酸镁、8g柠檬酸和1000mL去离子水,搅拌后置于灭菌罐中,在110℃灭菌10min,得到培养基,按接种量10%将黄单胞杆菌接种到培养基中,随后转移至培养箱中,在40℃、130r/min下培养3天,然后置于离心机中,在1300r/min下离心30min,收集上清液,即黄单胞杆菌菌液;然后依次称取40g淀粉、8g蛋白胨、4g硝酸钠和1000mL去离子水,搅拌均匀后转移至灭菌罐中,在110℃灭菌20min,得到发酵培养基,随后转移至发酵罐中,待发酵培养基温度降至40℃后,取300mL上述黄单胞杆菌菌液加入到发酵罐中,在40℃下发酵4天,待发酵结束升温至110℃,搅拌10min,随后收集发酵液,并置于离心机中,在7000r/min下离心40min,收集上清液,备用;再称取300g新鲜牛骨,用去离子水洗涤干净,随后放入发酵罐中,取沼气液过滤,收集滤液,取2L滤液加入到发酵罐中,控制温度在40℃,密闭发酵3天,发酵结束,升温至110℃,搅拌灭菌30min,将发酵后的牛骨取出,收集发酵液,并置于离心机中,在6000r/min下离心40min,收集上清液,将上清液加入到烧杯中,再加入4g活性炭,静置2h,过滤,得到滤液,备用;称取5g氧化锌、4g羧甲基纤维素、8g碳酸钙加入到粉碎机中进行粉碎,过200目筛,得到混合粉末;最后按重量份数计,称取50份备用的上清液、30份备用的滤液、8份上述混合粉末、5份硬脂酸钠、3份十二烷基苯磺酸钠、3份二月桂酸二丁基锡加入到搅拌机中,在12000r/min下搅拌3h,得到医用包装纸表面施胶剂。First, weigh 30g of starch, 5g of sodium nitrate, 4g of potassium dihydrogen phosphate, 0.6g of magnesium sulfate, 8g of citric acid and 1000mL of deionized water, stir and place in a sterilizing tank, and sterilize at 110°C for 10 minutes to obtain a culture medium. Xanthomonas was inoculated into the culture medium according to 10% of the inoculation amount, then transferred to an incubator, cultured at 40°C and 130r/min for 3 days, then placed in a centrifuge, and centrifuged at 1300r/min for 30min. Collect the supernatant, that is, the Xanthomonas bacteria liquid; then weigh 40g starch, 8g peptone, 4g sodium nitrate and 1000mL deionized water in sequence, stir them evenly, transfer them to a sterilizing tank, and sterilize at 110°C for 20min to obtain The fermentation medium was then transferred to a fermenter. After the temperature of the fermentation medium dropped to 40°C, 300 mL of the above-mentioned Xanthomonas bacteria liquid was added to the fermenter, and fermented at 40°C for 4 days. After the fermentation was completed, the temperature was raised to Stir at 110°C for 10 minutes, then collect the fermentation broth, put it in a centrifuge, and centrifuge it at 7000r/min for 40 minutes, collect the supernatant, and set aside; then weigh 300g of fresh bovine bone, wash it with deionized water, and put it in the Put it into the fermenter, filter the biogas liquid, collect the filtrate, take 2L filtrate and add it to the fermenter, control the temperature at 40°C, and ferment in a sealed container for 3 days. Take out the bovine bone, collect the fermented liquid, put it in a centrifuge, centrifuge at 6000r/min for 40min, collect the supernatant, put the supernatant into a beaker, add 4g of activated carbon, let stand for 2h, and filter to obtain the filtrate , for subsequent use; take 5g zinc oxide, 4g carboxymethyl cellulose, 8g calcium carbonate and join in the pulverizer to pulverize, cross 200 mesh sieves, obtain mixed powder; Clear liquid, 30 parts of standby filtrate, 8 parts of the above mixed powder, 5 parts of sodium stearate, 3 parts of sodium dodecylbenzenesulfonate, and 3 parts of dibutyltin dilaurate are added to the mixer, and the mixture is mixed at 12000r/min Stir for 3 hours to obtain the surface sizing agent for medical packaging paper.

