[go: up one dir, main page]

CN1064082C - Bioenzyme used for dismounting pictures and the method therefor - Google Patents

Bioenzyme used for dismounting pictures and the method therefor Download PDF

Info

Publication number
CN1064082C
CN1064082C CN94106354A CN94106354A CN1064082C CN 1064082 C CN1064082 C CN 1064082C CN 94106354 A CN94106354 A CN 94106354A CN 94106354 A CN94106354 A CN 94106354A CN 1064082 C CN1064082 C CN 1064082C
Authority
CN
China
Prior art keywords
solution
enzyme
bricks
unmounting
aqueous solution
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.)
Expired - Fee Related
Application number
CN94106354A
Other languages
Chinese (zh)
Other versions
CN1113516A (en
Inventor
程建芳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beijing Union University
Original Assignee
Beijing Union University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beijing Union University filed Critical Beijing Union University
Priority to CN94106354A priority Critical patent/CN1064082C/en
Publication of CN1113516A publication Critical patent/CN1113516A/en
Application granted granted Critical
Publication of CN1064082C publication Critical patent/CN1064082C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Enzymes And Modification Thereof (AREA)
  • Detergent Compositions (AREA)
  • Paper (AREA)

Abstract

用生物酶素制成的揭裱液及其揭裱去污的方法。该揭裱液包括两种互相配合使用的酶溶液;由粉剂溶菌酶和水按每100ml溶液中含有120-220u活力的配比所配制成的溶菌酶水溶液,由粉剂α-淀粉酶和水按每100ml溶液中含有30-90u活力的配比所配制成α-淀粉酶水溶液,其揭裱方法分为干法和湿法,干法为涂刷一恒温法,湿法为浸泡法,可对被微生物分泌物、尘埃、粘结剂等污物破坏的“档案砖”进行揭裱去污,具有快速、方便、安全、经济的优点。The unmounting solution made of biological enzyme and the method for unmounting and decontamination thereof. The mounting fluid includes two kinds of enzyme solutions used in conjunction with each other; the lysozyme aqueous solution prepared by the ratio of 120-220u activity in every 100ml solution by powder lysozyme and water, and the powder α-amylase and water by Each 100ml solution contains 30-90u activity ratio to prepare α-amylase aqueous solution. The unmounting method is divided into dry method and wet method. The dry method is brushing-constant temperature method, and the wet method is soaking method. The decontamination of "archive bricks" damaged by microbial secretions, dust, adhesives and other dirt has the advantages of fast, convenient, safe and economical.

Description

生物酶素揭裱液及其揭裱方法Bioenzyme unmounting liquid and its unmounting method

本发明涉及到用生物酶素制成的揭裱液及其揭裱去污的方法。The invention relates to a mounting solution made of biozyme and a method for decontaminating the mounting.

在古籍档案文献中,载体材料大部分是手工纸,手工纸的主要成份是纤维素。然而随着时间的推移,档案典籍在保存和使用过程中,不可避免地遭到多方面的损害。除光照、有害气体、温湿变化外,还受到较严重的污物破坏,该污物包括:微生物的分泌物,油斑、色斑、尘埃及陈腐的粘性剂。其中微生物分泌物、尘埃、粘结剂等对档案破坏较为严重。档案典籍在潮湿条件下,粘结剂及分泌物易与灰尘、有害气体发生反应,纸张在自身和外界的压力下,页与页之间就会紧紧粘结在一起,使档案卷书变得又硬又脆,形同砖头,故称之为“档案砖”或“文献砖”。传统的揭裱法有干法、湿法和高湿蒸熏法。干法就是利用薄竹片插到粘结不严重的历史文献的页与页之间的空隙中,让竹片贴紧底页,左右移动分离文献页与页之间粘连之处,使之分离。此法适用于粘结不严重的档案。湿法是利用热水或开水冲洗“档案砖”内外部的污物。此法适用于档案文件内的泥斑和较轻的粘结剂污物。高温蒸熏法是把粘结得又硬又结实的“档案砖”,放在锅内,利用高温蒸汽熏掉“档案砖”内的污物。但对于微生物污染严重的“档案砖”,其污物化学稳定性能强,难溶或不溶于水,对高温也不敏感,往往只能揭开一部分污物粘连在一起的档案纸张,并会使珍贵档案文献的纸张变得非常脆化,不易保存。综上所述传统的揭裱法存在以下几个缺点:由于手工操作,十分麻烦,揭裱时间缓慢,已远远不能满足堆积如山待修字画的需求;还是由于手工操作,只能凭个人经验,不便掌握,有时操作不当有损坏珍贵文物的危险。因此有必要去寻找一种快速、方便、安全、经济的方法去取代这种缓慢、麻烦、危险、不经济的传统揭裱去污方法。In the archives of ancient books, most of the carrier materials are handmade paper, and the main component of handmade paper is cellulose. However, with the passage of time, archival classics are inevitably damaged in many ways in the process of preservation and use. In addition to light, harmful gases, and temperature and humidity changes, it is also damaged by serious dirt, which includes: microbial secretions, oil spots, stains, dust, and stale viscous agents. Among them, microbial secretions, dust, adhesives, etc. are more serious damage to archives. Under humid conditions, the adhesives and secretions of archives and classics are easy to react with dust and harmful gases. Under the pressure of itself and the outside world, the pages of the paper will be tightly bonded together, making the archives book They are hard and brittle, like bricks, so they are called "archive bricks" or "documentary bricks". Traditional exposing methods include dry method, wet method and high-humidity fumigation method. The dry method is to insert a thin bamboo piece into the gap between the pages of historical documents that are not seriously bonded, let the bamboo piece stick to the bottom page, move left and right to separate the adhesion between the pages of the document, and separate them . This method is suitable for files that are not seriously bonded. The wet method is to use hot water or boiling water to wash the dirt inside and outside the "archive brick". This method is suitable for mud spots and lighter adhesive soiling in archival documents. The high-temperature fumigation method is to put the hard and strong "archive bricks" in the pot, and use high-temperature steam to fumigate the dirt in the "archive bricks". However, for "archive bricks" with serious microbial contamination, the dirt has strong chemical stability, is insoluble or insoluble in water, and is not sensitive to high temperatures. The paper of precious archival documents becomes very brittle and difficult to preserve. To sum up, the traditional unmounting method has the following disadvantages: due to manual operation, it is very troublesome, and the unmounting time is slow, which is far from meeting the needs of piles of calligraphy and paintings waiting to be repaired; or due to manual operation, only personal experience can be used. , It is inconvenient to master, and sometimes improper operation may damage precious cultural relics. Therefore it is necessary to find a fast, convenient, safe and economical method to replace this slow, cumbersome, dangerous and uneconomical traditional decontamination method.

