CN116100836A - A kind of preparation technology of film-coated fabric adopting stripping method - Google Patents
A kind of preparation technology of film-coated fabric adopting stripping method Download PDFInfo
- Publication number
- CN116100836A CN116100836A CN202310110477.4A CN202310110477A CN116100836A CN 116100836 A CN116100836 A CN 116100836A CN 202310110477 A CN202310110477 A CN 202310110477A CN 116100836 A CN116100836 A CN 116100836A
- Authority
- CN
- China
- Prior art keywords
- film
- fabric
- pretreated
- adopting
- adhesive layer
- 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
Images
Classifications
-
- 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
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
- B32B27/283—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polysiloxanes
-
- 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
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/02—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
- B29C65/18—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using heated tools
-
- 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
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/48—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding
- B29C65/52—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding characterised by the way of applying the adhesive
-
- 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
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/40—General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
- B29C66/41—Joining substantially flat articles ; Making flat seams in tubular or hollow articles
-
- 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
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/80—General aspects of machine operations or constructions and parts thereof
- B29C66/83—General aspects of machine operations or constructions and parts thereof characterised by the movement of the joining or pressing tools
- B29C66/834—General aspects of machine operations or constructions and parts thereof characterised by the movement of the joining or pressing tools moving with the parts to be joined
- B29C66/8341—Roller, cylinder or drum types; Band or belt types; Ball types
- B29C66/83411—Roller, cylinder or drum types
- B29C66/83413—Roller, cylinder or drum types cooperating rollers, cylinders or drums
-
- 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
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
-
- 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
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
- B29C71/0081—After-treatment of articles without altering their shape; Apparatus therefor using an electric field, e.g. for electrostatic charging
-
- 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
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
- B29C71/04—After-treatment of articles without altering their shape; Apparatus therefor by wave energy or particle radiation, e.g. for curing or vulcanising preformed articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D7/00—Producing flat articles, e.g. films or sheets
- B29D7/01—Films or sheets
-
- 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
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/12—Layered products comprising a layer of synthetic resin next to a 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
- 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
-
- 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
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3802—Low-molecular-weight compounds having heteroatoms other than oxygen having halogens
- C08G18/3814—Polyamines
-
- 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
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/4816—Two or more polyethers of different physical or chemical nature mixtures of two or more polyetherpolyols having at least three hydroxy groups
-
- 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
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6681—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38
- C08G18/6685—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3225 or polyamines of C08G18/38
-
- 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
- C09J175/08—Polyurethanes from polyethers
-
- 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
- B32B2262/02—Synthetic macromolecular fibres
- B32B2262/0253—Polyolefin 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
- B32B2262/02—Synthetic macromolecular fibres
- B32B2262/0276—Polyester fibres
- B32B2262/0284—Polyethylene terephthalate [PET] or polybutylene terephthalate [PBT]
-
- 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
- B32B2262/06—Vegetal fibres
- B32B2262/062—Cellulose fibres, e.g. cotton
- B32B2262/065—Lignocellulosic fibres, e.g. jute, sisal, hemp, flax, bamboo
-
- 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
- B32B2307/30—Properties of the layers or laminate having particular thermal properties
- B32B2307/304—Insulating
-
- 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
- B32B2307/70—Other properties
- B32B2307/724—Permeability to gases, adsorption
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
- Y02P70/62—Manufacturing or production processes characterised by the final manufactured product related technologies for production or treatment of textile or flexible materials or products thereof, including footwear
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
Abstract
Description
技术领域technical field
本发明涉及覆膜面料技术领域,尤其涉及一种采用剥离方式的覆膜面料制备工艺。The invention relates to the technical field of film-coated fabrics, in particular to a process for preparing film-covered fabrics in a stripping manner.
背景技术Background technique
随着生活水平的提高,人们对面料的功能需求日益多样化,覆膜面料即是一种较为新型的面料,其具有防风特性,用于制造防风服等功能性服装。With the improvement of living standards, people have increasingly diversified functional requirements for fabrics. Laminated fabrics are a relatively new type of fabrics, which have windproof properties and are used to manufacture functional clothing such as windproof clothing.
目前除了对覆膜材料的选用外,织物-覆膜的制备工艺也是面料研发中需解决的问题,传统选用热粘合方法,粘合中需要通过加热令粘合胶软化,但加热过程不但需要消耗较大量电力能源,而且胶质经过高温加热后产生对人体和环境有害的挥发性气体,不符合环保要求。另外现有覆膜面料将高分子薄膜复合在面料层上,利用高分子薄膜遮挡面料层的孔隙,起到防风作用,但是这种覆膜面料的透气性很差。At present, in addition to the selection of film materials, the preparation process of fabric-film is also a problem to be solved in the research and development of fabrics. The traditional thermal bonding method is used, and the adhesive needs to be softened by heating during bonding. However, the heating process not only requires It consumes a large amount of electric energy, and the colloid produces volatile gases that are harmful to the human body and the environment after being heated at a high temperature, which does not meet environmental protection requirements. In addition, the existing film-coated fabrics compound the polymer film on the fabric layer, and utilize the polymer film to block the pores of the fabric layer to play a windproof effect, but the air permeability of this film-coated fabric is very poor.
目前为了增加覆膜面料的透气性,采用具有微孔结构的高分子薄膜,以平衡防风性能和透气性能,但是具有微孔结构的高分子薄膜在热粘合过程中,同样存在热粘合温度高,同时微孔分布匀度难以控制,进而导致覆膜面料的透气效果难以保持稳定的问题。At present, in order to increase the air permeability of the coated fabric, a polymer film with a microporous structure is used to balance the windproof performance and air permeability. However, the polymer film with a microporous structure also has a thermal bonding temperature during the thermal bonding process. At the same time, it is difficult to control the uniformity of micropore distribution, which leads to the problem that the breathability of the film-coated fabric is difficult to maintain stability.
发明内容Contents of the invention
本发明的目的是为了解决现有技术中存在的缺点,而提出的一种采用剥离方式的覆膜面料制备工艺。The object of the present invention is to solve the shortcomings in the prior art, and propose a method for preparing film-coated fabrics in a stripping manner.
