CN102219550B - Stone paper for maintaining cement mortar and preparation method thereof - Google Patents
Stone paper for maintaining cement mortar and preparation method thereof Download PDFInfo
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- CN102219550B CN102219550B CN 201110077964 CN201110077964A CN102219550B CN 102219550 B CN102219550 B CN 102219550B CN 201110077964 CN201110077964 CN 201110077964 CN 201110077964 A CN201110077964 A CN 201110077964A CN 102219550 B CN102219550 B CN 102219550B
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- 239000004575 stone Substances 0.000 title claims abstract description 21
- 239000011083 cement mortar Substances 0.000 title claims abstract description 8
- 238000002360 preparation method Methods 0.000 title abstract description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 29
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 24
- 239000004567 concrete Substances 0.000 abstract description 22
- 229920000092 linear low density polyethylene Polymers 0.000 abstract description 16
- 239000004707 linear low-density polyethylene Substances 0.000 abstract description 16
- 239000004831 Hot glue Substances 0.000 abstract description 15
- 239000006087 Silane Coupling Agent Substances 0.000 abstract description 15
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract description 12
- 239000000377 silicon dioxide Substances 0.000 abstract description 12
- 238000005336 cracking Methods 0.000 abstract description 7
- 229920003023 plastic Polymers 0.000 abstract description 5
- 239000004033 plastic Substances 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 4
- 239000004570 mortar (masonry) Substances 0.000 abstract description 4
- 229920000642 polymer Polymers 0.000 abstract description 4
- 230000008020 evaporation Effects 0.000 abstract description 3
- 238000001704 evaporation Methods 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 3
- 239000002253 acid Substances 0.000 abstract description 2
- 238000004132 cross linking Methods 0.000 abstract 1
- 230000001681 protective effect Effects 0.000 abstract 1
- 238000001179 sorption measurement Methods 0.000 abstract 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 abstract 1
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 26
- -1 polyethylene Polymers 0.000 description 20
- 239000000440 bentonite Substances 0.000 description 15
- 229910000278 bentonite Inorganic materials 0.000 description 15
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 15
- 239000004698 Polyethylene Substances 0.000 description 14
- 229920000573 polyethylene Polymers 0.000 description 14
- 239000004593 Epoxy Substances 0.000 description 13
- 235000021355 Stearic acid Nutrition 0.000 description 13
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 13
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 13
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 13
- 239000008117 stearic acid Substances 0.000 description 13
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 12
- 239000000843 powder Substances 0.000 description 12
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 8
- 229950011392 sorbitan stearate Drugs 0.000 description 8
- 238000005266 casting Methods 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000001993 wax Substances 0.000 description 7
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 238000003490 calendering Methods 0.000 description 6
- 230000018044 dehydration Effects 0.000 description 6
- 238000006297 dehydration reaction Methods 0.000 description 6
- 239000001294 propane Substances 0.000 description 6
- UHGGERUQGSJHKR-VCDGYCQFSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;octadecanoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCCCCCCCCCCCC(O)=O UHGGERUQGSJHKR-VCDGYCQFSA-N 0.000 description 5
- 244000025254 Cannabis sativa Species 0.000 description 4
- JETSKDPKURDVNI-UHFFFAOYSA-N [C].[Ca] Chemical compound [C].[Ca] JETSKDPKURDVNI-UHFFFAOYSA-N 0.000 description 4
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 4
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 4
- 238000010276 construction Methods 0.000 description 3
- 238000012423 maintenance Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229910021532 Calcite Inorganic materials 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 230000002902 bimodal effect Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- UCEHPOGKWWZMHC-UHFFFAOYSA-N dioctyl cyclohex-3-ene-1,2-dicarboxylate Chemical compound CCCCCCCCOC(=O)C1CCC=CC1C(=O)OCCCCCCCC UCEHPOGKWWZMHC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
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- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
技术领域 technical field
本发明涉及一种建筑材料。The present invention relates to a building material.
