CN101313188B - 液化天然气流的处理方法和相关装置 - Google Patents
液化天然气流的处理方法和相关装置 Download PDFInfo
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- CN101313188B CN101313188B CN2006800437214A CN200680043721A CN101313188B CN 101313188 B CN101313188 B CN 101313188B CN 2006800437214 A CN2006800437214 A CN 2006800437214A CN 200680043721 A CN200680043721 A CN 200680043721A CN 101313188 B CN101313188 B CN 101313188B
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- heat exchanger
- cryogenic fluid
- natural gas
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- 238000000034 method Methods 0.000 title claims abstract description 33
- 239000003949 liquefied natural gas Substances 0.000 title claims description 58
- 238000009434 installation Methods 0.000 title 1
- 239000007788 liquid Substances 0.000 claims abstract description 26
- 238000001816 cooling Methods 0.000 claims abstract description 19
- 239000012530 fluid Substances 0.000 claims description 71
- 238000005057 refrigeration Methods 0.000 claims description 43
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 38
- 239000007789 gas Substances 0.000 claims description 30
- 230000006835 compression Effects 0.000 claims description 26
- 238000007906 compression Methods 0.000 claims description 26
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 20
- 239000003345 natural gas Substances 0.000 claims description 18
- 206010042674 Swelling Diseases 0.000 claims description 12
- 230000008961 swelling Effects 0.000 claims description 12
- 239000001294 propane Substances 0.000 claims description 10
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 238000003672 processing method Methods 0.000 claims description 6
- 239000000284 extract Substances 0.000 claims description 5
- 238000011144 upstream manufacturing Methods 0.000 claims description 5
- 230000008016 vaporization Effects 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- 239000013526 supercooled liquid Substances 0.000 claims description 4