本发明的目的是实现一种生物酶素制成的揭裱液及其揭裱去污的方法,是用生物酶素制成揭裱液,使用该揭裱液去揭裱、去污,具有快速、方便、安全、经济的优点。The purpose of the present invention is to realize a kind of demounting liquid that biological enzyme element is made and the method for decontaminating and decontaminating thereof, be to make demounting liquid with biological enzyme element, use this demounting liquid to remove mounting, decontamination, have Fast, convenient, safe and economical advantages.

本发明是通过下述方式实现的:用生物酶素制成的含酶水溶液作为“档案砖”、“文献砖”的揭裱液,可以对受到污物破坏的“档案砖”或“文献砖”进行揭裱去污。The present invention is achieved in the following manner: the enzyme-containing aqueous solution made of biological enzymes is used as the mounting solution for "archive bricks" and "document bricks", which can be used for "archive bricks" or "document bricks" damaged by dirt. "Carry out exposing and decontaminating.

由于受到污物破坏的“档案砖”或“文献砖”的种类不同,例如象古字画,皇榜一类,或是象案卷、奏本、古书一类的;存放地点不同;纸张性质的不同,因此实际上污物对古藉、档案、文献的破坏是十分复杂的。但从破坏“档案砖”或“文献砖”的污物的角度上来分析,污物可以分为三种类型:(1)纯淀粉粘结剂污物,(2)纯微生物的分泌物,(3)淀粉粘结剂、灰尘与微生物的共同作用。利用酶液进行揭裱去污,是利用酶对污物进行反应的机理,例如利用酶素对淀粉浆糊污物的水解反应,可对纯淀粉粘结剂污物进行处理,而不同性能的酶素,对不同的污物的反应又有专一性,因此本发明的生物酶素揭裱液根据受到污物破坏的“档案砖”或“文献砖”被破坏的不同情况和程度,配制了三种含有不同成分酶素的揭裱液。Due to the different types of "archive bricks" or "document bricks" damaged by dirt, such as ancient calligraphy and paintings, imperial lists, or files, memorials, and ancient books; different storage locations; different paper properties , so in fact, the damage of dirt to ancient borrowings, archives, and documents is very complicated. However, from the perspective of the dirt that destroys "archive bricks" or "document bricks", the dirt can be divided into three types: (1) pure starch binder dirt, (2) secretions of pure microorganisms, ( 3) The joint action of starch binder, dust and microorganisms. The use of enzyme liquid to decontaminate is the mechanism of using enzymes to react with dirt. For example, the use of enzymes to hydrolyze starch paste dirt can treat pure starch binder dirt, and different properties Enzymes have specificity in response to different dirt, so the bioenzyme mounting solution of the present invention is prepared according to the different situations and degrees of destruction of "archive bricks" or "document bricks" damaged by dirt. Three kinds of mounting solutions containing different enzymes were prepared.

生物酶素揭裱液1号,适用于受到陈腐淀粉粘结剂、灰尘等污物破坏的“档案砖”或“文献砖”。该生物酶素揭裱液1号包括下述两种互相配合使用的酶溶液:Bioenzyme Mounting Solution No. 1 is suitable for "archive bricks" or "documentary bricks" damaged by stale starch binders, dust and other dirt. The bioenzyme mounting solution No. 1 includes the following two enzyme solutions used in conjunction with each other:

(1)将粉剂溶菌酶和水按每100ml溶液中含有120-220u活力的配比所配制成的溶菌酶水溶液,该溶液的PH为5.8-6.8,存放温度为0℃-10℃;(1) The aqueous solution of lysozyme prepared by mixing powdered lysozyme and water according to the ratio of 120-220u activity per 100ml solution, the pH of the solution is 5.8-6.8, and the storage temperature is 0°C-10°C ℃;

(2)将粉剂a-淀粉酶和水按每100ml溶液中含有30-90u活力的配比所配制成a-淀粉酶水溶液,该溶液的PH为7-7.8,存放温度为0℃-10℃。(2) Prepare the a-amylase aqueous solution by mixing powder a-amylase and water according to the ratio of 30-90u activity per 100ml solution, the pH of the solution is 7-7.8, and the storage temperature is 0°C- 10°C.

