CN115181527A - 一种抗老化抗菌帐篷面料粘结胶组合物及其制备方法 - Google Patents
一种抗老化抗菌帐篷面料粘结胶组合物及其制备方法 Download PDFInfo
- Publication number
- CN115181527A CN115181527A CN202210627265.9A CN202210627265A CN115181527A CN 115181527 A CN115181527 A CN 115181527A CN 202210627265 A CN202210627265 A CN 202210627265A CN 115181527 A CN115181527 A CN 115181527A
- Authority
- CN
- China
- Prior art keywords
- percent
- compound
- adhesive composition
- tackifier
- aging
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 28
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 20
- 230000003712 anti-aging effect Effects 0.000 title claims abstract description 19
- 238000002360 preparation method Methods 0.000 title claims abstract description 10
- 239000004835 fabric adhesive Substances 0.000 title claims description 13
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims abstract description 45
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 45
- 150000001875 compounds Chemical class 0.000 claims abstract description 26
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000003063 flame retardant Substances 0.000 claims abstract description 25
- 239000003242 anti bacterial agent Substances 0.000 claims abstract description 24
- 239000000853 adhesive Substances 0.000 claims abstract description 20
- 230000001070 adhesive effect Effects 0.000 claims abstract description 20
- 229910001404 rare earth metal oxide Inorganic materials 0.000 claims abstract description 15
- 238000002844 melting Methods 0.000 claims abstract description 12
- 230000008018 melting Effects 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical compound [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000004744 fabric Substances 0.000 claims abstract description 8
- 239000000463 material Substances 0.000 claims description 48
- 238000005266 casting Methods 0.000 claims description 44
- 238000002156 mixing Methods 0.000 claims description 28
- 229920000058 polyacrylate Polymers 0.000 claims description 24
- 239000002245 particle Substances 0.000 claims description 21
- 238000001816 cooling Methods 0.000 claims description 14
- 238000001035 drying Methods 0.000 claims description 14
- 229920003023 plastic Polymers 0.000 claims description 14
- 239000004033 plastic Substances 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 14
