TW201726B - - Google Patents

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TW201726B
TW201726B TW80103477A TW80103477A TW201726B TW 201726 B TW201726 B TW 201726B TW 80103477 A TW80103477 A TW 80103477A TW 80103477 A TW80103477 A TW 80103477A TW 201726 B TW201726 B TW 201726B
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Taiwan
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composition
powder
polymer
item
component
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TW80103477A
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Chinese (zh)
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Dai Ichi Kogyo Seiyaku Co Ltd
Daiichi Sairamo Kk
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Priority claimed from JP1287708A external-priority patent/JPH03150257A/en
Application filed by Dai Ichi Kogyo Seiyaku Co Ltd, Daiichi Sairamo Kk filed Critical Dai Ichi Kogyo Seiyaku Co Ltd
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Publication of TW201726B publication Critical patent/TW201726B/zh

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Description

A6 B6 £01*726 五、發明説明() 本發明係有關一種製備燒結體的可射出壓縮組合物, 該組合物含有一種無機粉末及一種特定之有機接著劑;特 別言之,本發明之可射出壓縮組合物具有良好之可射出壓 縮性並且於燒結中自壓縮初胚移去接著劑的性能良好,使 得生成之燒結體幾乎不會產生如翹曲和破裂之缺陷,且於 高產出時具有良好的結構穩定性;本發明亦有關於由該組 合物製備形成的燒結體。 燒結體係將無機粉末和有機接著劑之混合物壓縮再予 Μ燒結;近年來,陶瓷界製備陶瓷產物係先将陶瓷粉末和 有機接著劑混合,使混合物具有可塑性,再將之射出壓縮 形成壓縮初胚,移去接箸劑並予Μ燒结;該陶瓷產物逐漸 應用於汽車之引擎零件上,並且其具有的特色是部分複雜 形狀之產物能於工業上大量生產製造。 有機接箸劑和陶瓷粉末之均勻分散性有關,此外亦和 與其混合之粉末流動性、壓縮初胚之強度,以及自緣色壓 縮睡移去接著劑的容易性(接著劑去除性)有關;因此, 如果不適當選擇接著劑之棰類和用量,則不能生成良好之 燒結體,舉例來說,如果陶瓷粉末不能在有機接著劑中充 分均勻分散,產生的壓缩體或燒結體很容易發生如翹曲和 破裂之缺陷,同時壓编體的強度亦會降低;同時,如果有 機接著劑具有差的熱穩定性,其會於射出模製機的圓柱内 變質,並且壓縮組合物的流動性不穩定,於是不能產生良 好之射出壓縮體,有時陶瓷粉末和有機接著劑甚至會分離 ;如果使用過量接著劑,則很難避免發泡和破裂的產生, 表紙張尺茂適用中國國家標準(CNS)甲.1規格(210 X 297公騖) _ 3 - 81.9.25,000 (請先閲讀背面之注意事項再填寫本頁) .裝_ 訂 經濟部中央標準局員工消費合作社印皙 經濟部中央標準局员工消費合作社印製 A6 B6__ 五、發明説明() 此係因爲於移去接著劑的步驟中壓縮體內部產生大量之氣 aat» 體0 使用於壓縮陶瓷粉末之有機接箸劑沿用的有锻類和聚 合體、聚合體包括如乙烯-丙烯酸乙酯共聚物(EVA)、聚 苯乙烯、不規則聚丙烯(APP〉、聚乙烯以及丙烯酸和甲基 丙烯酸聚合體;製備燒結體之有機接著劑須具有良好之待 性如可壓縮性(如壓縮穩定性、模型釋出特性Μ及無機粉 末和接箸劑結合時之粉末滾動性)、壓縮初胚之強度、燒 結前熱分解壓縮初胚之接著劑去除性,以及烧結時之形狀 維持性和所殘留之破量,但是,該接著劑各有其®缺點, 並不能皆符合上述吾人所需之待性。 一般而言,聚合物接箸劑具有較佳之可壓缩性,但是 具有較差之去除性,舉例來說,乙烯-乙酸乙烯酯共聚物 (EVA)具有優良的粉末流動性,並使形成的壓縮髏具有高 強度,酋其與陶瓷粉末混合時具有適當的可塑性且不損其 流動性;但是,當策熱分解移去壓縮體中之接著劑時,於 2001會有乙酸氣體產生使得發泡和破裂之現嫌易於產生 Ο 類似於EVA乙烯-丙烯酸乙酯共聚物亦具有高強度, 且其與陶瓷粉末或金羼粉末混合時壓缩體具有適當的可塑 性且不損其流動性;但是,如果其大量使用時,吾人在利 用熱分解法移除接著劑時,壓縮物會產生明顯的發泡現象 和裂痕,因此,欲移除接著劑而不損及壓縮物是非常固難 的。同時,聚苯乙烯、丙烯酸和甲基丙烯睃聚合物(如聚 用中國國家橒準(CNS)甲4规格(210 X 297公兑) _ 4 _ 81-9.25,000 (請先閲讀背面之注意事項再塡寫本頁) 裝_ 訂. 201726 經濟部中央標準局員工消費合作社印髮 A6 B6 五、發明説明() 甲基丙烯酸異丁酯)和陶瓷粉末及金屬粉末亦具有優良之 接著效果,且形成的壓编初胚具有高的強度;持別而言, 它們可有效防止薄層部分損傷,並使壓縮初胚維持優良的 形狀;該接著劑亦具有優秀的熱分解性,使其較易脫離壓 縮體;但是,當其大量使用時,其與金属粉末形成的混合 物具有較差的流動性,並且於射出模製時會產生填料的短 缺和焊接線。 不規則聚丙烯和陶瓷粉末混合物具有良好之流動性; 並且較易射出模製,生成之K縮初胚具有足夠的強度便於 處理(日本專利申請Kokoku第51-29170號);但是,其在 接箸劑去除性方面較差。 蠟類接著劑如石蟠和聚合物接著劑相比,具有較佳的 去除性,但是其於高壓下流動性不穩定,使其可射出壓縮 性較差;並且由於其係較低分子量之化合物,得到的壓縮 初胚強度較低。 為了得到令人滿意性質的接著劑,因此吾人將具有不 同性質接著劑二或多棰以良好的分配比例結合,但是由於 該些接著劑具有不同的型式和軟化點,並且其溶解性和兼 容性亦不能令人滿意,使得不能得到均勻之混合物,或者 需要棰長的混合時間;一般而言,如果將二或多種接著劑 混合而不足以形成均勻混合物,則需要花費較多的時間決 定壓縮條件,因爲混合物的流動性不安定;同時,因為形 成的壓縮物均勻性不一,則使用非均勻之接箸劑混合物易 引起燒結體的破裂並影道壓縮體結構的穩定。 (請先閲讀背面之注意事項再塡寫本頁) 丨裝_ 訂 本纸張尺/t適用中國國家橒準(CNS)甲4規樁(2〗0 X 297 y楚) -5 - 81.9.25,000 A6 B6 £01728 五、發明説明() (請先閲讀背面之注意事項再填寫本頁) 本發明的目的就是提供一檑適於製備無機粉末燒結體 之可射出模製組合物,該無機粉末包括陶瓷粉末或金屬粉 末係藉射出模製注製成,其具有均勻的待性分配,包括可 射出壓縮性、壓縮初胚之強度,燒結前藉熱分解法將接著 劑去除之去除性;同時,於高產出率時,得到之燒結體不 會產生如翹曲、破裂和凹陷之缺點。 本發明之另一目的係提供一棰不具缺點之陶瓷粉末或 金羼粉末之燒结體。 由下文將可對本發明該些目的有更深的認識。 經濟部中央標準局β工消費合作社印- 根據本發明,係提供一棰適於製備燒結涯之可射出模 製組合物,該組合物包括一種無機粉末和一種有機接箸劑 ,該接箸劑包含45〜80wt.%之合成丙烯酸聚合物和10〜 50wt.%之蟠類,該蟠類之熔點至多為100C並和該合成 丙烯酸聚合物相容;該無機粉末和有機接著劑之醱積比為 0.65/ 0.35至0.25/ 0.75 ;合成之丙烯酸聚合物係一種懸 浮聚合產物*係將選自含有乙烯-乙酸乙烯酯共聚物和乙 烯-丙烯酸乙酯共聚物之聚合物成分U)溶解於丙烯酸酯 單體或甲基丙烯酸酯單體或是該二單醱之混合物Μ及苯乙 烯化合物之單體成分(b),然後在含有分散劑之媒介液中 攪拌得到之溶液、再將該分散液懸浮聚合。 第1至第4圖係丙烯酸聚合物的縮影片,該聚合物先 經溶劑作浸蝕處理,再利用倍數5,000的掃描電子顯撤鏡 観察其内部結構;其中第1和第3圖係本發明合成丙烯酸 聚合物的縮影片;第2和第4圖係摻合二或多種聚合物裂 本紙張尺廑適用中园國家標準(CNS)甲4規格(2丨0 X 297公%) —6 81.9.25,000A6 B6 £ 01 * 726 5. Description of the invention () The present invention relates to an injection-compression composition for preparing a sintered body. The composition contains an inorganic powder and a specific organic adhesive; in particular, the invention can The injection compression composition has good injection compressibility and the performance of removing the adhesive from the compressed initial embryo during sintering is good, so that the resulting sintered body hardly has defects such as warpage and cracking, and at high output It has good structural stability; the invention also relates to a sintered body prepared from the composition. The sintering system compresses the mixture of inorganic powder and organic adhesive and then sinters it; in recent years, the ceramic industry prepares ceramic products by first mixing ceramic powder and organic adhesive to make the mixture plastic, and then ejecting and compressing it to form a compressed initial embryo , Remove the scavenger and sinter M; this ceramic product is gradually used in automotive engine parts, and its characteristic is that some products with complex shapes can be mass produced in industry. The organic scavenger is related to the uniform dispersion of the ceramic powder, and is also related to the fluidity of the powder mixed with it, the strength of the compressed initial embryo, and the ease of removing the adhesive from the natural color compression sleep (adhesive removal); Therefore, if the type and amount of the adhesive are not properly selected, a good sintered body cannot be produced. For example, if the ceramic powder cannot be sufficiently uniformly dispersed in the organic adhesive, the resulting compressed body or sintered body is likely to occur. The defects of warpage and cracking, meanwhile, the strength of the press-knitted body will also decrease; meanwhile, if the organic adhesive has poor thermal stability, it will deteriorate in the cylinder of the injection molding machine, and the fluidity of the compressed composition will not It is stable, so it can not produce good injection compression body, and sometimes ceramic powder and organic adhesive may even separate; if excessive adhesive is used, it is difficult to avoid the occurrence of foaming and cracking. The surface paper ruler is applicable to the Chinese National Standard (CNS ) A.1 specifications (210 X 297 male) _ 3-81.9.25,000 (please read the precautions on the back before filling out this page). 装 _ Order in the Ministry of Economic Affairs Standards Bureau Employee Consumer Cooperative Yinxi Ministry of Economic Affairs Central Standards Bureau Employee Consumer Cooperative printed A6 B6__ 5. Description of the invention () This is because a large amount of gas is generated inside the compression body during the step of removing the adhesive aat »Body 0 is used for compression Organic powders for ceramic powders are used in forging and polymers. Polymers include, for example, ethylene-ethyl acrylate copolymer (EVA), polystyrene, irregular polypropylene (APP>, polyethylene, acrylic and methyl Acrylic polymer; the organic adhesive used to prepare the sintered body must have good hospitality, such as compressibility (such as compression stability, mold release characteristics M, and powder rolling when the inorganic powder is combined with the scintillator), initial compression embryo The strength, the removability of the adhesive before thermal decomposition and compression of the initial embryo before sintering, as well as the shape maintenance during sintering and the amount of breakage remaining, but each of