CN101787110B - Photoelastic plastic material and preparation method - Google Patents
Photoelastic plastic material and preparation method Download PDFInfo
- Publication number
- CN101787110B CN101787110B CN2009102153068A CN200910215306A CN101787110B CN 101787110 B CN101787110 B CN 101787110B CN 2009102153068 A CN2009102153068 A CN 2009102153068A CN 200910215306 A CN200910215306 A CN 200910215306A CN 101787110 B CN101787110 B CN 101787110B
- Authority
- CN
- China
- Prior art keywords
- solution
- photoelastic
- epoxy
- plastic material
- preparation
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 37
- 239000004033 plastic Substances 0.000 title claims abstract description 26
- 238000002360 preparation method Methods 0.000 title claims abstract description 12
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims abstract description 32
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000002994 raw material Substances 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 238000003756 stirring Methods 0.000 claims description 19
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 238000005266 casting Methods 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 5
- 239000012535 impurity Substances 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims 7
- 229920005989 resin Polymers 0.000 claims 6
- 239000011347 resin Substances 0.000 claims 6
- 238000007711 solidification Methods 0.000 claims 2
- 230000008023 solidification Effects 0.000 claims 2
- MNAHQWDCXOHBHK-UHFFFAOYSA-N 1-phenylpropane-1,1-diol Chemical compound CCC(O)(O)C1=CC=CC=C1 MNAHQWDCXOHBHK-UHFFFAOYSA-N 0.000 claims 1
- CMEWLCATCRTSGF-UHFFFAOYSA-N N,N-dimethyl-4-nitrosoaniline Chemical compound CN(C)C1=CC=C(N=O)C=C1 CMEWLCATCRTSGF-UHFFFAOYSA-N 0.000 claims 1
- 239000004902 Softening Agent Substances 0.000 claims 1
- -1 chloropropionate alkene Chemical class 0.000 claims 1
- 238000001879 gelation Methods 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000008240 homogeneous mixture Substances 0.000 claims 1
- 238000003754 machining Methods 0.000 claims 1
- 239000000155 melt Substances 0.000 claims 1
- 238000001556 precipitation Methods 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 abstract description 20
- 229920000647 polyepoxide Polymers 0.000 abstract description 20
- 238000000034 method Methods 0.000 abstract description 16
- 238000004458 analytical method Methods 0.000 abstract description 4
- 238000005516 engineering process Methods 0.000 abstract description 3
- 229910000831 Steel Inorganic materials 0.000 abstract description 2
- 230000007547 defect Effects 0.000 abstract description 2
- 238000011068 loading method Methods 0.000 abstract description 2
- 239000010959 steel Substances 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 30
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 8
- 238000000137 annealing Methods 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 239000008029 phthalate plasticizer Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 239000002893 slag Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- BEFWKRMPVGUNOB-UHFFFAOYSA-N 2-chloro-3-methyloxirene Chemical compound CC1=C(Cl)O1 BEFWKRMPVGUNOB-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000005489 elastic deformation Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
Images
Landscapes
- Epoxy Resins (AREA)
Abstract
本发明涉及一种光弹塑性材料及制备方法,属于材料领域。包括下列原料的质量比:环氧树脂∶顺丁烯二酸酐∶邻苯二甲酸二丁脂=80-100∶24-60∶32-80。本发明可以用来模拟在小弹塑性变形下,一些复杂构件的受力状态分析,如研究构件(如钢轨、钢板)矫直过程中的残余应力研究等,光弹塑性法显出了极大的优越性,不但有效、方便,而且也是最经济的方法。原有的光弹技术缺陷织只局限于加载过程应力、应变的研究,不能研究卸载后的应力、应变状态。采用本发明光弹塑性材料在数码光弹仪上加载获取等色线后卸载,观察卸载后光弹塑性材料中条纹数的变化情况,该材料能够使研究构件残余应力随时间变化且保留15分钟。
The invention relates to a photoelastic plastic material and a preparation method, belonging to the field of materials. The mass ratio of the following raw materials is included: epoxy resin:maleic anhydride:dibutyl phthalate=80-100:24-60:32-80. The present invention can be used for simulating under the small elasto-plastic deformation, the force state analysis of some complex components, such as the residual stress research in the straightening process of the research components (such as rails, steel plates), etc., the photoelastoplastic method shows great It is not only effective and convenient, but also the most economical method. The defect of the original photoelastic technology is only limited to the research of stress and strain in the loading process, and cannot study the state of stress and strain after unloading. Use the photoelastic plastic material of the present invention to load and obtain isochromatic lines on a digital photoelastic instrument and then unload it, observe the change of the number of stripes in the photoelastic plastic material after unloading, the material can make the residual stress of the research component change with time and keep it for 15 minutes .
