CN105142762B - 包含多级净化的渗透驱动膜***的改进 - Google Patents
包含多级净化的渗透驱动膜***的改进 Download PDFInfo
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- 238000000746 purification Methods 0.000 title abstract description 10
- 230000003204 osmotic effect Effects 0.000 title description 10
- 230000006872 improvement Effects 0.000 title description 2
- 238000001223 reverse osmosis Methods 0.000 claims abstract description 104
- 150000003839 salts Chemical class 0.000 claims abstract description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000002994 raw material Substances 0.000 claims description 35
- 230000014759 maintenance of location Effects 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 19
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- 239000003085 diluting agent Substances 0.000 claims description 10
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- 238000001764 infiltration Methods 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000002519 antifouling agent Substances 0.000 claims description 4
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- 206010000234 Abortion spontaneous Diseases 0.000 claims 1
- 208000015994 miscarriage Diseases 0.000 claims 1
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- 239000007788 liquid Substances 0.000 abstract description 25
- 238000001728 nano-filtration Methods 0.000 abstract description 12
- 239000000463 material Substances 0.000 abstract description 7
- 239000010408 film Substances 0.000 description 50
- 235000002639 sodium chloride Nutrition 0.000 description 45
- 239000012528 membrane Substances 0.000 description 26
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 20
- 230000002706 hydrostatic effect Effects 0.000 description 16
- 230000005764 inhibitory process Effects 0.000 description 12
- 239000011780 sodium chloride Substances 0.000 description 10
- 238000010612 desalination reaction Methods 0.000 description 8
- 238000004064 recycling Methods 0.000 description 8
- 239000002699 waste material Substances 0.000 description 7
