CN116141703A - 一种聚氨酯增韧环氧基阻尼复合材料及其制备方法 - Google Patents
一种聚氨酯增韧环氧基阻尼复合材料及其制备方法 Download PDFInfo
- Publication number
- CN116141703A CN116141703A CN202310410319.0A CN202310410319A CN116141703A CN 116141703 A CN116141703 A CN 116141703A CN 202310410319 A CN202310410319 A CN 202310410319A CN 116141703 A CN116141703 A CN 116141703A
- Authority
- CN
- China
- Prior art keywords
- composite material
- damping
- polyurethane
- nitrile rubber
- preparing
- 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.)
- Pending
Links
- 238000013016 damping Methods 0.000 title claims abstract description 79
- 239000002131 composite material Substances 0.000 title claims abstract description 41
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 27
- 239000004814 polyurethane Substances 0.000 title claims abstract description 27
- 239000004593 Epoxy Substances 0.000 title claims abstract description 22
- 238000002360 preparation method Methods 0.000 title claims abstract description 12
- 239000000463 material Substances 0.000 claims abstract description 38
- 229920000459 Nitrile rubber Polymers 0.000 claims abstract description 36
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 34
- 239000004917 carbon fiber Substances 0.000 claims description 34
- 239000003365 glass fiber Substances 0.000 claims description 34
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 30
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 28
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 28
- 239000003822 epoxy resin Substances 0.000 claims description 25
- 229920000647 polyepoxide Polymers 0.000 claims description 25
- 238000001035 drying Methods 0.000 claims description 17
- 239000005543 nano-size silicon particle Substances 0.000 claims description 15
- 235000012239 silicon dioxide Nutrition 0.000 claims description 15
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 14
- 239000004744 fabric Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 12
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 claims description 10
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 8
- 230000001680 brushing effect Effects 0.000 claims description 8
- 238000002791 soaking Methods 0.000 claims description 8
- 238000003756 stirring Methods 0.000 claims description 5
- 230000002194 synthesizing effect Effects 0.000 claims description 5
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 claims description 4
- 238000007598 dipping method Methods 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims description 4
- PISLZQACAJMAIO-UHFFFAOYSA-N 2,4-diethyl-6-methylbenzene-1,3-diamine Chemical compound CCC1=CC(C)=C(N)C(CC)=C1N PISLZQACAJMAIO-UHFFFAOYSA-N 0.000 claims description 3