Description
技术领域technical field
本发明涉及一种光弹塑性材料及制备方法,特点是涉及一种在小弹塑变形条件下构件残余应力的光弹塑性材料,属于材料领域。The invention relates to a photoelastic plastic material and a preparation method thereof, and is characterized in that it relates to a photoelastic plastic material with component residual stress under the condition of small elastic plastic deformation, and belongs to the field of materials.
背景技术Background technique
光弹性法获得结构物的各种力学量是工程技术中的基本问题,虽然在工程力学中已经建立了一系列理论分析的方法,但是在很多高新技术领域中所需用的结构物,几何形状特别复杂,载荷情况和工作环境(高温、高压、地下、液中、强磁场、强辐射、动态等)也越来越多样,致使理论分析十分困难;因此,采用实验的办法就显得尤为重要,甚至是唯一的手段了。该方法适用于弹性变形条件下,构件卸载后应力-应变状态随即消失。Obtaining various mechanical quantities of structures by photoelasticity is a basic problem in engineering technology. Although a series of theoretical analysis methods have been established in engineering mechanics, structures and geometric shapes required in many high-tech fields It is particularly complex, and the load conditions and working environments (high temperature, high pressure, underground, liquid, strong magnetic field, strong radiation, dynamics, etc.) are becoming more and more diverse, making theoretical analysis very difficult; therefore, it is particularly important to use experimental methods. Even the only means. This method is suitable for elastic deformation conditions, and the stress-strain state disappears immediately after the member is unloaded.
光塑性法是建立在经典光弹性概念基础上,应用合适的聚合物材料制作模型进行实验,以确定原型结构的弹塑性应力、应变状态的实验方法,根据研究对象和变形程度的不同,光塑性主要是研究结构在大塑性变形下,卸载后的残余应变状态的光塑性法。The photoplastic method is based on the classic concept of photoelasticity. It uses suitable polymer materials to make models for experiments to determine the elastic-plastic stress and strain state of the prototype structure. According to the different research objects and deformation degrees, photoplastic It is mainly a photoplastic method to study the residual strain state of the structure after unloading under large plastic deformation.
由于光弹性法的局限性以及工程实际存在大量的弹塑性和大塑性变形问题,因而光塑性法具有直观、方便、经济等优点的光塑性法近年来受到了极大重视,取得了较快发展。Due to the limitations of the photoelastic method and the fact that there are a large number of elastic-plastic and large plastic deformation problems in engineering, the photoplastic method, which has the advantages of intuition, convenience, and economy, has received great attention in recent years and has achieved rapid development. .
发明内容Contents of the invention
本发明的目的在于提供一种在小弹塑变形条件下,可用于研究构件残余应力,并且卸载后仍然保留应力、应变状态的光弹塑性材料及制备方法。The object of the present invention is to provide a photoelastoplastic material that can be used to study the residual stress of components under the condition of small elastic-plastic deformation, and still retain the state of stress and strain after unloading, and its preparation method.