一种采用剥离方式的覆膜面料制备工艺,包括如下步骤:A preparation process for film-coated fabrics in a stripping manner, comprising the steps of:
S1、按重量份将40-60份聚醚三元醇MN-500、20-40份聚醚三元醇EP-330N、1-2份4,4'-亚甲基二(2-氯苯胺)、1-2份均泡剂、5-12份聚氧化乙烯甘油醚、0.1-1份催化剂、1-10份水加入至混料罐中,在温度30-50℃搅拌,加入20-60份异氰酸酯预聚物继续搅拌10-60s,得到活性粘合层;S1. By weight, 40-60 parts of polyether triol MN-500, 20-40 parts of polyether triol EP-330N, 1-2 parts of 4,4'-methylenebis(2-chloroaniline ), 1-2 parts of foam stabilizer, 5-12 parts of polyoxyethylene glyceryl ether, 0.1-1 part of catalyst, 1-10 parts of water are added to the mixing tank, stirred at a temperature of 30-50 °C, and 20-60 One part of isocyanate prepolymer continues to stir for 10-60s to obtain an active adhesive layer;
S2、将基材布料、有机硅薄膜分别采用等离子体技术处理,处理过程中,采用常压直流辉光放电,分别得到预处理基材布料、预处理有机硅薄膜;S2. The substrate fabric and the organic silicon film are respectively treated with plasma technology. During the treatment process, the normal pressure DC glow discharge is used to obtain the pretreated substrate fabric and the pretreated organic silicon film respectively;
S3、将活性粘合层采用滚筒花纹上胶至预处理基材布料表面,成型,采用激光器在粘合层表面激光扫射,得到微孔阵列的三维预处理基材布料,然后在粘合层另一侧附上预处理有机硅薄膜,采用上压辊和下压辊加热压碾,其中上压辊温度为70-80℃,得到覆膜面料。S3. Glue the active adhesive layer to the surface of the pretreated substrate cloth with a roller pattern, shape it, and use a laser to scan the surface of the adhesive layer to obtain a three-dimensional pretreated substrate cloth with a microhole array, and then place it on the adhesive layer. A pre-treated silicone film is attached to one side, and the upper pressing roller and the lower pressing roller are used to heat and press, wherein the temperature of the upper pressing roller is 70-80°C to obtain a coated fabric.
优选地,在S1中,所述催化剂为有机锡催化剂,优选为二月桂酸二丁基锡。Preferably, in S1, the catalyst is an organotin catalyst, preferably dibutyltin dilaurate.
优选地,在S1中,所述均泡剂为均泡剂L2580。Preferably, in S1, the foam stabilizer is foam stabilizer L2580.
优选地,在S2中,放电过程中,放电功率为85-110W,极板间距为2-4mm,处理速度为60-80mm/min,处理时间为2-4min,工作气体包括氦气和氧气,氦气与氧气的流量比为10:1-4ml/min。Preferably, in S2, during the discharge process, the discharge power is 85-110W, the electrode plate spacing is 2-4mm, the processing speed is 60-80mm/min, the processing time is 2-4min, and the working gas includes helium and oxygen, The flow ratio of helium to oxygen is 10:1-4ml/min.
优选地,在S2中,所述有机硅薄膜为有机硅PDMS薄膜,厚度为50μm。Preferably, in S2, the organosilicon film is an organosilicon PDMS film with a thickness of 50 μm.
优选地,在S2中,所述基材布料为涤纶、棉纶、棉的一种。Preferably, in S2, the base material fabric is one of polyester, cotton and cotton.
优选地,在S3中,预处理基材布料表面施胶量为5-12g/m2。Preferably, in S3, the amount of sizing agent on the surface of the pretreated substrate cloth is 5-12g/m 2 .
优选地,在S3中,激光器的波长为1064nm、脉冲能量为0.5mJ。Preferably, in S3, the wavelength of the laser is 1064 nm, and the pulse energy is 0.5 mJ.
一种覆膜面料,采用所述覆膜面料制备工艺制成。A film-coated fabric is made by adopting the preparation process of the film-coated fabric.
本发明的技术效果如下所示:Technical effect of the present invention is as follows:
本发明中,异氰酸酯基与水反应生成脲键和二氧化碳,配合L2580均泡剂、聚氧化乙烯甘油醚形成的活性粘合层,由于大分子聚醚的柔性链间含有大量空隙结构,占据空间位置大,形成的活性粘合层不仅柔韧性极高,同时上胶至预处理基材布料表面,由于通过等离子体处理可有效对基材布料表面进行活化,两者亲和性好,经过成型后粘合层表面进行激光扫射,可有效增加粘合层表面粗糙度,进一步与预处理有机硅薄膜结合经过热压碾,在有效降低压碾温度的前提下,相互间结合强度高,面料不仅力学性能优异,同时在保证保温性能的基础上,透气、透湿性能优异。In the present invention, the isocyanate group reacts with water to generate urea bonds and carbon dioxide, and the active adhesive layer formed by cooperating with L2580 foam stabilizer and polyoxyethylene glycerol ether occupies a spatial position due to the large number of void structures between the flexible chains of macromolecular polyether. Large, the active adhesive layer formed is not only extremely flexible, but also glued to the surface of the pretreated substrate fabric. Because the plasma treatment can effectively activate the surface of the substrate fabric, the two have good affinity. After molding Laser scanning on the surface of the adhesive layer can effectively increase the surface roughness of the adhesive layer. It is further combined with the pretreated silicone film and subjected to hot rolling. Under the premise of effectively reducing the rolling temperature, the mutual bonding strength is high, and the fabric is not only mechanical The performance is excellent, and at the same time, on the basis of ensuring the thermal insulation performance, the air permeability and moisture permeability are excellent.