these adhesives has its own shortcomings and cannot all meet the above needs. In general, polymer scavengers have better compressibility, but have poorer removability, for example, ethylene-vinyl acetate copolymer ( EVA) has excellent powder fluidity, and makes the formed compressed skull with high strength. When mixed with ceramic powder, it has appropriate plasticity and does not damage its fluidity; however, when the thermal decomposition is removed from the compressed body In 2001, acetic acid gas will be generated, which may cause foaming and cracking. It is likely to be generated. Similar to EVA ethylene-ethyl acrylate copolymer, it also has high strength, and when it is mixed with ceramic powder or gold powder, the compressed body has Appropriate plasticity without compromising its fluidity; however, if it is used in large quantities, when the adhesive is removed by thermal decomposition, the compressed product will have obvious foaming phenomena and cracks. Therefore, if you want to remove the adhesive It is very hard not to damage the compressed material. At the same time, polystyrene, acrylic and methacrylic polymers (such as the Chinese National Standards (CNS) A 4 specifications (210 X 297 conversion) _ 4 _ 81 -9.25,000 (please read the precautions on the back before writing this page) to install _ order. 201726 A6 B6 issued by the Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs 5. Description of the invention () Isobutyl methacrylate) and Porcelain powder and metal powder also have excellent adhesion effect, and the formed primary woven embryos have high strength; in other words, they can effectively prevent damage to the thin layer and maintain the compressed primary embryos in an excellent shape; The agent also has excellent thermal decomposition properties, making it easier to break away from the compression body; however, when it is used in large amounts, the mixture formed with the metal powder has poor fluidity, and it will produce a shortage of filler and injection molding Welding line. The irregular polypropylene and ceramic powder mixture has good fluidity; and it is easier to injection mold, and the resulting K shrinkage embryo has sufficient strength to be easily handled (Japanese Patent Application Kokoku No. 51-29170); however, it is The removability of the scavenger is poor. Compared with polymer adhesives, wax adhesives such as Shipan have better removal properties, but their fluidity under high pressure is unstable, making them less compressible; and because they are lower molecular weight compounds, The strength of the obtained compressed initial embryo is low. In order to obtain adhesives with satisfactory properties, we will combine two or more adhesives with different properties in a good distribution ratio, but because these adhesives have different types and softening points, and their solubility and compatibility It is also unsatisfactory, making it impossible to obtain a homogeneous mixture, or requiring a long mixing time; in general, if two or more adhesives are not enough to form a homogeneous mixture, it takes more time to determine the compression conditions Because the fluidity of the mixture is not stable; at the same time, because the uniformity of the formed compressed material is not uniform, the use of a non-uniform mixture of corrosion agents can easily cause the sintered body to crack and affect the stability of the compressed body structure. (Please read the precautions on the back before writing this page) 丨 Installation_ The paper ruler / t is applicable to China National Standards (CNS) A 4 gauge pile (2〗 0 X 297 y Chu) -5-81.9. 25,000 A6 B6 £ 01728 5. Description of the invention () (Please read the precautions on the back before filling in this page) The purpose of the present invention is to provide an injection moldable composition suitable for the preparation of sintered bodies of inorganic powder, the inorganic powder Including ceramic powder or metal powder is injection molded by injection molding, which has uniform standby distribution, including injection compressibility, strength of compressed initial embryo, removal of adhesive by thermal decomposition method before sintering; meanwhile At high output rates, the resulting sintered body does not suffer from defects such as warpage, cracking, and dents. Another object of the present invention is to provide a sintered body of ceramic powder or gold powder without defects. The purpose of the present invention will be better understood from the following. Printed by β-Consumer Cooperative Society, Central Bureau of Standards, Ministry of Economic Affairs-According to the present invention, an injection moldable composition suitable for the preparation of sintering is provided, the composition comprising an inorganic powder and an organic scavenger, the scavenger Contains 45 ~ 80wt.% Synthetic acrylic polymer and 10 ~ 50wt.% Flats, the melting point of the flats is at most 100C and is compatible with the synthetic acrylic polymer; the ratio of the inorganic powder to organic adhesive 0.65 / 0.35 to 0.25 / 0.75; the synthetic acrylic polymer is a suspension polymerization product * is a polymer component U) selected from the group consisting of ethylene-vinyl acetate copolymer and ethylene-ethyl acrylate copolymer dissolved in acrylate The monomer or methacrylate monomer or the mixture of the two monomers M and the monomer component (b) of the styrene compound, and then the resulting solution is stirred in a vehicle liquid containing a dispersant, and then the dispersion is suspended polymerization. Figures 1 to 4 are miniatures of acrylic polymers. The polymer is first etched by a solvent, and then its internal structure is examined using a scanning electron magnification of 5,000; Figures 1 and 3 are synthesized by the present invention Acrylic polymer miniature film; Figures 2 and 4 are blended with two or more polymers. The size of the paper is applicable to the Central Park National Standard (CNS) A 4 specification (2 丨 0 X 297%) — 6 81.9. 25,000

經濟部中央標準局員工消費合作社印¾ '發明説明() 備而成的混雜聚合物縮影片。 與特定有機接著劑結合製備本發明之可射出壓縮組口 物之無機粉末並不特別予Μ限制只要其為適用於堍结體之 無機粉末,待別言之,該金羼粉末較好為球粒型或類似球 形,平均粒徑約0.1〜50/um,Μ無機粉末之填充密度和壓 縮組成物的流動性觀點而言,尤以平均粒為0.1〜20// m為 待別佳。 無機粉末之代表性例子包括金羼粉末如鐵、鐵合金( 如鐵鎳合金)、鐵鈷合金或不锈鏑、鋳、鋁合金或銅合金 ;及氧化陶瓷粉末如礬石、锆石、富鋁、紅柱石Uullite )、钛鐵礦或鐵酸鹽(ferrite);氮化陶瓷粉末如氮化矽 、気化鋁或気化硼;碳化陶瓷粉末如碩化矽、磺化鋁或磺 化鋳;以及一種金羼互化物如钛-鋁合金;一棰磷酸化物 粉末如磷灰石之類。 無機粉末除了金羼外亦可包含1〜50%體積之金饜或 無機物質鰌維或晶絲;舉例而言,金屬包括有網、不锈鏑 、鎔、鎂、鎳、钛、铍、鎢、鉬和硼;非金羼之無機物質 有礬石、锆石、磺化矽、碳化晒、氮化矽、氮化硼和気化 鋁。 本發明所使用之無機接箸劑至少包含二種成分,一般 而言包括45〜80wt. %之合成丙烯酸聚合物和10〜50wt. % (較好是15〜40wt·%)之蟠類,該蠟類之熔點至多100 它並可用合成丙烯酸聚合物相容;上述混合之有機接箸劑 亦包含0〜40wt·%,較好是〇〜25wt.%之添加物,包括有 本纸張尺度適用中a國家橒準(CNS)甲4規格 (210 X 297公兑) _ 7 - 81.9.25,000 (請先閲讀背面之注意事項再填寫本頁) 裝_ 訂. - 經濟部中央標準局MT工消費合作社印3衣 五、發明説明( !^L· 塑化劑如呔睃酯化物、潤滑劑或模釋出劑如較高级脂肪睃 、以改善無機粉末表面潤溼性之界面活性劑,和表面處理 劑(偶合劑)。 合成丙烯酸聚合物、蛹和選擇性添加物可先行混合形 成有機接著劑再加至無機粉末,或者其値別加至無機粉末 中Ο 合成丙烯酸聚合物和摻合之聚合物比較具有優秀均匀 之结構;同時其在壓縮組合物方面亦有較佳之滾動性,並 且對壓縮初胚有較佳之去除性,此外,對於接合金羼徹粒 亦有優秀之效果;若使用該合成丙烯酸聚合物會使形成之 組成物具有足夠的滾動性,同時製備而得之壓缩初胚具有 足夠的強度和塑性。 合成丙烯酸聚合物係將聚合物成分(d),包括乙烯-乙睃乙烯酯共聚物和/或乙烯-丙烯睃乙酯共聚物和一種 聚合起始劑溶解於單體成分(b),包括丙烯酸酯或甲基丙 烯睃酯或是該二單體之混合物Μ及苯乙烯,然後在含有分 散劑之溶液媒介中攪拌形成之溶液,再懸浮聚合形成的分 散液;如偶有需要亦可於上述容液中加入鍊轉移劑。 因合成丙烯酸聚合物係先將EVA和/#ΕΕΑ溶解於單 體成分、再於媒介溶液中攪拌。鳙谬,^^術以猶如一棰 聚合物合金,其中由單體成分(b)形成合物均勻分散 於聚合物成分(a)中,如第1圃和第3画所示之合成丙稀 酸聚合物撤粒之縮影片,該聚合物係經溶劑浸蝕以顯示其 內部結構;合成丙烯酸聚合物較摻合之聚合物更易決定於 (請先閲讀背面之注意事項再填寫本頁) _裝· 訂· 衣紙張尺茂適用中囚國家橒準(CNS)甲4規格(210 X 297公縫) 一 8 — 81.9.25,000 經濟部中央標準局貝工消費合作社印*-|农 01726 Λ6 __B6__ 五、發明説明() 壓縮組合物時所需之條件(比較第2和第4圖),並且組 合物的流動性較搔定,因此在高產出率時只會稍微地散播 形成良好之燒結體。 