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TW200806468A - Resin coated metal plate having excellent electromagnetic wave shielding property - Google Patents

Resin coated metal plate having excellent electromagnetic wave shielding property Download PDF

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Publication number
TW200806468A
TW200806468A TW096117257A TW96117257A TW200806468A TW 200806468 A TW200806468 A TW 200806468A TW 096117257 A TW096117257 A TW 096117257A TW 96117257 A TW96117257 A TW 96117257A TW 200806468 A TW200806468 A TW 200806468A
Authority
TW
Taiwan
Prior art keywords
resin film
resin
steel sheet
ppit
conductivity
Prior art date
Application number
TW096117257A
Other languages
Chinese (zh)
Other versions
TWI347886B (en
Inventor
Takeshi Watase
Yasuo Hirano
Tetsuya Igarashi
Original Assignee
Kobe Steel Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kobe Steel Ltd filed Critical Kobe Steel Ltd
Publication of TW200806468A publication Critical patent/TW200806468A/en
Application granted granted Critical
Publication of TWI347886B publication Critical patent/TWI347886B/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C26/00Coating not provided for in groups C23C2/00 - C23C24/00
    • C23C26/02Coating not provided for in groups C23C2/00 - C23C24/00 applying molten material to the substrate
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/04Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/06Zinc or cadmium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/32Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer
    • C23C28/322Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer only coatings of metal elements only
    • C23C28/3225Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer only coatings of metal elements only with at least one zinc-based layer
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K9/00Screening of apparatus or components against electric or magnetic fields

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Inorganic Chemistry (AREA)
  • Laminated Bodies (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)

Abstract

To provide a new resin-coated metal plate which can exert excellent performance of shielding electromagnetic waves by improving the conductivity of the resin-coated metal plate and preferably exert the good characteristics even under light-contact conditions. The plate is surface-coated with a resin film, and the resin film meets the condition (1) PPIt ≥ 70 (wherein, PPIt is the number of peak-trough counts, with the half of the peak count level (2H) equal to the thickness t (μm) of the resin film, for PPI (Peaks Per Inch) defined by SAE J911-1986).

Description

200806468 ’ (1) 九、發明說明 【發明所屬之技術領域】 本發明涉及電磁波遮蔽性(導電性)優異的樹脂塗敷 金屬板。本發明的樹脂塗敷金屬板例如在壓力10〜 1 2g/mm2左右的輕接觸下(輕壓力下)也能夠發揮良好的 導電性,所以例如適用於電子、電氣、光學設備等(以下 有時以電子設備爲代表)的框體等的構成原材。 【先前技術】 隨著電子設備的高性能化、小型化的進步,爲了不使 電子設備內部產生的電磁波浅露到外部,或不使從電子設 備外部侵入的電磁波侵入到內部,而要求電子設備等的框 體具有優異的電磁波遮蔽性。 爲了提高電子設備框體的電磁波遮蔽性,推薦使用例 如電鑛錄鋼板寺導電性優異的材料。由此,雖然能夠衰減 Φ 例如從鋼板彼此的間隙漏出的電磁波,但是存在不能夠有 效地防止例如來自空氣孔和佈線孔的電磁波的洩露的問題 〇 . 另一方面,在日本特開2005-21 572號公報中,公開 了一種至少在鋼板的背面(構成框體的內部側面)以規定 的厚度被覆有含有磁性粉末等電磁波吸收添加劑的磁性塗 膜的樹脂塗敷金屬板。由此認爲,因爲框體內部產生的電 磁波由上述金屬板多重反射等而被吸收,所以最終能夠發 揮衰減從空氣孔等向框體外部洩漏的電磁波的效果。 5- (2) (2)200806468 另外,在日本特開2004- 1 5608 1號公報、日本特開 2005-23 853 5號公報以及日本特開2004-277876號公報中 ,公開了如下技術:特別是通過控制樹脂塗敷金屬板的樹 脂皮膜的厚度和表面粗糙度、金屬板的粗糙度,提高導電 性,由此實現電磁波遮蔽性的提高。 其中,在日本特開2004- 1 5608 1號公報中,公開了一 種通過適當地控制皮膜形成後的中心線平均粗糙度(Ra ) 和皮膜平均厚度的關係而提高了電磁波遮蔽性的表面處理 鋼板。其中,根據如下的認識而確定了 Ra和皮膜平均厚 度的關係式,即,皮膜的導電性由皮膜厚度相對地變薄的 凸部分的膜厚決定,平均皮膜厚度相同程度時,增大Ra 則皮膜的導電性提高。 在日本特開2005_23 8 5 3 5號公報中,公開了一種作爲 鍍覆原材板使用適當地控制了表面粗糙度Ra和PPI並利 用放電加工輥進行了調質軋製的鋼板,從而提高了導電性 的表面處理鋼板。其中,與所述日本特開20 04-156081號 公報同樣,記載有皮膜的導電性由凸部分的皮膜膜厚決定 。此外,記載有在Ra相同程度時,高PPI的鍍覆原材板 與低PPI的鍍覆原材板相比,在粗糙度曲線的平均線方向 上,超過割線水準(cut level )的峰値數變多,所以在高 PPI的表面處理鋼板的凸部分,更多存在局部膜厚薄的部 分,從而改善導電性。 在日本特開2004-277876號公報中,公開有一種通過 適當地控制表面處理後的鋼板的表面粗糙度(算術平均粗 -6 - (3) (3)200806468 糙度Ra )而確保良好的接地性的表面處理鋅系鍍覆鋼板 。其中’還記載有若適當地控制濾波中心線波形(Wca ) 則能夠提高接地性的情況。 隨著電子設備的高性能化,對提高電磁波遮蔽性的要 求曰益高漲。此外,以削減成本爲目的,強烈希望提供能 夠省略、簡化墊片和銅彈簧等的電磁波遮罩應對部件,在 輕接觸下也能發揮優異的導電性,電磁波遮蔽性提高的樹 脂塗敷金屬板。 【發明內容】 本發明鑒於上述事情而進行,其目的在於,提供一種 新型的樹脂塗敷金屬板,其通過提高樹脂塗敷金屬板的導 電性而能夠發揮優異的電磁波遮蔽性,最佳爲在輕接觸下 也能夠發揮良好的特性。 可解決上述課題的本發明的樹脂塗敷金屬板是在金屬 板的表面被覆有樹脂皮膜的樹脂塗敷金屬板,所述樹脂皮 膜滿足下述(1 )的必要條件, PPIt^ 70 PPIt 表示在 SAE J911-19 86 中記載的 PPI ( Peaks Per Inch)中,將峰値計數水準(2H)的1/2作爲樹脂皮膜的 厚度ί(μιη)時的峰-谷計數的數目。 在最佳的實施方式中,所述樹脂皮膜的玻璃轉變點( 200806468 (4)(1) In the present invention, the present invention relates to a resin-coated metal sheet excellent in electromagnetic shielding properties (electrical conductivity). The resin-coated metal sheet of the present invention can exhibit excellent electrical conductivity even under light contact (at a light pressure) of, for example, a pressure of about 10 to 12 g/mm 2 , and is therefore suitable for use in, for example, electronic, electrical, and optical equipment (hereinafter sometimes). A frame made of a frame or the like represented by an electronic device. [Prior Art] With the advancement of the high-performance and miniaturization of electronic devices, electronic devices are required to prevent electromagnetic waves generated inside the electronic devices from being exposed to the outside or electromagnetic waves intruding from the outside of the electronic devices. The frame has excellent electromagnetic shielding. In order to improve the electromagnetic shielding of the electronic device housing, it is recommended to use a material having excellent conductivity, such as the electric mining record steel plate. Therefore, although it is possible to attenuate Φ, for example, electromagnetic waves leaking from the gap between the steel sheets, there is a problem that leakage of electromagnetic waves such as from the air holes and the wiring holes cannot be effectively prevented. On the other hand, in Japanese Patent Laid-Open No. 2005-21 Japanese Laid-Open Patent Publication No. 572 discloses a resin-coated metal sheet in which a magnetic coating film containing an electromagnetic wave absorbing additive such as magnetic powder is coated on a back surface of a steel sheet (the inner side surface of the casing) at a predetermined thickness. Therefore, it is considered that the electromagnetic wave generated inside the casing is absorbed by the above-described metal plate multiple reflection or the like, so that the effect of attenuating electromagnetic waves leaking from the air hole or the like to the outside of the casing can be finally achieved. In the following, the following technique is disclosed in Japanese Laid-Open Patent Publication No. 2004-158810, the Japanese Patent Publication No. 2005-23 853, and the Japanese Patent Publication No. 2004-277876. By controlling the thickness of the resin film of the resin-coated metal sheet, the surface roughness, and the roughness of the metal plate, the conductivity is improved, thereby improving the electromagnetic wave shielding property. In Japanese Laid-Open Patent Publication No. 2004-158018, a surface-treated steel sheet having improved electromagnetic wave shielding properties by appropriately controlling the relationship between the center line average roughness (Ra) and the average thickness of the film after formation of the film is disclosed. . Here, the relationship between the Ra and the average thickness of the film is determined according to the following knowledge, that is, the conductivity of the film is determined by the film thickness of the convex portion in which the film thickness is relatively thin, and when the average film thickness is the same, the Ra is increased. The conductivity of the film is improved. In Japanese Laid-Open Patent Publication No. 2005_23 8 5 3 5, a steel sheet which is subjected to temper rolling by appropriately controlling the surface roughness Ra and PPI and using an electric discharge machining roll as a plated raw material sheet is disclosed. Conductive surface treated steel sheet. In the same manner as in the above-mentioned Japanese Patent Publication No. 20 04-156081, the conductivity of the film is determined by the film thickness of the convex portion. Further, it is described that when the Ra is the same level, the plated raw material plate having a high PPI exceeds the cut line peak in the average line direction of the roughness curve as compared with the plated raw material plate having a low PPI. Since the number is increased, the convex portion of the surface of the steel sheet is treated with a high PPI, and there is more a portion having a thin portion of the local film thickness, thereby improving conductivity. In Japanese Laid-Open Patent Publication No. 2004-277876, it is disclosed that a good grounding is ensured by appropriately controlling the surface roughness (arithmetic mean coarseness - 6 - (3) (3) 200,806,468 roughness Ra) of the surface-treated steel sheet. Sexual surface treatment of zinc-based plated steel. The case where the grounding property can be improved by appropriately controlling the filter center line waveform (Wca) is also described. With the high performance of electronic devices, the demand for improving the shielding of electromagnetic waves is greatly increased. In addition, in order to reduce the cost, it is strongly desired to provide a resin-coated metal sheet which can eliminate the simplification of the electromagnetic wave shielding member such as a gasket and a copper spring, and which exhibits excellent electrical conductivity and electromagnetic wave shielding property under light contact. In view of the above, an object of the present invention is to provide a novel resin-coated metal sheet which can exhibit excellent electromagnetic shielding properties by improving the conductivity of a resin-coated metal sheet. Good characteristics can also be achieved under light contact. The resin-coated metal sheet of the present invention which solves the above-described problems is a resin-coated metal sheet coated with a resin film on the surface of a metal sheet, and the resin film satisfies the requirements of the following (1), and PPIt^ 70 PPIt indicates In PPI (Peaks Per Inch) described in SAE J911-19, the number of peak-to-valley counts when 1/2 of the peak value (2H) is taken as the thickness ί(μιη) of the resin film. In a preferred embodiment, the glass transition point of the resin film (200806468 (4)