本发明不仅热压温度低,同时最大程度地保持了原来面料结构内纱线的相对运动自由度,从而保持其拉伸、剪切弹性和弯曲柔性,令复合面料呈现轻、薄、柔、弹的特征,保障了触肤舒适度和人体运动的自由度,同时可以平衡保温性能和透气性能,且透气孔的孔径、分布匀度均可通过对相应的参数进行精确控制,达到透气透湿效果稳定,产品一致性高的优点。The invention not only has a low hot-pressing temperature, but also maintains the relative freedom of movement of the yarns in the original fabric structure to the greatest extent, so as to maintain its stretching, shear elasticity and bending flexibility, so that the composite fabric is light, thin, soft and elastic. The characteristics of the skin-touching comfort and the freedom of human body movement are guaranteed, and at the same time, it can balance the thermal insulation performance and air permeability, and the pore size and distribution uniformity of the air holes can be precisely controlled by the corresponding parameters to achieve the breathable and moisture-permeable effect. The advantages of stability and high product consistency.
附图说明Description of drawings
图1为实施例5与对比例1-2所得面料的传热系数、保温率测试图。Fig. 1 is the heat transfer coefficient of the fabric obtained in embodiment 5 and comparative example 1-2, the heat retention rate test chart.
图2为实施例5与对比例1-2所得面料的克罗值测试图。Fig. 2 is the Cro value test figure of the fabric obtained in embodiment 5 and comparative example 1-2.
图3为实施例5与对比例1-2所得面料的透气透湿性能测试图。Fig. 3 is the air and moisture permeability test chart of the fabrics obtained in Example 5 and Comparative Examples 1-2.
具体实施方式Detailed ways
下面结合具体实施例对本发明作进一步解说。The present invention will be further explained below in conjunction with specific embodiments.
实施例1Example 1
一种采用剥离方式的覆膜面料制备工艺,包括如下步骤:A preparation process for film-coated fabrics in a stripping manner, comprising the steps of:
S1、将40kg聚醚三元醇MN-500、20kg聚醚三元醇EP-330N、1kg4,4'-亚甲基二(2-氯苯胺)、1kg均泡剂L2580、5kg聚氧化乙烯甘油醚、0.1kg二月桂酸二丁基锡、1kg水加入至混料罐中,在温度30℃搅拌10min,加入20kg异氰酸酯预聚物继续搅拌10s,得到活性粘合层;S1, 40kg polyether triol MN-500, 20kg polyether triol EP-330N, 1kg4,4'-methylenebis(2-chloroaniline), 1kg foam stabilizer L2580, 5kg polyoxyethylene glycerin Add ether, 0.1kg of dibutyltin dilaurate, and 1kg of water into the mixing tank, stir at 30°C for 10min, add 20kg of isocyanate prepolymer and continue stirring for 10s to obtain an active adhesive layer;
所述异氰酸酯预聚物为异氰酸预聚合物(9048-57-1),品牌:国产湖北;The isocyanate prepolymer is an isocyanate prepolymer (9048-57-1), brand: domestic Hubei;
S2、将涤纶布料、有机硅薄膜分别采用等离子体技术处理,处理过程中,采用常压直流辉光放电,放电功率为85W,极板间距为2mm,处理速度为60mm/min,处理时间为2min,工作气体包括氦气和氧气,氦气与氧气的流量比为10:14ml/min,分别得到预处理基材布料、预处理有机硅薄膜;S2. The polyester cloth and the organic silicon film are respectively treated with plasma technology. During the treatment process, the normal voltage DC glow discharge is used, the discharge power is 85W, the distance between the plates is 2mm, the treatment speed is 60mm/min, and the treatment time is 2min , the working gas includes helium and oxygen, the flow ratio of helium and oxygen is 10:14ml/min, and the pretreated substrate cloth and the pretreated silicone film are respectively obtained;
所述有机硅薄膜为有机硅PDMS薄膜,厚度为50μm,购自杭州圭臬新材料科技有限公司。The organosilicon film is an organosilicon PDMS film with a thickness of 50 μm, purchased from Hangzhou Guibiao New Material Technology Co., Ltd.
S3、将活性粘合层采用滚筒花纹上胶至预处理基材布料表面,施胶量为5g/m2,成型,采用波长为1064nm、脉冲能量为0.5mJ激光器在粘合层表面激光扫射,得到微孔阵列的三维预处理基材布料,然后在粘合层另一侧附上预处理有机硅薄膜,采用上压辊和下压辊加热压碾,其中上压辊温度为70℃,得到覆膜面料。S3. Glue the active adhesive layer to the surface of the pretreated substrate cloth with a roller pattern, the glue amount is 5g/m 2 , and shape it. Use a laser with a wavelength of 1064nm and a pulse energy of 0.5mJ to scan the surface of the adhesive layer. The three-dimensional pretreated substrate cloth with micropore array was obtained, and then the pretreated silicone film was attached on the other side of the adhesive layer, and the upper and lower pressing rollers were used to heat and press, wherein the temperature of the upper pressing roller was 70°C, and the obtained Laminated fabric.