- 238000009834 vaporization Methods 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 239000000110 cooling liquid Substances 0.000 claims description 2
- 239000002737 fuel gas Substances 0.000 claims description 2
- 238000004821 distillation Methods 0.000 abstract description 4
- 239000002826 coolant Substances 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 238000010586 diagram Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 241000282326 Felis catus Species 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000004781 supercooling Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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Abstract
本方法中,在所述第一热交换器(19)内,通过与制冷流体(83)热交换来冷却液化天然气流(11)。使制冷流体(83)经受半开式的第二制冷循环(21),该第二制冷循环独立于所述第一制冷循环(17)。所述方法包括将过冷液化天然气流(59)引入蒸馏塔(49)内的步骤,以及回收所述蒸馏塔(49)顶部的气体流(69)的步骤。所述第二制冷循环(21)包括:由顶部的气体流(69)的一部分形成制冷流体流(73)的步骤;压缩所述制冷流体流(73)到一高压的步骤;然后将被压缩的制冷流体流(75)的一部分(81)膨胀以形成基本液态的过冷流(83)的步骤。所述基本液态的过冷流(83)在所述第一热交换器(19)内被汽化。
Description
技术领域
本发明涉及通过第一制冷循环冷却得到的液化天然气(GNL)流的处理方法,该方法包括以下步骤:
(a)将温度低于-100℃的液化天然气流引入第一热交换器内;
(b)在所述第一热交换器内,通过与制冷流体热交换来使液化天然气流过冷,以形成过冷的液化天然气流;以及
(c)使制冷流体经受半开式的第二制冷循环,该第二制冷循环独立于所述第一制冷循环。
背景技术
由文件US-B-6 308 531知道上述类型的一种方法,在该方法中,天然气流通过第一制冷循环被液化,所述第一制冷循环使烃混合物冷凝和汽化。所得天然气的温度约为-100℃。然后,将所述天然气制品通过半开式的称为“反向布雷顿循环(cycle de Brayton inversé)”类型的第二制冷循环过冷到约-170℃,所述第二制冷循环包括级式压缩机和气体膨胀涡轮。
这样的方法不完全令人满意。实际上,所述称为反向布雷顿循环的最大效率限制在约40%。另外,其半开式循环的运行难于实施。
发明内容
本发明的目的是提出液化天然气流的一自主(autonome)处理方法,该方法具有改善的效率并能轻易地在各种结构单元中实施。
因此,本发明是上述类型的一种处理方法,其特征在于,所述方法包括以下步骤:
(d)在中间涡轮内动力膨胀过冷的液化天然气流,同时保持该过冷的液化天然气流基本呈液态;
(e)将出自所述中间涡轮的流冷却和膨胀,然后将其引入到蒸馏塔内;
(f)回收在所述蒸馏塔基部的被除氮的液化天然气流,并回收在所述蒸馏塔顶部的气体流;以及
(g)在级式压缩机内压缩顶部的气体流,并在所述压缩机的中间压力级处提取被压缩到中间压力PI的顶部的气体流的第一部分,以形成可燃气体流;
并且,其特征在于,所述第二制冷循环包括以下步骤:
(i)由被压缩到中间压力PI的顶部气体的第二部分形成初始的制冷流体流;
(ii)压缩初始的制冷流体流到高于所述中间压力PI的高压PH,以形成被压缩的制冷流体流;
(iii)在第二热交换器内冷却被压缩的制冷流体流;
(iv)将出自所述第二热交换器的被压缩的制冷流体流分为主要的冷却流和液化天然气过冷流;