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 3
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 3
- 238000009941 weaving Methods 0.000 claims description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 239000005056 polyisocyanate Substances 0.000 claims description 2
- 229920001228 polyisocyanate Polymers 0.000 claims description 2
- -1 polymethylene Polymers 0.000 claims description 2
- 229920006389 polyphenyl polymer Polymers 0.000 claims description 2
- 239000002105 nanoparticle Substances 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 14
- 229920006168 hydrated nitrile rubber Polymers 0.000 description 6
- 238000005470 impregnation Methods 0.000 description 6
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 238000009940 knitting Methods 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 229930185605 Bisphenol Natural products 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 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 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/04—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
- B29C70/28—Shaping operations therefor
- B29C70/30—Shaping by lay-up, i.e. applying fibres, tape or broadsheet on a mould, former or core; Shaping by spray-up, i.e. spraying of fibres on a mould, former or core
- B29C70/38—Automated lay-up, e.g. using robots, laying filaments according to predetermined patterns
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B13/00—Conditioning or physical treatment of the material to be shaped
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B15/00—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00
- B29B15/08—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00 of reinforcements or fillers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B15/00—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00
- B29B15/08—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00 of reinforcements or fillers
- B29B15/10—Coating or impregnating independently of the moulding or shaping step
- B29B15/12—Coating or impregnating independently of the moulding or shaping step of reinforcements of indefinite length
- B29B15/122—Coating or impregnating independently of the moulding or shaping step of reinforcements of indefinite length with a matrix in liquid form, e.g. as melt, solution or latex
- B29B15/125—Coating or impregnating independently of the moulding or shaping step of reinforcements of indefinite length with a matrix in liquid form, e.g. as melt, solution or latex by dipping
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/02—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