- 238000010586 diagram Methods 0.000 description 5
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
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- 238000004519 manufacturing process Methods 0.000 description 3
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- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000003491 array Methods 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
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- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000010979 pH adjustment Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
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- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
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- UBXAKNTVXQMEAG-UHFFFAOYSA-L strontium sulfate Chemical compound [Sr+2].[O-]S([O-])(=O)=O UBXAKNTVXQMEAG-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 102000015863 Nuclear Factor 90 Proteins Human genes 0.000 description 1
- 108010010424 Nuclear Factor 90 Proteins Proteins 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000011469 building brick Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
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- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000006298 dechlorination reaction Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 238000009292 forward osmosis Methods 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- TVHALOSDPLTTSR-UHFFFAOYSA-H hexasodium;[oxido-[oxido(phosphonatooxy)phosphoryl]oxyphosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O TVHALOSDPLTTSR-UHFFFAOYSA-H 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 235000011147 magnesium chloride Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000009938 salting Methods 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 229940065287 selenium compound Drugs 0.000 description 1
- 150000003343 selenium compounds Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
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Classifications
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Abstract
一种用于净化高浓度原料液的实例水净化***包含高截留率正渗透模块、一或多个低截留率模块及高截留率反渗透模块。所述低截留率模块可具有不同的截留率水平。所述***可由一或多个泵加压。所述低截留率模块中的一或多者可包含一或多个纳滤NF膜。汲取液可包含单价盐、多价盐或两者的组合。
Description
交叉引用
本申请案主张2013年3月15日申请的第61/794,537号美国临时申请案的早先申请日期的权益,所述申请案的全文出于任何目的而以引用的方式并入本文中。
技术领域
本文中描述的实例涉及可用于正渗透(FO)或反渗透(RO)或大体上任何分离过程的分离***、元件及方法。
政府赞助
本发明在由国防部授权的合同号为W911NF-09-C-0079下受政府的支持。政府对本发明具有某些权利。
背景技术
对于渗透预处理,较高汲取液渗透势实质上增加***的原料浓度操作窗。常规***通常具有对用于反渗透(RO)的汲取液浓度的限制。
在RO***中,可处理的最大原料盐度受汲取液的最大盐度限制。汲取液通常受限于80,000ppm的高点,这是由于任何较大浓度将需要将使膜破裂的RO静水压力。最大RO操作静水压力通常在1000与1200psi之间。以下大体上解释此限制。跨越RO膜的通量与活性膜压力成正比。活性膜压力为跨越RO膜的静水压力差(通常为到近大气渗透物的800psi原料)减去跨越RO膜的渗透压力差(通常为500psi到近0psi渗透物的原料)。可通过改变前述值中的任何者调整活性膜压力。虽然原料的渗透压力可在***中容易地调整,但渗透物的渗透压力通常固定为近零,且为RO膜的抑制的函数(被定义为1减去进入渗透物的盐的分数,典型RO抑制大于99%)。
因此,与膜驱动***相比,能够处理浓度超过80,000ppm的原料液的净化***通常使用热变及相变,从而引起大占据面积、高能量需求及高资金***成本。当原料总溶解溶质(TDS)大于80,000ppm时或当必须将较低TDS原料液处理为具有超过80,000ppm的废料的高回收(例如,零液体排放应用)时使用这些***。
发明内容
本文中揭示用于净化的设备、***及方法的实例。举例来说,一种设备可包含:可接收原料流及高浓度汲取流以产生第一流的正渗透模块;可加压于所述第一流的泵;可接收所述经加压第一流以产生所述高浓度汲取流及低浓度汲取流的低抑制膜模块;及可接收所述低浓度流以产生产物流及截留流的反渗透模块。来自所述反渗透流的所述截留流可与所述第一流组合且被提供到所述低抑制模块。所述汲取流可包含多价盐。
一种实例***可包含:可经配置以接收汲取流及原料流以产生第一流的正渗透级;经配置以接收所述第一流且产生输出流的串联连接的多个低抑制级;及可接收所述输出流以产生截留流及产物流的反渗透级。所述低抑制级可各自产生截留流且将所述截留流提供到前一低抑制级。
又一实例,一种方法可包含:将汲取流提供到正渗透模块;将原料流提供到所述正渗透模块;用所述正渗透模块过滤所述原料流,此可产生第一流;加压于所述第一流;用低抑制模块过滤所述经加压第一流,此可产生稀释流;及用反渗透模块过滤所述稀释流,此可产生产物流。所述方法可进一步包含将阻垢剂或防污剂添加到所述原料流。
附图说明
图1为根据本发明的实施例的净化***的框图。
图2为根据本发明的另一实施例的净化***的框图。
图3为根据本发明的又一实施例的净化***的框图。
具体实施方式
下文陈述某些细节以提供对本发明的实施例的充分理解。然而,所属领域的技术人员应清楚,可在无需这些特定细节的情况下实践本发明的实施例。在一些情况下,尚未详细地展示众所周知的化学结构、化学成分、分子、材料、制造组件、控制***、电子组件、时序协议及软件操作以避免不必要地混淆本发明所描述的实施例。
在本文中描述的实例中,可使用以两个或两个以上模块的阵列深入地分级的纳滤(NF)及/或反渗透(RO)膜模块且允许上游级中的NF或RO膜的渗透物侧上的盐浓度增加来克服对用于RO及高压RO的汲取液浓度的现有限制。以此方式,跨越每一RO膜的有效浓度差与所需施加的液压压力一起减小。可以若干方式产生RO膜的渗透物侧上增加的盐浓度,所述方式包含利用较少选择性RO膜或具有4个通口(例如,汲取物入口/出口、渗透物入口/出口)的RO膜样式。由于回收的倍增性质而通常不进行RO模块的此分级,此意味着总***回收率可能非常低。本文中描述的实例的优点及常规***的任何所描述缺点不希望为限制性的,且经提供以辅助理解。应理解,一些实例可不展现所有或甚至任何所描述优点。此外,一些实例可不解决常规***的所有或甚至任何所描述缺点。