(v)先在第三热交换器内、然后在所述第一热交换器内冷却液化天然气过冷流;
(vi)将出自所述第一热交换器的过冷流膨胀达到小于所述中间压力PI的低压,以形成基本为液态的液化天然气的过冷流;
(vii)在所述第一热交换器内,汽化基本为液态的液化天然气的过冷流,以形成被加热的过冷流;
(viii)在主涡轮内,将主要的冷却流基本膨胀到所述低压PB,并将出自所述主涡轮的主冷却流与被加热的过冷流混合,以形成混合流;
(ix)先在所述第三热交换器内、然后在所述第二热交换器内相继地加热混合流,以形成被加热的混合流;以及
(x)将被加热的混合流引入到所述压缩机内,至位于所述中间压力级上游的低压级。
根据本发明的方法可包括以下的一个或多个特征,所述特征单独地应用或按所有技术上可能的组合加以应用:
-所述高压PH介于大约40巴至100巴之间,优选在大约50巴至80巴之间,且尤其在大约60巴至75巴之间;
-所述低压PB低于大约20巴;
-在所述步骤(vi),在液体膨胀涡轮内,将出自所述第一热交换器的过冷流动力膨胀;
-在所述步骤(ii),在联接所述主涡轮的辅助压缩机内,至少部分地压缩初始的制冷流体流;
-在所述步骤(i),将C2烃流引入到所述压缩机内,以形成初始的制冷流体流的一部分;
-在所述步骤(iii),使被压缩的制冷流体流与在所述第二热交换器内流通的次级制冷流体进行热交换,次级制冷流体经受第三制冷循环,在该第三制冷循环中,次级制冷流体在所述第二热交换器的出口处被压缩,使次级制冷流体冷却并且至少部分地冷凝,然后使次级制冷流体在所述第二热交换器内汽化之前进行膨胀;
-次级制冷流体包含丙烷,并且还可能包含乙烷;以及
-在所述步骤(e)的膨胀之前,将出自所述中间涡轮的流与天然气补给流混合,所述天然气补给流在第四热交换器内与顶部的气体流热交换而被冷却;以及
-顶部气体的C2 +含量使得被所述第二热交换器冷却的流为纯气态。
本发明的目的还为了通过第一制冷循环冷却得到的液化天然气流的处理设备,该设备包括:
-液化天然气流过冷部件,其包括使液化天然气流与制冷流进行热交换的第一热交换器;以及
-半开式的第二制冷循环,其独立于所述第一制冷循环,
其特征在于,所述设备包括:
-中间涡轮,其使出自所述第一热交换器的过冷液化天然气流动力膨胀;
-冷却和膨胀部件,其使出自所述中间涡轮的流冷却和膨胀;
-蒸馏塔,其与所述冷却和膨胀部件连接;
-回收所述蒸馏塔基部的除氮液化天然气流的部件,和回收所述 蒸馏塔顶部的气体流的部件;
-级式压缩机,其与回收所述蒸馏塔顶部的气体流的部件相连;以及
-为形成可燃气体而提取顶部的气体流的第一部分的部件,其安插在所述压缩机的中间压缩级处;
并且,其特征在于,所述第二制冷循环包括:
-由压缩至中间压力的顶部气体的第二部分形成初始的制冷流体流的部件;
--初始的制冷流体流的压缩部件,其将初始的制冷流体流压缩到高于所述中间压力的高压,以形成被压缩的制冷流体流;
-第二热交换器,用以冷却被压缩的制冷流体流;
-分离部件,其将出自所述第二热交换器的被压缩的制冷流体流分离为主要的冷却流和液化天然气的过冷流;
-第三热交换器,用以冷却所述过冷流;
-将出自所述第三热交换器的过冷流引入所述第一热交换器的部件;
-出自所述第一热交换器的过冷流的膨胀部件,其使所述过冷流膨胀达到小于所述中间压力的低压,以形成基本液态的液化天然气过冷流;
-基本液态的液化天然气过冷流的流通部件,其使基本液态的液化天然气过冷流在所述第一热交换器内流通,以形成被加热的过冷流;
-主膨胀涡轮,其使主要的冷却流基本膨胀到所述低压;
-混合部件,其使出自所述主涡轮的冷却流与被加热的过冷流进行混合以形成混合流;
-混合流的流通部件,其使混合流先在所述第三热交换器内、然后在所述第二热交换器内相继地流通,以形成被加热的混合流;
-将被加热的混合流引入到所述压缩机内,至位于所述中间压力级上游的低压级的部件。
根据本发明的所述方法可包括以下的一个或多个特征,所述特征可单独地应用或按所有技术上可能的组合应用:
-所述高压PH介于大约40巴至100巴之间,优选地在大约50巴至80巴之间,且尤其是在大约60巴至75巴之间;
-所述低压PB小于大约20巴;
-出自所述第一热交换器的过冷流的膨胀部件包括液体膨胀涡轮;
-所述的初始的制冷流体流的压缩部件包括辅助压缩机,该辅助压缩机与所述主涡轮联接;
-所述第二制冷循环包括将C2烃流引入到所述压缩机以形成初始的制冷流体流的一部分的部件;
