CN111283946A - Material foaming method for in-mold foaming molding - Google Patents
Material foaming method for in-mold foaming molding Download PDFInfo
- Publication number
- CN111283946A CN111283946A CN202010103940.9A CN202010103940A CN111283946A CN 111283946 A CN111283946 A CN 111283946A CN 202010103940 A CN202010103940 A CN 202010103940A CN 111283946 A CN111283946 A CN 111283946A
- Authority
- CN
- China
- Prior art keywords
- mold
- plastic particles
- foaming
- foaming method
- supercritical fluid
- 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
Images
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
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/02—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete 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
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/3403—Foaming under special conditions, e.g. in sub-atmospheric pressure, in or on a liquid
-
- 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
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/3461—Making or treating expandable particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0005—Condition, form or state of moulded material or of the material to be shaped containing compounding ingredients
Landscapes
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
技术领域technical field
本发明涉及物理发泡方法,尤其是涉及一种在模内发泡成型的物料发泡方法。The invention relates to a physical foaming method, in particular to a material foaming method for in-mold foaming.
背景技术Background technique
在发泡成型过程或发泡聚合物材料中,通过物理发泡剂或化学发泡剂的添加与反应,形成了蜂窝状或多孔状结构。发泡成型的基本步骤是形成泡核、泡核生长或扩大以及泡核的稳定。In the foam molding process or foamed polymer material, a cellular or cellular structure is formed through the addition and reaction of physical or chemical blowing agents. The basic steps of foam molding are the formation of the cell nucleus, the growth or expansion of the cell nucleus, and the stabilization of the cell nucleus.
中国专利CN109517262A公开了一种全程保压的超临界流体发泡方法,该超临界流体发泡方法是在储料罐中制作渗透后塑胶粒,然后通过注塑机或者挤出机将产品注塑或挤出成型。然而,注塑机和挤出机的成本较高,上述设备的购买和检修将大大增加发泡工艺的整体成本。Chinese patent CN109517262A discloses a supercritical fluid foaming method with full pressure maintaining. The supercritical fluid foaming method is to make infiltrated plastic pellets in a storage tank, and then inject or extrude the product through an injection molding machine or an extruder. out of shape. However, the cost of injection molding machines and extruders is high, and the purchase and maintenance of the above equipment will greatly increase the overall cost of the foaming process.
中国专利CN110157086A公开了一种直接在模内形成发泡产品的物理发泡方法,该物理发泡方法将模具放入压力釜中,压力釜泄压时半成品在模内直接进行1:1发泡。然而,上述物理发泡方法的型胚还是需要通过射出机、挤出机或模压机制作,因此同样制约了发泡工艺成本的降低。此外,上述物理发泡方法在常温下进行1:1发泡,发泡效率低。Chinese patent CN110157086A discloses a physical foaming method for directly forming a foamed product in a mold. In the physical foaming method, the mold is put into an autoclave, and the semi-finished product is directly foamed in the mold at a ratio of 1:1 when the autoclave is depressurized. . However, the parison of the above-mentioned physical foaming method still needs to be produced by an injection machine, an extruder or a molding machine, which also restricts the reduction of the cost of the foaming process. In addition, the above-mentioned physical foaming method performs 1:1 foaming at normal temperature, and the foaming efficiency is low.
发明内容SUMMARY OF THE INVENTION
本发明技术方案是针对上述情况的,为了解决上述问题而提供一种在模内发泡成型的物料发泡方法,所述发泡方法包括以下步骤:The technical solution of the present invention is aimed at the above-mentioned situation, and in order to solve the above-mentioned problems, a material foaming method for foaming molding in a mold is provided, and the foaming method comprises the following steps:
步骤A、将塑胶粒导入模具内部;Step A. Introduce the plastic pellets into the mold;
步骤B、加压加热装置对模具施压并加热,若塑胶粒为聚烯烃材料,则进行步骤C,若塑胶粒为热塑性弹性体,则直接进行步骤D;Step B, the pressure heating device applies pressure to and heats the mold, if the plastic pellets are polyolefin materials, proceed to step C, and if the plastic pellets are thermoplastic elastomers, proceed directly to step D;
步骤C、在模具中用超临界流体进行高压浸渗,超临界流体浸渗塑胶粒,得到超临界流体浸渗的塑胶粒;Step C, carry out high pressure impregnation with supercritical fluid in the mold, and supercritical fluid impregnates plastic particles to obtain plastic particles infiltrated by supercritical fluid;
步骤D、泄压后,塑胶粒在模具内部1:1发泡成型,发泡成型后冷却模具,模具冷却后进行开模操作,取出发泡产品。Step D. After the pressure is released, the plastic pellets are foamed and molded in the mold at a ratio of 1:1, the mold is cooled after the foaming molding, and the mold is cooled to perform a mold opening operation, and the foamed product is taken out.
