TWI851501B - Control Methods for Seawater Minerals - Google Patents
Control Methods for Seawater Minerals Download PDFInfo
- Publication number
- TWI851501B TWI851501B TW112150082A TW112150082A TWI851501B TW I851501 B TWI851501 B TW I851501B TW 112150082 A TW112150082 A TW 112150082A TW 112150082 A TW112150082 A TW 112150082A TW I851501 B TWI851501 B TW I851501B
- Authority
- TW
- Taiwan
- Prior art keywords
- seawater
- concentration
- ions
- concentrate
- ion concentration
- Prior art date
Links
- 239000013535 sea water Substances 0.000 title claims abstract description 234
- 238000000034 method Methods 0.000 title claims abstract description 25
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims abstract description 21
- 239000011707 mineral Substances 0.000 title claims abstract description 21
- 229910052796 boron Inorganic materials 0.000 claims abstract description 91
- -1 boron ions Chemical class 0.000 claims abstract description 89
- 239000012141 concentrate Substances 0.000 claims abstract description 77
- 229910001425 magnesium ion Inorganic materials 0.000 claims abstract description 74
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 claims abstract description 72
- 230000001105 regulatory effect Effects 0.000 claims abstract description 31
- 239000003957 anion exchange resin Substances 0.000 claims abstract description 19
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 claims description 24
- 229910001424 calcium ion Inorganic materials 0.000 claims description 24
- 238000001223 reverse osmosis Methods 0.000 claims description 21
- 150000002500 ions Chemical class 0.000 claims description 18
- 238000001914 filtration Methods 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 5
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 4
- 238000010790 dilution Methods 0.000 claims description 3
- 239000012895 dilution Substances 0.000 claims description 3
- 238000011033 desalting Methods 0.000 claims description 2
- 238000010025 steaming Methods 0.000 claims description 2
- 239000003651 drinking water Substances 0.000 abstract description 6
- 235000020188 drinking water Nutrition 0.000 abstract description 6
- 230000008520 organization Effects 0.000 abstract description 4
- 230000000052 comparative effect Effects 0.000 description 15
- 230000014759 maintenance of location Effects 0.000 description 12
- 229910001415 sodium ion Inorganic materials 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 229910001414 potassium ion Inorganic materials 0.000 description 9
- 239000002384 drinking water standard Substances 0.000 description 8
- 239000012528 membrane Substances 0.000 description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
- 230000001143 conditioned effect Effects 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 4
- 230000006837 decompression Effects 0.000 description 4
- 238000010612 desalination reaction Methods 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- OBSLWIKITOYASJ-YDEIVXIUSA-N (3r,4r,5s,6r)-6-(hydroxymethyl)-3-(methylamino)oxane-2,4,5-triol Chemical group CN[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O OBSLWIKITOYASJ-YDEIVXIUSA-N 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical group CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 description 3
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 3
- 238000009360 aquaculture Methods 0.000 description 3
- 244000144974 aquaculture Species 0.000 description 3
- 235000013361 beverage Nutrition 0.000 description 3
- 238000010411 cooking Methods 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000000909 electrodialysis Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000001728 nano-filtration Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910001576 calcium mineral Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000009388 chemical precipitation Methods 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009616 inductively coupled plasma Methods 0.000 description 1
- 238000002354 inductively-coupled plasma atomic emission spectroscopy Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910001607 magnesium mineral Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Landscapes
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
一種海水礦物質的調控方法,包含以下步驟:提供一種海水濃縮液,以及使該海水濃縮液通過用於吸附硼離子的陰離子交換樹脂,以獲得經處理海水濃縮液。該海水濃縮液含有最低濃度為140 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子。該經處理海水濃縮液含有濃度低於60 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子。本發明之海水礦物質的調控方法可於維持鎂離子原有濃度下有效降低硼離子濃度,且所製得的經處理海水濃縮液可供製備符合世界衛生組織規範的飲用水。A method for regulating seawater minerals comprises the following steps: providing a seawater concentrate, and passing the seawater concentrate through an anion exchange resin for adsorbing boron ions to obtain a treated seawater concentrate. The seawater concentrate contains a minimum boron ion concentration of 140 mg/L and a minimum magnesium ion concentration of 40,000 mg/L. The treated seawater concentrate contains a boron ion concentration of less than 60 mg/L and a minimum magnesium ion concentration of 40,000 mg/L. The seawater mineral control method of the present invention can effectively reduce the boron ion concentration while maintaining the original magnesium ion concentration, and the prepared treated seawater concentrate can be used to prepare drinking water that meets the standards of the World Health Organization.
Description
本發明是關於一種海水處理方法,特別是指一種海水礦物質的調控方法。The present invention relates to a method for treating seawater, and more particularly to a method for regulating seawater minerals.
位在海平面下200公尺以下的深層海水因陽光無法穿透而無法進行光合作用,進而可以保留較高含量的無機營養鹽。目前深層海水已被廣泛應用於飲料、食品、醫藥品及水產養殖等領域,如此也讓深層海水的純化及處理成為業界研發重點。Deep seawater below 200 meters below sea level cannot photosynthesize because sunlight cannot penetrate, so it can retain a higher content of inorganic nutrients. Currently, deep seawater has been widely used in beverages, food, medicines and aquaculture, making the purification and treatment of deep seawater a research focus in the industry.
在深層海水所含的離子中,以鎂離子與鈣離子最受關注,因為在人體中,鎂離子與鈣離子的含量比例會影響肌肉組織、神經系統等運作。以成年人而言,衛生署建議每日需攝取之鎂及鈣等礦物質含量為:含量315-350 mg/天的鎂,及含量1000 mg/天的鈣。基於前述考量,許多關於如何維持深層海水中的鎂離子與鈣離子含量的文獻及專利被報導。例如,中華民國專利公告TW I428292B即提出一種海水濃縮液的製備方法,包含將一濃縮滷水透過二價陰離子膜進行電透析處理,以得到一脫除硫酸根離子礦物質水;接著對該脫除硫酸根離子礦物質水施予濃縮及分離處理,取得一海水濃縮液及礦物質鹽。該海水濃縮液具有低含量的硫酸根離子及鈉離子、以及高含量的鎂離子與鈣離子。此專利公告主要是希望製得具有低含量硫酸根離子及鈉離子,並同時含有高含量鎂離子及鈣離子的海水濃縮液。Among the ions contained in deep seawater, magnesium and calcium ions are of greatest concern, because in the human body, the ratio of magnesium to calcium ions affects the functioning of muscle tissue, the nervous system, etc. For adults, the Department of Health recommends a daily intake of magnesium and calcium minerals of 315-350 mg/day of magnesium and 1000 mg/day of calcium. Based on the above considerations, many literatures and patents have been reported on how to maintain the magnesium and calcium ion content in deep seawater. For example, the patent publication of the Republic of China TW I428292B proposes a method for preparing a seawater concentrate, which includes subjecting a concentrated brine to electrodialysis through a divalent anion membrane to obtain a sulfate-free mineral water; then the sulfate-free mineral water is subjected to concentration and separation treatment to obtain a seawater concentrate and mineral salts. The seawater concentrate has a low content of sulfate ions and sodium ions, and a high content of magnesium ions and calcium ions. This patent announcement is mainly intended to produce a seawater concentrate having low content of sulfate ions and sodium ions, and high content of magnesium ions and calcium ions.