本發明使用之乙烯-乙酸乙烯酯共聚物(EVA)非特別 限定,可爲任何商業化生產之棰類;乙烯和乙酸乙烯酯形 成共聚物的重量比為85/ 15至50/50,較好係80/ 20至60 /40;因為重量比如果超過85/15,即難溶解於單體成分 (b>中;若低於50/ 50,不易形成有用之共聚物並會降低 壓縮初胚的強度;從溶解於單膿成分(M之共聚物溶液 的黏度觀點而言,EVA較好具有約10至500之熔化率;從 壓縮龌的流動性和壓縮初胚強度觀點而言,EVA較好具 有約20至400之熔化率。 本發明使用之乙烯-丙烯睃乙酯共聚物(EEA)非特定 限定,可為商業化生產之棰類任一;乙烯和丙烯酸乙酯形 成的共聚物重量比為85/ 15至50/ 50,尤Μ 80/ 20至60/ 40為佳;因為重量比若超過85/ 15,則難溶解於單體(b) 中;若低於50/50,不易形成有用之共聚物並且會降低壓 縮初胚之強度;由溶解於單體成分(b〉形成的共聚物溶液 觀酤而言,EEA較好具有約10至2000之熔化率;從壓縮體 的流動性和壓縮初旺強度観點而言,EEA較好具有約100 至1500之熔化率。 單體成分(b)中的丙烯酸酯和甲基丙烯酸酯非特別限 定;但從壓縮時粉末流動性、壓縮初胚之強度和接著劑去 除率的觀點來看,較好是和具有1至8個碳的醇類形成的 (請先閲讀背面之注意事項再填窝本頁) .-—丨装. 訂. 本紙張尺度適用中®國家樣準(CNS)甲4規格(2〗0\ 297 2:兑) 一 9 — 81.9.25,000 201728 A6 一 __B6__ 五、發明説明() (請先閲讀背面之注意事項再塡寫本頁) 丙烯睃酯或甲基丙烯酸酯為佳,舉例來說有具有l-。烷 基之(甲基)丙烯酸正烷基化物、(甲基)丙烯酸異丙酯 、(甲基)丙烯酸異丁酯、(甲基)丙烯酸三级丁酯、( 甲基)丙烯酸2-乙基己酯、(甲基)丙烯酸2-甲氧乙酯、 (甲基)丙烯酸2-乙氧乙酯之類,其中以具有L-C*烷基 之(甲基)丙烯酸正烷基化物、(甲基)丙烯酸異丙酯和 (甲基)丙烯睃異丁酯較佳,亦可將其混合或單獨使用。 (甲基)丙烯酸酯類能與苯乙烯化物混合使用,代表 性的例子有苯乙烯、α-甲基笨乙烯、對-甲基苯乙烯和 乙烯基苯乙烯,其含量較好不超過(甲基)丙烯酸酯和其 混合物缠重量的80%,笨乙烯化物含量愈多,接著劑的流 動性就愈差,所Μ使用高比例之苯乙烯化物易降低可壓縮 性。 其它如丙烯酸、甲基丙烯酸、乙酸乙烯酯和氯化乙烯 之單體亦可微置存於成分(b)中,衹要不損及用作接箸劑 之聚合物所需之特性。 經濟部中央標準局員工消費合作社印製 聚合物成分U)和單體成分(b)的重量比率約為5/95 至80/ 20,較佳為20/ 80至70/ 30;當重量比低於5/95, 壓縮時粉末流動性即嫌不足,而導致壓縮失敗;若超過80 /20,以熱分解移去接箸劑時會有發泡產生,而降低堍結 體之強度,並使接著劑的去除和處理變得困難。 較好使用一種可溶於油類之聚合起始劑,使聚合反應 在油滴分散於媒介溶液的條件下進行,如此,聚合物成分 (d)和單體成分(b)形成的聚合物之聚合徹粒均勻摻合; 本紙張尺度適用中國國家橒準(CNS)甲.1規格(210 X 297 ) 8i.9.25,000 五、發明説明() 代表性聚合起始劑包括有機過氧化物如苯甲醯過氧化物、 十二醯過氧化物或2-乙基過氧己酸三级丁酯,或偶気化物 如隅氮異丁酶或偶氮雙二甲基戊Μ及其它可溶於油類 之聚合起始劑,或者是該些起始劑單獨或混合使用,其含 量约爲0.05〜1_5份、較佳係0.1〜0.6份,其係以1〇〇份 之單體成分(b)重量為準。 聚合反應中用來控制分子置之鏈移轉劑代表例子有硫 醇如十二基硫醇、三级辛基碕醇、α-甲基苯乙烯和其二 聚物,該些移轉劑可混合或單獨使用,其含量約為0.01〜 1份、較好係0.03〜0.5份,Μ100份之單體成分(b)重 量爲準。 理想狀況是聚合物成分<d>完全溶解於單體成分(b) 中,使反應均勻進行,而生成均勻組成之聚合物;溶解方 式並不特別限制;當聚合起始劑溶解時,溶解溫度應低於 起始劑的分解溫度,溶液於含有分散劑之媒介中攪拌,再 將形成的懸浮液懸浮聚合。 經濟部t央標準局員工消費合作社印- 用於本發明之已知分散劑代表例子包括具有高分子董 之可溶於水有機化物如聚乙烯醇、羥乙基继維素或聚乙烯 基笕五園酮,以及一棰陰離子界面话性劑和一種微溶於水 之無機化物細粉末之结合物,該無機化物如a基式磷灰石 或焦磷酸鎂;該分散劑3含量約爲0.1〜1份,較佳是0.2 〜0.5份,M100份之媒介液重量為準。 聚合物成分(d〉和起始劑有時亦可含鐽移轉劑溶解於 單體成分(b>中形成之溶液於介質液中攪拌,該介質液可 81.9.25.000 (請先閲讀背面之注意事項再塡寫本頁) 本紙張尺茂適用中囚阀家橒準(CNS) T .ί規格(210 X 297 λ'釐) 201728 Afi A6 Γ— --- B6 Α、發明説明() (請先W讀背面之注意事項再填窝本頁) 為水,含虽約為30〜120份、铰好係50〜100份,M100 份之介質液重量為準。 懸浮聚合反應條件並不恃別限定,約以一般之方法即 可,聚合溫度根據所用之聚合起始劑分解溫度而定,一般 係於501〜130¾進行2〜10小時。 得到之懸浮聚合產物係合成之聚合物,其中單體成分 (b〉形成的聚合物均勻分散於聚合物成分(a)中,如第1 圖和第3圖所示之縮影Η,該聚合徹粒係根據本發明所製 備,經由溶劑浸蝕處理以顯示其内部結構。 根據本發明製備之合成聚合物係作為一棰裂備無機粉 末燒結體之接箸劑,無機粉末包含金羼粉末或陶瓷粉末, 且該聚合物具有上述之優點;本發明中,合成丙烯酸聚合 物係和蠟结合;蠟之效果在於使聚合物易和無機粉末捏合 ,使無機粉末均勻分散於合成丙烯睃聚合物中,並使形成 之壓縮組合物具有可塑性;同時,吾人若使用合成丙烯酸 聚合物和蟠與無機粉末結合,此棰情況與單播使用二者之 比較,能降低有機接著劑之使用量。 經濟部中央樣準局S工消費合作社印製 蟠類之熔點至多爲100=,並和本發明使用之合成丙 烯酸聚合物具有相容性;若其熔點离於100Ό ,則其與合 成丙烯酸聚合物结合形成之有機接瞢劑躭會具有离的熔點 ,並且其流動性會不足,因此不易降低有櫬接著劑之用量 ;此外,若液體蠟之熔點低於一般溫度且固體锄和合成丙 烯酸樹脂不相容,具不會得到上述之效果;因為前者於壓 縮時不能得到良好之壓縮體強度和模釋出性;而後者使無 81.9.25,000 本紙張尺度適用中國國家揉準(CNS)甲4規格(210 X 297父兑) A6 B6 %oine 五、發明説明() (請先閲讀背面之注意事項再填寫本頁) 機粉末不易分散於有機接箸劑中。 锄於本發明有機接箸劑中之含量爲10〜50wt.% ,較 好是15〜40wt.% ,以有機接箸劑之重量為準;若低於10 wt.% ,則不能得到上述之效果;若超過50wt.% ,蟠缺 乏強度之嚴重缺點會明顯地表現出來,因此當壓縮初胚 自楔釋出時易斷裂,並且形成之壓縮初胚強度不足以承 受一般之操作處理。 本發明可兼用天然蠘類和合成蟠類,舉例而言有石蟠 、微晶播、聚乙稀播、蜜播(bees wax)、巴西嫌(carnan-ba wax)、和褐媒播(montan wax)之類。 本發明之可射出歷縮組合物包含無機粉末和有機接著 劑,該有機接著劑包含合成丙烯酸聚合物和蟠之基本成分 ,其粉末和接著劑的體積比為0.65/ 0.35至0.25/0 ·75 ; 計算公式如下 W P/ D P W b/ D b 體積比=- - WP/DP+Wb/Db Wp/Dp+Wb/Db 其中Wp係無機粉末重量,Dp係無機粉末比重; 經濟部中央櫺準局员工消費合作社印"Printed by the Employee Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs ¾ 'Instruction for Invention () Prepared hybrid polymer shrink film. The inorganic powder capable of injecting the compressed composition of the present invention in combination with a specific organic adhesive is not particularly limited as long as it is an inorganic powder suitable for beetle bodies, to be otherwise stated, the gold powder is preferably a ball The particle type or spherical shape, the average particle size is about 0.1 ~ 50 / um, from the viewpoint of the packing density of the M inorganic powder and the fluidity of the compressed composition, the average particle size is particularly preferably 0.1 ~ 20 // m. Representative examples of inorganic powders include gold powders such as iron, iron alloys (such as iron-nickel alloys), iron-cobalt alloys or stainless dysprosium, aluminum alloys, or copper alloys; and oxide ceramic powders such as alum, zircon, and aluminum-rich , Andalusite Uullite), ilmenite or ferrite; nitrided ceramic powders such as silicon nitride, aluminum or boron; carbonized ceramic powders such as master silicon, aluminum sulfonate or sulfonate; and a Jinyi intermetallic compound such as titanium-aluminum alloy; a batch of phosphate powder such as apatite and the like. The inorganic powder can also contain 1-50% by volume of golden noodles or inorganic materials such as koji or crystal wires; for example, metals include mesh, stainless dysprosium, dysprosium, magnesium, nickel, titanium, beryllium, and tungsten. , Molybdenum and boron; non-golden inorganic substances include alum, zircon, sulfonated silicon, carbonized solar, silicon nitride, boron nitride and aluminum nitride. The inorganic scavenger used in the present invention contains at least two components, generally including 45 ~ 80wt.% Of synthetic acrylic polymer and 10 ~ 50wt.% (Preferably 15 ~ 40wt ·%) of the flats, the The melting point of waxes is at most 100 It is compatible with synthetic acrylic polymers; the above-mentioned mixed organic scavengers also contain 0 ~ 40wt ·%, preferably 〇 ~ 25wt.% Of additives, including the paper size applicable China National Standards (CNS) Grade A 4 (210 X 297 conversion) _ 7-81.9.25,000 (please read the precautions on the back before filling out this page) _ order.-MT consumption of the Central Bureau of Standards of the Ministry of Economic Affairs Cooperative Society Printed 3 Clothing V. Description of Invention (! ^ L · Plasticizers such as esters, lubricants or mold release agents such as higher-grade fats, surfactants to improve the wettability of inorganic powder surfaces, and surfaces Treatment agent (coupling agent). Synthetic acrylic polymer, pupa and optional additives can be mixed to form an organic adhesive before adding to the inorganic powder, or its value is added to the inorganic powder. Synthetic acrylic polymer and blending polymerization The object has an excellent uniform structure; at the same time Compressed composition also has better rolling properties, and better removal of compressed primary embryos. In addition, it also has excellent effects on the bonding of Jinluo tablets; if the synthetic acrylic polymer is used, the resulting composition will have Sufficient rollability, and the compressed primary embryos prepared at the same time have sufficient strength and plasticity. Synthetic acrylic polymer is based on polymer component (d), including ethylene-ethylene vinyl ester copolymer and / or ethylene-propylene vinyl acetate The ester copolymer and a polymerization initiator are dissolved in the monomer component (b), including acrylate or methacrylic acid ester or a mixture of the two monomers M and styrene, and then stirred in a solution medium containing a dispersant The resulting solution is then resuspended to form a dispersion liquid; if occasionally necessary, a chain transfer agent can be added to the above-mentioned liquid solution. Because synthetic acrylic polymer first dissolves EVA and / # ΕΕΑ in the monomer component and then in the medium Stir in the solution. It is like a polymer alloy, in which the compound formed by the monomer component (b) is uniformly dispersed in the polymer component (a), as shown in the first garden and the third painting The shrinking film