TW200902767A - Electrode for membrane electrolysis cells - Google Patents
Electrode for membrane electrolysis cells Download PDFInfo
- Publication number
- TW200902767A TW200902767A TW097115149A TW97115149A TW200902767A TW 200902767 A TW200902767 A TW 200902767A TW 097115149 A TW097115149 A TW 097115149A TW 97115149 A TW97115149 A TW 97115149A TW 200902767 A TW200902767 A TW 200902767A
- Authority
- TW
- Taiwan
- Prior art keywords
- electrode
- electrolytic cell
- item
- groove
- representative
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
- C25B11/02—Electrodes; Manufacture thereof not otherwise provided for characterised by shape or form
- C25B11/03—Electrodes; Manufacture thereof not otherwise provided for characterised by shape or form perforated or foraminous
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
- C25B11/02—Electrodes; Manufacture thereof not otherwise provided for characterised by shape or form
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/14—Alkali metal compounds
- C25B1/16—Hydroxides
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/24—Halogens or compounds thereof
- C25B1/26—Chlorine; Compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/34—Simultaneous production of alkali metal hydroxides and chlorine, oxyacids or salts of chlorine, e.g. by chlor-alkali electrolysis
- C25B1/46—Simultaneous production of alkali metal hydroxides and chlorine, oxyacids or salts of chlorine, e.g. by chlor-alkali electrolysis in diaphragm cells
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
- C25B9/17—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof
- C25B9/19—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof with diaphragms
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
Landscapes
- Chemical & Material Sciences (AREA)
- Metallurgy (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Electrodes For Compound Or Non-Metal Manufacture (AREA)
- Electrolytic Production Of Metals (AREA)
- Secondary Cells (AREA)
- Primary Cells (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
200902767 九、發明說明: 【發明所屬之技術領域】 本發明係關於電化學應用之電極,尤指在金屬載體上 作的隔膜電解池用之電極。 【先前技術】 在利用離子交換隔膜加以分開的電解池内進行之電解過 程’,最具相關的工業上電化學用途。此等用途有些例是鹼 ,屬匕物塩水電解(减氯電解),尤指氯化納迄水電解,以 生產氯和苛性鈉’以及塩酸溶液電解。 、在以下說明申,係參照氯化鈉電解做為總體生產上最且 代表性之例,但本發明不限於此等用途。 八 在隔膜魏電射,電解池之陽極室是·離子交 $,與陰極室分開。轉池之陽極室加氣化魏水,例如濃 的;在陽極表面發生釋出氣,電流密度通常不超過 k^/m,而塩水自然消耗到出口濃度往往在施和22 離子電場傳送越過隔膜,到陰極室,在此產生 Γ ΐ度通常不高於33%重量。苛性生成物即萃 ,’在電解料_蒸發加以濃縮。在陰極絲亦發生^ ΐ: ϊίί低iitt會導致工f設計在較高電流密度操 售廠在在在3 作業,而新廉則在約5 設計中的電流趨向進一步提高到6 kW或 辦,會成目、式釋出,其流量隨電流密度增加而遞 二S ’/_之機械完整性有潜在危險:因 ==電 =:,:,,增加在二匚= =釋=隨後酸化,而;部釋放==層農= 累積、乳累積、被捕紐水、酸化)的組合,遭致隔膜^ 5 200902767 ίί電ίίί在ίίΓ陽極和隔膜間的間隙區,形成氣泡, 、、農情況下,液體滞留導致苛性生成物 構學結 表=二 極界面促進塩水循環,以免在界面因消^ 情不規騎極表面,以改進垣水供應至陽極。 交換===;:某==所:防離子 ⑦有最佳功用,以副目前市=== 制,ϊίί::ί=ϊ解、f用之電極’克服先前技術之限 f,此⑽能用電X可能 【發明内容】 本發明各種層面列在附帶申請專利範圍。 凹溝了金η屬基體上所得電極’有複數局部平行 至〇.5二 酿’相鄰凹溝間距離(間距)〇.〇1 200902767 局部平行凹溝意指複數開放或封 以平直行二溝之途徑可假設 ㈣ΐί電構’呈直線或任何形狀的曲率。在-且= 交又。’