进一步,所述超临界流体包括二氧化碳、水、甲烷、乙烷、乙烯、丙烯、甲醇、乙醇、丙酮、氮气中的一种或多种。Further, the supercritical fluid includes one or more of carbon dioxide, water, methane, ethane, ethylene, propylene, methanol, ethanol, acetone, and nitrogen.
进一步,高压渗透的压强范围为5~60MPa,温度范围为比塑胶粒软化点高5℃至比塑胶粒熔点低3℃,渗透持续时间为0.5~8h。Further, the pressure range of the high pressure infiltration is 5-60MPa, the temperature range is 5°C higher than the softening point of the plastic pellets to 3°C lower than the melting point of the plastic pellets, and the infiltration duration is 0.5-8h.
进一步,在所述步骤D中,模具内部的温度范围为比塑胶粒熔点低25℃至比塑胶粒熔点高25℃,在泄压前,模具内部的压强范围为大于0.1MPa并且小于或等于40MPa,保压时间为0.2~5h;在泄压后,发泡持续时间为5~10min,模具冷却至40℃以下后进行开模操作。Further, in the step D, the temperature range inside the mold is 25°C lower than the melting point of the plastic pellets to 25°C higher than the melting point of the plastic pellets, and before the pressure is released, the pressure range inside the mold is greater than 0.1 MPa and less than or equal to 40 MPa , the pressure holding time is 0.2~5h; after the pressure is released, the foaming duration is 5~10min, and the mold is cooled to below 40 ℃ before the mold opening operation.
进一步,若塑胶粒为聚烯烃材料,在步骤A之前,还进行以下步骤:步骤E、使塑胶粒发生交联反应,得到交联的塑胶粒。Further, if the plastic particles are polyolefin materials, before step A, the following steps are further performed: step E, crosslinking the plastic particles to obtain cross-linked plastic particles.
进一步,在所述步骤E中,交联反应以化学交联方式或电子束辐照方式进行。Further, in the step E, the cross-linking reaction is carried out by chemical cross-linking or electron beam irradiation.
进一步,聚烯烃组合物包括聚烯烃材料,所述聚烯烃组合物材料还掺杂有交联剂、填充剂、助剂中的一种或多种。Further, the polyolefin composition includes a polyolefin material, and the polyolefin composition material is further doped with one or more of a crosslinking agent, a filler, and an auxiliary agent.
进一步,聚烯烃材料包括乙烯~乙酸乙烯酯共聚物(EVA)、聚烯烃弹性体(POE)、低密度聚乙烯(LDPE)、三元乙丙橡胶(EPDM)中的一种或多种。Further, the polyolefin material includes one or more of ethylene-vinyl acetate copolymer (EVA), polyolefin elastomer (POE), low density polyethylene (LDPE), and ethylene propylene diene rubber (EPDM).
进一步,热塑性弹性体包括热塑性聚氨酯(TPU)、热塑性聚酯弹性体(TPEE)、嵌段聚醚酰胺弹性体(Pebax)、聚乙烯(PE)、聚丙烯(PP)中的一种或多种。Further, the thermoplastic elastomer includes one or more of thermoplastic polyurethane (TPU), thermoplastic polyester elastomer (TPEE), block polyetheramide elastomer (Pebax), polyethylene (PE), and polypropylene (PP). .
