CN85103305A - Fuel cell - Google Patents
Fuel cell Download PDFInfo
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- CN85103305A CN85103305A CN85103305.9A CN85103305A CN85103305A CN 85103305 A CN85103305 A CN 85103305A CN 85103305 A CN85103305 A CN 85103305A CN 85103305 A CN85103305 A CN 85103305A
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- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
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Abstract
Fuel cell (8) includes fuel electrode, oxidant electrode and is placed in two interelectrode electrolyte.For making the quantity of methyl alcohol in the conduit (9) of fuel cell (8) fueling controlled, locate to settle a methanol concentration control device (10) at conduit (9), borrow the open circuit voltage of cell (15) in the detection (10) such as the Open Circuit Potential of oxidant cell (2) to control.
Description
The invention relates to fuel cell, more particularly, about methanol-air acidic electrolyte bath fuel cell.
Fuel cell is input fuel and an oxidant, carries out electrochemical reaction on electrode, directly produces electric energy, and it is used as always a kind ofly has high efficiency novel energy and look forward to.Particularly as the small size energy movably, methanol-air acidic electrolyte bath fuel cell is more noticeable in the fuel cell that uses liquid fuel.Methyl alcohol can be easily from microbial fermentation, and lique faction of coal and make ， And and operate easily is so people's expectation drops into actual the use with methanol fuel cell.
In the fuel of input fuel cell, the concentration of methyl alcohol is exported to closing weight for the rated power of keeping fuel cell.When methanol concentration is lower than setting, then power output will reduce naturally; When methanol concentration increases, just reached specified power output.Yet, because electric osmose and diffusion etc. are former thereby by electrolytical methyl alcohol the more, on oxidant electrode, be consumed also just the more.So the utilance of methyl alcohol just reduces.
For this reason, in order to keep not fluctuation of power output, it is constant in the scope of predesignating to keep methanol concentration during the fuel input.
Fig. 2 sees from Japanese patent laid-open publication gazette 56-118273 number (1981) being entitled as " concentration sensor of fuel cell ", proposed to detect the early stage technology of methanol concentration in the fuel, promptly in fuel cell, constitute a small fuel cell separately, fuel input fuel cell is to produce electric energy, and the concentration of methyl alcohol then detects and controls according to the electromotive force of this small fuel cell in the fuel at this moment.
Early stage technology provides air and liquid electrolyte to oxidant electrode, because it requires air to emerge so air chamber of needs through electrolyte.
The purpose of this invention is to provide a kind of fuel cell, the concentration and the control methanol concentration that wherein comprise methyl alcohol in the fuel that detects the input fuel cell keep constant device, and do not need to install complicated air chamber, thereby keep the power stability of output, do not fluctuate.
The inventor has in depth studied the progress of fuel cell.Found that when temperature of fuel cell is 50 °～60 ℃ the open circuit voltage of battery (being shown in the Fig. 2 that is attached to the back) is relevant with methanol concentration, is shown in Fig. 4.When oxidant electrode was immersed in the fuel that contains electrolyte (anolyte), the relation of open circuit voltage and fuel methanol concentration shown in Figure 9 was shown in Fig. 5 in addition.These have all pointed out the index with the enough do indications of the corresponding open circuit voltage of methanol concentration and energy of position methanol concentration, as Fig. 4 and shown in Figure 5.
The present invention utilizes above-mentioned concentration dependence, and a device is set uniquely, in this device, and the concentration that the concentration stabilize of utilizing the Open Circuit Potential of the open circuit voltage of cell and oxidant electrode to control methyl alcohol in the input fuel is being predesignated.The present invention notices that methanol concentration depends on that it sees through and be mixed into the quantity of air electrode (being shown in Fig. 2 or Fig. 9 of being attached to the back), does not have complicated air chamber in this kind structure.
The present invention includes following three systems (1)～(3):
(1) cell (is shown in Fig. 2 and Fig. 7, be attached to the back) be placed on the fuel input channel of fuel cell, detect the open circuit voltage of cell, new methyl alcohol replenishes into the open circuit voltage of predesignating to keep, thereby makes the fuel input fuel cell of concentration stabilize in predesignating scope.(2) cells (being shown in Fig. 6 and Fig. 8 of being attached to the back) are placed on the fuel input channel of fuel cell, settle one to make methyl alcohol keep it to give the cell of first normal concentration (for example 1 mol) again, detect the open circuit voltage of each cell respectively, the control methanol feeding, make the open circuit voltage energy of two batteries identical, methanol concentration keeps being stabilized in the concentration of predesignating in the fuel of importing fuel cell thereby make.(3) as Fig. 9 of being attached to the back and shown in Figure 11, anolyte and oxidant electrode keep in touch, and reduce according to current potential that kind and measure methanol concentration, re-enter methyl alcohol according to measuring-signal to fuel cell simultaneously, thereby methanol concentration is remained unchanged.