電c表面呈現局部平行凹溝,有封_狀,彼此^復 =界定之電極有益於任何電解應用, 離子父換賴直接接觸;以舰電脾 、=作業時與 與其有凹溝的表面組合,直接接觸隔^述電極可200902767 IX. Description of the Invention: [Technical Field] The present invention relates to an electrode for electrochemical applications, and more particularly to an electrode for a diaphragm electrolytic cell used on a metal carrier. [Prior Art] The electrolysis process carried out in an electrolytic cell separated by an ion exchange membrane, the most relevant industrial electrochemical use. Some of these uses are alkalis, which are sputum water electrolysis (chlorine reduction electrolysis), especially sodium chloride water electrolysis, to produce chlorine and caustic soda and tannic acid solution electrolysis. In the following description, sodium chloride electrolysis is referred to as the most representative and representative example of the overall production, but the present invention is not limited to such use. Eight In the diaphragm Wei, the anode chamber of the electrolytic cell is · ion exchange $, separated from the cathode chamber. The anode chamber of the rotary tank is filled with gasified Wei water, for example, concentrated; the gas is released on the surface of the anode, and the current density usually does not exceed k^/m, while the natural consumption of the hydrophobic water to the outlet concentration is often transmitted across the membrane at the application of the 22 ion electric field to The cathode chamber, where the degree of enthalpy is usually not higher than 33% by weight. The caustic product is extracted, and is concentrated in the electrolytic material. In the cathode wire also occurs ^ ΐ: ϊ ίί low iitt will cause the work f design at the higher current density of the operating plant in the 3 operations, while the new cheaper in the 5 design of the current trend is further increased to 6 kW or do, Will be released, the release, the flow rate increases with the current density and the mechanical integrity of the two S ' / _ is potentially dangerous: because = = electricity =:,:,, increase in the second = = release = subsequent acidification, And the combination of the partial release == layer farming = accumulation, milk accumulation, trapped new water, acidification), caused by the diaphragm ^ 5 200902767 ίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίίί Under the condition, the liquid retention leads to the formation of the caustic formation table = the two-pole interface promotes the hydrophobic circulation, so as to avoid the riding of the pole surface due to the elimination of the interface, so as to improve the supply of the hydrophobic water to the anode. Exchange ===;: Some ==: Anti-Ion 7 has the best function, with the current market === system, ϊίί:: ί=ϊ,f electrode used to overcome the limitations of the prior art f, this (10) It is possible to use electricity X. [Invention] Various aspects of the invention are listed in the scope of the accompanying claims. The groove obtained on the base of the gold η genus has a plurality of partial parallel to 〇.5 two brewing 'distance between adjacent grooves (pitch) 〇.〇1 200902767 Partial parallel groove means plural open or sealed with straight line two The path of the trench can be assumed to be (4) 电 电 structure 'curvature in a straight line or any shape. In - and = pay again. 'Electric c surface presents a local parallel groove, there is a seal _ shape, each other = the defined electrode is beneficial for any electrolysis application, the ion father for direct contact; for the ship spleen, = when working and with a grooved surface Combination, direct contact with the electrode