背景技术 Background technique
中国经济正处于高速发展阶段,我国的高速公路、大型工程建设、尤其是大城市地铁工程建设也在蓬勃发展,目前已居世界前列。在大型工程的过程中,也存在着一些有待解决的技术问题,如混凝土浇注后表面的开裂问题,高速公路混凝土浇注后路基表面的开裂问题和抗形变能力;严寒地区施工过程所需抗冻融问题等等。攻克技术难关必须依靠科技进步,采用先进技术,包括新材料的应用。China's economy is in a stage of rapid development, and my country's highways, large-scale engineering construction, especially metropolitan subway engineering construction are also booming, and are now at the forefront of the world. In the process of large-scale projects, there are also some technical problems to be solved, such as the cracking problem of the surface after concrete pouring, the cracking problem and deformation resistance of the subgrade surface after expressway concrete pouring; the freezing and thawing resistance required for construction in severe cold areas Questions and more. To overcome technical difficulties, we must rely on scientific and technological progress and adopt advanced technologies, including the application of new materials.
炎热天气通常会造成混凝土塑性收缩开裂,如果周围环境引起混凝土表面水分快速蒸发,塑性收缩开裂也会随时发生,一旦混凝土表面蒸发的水分大于泌水速度就会产生开裂,因为这使得表面出现快速的干燥收缩和拉应力,产生不规则形状的裂纹。塑性收缩裂纹塑有时在新拌混凝土浇注后不久就在表面出现,而有时却在修整时或修整后不久产生。采取预防措施,如需要在砂浆表面定时浇水,覆盖塑料薄膜,植物草等可以减少这些主要在水平表面出现的裂缝,但需耗费大量的人力和物力,尤其是大型工程,在实际操作中还存在一定的难度。Hot weather usually causes plastic shrinkage and cracking of concrete. If the surrounding environment causes rapid evaporation of moisture on the concrete surface, plastic shrinkage cracking will also occur at any time. Once the evaporated water on the concrete surface is greater than the bleeding speed, cracking will occur, because this makes the surface appear rapid. Drying shrinkage and tensile stress produce irregularly shaped cracks. Plastic shrinkage cracks sometimes appear on the surface shortly after the fresh concrete is poured, and sometimes they occur during or shortly after finishing. Taking preventive measures, such as regular watering on the mortar surface, covering plastic film, planting grass, etc., can reduce the cracks that mainly appear on the horizontal surface, but it takes a lot of manpower and material resources, especially for large-scale projects. There are certain difficulties.
发明内容 Contents of the invention
本发明的目的是提供一种用于水泥砂浆养护的石头纸及其制备方法,以克服现有技术存在的上述缺陷。The object of the present invention is to provide a kind of stone paper used for cement mortar maintenance and its preparation method, to overcome the above-mentioned defects existing in the prior art.
所述的用于水泥砂浆养护的石头纸,包括如下重量份的组分:The stone paper used for cement mortar maintenance includes the following components by weight:
所述重质碳酸钙方解石粉,细度为1500~2000目;The ground calcium carbonate calcite powder has a fineness of 1500-2000 mesh;
二氧化硅微粉主要指标:SiO2含量83~96%、平均粒径0.15~0.335um、比表面积15~22m2/g、火山灰活性指数>86%自然堆积密度180~240kg/m3;Main indicators of silica powder: SiO 2 content 83-96%, average particle size 0.15-0.335um, specific surface area 15-22m 2 /g, pozzolanic activity index> 86%, natural bulk density 180-240kg/m 3 ;
所述烷偶联剂为r-甲基丙烯酰氧基丙基三甲氧基硅烷;The alkane coupling agent is r-methacryloxypropyltrimethoxysilane;