隨著深層海水在保健與醫療用途的應用增加,深層海水中的過量硼離子被發現在長期進入人體後會誘發許多疾病,因此,如何有效去除深層海水中的過量硼離子成為另一研發重點項目。世界衛生組織(WHO)於飲用水水質標準所規定之硼離子限制值為0.5 mg/L,而歐盟規定之硼離子限制值為1 mg/L。惟,綜觀現有的海水除硼技術 [包含多段逆滲透(Reverse Osmosis,RO)、電透析、吸附法、化學沉澱法與離子交換樹脂等技術],這些技術無法順利在維持鎂離子原有濃度下有效降低硼含量,也無法工業化大量處理。以多段逆滲透為例,雖然使用多段逆滲透處理海水的技術可以去除海水中的硼離子,但對於所有離子沒有選擇性差異,在去除硼離子的同時,也會同時去除鎂離子、鈣離子等離子,所以多段式逆滲透技術無法有效維持深層海水中的鎂離子含量。As deep seawater is increasingly used for health and medical purposes, it has been found that excessive boron ions in deep seawater can induce many diseases after long-term exposure to the human body. Therefore, how to effectively remove excess boron ions in deep seawater has become another key research and development project. The World Health Organization (WHO) stipulates a boron ion limit of 0.5 mg/L in its drinking water quality standards, while the EU stipulates a boron ion limit of 1 mg/L. However, looking at the existing seawater boron removal technologies [including multi-stage reverse osmosis (RO), electrodialysis, adsorption, chemical precipitation and ion exchange resin technologies], these technologies cannot effectively reduce the boron content while maintaining the original concentration of magnesium ions, nor can they be industrialized for large-scale treatment. Taking multi-stage reverse osmosis as an example, although the technology of using multi-stage reverse osmosis to treat seawater can remove boron ions in seawater, there is no selectivity difference for all ions. While removing boron ions, magnesium ions, calcium ions and other ions will also be removed at the same time, so multi-stage reverse osmosis technology cannot effectively maintain the magnesium ion content in deep seawater.
鑒於現有方法無法在維持鎂離子原有濃度下有效降低硼離子濃度,所以,業界仍亟需尋找更佳的海水除硼方法。Since existing methods cannot effectively reduce the concentration of boron ions while maintaining the original concentration of magnesium ions, the industry is still in urgent need of finding better methods for removing boron from seawater.
因此,本發明的目的,即在提供一種海水礦物質的調控方法,該方法可於維持鎂離子原有濃度下有效降低硼離子濃度,且所製得的經處理海水濃縮液可供製備符合世界衛生組織規範的飲用水。Therefore, the purpose of the present invention is to provide a method for regulating seawater minerals, which can effectively reduce the concentration of boron ions while maintaining the original concentration of magnesium ions, and the obtained treated seawater concentrate can be used to prepare drinking water that meets the standards of the World Health Organization.
於是,本發明海水礦物質的調控方法,包含以下步驟: 提供一種海水濃縮液,該海水濃縮液含有最低濃度為140 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子;及 使該海水濃縮液通過一用於吸附硼離子的陰離子交換樹脂,以獲得一經處理海水濃縮液,其中,該經處理海水濃縮液含有濃度低於60 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子。 Therefore, the seawater mineral control method of the present invention comprises the following steps: Providing a seawater concentrate containing a minimum boron ion concentration of 140 mg/L and a minimum magnesium ion concentration of 40,000 mg/L; and Passing the seawater concentrate through an anion exchange resin for adsorbing boron ions to obtain a treated seawater concentrate, wherein the treated seawater concentrate contains a boron ion concentration of less than 60 mg/L and a minimum magnesium ion concentration of 40,000 mg/L.
於本發明的一些具體例中,該海水濃縮液含有濃度範圍為140~300 mg/L的硼離子。In some specific embodiments of the present invention, the concentrated seawater contains boron ions in a concentration range of 140-300 mg/L.
於本發明的一些具體例中,該海水濃縮液含有濃度範圍為40,000~120,000 mg/L的鎂離子。In some specific embodiments of the present invention, the concentrated seawater contains magnesium ions in a concentration range of 40,000-120,000 mg/L.
於本發明的一些具體例中,該海水濃縮液還含有濃度範圍為120~19,000 mg/L的鈣離子。In some specific embodiments of the present invention, the concentrated seawater further contains calcium ions in a concentration range of 120-19,000 mg/L.
於本發明的一些具體例中,該海水濃縮液的pH值範圍為6~7。In some specific embodiments of the present invention, the pH value of the concentrated seawater is in the range of 6-7.
於本發明的一些具體例中,該經處理海水濃縮液的最低總硬度為186,500 mg/L。In some embodiments of the present invention, the minimum total hardness of the treated seawater concentrate is 186,500 mg/L.
於本發明的一些具體例中,該海水濃縮液是將深層海水進行逆滲透步驟、低溫減壓濃縮步驟、蒸煮脫鹽步驟、離子調合步驟及過濾步驟所獲得。In some specific examples of the present invention, the seawater concentrate is obtained by subjecting deep seawater to a reverse osmosis step, a low-temperature pressure reduction concentration step, a cooking and desalination step, an ion blending step, and a filtration step.
於本發明的一些具體例中,該深層海水為位於海平面下200公尺以下的海水,該深層海水的硬度範圍為6,000~7,000 mg/L,及矽酸鹽最低濃度為20 μM。In some specific examples of the present invention, the deep seawater is seawater located below 200 meters below sea level, the hardness of the deep seawater ranges from 6,000 to 7,000 mg/L, and the minimum concentration of silicate is 20 μM.
於本發明的一些具體例中,本發明調控方法還包含一稀釋步驟,該稀釋步驟是將該經處理海水濃縮液進行稀釋,以獲得一經調控海水,該經調控海水含有濃度低於0.5 mg/L的硼離子。In some specific examples of the present invention, the control method of the present invention further comprises a dilution step, wherein the treated seawater concentrate is diluted to obtain a regulated seawater, wherein the regulated seawater contains a boron ion concentration of less than 0.5 mg/L.