- 239000002390 adhesive tape Substances 0.000 claims description 13
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 claims description 13
- 229910000420 cerium oxide Inorganic materials 0.000 claims description 12
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 claims description 12
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 claims description 12
- 238000013329 compounding Methods 0.000 claims description 10
- 229940043810 zinc pyrithione Drugs 0.000 claims description 10
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 claims description 10
- QHNCWVQDOPICKC-UHFFFAOYSA-N copper;1-hydroxypyridine-2-thione Chemical compound [Cu].ON1C=CC=CC1=S.ON1C=CC=CC1=S QHNCWVQDOPICKC-UHFFFAOYSA-N 0.000 claims description 8
- 238000005520 cutting process Methods 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 238000004321 preservation Methods 0.000 claims description 8
- 239000000498 cooling water Substances 0.000 claims description 7
- 238000003825 pressing Methods 0.000 claims description 7
- 238000007493 shaping process Methods 0.000 claims description 7
- 229920000877 Melamine resin Polymers 0.000 claims description 4
- 229920000388 Polyphosphate Polymers 0.000 claims description 4
- 229910001377 aluminum hypophosphite Inorganic materials 0.000 claims description 4
- 239000002131 composite material Substances 0.000 claims description 4
- CQYBWJYIKCZXCN-UHFFFAOYSA-N diethylaluminum Chemical compound CC[Al]CC CQYBWJYIKCZXCN-UHFFFAOYSA-N 0.000 claims description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 4
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 claims description 4
- 239000001205 polyphosphate Substances 0.000 claims description 4
- 235000011176 polyphosphates Nutrition 0.000 claims description 4
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- 239000012948 isocyanate Substances 0.000 claims description 2
- 150000002513 isocyanates Chemical class 0.000 claims description 2
- 229920005906 polyester polyol Polymers 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 230000032683 aging Effects 0.000 abstract description 9
- 230000003115 biocidal effect Effects 0.000 abstract description 2
- 230000007613 environmental effect Effects 0.000 abstract description 2
- 229910052761 rare earth metal Inorganic materials 0.000 abstract description 2