所述的线性低密度聚乙烯的商品牌号为LLDPE,密度为0.92~0.93,熔体指数MI0.3~0.6,优选双峰型;The trade name of the linear low density polyethylene is LLDPE, the density is 0.92-0.93, the melt index MI0.3-0.6, preferably bimodal;
所述热熔胶为乙烯-醋酸乙烯共聚体型,简称EVA,熔点85~105℃;The hot melt adhesive is ethylene-vinyl acetate copolymer, referred to as EVA, with a melting point of 85-105°C;
进一步,包括如下的组分:Further, include the following components:
所述膨润土细度为1200~1500目;The fineness of the bentonite is 1200-1500 mesh;
所述改性聚乙烯蜡为聚酰胺改性聚乙烯微粉化蜡,采用科莱恩公司牌号为9615A的产品;The modified polyethylene wax is polyamide-modified polyethylene micronized wax, which is a product of 9615A from Clariant;
所述的用于水泥砂浆养护的石头纸的制备方法,包括如下步骤:The preparation method of the described stone paper that is used for cement mortar maintenance, comprises the steps:
将重质碳钙、活性二氧化硅微粉、亚磷酸三苯酯和硅烷偶联剂,在130~150℃下混合30~60分钟、再加入线性低密度聚乙烯、热熔胶、硬脂酸、环氧四氢邻苯二甲酸二辛酯、改性聚乙烯蜡、膨润土、油酸酰胺和失水山梨醇硬脂酸酯,混合30~60分钟,然后送入170~185℃塑化机塑化,175~185℃挤出机流延,170~185℃四轴压延机压延成?0.10~0.12mm的石头纸,降温后,再经25±2℃,相对湿度60±2%条件下平衡25~30分钟,即可获得产品。Mix heavy calcium carbon, activated silica micropowder, triphenyl phosphite and silane coupling agent at 130-150°C for 30-60 minutes, then add linear low-density polyethylene, hot melt adhesive, stearic acid , Epoxy dioctyl tetrahydrophthalate, modified polyethylene wax, bentonite, oleic acid amide and sorbitan stearate, mixed for 30-60 minutes, and then sent to a plasticizer at 170-185°C Plasticizing, 175~185℃ extruder casting, 170~185℃ four-axis calender rolling into? 0.10-0.12mm stone paper, after cooling down, then equilibrate for 25-30 minutes under the conditions of 25±2°C and relative humidity of 60±2%, and then the product can be obtained.
本发明的水泥砂浆养护的石头纸以高分子聚合物为基材原料,对碳酸钙和活性二氧化硅微粉进行复合改性,并添加其他添加剂,利用高分子界面化学原理和高分子改性的特点,经特殊工艺处理后,采用聚合物混合、填料复合改性、聚合物与填料塑化、挤出流延、压延成型工艺制成。在混凝土浇注后直接酸覆盖在混凝土表面,利用石头纸中膨润土吸水膨胀的原理和石头纸中活性二氧化硅微粉在硅烷偶联剂的作用下,与砂浆表面进行交联吸附,形成一层保护膜,控制混凝土表面水分快速蒸发,预防塑性收缩开裂。The stone paper maintained by cement mortar of the present invention uses high-molecular polymer as the base material, carries out compound modification on calcium carbonate and active silica micropowder, and adds other additives, utilizes the principle of high-molecular interface chemistry and high-molecular modification Features: After special processing, it is made by polymer mixing, filler compound modification, polymer and filler plasticization, extrusion casting, and calendering. After the concrete is poured, the acid is directly covered on the surface of the concrete. Using the principle of bentonite in the stone paper to absorb water and expand, and the active silica powder in the stone paper under the action of the silane coupling agent, it is cross-linked and adsorbed on the surface of the mortar to form a layer of protection. Membrane to control the rapid evaporation of moisture on the concrete surface and prevent plastic shrinkage cracking.
具体实施方式 Detailed ways
实施例中,如无特别说明,均为重量份。In the examples, unless otherwise specified, all are parts by weight.
