WO2012060036A1 - 淡水化装置を用いて塩水を淡水化する方法 - Google Patents
淡水化装置を用いて塩水を淡水化する方法 Download PDFInfo
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- WO2012060036A1 WO2012060036A1 PCT/JP2011/004715 JP2011004715W WO2012060036A1 WO 2012060036 A1 WO2012060036 A1 WO 2012060036A1 JP 2011004715 W JP2011004715 W JP 2011004715W WO 2012060036 A1 WO2012060036 A1 WO 2012060036A1
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/02—Treatment of water, waste water, or sewage by heating
- C02F1/04—Treatment of water, waste water, or sewage by heating by distillation or evaporation
- C02F1/043—Details
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/02—Treatment of water, waste water, or sewage by heating
- C02F1/04—Treatment of water, waste water, or sewage by heating by distillation or evaporation
- C02F1/14—Treatment of water, waste water, or sewage by heating by distillation or evaporation using solar energy
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/08—Seawater, e.g. for desalination
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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
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A20/00—Water conservation; Efficient water supply; Efficient water use
- Y02A20/124—Water desalination
-
- 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
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A20/00—Water conservation; Efficient water supply; Efficient water use
- Y02A20/124—Water desalination
- Y02A20/138—Water desalination using renewable energy
- Y02A20/142—Solar thermal; Photovoltaics
Definitions
- the present invention relates to a method for desalinating salt water using a desalination apparatus.
- Patent Document 1 discloses a sand filter for filtering seawater to remove solids in seawater.
- Patent Document 2 discloses that water repellency is applied to a filtering agent composed of porous particles (particularly paragraph 0017).
- An object of the present invention is to provide a method for desalinating salt water using a desalination apparatus.
- the desalination apparatus includes a breathable sheet, a water repellent particle layer, and a tank layer inside the container, the tank layer is located at the bottom of the container, and the breathable sheet is disposed between the water repellent particle layer and the tank layer. It is sandwiched between.
- the breathable sheet has through holes, the water-repellent particle layer is composed of a plurality of dense water-repellent particles, and the surface of the water-repellent particles has a water-repellent film.
- the salt water is desalinated by the method comprising
- FIG. 1 shows a desalination apparatus according to the invention.
- filtration means that a liquid containing solids passes through a porous material and removes the solids. The solid is not dissolved in the liquid.
- the term “desalination” is to obtain fresh water from seawater in which impurities such as ions are dissolved. That is, removing salt from seawater. The salt is dissolved in seawater.
- filtration should not be used to mean removing impurities dissolved in a liquid.
- FIG. 1 shows a desalination apparatus according to the invention.
- the desalination apparatus includes a container 1, a breathable sheet 2, a water repellent particle layer 3, and a tank layer 5.
- the breathable sheet 2, the water repellent particle layer 3, and the tank layer 5 are provided inside the container 1.
- the tank layer 5 is located in the lower part inside the container 1. That is, the tank layer 5 is sandwiched between the bottom surface of the container 1 and the breathable sheet 2.
- the tank layer 5 is usually filled with air.
- the preferred height of the tank layer 5 is not less than 5 cm and not more than 15 cm.
- the breathable sheet 2 has a through hole.
- a preferable shape of the through hole is a circle. Examples of the cross-sectional area of the through holes is 3.14 mm 2 or more 78.5 mm 2 or less. If the diameter is less than 1 mm, it may be difficult for gas to pass through the breathable sheet 2. On the other hand, if the diameter exceeds 5 mm, the particles constituting the water-repellent particle layer 3 may fall into the tank layer 5 through the through holes.
- the number of through holes is not limited.
- the preferred material for the breathable sheet 2 is resin.
- An example of the resin is polyvinyl chloride.
- the preferable thickness of the air permeable sheet 2 is 0.5 mm or more and 5 mm or less.
- the periphery of the breathable sheet 2 is adhered to the inner wall surface of the container 1 using an adhesive. That is, the periphery of the breathable sheet 2 is in contact with the inner wall surface of the container 1.
- the water repellent particle layer 3 is provided on the upper surface of the breathable sheet 2.
- the water repellent particle layer 3 is composed of a plurality of water repellent particles.
- a plurality of water-repellent particles are densely formed to form the water-repellent particle layer 3. That is, the surface of one water-repellent particle is in contact with the surfaces of a plurality of other water-repellent particles.
- Each water repellent particle includes a particle and a water repellent film.
- the particles are preferably sand particles.