在医用纸的一侧边缘处涂抹一圈本发明制备的表面施胶剂,然后将薄膜覆盖到涂有施胶剂的医用纸上,然后在160℃、6kPa下热封5s,预留一边作为封口,形成纸袋,然后将包装物装入纸袋中,然后将开口一端进行热封即可,使用时只要在纸袋开启端从两层纸粘合处剥离即可打开。Apply a circle of the surface sizing agent prepared by the present invention on one edge of the medical paper, then cover the film on the medical paper coated with the sizing agent, then heat seal at 160°C and 6kPa for 5s, and reserve one side as Seal it to form a paper bag, then put the packaging into the paper bag, and then heat seal the opening end. When in use, just peel off the opening end of the paper bag from the adhesive part of the two layers of paper to open it.

实例3Example 3

首先称取25g淀粉、4g硝酸钠、3g磷酸二氢钾、0.5g硫酸镁、7g柠檬酸和900mL去离子水,搅拌后置于灭菌罐中,在105℃灭菌8min,得到培养基,按接种量9%将黄单胞杆菌接种到培养基中,随后转移至培养箱中,在35℃、125r/min下培养2.5天,然后置于离心机中,在1250r/min下离心25min,收集上清液,即黄单胞杆菌菌液;然后依次称取35g淀粉、7g蛋白胨、3g硝酸钠和900mL去离子水,搅拌均匀后转移至灭菌罐中,在105℃灭菌15min,得到发酵培养基,随后转移至发酵罐中,待发酵培养基温度降至35℃后,取250mL上述黄单胞杆菌菌液加入到发酵罐中,在35℃下发酵3.5天,待发酵结束升温至105℃,搅拌8min,随后收集发酵液,并置于离心机中,在6500r/min下离心35min,收集上清液,备用;再称取250g新鲜牛骨,用去离子水洗涤干净,随后放入发酵罐中,取沼气液过滤,收集滤液,取1.5L滤液加入到发酵罐中,控制温度在35℃,密闭发酵2.5天,发酵结束,升温至105℃,搅拌灭菌25min,将发酵后的牛骨取出,收集发酵液,并置于离心机中,在5500r/min下离心35min,收集上清液,将上清液加入到烧杯中,再加入3g活性炭,静置1.5h,过滤,得到滤液,备用;称取4g氧化锌、3g羧甲基纤维素、7g碳酸钙加入到粉碎机中进行粉碎,过150目筛,得到混合粉末;最后按重量份数计,称取45份备用的上清液、25份备用的滤液、6份上述混合粉末、4份硬脂酸钠、2份十二烷基苯磺酸钠、2份二月桂酸二丁基锡加入到搅拌机中,在11000r/min下搅拌2.5h,得到医用包装纸表面施胶剂。First weigh 25g of starch, 4g of sodium nitrate, 3g of potassium dihydrogen phosphate, 0.5g of magnesium sulfate, 7g of citric acid and 900mL of deionized water, put them in a sterilizing tank after stirring, and sterilize at 105°C for 8 minutes to obtain a culture medium. Xanthomonas was inoculated into the culture medium according to the inoculation amount of 9%, and then transferred to an incubator, cultured at 35°C and 125r/min for 2.5 days, then placed in a centrifuge, and centrifuged at 1250r/min for 25min. Collect the supernatant, that is, the Xanthomonas bacteria liquid; then weigh 35g starch, 7g peptone, 3g sodium nitrate and 900mL deionized water in sequence, stir them evenly, transfer them to a sterilizing tank, and sterilize at 105°C for 15 minutes to obtain The fermentation medium was then transferred to a fermenter. After the temperature of the fermentation medium dropped to 35°C, 250 mL of the above-mentioned Xanthomonas bacterium liquid was added to the fermenter, and fermented at 35°C for 3.5 days. After the fermentation was completed, the temperature was raised to Stir at 105°C for 8 minutes, then collect the fermentation broth, put it in a centrifuge, and centrifuge it at 6500r/min for 35 minutes, collect the supernatant, and set aside; then weigh 250g of fresh bovine bone, wash it with deionized water, and put it in the Put it into the fermenter, filter the biogas liquid, collect the filtrate, take 1.5L filtrate and add it to the fermenter, control the temperature at 35°C, and ferment in a sealed container for 2.5 days. Take out the bovine bone, collect the fermentation liquid, put it in a centrifuge, centrifuge at 5500r/min for 35min, collect the supernatant, add the supernatant to a beaker, add 3g of activated carbon, let stand for 1.5h, filter, Obtain filtrate, standby; Weigh 4g zinc oxide, 3g carboxymethyl cellulose, 7g calcium carbonate and join in pulverizer and pulverize, cross 150 mesh sieves, obtain mixed powder; Finally, count 45 parts by weight for standby The supernatant, 25 parts of standby filtrate, 6 parts of the above-mentioned mixed powder, 4 parts of sodium stearate, 2 parts of sodium dodecylbenzenesulfonate, and 2 parts of dibutyltin dilaurate are added to the mixer, at 11000r/ Stir for 2.5 hours at 1 min to obtain the surface sizing agent for medical packaging paper.