- 150000002910 rare earth metals Chemical class 0.000 abstract description 2
- 239000007787 solid Substances 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 5
- 241000588724 Escherichia coli Species 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 238000009958 sewing Methods 0.000 description 3
- 229940100555 2-methyl-4-isothiazolin-3-one Drugs 0.000 description 2
- 229940100484 5-chloro-2-methyl-4-isothiazolin-3-one Drugs 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- 241000270923 Hesperostipa comata Species 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- FENRSEGZMITUEF-ATTCVCFYSA-E [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].OP(=O)([O-])O[C@@H]1[C@@H](OP(=O)([O-])[O-])[C@H](OP(=O)(O)[O-])[C@H](OP(=O)([O-])[O-])[C@H](OP(=O)(O)[O-])[C@H]1OP(=O)([O-])[O-] Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].OP(=O)([O-])O[C@@H]1[C@@H](OP(=O)([O-])[O-])[C@H](OP(=O)(O)[O-])[C@H](OP(=O)([O-])[O-])[C@H](OP(=O)(O)[O-])[C@H]1OP(=O)([O-])[O-] FENRSEGZMITUEF-ATTCVCFYSA-E 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- -1 polytetrafluoroethylene Polymers 0.000 description 1
- 229940083982 sodium phytate Drugs 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4018—Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
- C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/04—Non-macromolecular additives inorganic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/08—Macromolecular additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/35—Heat-activated
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
- C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/40—Adhesives in the form of films or foils characterised by release liners
- C09J7/403—Adhesives in the form of films or foils characterised by release liners characterised by the structure of the release feature
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/221—Oxides; Hydroxides of metals of rare earth metal
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/221—Oxides; Hydroxides of metals of rare earth metal
- C08K2003/2213—Oxides; Hydroxides of metals of rare earth metal of cerium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/358—Applications of adhesives in processes or use of adhesives in the form of films or foils for garments and textiles
Abstract