於本發明的一些具體例中,該經調控海水含有濃度範圍為240~300 mg/L的鎂離子。In some embodiments of the present invention, the regulated seawater contains magnesium ions in a concentration range of 240-300 mg/L.
本發明的功效在於:本發明透過使用含有最低濃度為140 mg/L的硼離子以及最低濃度為40,000 mg/L的鎂離子之海水濃縮液,再通過用於吸附硼離子的陰離子交換樹脂後,可在維持鎂離子原有濃度下有效降低硼離子濃度。本發明海水濃縮液可供製備符合世界衛生組織規範的飲用水、或用於其他領域(如其他飲料、食品、醫藥品及水產養殖等)。The efficacy of the present invention is that the present invention uses a seawater concentrate containing a minimum boron ion concentration of 140 mg/L and a minimum magnesium ion concentration of 40,000 mg/L, and then passes through an anion exchange resin for adsorbing boron ions to effectively reduce the boron ion concentration while maintaining the original magnesium ion concentration. The seawater concentrate of the present invention can be used to prepare drinking water that meets the standards of the World Health Organization, or used in other fields (such as other beverages, food, pharmaceuticals and aquaculture, etc.).
本發明海水礦物質的調控方法,包含以下步驟:提供一種海水濃縮液,以及使該海水濃縮液通過一用於吸附硼離子的陰離子交換樹脂,以獲得一經處理海水濃縮液。該海水濃縮液含有最低濃度為140 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子。該經處理海水濃縮液含有濃度低於60 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子。The seawater mineral control method of the present invention comprises the following steps: providing a seawater concentrate, and passing the seawater concentrate through an anion exchange resin for adsorbing boron ions to obtain a treated seawater concentrate. The seawater concentrate contains a minimum boron ion concentration of 140 mg/L and a minimum magnesium ion concentration of 40,000 mg/L. The treated seawater concentrate contains a boron ion concentration of less than 60 mg/L and a minimum magnesium ion concentration of 40,000 mg/L.
本發明所提及的「海水礦物質」一詞泛指任何由海水進行處理所獲得的礦物質,例如但不限於含鎂離子、鈣離子、或鉀離子等礦物質。The term "seawater mineral" mentioned in the present invention refers to any mineral obtained by processing seawater, such as but not limited to minerals containing magnesium ions, calcium ions, or potassium ions.
本發明所提及的「最低濃度為140 mg/L」代表濃度≧140 mg/L;而「最低濃度為40,000 mg/L」是指濃度≧40,000 mg/L。「濃度低於60 mg/L」是指濃度< 60 mg/L。The "minimum concentration of 140 mg/L" mentioned in the present invention means the concentration is ≥ 140 mg/L; and the "minimum concentration of 40,000 mg/L" means the concentration is ≥ 40,000 mg/L. "Concentration less than 60 mg/L" means the concentration is less than 60 mg/L.
本發明所提及的「深層海水」泛指位於海洋斜溫層的海水、或位於海平面下200公尺以下的海水。較佳地,該深層海水為位於海平面下200公尺以下的海水,該深層海水的硬度範圍為6,000~7,000 mg/L,及矽酸鹽最低濃度為20 μM。The "deep seawater" mentioned in the present invention generally refers to seawater located in the ocean thermocline layer, or seawater located below 200 meters below sea level. Preferably, the deep seawater is seawater located below 200 meters below sea level, the hardness range of the deep seawater is 6,000-7,000 mg/L, and the minimum silicate concentration is 20 μM.
較佳地,該海水濃縮液是將海水進行處理後所獲得。上述的「處理」須滿足可獲得含有最低濃度為140 mg/L的硼離子以及最低濃度為40,000 mg/L的鎂離子之海水濃縮液的條件。該處理包含但不限於:逆滲透步驟、低溫減壓濃縮步驟、蒸煮脫鹽步驟、離子調合步驟、過濾步驟等。該逆滲透步驟,例如使海水通過一逆滲透過濾循環設備,該逆滲透過濾循環設備可包括一或多個以串聯或並聯連接、並含有多道式過濾膜的逆滲透過濾裝置。該低溫減壓濃縮步驟,例如將海水放置於低溫真空濃縮裝置進行低溫減壓濃縮,以得到濃縮海水。該蒸煮脫鹽步驟,例如使海水導入一蒸煮設備中;並使海水在低壓環境下加熱,以讓水分沸騰汽化,同時讓海水中的碳酸鹽類、硫酸鹽類及氯化鹽類等鹽類達到過飽和,進而持續使海水析出結晶至所需的組成濃度。該離子調合步驟,是使用去離子水來稀釋經過蒸煮脫鹽後的海水至所需組成濃度。該過濾步驟是使海水通過一微奈米膜進行過濾。Preferably, the seawater concentrate is obtained by treating seawater. The above-mentioned "treatment" must satisfy the conditions for obtaining a seawater concentrate containing a minimum boron ion concentration of 140 mg/L and a minimum magnesium ion concentration of 40,000 mg/L. The treatment includes but is not limited to: reverse osmosis step, low temperature and reduced pressure concentration step, cooking and desalination step, ion blending step, filtration step, etc. The reverse osmosis step, for example, allows the seawater to pass through a reverse osmosis filtration circulation device, which may include one or more reverse osmosis filtration devices connected in series or in parallel and containing multi-pass filter membranes. The low-temperature decompression concentration step, for example, places the seawater in a low-temperature vacuum concentration device for low-temperature decompression concentration to obtain concentrated seawater. The desalination step, for example, introduces seawater into a desalination device; and heats the seawater under low pressure to boil and vaporize the water, while allowing carbonates, sulfates, chlorides and other salts in the seawater to reach supersaturation, and then continuously precipitates and crystallizes the seawater to the desired composition concentration. The ion blending step uses deionized water to dilute the desalinated seawater to the desired composition concentration. The filtering step is to filter the seawater through a micro-nano membrane.