和不錄鋼。基體可呈任何幾何形狀:做為 =口J 凹溝表面可設在沖屢或拉模之片材上, ^ ’有 結構電軸線轉動,亦稱為百葉窗式電極。· 旨在魏電解池_做陽極以釋出氣時減其 3特別有用於减氯電解池’無論釋放氯用所 用的陰極,尤其是與有凹溝絲組合時 隔= 平行延伸跨齡結狀餘凹料言,凹 tiff t從表面釋放的氣泡有改進之循環。按二 發明人觀〒,在有凹溝表面 ,,全然可接受之電解池電壓。現場測試,在=電解3 度低於2GG g/l (尤其是降到15〇的)可得優肆果性/ 成物濃度在33%以上(尤其是37%),維 的 差高於3000 Pa (尤其是達1〇〇〇〇 pa) 力 時,在此等條件通常導致隔膜快速劣化。 別认、電極 不願受到任何特殊理論之限制,可假設在上述凹溝表面 200902767 所得電極,得以特別有效率釋放氣泡,且與 溝電極比較之下,可能是目密實的裝填 ^ 細管傳送現象,與電解質循環相反。 冑有利於毛 f 成本ii技ΪΓ寻電極較之技術上已知之其他有凹溝表面, ^本銳降,其特徵為凹赫度高好,非單純研磨所得竟其 【實施方式】 實施你>丨1. 麯股ί張1 Γ1厚,600 mm x 800 mm寬的鈦級1片材, 職^深tii磨輪加以侵姓處理,所有樣片上均得間距〇.2 網狀幾何开:溝,片材f照已知技術拉撐’得扁菱形 俨铲皮二2對角1〇mmx 5««11,移動步距1.5111111。拉 1牙Γ戶Γ元成時’以表面測定器測得凹溝顯示平均深度,如第And do not record steel. The base body can be of any geometric shape: as the mouth of the mouth J, the surface of the groove can be set on the sheet of the punch or the die, and the structure of the structure is rotated, also known as the louver electrode. · Designed for the Wei electrolysis cell _ to do the anode to reduce the gas when it is released 3 especially for the chlorine reduction electrolytic cell 'no matter the cathode used for the release of chlorine, especially when combined with the grooved wire = the parallel extension of the cross-age knot In the concave state, the concave tiff t has an improved cycle of bubbles released from the surface. According to the second inventor's view, on the surface of the groove, the electrolytic cell voltage is fully acceptable. On-site testing, at = 3 degrees below 2 GG g / l (especially down to 15 )) can achieve superior fruit / product concentration above 33% (especially 37%), the difference in dimensional is higher than 3000 When Pa (especially up to 1 〇〇〇〇pa) force, these conditions usually cause the diaphragm to deteriorate rapidly. Do not recognize, the electrode is not willing to be limited by any special theory, it can be assumed that the electrode obtained on the surface of the groove above 200902767 can release the bubble particularly efficiently, and compared with the groove electrode, it may be a dense filling phenomenon. Contrary to the electrolyte cycle.胄 胄 胄 胄 ii ii ii ii ii ii ii ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ΪΓ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ;丨1. 曲张ί1 Γ1 thick, 600 mm x 800 mm wide titanium grade 1 sheet, job ^ deep tii grinding wheel to invade the surname, all the swatches have a spacing 〇.2 mesh geometry open: ditch , sheet f according to the known technology to pull 'de flat diamond 俨 shovel skin 2 2 diagonal 1 〇 mmx 5 « «11, moving step 1.5111111. Pulling a 1 Γ Γ Γ ’ ’ ’ 以 以 以 以 以 以 以 以 以 以 以 以 以 以 以 以