本发明公开了一种抗老化抗菌帐篷面料粘结胶组合物及其制备方法,由如下重量百分比的组分组成:熔点为60‑130℃的热塑性聚氨酯TPU70‑85%,复配磷氮类阻燃剂6‑10%,纳米稀土氧化物2‑5%,复配抗菌剂1‑3%和增粘剂6‑12%。本发明提供一种固体胶带状改性热塑性聚氨酯粘合剂,主要由热塑性聚氨酯TPU、阻燃剂、稀土、增粘剂、抗菌剂,具有阻燃、抗紫外老化、防水、粘结强度高、环保、抗菌等优点,完全符合帐篷新技术新工艺要求。
Description
技术领域
本发明属于胶粘剂材料技术领域,具体涉及一种抗老化抗菌帐篷面料粘结胶组合物及其制备方法。
背景技术
传统帐篷帐面制作简易流程为:布料裁剪、布料搭接针线缝制、针缝处单面粘合防水带热。由流程可知,涉及三个步骤,两台设备(缝纫机、热封机),这些设备的运行需要场地和人员;随着中国人口红利下降,用工成本增高,企业负担增大;因此,通过推陈出新,改变传统帐篷帐面制作工艺,减少人员的投入,实现节约用工成本,成了帐篷企业技术开发的重要方向。
通过引入粘合胶带材料,采用热粘合方式,取代搭接针缝工艺再热封防水带工艺,将两道工序缩短为一道工序;既减少了设备机台数量,又减少了操作人员数量,实现技术进步优化成本的目的。
CN 1519094A公开了一种聚氨酯一聚四氟乙烯共同拉伸复合膜的制备方法,其技术方案采用溶剂将热塑性聚氨酯溶解,制备一定浓度的聚氨酯溶液,然后将其涂覆于聚四氟乙烯基带上,再将基带浸于水中或于70~160℃中烘干,该薄膜可用于保温内衣、运动服、帐篷等的粘合。CN 107603556 A公开了一种帐篷用热熔胶的制备方法,该方法将二聚酸和苯混合,加热沸腾8~12min,随后加入无水硫酸镁,制得无水二聚酸;然后再加入已内酰胺、异佛尔酮二胺、植酸钠、六甲基二硅胺、浓硫酸于230~240℃下保温保压160~200min,制得粘合剂,该粘合剂对帐篷粘结力强,可延长帐篷的使用寿命。
从以上专利可知,所涉及的帐篷用粘合剂均为含有机溶剂的粘合胶,有些甚至涉及致癌物质苯,环保性差,不符合密闭空间作业使用。
发明内容
本发明目的在于克服现有技术缺陷,提供一种抗老化抗菌帐篷面料粘结胶组合物。
本发明的另一目的在于提供上述抗老化抗菌帐篷面料粘结胶组合物的制备方法。
本发明的技术方案如下:
一种抗老化抗菌帐篷面料粘结胶组合物,由如下重量百分比的组分组成:
其中,热塑性聚氨酯TPU为聚酯多元醇、聚醚多元醇与异氰酸酯MDI的聚合物,复配磷氮类阻燃剂由二乙基次磷酸铝和三聚氰胺聚磷酸盐复配而成,纳米稀土氧化物为纳米氧化铈或纳米氧化镧,增粘剂为丙烯酸酯聚合物和/或环氧丙烯酸酯聚合物。
在本发明的一个优选实施方案中,所述复配抗菌剂由吡啶硫酮锌、吡啶硫酮铜、5-氯-2-甲基-4-异噻唑啉-3-酮和2-甲基-4-异噻唑啉-3-酮中的至少两种复配而成。
进一步优选的,所述复配抗菌剂由吡啶硫酮锌、吡啶硫酮铜、5-氯-2-甲基-4-异噻唑啉-3-酮和2-甲基-4-异噻唑啉-3-酮中的两种以0.8-1.2:08-1.2的质量比复配而成。
在本发明的一个优选实施方案中,所述热塑性聚氨酯TPU的熔点为70-110℃。
在本发明的一个优选实施方案中,所述复配磷氮类阻燃剂由二乙基次磷酸铝和三聚氰胺聚磷酸盐以1-1.5∶0.8-1.2的质量比复配而成。
在本发明的一个优选实施方案中,所述丙烯酸酯聚合物的分子量为60000-64000,所述环氧丙烯酸酯聚合物的分子量为50000-53000。
在本发明的一个优选实施方案中,由如下重量百分比的组分组成:
其中,纳米稀土氧化物为纳米氧化镧,增粘剂为分子量为63000的丙烯酸酯聚合物,复配抗菌剂由吡啶硫酮锌和5-氯-2-甲基-4-异噻唑啉-3-酮以1∶1的质量比复配而成。
在本发明的一个优选实施方案中,由如下重量百分比的组分组成:
其中,纳米稀土氧化物为纳米氧化铈,增粘剂为分子量为52000的环氧丙烯酸酯聚合物,复配抗菌剂由吡啶硫酮锌和吡啶硫酮铜以1∶1的质量比复配而成。
在本发明的一个优选实施方案中,由如下重量百分比的组分组成:
其中,纳米稀土氧化物为纳米氧化铈,增粘剂由分子量为52000的环氧丙烯酸酯聚合物和分子量为63000的丙烯酸酯聚合物以1∶1的质量比复配而成,复配抗菌剂由吡啶硫酮锌和吡啶硫酮铜以1∶1的质量比复配而成。
上述抗老化抗菌帐篷面料粘结胶组合物的制备方法,包括如下步骤:
(1)将热塑性聚氨酯TPU与增粘剂以300-500rpm的搅拌速度分散20~30min,混合均匀;
(2)将步骤(1)所得的物料料倒入双螺杆挤出机的进料槽中;
(3)将复配磷氮类阻燃剂、纳米稀土氧化物和复配抗菌剂搅拌混合均匀,再倒入上述双螺杆挤出机侧部的喂料槽中;
(4)用上述双螺杆挤出机将步骤(1)和步骤(3)所得的物料混合均匀,采用冷却水方式冷却,经造粒和干燥至含水率小于0.03%控制含水率小于0.03%,获得料粒;
(5)将步骤(4)所得的料粒导入流延机进料口,并流延至带有游离纸的流延辊面上,形成薄膜,对薄膜施加压力,使得薄膜平整的贴附于游离纸上,将薄膜随流延辊移动通过冷却装置,进而将薄膜定型,获得流延膜卷材,获得流延膜卷材;
(6)将步骤(5)所得的流延膜卷材切成固定需求的胶带,并用塑料袋真空塑封保存。
在本发明的一个优选实施方案中,所述干燥温度为70-90℃。
本发明的有益效果是:
1、本发明提供一种固体胶带状改性热塑性聚氨酯粘合剂,主要由热塑性聚氨酯TPU、阻燃剂、稀土、增粘剂、抗菌剂,具有阻燃、抗紫外老化、防水、粘结强度高、环保、抗菌等优点,完全符合帐篷新技术新工艺要求。
2、本发明制备工艺简便、环保,可应用于帐篷、服装、鞋等材料。