About (3), as be attached to the shown in Figure 9 of back, it is possible setting up such system, wherein relative with oxidant electrode counter electrode and oxidant electrode are immersed in the same anolyte, perhaps as being attached to the shown in Figure 11 of back, set up such system, its septation, as amberplex, insert between oxidant electrode and the counter electrode, anolyte circulates between barrier film and oxidant electrode, and the space between barrier film and the counter electrode then adds standard liquid, as contains the methyl alcohol of fixed amount or as the reference anolyte of electrolytical aqueous sulfuric acid.Say again, 2-cell system can accomplish, in this system, the arrangement of reference methanol concentration battery (its methanol concentration can remain zero well) is the same with aforementioned system (2), voltage difference to reference cell and tested battery judges, thereby measures the methanol concentration of anode of fuel cell electrolyte.Any material as long as be that chemically stable ， And can conduct electricity for electrolyte, all can be used as the counter electrode material in the system that (3) bar narrates.
Fig. 1 is applied to the perspective illustration that the methanol fuel cell of methanol concentration control device is housed of the present invention.
Fig. 2 is the structural representation of methanol concentration control device (I).
Fig. 3 is that current density-current potential (i-E) curve is used for estimating electrode and cell voltage (potential difference) performance.
Fig. 4 is the characteristic curve of cell among Fig. 2, the methanol concentration of expression fuel and the relation between the open circuit voltage.
Fig. 5 is the Open Circuit Potential of oxidant electrode among Fig. 9 and the relation curve of methanol concentration.
Fig. 6 is the structural representation of methanol concentration control device (II).
Fig. 7 is the structural representation of methanol concentration control device (III).
Fig. 8 is the structural representation of methanol concentration control device (IV).
Fig. 9 is the structural representation of methanol concentration control device (V).
Figure 10 is that the concentration of methanol concentration control device (V) among Fig. 9 detects characteristic curve.
Figure 11 is the structural representation of methanol concentration control device (VI).
Figure 12 be methanol concentration control device (I), (IV) and (V) are housed respectively fuel cell when current density is 60 milliamperes/square centimeter, the relation curve of discharge time and cell voltage and battery temperature.
Being used for fuel cell of the present invention is methanol fuel cell, settles the device of methanol concentration in the control fuel on fuel feed channel.
Referring to Fig. 1, the battery pile 8 usefulness fuel electrodes and the oxidant electrode that are piled by 33 cells constitute.
(CMV, Asahi Garasu produces) inserts between the electrode as electrolyte the amberplex that contains 3 mol sulfuric acid.On the conduit 9 of battery pile 8 input fuel, methanol concentration control device 10 is housed.The fuel (sulfuric acid that contains 1.5 mol) that leads to through the battery pile circulation is stored in the fuel tank 11.(2: 1) methanol-water is stored in the fuel tank 13, according to the signal from the methanol concentration control device, is imported by methanol-water feed conduit 12 through the new methyl alcohol that charging hole 14 is supplied with.
Referring to Fig. 2, each fuel electrode 1 and oxidant electrode 2 all are cut into 10 * 10 millimeters thin slice in the cell 15, the amberplex 3 that contains sulfuric acid is inserted between the electrode tightly as electrolyte, and the fuel concentration of so just having made methanol concentration control device (I) detects partly 22.
In this fuel cell, the carbon carrier of porous, for example graphite or oven process carbon black are used for electrode, and catalyst adopts platinum, ruthenium or the material of platiniferous, ruthenium wherein.The preparation method can be the catalyst method for making of any common usefulness, as sedimentation, infusion process, intervention method and kneading.The manufacture method of electrode is to coat catalyst paste on the porous, electrically conductive matrix, dry then and oven dry.The preparation of catalyst paste is that distilled water and adhesive (for example polytetrafluoroethylene) are added in the catalyst powder, and kneading mixture forms then.