片,=理,二張1 mm厚,而600 mm X 800 mm寬之鎳 經脫脂,以同樣侵蝕處理,隨即拉撐,得一致的幾何形 200902767 ίίί棒絲面败賴咖示平均深 樣品内徑 ΓΜ------ 凹溝深度(mm) U 1 0.002 — {JZ 0.01 0.05 Γ0_, 鬥上返樣品),分別標為AO和 列後,按ίΐϋ知方式’用金剛石噴砂’稍後在HC1内餘 磨光處^ _拉撐處理;但在此财不再進行附加 ί 極釋和鈦氧2化物為基礎之觸媒,供陽 因塗佈步驟引起任何重大變異。尽職置凹溝冰度,未見 f施你丨2 舰5==1之=’切片成15°一。〇 ίίΓίΠ複餘細各站裝設—隔職解=適 =°n 982,美國杜邦公司製品)直接接觸。表ff= 试’啟用全部電解池,陽極和 人仃=用可命測 較普通的工聿實況爵并,、口,製程條件遠 對於製程電if声疋離子交換隔膜衰減時間,以相 脖門ί Ϊ 4度之初始值言’電解池電壓提高G5 V所雷 時間计。製程條件如下: .V所而 —在陽極室出口的塩水濃度:150g/1 一苛性鈉生成物濃度,重量計:37% —跨越二室之壓力差:5000Pa 電 掛度· 12 kA/n^ 所得結果列於表3 ·· 9 200902767 表3Sheet, = rational, two sheets 1 mm thick, and 600 mm X 800 mm wide nickel is degreased, treated with the same erosion, then pulled, and the consistent geometry 200902767 ίίί 丝 面 咖 咖 咖 咖 平均 平均Diameter ΓΜ groove depth (mm) U 1 0.002 — {JZ 0.01 0.05 Γ0_, bucket back sample), marked as AO and column, respectively, according to the way ' 'with diamond blasting' later The residual polishing of HC1 is _ strutting treatment; however, there is no additional ί extreme release and titanium oxide based catalyst, which will cause any significant variation in the coating process. Dedicated to the gutter ice, not seen f 丨 2 5 5 = =1 = ' sliced into 15 ° one. 〇 Γ ίίί Γ Π 细 各 各 各 各 — — — — — — — — — — — 隔 隔 隔 隔 隔 隔 隔 隔 隔 隔 隔 隔 ° ° Table ff= Test 'Enable all electrolytic cells, anode and human 仃 = use the measurable normal workmanship, the mouth, the process conditions are far away from the process electric if sono ion exchange diaphragm decay time, to the neck door ί Ϊ The initial value of 4 degrees says that the electrolytic cell voltage is increased by the G5 V thunder time meter. The process conditions are as follows: .V - the concentration of hydrophobic water at the outlet of the anode chamber: 150g / 1 concentration of caustic soda, weight: 37% - pressure difference across the two chambers: 5000Pa electric suspension degree · 12 kA / n ^ The results are shown in Table 3. ·· 9 200902767 Table 3
Test number Anode Cathode Duration (h) 1 AO CO 514 2 AO CO 562 3 AO C2 580 4 A0 C3 565 5 A1 CO 729 6 A2 CO 904 7 A3 CO 1213 8 A4 CO 1417 9 A5 CO 866 10 A6 CO 578 11 A2 C1 940 12 A3 C1 1283 13 A4 C1 1646 14 A5 C1 1108 15 A1 C2 887 16 A2 C2 959 17 A3 C2 1682 18 A4 C2 1704 19 A5 C2 1011 20 A6 C2 622 21 A3 C3 1088 22 A4 C3 1544 23 A3 C1 1305 24 A4 C1 1593 實施例3 一電解池同實施例2,裝設陽極樣品A4和陰極樣品 C2,第二類似電解池裝設無凹溝陽極樣品A0和無凹溝陰極 樣品C0,在製程條件經使用壽命測試,比通常工業實況更嚴 A-h 可。 製程條件設定如下: —在陽極室出口的塩水濃度:180 g/1 一苛性鈉生成物濃度,重量計:35% 一跨越二室之壓力差:4000 Pa 一電流密度:10kA/m2 200902767 =式約900小時後’裝設電極樣品A〇和c〇 ί'ίΐί,St隔膜逐漸劣化會造成電解池電壓強烈Ϊ升, 兩層開妹_,也會觀察到隔膜 ㈣陰極C2的電解池,在實際上一定電壓連 時後賴。電解轉解時,未賴隔膜劣化之 f 前述說明無法關本剌,本發啊舰不同且 鉍,不悖其範圍,惟以所附申請專利範圍為準。、]貫 在本案全文和ΐ請專利範II裡「包括」及其類似用語, 無思排除其他元件或添加劑的存在。 本說明書所含文獻討論、作用、材料、農置、論文 純為提供本發明之文脈,並非建議或表示其任一或:忐 先前技術基礎之一部份’或是本案各申請專利範圍優先^ 之前,與本發明相關領域内之通嘗一般知識。