具体实施方式
以下通过具体实施方式对本发明的技术方案进行进一步的说明和描述。
实施例1
(1)将熔点70℃的热塑性聚氨酯TPU(型号1070AP,购自浙江华峰)与丙烯酸酯聚合物(分子量63000)增粘剂按比例加入混料罐中,匀速搅拌,搅拌速度500r/min,分散20min,混合均匀,备用;
(2)将步骤(1)所得的物料倒入双螺杆挤出机进料槽中;
(3)将阻燃剂、纳米氧化镧、抗菌剂等按比例,加入混料罐中,搅拌均匀,再倒入上述双螺杆挤出机侧的喂料槽中;
(4)设置挤出温度和出料速率,利用双螺杆挤出机将步骤(2)和步骤(3)所得的物料混合均匀,采用冷却水方式冷却,造粒,然后及时放入恒温烘箱中干燥,设置干燥温度为80℃,控制含水率小于0.03%,获得料粒;
(5)将步骤(4)所得的料粒导入流延机进料口,并流延至带有游离纸的流延辊面上,形成薄膜,对薄膜施加压力,使得薄膜平整的贴附于游离纸上,将薄膜随流延辊移动通过冷却装置,进而将薄膜定型,获得流延膜卷材;
(6)将步骤(5)所得的流延膜卷材,切成固定需求的胶带,并用塑料袋真空塑封保存。
下表为本实施例胶带主要成分配比:
表1 实施例1各成分配比
序号 | 材料名称 | 质量百分比/% |
1 | 热塑性聚氨酯TPU | 85 |
2 | 阻燃剂 | 6 |
3 | 纳米氧化镧抗紫外老化剂 | 2 |
4 | ZPT、CIT(质量比1∶1) | 1 |
5 | 丙烯酸酯聚合物增粘剂 | 6 |
表2 实施例1粘结帐篷的各项性能
实施例2
(1)将熔点约90℃的热塑性聚氨酯TPU(型号1180A,购自巴斯夫)与环氧丙烯酸酯聚合物(分子量52000)增粘剂按比例加入混料罐中,匀速搅拌,搅拌速度300r/min,分散30min,混合均匀,备用;
(2)将步骤(1)所得的物料倒入双螺杆挤出机进料槽中;
(3)将阻燃剂、纳米氧化铈、抗菌剂等按比例,加入混料罐中,搅拌均匀,再倒入上述双螺杆挤出机侧的喂料槽中;
(4)设置挤出温度和出料速率,利用双螺杆挤出机将步骤(2)和步骤(3)所得的物料混合均匀,采用冷却水方式冷却,造粒,然后及时放入恒温烘箱中干燥,设置干燥温度为70℃,控制含水率小于0.03%,获得料粒;
(5)将步骤(4)所得的料粒导入流延机进料口,并流延至带有游离纸的流延辊面上,形成薄膜,对薄膜施加压力,使得薄膜平整的贴附于游离纸上,将薄膜随流延辊移动通过冷却装置,进而将薄膜定型,获得流延膜卷材;
(6)将步骤(5)所得的流延膜卷材,切成固定需求的胶带,并用塑料袋真空塑封保存。
下表为本实施例胶带主要成分配比:
表3 实施例2各成分配比
序号 | 材料名称 | 质量百分比/% |
1 | 热塑性聚氨酯TPU | 78 |
2 | 阻燃剂 | 8 |
3 | 纳米氧化铈抗紫外老化剂 | 3 |
4 | CPT、ZPT(质量比1∶1) | 2 |
5 | 环氧丙烯酸酯聚合物增粘剂 | 9 |
表4 实施例2粘结帐篷的各项性能
序号 | 项目 | 测试指标 | 执行标准 |
1 | 粘结强度,N | 350 | ISO 13935-2-2014 |
2 | 阻燃等级 | V-0 | UL 90 |
3 | 抗紫外老化性(无开胶、粉化),12月 | 通过 | 户外测试 |
4 | 抑菌圈大小(大肠杆菌抑菌率) | 28mm | —— |
实施例3
(1)将熔点110℃的热塑性聚氨酯TPU(型号1195A,购自巴斯夫)与增粘剂丙烯酸酯聚合物(分子量63000)和环氧丙烯酸酯聚合物(分子量52000)共混合物(质量比为1∶1),按比例加入混料罐中,匀速搅拌,搅拌速度400r/min,分散25min,混合均匀,备用;
(2)将步骤(1)所得的物料倒入双螺杆挤出机进料槽中;
(3)将阻燃剂、纳米氧化铈、抗菌剂等按比例,加入混料罐中,搅拌均匀,再倒入上述双螺杆挤出机侧的喂料槽中;
(4)设置挤出温度和出料速率,利用双螺杆挤出机将步骤(2)和步骤(3)所得的物料混合均匀,采用冷却水方式冷却,造粒,然后及时放入恒温烘箱中干燥,设置干燥温度为90℃,控制含水率小于0.03%,获得料粒;
(5)将步骤(4)所得的料粒导入流延机进料口,并流延至带有游离纸的流延辊面上,形成薄膜,对薄膜施加压力,使得薄膜平整的贴附于游离纸上,将薄膜随流延辊移动通过冷却装置,进而将薄膜定型,获得流延膜卷材;
(6)将步骤(5)所得的流延膜卷材,切成固定需求的胶带,并用塑料袋真空塑封保存。
下表为本实施例胶带主要成分配比:
表5 实施例3各成分配比
序号 | 材料名称 | 质量百分比/% |
1 | 热塑性聚氨酯TPU | 70 |
2 | 阻燃剂 | 10 |
3 | 纳米氧化铈抗紫外老化剂 | 5 |
4 | MIT、ZPT(质量比1∶1) | 3 |
5 | 混合增粘剂 | 12 |
表6 实施例3粘结帐篷的各项性能
序号 | 项目 | 测试指标 | 执行标准 |
1 | 粘结强度,N | 220 | ISO 13935-2-2014 |
2 | 阻燃等级 | V-0 | UL 90 |
3 | 抗紫外老化性(无开胶、粉化),12月 | 通过 | 户外测试 |
4 | 抑菌圈大小(大肠杆菌抑菌率) | 22mm | —— |
对比例4
(1)将熔点90℃的热塑性聚氨酯TPU(型号1180A,购自巴斯夫)与环氧丙烯酸酯聚合物(分子量52000)增粘剂按比例加入混料罐中,匀速搅拌,搅拌速度300r/min,分散30min,混合均匀,备用;