实施例1Example 1
重质碳酸钙65份、活性二氧化硅微粉10份、亚磷酸三苯酯0.1份、硅烷偶联剂3份、线性低密度聚乙烯30份、热熔胶5份、2,2-双(4-羟基苯基)丙烷0.3份、硬脂酸0.5份、环氧四氢邻苯二甲酸二辛酯0.5份、改性聚乙烯蜡0.2份、膨润土0.5份、油酸酰胺0.3份、失水山梨醇硬脂酸酯0.5份。65 parts of heavy calcium carbonate, 10 parts of active silica powder, 0.1 part of triphenyl phosphite, 3 parts of silane coupling agent, 30 parts of linear low density polyethylene, 5 parts of hot melt adhesive, 2,2-bis( 0.3 parts of 4-hydroxyphenyl)propane, 0.5 parts of stearic acid, 0.5 parts of dioctyl epoxy tetrahydrophthalate, 0.2 parts of modified polyethylene wax, 0.5 parts of bentonite, 0.3 parts of oleic acid amide, dehydration 0.5 parts of sorbitol stearate.
制备方法:Preparation:
将重质碳钙、活性二氧化硅微粉、亚磷酸三苯酯、硅烷偶联剂、在130℃下混合60分钟、再加入线性低密度聚乙烯、热熔胶、硬脂酸、环氧四氢邻苯二甲酸二辛酯、改性高密度聚乙烯蜡、膨润土、油酸酰胺、失水山梨醇硬脂酸酯继续混合30分钟,然后送入170℃塑化机塑化,170℃挤出机流延,170℃四轴压延机压延成0.12mm左右的石头纸,降温后,再经25±2℃,相对湿度60±2%平衡25分钟,获得产品。Mix heavy calcium carbonate, activated silica micropowder, triphenyl phosphite, silane coupling agent at 130°C for 60 minutes, then add linear low density polyethylene, hot melt adhesive, stearic acid, epoxy four Dioctyl hydrogen phthalate, modified high-density polyethylene wax, bentonite, oleic acid amide, and sorbitan stearate continued to mix for 30 minutes, then sent to a plasticizing machine at 170°C for plasticization, and extruded at 170°C Out of the machine, the four-axis calender is calendered at 170°C to form a stone paper of about 0.12mm. After cooling down, it is then equilibrated at 25±2°C and relative humidity of 60±2% for 25 minutes to obtain the product.
实施例2Example 2
重质碳酸钙55份、活性二氧化硅微粉20份、亚磷酸三苯酯0.2份、硅烷偶联剂4份、线性低密度聚乙烯20份、热熔胶10份、2,2-双(4-羟基苯基)丙烷0.4份、硬脂酸1份、环氧四氢邻苯二甲酸二辛酯1份、改性聚乙烯蜡0.3份、膨润土1份、油酸酰胺0.4份、失水山梨醇硬脂酸酯0.75份。。55 parts of heavy calcium carbonate, 20 parts of active silica powder, 0.2 parts of triphenyl phosphite, 4 parts of silane coupling agent, 20 parts of linear low density polyethylene, 10 parts of hot melt adhesive, 2,2-bis( 0.4 parts of 4-hydroxyphenyl)propane, 1 part of stearic acid, 1 part of epoxy tetrahydrophthalate dioctyl, 0.3 parts of modified polyethylene wax, 1 part of bentonite, 0.4 parts of oleic acid amide, dehydration 0.75 parts of sorbitol stearate. .
制备方法:Preparation:
将重质碳钙、活性二氧化硅微粉、亚磷酸三苯酯、硅烷偶联剂、在140℃下混合45分钟、再加入线性低密度聚乙烯、热熔胶、硬脂酸、环氧四氢邻苯二甲酸二辛酯、改性聚乙烯蜡、膨润土、油酸酰胺、失水山梨醇硬脂酸酯继续混合45分钟,然后送入173℃塑化机塑化,175℃挤出机流延,175℃四轴压延机压延成0.12mm左右的石头纸,降温后,再经25±2℃,相对湿度60±2%平衡30分钟后收卷包装。Mix heavy calcium carbon, active silica powder, triphenyl phosphite, silane coupling agent at 140°C for 45 minutes, then add linear low density polyethylene, hot melt adhesive, stearic acid, epoxy tetra Dioctyl hydrogen phthalate, modified polyethylene wax, bentonite, oleic acid amide, and sorbitan stearate continued to mix for 45 minutes, then sent to a plasticizing machine at 173°C for plasticization, and extruder at 175°C Casting, 175°C four-axis calender calendering into stone paper of about 0.12mm, after cooling down, then equilibrate at 25±2°C, relative humidity 60±2% for 30 minutes, then roll and pack.