Test number Anode Cathode Duration (h) 1 AO CO 514 2 AO CO 562 3 AO C2 580 4 A0 C3 565 5 A1 CO 729 6 A2 CO 904 7 A3 CO 1213 8 A4 CO 1417 9 A5 CO 866 10 A6 CO 578 11 A2 C1 940 12 A3 C1 1283 13 A4 C1 1646 14 A5 C1 1108 15 A1 C2 887 16 A2 C2 959 17 A3 C2 1682 18 A4 C2 1704 19 A5 C2 1011 20 A6 C2 622 21 A3 C3 1088 22 A4 C3 1544 23 A3 C1 1305 24 A4 C1 1593 Example 3 An electrolytic cell is the same as in Embodiment 2, and an anode sample A4 and a cathode sample C2 are installed. The second similar electrolytic cell is provided with a groove-free anode sample A0 and a groove-free cathode sample C0, in the process conditions. Life test, which is stricter than the normal industrial situation. The process conditions are set as follows: - the concentration of hydrophobic water at the outlet of the anode chamber: 180 g / 1 concentration of caustic soda, weight: 35%: pressure difference across two chambers: 4000 Pa, current density: 10 kA / m2 200902767 = After about 900 hours, the electrode samples A〇 and c〇ί'ίΐί were installed. The gradual deterioration of the St diaphragm caused the voltage of the electrolytic cell to rise sharply. The two layers of the cathode were also observed, and the electrolytic cell of the cathode (C) cathode C2 was also observed. In fact, certain voltages will depend on the time. When electrolysis is transferred, it does not depend on the deterioration of the diaphragm. f The above description cannot be closed. The ship is different and has no scope, but the scope of the attached patent application shall prevail. ,] In the full text of this case and in the Patent Model II, "including" and similar terms, without the exclusion of the existence of other components or additives. The literature discussion, role, materials, agricultural, and papers contained in this manual are purely to provide the context of the present invention, and are not suggested or indicated as either: or part of the prior art basis or the priority of each patent application in this case. Previously, general knowledge has been gained in the field related to the present invention.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT000980A ITMI20070980A1 (en) | 2007-05-15 | 2007-05-15 | ELECTRODE FOR ELECTROLYTIC MEMBRANE CELLS |
Publications (1)
Publication Number | Publication Date |
---|---|
TW200902767A true TW200902767A (en) | 2009-01-16 |
Family
ID=39874450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW097115149A TW200902767A (en) | 2007-05-15 | 2008-04-25 | Electrode for membrane electrolysis cells |
Country Status (24)
Country | Link |
---|---|
US (1) | US20100059389A1 (en) |
EP (1) | EP2147133B1 (en) |
JP (1) | JP5193287B2 (en) |
KR (1) | KR20100023873A (en) |
CN (1) | CN101707932B (en) |
AR (1) | AR066579A1 (en) |
AT (1) | ATE490354T1 (en) |
AU (1) | AU2008249990B2 (en) |
BR (1) | BRPI0811852A2 (en) |
CA (1) | CA2687319A1 (en) |
CL (1) | CL2008001402A1 (en) |
DE (1) | DE602008003789D1 (en) |
DK (1) | DK2147133T3 (en) |
EG (1) | EG25970A (en) |
ES (1) | ES2357080T3 (en) |
HK (1) | HK1143615A1 (en) |
IL (1) | IL201541A (en) |
IT (1) | ITMI20070980A1 (en) |
MX (1) | MX2009012314A (en) |
PL (1) | PL2147133T3 (en) |
PT (1) | PT2147133E (en) |
RU (1) | RU2436871C2 (en) |
TW (1) | TW200902767A (en) |
WO (1) | WO2008138945A2 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20110174242A1 (en) * | 2010-04-09 | 2011-07-21 | Mcconahay Fred E | Cylindrical hydrogen fuel generator having tubular cells with microscopic indentations |