- the water repellent film covers the surface of the particles.
- the water repellent film preferably comprises a fluorocarbon group represented by the chemical formula — (CF 2 ) n—.
- n is a natural number. Preferred n is 2 or more and 20 or less.
- the water repellent film is bonded to the particle by a covalent bond.
- the following chemical formula (I) represents a preferred water-repellent film.
- Q is hydrogen or fluorine
- M1 and m2 are independently a natural number of 0 or 1 or more.
- N is 2 or more and 20 or less.
- a preferable thickness of the water repellent particle layer 3 will be described later.
- An example of a method for producing water-repellent particles will be described below.
- a surfactant represented by the chemical formula CX 3 — (CH 2 ) m1 — (CF 2 ) n — (CH 2 ) m2 —SiX 3 is dissolved in a non-aqueous solvent to prepare a surfactant solution.
- X is a halogen, preferably chlorine.
- a plurality of particles are immersed in the surfactant solution to obtain a plurality of water-repellent particles.
- the obtained plurality of water-repellent particles are put in a container 1 having a breathable sheet 2. In this way, the plurality of water-repellent particles are stacked on the breathable sheet 2 to form the water-repellent particle layer 3.
- seawater is poured into the container 1 to form the seawater layer 4 on the upper surface of the water repellent particle layer 3. Due to the water repellency of the water repellent particle layer 3, the poured seawater does not flow down to the tank layer 5. That is, the poured seawater is stacked and maintained on the upper surface of the water-repellent particle layer 3 as the seawater layer 4.
- the preferred thickness of the water repellent particle layer 3 is 5 cm or more and 15 cm or less. If the water-repellent particle layer 3 is too thin, poured seawater may flow down to the tank layer 5. On the other hand, if the water repellent particle layer 3 is too thick, the breathable sheet 2 may be broken and come off the inner wall surface of the container 1 due to the weight of the water repellent particle layer 3 being too heavy.
- step (c) the seawater in the seawater layer 4 is heated. This causes the water contained in the seawater to evaporate. In this way, the water contained in the seawater becomes a gas, that is, water vapor.
- the seawater in the seawater layer 4 is heated by sunlight. It is also preferable that the heater heats the seawater in the seawater layer 4.
- the heated solid material can be supplied to the seawater layer 4 to heat the seawater.
- the solid is required to be insoluble in seawater.
- a preferred example of the solid is stone.
- the water vapor passes through the through holes provided in the breathable sheet 2 and reaches the inside of the tank layer 5.
- the water vapor is liquefied in the tank layer 5 to become liquid water.
- the water vapor is cooled in the tank layer 5 to become liquid water.
- the liquid water does not contain impurities contained in seawater.
- An example of the impurity is an ion. That is, the liquid water is fresh water.
- the water vapor that has passed through the gaps in the water-repellent particle layer 3 is liquefied at the bottom of the water-repellent particle layer 3 or the upper surface of the breathable sheet 2 and becomes liquid water.
- the liquid water passes through the through-hole provided in the breathable sheet 2 and dripped into the tank layer 5.
- the liquid water is also fresh water.
- the container 1 comprises a lid 7.
- the lid 7 does not allow the water vapor moving upward to escape from the container 1.
- the lid 7 is preferably transparent.
- the tank layer 5 can be cooled as necessary.
- Example 1 (Preparation of container 1) First, the container 1 was prepared.
- the container was a rectangular parallelepiped having a width of 10 cm, a height of 15 cm, and a depth of 10 cm.
- the material of the container 1 was polyvinyl chloride.
- the breathable sheet 2 was attached to the container 1.
- the breathable sheet 2 can also be defined as the breathable layer 2.
- the breathable layer 2 was a thin plate made of polyvinyl chloride having a thickness of 1 mm. Several holes were pre-formed by cones in the thin plate. Each hole had a diameter of approximately 3 mm.
- the thin plate was adhered to the inside of the container 1 by an adhesive (trade name Cemedine, manufactured by Cemedine Co., Ltd.) to form a breathable layer 2 and a tank 5. The distance between the bottom of the container 1 and the breathable layer 2 was 8 cm.
- the water repellent particles were prepared according to the procedure disclosed in US Pat. No. 5,527,0080, which is incorporated herein.
- Sand with the trade name “Toyoura Sand” was purchased from Toyoura Silica Mining Co., Ltd.
- the sand was washed with acetone to remove surface impurities. Thereafter, the sand was stored under a dry nitrogen atmosphere.