采用上述技术方案后,本发明的效果是:上述发泡方法并不需要使用注塑机或者挤出机,同时也不必设置缓冲罐,大大降低了材料发泡的设备成本。此外,上述发泡方法采用了加热的方式,材料发泡时处于熔融或软化状态,发泡效率高,可使塑胶粒充分发泡成型。After the above technical solution is adopted, the effect of the present invention is that the above foaming method does not need to use an injection molding machine or an extruder, and also does not need to set a buffer tank, which greatly reduces the equipment cost of material foaming. In addition, the above foaming method adopts a heating method, and the material is in a molten or softened state when foaming, and the foaming efficiency is high, and the plastic particles can be fully foamed and formed.
附图说明Description of drawings
图1为本发明涉及的采用压力釜的发泡设备的示意图;Fig. 1 is the schematic diagram of the foaming equipment that adopts the autoclave involved in the present invention;
图2为本发明涉及的采用模压机的发泡设备的示意图。FIG. 2 is a schematic diagram of a foaming device using a molding press according to the present invention.
具体实施方式Detailed ways
下面通过实施例对本发明技术方案进一步的描述:The technical scheme of the present invention is further described below by the examples:
本发明提供一种在模内发泡成型的物料发泡方法,如图1和图2所示,该发泡方法使用的设备包括:储料罐1、传输管路2、加压加热装置3和模具4,传输管路2的一端与储料罐1内部连通,另一端与模具4内部连通,模具4位于加压加热装置3内部,传输管路2中具有阀门20。在本实施例中,加压加热装置3可以为压力釜或模压机(也称油压机)。当加压加热装置3为压力釜时,模具4具有通孔40;当加压加热装置3为模压机时,模压机具有高压管路30,高压管路30与模具4内部连通。The present invention provides a material foaming method for in-mold foaming. As shown in Figures 1 and 2, the equipment used in the foaming method includes: a
该发泡方法包括以下步骤:The foaming method includes the following steps:
步骤A、打开传输管路2的阀门20,将塑胶粒通过传输管路2从储料罐1导入模具4内部;Step A, open the
步骤B、加压加热装置3对模具4施压并加热,若塑胶粒为聚烯烃材料,则进行步骤C,若塑胶粒为热塑性弹性体,则直接进行步骤D;Step B, the
步骤C、在模具中用超临界流体进行高压浸渗,超临界流体通过高压管路30或模具的通孔40浸渗塑胶粒,得到超临界流体浸渗的塑胶粒;Step C, high-pressure impregnation is carried out with supercritical fluid in the mold, and the supercritical fluid infiltrates the plastic particles through the high-
步骤D、泄压后,塑胶粒在模具4内部1:1发泡成型,发泡成型后冷却模具4,模具4冷却后进行开模操作(即将模具的上模和下模分离),取出发泡产品。Step D, after pressure relief, the plastic pellets are foamed and molded in the
作为一种优选的方案,若塑胶粒为聚烯烃材料,在步骤A之前,还进行以下步骤:步骤E、使塑胶粒发生交联反应,得到交联的塑胶粒。As a preferred solution, if the plastic particles are polyolefin materials, before step A, the following steps are also performed: step E, crosslinking the plastic particles to obtain cross-linked plastic particles.
上述发泡方法并不需要使用注塑机或者挤出机,同时也不必设置缓冲罐,大大降低了材料发泡的设备成本。此外,上述发泡方法采用了加热的方式,材料发泡时处于熔融或软化状态,发泡效率高,可使塑胶粒充分发泡成型。The above-mentioned foaming method does not need to use an injection molding machine or an extruder, and also does not need to set a buffer tank, which greatly reduces the equipment cost of material foaming. In addition, the above foaming method adopts a heating method, and the material is in a molten or softened state when foaming, and the foaming efficiency is high, and the plastic particles can be fully foamed and formed.
-导入塑胶粒--Introduction of plastic pellets-
打开传输管路的阀门,将塑胶粒通过传输管路从储料罐导入模具内部。Open the valve of the transfer line, and introduce the plastic pellets from the storage tank into the mold through the transfer line.
可用于本发明的超临界流体发泡方法的塑胶粒包括聚烯烃组合物和热塑性弹性体。Plastic pellets useful in the supercritical fluid foaming method of the present invention include polyolefin compositions and thermoplastic elastomers.