- B32B5/026—Knitted fabric
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/02—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
- B32B5/08—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer the fibres or filaments of a layer being of different substances, e.g. conjugate fibres, mixture of different fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/22—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed
- B32B5/24—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer
- B32B5/26—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer another layer next to it also being fibrous or filamentary
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/20—All layers being fibrous or filamentary
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/02—Coating on the layer surface on fibrous or filamentary layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/26—Polymeric coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/02—Composition of the impregnated, bonded or embedded layer
- B32B2260/021—Fibrous or filamentary layer
- B32B2260/023—Two or more layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/04—Impregnation, embedding, or binder material
- B32B2260/048—Natural or synthetic rubber
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/10—Inorganic fibres
- B32B2262/101—Glass fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/10—Inorganic fibres
- B32B2262/106—Carbon fibres, e.g. graphite fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/14—Mixture of at least two fibres made of different materials
- B32B2262/152—Knitted fabric
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/56—Damping, energy absorption
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2363/00—Characterised by the use of epoxy resins; Derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2415/00—Characterised by the use of rubber derivatives
-
- 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
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/06—Elements
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
- C08K7/26—Silicon- containing compounds
-
- 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
- C08K9/00—Use of pretreated ingredients
- C08K9/08—Ingredients agglomerated by treatment with a binding agent
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T50/00—Aeronautics or air transport
- Y02T50/40—Weight reduction
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Composite Materials (AREA)
- Robotics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Textile Engineering (AREA)
- Reinforced Plastic Materials (AREA)