- a fluorocarbon-based silane-based surfactant (chemical formula: CF 3 (CF 2 ) 7 (CH 2 ) 2 SiCl 3 , 5 ml) is added to a non-aqueous solvent (source: Sumitomo 3M Limited, trade name: HFE7200, 500 ml) to prepare a surfactant solution.
- a non-aqueous solvent source: Sumitomo 3M Limited, trade name: HFE7200, 500 ml
- the water repellent particles were supplied to the container 1 to form a water repellent particle layer 3 having a thickness of 10 cm.
- the inventor has checked that the water-repellent particles do not pass through the holes formed in the breathable layer 2.
- the heater was wound around the outer peripheral surface of the container 1 so that a heater (trade name silicon rubber heater manufactured by OHM Heater Co., Ltd.) surrounds the seawater layer 4. A thermometer was provided in the seawater layer 4. The heater was turned on and the simulated seawater was heated to 67 ° C. Thereafter, the container 1 was left for 11 hours. Since neither the heating device nor the cooling device was provided in the tank 5, the temperature in the tank 5 probably remained at room temperature (22 ° C.).
- the inventor drank water accumulated in the tank 5. The salty taste was not felt.
- Example 2 instead of the heater, a heating lamp (Iwasaki Electric Co., Ltd., eye infrared bulb) was used. The simulated seawater was heated to 43 ° C. Furthermore, the outer peripheral surface of the tank layer 5 was surrounded by a cooling agent.
- a heating lamp Iwasaki Electric Co., Ltd., eye infrared bulb
- Example 2 the speed of water accumulated in the tank layer 5 was faster than that in Example 1.
- the salinity of water accumulated in the tank 5 was 0.0%.
- the inventor drank the water accumulated in the tank 5 also in Example 2.
- the salty taste was not felt.
- Example 1 An experiment similar to Example 1 was performed except that sand having a trade name of “Toyoura sand” was used in place of the water-repellent particles. Needless to say, the sand did not have water repellency.
- the salinity of the water falling into the tank 5 was 3.5%.
- the inventor drank water in the tank 5 in Comparative Example 1 as well. A salty taste was felt.
- the present invention achieves seawater demineralization. Instead of sea water, salt water can be used.
- Container 2 Breathable sheet (breathable layer) 3 Water repellent particle layer 4 Seawater layer 5 Tank layer 7 Lid
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- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heat Treatment Of Water, Waste Water Or Sewage (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
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Abstract
Description
用語「濾過」とは、固体を含有する液体が多孔質の物質を通過し、当該固体を除去することを意味する。当該固体は、当該液体に溶解していない。
(工程(a))
まず、淡水化装置が用意される。図1は、本発明による淡水化装置を示す。淡水化装置は、容器1、通気性シート2、撥水粒子層3、およびタンク層5を具備する。通気性シート2、撥水粒子層3、およびタンク層5は、容器1の内部に設けられる。