实施例2Example 2
一种采用剥离方式的覆膜面料制备工艺,包括如下步骤:A preparation process for film-coated fabrics in a stripping manner, comprising the steps of:
S1、将60kg聚醚三元醇MN-500、40kg聚醚三元醇EP-330N、2kg4,4'-亚甲基二(2-氯苯胺)、2kg均泡剂L2580、12kg聚氧化乙烯甘油醚、1kg二月桂酸二丁基锡、10kg水加入至混料罐中,在温度50℃搅拌30min,加入60kg异氰酸酯预聚物继续搅拌60s,得到活性粘合层;S1, 60kg polyether triol MN-500, 40kg polyether triol EP-330N, 2kg4,4'-methylenebis(2-chloroaniline), 2kg foam stabilizer L2580, 12kg polyoxyethylene glycerin Add ether, 1kg dibutyltin dilaurate, and 10kg water into the mixing tank, stir at a temperature of 50°C for 30min, add 60kg of isocyanate prepolymer and continue stirring for 60s to obtain an active adhesive layer;
所述异氰酸酯预聚物为异氰酸预聚合物(9048-57-1),品牌:国产湖北;The isocyanate prepolymer is an isocyanate prepolymer (9048-57-1), brand: domestic Hubei;
S2、将涤纶布料、有机硅薄膜分别采用等离子体技术处理,处理过程中,采用常压直流辉光放电,放电功率为110W,极板间距为4mm,处理速度为80mm/min,处理时间为4min,工作气体包括氦气和氧气,氦气与氧气的流量比为10:4ml/min,分别得到预处理基材布料、预处理有机硅薄膜;S2. The polyester cloth and the organic silicon film are respectively treated by plasma technology. During the treatment process, the normal voltage DC glow discharge is adopted, the discharge power is 110W, the distance between the plates is 4mm, the treatment speed is 80mm/min, and the treatment time is 4min , the working gas includes helium and oxygen, the flow ratio of helium and oxygen is 10:4ml/min, and the pretreated substrate cloth and the pretreated silicone film are respectively obtained;
所述有机硅薄膜为有机硅PDMS薄膜,厚度为50μm,购自杭州圭臬新材料科技有限公司。The organosilicon film is an organosilicon PDMS film with a thickness of 50 μm, purchased from Hangzhou Guibiao New Material Technology Co., Ltd.
S3、将活性粘合层采用滚筒花纹上胶至预处理基材布料表面,施胶量为12g/m2,成型,采用波长为1064nm、脉冲能量为0.5mJ激光器在粘合层表面激光扫射,得到微孔阵列的三维预处理基材布料,然后在粘合层另一侧附上预处理有机硅薄膜,采用上压辊和下压辊加热压碾,其中上压辊温度为80℃,得到覆膜面料。S3. Glue the active adhesive layer to the surface of the pretreated substrate cloth with a roller pattern, the glue amount is 12g/m 2 , and shape it. Use a laser with a wavelength of 1064nm and a pulse energy of 0.5mJ to scan the surface of the adhesive layer. The three-dimensional pretreated substrate cloth with micropore array was obtained, and then the pretreated silicone film was attached on the other side of the adhesive layer, and the upper and lower pressing rollers were used to heat and press, wherein the temperature of the upper pressing roller was 80°C. Laminated fabric.
实施例3Example 3
一种采用剥离方式的覆膜面料制备工艺,包括如下步骤:A preparation process for film-coated fabrics in a stripping manner, comprising the steps of:
S1、将45kg聚醚三元醇MN-500、22kg聚醚三元醇EP-330N、1.3kg4,4'-亚甲基二(2-氯苯胺)、1.2kg均泡剂L2580、6kg聚氧化乙烯甘油醚、0.2kg二月桂酸二丁基锡、2kg水加入至混料罐中,在温度32℃搅拌15min,加入30kg异氰酸酯预聚物继续搅拌10-60s,得到活性粘合层;S1. Mix 45kg polyether triol MN-500, 22kg polyether triol EP-330N, 1.3kg 4,4'-methylenebis(2-chloroaniline), 1.2kg foam stabilizer L2580, 6kg polyoxygen Add ethylene glyceryl ether, 0.2kg dibutyltin dilaurate, and 2kg water into the mixing tank, stir at a temperature of 32°C for 15min, add 30kg of isocyanate prepolymer and continue stirring for 10-60s to obtain an active adhesive layer;
所述异氰酸酯预聚物为异氰酸预聚合物(9048-57-1),品牌:国产湖北;The isocyanate prepolymer is an isocyanate prepolymer (9048-57-1), brand: domestic Hubei;
S2、将棉纶布料、有机硅薄膜分别采用等离子体技术处理,处理过程中,采用常压直流辉光放电,放电功率为90W,极板间距为3mm,处理速度为65mm/min,处理时间为2.5min,工作气体包括氦气和氧气,氦气与氧气的流量比为10:1.5ml/min,分别得到预处理基材布料、预处理有机硅薄膜;S2. The cotton cloth and the organic silicon film are respectively treated with plasma technology. During the treatment process, normal voltage DC glow discharge is adopted, the discharge power is 90W, the distance between the plates is 3mm, the treatment speed is 65mm/min, and the treatment time is 2.5min, the working gas includes helium and oxygen, the flow ratio of helium and oxygen is 10:1.5ml/min, and the pretreated substrate fabric and the pretreated silicone film are respectively obtained;
所述有机硅薄膜为有机硅PDMS薄膜,厚度为50μm,购自杭州圭臬新材料科技有限公司。The organosilicon film is an organosilicon PDMS film with a thickness of 50 μm, purchased from Hangzhou Guibiao New Material Technology Co., Ltd.
S3、将活性粘合层采用滚筒花纹上胶至预处理基材布料表面,施胶量为7g/m2,成型,采用波长为1064nm、脉冲能量为0.5mJ激光器在粘合层表面激光扫射,得到微孔阵列的三维预处理基材布料,然后在粘合层另一侧附上预处理有机硅薄膜,采用上压辊和下压辊加热压碾,其中上压辊温度为72℃,得到覆膜面料。S3. Glue the active adhesive layer to the surface of the pretreated substrate cloth with a roller pattern, the glue amount is 7g/m 2 , and shape it. Use a laser with a wavelength of 1064nm and a pulse energy of 0.5mJ to scan the surface of the adhesive layer. The three-dimensional pretreated substrate cloth with micropore array was obtained, and then the pretreated silicone film was attached on the other side of the adhesive layer, and the upper pressing roller and the lower pressing roller were used to heat and press, wherein the temperature of the upper pressing roller was 72°C, and the obtained Laminated fabric.