实施例3Example 3
重质碳酸钙45份、活性二氧化硅微粉30份、亚磷酸三苯酯0.3份、硅烷偶联剂5份、线性低密度聚乙烯25份、热熔胶8份、2,2-双(4-羟基苯基)丙烷0.5份、硬脂酸1.5份、环氧四氢邻苯二甲酸二辛酯1.5份、改性聚乙烯蜡0.4份、膨润土1.5份、油酸酰胺0.5份、失水山梨醇硬脂酸酯1份。45 parts of heavy calcium carbonate, 30 parts of active silica powder, 0.3 parts of triphenyl phosphite, 5 parts of silane coupling agent, 25 parts of linear low density polyethylene, 8 parts of hot melt adhesive, 2,2-bis( 0.5 parts of 4-hydroxyphenyl) propane, 1.5 parts of stearic acid, 1.5 parts of dioctyl epoxy tetrahydrophthalate, 0.4 parts of modified polyethylene wax, 1.5 parts of bentonite, 0.5 parts of oleic acid amide, dehydration 1 part of sorbitan stearate.
制备方法:Preparation:
将重质碳钙、活性二氧化硅微粉、亚磷酸三苯酯、硅烷偶联剂、在150℃下混合30分钟、再加入线性低密度聚乙烯、热熔胶、硬脂酸、环氧四氢邻苯二甲酸二辛酯、改性聚乙烯蜡、膨润土、油酸酰胺、失水山梨醇硬脂酸酯继续混合60分钟,然后送入176℃塑化机塑化,179℃挤出机流延,180℃四轴压延机压延成0.11mm左右的石头纸,降温后,再经25±2℃,相对湿度60±2%平衡25分钟后收卷包装。Mix heavy calcium carbonate, activated silica micropowder, triphenyl phosphite, silane coupling agent at 150°C for 30 minutes, then add linear low density polyethylene, hot melt adhesive, stearic acid, epoxy four Dioctyl hydrogen phthalate, modified polyethylene wax, bentonite, oleic acid amide, and sorbitan stearate continued to mix for 60 minutes, then sent to a plasticizing machine at 176°C for plasticization, and extruder at 179°C Casting, 180°C four-axis calender calendering into stone paper of about 0.11mm, after cooling down, then equilibrate at 25±2°C, relative humidity 60±2% for 25 minutes, then roll and pack.
实施例4Example 4
重质碳酸钙60份、活性二氧化硅微粉15份、亚磷酸三苯酯0.1份、硅烷偶联剂3份、线性低密度聚乙烯22份、热熔胶10份、2,2-双(4-羟基苯基)丙烷0.6份、硬脂酸0.5份、环氧四氢邻苯二甲酸二辛酯1.5份、改性聚乙烯蜡0.5份、膨润土1.5份、油酸酰胺0.6份、失水山梨醇硬脂酸酯0.75份。。60 parts of heavy calcium carbonate, 15 parts of active silica powder, 0.1 part of triphenyl phosphite, 3 parts of silane coupling agent, 22 parts of linear low density polyethylene, 10 parts of hot melt adhesive, 2,2-bis( 0.6 parts of 4-hydroxyphenyl) propane, 0.5 parts of stearic acid, 1.5 parts of dioctyl epoxy tetrahydrophthalate, 0.5 parts of modified polyethylene wax, 1.5 parts of bentonite, 0.6 parts of oleic acid amide, dehydration 0.75 parts of sorbitol stearate. .
