ADHESION BETWEEN BASE MATERIAL AND RESILIENT MATERIAL LAYER
20250313716 ยท 2025-10-09
Inventors
Cpc classification
B05D2401/30
PERFORMING OPERATIONS; TRANSPORTING
B05D2451/00
PERFORMING OPERATIONS; TRANSPORTING
C08J2483/06
CHEMISTRY; METALLURGY
B29C2045/14868
PERFORMING OPERATIONS; TRANSPORTING
C08J7/043
CHEMISTRY; METALLURGY
C08J7/06
CHEMISTRY; METALLURGY
B29K2083/005
PERFORMING OPERATIONS; TRANSPORTING
B05D2401/33
PERFORMING OPERATIONS; TRANSPORTING
B05D7/02
PERFORMING OPERATIONS; TRANSPORTING
B05D2401/30
PERFORMING OPERATIONS; TRANSPORTING
B29C45/14311
PERFORMING OPERATIONS; TRANSPORTING
B05D2401/33
PERFORMING OPERATIONS; TRANSPORTING
B05D1/62
PERFORMING OPERATIONS; TRANSPORTING
B05D2451/00
PERFORMING OPERATIONS; TRANSPORTING
B05D2201/00
PERFORMING OPERATIONS; TRANSPORTING
C09D183/06
CHEMISTRY; METALLURGY
C08J7/042
CHEMISTRY; METALLURGY
C08J2383/06
CHEMISTRY; METALLURGY
B05D2350/60
PERFORMING OPERATIONS; TRANSPORTING
International classification
C09D183/06
CHEMISTRY; METALLURGY
Abstract
Embodiments relate to improving the adhesion between a base substrate and a resilient material layer. Plasma-enhanced chemical vapor deposition (PECVD) is performed to deposit a silicon compound layer on a base substrate. A resilient material layer is formed on the surface of the silicon compound layer. An object formed by the method may include the base substrate, a silicon compound layer on the base substrate, and the resilient material layer on a surface of the silicon compound layer. By having a silicon compound layer with a surface roughness and thickness, adhesion between the base substrate and the resilient material layer can be significantly improved.
Claims
1. A method, comprising: performing plasma-enhanced chemical vapor deposition (PECVD) to deposit a silicon compound layer on a base substrate of an article of manufacture; and forming a resilient material layer on a surface of the silicon compound layer.
2. The method of claim 1, wherein a thickness of the silicon compound layer is less than 1000 nm but more than 50 nm.
3. The method of claim 2, wherein a surface roughness of the silicon compound layer is between 50 nm and 600 nm in units of Ra.
4. The method of claim 1, wherein the silicon compound layer is a SiO.sub.xC.sub.yH.sub.z layer.
5. The method of claim 4, wherein the SiO.sub.xC.sub.yH.sub.z layer comprises 28-30 wt % of silicon, 60-65 wt % of oxygen, 0-1 wt % of carbon and 6-9 wt % of hydrogen.
6. The method of claim 1, wherein the base substrate comprises at least one of thermo-plastic polymer, thermo-setting polymer, silicone rubber, metals, and glass.
7. The method of claim 6, wherein the thermo-plastic polymer is at least one of polypropylene (PP), polyester sulfone (PES), polyphenyl sulfone (PPSU), polyamide (PA), tritan, polycarbonate (PC), and nylon.
8. The method of claim 1, wherein the resilient material layer is a material selected from a group consisting of liquid silicone rubber (LSR), heat cured rubber (HCR) silicone, and a combination thereof.
9. The method of claim 1, wherein the base substrate is PPSU, and the resilient material layer is silicone rubber.
10. The method of claim 1, wherein performing the PECVD comprises reacting a precursor hexamethyldisiloxane (HMDSO) with a reactivity gas oxygen (O.sub.2) under plasma.
11. The method of claim 1, wherein forming the resilient material layer comprises injecting a liquid form of resilient material into a mold placed with the base substrate that is deposited with the resilient material layer.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0027]
[0028]
[0029]
[0030]
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DETAILED DESCRIPTION OF EMBODIMENTS
[0034] Embodiments are described herein with reference to the accompanying drawings. Principles disclosed herein may, however, be embodied in many different forms and should not be construed as being limited to the embodiments set forth herein. In the description, details of well-known features and techniques may be omitted to avoid unnecessarily obscuring the features of the embodiments. In the drawings, like reference numerals in the drawings denote like elements. The shape, size and regions, and the like, of the drawing may be exaggerated for clarity.