The performance of the electrode that makes is estimated with current density-potential curve (i-E).As shown in Figure 3, when electric current by the time, the current potential of fuel electrode I is to the direction expansion that increases (among the figure upwards), the oxidant electrode II is to the direction expansion that reduces (among the figure downwards), this is because the hysteresis of reaction, due to the internal resistance etc.The electrical potential difference of electrode I and II promptly is the voltage III of battery.The cell voltage height, even if electric current when output arranged, its voltage does not reduce yet, such battery is the battery of high-output power.IV is that electric current is zero to be the open circuit voltage when not connecing load between the electrode among Fig. 3.
Figure 6 shows that methanol concentration control device (II).Cell 23 is equipped with standard electrolyte solution (161), fuel electrode (111), amberplex (311) and oxidant electrode (211), be contained in second fuel concentration test section 221, it fits together with another cell 15, and this cell 15 is contained in first concentration shown in Figure 2 and divides in 22.Cell 23 has been full of the fuel of supplying with the predetermined methanol concentration (1 mol) of battery pile 8. Cell 15 and 23 open circuit voltage detect by lead 20 usefulness voltmeters 17 respectively, and the input valve 19 of methanol-water is by compensation arrangement 18 keyings, so the open circuit voltage of cell 15 and 23 can equate.Because the setting of methanol concentration control device (II) can make the methanol concentration of the fuel of input battery pile 8 be controlled at 1 mol ± 0.1 mol.The fuel cell note of Fig. 6 is made F.
Methanol concentration control device (III) is shown in Fig. 7, and it is similar to the control device that is shown in Fig. 2 (I), and different just oxidant electrodes 2 are placed in the atmosphere.Like this, the methanol concentration of the anolyte of supply battery pile 8 can be controlled in the scope of 0.8 mol-1.2 mol.
Methanol concentration control device (IV) is shown in Fig. 8, and it is similar to the control device that is shown in Fig. 7 (III), and the assembling of different is second fuel concentration test section 221 is different with first fuel concentration test section 22 of Fig. 7.Be shown in the similar of oxidant electrode 211 and Fig. 6 in second fuel concentration test section 221 of Fig. 8, the oxidant electrode 211 of different is Fig. 8 is to be placed in the atmosphere.
Like this, the methanol concentration of the anolyte of supply battery pile 8 can be controlled between 0.9 mol-1.1 mol.
The characteristics that are shown in the methanol concentration control device (V) of Fig. 9 be its methanol concentration test section 222 have following some be different from the methanol concentration test section shown in Fig. 2 and Fig. 6.
At first, concentration part is placed on the arm that anolyte flows through, and this just can make the checkout gear miniaturization.Secondly, test section 222 is made up of oxidant electrode 2 and counter electrode 24.Oxidant electrode 2 is the small pieces with the original oxidant electrode same size of fuel cell, and counter electrode then is a graphite pole piece.
What can be used as counter electrode 24 also has: noble metal such as platinum, gold, iridium, rhodium, ruthenium and osmium, base metal be as lead, niobium, tantalum, zirconium and hafnium, carbon material such as graphite.The state of material therefor can be intensive pole piece formula, as metal parallel plate electrode electrode, the electrode of surperficial coated platinum black and so on, or with the fuel electrode or the similar porous electrode of oxidant electrode of fuel cell.About septate structure between counter electrode and the oxidant electrode, a kind of like this structure also is fine, and promptly its counter electrode also makes oxidant electrode, to its air supply ， And with corresponding as the oxidant electrode of behavior electrode.Because cell and oxidant electrode-counter electrode in this device needn't produce electric energy, therefore do not need external power source.Owing to taked these measures, the concentration of the fuel methanol of fueling battery just can be controlled, make its constant in the concentration range of predesignating the output voltage of ， And and fuel cell also can remain unchanged.For constant sulfuric acid concentration, the graphite basicly stable current potential of performance is and irrelevant with methanol concentration, and result's two interelectrode voltages just change with the concentration of methyl alcohol in the anolyte.This result's a example is shown in Figure 10.Established well according to the relation between Figure 10 methanol concentration and the detection signal.Therefore, predesignate concentration or during when reaching than the corresponding detection voltage of its low concentration, just reach the voltage predesignated or when higher than it, just provide the signal of starting fluid inlet valve 19, so the methanol concentration of anolyte can be controlled in 0.8～1.2 mol.Fuel cell note in this example is made I.