在医用纸的一侧边缘处涂抹一圈本发明制备的表面施胶剂,然后将薄膜覆盖到涂有施胶剂的医用纸上,然后在155℃、5kPa下热封4s,预留一边作为封口,形成纸袋,然后将包装物装入纸袋中,然后将开口一端进行热封即可,使用时只要在纸袋开启端从两层纸粘合处剥离即可打开。Apply a circle of surface sizing agent prepared by the present invention on one edge of medical paper, then cover the film on the medical paper coated with sizing agent, heat seal at 155°C and 5kPa for 4s, and reserve one side as Seal it to form a paper bag, then put the packaging into the paper bag, and then heat seal the opening end. When in use, just peel off the opening end of the paper bag from the adhesive part of the two layers of paper to open it.

Claims (1)

1. a kind of preparation method of medical packing paper Cypres, it is characterised in that specifically preparation process is:
(1)Weigh 20~30g starch, 3~5g sodium nitrate, 2~4g potassium dihydrogen phosphates, 0.4~0.6g magnesium sulfate, 6~8g lemons Acid and 800~1000mL deionized waters, are placed in sterilization tank after stirring, and sterilize 5~10min at 100~110 DEG C, is cultivated Base, Xanthomonas campestris is inoculated into culture medium by inoculum concentration 8~10%, is subsequently transferred in incubator, 30~40 DEG C, 120 Cultivate 2~3 days, be subsequently placed in centrifuge under~130r/min, 20~30min is centrifuged under 1200~1300r/min, collect Supernatant, i.e. Xanthomonas campestris bacterium solution;
(2)30~40g starch, 6~8g peptones, 2~4g sodium nitrate and 800~1000mL deionized waters are weighed successively, are stirred It is transferred to after uniformly in sterilization tank, sterilize 10~20min at 100~110 DEG C, obtains fermentation medium, is subsequently transferred to ferment In tank, after fermentation medium temperature is down to 30~40 DEG C, the above-mentioned Xanthomonas campestris bacterium solutions of 200~300mL are taken to be added to fermentation In tank, fermented 3~4 days at 30~40 DEG C, treat that fermentation ends are warming up to 100~110 DEG C, stirred 5~10min, then collect Zymotic fluid, it is placed in centrifuge, 30~40min is centrifuged under 6000~7000r/min, collects supernatant, it is standby;
(3)The fresh ox bones of 200~300g are weighed, is washed with deionized totally, is subsequently placed into fermentation tank, takes methane liquid mistake Filter, filtrate is collected, takes 1~2L filtrates to be added in fermentation tank, control temperature sealed fermenting 2~3 days, is fermented at 30~40 DEG C Terminate, be warming up to 100~110 DEG C, stirring 20~30min of sterilizing, the ox bone after fermentation taken out, zymotic fluid is collected, is placed in In centrifuge, 30~40min is centrifuged under 5000~6000r/min, supernatant is collected, supernatant is added in beaker, then 2~4g activated carbons are added, 1~2h is stood, filtering, obtains filtrate, it is standby;
(4)Weigh 3~5g zinc oxide, 2~4g carboxymethyl celluloses, 6~8g calcium carbonate to be added in pulverizer and crushed, mistake 100~200 mesh sieves, obtain mixed-powder;
(5)Count in parts by weight, weigh 40~50 parts of steps(2)Standby supernatant, 20~30 parts of steps(3)Standby filter Liquid, 5~8 parts of above-mentioned mixed-powders, 3~5 parts of odium stearate, 1~3 part of neopelex, 1~3 part of tin dilaurate two Butyl tin is added in mixer, and 2~3h is stirred under 10000~12000r/min, obtains medical packing paper Cypres.
CN201610746866.6A 2016-08-29 2016-08-29 A kind of preparation method of medical packing paper Cypres Expired - Fee Related CN106168004B (en)

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