WO2014052928A1 (en) * | 2012-09-28 | 2014-04-03 | Hydrogen Injection Technology, Inc. | Supplementary hydrogen fuel system |
FI125711B (en) * | 2012-12-21 | 2016-01-15 | Outotec Oyj | Electrode for an electrolytic process |
JP6234754B2 (en) * | 2013-09-18 | 2017-11-22 | 株式会社神戸製鋼所 | Electrode metal plate and electrode |
WO2016043072A1 (en) * | 2014-09-19 | 2016-03-24 | 株式会社 東芝 | Electrolytic device, electrode unit, and method for generating electrolytic water |
EP3854912A4 (en) * | 2018-09-21 | 2021-11-24 | Asahi Kasei Kabushiki Kaisha | Electrode for electrolysis, and laminate |
CN109457270A (en) * | 2018-12-29 | 2019-03-12 | 西安泰金工业电化学技术有限公司 | A kind of preparation method of ti-based coating Ni―Ti anode |
WO2021014940A1 (en) * | 2019-07-23 | 2021-01-28 | マクセルホールディングス株式会社 | Electrode for bubble generation, and method for forming surface of electrode for bubble generation |
CN110441539B (en) * | 2019-08-21 | 2023-08-01 | 东软威特曼生物科技(沈阳)有限公司 | Reaction cup holder for solid direct heating type or air bath type reaction disk and full-automatic biochemical analyzer |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3361656A (en) * | 1966-05-16 | 1968-01-02 | Hooker Chemical Corp | Wicking electrode for an electrolytic cell |
US3589942A (en) * | 1966-12-22 | 1971-06-29 | Cons Natural Gas Svc | Bipolar collector plates |
US4056452A (en) * | 1976-02-26 | 1977-11-01 | Billings Energy Research Corporation | Electrolysis apparatus |
DE2926776C2 (en) * | 1979-07-03 | 1984-03-15 | Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt | Fuel and / or electrolysis cell |
JPS6016518B2 (en) * | 1980-07-31 | 1985-04-25 | 旭硝子株式会社 | Ion exchange membrane electrolyzer |
JPS60501364A (en) * | 1983-03-30 | 1985-08-22 | イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− | Improved electrolysis method for brine containing iodide impurities |
JPS6049718B2 (en) * | 1983-08-12 | 1985-11-05 | 旭硝子株式会社 | Alkali chloride electrolyzer |
DD244769B3 (en) * | 1985-12-23 | 1991-08-08 | Eilenburger Chemie-Werk Gmbh,De | DEVICE FOR CARRYING OUT ELECTROCHEMICAL PROCESSES |
BR9000773A (en) * | 1989-02-28 | 1991-01-22 | Du Pont | PROCESS FOR THE MANUFACTURE OF A CATIO EXCHANGE MEMBRANE; PROCESS FOR THE MANUFACTURE OF A COATED FABRIC; PROCESS FOR THE MANUFACTURE OF A COATED YARN; CATION EXCHANGE MEMBRANE; PERFECT PROCESS FOR THE ELECTROLYSIS OF AN ALKALINE METAL HALIDE; CATION EXCHANGE FABRIC AND CATION EXCHANGE YARN |
SE465966B (en) * | 1989-07-14 | 1991-11-25 | Permascand Ab | ELECTRIC FOR ELECTRIC LIGHTING, PROCEDURE FOR ITS MANUFACTURING AND APPLICATION OF THE ELECTRODE |
TW197475B (en) * | 1990-12-26 | 1993-01-01 | Eltech Systems Corp | |
SE505714C2 (en) * | 1991-09-19 | 1997-09-29 | Permascand Ab | Electrode with channel forming wires, methods of making the electrode, electrolytic cell provided with the electrode and methods of electrolysis |
JPH08302492A (en) * | 1995-04-28 | 1996-11-19 | Permelec Electrode Ltd | Electrolytic cell using gas diffusion electrode |