[0035] Embodiments relate to articles of manufacture having a base substrate bonded to a resilient material layer and method for manufacturing such articles. A silicon compound layer with a predefine degree of surface roughness is deposited on the base substrate, and the resilient material layer is disposed on the silicon compound layer to enhance adhesion between the base substrate and the resilient material layer. The silicon compound layer of an average thickness less 1000 nm, and surface roughness of 50 nm to 600 nm in units of Ra may be deposited using a plasma-enhanced chemical vapor deposition (PECVD) method. Such articles of manufacture may be used as a high heat-resistance part (e.g., car parts and electronic components) or components that are transparent and chemically safe (e.g., baby bottles, goggles and bathroom products).
Method of Bonding Resilient Material Layer to Base Substrate
[0036]
[0037] First, a base substrate is prepared 102 for an object. The base substrate may be formed from at least one of thermo-plastic polymer, thermo-setting polymer, silicone rubber, metals such as stainless steel, aluminum, gold, silver, copper, iron, inorganic materials such as aluminum oxide, titanium oxide and glass. In particular, when the base substrate includes thermo-plastic polymer, the base substrate may be formed of at least one of polypropylene (PP), polyester sulfone (PES), polyphenyl sulfone (PPSU), polyamide (PA), tritan, polycarbonate (PC), and nylon. These thermo-plastic polymers have high heat-resistance and impact resistance. Thus, base substrates including thermo-plastic polymer may be advantageous in applications for medical devices, baby products, kitchen products, and the like that require repetitive sterilization with high temperature and moisture.
[0038] Then, a deposition method is performed 104 to deposit a silicon compound layer on the base substrate. The silicon compound layer may be a layer of SiO.sub.xC.sub.yH.sub.z which is predominantly silicon dioxide. In particular, the SiO.sub.xC.sub.yH.sub.z layer has an average thickness below 1000 nm and a surface roughness from 50 nm to 600 nm in units of Ra. Ra indicates the arithmetic average of the absolute values of the profile height deviations from the mean line of a surface of the layer. The range of surface roughness and the thickness of the SiO.sub.xC.sub.yH.sub.z effective to the adhesion of silicone to the base substrate was determined based on experiments described below in detail with reference to
[0039] The surface roughness of the silicon compound layer (e.g., SiO.sub.xC.sub.yH.sub.z layer) may be measured using an atomic force microscopy (AFM) as described, for example, in Ichiko Misuzu et al., Profile Surface Roughness Measurement Using Metrological Atomic Force Microscope and Uncertainty Evaluation, 11.sup.th Laser Metrology for Precision Measurement and Inspection in Industry 2014 (Sep. 2-5, 2014), which is incorporated by reference herein in its entirety. The surface roughness of the examples described below with reference to
[0040] The thickness of the silicon compound layer (e.g., SiO.sub.xC.sub.yH.sub.z layer) may be determined by analyzing the images of the scanning electron microscope (SEM). First, the surface of the substrate with or without the silicon compound is pre-treated with platinum coating to prevent any damage to the silicon compound layer. Then, the pre-treated surface is processed using focused ion beam (FIB). The cross section of the surface treated with the FIB is then captured using the SEM. Pixels of the captured image are then analyzed to determine thicknesses at multiple points in the image. An average value of the thicknesses at the multiple points is taken as the thickness of the silicon compound layer.
[0041] In one embodiment, the silicon compound layer having surface roughness is achieved by performing plasma-enhanced chemical deposition (PECVD) to deposit the silicon compound layer. In one instance, the PECVD process may be performed under relatively low-temperature and low-pressure conditions to obtain the desired surface roughness of the silicon compound layer on the base substrate. The pressure for the PECVD process may be from 110.sup.2 to 1 Torr, and the temperature of the base substrate during at least a part or entirety of the PECVD process may be from 50 C. to 200 C. A Si-containing precursor gas and a reactivity gas may be used in the PECVD process. The Si-containing precursor is hexamethyldisiloxane (HMDSO) and the reactivity gas is oxygen (O.sub.2).