Abstract
本发明提供了一种聚氨酯增韧环氧基阻尼复合材料及其制备方法,该方法使用碳纤维和玻璃纤维增强树脂基预浸料,提高了材料的力学性能。此外,使用氢化丁腈橡作为阻尼材料、引入纳米颗粒还可以改善复合材料的阻尼性能。
Description
技术领域
本发明属于复合材料制备技术领域,尤其是涉及一种聚氨酯增韧环氧基阻尼复合材料及其制备方法。
背景技术
在航空航天、汽车和住宅结构中,将粘弹性阻尼材料插入结构表面以降低振动和噪声,当结构受到弯曲振动时,约束阻尼层会发生剪切变形,结构通过剪切变形耗散能量以增加其阻尼。现有的一些复合阻尼材料注重阻尼性能的同时往往会忽略复合阻尼材料的力学性能的问题,因此,需要提出一种新的复合材料,以提高阻尼性能和力学性能,延长其使用寿命。
发明内容
有鉴于此,本发明旨在提出一种聚氨酯增韧环氧基阻尼复合材料及其制备方法,以解决上述问题。
为达到上述目的,本发明的技术方案是这样实现的:
一种聚氨酯增韧环氧基阻尼复合材料的制备方法,该方法包括如下步骤:
1)将阻尼材料氢化丁腈橡胶充分溶解,之后将玻璃纤维和碳纤维分别浸泡在氢化丁腈橡胶中,并对浸泡后的玻璃纤维和碳纤维进行烘干;
2)将浸泡后的玻璃纤维和碳纤维编织成混合织物;
3)使用聚氨酯对环氧树脂进行增韧改性,之后用增韧改性的环氧树脂浸渍步骤2)得到的混合织物制成预浸料;
4)将氢化丁腈橡胶充分溶解,并添加纳米二氧化硅后搅拌,之后将其涂刷或喷涂在预浸料的上下表面,得到阻尼材料,氢化丁腈橡胶与纳米二氧化硅的质量比为100:(1-10);
5)将步骤3)制备的预浸料与步骤4)制备的阻尼材料分层叠放铺层,之后采用高压釜工艺,固化得到阻尼复合材料。
进一步,步骤1)和步骤4)中,使用四氢呋喃溶解氢化丁腈橡胶,玻璃纤维的直径为6-15μm,碳纤维的直径为5-8μm。
进一步,步骤1)中浸泡时间为30-50min,烘干温度为80-90℃,烘干时间为12-24h。
进一步,步骤2)先将玻璃纤维与碳纤维合成一股再进行编织,玻璃纤维与碳纤维的数量比例为1:4-10,编织的混合织物的厚度为1-3mm。
进一步,步骤3)中,先利用异氰酸酯制备聚氨酯预聚体,再利用聚氨酯预聚体与环氧树脂反应得到聚氨酯改性环氧树脂,异氰酸酯为甲苯二异氰酸酯、二苯甲烷二异氰酸酯、多亚甲基多苯基多异氰酸酯或己二异氰酸酯中的任一种,环氧树脂为双酚F型环氧树脂或双酚S型环氧树脂。
进一步,步骤3)中浸渍的时间为30-60min,浸渍后需进行烘干,烘干的温度为80-90℃。
进一步,步骤4)中涂刷或喷涂的厚度为0.15-0.3mm。
进一步,步骤5)中,预浸料为6-10偶数层,阻尼材料为2-4层,预浸料与阻尼材料的铺层方式为[0/G/0/G/……/0/0/0/0]或[0/0/……G/0/G/0/……/0/0],其中G为阻尼材料,0为预浸料。
进一步,步骤5)中使用的固化剂为4,4’-二氨基二苯甲烷或二乙基甲苯二胺中的一种;固化温度在110-130℃,固化压力2MPa,固化时间1.5-2.5h。
本发明还提供了一种由上述所述的制备方法制备的聚氨酯增韧环氧基阻尼复合材料。
相对于现有技术,本发明所述的聚氨酯增韧环氧基阻尼复合材料具有以下优势:
本发明所述的聚氨酯增韧环氧基阻尼复合材料使用碳纤维和玻璃纤维增强树脂基预浸料,提高了材料的力学性能。此外,使用氢化丁腈橡作为阻尼材料、引入纳米颗粒还可以改善复合材料的阻尼性能。
具体实施方式
需要说明的是,在不冲突的情况下,本发明中的实施例及实施例中的特征可以相互组合。
下面将结合实施例来详细说明本发明。
实施例1
一种聚氨酯增韧环氧基阻尼复合材料的制备方法,该方法包括如下步骤:
1)使用四氢呋喃充分溶解阻尼材料氢化丁腈橡胶HNBR,四氢呋喃与氢化丁腈橡胶的质量比为4:1,静置24h,阻尼材料必须完全溶解;之后将玻璃纤维和碳纤维分别浸泡在氢化丁腈橡中50min,并对浸泡后的玻璃纤维和碳纤维进行烘干,烘干温度为80℃,烘干时间为18h;玻璃纤维的直径为8μm,碳纤维的直径为5μm;
2)先将浸泡后的玻璃纤维与碳纤维合成一股再进行编织,玻璃纤维与碳纤维的数量比例为1:4,编织的混合织物的厚度为1.5mm;
3)首先将聚乙二醇(PEG)和甲苯二异氰酸酯反应生成端异氰酯基预聚体,然后由端异氰酯基预聚体与双酚F型环氧树脂进行接枝反应,制备增韧环氧树脂;之后用增韧改性的环氧树脂浸渍步骤2)得到的混合织物制成预浸料,浸渍的时间为60min,浸渍后需进行烘干,烘干的温度为90℃;
4)使用四氢呋喃充分溶解阻尼材料氢化丁腈橡胶HNBR,四氢呋喃与氢化丁腈橡胶的质量比为4:1,静置24h,阻尼材料必须完全溶解;然后添加纳米二氧化硅后搅拌均匀,之后将其涂刷在预浸料的上下表面,涂刷厚度为0.15mm,得到阻尼材料,氢化丁腈橡胶与纳米二氧化硅的质量比为100:3;
5)将步骤3)制备的预浸料与步骤4)制备的阻尼材料分层叠放铺层,采用[0/G/0/G/0/G/0/0/0/0/0/0/0]的放置方式,之后放入高压釜中,使用的固化剂为4,4’-二氨基二苯甲烷,温度在120℃,固化压力2MPa,时间为2h,固化得到阻尼复合材料。
实施例2
一种聚氨酯增韧环氧基阻尼复合材料的制备方法,该方法包括如下步骤:
1)使用四氢呋喃充分溶解阻尼材料氢化丁腈橡胶HNBR,四氢呋喃与氢化丁腈橡胶的质量比为4:1,静置24h,阻尼材料必须完全溶解;之后将玻璃纤维和碳纤维分别浸泡在氢化丁腈橡中45min,并对浸泡后的玻璃纤维和碳纤维进行烘干,烘干温度为85℃,烘干时间为20h;玻璃纤维的直径为10μm,碳纤维的直径为5μm;
2)先将浸泡后的玻璃纤维与碳纤维合成一股再进行编织,玻璃纤维与碳纤维的数量比例为1:7,编织的混合织物的厚度为1.9mm;
3)首先将聚丙二醇和二苯甲烷二异氰酸酯反应生成聚氨酯预聚体,然后由聚氨酯预聚体与双酚S型环氧树脂进行接枝反应,制备增韧环氧树脂;之后用增韧改性的环氧树脂浸渍步骤2)得到的混合织物制成预浸料,浸渍的时间为60min,浸渍后需进行烘干,烘干的温度为90℃;
4)使用四氢呋喃充分溶解阻尼材料氢化丁腈橡胶HNBR,四氢呋喃与氢化丁腈橡胶的质量比为4:1,静置24h,阻尼材料必须完全溶解;然后添加纳米二氧化硅后搅拌均匀,之后将其涂刷在预浸料的上下表面,涂刷厚度为0.2mm,得到阻尼材料,氢化丁腈橡胶与纳米二氧化硅的质量比为100:6;