-所述第二热交换器包括次级制冷流体的流通部件,所述设备包括第三制冷循环,该第三制冷循环包括:次级压缩部件,其压缩出自所述第三热交换器的次级制冷流体;出自所述次级压缩部件的次级制冷流体的次级冷却和膨胀部件;以及,将出自所述次级膨胀部件的次级制冷流体引入所述第二热交换器内的部件;以及
-次级制冷流体包含丙烷,并且还可能包含乙烷;以及
-所述设备包括:将过冷的液化天然气流与天然气的补给流混合的部件;以及第四热交换器,用以使补给流与顶部的气体流进行热交换。
附图说明
现参照附图描述本发明的实施例,其中:
-图1是根据本发明的第一设备的运行框图;
-图2是示出图1设备的第二制冷循环根据所述第一热交换器入口处的液化天然气温度的效率曲线图;
-图3是类似图1的按本发明的第二设备的示意图;
-图4是类似图1的按本发明的第三设备的示意图;及
-图5是类似图1的按本发明的第四设备的示意图。
具体实施方式
如图1所示的根据本发明的第一过冷设备9,用于从温度被带到低于-90℃的初始的液化天然气(GNL)流11制备除氮液化天然气流13。所述设备9还制备富氮的可燃气体流16。
如图1所示,所述初始的液化天然气流11由天然气液化单元15产生,该液化单元15包括第一制冷循环17。所述第一制冷循环17例如包括一循环,该循环具有烃混合物的冷凝和汽化部件。
所述设备9包括:第一过冷热交换器19;独立于所述第一循环17的半开式第二制冷循环21;以及除氮单元23。
所述第二制冷循环21包括级式压缩装置25,该级式压缩装置具有多个压缩级27。每个所述压缩级27包括一压缩机29和一冷却器31。
所述第二循环21还包括:第二热交换器33;第三热交换器35;膨胀阀37;以及辅助压缩机39,所述辅助压缩机39与主膨胀涡轮41联接。所述第二循环21还包括辅助冷却器43。
在图1所示的实例中,所述级式压缩装置25包括四个压缩机29。所述四个压缩机29由相同的外部能量源45驱动。所述能量源45例如是燃气涡轮式发动机。
所述冷却器31和43由水和/或空气冷却。
所述除氮单元23包括:中间的液压涡轮47,该涡轮47与流产生器48联接;蒸馏塔49;塔顶的热交换器51;以及塔基部的热交换器53。所述除氮单元23还包括排出除氮液化天然气13的排出泵55。
在整个下文中,同一附图标记表示液流和运输液流的管道,所考虑的压力是绝对压力,并且所考虑的百分比是摩尔百分比。
出自所述液化单元15的初始的液化天然气流11的温度低于-90℃,例如为-130℃。该流11例如包括大致5%的氮、90%的甲烷以及5%的乙烷,并且其流量为50000kmol/h。
所述液化天然气流11被引入到所述第一热交换器19内,在该第一热交换器中被过冷到-150℃的温度,以产生过冷的液化天然气流57。
所述流57然后被引入到所述液压涡轮47内,并动力膨胀到一低压以形成膨胀流59。所述膨胀流59主要为液态,也就是说它包含少于2%摩尔的气体。所述膨胀流59在基部热交换器53内被冷却,然后被引入到膨胀阀61,在该膨胀阀它形成供给所述蒸馏塔49的流64。
在蒸馏低压下,所述流64从所述蒸馏塔49的顶部被引入。该蒸 馏低压略高于大气压。在本实例中,该低压为1.25巴,且所述流64的温度约为-165℃。
天然气的补给流63与所述初始的液化天然气流11基本具有相同的成分,该补给流63在所述顶部交换器51内被冷却,然后在阀65内被膨胀,并在所述阀61的上游与膨胀的过冷液化天然气流59混合。
重沸流68在一中间级Ni从所述蒸馏塔49提取,该中间级Ni位于所述蒸馏塔的底部附近。所述流68被引入到所述交换器53内,并在被引入到所述蒸馏塔49内所述中间级Ni的下面之前,通过与所述膨胀的过冷液化天然气流59热交换而被加热。
包含少于1%的氮的液态的基部流67提取自所述蒸馏塔49。所述基部流67被所述泵55泵吸入,以形成所述去氮的液化天然气流13,该流13用于被送至一储存器。
包含近50%的氮的气态顶部流69提取自所述蒸馏塔49。所述流69在所述顶部交换器51内与所述补给流63热交换而被加热,以形成被加热的顶部流71。该流71被引入到所述压缩装置25的第一级27A内。
所述被加热的顶部流71在所述压缩装置25的第一级27A和第二级27B中相继地被压缩到大致一循环低压PB,然后在被引入到所述第四压缩级27D之前在所述第三压缩级27C内被压缩。在压缩机的每个压缩级27中,所述顶部流71在所述压缩机29内受到压缩,继而在相关联的冷却器31内被冷却至约35℃的温度。
在所述第四压缩级27D内被压缩的所述顶部流的第一部分16在中间压力PI,被提取自所述压缩机29D,以形成所述可燃气体流。
所述中间压力PI例如高于20巴,且优选大致等于30巴。所述循环低压PB例如低于20巴。