[0042] The silicon compound layer formed by such PECVD process may be a SiO.sub.xC.sub.yH.sub.z layer. In one or more embodiments, the ratio of silicon, oxygen, carbon and hydrogen is in the range of 28-30 wt %, 60-65 wt %, 0-1 wt % and 6-9 wt %, respectively. The composition of the silicon compound layer may be determined, for example, using Rutherford Backscattering Spectrometry (RBS)-Elastic Recoil Detection (ERD) method, as well known in the art.
[0043] Returning to
[0044] In one embodiment, plasma treatment is performed on the surface of the base substrate before depositing the silicon compound layer. Performing plasma treatment reduces contamination or other particles on the base substrate, and results in improved adhesion between the base substrate and the deposited silicon compound layer.
[0045] Further, an ionization process may be performed on a surface of the silicon compound layer before forming the resilient material layer. Although the relative high surface roughness of the silicon compound layer improves physical and mechanical adhesion with the resilient material layer, performing an ionization process can further improve adhesion by increasing the surface energy of the surface of the silicon compound layer.
Composite Structure
[0046]
[0047] The base substrate 110 forms as a base material for the composite structure 100, and may be formed from materials and properties described in conjunction with step 102 of the method illustrated in
[0048] The silicon compound layer 130 is formed between the base substrate 110 and the resilient material layer 120, and is formed from materials and properties described in conjunction with step 104 of the method illustrated in
Experimental Results
[0049] In the following examples, adhesion of silicone to a container of a baby bottle made of PPSU using a SiO.sub.xC.sub.yH.sub.z layer was tested. In the examples, ionization procedure was performed to activate the surface of the PPSU and then a PECVD process involving HMDSO as the Si-containing precursor and O.sub.2 as the reactivity gas was used to form the SiO.sub.xC.sub.yH.sub.z layer. Then the PPSU substrate in the form of a baby bottle with the SiO.sub.xC.sub.yH.sub.z layer is placed in a mold of an injection molding machine, and then the mold is filled with LSR silicone. The PPSU substrate with the LSR silicone is then cooled to cure the silicone. After attaching the silicone to the PPSU via the SiO.sub.xC.sub.yH.sub.z layer, the baby bottle was immersed in a boiling water for a predetermined amount of time at pressure of 2 atm to determine if the adhesion between the PPSU and the silicone was maintained. No separate adhesive was placed between the SiOxCyHz layer and the silicone to attach the silicone to the PPSU substrate.
[0050]
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[0055] Experiments were also performed using materials other than PPSU as a base substrate. Specifically, lap-shear tests according to ASTM D1002 was performed using two specimen pieces where each of the specimen piece was deposited with a silicon compound layer (e.g., SiOxCyHz layer). LSR was then coated on a surface of one specimen piece deposited with the silicon compound layer. The other specimen piece was then overlapped with the surface deposited with the silicon compound layer facing the LSR coated surface. The specimen pieces were pressed so that the LSR reached a predetermined thickness (e.g., 1 mm), and then baked to cure the LSR into silicone. Then the two specimen pieces were pulled in opposite directions to test the failure shear force at the overlapping part of the specimen pieces.
[0056] Maximum shear force before the failure was measured for different materials (e.g., polycarbonate, glass, polypropylene, and stainless steel) as the specimen materials to test applicability of the silicon compound to these materials. The SiOxCyHz layers were deposited under similar PECVD conditions as examples of
TABLE-US-00001 TABLE 1 Maximum Maximum Shear Shear Force Force without with SiOxCyHz SiOxCyHz Sample layer layer Material (unit: Newton) (unit: Newton) Polycarbonate 91.7 N 1620.7 N Glass 209.3 N 410 N Polypropylene 136.7 N 967 N Stainless steel 4 N 2765.3 N (SUS304)
[0057] As shown in Table 1, there was a considerable increase in the maximum shear force when the SiOxCyHz layer was deposited on the sample materials. In the case of stainless steel, the increased shear force due to deposition of the SiOxCyHz layer was approximately 691 times. Although only PPSU, polycarbonate, glass, polypropylene and stainless steel were used as the materials of the basis substrate, similar results are expected in other materials.
[0058] Although the present disclosure has been described above with respect to several embodiments, various modifications can be made within the scope of the disclosure. Accordingly, the disclosure described above is intended to be illustrative, but not limiting.