技术解决方案:本发明包括下列原料的质量比:环氧树脂∶顺丁烯二酸酐∶邻苯二甲酸二丁脂=80-100∶24-60∶32-80;Technical solution: the present invention comprises the mass ratio of following raw materials: epoxy resin: maleic anhydride: dibutyl phthalate=80-100: 24-60: 32-80;
制备方法如下:(1)将上述环氧树脂倒入烧杯中,然后连同烧杯放进100℃-120℃的水浴锅中煮沸40-60分钟,并不断搅拌,以挥发杂质和沉淀渣子;The preparation method is as follows: (1) Pour the above-mentioned epoxy resin into a beaker, and then put the beaker into a water bath at 100°C-120°C and boil for 40-60 minutes while stirring continuously to volatilize impurities and precipitate slag;
(2)将水浴锅内水温降温到50~60℃,在水浴后的环氧树脂中加入顺丁烯二酸酐固化剂,并沿一个方向均匀搅拌20-30分钟,制成均匀混合溶液A;(2) Cool the water temperature in the water bath to 50-60°C, add a maleic anhydride curing agent to the epoxy resin after the water bath, and stir evenly in one direction for 20-30 minutes to make a uniform mixed solution A;
(3)取上述邻苯二甲酸二丁脂增塑剂倒入烧杯,在电炉子上水浴加热至固化剂完全融化,温度控制在80℃-95℃,制成溶液B;(3) Take the above-mentioned dibutyl phthalate plasticizer and pour it into a beaker, heat it in a water bath on an electric stove until the curing agent is completely melted, and control the temperature at 80°C-95°C to make solution B;
(4)将步骤(2)的溶液A与步骤(3)的溶液B进行混合,制成C溶液,在C溶液中加入N-N-二甲基苯胺催化剂,催化剂的加入量为C溶液总重量的0.5-1.0%,加入时边倒边沿一个方向均匀搅拌,温度控制在50~60℃之间,搅拌20-30分钟后,制成D溶液,将D溶液倒入模具,放入恒温在40-65℃的烘箱中,静放40-60分钟,待没有气泡时,进行浇铸;(4) Solution A of step (2) is mixed with solution B of step (3) to make C solution, and N-N-dimethylaniline catalyst is added in C solution, and the addition amount of catalyst is C solution gross weight 0.5-1.0%, when adding, stir evenly in one direction while pouring, the temperature is controlled between 50-60°C, after stirring for 20-30 minutes, make D solution, pour D solution into the mold, put it into the constant temperature at 40- In an oven at 65°C, let it stand for 40-60 minutes, and cast when there are no bubbles;
(5)浇铸完成后,把模具放进烘干箱内恒温在42~44℃进行第一次固化处理,固化时间48-72小时,待模型完全胶凝后脱模,再进行第二次120℃的固化处理,固化时间10-15小时,得到成品材料。(5) After the casting is completed, put the mold into a drying oven at a constant temperature of 42-44°C for the first curing treatment. The curing time is 48-72 hours. After the model is completely gelled, the mold is demoulded, and then the second 120 The curing treatment at ℃, the curing time is 10-15 hours, and the finished material is obtained.
(6)将成品材料进行机加工,在光弹仪上观察是否有初应力,如果有初应力要进行退火处理。(6) Machine the finished material, observe whether there is initial stress on the photoelasticometer, and if there is initial stress, annealing treatment is required.
本发明包括下列原料的质量比:环氧树脂∶顺丁烯二酸酐∶邻苯二甲酸二丁脂=100∶30-50∶40-70。The present invention includes the mass ratio of the following raw materials: epoxy resin:maleic anhydride:dibutyl phthalate=100:30-50:40-70.
本发明包括下列原料的质量比:环氧树脂∶顺丁烯二酸酐∶邻苯二甲酸二丁脂=80∶24-48∶32-64。The present invention includes the mass ratio of the following raw materials: epoxy resin: maleic anhydride: dibutyl phthalate = 80: 24-48: 32-64.
环氧树脂为双酚A与环氧氯丙烯的低分子量聚合物。Epoxy resin is a low molecular weight polymer of bisphenol A and epichlorohydrin.