制备方法:Preparation:
将重质碳钙、活性二氧化硅微粉、亚磷酸三苯酯、硅烷偶联剂、在135℃下混合30分钟、再加入线性低密度聚乙烯、热熔胶、硬脂酸、环氧四氢邻苯二甲酸二辛酯、改性聚乙烯蜡、膨润土、油酸酰胺、失水山梨醇硬脂酸酯继续混合60分钟,然后送入180℃塑化机塑化,180℃挤出机流延,180℃四轴压延机压延成0.12mm左右的石头纸,降温后,再经25±2℃,相对湿度60±2%平衡30分钟后收卷包装。Mix heavy calcium carbonate, activated silica micropowder, triphenyl phosphite, silane coupling agent at 135°C for 30 minutes, then add linear low density polyethylene, hot melt adhesive, stearic acid, epoxy four Dioctyl hydrogen phthalate, modified polyethylene wax, bentonite, oleic acid amide, and sorbitan stearate continued to mix for 60 minutes, and then sent to a 180°C plasticizing machine for plasticization, and a 180°C extruder Casting, 180°C four-axis calender calendering into stone paper of about 0.12mm, after cooling down, then balance at 25±2°C, relative humidity 60±2% for 30 minutes, then roll and pack.
实施例5Example 5
重质碳酸钙50份、活性二氧化硅微粉25份、亚磷酸三苯酯0.2份、硅烷偶联剂4份、线性低密度聚乙烯28份、热熔胶7份、2,2-双(4-羟基苯基)丙烷0.5份、硬脂酸1份、环氧四氢邻苯二甲酸二辛酯1份、改性聚乙烯蜡0.6份、膨润土1份、油酸酰胺0.4份、失水山梨醇硬脂酸酯0.6份。50 parts of heavy calcium carbonate, 25 parts of active silica powder, 0.2 part of triphenyl phosphite, 4 parts of silane coupling agent, 28 parts of linear low density polyethylene, 7 parts of hot melt adhesive, 2,2-bis( 0.5 parts of 4-hydroxyphenyl)propane, 1 part of stearic acid, 1 part of epoxy tetrahydrophthalate dioctyl, 0.6 parts of modified polyethylene wax, 1 part of bentonite, 0.4 parts of oleic acid amide, dehydration 0.6 parts of sorbitol stearate.
制备方法:Preparation:
将重质碳钙、活性二氧化硅微粉、亚磷酸三苯酯、硅烷偶联剂、在145℃下混合45分钟、再加入线性低密度聚乙烯、热熔胶、硬脂酸、环氧四氢邻苯二甲酸二辛酯、改性聚乙烯蜡、膨润土、油酸酰胺、失水山梨醇硬脂酸酯继续混合45分钟,然后送入185℃塑化机塑化,180℃挤出机流延,185℃四轴压延机压延成0.10mm左右的石头纸,降温后,再经25±2℃,相对湿度60±2%平衡25分钟后收卷包装。Mix heavy calcium carbon, active silica powder, triphenyl phosphite, silane coupling agent at 145°C for 45 minutes, then add linear low density polyethylene, hot melt adhesive, stearic acid, epoxy tetra Dioctyl hydrogen phthalate, modified polyethylene wax, bentonite, oleic acid amide, and sorbitan stearate continued to mix for 45 minutes, and then sent to a plasticizing machine at 185°C for plasticization, and extruder at 180°C Casting, calendering at 185°C with a four-axis calender to form stone paper of about 0.10mm, after cooling down, then balance at 25±2°C and relative humidity of 60±2% for 25 minutes, then roll and pack.
实施例6Example 6
重质碳酸钙50份、活性二氧化硅微粉25份、亚磷酸三苯酯0.3份、硅烷偶联剂5份、线性低密度聚乙烯24份、热熔胶9份、2,2-双(4-羟基苯基)丙烷0.5份、硬脂酸1.5份、环氧四氢邻苯二甲酸二辛酯1.5份、改性聚乙烯蜡0.4份、膨润土1.5份、油酸酰胺0.4份、失水山梨醇硬脂酸酯0.9份。50 parts of heavy calcium carbonate, 25 parts of active silica powder, 0.3 parts of triphenyl phosphite, 5 parts of silane coupling agent, 24 parts of linear low density polyethylene, 9 parts of hot melt adhesive, 2,2-bis( 0.5 parts of 4-hydroxyphenyl)propane, 1.5 parts of stearic acid, 1.5 parts of dioctyl epoxy tetrahydrophthalate, 0.4 parts of modified polyethylene wax, 1.5 parts of bentonite, 0.4 parts of oleic acid amide, dehydration 0.9 part of sorbitol stearate.