5)将步骤3)制备的预浸料与步骤4)制备的阻尼材料分层叠放铺层,采用[0/0/0/0/G/0/G/0/G/0/0/0/0]的放置方式,之后放入高压釜中,使用的固化剂为二乙基甲苯二胺,温度在120℃,固化压力2MPa,时间为2.2h,固化得到阻尼复合材料。
实施例3
一种聚氨酯增韧环氧基阻尼复合材料的制备方法,该方法包括如下步骤:
1)使用四氢呋喃充分溶解阻尼材料氢化丁腈橡胶HNBR,四氢呋喃与氢化丁腈橡胶的质量比为4:1,静置24h,阻尼材料必须完全溶解;之后将玻璃纤维和碳纤维分别浸泡在氢化丁腈橡中30min,并对浸泡后的玻璃纤维和碳纤维进行烘干,烘干温度为90℃,烘干时间为24h;玻璃纤维的直径为13μm,碳纤维的直径为8μm;
2)先将浸泡后的玻璃纤维与碳纤维合成一股再进行编织,玻璃纤维与碳纤维的数量比例为1:8,编织的混合织物的厚度为2.3mm;
3)首先将聚乙二醇(PEG)和己二异氰酸酯反应生成聚氨酯预聚体,然后由聚氨酯预聚体与双酚F型环氧树脂进行接枝反应,制备增韧环氧树脂;之后用增韧改性的环氧树脂浸渍步骤2)得到的混合织物制成预浸料,浸渍的时间为60min,浸渍后需进行烘干,烘干的温度为90℃;
4)使用四氢呋喃充分溶解阻尼材料氢化丁腈橡胶HNBR,四氢呋喃与氢化丁腈橡胶的质量比为4:1,静置24h,阻尼材料必须完全溶解;然后添加纳米二氧化硅后搅拌均匀,之后将其涂刷在预浸料的上下表面,涂刷厚度为0.25mm,得到阻尼材料,氢化丁腈橡胶与纳米二氧化硅的质量比为100:10;
5)将步骤3)制备的预浸料与步骤4)制备的阻尼材料分层叠放铺层,采用[0/G/0/G/0/G/0/0/0/0/0]的放置方式,之后放入高压釜中,使用的固化剂为4,4’-二氨基二苯甲烷,温度在130℃,固化压力2MPa,时间为2.5h,固化得到阻尼复合材料。
对比例1
在上述实施例1的基础上,去掉纳米二氧化硅制得阻尼复合材料。
对比例2
在上述实施例1的基础上,氢化丁腈橡胶与纳米二氧化硅的质量比为100:20制得阻尼复合材料。
对比例3
在上述实施例1的基础上,步骤3)仅使用双酚F型环氧树脂制成预浸料,最后制得阻尼复合材料。
对比例4
在上述实施例1的基础上,仅使用玻璃纤维。
对比例5
在上述实施例1的基础上,仅使用碳纤维。
对比例6
在上述实施例1的基础上,玻璃纤维与碳纤维的数量比例为1:1。
对比例7
在上述实施例1的基础上,直接使用未经氢化丁腈橡胶浸泡的玻璃纤维和碳纤维编织成混合织物。
对照组
在上述实施例1的基础上,不使用阻尼材料氢化丁腈橡胶。
表1 实施例及对比例性能测试
注:阻尼系数为实施例或对比例与对照组的相对阻尼系数。
从表1中发现,实施例1-3所制备的阻尼复合材料的阻尼性能和力学性能都优于对比例1-7和对照组。从实施例和对比例1-2可知,添加纳米二氧化硅并保证添加的比例在本申请设置的范围内,可改善复合材料的阻尼性能。从实施例和对比例3可知,使用聚氨酯改性的环氧树脂的力学性能能够得到改善。从实施例和对比例4-6可知,同时使用玻璃纤维与碳纤维并保证玻璃纤维与碳纤维添加的比例在本申请设置的范围内,可改善复合材料的力学性能。从实施例和对比例7可知,预先使用氢化丁腈橡胶浸泡玻璃纤维和碳纤维可以提高复合材料的阻尼性能。
以上所述仅为本发明的较佳实施例而已,并不用以限制本发明,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (10)
1.一种聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:该方法包括如下步骤:
1)将阻尼材料氢化丁腈橡胶充分溶解,之后将玻璃纤维和碳纤维分别浸泡在氢化丁腈橡胶中,并对浸泡后的玻璃纤维和碳纤维进行烘干;
2)将浸泡后的玻璃纤维和碳纤维编织成混合织物;
3)使用聚氨酯对环氧树脂进行增韧改性,之后用增韧改性的环氧树脂浸渍步骤2)得到的混合织物制成预浸料;
4)将氢化丁腈橡胶充分溶解,并添加纳米二氧化硅后搅拌,之后将其涂刷或喷涂在预浸料的上下表面,得到阻尼材料,氢化丁腈橡胶与纳米二氧化硅的质量比为100:(1-10);
5)将步骤3)制备的预浸料与步骤4)制备的阻尼材料分层叠放铺层,之后采用高压釜工艺,固化得到阻尼复合材料。
2.根据权利要求1所述的聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:步骤1)和步骤4)中,使用四氢呋喃溶解氢化丁腈橡胶,玻璃纤维的直径为6-15μm,碳纤维的直径为5-8μm。
3.根据权利要求1所述的聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:步骤1)中浸泡时间为30-50min,烘干温度为80-90℃,烘干时间为12-24h。
4.根据权利要求1所述的聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:步骤2)先将玻璃纤维与碳纤维合成一股再进行编织,玻璃纤维与碳纤维的数量比例为1:(4-10),编织的混合织物的厚度为1-3mm。
5.根据权利要求1所述的聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:步骤3)中,先利用异氰酸酯制备聚氨酯预聚体,再利用聚氨酯预聚体与环氧树脂反应得到聚氨酯改性环氧树脂,异氰酸酯为甲苯二异氰酸酯、二苯甲烷二异氰酸酯、多亚甲基多苯基多异氰酸酯或己二异氰酸酯中的任一种,环氧树脂为双酚F型环氧树脂或双酚S型环氧树脂。
6.根据权利要求1所述的聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:步骤3)中浸渍的时间为30-60min,浸渍后需进行烘干,烘干的温度为80-90℃。
7.根据权利要求1所述的聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:步骤4)中涂刷或喷涂的厚度为0.15-0.3mm。