Tg)在60°C以下。 在最佳的實施方式中,所述金屬板是鋅和鐵族元 合金鍍覆鋼板。 在最佳的實施方式中,所述金屬板是合金化熔融 鋼板。 本發明的樹脂塗敷金屬板因爲如上述構成,所以 還能夠提高輕接觸下的導電性,實現良好的電磁波遮 【實施方式】 本發明者爲了提供例如在壓力10〜12g/mm2左右 接觸下(輕壓力下)也能夠發揮良好的導電性,電磁 蔽性佳的樹脂塗敷金屬板,而從樹脂皮膜和金屬板( 板)雙方的側面進行了硏究。 本發明者通過多次基礎實驗,其結果明確表明, • 脂皮膜相關,樹脂皮膜的變形能越大(即,樹脂皮膜 ),導電性越提高。而且,發現爲了促進樹脂皮膜的 ,(1 )控制樹脂皮膜的形狀最有效,爲此設定所謂 (每1英寸的超過皮膜厚度t的峰谷數,在後面詳述 獨自的指標,並且,(2 )根據樹脂皮膜的形狀,適 控制樹脂皮膜的玻璃轉變點(Tg )也有效,由此完成 發明。 另一方面,發現與金屬板(原材板)相關,與歷 用的電鍍鋅鋼板相比,最佳爲使用鋅和鐵族元素(F e 素的 鍍鋅 例如 蔽性 的輕 波遮 原材 與樹 越軟 變形 PPIt )的 當地 了本 來通 、Co (5) 200806468 、N i )合金化的鍍覆鋼板(以下,有時稱爲“鋅-鐵元素的 合金鍍覆鋼板”),其中,考慮到削減成本,更佳爲使用 鋅和鐵通過熔融鍍覆法而合金化的合金化熔融鍍鋅鋼板。 爲了得到電磁波遮蔽性佳的樹脂塗敷金屬板,如上所 述,可以實施樹脂皮膜的變形能促進方法,以進一步提高 電磁波遮蔽性爲目的,最佳爲進一步適當地控制金屬板的 種類。 # 在本說明書中,所謂“電磁波遮蔽性佳,,是指無論電子 設備的內部外部都能夠防止電磁波的洩漏的特性(作用效 果)。 另一方面,在本說明書中,所謂“電磁波吸收性”是指 爲了提高所謂電磁波遮蔽性的特性而對金屬板(原材板) 等要求的特性。電磁波吸收性優異的金屬板,例如能夠減 少來自空氣孔和佈線孔的洩漏電磁波,所以電磁波遮蔽性 佳。 • 以下,對樹脂皮膜的變形能促進方法,以及金屬板的 最佳種類進行詳細說明。 (樹脂皮膜的變形能促進方法) (1 )樹脂皮膜的形狀控制(樹脂皮膜的PPIt 2 70 ) 在本發明中,爲了使“樹脂皮膜的變形能越大(樹脂 皮膜的硬度越小)越提高導電性”的技術思想具體化,而 確定以下詳述的所謂PPIt的參數。爲了促進樹脂皮膜的 變形能,適當地控制樹脂皮膜自身的硬度的方法最有效, -9 - (6) 200806468 但是測定被覆在金屬板上的樹脂皮膜的硬度極爲困難,因 此,在本發明中,並非控制樹脂皮膜的硬度,而是控制樹 脂皮膜的形狀(在此,是PPIt)。 樹脂塗敷金屬板一般在樹脂皮膜的厚度大時金屬板的 凹凸不產生影響。但是,樹脂皮膜薄時金屬板的凹凸對樹 脂皮膜厚的影響程度大,在金屬板凸部有樹脂皮膜變薄的 傾向,樹脂皮膜的厚度根據位置而變動。 0 PPIt是將美國的SAE J91 1-JUN86 ( 1 98 6 )中規格化 的PPI ( Peaks Per Inch)的峰値計數水準變換爲樹脂皮膜 的厚度t ( μιη )而成的,作爲表示樹脂皮膜的變形能的指 標由本發明者獨自確定。 以下,參照圖1說明SAE規格的ΡΡΙ和本發明所規定 的PPIt的不同點。 首先,所謂SAE規格的PPI是指,從抽出曲線f(x)的 平均線分別向正(+)負(-)的兩方向設定一定的基準水 ® 準Η (因此,正負間的基準水準的寬度=2H ),將超過負 的基準水準(-H,谷部分)並超過正的基準水準(+H,峰 部分)時記爲“1計數,’時,每1英寸(25.4mm)的計數數 .目(峰-谷計數的數目)。在此,正負間的基準水準的寬 度(2H )被稱爲峰値計數水準,是固定値,通常定爲 2H = 50pinch 〇 相對於此,本發明所規定的PPIt不使正負間的基準 水準的寬度(2H )如上述爲固定値,而是基於樹脂皮膜的 厚度t ( μπι )來設定。即,在圖1中,通過設H = t,從而 -10- (7) (7)200806468 對於PPIt,測定超過樹脂皮膜的厚度t的峰·谷計數的數 目。這是考慮到在樹脂皮膜的凹凸部分中’能夠發揮導電 性的部分(導通點)是樹脂皮膜的厚度薄的峰部分(凸部 分),樹脂皮膜的厚度厚的凹部分不會成爲導通點’從而 設定的。還有,對於t而言,通過後述的方法求得樹脂層 的平均厚度,從而使用其値。在圖1中,橫軸是測定距離 ,抽出曲線是抽出覆蓋金屬板的樹脂皮膜表面的凹凸。根 據本發明,以樹脂皮膜的厚度薄的峰部分的數目變多的方 式測定根據樹脂皮膜的厚度t的峰-谷計數的數目,因此與 使用PPI的現有方法相比,能夠高精度地評價和導電性的 關係。 即,例如,如所述的日本特開2005-23 853 5號公報, 在使用SAE規格的PPI的方法中,即使有樹脂皮膜的膜厚 厚的凸部分,超過規定的峰値計數水準(2H )的也全部被 計數。但是,導電性由樹脂皮膜的厚度薄的凸部分(峰部 分)的皮膜的厚度決定,樹脂皮膜的膜厚厚的峰部分不會 成爲導通點,因此在完全不考慮樹脂皮膜的厚度僅測定峰 谷計數的數目的上述方法中,不能夠正確地把握和導電性 的關係。 相對於此,在本發明中,如上述,將測定根據樹脂皮 膜的厚度的峰-谷計數的數目的“PPIt”用作導電性的指標, 所以能夠正確地把握成爲導通點的部分。在導通點部分( 峰部分)很薄地被覆的樹脂皮膜與金屬板相比非常柔軟, 因此即使在輕接觸下該樹脂皮膜也會變形,從而能夠得到 -11 - (8) (8)200806468 優異的導電性。 爲了能夠有效地發揮基於PpIt的控制的樹脂皮膜的 變形能促進作用,確保優異的導電性’而將PPIt設爲70 以上。PPIt低於70時,如後述的實施例所示,不能得到 優異的導電性。PPIt越大越好’由此,能夠增加可成爲導 通點的峰部分的數目。另外,如果增加峰部分的數目,則 向峰部分施加的局部的壓力上升,其結果,樹脂皮膜整體 容易變形,因此能夠促進輕接觸下的變形。PMt例如最佳 爲100以上,更佳爲120以上,最優爲150以上。還有, PPIt的上限沒有特別限定,但是PPIT變得過大時,產生 樹脂皮膜的不均,難以使附著量均勻,另外,外觀變得不 穩定,考慮到這些,最佳大致設在500以下,更佳爲400 以下,最優爲3 〇 0以下。 PPIt的控制方法,在後面進行詳述。 作爲構成樹脂皮膜的基材樹脂,例如能夠列舉出聚酯 系樹脂、丙烯系樹脂、聚氨酯系樹脂、聚烯烴系樹脂、氟 系樹脂、矽系樹脂、以及這些樹脂的混合物或改性的樹脂 等。還有,本發明的樹脂塗敷金屬板主要用於電子設備的 框體,若考慮到更要求具有彎曲加工性、皮膜密接性、耐 蝕性等特性,則最佳爲聚酯樹脂或改性聚酯樹脂(例如, 不飽和聚酯樹脂中添加環氧樹脂而改性的樹脂)。 樹脂皮膜在所述的基材樹脂之外,還可以含有架橋劑 。架橋劑的種類只要是樹脂塗敷金屬板中一般使用的就沒 有特別限定’例如,能夠列舉出三聚氰胺系化合物、異氰 -12- 200806468 (9) 酸鹽系化合物等。這些可以單獨使用也可以並用。架橋劑 的含量(合計量)最佳爲大致在〇·5〜30質量%的範圍內 (2 )樹脂皮膜的玻璃轉變點(Tg )的控制 根據本發明,通過如上述(1 )那樣控制樹脂皮膜的 形狀(PP It )能夠促進樹脂皮膜的變形,其結果能夠提高 # 導電性,但是以進一步提高特性爲目的,最佳爲將樹脂皮 膜的玻璃轉變點(Tg )控制在60°c以下。樹脂皮膜的Tg 的控制,特別是樹脂皮膜的PPIt在大約70〜250的範圍 內時能夠有效發揮,由此,能夠進一步提高樹脂皮膜的變 形能促進作用(參照後述的實施例)。相對於此,樹脂皮 膜的PPIt例如在大約3 50以上非常大時,不論樹脂皮膜 的Tg,由於能夠最大限度地發揮樹脂皮膜的PPIt控制的 變形能促進作用,所以即使樹脂皮膜的Tg超過60°C,也 • 能夠得到期望的導電性。 在此,所謂樹脂皮膜的Tg是指樹脂皮膜整體的Tg。 如後面詳細說明,在樹脂皮膜中,除了構成塗膜的基材樹 脂和架橋劑之外,還可含有防鏽劑和消光劑、顏料等公知 的添加劑,由於Tg不受防鏽劑等的無機化合物的影響, 因此樹脂皮膜的Tg實質上由使用的基材樹脂和架橋劑的 種類和添加量決定。 因此,爲了控制樹脂皮膜的Tg,根據作爲主成分的 基材樹脂和架橋劑的種類,適當調節配合量即可。樹脂皮 -13- 200806468 (10) 膜的Tg很大程度上由基材樹脂的Tg支配。另外,基材樹 脂的含量越比架橋劑多,樹脂皮膜的Tg越有下降的傾向 ,相反,基材樹脂的含量越比架橋劑少,就越有上升的傾 向。對於樹脂皮膜的Tg控制,考慮到上述方面,首先, 選擇具有與作爲目標的Tg接近的Tg的基材樹脂,將該基 材樹脂和架橋劑配合,而將樹脂皮膜的Tg控制在規定範 圍內即可。 # 以下,作爲本發明使用的樹脂皮膜的代表例,如後述 實施例所示,列舉作爲基材樹脂使用聚酯系樹脂,作爲架 橋劑使用三聚氰胺系樹脂的情況,對Tg的控制方法進行 具體的說明。 作爲聚酯系樹脂,代表性的可以列舉例如東洋紡績( 株)製的 Vylon系列。具体地說,能够列舉出:Vylon 103 ( Tg :大約 4 7°C ) 、Vylon 2 00 ( Tg :大約 67〇C )、Tg) is below 60 °C. In a preferred embodiment, the metal sheet is a zinc and iron group alloy plated steel sheet. In a preferred embodiment, the metal sheet is an alloyed molten steel sheet. Since the resin-coated metal sheet of the present invention has the above-described configuration, it is possible to improve the electrical conductivity under light contact and achieve good electromagnetic wave shielding. [Inventors] The present inventors have provided contact with, for example, a pressure of about 10 to 12 g/mm 2 ( Under light pressure, it is also possible to exhibit good electrical conductivity, and the resin having good electromagnetic shielding properties is coated with a metal plate, and the side surfaces of both the resin film and the metal plate (plate) are inspected. The inventors have conducted a plurality of basic experiments, and the results clearly show that • the fat film is related, and the deformation energy of the resin film is larger (that is, the resin film), and the conductivity is improved. In addition, it is found that in order to promote the resin film, (1) the shape of the resin film is controlled to be the most effective, and the number of peaks and valleys exceeding the film thickness t per one inch is set, and the individual index is described in detail later, and (2) According to the shape of the resin film, it is also effective to control the glass transition point (Tg) of the resin film, thereby completing the invention. On the other hand, it has been found that it is related to the metal plate (raw material plate) and compared with the conventional electrogalvanized steel sheet. It is best to use zinc and iron elements (galvanized by Fe, such as the opaque light-shielding material and the softer deformation of the tree PPIt). The local alloy, Co (5) 200806468, N i ) alloying A plated steel sheet (hereinafter sometimes referred to as "zinc-iron alloy-plated steel sheet"), in which alloying melting by alloying by zinc and iron is more preferable in consideration of cost reduction. Galvanized steel. In order to obtain a resin-coated metal sheet having excellent electromagnetic shielding properties, as described above, it is possible to carry out a method for promoting the deformation of the resin film to further improve electromagnetic shielding properties, and it is preferable to further appropriately control the type of the metal plate. In the present specification, "the electromagnetic wave shielding property is good, and it is a characteristic (action effect) that can prevent leakage of electromagnetic waves regardless of the inside and outside of the electronic device. On the other hand, in the present specification, "electromagnetic wave absorption" It is a characteristic required for a metal plate (raw material plate), etc. in order to improve the characteristic of the electromagnetic shielding property. The metal plate excellent in electromagnetic wave absorption can reduce the leakage electromagnetic wave from the air hole and the wiring hole, for example, and it is excellent in electromagnetic shielding. In the following, the method for promoting the deformation of the resin film and the optimum type of the metal plate will be described in detail. (The method for promoting the deformation of the resin film) (1) The shape control of the resin film (PPIt 2 70 of the resin film) In the present invention, in order to embody the technical idea that "the deformation energy of the resin film is larger (the hardness of the resin film is smaller) and the conductivity is improved", the parameter of PPIt described below is determined. In order to promote the deformation of the resin film. The method of properly controlling the hardness of the resin film itself is most effective, -9 - (6) 200806468 but It is extremely difficult to measure the hardness of the resin film coated on the metal plate. Therefore, in the present invention, the hardness of the resin film is not controlled, but the shape of the resin film (here, PPIt) is controlled. The resin-coated metal plate is generally When the thickness of the resin film is large, the unevenness of the metal plate is not affected. However, when the resin film is thin, the unevenness of the metal plate has a large influence on the thickness of the resin film, and the resin film is thinned at the convex portion of the metal plate, and the thickness of the resin film tends to be small. It varies depending on the position. 0 PPIt is obtained by converting the peak value of PPI (Peaks Per Inch) normalized in SAE J91 1-JUN86 (1 98 6 ) in the United States to the thickness t ( μιη ) of the resin film. The index indicating the deformation energy of the resin film is determined by the inventors. The difference between the SAE standard and the PPIt specified in the present invention will be described below with reference to Fig. 1. First, the PPI of the SAE standard refers to the extraction curve f. The average line of (x) sets a certain reference water® quasi-Η in both directions of positive (+) negative (-) (so the width of the reference level between positive and negative = 2H) will exceed the negative When the quasi-level (-H, valley portion) exceeds the positive reference level (+H, peak portion), it is recorded as "1 count, ', every 1 inch (25.4 mm) count. Mesh (peak-to-valley count) number). Here, the width (2H) of the reference level between positive and negative is called the peak 値 count level, and is fixed 値, which is usually set to 2H = 50pinch. In contrast, the PPIt specified in the present invention does not make the reference level between positive and negative. The width (2H) is set as the fixed crucible as described above, but based on the thickness t (μπι) of the resin film. That is, in Fig. 1, by setting H = t, -10-(7)(7)200806468 for PPIt, the number of peak-to-valley counts exceeding the thickness t of the resin film was measured. In this case, it is considered that a portion (conduction point) capable of exhibiting conductivity in the uneven portion of the resin film is a peak portion (convex portion) having a thin thickness of the resin film, and a concave portion having a thick thickness of the resin film does not become a conduction point' Thus set. Further, in t, the average thickness of the resin layer was determined by the method described later, and the crucible was used. In Fig. 1, the horizontal axis represents the measurement distance, and the extraction curve is the unevenness of the surface of the resin film covering the metal plate. According to the present invention, the number of peak-to-valley counts according to the thickness t of the resin film is measured so that the number of peak portions having a small thickness of the resin film is increased. Therefore, compared with the conventional method using PPI, it is possible to evaluate the sum with high precision. The relationship of electrical conductivity. In other words, in the method of using the PPI of the SAE standard, the convex portion having a thick film thickness of the resin film exceeds a predetermined peak value level (2H, for example, in the above-mentioned Japanese Patent Publication No. 2005-238535). ) are all counted. However, the conductivity is determined by the thickness of the film of the convex portion (peak portion) having a small thickness of the resin film, and the peak portion of the thickness of the resin film does not become a conduction point. Therefore, only the peak is measured regardless of the thickness of the resin film. In the above method of the number of valley counts, the relationship with the conductivity cannot be accurately grasped. On the other hand, in the present invention, as described above, "PPIt" which measures the number of peak-to-valley counts according to the thickness of the resin film is used as an index of conductivity, so that the portion to be a conduction point can be accurately grasped. The resin film which is thinly covered in the conduction point portion (peak portion) is very soft compared to the metal plate, so that the resin film is deformed even under light contact, and excellent -11 - (8) (8) 200806468 can be obtained. Electrical conductivity. In order to effectively exhibit the deformation energy-promoting action of the resin film controlled by PpIt, the excellent conductivity is ensured, and PPIt is made 70 or more. When PPIt is less than 70, excellent conductivity cannot be obtained as shown in the examples described later. The larger the PPIt, the better. Thus, the number of peak portions that can become the conduction point can be increased. Further, when the number of peak portions is increased, the local pressure applied to the peak portion is increased, and as a result, the entire resin film is easily deformed, so that deformation under light contact can be promoted. The PMt is, for example, preferably 100 or more, more preferably 120 or more, and most preferably 150 or more. In addition, the upper limit of the PPIt is not particularly limited. However, when the PPIT is too large, unevenness of the resin film occurs, and it is difficult to make the adhesion amount uniform, and the appearance is unstable. In view of these, it is preferably set to be approximately 500 or less. More preferably 400 or less, and most preferably 3 〇 0 or less. The control method of PPIt will be described in detail later. Examples of the base resin constituting the resin film include a polyester resin, a propylene resin, a urethane resin, a polyolefin resin, a fluorine resin, a fluorene resin, and a mixture of these resins or a modified resin. . Further, the resin-coated metal sheet of the present invention is mainly used for a frame of an electronic device, and it is preferably a polyester resin or a modified poly group in consideration of characteristics such as bending workability, film adhesion, and corrosion resistance. An ester resin (for example, a resin modified by adding an epoxy resin to an unsaturated polyester resin). The resin film may further contain a bridging agent in addition to the base resin. The type of the bridging agent is not particularly limited as long as it is generally used in the resin-coated metal sheet. For example, a melamine-based compound, an isocyanide-12-200806468 (9) acid-based compound, and the like can be given. These can be used alone or in combination. The content (total amount) of the bridging agent is preferably in the range of approximately 5 to 30% by mass. (2) Control of the glass transition point (Tg) of the resin film According to the present invention, the resin is controlled as in the above (1) The shape of the film (PP It ) can promote the deformation of the resin film, and as a result, the conductivity can be improved. However, for the purpose of further improving the properties, it is preferable to control the glass transition point (Tg) of the resin film to 60° C. or less. In the control of the Tg of the resin film, particularly when the PPIt of the resin film is in the range of about 70 to 250, the deformation promoting effect of the resin film can be further improved (see the examples described later). On the other hand, when the PPIt of the resin film is extremely large, for example, at about 3 50 or more, the deformation of the resin film can be maximized regardless of the Tg of the resin film, so that the Tg of the resin film exceeds 60°. C, also • The desired conductivity can be obtained. Here, the Tg of the resin film means the Tg of the entire resin film. As described in detail later, in the resin film, in addition to the base resin and the bridging agent constituting the coating film, a known additive such as a rust preventive, a matting agent, or a pigment may be contained, and the Tg is not affected by the inorganic agent such as a rust preventive agent. The influence of the compound is such that the Tg of the resin film is substantially determined by the type and amount of the base resin and the bridging agent to be used. Therefore, in order to control the Tg of the resin film, the blending amount may be appropriately adjusted depending on the type of the base resin and the bridging agent as the main component. Resin skin -13- 200806468 (10) The Tg of the film is largely governed by the Tg of the base resin. Further, the content of the base resin is more than that of the bridging agent, and the Tg of the resin film tends to decrease. On the contrary, the content of the base resin is less than that of the bridging agent, and the tendency to rise is increased. In consideration of the above aspects, in order to control the Tg of the resin film, first, a base resin having a Tg close to the target Tg is selected, and the base resin and the bridging agent are blended to control the Tg of the resin film within a predetermined range. Just fine. In the following, as a representative example of the resin film used in the present invention, a polyester resin is used as the base resin, and a melamine resin is used as the bridging agent, and the method for controlling the Tg is specifically described. Description. Typical examples of the polyester-based resin include the Vylon series manufactured by Toyobo Co., Ltd. Specifically, it can be exemplified by Vylon 103 (Tg: about 47 ° C) and Vylon 2 00 (Tg: about 67 〇 C).