Figure 11 shows that methanol concentration control device (VI) with shown in Figure 9 basic identical, but it has individual outstanding feature, promptly amberplex dividing plate 3 is placed between air electrode 2 and the counter electrode 24.Fill with the standard anode electrolyte through harmonizing in space between dividing plate 3 and the counter electrode 24.Air electrode 2 and counter electrode 24 are respectively air electrode and the methyl alcohol electrode small pieces of forming fuel cell pack 8.In this example, counter electrode 24 always places the fixedly solution of component, so its current potential is constant, so potential difference is the correlation that cell voltage demonstrates methanol concentration as shown in Figure 10 between two electrodes.Like this, rely on same system, the methanol concentration of anolyte can be controlled in the scope of 0.7～1.2 mol.This routine fuel cell note is made J.
The present invention is used for the oxidant electrode of methanol concentration control device and the preparation method of fuel electrode is described as follows:
Catalyst preparation example 1:
The potassium hydroxide solution of 50 milliliter 37% formalin and 100 milliliter 50% added (the oven process carbon black: the CSX-150A2 that Cabot company produces), and then add distilled water, making its volume is 500 milliliters, agitating solution in the 20 gram carbon dusts.During stirring, solution is cooled to 0 ± 2 ℃.28 gram platinum chlorides and 14 gram ruthenic chlorides are dissolved in distilled water, and making liquor capacity is 500 milliliters, this solution is added in the solution that obtains previously, keeps 0 ± 2 ℃ of temperature at that time.After adding finished, solution returned back to room temperature.Then 35 °～40 ℃ stir abouts 2 hours, again 55 °～60 ℃ stir abouts 2 hours.After stirring end, use the distilled water washed solid, cyclic washing to the pH value of dope becomes 7 or lower.Filter cake after the washing promptly obtains fuel electrode catalyst A with drier 80 ℃ of intensive dryings.
Catalyst preparation example 2:
With 1 liter of (1: 1) methyl alcohol-H
2In the O adding 15 gram carbon dusts (the oven process carbon black, CSX-150A2).Then, dissolve in 31 gram platinum chlorides, the solution of heating gained was 70 ℃ of stir abouts 5 hours.After stirring end,, become 7 or lower until PH with distilled water cyclic washing solid matter.Filter cake (80 ℃) after the dry washing promptly obtains the oxidant electrode catalyst B.
Example 1:
Get the powder of 1.15 gram catalyst A, add 2 ml distilled waters, evenly the mixture kneading.Then, add 1 milliliter of tetrafluoroethene liquid (the polytetrafluoroethyldispersion dispersion D1 that Daikin is produced is diluted to 2.5 times), mix.The pasty state catalyst that obtains is coated in equably on 100 * 128 millimeters the porous carbon matrix (the Kureca paper E-715 that Kureha Kagaku produces).After the catalyst air drying, substrate was toasted about 30 minutes in 300 ℃ in blanket of nitrogen.The substrate that toasted can use as fuel electrode.
Example 2:
Get the powder of 0.77 gram catalyst B, add distilled water, kneading mixture.Then, add 0.55 milliliter of polytetrafluoroethyldispersion dispersion, the mixture that obtains is coated on 100 * 128 millimeters the porous carbon matrix.After mixture was used the air drying, substrate toasted about 30 minutes in 300 ℃ in air.So just obtained oxidant electrode.
Fuel cell E, F, G, H, I and J have stood 100 hours continuous working test, and the current density of battery is 60 milliamperes/centimetre
2The tanks 11 of each sample is full of the anolyte of being made up of the sulfuric acid of the methyl alcohol of 1 mol and 1.5 mol, 13 methyl alcohol that are full of (2: 1) of tanks: water.The result of E, H and I represents IV (fuel cell E), V (fuel cell H) and the VI (fuel cell I) among Figure 12 respectively.Among individual fuel cells E, H and the I any one can both keep its power output constant.In addition, the temperature of battery is also constant.About fuel cell F, G and J, figure explanation of no use, no matter their result is power output, or battery temperature, all similar with the result of battery E, H and I.