IT1279069B1 (en) * | 1995-11-22 | 1997-12-04 | Permelec Spa Nora | IMPROVED ELECTRODE TYPE FOR ION EXCHANGE MEMBRANE ELECTROLYZERS |
US5653857A (en) * | 1995-11-29 | 1997-08-05 | Oxteh Systems, Inc. | Filter press electrolyzer electrode assembly |
JP2001152380A (en) * | 1999-11-29 | 2001-06-05 | Tokuyama Corp | Ion-exchange membrane electrolytic cell |
ES2533254T3 (en) * | 2002-11-27 | 2015-04-08 | Asahi Kasei Chemicals Corporation | Bipolar electrolytic cell, without interstices |
DE102005006555A1 (en) * | 2005-02-11 | 2006-08-17 | Uhdenora S.P.A. | Electrode for electrolysis cells |
-
2007
- 2007-05-15 IT IT000980A patent/ITMI20070980A1/en unknown
-
2008
- 2008-03-14 CL CL200801402A patent/CL2008001402A1/en unknown
- 2008-04-25 TW TW097115149A patent/TW200902767A/en unknown
- 2008-05-14 PL PL08759575T patent/PL2147133T3/en unknown
- 2008-05-14 PT PT08759575T patent/PT2147133E/en unknown
- 2008-05-14 JP JP2010507912A patent/JP5193287B2/en not_active Expired - Fee Related
- 2008-05-14 DE DE602008003789T patent/DE602008003789D1/en active Active
- 2008-05-14 WO PCT/EP2008/055887 patent/WO2008138945A2/en active Application Filing
- 2008-05-14 RU RU2009146284/07A patent/RU2436871C2/en not_active IP Right Cessation
- 2008-05-14 CA CA002687319A patent/CA2687319A1/en not_active Abandoned
- 2008-05-14 DK DK08759575.7T patent/DK2147133T3/en active
- 2008-05-14 MX MX2009012314A patent/MX2009012314A/en active IP Right Grant
- 2008-05-14 ES ES08759575T patent/ES2357080T3/en active Active
- 2008-05-14 CN CN2008800158766A patent/CN101707932B/en not_active Expired - Fee Related
- 2008-05-14 KR KR1020097026193A patent/KR20100023873A/en not_active Application Discontinuation
- 2008-05-14 BR BRPI0811852-3A2A patent/BRPI0811852A2/en not_active IP Right Cessation
- 2008-05-14 AU AU2008249990A patent/AU2008249990B2/en not_active Ceased
- 2008-05-14 AT AT08759575T patent/ATE490354T1/en active
- 2008-05-14 EP EP08759575A patent/EP2147133B1/en not_active Not-in-force
- 2008-05-15 AR ARP080102058A patent/AR066579A1/en unknown
-
2009
- 2009-10-15 IL IL201541A patent/IL201541A/en not_active IP Right Cessation
- 2009-11-11 EG EG2009111668A patent/EG25970A/en active
- 2009-11-13 US US12/617,773 patent/US20100059389A1/en not_active Abandoned
-
2010
- 2010-10-28 HK HK10110136.2A patent/HK1143615A1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
HK1143615A1 (en) | 2011-01-07 |
AR066579A1 (en) | 2009-08-26 |
JP2010526938A (en) | 2010-08-05 |
KR20100023873A (en) | 2010-03-04 |
ES2357080T3 (en) | 2011-04-18 |
CA2687319A1 (en) | 2008-11-20 |
MX2009012314A (en) | 2009-12-03 |
CN101707932B (en) | 2011-07-27 |
AU2008249990A1 (en) | 2008-11-20 |
BRPI0811852A2 (en) | 2014-11-18 |
PT2147133E (en) | 2011-02-24 |
CN101707932A (en) | 2010-05-12 |
ATE490354T1 (en) | 2010-12-15 |
EG25970A (en) | 2012-11-13 |
ITMI20070980A1 (en) | 2008-11-16 |
DE602008003789D1 (en) | 2011-01-13 |
EP2147133A2 (en) | 2010-01-27 |
CL2008001402A1 (en) | 2008-08-22 |
IL201541A (en) | 2013-03-24 |