实施例4Example 4
一种采用剥离方式的覆膜面料制备工艺,包括如下步骤:A preparation process for film-coated fabrics in a stripping manner, comprising the steps of:
S1、将55kg聚醚三元醇MN-500、35kg聚醚三元醇EP-330N、1.8kg4,4'-亚甲基二(2-氯苯胺)、1.6kg均泡剂L2580、10kg聚氧化乙烯甘油醚、0.7kg二月桂酸二丁基锡、8kg水加入至混料罐中,在温度45℃搅拌24min,加入55kg异氰酸酯预聚物继续搅拌50s,得到活性粘合层;S1. Mix 55kg polyether triol MN-500, 35kg polyether triol EP-330N, 1.8kg 4,4'-methylene bis(2-chloroaniline), 1.6kg foam stabilizer L2580, 10kg polyoxygen Add ethylene glyceryl ether, 0.7kg dibutyltin dilaurate, and 8kg water into the mixing tank, stir at a temperature of 45°C for 24min, add 55kg of isocyanate prepolymer and continue stirring for 50s to obtain an active adhesive layer;
所述异氰酸酯预聚物为异氰酸预聚合物(9048-57-1),品牌:国产湖北;The isocyanate prepolymer is an isocyanate prepolymer (9048-57-1), brand: domestic Hubei;
S2、将棉纶布料、有机硅薄膜分别采用等离子体技术处理,处理过程中,采用常压直流辉光放电,放电功率为105W,极板间距为4mm,处理速度为75mm/min,处理时间为3min,工作气体包括氦气和氧气,氦气与氧气的流量比为10:3ml/min,分别得到预处理基材布料、预处理有机硅薄膜;S2. The cotton fabric and the organic silicon film are respectively treated with plasma technology. During the treatment process, normal voltage DC glow discharge is adopted, the discharge power is 105W, the distance between the plates is 4mm, the treatment speed is 75mm/min, and the treatment time is 3min, the working gas includes helium and oxygen, the flow ratio of helium and oxygen is 10:3ml/min, and the pretreated substrate cloth and the pretreated silicone film are respectively obtained;
所述有机硅薄膜为有机硅PDMS薄膜,厚度为50μm,购自杭州圭臬新材料科技有限公司。The organosilicon film is an organosilicon PDMS film with a thickness of 50 μm, purchased from Hangzhou Guibiao New Material Technology Co., Ltd.
S3、将活性粘合层采用滚筒花纹上胶至预处理基材布料表面,施胶量为10g/m2,成型,采用波长为1064nm、脉冲能量为0.5mJ激光器在粘合层表面激光扫射,得到微孔阵列的三维预处理基材布料,然后在粘合层另一侧附上预处理有机硅薄膜,采用上压辊和下压辊加热压碾,其中上压辊温度为78℃,得到覆膜面料。S3. Glue the active adhesive layer to the surface of the pretreated substrate cloth with a roller pattern, the glue amount is 10g/m 2 , and shape it. Use a laser with a wavelength of 1064nm and a pulse energy of 0.5mJ to scan the surface of the adhesive layer. The three-dimensional pretreated substrate cloth with micropore array was obtained, and then the pretreated silicone film was attached on the other side of the adhesive layer, and the upper and lower pressing rollers were used to heat and press, wherein the temperature of the upper pressing roller was 78°C, and the obtained Laminated fabric.
实施例5Example 5
一种采用剥离方式的覆膜面料制备工艺,包括如下步骤:A preparation process for film-coated fabrics in a stripping manner, comprising the steps of:
S1、将50kg聚醚三元醇MN-500、30kg聚醚三元醇EP-330N、1.6kg4,4'-亚甲基二(2-氯苯胺)、1.5kg均泡剂L2580、8kg聚氧化乙烯甘油醚、0.5kg二月桂酸二丁基锡、5kg水加入至混料罐中,在温度40℃搅拌20min,加入40kg异氰酸酯预聚物继续搅拌50s,得到活性粘合层;S1. Mix 50kg of polyether triol MN-500, 30kg of polyether triol EP-330N, 1.6kg of 4,4'-methylene bis(2-chloroaniline), 1.5kg of foam stabilizer L2580, and 8kg of polyoxygen Add ethylene glyceryl ether, 0.5kg dibutyltin dilaurate, and 5kg water into the mixing tank, stir at a temperature of 40°C for 20min, add 40kg of isocyanate prepolymer and continue stirring for 50s to obtain an active adhesive layer;
所述异氰酸酯预聚物为异氰酸预聚合物(9048-57-1),品牌:国产湖北;The isocyanate prepolymer is an isocyanate prepolymer (9048-57-1), brand: domestic Hubei;
S2、将棉纶布料、有机硅薄膜分别采用等离子体技术处理,处理过程中,采用常压直流辉光放电,放电功率为100W,极板间距为3mm,处理速度为70mm/min,处理时间为3min,工作气体包括氦气和氧气,氦气与氧气的流量比为10:3ml/min,分别得到预处理基材布料、预处理有机硅薄膜;S2. The cotton cloth and the organic silicon film are respectively treated with plasma technology. During the treatment process, normal voltage DC glow discharge is adopted, the discharge power is 100W, the distance between the plates is 3mm, the treatment speed is 70mm/min, and the treatment time is 3min, the working gas includes helium and oxygen, the flow ratio of helium and oxygen is 10:3ml/min, and the pretreated substrate cloth and the pretreated silicone film are respectively obtained;
所述有机硅薄膜为有机硅PDMS薄膜,厚度为50μm,购自杭州圭臬新材料科技有限公司。The organosilicon film is an organosilicon PDMS film with a thickness of 50 μm, purchased from Hangzhou Guibiao New Material Technology Co., Ltd.
S3、将活性粘合层采用滚筒花纹上胶至预处理基材布料表面,施胶量为10g/m2,成型,采用波长为1064nm、脉冲能量为0.5mJ激光器在粘合层表面激光扫射,得到微孔阵列的三维预处理基材布料,然后在粘合层另一侧附上预处理有机硅薄膜,采用上压辊和下压辊加热压碾,其中上压辊温度为75℃,得到覆膜面料。S3. Glue the active adhesive layer to the surface of the pretreated substrate cloth with a roller pattern, the glue amount is 10g/m 2 , and shape it. Use a laser with a wavelength of 1064nm and a pulse energy of 0.5mJ to scan the surface of the adhesive layer. The three-dimensional pretreated substrate cloth with micropore array was obtained, and then the pretreated silicone film was attached on the other side of the adhesive layer, and the upper pressing roller and the lower pressing roller were used to heat and press, wherein the temperature of the upper pressing roller was 75°C, and the obtained Laminated fabric.