所述顶部流的第二部分73继续在所述压缩机29D内被压缩到大致等于50巴的平均压力,以形成一初始的制冷流体流。
所述流73在所述交换器31D内被冷却,然后被引入到所述辅助压缩机39。
所述初始的制冷流体流73的流量远高于所述可燃气体流16的流 量。这两个流量之比在本实例中大致等于6.5。
然后,所述流73在所述压缩机39内被压缩达到循环高压PH。该高压在40巴至100巴之间,优选在50巴至80巴之间,且有利地在60巴至75巴之间。
出自所述压缩机39的流73,在通过所述冷却器43后,形成被压缩的制冷流体流75。所述顶部流69包含质量百分比少于5%的C2 +烃,使得所述流75为纯气态。当所述高压高于大约60巴时,所述流75是一超临界流体。
接着,所述流75在所述第二热交换器33内被冷却,并在该交换器33的出口处被分为少数的液化天然气过冷流77和主要的多数冷却流79。这两流的流量比约为0.5。
所述过冷流77先在所述第三交换器35内、然后在所述第一交换器19内被冷却,以形成冷却的过冷流81。所述流81在所述阀37内被膨胀达到所述循环低压PB,所述流81以基本液态的过冷流83的形式-也就是包含的气体少于10%摩尔-离开所述阀37。
然后,所述流83被引入到所述第一交换器19内,在此通过与所述流81和所述初始的液化天然气流11热交换而被汽化和冷却,以便在所述第一交换器19的出口处形成被加热的过冷流85。
气态的主要流79在所述涡轮41内被膨胀达到大致循环低压PB,并与出自所述第一交换器19的被加热流85混合,以形成混合流87。接着,所述混合流87相续地被引入到所述第三交换器35内、然后是所述第二交换器33内,在此处,所述混合流87通过热交换关系分别冷却所述过冷流77和所述被压缩的制冷流体流75。
接着,出自所述交换器33的被加热的混合流89基本在低压PB,在第三压缩级27C的入口处被引入到所述压缩装置25内。
作为说明,下表给出循环高压PH大致等于75巴时的压力值、温度和流量。
表1
流 | 温度℃ | 压力(巴) | 流量(kmol/h) |
11 | -130.0 | 49.1 | 50000 |
13 | -161.1 | 5.3 | 46724 |
16 | 67.0 | 30.0 | 4876 |
57 | -150.0 | 49.0 | 50000 |
59 | -150.7 | 5.0 | 50000 |
63 | -34.0 | 50.0 | 1600 |
64 | -164.9 | 1.3 | 51600 |
67 | -161.1 | 1.2 | 46724 |
69 | -165.2 | 1.2 | 4876 |
71 | -48.6 | 1.2 | 4876 |
73 | 124.0 | 50.9 | 31768 |
75 | 35.0 | 74.7 | 31768 |
77 | -38.2 | 74.2 | 11496 |
79 | -38.2 | 74.2 | 20272 |
81 | -150.0 | 73.6 | 11496 |
83 | -155.2 | 11.0 | 11496 |
85 | -132.0 | 10.9 | 11496 |
87 | -130.3 | 10.9 | 31768 |
89 | 34.38 | 10.7 | 31768 |
在图2中,在按本发明的方法中的循环21的效率曲线91根据液化天然气流11的温度值而示出。如该图所示,所述效率高于44%,相对使用称为半开式的反向布雷顿循环的现有技术的方法,这构成显著的收益。
该结果用简单的方式得到,因为不需要设置制冷流体的制备及储存部件,所述制冷流体73连续地由所述设备9输送。
本发明所示的方法和设备9或可用于新的液化单元,或可用于优化现有液化天然气制备单元的性能。在上述后一种情况中,对于相等的消 耗功率下,除氮液化天然气的制备可提高5%到20%。根据本发明的方法和设备9还可用于提取天然气液体(LGN)的方法中产生的液化天然气的过冷和除氮。
图3所示的设备99不同于第一设备9之处在于,位于所述第一交换器下游的所述膨胀阀37被一动力膨胀涡轮101替代,该膨胀涡轮与流产生器103联接。
此外,该设备中的液化天然气流的处理方法除数值以外,与所述设备9中实施的方法一样。
图3中虚线示出的变型中,乙烷流92与所述被加热的混合流89在该混合流89被引入所述第三压缩级27C之前进行混合。
所述循环21的效率因而进一步被提高,如图2的曲线93所示出的。