通过将多个反渗透(RO)器皿与正渗透预处理配对,一些实例中的总***回收率可与RO***回收率解耦。在一些实例中,与在未使用FO预处理***的情况下的回收率相比,正渗透(FO)预处理与多级NF及/或RO的耦合允许总***水回收率增加。
在图1的框图中说明根据本发明的实施例的实例净化***10。***10可能够通过以高于原料100的浓度再产生汲取液105而处理超过80,000ppm浓度的原料液100。虽然在一些实施例中可能需要超过1200psi的静水压力以通过将再浓缩断开成两个或两个以上级(每一级可在低于膜的爆裂压力的静水压力下操作)在一个级中用RO膜的阵列再浓缩此汲取液。高压RO元件通常为额定1800psi,但当可减轻污物形成及污垢形成时可高达3000psi。
在一些实例中,将再浓缩分离成多个级可使用一或多个中压驱动脱盐膜。虽然跨越这些膜的静水压力或渗透压力差相对于常规RO膜的限制可不增加,但还可通过增加渗透物渗透压力增加原料渗透压力,此可使两个流之间的渗透压力差保持恒定。可使用相对于常规RO膜(例如NR膜或松散RO膜)具有减小的盐截留率的膜。
返回到图1,***10说明可能够将高浓度原料处理成小于120kppm的浓度的两级FO/RO***。所述***可使用氯化钠汲取溶质,但可以单一形式或以组合形式而与其它汲取溶质一起被利用。所述***包含三个膜阵列:FO模块103、低抑制压力驱动脱盐模块110(LR),及RO模块116。FO模块103通常包含并联布置、串联布置或两者的组合的FO膜阵列。通常可使用任何适合的RO膜。FO模块103通常可具有高盐截留率(例如,通常大于95%)。LR模块110通常包含具有小于RO的盐截留率(例如,其通常为99%或更大)的膜阵列。LR模块中的膜阵列可被串联布置、并联布置或其组合。通常,所述模块的盐截留率(例如,氯化钠抑制)可小于90%,在一些实例中小于80%,在一些实例中小于70%,在一些实例中小于60%,在一些实例中小于50%。RO模块116通常包含并联布置、串联布置或两者的组合的RO膜阵列。通常可使用任何适合的RO膜。RO模块可具有高抑制(例如,通常大于99%)。
在实例操作期间,高浓度原料流102进入FO模块103,在FO模块103处,高浓度原料流102被脱水且作为截留流104而离开***。通常,可将任何流用作原料流,包含但不限于海水或废水。高浓度汲取流105(例如,120kppm)以可为近大气的压力流动(例如,1MGD),进入FO模块103,此吸收质量且变得稀释,从而作为具有减小的浓度(例如,80kppm)的第一流106而离开,且高浓度汲取流105以可为近大气的压力流动(例如,1.5MGD)。此流的浓度可能太高而不能用单级RO进行回收。接着可由泵107(其可能为高压泵)加压(例如,1000psi)于所述流,接着与具有流率(例如,0.5MGD)的邻近反渗透截留(例如,卤水)流117(其可为高压流)组合,从而形成具有流率(例如,2MGD)的流109。所述压力可保持上升(例如,1000psi)。流109可与低截留率压力驱动盐截留模块110(LR)接触,低抑制压力驱动盐截留模块110(LR)可具有(例如)50%的截留率及50%的回收率。在其它实例中,模块110的盐截留率(例如,氯化钠截留率)可小于40%、小于50%、小于60%、小于70%、小于80%,或在一些实例中小于90%。在其它实例中,模块110的回收率可小于90%、小于70%、小于50%、小于30%且大于10%。与其中(例如)50%回收引起约为原料流的浓度两倍的截留流在高TDS处限制回收的RO膜对比,LR膜将由于散装盐跨越所述膜进行转移而具有小于两倍的原料流的浓度,从而允许比典型RO膜高的回收比率。流109的静水压力可克服跨越膜的平均浓度差(例如,40kppm乘300psi),从而产生流动(例如,1MGD)且可具有近大气的压力的低浓度流113(例如,40kppm),及可流动(例如,1MGD)且具有较高压力(例如,1000psi)的高浓度汲取流111(例如,120kppm)。
此流的压力可跨越能量回收装置112(例如,液压电动机)而减低,从而形成可被馈送到FO膜阵列103的低压高浓度汲取流105。接着可由泵114将低浓度流113加压到较高压力(例如,1000psi),从而形成流115。将此流馈送到可具有高截留率(例如,大于99%、大于98%、大于97%、大于95%,或在一些实例中大于90%)的级2RO模块116。静水压力可克服跨越膜的平均浓度差(例如,40kppm乘300psi)且可产生高质量产物流118。
产物流118可具有几乎0kppm(例如,350ppm)的浓度、0.5MGD的流量及近大气的压力。RO模块116还可产生反渗透截留流117,反渗透截留流117可与流108组合且如上文所论述而被再循环。反渗透截留流117可具有80kppm的浓度、0.5MGD的流量及1000psi的压力。