对比例1Comparative example 1
一种采用剥离方式的覆膜面料制备工艺,包括如下步骤:A preparation process for film-coated fabrics in a stripping manner, comprising the steps of:
S1、将棉纶布料、有机硅薄膜分别采用等离子体技术处理,处理过程中,采用常压直流辉光放电,放电功率为100W,极板间距为3mm,处理速度为70mm/min,处理时间为3min,工作气体包括氦气和氧气,氦气与氧气的流量比为10:3ml/min,分别得到预处理基材布料、预处理有机硅薄膜;S1. The cotton cloth and the organic silicon film are respectively treated with plasma technology. During the treatment process, normal voltage DC glow discharge is adopted, the discharge power is 100W, the distance between the plates is 3mm, the treatment speed is 70mm/min, and the treatment time is 3min, the working gas includes helium and oxygen, the flow ratio of helium and oxygen is 10:3ml/min, and the pretreated substrate cloth and the pretreated silicone film are respectively obtained;
所述有机硅薄膜为有机硅PDMS薄膜,厚度为50μm,购自杭州圭臬新材料科技有限公司。The organosilicon film is an organosilicon PDMS film with a thickness of 50 μm, purchased from Hangzhou Guibiao New Material Technology Co., Ltd.
S2、将聚氨酯胶粘剂采用滚筒花纹上胶至预处理基材布料表面,施胶量为10g/m2,成型,采用波长为1064nm、脉冲能量为0.5mJ激光器在粘合层表面激光扫射,得到微孔阵列的三维预处理基材布料,然后在粘合层另一侧附上预处理有机硅薄膜,采用上压辊和下压辊加热压碾,其中上压辊温度为75℃,得到覆膜面料。S2. Glue the polyurethane adhesive to the surface of the pretreated substrate cloth with a roller pattern, the glue amount is 10g/m 2 , and shape it. Use a laser with a wavelength of 1064nm and a pulse energy of 0.5mJ to scan the surface of the adhesive layer to obtain a micro The three-dimensional pretreatment of the base material cloth of the hole array, and then attach the pretreatment silicone film on the other side of the adhesive layer, and use the upper pressing roller and the lower pressing roller to heat and press, and the temperature of the upper pressing roller is 75°C to obtain the coating fabric.
所述聚氨酯胶粘剂购自温州国仕邦高分子材料有限公司,型号为5693聚氨酯胶粘剂;The polyurethane adhesive is purchased from Wenzhou Guoshibang Polymer Material Co., Ltd., and the model is 5693 polyurethane adhesive;
对比例2Comparative example 2
一种采用剥离方式的覆膜面料制备工艺,包括如下步骤:A preparation process for film-coated fabrics in a stripping manner, comprising the steps of:
S1、将50kg聚醚三元醇MN-500、30kg聚醚三元醇EP-330N、1.6kg4,4'-亚甲基二(2-氯苯胺)、1.5kg均泡剂L2580、8kg聚氧化乙烯甘油醚、0.5kg二月桂酸二丁基锡、5kg水加入至混料罐中,在温度40℃搅拌20min,加入40kg异氰酸酯预聚物继续搅拌10-60s,得到活性粘合层;S1. Mix 50kg of polyether triol MN-500, 30kg of polyether triol EP-330N, 1.6kg of 4,4'-methylene bis(2-chloroaniline), 1.5kg of foam stabilizer L2580, and 8kg of polyoxygen Add ethylene glyceryl ether, 0.5kg dibutyltin dilaurate, and 5kg water into the mixing tank, stir at a temperature of 40°C for 20min, add 40kg of isocyanate prepolymer and continue stirring for 10-60s to obtain an active adhesive layer;
所述异氰酸酯预聚物为异氰酸预聚合物(9048-57-1),品牌:国产湖北;The isocyanate prepolymer is an isocyanate prepolymer (9048-57-1), brand: domestic Hubei;
S2、将活性粘合层采用滚筒花纹上胶至棉纶布料表面,施胶量为10g/m2,成型,采用波长为1064nm、脉冲能量为0.5mJ激光器在粘合层表面激光扫射,得到微孔阵列的三维预处理基材布料,然后在粘合层另一侧附上有机硅薄膜,采用上压辊和下压辊加热压碾,其中上压辊温度为75℃,得到覆膜面料;S2. Glue the active adhesive layer to the surface of the cotton fabric with a roller pattern, the glue amount is 10g/m 2 , and shape it. Use a laser with a wavelength of 1064nm and a pulse energy of 0.5mJ to scan the surface of the adhesive layer to obtain a micro The three-dimensional pretreatment of the base material fabric of the hole array, and then attaching a silicone film on the other side of the adhesive layer, heating and rolling with the upper pressing roller and the lower pressing roller, wherein the temperature of the upper pressing roller is 75°C, to obtain the coated fabric;
所述有机硅薄膜为有机硅PDMS薄膜,厚度为50μm,购自杭州圭臬新材料科技有限公司。The organosilicon film is an organosilicon PDMS film with a thickness of 50 μm, purchased from Hangzhou Guibiao New Material Technology Co., Ltd.
测试test
1、保温性能测试1. Thermal insulation performance test
将覆膜面料缝制成袋,针密选取9针/cm,将含绒量为75%的白鸭绒充入袋中,袋口缝制完整,得到尺寸为40cm×40cm的羽绒包,含绒量为50g,然后进行保温性能测试。Sew the film-coated fabric into a bag with a needle density of 9 stitches/cm, fill the bag with white duck down with a down content of 75%, and sew the bag mouth completely to obtain a down bag with a size of 40cm×40cm, including down The amount is 50g, and then the insulation performance test is carried out.