本发明就是基于光弹法和光塑性法两种方法之间,主要用于是研究结构在小弹塑性变形下,卸载后仍然保留应力、应变状态的光弹塑性法,通过改变光弹性材料的配比,制备了光弹塑性应力材料。实验结果表明:利用光弹塑性法可以用来模拟在小弹塑性变形下,一些复杂构件的受力状态分析,如研究构件(如钢轨、钢板)矫直过程中的残余应力研究等,光弹塑性法显出了极大的优越性,不但有效、方便,而且也是最经济的方法。原有的光弹技术缺陷织只局限于加载过程应力、应变的研究,不能研究卸载后的应力、应变状态。采用本发明光弹塑性材料在数码光弹仪上加载获取等色线后卸载,观察卸载后光弹塑性材料中条纹数的变化情况,该材料能够使研究构件残余应力随时间变化且至少保留15分钟。The present invention is based on the two methods of photoelasticity and photoplasticity. It is mainly used to study the photoelasticity and plasticity of the structure that still retains the state of stress and strain after unloading under small elastic-plastic deformation. By changing the ratio of photoelastic materials , prepared photoelastoplastic stress materials. The experimental results show that the photoelastic-plastic method can be used to simulate the force state analysis of some complex components under small elastic-plastic deformation, such as the research on the residual stress in the straightening process of components (such as rails and steel plates). The plastic method shows great advantages, not only effective, convenient, but also the most economical method. The defect of the original photoelastic technology is limited to the research of stress and strain in the loading process, and cannot study the state of stress and strain after unloading. The photoelastic plastic material of the present invention is loaded on a digital photoelastic instrument to obtain isochromatic lines and then unloaded to observe the change of the number of stripes in the photoelastic plastic material after unloading. This material can make the residual stress of the research component change with time and retain at least 15 minute.
附图说明Description of drawings
图1本发明为光弹塑性材料圆盘在不同受力条件下的等色线条纹图;Fig. 1 the present invention is the isochromatic line fringe figure of photoelastoplastic material disc under different stress conditions;
图2本发明光弹塑性材料圆盘在不同受力条件下的等差线条纹图;Fig. 2 is the contour fringe diagram of the photoelastoplastic material disc of the present invention under different stress conditions;
图3为本发明光弹塑性材料卸载之后每隔一分钟的等色线图;Fig. 3 is an isochromatic line diagram every minute after photoelastoplastic material of the present invention is unloaded;
图4为本发明的固化图;Fig. 4 is the curing figure of the present invention;
图5为本发明退火曲线图。Fig. 5 is an annealing curve diagram of the present invention.
具体实施方式Detailed ways
实施例1Example 1
本发明包括下列原料的质量比:环氧树脂∶顺丁烯二酸酐∶邻苯二甲酸二丁脂=100∶30∶40;环氧树脂为双酚A与环氧氯丙烯的低分子量聚合物。The present invention comprises the mass ratio of following raw material: epoxy resin: maleic anhydride: dibutyl phthalate=100: 30: 40; Epoxy resin is the low molecular weight polymer of bisphenol A and epoxy chloropropene .
制备方法如下:(1)将上述100克环氧树脂倒入烧杯中,然后连同烧杯放进100℃的水浴锅中煮沸50分钟,并不断搅拌,以挥发杂质和沉淀渣子;The preparation method is as follows: (1) Pour the above-mentioned 100 grams of epoxy resin into a beaker, then put the beaker into a water bath at 100°C and boil for 50 minutes, and keep stirring to volatilize impurities and precipitate slag;
(2)将水浴锅内水温降温到55℃,在水浴后的环氧树脂中加入30克顺丁烯二酸酐固化剂,并沿一个方向均匀搅拌20-分钟,制成均匀混合溶液A;(2) Cool the water temperature in the water bath to 55°C, add 30 grams of maleic anhydride curing agent to the epoxy resin after the water bath, and stir evenly in one direction for 20-minutes to make a uniform mixed solution A;
(3)取上述40克邻苯二甲酸二丁脂增塑剂倒入烧杯,在电炉子上水浴加热至增塑剂完全融化,温度控制在85℃,制成溶液B;(3) Take the above-mentioned 40 grams of dibutyl phthalate plasticizer and pour it into a beaker, heat it in a water bath on an electric stove until the plasticizer is completely melted, and the temperature is controlled at 85° C. to make solution B;
(4)将步骤(2)的溶液A与步骤(3)溶液B的进行混合,制成C溶液,在C溶液中加入0.2克N-N-二甲基苯胺催化剂,边倒边沿一个方向均匀搅拌,温度控制在52℃之间,搅拌20分钟后,制成D溶液,将D溶液倒入模具,放入恒温在42℃的烘箱中,静放40分钟,待没有气泡时,进行浇铸;(4) Mix solution A of step (2) with solution B of step (3) to make solution C, add 0.2 gram of N-N-dimethylaniline catalyst in solution C, stir evenly in one direction while pouring, The temperature is controlled at 52°C, and after stirring for 20 minutes, the D solution is made, and the D solution is poured into the mold, placed in an oven with a constant temperature of 42°C, and left for 40 minutes. When there are no bubbles, cast;
(5)浇铸完成后,把模具放进烘干箱内恒温在42℃进行第一次固化处理,固化时间50小时,待模型完全胶凝后脱模,再进行第二次120℃的固化处理,固化时间12小时,得到成品材料。(5) After the casting is completed, put the mold into a drying oven at a constant temperature of 42°C for the first curing treatment. The curing time is 50 hours. After the model is completely gelled, the mold is demoulded, and then the second curing treatment at 120°C is performed. , the curing time is 12 hours, and the finished material is obtained.