DK2147133T3 (en) | 2011-02-28 |
IL201541A0 (en) | 2010-05-31 |
WO2008138945A3 (en) | 2009-01-15 |
JP5193287B2 (en) | 2013-05-08 |
PL2147133T3 (en) | 2011-05-31 |
RU2436871C2 (en) | 2011-12-20 |
WO2008138945A2 (en) | 2008-11-20 |
AU2008249990B2 (en) | 2012-02-02 |
US20100059389A1 (en) | 2010-03-11 |
EP2147133B1 (en) | 2010-12-01 |
RU2009146284A (en) | 2011-06-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TW200902767A (en) | Electrode for membrane electrolysis cells | |
Dresp et al. | Direct electrolytic splitting of seawater: opportunities and challenges | |
CA3018074C (en) | Anode for alkaline water electrolysis and method for producing anode for alkaline water electrolysis | |
CN105734600B (en) | A kind of device and method of the double electrolytic cell two-step method water electrolysis hydrogen productions of three-electrode system | |
CN105420748B (en) | A kind of method and device of the two-step method water electrolysis hydrogen production based on three-electrode system | |
Bolar et al. | Progress in theoretical and experimental investigation on seawater electrolysis: opportunities and challenges | |
CN107075701B (en) | Electrolysis unit and electrolysis ozone water making device | |
CN107002262B (en) | Oxygen anode | |
US9315908B2 (en) | Electrolytic cell for producing chlorine—sodium hydroxide and method of producing chlorine—sodium hydroxide | |
JP5178959B2 (en) | Oxygen gas diffusion cathode, electrolytic cell using the same, chlorine gas production method, and sodium hydroxide production method | |
JP2016540118A (en) | Electrochemical cell with graphene-covered electrode | |
KR102529087B1 (en) | Alkaline water electrolysis method and anode for alkaline water electrolysis | |
KR101584725B1 (en) | Alkaline anion exchange membrane water electrolyzer using Ni electrodeposited hydrophilic porous carbon material and method for preparing the same | |
Feng et al. | Recent progress in seawater electrolysis for hydrogen evolution by transition metal phosphides | |
JP6788378B2 (en) | Water electrolysis cell and multi-pole water electrolysis tank | |
WO2015154712A1 (en) | Excess microbubble hydrogen preparation device | |
JP2010509050A (en) | Extraction of platinum group metals from spent catalyst by electrochemical method | |
CN107670667A (en) | It is a kind of to be used to analyse nanoporous Ni Fe bimetallic layered hydroxide electrocatalysis materials of oxygen and its preparation method and application | |
KR102373090B1 (en) | Alkaline water electrolysis method and anode for alkaline water electrolysis | |
CN109534457B (en) | Electrolysis electrode | |
JP6438205B2 (en) | Water electrolysis cell | |
JP2010174346A (en) | Electrolytic bath for ion exchange membrane method and method of manufacturing the same | |
CN114990603B (en) | Ion exchange membrane electrolyzer | |
Lin et al. | Hydrogen production from seawater splitting enabled by on-line flow-electrode capacitive deionization | |
CN105132980B (en) | A kind of lead silver alloy anode surface recombination ceramic film film build method |