The touch upon oxidant of input of the present invention is an air, because it also is applicable to atmospheric air, so it does not need air chamber.Temperature compensation means of Technology Need in the past detects compensation temperature, and the present invention when working temperature is 40～60 ℃ without any need for temperature compensation means.Because methanol concentration control device of the present invention can be controlled methanol concentration with the open circuit voltage of electrode, it can or not have chemical reaction State Control methanol concentration at the fuel cell no-load condition.Therefore, control device of the present invention compensates the rising or the decline of the battery temperature that the chemical reaction by fuel cell causes without any need for temperature compensation means.In the former technology, methyl alcohol is indoor by the barrier film entrained air inevitably, and therefore fresh electrolyte (not containing methyl alcohol) need constantly add in the air chamber and go.On the other hand, the present invention measures methanol concentration according to the above-mentioned methyl alcohol quantity that sees through Ge Mo And entrained air electrode.In the former technology, electrode is done the effective surface area that (as the platinum lead) is difficult to strengthen active material with lead.On the contrary, the present invention adopts the big catalyst of effective surface area, makes the same active material that uses in fuel cell pack have polymolecularity.
Claims (12)
1, a kind of fuel cell includes fuel electrode and the oxidant electrode arranged in opposite directions; Electrolyte between two electrodes; Partly to the concentration device of fuel cell fueling, fuel cell is characterised in that said device is made up of following from supply of fuel in control:
Fuel concentration test section (22,221) comprises fuel electrode (1), and one main surface part of fuel direct and before the above-mentioned fuel cell of supply (8) contacts; Oxidant electrode (2), an one main surface directly contacts with air; Electrolyte (3), its two main surfaces directly contact with another main surface of above-mentioned fuel electrode (1) and another main surface of above-mentioned oxidant electrode (2) respectively;
Instrument (17) detects the potential difference between above-mentioned two electrodes (1,2),
The fuel that device (18) control is supplied with to fuel cell (8) by supply of fuel part (13) makes above-mentioned potential difference keep a steady state value.
2, a kind of according to claim 1 described fuel cell, it is characterized in that said fuel is a kind of liquid fuel.
3, a kind of according to claim 2 described fuel cells, it is characterized in that said liquid fuel is a methyl alcohol.
4, a kind of according to claim 1 described fuel cell, it is characterized in that in fuel concentration test section (22,221) in fuel electrode (1) and the oxidant electrode (2), have at least a kind of electrode to contain a kind of porous conductive material, it contains a kind of element of periodic table VI and VIII family at least; Or containing a kind of conductive powder, a kind of element ， And that this powder contains periodic table VI and VIII family at least contains adhesive.
5, a kind of according to claim 1 described fuel cell, it is characterized in that said electrolyte (3) is made of amberplex.
6, a kind of according to claim 4 described fuel cells, it is characterized in that said adhesive is a hydrophobic adhesive.
7, a kind of fuel cell includes fuel electrode and the oxidant electrode that is arranged in the electrolyte both sides in opposite directions and controls the control device that flows to the fuel concentration of fuel cell from the part of the fuel supply.
Fuel cell is characterised in that said device is made up of following:
Fuel cell concentration branch (222) comprises oxidant electrode (2), and it directly contacts with air with a main surface; Counter electrode (24), it is placed in the opposite of said oxidant electrode (2); The fuel that another main surface of oxidant electrode (2) and the space contain between the counter electrode are supplied with to fuel cell (8) contains electrolyte in the fuel.On another main surface of oxidant electrode (2), fuel and oxidant directly react, and cause that electrode potential reduces, and just can measure fuel concentration by this phenomenon, the voltmeter (17) of potential difference between the measurement electrode (2,24),
Device (18) is controlled the fuel that from the part of the fuel supply (13) flow to fuel cell (8) by said current potential being remained on a steady state value.
8, a kind of according to claim 7 described fuel cells, it is characterized in that said fuel is a kind of liquid fuel.
9, a kind of according to claim 8 described fuel cells, it is characterized in that said liquid fuel is a methyl alcohol.
10, a kind of fuel cell according to claim 7 defineds is characterized in that the oxidant electrode of said fuel concentration test section (222) comprises a kind of porous conductive material, and it contains a kind of element of periodic table VI family and VIII family at least; Or containing a kind of conductive powder, this powder contains a kind of element ， And of periodic table VI family and VIII family at least and contains adhesive.
11, a kind of according to claim 10 described fuel cells, it is characterized in that said adhesive is a hydrophobic adhesive.
