This Application claims priority of Taiwan Patent Application No. 098112619, filed on Apr. 16, 2009, the entirety of which is incorporated by reference herein.
1. Field of the Invention
The present invention relates to a hydrogen supply device, and in particular relates to a fuel cell utilizing the same.
2. Description of the Related Art
Portable energy is required in digital products such as laptop computers, walkmans, cameras, and the likes. Desired portable energy characteristics include low cost, long energy supply, small size, light weight, and operational under a variety of environmental conditions. One type of portable energy, a conventional fuel cell, is economical and provides long energy supply. However, conventional fuel cells are limited by the inability for hydrogen supply to comply with the characteristics of desired portable energy, thus difficulty occurs when attempting to apply them to portable electronic products. Chemical hydrogen storage material can serve as a hydrogen source due to high hydrogen storage density. Solid hydrogen materials are currently popular. When a solid hydrogen fuel (combination of catalyst and sodium boron hydride) is selected, water is required for reaction to form the hydrogen as shown in Formula I below. However, the hydrogen generating mechanism has two major problems. First, difficulty occurs when attempting to provide a stable hydrogen generation rate. Thus, methods include complicated devices that dramatically increase volume and cost of the hydrogen supply device.
Taiwan Patent No. 98108205, however, disclosed by the inventors of this invention, discloses a more simplified method for stabilizing hydrogen generation rates.
Secondly, the hydrogen supply device is required to be fastened in one direction. Specifically, if the hydrogen supply device is inverted, tilted, or shaken, the water in the hydrogen supply device may flow to the fuel cell, thereby containing the MEA film in the fuel cell, which degrades performance. As such, portability of the fuel cell is a problem. While, those skilled in the art may adopt a hydrophobic gas-liquid separation membrane to permeate hydrogen and block water. However, fuel cell costs are increased due to expensive membrane. Furthermore, the gas-liquid separation membrane cannot totally contain the liquid water. Due to the hydrogen pressure, a little bit of water may be extruded through the membrane to degrade fuel cell performance. Accordingly, a totally solid hydrogen supply device is called for in fuel cells.
The invention provides a hydrogen supply device, comprising a super water absorbent material for containing water, alcohol, or combinations thereof; and a solid hydrogen fuel directly contacting the super water absorbent material to generate hydrogen.
A detailed description is given in the following embodiments with reference to the accompanying drawings.
The present invention can be more fully understood by reading the subsequent detailed description and examples with references made to the accompanying drawings, wherein:
The following description is of the best-contemplated mode of carrying out the invention. This description is made for the purpose of illustrating the general principles of the invention and should not be taken in a limiting sense. The scope of the invention is best determined by reference to the appended claims.
The invention provides a hydrogen supply device, including a super water absorbent material to absorb water, alcohol, or combinations thereof; and solid hydrogen fuel directly contacting the super water absorbent material to generate hydrogen. The super water absorbent material can be a polymer such as polyacrylate, poly(ethylene glycol), ethylene vinyl acetate, polyurethane, poly(ethylene oxide), starch graft copolymer, or rubber blend. A little super water absorbent material may absorb a huge amount of water. For example, 1 g of sodium polyacrylate can absorb at least 25 g of water.
The solid hydrogen fuel of the invention includes a solid catalyst, solid hydride, and hydrophobic elastomer polymer. The solid hydride can be alkali/alkaline metal boron hydride, metal hydride, boron nitrogen hydride, or combinations thereof. The metal boron hydride includes NaBH4, LiBH4, Ca(BH4)2, MgBH4, KBH4, or Al(BH4)3. The metal hydride includes LiH, NaH, or CaH2 and the boron nitrogen hydride includes ammonia borane, diborane, diamino diborane, H2B(NH3)2BH4, poly(amino borane), borazine, borane-morpholine complex, or borane-tetrahydrofuran complex. The solid catalyst can be Ru, Co, Ni, Cu, Fe, or combinations thereof, and the hydrophobic elastomer polymer includes silicone, rubber, or silicone rubber. The solid catalyst and the solid hydride are ball-grinded at high speeds, and then added the hydrophobic elastomer polymer to complete the flexible solid hydrogen fuel. For the detailed formula and manufacturing thereof, reference can be made to Taiwan Patent Application No. 98108205.
As shown in
The described water absorbent polymer may absorb liquid at a hundred times that of its original weight, and the absorbed liquid is contained without flowing out of the polymer. However, the water absorbent polymer has low water absorbent rate, it needs a longer time to form a hydrogel solid. In another embodiment, the water absorbent material further includes a water absorbent cotton material to compensate for the slow water absorbent rate. The water absorbent cotton material has high water absorbent rate, however, it cannot totally contain water and its water absorbent amount is low. For simultaneously possessing the advantages such as having a huge absorbent amount, containing liquid, and having a fast absorbent rate, an appropriate amount of water absorbent polymer can be added on the water absorbent cotton surface to complete a sheet of water absorbent material 23, as shown in
Subsequently, the solid hydrogen fuel is cut to be a sheet. Because the solid hydrogen fuel contains hydrophobic elastomer polymer, the sheet of solid hydrogen fuel 25 is flexible. The sheet of the solid hydrogen fuel 25 and the sheet of the water absorbent material 23 are stacked and rolled to form a rod-like object 27, as shown in
As shown in
1 g of water absorbent polymer (sodium polyacrylate) was charged in a vessel and then added 25 g of water. After 10 minutes, a non-flowable hydrogel was formed.
Referring to Taiwan Patent Application No. 98108205, solid hydride (NaBH4) and solid catalyst (Co2+/IR-120) were ball-grinded at a high speed, and then added silicone rubber to complete a flexible solid hydrogen fuel. The solid hydrogen fuel was pelletized to form pellets. Each pellet included 1 g of solid hydride, 0.1 g of solid catalyst, and 0.1 g of silicone rubber.
Two of the previously described pellets were charged on the described hydrogel, and the solid hydrogen fuel absorbed water and reacted to generate hydrogen. The hydrogen generation rate versus time thereof was measured and is shown in
0.5 g of water absorbent polymer (sodium polyacrylate) was uniformly dispersed on a 5 cm*13 cm*0.05 cm cosmetic cotton (KK-II, commercially available from Yani international corporation, Taiwan) to form a sheet of the water absorbent material.
Referring to Taiwan Patent Application No. 98108205, solid hydride (NaBH4) and solid catalyst (Co2+/IR-120) were ball-grinded at a high speed, and then added silicone rubber to complete a flexible solid hydrogen fuel. The solid hydrogen fuel was pressed and cut to form a sheet of the solid hydrogen fuel (4 cm*11 cm*0.1 cm).
The sheet of the solid hydrogen fuel and the sheet of the water absorbent material were stacked and rolled to form a rod-like object. The rod-like object was charged in a vessel and added 20 g of water, such that the water absorbent material absorbed water rapidly. After 5 minutes, the redundant water was poured from the vessel. Subsequently, the hydrogen generation rate versus time thereof was measured and is shown in
In Examples 1 and 2, no water flowed out from the vessel when inverted or tilted during the start of hydrogen generation rate measurement. Moreover, inverting or tilting the vessel did not influence the hydrogen generation rate. Accordingly, the problems such as the liquid flowing from the hydrogen supply device into the fuel cell was disappeared and a gas-liquid separation membrane as in prior art was not utilized.
While the invention has been described by way of example and in terms of the preferred embodiments, it is to be understood that the invention is not limited to the disclosed embodiments. To the contrary, it is intended to cover various modifications and similar arrangements (as would be apparent to those skilled in the art). Therefore, the scope of the appended claims should be accorded the broadest interpretation so as to encompass all such modifications and similar arrangements.
Number | Date | Country | Kind |
---|---|---|---|
98112619 A | Apr 2009 | TW | national |
Number | Name | Date | Kind |
---|---|---|---|
7344571 | Bae et al. | Mar 2008 | B2 |
20020182459 | Hockaday et al. | Dec 2002 | A1 |
20030228252 | Shurtleff | Dec 2003 | A1 |
20040071630 | Jorgensen | Apr 2004 | A1 |
20060237688 | Zimmermann | Oct 2006 | A1 |
20060257313 | Cisar et al. | Nov 2006 | A1 |
20070253875 | Koripella et al. | Nov 2007 | A1 |
20080102024 | Bae et al. | May 2008 | A1 |
20080299420 | Kelley et al. | Dec 2008 | A1 |
20080299423 | Laven | Dec 2008 | A1 |
Number | Date | Country |
---|---|---|
101327907 | Dec 2008 | CN |
101327907 | Dec 2008 | CN |
101327909 | Dec 2008 | CN |
2 048 110 | Apr 2009 | EP |
I229471 | Sep 2005 | TW |
200806392 | Feb 2008 | TW |
WO 2008132986 | Nov 2008 | WO |
Number | Date | Country | |
---|---|---|---|
20100266910 A1 | Oct 2010 | US |