制备方法:Preparation:
将重质碳钙、活性二氧化硅微粉、亚磷酸三苯酯、硅烷偶联剂、在140℃下混合60分钟、再加入线性低密度聚乙烯、热熔胶、硬脂酸、环氧四氢邻苯二甲酸二辛酯、改性聚乙烯蜡、膨润土、油酸酰胺、失水山梨醇硬脂酸酯继续混合30分钟,然后送入180℃塑化机塑化,182℃挤出机流延,185℃四轴压延机压延成0.10mm左右的石头纸,降温后,再经25±2℃,相对湿度60±2%平衡30分钟后收卷包装。Mix heavy calcium carbon, activated silica powder, triphenyl phosphite, and silane coupling agent at 140°C for 60 minutes, then add linear low-density polyethylene, hot melt adhesive, stearic acid, and epoxy tetra Dioctyl hydrogen phthalate, modified polyethylene wax, bentonite, oleic acid amide, and sorbitan stearate continued to mix for 30 minutes, then sent to a plasticizing machine at 180°C for plasticization, and extruder at 182°C Casting, 185°C four-axis calender calenders into stone paper of about 0.10mm, after cooling down, then balance at 25±2°C, relative humidity 60±2% for 30 minutes, then roll and pack.
应用实施例7Application Example 7
目前还没有混凝土养护纸的国家或行业标准,只能根据纸类常用测试方法对实施例进行实际测定,采用的检测方法,可参见有关标准:GBT 13023-2008瓦楞(原纸)、QBT3805-1999聚氯乙烯壁纸、JGJ 70-2009建筑砂浆基本性能试验方法,结果见表1和表2。At present, there is no national or industry standard for concrete curing paper, and the actual measurement of the examples can only be carried out according to the commonly used test methods for paper. For the detection methods used, please refer to the relevant standards: GBT 13023-2008 corrugated (base paper), QBT3805-1999 poly Vinyl chloride wallpaper, JGJ 70-2009 building mortar basic performance test method, the results are shown in Table 1 and Table 2.
表一Table I
应用试验:大型广场浇注混凝土为对象,进行实际应用,时间为4月中旬,晴天,环境温度为18~24℃:大型广场混凝土浇注30分钟后,在混凝土表面立即覆盖本发明的养护纸,对比1为用植物草覆盖混凝土;对比2为露天混凝土;通过对混凝土表面进行测定:Application test: large-scale square pouring concrete is the object, and the time is mid-April, sunny, and the ambient temperature is 18-24°C: 30 minutes after the large-scale square concrete is poured, the curing paper of the present invention is immediately covered on the concrete surface, and compared 1 is covering concrete with plant grass; comparison 2 is open-air concrete; by measuring the concrete surface:
表二Table II
从实际应用可以得出结论,使用养护石头纸养护的混凝土,在48小时期间只需要浇水一次,6个月后表面光滑,无裂缝。而使用植物草覆盖的混凝土在48小时期间浇水三次、露天的混凝土在在48小时期间浇水四次,28天后仍出现了轻微裂缝,同时使用植物草还需要人工清理现场,耗时耗力;露天的还需要多浇一次水仍未达到预期效果。从应用试验说明本发明的水泥浆养护石头纸达到了预期的效果。From the practical application, it can be concluded that the concrete cured with curing stone paper only needs to be watered once within 48 hours, and the surface is smooth without cracks after 6 months. However, the concrete covered with plant grass was watered three times in 48 hours, and the concrete in the open air was watered four times in 48 hours. After 28 days, slight cracks still appeared. At the same time, the use of plant grass also required manual cleaning of the site, which was time-consuming and labor-intensive. ; The open air still needs to be watered one more time and the expected effect has not yet been achieved. It is shown from the application test that the cement slurry curing stone paper of the present invention has achieved the desired effect.
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