更佳地,該海水濃縮液是將深層海水進行逆滲透步驟、低溫減壓濃縮步驟、蒸煮脫鹽步驟、離子調合步驟及過濾步驟所獲得。更具體而言,該深層海水是通過以下步驟而獲得:(1)使深層海水通過一含有多個逆滲透過濾裝置的逆滲透過濾設備,並利用該等逆滲透過濾裝置進行深層海水的脫水及礦物質截留,並進一步讓深層海水中的礦物質濃度濃縮至適合後續步驟的濃度,以獲得第一經處理海水,其中,較佳地,第一經處理海水的最低總硬度為8,000 mg/L;(2) 將該第一經處理海水導入一低溫真空濃縮裝置進行低溫減壓濃縮(例如溫度為60°C、壓力為600 mmHg),得到一第二經處理海水;(3)使該第二經處理海水導入一蒸煮設備,而後讓該第二經處理海水於低壓環境下進行加熱 (例如溫度為120°C、壓力為760 mmHg),以讓所含水分沸騰汽化,並讓鹽類呈現過飽和而持續結晶析出之狀態,待該第二經處理海水持續結晶析出至所需之離子濃度,最後過濾取出液體,並獲得一第三經處理海水,其中,較佳地,該第三經處理海水的最低總硬度為300,000 mg/L,鎂離子最低濃度為70,000 mg/L,硼離子最低濃度為250 mg/L;(4)利用去離子水稀釋該第三經處理海水,以調整第三經處理海水所含的離子濃度,進而獲得一第四經處理海水,其中,較佳地,該第四經處理海水的最低總硬度為165,000 mg/L,鎂離子最低濃度為40,000 mg/L,硼離子最低濃度為140 mg/L;(5)使該第四經處理海水通過一奈米過濾膜(如孔徑0.2 μm)進行過濾,得到該海水濃縮液。More preferably, the seawater concentrate is obtained by subjecting deep seawater to a reverse osmosis step, a low-temperature reduced-pressure concentration step, a steaming and desalting step, an ion blending step, and a filtering step. More specifically, the deep seawater is obtained by the following steps: (1) passing the deep seawater through a reverse osmosis filtration device comprising a plurality of reverse osmosis filtration devices, and utilizing the reverse osmosis filtration devices to dehydrate the deep seawater and intercept minerals, and further concentrating the mineral concentration in the deep seawater to a concentration suitable for subsequent steps, so as to obtain a first treated seawater, wherein, preferably, the first treated seawater has a minimum total hardness of 8,000 mg/L; (2) introducing the first treated seawater into a low-temperature vacuum concentration device for low-temperature decompression concentration (e.g., a temperature of 60°C and a pressure of 600°C); (3) introducing the second treated seawater into a boiling device, and then heating the second treated seawater in a low pressure environment (e.g., a temperature of 120°C and a pressure of 760 mmHg) to allow the water contained therein to boil and vaporize, and to allow the salts to be supersaturated and continuously crystallize, and wait for the second treated seawater to continuously crystallize to a desired ion concentration, and finally filter out the liquid to obtain a third treated seawater, wherein, preferably, the third treated seawater has a minimum total hardness of 300,000 mg/L, a minimum magnesium ion concentration of 70,000 mg/L, and a minimum boron ion concentration of 250 (4) diluting the third treated seawater with deionized water to adjust the ion concentration of the third treated seawater to obtain a fourth treated seawater, wherein, preferably, the fourth treated seawater has a minimum total hardness of 165,000 mg/L, a minimum magnesium ion concentration of 40,000 mg/L, and a minimum boron ion concentration of 140 mg/L; (5) filtering the fourth treated seawater through a nanofiltration membrane (e.g., with a pore size of 0.2 μm) to obtain the seawater concentrate.
該海水濃縮液含有最低濃度為140 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子。較佳地,該海水濃縮液含有濃度範圍為140~300 mg/L的硼離子。更佳地,該海水濃縮液含有濃度範圍為40,000~120,000 mg/L的鎂離子。除維持鎂離子的含量外,其餘礦物質離子含量也可以視需要進行維持,例如鈣離子、鈉離子、磷離子等。又更佳地,該海水濃縮液還含有濃度範圍為120~19,000 mg/L的鈣離子;再又更佳地,該海水濃縮液還含有濃度範圍為120~13,000 mg/L的鈣離子。The seawater concentrate contains a minimum boron ion concentration of 140 mg/L and a minimum magnesium ion concentration of 40,000 mg/L. Preferably, the seawater concentrate contains a boron ion concentration in the range of 140-300 mg/L. More preferably, the seawater concentrate contains a magnesium ion concentration in the range of 40,000-120,000 mg/L. In addition to maintaining the content of magnesium ions, the content of other mineral substances, such as calcium ions, sodium ions, phosphorus ions, etc., can also be maintained as needed. More preferably, the concentrated seawater further contains calcium ions in a concentration range of 120-19,000 mg/L; even more preferably, the concentrated seawater further contains calcium ions in a concentration range of 120-13,000 mg/L.
需特別說明的是,當海水濃縮液含有濃度為140 mg/L以下的硼離子時,即使同樣通過一用於吸附硼離子的陰離子交換樹脂,也無法獲得有效降低硼離子濃度,這是因為用於吸附硼離子的陰離子交換樹脂具有交換高濃度硼離子的特性,所以當硼離子濃度過低時,陰離子交換樹脂將無法吸附硼離子而無法有效去除硼離子。其次,當海水濃縮液含有濃度為40,000 mg/L以下的鎂離子時,即使同樣通過該陰離子交換樹脂,將無法獲得含有高鎂離子濃度的經處理海水濃縮液。It should be noted that when the seawater concentrate contains boron ions at a concentration below 140 mg/L, even if it is passed through an anion exchange resin for adsorbing boron ions, the boron ion concentration cannot be effectively reduced. This is because the anion exchange resin for adsorbing boron ions has the characteristic of exchanging high-concentration boron ions. Therefore, when the boron ion concentration is too low, the anion exchange resin will not be able to adsorb boron ions and cannot effectively remove boron ions. Secondly, when the seawater concentrate contains magnesium ions at a concentration of 40,000 mg/L or less, it is not possible to obtain a treated seawater concentrate containing a high magnesium ion concentration even if it passes through the anion exchange resin.
較佳地,該海水濃縮液的pH值範圍為6~7。於本發明的一些具體例中,該海水濃縮液的pH值範圍為6.8。Preferably, the pH value of the concentrated seawater is in the range of 6 to 7. In some embodiments of the present invention, the pH value of the concentrated seawater is in the range of 6.8.
較佳地,該海水濃縮液的最低總硬度為165,000 mg/L。Preferably, the seawater concentrate has a minimum total hardness of 165,000 mg/L.