8.根据权利要求1所述的聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:步骤5)中,预浸料为6-10偶数层,阻尼材料为2-4层,预浸料与阻尼材料的铺层方式为[0/G/0/G/……/0/0/0/0]或[0/0/……G/0/G/0/……/0/0],其中G为阻尼材料,0为预浸料。
9.根据权利要求1所述的聚氨酯增韧环氧基阻尼复合材料的制备方法,其特征在于:步骤5)中使用的固化剂为4,4’-二氨基二苯甲烷或二乙基甲苯二胺中的一种;固化温度在110-130℃,固化压力2MPa,固化时间1.5-2.5h。
10.一种由权利要求1-9任一项所述的制备方法制备的聚氨酯增韧环氧基阻尼复合材料。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202310410319.0A CN116141703A (zh) | 2023-04-18 | 2023-04-18 | 一种聚氨酯增韧环氧基阻尼复合材料及其制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202310410319.0A CN116141703A (zh) | 2023-04-18 | 2023-04-18 | 一种聚氨酯增韧环氧基阻尼复合材料及其制备方法 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN116141703A true CN116141703A (zh) | 2023-05-23 |
Family
ID=86373944
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202310410319.0A Pending CN116141703A (zh) | 2023-04-18 | 2023-04-18 | 一种聚氨酯增韧环氧基阻尼复合材料及其制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN116141703A (zh) |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101786356A (zh) * | 2010-01-25 | 2010-07-28 | 张博明 | 一种共固化高阻尼复合材料的制备方法 |
CN102700203A (zh) * | 2012-06-15 | 2012-10-03 | 哈尔滨工业大学 | 一种具有压电阻尼的碳纤维复合材料层合板及其制备方法 |
CN103113604A (zh) * | 2013-01-28 | 2013-05-22 | 北京化工大学常州先进材料研究院 | 一种聚氨酯预聚体改善中低温固化预浸料层间剪切强度的制备方法 |
CN104497484A (zh) * | 2014-12-12 | 2015-04-08 | 天津大学 | 一种三维编织橡胶涂层碳纤维增强复合材料的制备方法 |
CN105690792A (zh) * | 2015-08-24 | 2016-06-22 | 青岛理工大学 | 带粘弹性薄膜的低温共固化高阻尼复合材料构件制作工艺 |
CN106398613A (zh) * | 2016-06-23 | 2017-02-15 | 吴迪 | 一种复合增韧改性环氧结构胶的制备方法 |
CN106519706A (zh) * | 2016-10-10 | 2017-03-22 | 芜湖市鸿坤汽车零部件有限公司 | 一种汽车用含纳米空心粒子的丁腈橡胶复合阻尼材料及其制备方法 |
CN106519132A (zh) * | 2016-10-10 | 2017-03-22 | 芜湖市鸿坤汽车零部件有限公司 | 一种汽车用具有高粘结强度的丁腈橡胶阻尼材料及其制备方法 |
CN107938113A (zh) * | 2017-12-26 | 2018-04-20 | 芜湖市长江起重设备制造有限公司 | 一种表面涂覆淀粉复合氢化丁腈橡胶的纤维的制备方法 |
CN109776893A (zh) * | 2019-01-21 | 2019-05-21 | 青岛理工大学 | 氨酚醛树脂基中温共固化的嵌入式大阻尼复合材料及其制备工艺 |
CN114013151A (zh) * | 2021-11-19 | 2022-02-08 | 成都迈科高分子材料股份有限公司 | 一种梯度多层阻尼材料及其制备方法 |
CN114716743A (zh) * | 2022-03-25 | 2022-07-08 | 成都飞机工业(集团)有限责任公司 | 一种氢化丁腈橡胶补强剂及其制备方法、应用 |
CN114957741A (zh) * | 2021-12-29 | 2022-08-30 | 江苏志纤复能科技有限公司 | 一种新型低温共固化高阻尼复合材料及其制备方法 |
CN115109281A (zh) * | 2022-08-26 | 2022-09-27 | 潍坊科技学院 | 一种碳纳米管增强共固化阻尼复合材料及其制备方法 |
-
2023
- 2023-04-18 CN CN202310410319.0A patent/CN116141703A/zh active Pending
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101786356A (zh) * | 2010-01-25 | 2010-07-28 | 张博明 | 一种共固化高阻尼复合材料的制备方法 |
CN102700203A (zh) * | 2012-06-15 | 2012-10-03 | 哈尔滨工业大学 | 一种具有压电阻尼的碳纤维复合材料层合板及其制备方法 |
CN103113604A (zh) * | 2013-01-28 | 2013-05-22 | 北京化工大学常州先进材料研究院 | 一种聚氨酯预聚体改善中低温固化预浸料层间剪切强度的制备方法 |
CN104497484A (zh) * | 2014-12-12 | 2015-04-08 | 天津大学 | 一种三维编织橡胶涂层碳纤维增强复合材料的制备方法 |