可将纳滤(NF)膜用作模块110中的中间级1压力驱动盐截留膜阵列。与趋向于以比单价盐高的百分比截留多价盐的RO膜不同,NF膜可以比多价盐高的百分比截留单价盐。此可通过具有包含单价盐(例如,氯化钠或氯化锂)及多价盐(例如,氯化镁、氯化钙、硫酸镁或磷酸钠)两者的汲取溶质予以充分利用。举例来说,NF膜可以70%截留单价盐且以30%截留多价盐,但在其它实例中可使用其它截留百分比。当进入模块110时,多价盐可更可能在低浓度流113中离开所述模块,且单价盐可更可能在高浓度汲取流111中离开所述模块。
因此,级2RO模块116可为脱盐流115,脱盐流115的盐主要为多价盐,此可引起较高质量的较低TDS产物流118。在另一实例中,NF膜可比单价盐更好地抑制多价盐,此可引起较高的特定RO通量。在其它实例中,FO模块103可接收汲取液流105,汲取液流105的盐主要为单价盐,此可引起比用多价盐所达到的通量高的特定通量。
表1含有用于图1所说明的***中的不同点的实例流率、静水压力及溶质浓度。表1中给出的值为示范性的且不应被解释为将本发明的实施例限于所给出的值。在其它实例中,可使用流率、静水压力及溶质浓度的其它值。
表1:用于两级FO/RO***10的示范性值
图1中的元件编号 | 流量(MGD) | 静水压力(psi) | 浓度(ppm) | |
原料 | 102 | 0.63 | 5.0 | 35,000 |
原料废料 | 104 | 0.13 | 0.0 | 105,000 |
FO汲取废料 | 106 | 1.50 | 0.5 | 80,000 |
经加压FO汲取废料 | 108 | 1.50 | 980 | 80,000 |
级1LR汲取原料 | 109 | 2.00 | 980 | 80,000 |
级1LR汲取废料 | 111 | 1.00 | 965 | 120,000 |
FO汲取原料 | 105 | 1.00 | 3.0 | 120,000 |
级1LR渗透物 | 113 | 1.00 | 0.5 | 40,000 |
级2RO原料 | 115 | 1.00 | 1000 | 40,000 |
级2RO废料 | 117 | 0.50 | 985 | 80,000 |
***渗透物 | 118 | 0.50 | 0.0 | 350 |
图2说明根据本发明的实施例的三级***20的框图。三级FO RO***20可能够将高浓度原料处理为小于160kppm的浓度。所述***被认为具有氯化钠汲取溶质,但可以单一形式或以与包含氯化钠的其它溶质(例如,多价物)组合的形式而与其它汲取溶质一起被利用。***20可包含四个膜阵列:具有高抑制(例如,通常大于95%)的FO模块103、具有小于RO的抑制(例如,通常为33%)的中间级1压力驱动脱盐膜阵列(例如,LR模块)125、具有小于RO的抑制(例如,通常为50%)的中间级2压力驱动脱盐膜阵列(例如,LR模块)132,及具有高抑制(例如,通常大于99%)的最终级3RO模块137。
在操作期间,高浓度原料流102可进入FO模块103,在FO模块103处,高浓度原料流102被脱水且作为废料或废物流104而离开***。高浓度汲取流120(例如,160kppm)以可为近大气的压力流动(例如,1.5MGD),进入FO模块103,此吸收质量且变得稀释,从而作为流121(例如,120kppm)而离开,其中增加流量(例如,2MGD)具有可为近大气的压力。此流的浓度可能太高而不能用单级或双级RO进行回收。接着可由泵122将所述流加压到较高压力(例如,1000psi),接着与邻近高压流133组合,从而形成流124,其具有增加的流量(例如,3MGD),但具有相同的压力(例如,1000psi)。流124可与可具有33%的抑制的LR模块125接触。静水压力(例如,1000psi)可克服跨越膜的平均浓度差(例如,60kppm乘300psi),从而产生具有减小的流量(例如,1.5MGD)且可具有为近大气的压力的低浓度流128(例如,80kppm)。LR模块125还可产生具有减小的流量(例如,1.5MGD)及较高压力(例如,1000psi)的高浓度汲取流126(例如,160kppm)。
流126的压力可跨越液压电动机(能量回收装置)127而减低,从而形成可被馈送到FO膜阵列103的流120。接着可由第二泵129加压(例如,1000psi)于低浓度流128,从而形成流130。接着将此流130与邻近高压流138组合,从而形成具有增加的流量(例如,2MGD)的流131。流131与可具有50%的抑制的LR模块132接触。静水压力(例如,1000psi)可克服跨越膜的平均浓度差(例如,60kppm乘300psi),从而产生具有减小的流量(例如,1GMD)且可具有为近大气的压力的稀释流134(例如,40kppm),及可具有减小的流量(例如,1GMD)及较高压力(例如,1000psi)的高浓度抑制流133(例如,120kppm)。此高浓度抑制流133可与如上文所描述的流123组合且被再循环。可接着由第三泵135加压(例如,1000psi)于稀释流134,从而形成流136。此流136被馈送到可具有大于99%的抑制的级3RO模块137。静水压力(例如,1000psi)可克服跨越膜的平均浓度差(例如,60kppm乘300psi),从而产生可具有几乎0kppm的浓度、0.5MGD的流量及近大气的压力的高质量产物流118。RO模块137还可产生反渗透截留流138,其可具有80kppm的浓度、0.5MGD的流量及1000psi的压力。此反渗透截留流138可与如上文所描述的流130组合且被再循环。
表2含有用于图2所说明的***中的不同点的实例流率、静水压力及溶质浓度。表2中给出的值为示范性的且不应被解释为将本发明的实施例限于所给出的值。流率、静水压力及溶质浓度的其它值可为可能的。
表2:用于三级FO/RO***20的示范性值
虽然图1及2中已分别展示两级***及三级***,但在其它实例中可使用任何数目个级。通常,实例***包含FO模块,FO模块的汲取流输出被提供到具有低抑制压力驱动脱盐膜的一个或一系列LR模块。每一LR模块可产生被提供到所述系列中的下一LR模块或提供到稍后RO模块的低浓度流,及被反馈到最后级(例如,FO模块汲取或到早先LR模块)的较高浓度流。提供后续RO模块,所述RO模块从所述系列中的最后LR模块接收低浓度流,从而提供产物流。
包含于图1及2所说明的***10及20中的本文中描述的实例的原料及汲取水可具有额外预处理来以高回收率移除增加浓度的污垢或污物。回收率为渗透物流(X)除以原料流(Y)的比率。污垢可包含但不限于:碳酸钙、碳酸钠、硅石、石膏、硫酸钡、硫酸锶及氟化钙。污物可包含但不限于:小型有机分子、颗粒或胶体,或生物膜生长。可用阻垢剂或防污剂处理原料及汲取水以防止FO膜或RO膜的污垢形成或污物形成。阻垢剂可包含浓缩聚磷酸盐、有机磷酸盐及聚电解质。可通过添加亚硫酸氢钠来实现原料水的脱氯。可升高原料水及汲取物的pH以移除硬度及碱度或增加弱电离阴离子的截留,例如硼酸盐、氰化物、氟化物及某些砷或硒化合物。可降低原料水及汲取物的pH以减小污垢形成。原料或汲取物中的任一者可取决于原料水、操作参数(例如,回收率)及所要***渗透物质量而具有以任何组合及以任何次序的额外阻垢剂、防污剂、pH调整、除气。
可在批次模式中完成汲取流的污垢及污物移除过程(例如pH调整),在批次模式中,当污垢及污物移除过程完成时,汲取回路被排干且用另一汲取液替换。还可在半批次模式中完成污垢及污物移除过程,使得每次针对处理来移除汲取回路的小部分。可独立地调整正渗透膜及反渗透膜的截留以及污垢形成及污物形成倾向。接着可优化所述***以如针对特定应用所希望而最小化耗材且最大化总效率。
与传统反渗透***不同,图1及2所展示的FO/RO***的汲取液复合物可经调谐以优化所述***的性能。汲取液可为具有来自反渗透膜的高截留率的任何水溶液。汲取溶质可优选地为无机盐,例如氯化钠、氯化镁、硫酸镁、硫酸钠或磷酸钠。汲取溶质可为单价或多价。汲取液可为盐(单价或多价两者)的混合物。低截留率反渗透膜(例如包含于LR模块中的低截留率反渗透膜)可为用于高氯化钠截留率(例如,大于99%)的标准反渗透膜,例如DOWSW30膜。低截留率反渗透膜可为具有适度氯化钠截留率(大于80%)及高多价截留率(例如,大于90%)的纳滤膜,例如DOW NF90。低截留率反渗透膜可为磺化聚砜纳滤膜,例如海德能(Hydranautics)HydraCoRe70。
在图1及2所说明的两个***中,可包含于LR模块中的低截留率反渗透膜可通过化学地处理标准反渗透膜而调谐。在一些实例中,低截留率反渗透膜可为具有聚酰胺选择性层的薄膜复合膜。可减小聚酰胺层的交联密度,从而增加透盐率(减小选择性)且增加渗水性。举例来说,可将DOW SW30膜暴露到1000ppm次氯酸钠溶液达10分钟到6小时且接着用硫酸氢钠或水进行冲洗。可将所述膜的氯化钠截留率从99%减小到10%。经处理膜可具有高的多价盐截留率。可取决于所述膜对单价盐及多价盐的相对截留率及优选操作参数来选择单价盐及多价盐的汲取溶质复合物及反渗透膜。
图3中说明根据本发明的原理的多通口净化***30。在此实例中,汲取液300由泵305带到第一RO元件315的第一通口310。来自第一RO元件315的截留流355被减压且由能量回收装置370返回到汲取液作为浓缩流360。渗透物320由泵325加压且被递送到第二RO元件335中的输入通口330。产物作为流340而离开RO元件335。截留流345由能量回收装置365减压且被返回到第一RO元件315中的第二通口350。
在图3所展示的实例实施例中,渗透预处理可与多个RO级及4通口RO元件一起被使用。4通口RO元件可允许盐溶液通过RO1的渗透物通道而循环,此可减低跨越膜RO1的有效渗透压差。器皿RO2可利用标准3通口RO元件。中间汲取液的浓度可在入口汲取液浓度与产物水之间。在两级***中,此浓度可约为入口汲取液与产物水浓度之间的差的一半。在此实例中,跨越每一RO元件的盐度差可仅约为从入口到产物的总盐度减小的一半。
在无FO预处理的此多级RO***的水回收单独为RO步骤中的每一者的水回收的产物。对于其中RO步骤中的每一者的水回收为10%的***,总***水回收仅为1%。然而,当FO预处理***耦合到多级RO***时,整个***的总回收等于FO回路的水回收且独立于所述***的RO部分的水回收,因此其可大于1%。
从前述应了解,尽管本文中已出于说明的目的而描述本发明的特定实施例,但在不背离本发明的精神及范围的情况下可做出各种修改。
Claims (25)
1.一种用于分离的设备,其包括:
经配置以接收原料流及高浓度汲取流的正渗透模块,其中所述正渗透模块进一步经配置以从所述原料流及所述高浓度汲取流产生包括水的第一流;
经配置以加压于所述第一流的泵;
具有小于90%的盐截留率、经配置以接收所述经加压第一流且产生所述高浓度汲取流及低浓度流的低截留率膜模块;及
经配置以接收所述低浓度流且产生产物流及反渗透截留流的反渗透模块;
其中使所述反渗透截留流循环以形成所述高浓度汲取流的一部分。
2.根据权利要求1所述的设备,其进一步包括经配置以加压于被提供到所述反渗透模块的所述低浓度流的第二泵。
3.根据权利要求1所述的设备,其中所述第一流被加压到小于3000psi。
4.根据权利要求1所述的设备,其进一步包括经配置以减小由所述低截留率模块产生的所述高浓度汲取流的压力的能量回收装置。
5.根据权利要求4所述的设备,其中所述能量回收装置及所述泵为集成组件。
6.根据权利要求1所述的设备,其进一步包括经配置以将所述原料流提供到所述正渗透模块的进料泵。
7.根据权利要求1所述的设备,其中所述反渗透截留流与被提供到所述低截留率模块的所述第一流组合。
8.根据权利要求1所述的设备,其中所述低截留率模块具有小于90%的回收率。
9.根据权利要求1所述的设备,其中所述低截留率模块包括具有小于90%的盐截留率的膜。
10.根据权利要求1所述的设备,其进一步包括经配置以将溶质提供到所述高浓度汲取流的计量泵。
11.根据权利要求10所述的设备,其中所述溶质包括多价盐。
12.根据权利要求10所述的设备,其中所述溶质包括单价盐。
13.根据权利要求1所述的设备,其中所述低浓度流被提供到经配置以产生稀释流及截留流的第二低截留率模块,且其中所述反渗透模块经配置以接收所述稀释流。
14.根据权利要求13所述的设备,其中所述截留流与被提供到所述低截留率模块的所述第一流组合。
15.根据权利要求13所述的设备,其中所述反渗透截留流与被提供到所述第二低截留率模块的所述低浓度流组合。
16.根据权利要求13所述的设备,其进一步包括经配置以加压于被提供到所述反渗透模块的所述稀释流的第三泵。
17.一种用于分离的方法,其包括:
将汲取流提供到正渗透模块;
将原料流提供到所述正渗透模块;
用所述正渗透模块过滤所述原料流以产生第一流;
加压于所述第一流;
用具有小于90%的盐截留率的低截留率模块过滤所述经加压第一流以产生稀释流和所述汲取流;
用反渗透模块过滤所述稀释流以产生产物流和反渗透截留流;及
使所述反渗透截留流循环以形成所述汲取流的一部分。
18.根据权利要求17所述的方法,其进一步包括:
用所述反渗透模块产生截留流;及
组合所述截留流与所述第一流。
19.根据权利要求17所述的方法,其进一步包括将溶质添加到所述汲取流。
20.根据权利要求19所述的方法,其中所述溶质包括单价盐。
21.根据权利要求19所述的方法,其中所述溶质包括多价盐。
22.根据权利要求17所述的方法,其进一步包括:
用第二低截留率模块过滤所述稀释流以产生低浓度流;及
将所述低浓度流提供到所述反渗透模块。
23.根据权利要求17所述的方法,其进一步包括将阻垢剂添加到所述原料流。
24.根据权利要求17所述的方法,其进一步包括将防污剂添加到所述原料流。
25.根据权利要求17所述的方法,其进一步包括移除污垢。
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CN105188889A (zh) | 2015-12-23 |
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US10500544B2 (en) | 2019-12-10 |
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