Vylon 220 ( Tg :大約 53°C ) 、Vylon 240 ( Tg :大約 60 # °C ) 、Vylon 245 ( Tg :大約 60°C ) 、Vylon 270 ( Tg :大 約 67°C ) 、Vylon 280 ( Tg :大約 6 8 °C ) 、Vylon 290 ( Tg :大約 7 2°C ) 、Vylon 2 96 ( Tg :大約 71 °C ) 、Vylon 300 ( Tg :大約 7°C ) 、Vylon 500 ( Tg :大約 4 °C )、Vylon 220 (Tg: about 53 ° C), Vylon 240 (Tg: about 60 # °C), Vylon 245 (Tg: about 60 ° C), Vylon 270 (Tg: about 67 ° C), Vylon 280 (Tg: About 6 8 ° C), Vylon 290 (Tg: about 7 2 ° C), Vylon 2 96 (Tg: about 71 ° C), Vylon 300 (Tg: about 7 ° C), Vylon 500 (Tg: about 4 °) C),

Vylon 5 30 ( Tg ··大約 5°C ) 、Vylon 5 5 0 ( Tg :大約-15 °C )、Vylon 5 60 ( Tg :大約 7°C) 、Vylon 600 ( Tg :大約 4 7〇C ) 、Vylon 630 ( Tg :大約 7 °C ) 、Vylon 650 ( Tg : 大約 l〇°C ) 、Vylon GK110 ( Tg :大約 5 0 °C ) > VylonVylon 5 30 (Tg ·· about 5°C), Vylon 5 5 0 (Tg: about -15 °C), Vylon 5 60 (Tg: about 7°C), Vylon 600 (Tg: about 4 7〇C) , Vylon 630 (Tg: about 7 °C), Vylon 650 (Tg: about l〇 °C), Vylon GK110 (Tg: about 50 °C) > Vylon

GK130(Tg:大約 15°C ) 、Vylon GK140 (Tg:大約 20°C •14- (11) 200806468 )、Vylon GK1 50 ( Tg :大約 2 01: ) 、Vylon GK1 8 0 ( Tg :大約 0°C ) 、Vylon GK190 ( Tg :大約 1 1 °C ) 、VylonGK130 (Tg: about 15 ° C), Vylon GK140 (Tg: about 20 ° C • 14- (11) 200806468 ), Vylon GK1 50 ( Tg : about 2 01 : ) , Vylon GK1 8 0 ( Tg : about 0 ° C), Vylon GK190 (Tg: approx. 1 1 °C), Vylon

GK250 ( Tg :大約 60〇C ) 、Vylon GK3 3 0 ( Tg :大約 16°C )、Vylon GK590 ( Tg :大約 15 °C ) 、Vylon GK640 ( Tg :大約 79°C ) 、Vylon GK680 ( Tg :大約 1 0 °C ) 、Vylon GK780 ( Tg :大約 36°C ) 、Vylon GK 8 1 0 ( T g :大約 4 61: )、Vylon GK8 80 ( Tg :大約 84°C ) 、Vylon GK890 ( TgGK250 (Tg: about 60〇C), Vylon GK3 3 0 (Tg: about 16°C), Vylon GK590 (Tg: about 15 °C), Vylon GK640 (Tg: about 79°C), Vylon GK680 (Tg: About 10 °C), Vylon GK780 (Tg: about 36 °C), Vylon GK 8 1 0 (T g: about 4 61: ), Vylon GK8 80 (Tg: about 84 ° C), Vylon GK890 (Tg

:大約 17 °C) 、VylonBX1001(Tg:大約-18°C)等。該 些Tg是產品目錄中記載的温度。 作爲三聚氰胺系樹脂例如可以列舉住友化學(株)製 SUMIMAL M-40ST 等。 在後述的實施例中,爲了將樹脂皮膜的Tg控制爲規 定値(1 0°C、25°c、40°C、60°c、75°C ),而從所述聚酯 系樹脂中選擇具有與規定値Tg接近的Tg的聚酯系樹脂, 並和三聚氰胺系樹脂進行了配合。具體地說’如下述表1 所示。 -15- (12) 200806468 【表1】 樹脂皮 膜的 Tg(°C) 基材樹脂A 架橋劑B 配合比率 (質量比率) 種類 Tg(°C) 10 東洋紡績(株)製的Vylon 650 10 住友化學㈱) 製的 SUMIMALM- 40ST A : B=100 : 20 25 東洋紡績(株)製的Vylon GK140 20 40 東洋紡績(株)製的Vylon GK780 36 60 東洋紡績(株)製的Vylon 245 60 75 東洋紡績(株)製的Vylon 290 72: approximately 17 ° C), Vylon BX1001 (Tg: approximately -18 ° C), etc. These Tg are the temperatures stated in the catalog. Examples of the melamine-based resin include SUMIMAL M-40ST manufactured by Sumitomo Chemical Co., Ltd., and the like. In the examples described later, in order to control the Tg of the resin film to a predetermined enthalpy (10 ° C, 25 ° C, 40 ° C, 60 ° C, 75 ° C), the polyester resin is selected from the polyester resin. A polyester resin having a Tg close to the predetermined 値Tg is blended with a melamine resin. Specifically, 'as shown in Table 1 below. -15- (12) 200806468 [Table 1] Tg (°C) of the resin film Base resin A bridging agent B Mixing ratio (mass ratio) Type Tg (°C) 10 Vylon 650 10 manufactured by Toyobo Co., Ltd. Sumitomo SIIMALM- 40ST A manufactured by Chemical Co., Ltd.: B=100: 20 25 Vylon GK140, manufactured by Toyobo Co., Ltd. 20 40 Vylon GK780, manufactured by Toyobo Co., Ltd. 60 60 Vylon 245 60 75, manufactured by Toyobo Co., Ltd. Vylon 290 72, manufactured by Kasei Co., Ltd.