(2)将步骤(1)所得的物料倒入双螺杆挤出机进料槽中;
(3)将阻燃剂、纳米氧化铈、抗菌剂等按比例,加入混料罐中,搅拌均匀,再倒入上述双螺杆挤出机侧的喂料槽中;
(4)设置挤出温度和出料速率,利用双螺杆挤出机将步骤(2)和步骤(3)所得的物料混合均匀,采用冷却水方式冷却,造粒,然后及时放入恒温烘箱中干燥,设置干燥温度为70℃,控制含水率小于0.03%,获得料粒;
(5)将步骤(4)所得的料粒导入流延机进料口,并流延至带有游离纸的流延辊面上,形成薄膜,对薄膜施加压力,使得薄膜平整的贴附于游离纸上,将薄膜随流延辊移动通过冷却装置,进而将薄膜定型,获得流延膜卷材;
(6)将步骤(5)所得的流延膜卷材,切成固定需求的胶带,并用塑料袋真空塑封保存。
下表为本对比例胶带主要成分配比:
表7 对比例4各成分配比
表8 对比例4粘结帐篷的各项性能
序号 | 项目 | 测试指标 | 执行标准 |
1 | 粘结强度,N | 120 | ISO 13935-2-2014 |
2 | 阻燃等级 | V-0 | UL 90 |
3 | 抗紫外老化性(无开胶、粉化),10月 | 通过 | 户外测试 |
4 | 抑菌圈大小(大肠杆菌抑菌率) | 22mm | —— |
对比例5
(1)将熔点90℃的热塑性聚氨酯TPU(型号1180A,购自巴斯夫)与环氧丙烯酸酯聚合物(分子量52000)增粘剂按比例加入混料罐中,匀速搅拌,搅拌速度300r/min,分散30min,混合均匀,备用;
(2)将步骤(1)所得的物料倒入双螺杆挤出机进料槽中;
(3)将阻燃剂、纳米氧化铈、抗菌剂等按比例,加入混料罐中,搅拌均匀,再倒入上述双螺杆挤出机侧的喂料槽中;
(4)设置挤出温度和出料速率,利用双螺杆挤出机将步骤(2)和步骤(3)所得的物料混合均匀,采用冷却水方式冷却,造粒,然后及时放入恒温烘箱中干燥,设置干燥温度为70℃,控制含水率小于0.03%,获得料粒;
(5)将步骤(4)所得的料粒导入流延机进料口,并流延至带有游离纸的流延辊面上,形成薄膜,对薄膜施加压力,使得薄膜平整的贴附于游离纸上,将薄膜随流延辊移动通过冷却装置,进而将薄膜定型,获得流延膜卷材;
(6)将步骤(5)所得的流延膜卷材,切成固定需求的胶带,并用塑料袋真空塑封保存。
下表为本对比例胶带主要成分配比:
表9 对比例5各成分配比
表10 对比例5粘结帐篷的各项性能
序号 | 项目 | 测试指标 | 执行标准 |
1 | 粘结强度,N | 220 | ISO 13935-2-2014 |
2 | 阻燃等级 | V-2 | UL 90 |
3 | 抗紫外老化性(无开胶、粉化),8月 | 通过 | 户外测试 |
4 | 抑菌圈大小(大肠杆菌抑菌率) | 15mm | —— |
以上所述,仅为本实施例的较佳实施例而已,故不能依此限定本实施例实施的范围,即依本实施例专利范围及说明书内容所作的等效变化与修饰,皆应仍属本实施例涵盖的范围内。
Claims (11)
1.一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:由如下重量百分比的组分组成:
熔点为60-130℃的热塑性聚氨酯TPU 70-85%
复配磷氮类阻燃剂 6-10%
纳米稀土氧化物 2-5%
复配抗菌剂 1-3%
增粘剂 6-12%
其中,热塑性聚氨酯TPU为聚酯多元醇、聚醚多元醇与异氰酸酯MDI的聚合物,复配磷氮类阻燃剂由二乙基次磷酸铝和三聚氰胺聚磷酸盐复配而成,纳米稀土氧化物为纳米氧化铈或纳米氧化镧,增粘剂为丙烯酸酯聚合物和/或环氧丙烯酸酯聚合物。
2.如权利要求1所述的一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:所述复配抗菌剂由吡啶硫酮锌、吡啶硫酮铜、5-氯-2-甲基-4-异噻唑啉-3-酮和2-甲基-4-异噻唑啉-3-酮中的至少两种复配而成。
3.如权利要求2所述的一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:所述复配抗菌剂由吡啶硫酮锌、吡啶硫酮铜、5-氯-2-甲基-4-异噻唑啉-3-酮和2-甲基-4-异噻唑啉-3-酮中的两种以0.8-1.2: 08-1.2的质量比复配而成。
4.如权利要求1所述的一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:所述热塑性聚氨酯TPU的熔点为70-110℃。
5.如权利要求1所述的一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:所述复配磷氮类阻燃剂由二乙基次磷酸铝和三聚氰胺聚磷酸盐以1-1.5: 0.8-1.2的质量比复配而成。
6.如权利要求1所述的一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:所述丙烯酸酯聚合物的分子量为60000-64000,所述环氧丙烯酸酯聚合物的分子量为50000-53000。
7.如权利要求1所述的一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:由如下重量百分比的组分组成:
熔点为70℃的热塑性聚氨酯TPU 85%
复配磷氮类阻燃剂 6%
纳米稀土氧化物 2%
复配抗菌剂 1%
增粘剂 6%
其中,纳米稀土氧化物为纳米氧化镧,增粘剂为分子量为63000的丙烯酸酯聚合物,复配抗菌剂由吡啶硫酮锌和5-氯-2-甲基-4-异噻唑啉-3-酮以1: 1的质量比复配而成。