該海水濃縮液通過該陰離子交換樹脂,以獲得該經處理海水濃縮液。該陰離子交換樹脂是用於吸附硼離子,例如,具有N-甲基葡萄糖胺官能基之陰離子交換樹脂或大孔隙苯乙烯樹脂。較佳地,該陰離子交換樹脂是具有N-甲基葡萄糖胺官能基之陰離子交換樹脂。該具有N-甲基葡萄糖胺官能基之陰離子交換樹脂對於硼酸或硼酸根離子具有高度專一性的吸附效果。The seawater concentrate passes through the anion exchange resin to obtain the treated seawater concentrate. The anion exchange resin is used to adsorb boron ions, for example, an anion exchange resin with N-methylglucamine functional groups or a macroporous styrene resin. Preferably, the anion exchange resin is an anion exchange resin with N-methylglucamine functional groups. The anion exchange resin with N-methylglucamine functional groups has a highly specific adsorption effect on boric acid or borate ions.
該經處理海水濃縮液含有濃度低於60 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子。較佳地,該經處理海水濃縮液含有濃度低於60 mg/L的硼離子,以及最低濃度為40,000 mg/L的鎂離子。The treated seawater concentrate contains boron ions at a concentration of less than 60 mg/L and magnesium ions at a minimum concentration of 40,000 mg/L. Preferably, the treated seawater concentrate contains boron ions at a concentration of less than 60 mg/L and magnesium ions at a minimum concentration of 40,000 mg/L.
較佳地,該經處理海水濃縮液的最低總硬度為186,500 mg/L。Preferably, the treated seawater concentrate has a minimum total hardness of 186,500 mg/L.
較佳地,本發明海水礦物質的調控方法還包含一稀釋步驟,該稀釋步驟是將該經處理海水濃縮液進行稀釋,以獲得一經調控海水,該經調控海水含有濃度低於0.5 mg/L的硼離子。Preferably, the seawater mineral control method of the present invention further comprises a dilution step, wherein the treated seawater concentrate is diluted to obtain a regulated seawater, wherein the regulated seawater contains a boron ion concentration of less than 0.5 mg/L.
較佳地,該經調控海水含有濃度範圍為240~300 mg/L的鎂離子。除了上述濃度範圍外,鎂離子濃度範圍也可以視後續應用需求進行調整,例如濃度範圍為5~300 mg/L,具體濃度例如但不限於7.1、23.6、70.9、141.8 mg/L及260 mg/L等。Preferably, the regulated seawater contains magnesium ions in a concentration range of 240-300 mg/L. In addition to the above concentration range, the magnesium ion concentration range can also be adjusted according to subsequent application requirements, for example, the concentration range is 5-300 mg/L, and specific concentrations are, for example, but not limited to, 7.1, 23.6, 70.9, 141.8 mg/L and 260 mg/L.
該經調控海水可用於飲料、食品、醫藥品及水產養殖等領域。上述的海水濃縮液也可以直接運用於上述各個領域。 [ 實施例 ] The regulated seawater can be used in beverages, food, medicines, aquaculture and other fields. The above-mentioned seawater concentrate can also be directly used in the above-mentioned fields. [ Example ]
本發明將就以下實施例作進一步說明,但應瞭解的是,該實施例僅為例示說明之用,而不應被解釋為本發明實施之限制。The present invention will be further described with respect to the following embodiments, but it should be understood that the embodiments are only for illustrative purposes and should not be interpreted as limitations on the implementation of the present invention.
以下實施例和比較例皆使用深層海水,並利用下面的儀器進行性質測試: 1. 該深層海水是位於海平面下200公尺以下的深層海水。此深層海水具有6,000~7,000 mg/L的總硬度,以及最低濃度為20μM的矽酸鹽。 2. 離子濃度(mg/L)、硬度(mg/L):利用感應偶合電漿原子發射光譜儀(ICP-OES,Perkin Elmeroptima 2100DV)進行量測。 3. pH值:利用pH酸鹼度測量儀進行量測。 The following examples and comparative examples all use deep seawater and use the following instruments for property testing: 1. The deep seawater is deep seawater located below 200 meters below sea level. This deep seawater has a total hardness of 6,000~7,000 mg/L and a minimum silicate concentration of 20μM. 2. Ion concentration (mg/L), hardness (mg/L): measured using an inductively coupled plasma atomic emission spectrometer (ICP-OES, Perkin Elmeroptima 2100DV). 3. pH value: measured using a pH acidity meter.
[ 實施例 1]1. 海水濃縮液的製備: (1) 使深層海水通過一逆滲透過濾設備 [美國安邁科技公司(AMI)製造,型號為M-S4040A],俾以進行深層海水的脫水及礦物質截留,並進一步讓礦物質濃度增加,獲得第一經處理海水(最低總硬度為8,000 mg/L)。 (2) 將該第一經處理海水導入一低溫減壓濃縮裝置,並於溫度60°C及壓力600 mmHg下進行濃縮,獲得一第二經處理海水。 (3) 使該第二經處理海水導入一蒸煮設備(不銹鋼蒸氣迴轉鍋,台灣豐隆鐵工廠製造,型號為560L)。而後讓該第二經處理海水於溫度120°C及壓力760 mmHg下進行加熱,以讓所含水分沸騰汽化,並讓鹽類呈現過飽和而持續結晶析出之狀態,待該第二經處理海水持續結晶析出至所需之離子濃度,最後過濾取出液體,並獲得一第三經處理海水。該第三經處理海水的最低總硬度為300,000 mg/L,鎂離子最低濃度為70,000 mg/L,硼離子最低濃度為250 mg/L。 (4) 利用去離子水稀釋該第三經處理海水,以調整第三經處理海水所含的離子濃度,進而獲得一第四經處理海水。該第四經處理海水的最低總硬度為165,000 mg/L,鎂離子最低濃度為40,000 mg/L,硼離子最低濃度為140 mg/L。 (5) 使該第四經處理海水通過一奈米過濾膜[孔徑0.2 μm,美國安邁科技公司(AMI)製造,型號為M-N4040A5]進行過濾,得到該海水濃縮液。該海水濃縮液含有濃度45,441 mg/L的鎂離子、濃度130 mg/L的鈣離子、及濃度142.6 mg/L的硼離子。該海水濃縮液的pH值為6.8。 2. 經處理海水濃縮液的製備: 以溫度25°C、批次處理量300 L以及流量100 L/h為控制條件,使上述的海水濃縮液通用一含有N-甲基葡萄糖胺官能基的陰離子交換樹脂管柱 (樹脂填充量為16.5 L,美國杜邦公司製造,型號為IRA743),得到實施例1的經處理海水濃縮液。該經處理海水濃縮液含有濃度為45,441 mg/L的鎂離子及濃度為24.5 mg/L的硼離子。該經處理海水濃縮液的總硬度為187,450 mg/L。 3. 經調控海水的製備: 利用逆滲透過濾水進行上述實施例1之經處理海水濃縮液的稀釋,以獲得一經調控海水。該經調控海水含有濃度為270 mg/L的鎂離子、濃度為0.15 mg/L的硼離子、濃度為2,000 mg/L的鈉離子及濃度為2,000 mg/L的鉀離子。 [ Example 1] 1. Preparation of seawater concentrate: (1) Deep seawater is passed through a reverse osmosis filtration device [manufactured by AMI, Inc., USA, model number M-S4040A] to dehydrate the deep seawater and retain minerals, and further increase the mineral concentration to obtain a first treated seawater (minimum total hardness of 8,000 mg/L). (2) The first treated seawater is introduced into a low-temperature decompression concentration device and concentrated at a temperature of 60°C and a pressure of 600 mmHg to obtain a second treated seawater. (3) The second treated seawater is introduced into a cooking device (a stainless steel steam rotary pot, manufactured by Taiwan Fenglong Iron Works, model 560L). The second treated seawater is then heated at a temperature of 120°C and a pressure of 760 mmHg to allow the water contained therein to boil and vaporize, and to allow the salts to be supersaturated and continuously crystallize and precipitate. The second treated seawater continues to crystallize and precipitate to the desired ion concentration, and finally the liquid is filtered out to obtain a third treated seawater. The third treated seawater has a minimum total hardness of 300,000 mg/L, a minimum magnesium ion concentration of 70,000 mg/L, and a minimum boron ion concentration of 250 mg/L. (4) The third treated seawater is diluted with deionized water to adjust the ion concentration of the third treated seawater, thereby obtaining a fourth treated seawater. The fourth treated seawater has a minimum total hardness of 165,000 mg/L, a minimum magnesium ion concentration of 40,000 mg/L, and a minimum boron ion concentration of 140 mg/L. (5) The fourth treated seawater is filtered through a nanofiltration membrane [pore size 0.2 μm, manufactured by AMI, USA, model number M-N4040A5] to obtain the seawater concentrate. The seawater concentrate contains magnesium ions at a concentration of 45,441 mg/L, calcium ions at a concentration of 130 mg/L, and boron ions at a concentration of 142.6 mg/L. The pH value of the seawater concentrate is 6.8. 2. Preparation of treated seawater concentrate: The above-mentioned seawater concentrate was subjected to an anion exchange resin column containing N-methylglucosamine functional groups (resin filling volume of 16.5 L, manufactured by DuPont, USA, model IRA743) under the control conditions of temperature 25°C, batch processing volume 300 L and flow rate 100 L/h to obtain the treated seawater concentrate of Example 1. The treated seawater concentrate contained magnesium ions at a concentration of 45,441 mg/L and boron ions at a concentration of 24.5 mg/L. The total hardness of the treated seawater concentrate was 187,450 mg/L. 3. Preparation of conditioned seawater: The treated seawater concentrate of Example 1 was diluted by reverse osmosis filtration to obtain conditioned seawater. The conditioned seawater contained 270 mg/L of magnesium ions, 0.15 mg/L of boron ions, 2,000 mg/L of sodium ions, and 2,000 mg/L of potassium ions.
[ 實施例 2]除了將流量調整為600 mg/L之外,其餘步驟及條件皆與實施例1相同,實施例2所製得的經處理海水濃縮液含有濃度為42,715 mg/L的鎂離子及濃度為53.7 mg/L的硼離子,該經處理海水濃縮液的總硬度為187,450 mg/L。利用逆滲透過濾水進行上述實施例2之經處理海水濃縮液的稀釋,以獲得一經調控海水。所製得的該經調控海水含有濃度為270 mg/L的鎂離子、濃度為0.32 mg/L的硼離子、濃度為2,000 mg/L的鈉離子及濃度為2,000 mg/L的鉀離子。 [ Example 2] Except for adjusting the flow rate to 600 mg/L, the remaining steps and conditions are the same as those of Example 1. The treated seawater concentrate prepared in Example 2 contains 42,715 mg/L of magnesium ions and 53.7 mg/L of boron ions, and the total hardness of the treated seawater concentrate is 187,450 mg/L. The treated seawater concentrate of Example 2 is diluted by reverse osmosis filtered water to obtain a regulated seawater. The conditioned seawater thus produced contained magnesium ions at a concentration of 270 mg/L, boron ions at a concentration of 0.32 mg/L, sodium ions at a concentration of 2,000 mg/L and potassium ions at a concentration of 2,000 mg/L.
[ 比較例 1]將深層海水進行雜質過濾,得到純化海水。該純化海水含有濃度1,300 mg/mL的鎂離子、濃度4-5 mg/mL的硼離子及濃度500 mg/mL的鈣離子。該純化海水的pH值為7.8~8.5。 以溫度25°C、批次處理量300 L以及流量100 L/h為控制條件,使上述的純化海水通用一含有N-甲基葡萄糖胺官能基的陰離子交換樹脂管柱 (樹脂填充量為16.5 L),得到比較例1的經處理海水。該經處理海水含有濃度為1,300 mg/L的鎂離子及濃度為1~2 mg/L的硼離子。 利用逆滲透過濾水進行上述比較例1之經處理海水的稀釋,以獲得一經調控海水。該經調控海水含有濃度為270 mg/L的鎂離子、濃度為0.42 mg/L的硼離子、濃度為15,000 mg/L的鈉離子及濃度為450 mg/L的鉀離子。 [ Comparative Example 1] Deep seawater was filtered to obtain purified seawater. The purified seawater contained magnesium ions at a concentration of 1,300 mg/mL, boron ions at a concentration of 4-5 mg/mL, and calcium ions at a concentration of 500 mg/mL. The pH value of the purified seawater was 7.8-8.5. Under the control conditions of temperature 25°C, batch processing volume 300 L, and flow rate 100 L/h, the purified seawater was subjected to an anion exchange resin column containing N-methylglucosamine functional groups (resin filling volume of 16.5 L) to obtain the treated seawater of Comparative Example 1. The treated seawater contained 1,300 mg/L of magnesium ions and 1-2 mg/L of boron ions. The treated seawater of Comparative Example 1 was diluted with reverse osmosis filtered water to obtain regulated seawater. The regulated seawater contained 270 mg/L of magnesium ions, 0.42 mg/L of boron ions, 15,000 mg/L of sodium ions, and 450 mg/L of potassium ions.