樹脂皮膜的Tg可使用DSC (示差掃描熱量計)通過 常規方法進行測定。 如果從促進樹脂皮膜的變形能提高導電性的觀點出發 ,樹脂皮膜的Tg越低越好,例如,最佳爲在5 5 °C以下, 更佳在50°C以下,最優在45°C以下。 還有,Tg的下限從導電性的觀點出發沒有特別限定 ,Tg低時電子設備的框體所要求的電磁波遮蔽性以外的 特性(例如,耐瑕疵性和耐鈾性等)降低,因此大致最佳 爲l〇°C以上,更佳爲15°C以上,最優爲20°C以上。 (金屬板的種類) 爲了得到電磁波遮蔽性佳的樹脂塗敷金屬板,如前所 述,控制樹脂皮膜的形狀,或最佳爲進一步控制樹脂皮膜 -16- (13) (13)200806468 的Tg即可,但是通過如下這樣控制金屬板的種類也能夠 提高電磁波吸收性,其結果,能夠進一步提高電磁波遮蔽 性。另外,如下所示,通過使用硬度大(金屬板的變形能 小)的金屬板能夠促進樹脂皮膜的變形,還有提高導電性 的傾向,因此,其結果認爲能夠得到良好的電磁波遮蔽性 〇 作爲本發明使用的金屬板,與現有的廣泛應用的電鍍 鋅鋼板相比,最佳爲鋅和鐵族元素(Fe、Co、Ni )合金化 的鍍覆鋼板(鋅-鐵族元素的合金鍍覆鋼板)。 作爲鋅-鐵族元素的合金鍍覆鋼板,可列舉Zn和Fe 的合金鍍覆鋼板、Zn和Ni的合金鍍覆鋼板、Zn和Co的 合金鍍覆鋼板。如果從確保電磁波吸收性的觀點出發,Fe 、Ni、Co含量均最佳爲大致控制在5〜20質量%的範圍內 。還有,鍍覆的方法沒有特別限定,通過熔融鍍覆法、電 鍍法中任一方法均可得到。還有,熔融鍍覆法、電鍍法的 詳細的鍍覆條件沒有特別限定,可以採用合金化所通常使 用的方法。 若考慮電磁波吸收性,則鍍覆的附著量越少越好,例 如,最佳爲50g/m2以下,更佳爲40g/m2以下,更佳爲 35g/m2以下,最優爲3〇mg/m2以下。鍍覆附著量的下限從 電磁波吸收性的觀點出發沒有特別限定,但如果考慮到耐 飩性等,則例如最佳爲5 g / m 2,最優爲1 〇 g / m 2。 此外,若考慮成本等,則最佳爲使用可以廉價且簡便 製造的合金化熔融鍍鋅鋼板(通過熔融鍍覆法使Zn和Fe -17- (14) 200806468 合金化的鋼板)。 如上所述,本發明中作爲金屬板推薦使用合金 鋼板,此外,也可以使用鍍覆附著量控制在大約 以下的純鋅鍍覆鋼板或冷軋鋼板。這是因爲,這些 具有優異的電磁波吸收作用,能夠實現希望的導電 照後述的實施例)。另外,如上所述,通過使用不 金化的鋼板,能夠回避合金化鋼板使用中的問題( 彎曲加工時產生的裂紋等的破裂和剝離等)。 例如,如果使用不進行鍍覆的冷軋鋼板,則可 加工嚴格的用途。特別是如果僅從提高電磁波吸收 點出發,可知與合金化鋼板相比冷軋鋼板具有優異 波吸收性(參照後述實施例)。但是,冷軋鋼板的 差,如果考慮用於電子設備的框體,則其綜合特性 ,因此與冷軋鋼板相比最佳爲使用合金化鍍覆鋼板 另一方面,如果使用純鋅鍍覆鋼板,則能夠用 劇烈並且要求耐蝕性的用途。爲了有效地發揮耐触 覆附著量最佳爲大約3g/m2以上,更佳爲6g/m2以 有,若考慮到電磁波吸收性,則鍍覆附著量的上限 15g/m2,更佳爲 12g/m2,最優爲 10g/m2。 以上,對表徵本發明的樹脂皮膜的必要條件和 的種類進行了說明。 樹脂皮膜的厚度(平均厚度)最佳爲大致在 3 . Ομιη的範圍內。如果厚度在上述範圍之外,則電 的框體所要求的電磁波遮蔽性以外的特性(彎曲加 化鍍覆 1 5 g/m2 鋼板也 性(參 進行合 例如, 以用於 性的觀 的電磁 耐蝕性 評價低 〇 於加工 性,鍍 上。還 最佳爲 金屬板 0· 1〜 子設備 工性、 -18 - (15) 200806468 根據所使 等也有所 0 · 2 μιη 以 〇 算的方法 微鏡觀察 設備的框 這是因爲 。當然, 還可以含 等)° 添加劑) 性粉末, 粉末等。 系鐵氧體 金屬粉末 3 5 %以上 合金)等 皮膜密接性、耐蝕性等)下降。樹脂皮膜的厚度 用的基材樹脂和金屬板的種類、金屬板的粗糙度 不同,難以進行唯一地確定,但是更佳爲大致在 上2.0μπι以下,更佳爲在0.3μιη以上1.5μιη以下 樹脂皮膜的厚度可根據皮膜重量通過比重換 進行測定,或者也可以對樹脂皮膜的截面進行顯 (SEM照片觀察)而進行測定。 φ 樹脂皮膜形成在金屬板的至少背面(從電子 體觀察,非外側(外部氣體側)的內側)即可。 電磁波遮蔽性在電子設備構件的內側會產生問題 也可以形成在金屬板的表背側。 樹脂皮膜除所述的基材樹脂和架橋劑之外, 有公知的添加劑(例如,防鏽劑、消光劑、顏料 樹脂皮膜還可以含有磁性粉末(電磁波吸收 ,由此,能夠進一步提高電磁波遮蔽性。作爲磁 • 可列舉出代表性的軟磁性鐵氧體粉末和磁性金屬 作爲軟磁性鐵氧體粉末例如可列舉軟磁性Ni-Zn 粉末和Mn-Zii系鐵氧體粉末等。另外,作爲磁性 例如可列舉坡莫合金(Ni-Fe系合金中Ni含量在 的合金)和鐵砂銘合金(Sendust) ( Si-Al-Fe系 。它們可以單獨使用或並用。 磁性粉末的含量(合計量)最佳爲大致在20〜60質 量%的範圍內。含量低於20質量%時,不能有效地發揮上 述作用,另一方面,超過60質量%時,電子設備構件用樹 200806468 (16) 脂塗敷鋼板所要求的特性(彎曲加工性、皮膜密接性以及 耐蝕性)有劣化的傾向。磁性粉末的含量例如根據使用的 磁性粉末的種類和形狀、樹脂皮膜的厚度等也有所不同, 難以唯一地進行確定,但是更佳爲大致在25質量%以上 5〇質量%以下,最優爲30質量%以上45質量%以下。 上述磁性粉末最佳爲平均粒徑在1 5 μπι以下,以盡可 能除去大粒徑(例如,20μπι以上)的粉末爲佳。由此, Φ 磁性塗膜的形成變得容易,能夠抑制加工性、耐鈾性的降 低。 在此,上述磁性粉末的平均粒徑是指,通過一般的粒 度分佈計測定分級後的磁性粉末粒子的粒度分佈,根據其 測定結果算出的來自小粒徑側的積算値5 0%的粒度(D50 )。該粒度分布可通過對磁性粉末粒子照射光而產生的衍 射和散射的强度圖案進行測定,作爲該粒度分布計例如例 示有日機裝社製的 Microtrac 9220FRA 或 Microtrac HRA # 等。 還有,滿足上述最佳平均粒徑的磁性粉末也可以使用 市場商品。例如,可列舉Ni-Zn系軟磁性鐵氧體[户田工 業(株)製 BSN-125、平均粒徑 13·0μιη]、坡莫合金( 78%Ni)[日本 Atomize加工(株)製 SFR-PC78、平均粒 徑5·7μπι]、坡莫合金(45%Ni )[日本Atomize加工(株) 製 SFR-PB45、平均粒徑 5.8μπι]、鐵矽鋁合金[日本 Atomize 加工(株)製 SFR_FeSiAl( 84.5-10-5.5)、平均 粒徑6.9μιη]等。 -20- (17) 200806468 爲了進一步提高樹脂塗敷金屬板的電磁波遮蔽性,也 可以在樹脂皮膜中添加導電性賦予劑。作爲導電性賦予劑 例如可列舉Ag、Zn、Fe、Ni、Cu等的金屬單體或FeP等 的金屬化合物。其中,特別佳的是Ni。還有,其形狀沒有 特別限定,但是爲了得到更優異的導電性,例如推薦使用 鱗片狀的結構。 樹脂皮膜中所含的導電性賦予劑的含量最佳大致爲20 # 〜40質量%。嚴格來說,可以根據使用的磁性粉末的種類 等適當地調整其添加量。例如,作爲磁性粉末使用軟磁性 鐵氧體粉末時,以盡可能多(例如25質量%以上)添加導 電性賦予劑爲佳。另外,作爲磁性粉末使用磁性金屬粉末 時,以盡可能少(例如3 0質量%以下)添加導電性賦予劑 爲佳。 另一方面,如果考慮導電性賦予劑與上述磁性粉末同 樣有可能對加工性等帶來不良影響,則磁性塗膜中所含的 ® 導電性賦予劑和磁性粉末的合計含量最佳大致在60質量% 以下的範圍內。 金屬板以提高耐触性、提高和樹脂皮膜的密接性等爲 目的,可以實施鉻酸鹽處理或磷酸鹽處理等表面處理(襯 底處理)。或者,考慮到環境污染等也可以使用未進行鉻 酸鹽處理的金屬板,實施了任一種襯底處理的金屬板都包 含於本發明的範圍內。 進行上述襯底處理時,考慮到導電性等,襯底處理的 附著量最佳大致爲3 0 0mg/m2以下,最佳爲2〇〇mg/m2以下 -21 - (18) (18)200806468 ,更佳爲150mg/m2以下,最優爲i〇〇mg/m2以下。 另外,非鉻酸鹽處理的方法沒有特別限定,進行通常 使用的公知的襯底處理即可。具體地說,推薦單獨或並用 磷酸鹽系、二氧化矽系 '鈦系、銷系等的襯底處理。 還有,一般進行非絡酸鹽處理時,耐蝕性降低,所以 以提高耐蝕性爲目的,在塗膜中或襯底處理時,可以使用 防鏽劑。作爲上述防鏽劑可列舉二氧化矽系化合物、磷酸 鹽系化合物、亞磷酸鹽系化合物、聚磷酸鹽系化合物、硫 系有機化合物、苯並三唑、丹寧酸、鉬酸鹽系化合物、鎢 酸鹽系化合物、釩系化合物、矽烷耦合劑等,能夠單獨或 並用它們。尤其最佳的是二氧化矽系化合物(例如鈣離子 交換二氧化矽等)和磷酸鹽系化合物、亞磷酸鹽系化合物 、聚磷酸鹽系化合物(例如三聚磷酸鋁等)的並用,推薦 在以質量比率計0.5: 9.5〜9.5: 0.5 (更佳爲1: 9〜9: 1 )的範圍內並用二氧化矽系化合物(磷酸鹽系化合物、亞 磷酸鹽系化合物、或聚磷酸鹽系化合物)。通過控制在該 範圍,能夠確保希望的耐蝕性和加工性雙方。 通過上述防鏽劑的使用,能夠確保非鉻酸鹽處理金屬 板的耐蝕性,但是相反由於防鏽劑的添加也導致加工性降 低。爲此,作爲塗膜的形成成分,特別推薦將環氧改性聚 酯系樹脂及/或酚衍生物導入骨架的聚酯系樹脂、及架橋 劑(最佳爲異氰酸鹽系樹脂及/或三聚氰胺系樹脂,更佳 兩者並用)組合使用。 其中,將環氧改性聚酯系樹脂及/或酚衍生物導入骨 -22- (19) (19)200806468 架的聚酯系樹脂(例如,將雙酚A導入骨架的聚酯系樹脂 等)與聚酯系樹脂相比,耐蝕性以及塗膜密接性優異。 另一方面’異氰酸鹽系架橋劑有提高加工性的作用( 是指提高加工後的外觀的作用,在後述的實施例中,以密 接性彎曲試驗中的裂紋數進行評價),由此,即使添加了 防鏽劑也能夠確保優異的加工性。 另外’三聚氰胺系架橋劑具有優異的耐蝕性。因此, 在本發明中,通過與所述的防鏽劑並用,能夠得到非常良 好的耐蝕性。 可以單獨使用這些異氰酸鹽系架橋劑及三聚氰胺系架 橋劑’但並用時能夠進一步提高非鉻酸鹽處理金屬板的加 工性和耐飩性。具體地說,相對於異氰酸鹽系樹脂1 〇〇質 量部,推薦以5〜80質量部的比率含有三聚氰胺系樹脂。 在三聚氰胺系樹脂低於5質量部時,不能得到希望的耐蝕 性,另一方面,三聚氰胺系樹脂超過80質量部時,不能 良好地發揮異氰酸鹽系樹脂的添加帶來的效果,不能得到 希望的加工性提高作用。更佳爲相對於1 00質量部的異氰 酸鹽系樹脂,在10質量部以上40質量部以下,更佳爲15 質量部以上3 0質量部以下。 本發明的樹脂塗敷金屬板,在金屬板(還包括上述進 行了襯底處理的部分)的表面,被覆了含有上述各種添加 劑的樹脂皮膜,但根據需要,以賦予耐瑕疵性和耐指紋性 等爲目的,也可以在樹脂皮膜的表面形成實施了其他樹脂 皮膜的二層的皮膜結構。 -23- (20) (20)200806468 接著,說明製造本發明的樹脂塗膜金屬板的方法。 本發明的樹脂塗敷金屬板,在基材樹脂和架橋劑之外 ,將根據需要而含有各種添加劑的塗料用公知的塗敷方法 塗布在金屬板的表面,進行燒黏而獲得。 在此,爲了將樹脂皮膜的PPIt控制在本發明的範圍 (70以上),最佳如下控制原材板(金屬板)的表面粗糙 度(JIS B 060 1 ( 1 994 )所規定的算術平均粗糙度Ra,以 下簡稱爲Ra)和樹脂皮膜的形成方法(塗料的黏度和固 態量濃度、塗料的燒黏條件等)。 首先,作爲原材板的金屬板的Ra最佳大致控制在0.8 〜1·6μπι的範圍內。例如,作爲原材板使用鋼板時,若將 調質軋輥的Ra大致控制在0.6〜3.2 μιη的範圍內,將軋製 時的軋製率大致控制在0.3〜2.5 %的範圍內,則能夠將金 屬板的Ra控制在上述範圍內。在調質軋製工序中,用於 調質軋製的輥的表面形狀以高轉印率轉印到鍍覆原材板上 ,但是,如本發明,將非常薄的樹脂皮膜施加於鍍覆原材 板上時,鍍覆樹脂皮膜的表面形狀被認爲基本反映原材板 的表面形狀,因此,要適當地控制作爲原材板的金屬板的 Ra。軋製率基於調質軋輥的Ra確定於適當的範圍即可。 調質軋輥的Ra例如可使用噴九鈍化加工、放電鈍化 加工、鐳射鈍化加工等公知的加工方法進行適當的調節。 例如,使用噴九鈍化加工時,使用調整了粒度的磨削材調 整調質軋輥的表面粗糙度即可。 塗料的黏度,最佳以福特杯(ford cup ) No ·4計在10 -24- (21) (21)200806468 秒〜4 0秒的範圍內,更佳在1 5〜3 0秒的範圍內。在此, 意味著時間越短黏度越低。 例如,所使用的塗料的黏度以福特杯No.4計低於10 秒時,塗料容易侵入金屬板的谷部(凹部),因此,樹脂 皮膜的PPIt有減少的傾向。另一方面,所使用的塗料的 黏度以福特杯No.4計超過40秒時,金屬板的表面粗糙度 (凹凸的形狀)會對樹脂皮膜的形成帶來很大的影響,輕 接觸下的導電性有可能變得不穩定。 塗料的固態量濃度根據所使用的塗料的黏度和塗敷條 件等適當調整到易於塗布即可,但大致最佳在2〜20質量 %的範圍內,更佳在4〜16質量%的範圍內,最優在6〜12 質量%的範圍內。 燒黏條件例如考慮到根據塗料稀釋使用的溶劑的種類 等流入金屬板的谷部(凹部)的程度變化等,最佳大致在 1分鐘以內結束燒黏。 塗敷方法沒有特別限定,例如可以列舉清潔表面,根 據必要在實施有塗敷前處理(例如,磷酸鹽處理、鉻酸鹽 處理等)的長尺金屬帶表面上使用輥塗法、噴射法、幕塗 流動(curtain fl〇w )塗法等塗布塗料,使其通過熱風乾燥 爐進行乾燥的方法等。綜合考慮到被膜厚度的均勻性和處 理成本、塗敷效率等在實用上最佳的是輥塗法。 作爲適用本發明的樹脂塗敷金屬板的電子設備構件, 例如是在封閉空間內置發熱體的電子設備構件,該電子設 備構件還包括其外壁的全部或一部分由上述電子設備構件 -25- 200806468 (22)The Tg of the resin film can be measured by a conventional method using DSC (differential scanning calorimeter). The Tg of the resin film is preferably as low as possible from the viewpoint of improving the conductivity of the resin film, and for example, it is preferably at most 5 5 ° C, more preferably at most 50 ° C, and most preferably at 45 ° C. the following. In addition, the lower limit of Tg is not particularly limited from the viewpoint of conductivity, and when Tg is low, characteristics other than electromagnetic shielding properties required for the casing of the electronic device (for example, tamper resistance and uranium resistance) are lowered. Preferably, it is l〇°C or more, more preferably 15°C or more, and most preferably 20°C or more. (Type of metal plate) In order to obtain a resin-coated metal plate having excellent electromagnetic shielding properties, the shape of the resin film is controlled as described above, or it is optimal to further control the Tg of the resin film-16-(13)(13)200806468 However, the electromagnetic wave absorptivity can be improved by controlling the type of the metal plate as follows, and as a result, the electromagnetic wave shielding property can be further improved. In addition, as described below, by using a metal plate having a large hardness (the deformation energy of the metal plate is small), the deformation of the resin film can be promoted, and the conductivity tends to be improved. Therefore, it is considered that good electromagnetic wave shielding properties can be obtained. As a metal plate used in the present invention, a plated steel sheet (zinc-iron group alloy plating) which is preferably alloyed with zinc and an iron group element (Fe, Co, Ni) is preferable to the widely used electrogalvanized steel sheet. Covered steel plate). Examples of the alloy-plated steel sheet of the zinc-iron group element include an alloy-plated steel sheet of Zn and Fe, an alloy-plated steel sheet of Zn and Ni, and an alloy-plated steel sheet of Zn and Co. From the viewpoint of ensuring electromagnetic wave absorptivity, the Fe, Ni, and Co contents are preferably controlled to be substantially in the range of 5 to 20% by mass. Further, the method of plating is not particularly limited, and can be obtained by any of a hot-dip plating method and an electroplating method. Further, the detailed plating conditions of the hot-dip plating method and the plating method are not particularly limited, and a method generally used for alloying can be employed. When the electromagnetic wave absorptivity is considered, the amount of adhesion of the plating is preferably as small as possible, and for example, it is preferably 50 g/m 2 or less, more preferably 40 g/m 2 or less, still more preferably 35 g/m 2 or less, and most preferably 3 〇 mg / Below m2. The lower limit of the amount of plating adhesion is not particularly limited, but is preferably 5 g / m 2 , and most preferably 1 〇 g / m 2 , in view of resistance to enthalpy and the like. Further, in consideration of cost and the like, it is preferable to use an alloyed hot-dip galvanized steel sheet which is inexpensive and easy to manufacture (a steel sheet which is alloyed by Zn and Fe -17-(14) 200806468 by a hot-dip coating method). As described above, in the present invention, an alloy steel sheet is preferably used as the metal sheet, and a pure zinc plated steel sheet or a cold-rolled steel sheet having a plating adhesion amount of about or less may be used. This is because these have excellent electromagnetic wave absorbing effects and can realize desired conductive embodiments as will be described later. Further, as described above, by using a steel sheet which is not alloyed, it is possible to avoid problems in use of the alloyed steel sheet (cracking or peeling of cracks or the like which occur during bending processing). For example, if a cold-rolled steel sheet which is not plated is used, it can be processed for strict use. In particular, it has been found that the cold-rolled steel sheet has superior wave absorbability as compared with the alloyed steel sheet (see the examples described later). However, the difference in cold-rolled steel sheets, if considering the frame used for electronic equipment, is a comprehensive feature. Therefore, it is preferable to use alloyed plated steel sheets as compared with cold-rolled steel sheets. On the other hand, if pure zinc-plated steel sheets are used. It can be used in applications that are severe and require corrosion resistance. In order to effectively exhibit the contact-resistant adhesion amount, it is preferably about 3 g/m2 or more, more preferably 6 g/m2, and in consideration of electromagnetic wave absorptivity, the upper limit of the plating adhesion amount is 15 g/m2, more preferably 12 g/ M2 is optimally 10 g/m2. The necessary conditions and types for characterizing the resin film of the present invention have been described above. The thickness (average thickness) of the resin film is preferably in the range of approximately 3. Ομηη. If the thickness is outside the above range, the characteristics of the electromagnetic shielding of the electric frame are not the same as those of the electromagnetic shielding (bending plus plating of 15 g/m2 steel plate (see, for example, for electromagnetic observation) Corrosion resistance evaluation is lower than workability, plating. It is also best for metal plate 0· 1~ sub-workability, -18 - (15) 200806468 According to the so-called, etc., there are also 0 · 2 μιη The frame of the mirror observation device is because of course, it can also contain, etc.) additives, powders, powders, and the like. The ferrite metal powder (35% or more of the alloy) has a decreased film adhesion, corrosion resistance, and the like. The thickness of the base material resin and the metal plate for the thickness of the resin film is different from the roughness of the metal plate, and it is difficult to uniquely determine the thickness of the resin film. More preferably, it is approximately 2.0 μm or less, more preferably 0.3 μm or more and 1.5 μm or less. The thickness of the film can be measured by the specific gravity according to the weight of the film, or the cross section of the resin film can be measured (SEM observation). The φ resin film may be formed on at least the back surface of the metal plate (the inside of the non-outer side (outside gas side) as viewed from the electron body). The electromagnetic wave shielding property may cause problems on the inner side of the electronic device member or may be formed on the front and back sides of the metal plate. In addition to the base resin and the bridging agent, the resin film may have a known additive (for example, a rust preventive, a matting agent, or a pigment resin film may further contain a magnetic powder (electromagnetic wave absorption, whereby electromagnetic wave shielding can be further improved) Examples of the magnetic soft magnetic ferrite powder and the magnetic metal are soft magnetic ferrite powders, for example, soft magnetic Ni-Zn powder, Mn-Zii ferrite powder, etc. For example, permalloy (an alloy having a Ni content in a Ni-Fe alloy) and an iron alloy (Sendust) (Si-Al-Fe system) may be used alone or in combination. The content of the magnetic powder (total amount) is the most Preferably, it is in the range of 20 to 60% by mass. When the content is less than 20% by mass, the above effects cannot be effectively exerted. On the other hand, when it exceeds 60% by mass, the electronic device member is coated with the tree 200806468 (16). The properties required for the steel sheet (bending workability, film adhesion, and corrosion resistance) tend to deteriorate. The content of the magnetic powder depends, for example, on the type and shape of the magnetic powder used. The thickness of the resin film is also different, and it is difficult to determine uniquely. However, it is more preferably about 25% by mass or more and 5% by mass or less, and most preferably 30% by mass or more and 45% by mass or less. When the average particle diameter is 15 μm or less, it is preferable to remove a powder having a large particle diameter (for example, 20 μm or more) as much as possible. Thereby, formation of the Φ magnetic coating film is easy, and workability and uranium resistance can be suppressed from being lowered. Here, the average particle diameter of the magnetic powder is a particle size distribution of the magnetic powder particles after classification by a general particle size distribution meter, and the particle size of the 値50% from the small particle diameter side calculated based on the measurement result. (D50) The particle size distribution is measured by a diffraction pattern of the diffraction and scattering of the magnetic powder particles, and the particle size distribution meter is exemplified by Microtrac 9220FRA or Microtrac HRA # manufactured by Nikkiso Co., Ltd. In the case of the magnetic powder which satisfies the above-mentioned optimum average particle diameter, a commercially available product can also be used. For example, Ni-Zn-based soft magnetic ferrite can be cited [Toda Industry BSN-125, average particle size 13·0μιη], permalloy (78% Ni) [SFR-PC78, Atomize Processing Co., Ltd., average particle size 5·7μπι], permalloy (45% Ni) [SFR-PB45 manufactured by Atomize Processing Co., Ltd., average particle diameter 5.8 μm], iron-stained aluminum alloy [SFR_FeSiAl (84.5-10-5.5) manufactured by Atomize Processing Co., Ltd., average particle diameter 6.9 μm], etc. 20- (17) 200806468 In order to further improve the electromagnetic shielding properties of the resin-coated metal sheet, a conductivity imparting agent may be added to the resin film. Examples of the conductivity imparting agent include metal monomers such as Ag, Zn, Fe, Ni, and Cu, and metal compounds such as FeP. Among them, Ni is particularly preferred. Further, the shape thereof is not particularly limited, but in order to obtain more excellent conductivity, for example, a scaly structure is recommended. The content of the conductivity imparting agent contained in the resin film is preferably approximately 20 # to 40% by mass. Strictly speaking, the amount of addition can be appropriately adjusted depending on the kind of the magnetic powder to be used and the like. For example, when a soft magnetic ferrite powder is used as the magnetic powder, it is preferred to add a conductivity imparting agent as much as possible (for example, 25% by mass or more). Further, when a magnetic metal powder is used as the magnetic powder, it is preferred to add a conductivity imparting agent as little as possible (for example, 30% by mass or less). On the other hand, when the conductivity imparting agent is considered to have an adverse effect on the workability or the like as in the case of the magnetic powder, the total content of the conductive property imparting agent and the magnetic powder contained in the magnetic coating film is preferably about 60. Within the range of mass % or less. The metal plate may be subjected to a surface treatment (substrate treatment) such as chromate treatment or phosphate treatment for the purpose of improving the contact resistance and improving the adhesion to the resin film. Alternatively, a metal plate not subjected to chromate treatment may be used in consideration of environmental pollution or the like, and a metal plate subjected to any substrate treatment is included in the scope of the present invention. When performing the above substrate treatment, the adhesion amount of the substrate treatment is preferably about 300 mg/m2 or less, and most preferably 2 〇〇mg/m2 or less - 21 - (18) (18) 200806468 in consideration of conductivity and the like. More preferably, it is 150 mg/m2 or less, and most preferably i〇〇mg/m2 or less. Further, the method of non-chromate treatment is not particularly limited, and a known substrate treatment which is generally used may be carried out. Specifically, it is recommended to treat the substrate alone or in combination with a phosphate-based or cerium oxide-based "titanium system" or a pin system. Further, in general, when the non-base acid salt treatment is performed, the corrosion resistance is lowered. Therefore, for the purpose of improving the corrosion resistance, a rust preventive agent can be used in the coating film or the substrate treatment. Examples of the rust preventive agent include a cerium oxide compound, a phosphate compound, a phosphite compound, a polyphosphate compound, a sulfur organic compound, a benzotriazole, a tannic acid, and a molybdate compound. A tungstate compound, a vanadium compound, a decane coupling agent, etc. can be used individually or in combination. Particularly preferred is a combination of a cerium oxide-based compound (for example, calcium ion-exchanged cerium oxide) and a phosphate-based compound, a phosphite-based compound, or a polyphosphate-based compound (for example, aluminum tripolyphosphate). A cerium oxide compound (a phosphate compound, a phosphite compound, or a polyphosphate compound) is used in combination with a mass ratio of 0.5: 9.5 to 9.5: 0.5 (more preferably 1: 9 to 9: 1 ). ). By controlling in this range, both desired corrosion resistance and workability can be ensured. By the use of the above rust preventive agent, the corrosion resistance of the non-chromate-treated metal sheet can be ensured, but on the contrary, the workability is lowered due to the addition of the rust preventive agent. For this reason, as a component for forming a coating film, a polyester resin in which an epoxy-modified polyester resin and/or a phenol derivative is introduced into a skeleton, and a bridging agent (preferably an isocyanate resin and/or Or a melamine-based resin, preferably used in combination). Among them, an epoxy-modified polyester resin and/or a phenol derivative are introduced into a polyester resin of a bone-22-(19) (19)200806468 shelf (for example, a polyester resin in which bisphenol A is introduced into a skeleton, etc.) ) It is excellent in corrosion resistance and coating film adhesion compared with a polyester resin. On the other hand, the 'isocyanate bridging agent has an effect of improving the workability (refers to an effect of improving the appearance after processing, and is evaluated in the examples described later by the number of cracks in the adhesion bending test). Even if a rust inhibitor is added, excellent workability can be ensured. In addition, the melamine bridging agent has excellent corrosion resistance. Therefore, in the present invention, by using in combination with the above-mentioned rust preventive agent, very good corrosion resistance can be obtained. These isocyanate bridging agents and melamine-based bridging agents can be used singly, but when used in combination, the workability and the tamper resistance of the non-chromated metal sheets can be further improved. Specifically, it is recommended to contain the melamine-based resin in a ratio of 5 to 80 parts by mass with respect to the isocyanate-based resin 1 〇〇 mass portion. When the melamine resin is less than 5 parts by mass, the desired corrosion resistance cannot be obtained. On the other hand, when the melamine resin exceeds 80 parts by mass, the effect of the addition of the isocyanate resin cannot be satisfactorily exhibited, and the effect cannot be obtained. The desired processability is enhanced. More preferably, it is 10 parts by mass or more and 40 parts by mass or less, more preferably 15 parts by mass or more and 30 parts by mass or less, based on 100 parts by mass of the isocyanate-based resin. The resin-coated metal sheet of the present invention is coated with a resin film containing the above various additives on the surface of the metal plate (including the portion subjected to the substrate treatment described above), but imparts tamper resistance and fingerprint resistance as needed. For the purpose, a two-layer film structure in which another resin film is applied may be formed on the surface of the resin film. -23- (20) (20) 200806468 Next, a method of producing the resin-coated metal sheet of the present invention will be described. In the resin-coated metal sheet of the present invention, a coating material containing various additives as needed, in addition to the base resin and the bridging agent, is applied to the surface of the metal plate by a known coating method, and is obtained by baking. Here, in order to control the PPIt of the resin film within the scope of the present invention (70 or more), it is preferable to control the surface roughness of the raw material sheet (metal plate) as follows (the arithmetic mean roughness prescribed by JIS B 060 1 (1 994)) The degree Ra, hereinafter referred to as Ra) and the method of forming the resin film (viscosity and solid concentration of the coating, the burning condition of the coating, etc.). First, the Ra of the metal plate as the raw material plate is preferably controlled to be in the range of 0.8 to 1·6 μm. For example, when the steel sheet is used as the raw material sheet, if the Ra of the tempering roll is approximately controlled within the range of 0.6 to 3.2 μm, and the rolling ratio during rolling is approximately controlled within the range of 0.3 to 2.5%, it is possible to The Ra of the metal plate is controlled within the above range. In the temper rolling process, the surface shape of the roll for temper rolling is transferred to the plated raw material plate at a high transfer rate, but as in the present invention, a very thin resin film is applied to the plating. In the case of the raw material plate, the surface shape of the plated resin film is considered to substantially reflect the surface shape of the raw material plate, and therefore, Ra of the metal plate as the raw material plate is appropriately controlled. The rolling ratio is determined based on the Ra of the tempering roll in an appropriate range. The Ra of the tempering roll can be appropriately adjusted by, for example, a known processing method such as a spray passivation process, a discharge passivation process, or a laser passivation process. For example, when using a spray-passivation process, the surface roughness of the tempering roll can be adjusted using a grinding material having a particle size adjusted. The viscosity of the coating is preferably in the range of 10 -24- (21) (21)200806468 seconds to 40 seconds, preferably in the range of 1 5 to 30 seconds. . Here, it means that the shorter the time, the lower the viscosity. For example, when the viscosity of the coating material used is less than 10 seconds in Ford Cup No. 4, the paint easily penetrates into the valley portion (concave portion) of the metal sheet, and therefore the PPIt of the resin film tends to decrease. On the other hand, when the viscosity of the coating material used is more than 40 seconds in Ford Cup No. 4, the surface roughness (the shape of the unevenness) of the metal sheet greatly affects the formation of the resin film, under light contact. Conductivity may become unstable. The solid concentration of the coating material is appropriately adjusted to be easy to apply depending on the viscosity and coating conditions of the coating material to be used, but is preferably in the range of preferably 2 to 20% by mass, more preferably 4 to 16% by mass. The optimum is in the range of 6 to 12% by mass. The burnt-bonding condition is, for example, a change in the degree of the valley portion (concave portion) which flows into the metal sheet according to the type of the solvent used for the dilution of the paint, and the like, and it is preferable to finish the sticking in about one minute. The coating method is not particularly limited, and examples thereof include a cleaning surface, and if necessary, a roll coating method, a spray method, or a spray method on a surface of a long metal strip on which a pre-coating treatment (for example, a phosphate treatment, a chromate treatment, or the like) is performed. A method of applying a coating such as a curtain coating method to dry it in a hot air drying oven. The roll coating method is practically preferable in consideration of uniformity of film thickness and processing cost, coating efficiency, and the like. As an electronic device member to which the resin-coated metal sheet of the present invention is applied, for example, an electronic device member in which a heat generating body is built in an enclosed space, the electronic device member further including all or a part of an outer wall thereof by the above-described electronic device member -25-200806468 ( twenty two)