聚烯烃组合物包括聚烯烃材料,并且聚烯烃材料掺杂有交联剂、填充剂、助剂中的一种或多种。交联剂可以与聚烃类树脂相作用,在聚合物分子链之间形成桥键,变为三维结构的不溶性物质;填充剂可以改善物料性能,能增容、增重,降低物料的成本的固体物质;助剂可以提高主材料的流动性。其中,以聚烯烃材料的重量份为100phr计,交联剂的量可以为0.15phr–1.1phr,优选0.25phr~1.0phr,填充剂的量可以为30phr以下,助剂的量可以为10phr以下。The polyolefin composition includes a polyolefin material, and the polyolefin material is doped with one or more of a crosslinking agent, a filler, and an adjuvant. The cross-linking agent can interact with the polyhydrocarbon resin to form bridge bonds between the polymer molecular chains and become an insoluble substance with a three-dimensional structure; the filler can improve the properties of the material, increase the capacity, increase the weight, and reduce the cost of the material. Solid substance; additives can improve the fluidity of the main material. Wherein, based on the weight part of the polyolefin material as 100 phr, the amount of the crosslinking agent can be 0.15phr-1.1phr, preferably 0.25phr~1.0phr, the amount of the filler can be less than 30phr, and the amount of the auxiliary agent can be less than 10phr .
聚烯烃材料可以包括乙烯~乙酸乙烯酯共聚物(EVA)、聚烯烃弹性体(POE)、低密度聚乙烯(LDPE)、三元乙丙橡胶(EPDM)中的一种或多种。例如,聚烯烃材料可以为EVA,其中乙酸乙烯酯的摩尔含量为5%~40%,或者可以为EVA/POE的混合物,掺混比例为100/0.1~0.1/100,或者可以为聚烯烃材料与橡胶材料的共混物,例如EVA/POE/EPDM(三元乙丙橡胶)共混物,掺混比例为100/0.1/0.1~0.1/100/20。The polyolefin material may include one or more of ethylene-vinyl acetate copolymer (EVA), polyolefin elastomer (POE), low density polyethylene (LDPE), and ethylene propylene diene rubber (EPDM). For example, the polyolefin material can be EVA, wherein the molar content of vinyl acetate is 5% to 40%, or it can be a mixture of EVA/POE with a blending ratio of 100/0.1 to 0.1/100, or it can be a polyolefin material Blends with rubber materials, such as EVA/POE/EPDM (ethylene-propylene-diene rubber) blends, with a blending ratio of 100/0.1/0.1 to 0.1/100/20.
交联剂可以包括过氧化物,例如包括过氧化二异丙苯(DCP)、双叔丁基过氧化二异丙基苯(BIPB)中的一种或多种。The cross-linking agent may include peroxides, including, for example, one or more of dicumyl peroxide (DCP), bis-tert-butyl dicumyl peroxide (BIPB).
填充剂可以包括碳酸钙、滑石粉、锌氧粉、钛白粉中的一种或多种。The filler may include one or more of calcium carbonate, talc, zinc oxide powder, and titanium dioxide.
助剂可以包括石蜡、硬脂酸中的一种或多种。The adjuvant may include one or more of paraffin wax and stearic acid.
热塑性弹性体可以包括热塑性聚氨酯(TPU)、热塑性聚酯弹性体(TPEE)、嵌段聚醚酰胺弹性体(Pebax)、聚乙烯(PE)、聚丙烯(PP)中的一种或多种。The thermoplastic elastomer may include one or more of thermoplastic polyurethane (TPU), thermoplastic polyester elastomer (TPEE), block polyetheramide elastomer (Pebax), polyethylene (PE), polypropylene (PP).
-施压和加热--Pressure and heat-
打开传输管路的阀门,塑胶粒通过传输管路从储料罐传输至模具内部,加压加热装置内部对模具施压并加热,直到模具内部的压强和温度恒定。Open the valve of the transfer line, the plastic pellets are transferred from the storage tank to the inside of the mold through the transfer line, and the inside of the pressure heating device pressurizes and heats the mold until the pressure and temperature inside the mold are constant.