8.如权利要求1所述的一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:由如下重量百分比的组分组成:
熔点为90℃的热塑性聚氨酯TPU 78%
复配磷氮类阻燃剂 8%
纳米稀土氧化物 3%
复配抗菌剂 2%
增粘剂 9%
其中,纳米稀土氧化物为纳米氧化铈,增粘剂为分子量为52000的环氧丙烯酸酯聚合物,复配抗菌剂由吡啶硫酮锌和吡啶硫酮铜以1: 1的质量比复配而成。
9.如权利要求1所述的一种抗老化抗菌帐篷面料粘结胶组合物,其特征在于:由如下重量百分比的组分组成:
熔点为110℃的热塑性聚氨酯TPU 70%
复配磷氮类阻燃剂 10%
纳米稀土氧化物 5%
复配抗菌剂 3%
增粘剂 12%
其中,纳米稀土氧化物为纳米氧化铈,增粘剂由分子量为52000的环氧丙烯酸酯聚合物和分子量为63000的丙烯酸酯聚合物以1:1的质量比复配而成,复配抗菌剂由吡啶硫酮锌和吡啶硫酮铜以1: 1的质量比复配而成。
10.权利要求1至9中任一权利要求所述的一种抗老化抗菌帐篷面料粘结胶组合物的制备方法,其特征在于:包括如下步骤:
(1)将热塑性聚氨酯TPU与增粘剂以300-500rpm的搅拌速度分散20~30min,混合均匀;
(2)将步骤(1)所得的物料料倒入双螺杆挤出机的进料槽中;
(3)将复配磷氮类阻燃剂、纳米稀土氧化物和复配抗菌剂搅拌混合均匀,再倒入上述双螺杆挤出机侧部的喂料槽中;
(4)用上述双螺杆挤出机将步骤(1)和步骤(3)所得的物料混合均匀,采用冷却水方式冷却,经造粒和干燥至含水率小于0.03%控制含水率小于0.03%,获得料粒;
(5)将步骤(4)所得的料粒导入流延机进料口,并流延至带有游离纸的流延辊面上,形成薄膜,对薄膜施加压力,使得薄膜平整的贴附于游离纸上,将薄膜随流延辊移动通过冷却装置,进而将薄膜定型,获得流延膜卷材,获得流延膜卷材;
(6)将步骤(5)所得的流延膜卷材切成固定需求的胶带,并用塑料袋真空塑封保存。
11.如权利要求10所述的制备方法,其特征在于:所述干燥温度为70-90℃。
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210627265.9A CN115181527B (zh) | 2022-06-02 | 2022-06-02 | 一种抗老化抗菌帐篷面料粘结胶组合物及其制备方法 |
US17/975,081 US20230392058A1 (en) | 2022-06-02 | 2022-10-27 | Bonding composition and method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210627265.9A CN115181527B (zh) | 2022-06-02 | 2022-06-02 | 一种抗老化抗菌帐篷面料粘结胶组合物及其制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN115181527A true CN115181527A (zh) | 2022-10-14 |
CN115181527B CN115181527B (zh) | 2023-09-29 |
Family
ID=83513825
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202210627265.9A Active CN115181527B (zh) | 2022-06-02 | 2022-06-02 | 一种抗老化抗菌帐篷面料粘结胶组合物及其制备方法 |
Country Status (2)
Country | Link |
---|---|
US (1) | US20230392058A1 (zh) |
CN (1) | CN115181527B (zh) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4422140A1 (de) * | 1994-06-27 | 1996-01-11 | Mehler Vario System Gmbh | Zeltstoff insbesondere für den militärischen Bereich |
EP0950083A1 (en) * | 1997-01-06 | 1999-10-20 | Shell Internationale Researchmaatschappij B.V. | Pressure sensitive adhesives comprising thermoplastic polyurethanes |
CN104263259A (zh) * | 2014-09-18 | 2015-01-07 | 东莞市雄林新材料科技股份有限公司 | 一种低熔点高粘接强度tpu热熔胶膜及其制备方法 |
CN107033376A (zh) * | 2016-11-23 | 2017-08-11 | 广东聚航新材料研究院有限公司 | 一种抗菌型tpu流延膜制备方法 |
CN108715729A (zh) * | 2018-06-26 | 2018-10-30 | 段小宁 | 阻燃、抗菌性水性聚氨酯涂料和胶黏剂的制备方法 |
CN109096740A (zh) * | 2018-07-20 | 2018-12-28 | 山东诺威聚氨酯股份有限公司 | 抗菌抗静电tpu薄膜材料及其制备方法 |