用塗敷體構成的電子設備構件。作爲上述電子設備構件, 歹!J 舉有 CD、LD、DVD、CD-ROM、CD-RAM、PDP、LCD 等資訊記錄製品,個人電腦、汽車導航系統、車載AV等 „ 電氣、電子、通信相關製品,投影儀、電視機、錄影機' 遊戲機等AV設備,影印機、印表機等複印設備,空調室 外機等的電源盒罩、控制盒罩、自動售貨機、冰箱等。 [實施例] 以下,列舉實施例更具體地說明本發明,但本發明當 然不受下述實施例限定,在符合前後所述要旨的範圍內能 夠進行適當的變更而實施,這些均包含於本發明的技術範 圍內。 實施例1 (金屬板) 使用以下表示的各種金屬板(板厚全部爲0.6mm), 使調質軋輥的表面粗糙度(Ra)在0.6〜3.2 μπι的範圍內 變化,並且使軋製時的軋製率在〇 . 3〜1 . 5 %的範圍內變化 ,由此,使金屬板的表面粗糙度(Ra)在0.56〜1·35μιη 的範圍內變化。通過使砂粒粒度在# 50〜# 70的範圍內變 化,使用調整了粒度的磨削材進行噴九鈍化加工,由此使 調質軋輥的Ra變化。 在以下的記載中,“%”沒有特別限定是質量%的意思 。另外,鍍覆鋼板(EG、GI、GA、ZN、ZF )全部進行了 -26- (23) 200806468 兩面鍍覆。 EG ( 1 ):電鍍鋅鋼板 (單面鍍覆附著量20g/m2、Ra: 0.76pm) EG ( 2 ):電鍍鋅鋼板 (單面鍍覆附著量15g/m2、Ra : 0·78μπι) EG ( 3 ):電鍍鋅鋼板 (單面鍍覆附著量12g/m2、Ra : 0·75μπι) φ EG ( 4 ):電鍍鋅鋼板 (單面鍍覆附著量9g/m2、Ra: 0.80μιη) EG ( 5 ):電鍍鋅鋼板 (單面鍍覆附著量6g/m2、Ra : 0·76μηι ) EG ( 6 ):電鍍鋅鋼板 (單面鍍覆附著量3g/m2、Ra: 0.77μπ〇 GI :熔融鍍鋅鋼板 (單面鍍覆附著量60g/m2、Ra : 0·56μηι) # CR :冷軋鋼板(Ra : 0·86μπι ) GA ( 1 ):合金化熔融鍍鋅鋼板 (單面鍍覆附著量40g/m2、Fe : 10%、Ra : 1 . 3 4 μιη ) GA ( 2 ):合金化熔融鍍鋅鋼板 (單面鍍覆附著量40g/m2、Fe : 10%、Ra : 0.8 2 μ m ) GA ( 3 ):合金化熔融鍍鋅鋼板 (單面鍍覆附著量 35g/m2、Fe : 10%、Ra : -27- (24)200806468An electronic device component constructed of an applicator. As the above electronic device component, oh! J holds information recording products such as CD, LD, DVD, CD-ROM, CD-RAM, PDP, LCD, etc., personal computers, car navigation systems, car AV, etc. 电气 Electrical, electronic, communication related products, projectors, televisions, Video recorders such as AV equipment such as game machines, copying equipment such as photocopiers and printers, power box covers such as air conditioner outdoor units, control box covers, vending machines, refrigerators, etc. [Embodiment] Hereinafter, examples are more specific. The present invention is not limited by the following examples, and can be appropriately modified and implemented within the scope of the present invention. These are all included in the technical scope of the present invention. Plate) The surface roughness (Ra) of the tempering roll was changed within the range of 0.6 to 3.2 μm using various metal plates (the plate thickness was 0.6 mm) shown below, and the rolling ratio during rolling was made 〇 3 to 1. 5 % variation within the range, whereby the surface roughness (Ra) of the metal sheet is varied within the range of 0.56 to 1.35 μm. By changing the grain size of the sand within the range of #50 to #70 , use adjusted granularity In the following description, "%" is not particularly limited to mass%. In addition, the plated steel sheet (EG, GI, GA, ZN) is changed by the spray-cutting passivation process. , ZF ) All carried out -26- (23) 200806468 two-sided plating. EG (1): electro-galvanized steel sheet (single-side plating adhesion 20g / m2, Ra: 0.76pm) EG ( 2 ): electro-galvanized steel sheet ( Single-sided plating adhesion amount 15g/m2, Ra: 0·78μπι) EG (3): electro-galvanized steel sheet (single-side plating adhesion amount 12g/m2, Ra: 0·75μπι) φ EG ( 4 ): electrogalvanized steel sheet (single-side plating adhesion amount: 9g/m2, Ra: 0.80μιη) EG (5): electro-galvanized steel sheet (single-side plating adhesion amount: 6g/m2, Ra: 0·76μηι) EG (6): electrogalvanized steel sheet ( Single-sided plating adhesion amount 3g/m2, Ra: 0.77μπ〇GI: hot-dip galvanized steel sheet (single-side plating adhesion amount 60g/m2, Ra: 0·56μηι) # CR : cold-rolled steel sheet (Ra: 0·86μπι GA (1): Alloyed hot-dip galvanized steel sheet (single-side plating adhesion 40g/m2, Fe: 10%, Ra: 1. 3 4 μιη) GA ( 2 ): alloyed hot-dip galvanized steel sheet (single-sided Plating adhesion amount 40g/m2, Fe: 10%, Ra: 0.8 2 μ m ) GA ( 3): Alloyed hot-dip galvanized steel sheet (single-sided plating adhesion amount 35g/m2, Fe: 10%, Ra: -27- (24)200806468