of the synthetic acrylic polymer withdrawing the particles, the polymer is etched by the solvent to show its internal structure; the synthetic acrylic polymer is easier to determine than the blended polymer (please read the precautions on the back before filling in this Page) _Set · Order · Clothing paper size Mao applies to the Chinese prisoner National Standard (CNS) A 4 specifications (210 X 297 male seams) 1 8 — 81.9.25,000 Printed by Beigong Consumer Cooperatives, Central Bureau of Standards, Ministry of Economic Affairs *-| Agricultural 01726 Λ6 __B6__ V. Description of the invention () The conditions required to compress the composition (compare Figures 2 and 4), and the fluidity of the composition is relatively stable, so it will only be slightly spread at high output rates. Good sintered body. The ethylene-vinyl acetate copolymer (EVA) used in the present invention is not particularly limited, and may be any commercially produced type; the weight ratio of ethylene and vinyl acetate to form a copolymer is 85/15 to 50/50, preferably It is 80/20 to 60/40; if the weight ratio exceeds 85/15, it is difficult to dissolve in the monomer component (b>); if it is less than 50/50, it is not easy to form a useful copolymer and will reduce the compression of the embryo Strength; from the viewpoint of the viscosity of the copolymer solution dissolved in the single pus (M copolymer, EVA preferably has a melting rate of about 10 to 500; from the viewpoint of the fluidity of the compressed squat and the strength of the compressed initial embryo, EVA is better It has a melting rate of about 20 to 400. The ethylene-propylene ethyl acetate copolymer (EEA) used in the present invention is not particularly limited, and can be any of the commercially produced types; the weight ratio of the copolymer formed by ethylene and ethyl acrylate 85/15 to 50/50, especially M 80/20 to 60/40; because the weight ratio exceeds 85/15, it is difficult to dissolve in the monomer (b); if it is less than 50/50, it is not easy to form Useful copolymer and will reduce the strength of the compressed initial embryo; copolymer formed by dissolving in the monomer component (b> From a liquid perspective, EEA preferably has a melting rate of about 10 to 2000; from the viewpoint of fluidity and initial compression strength of the compressed body, EEA preferably has a melting rate of about 100 to 1500. Monomer composition ( The acrylic acid ester and methacrylic acid ester in b) are not particularly limited; however, from the viewpoint of powder fluidity during compression, strength of compressed primary embryos and adhesive removal rate, alcohols having 1 to 8 carbons are preferred Formed (please read the precautions on the back before filling the nest page) .-— 丨 Packing. Ordering. This paper size is applicable to China® National Standard (CNS) A 4 specifications (2〗 0 \ 297 2: Redeem) 1. 9 — 81.9.25,000 201728 A6 1. __B6__ 5. Description of the invention () (Please read the precautions on the back before writing this page) Acrylic acid ester or methacrylic acid ester is better, for example, it has l-. Alkyl (meth) acrylic acid n-alkylate, isopropyl (meth) acrylate, isobutyl (meth) acrylate, tertiary butyl (meth) acrylate, 2-ethyl (meth) acrylate Hexyl ester, 2-methoxyethyl (meth) acrylate, 2-ethoxyethyl (meth) acrylate, etc. (Meth) acrylic acid n-alkylate having LC * alkyl group, isopropyl (meth) acrylate and (meth) acrylic acid isobutyl ester are preferred, and they can also be mixed or used alone. (Methyl) Acrylic esters can be used in combination with styrenates. Representative examples are styrene, α-methyl stupid ethylene, p-methyl styrene and vinyl styrene, the content of which is preferably not more than (meth) acrylate and The weight of the mixture is 80%, the more the stupid vinyl compound content, the worse the flowability of the adhesive, so the use of a high proportion of styrene compound is easy to reduce the compressibility. Other monomers such as acrylic acid, methacrylic acid, vinyl acetate, and vinyl chloride can also be placed in component (b) as long as they do not impair the properties required by the polymer used as a scavenger. The weight ratio of the polymer component U) and the monomer component (b) printed by the Staff Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs is about 5/95 to 80/20, preferably 20/80 to 70/30; when the weight ratio is low On 5/95, the fluidity of the powder during compression is insufficient, which leads to compression failure; if it exceeds 80/20, there will be foaming when the pyrolysis agent is removed by thermal decomposition, which reduces the strength of the knot body and makes The removal and handling of the adhesive becomes difficult. It is preferable to use a polymerization initiator soluble in oil, so that the polymerization reaction is carried out under the condition that the oil droplets are dispersed in the vehicle solution. Thus, the polymer formed by the polymer component (d) and the monomer component (b) The polymer is thoroughly blended; this paper scale is applicable to the Chinese National Standard (CNS) A.1 specification (210 X 297) 8i.9.25,000 5. Description of the invention () Representative polymerization initiators include organic peroxides such as Benzoyl peroxide, dodecyl peroxide or tertiary butyl 2-ethylperoxyhexanoate, or azoides such as corner-nitroisobutyrase or azobisdimethylpentyl M and other soluble It is used as the polymerization initiator in oils, or these initiators are used alone or in combination, and its content is about 0.05 ~ 1-5 parts, preferably 0.1 ~ 0.6 parts, which is 100 parts of monomer component ( b) The weight shall prevail. Representative examples of chain transfer agents used to control molecular placement in polymerization reactions are mercaptans such as dodecyl mercaptan, tertiary octylbenzyl alcohol, α-methylstyrene, and their dimers. These transfer agents can be Mixed or used alone, the content is about 0.01 ~ 1 part, preferably 0.03 ~ 0.5 part, the weight of the monomer component (b) of Μ100 part shall prevail. The ideal situation is that the polymer component < d > is completely dissolved in the monomer component (b) to allow the reaction to proceed uniformly to produce a polymer of uniform composition; the dissolution method is not particularly limited; when the polymerization initiator dissolves, dissolves The temperature should be lower than the decomposition temperature of the initiator, the solution is stirred in the medium containing the dispersant, and then the suspension formed is polymerized in suspension. Printed by the Employee Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs-Representative examples of known dispersants for use in the present invention include water-soluble organic compounds such as polyvinyl alcohol, hydroxyethyl ketone or polyvinyl quin Five Yuan ketone, and a combination of an anionic interfacial agent and a fine powder of a slightly soluble inorganic compound such as a-based apatite or magnesium pyrophosphate; the content of the dispersant 3 is about 0.1 ~ 1 part, preferably 0.2 ~ 0.5 part, M100 part of the weight of the medium shall prevail. The polymer component (d> and the starter may sometimes contain a transfer agent dissolved in the monomer component (b >) and the solution formed in the medium liquid is stirred in the medium liquid, which can be 81.9.25.000 (please read the back page first Matters needing attention will be written on this page) This paper ruler is suitable for the prisoner housekeeper's standard (CNS) T .ί specification (210 X 297 λ '%) 201728 Afi A6 Γ— --- B6 Α, invention description () ( Please read the precautions on the back before filling the nest.) It is water, although it contains about 30 ~ 120 parts, hinged 50 ~ 100 parts, M100 part of the medium liquid weight is subject to. Suspension polymerization reaction conditions are not dependent It is not limited, and it can be about a general method. The polymerization temperature is determined according to the decomposition temperature of the polymerization initiator used, and it is generally carried out at 501 ~ 130¾ for 2 ~ 10 hours. The resulting suspension polymerization product is a synthetic polymer, in which the single The polymer formed by the body component (b> is uniformly dispersed in the polymer component (a), as shown in FIGS. 1 and 3 in the microcosm Η. The polymer pellet is prepared according to the present invention, and is subjected to a solvent etching treatment to It shows its internal structure. The synthetic polymer prepared according to the present invention is used as a Prepare the sintering agent of the inorganic powder sintered body. The inorganic powder contains gold powder or ceramic powder, and the polymer has the above advantages; in the present invention, the synthetic acrylic polymer is combined with wax; the effect of the wax is to make the polymer easy Knead with the inorganic powder to make the inorganic powder evenly dispersed in the synthetic propylene oxide polymer, and make the formed compressed composition have plasticity; at the same time, if we use a synthetic acrylic polymer and flat and inorganic powder combination, this situation and unicast Using the comparison between the two can reduce the amount of organic adhesives. The melting point of the scorpions printed by the Sigong Consumer Cooperative of the Central Bureau of Samples of the Ministry of Economic Affairs is at most 100 =, and is compatible with the synthetic acrylic polymers used in the present invention ; If its melting point is away from 100Ό, the organic binder formed by combining it with a synthetic acrylic polymer will have a melting point, and its fluidity will be insufficient, so it is not easy to reduce the amount of adhesive agent; In addition, if the liquid The melting point of the wax is lower than the normal temperature and the solid hoe is not compatible with the synthetic acrylic resin, so the above effects will not be obtained; because Those who are unable to obtain good compression body strength and mold releasability during compression; and the latter makes the 81.9.25,000 paper size not applicable to China National Standard (CNS) A 4 specifications (210 X 297 parent) A6 B6% oine V 2. Description of the invention () (Please read the precautions on the back before filling in this page) Machine powder is not easy to disperse in the organic scavenger. The content of the hoe in the organic scavenger of the present invention is 10 ~ 50wt.%, Preferably 15 ~ 40wt.%, Based on the weight of the organic scavenger; if it is less than 10wt.%, The above effects cannot be obtained; if it exceeds 50wt.%, The serious disadvantage of the lack of strength of the pan will obviously appear, so When the compressed primary embryo is released from the wedge, it is easy to break, and the strength of the compressed primary embryo formed is not enough to withstand the general handling. The present invention can be used in combination with natural beetles and synthetic panties, for example, stone pancreas, microcrystalline seed, polyethylene seed, bees wax, carnan-ba wax, and brown media (montan) wax) and the like. The injectable shrinkage composition of the present invention contains an inorganic powder and an organic adhesive. The organic adhesive contains the basic components of a synthetic acrylic polymer and a pan. The volume ratio of the powder to the adhesive is 0.65 / 0.35 to 0.25 / 0.75. ; The calculation formula is as follows: WP / DPW b / D b volume ratio =--WP / DP + Wb / Db Wp / Dp + Wb / Db where Wp is the weight of inorganic powder and Dp is the weight of inorganic powder; employees of the Central Bureau of the Ministry of Economic Affairs Consumer Cooperative Print "

Wb係有機接著劑重量,Db係有機接著劑比重。 若饉積比超過0.65/ 0.35,K缩組成物缺乏流動性, 且不能麽缩成所需形狀;若低於0.25/0.75,得到壓编初 胚之密度太低,所以燒結之壓缩體由於燒結時產生極大的 收縮,结構相當地不穩定,並且藉熱分解移去接著劑時會 產生大量氣體,使得斷裂和發泡之缺陷明顯產生。 本紙張尺度適用中因围家棵準(C.NS)甲4規格(2]0 X 29了 兌) 13 81.9.25,000 201728 AfiWb-based organic adhesive weight, Db-based organic adhesive specific gravity. If the product ratio exceeds 0.65 / 0.35, the K-shrinkable composition lacks fluidity and cannot be shrunk to the desired shape; if it is less than 0.25 / 0.75, the density of the compressed initial embryo is too low, so the sintered compressed body is sintered There is a great shrinkage, the structure is quite unstable, and a large amount of gas is generated when the adhesive is removed by thermal decomposition, so that the defects of fracture and foaming are obviously produced. This paper scale is applicable to C.NS A4 specifications (2) 0 X 29) 13 81.9.25,000 201728 Afi

Ab _ B6 五'發明説明() (請先閲讀背面之注意事項再塡寫本頁) 由本發明之可射出壓縮組合物製備陶瓷或金属之燒結 體係根據下列之方法,但並不特別限定;首先,無機粉末 如陶瓷或金屬粉末,和有機接箸劑於加熱下充分捏合,該 反應係藉由如壓力捏合器之捏合器使無機粉末均勻分散於 有機接箸劑中;形成的混合物形成如小球粒或粉化粗顆粒 之形狀,用以製成可射出壓縮組合物;將組合物利用一般 如塑模之已知方法及射出模製機射出壓缩成所需形狀;S 箸熱分解或其它方法移去壓縮體中之有機接著劑,於適當 的溫度環境下燒结成所需形狀之燒结體。 下述範例將對本發明更詳晝解釋,其中%和份數若未 特別證明皆以重量表示,須了解的是,本發明並不偈限於 下述範例。 參考範例1 (合成丙烯酸聚合之製備) 經濟部中央標準局8工消費合作社印S取 將700克甲基丙烯酸正丁酯(BMA)、500克苯乙烯和 0.35克正十二基硫酵置於5升之反應器中;加進300克乙 烯醺酸乙烯酯(EVA)〔Tosoh公司製造、商檷爲”Ultracen” 722〕,並攪拌之,加溫至75TC使EAV溶解於單體混合物 中,再將4.8克苯甲瞌過氣化物和0.25克遇氧笨甲酸三级 丁醋溶於其內;將1,840ml之去離子水和160b1之3%聚 乙烯酵混合加熱至80七製備形成含有分散_之溶液加至反 應器中、攪拌形成懸浮液;以氮氣取代聚合条統後,於80 C進行聚合反應5小時,再於110它進行反應2小時;冷 卻反應後之混合物,取出產生之聚合物,Μ水清洗、乾燥 ,形成白色球粒,其粒徑為0.3〜1.0mm;生成聚合物的固 本纸張尺度適用中國园家揉準(CNS)甲4規格(210 X 2fJ7公兑) -14 - 8】·9.25,0〇〇 A6 B6 201728 五、發明説明() (請先閱讀背面之注意事项再填寫本頁) 有鈷度[η ]爲0.70 (同30它之甲苯溶液),該聚合物下文 以“合成丙烯酸聚合物(Α)”表之。 參皇.範例2 (合成丙烯酸聚合物之製備) 將600克甲基丙烯酸正丁酯(ΒΜΑ〉和0.3克正十二基 硫醇置於5升反應器中,加熱至75Τ並攪拌之;再加入 900克乙烯-乙酸乙烯酯共聚物(EVA)〔Tosoh公司製造 、商裸為” Ultracen”722〕 和作為聚合起始劑之2.4克茉 甲醯過氧化物,其溶解於BMA中形成EVA-BMA溶液;將 1,840««丨之去離子水和160ml之3%聚乙烯酵溶液混合製 備形成含有分散劑之溶液加至反應器中攪拌,使EVA-BMA 於溶液中懸浮;将気氣取代聚合糸統後,於80C進行聚合 反應3小時,再於lOOt:進行反應2小時;冷卻反應混合 物,取出生成之聚合物,Μ水清洗並乾燥之;生成聚合物 係Μ球粒型式存在,粒徑落於0.3〜1mm,固有黏度[τι]爲 0.85 (同30¾之甲苯溶液),文後以“合成丙烯酸聚合物 (B) ”稱之。 參考範.M 3和4 (混合丙烯酸聚合物之製備) 經濟部中央樣準局員工消費合作社印焚 將同範例1之EVA以及分子量為300,000之聚甲基丙 烯酸丁酯和聚苯乙烯藉混合滾軋(mixing rlls)於15〇·〇 摻合30分鑊形成混合之丙烯睃聚合物(Α> ,該聚合物和合 成聚合物(Α)具有约略相同之组成和固有黏度。 然後,將同範例2之EVA Μ及分子置為300,000之聚 甲基丙烯酸丁酯藉混合滾軋於1401C摻合30分鐘形成混合 之丙烯酸聚合物(Β),該聚合物和合成聚合物(Β)具有約 本纸張尺茂適用中S因家標準(CNS)甲.丨規格(210 X 297公译) _1S- 81-9.25,000 A6 B6 五、發明説明() 略相同之組成和固有黏度。 將範例1和2生成之懸浮聚合產物,以及範例3和4 得到之摻合物浸於己烷2小時作浸蝕處理,以便觀察其内 部結構,吾人使用倍數5,000之掃描電子顯撤鏡觀察浸蝕 產物和摻合物,縮影片見於第1至第4圖,其中第1圖係 範例1之合成聚合物(A),第2圖係範例3之混合聚合物 (A),第3圖係範例2之合成聚合物(B),第4圖係範例 2之混合聚合物(B〉。 由第1和第2圖,吾人戡察到範例1之EVA-BMA-苯乙 烯懸浮聚合產物具有均勻分散之撤粒,並且範例1產物和 範例3摻合物的分散態有明顯的差異;由第3圖和第4圖 中,範例2之EVA-BMA憨浮聚合產物和範例4摻合物亦可 觀察到類似之差異發生。 節例1 經濟部中央標準局8工消費合作社印製 於100份平均粒徑為0.4wm之馨石粉(Sumitono化學 有限公司製造、商榡為”Alumina AES-ΙΓ)中加進12.35 份之合成丙烯酸聚合物(B>和4.75份之徹晶蠟(熔點爲84 它)以及1.90份之硬酯酸;將混合物於140T藉壓力捏合 器充分捏合1小時,切割成粒徑2〜4ββ之小球粒,形成礬 石粉和有機接箸劑體積比為0.59/0.41之陶瓷組合物,該 組合物係作射出壓縮之用。 於射出壓力500〜1300kg/cmB ,壓縮溫度120°〜160 它時將該陶瓷组成物壓縮,形成螺釘型式之壓縮體(以 JIS B-176法),該壓缩體高度為50mm,最大壁厚為5mm 81.9.25,000 (請先閱讀背面之注意事項存填寫本頁) 本紙張尺度適用中國國家標準(CNS)甲4規格(2】〇 X 297 W分) 201726 A6 B6 經濟部中央標準局W工消費合作杜印製 五、發明説明() 〇 將形成之壓縮體嵌入礬石粉中,並M 3〇r/hr之加熱 速率自20它加熱至140它。再M4t:/hr加熱速率自140T3 加熱至350¾,再以1010 /hr加熱至4501C ,再以30¾ / hr 加熱至600¾ ,使接箸劑分解去除;然後,將壓縮髏置於 堍結窯中加熱至16201C燒結,維持該溫度1小時;生成之 燒結壓縮體不具缺陷。 節例2 將10.4份之合成丙烯酸聚合物(Β>、4.0份之石蟠(熔 點爲500和1.6份之硬脂酸加入於100份比表面積為6 ma/g之部分穩化的锆石粉中(Dai_Ichi Kigenso Kagaku Kogyo Kabushiki Kaisha之產物,適商檫為”HSY-3.0”) ;將混合物於140¾充分捏合60分鐘後切割成粒徑2〜4bmd 之小球粒,形成锆石粉和有機接箸劑體積比為0.51/0.49 之陶瓷組合物,該組合物係作壓縮射出之用。 将該陶瓷组合物壓縮成螺釘型,同範例1之方法加熱 移除接著劑並燒結之,唯一改變的是壓縮體於燒結窯中加 熱至1500*0後須於該溫度下維持2小時,形成之燒結壓縮 體不具有如翹曲和破裂之缺陷。 節例3 將9.5份合成丙烯酸聚合物(Α)、5.0份之石蟠(熔 點為581C)和1.3份之呔酸二丁酯加入100份同範例2之 结石粉;於150=充分捏合6()分鐘後切割成粒徑2〜4ππβ之 小球粒,形成锆石粉和有機接箸劑體積比為〇 . 5 1 / 0 . 49之 (請先閲讀背面之注意事喟再填寫本頁) 丨裝· 訂. /f 適用中 a 囷家揉準(CNS)甲 4 规格(210 X 297 'Α'兌) -11 - 81.9.25,000 經濟部中央標準局貝工消費合作社印製 五、發明説明() 射出壓縮用之陶瓷組合物。 該陶瓷組合物壓縮成螺釘型,同範例1之方法將接著 劑加熱移除並焼結之,唯一改變的是壓縮體於燒结窯中加 熱至1500T:後須於該溫度下維持2小時,形成之良好燒結 壓縮髏不具有如翹曲和破裂之缺陷。 筋例4· 將6.6份之合成丙烯酸聚合物(A) ,1·8份之石蟠( 熔點69¾)和2.6份之肽酸二丁酯加入於100份之平均粒 徑為 8.之不诱銷粉中(Mitsubishi Seiko Kabushiki Kaisha之產物,商檫爲”SUS 304L”):於150Ό充分捏合 60分鐘形成射出壓縮用之金屬組合物,該組合物的不锈鏑 粉和有機接箸劑的髏積比爲0.53/ 0.47。 將該金羼組合物同範例1之方法壓縮成螟釘型。 得到之壓缩體嵌入於礬石粉中、並於氮氣中M /hr 之加熱速率自室溫加熱至120Ό ,然後再M /hr之速率 加熱至450"C,維持該溫度2小時以除去所含之接箸劑; 然後將該壓縮體置於真空燒結窯中、加熱至13501C,維持 該溫度1小時,形成燒結密度為98%及不具裂痕之良好燒 結體。 筘例B和ft 將70份之合成丙烯酸聚合物(B)、20份之石蟠(熔點 47Ό) ,Μ及10份之硬脂睃均勻混合製備成有機接箸劑。 將12份之該有機接著劑加入於100份之気化矽粉末中 (Ube工業有限公司製造、商橒為” SN-ESP”),該粉末含 本紙張尺茂適用中an家標準(CNS)甲4規格<210 X 297 _ 18 _ 81.9.25,000 (請先閱讀背面之注意事項再塡寫本頁) -—裝· 訂· 201^26 A6 B6 經濟部中央標準局员工消費合作社印製 五、發明説明() 有5%之Ya〇a和5%之AU03 ,並且其粒徑為0.1〜0-6 /_tm :再將12份之該有機接著劑加入於100份之Mn-Zn軟鐵酸鹽 粉末中(Toda Kogyo Kabushiki Kaisha之產物),該粉末 之平均粒徑為1.5wm;同範例1之方法進行捏合、壓縮和 接著劑之去除步驟;氮化矽和接箸劑賭積比為0.63/0.37 ;鐵酸鹽和接著劑之體積比為0.62/ 0.38。 以一般的燒結技術燒結壓縮體,形成之燒結壓縮體不 具如翹曲和破裂之缺陷。 筘例7 ft 將45份合成丙烯酸聚合物(A)、40份之石蟠(熔黠為 69t)和15份之呔酸二辛基酯均勻混合製備成一種有機接 箸劑。 將9分之該有機接著劑分別加至各100份平均粒徑為 l.Ow «η之磷化鎢粉末和平均粒徑為2〜5wm之羰基化鐵粉 末;同範例4之方法捏合混合物,形成一組合物的碳化鎢 和接著劑之體稹比為0.50/0.50 ;另一組合物的羰基化鐵 和接著劑的體積比為0.58/ 0.42;將該組合物同範例4之 方法壓縮並移除壓縮體所含之接著劑。 以一般之燒結技術燒結壓縮體,形成燒結密度爲98% 及不具缺陷之良好燒結體。 kh較範例1 重覆範例1之步驟,除了 Η混合丙烯酸聚合物(B)取 代合成丙烯酸聚合物(Β);结杲顯示其於射出壓縮時會發 生如倒注口之斷裂,並且和範例1比較其產出率下降約12 (請先閲讀背面之注意事項再塡寫本頁) 丨裝· 訂.Ab _ B6 Five 'Description of the invention () (Please read the precautions on the back before writing this page) The sintering system for preparing ceramics or metals from the injection-compression composition of the present invention is according to the following method, but it is not particularly limited; first , Inorganic powders such as ceramic or metal powders, and organic scavengers are sufficiently kneaded under heating, the reaction is by a kneader such as a pressure kneader to uniformly disperse the inorganic powder in the organic scintillator; the resulting mixture is formed as small The shape of pellets or pulverized coarse particles is used to make an injection-compression composition; the composition is injected into a desired shape using a known method such as plastic molding and an injection molding machine; S is thermally decomposed or other Method Remove the organic adhesive in the compressed body, and sinter it into a sintered body of the desired shape under an appropriate temperature environment. The following examples will explain the present invention in more detail, where% and parts are expressed by weight unless otherwise proven. It should be understood that the present invention is not limited to the following examples. Reference Example 1 (Preparation of Synthetic Acrylic Acid Polymerization) The Central Standards Bureau of the Ministry of Economic Affairs and Industry Co., Ltd. of India took 700 grams of n-butyl methacrylate (BMA), 500 grams of styrene, and 0.35 grams of n-dodecyl thiolease. In a 5 liter reactor; add 300 grams of ethylene vinyl acetate (EVA) [manufactured by Tosoh Corporation, commercially available as "Ultracen" 722], and stir it, heating to 75TC to dissolve EAV in the monomer mixture, Then dissolve 4.8 g of benzyl peroxide gasifier and 0.25 g of benzoic acid tertiary butyl vinegar in it; mix 1,840 ml of deionized water and 160b1 of 3% polyethylene leaven to 80% to prepare a dispersion containing dispersion _ The solution was added to the reactor and stirred to form a suspension; after replacing the polymerization system with nitrogen, the polymerization reaction was carried out at 80 C for 5 hours and then at 110 C for 2 hours; the mixture after cooling the reaction was taken out and the resulting polymerization was taken out Material, washed and dried with Μ water to form white spheres, the particle size of which is 0.3 ~ 1.0mm; the size of the solid paper that produces the polymer is suitable for the Chinese Gardener Kneading Standard (CNS) A 4 specifications (210 X 2fJ7 conversion) -14-8] 9.25, 〇〇〇A6 B6 201728 V. Description of the invention () (Please read the precautions on the back before filling in this page) The cobalt degree [η] is 0.70 (same as 30 toluene solution), the polymer is listed in the table below under “Synthetic Acrylic Polymer (Α)”. Samhuang. Example 2 (Preparation of Synthetic Acrylic Polymer) 600 g of n-butyl methacrylate (BMA) and 0.3 g of n-dodecyl mercaptan were placed in a 5 liter reactor, heated to 75T and stirred; Add 900 grams of ethylene-vinyl acetate copolymer (EVA) [manufactured by Tosoh Corporation, commercially available as "Ultracen" 722] and as a polymerization initiator 2.4 grams of jasmonic peroxide, which is dissolved in BMA to form EVA- BMA solution; mix 1,840 deionized water and 160ml of 3% polyethylene fermentation solution to form a solution containing a dispersant and add it to the reactor to stir, so that EVA-BMA is suspended in the solution; replace the polymerization with deuterium gas After the system, the polymerization reaction was carried out at 80C for 3 hours, then at 100t: for 2 hours; the reaction mixture was cooled, the resulting polymer was taken out, washed with M water and dried; the produced polymer was in the form of spherulites, particle size It falls within 0.3 ~ 1mm, and its intrinsic viscosity [τι] is 0.85 (same as 30¾ in toluene solution), which is called "Synthetic Acrylic Polymer (B)" later. Reference Fan. M 3 and 4 (Preparation of Mixed Acrylic Polymer) ) Employee consumption of the Central Bureau of Samples of the Ministry of Economic Affairs Zuosha Printing and Burning will mix the EVA of Example 1 and polybutyl methacrylate and polystyrene with a molecular weight of 300,000 by mixing rolling (mixing rlls) at 150 ° C for 30 minutes to form a mixed propylene oxide polymer. (Α>, the polymer and the synthetic polymer (Α) have approximately the same composition and intrinsic viscosity. Then, the EVA M of the same example 2 and the polybutyl methacrylate with a molecular weight of 300,000 are mixed and rolled at 1401C Blending for 30 minutes to form a mixed acrylic polymer (B), the polymer and the synthetic polymer (B) have about the size of the paper and apply to the S home standard (CNS) A. 丨 specifications (210 X 297 public translation ) _1S- 81-9.25,000 A6 B6 V. Description of the invention () Slightly the same composition and inherent viscosity. The suspension polymerization products produced in Examples 1 and 2 and the blends obtained in Examples 3 and 4 are immersed in hexane 2 Etching treatment for hours to observe its internal structure. We use a scanning electron microscope with a magnification of 5,000 to observe the etched products and admixtures. The thumbnail images are shown in Figures 1 to 4, where Figure 1 is the synthetic polymer of Example 1. (A), the second picture is the mixed polymerization of example 3 Compound (A), Figure 3 is the synthetic polymer (B) of Example 2, and Figure 4 is the mixed polymer (B> of Example 2). From Figures 1 and 2, we observed the EVA of Example 1. -The BMA-styrene suspension polymerization product has a uniformly dispersed threshing, and the dispersion state of the blend of the product of Example 1 and Example 3 is obvious; from Figure 3 and Figure 4, the EVA-BMA of Example 2 A similar difference can also be observed between the floating polymer product and the Example 4 blend. Example 1 Printed in 100 parts of Cinnamon powder (manufactured by Sumitano Chemical Co., Ltd., sold under the name "Alumina AES-ΙΓ") of 100 pieces of Cinnamon powder with an average particle size of 0.4wm, added 12.35 parts of synthetic acrylic acid Polymer (B > and 4.75 parts of crystalline wax (melting point of 84%) and 1.90 parts of stearic acid; the mixture was fully kneaded at 140T with a pressure kneader for 1 hour and cut into small particles with a particle size of 2 ~ 4ββ To form a ceramic composition with a volume ratio of alumite powder and organic scavenger of 0.59 / 0.41, which is used for injection compression. When the injection pressure is 500 ~ 1300kg / cmB and the compression temperature is 120 ° ~ 160, the ceramic The composition is compressed to form a screw-type compression body (according to JIS B-176 method). The height of the compression body is 50mm and the maximum wall thickness is 5mm 81.9.25,000 (please read the precautions on the back and fill in this page) The paper size Applicable to China National Standards (CNS) Grade 4 specifications (2) 〇X 297 W points) 201726 A6 B6 Central Ministry of Economic Affairs W Industrial and Consumer Cooperation Du Printing V. Description of invention () 〇The formed compressed body is embedded in alum powder , And M 3〇r / hr The heating rate is from 20 to 140. The M4t: / hr heating rate is from 140T3 to 350¾, then 1010 / hr to 4501C, and then 30¾ / hr to 600¾ to decompose and remove the scavenger; then, Place the compressed skull in a knot kiln and heat it to 16201C for sintering. Maintain the temperature for 1 hour; the resulting sintered compressed body has no defects. Section 2 10.4 parts of synthetic acrylic polymer (B>, 4.0 parts of stone pan (melting point Add 500 and 1.6 parts of stearic acid to 100 parts of partially stabilized zircon powder with a specific surface area of 6 ma / g (product of Dai_Ichi Kigenso Kagaku Kogyo Kabushiki Kaisha, suitable for commercial sassafras as "HSY-3.0"); The mixture was fully kneaded at 140¾ for 60 minutes and then cut into small spheres with a particle size of 2 to 4 bmd to form a ceramic composition with a volume ratio of 0.51 / 0.49 of zircon powder and organic scavenger, which was used for compression injection. The ceramic composition is compressed into a screw type, which is heated and removed by the same method as in Example 1 and sintered. The only change is that the compressed body must be maintained at this temperature for 2 hours after being heated to 1500 * 0 in the sintering kiln. Sintered compact body without Defects such as warping and cracking. Section 3 Add 9.5 parts of synthetic acrylic polymer (Α), 5.0 parts of stone pan (melting point of 581C) and 1.3 parts of dibutyl oxalate to 100 parts of stone powder of Example 2 ; After 150 = fully kneaded for 6 () minutes, cut into small spheres with a particle size of 2 ~ 4ππβ to form a volume ratio of zircon powder and organic scavenger of 0.5 1 / 0.49 (please read the note on the back first Please fill out this page again) 丨 Installation and ordering. / F Applicable a a Jiajia Jiazhun (CNS) A 4 specifications (210 X 297 'Α') -11-81.9.25,000 shellfish consumption of the Central Standards Bureau of the Ministry of Economic Affairs Printed by the cooperative. V. Description of the invention () The ceramic composition for injection compression. The ceramic composition is compressed into a screw shape. The adhesive is heated and removed in the same way as in Example 1. The only change is that the compressed body is heated to 1500T in the sintering kiln: after that, it must be maintained at this temperature for 2 hours. The well-formed sintered compression skull does not have defects such as warpage and cracking. Tendon example 4. Add 6.6 parts of synthetic acrylic polymer (A), 1 · 8 parts of stone pan (melting point 69¾) and 2.6 parts of dibutyl peptidate to 100 parts of an average particle size of 8. In the powder (product of Mitsubishi Seiko Kabushiki Kaisha, commercialized as "SUS 304L"): fully kneaded at 150Ό for 60 minutes to form a metal composition for injection compression, a stainless dysprosium powder of the composition and an organic scaffold The product ratio is 0.53 / 0.47. The Jin-Yu composition was compressed into a borer type in the same manner as in Example 1. The resulting compressed body was embedded in alum powder and heated at a heating rate of M / hr in nitrogen from room temperature to 120Ό, and then heated at a rate of M / hr to 450 " C, and maintained at this temperature for 2 hours to remove the contained connections. Scrap agent; The compressed body is then placed in a vacuum sintering kiln, heated to 13501C, and maintained at this temperature for 1 hour to form a good sintered body with a sintered density of 98% and no cracks. Reeds B and ft 70 parts of synthetic acrylic polymer (B), 20 parts of stone pan (melting point 47Ό), M and 10 parts of stearin were uniformly mixed to prepare an organic scavenger. Add 12 parts of the organic adhesive to 100 parts of the fumed silicon powder (manufactured by Ube Industrial Co., Ltd., "SN-ESP"), the powder contains the paper and the standard is applicable to the national standard (CNS) A 4Specifications < 210 X 297 _ 18 _ 81.9.25,000 (please read the precautions on the back before writing this page)--Pack · Order · 201 ^ 26 A6 B6 Printed by the Employee Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs Description of the invention () There are 5% of Ya〇a and 5% of AU03, and its particle size is 0.1 ~ 0-6 / _tm: then add 12 parts of the organic adhesive to 100 parts of Mn-Zn soft ferric acid In the salt powder (product of Toda Kogyo Kabushiki Kaisha), the average particle size of the powder is 1.5wm; the kneading, compression and adhesive removal steps are carried out in the same way as in Example 1; the bet ratio of silicon nitride and cement is 0.63 /0.37; The volume ratio of ferrite and adhesive is 0.62 / 0.38. The sintered compressed body is sintered by a general sintering technique, and the formed sintered compressed body does not have defects such as warpage and cracking. Reed 7 ft 45 parts of synthetic acrylic polymer (A), 40 parts of stone pan (69t of melt) and 15 parts of dioctyl oxate are evenly mixed to prepare an organic scavenger. Add 9 parts of the organic adhesive to each of 100 parts of tungsten phosphide powder with an average particle size of 1.0 W «η and iron carbonyl powder with an average particle size of 2 to 5 wm; knead the mixture with the method of Example 4, The volume ratio of the tungsten carbide and the adhesive forming the composition is 0.50 / 0.50; the volume ratio of the iron carbonylation of the other composition and the adhesive is 0.58 / 0.42; the composition is compressed and moved in the same way as Example 4 In addition to the adhesive contained in the compressed body. The sintered compact is sintered by the general sintering technology to form a good sintered body with a sintered density of 98% and no defects. kh repeats the steps of Example 1 more than Example 1, except that Η mixed acrylic polymer (B) replaces the synthetic acrylic polymer (B); Comparing its output rate dropped by about 12 (please read the precautions on the back before writing this page).

J-S 本纸張尺度適用令國國家標準(CNS)甲4规格(2Η) X 297 7^) - 1 9 - 81-9.25,000 A6 B6 經濟部中央標準局員工消費合作社印53 五、發明説明() hL較範例2 同範例3之步驟,除了 Μ混合丙烯酸聚合物(A)取代 合成之丙烯酸聚合物(Α> ;結果顯示其於射出壓·缩時會有 斷裂產生,同時於除去接箸劑時,該現象亦會發生;和範 例3相比其產出率約下降22%。 w.m mm 9. 除了將14份之石播(熔點58ΐ!)、2份之EVA和1扮 之肽酸二丁酯加入於100份之礬石粉中,其餘之射出壓縮 步驟皆同於範例1;當形成之壓縮體自模中取出時會受損 ,這是因為壓縮鱧的強度非常低,因此未生成良好之壓缩 髏。 卜卜.酧例4· 同範例1方法製備壓縮初胚,唯一改變的是於礬石 粉中衹加入合成丙烯酸聚合物)B),而仍維持相同的礬石 粉和接著劑體積比(0.59/0.41);由於其缺乏流動性,Μ 致不能得到令人滿意之壓縮初胚。 除了上述範例所用之成分外,其它如申請專利範圍所 述之其它成分亦可使用,結果亦大略相同。 (請先閱讀背面之注意事項再填寫本頁) 本纸張尺度適用中S a家橒準(CNS)甲.1规格(210 X 297 γ兌) 81.9.25,000JS This paper scale is applicable to the National Standards (CNS) A 4 specifications (2Η) X 297 7 ^)-1 9-81-9.25,000 A6 B6 Printed by the Employee Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economy 53 V. Description of invention ( ) HL compared with Example 2 is the same as Example 3, except that the M mixed acrylic polymer (A) replaces the synthetic acrylic polymer (Α>; the results show that it will break during injection pressure and shrinkage, and at the same time remove the cement This phenomenon will also occur; its output rate is about 22% lower than that of Example 3. wm mm 9. In addition to 14 parts of stone seed (melting point 58l!), 2 parts of EVA and 1 part of peptide acid diacid Butyl ester is added to 100 parts of alum powder, and the rest of the injection compression steps are the same as in Example 1; when the formed compression body is taken out from the mold, it will be damaged, because the strength of the compressed snakehead is very low, so it is not well formed Compressed skeleton. 卜卜. 酧 Example 4. Prepare the compressed primary embryo in the same way as Example 1, the only change is that only synthetic acrylic polymer is added to the alumina powder) B), while still maintaining the same volume ratio of alumina powder and adhesive (0.59 / 0.41); due to its lack of liquidity, M cannot be satisfied It means to compress the initial embryo. In addition to the ingredients used in the above examples, other ingredients as described in the patent application scope can also be used, and the results are roughly the same. (Please read the precautions on the back before filling in this page) This paper size is applicable to the standard of the Sa Family Standard (CNS) A.1 (210 X 297 γ) 81.9.25,000

Claims (1)

Α7 Β7 C7 D7 六、申請專利範圍 第80 103 477號申請案申請專利範圍修正本 修正日期:81年12月 1_ 一種適於製備燒結體之可射出模製組合物,該組合物 包含一種無機粉末和一種有機接箸劑,該接箸劑包含 45〜80wt_%之合成丙烯酸聚合物和1〇〜50wt.%之 蟠類,該蟠類之熔點至多為ιοου並和該合成丙烯酸 聚合物相容;該無機粉末和有機接著劑之體積比為 0.65/ 0.35至0.35/ 0.65 ;該合成之丙烯酸聚合物係 一種懸浮聚合產物,係將選自含有乙烯-乙酸乙烯酯 共聚物和乙烯-丙烯酸乙酯共聚物之聚合物成分(a) 溶解於丙烯酸酯單體或甲基丙烯酸酯單鼸或是該二單 體之混合物以及苯乙烯化合物之單體成分(b),然後 在含有分散劑之媒介液中搜伴得到之溶液,再將該分 散液懸浮聚合。 2·如申請專利範園第丨項所述之組合物,其中該無機粉 末係一棰陶瓷粉末或金饜粉末。 3.如申謓專利範圍第1項所述之組合物,其中該有機接 箸劑包含至多40wt. %之添加物,該添加物係選自塑 化劑、潤滑劑、界面活性劑和偶合劑。 4·如申請專利範圍第1項所述之组合物,其中該有機接 著劑的蠟含量為15〜40wt.% 。 5.如申請專利範圍第1項所述之组合物,其中溶解於成 分(b)之成分U)溶液包含可溶於油之聚合起始劑。 6·如申請專利範圍第1項所述之組合物,其中溶解於成 本紙張尺茂適用中國國家標準(CNS)甲4規格(2】〇 X 2(j7 乂-缝) (請先閲讀背面之注意事項再填窝本頁) 丨装‘ 訂· 經濟部中央櫺準局工消費合作杜印製 81.9.10,000 ^017S6 A7 B7 C7 D7 a、申請專利範团 (請先閱讀背面之注意事項再場寫本頁) 分(b)之成分(a)溶液包含一種鍵轉移劑。 如申請專利範圍第1項所述之組合物,其中聚合物成 分U〉和單體成分(b)之重g比率為5/95至80/20。 8 · —種燒結體,其係如申請專利範圍第1項所述之 組合物之壓縮初胚再經嬈結而得。 經 濟 部 中 央 m 準 M, 工 消 费 合 作 社 印 本纸張尺茂通用中囿S家丨累準(CNS)甲4規格 (210 x 297公兑Α7 Β7 C7 D7 VI. Application for Patent Scope No. 80 103 477 Application for Patent Scope Amendment Date of this amendment: December 81, 1_ An injection moldable composition suitable for preparing a sintered body, the composition containing an inorganic powder And an organic scavenger, the scavenger contains 45 ~ 80wt_% synthetic acrylic polymer and 10 ~ 50wt.% Flats, the melting point of the flats is at most ιοου and compatible with the synthetic acrylic polymer; The volume ratio of the inorganic powder and the organic adhesive is 0.65 / 0.35 to 0.35 / 0.65; the synthetic acrylic polymer is a suspension polymerization product, which is selected from copolymers containing ethylene-vinyl acetate copolymer and ethylene-ethyl acrylate copolymer The polymer component (a) is dissolved in the acrylate monomer or methacrylate monomer or the mixture of the two monomers and the monomer component (b) of the styrene compound, and then searched in the vehicle liquid containing the dispersant Accompanying the resulting solution, the dispersion is then suspended and polymerized. 2. The composition as described in item 丨 of the patent application park, wherein the inorganic powder is a ceramic powder or gold powder. 3. The composition as described in item 1 of the Shenhua patent scope, wherein the organic scavenger contains up to 40 wt.% Of additives, which are selected from plasticizers, lubricants, surfactants and coupling agents . 4. The composition as described in item 1 of the patent application scope, wherein the wax content of the organic adhesive is 15-40 wt.%. 5. The composition as described in item 1 of the scope of patent application, wherein the solution of component U) dissolved in component (b) contains an oil-soluble polymerization initiator. 6. The composition as described in item 1 of the scope of the patent application, in which the paper dissolved in the cost paper is applicable to the Chinese National Standard (CNS) A 4 specifications (2) 〇X 2 (j7 乂-seam) (please read the back (Notes are to be filled in this page) 丨 Installed '' Ordered by the Ministry of Economic Affairs Central Bureau of Industry and Consumer Cooperation Du Printed 81.9.10,000 ^ 017S6 A7 B7 C7 D7 a, apply for a patent model group (please read the notes on the back before the show (This page is written) The component (a) solution of sub- (b) contains a bond transfer agent. The composition as described in item 1 of the patent application, wherein the ratio of the weight g of the polymer component U> and the monomer component (b) is It is 5/95 to 80/20. 8. A kind of sintered body, which is obtained by compressing the initial embryo of the composition as described in item 1 of the patent application scope and then knotting. Central Ministry of Economic Affairs m quasi-M, industrial consumption Cooperative Society Printed Paper, Ruler, Universal, General, Family, Home, Standard (CNS), Grade A (210 x 297)
TW80103477A 1989-11-04 1991-05-02 TW201726B (en)

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JP1287708A JPH03150257A (en) 1989-11-04 1989-11-04 Composition for injection molding and sintered material obtained therefrom

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