生物酶素揭裱液2号,适用于受到微生物、害虫的分泌物及灰尘等污物破坏的“档案砖”或“文献砖”,生物酶素揭裱液2号包括下述两种互相配合使用的复合酶溶液:Bioenzyme Mounting Solution No. 2 is suitable for "archive bricks" or "documentary bricks" damaged by microorganisms, pest secretions, dust and other dirt. Biozyme Mounting Solution No. 2 includes the following two kinds of mutual Compound enzyme solution used:

(1)溶菌酶、糖化酶的复合水溶液,是将粉剂溶菌酶和水按每100ml溶液中含有150-250u活力的配比配制的溶菌酶水溶液,该溶液的PH为5.8-6.8,再将液剂糖化酶和水按每100ml溶液中含有30-90u活力的配比配制的糖化酶水溶液,该溶液的PH为6.0-6.7,最后将上述两种酶溶液按1∶1等体积混合而制成的,该复合酶溶液的存放温度为0℃-10℃;(1) The composite aqueous solution of lysozyme and glucoamylase is a lysozyme aqueous solution prepared by powder lysozyme and water according to the ratio of 150-250u activity per 100ml solution, and the pH of the solution is 5.8-6.8 , and then the solution of glucoamylase and water according to the ratio of 30-90u activity in each 100ml solution to prepare the glucoamylase aqueous solution, the pH of the solution is 6.0-6.7, and finally the above two enzyme solutions are mixed by 1 : 1 is prepared by mixing equal volumes, and the storage temperature of the complex enzyme solution is 0°C-10°C;

(2)胰蛋白酶、枯草杆菌中性蛋白酶的复合水溶液,是将粉剂胰蛋白酶和水按每100ml溶液中含有100-200u活力的配比配制的胰蛋白酶水溶液,该溶液的PH为7.0-7.7,再将粉剂枯草杆菌中性蛋白酶和水按每100ml溶液中含有120-220u活力的配比配制的枯草杆菌中性蛋白酶水溶液,该溶液的PH为7.0-7.8,最后将上述两种酶溶液按1∶1等体积混合而制成的,该复合酶溶液的存放温度为0℃-10℃。(2) The composite aqueous solution of trypsin and bacillus subtilis neutral protease is the trypsin aqueous solution prepared by powder trypsin and water according to the ratio of 100-200u activity in every 100ml solution, and the pH of this solution is 7.0- 7.7, then powder bacillus subtilis neutral protease and water are prepared by the ratio of 120-220u activity in every 100ml solution to prepare bacillus subtilis neutral protease aqueous solution, the pH of this solution is 7.0-7.8, finally It is prepared by mixing the above two enzyme solutions in an equal volume ratio of 1:1, and the storage temperature of the composite enzyme solution is 0°C-10°C.

生物酶素揭裱液3号,适用于受到淀粉粘结剂,微生物、害虫的分泌物及灰尘等污物破坏的“档案砖”或“文献砖”,该生物酶素揭裱液3号包括下述两种互相配合使用的复合酶溶液:Bioenzyme Mounting Solution No. 3 is suitable for "archive bricks" or "documentary bricks" damaged by starch binders, secretions of microorganisms, pests, and dust. The Bioenzyme Mounting Solution No. 3 includes The following two complex enzyme solutions are used in conjunction with each other:

(1)溶菌酶、糖化酶的复合水溶液,是将粉剂溶菌酶和水按每100ml溶液中含有120-220u活力的配比配制的溶菌酶水溶液,该溶液的PH为6.0-6.7,再将液剂糖化酶和水按每100ml溶液中含有30-90u活力的配比配制的糖化酶水溶液,该溶液的PH为5.8-6.8,最后将上述两种酶溶液按1∶1等体积混合而制成的,该复合酶溶液的存放温度为0℃-10℃;(1) The composite aqueous solution of lysozyme and glucoamylase is a lysozyme aqueous solution prepared by mixing powdered lysozyme and water according to the ratio of 120-220u activity per 100ml solution, and the pH of the solution is 6.0-6.7 , and then the solution of glucoamylase and water according to the ratio of 30-90u activity in each 100ml solution to prepare the glucoamylase aqueous solution. The pH of the solution is 5.8-6.8, and finally the above two enzyme solutions : 1 is prepared by mixing equal volumes, and the storage temperature of the complex enzyme solution is 0°C-10°C;

(2)a-淀粉酶、胰蛋白酶,枯草杆菌中性蛋白酶的复合水溶液,是将粉剂a-淀粉酶和水按每100ml溶液中含有30-90u活力的a-淀粉酶水溶液,该溶液的PH为7.0-7.5,将粉剂胰蛋白酶和水按每100ml溶液中含有120-220u活力的配比配制的胰蛋白酶水溶液,该溶液的PH为7.0-7.8,再将粉剂枯草杆菌中性蛋白酶和水按100ml溶液中含有120-220u活力的配比配制的枯草杆菌中性蛋白酶水溶液,该溶液的PH为7.0-7.6,最后将上述三种酶溶液按1∶1∶1等体积混合而制成的,该复合酶溶液的存放温度为0℃-10℃。(2) α-amylase, trypsin, the composite aqueous solution of bacillus subtilis neutral protease, is that powder α-amylase and water contain the α-amylase aqueous solution of 30-90u activity in every 100ml solution, the pH of this solution If the pH of the solution is 7.0-7.5, the trypsin aqueous solution prepared by mixing powder trypsin and water according to the ratio of 120-220u activity per 100ml solution, the pH of the solution is 7.0-7.8, and then the powder Bacillus subtilis neutral protease and water contain the bacillus subtilis neutral protease aqueous solution prepared by the proportioning ratio of 120-220u activity in 100ml solution, the pH of this solution is 7.0-7.6, finally the above three kinds of enzyme solutions are pressed by 1 : 1:1 mixed with equal volumes, the storage temperature of the complex enzyme solution is 0°C-10°C.

上述生物酶素揭裱液一般存放在黄色玻璃瓶中,保存在0℃-10℃温度条件下,使用有效期在10个月以内。The above-mentioned bioenzyme unmounting solution is generally stored in a yellow glass bottle at a temperature of 0°C-10°C, and the validity period is within 10 months.

生物酶素揭裱液1号、2号、3号的揭裱方法可分为干法和湿法两种。The mounting methods of Biozyme Mounting Solution No. 1, No. 2, and No. 3 can be divided into dry method and wet method.

干法:每种标号的生物酶素揭裱液都是按下述方式进行揭裱操作的,按照其中酶液的序号(1)、(2)的顺序,用所述的序号(1)酶溶液、序号(2)酶溶液分先后对“档案、文献砖”进行涂刷-恒温的操作,该涂刷-恒温操作过程为:先用所述酶溶液在“档案、文献砖”上涂刷,再用纯植物纤维布包裹好,然后放入35℃-40℃恒温箱内恒温10-30分钟,所述序号(1)的酶溶液所进行的涂刷-恒温的操作次数为1-2次,所述序号(2)的酶溶液所进行的涂刷-恒温的操作次数为1-2次,整个涂刷-恒温操作完成后,经撤潮,待“档案、文献砖”的含湿量为30-40%时,即可进行揭裱,揭裱后的每页纸上喷涂含有新洁尔灭防霉剂的水溶液。该水溶液是由新洁尔灭防霉剂与水配制成,该水溶液含0.1%(重量百分比)的新洁尔灭防霉剂。涂刷-恒温操作中所用的纯植物纤维布为棉、毛、麻等植物纤维制成的布料。该干法适用于“档案砖”、“文献砖”的强度较差的纸张揭裱。Dry method: each label of bioenzyme unmounting solution is carried out in the following way, according to the order of the serial numbers (1) and (2) of the enzyme solution, use the serial number (1) enzyme Solution, serial number (2) Enzyme solution carries out brushing-constant temperature operation to "archives and document bricks" successively, the brushing-constant temperature operation process is: first use the enzyme solution to brush on "archives and document bricks" , then wrap it with pure plant fiber cloth, then put it into a 35°C-40°C constant temperature box for 10-30 minutes, and the number of brushing-constant temperature operations carried out by the enzyme solution of the serial number (1) is 1-2 times, the number of operations of the brushing-constant temperature carried out by the enzyme solution of the serial number (2) is 1-2 times. When the amount is 30-40%, it can be unmounted, and each page of paper after unmounted is sprayed with an aqueous solution containing bromogeramine antifungal agent. The aqueous solution is prepared from bromogeramine antifungal agent and water, and the aqueous solution contains 0.1% (percentage by weight) of the bromogeramine antifungal agent. The pure plant fiber cloth used in the brushing-constant temperature operation is the cloth made of plant fibers such as cotton, wool and hemp. This dry method is suitable for unmounting paper with poor strength of "archive bricks" and "document bricks".

湿法:每种标号的生物酶素揭裱液都是按下述方式进行揭裱操作的,按照其中酶液的序号(1)、(2)的顺序,将“档案、文献砖”分先后各一次浸泡在所述的序号(1)酶溶液、序号(2)酶溶液中,浸泡的温度为35℃-40℃,每次浸泡15-25分钟,每次浸泡完毕后都用清水冲洗净,最后经撤潮,待“档案、文献砖”的含湿量为30-40%时,即可进行揭裱。该湿法适用于“档案、文献砖”的强度较好纸张揭裱。Wet method: each type of bioenzyme demounting solution is demounted in the following way, according to the sequence of the serial numbers (1) and (2) of the enzyme solution, the "archives and literature bricks" are sorted Soak in the enzyme solution of serial number (1) and enzyme solution of serial number (2) each time, the soaking temperature is 35°C-40°C, soak for 15-25 minutes each time, rinse with water after each soaking Clean, and finally after the tide is removed, when the moisture content of the "archive and document bricks" is 30-40%, it can be unmounted. This wet method is suitable for unmounting of paper with better strength for "archives and literature bricks".

下面用实施例再进一步说明。Further illustrate with embodiment below again.

实施例1:Example 1:

制备生物酶素揭裱液1号,适用于受到淀粉粘结剂、灰尘等污物破坏的“档案、文献砖”。将粉剂溶菌酶和水按每100ml溶液中含有200u活力的配比所配制成溶菌酶水溶液,PH为6.3;将粉剂a-淀粉酶和水按每100ml溶液中含有50u活力的配比配制成a-淀粉酶水溶液,PH为7.3。Prepare Bioenzyme Mounting Solution No. 1, which is suitable for "archives and literature bricks" damaged by starch binders, dust and other dirt. Prepare powdered lysozyme and water according to the ratio of 200u activity per 100ml solution to make lysozyme aqueous solution, pH is 6.3; prepare powder a-amylase and water according to the ratio of 50u activity per 100ml solution into a-amylase aqueous solution, pH 7.3.

用干法对纸张强度较差的“档案、文献砖”进行揭裱。将溶菌酶水溶液涂刷在“档案、文献砖”内,用纯植物纤维布将已被酶液浸湿的“档案、文献砖”包裹好,再放入37℃的恒温箱内,20分钟后取出,拆去包裹用的纯植物纤维布,再用溶菌酶水溶液涂刷一遍,用纯植物纤维布包裹好后,又一次放入上述温度的恒温箱内,10分钟后取出,拆去包裹用的纯植物纤维布,再用a-淀粉酶水溶液涂刷一遍,用干净的纯植物纤维布包裹好后,放入37℃恒湿箱内,20分钟后取出,拆去包裹用的纯植纤维布,再用a-淀粉酶水溶液又涂刷一遍,用纯植物纤维布包裹好后,又一次放入37℃的恒温箱内,20分钟后取出,拆去包裹用的纯植物纤维布,经撤潮,待“档案、文献砖”的含湿量为30-40%时,可进行揭裱,只要稍加一点拉力,此时“档案、文献砖”的纸张的页与页之间可完全分离。为防止“档案、文献砖”的纸张再次发生霉害可在揭开的纸页上喷涂含有新洁尔灭防霉剂的水溶液,该水溶液是由新洁尔灭防霉剂与水配制成,该水溶液含0.1%(重量百分比)的新洁尔灭防霉剂。Use the dry method to unmount the "archive and document bricks" with poor paper strength. Paint the lysozyme aqueous solution on the "archives and literature bricks", wrap the "archives and literature bricks" soaked in the enzyme solution with pure plant fiber cloth, and then put them in a constant temperature box at 37°C. After 20 minutes Take it out, remove the pure plant fiber cloth used for wrapping, and then brush it again with lysozyme aqueous solution, wrap it with pure plant fiber cloth, put it in the incubator at the above temperature again, take it out after 10 minutes, and remove it for wrapping Pure plant fiber cloth, then brush it again with a-amylase aqueous solution, wrap it with a clean pure plant fiber cloth, put it in a 37°C constant humidity box, take it out after 20 minutes, and remove the pure plant fiber for wrapping cloth, then brush it again with a-amylase aqueous solution, wrap it with pure plant fiber cloth, put it in the incubator at 37°C again, take it out after 20 minutes, remove the pure plant fiber cloth for wrapping, and Withdraw the tide, and when the moisture content of the "archives and literature bricks" is 30-40%, it can be unmounted. As long as a little pulling force is applied, the pages of the "archives and literature bricks" can be completely sealed. separate. In order to prevent mildew on the paper of "archives and literature bricks", an aqueous solution containing bromogeramine antifungal agent can be sprayed on the uncovered paper pages. % (percentage by weight) of the bromogermic antifungal agent.

用湿法对纸张强度较好的“档案、文献砖”进行揭裱。将“档案、文献砖”浸入在溶菌酶水溶液中,浸泡的温度为37℃,20分钟后取出,用清水冲洗,再将冲洗后的“档案、文献砖”浸入a-淀粉酶水溶液中,浸泡的温度为37℃,20分钟后取出,用清水冲洗后,经撤潮,待“档案、文献砖”的含湿量为30-40%时,可进行揭裱。Use the wet method to unmount the "archive and document bricks" with good paper strength. Immerse the "archives and literature bricks" in the lysozyme aqueous solution at a temperature of 37°C, take them out after 20 minutes, rinse them with clean water, and then immerse the rinsed "archives and literature bricks" in the a-amylase aqueous solution, soak The temperature is 37°C, take it out after 20 minutes, rinse with clean water, and remove the moisture. When the moisture content of the "archive and document brick" is 30-40%, it can be unmounted.

实施例2:Example 2:

制备生物酶素揭裱液2号,适用于受到微生物、害虫的分泌物及灰尘等污物破坏的“档案、文献砖”。将粉剂溶菌酶和水按每100ml溶液中含有200u活力的配比所配制成溶菌酶水溶液,PH为6.2;再将液剂糖化酶和水按每100ml溶液中含有50u活力的配比配制成糖化酶水溶液,PH为6.2。并将上述两种酶溶液按1∶1等体积混合而制成复合酶溶液(1);将粉剂胰蛋白酶和水按每100ml溶液中含有160u活力的配比配制的胰蛋白酶水溶液,PH为7.3,再将粉剂枯草杆菌中性蛋白酶和水按每100ml溶液中含有160u活力的配比配制的枯草杆菌中性蛋白酶水溶液,PH为7.3,将上述两种酶溶液按1∶1等体积混合而制成复合酶溶液(2)。Prepare bioenzyme unmounting solution No. 2, which is suitable for "archives and literature bricks" damaged by microorganisms, pest secretions, dust and other dirt. Prepare powdered lysozyme and water according to the ratio of 200u activity per 100ml solution to make lysozyme aqueous solution, pH is 6.2; then prepare liquid glucoamylase and water according to the ratio of 50u activity per 100ml solution into an aqueous solution of glucoamylase with a pH of 6.2. And above-mentioned two kinds of enzyme solutions are mixed by 1: 1 equivolume and make compound enzyme solution (1); The trypsin aqueous solution prepared by the proportioning ratio that contains 160u activity in every 100ml solution with powder trypsin and water, pH is 7 .3, then powder Bacillus subtilis neutral protease and water according to the ratio of 160u activity in each 100ml solution to prepare the Bacillus subtilis neutral protease aqueous solution, the pH is 7.3, and the above two enzyme solutions are mixed at a ratio of 1:1, etc. Volume mixing to make complex enzyme solution (2).

用干法对纸张强度较差的“档案、文献砖”进行揭裱。其操作过程和实施例1中的干法操作过程基本相同,只是恒温箱的温度控制不同,为38℃,其它条件都相同。即序号(1)的复合酶溶液所进行的涂刷-恒温的操作次数为2次,第一次恒温的时间为20分钟,第二次恒温的时间为10分钟,而后的序号(2)的复合酶溶液所进行的涂刷-恒温的操作次数也为2次,每次恒温的时间分别为20分钟。上述恒温过程中所用的恒温箱的温度均为38℃。最后在“档案、文献砖”的含湿量为30-40%时进行揭裱,揭裱后的每页纸上喷涂含有新洁尔灭防霉剂的水溶液,该水溶液含0.1%(重量百分比)的新洁尔灭防霉剂。Use the dry method to unmount the "archive and document bricks" with poor paper strength. Its operating process is basically the same as the dry process in Example 1, except that the temperature control of the incubator is different, which is 38° C., and other conditions are the same. That is, the number of brushing-constant temperature operations carried out by the compound enzyme solution of serial number (1) is 2 times, the time of constant temperature for the first time is 20 minutes, the time of constant temperature for the second time is 10 minutes, and then the time of serial number (2) The number of brushing-constant temperature operations performed by the compound enzyme solution is also 2 times, and the time for each constant temperature is 20 minutes. The temperature of the constant temperature box used in the above constant temperature process is 38°C. Finally, when the moisture content of "archives and literature bricks" is 30-40%, unmounting is carried out, and each page of paper after unmounting is sprayed with an aqueous solution containing bromogeramine antifungal agent, which contains 0.1% (percentage by weight) The new geramine antifungal agent.

用湿法对纸张强度较好的“档案、文献砖”进行揭裱。其操作过程和实施例1中的湿法操作过程基本相同,只是浸泡的温度控制不同,为38℃,其它条件都相同。即将“档案、文献砖”分先后各一次浸入在序号(1)的复合酶溶液、序号(2)的复合酶溶液中,浸入时酶溶液的温度为38℃,每次浸入20分钟,每次浸入过程完毕后都用清水冲洗净,最后经撤潮,待“档案、文献砖”的含湿量为30-40%时,可进行揭裱。Use the wet method to unmount the "archive and document bricks" with good paper strength. Its operating process is basically the same as the wet operating process in Example 1, except that the soaking temperature control is different, which is 38° C., and other conditions are all the same. That is to say, the "archives and literature bricks" are immersed in the compound enzyme solution of serial number (1) and the compound enzyme solution of serial number (2) one at a time. Rinse with clear water after the immersion process is completed, and finally remove the moisture, and when the moisture content of the "archive and document bricks" is 30-40%, it can be unmounted.

实施例3Example 3

制备生物酶素揭裱液3号,适用于受到淀粉粘结剂,微生物、害虫的分泌物及灰尘等污物破坏的“档案、文献砖”。将粉剂溶菌酶和水按每100ml溶液中含有200u活力的配比所配制成溶菌酶水溶液,PH为6.3;再将液剂糖化酶和水按每100ml溶液中含有50u活力的配比配制成糖化酶水溶液,PH为6.3。并将上述两种酶溶液按1∶1等体积混合而制成复合酶溶液(1);将粉剂a-淀粉酶和水按每100ml溶液中含有50u活力的配比配制a-淀粉酶水溶液,PH为7.4,将粉剂胰蛋白酶和水按每100ml溶液中含有160u活力的配比配制成胰蛋白酶水溶液,PH为7.4,再将粉剂枯草杆菌中性蛋白酶和水按100ml溶液中含有160u活力的配比配制成枯草杆菌中性蛋白酶水溶液,PH为7.4,最后将上述三种酶溶液按1∶1∶1等体积混合而制成复合酶溶液(2)。Prepare Bioenzyme Mounting Solution No. 3, which is suitable for "archives and literature bricks" damaged by starch binders, secretions of microorganisms, pests, and dust. Prepare powdered lysozyme and water according to the ratio of 200u activity per 100ml solution to prepare lysozyme aqueous solution, pH is 6.3; then prepare liquid glucoamylase and water according to the ratio of 50u activity per 100ml solution into an aqueous solution of glucoamylase with a pH of 6.3. And above-mentioned two kinds of enzyme solutions are mixed by 1: 1 equivolume and make compound enzyme solution (1); Powder a-amylase and water contain the proportioning preparation a-amylase aqueous solution of 50u activity in every 100ml solution, The pH is 7.4, the powder trypsin and water are formulated into a trypsin aqueous solution according to the ratio of 160u activity per 100ml solution, and the pH is 7.4, then the powder Bacillus subtilisin neutral protease and water are mixed with 100ml solution containing The ratio of 160u activity is prepared into an aqueous solution of Bacillus subtilis neutral protease, with a pH of 7.4, and finally the above three enzyme solutions are mixed in equal volumes of 1:1:1 to prepare a complex enzyme solution (2).

用干法对纸张强度较差的“档案、文献砖”进行揭裱。其操作过程和实施例2中的干法操作过程相同,涂刷—恒温操作次数,恒温时间、恒温箱的温度都相同。Use the dry method to unmount the "archive and document bricks" with poor paper strength. Its operating process is the same as the dry process in Example 2, the number of brushing-constant temperature operations, the constant temperature time, and the temperature of the incubator are all the same.

用湿法对纸张强度较好的“档案、文献砖”进行揭裱。其操作过程和实施例2中的湿法操作过程相同,浸入次数、浸泡时间、浸泡的温度都相同。Use the wet method to unmount the "archive and document bricks" with good paper strength. Its operating process is the same as the wet operating process in Example 2, and the dipping times, soaking time, and soaking temperature are all the same.

采用生物酶素法水解处理“档案、文献砖”的污物,揭裱效果极为明显。用生物酶素揭裱的方法不仅避免了传统高温蒸熏对档案纸张的损坏,而且处理后对历史文献无任何副作用。因为揭裱液中的酶素无毒、无味、无腐蚀。酶素的筛选、提纯完全来自于天然,而且酶溶液的PH值为弱碱性,经实验表明,在档案典籍纸张中残留弱碱成分,对档案纸张的寿命有利无害,因为它可以不断中和掉以后档案中再次产生的酸性成分。对档案的安全是有利的。此外本发明的揭裱液对碳素成分的字迹材料几乎无影响。Using bio-enzyme method to hydrolyze the dirt of "archives and literature bricks", the effect of exposing and mounting is extremely obvious. The method of unmounting with biological enzymes not only avoids the damage to the archive paper caused by traditional high-temperature fumigation, but also has no side effects on historical documents after treatment. Because the enzyme in the mounting solution is non-toxic, tasteless and non-corrosive. The screening and purification of enzymes are completely natural, and the pH value of the enzyme solution is weakly alkaline. Experiments have shown that residual weak alkaline components in archival paper are beneficial and harmless to the life of archival paper, because it can be continuously neutralized. And the acidic components that regenerate in the archives after dropping. It is beneficial to the security of files. In addition, the mounting liquid of the present invention has almost no influence on the writing materials of carbon components.

采用生物酶素方法处理粘结成砖的历史档案或历史文献,由于分析“档案、文献砖”内的污物成分和性质;有的放矢的选择适合的酶素液,去除粘在一起的污物非常彻底,使档案纸张页与页之间完全分离。The biological enzyme method is used to treat historical archives or historical documents bonded into bricks. Due to the analysis of the dirt components and properties in the "archives and document bricks", it is very easy to remove the sticky dirt by selecting a suitable enzyme solution. Thorough, with complete separation of archival paper pages from page to page.

采用生物酶素方法修得抢救历史档案文献,是一种科学、经济的办法。可以省工、省时,可达到最佳效果。It is a scientific and economical method to repair and salvage historical archives and documents using the biological enzyme method. It can save labor and time and achieve the best effect.

我国是一个文明古国,要修复、抢救的历史文献、档案很多,因此本发明的揭裱液及其揭裱方法的应用范围很广,具有广泛的社会应用性。my country is an ancient civilization country, and there are many historical documents and files to be repaired and rescued. Therefore, the mounting fluid and mounting method of the present invention have a wide range of applications and have extensive social applicability.

Claims (3)

1、一种生物酶素揭裱液,其特征在于包括下述两种互相配合使用的酶溶液:1, a kind of biological enzyme element unmounting liquid, it is characterized in that comprising the enzyme solution that following two kinds cooperate with each other: (1)将粉剂溶菌酶和水按每100ml溶液中含有120-220u活力的配比所配制成的溶菌酶水溶液,该溶液的PH为5.8-6.8,存放温度为0℃-10℃;(1) The aqueous solution of lysozyme prepared by mixing powdered lysozyme and water according to the ratio of 120-220u activity per 100ml solution, the pH of the solution is 5.8-6.8, and the storage temperature is 0°C-10°C ℃; (2)将粉剂a-淀粉酶和水按每100ml溶液中含有30-90u活力的配比所配制成a-淀粉酶水溶液,该溶液的PH为7-7.8,存放温度为0℃-10℃。(2) Prepare the a-amylase aqueous solution by mixing powder a-amylase and water according to the ratio of 30-90u activity per 100ml solution, the pH of the solution is 7-7.8, and the storage temperature is 0°C- 10°C. 2、权利要求1所述的生物酶素揭裱液的揭裱方法,其特征在于按照其中酶液的序号(1)、(2)的顺序,用所述的序号(1)酶溶液、序号(2)酶溶液分先后对“档案、文献砖”进行涂刷-恒温的操作,该涂刷-恒温操作过程为:先用所述酶溶液在“档案、文献砖”上涂刷,再用纯植物纤维布包裹好,然后放入35℃-40℃恒温箱内恒温10-30分钟,所述序号(1)的酶溶液所进行的涂刷-恒温的操作次数为1-2次,所述序号(2)的酶溶液所进行的涂刷-恒温的操作次数为1-2次,整个涂刷-恒温操作完成后,经撤潮,待“档案、文献砖”的含湿量为30-40%时,即可进行揭裱,揭裱后的每页纸上喷涂含有新洁尔灭防霉剂的水溶液。2, the method for unmounting of the described bioenzyme unmounting solution of claim 1, it is characterized in that according to the sequence number (1), (2) of enzyme liquid wherein, use described serial number (1) enzyme solution, serial number (2) Enzyme solution carries out brushing-constant temperature operation to "archives, literature bricks" successively, and this brushing-constant temperature operation process is: first brush on "archives, literature bricks" with described enzyme solution, and then use Wrap it with pure plant fiber cloth, then put it into a 35°C-40°C incubator to keep the temperature constant for 10-30 minutes, and the number of times of brushing-constant temperature operation carried out by the enzyme solution of the serial number (1) is 1-2 times. The operation times of brushing-constant temperature carried out by the enzyme solution of the serial number (2) is 1-2 times. When the temperature is -40%, it can be unmounted, and each page after unmounted is sprayed with an aqueous solution containing bromogeril antifungal agent. 3、权利要求1所述的生物酶素揭裱液的揭裱方法,其特征在于按照其中酶液的序号(1)、(2)的顺序,将‘档案、文献砖“分先后各一次浸泡在所述的序号(1)酶溶液、序号(2)酶溶液中,浸泡的温度为35℃-40℃,每次浸泡15-25分钟,每次浸泡完毕后都用清水冲洗净,最后经撤潮,待“档案、文献砖”的含湿量为30-40%时,即可进行揭裱。3. The method for unmounting of the bio-enzyme unmounting solution according to claim 1 is characterized in that according to the order of the serial numbers (1) and (2) of the enzyme solution, the 'archives and literature bricks' are soaked once in succession In the enzyme solution of the serial number (1) and the enzyme solution of the serial number (2), the soaking temperature is 35°C-40°C, soaking for 15-25 minutes each time, rinsing with clear water after each soaking, and finally After the tide is withdrawn, when the moisture content of the "archive and document bricks" is 30-40%, the mounting can be carried out.
CN94106354A 1994-06-14 1994-06-14 Bioenzyme used for dismounting pictures and the method therefor Expired - Fee Related CN1064082C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN94106354A CN1064082C (en) 1994-06-14 1994-06-14 Bioenzyme used for dismounting pictures and the method therefor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN94106354A CN1064082C (en) 1994-06-14 1994-06-14 Bioenzyme used for dismounting pictures and the method therefor