12, a kind of according to claim 7 described fuel cells, it is characterized in that amberplex (3) is placed between oxidant electrode (2) and the counter electrode (24); Be full of the standard electrolyte solvent between barrier film (3) and the counter electrode (24).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN85103305A CN1006431B (en) | 1985-04-30 | 1985-04-30 | Fuel cell |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN85103305A CN1006431B (en) | 1985-04-30 | 1985-04-30 | Fuel cell |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN85103305A true CN85103305A (en) | 1987-06-03 |
| CN1006431B CN1006431B (en) | 1990-01-10 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN85103305A Expired CN1006431B (en) | 1985-04-30 | 1985-04-30 | Fuel cell |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1006431B (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1303715C (en) * | 2000-07-18 | 2007-03-07 | 摩托罗拉公司 | Direct methanol fuel cell system |
| CN100367554C (en) * | 2003-01-08 | 2008-02-06 | 株式会社尼康 | Electronic apparatus and its operation controllig method |
| CN100384005C (en) * | 2003-06-17 | 2008-04-23 | 乐金电子(天津)电器有限公司 | Nourrice tank changing time announcement device and method for fuel cell |
| CN100424919C (en) * | 2004-07-30 | 2008-10-08 | 三洋电机株式会社 | Fuel cell system and method of controlling fuel cell |
| CN100434911C (en) * | 2005-06-02 | 2008-11-19 | 英属盖曼群岛商胜光科技股份有限公司 | Method in use for direct methanol fuel cells for calculating concentration of fuel |
| CN100434904C (en) * | 2005-12-14 | 2008-11-19 | 英属盖曼群岛商胜光科技股份有限公司 | Method for computing concentration of liquid fuel battery |
| CN100464461C (en) * | 2006-02-22 | 2009-02-25 | 英属盖曼群岛商胜光科技股份有限公司 | Fuel supply method for liquid fuel cell |
| CN101464425A (en) * | 2007-12-19 | 2009-06-24 | 财团法人工业技术研究院 | Fuel concentration measuring method |
| CN100530802C (en) * | 2005-09-14 | 2009-08-19 | 株式会社日立制作所 | Electronic equipment with cell-power supply unit |
| CN101116213B (en) * | 2005-02-10 | 2012-10-10 | 索尼株式会社 | Electrochemical energy generator and its driving method |
| CN102723512A (en) * | 2003-07-29 | 2012-10-10 | 法商Bic公司 | Fuel cartridge with flexible liner |
| US8501491B2 (en) | 2007-11-27 | 2013-08-06 | Industrial Technology Research Institute | Method of measuring concentration of fuel |
-
1985
- 1985-04-30 CN CN85103305A patent/CN1006431B/en not_active Expired
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1303715C (en) * | 2000-07-18 | 2007-03-07 | 摩托罗拉公司 | Direct methanol fuel cell system |
| CN100367554C (en) * | 2003-01-08 | 2008-02-06 | 株式会社尼康 | Electronic apparatus and its operation controllig method |
| CN100384005C (en) * | 2003-06-17 | 2008-04-23 | 乐金电子(天津)电器有限公司 | Nourrice tank changing time announcement device and method for fuel cell |
| CN102723512B (en) * | 2003-07-29 | 2014-10-15 | 法商Bic公司 | Fuel cartridge with flexible liner |
| CN102723512A (en) * | 2003-07-29 | 2012-10-10 | 法商Bic公司 | Fuel cartridge with flexible liner |
| CN100424919C (en) * | 2004-07-30 | 2008-10-08 | 三洋电机株式会社 | Fuel cell system and method of controlling fuel cell |
| CN101116213B (en) * | 2005-02-10 | 2012-10-10 | 索尼株式会社 | Electrochemical energy generator and its driving method |
| CN100434911C (en) * | 2005-06-02 | 2008-11-19 | 英属盖曼群岛商胜光科技股份有限公司 | Method in use for direct methanol fuel cells for calculating concentration of fuel |
| CN100530802C (en) * | 2005-09-14 | 2009-08-19 | 株式会社日立制作所 | Electronic equipment with cell-power supply unit |
| CN100434904C (en) * | 2005-12-14 | 2008-11-19 | 英属盖曼群岛商胜光科技股份有限公司 | Method for computing concentration of liquid fuel battery |
| CN100464461C (en) * | 2006-02-22 | 2009-02-25 | 英属盖曼群岛商胜光科技股份有限公司 | Fuel supply method for liquid fuel cell |
| US8501491B2 (en) | 2007-11-27 | 2013-08-06 | Industrial Technology Research Institute | Method of measuring concentration of fuel |
| CN101464425A (en) * | 2007-12-19 | 2009-06-24 | 财团法人工业技术研究院 | Fuel concentration measuring method |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1006431B (en) | 1990-01-10 |
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