CN105690792A (zh) * | 2015-08-24 | 2016-06-22 | 青岛理工大学 | 带粘弹性薄膜的低温共固化高阻尼复合材料构件制作工艺 |
CN106398613A (zh) * | 2016-06-23 | 2017-02-15 | 吴迪 | 一种复合增韧改性环氧结构胶的制备方法 |
CN106519706A (zh) * | 2016-10-10 | 2017-03-22 | 芜湖市鸿坤汽车零部件有限公司 | 一种汽车用含纳米空心粒子的丁腈橡胶复合阻尼材料及其制备方法 |
CN106519132A (zh) * | 2016-10-10 | 2017-03-22 | 芜湖市鸿坤汽车零部件有限公司 | 一种汽车用具有高粘结强度的丁腈橡胶阻尼材料及其制备方法 |
CN107938113A (zh) * | 2017-12-26 | 2018-04-20 | 芜湖市长江起重设备制造有限公司 | 一种表面涂覆淀粉复合氢化丁腈橡胶的纤维的制备方法 |
CN109776893A (zh) * | 2019-01-21 | 2019-05-21 | 青岛理工大学 | 氨酚醛树脂基中温共固化的嵌入式大阻尼复合材料及其制备工艺 |
CN114013151A (zh) * | 2021-11-19 | 2022-02-08 | 成都迈科高分子材料股份有限公司 | 一种梯度多层阻尼材料及其制备方法 |
CN114957741A (zh) * | 2021-12-29 | 2022-08-30 | 江苏志纤复能科技有限公司 | 一种新型低温共固化高阻尼复合材料及其制备方法 |
CN114716743A (zh) * | 2022-03-25 | 2022-07-08 | 成都飞机工业(集团)有限责任公司 | 一种氢化丁腈橡胶补强剂及其制备方法、应用 |
CN115109281A (zh) * | 2022-08-26 | 2022-09-27 | 潍坊科技学院 | 一种碳纳米管增强共固化阻尼复合材料及其制备方法 |
Non-Patent Citations (1)
Title |
---|
丁永涛: "高分子复合材料研究新进展", 黄河水利出版社, pages: 84 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2010227757B2 (en) | Prepregs and molded bodies produced from same | |
KR101868177B1 (ko) | 용액 중 폴리우레탄 조성물을 기재로 하는 저장-안정성 폴리우레탄 프리프레그를 제조하는 방법 및 그로부터 제조된 성형체 | |
KR101891830B1 (ko) | 프리프레그 및 저온에서 이로부터 제조된 성형체 | |
CN103201102B (zh) | 用于纤维强化复合材料的环氧树脂组合物、预浸料坯和纤维强化复合材料 | |
JP6000852B2 (ja) | 風力発電プラントにおける層状上部構造物の使用 | |
RU2013136330A (ru) | Заготовки из композиционного материала и изготовленные из них формованные детали, а также формованные детали, изготовленные непосредственно на основе гидроксифункционализированных (мет) акрилатов, которые термореактивно сшиваются с помощью уретдионов | |
KR20140024333A (ko) | 액체 수지 성분을 함유하는 폴리우레탄 조성물로 제조된 저장-안정성 폴리우레탄 프리프레그 및 그로부터 제조된 성형 부품 | |
KR102481812B1 (ko) | 폴리이소시아누레이트 기재 중합체 및 섬유 강화된 복합재 | |
CN109867916A (zh) | 植物纤维增强树脂基复合材料及其制备方法 | |
CN112204064B (zh) | 用于生产异氰脲酸酯聚合物的胺催化剂的加合物 | |
CN1401680A (zh) | 一种硬质聚氨酯浇注材料 | |
CN116141703A (zh) | 一种聚氨酯增韧环氧基阻尼复合材料及其制备方法 | |
CN116082797B (zh) | 一种高模量热塑环氧树脂组合物及其制备方法 | |
CN1143661A (zh) | 常温固化聚氨酯增韧环氧树脂胶粘剂的制备 | |
CN114874607B (zh) | 一种轴承用聚氨酯及其制备方法 | |
CN113897032B (zh) | 一种用于纤维缠绕的环氧树脂复合材料及其制备方法 | |
CN114196165B (zh) | 一种改性黄麻纤维增强生物基环氧树脂复合材料的制备方法 | |
AU2021217266A1 (en) | Molding material and fiber reinforced composite material | |
CN116253852B (zh) | 一种改性热塑性聚氨酯弹性体的制备方法 | |
CN115181231B (zh) | 一种液体组合物和由其制备的预浸料和复合材料 | |
CN113736218B (zh) | 一种用于补强船体的预浸料树脂及其制备方法与应用 | |
CN116574359B (zh) | 一种抗冲击的改性环氧树脂及其制备工艺 | |
CN116120714A (zh) | 一种环氧树脂基预浸料的制备方法与应用 | |
CN118772585A (zh) | 一种适用于hp-rtm工艺的抗冲击环氧树脂组合物及其制备方法和应用 | |
CN116948132A (zh) | 一种综合性能优异的改性玄武岩纤维/聚氨酯减振降噪材料及其制备方法 |
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 | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20230523 |