Publications (2)

Publication Number Publication Date
CN1113516A CN1113516A (en) 1995-12-20
CN1064082C true CN1064082C (en) 2001-04-04

Family

ID=5032502

Family Applications (1)

Application Number Title Priority Date Filing Date
CN94106354A Expired - Fee Related CN1064082C (en) 1994-06-14 1994-06-14 Bioenzyme used for dismounting pictures and the method therefor

Country Status (1)

Country Link
CN (1) CN1064082C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109944114A (en) * 2019-04-01 2019-06-28 广州百立可科技有限公司 A kind of archives brick restorative procedure

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102877299B (en) * 2012-10-22 2014-07-23 中国科学技术大学 Application of superoxide dismutase and trehalose mixture for textile ashing reaction inhibitor to textiles
CN104532679B (en) * 2014-12-11 2016-06-22 首都博物馆 Biology takes off spreader application in painting and calligraphy historical relic restoration and protection
CN105695113B (en) * 2016-03-07 2019-01-01 辽宁大学 Paper relics mildew bio-enzyme cleaning agent and application thereof
CN105755900B (en) * 2016-03-07 2017-09-12 辽宁大学 Paper relics mildew cleaning method
CN106274260A (en) * 2016-08-20 2017-01-04 陕西师范大学 Antiquated calligraphy and painting draws that the heart is lossless tears off method
CN107789619A (en) * 2016-08-30 2018-03-13 山东威高药业股份有限公司 A kind of alimentary canal mucus cleaning agent

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN87104540A (en) * 1986-06-30 1988-02-24 武田药品工业株式会社 The production of human lysozyme
CN1030999A (en) * 1987-07-13 1989-02-08 西屋电气公司 Vacuum Circuit Breaker Contacts
CN1043740A (en) * 1989-11-22 1990-07-11 华南农业大学 Lysozyme production method
CN1051188A (en) * 1989-10-05 1991-05-08 生物信息公司 Biodegradable films and preparation method thereof
CN1080817A (en) * 1992-05-29 1994-01-19 美国玉米产品公司 Remove the method for remaining cyclodextrin

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN87104540A (en) * 1986-06-30 1988-02-24 武田药品工业株式会社 The production of human lysozyme
CN1030999A (en) * 1987-07-13 1989-02-08 西屋电气公司 Vacuum Circuit Breaker Contacts
CN1051188A (en) * 1989-10-05 1991-05-08 生物信息公司 Biodegradable films and preparation method thereof
CN1043740A (en) * 1989-11-22 1990-07-11 华南农业大学 Lysozyme production method
CN1080817A (en) * 1992-05-29 1994-01-19 美国玉米产品公司 Remove the method for remaining cyclodextrin

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109944114A (en) * 2019-04-01 2019-06-28 广州百立可科技有限公司 A kind of archives brick restorative procedure
CN109944114B (en) * 2019-04-01 2022-06-28 广州百立可科技有限公司 File brick repairing method

Also Published As

Publication number Publication date
CN1113516A (en) 1995-12-20

Similar Documents

Publication Publication Date Title
CN1064082C (en) Bioenzyme used for dismounting pictures and the method therefor
Adams et al. Characterization of extracellular Mn2+-oxidizing activity and isolation of an Mn2+-oxidizing protein from Leptothrix discophora SS-1
Zobell The effect of solid surfaces upon bacterial activity
DE1905681B2 (en) STABILIZED ENZYME PREPARATION AND METHOD FOR ITS MANUFACTURING
CN116037212A (en) 2-AIA@MOF-808 composite material for photocatalytic degradation of organophosphorus compound
GB9424711D0 (en) Composition for surface treatment
CN104745567B (en) A kind of immobilization gemma laccase and its preparation and application
Ghisalba et al. Microbial degradation and utilization of selected organophosphorus compounds--strategies and applications.
US5414196A (en) Method of decontaminating a cementitious surface
JP2018529012A (en) Bio-cleaning kit and method for removing biofilm from a substrate
US6121039A (en) Composition, method and apparatus for safe disposal of oil contaminated filter media
CN100493930C (en) Biological cleaning and restoration of paper cultural relics
Decoux Enzymes used for adhesive removal in paper conservation: a literature review
Aumen et al. Impact of nitrogen and phosphorus on [14C] lignocellulose decomposition by stream wood microflora
CN113088512B (en) Complex enzyme, and preparation method, regeneration method and application thereof
Godon et al. Effect of a siliceous additive in a clay engineered barrier on aqueous corrosion of R7T7 nuclear waste glass
CN115836680A (en) Carbomer mildew-removing gel reagent and preparation method thereof
CN111057645B (en) Microbial storage device for food decomposition and storage method thereof
Schwarz A Pre-packaged alpha-Amylase Poulticing System: Albertina-Kompresse
Kennedy et al. Water-insoluble papain conjugates of titanium (IV)-activated supports
CN1218835A (en) Regenerating method for powdered active carbon in sugar making by enzymolysis of starch
EP0842910A3 (en) Binder based on waterglass solution, process for its preparation and its utilisation
CN106380097A (en) Method for preparation of water-retaining high viscosity gypsum powder from desulfurized gypsum
IMMOBILISATION 4DJ, UK
CN115945442A (en) Hydrogen peroxide soaking and flushing process for bone tissues

Legal Events

Date Code Title Description
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C06 Publication
PB01 Publication
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee