M436834 五、新型說明： 【新型所屬之技術領域】 本新型是有關於一種分離裝置，特別是指一種電泳分 離裝.置。 【先前技術】 一般的蛋白質經酸或酵素水解後，產生不同分子量的 胜肽與胺基酸’上述的產物可做為微生物的培養液或植物 的營養源’但使用一般膠過濾方式的分離速度較慢、分離 2：少，且不易大量製備；而離心方式則因為難以認定分配 層如何區隔’而不易有效收集所需的胜肽或胺基酸，因此 ，開發有效分離不同分子量的胜肽與胺基酸的裝置仍存在 一大需求。 【新型内容】 因此，本新型之目的，即在提供一種可以簡單分離複 數可受電場泳動物質的電泳分離裝置。 於是，本新型電泳分離裝置，適用於分離複數可受電 場泳動的物質，該電泳分離裝置包含一電泳槽及一第一隔 離壁。 网 該電泳槽包括二電性相異的電極組。 該第一隔離壁包括複數穿孔，該第-隔離壁介於該等 物質與至少一電極組之間。 本新型之功效在於：藉由該第一隔離壁介於該等物質 與至少-電極組之間且配合該等電極組形成電場，而產生 簡單分離該等物質的效果。 3 M436834 【實施方式】 有關本新型之前述及其他技術内容、特點與功效，在 以下配合參考圖式之五個較佳實施例的詳細說明中，將可 清楚的呈現。 在本新型被詳細描述之前，要注意的是，在以下的說 明内容中’類似的元件是以相同的編號來表示。 參閱圖1，本新型電泳分離裝置，適用於分離複數可受 電場泳動的物質（圖未示），該等物質包含蛋白質原料經酸或 酵素水解後產生，且具有不同分子量與電荷的胜肽、胺基 酸，及或在收集蛋白質原料時混入的電解質，如鈉離子 (Na+)、氣離子（Cl·)、氨態氮（NH4+)與亞硝氨（Ν〇2·)。以黃豆 蛋白加工處理為例，黃豆蛋白質經過黴菌醱酵製成的納豆 §含胜肽、胺基酸，而加鹽分解製成的醬油除了包含胜狀 、胺基酸外，還包含鈉離子（Na+)、氣離子（ci_)。 >閱圖1與圖2，本新型的第一較佳實施例包含一電泳 軋1、一隔離單元2，及一直流電源組3。 β電冰槽1包括—槽本體u及：電極棒12。該等電極 =12分別安裝在_本體u二對向側，且分別電連接該直 ^源組3的二電性相異的電極端Η。值得說明的是，該 荨電極棒12也可以相對皮 源細^& 、本^ fK千面刀別上、下設置，該直流電 …‘·也可以為一交流轉換直流的電壓沔夫干、 達到前述相同的功效。 電壓源(圖未不)’也可以 該隔離單元2為—齡这斗上 孔川的第一隔離壁第式^膜，包括一具有複數穿 °亥第—隔離壁21圍繞一軸線][界 4 定一容置該等物質的儲料空間22，並形成二開口 23、。 使用者利用該第-較佳實施例進行醬油中納離子、氛 離子與胜肽、胺基酸分離時，先選定具有適當穿孔211孔徑 的該隔離單元2並封閉其申一聞 ' Ψ開口 24，再將已加鹽處理的 黃豆蛋白質製成的醬油經另一 力開口 23裝入該隔離單元2 儲料空間22中，再使該另一開口 23封閉。 在β亥槽本體11内注水，且將兮隨雜留_ Η·將及離早TL 2置於該槽本 體时’配合該直流電源組3的供電，能使帶有不同電荷 的納離子、_子受到電場較而分躲料電極棒12方 向泳動，由於，該隔離單亓？ _早兀2的弟一隔離壁^介於該等物 質與該專電極棒12之間，可脾兮楚‘所广、 Π 7將5玄專物質區分成可通過該等 穿孔211的鈉離子、氯離子，盥 丁 ’、留存在该儲料空間22中的 胜狀、胺基酸，而產生簡嵐八触外垃併 座王間早刀離忒等物質的效果。需要說 明的是，該寻穿孔211的孔徑大小可視欲分離的物質分子量 以、調整。另外’該電泳槽1不需特別控溫，但為避免該 寺物質在分離過程中腐敗，兮齋、1 4抵 ㈣敗忒電泳槽1可控溫在15〇C以下 0 參閱圖3»本新型的—i., 的弟一較佳貫施例是類似於該第一 較佳實施例，其主要差異之處在於： 該隔離單元4為一營式车潘替 '牛透膜，包括一具有複數穿孔 川的第-隔離壁41及一底壁42.，該第—隔離壁Μ圍繞一 軸線Π界定一容置該等物質的儲料空間43,並形成二開口 44、45,該底壁42連接該其中一開口 45。 如此，該第二較佳實施例也可達到與上述第一較佳實 M436834 施例相同的目的與功效’而且，選用不_式的隔離單元4 ，可產生持續添加已經過酸水解或酵素水解成包含胜肽與 胺基酸後的蛋白質原料的效果。 ㈣4,本新型的一第三較佳實施例是類似於該第二 較佳貫施例，其主要差異之處在於： 該隔離單元5為—網籃，包括—具有複數穿孔川的第 -隔離壁51及一具有複數穿孔521的底壁52，該第一隔離 壁圍繞-軸線m界定一容置該等物質的儲料空間”， 並形成二開口 54、55,該底壁52連接該其中—開口 5卜i 當使用者欲利用該第三較佳實施例純化一蛋白質膠體（ 又稱膠原蛋㈣，_agen pept叫時，先㈣畜產或水產 生物屠體的外皮、肋肉或内臟，利用加熱或酸驗處理將蛋 白質膠體初步分離出來，由於，該蛋白質膠體的蛋白胜肽 在室溫時因收摺而形成不帶電的立體結構，因此可以將該 蛋白質膠體放置在該隔離單元5的儲料空間幻中。 配合該直流電源組3的供電，能使收集該蛋白質膠體 時混入的雜質，如胜肽、胺基酸、氨態氮與亞硝氨等受到β 電場驅使而分別往該等電極棒12方向泳動，而純化該蛋白 質膠體。 如此，忒第二較佳實施例也可達到與上述第二較佳實 加例相同的目的與功效，而且，可對膠體進行純化處理， 而產生簡單分離該等物質的效果。 參閱圖5,本新型的—第四較佳實施例包含一電泳槽6 、一包括複數穿礼711的第一隔離壁71、二包括複數^孔 四洩料閥74，及一直流電 721、731的第二隔離壁72、73 源組3。 /电泳才曰6包括-槽本體61及二電極棒62、63。該等 棒2 63为別安裝在該槽本體61二對向側，且分別 電連接:亥直机電源組3的二電性相異的電極端B。 “亥第離壁71與該等第二隔離壁72、73分別為一 :透膜板’ 4第-_壁71的外周緣712與該等第二隔離 土 72 73的外周緣722、732分別部分連接該槽本體η的 内土面611 ’該第-隔離壁71與該第二隔離壁72、73將該 槽本體61區隔成—介於該電極棒62與該第二隔離壁72之 間的第-分料區64、一介於該第二隔離壁Μ與第一隔離壁 1之間的第一分料區65、一介於第一隔離壁71與該第二 同離土 73之間的第三分料區66，及一介於該第二隔離壁 73與该電極棒63之間的第四分料區67。該等⑽閥74分 別連接該槽本體61的第—分料$ 64、第二分料區&、第 —刀料區66，及第四分料區67。需要說明的是，該槽本體 1的内J面611 π^可形成三分別卡合該第一隔離壁7ι與該 #第二隔離壁72、73外周緣712、722、732的卡槽(圖未示 )’利用該第一隔離壁71與該等第二隔離壁72、73可抽換 地貼處該槽本體61的内壁面611，產生方便更換與清 效果。 ^ 當使用者欲使用該第四較佳實施例收集多種不同分子 量區間的胜肽或胺基酸時，可將已經過酸水解或酵素水解 成包含胜肽與胺基酸後的蛋白質原料放入該等分料區㈠、 M436834 65 ' 66、67其中之一。在該槽本體61内注水，配合該直流 電源組3的供電’能使帶有不同電荷的胜肽、胺基酸受到 电場驅使而力別往該等電極棒62、63方向泳動，由於，該 第一隔離壁71與該第二隔離壁72、73分別介於該等物質 與該等電極棒62、63之間，利用該等穿孔711、721、731 的孔徑選用，可將該等物質區分至該等分料區64、65、66 67中，當分離處理完成後，經由該等洩料閥74收集不同 分子量區間的胜肽或胺基酸。 如此，該第四較佳實施例也可達到與上述第一較佳實· 施例相同的目的與功效，而且，可利用該等分料區64、65 、66、67收集不同分子量區間的物質，而產生簡單分離該 等物質的效果。 參閱圖6,本新型的一第五較佳實施例是類似於該第四 較佳實施例，其主要差異之處在於： _八直流電源組8包括二直流電源、81。該電泳槽6還包括 Λ 有第收料部681及一第二收料部682的收料 ^組68、四分別介於該電泳槽6的槽本體61與該等收料部籲 的第收料。[5 681與第二收料部682間的隔離閥門69 ’及四分別連接該等收料部組68的第一收料部681盘第二 收料部682的洩料閥610。 八 6亥專電極組62、63八2丨丨、吾η 士 6 刀別還具有一設置在該等收料部組 的第一收料部681的第一雷搞ο 等收 #電極621、631，及一設置在該 寺從枓部組68的第-妝社加< 等 第—收抖部682的第二電極622、632。該 笔極组62、63的第—带η! 幻弟電極621、631與第二電極 622、 8 M436834 632分別連接二電連接料直流電源8ι的二電性相 極端811。 ％ 如此，該第五較佳實施例也可達到與上述第四較佳實 施例相同的目的與功效，而且，可利用該等隔離閥門69的 調節，搭配該等電極组62、63的第一電極621、⑶與第 二電極622、632施加電場，產生連續作業的效果。M436834 V. New description: [New technical field] The present invention relates to a separation device, in particular to an electrophoretic separation device. [Prior Art] Generally, proteins are hydrolyzed by acid or enzyme to produce peptides of different molecular weights and amino acids. 'The above products can be used as a culture medium for microorganisms or a nutrient source for plants' but using a general gel filtration method. Slower, separation 2: less, and not easy to prepare in large quantities; while centrifugation is difficult to identify how the distribution layer is separated 'not easy to effectively collect the desired peptide or amino acid, therefore, develop a peptide that effectively separates different molecular weights There is still a great need for a device with an amino acid. [New content] Therefore, the object of the present invention is to provide an electrophoretic separation device which can easily separate a plurality of substances which can be subjected to electric field migration. Therefore, the novel electrophoretic separation device is suitable for separating a plurality of substances that can be subjected to electric field movement, and the electrophoresis separation device comprises an electrophoresis tank and a first partition wall. The electrophoresis tank comprises two electrically different electrode groups. The first dividing wall includes a plurality of perforations, the first dividing wall being interposed between the substance and the at least one electrode set. The effect of the novel is that the first partition wall is interposed between the substances and at least the electrode group and forms an electric field with the electrode groups to produce an effect of simply separating the substances. 3 M436834 [Embodiment] The above and other technical contents, features and effects of the present invention will be apparent from the following detailed description of the preferred embodiments. Before the present invention is described in detail, it is to be noted that in the following description, similar elements are denoted by the same reference numerals. Referring to Fig. 1, the novel electrophoresis separation device is suitable for separating a plurality of substances (not shown) which are capable of being driven by an electric field, and the substances include peptides having different molecular weights and charges, which are produced by hydrolysis of acid materials or enzymes. An amino acid, and an electrolyte mixed in the collection of protein materials, such as sodium ions (Na+), gas ions (Cl·), ammonia nitrogen (NH4+), and nitrosamine (Ν〇2·). Taking the processing of soybean protein as an example, the natto § containing the peptide and the amino acid produced by the mold fermentation of the soybean protein, and the soy sauce prepared by the decomposition of the salt contains sodium ions in addition to the triumphant and amino acid ( Na+), gas ion (ci_). > Referring to Figures 1 and 2, a first preferred embodiment of the present invention comprises an electrophoretic rolling 1, an isolation unit 2, and a DC power supply unit 3. The beta electric ice tank 1 includes a groove body u and an electrode rod 12. The electrodes =12 are respectively mounted on the opposite sides of the _ body u, and are respectively electrically connected to the two-electrode different electrode terminals of the direct source group 3. It is worth noting that the 荨 electrode rod 12 can also be placed on the top and bottom of the 源 源 , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Achieve the same effect as described above. The voltage source (not shown) can also be the isolation unit 2 being the first partition wall of the upper body of the bucket, including a plurality of through holes - the partition wall 21 surrounds an axis] 4 A storage space 22 for accommodating the substances is formed, and two openings 23 are formed. When the user separates the nano ions and the ionic ions from the peptide and the amino acid in the soy sauce by using the first preferred embodiment, the isolation unit 2 having the appropriate perforation 211 aperture is first selected and the sputum opening 24 is closed. Then, the soy sauce made of the salted soybean protein is loaded into the storage unit 22 of the isolation unit 2 through another force opening 23, and the other opening 23 is closed. Water is injected into the β-hump body 11, and the cesium is mixed with _ Η · and the early TL 2 is placed in the groove body. 'With the power supply of the DC power source group 3, nano ions with different charges can be The _ sub-subject is moved by the electric field in the direction of the electrode rod 12, because of the isolation unit? _ 兀 兀 的 的 的 隔离 隔离 ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ , chloride ion, 盥丁', the succulent, amino acid remaining in the storage space 22, and the effect of the simple eight-touch outside and the king's early knife away from the sputum. It should be noted that the pore size of the perforation 211 can be adjusted according to the molecular weight of the substance to be separated. In addition, the electrophoresis tank 1 does not need special temperature control, but in order to avoid the corruption of the temple material in the separation process, the 兮 、, 14 4 (4) defeated the electrophoresis tank 1 can control the temperature below 15 〇 C 0 See Figure 3»本A preferred embodiment of the new type - i., is similar to the first preferred embodiment, the main difference being that: the isolation unit 4 is a camper car Pant' cattle membrane, including a a first partition wall 41 having a plurality of perforated tubes and a bottom wall 42. The first partition wall defines a storage space 43 for accommodating the materials around an axis, and forms two openings 44, 45. A wall 42 connects the one of the openings 45. Thus, the second preferred embodiment can achieve the same purpose and effect as the first preferred embodiment of M436834 above. Moreover, the isolation unit 4 of the non-type type can be selected to produce continuous acid hydrolysis or enzymatic hydrolysis. The effect of a protein material containing a peptide and an amino acid. (4) 4, a third preferred embodiment of the present invention is similar to the second preferred embodiment, and the main difference is that: the isolation unit 5 is a basket, including - a first isolation having a plurality of perforations a wall 51 and a bottom wall 52 having a plurality of perforations 521 defining a storage space for accommodating the substance around the axis m and forming two openings 54, 55 which connect the bottom wall 52 - opening 5, i when the user wants to use the third preferred embodiment to purify a protein colloid (also known as collagen egg (4), _agen pept, first (four) the skin, ribs or internal organs of the carcass of the livestock or water-generating material, The protein colloid is initially separated by heating or acid treatment, because the protein peptide of the protein colloid forms an uncharged three-dimensional structure at room temperature, so that the protein colloid can be placed in the isolation unit 5. The storage space is illusory. In combination with the power supply of the DC power source group 3, impurities mixed in the collection of the protein colloid, such as peptide, amino acid, ammonia nitrogen and nitrosamine, are driven by the beta electric field. Isoelectric rod 12 The protein colloid is purified by migrating. Thus, the second preferred embodiment can achieve the same purpose and efficacy as the above second preferred embodiment, and the colloid can be purified to produce a simple separation. The effect of the material is as follows. Referring to FIG. 5, the fourth preferred embodiment of the present invention comprises an electrophoresis tank 6, a first partition wall 71 including a plurality of shields 711, and a plurality of four blowdown valves 74, and The second isolation wall 72, 73 of the DC power source 721, 731 is the source group 3. The electrophoresis module 6 includes a --slot body 61 and two-electrode rods 62, 63. The rods 2 63 are mounted on the slot body 61. To the side, and electrically connected respectively: two electrically different electrode ends B of the helicopter power supply group 3. "The first wall 71 and the second partition walls 72, 73 are respectively: a diaphragm" 4 The outer peripheral edge 712 of the first--wall 71 and the outer peripheral edges 722, 732 of the second spacers 72 73 are partially connected to the inner surface 611 of the groove body η, respectively. The first-isolation wall 71 and the second partition wall 72 , the groove body 61 is partitioned into a first-division region 64 between the electrode rod 62 and the second partition wall 72, a first dosing zone 65 between the second partition wall and the first partition wall 1, a third dosing zone 66 between the first partition wall 71 and the second dissimilar soil 73, and a medium a fourth dosing zone 67 between the second partition wall 73 and the electrode rod 63. The (10) valves 74 are respectively connected to the first portion of the trough body 61 by $64, the second dosing area & - a tooling area 66, and a fourth materializing zone 67. It should be noted that the inner J surface 611 π of the groove body 1 can form three to respectively engage the first partition wall 7ι and the # second partition wall 72. a card slot (not shown) of the outer peripheral edges 712, 722, and 732 of the outer peripheral edge 712, 722, and 732 is detachably attached to the inner wall surface 611 of the groove body 61 by the first partition wall 71 and the second partition walls 72 and 73, thereby generating Easy to change and clear. ^ When the user wants to use the fourth preferred embodiment to collect a plurality of peptides or amino acids of different molecular weight ranges, the protein material which has been hydrolyzed or hydrolyzed to contain the peptide and the amino acid can be placed. One of the distribution zones (1), M436834 65 '66, 67. Water is injected into the tank body 61, and the power supply of the DC power source group 3 can be used to enable the peptides and amino acids with different charges to be driven by the electric field and force to move toward the electrode rods 62 and 63. The first partition wall 71 and the second partition wall 72, 73 are respectively interposed between the substances and the electrode rods 62, 63, and the holes are selected by using the holes 711, 721, and 731. Distinguishing into the dosing zones 64, 65, 66 67, after the separation process is completed, peptides or amino acids of different molecular weight ranges are collected via the blowdown valves 74. Thus, the fourth preferred embodiment can achieve the same purpose and efficacy as the first preferred embodiment described above, and the materials of different molecular weight ranges can be collected by using the different distribution zones 64, 65, 66, and 67. , resulting in the effect of simply separating the substances. Referring to Figure 6, a fifth preferred embodiment of the present invention is similar to the fourth preferred embodiment. The main difference is that the _ eight DC power supply unit 8 includes two DC power supplies 81. The electrophoresis tank 6 further includes a receiving group 68 having a first receiving portion 681 and a second receiving portion 682, and a receiving portion 68 of the electrophoresis tank 6 and a receiving portion of the receiving portion material. The isolation valve 69' between the 5 681 and the second receiving portion 682 and the discharge valve 610 of the second receiving portion 682 of the first receiving portion 681 of the receiving portion group 68 are respectively connected. The eight-six-electrode special electrode group 62, 63 八 2 丨丨, and the η 士 士 6 knife also have a first thundering device 681 disposed in the first receiving portion 681 of the receiving portion group, 631, and a second electrode 622, 632 disposed in the temple from the first part of the temple group 68. The first band η! phantom electrodes 621, 631 and the second electrodes 622, 8 M436834 632 of the pen electrode groups 62, 63 are respectively connected to the two-electrode phase extremes 811 of the two-wire DC power source 8ι. Thus, the fifth preferred embodiment can achieve the same purpose and effect as the above-described fourth preferred embodiment, and the adjustment of the isolation valves 69 can be utilized to match the first of the electrode groups 62, 63. An electric field is applied to the electrodes 621, (3) and the second electrodes 622, 632 to produce an effect of continuous operation.
歸納上述’本新型電泳分離裝置可獲致下述功效及優 點，故確實能達到本新型之目的： 一、 本新型藉由該第一隔離壁21、41、51、7丨介於該 等物貝與其中f極棒12、62、63之間且配合該等電極棒 U、62、63形成電場’而產生簡單分離該等物質的效果。 二、 本新型利用不同形式的隔離單元4、5，可分別產 生持續添加該等物質與對膠體形式的該等物質進行純化處 理的效果。In summary, the above-mentioned 'electrophoretic separation device can achieve the following functions and advantages, so it can achieve the purpose of the novel: 1. The novel is separated by the first partition wall 21, 41, 51, 7 An electric field is formed between the f-poles 12, 62, 63 and the electrode rods U, 62, 63 to form a simple separation of the substances. Second, the present invention utilizes different forms of isolation units 4, 5, which respectively produce the effect of continuously adding such substances and purifying the substances in colloidal form.
三、 本新型藉由該等分料區64、65、66、67收集不同 分子量區間的物質’而產生簡單分離該等物質的效果。 四、 本新型利用該等隔離閥門69的調節，搭配該等電 極組62、63的第一電極621、631與第二電極622、㈣施 加電場，產生連續作業的效果。 二惟以上所述者，僅為本新型之較佳實施例而已，當不 j以此限定本新型實施之範圍，即大凡依本新型申請專利 軏圍及新型說明内容所作之簡單的等效變化與修飾，皆仍 屬本新型專利涵蓋之範圍内。 【圖式簡單說明】 9 M436834 圖1是本新型電泳分離裝置一第一較佳實施例的立體 圖， 圖2是該第一較佳實施例的一隔離單元的剖視圖； 圖3是本新型電泳分離裝置一第二較佳實施例的立體 圖， 圖4是本新型電泳分離裝置一第三較佳實施例的立體 圖， 圖5是本新型電泳分離裝置一第四較佳實施例的立體 圖；及 圖6是本新型電泳分離裝置一第五較佳實施例的剖視 圖。 10 M436834 【主要元件符號說明】3. The present invention produces the effect of simply separating the materials by collecting the materials of different molecular weight ranges by the respective distribution zones 64, 65, 66, 67. 4. The present invention utilizes the adjustment of the isolation valves 69, the first electrodes 621, 631 and the second electrodes 622, (4) of the electrode groups 62, 63 to apply an electric field, thereby producing the effect of continuous operation. The above is only the preferred embodiment of the present invention, and does not limit the scope of the implementation of the present invention, that is, the simple equivalent change of the patent application scope and the new description content of the present invention. And modifications are still within the scope of this new patent. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a perspective view of a first preferred embodiment of the electrophoretic separation device of the present invention, FIG. 2 is a cross-sectional view of an isolation unit of the first preferred embodiment; FIG. FIG. 4 is a perspective view of a third preferred embodiment of the electrophoretic separation device of the present invention, and FIG. 5 is a perspective view of a fourth preferred embodiment of the electrophoretic separation device of the present invention; and FIG. It is a cross-sectional view of a fifth preferred embodiment of the novel electrophoretic separation device. 10 M436834 [Main component symbol description]
1 ..........電泳槽 11 .........槽本體 12 .........電極棒 2 ..........隔離單元 21 .........第一隔離壁 211 .......穿孔 22 .........儲料空間 23 .........開口 24 .........開口 3 ..........直流電源組 31.........電極端 4 ..........隔離單元 41 .........第一隔離壁 411 .......複數穿孔 42 .........底壁 43 .........儲料空間 44 .........開口 45 .........開口 5 ..........隔離單元 51 .........第一隔離壁 511 .......穿礼 52 .........底壁 521 .......穿礼 53 .........儲料空間 54 .........開口 55 .........開口 6 ..........電泳槽 61.........槽本體 611 .......内壁面 6 2.........電極棒 63 .........電極棒 64 .........第一分料區 6 5.........弟二分料區 66 .........第三分料區 67 .........第四分料區 68 .........收料部組 681 .......第一收料部 682 .......第二收料部 69 .........隔離閥門 610.......洩料閥 71 .........第一隔離壁 711 .......穿孔 712 .......外周緣 72 .........第二隔離壁 721 .......穿孔 722 .......外周緣 11 M436834 73 .........第二隔離壁 731 .......穿孔 732 .......外周緣 74 .........洩料閥 8 ..........直流電源組 81.........直流電源 811 .......電極端 I ...........軸線 II ..........軸線 III ........軸線 121 ..........electrophoresis tank 11 .... tank body 12 ... ... electrode rod 2 .......... isolation unit 21 .........first partition wall 211 ....perforation 22 ... ... storage space 23 ... ... opening 24 .. .......opening 3 ..........DC power supply group 31.........electrode end 4 .......... isolation unit 41 .. .......first partition wall 411.......plural perforation 42 ......... bottom wall 43 ... ... storage space 44 ... ... opening 45 ... ... opening 5 .......... isolation unit 51 ... ... first partition wall 511 .... ... wearing a gift 52 ......... bottom wall 521 ....... wearing a gift 53 ... ... storage space 54 ......... Opening 55 .... opening 6 ..... electrophoresis tank 61 .... tank body 611 .... inner wall surface 6 2. ........electrode rod 63 .........electrode rod 64 .........the first material area 6 5......different Feed zone 66 .... third dosing zone 67 .... fourth dosing zone 68 ... ... receiving section 681 ... ....first receiving portion 682.......second receiving portion 69 ....isolation valve 610.......blowing valve 71 .... ..... first partition wall 711 .... perforation 712 ....... outer circumference 72 ....... ..Second partition wall 721 . . . perforation 722 ....... outer circumference 11 M436834 73 ......... second partition wall 731 .... perforation 732 .......outer circumference 74 .........Blowing valve 8 ..........DC power supply group 81.........DC power supply 811 .......electrode end I ...........axis II ..........axis III ........axis 12