[ 比較例 2]使深層海水通過孔徑1 μm的過濾膜進行粗過濾,之後再通過第一道逆滲透膜[美國安邁科技公司(AMI)製造,型號為M-S4040A]進行淡化,得到一次淡化海水。該一次淡化海水再通過第二道逆滲透膜[美國安邁科技公司(AMI)製造,型號為M-S4040A],得到二次淡化海水。該二次淡化海水含有濃度小於1 mg/L的鎂離子、濃度4-5 mg/L的硼離子及濃度小於1 mg/L的鈣離子。 以溫度25°C、批次處理量300 L以及流量100 L/h為控制條件,使上述的二次淡化海水通用一含有N-甲基葡萄糖胺官能基的陰離子交換樹脂管柱 (樹脂填充量為16.5 L),得到比較例2的經處理海水。該經處理海水含有濃度小於1 mg/L的鎂離子、及濃度為0.8~1.5 mg/L的硼離子。 利用逆滲透過濾水進行上述比較例2之經處理海水的稀釋,以獲得一經調控海水。該經調控海水含有濃度小於1 mg/L的鎂離子、濃度為0.8~1.5 mg/L的硼離子、濃度小於10 mg/L的鈉離子及濃度小於10 mg/L的鉀離子。 [ Comparative Example 2] Deep seawater is coarsely filtered through a filter membrane with a pore size of 1 μm, and then desalinated through a first reverse osmosis membrane [manufactured by AMI, USA, model M-S4040A] to obtain primary desalinated seawater. The primary desalinated seawater is then passed through a second reverse osmosis membrane [manufactured by AMI, USA, model M-S4040A] to obtain secondary desalinated seawater. The secondary desalinated seawater contains magnesium ions with a concentration of less than 1 mg/L, boron ions with a concentration of 4-5 mg/L, and calcium ions with a concentration of less than 1 mg/L. With the temperature of 25°C, the batch processing volume of 300 L and the flow rate of 100 L/h as the control conditions, the secondary desalinated seawater was used in an anion exchange resin column containing N-methylglucosamine functional groups (resin filling volume of 16.5 L) to obtain the treated seawater of Comparative Example 2. The treated seawater contained magnesium ions with a concentration of less than 1 mg/L and boron ions with a concentration of 0.8-1.5 mg/L. The treated seawater of Comparative Example 2 was diluted with reverse osmosis filtered water to obtain a regulated seawater. The conditioned seawater contains magnesium ions at a concentration of less than 1 mg/L, boron ions at a concentration of 0.8-1.5 mg/L, sodium ions at a concentration of less than 10 mg/L and potassium ions at a concentration of less than 10 mg/L.
將上述實施例1、比較例1及比較例2進行比較如下表1,其中,鎂離子保留率及硼離子去除率的計算公式如下(以海水濃縮液為例):
鎂離子保留率(%)=(經處理海水濃縮液所含鎂離子濃度/海水濃縮液所含鎂離子濃度)×100%
硼離子去除率(%)=[(海水濃縮液所含硼離子濃度–經處理海水濃縮液所含硼離子濃度)/海水濃縮液所含硼離子濃度]×100%
表1
依據表1結果來看,雖然比較例1及比較例2亦可保留鎂離子及去除硼離子,但最終所製得的經調控海水皆無法符合WTO的飲用水標準。就比較例1而言,雖然鎂離子濃度及硼離子濃度皆符合標準,但因為比較例1的深層海水並未經過較嚴密的過濾、或其他濃縮純化步驟,導致純化海水的鈉離子嚴重超標,且深層海水也可能含有其他金屬離子,因此,該純化海水無法直接作為飲用水使用。就比較例2而言,比較例2的經調控海水雖然含有符合標準的鈉離子濃度和鉀離子濃度,但因為硼離子濃度過高,而無法符合WTO的飲用水標準。再就實施例1來看,實施例1的經調控海水不但可以維持較高濃度的鎂離子、符合標準濃度的鈉離子和鉀離子,還含有符合標準之低濃度硼離子,故實施例1之經調控海水可作為飲用水使用。According to the results in Table 1, although Comparative Example 1 and Comparative Example 2 can also retain magnesium ions and remove boron ions, the regulated seawater finally produced cannot meet the WTO drinking water standards. For Comparative Example 1, although the magnesium ion concentration and boron ion concentration both meet the standards, because the deep seawater in Comparative Example 1 has not undergone more rigorous filtration or other concentration and purification steps, the sodium ion in the purified seawater seriously exceeds the standard, and the deep seawater may also contain other metal ions. Therefore, the purified seawater cannot be used directly as drinking water. As for Comparative Example 2, although the regulated seawater of Comparative Example 2 contains sodium ion concentration and potassium ion concentration that meet the standards, the boron ion concentration is too high and cannot meet the WTO drinking water standard. As for Example 1, the regulated seawater of Example 1 can not only maintain a relatively high concentration of magnesium ions, sodium ions and potassium ions that meet the standard concentrations, but also contains a low concentration of boron ions that meet the standards, so the regulated seawater of Example 1 can be used as drinking water.
再將實施例1及實施例2之結果整理如下表2:
表2
依據表2結果來看,實施例2因為調高6倍流量(由100 L/h增加至600 L/h),雖然導致鎂離子保留率及硼離子去除率降低,且最後獲得的經調控海水的硼離子濃度也有些提高,不過,最後製得之經調控海水仍符合WTO的飲用水標準。由實施例2結果也顯示,本發明的調控方法可以大量處理深層海水,並可在維持較高鎂離子濃度下有效降低硼離子濃度,進而獲得符合WTO飲用水標準的經調控海水。According to the results in Table 2, Example 2 increases the flow rate by 6 times (from 100 L/h to 600 L/h), which results in a decrease in the magnesium ion retention rate and the boron ion removal rate, and the boron ion concentration of the regulated seawater is also slightly increased. However, the regulated seawater still meets the WTO drinking water standard. The results of Example 2 also show that the regulation method of the present invention can treat deep seawater in large quantities, and can effectively reduce the boron ion concentration while maintaining a relatively high magnesium ion concentration, thereby obtaining regulated seawater that meets the WTO drinking water standard.