作为一种优选的方案,加压加热装置为模压机。与压力釜相比,由于模压机热传导快,因此模压机需提供的加热温度相对较低,比较节能;此外,由于模压机导热性好,因此浸渗时间短,并且产品拿取方便,可大大提高生产效率。As a preferred solution, the pressure heating device is a molding machine. Compared with the autoclave, due to the fast heat conduction of the molding machine, the heating temperature that the molding machine needs to provide is relatively low, which is more energy-saving; in addition, due to the good thermal conductivity of the molding machine, the impregnation time is short, and the product is easy to take, which can greatly reduce the energy consumption. Increase productivity.
-浸渗塑胶粒--Infiltrated plastic pellets-
在模具中用超临界流体进行高压浸渗,超临界流体通过高压管路或模具的通孔浸渗塑胶粒,得到超临界流体浸渗的塑胶粒。其中,超临界流体可以包括二氧化碳、水、甲烷、乙烷、乙烯、丙烯、甲醇、乙醇、丙酮、氮气中的一种或多种。高压渗透的压强范围为5~60MPa,温度范围为比塑胶粒软化点高5℃至比塑胶粒熔点低3℃,渗透持续时间为0.5~8h。在所得的超临界流体浸渗的塑胶粒中,塑胶粒的超临界流体渗透量以重量计为1~10%。当高压浸渗的温度接近原料的熔点,原料将变成熔融状态,无法顺利浸渗超临界流体;当高压浸渗的温度接近原料的软化温度,原料呈现较硬的状态(即强度太高),超临界流体无法留在原料中。The supercritical fluid is used for high-pressure infiltration in the mold, and the supercritical fluid infiltrates the plastic particles through the high-pressure pipeline or through holes of the mold to obtain the supercritical fluid-impregnated plastic particles. The supercritical fluid may include one or more of carbon dioxide, water, methane, ethane, ethylene, propylene, methanol, ethanol, acetone, and nitrogen. The pressure range of high pressure infiltration is 5-60MPa, the temperature range is 5°C higher than the softening point of the plastic pellets to 3°C lower than the melting point of the plastic pellets, and the duration of infiltration is 0.5-8h. In the obtained supercritical fluid-impregnated plastic particles, the supercritical fluid permeation amount of the plastic particles is 1-10% by weight. When the temperature of high-pressure infiltration is close to the melting point of the raw material, the raw material will become a molten state, and the supercritical fluid cannot be infiltrated smoothly; when the temperature of high-pressure infiltration is close to the softening temperature of the raw material, the raw material will be in a relatively hard state (that is, the strength is too high). , the supercritical fluid cannot remain in the raw material.
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202010103940.9A CN111283946A (en) | 2020-02-20 | 2020-02-20 | Material foaming method for in-mold foaming molding |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202010103940.9A CN111283946A (en) | 2020-02-20 | 2020-02-20 | Material foaming method for in-mold foaming molding |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN111283946A true CN111283946A (en) | 2020-06-16 |
Family
ID=71028326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202010103940.9A Pending CN111283946A (en) | 2020-02-20 | 2020-02-20 | Material foaming method for in-mold foaming molding |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN111283946A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112895307A (en) * | 2021-03-11 | 2021-06-04 | 爱驰汽车有限公司 | Method and equipment for manufacturing spoiler |
| US20240391144A1 (en) * | 2023-05-26 | 2024-11-28 | Dongguan Hailex New Material Science And Technology Co., Ltd | Supercritical In-mold Foam Forming Device with Pretreatment Function and Foaming Method Thereof |
| US12458103B2 (en) | 2018-09-07 | 2025-11-04 | Skechers U.S.A., Inc. Ii | Foamed sole components and method for making a sole with foamed sole components |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040080070A1 (en) * | 2002-10-23 | 2004-04-29 | Industrial Technology Research Institute | Method of manufacturing polymeric foam using supercritical fludis |
| CN107099129A (en) * | 2017-05-05 | 2017-08-29 | 宁波格林美孚新材料科技有限公司 | A kind of moulding process of composite thermoplastic polyurethane elastomer expanded material |
| CN208118254U (en) * | 2018-03-07 | 2018-11-20 | 泉州师范学院 | A kind of macromolecule polymer material supercritical fluid foam device |
-
2020
- 2020-02-20 CN CN202010103940.9A patent/CN111283946A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040080070A1 (en) * | 2002-10-23 | 2004-04-29 | Industrial Technology Research Institute | Method of manufacturing polymeric foam using supercritical fludis |