(6)将成品材料进行机加工,在光弹仪上观察是否有初应力,如果有初应力要进行退火处理。(6) Machine the finished material, observe whether there is initial stress on the photoelasticometer, and if there is initial stress, annealing treatment is required.
光弹塑性材料在数码光弹仪上加载获取等色线后卸载,观察卸载后光弹塑性材料中条纹数的变化情况,该材料能够使研究构件残余应力随时间变化且保留15分钟。The photoelastic plastic material is loaded on the digital photoelastic instrument to obtain the isochromatic line and then unloaded, and the change of the number of stripes in the photoelastic plastic material after unloading is observed. This material can make the residual stress of the research component change with time and keep it for 15 minutes.
实施例2Example 2
本发明包括下列原料环氧树脂∶顺丁烯二酸酐∶邻苯二甲酸二丁脂,原料的质量比为环氧树脂∶顺丁烯二酸酐∶邻苯二甲酸二丁脂=90∶50∶60;其中:环氧树脂为双酚A与环氧氯丙烯的低分子量聚合物。The present invention comprises following raw material epoxy resin: maleic anhydride: dibutyl phthalate, and the mass ratio of raw material is epoxy resin: maleic anhydride: dibutyl phthalate=90:50: 60; wherein: the epoxy resin is a low molecular weight polymer of bisphenol A and epichlorohydrin.
制备方法如下:(1)将上述90克环氧树脂倒入烧杯中,然后连同烧杯放进100℃的水浴锅中煮沸50分钟,并不断搅拌,以挥发杂质和沉淀渣子;The preparation method is as follows: (1) Pour the above-mentioned 90 grams of epoxy resin into a beaker, then put the beaker into a water bath at 100°C and boil for 50 minutes, and keep stirring to volatilize impurities and precipitate slag;
(2)将水浴锅内水温降温到55℃,在水浴后的环氧树脂中加入50克顺丁烯二酸酐固化剂,并沿一个方向均匀搅拌20分钟,制成均匀混合溶液A;(2) Cool the water temperature in the water bath to 55°C, add 50 grams of maleic anhydride curing agent to the epoxy resin after the water bath, and stir evenly in one direction for 20 minutes to make a uniform mixed solution A;
(3)取上述60克邻苯二甲酸二丁脂增塑剂倒入烧杯,在电炉子上水浴加热至增塑剂完全融化,温度控制在75℃,制成溶液B;(3) Take the above-mentioned 60 grams of dibutyl phthalate plasticizer and pour it into a beaker, heat it in a water bath on an electric stove until the plasticizer is completely melted, and the temperature is controlled at 75° C. to make solution B;
(4)将步骤(2)的溶液A与步骤(3)溶液B的进行混合,制成C溶液,在C溶液中加入0.1克N-N-二甲基苯胺催化剂,边倒边沿一个方向均匀搅拌,温度控制在52℃之间,搅拌20分钟后,制成D溶液,将D溶液倒入模具,放入恒温在42℃的烘箱中,静放40分钟,待没有气泡时,进行浇铸;(4) Mix solution A of step (2) with solution B of step (3) to make solution C, add 0.1 gram of N-N-dimethylaniline catalyst in solution C, stir evenly in one direction while pouring, The temperature is controlled at 52°C, and after stirring for 20 minutes, the D solution is made, and the D solution is poured into the mold, placed in an oven with a constant temperature of 42°C, and left for 40 minutes. When there are no bubbles, cast;
(5)浇铸完成后,把模具放进烘干箱内恒温在42℃进行第一次固化处理,固化时间50小时,待模型完全胶凝后脱模,再进行第二次120℃的固化处理,固化时间12小时,得到成品材料。(5) After the casting is completed, put the mold into a drying oven at a constant temperature of 42°C for the first curing treatment. The curing time is 50 hours. After the model is completely gelled, the mold is demoulded, and then the second curing treatment at 120°C is performed. , the curing time is 12 hours, and the finished material is obtained.