工程(b)では、容器1に海水が注がれ、撥水粒子層3の上面上に海水層4を形成する。撥水粒子層3の撥水性のため、注がれた海水はタンク層5に流れ落ちない。すなわち、注がれた海水は、海水層4として撥水粒子層3の上面上に積み重ねられて維持される。
工程(c)では、海水層4の海水が加熱される。これは、海水に含まれる水が蒸発することをもたらす。このようにして、海水に含まれる水は気体、すなわち、水蒸気になる。
当該水蒸気は、上方向だけでなく、下方向にも移動する。下方向に移動する水蒸気は、撥水粒子層3を通り抜ける。厳密には、当該水蒸気は、撥水粒子層3を構成する複数の撥水性粒子の間に形成されている隙間を通り抜ける。このようにして、水蒸気は通気性シート2の上面に到達する。
(容器1の用意)
まず、容器1を用意した。当該容器は幅10cm、高さ15cm、および奥行き10cmの直方体であった。容器1の材質はポリ塩化ビニルであった。
次に、容器1に通気性シート2が取り付けられた。通気性シート2は、通気性層2と規定することも出来る。通気性層2は、1mmの厚みを有するポリ塩化ビニルからなる薄板であった。当該薄板に錐によりいくつかの孔が前もって形成された。各孔は、おおよそ3mmの直径を有していた。当該薄板が、接着剤(セメダイン社製、商品名雨どい用セメダイン)により、容器1の内部に接着され、通気性層2およびタンク5を形成した。容器1の底および通気性層2の間の距離は、8cmであった。
撥水性粒子は、米国特許第5270080号(これは本願に組み込まれる)に開示された手順に従って調製された。「豊浦砂」の商品名を有する砂が豊浦珪石鉱業株式会社より購入された。砂はアセトンにより洗浄され、表面の不純物を除去した。その後、砂は乾燥窒素雰囲気下にて保管された。
塩化ナトリウム(関東化学株式会社から入手)が水道水に溶解され、3.5%の塩分濃度を有する模擬海水を調製した。当該模擬海水が容器1に注がれた。模擬海水は撥水性撥水粒子層3の上面上に溜まり、3cmの厚みを有する海水層4が形成された。模擬海水が撥水性撥水粒子層3の下面から下方向に向かって滴ることはなかった。最後に、フタ7を容器1に載せた。
ヒーター(オーエムヒーター株式会社製、商品名シリコンラバーヒーター)が海水層4を囲むように、当該ヒーターが容器1の外周面に巻かれた。海水層4の中に温度計が設けられた。ヒーターに電源を入れ、模擬海水を67℃に加温した。その後、11時間、容器1は放置された。タンク5には加熱装置および冷却装置のいずれもが設けられなかったので、タンク5内の温度はおそらく室温(22℃)のままであった。
ヒーターに代えて、加熱用ランプ(岩崎電気株式会社、アイ赤外線電球)が用いられた。模擬海水は、43℃に加温された。さらに、タンク層5の外周面が保冷剤により囲まれた。
撥水性粒子に代えて、「豊浦砂」の商品名を有する砂を用いたこと以外は、実施例1と同様の実験が行われた。いうまでもないが、当該砂は撥水性を有していなかった。
2 通気性シート(通気性層)
3 撥水粒子層
4 海水層
5 タンク層
7 フタ
Claims (9)
- 淡水化装置を用いて塩水を淡水化する方法であって、
前記淡水化装置を用意する工程(a)と、
前記淡水化装置は、
容器と、
通気性シートと、
撥水粒子層と、
タンク層と、を具備し、
前記通気性シート、前記撥水粒子層、および前記タンク層は、前記容器の内部に設けられており、
前記タンク層は、前記容器の内部の下部に位置しており、
前記通気性シートは、前記撥水粒子層と前記タンク層との間に挟まれており、
前記通気性シートは、貫通孔を具備しており、
前記撥水粒子層は、複数の撥水性粒子から構成されており、
前記各撥水性粒子の表面は、撥水膜を具備しており、
前記複数の撥水性粒子は密集しており、
前記容器に塩水を注ぎ、前記撥水粒子層の表面上に前記塩水を配置させる工程(b)と、
前記塩水を加熱し、前記塩水を蒸発させて水蒸気にする工程(c)と、
前記水蒸気を液化し、前記タンク層に前記淡水を得る工程(d)と、
を含む、淡水化する方法。 - 前記水蒸気の少なくとも一部が、前記工程(c)の後、かつ前記工程(d)の前に、前記容器の下部に向かって移動する、
請求項1に記載の方法。 - 前記容器は、さらにフタを具備する、
請求項1に記載の方法。 - 前記工程(c)において、前記塩水は太陽光によって加熱される、
請求項1に記載の方法。 - 前記工程(c)において、前記塩水はヒーターによって加熱される、
請求項1に記載の方法。 - 前記タンク層の外周面が冷却される、
請求項1に記載の方法。 - 前記タンク層の外周面が保冷剤により囲まれる、
請求項6に記載の方法。 - 前記撥水膜が化学式-(CF2)n-によって表されるフッ化炭素基を具備する、
請求項1に記載の方法。 - 前記塩水が海水である、
請求項1に記載の方法。
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JP2012511860A JP5045863B2 (ja) | 2010-11-05 | 2011-08-25 | 淡水化装置を用いて塩水を淡水化する方法 |
CN201180011522.6A CN102781845B (zh) | 2010-11-05 | 2011-08-25 | 使用淡水化装置淡化盐水的方法 |
US13/372,098 US8652303B2 (en) | 2010-11-05 | 2012-02-13 | Method for desalinating saltwater with desalination device |
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US13/372,098 Continuation US8652303B2 (en) | 2010-11-05 | 2012-02-13 | Method for desalinating saltwater with desalination device |
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Cited By (7)
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WO2014103289A1 (ja) * | 2012-12-27 | 2014-07-03 | パナソニック株式会社 | 淡水化システムにおいて用いる測定システム、淡水化システム、及び淡水化方法 |
WO2014112022A1 (ja) * | 2013-01-18 | 2014-07-24 | パナソニック株式会社 | 淡水化システム及び淡水化方法 |
WO2014141643A1 (ja) * | 2013-03-11 | 2014-09-18 | パナソニック株式会社 | 淡水化システム及び淡水化方法 |
WO2014148010A1 (ja) * | 2013-03-18 | 2014-09-25 | パナソニック株式会社 | 淡水化装置及び淡水化方法 |
WO2014148009A1 (ja) * | 2013-03-19 | 2014-09-25 | パナソニック株式会社 | 淡水化装置、それを備える淡水化システム及び淡水化方法 |
WO2014156124A1 (ja) * | 2013-03-28 | 2014-10-02 | パナソニック株式会社 | 水量制御方法及び淡水化システム |
WO2014156084A1 (ja) * | 2013-03-29 | 2014-10-02 | パナソニック株式会社 | 淡水化装置及び淡水化方法 |
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- 2011-08-25 JP JP2012511860A patent/JP5045863B2/ja not_active Expired - Fee Related
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CN104220382A (zh) * | 2012-12-27 | 2014-12-17 | 松下电器产业株式会社 | 淡水化系统中所使用的测定系统、淡水化系统、以及淡水化方法 |
US9873618B2 (en) | 2012-12-27 | 2018-01-23 | Panasonic Intellectual Property Management Co., Ltd. | Measurement system included in desalination system, desalination system, and desalination method |
WO2014103289A1 (ja) * | 2012-12-27 | 2014-07-03 | パナソニック株式会社 | 淡水化システムにおいて用いる測定システム、淡水化システム、及び淡水化方法 |
JP5799265B2 (ja) * | 2012-12-27 | 2015-10-21 | パナソニックIpマネジメント株式会社 | 淡水化システムにおいて用いる測定システム、淡水化システム、及び淡水化方法 |
WO2014112022A1 (ja) * | 2013-01-18 | 2014-07-24 | パナソニック株式会社 | 淡水化システム及び淡水化方法 |
US9822019B2 (en) | 2013-01-18 | 2017-11-21 | Panasonic Intellectual Property Management Co., Ltd. | Desalination system and desalination method |
JP5689213B2 (ja) * | 2013-01-18 | 2015-03-25 | パナソニックIpマネジメント株式会社 | 淡水化システム及び淡水化方法 |
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JP5621073B1 (ja) * | 2013-03-11 | 2014-11-05 | パナソニック株式会社 | 淡水化システム及び淡水化方法 |
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JP5659331B1 (ja) * | 2013-03-18 | 2015-01-28 | パナソニック株式会社 | 淡水化装置及び淡水化方法 |
WO2014148010A1 (ja) * | 2013-03-18 | 2014-09-25 | パナソニック株式会社 | 淡水化装置及び淡水化方法 |
JP5838366B2 (ja) * | 2013-03-19 | 2016-01-06 | パナソニックIpマネジメント株式会社 | 淡水化方法 |
WO2014148009A1 (ja) * | 2013-03-19 | 2014-09-25 | パナソニック株式会社 | 淡水化装置、それを備える淡水化システム及び淡水化方法 |
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WO2014156124A1 (ja) * | 2013-03-28 | 2014-10-02 | パナソニック株式会社 | 水量制御方法及び淡水化システム |
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JP5617064B1 (ja) * | 2013-03-28 | 2014-10-29 | パナソニック株式会社 | 水量制御方法及び淡水化システム |
WO2014156084A1 (ja) * | 2013-03-29 | 2014-10-02 | パナソニック株式会社 | 淡水化装置及び淡水化方法 |
US9862621B2 (en) | 2013-03-29 | 2018-01-09 | Panasonic Intellectual Property Management Co., Ltd. | Desalination apparatus and desalination method |
JP5621074B1 (ja) * | 2013-03-29 | 2014-11-05 | パナソニック株式会社 | 淡水化装置及び淡水化方法 |
Also Published As
Publication number | Publication date |
---|---|
CN102781845B (zh) | 2014-10-22 |
US20120138448A1 (en) | 2012-06-07 |
JP5045863B2 (ja) | 2012-10-10 |
CN102781845A (zh) | 2012-11-14 |
US8652303B2 (en) | 2014-02-18 |
JPWO2012060036A1 (ja) | 2014-05-12 |
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