| CN107099129A (en) * | 2017-05-05 | 2017-08-29 | 宁波格林美孚新材料科技有限公司 | A kind of moulding process of composite thermoplastic polyurethane elastomer expanded material |
| CN208118254U (en) * | 2018-03-07 | 2018-11-20 | 泉州师范学院 | A kind of macromolecule polymer material supercritical fluid foam device |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12458103B2 (en) | 2018-09-07 | 2025-11-04 | Skechers U.S.A., Inc. Ii | Foamed sole components and method for making a sole with foamed sole components |
| US12520904B2 (en) | 2018-09-07 | 2026-01-13 | Skechers U.S.A., Inc. Ii | Foamed sole components and method for making a sole with foamed sole components |
| CN112895307A (en) * | 2021-03-11 | 2021-06-04 | 爱驰汽车有限公司 | Method and equipment for manufacturing spoiler |
| US20240391144A1 (en) * | 2023-05-26 | 2024-11-28 | Dongguan Hailex New Material Science And Technology Co., Ltd | Supercritical In-mold Foam Forming Device with Pretreatment Function and Foaming Method Thereof |
| US12403636B2 (en) * | 2023-05-26 | 2025-09-02 | Dongguan Hailex New Material Science And Technology Co., Ltd | Supercritical in-mold foam forming device with pretreatment function and foaming method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN109135033A (en) | High molecular material physical foaming method and foaming product | |
| US6303666B1 (en) | Process for the production of expanded olefinic thermoplastic elastomer products | |
| CN110157086A (en) | A kind of physical foaming method forming foamed products directly in mould | |
| CN111283946A (en) | Material foaming method for in-mold foaming molding | |
| CN109438821A (en) | A kind of high thermal conductivity graphene modified EVA foamed material and preparation method thereof | |
| CN108299744A (en) | Rubber composition, and the application in foaming product and production method | |
| CN110041624B (en) | TPV material and preparation method and application method thereof | |
| KR101839434B1 (en) | Method of manufacturing midsole | |
| CN104031311A (en) | Formula and preparation process of rubber-synthesizing crosslinked polymer | |
| CN111019183B (en) | Micro-crosslinked elastomer foam material, and preparation method and application thereof | |
| CN105001505A (en) | Formula and preparation technology for ternary rubber synthetic cross-linked polymer | |
| CN105218850A (en) | The preparation method of a kind of high-elastic thermoplastic polyurethane foam's particle and formed body thereof | |
| CN109517262A (en) | A kind of supercritical fluid foaming method of whole process pressure maintaining | |
| CN106147036A (en) | The expanded material of a kind of recyclable recycling and manufacture method thereof | |
| CN102924802B (en) | POE (polyolefin elastomer)/EPDM (Ethylene-Propylene-Diene Monomer)/REC (Rectorite) composite foam material and preparation method thereof | |
| JP4465898B2 (en) | Manufacturing method of foam molded product | |
| CN107107409A (en) | The manufacture method of polypropylene-based expanded moldings and polypropylene-based expanded moldings | |
| CN109021379B (en) | Radiation crosslinking polypropylene foaming material, preparation method and application thereof | |
| CN104385479A (en) | Method for preparing TPU foamed beads by continuous extrusion foaming | |
| CN109485984A (en) | A kind of foaming method of Polymer Physics foamed material | |
| CN116655992A (en) | A kind of TPEE supercritical microcellular injection foaming material and its preparation method and application | |
| CN101835829B (en) | Polypropylene-based resin expanded particles and expanded molded articles | |
| CN108884261A (en) | The manufacturing method of polyethylene-based resin foamed particle and the manufacturing method of polyethylene-based resin foamed-mold product | |
| TWI858840B (en) | Method for making a foamed shoe body by using a foamed mixture mixed with phase change material | |
| CN107627527A (en) | The preparation method of copolymerized polymer foam with hydrophilic units |
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: 20200616 |