(6)将成品材料进行机加工,在光弹仪上观察是否有初应力,如果有初应力要进行退火处理。(6) Machine the finished material, observe whether there is initial stress on the photoelasticometer, and if there is initial stress, annealing treatment is required.
光弹塑性材料在数码光弹仪上加载获取等色线后卸载,观察卸载后光弹塑性材料中条纹数的变化情况,该材料能够使研究构件残余应力随时间变化且保留15分钟。The photoelastic plastic material is loaded on the digital photoelastic instrument to obtain the isochromatic line and then unloaded, and the change of the number of stripes in the photoelastic plastic material after unloading is observed. This material can make the residual stress of the research component change with time and keep it for 15 minutes.
实施例3Example 3
本发明包括下列原料质量比:环氧树脂∶顺丁烯二酸酐∶邻苯二甲酸二丁脂=80∶40∶50;其中:环氧树脂为双酚A与环氧氯丙烯的低分子量聚合物。The present invention comprises following raw material mass ratio: epoxy resin: maleic anhydride: dibutyl phthalate=80: 40: 50; Wherein: epoxy resin is the low molecular weight polymerization of bisphenol A and epoxy chloropropene thing.
制备方法如下:(1)将上述80克环氧树脂倒入烧杯中,然后连同烧杯放进100℃的水浴锅中煮沸50分钟,并不断搅拌,以挥发杂质和沉淀渣子;The preparation method is as follows: (1) Pour the above-mentioned 80 grams of epoxy resin into a beaker, then put the beaker into a water bath at 100° C. and boil for 50 minutes while stirring continuously to volatilize impurities and precipitate slag;
(2)将水浴锅内水温降温到55℃,在水浴后的环氧树脂中加入40克顺丁烯二酸酐固化剂,并沿一个方向均匀搅拌20分钟,制成均匀混合溶液A;(2) Cool the water temperature in the water bath to 55°C, add 40 grams of maleic anhydride curing agent to the epoxy resin after the water bath, and stir evenly in one direction for 20 minutes to make a uniform mixed solution A;
(3)取上述50克邻苯二甲酸二丁脂增塑剂倒入烧杯,在电炉子上水浴加热至增塑剂完全融化,温度控制在75℃,制成溶液B;(3) Take the above-mentioned 50 grams of dibutyl phthalate plasticizer and pour it into a beaker, heat it in a water bath on an electric stove until the plasticizer is completely melted, and the temperature is controlled at 75° C. to make solution B;
(4)将步骤(2)的溶液A与步骤(3)溶液B的进行混合,制成C溶液,在C溶液中加入0.1克N-N-二甲基苯胺催化剂,边倒边沿一个方向均匀搅拌,温度控制在52℃之间,搅拌20分钟后,制成D溶液,将D溶液倒入模具,放入恒温在40℃的烘箱中,静放40分钟,待没有气泡时,进行浇铸;(4) Mix solution A of step (2) with solution B of step (3) to make solution C, add 0.1 gram of N-N-dimethylaniline catalyst in solution C, stir evenly in one direction while pouring, The temperature is controlled at 52°C, and after stirring for 20 minutes, the D solution is made, and the D solution is poured into the mold, placed in an oven with a constant temperature of 40°C, and left for 40 minutes. When there are no bubbles, cast;
(5)浇铸完成后,把模具放进烘干箱内恒温在42℃进行第一次固化处理,固化时间55小时,待模型完全胶凝后脱模,再进行第二次110℃的固化处理,固化时间15小时,得到成品材料。(5) After the casting is completed, put the mold into a drying oven at a constant temperature of 42°C for the first curing treatment. The curing time is 55 hours. After the model is completely gelled, the mold is demoulded, and then the second curing treatment at 110°C is performed. , the curing time is 15 hours, and the finished material is obtained.