1 . 3 2 μιη ) GA ( 4 ):合金化熔融鍍鋅鋼板 (單面鍍覆附著量30g/m2、Fe : 10%、 1 . 3 5 μιη ) GA ( 5 ):合金化熔融鍍鋅鋼板 (單面鍍覆附著量25g/m2、Fe : 1 〇 %、 1 . 3 0 μιη ) φ ΖΝ : Zn-Ni合金化電鍍鋼板 (單面鍍覆附著量20g/m2、Ni· : 10%、 0.8 3 μιη ) Z F : Ζ η - F e合金化電鍍鋼板 (單面鍍覆附著量20g/m2、Fe : 10%、 0.81 μιη ) (樹脂皮膜的調製) # 準備含有表1所示成分的各種塗料,在金屬板上 了條形塗膜(bar coat )塗敷。作爲稀釋劑使用了二 和環己酮的混合溶劑(1 : 1 )。樹脂皮膜的厚度通過 稀釋塗料的固態量濃度和條形塗膜塗敷中使用的條形 數,而使其在0.3〜2.4μιη的範圍內變化。 塗布上述的塗料後,在以下的條件下進行了燒黏 熱風乾燥爐的通過時間(爐內時間):50秒 熱風乾燥爐的到達板溫:2 3 0 °C1 . 3 2 μιη ) GA ( 4 ): Alloyed hot-dip galvanized steel sheet (single-side plating adhesion amount 30 g/m 2 , Fe : 10%, 1. 3 5 μιη ) GA ( 5 ): alloyed hot-dip galvanized steel sheet (Single-side plating adhesion amount 25g/m2, Fe: 1 〇%, 1.30 μιη) φ ΖΝ : Zn-Ni alloyed plated steel sheet (single-side plating adhesion amount 20g/m2, Ni·: 10%, 0.8 3 μιη ) ZF : Ζ η - F e alloyed plated steel sheet (single-side plating adhesion amount: 20g/m2, Fe: 10%, 0.81 μιη) (Preparation of resin film) # Prepare various materials containing the components shown in Table 1. The coating was applied to a metal bar with a bar coat. As the diluent, a mixed solvent of dioxanone (1:1) was used. The thickness of the resin film was varied in the range of 0.3 to 2.4 μm by diluting the solid concentration of the coating material and the number of bars used in the coating of the strip coating film. After coating the above coating, the passing time of the hot air drying oven was carried out under the following conditions (in-furnace time): 50 seconds. The arrival temperature of the hot air drying oven was 2 3 0 °C.

Ra :Ra :

Ra :Ra :

Ra ··Ra ··

Ra : 進行 甲苯 改變 的支 -28- (25) (25)200806468 (樹脂皮膜的評價) (T g的測定) 樹脂皮膜的Tg基於JIS K 7121用示差掃描熱量計( 商品名:Thermo Plus DSC8230、(株)Rigaku 製)進行 了测定。具體地說,將從如上所述製作的樹脂塗敷金屬板 中獲取的樹脂皮膜置於示差掃描熱量計,冷卻到-100°c, 穩定之後,以2(TC /分鐘的速度升溫至180°c,然後從所 得的D S C曲線求出玻璃轉變溫度(Tg )。 (PPIt的測定) 對於PPIt而言,在美國的SAE J91 1-JUN86 ( 1 98 6 ) 中規格化的PPI中,以樹脂皮膜的平均厚度(μιη)爲基準 高度,算出了樹脂塗敷金屬板的PPIt。 測定條件爲截止値:〇 · 8 mm,觸針前端半徑R : 2 μιη ( 將觸針部分看作球),測定長度:2 5 · 4mm。實際上,考慮 測定誤差(士〇 .4mm ),在26.2mm的範圍內橫截觸針。另 外,測定位置任意選擇1 〇個位置,將其平均値作爲PPIt 。測定位置在同一方向合計選擇5個位置,在與該方向垂 直的方向合計選擇5個位置。 樹脂皮膜的平均厚度用以下所示的方法求出。首先, 在塗料中以1〜10重量%的重量比率添加氧化矽(si〇2) 作爲標記(marker ),通過螢光X射線分析法測定了 Si 附著量。在測定S i附著量時,預先作成表示§ i量和螢光 X射線強度的關係的檢量線,基於該檢量線,測定了 Μ -29- (26) 200806468 附著量。 接著’如上所述,根據測定的S i附著量,進行比重 換算而算出樹脂皮膜的重量,求出了平均厚度t ( μηι )。 具體的換算方法如下所述。Ra : Branches for the change of toluene -28- (25) (25)200806468 (Evaluation of resin film) (Measurement of T g) The Tg of the resin film is based on a differential scanning calorimeter according to JIS K 7121 (product name: Thermo Plus DSC8230, The measurement was carried out by Rigaku Co., Ltd. Specifically, the resin film obtained from the resin-coated metal sheet produced as described above was placed in a differential scanning calorimeter, cooled to -100 ° C, and stabilized, and then heated to 180 ° at a rate of 2 (TC / min). c, and then the glass transition temperature (Tg) is obtained from the obtained DSC curve. (Measurement of PPIt) For PPIt, a resin film is standardized in the PPI of SAE J91 1-JUN86 (1 98 6 ) in the United States. The average thickness (μιη) was taken as the reference height, and the PPIt of the resin-coated metal plate was calculated. The measurement conditions were cutoff 値: 〇·8 mm, and the tip end radius R: 2 μιη (the stylus portion was regarded as a ball), and the measurement was performed. Length: 2 5 · 4 mm. Actually, considering the measurement error (±4 mm), cross-contact the needle in the range of 26.2 mm. In addition, the measurement position is arbitrarily selected from 1 position and the average 値 is taken as PPIt. Five positions are selected in total in the same direction, and five positions are selected in total in the direction perpendicular to the direction. The average thickness of the resin film is obtained by the method described below. First, the weight is 1 to 10% by weight in the paint. Ratio of strontium oxide added Si〇2) The amount of Si adhesion was measured by a fluorescent X-ray analysis method as a marker. When measuring the amount of attachment of Si, a calibration curve indicating the relationship between the amount of § i and the intensity of fluorescent X-rays was prepared in advance. Based on the calibration curve, the amount of adhesion of Μ -29-(26) 200806468 was measured. Then, as described above, the weight of the resin film was calculated from the measured amount of Si deposition, and the average thickness t was obtained. Μηι ) The specific conversion method is as follows.

樹脂皮膜的平均厚度ί(μπι) = {A/(BxCxD) } xlOOO φ 式中,The average thickness of the resin film ί(μπι) = {A/(BxCxD) } xlOOO φ where

Si 附著量(mg/m2) B = 2 8/ 6 0 ( Si/Si02) c二Si〇2的重量比率 D =樹脂皮膜的比重(g/cm3) 將如上所述而得到的樹脂皮膜的平均厚度(t )作爲 正負各自的基準水準(峰値計數水準),測定每一英寸存 在的超過皮膜厚度t的峰谷數,從而求出了 PP It。 (導電性的評價) _ 使用測試器〔(株)Casutama製多用途測試器CX- 250〕,如下測定了樹脂塗敷金属板的表面的電阻。 如圖5所示,將端子保持45。的角度,同時以30mm/ 秒的平均速度使其在樹脂塗敷金屬板的表面滑動(測定長 度100mm )。測定時的壓力是在僅有端子的自重(7g)的 輕接觸下進行的。從測定開始經過1秒以上,測定値(電 阻値)穩定之後讀取了測定値。 -30- (27) (27)200806468 變換測定位置進行合計2 0次與上述相同的操作,將 其平均値作爲電阻値。 在本實施例中’將如上所述得到的電阻値低於〗〇〇Ω 的評價爲導電性優異(合格),電阻値在1 0 0 Ω以上的評 價爲導電性差(不合格)。電阻値越大,導電性越差。 還有,本實施例的評價方法,在電阻値測定時的壓力 處於10〜12g/mm2的範圍內和評價輕接觸下的導電性方面 ,與所述日本特開2004-156081號公報、日本特開2005-23 8 5 3 5號公報、特開2004-277876號公報中記載的導電性 評價方法不同。在這些文献中,均是使用三菱油化(株) 製的Loresta AP或GP作爲表面電阻測試器,使用ASP或 LSP探針作爲測定探針價導電性,算出測定時的探針的壓 力’大致爲33〜460g/mm2,與本實施例相比非常高。 (電磁波吸收性的評價) 圖2是說明對樹脂塗敷金屬板的電磁波吸收性進行評 價的方法的圖。如圖2所示,在長方體形狀的框體1內, 設置有高頻環形天線5,磁場結合而構成。高頻環形天線 5經由連接器(未圖示)連接在同軸電纜6的一端,同軸 電纜6的另一端與網路分析器7連接。在網路分析器7中 ’一邊掃過頻率一邊產生電磁波,經由同軸電纜6、高頻 環形天線5輸入框體1內(高頻輸入波:箭頭B)。在框 體1的共振頻率中,由於積蓄輸入的電磁波,因此能夠觀 察反射量減少的特性(參照圖3 )。於是,由箭頭C表示 -31 - 200806468 (28) 的高頻反射波作爲觀察値輸入網路分析器7 (高頻反射波 :箭頭C )。 此時,如果計測框體1中的由下式(2 )求出的Q値 ,則可知框體1內積蓄的能量的大小。還有,從下式(2 )求出的Q値是從根據導納軌道滿足的條件而求出的頻率 差Af和共振頻率fr算出的値(例如,中島將光著“森北電 工學系列3微波工學-基礎和原理森北出版株式會社發行 _ ,第 159 〜163 頁)。 Q 値= fr/Af ....(2) 這表示從上式(2 )求出的Q値越小框體1內積蓄的 能量越少。因此,Q値越小,從框體i向內部反射的電磁 場能級也越小。 此時的狀況模式地表不在圖4中,該圖表示所謂Ez ^ = 0、TE0 1 1的最低頻率的共振模式的電磁場分佈,圖中, E是局頻磁場,F是高頻電場。上述Ez是z方向的電場強 • 度的意思,TEou表示共振模式的電磁場分佈的姿態。該 • TE意味著在z方向波前進,其橫向存在電場。附加字 t〇ll”表示相對於X、y、z方向,在y和Z方向上存在一 個電場強度分佈,在X方向上電場強度分佈不變化(例如 ’參照上述文獻第141〜144頁)。 另外,圖4所示的電磁場分佈以下式表示。Si adhesion amount (mg/m2) B = 2 8/ 6 0 (Si/Si02) c Weight ratio of diSi〇2 D = specific gravity of resin film (g/cm3) Average of resin film obtained as described above The thickness (t) was used as a reference level for each of the positive and negative (peak enthalpy level), and the number of peaks and valleys exceeding the film thickness t per inch was measured to determine PP It. (Evaluation of Conductivity) _ The resistance of the surface of the resin-coated metal plate was measured as follows using a tester [manufactured by Casuyama Co., Ltd. CX-250]. As shown in FIG. 5, the terminal is held at 45. At the same time, it was slid on the surface of the resin-coated metal plate at an average speed of 30 mm/sec (measurement length 100 mm). The pressure at the time of measurement was carried out under light contact of only the terminal weight (7 g). The measurement enthalpy was read after the measurement of enthalpy (resistance enthalpy) was completed for 1 second or more from the start of the measurement. -30- (27) (27)200806468 The measurement position was changed to perform the same operation as above for a total of 20 times, and the average 値 was used as the resistance 値. In the present embodiment, the evaluation of the electric resistance 値 obtained as described above was lower than 〇〇 Ω, and the electric conductivity was excellent (pass), and the evaluation of the electric resistance 値 of 100 Ω or more was poor in conductivity (failed). The larger the resistance, the worse the conductivity. In addition, in the evaluation method of the present embodiment, the pressure at the time of resistance 値 measurement is in the range of 10 to 12 g/mm 2 and the conductivity under light contact is evaluated, and the above-mentioned Japanese Patent Laid-Open Publication No. 2004-156081, Japan The conductivity evaluation methods described in JP-A-2005-277876 are different. In these documents, Loreta AP or GP manufactured by Mitsubishi Petrochemical Co., Ltd. was used as a surface resistance tester, and ASP or LSP probe was used as the probe probe conductivity, and the pressure of the probe at the time of measurement was calculated. It is 33 to 460 g/mm 2 and is very high compared to this embodiment. (Evaluation of electromagnetic wave absorptivity) Fig. 2 is a view for explaining a method of evaluating electromagnetic wave absorptivity of a resin-coated metal plate. As shown in FIG. 2, in the rectangular parallelepiped casing 1, a high-frequency loop antenna 5 is provided, and a magnetic field is combined. The high frequency loop antenna 5 is connected to one end of the coaxial cable 6 via a connector (not shown), and the other end of the coaxial cable 6 is connected to the network analyzer 7. In the network analyzer 7, an electromagnetic wave is generated while sweeping the frequency, and is input into the casing 1 via the coaxial cable 6 and the high-frequency loop antenna 5 (high-frequency input wave: arrow B). In the resonance frequency of the casing 1, since the input electromagnetic wave is accumulated, it is possible to observe the characteristic of the decrease in the amount of reflection (see Fig. 3). Then, the high-frequency reflected wave of -31 - 200806468 (28) is indicated by the arrow C as the observation 値 input network analyzer 7 (high-frequency reflected wave: arrow C). At this time, when Q値 obtained by the following formula (2) in the measurement frame 1 is measured, the amount of energy accumulated in the casing 1 is known. Further, Q 求出 obtained from the following formula (2) is a 算出 calculated from the frequency difference Af obtained by the condition satisfied by the admittance orbit and the resonance frequency fr (for example, Nakajima will be lighted "Senbei Electrotechnical Series 3 Microwave Engineering - Foundation and Principles issued by Moribe Publishing Co., Ltd. _ , pp. 159 ~ 163.) Q 値 = fr / Af .... (2) This means that the smaller the Q 求出 from the above equation (2) The smaller the energy accumulated in the body 1. Therefore, the smaller the Q値, the smaller the electromagnetic field level reflected from the frame i to the inside. The situation pattern at this time is not shown in Fig. 4, which shows the so-called Ez ^ = 0 The electromagnetic field distribution of the resonance mode of the lowest frequency of TE0 1 1 , where E is a local frequency magnetic field and F is a high frequency electric field. The above Ez is the meaning of the electric field strength in the z direction, and TEou represents the electromagnetic field distribution of the resonance mode. Attitude. The TE means that the wave advances in the z direction, and there is an electric field in the lateral direction. The additional word t〇ll” indicates that there is an electric field intensity distribution in the y and Z directions with respect to the X, y, and z directions, in the X direction. The electric field intensity distribution does not change (for example, 'refer to pages 141 to 144 of the above-mentioned documents). In addition, the electromagnetic field distribution shown in FIG. 4 is represented by the following formula.

Hz ^ H011 · cos ( ky · y ) · sin ( kz · z) -32» (29) 200806468Hz ^ H011 · cos ( ky · y ) · sin ( kz · z) -32» (29) 200806468

Hy= ( -kz · ky/kc2) · Η〇ιι· sin(ky· y) · cos ( kz • z )Hy= ( -kz · ky/kc2) · Η〇ιι· sin(ky· y) · cos ( kz • z )

Ex=(-jcopky/kc2) · H 〇 11 · s i n ( k y · y ) · sin ( kz · z ) 在此,ky=^K/b、kz^w/c、kc=ky。b、c 是圖 4 的長 方體(框體1)的y、z方向的長度,j是虛數,ω是各頻 率,μ是空氣的導磁率… φ 本發明者們製作了能夠將試樣鋼板所占內面的比率提 高到100%附近(即,直到框體內面的整個面)的框體。 圖6是表示構成該框體的SUS制框架(架體)的說明圖, 圖6(a)是俯視圖,圖6(b)是主視圖,圖6(c)是左 視圖。還有,該框架構成爲上下左右對稱,因此,仰視圖 、後視圖、右視圖分別與俯視圖(圖6 ( a ))、主視圖( 圖6 ( b ))、左視圖(圖6 ( c ))同樣表現。 在圖6所示的框架上,貼附(安裝螺釘)圖7、8 • 所示的試樣鋼板以及SUS板形成框體(240x 1 80x90mm) 。還有,圖7 ( a )是配置於框架的正面、背面部分的試樣 鋼板(2片),圖7(b)是配置於框架的左右側面部分的試 樣鋼板(2片),圖8 ( a)是配置於上面部分的SUS板, 圖8(b)是配置於底面部分的SUS板。 根據如上所述的構成,如果製作框體,則試樣鋼板能 夠占其內面直到接近100%的比例。另外,安裝螺釘其間 距設爲20〜40mm,降低了接觸電阻,因此,需要多個止 動螺釘。止動螺釘通過管理轉矩,能夠提高Q値測定的再 -33- (30) 200806468 現性。使用這種框體測定Q値(所述圖2),並由下式算 出了電磁波吸收性。 試樣鋼板的電磁波吸收性(dB)= l〇xl〇g1G(〔 EG)/〔 A)) 其中,〔EG〕:成爲基板的电鍍鋅鋼板的Q値 〔A〕:試樣鋼板的Q値 評價爲由上述方法算出的値(dB )越高,電磁波吸收 性越優異。在本實施例中,如上所述算出的値在3.0dB以 上的評價爲電磁波吸收性優異(合格),低於3.0dB的評 價爲電磁波吸收性差(不合格)。評價爲上述算出値越大 電磁波吸收性越優異。 這些結果一倂記錄於表2和表3中。 還有,在表2和表3中,設有綜合評價欄,按下述基 ^ 準進行了綜合評價。綜合評價爲◎或〇的爲“本發明例”。 ◎:導電性和電磁波吸收性雙方合格 〇:導電性合格電磁波吸收性不合格 X :導電性不合格電磁波吸收性合格,或導電性和電 磁波吸收性雙方不合格 -34- (31)200806468 【表2】Ex=(-jcopky/kc2) · H 〇 11 · s i n ( k y · y ) · sin ( kz · z ) Here, ky=^K/b, kz^w/c, and kc=ky. b, c is the length in the y and z directions of the rectangular parallelepiped (frame 1) of Fig. 4, j is an imaginary number, ω is the frequency, and μ is the magnetic permeability of the air... φ The inventors have made the sample steel plate The ratio of the inner surface is increased to around 100% (i.e., until the entire surface of the inner surface of the frame). Fig. 6 is an explanatory view showing a SUS frame (frame) constituting the frame, Fig. 6(a) is a plan view, Fig. 6(b) is a front view, and Fig. 6(c) is a left side view. Further, the frame is configured to be vertically symmetrical, so that the bottom view, the rear view, and the right view are respectively a top view (Fig. 6 (a)), a main view (Fig. 6 (b)), and a left view (Fig. 6 (c) ) Same performance. On the frame shown in Fig. 6, the sample steel plate and the SUS plate shown in Figs. 7 and 8 are attached (mounting screws) to form a frame (240 x 1 80 x 90 mm). Further, Fig. 7(a) is a sample steel plate (two pieces) disposed on the front and back portions of the frame, and Fig. 7(b) is a sample steel plate (two pieces) disposed on the left and right side surface portions of the frame, Fig. 8 (a) is a SUS plate disposed on the upper portion, and (b) is a SUS plate disposed on the bottom surface portion. According to the configuration described above, if the frame is produced, the sample steel sheet can occupy the inner surface up to a ratio of approximately 100%. In addition, the mounting screws have a pitch of 20 to 40 mm, which reduces the contact resistance, and therefore requires a plurality of stopper screws. The set screw can improve the Q値 measurement by managing the torque. -33- (30) 200806468 Present. Using this frame, Q 値 (the above Fig. 2) was measured, and electromagnetic wave absorptivity was calculated from the following formula. Electromagnetic wave absorptivity (dB) of the sample steel sheet = l〇xl〇g1G([EG)/[A)) where [EG]: Q値[A] of the electrogalvanized steel sheet to be the substrate: Q of the sample steel sheet The 値 evaluation is that the higher the enthalpy (dB) calculated by the above method, the more excellent the electromagnetic wave absorptivity. In the present embodiment, the evaluation of enthalpy calculated as described above above 3.0 dB is excellent in electromagnetic wave absorptivity (pass), and the evaluation below 3.0 dB is poor in electromagnetic wave absorptivity (failed). The evaluation was as described above, and the larger the electromagnetic enthalpy, the more excellent the electromagnetic wave absorptivity. These results are collectively recorded in Tables 2 and 3. In addition, in Tables 2 and 3, a comprehensive evaluation column is provided, and a comprehensive evaluation is performed based on the following criteria. The comprehensive evaluation of ◎ or 〇 is "an example of the present invention". ◎: Both conductivity and electromagnetic wave absorption are acceptable. 导电 导电 导电 导电 导电 导电 导电 导电 导电 导电 导电 导电 : : : : : : : : : : : : : : : : : : : : : : : X X X X X X X X X X X X X X X X 2】

N.o 原材板 樹脂皮膜 導, 鬣性 電磁波吸收性 綜合 評價 Tg(°C) 平均厚 度(μπι) PPIt 電阻値 (Ω) 評價 値dB) 評價 1 0.3 351 8 〇 3.29 〇 ◎ 2 0.5 300 15 〇 3.31 〇 ◎ 3 0.7 242 21 〇 3.25 〇 ◎ 4 40 1.0 184 28 〇 3.28 〇 ◎ 5 1.2 146 32 〇 3.30 〇 ◎ 6 1.6 107 60 〇 3.29 〇 ◎ 7 1.9 80 80 〇 3.27 〇 ◎ S GA 2.4 51 100以上 X 3.22 〇 X 9 (1) 10 1.9 78 57 〇 3.27 〇 ◎ 10 25 1.9 82 65 〇 3.29 〇 ◎ 11 60 1.9 81 86 〇 3.30 〇 ◎ 12 75 1.9 83 97 〇 3.28 〇 ◎ 13 10 1.0 180 8 〇 3.31 〇 ◎ 14 25 1.0 182 16 〇 3.27 〇 ◎ 15 60 1.0 179 34 〇 3.29 〇 ◎ 16 75 1.0 185 50 〇 3.24 〇 ◎ 17 0.3 262 21 〇 3.31 〇 ◎ 18 0.5 190 32 〇 3.26 〇 ◎ 19 40 0.7 138 40 〇 3.24 〇 ◎ 20 0.9 80 79 〇 3.27 〇 ◎ 21 1.0 61 100以上 X 3.30 〇 X 22 GA 10 0.9 77 59 〇 3.28 〇 ◎ 23 25 0.9 78 67 〇 3.29 〇 ◎ 24 (2) 60 0.9 80 85 〇 3.25 〇 ◎ 25 75 0.9 78 93 〇 3.24 〇 ◎ 26 10 0.7 135 18 〇 3.26 〇 ◎ 27 25 0.7 140 27 〇 3.28 〇 ◎ 28 60 0.7 145 50 〇 3.31 〇 ◎ 29 75 0.7 141 71 〇 3.21 〇 ◎ 30 GA⑶ 40 0.6 280 17 〇 3.45 〇 ◎ 31 GA(4) 40 0.6 310 13 〇 3.65 〇 ◎ 32 〇A(5) 40 0.6 298 16 〇 3.86 〇 ◎ -35- (32)200806468No Raw material sheet resin film guide, comprehensive evaluation of 电磁 electromagnetic wave absorption Tg (°C) Average thickness (μπι) PPIt resistance 値 (Ω) Evaluation 値 dB) Evaluation 1 0.3 351 8 〇 3.29 〇 ◎ 2 0.5 300 15 〇 3.31 〇 ◎ 3 0.7 242 21 〇 3.25 〇 ◎ 4 40 1.0 184 28 〇 3.28 〇 ◎ 5 1.2 146 32 〇 3.30 〇 ◎ 6 1.6 107 60 〇 3.29 〇 ◎ 7 1.9 80 80 〇 3.27 〇 ◎ S GA 2.4 51 100 or more X 3.22 〇X 9 (1) 10 1.9 78 57 〇 3.27 〇 ◎ 10 25 1.9 82 65 〇 3.29 〇 ◎ 11 60 1.9 81 86 〇 3.30 〇 ◎ 12 75 1.9 83 97 〇 3.28 〇 ◎ 13 10 1.0 180 8 〇 3.31 〇 ◎ 14 25 1.0 182 16 〇 3.27 〇 ◎ 15 60 1.0 179 34 〇 3.29 〇 ◎ 16 75 1.0 185 50 〇 3.24 〇 ◎ 17 0.3 262 21 〇 3.31 〇 ◎ 18 0.5 190 32 〇 3.26 〇 ◎ 19 40 0.7 138 40 〇 3.24 〇◎ 20 0.9 80 79 〇3.27 〇◎ 21 1.0 61 100 or more X 3.30 〇X 22 GA 10 0.9 77 59 〇3.28 〇◎ 23 25 0.9 78 67 〇3.29 〇◎ 24 (2) 60 0.9 80 85 〇3.25 〇 ◎ 25 75 0.9 78 93 3.24 〇 ◎ 26 10 0.7 135 18 〇 3.26 〇 ◎ 27 25 0.7 140 27 〇 3.28 〇 ◎ 28 60 0.7 145 50 〇 3.31 〇 ◎ 29 75 0.7 141 71 〇 3.21 〇 ◎ 30 GA (3) 40 0.6 280 17 〇 3.45 〇 ◎ 31 GA(4) 40 0.6 310 13 〇3.65 〇◎ 32 〇A(5) 40 0.6 298 16 〇3.86 〇◎ -35- (32)200806468

【表3】 樹脂皮膜 導電性 電磁波吸收性 綜合 評價 N.o 原材板 Tg(°C) 平均厚 度(μιη) PPIt 電阻値(Ω) 評價 傲dB) 評價 33 0.6 147 39 〇 0.01 X 〇 34 40 0.9 120 60 〇 -0.02 X 〇 35 1.0 71 88 〇 0.03 X 〇 36 10 1.0 74 68 〇 0.01 X 〇 37 25 1.0 72 80 〇 0.02 X 〇 38 EG(1) 60 1.0 75 90 〇 0.00 X 〇 39 75 1.0 76 98 〇 -0.01 X 〇 40 10 0.6 150 18 〇 0.01 X 〇 41 25 0.6 142 27 〇 -0.01 X 〇 42 60 0.6 153 50 〇 0.02 X 〇 43 75 0.6 146 71 〇 0.03 X 〇 44 EG⑵ 40 0.6 150 40 〇 0.51 X 〇 45 EG(3) 40 0.6 146 41 〇 0.73 X 〇 46 EG(4) 40 0.5 149 39 〇 0.98 X 〇 47 EG(5) 40 0.6 156 37 〇 1.32 X 〇 48 EG(6) 40 0.6 143 42 〇 1.78 X 〇 49 ZN 40 0.6 163 35 〇 3.40 〇 ◎ 50 ZF 40 0.6 158 36 〇 3.97 〇 ◎ 51 40 0.5 179 41 〇 -0.54 X 〇 52 1.1 47 100以上 X -0.56 X X 53 GI 10 0.5 175 20 〇 -0.60 X 〇 54 25 0.5 172 28 〇 -0.57 X 〇 55 60 0.5 180 55 〇 -0.54 X 〇 56 75 0.5 184 69 〇 -0.58 X 〇 57 0.5 178 38 〇 4.11 〇 ◎ 58 40 1.2 76 78 〇 4.12 〇 ◎ 59 1.6 53 100以上 X 4.15 〇 X 60 10 1.2 78 56 〇 4.13 〇 ◎ 61 25 1.2 75 67 〇 4.16 〇 ◎ 62 CR 60 1.2 73 84 〇 4.12 〇 ◎ 63 75 1.2 76 97 〇 4.12 〇 ◎ 64 10 0.5 178 19 〇 4.12 〇 ◎ 65 25 0.5 175 26 〇 4.14 〇 ◎ 66 60 0.5 170 55 〇 4.09 〇 ◎ 67 75 0.5 173 82 〇 4.11 〇 ◎ -36- (33) (33)200806468 從這些結果可以進行如下考察。 首先,對作爲鍍覆原材板使用了合金化熔融鍍鋅鋼板 的結果(表2的Νο·1〜32)進行考察。在本實施例中,使 用鍍覆附著量不同的合計5種原材板(GA ( 1 )〜GA ( 5 ))評價了導電性和電磁波吸收性。 其中,No. 1〜16是作爲鍍覆原材板使用了合金化熔融 鍍鋅鋼板(鍍覆附著量40g/m2、Fe : 10% )的例子。它們 均使用了合金化熔融鍍鋅鋼板,因此能夠得到良好的電磁 波吸收性。 如表2所示可知,PPIt控制在70以上的No.l〜7、9 〜16與PPIt不滿足本發明的範圍的N 〇.8相比,導電性均 優異。詳細地說,PPIT越大基本上電阻値越小,導電性 具有提筒的傾向。 另外,對樹脂皮膜的Tg和電阻値的關係進行考察時 ,如下所述。 首先,對樹脂皮膜的平均厚度爲1.9μιη的情況進行考 察。Νο·7 ( Tg = 40°C ) 、Νο·9 ( Tg = 1 (TC ) ' No.10 ( Tg =25〇C ) > No.11 ( Tg= 60°C ) 、N o · 12 ( T g = 7 5 〇C )的 PPIt均爲大約78〜83,設定在本發明所規定的下限値( 70 )附近,但是,比較硏究它們的電阻値時可見,Tg越 低基本上電阻値也越小,導電性具有提高的傾向。 同樣的傾向在樹脂皮膜的平均厚度爲Ι.Ομπι時也可以 看到。No.4(Tg=40°C) 、No.l3(Tg=10°C) > No.14 ( -37- 200806468 (34)[Table 3] Comprehensive evaluation of conductive electromagnetic wave absorptivity of resin film No T2 (°C) Average thickness (μιη) PPIt Resistance 値 (Ω) Evaluation proud dB) Evaluation 33 0.6 147 39 〇0.01 X 〇34 40 0.9 120 60 〇-0.02 X 〇35 1.0 71 88 〇0.03 X 〇36 10 1.0 74 68 〇0.01 X 〇37 25 1.0 72 80 〇0.02 X 〇38 EG(1) 60 1.0 75 90 〇0.00 X 〇39 75 1.0 76 98 〇-0.01 X 〇40 10 0.6 150 18 〇0.01 X 〇41 25 0.6 142 27 〇-0.01 X 〇42 60 0.6 153 50 〇0.02 X 〇43 75 0.6 146 71 〇0.03 X 〇44 EG(2) 40 0.6 150 40 〇0.51 X 〇45 EG(3) 40 0.6 146 41 〇0.73 X 〇46 EG(4) 40 0.5 149 39 〇0.98 X 〇47 EG(5) 40 0.6 156 37 〇1.32 X 〇48 EG(6) 40 0.6 143 42 〇1.78 X 〇49 ZN 40 0.6 163 35 〇3.40 〇◎ 50 ZF 40 0.6 158 36 〇3.97 〇◎ 51 40 0.5 179 41 〇-0.54 X 〇52 1.1 47 100 or more X -0.56 XX 53 GI 10 0.5 175 20 〇 -0.60 X 〇54 25 0.5 172 28 〇-0.57 X 〇55 60 0.5 180 55 〇-0.54 X 〇56 75 0.5 184 69 〇-0 .58 X 〇57 0.5 178 38 〇4.11 〇◎ 58 40 1.2 76 78 〇4.12 〇◎ 59 1.6 53 100 or more X 4.15 〇X 60 10 1.2 78 56 〇4.13 〇◎ 61 25 1.2 75 67 〇4.16 〇◎ 62 CR 60 1.2 73 84 〇 4.12 〇 ◎ 63 75 1.2 76 97 〇 4.12 〇 ◎ 64 10 0.5 178 19 〇 4.12 〇 ◎ 65 25 0.5 175 26 〇 4.14 〇 ◎ 66 60 0.5 170 55 〇 4.09 〇 ◎ 67 75 0.5 173 82 〇 4.11 〇◎ -36- (33) (33)200806468 These results can be examined as follows. First, the results of using the alloyed hot-dip galvanized steel sheet as the plated raw material sheet (Νο·1 to 32 in Table 2) were examined. In the present embodiment, conductivity and electromagnetic wave absorptivity were evaluated using a total of five kinds of raw material sheets (GA (1) to GA (5)) having different plating adhesion amounts. Among them, No. 1 to 16 are examples in which an alloyed molten galvanized steel sheet (plating adhesion amount: 40 g/m2, Fe: 10%) is used as a plated raw material sheet. Since they are all alloyed hot-dip galvanized steel sheets, good electromagnetic absorption can be obtained. As shown in Table 2, No. 1 to 7, 9 to 16 in which PPIt was controlled at 70 or more was superior in conductivity to N 〇.8 in which PPIt did not satisfy the range of the present invention. In detail, the larger the PPIT, the smaller the resistance 値, and the conductivity has a tendency to lift the cylinder. Further, when the relationship between the Tg of the resin film and the electric resistance 値 is examined, it is as follows. First, the case where the average thickness of the resin film was 1.9 μm was examined. Νο·7 ( Tg = 40°C ), Νο·9 ( Tg = 1 (TC ) ' No.10 ( Tg =25〇C ) > No.11 ( Tg= 60°C ) , N o · 12 ( The PPIt of T g = 7 5 〇C ) is about 78 to 83, which is set near the lower limit 70( 70 ) prescribed by the present invention, but it can be seen when comparing their resistance 値, and the lower the Tg is substantially the resistance 値The smaller the conductivity, the higher the conductivity. The same tendency is observed when the average thickness of the resin film is Ι.Ομπι. No. 4 (Tg = 40 ° C), No. l3 (Tg = 10 ° C) ) > No.14 ( -37- 200806468 (34)

Tg= 25〇C ) 、No.l5(Tg=60°C) 、No.l6(Tg=75°C)的 PPIt均爲大約179〜185,控制在本發明所規定的範圍內 (PPIt 2 7 0 ),但是比較硏究它們的電阻値時可見,Tg越 低基本上電阻値也越小,導電性具有提高的傾向。 在作爲鍍覆原材板使用了鍍覆附著量與所述GA(1) 不同的GA(2)的例子(Νο·17〜29)中,也同樣看到了 與上述同樣的傾向。The PPIt of Tg=25〇C), No.l5 (Tg=60°C) and No.l6 (Tg=75°C) are all about 179~185, and the control is within the range specified by the present invention (PPIt 2 7). 0), but when the resistance 値 is compared, the lower the Tg, the smaller the resistance 基本上, and the higher the conductivity. In the example (Νο·17 to 29) in which the amount of plating adhesion is different from that of the above-described GA (1) (Νο· 17 to 29), the same tendency as described above is similarly observed.

• 另外,作爲鍍覆原材板使用了鍍覆附著量不同的GA (3 )〜GA ( 5 )的Νο·30〜32,PPIt滿足本發明的範圍, 因此,能夠確保良好的導電性。由於它們使用合金化熔融 鍍鋅鋼板,因此電磁波吸收性也優異。 另一*方面’表3的Νο·49和50是作爲鑛覆原材板使 用了上述以外的鋅和鐵族元素的合金鍍覆鋼板的例子。詳 細地說,No. 49是使用了通過電鍍法使Ζη和Ni合金化的 鋼板的例子,Νο·50是使用了通過電鍍法使Zn和Fe合金 Φ 化的鋼板的例子,不過它們的PPIt均滿足本發明的範圍 ,因此能夠確保良好的導電性,並且電磁波吸收性也優異 〇 另一方面,表3的No.33〜48是作爲鍍覆原材板使用 了電鍍鋅鋼板的例子。本實施例中,使用鍍覆附著量不同 的合計6種原材板(EG(1)〜EG(6))對導電性和電 磁波吸收性進行了評價。 如表3所示’上述鋼板的ppit均控制在7〇以上,因 此,導電性優異。詳細地說可見,PPIt越大基本上電阻値 -38- (35) 200806468 越小,導電性具有提高的傾向。 與此相對,通過實驗確認到PPIt不滿足本發明 的使用任意鍍覆原材板時導電性均差(表中未顯示) 另外,考察樹脂皮膜的T g和電阻値的關係時, 所述。 首先,對樹脂皮膜的平均厚度爲Ι.Ομπι的情況進 察。表 3 的 Ν 〇 · 3 5 ( T g = 4 0 °C ) 、Ν ο · 3 6 ( T g = 1 0 °C No.37 ( Tg = 25C ) 、Νο·38 ( TTg: 60〇C ) 、No.39 ( 75C)的PPIt均大約爲71〜76,設定在本發明所規 下限値(PP It二70 )附近,但是比較硏究它們的電阻 可見,Tg越低基本上電阻値也越小,導電性具有提 傾向。 在樹脂皮膜的平均厚度爲0.6μιη時也看到了同樣 向。Νο·33 ( Tg = 40〇C ) 、Νο·40 ( Tg = 1 0 〇C ) 、No.In addition, as the plated raw material plate, Νο·30 to 32 of GA (3) to GA (5) having different plating adhesion amounts are used, and PPIt satisfies the scope of the present invention, so that good electrical conductivity can be ensured. Since they use an alloyed molten galvanized steel sheet, electromagnetic wave absorbability is also excellent. In another aspect, Νο. 49 and 50 of Table 3 are examples of alloy-plated steel sheets using zinc and iron group elements other than the above-described mineral-coated raw material sheets. Specifically, No. 49 is an example of a steel sheet in which Ζη and Ni are alloyed by an electroplating method, and Νο·50 is an example of a steel sheet in which Zn and Fe alloys are Φ by electroplating, but their PPIts are In the range of the present invention, it is possible to ensure good electrical conductivity and to be excellent in electromagnetic wave absorptivity. On the other hand, Nos. 33 to 48 of Table 3 are examples in which an electrogalvanized steel sheet is used as a plated raw material plate. In the present embodiment, conductivity and electromagnetic wave absorptivity were evaluated using a total of six kinds of raw material sheets (EG(1) to EG(6)) having different plating adhesion amounts. As shown in Table 3, the pipp of the above-mentioned steel sheet was controlled to be 7 Å or more, and therefore, the electric conductivity was excellent. In detail, it can be seen that the larger the PPIt is, the more the resistance 値 -38-(35) 200806468 is, the smaller the conductivity is. On the other hand, it was confirmed by experiments that PPIt does not satisfy the use of any of the plated raw material sheets of the present invention, and the conductivity is poor (not shown in the table). Further, when the relationship between the T g and the resistance 値 of the resin film is examined, the above is considered. First, the case where the average thickness of the resin film is Ι.Ομπι is observed. Table 3 Ν 〇 · 3 5 ( T g = 4 0 °C ) , ο ο · 3 6 ( T g = 1 0 °C No.37 ( Tg = 25C ) , Νο·38 ( TTg: 60〇C ) The PPIt of No. 39 (75C) is about 71 to 76, which is set near the lower limit of the invention (PP It II 70), but the resistance is visible. The lower the Tg, the more the resistance is. Small, the conductivity has a tendency to lift. When the average thickness of the resin film is 0.6 μm, the same direction is also observed. Νο·33 (Tg = 40〇C), Νο·40 (Tg = 1 0 〇C), No.

T g — 2 5 °C ) ' No.42 ( Tg=60°C ) ' No.43 ( Tg = 75 °C PPIt均大約爲142〜153,控制在本發明所規定的範 (PPIt- 70 ),但比較硏究它們的電阻値時可見,丁§ 基本上電阻値也越小,導電性具有提高的傾向。 表3的No.5 1〜56是作爲鑛覆原材板使用了熔融 鋼板的例子。 其中,PPIt滿足本發明的範圍的No.51、53〜56 滿足本發明的範圍的No. 52相比,導電性優異。 還有,上述鋼板均使用了熔融鍍鋅鋼板,所以電 吸收性差。 範圍 〇 如下 行考 )> Tg- 定的 値時 闻的 的傾 41 ( )的 圍內 越低 鍍鋅 與不 磁波 -39- (36) 200806468 表3的No .57〜67是作爲鍍覆原材板使用了冷軋鋼板 的例子。 其中,PPIt滿足本發明的範圍的No. 57〜58、60〜67 與不滿足本發明的範圍的No. 59相比,導電性優異。 另外,上述鋼板均使用了冷軋鋼板,因此,與使用了 合金化鍍覆鋼板的情況相比,能夠得到良好的電磁波吸收 性。 【圖式簡單說明】 圖1是用於說明S A E規格的P PI的槪念的圖。 圖2是說明塗敷鋼板的電磁波吸收性能的評價方法的 圖。 圖3是說明輸入的電磁波因框體的共振頻率而反射量 變少的狀態的圖。 •圖4是模式地表示測定電磁波吸收性時的狀態的說明 # 圖。 圖5是用於說明樹脂塗敷金屬板的導電性的測定方法 的圖。 圖6是表示構成用於測定電磁波吸收性的框體的s u S 制框架(架體)的說明圖。 圖7是表示配置在框架的左右側面部分的試樣鋼板的 形狀的說明圖。 圖8是表示配置在框架的上面部分和底面部分的試樣 鋼板的形狀的說明圖。 -40 - (37) (37)200806468T g — 2 5 ° C ) ' No. 42 ( Tg = 60 ° C ) ' No. 43 ( Tg = 75 ° C PPIt is approximately 142 to 153, controlled in the scope of the invention (PPIt- 70) However, when comparing their resistance 値, it is obvious that the resistance 値 is basically smaller, and the conductivity tends to increase. No. 5 1 to 56 of Table 3 is a molten steel sheet used as a mineral-coated raw material sheet. In the case where the PPIt satisfies the scope of the present invention, No. 51 and 53 to 56 are excellent in electrical conductivity as compared with No. 52 which satisfies the scope of the present invention. Further, since the steel sheets are all made of a hot-dip galvanized steel sheet, electrosorption is performed. Poor. The range is as follows:) Tg- 値 値 闻 41 41 41 ( ( ( ( ( ( ( ( ( ( ( ( ( ( - - - - - - - - - - - - - - - - - - - - - - - - - - - - - An example of a cold rolled steel sheet is used for the plated raw material sheet. Among them, No. 57 to 58, 60 to 67 in which PPIt satisfies the scope of the present invention is superior in conductivity to No. 59 which does not satisfy the scope of the present invention. Further, since all of the steel sheets described above are cold-rolled steel sheets, good electromagnetic wave absorption can be obtained as compared with the case of using alloyed plated steel sheets. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a view for explaining the concept of P PI of the S A E standard. Fig. 2 is a view for explaining a method of evaluating electromagnetic wave absorption performance of a coated steel sheet. Fig. 3 is a view for explaining a state in which the amount of reflection of the input electromagnetic wave is small due to the resonance frequency of the casing. Fig. 4 is a view schematically showing a state in which electromagnetic wave absorptivity is measured. Fig. 5 is a view for explaining a method of measuring conductivity of a resin-coated metal sheet. Fig. 6 is an explanatory view showing a s u S frame (frame) constituting a casing for measuring electromagnetic wave absorptivity. Fig. 7 is an explanatory view showing the shape of a sample steel sheet disposed on the left and right side surface portions of the frame. Fig. 8 is an explanatory view showing the shape of a sample steel sheet disposed on the upper portion and the bottom portion of the frame. -40 - (37) (37)200806468

【主要元件符號說明】 1 :框體 5 :高頻環形天線 6 :同軸電纜 7 :網路分析器 -41[Main component symbol description] 1 : Frame 5 : High frequency loop antenna 6 : Coaxial cable 7 : Network analyzer -41

Claims (1)

(1) 200806468 十、申請專利範圍 1·一種樹脂塗敷金屬板,其在金屬板表面被覆樹脂皮 膜而成,其特徵在於, 上述樹脂皮膜滿足下式(1 )的必要條件, PPIt- 70 ...... ( 1 ) PPIt 表不在 SAE J91 1 -1986 中記載的 ppi(peaks Per Inch) 中’將峰値計數水準(2H)的1/2作爲樹脂皮膜的厚度 ί(μπι)時的峰-谷計數的數目。 2·如申請專利範圍第1項所記載的樹脂塗敷金屬板, 其中, 上述樹脂皮膜的玻璃轉變點(Tg)在60 °C以下。 3 .如申請專利範圍第1項所記載的樹脂塗敷金屬板, 其中, Φ 上述金屬板是鋅和鐵族元素的合金鍍覆鋼板。 4·如申請專利範圍第1〜3項中任一項所記載的樹脂 塗敷金屬板,其中, 上述金屬板是合金化熔融鍍鋅鋼板。 -42-(1) 200806468 X. Patent Application No. 1. A resin-coated metal sheet obtained by coating a resin film on a surface of a metal sheet, wherein the resin film satisfies the requirement of the following formula (1), PPIt-70. ..... (1) The PPIt table is not in the ppi (peaks Per Inch) described in SAE J91 1 -1986, when 1/2 of the peak level (2H) is used as the thickness of the resin film ί(μπι) The number of peak-to-valley counts. The resin-coated metal sheet according to the first aspect of the invention, wherein the resin film has a glass transition point (Tg) of 60 ° C or lower. The resin-coated metal sheet according to the first aspect of the invention, wherein the metal sheet is an alloy-plated steel sheet of zinc and an iron group element. The resin-coated metal sheet according to any one of claims 1 to 3, wherein the metal sheet is an alloyed hot-dip galvanized steel sheet. -42-
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