对实施例5与对比例1-2制备的面料采用YG606D平板式保温仪对羽绒包进行保温性测试,具体测试方法为:The fabrics prepared in Example 5 and Comparative Example 1-2 are tested for the thermal insulation of the down bag by using a YG606D plate type heat preservation instrument. The specific test method is:
在恒温恒湿条件下进行一次空白实验后,将试样覆盖于试验板上,对试样进行预热,预热时间为30min,预热结束后仪器自动进入有样实验,测试各类羽绒包的传热系数、克罗值以及保温率。对同一个试样再次进行数据测试时,无需再对试样进行预热。After a blank test under constant temperature and humidity conditions, the sample is covered on the test board, and the sample is preheated. The preheating time is 30 minutes. After the preheating, the instrument automatically enters the sample test to test various down bags. The heat transfer coefficient, Cro value and heat retention rate. When data testing is performed on the same sample again, there is no need to preheat the sample.
每次有样实验开机之前,必须进行一次空白实验,减少实验误差,使实验数据更为精确。本实验对各类羽绒包均测试5次,取平均值作为最终实验结果,其中传热系数和保温率的测试结果如图1所示,克罗值测试结果如图2所示。Before each sample experiment is started, a blank experiment must be carried out to reduce the experimental error and make the experimental data more accurate. In this experiment, all kinds of down bags were tested 5 times, and the average value was taken as the final experimental result. The test results of heat transfer coefficient and heat preservation rate are shown in Figure 1, and the test results of Cro value are shown in Figure 2.
2、透气、透湿性能测试2. Breathability and moisture permeability test
对实施例5与对比例1-2制品进行透气性能测试,测试过程中,参考GB/T5453-1997《纺织品织物透气性的测定》,选取面料不同部位并避开面料的边缘以及褶皱处对面料进行透气性测试,压降选择为100Pa,测试面积为20cm2,测试模式为自动。不同面料各测试5次,取平均值为最终测试结果,测试结果如图3所示。Carry out breathability test to embodiment 5 and comparative example 1-2 products, in the test process, with reference to GB/T5453-1997 " the mensuration of the air permeability of textile fabric ", select different parts of fabric and avoid the edge of fabric and fold place to fabric Carry out the air permeability test, the pressure drop is selected as 100Pa, the test area is 20cm 2 , and the test mode is automatic. Different fabrics were tested 5 times, and the average value was taken as the final test result. The test results are shown in Figure 3.
对实施例5与对比例1-2制品进行透湿性能测试,测试过程中,参照GB/T12704.2-2009《纺织品织物透湿性测试方法第2部分:吸湿法》进行透湿性测试,测试结果如图3所示。The products of Example 5 and Comparative Example 1-2 were tested for moisture permeability. During the test, the moisture permeability test was carried out with reference to GB/T12704.2-2009 "Test Method for Moisture Permeability of Textile Fabrics Part 2: Moisture Absorption Method", and the test results As shown in Figure 3.
3、拉伸性能测试3. Tensile performance test
对实施例5与对比例1-2制品进行拉伸性能测试,测试过程中,在标准大气条件下将面料调湿24h,然后采用YG026D型电子式强力仪对面料进行拉伸性能测试,其中测试夹距设定为10mm,拉伸速度为50mm/min。每种面料均取5组平均值为最终测试结果,测试结果如表1所示。The products of Example 5 and Comparative Example 1-2 were tested for tensile properties. During the test, the fabric was conditioned for 24 hours under standard atmospheric conditions, and then the YG026D electronic strength tester was used to test the tensile properties of the fabric. The clamping distance is set to 10mm, and the stretching speed is 50mm/min. Each fabric takes 5 groups of average values as the final test results, and the test results are shown in Table 1.
以上所述,仅为本发明较佳的具体实施方式,但本发明的保护范围并不局限于此,任何熟悉本技术领域的技术人员在本发明揭露的技术范围内,根据本发明的技术方案及其发明构思加以等同替换或改变,都应涵盖在本发明的保护范围之内。The above is only a preferred embodiment of the present invention, but the scope of protection of the present invention is not limited thereto, any person familiar with the technical field within the technical scope disclosed in the present invention, according to the technical solution of the present invention Any equivalent replacement or change of the inventive concepts thereof shall fall within the protection scope of the present invention.
Claims (9)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202310110477.4A CN116100836B (en) | 2023-02-13 | 2023-02-13 | A process for preparing film-coated fabric by peeling method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202310110477.4A CN116100836B (en) | 2023-02-13 | 2023-02-13 | A process for preparing film-coated fabric by peeling method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN116100836A true CN116100836A (en) | 2023-05-12 |
| CN116100836B CN116100836B (en) | 2025-05-06 |
Family
ID=86265210
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202310110477.4A Active CN116100836B (en) | 2023-02-13 | 2023-02-13 | A process for preparing film-coated fabric by peeling method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN116100836B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117841397A (en) * | 2023-12-29 | 2024-04-09 | 东莞市特普优环保新材料有限公司 | A kind of preparation method of PET-TPU composite film |
Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5527616A (en) * | 1993-02-09 | 1996-06-18 | Toyo Seikan Kaisha Ltd. | Laminate for flexible packaging and a process for preparing the same |
| US20020048601A1 (en) * | 2000-07-07 | 2002-04-25 | Anestic Aps | Suppository and composition comprising at least one polyethylene glycol |
| US20070141113A1 (en) * | 2005-10-21 | 2007-06-21 | Bezwada Biomedical, Llc | Unsymmetrical aromatic ether diacids and absorbable polymers therefrom |
| CN101333771A (en) * | 2008-07-29 | 2008-12-31 | 瑞安市博业激光应用技术有限公司 | Method of preparing fibre composite sheet |
| CN101379240A (en) * | 2006-02-03 | 2009-03-04 | 巴斯夫欧洲公司 | Method for treating a substrate |
| CN102719187A (en) * | 2012-07-10 | 2012-10-10 | 湖北工程学院 | Single-component asphalt polyurethane waterproof coating and preparation method thereof |
| CN108049185A (en) * | 2018-02-13 | 2018-05-18 | 山东星宇手套有限公司 | A kind of oiliness PU- butyronitrile two-layer compound rubber gloves and its manufacturing method |