[ 實施例 3~7]除了分別將流量調整為60 mg/L、200 mg/L、300 mg/L、400 mg/L及500 mg/L之外,其餘步驟及條件皆與實施例1相同,實施例3~7所製得的經處理海水濃縮液所含有的離子濃度如下表3。鎂離子保留率及硼離子去除率依據上述[0041]段計算,而鈣離子保留率計算公式如下,最後將結果整理於表3中。 鈣離子保留率(%)=(經處理海水濃縮液所含鈣離子濃度/海水濃縮液所含鈣離子濃度)×100% [ Examples 3-7] Except for adjusting the flow rate to 60 mg/L, 200 mg/L, 300 mg/L, 400 mg/L and 500 mg/L, the remaining steps and conditions are the same as those of Example 1. The ion concentrations of the treated seawater concentrates obtained in Examples 3-7 are shown in Table 3. The magnesium ion retention rate and the boron ion removal rate are calculated according to the above paragraph [0041], and the calcium ion retention rate is calculated as follows. The results are summarized in Table 3. Calcium ion retention rate (%) = (calcium ion concentration in treated seawater concentrate/calcium ion concentration in seawater concentrate) × 100%
表3
由表3來看,利用本發明方法可在鎂離子保留率為94%以上,有效達到62.3%~85.3%之硼離子去除率。雖然流量的增加會影響鎂離子及鈣離子的保留率、及硼離子去除率,但由表2之實施例1及2的結果來看,最終製得的經調控海水仍會符合WTO的飲用水標準,可見流量控制在600 L/h以下皆可讓經調控海水符合WTO的飲用水標準。From Table 3, the present invention can effectively achieve a boron ion removal rate of 62.3% to 85.3% with a magnesium ion retention rate of more than 94%. Although the increase in flow rate will affect the retention rate of magnesium ions and calcium ions, and the boron ion removal rate, from the results of Examples 1 and 2 in Table 2, the final regulated seawater will still meet the WTO drinking water standards. It can be seen that the regulated seawater can meet the WTO drinking water standards when the flow rate is controlled below 600 L/h.
綜上所述,本發明海水礦物質的調控方法透過使用含有最低濃度為140 mg/L的硼離子以及最低濃度為40,000 mg/L的鎂離子之海水濃縮液,再通過用於吸附硼離子的陰離子交換樹脂後,可在維持鎂離子原有濃度下有效降低硼離子濃度,故確實能達成本發明的目的。In summary, the seawater mineral control method of the present invention uses a concentrated seawater solution containing a minimum boron ion concentration of 140 mg/L and a minimum magnesium ion concentration of 40,000 mg/L, and then passes through an anion exchange resin for adsorbing boron ions. The boron ion concentration can be effectively reduced while maintaining the original magnesium ion concentration, so the purpose of the present invention can be achieved.
惟以上所述者,僅為本發明的實施例而已,當不能以此限定本發明實施的範圍,凡是依本發明申請專利範圍及專利說明書內容所作的簡單等效變化與修飾,皆仍屬本發明專利涵蓋的範圍內。However, the above is only an example of the implementation of the present invention, and it cannot be used to limit the scope of the implementation of the present invention. All simple equivalent changes and modifications made according to the scope of the patent application of the present invention and the content of the patent specification are still within the scope of the patent of the present invention.
無without
無without
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW112150082A TWI851501B (en) | 2023-12-21 | 2023-12-21 | Control Methods for Seawater Minerals |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW112150082A TWI851501B (en) | 2023-12-21 | 2023-12-21 | Control Methods for Seawater Minerals |
Publications (1)
Publication Number | Publication Date |
---|---|
TWI851501B true TWI851501B (en) | 2024-08-01 |
Family
ID=93283852
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW112150082A TWI851501B (en) | 2023-12-21 | 2023-12-21 | Control Methods for Seawater Minerals |
Country Status (1)
Country | Link |
---|---|
TW (1) | TWI851501B (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20090061174A (en) * | 2007-12-11 | 2009-06-16 | 주식회사 워터비스 | Method for producing mineral water from deep ocean water with anion exchange resin |
KR20160004063A (en) * | 2014-07-02 | 2016-01-12 | 한국해양과학기술원 | Removal system of sulfate in seawater using ion exchange resin |
WO2021131156A1 (en) * | 2019-12-25 | 2021-07-01 | オルガノ株式会社 | Water treatment system and water treatment method |
CN117139350A (en) * | 2023-09-05 | 2023-12-01 | 中国海洋大学 | Deep sea sediment processing method |
-
2023
- 2023-12-21 TW TW112150082A patent/TWI851501B/en active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20090061174A (en) * | 2007-12-11 | 2009-06-16 | 주식회사 워터비스 | Method for producing mineral water from deep ocean water with anion exchange resin |
KR20160004063A (en) * | 2014-07-02 | 2016-01-12 | 한국해양과학기술원 | Removal system of sulfate in seawater using ion exchange resin |
WO2021131156A1 (en) * | 2019-12-25 | 2021-07-01 | オルガノ株式会社 | Water treatment system and water treatment method |
CN117139350A (en) * | 2023-09-05 | 2023-12-01 | 中国海洋大学 | Deep sea sediment processing method |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Sahli et al. | Fluoride removal for underground brackish water by adsorption on the natural chitosan and by electrodialysis | |
KR100732066B1 (en) | Method for extracting minerals of high purity from deep ocean water by using low temperature vacuum crystallization | |
US8758626B2 (en) | Water purification cartridge using zirconium ion-exchange sorbents | |
KR101639848B1 (en) | The manufacturing process of high hardness drinking water using NF/RO/ED membrane connection system | |
US20130115335A1 (en) | Preparation method of weakly basic, ionized, mineralization and healthy drinking water | |
CN104071808A (en) | Method for preparing industrial salt through separation, evaporation and crystallization of coal chemical strong brine | |
KR20160004063A (en) | Removal system of sulfate in seawater using ion exchange resin | |
WO2008153274A1 (en) | Preparation method of mineral water and mineral salt from deep ocean water | |
JP2005342664A (en) | Method for producing mineral water | |
JP5584321B1 (en) | Operation method of medical purified water production equipment | |
KR101689059B1 (en) | Removal of anions and conversion technology of carbonate ions from seawater | |
TWI851501B (en) | Control Methods for Seawater Minerals | |
KR101367477B1 (en) | Method for separate manufacturing of mineral salts (calcium and magnesium salts) isolated from alkaline water by electrolysis of sea water and mineral water | |
CN106186490A (en) | A kind of cold boiled water production technology | |
CN112679021B (en) | Salt-making method by using seawater | |
KR101896227B1 (en) | Method for preparing mineral water with high hardness using deep sea water or saline groundwater | |
KR100992428B1 (en) | Method of mineral water manufacture through efficient mineral control and removal of anion by nf membrane | |
Madrona et al. | The potential of different saline solution on the extraction of the Moringa oleifera seed's active component for water treatment | |
KR20140073609A (en) | The method for producing drinking water using deep sea water | |
CN102786566A (en) | Method for absorbing and purifying stevioside through multiple-column secondary resin series connection | |
JP2006142265A (en) | High-concentration mineral liquid manufacturing method and manufacturing apparatus | |
KR100899014B1 (en) | Preparation method of natural mineral salt from deep ocean water | |
CN108996521B (en) | Process for producing high-purity refined salt by using selective electrodialysis concentrated brine | |
JP2006007084A (en) | Mineral composition, manufacturing method therefor and usage thereof | |
KR100955004B1 (en) | Method for producing mineral salt with mineral materials |