(6)将成品材料进行机加工,在光弹仪上观察是否有初应力,如果有初应力要进行退火处理。(6) Machine the finished material, observe whether there is initial stress on the photoelasticometer, and if there is initial stress, annealing treatment is required.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2009102153068A CN101787110B (en) | 2009-12-21 | 2009-12-21 | Photoelastic plastic material and preparation method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2009102153068A CN101787110B (en) | 2009-12-21 | 2009-12-21 | Photoelastic plastic material and preparation method |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101787110A CN101787110A (en) | 2010-07-28 |
CN101787110B true CN101787110B (en) | 2011-07-27 |
Family
ID=42530497
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2009102153068A Expired - Fee Related CN101787110B (en) | 2009-12-21 | 2009-12-21 | Photoelastic plastic material and preparation method |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101787110B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106928657A (en) * | 2017-03-17 | 2017-07-07 | 河南理工大学 | A kind of production method of the epoxy resin board for photoelastic experiment test |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103698182B (en) * | 2013-12-20 | 2017-02-08 | 华南理工大学 | Photo-elastic particle material with small particle diameter and preparation method thereof |
CN113248866B (en) * | 2021-03-25 | 2023-09-01 | 合肥磐石智能科技股份有限公司 | Plastic sheet for stress demonstration |
CN117400538A (en) * | 2023-12-11 | 2024-01-16 | 华侨大学 | Three-dimensional photoelastic model rapid forming method combined with 3D printing |
-
2009
- 2009-12-21 CN CN2009102153068A patent/CN101787110B/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106928657A (en) * | 2017-03-17 | 2017-07-07 | 河南理工大学 | A kind of production method of the epoxy resin board for photoelastic experiment test |
Also Published As
Publication number | Publication date |
---|---|
CN101787110A (en) | 2010-07-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101787110B (en) | Photoelastic plastic material and preparation method | |
CN101733402A (en) | Gel injection molding method for high-gravity alloy | |
CN100408232C (en) | A kind of Ti6Al4V alloy gel injection molding method | |
CN102585106A (en) | Unsaturated polyester resin for die pressing and preparation method thereof | |
CN105238991A (en) | Nodular cast iron with high elongation and heat treatment process of nodular cast iron | |
CN105907107A (en) | Precision casting concocted wax and treatment process | |
CN108893689A (en) | Inconel718 alloy disc forging homogenizes manufacturing method | |
CN106280278A (en) | Dry-type transformer or dry type mutual inductor speed cured epoxy resin castable and preparation and application thereof | |
CN106881445B (en) | A kind of furan resin casting is with applying curing agent and preparation method thereof | |
CN110648815B (en) | A magnetorheological elastomer capable of precisely controlling the axial distribution of magnetic particles and its preparation method | |
CN110952046B (en) | Ironwork and forming process thereof | |
CN106365530A (en) | A large concrete structure simulation model material and its preparation method | |
KR101407340B1 (en) | Balance weight that can be reused for washing of the preparation method | |
CN109047670A (en) | Salt core preparation method | |
CN105689635A (en) | Curing agent for casting furan resin | |
CN104070141A (en) | Rare earth coated and magnesium oxide based ceramic core | |
CN107663379A (en) | Die casting machine Special wear-resistant anti-static material | |
CN213701755U (en) | An intelligent casting line quality management system | |
JPS63264625A (en) | Mold-making resinous material for molding | |
CN104815957A (en) | Novel precision investment casting process | |
CN104387788A (en) | Casting materials and casting method for 35kV-grade large-capacity dry main transformer coil | |
CN103658522B (en) | Small-sized fermentation tank precision casting technology | |
CN115521398A (en) | Organic radiation-proof material and formula and preparation method thereof | |
CN105622927B (en) | A kind of cross-linking modified method of phenoxy resin | |
CN104072153B (en) | The magnesium oxide-based ceramic core of a kind of Lanthanum trichloride clad nano |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20110727 Termination date: 20131221 |