| CN109703076A (en) * | 2018-12-26 | 2019-05-03 | 浙江东进新材料有限公司 | A kind of preparation method of air pillow fabric |
| CN111516337A (en) * | 2020-05-21 | 2020-08-11 | 江苏金太阳纺织科技股份有限公司 | Multifunctional fabric and preparation method thereof |
| JP2021031637A (en) * | 2019-08-28 | 2021-03-01 | 第一工業製薬株式会社 | Two-pack curable adhesive |
| WO2021200500A1 (en) * | 2020-03-31 | 2021-10-07 | 大日本印刷株式会社 | Decorative sheet for recoating, and decorative sheet coloring method using same |
| KR102398019B1 (en) * | 2021-07-16 | 2022-05-16 | (주) 페트로산업 | Flexible urethane waterproofing material with high adhesion, dual complex waterproof sheet including the same and complex waterproofing method using the same |
-
2023
- 2023-02-13 CN CN202310110477.4A patent/CN116100836B/en active Active
Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5527616A (en) * | 1993-02-09 | 1996-06-18 | Toyo Seikan Kaisha Ltd. | Laminate for flexible packaging and a process for preparing the same |
| US20020048601A1 (en) * | 2000-07-07 | 2002-04-25 | Anestic Aps | Suppository and composition comprising at least one polyethylene glycol |
| US20070141113A1 (en) * | 2005-10-21 | 2007-06-21 | Bezwada Biomedical, Llc | Unsymmetrical aromatic ether diacids and absorbable polymers therefrom |
| CN101379240A (en) * | 2006-02-03 | 2009-03-04 | 巴斯夫欧洲公司 | Method for treating a substrate |
| CN101333771A (en) * | 2008-07-29 | 2008-12-31 | 瑞安市博业激光应用技术有限公司 | Method of preparing fibre composite sheet |
| CN102719187A (en) * | 2012-07-10 | 2012-10-10 | 湖北工程学院 | Single-component asphalt polyurethane waterproof coating and preparation method thereof |
| CN108049185A (en) * | 2018-02-13 | 2018-05-18 | 山东星宇手套有限公司 | A kind of oiliness PU- butyronitrile two-layer compound rubber gloves and its manufacturing method |
| CN109703076A (en) * | 2018-12-26 | 2019-05-03 | 浙江东进新材料有限公司 | A kind of preparation method of air pillow fabric |
| JP2021031637A (en) * | 2019-08-28 | 2021-03-01 | 第一工業製薬株式会社 | Two-pack curable adhesive |
| WO2021200500A1 (en) * | 2020-03-31 | 2021-10-07 | 大日本印刷株式会社 | Decorative sheet for recoating, and decorative sheet coloring method using same |
| CN111516337A (en) * | 2020-05-21 | 2020-08-11 | 江苏金太阳纺织科技股份有限公司 | Multifunctional fabric and preparation method thereof |
| KR102398019B1 (en) * | 2021-07-16 | 2022-05-16 | (주) 페트로산업 | Flexible urethane waterproofing material with high adhesion, dual complex waterproof sheet including the same and complex waterproofing method using the same |
Non-Patent Citations (2)
| Title |
|---|
| 朱传方: "有机精细化工选论", 31 December 1991, 华中师范大学出版社, pages: 210 - 212 * |
| 约瑟夫·海伦: "包装工程手册", 31 December 1986, 上海东方印刷厂, pages: 223 - 225 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117841397A (en) * | 2023-12-29 | 2024-04-09 | 东莞市特普优环保新材料有限公司 | A kind of preparation method of PET-TPU composite film |
Also Published As
| Publication number | Publication date |
|---|---|
| CN116100836B (en) | 2025-05-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR960002714B1 (en) | Elastic, laminated, waterproof, moisture-permeable fabric | |
| KR101029309B1 (en) | Polyurethane foam sheet and manufacturing method of laminate sheet using same | |
| KR101131583B1 (en) | Manufacturing method of fabric with hotmelt stacking structure using moisture curing adhesive | |
| CN102268820A (en) | Preparation method of anti-ultraviolet knitted coated fabric | |
| CN109043709B (en) | Moisture-permeable and breathable fabrics for outdoor clothing | |
| CN116100836A (en) | A kind of preparation technology of film-coated fabric adopting stripping method | |
| WO2017177483A1 (en) | Silicon silk wadding product and preparation method therefor | |
| CN107794777A (en) | A kind of preparation method of ventilative moisture absorption PU leather | |
| CN113439984B (en) | A kind of heating wear-resistant carpet and preparation method thereof | |
| CN1220586C (en) | Manufacturing method of continuous roll type elastic cloth laminated rubber material | |
| CN111572163B (en) | Preparation method of environment-friendly leather base cloth | |
| JP3196139B2 (en) | Manufacturing method of artificial leather | |
| CN112064169A (en) | Crease-resistant breathable suit fabric | |
| CN112501767B (en) | Integrated trousers and production process thereof | |
| CN113322683B (en) | Hard composite artificial leather capable of being embossed and preparation method thereof | |
| CN101029456B (en) | A kind of elastic nonwoven material base material and its manufacturing method | |
| TW558501B (en) | A manufacturing method for adhering an elastomeric cloth with rubber in a continuous roll | |
| CN113322684A (en) | Artificial leather capable of being directly embossed and preparation method thereof | |
| CN111041854A (en) | Clothing adhesive interlining and production method thereof | |
| CN114438799A (en) | Process for preparing waterborne polyurethane embossed synthetic leather bass by one-step method | |
| CN111575908A (en) | A kind of preparation method of environment-friendly clothing base cloth | |
| TWI808560B (en) | Method for Improving Thermal Performance of Chemical Fiber Filling Material and Chemical Fiber Filling Material | |
| KR20190030594A (en) | Artificial leather and its manufacturing method | |
| TWI284162B (en) | Fabric formed with multi-layered PU film and with bactericidal fungicidal properties and method for producing the same | |
| KR20190030595A (en) | The method of Artificial leather and the Artificial leather manufactred thereform |
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 |