-
2022
- 2022-06-02 CN CN202210627265.9A patent/CN115181527B/zh active Active
- 2022-10-27 US US17/975,081 patent/US20230392058A1/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4422140A1 (de) * | 1994-06-27 | 1996-01-11 | Mehler Vario System Gmbh | Zeltstoff insbesondere für den militärischen Bereich |
EP0950083A1 (en) * | 1997-01-06 | 1999-10-20 | Shell Internationale Researchmaatschappij B.V. | Pressure sensitive adhesives comprising thermoplastic polyurethanes |
CN104263259A (zh) * | 2014-09-18 | 2015-01-07 | 东莞市雄林新材料科技股份有限公司 | 一种低熔点高粘接强度tpu热熔胶膜及其制备方法 |
CN107033376A (zh) * | 2016-11-23 | 2017-08-11 | 广东聚航新材料研究院有限公司 | 一种抗菌型tpu流延膜制备方法 |
CN108715729A (zh) * | 2018-06-26 | 2018-10-30 | 段小宁 | 阻燃、抗菌性水性聚氨酯涂料和胶黏剂的制备方法 |
CN109096740A (zh) * | 2018-07-20 | 2018-12-28 | 山东诺威聚氨酯股份有限公司 | 抗菌抗静电tpu薄膜材料及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN115181527B (zh) | 2023-09-29 |
US20230392058A1 (en) | 2023-12-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105155297B (zh) | 一种水性聚氨酯含浸超细纤维合成革贝斯的制备方法 | |
CN104031596A (zh) | 一种低成型温度水性聚氨酯胶粘剂及其制备方法 | |
CN106543553B (zh) | 一种聚丙烯镀铝膜专用料及其制备方法 | |
CN103757931A (zh) | 一种阻燃型浸胶帆布的浸渍液及其制备方法 | |
CN115181527B (zh) | 一种抗老化抗菌帐篷面料粘结胶组合物及其制备方法 | |
CN105315652A (zh) | 一种高粘合强度透气抑菌tpu复合膜及其制备方法 | |
CN103483549A (zh) | 用于织物整理的水性聚氨酯的制备方法 | |
CN107447533A (zh) | 一种聚酯阻燃帆布的制备方法 | |
JPH04228616A (ja) | ポリアミドの可染性を改質する方法 | |
CN112593309A (zh) | 聚乳酸锦纶复合纤维的制备方法及聚乳酸锦纶复合纤维 | |
CN112500700A (zh) | 一种可吹塑耐候尼龙组合物及其制备方法 | |
CN111286282A (zh) | 一种新型环氧胶膜及其制备方法 | |
CN108164809B (zh) | 一种抗滴落的一体膨胀型无卤阻燃剂及其制备方法 | |
CN105801813B (zh) | 超细纤维含浸用聚氨酯树脂及其制备方法 | |
CN106905753A (zh) | 一种适用于合成革的水性防针孔剂 | |
CN109280366A (zh) | 一种抗菌性防水透湿聚氨酯薄膜的制备方法 | |
CN106279622A (zh) | 一种弱溶剂型脂肪族面层用聚氨酯树脂 | |
CN107964162A (zh) | 一种发光塑料藤的制备方法 | |
CN104177792B (zh) | Pet多功能光亮母粒 | |
CN102492336A (zh) | 无苯、低毒、不燃、不爆可剥性电镀保护涂料及其制备方法 | |
EP0354319A1 (de) | Substituierte 3-(N-Imidazolyl)-propion-säurehydrazide, ihre Verwendung als Härtungsmittel in Epoxidharzzusammensetzungen, sie enthaltende härtbare Epoxidharzzusammensetzungen und Epoxidharzformkörper | |
CN116535856B (zh) | 一种抗菌pi复合材料及其制备方法 | |
CN109487566A (zh) | 一种复合塑料编织袋的内部直接涂覆工艺及其制备方法 | |
CN109233710A (zh) | 一种具有高玻璃化转变温度、高温粘结性的绝缘材料及其制备方法 | |
CN111394049A (zh) | 一种高性能环保型胶粘剂及其制备工艺 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |