TW201006872A - Electromagnetic wave absorber containing ferric powder and preparation method thereof - Google Patents
Electromagnetic wave absorber containing ferric powder and preparation method thereof Download PDFInfo
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- TW201006872A TW201006872A TW97130103A TW97130103A TW201006872A TW 201006872 A TW201006872 A TW 201006872A TW 97130103 A TW97130103 A TW 97130103A TW 97130103 A TW97130103 A TW 97130103A TW 201006872 A TW201006872 A TW 201006872A
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- iron powder
- electromagnetic wave
- absorbing material
- wave absorbing
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- 239000006096 absorbing agent Substances 0.000 title claims abstract description 17
- 239000000843 powder Substances 0.000 title abstract description 13
- 238000002360 preparation method Methods 0.000 title abstract description 10
- 229920005989 resin Polymers 0.000 claims abstract description 24
- 239000011347 resin Substances 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 16
- 238000002156 mixing Methods 0.000 claims abstract description 16
- 239000007788 liquid Substances 0.000 claims abstract description 5
- 238000001816 cooling Methods 0.000 claims abstract description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 100
- 239000011358 absorbing material Substances 0.000 claims description 35
- 239000002245 particle Substances 0.000 claims description 11
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
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- 229920001225 polyester resin Polymers 0.000 claims description 2
- 239000004645 polyester resin Substances 0.000 claims description 2
- 239000004925 Acrylic resin Substances 0.000 claims 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 claims 1
- 241000239226 Scorpiones Species 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 235000021419 vinegar Nutrition 0.000 claims 1
- 239000000052 vinegar Substances 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 17
- 238000005516 engineering process Methods 0.000 abstract description 4
- 239000002002 slurry Substances 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 17
- 238000012360 testing method Methods 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 238000003756 stirring Methods 0.000 description 9
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 8
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- 244000132059 Carica parviflora Species 0.000 description 6
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- 239000003814 drug Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 229940079593 drug Drugs 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000001878 scanning electron micrograph Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012762 magnetic filler Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000011265 semifinished product Substances 0.000 description 2
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 241000208340 Araliaceae Species 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- PFZCZKYOFNEBAM-UHFFFAOYSA-N [Fe].[Sr] Chemical compound [Fe].[Sr] PFZCZKYOFNEBAM-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000011268 mixed slurry Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
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- 238000010998 test method Methods 0.000 description 1
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- Soft Magnetic Materials (AREA)
- Shielding Devices Or Components To Electric Or Magnetic Fields (AREA)
Abstract
Description
201006872 九、發明說明: 【發明所屬之技術領域】 本發明係有關於一種電磁波吸收物及其製備方法,特別是指一種含鐵 粉之電磁波吸收物及其製備方法,其係應用於吸收電磁波之領域。 【先前技術】 中華民國專利469283中申明之介電性電磁波吸收材枓之製造方法是於 液態聚胺基甲酸脂(PU)樹脂中添加導電碳黑、碳粉、導電纖維及中空玻璃 參球(microballoons),經兩階段特殊裝置混合成漿狀半成品,再將半成品以 適當模具製成電磁波吸收材,但該製造方法因混合後之藥漿(slurry)黏度 大首先以樹脂混合部份碳黑以特殊設計的3〇〇〇_6〇〇〇rpm高速研磨機分散, 再添加碳粉、導電纖維及中空球此時藥漿黏度大增,改用3〇〇_6〇〇rpm低速 高黏度攪拌機充分混合後再塗佈成試片,具有製程及設備較繁複之缺點。 中華民國專利567643中申明之改良型Salisbury Screen式電磁波吸收材 其中第一層為電性均質耗損材,第二層為低介電常數材以兩種材料複合成 再加上反射層組合成之電磁波吸收材,但由於其為三層材料,故在製作上 比單層材料之製程繁複。中華民國專利566077中申明以多層中空碳球含量 ❿ 5-50wt%混合樹脂製成電磁波吸收材,但目前多層中空碳球多為實驗室產 品’價格高,也不符合大量生產之需求。201006872 IX. Description of the Invention: [Technical Field] The present invention relates to an electromagnetic wave absorbing material and a preparation method thereof, and particularly to an electromagnetic wave absorbing material containing iron powder and a preparation method thereof, which are applied to absorbing electromagnetic waves field. [Prior Art] The manufacturing method of the dielectric electromagnetic wave absorbing material described in the Republic of China Patent No. 469283 is to add conductive carbon black, carbon powder, conductive fibers, and hollow glass ginseng balls to a liquid polyurethane resin (PU) resin. Microballoons), which are mixed into a slurry semi-finished product by a two-stage special device, and then the semi-finished product is made into an electromagnetic wave absorbing material by a suitable mold, but the manufacturing method is mainly because the viscosity of the mixed slurry is first mixed with the resin by the resin. Specially designed 3〇〇〇_6〇〇〇rpm high-speed grinding machine disperses, then add carbon powder, conductive fiber and hollow ball. At this time, the viscosity of the slurry is greatly increased, and the low-speed high-viscosity mixer with 3〇〇_6〇〇rpm is used instead. After fully mixing, it is coated into a test piece, which has the disadvantages of complicated process and equipment. The improved Salisbury Screen type electromagnetic wave absorbing material declared in the Republic of China Patent No. 567643, wherein the first layer is an electrically homogeneous lossy material, and the second layer is a low dielectric constant material which is a composite of two materials and an electromagnetic wave combined with a reflective layer. Absorbent material, but because it is a three-layer material, it is more complicated to manufacture than a single-layer material. The Republic of China Patent No. 566077 states that electromagnetic wave absorbing materials are made of multi-layer hollow carbon spheres ❿ 5-50wt% mixed resin, but currently multi-layer hollow carbon spheres are mostly laboratory products, which are expensive and do not meet the needs of mass production.
且目前一些電磁波吸收材使用之鐵粉主要為球狀之羰基鐵粉,平均粒 徑約1-10 Microns,鐵粉比重高且球狀鐵粉的視密度大,在含球狀鐵粉的 電磁波吸收材配方裡鐵粉添加置要大於7〇%重量百分比才能做出具1〇册反 射損失的材料,因此造成電磁波吸收材單位面積重量太高,不人 技產業對材料輕、薄之需求。 Q 綜合上述,本發明人提供一種含鐵粉之電磁波吸收物及其製備方法, 其能解決習知技術製程及設備較繁複、價格高不符合大量生產之需求及電 磁波吸收材單位面積重量太高,不符合科技產業對材料輕、薄之需求的缺 201006872At present, the iron powder used in some electromagnetic wave absorbing materials is mainly spherical carbonyl iron powder, the average particle diameter is about 1-10 Microns, the iron powder has a high specific gravity and the spherical iron powder has a large apparent density, and the electromagnetic wave containing the spherical iron powder. In the formula of the absorbent material, the iron powder is added to be more than 7% by weight to make a material with a loss of reflection of the book. Therefore, the weight per unit area of the electromagnetic wave absorbing material is too high, and the demand for the material is light and thin. Q In summary, the present inventors provide an electromagnetic wave absorbing material containing iron powder and a preparation method thereof, which can solve the complicated process and equipment of the prior art, the high price does not meet the demand of mass production, and the unit weight of the electromagnetic wave absorbing material is too high. , does not meet the lack of demand for light and thin materials in the technology industry 201006872
【發明内容】 法 輕、薄之需求。 本發明之轉目的’在雜供—種含輸之電磁波魏滅其製備方 ’該含鐵粉之電磁波吸收物單位面積重量較低,故能敲科技產業材料 本發明之另-目的’在於提供—種含鐵粉之電磁舰㈣及其製備方 法,該含鐵粉之電磁波吸收物之製備方法具有製程及所需設備簡單之優點。 ❹[Summary of the Invention] The demand for light and thin. The object of the present invention is that the electromagnetic wave absorbing material of the iron-containing powder has a low basis weight, so that it can knock the technology industry material, and the other object of the present invention is to provide An electromagnetic ship (four) containing iron powder and a preparation method thereof, the preparation method of the electromagnetic wave absorber containing iron powder has the advantages of a simple process and a required equipment. ❹
、土 之又一目的’在於提供一種含鐵粉之電磁波吸收物及其製備方 法,其價格較低,故能符合大量生產之需求。 本發明提供-種含麟之電雜做物及其製财法。該含鐵粉之 磁波吸收物’其包括:4G~7G重量百分率之樹脂;及別,重量百分 率之鐵粉;其中該鐵粉之視密度為0. 5〜0. 8 g/cc。 該含鐵粉之電磁波吸㈣之製備紐,脉驟包括:⑴紐態樹脂和 鐵粉混合均勻,及⑵熟化冷卻後,即得到含鐵粉之電磁波吸收物;其 中該鐵粉之視密度為〇. 5〜〇. 8 g/cc。 茲為使貴審查委員對本發明之技術特徵及所達成之功效更有進一步 之瞭解與涊識,謹佐以較佳之實施例圖及配合詳細之說明,說明如後: 【實施方式】 本發明含鐵粉之電磁波吸收物,其包括:4〇〜7〇重量百分率之樹 脂;及30〜60重量百分率之鐵粉。 其中該鐵粉為珊瑚狀或鹿角狀’該鐵粉之視密度為〇5〜〇.8 g/cc 及該鐵粉之平均粒徑為30〜60μηι。該鐵粉之較佳視密度為0.53 g/cc及 較佳之平均粒徑為43.0μιη。 其中該樹脂係選自環氧樹脂、聚胺基曱酸脂樹脂、聚甲基丙烯酸 酯樹脂、矽樹脂及聚酯樹脂所組成之群組之其中之一者。且鵁鐵粉較 201006872 佳之重量百分率為42〜50%。 ’其步驟包括(如第一 本發明含鐵粉之電磁波吸收物之製備方法 圖所示): S11將液態樹脂和鐵粉混合均勻得到含鐵粉之電磁波吸收組成 物;及 S12熟化冷卻後,即得到含鐵粉之電磁波吸收物。 其中該鐵粉為珊瑚狀或鹿角狀。Another purpose of the soil is to provide an electromagnetic wave absorbing material containing iron powder and a preparation method thereof, which are low in price and can meet the demand for mass production. The invention provides a kind of electric hybrid material containing Lin and its method of making money. 5 克。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。. The preparation of the electromagnetic powder containing iron powder (4) includes: (1) uniformly mixing the resin and the iron powder, and (2) obtaining the electromagnetic wave absorption product containing the iron powder after the cooling is matured; wherein the apparent density of the iron powder is 〇. 5~〇. 8 g/cc. For a better understanding and understanding of the technical features and the efficacies of the present invention, the preferred embodiments and the detailed description are as follows: [Embodiment] The present invention includes An electromagnetic wave absorber of iron powder comprising: 4 〇 to 7 〇 by weight of a resin; and 30 to 60% by weight of iron powder. The iron powder is coral-like or staghorn-shaped. The apparent density of the iron powder is 〇5 to 8.8 g/cc and the average particle diameter of the iron powder is 30 to 60 μm. The iron powder preferably has an apparent density of 0.53 g/cc and preferably has an average particle diameter of 43.0 μm. The resin is one selected from the group consisting of epoxy resins, polyamine phthalic acid resins, polymethacrylate resins, enamel resins, and polyester resins. And the weight percentage of strontium iron powder is better than 201006872, which is 42~50%. 'The steps thereof include (as shown in the first method for preparing an electromagnetic wave absorber containing iron powder according to the present invention): S11 is a mixture of a liquid resin and an iron powder to obtain an electromagnetic wave absorbing composition containing iron powder; and S12 is matured and cooled. That is, an electromagnetic wave absorbing material containing iron powder is obtained. The iron powder is coral or staghorn.
❿ 其中該含鐵粉之電磁波吸收物包括4〇〜7〇重量百分率之樹脂及 30-60重量百分率之鐵粉。 其中步驟sn後更包括一灌入模具之步驟。 其中該含鐵粉之電磁波吸收物之厚度為0.5〜5.0_,且在2〜18GHZ 之頻率範圍具有10dB以上之反射損失。 其中該含鐵粉之電磁波吸收物之較佳厚度為 實施例及比較例 本發明使用之珊瑚狀鐵粉其SEM圖像如第二圖所示,製作方法為 以草酸鐵絲料於娜〜⑹此减氣_ 2〜4小_得,外觀形狀如珊 瑚或鹿角之長條多肖狀’視密度為0.5〜G.8gAx,以CGulterLS-230雷射 粒徑分析儀測量,平均粒徑為3〇〜6〇μιη。 本發明之較佳實施例於環氧樹脂中添加珊瑚狀鐵粉(本發明所製作 的原料產品,編號Τ2,視密度〇.53g/cc,平均粒徑43·0μπι)及比較例係 於環氧樹脂中添加羰基鐵粉作填料,再以一般三滾筒機(滾筒之間隙為 0· 1mm)來混料使藥漿混合均勻後,將藥漿倒入1 $ cmx 1 $ cm金屬模子中, 上下放鋁板,以夾子夾住,以80°C烘2小時後取出,冷卻後除去鋁板 將電磁波吸收材成品取出,經修飾後量測厚度、重量。 微波反射損失(Return Loss)量測方法採用自由空間(free space)測試 法’頻率範圍(2-18GHz),使用微波網路分析儀Hp 8722ES及Damaskos 公司free space量測夹具’以相同試片大小15cmxl5cm金屬片$上待測 201006872 位置’先校正水平,調整天線入射角度(21。)測原始反射量,接著換試片 並以該金屬片當反射面再量測試片之反射損失衰減強度,反射損失愈大 代表電磁波吸收效果愈好。 為更詳細描述本發明,以下特舉幾個實施例及比較例說明如後。表 一為本發明實施例及比較例使用之磁性填充料的來源及規格: 表一本發明實施例及比較例使用之磁性填充料 品名 來源 規格 珊瑚狀鐵 粉 本發明所製作 平均粒徑:43.0 Microns 視密度:0.53 g/cc 羰基鐵粉 (S3700) 美 International Specialty Products 公司 平均粒徑:2.5 microns 視密度:2.5g/cc 實施例1 將50.0g液態環氧樹脂及珊瑚狀鐵粉5〇 〇g加入25〇ml混料容器 總配料量IGGg),先以勝棒勝丨_2分鐘,再以—般三滾筒機來 此料5次使藥漿混合均勻後,取7〇 〇g藥聚,將藥聚倒入 ❿em金屬鮮巾’以8G°C供2小時後取$則,經修飾後量測重量為 6曰〇.〇g ’厚度為LW ’單位面積重量為2 7Kg/_,微波反射損失 里測如第二圖所不’兩峰值在1G()GH2,其反射損失為144册。 比較例1 將6〇.〇g液態環氧樹脂及幾基鐵粉M〇 〇g加入25編混料容器中(總配 =量200g) ’先以麟棒赫μ2分鐘伽一般三滾筒機來混料$次使藥 漿混合均勻後,取130.0g藥聚,將藥聚倒入15 ·ΐ5⑽金屬模子中,以 8〇 C烘2小時後取出試片,經修飾後量剛重量為ii3 〇g,厚度為2力麵,單 位面積重量為5.GKg/mxm,微波反射損失量測如第四_示,高峰值在 10-lGHz,其反射損失為15 6dB。 201006872 _ 實施例2 將58.0g液態環氧樹脂及珊瑚狀鐵粉42 〇g加入25〇ml混料容器中(總 配料量100g) ’先以攪拌棒攪拌1-2分鐘,再以一般三滾筒機來混料5次使 藥漿混合均勻後’取500g藥漿’將藥漿倒入15 cmxl5 cm金屬模子中,以 8〇°C供2小時後取出試片,經修飾後量測重量為44.0g,厚度為l.lmm,單 位面積重量為2.0Kg/mxm,微波反射損失量測如第五圖所示,高峰值在 14.4GHz,其反射損失為16 4dB。 比較例2 φ 將30.0g液態環氧樹脂及羰基鐵粉7〇.〇g加入250ml混料容器中(總配 料量100g),先以攪拌棒攪拌丨_2分鐘,再以一般三滾筒機來混料5次使藥 漿混合均勻後,取85.0g藥漿,將藥漿倒入丨5 cmx 15 cm金屬模子中,以8〇t>c 烘2小時後取出試片,經修飾後量測重量為75 〇g ,厚度為12mm,單位面 積重量為3.3Kg/mxm,微波反射損失量測如第六圖所示,高峰值在 15.2GHz,其反射損失為15.ldB。 實施例3 將100.〇g液態環氧樹脂及珊蝴狀鐵粉lOO.Og加入250ml混料容器中(總 配料量200g),先以攪拌棒攪拌丨_2分鐘,再以一般三滾筒機來混料$次使 φ 藥漿混合均勻後,取130.〇g藥漿,將藥漿倒入15 cm><15 cm金屬模子中,以 80°C烘2小時後取出試片,經修飾後量測重量為113 〇g,厚度為2 5mm , 單位面積重量為5.0Kg/mxm,微波反射損失量測如第七圖所示,高峰值在 6.0GHz,其反射損失為23.8dB。 比較例3 將60.0g液態環氧樹脂及羰基鐵粉14〇 〇g加入25〇ml混料容器中(總配 料量200g),先以攪拌棒攪拌丨_2分鐘,再以一般三滚筒機來混料5次使藥 漿混合均勻後,取185.0g藥漿,將藥漿倒入15 cmxl5 cm金屬模子中,以 80°C烘2小時後取出試片,經修飾後量測重量為178 〇g,厚度為3 〇mm, 單位面積重量為7.9Kg/mxm,微波反射損失量測如第八圖所示,高峰值在 201006872 6.0GHz ’其反射損失為11 9dB。 實施例4 將l〇〇.〇g液態環氧樹脂及珊蝴狀鐵粉lOO.Og加入250ml混料容器中(總 配料量20〇g),先以攪拌棒攪拌1-2分鐘,再以一般三滚筒機來混料5次使 藥漿混合均勻後’取194.0g藥漿,將藥漿倒入15 cmx 15 cm金屬模子中,以 80°C烘2小時後取出試片,經修飾後量測重量為1804g,厚度為44mm, 單位面積重量為8.0Kg/mxm,微波反射損失量測如第九圖所示,高峰值在 3.0GHz,其反射損失為i4.5dB。 比較例4 將120.0g液態環氧樹脂及羰基鐵粉28〇.〇g加入500m卜混料容器中(總 配料量40〇g) ’先以攪拌棒攪拌1-2分鐘’再以一般三滚筒機來混料5次使 藥漿混合均勻後,取360.0g藥漿,將藥漿倒入15 cmxl5 cm金屬模子中,以 80°C烘2小時後取出試片,經修飾後量測重量為344 〇g,厚度為62mm, 單位面積重量為15_3Kg/mxm ’微波反射損失量測如第十圖所示,高峰值在 3*0GHz ’其反射損失為14.2dB。 表二至表五為本發明上述之實施例與比較例及英國BAE公司產品在 X(8-12GHz),Ku(12-18GHz),C(4-8GHz),S(2-4GHz)相同頻段^的比較 表’由表中發現在相同的頻段下實施例試片之反射損失近似或大於比較 例試片之反射損失,顯示本發明含鐵粉之電磁波吸收物具有較佳的電磁 波吸收效果,且實施例試片的厚度及單位面積重皆較比較例試片小許 夕,又,本發明實施例試片和BAE公司產品比較除s頻段厚度稍大外其 餘厚度及單位面積重皆優於BAE公司產品。 201006872 ❿❿ The electromagnetic wave absorbing material of the iron powder comprises 4 〇 to 7 〇 by weight of the resin and 30 to 60% by weight of the iron powder. The step sn further includes a step of filling the mold. The electromagnetic wave absorbing material of the iron powder has a thickness of 0.5 to 5.0 Å and a reflection loss of 10 dB or more in a frequency range of 2 to 18 GHz. The preferred thickness of the electromagnetic wave absorbing material containing the iron powder is the SEM image of the coral iron powder used in the present invention. The SEM image is as shown in the second figure, and the method is as follows: Deflated _ 2 ~ 4 small _ get, the appearance of the shape such as coral or antler strips more than the shape of the visual density of 0.5 ~ G.8gAx, measured by the CGulterLS-230 laser particle size analyzer, the average particle size of 3 〇 ~6〇μιη. In a preferred embodiment of the present invention, a coral-like iron powder (a raw material produced by the present invention, No. 2, apparent density 〇.53 g/cc, average particle diameter 43·0 μπι) and a comparative example are attached to the epoxy resin. Add carbonyl iron powder as a filler to the oxygen resin, and then mix the slurry with a general three-roller machine (the gap of the roller is 0·1 mm), and then pour the slurry into a metal mold of 1 $ cmx 1 $ cm. The aluminum plate was placed up and down, clamped with a clip, and baked at 80 ° C for 2 hours, and then taken out. After cooling, the aluminum plate was removed to take out the electromagnetic wave absorbing material, and the thickness and weight were measured after modification. The microwave loss loss (Return Loss) measurement method uses the free space test method 'frequency range (2-18 GHz), using the microwave network analyzer Hp 8722ES and the Damaskos free space measurement fixture 'with the same test piece size 15cmxl5cm metal piece on the test 201006872 position 'first correction level, adjust the antenna incident angle (21.) to measure the original reflection amount, then change the test piece and use the metal piece as the reflection surface to re-measure the reflection loss attenuation intensity of the test piece, reflection The greater the loss, the better the electromagnetic wave absorption effect. In order to describe the present invention in more detail, the following specific examples and comparative examples are described below. Table 1 shows the source and specifications of the magnetic filler used in the examples and comparative examples of the present invention: Table 1 Magnetic fillers used in the examples and comparative examples of the present invention. Source name Coral iron powder The average particle diameter of the invention is 43.0. Microns apparent density: 0.53 g/cc carbonyl iron powder (S3700) US International Specialty Products company average particle size: 2.5 microns apparent density: 2.5g/cc Example 1 50.0g liquid epoxy resin and coral iron powder 5〇〇 g Add 25 〇ml mixing container total amount of IGGg), first win _2 minutes with the winning stick, then use the same three-roller machine to make the material mix 5 times, then take 7 〇〇g medicine Pour the medicine into the ❿em metal fresh towel' for 8 hours at 8G °C, and then measure the weight to 6 曰〇. 〇g 'thickness is LW' unit area weight is 2 7Kg / _, The microwave reflection loss is measured as shown in the second figure. The two peaks are at 1G() GH2, and the reflection loss is 144. Comparative Example 1 Add 6 〇.〇g liquid epoxy resin and several base iron powder M〇〇g to 25-mixed mixing container (total = 200g) 'Firstly, with a lininger 2 minute gamma general three-roller After mixing the drug for 10 times, take 130.0 g of the drug, collect the drug into a 15 · 5 (10) metal mold, and bake at 8 ° C for 2 hours, then take out the test piece. After modification, the weight is ii3 〇 g, the thickness is 2 force surface, the weight per unit area is 5.GKg/mxm, the microwave reflection loss measurement is as shown in the fourth figure, the high peak is at 10 lGHz, and the reflection loss is 15 6 dB. 201006872 _ Example 2 Add 58.0g liquid epoxy resin and coral iron powder 42 〇g to 25〇ml mixing container (total dosage 100g) 'First stir with stirring rod for 1-2 minutes, then use general three roller After the machine is mixed for 5 times, the slurry is evenly mixed, and then the sample is taken into a 15 cm x 15 cm metal mold. The sample is taken at 8 ° C for 2 hours, and the test piece is taken out. 44.0g, thickness llmm, weight per unit area is 2.0Kg/mxm, microwave reflection loss measurement as shown in the fifth figure, high peak at 14.4GHz, and its reflection loss is 16 4dB. Comparative Example 2 φ 30.0g of liquid epoxy resin and carbonyl iron powder 7〇.〇g were added to a 250ml mixing container (total amount of 100g), first stirred with a stir bar for _2 minutes, then with a general three-roller machine After mixing the mixture for 5 times, 85.0 g of the slurry was taken, and the slurry was poured into a 5 cm x 15 cm metal mold, and baked for 8 hours at 8 〇t>c, and the test piece was taken out and measured. The weight is 75 〇g, the thickness is 12mm, and the weight per unit area is 3.3Kg/mxm. The microwave reflection loss is measured as shown in the sixth figure. The high peak is at 15.2GHz and the reflection loss is 15.ldB. Example 3 100. 〇g liquid epoxy resin and mushroom iron powder 100.Og was added to a 250ml mixing container (total dosage of 200g), first stirred with a stir bar for _2 minutes, then with a general three-roller After mixing the φ slurry for a uniform time, take 130. 〇g of the slurry, pour the slurry into a 15 cm><15 cm metal mold, and dry at 80 °C for 2 hours, then take out the test piece. After the modification, the measured weight was 113 〇g, the thickness was 25 mm, and the weight per unit area was 5.0 Kg/mxm. The microwave reflection loss was measured as shown in the seventh figure, and the high peak was at 6.0 GHz, and the reflection loss was 23.8 dB. Comparative Example 3 60.0 g of liquid epoxy resin and 14 gram of carbonyl iron powder were added to a 25 〇ml mixing container (total amount of 200 g), first stirred with a stir bar for _2 minutes, and then with a general three-roller machine. After mixing the mixture for 5 times, 185.0 g of the slurry was taken, and the slurry was poured into a 15 cm x 15 cm metal mold, and the test piece was taken out after drying at 80 ° C for 2 hours. After the modification, the measured weight was 178 〇. g, the thickness is 3 〇mm, the weight per unit area is 7.9Kg/mxm, the microwave reflection loss is measured as shown in the eighth figure, and the high peak at 201006872 6.0GHz 'the reflection loss is 11 9dB. Example 4 Add l〇〇.〇g liquid epoxy resin and butterfly iron powder 100.Og into a 250ml mixing container (total dosage of 20〇g), first stir with a stir bar for 1-2 minutes, then Generally, the three-roller machine mixes the mixture 5 times to make the slurry evenly mixed, then take 194.0 g of the slurry, pour the slurry into a 15 cm x 15 cm metal mold, and dry it at 80 ° C for 2 hours, then take out the test piece and modify it. The measured weight was 1804 g, the thickness was 44 mm, the weight per unit area was 8.0 Kg/mxm, and the microwave reflection loss measurement was as shown in the ninth figure. The high peak value was 3.0 GHz, and the reflection loss was i4.5 dB. Comparative Example 4 120.0 g of liquid epoxy resin and carbonyl iron powder 28 〇.〇g were added to a 500 m mixing container (total amount of 40 〇g) 'First stir with a stirring bar for 1-2 minutes' and then with a general three roller After the machine was mixed 5 times to mix the slurry evenly, 360.0 g of the slurry was taken, and the slurry was poured into a 15 cm x 15 cm metal mold, and the test piece was taken out after drying at 80 ° C for 2 hours. After the modification, the weight was measured. 344 〇g, thickness 62mm, weight per unit area 15_3Kg/mxm 'The microwave reflection loss measurement is shown in the tenth figure, and the high peak value is 3*0GHz' and its reflection loss is 14.2dB. Tables 2 to 5 show the above-mentioned embodiments and comparative examples of the present invention and the British BAE products in the same frequency band of X (8-12 GHz), Ku (12-18 GHz), C (4-8 GHz), S (2-4 GHz). The comparison table of ^ is found in the table to show that the reflection loss of the test piece in the same frequency band is similar to or larger than the reflection loss of the test piece of the comparative example, and the electromagnetic wave absorption product containing the iron powder of the present invention has a better electromagnetic wave absorption effect. Moreover, the thickness and the unit area weight of the test piece are smaller than those of the comparative test piece, and the thickness of the test piece and the BAE company of the embodiment of the present invention are superior to those of the BAE company except that the thickness of the s-band is slightly larger. BAE products. 201006872 ❿
表二實施例1與吃整里丄及BAE公司產品比較表 實施例1 比較例1 BAE公司型號WMX3 厚度(mm) 1.5 2.0 2.3 單位面積重(Kg/mxm) 2.7 5.0 7.3 反射損失高峰值 (GHz/dB) 10.0/14.4 —------ 10.1/15.6 — 頻段 ------__ X X 表三實施例2與比較例2及BAE公司產品比較表 實施例1 比較例1 BAE公司型號WMX3 厚度(mm) 1.1 1.2 2.0 單位面積重(Kg/mxm) 2.0 3.3 6.0 反射損失高峰值 (GHz/dB) 14.4/16.4 —-一 ·_. — · 15.2/15.1 — 頻段 Ku Ku Ku 表四實施例3 J 3^BAE公司產品比較表 實施例1 比較例1 BAE公司型號WMX3 厚度(mm) 2.5 〜 3.0 3.3 單位面積重(Kg/mxm) 5.0 7.9 15.5 反射損失高峰值 (GHz/dB) 6.0/23.8 ^' 6.0/11.9 — 頻段 C C C 表五實施例4 J 契比較例4及BAE公司產r 右比較表 貫施例1 比較例1 BAE公司型號WMX3 厚度(mm) 4.4 6.2 3.8 單位面積重(Kg/mxm) 8.0 15.3 17.0 反射損失高每值 (GHz/dB) 頻段 3.0/14.5、^ 3.0/14.2 ~S ~ S 綜上所述,本發明具有以下之優點: 本發明含鐵粉之電磁奴收物單位面積重低,缝騎·科技產業材 201006872 料輕、薄之需求。 2·:輪饱祕㈣驗細伽嫩備簡單之 價格低i鐵電磁波魏物及其製備方法,*紐财线球,故其 價格低廉,能符合大量生產之需求。 國車!為—具雜酿、進步性料供«上桐者,應符合我 准專利,至感為3要件無疑,轰依法提出發明專利申請,祈均局早曰賜Table 2 Comparison of Example 1 with Eater and BAE Company Example 1 Comparative Example 1 BAE Model WMX3 Thickness (mm) 1.5 2.0 2.3 Unit Weight (Kg/mxm) 2.7 5.0 7.3 High Reflection Peak Loss (GHz /dB) 10.0/14.4 —------ 10.1/15.6 — Band ------__ XX Table 3 Example 2 and Comparative Example 2 and BAE Company Product Comparison Table Example 1 Comparison Example 1 BAE Model WMX3 Thickness (mm) 1.1 1.2 2.0 Weight per unit area (Kg/mxm) 2.0 3.3 6.0 High peak value of reflection loss (GHz/dB) 14.4/16.4 —-一·_. — · 15.2/15.1 — Band Ku Ku Ku Table 4 Implementation Example 3 J 3^BAE product comparison table Example 1 Comparative example 1 BAE company model WMX3 Thickness (mm) 2.5 ~ 3.0 3.3 Unit weight (Kg/mxm) 5.0 7.9 15.5 High reflection loss peak (GHz/dB) 6.0/ 23.8 ^' 6.0/11.9 - Band CCC Table 5 Example 4 J Comparison Example 4 and BAE Company r Right Comparison Table 1 Comparison Example 1 BAE Model WMX3 Thickness (mm) 4.4 6.2 3.8 Unit Weight (Kg /mxm) 8.0 15.3 17.0 High reflection loss per value (GHz/dB) Band 3.0/14.5, ^ 3.0/14.2 ~S ~ S In summary, the present invention The following advantages: the present invention contain iron slave electromagnetic closing weight per unit area was low, the seam ride-technology industry materials 201,006,872 material lighter, thinner demand. 2·: Round full of secrets (four) inspection fine Gane tender simple price low i iron electromagnetic wave Weiwu and its preparation method, * New Zealand line ball, so its low price, can meet the needs of mass production. National car! For the stuffy, progressive material supply «On the Tong, should meet my quasi-patent, to the sense of 3 elements undoubtedly, blasting the invention patent application, praying for the Bureau
"淮以上所述纟’僅為本發明較佳實施例而已,並非用來限定本發明實 範圍故舉凡依本發明申請專利範圍所述之特徵及精神所為之均等變 化與修飾,均應包括於本發明之憎專纖圍内。 【圖式簡單說明】 第-圖為本發明含鐵粉之電磁波魏物之製備方法之步驟流程圖。 第二圖本發明鐵粉呈珊瑚狀之SEM圖。 第三圖為本發明實關丨之麵粉之電磁纽收物樣波反射損失 特性圖。 第四圖為本發_較例1之含縣鐵粉之電磁波吸收物之微波反射 損失特性圖。 第五圖為本發明實施例2之含鐵粉之電磁波吸收物之微波反射損失 特性圖。 第六圖為本發明比較例2之含羰基鐵粉之電磁波吸收物之微波反射 損失特性圖。 第七圖為本發明實施例3之含鐵粉之電磁波吸收物之微波反射損失 特性圖。 第八圖為本發明比較例3之含羰基鐵粉之電磁波吸收物之微波反射 損失特性圖。 12 201006872 第九圖為本發明實施例4之含鐵粉之電磁波吸收物之微波反射損失 特性圖。 第十圖為本發明比較例4之含羰基鐵粉之電磁波吸收物之微波反射 損失特性圖。 【主要元件符號說明】 無 ❹The above description is only for the preferred embodiment of the present invention, and is not intended to limit the scope of the present invention, and the equivalents and modifications of the features and spirits described in the claims of the present invention should be included. In the 憎 special fiber circumference of the present invention. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a flow chart showing the steps of a method for preparing an electromagnetic wave containing iron powder according to the present invention. The second figure shows the SEM image of the iron powder of the present invention. The third figure is a characteristic diagram of the sample wave reflection loss of the electromagnetic contact of the flour of the present invention. The fourth graph is a microwave reflection loss characteristic diagram of the electromagnetic wave absorber of the iron powder containing the iron powder of the present invention. Fig. 5 is a graph showing the microwave reflection loss characteristics of the electromagnetic wave absorber containing iron powder according to Example 2 of the present invention. Fig. 6 is a graph showing the microwave reflection loss characteristics of the electromagnetic wave absorbing material containing carbonyl iron powder of Comparative Example 2 of the present invention. Fig. 7 is a graph showing the microwave reflection loss characteristics of the electromagnetic wave absorbing material containing iron powder according to Example 3 of the present invention. Fig. 8 is a graph showing the microwave reflection loss characteristics of the electromagnetic wave absorbing material containing carbonyl iron powder of Comparative Example 3 of the present invention. 12 201006872 The ninth graph is a graph showing the microwave reflection loss of the electromagnetic wave absorber containing iron powder according to Example 4 of the present invention. Fig. 10 is a graph showing the microwave reflection loss characteristics of the electromagnetic wave absorbing material containing carbonyl iron powder of Comparative Example 4 of the present invention. [Main component symbol description] None ❹
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| JP2006505483A (en) * | 2002-11-26 | 2006-02-16 | カーボン ナノテクノロジーズ インコーポレーテッド | Carbon nanotube fine particles, composition and method of use thereof |
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