图4示出根据本发明的第三设备104。该设备104不同于所述第二设备99之处在于:该设备104另外包括封闭的第三制冷循环105,该第三制冷循环独立于第一循环17和第二循环21。
所述第三循环105包括:次级压缩机107;次级第一冷却器109A和次级第二冷却器109B;膨胀阀111;以及分离瓶113。
该循环借助丙烷构成的次级制冷流体流115实现。在低压的气态流115被引入所述压缩机107内,然后在所述冷却器109A和109B内被冷却并压缩达到高压,以形成部分液态的丙烷流117。该流117在所述交换器33内被冷却,然后被引入所述膨胀阀111内,在其中该流被膨胀并形成膨胀的两相丙烷流119。
所述流119被引入到所述分离瓶113,以形成提取自所述瓶113基部的液态馏分121。所述馏分(fraction)121被引入所述交换器33内,在此,所述馏分121在被引入到所述瓶113中之前,在所述交换器33内通过与所述流117和所述被压缩的制冷流体流75热交换而被汽化。
出自所述瓶113顶部的气态馏分形成所述气态丙烷流115。
如图2的曲线123所示,相对所述第一设备9中所实施的方法的效率,所述循环21的效率此时平均提高4%。
图5示出根据本发明的第四设备125,其与图4所示的设备的不同在于:所述第三制冷循环105没有所述分离瓶113。因此,出自所述阀111的流119直接被引入到所述第二交换器33,并在该交换器内被完全汽化。
此外,所述制冷流体115由乙烷和丙烷的混合物组成。所述流体115内的乙烷含量基本等于丙烷含量。
如图2的曲线126所示,当温度低于-130℃时,相对所述第三设备104中所实施的方法的效率,所述第二制冷循环的平均效率因而被提高约0.5%。考虑所述涡轮47产生的能量,相对图1所示装置的总效率为47.5%、图3所示装置的总效率为47.6%、以及图4所示装置的总效率为49.6%,图5所示装置的总效率略高于50%。
Claims (25)
1.通过第一制冷循环(17)冷却得到的液化天然气流(11)的处理方法,该方法包括以下步骤:
(a)将温度低于-100℃的液化天然气流(11)引入第一热交换器(19)内;
(b)在所述第一热交换器内,通过与制冷流体(83)热交换来使液化天然气流(11)过冷,以形成过冷的液化天然气流(57);以及
(c)使制冷流体(83)经受半开式的第二制冷循环(21),该第二制冷循环独立于所述第一制冷循环(17),
其特征在于,所述方法包括以下步骤:
(d)在中间涡轮(47)内动力膨胀过冷的液化天然气流(57),同时保持该过冷的液化天然气流基本呈液态;
(e)将出自所述中间涡轮(47)的流(59)冷却和膨胀,然后将其引入到蒸馏塔(49)内;
(f)回收在所述蒸馏塔(49)的基部的被除氮的液化天然气流(67),并回收在所述蒸馏塔(49)的顶部的气体流(69);以及
(g)在级式压缩机(25)内压缩顶部气体流(69),并自所述压缩机(25)的中间压力级(29D)提取被压缩到中间压力PI的顶部气体流(69)的第一部分(16),以形成可燃气体流;
并且,其特征还在于,所述第二制冷循环(21)包括以下步骤:
(i)由被压缩到中间压力PI的顶部气体(69)的第二部分形成初始的制冷流体流(73);
(ii)压缩初始的制冷流体流(73)到高于所述中间压力PI的高压PH,以形成被压缩的制冷流体流(75);
(iii)在第二热交换器(33)内冷却被压缩的制冷流体流(75);
(iv)将出自所述第二热交换器(33)的被压缩的制冷流体流(75)分为主要的冷却流(79)和液化天然气过冷流(77);
(v)先在第三热交换器(35)内、然后在所述第一热交换器(19)内冷却液化天然气过冷流(77);
(vi)将出自所述第一热交换器(19)的过冷流(81)膨胀达到小于所述中间压力PI的低压PB,以形成基本为液态的液化天然气的过冷流(83);
(vii)在所述第一热交换器(19)内,汽化基本为液态的液化天然气的过冷流(83),以形成被加热的过冷流(85);
(viii)在主涡轮(41)内,将主要的冷却流(79)基本膨胀到所述低压PB,并将出自所述主涡轮(41)的冷却流与被加热的过冷流(85)混合,以形成混合流(87);
(ix)先在所述第三热交换器(35)内、然后在所述第二热交换器(33)内相继地加热混合流(87),以形成被加热的混合流(89);以及
(x)将被加热的混合流(89)引入到所述压缩机(25)内,至位于所述中间压力级(29D)上游的低压级(29C)。
2.根据权利要求1所述的方法,其特征在于,所述高压PH介于40巴至100巴之间。
3.根据权利要求1或2所述的方法,其特征在于,所述低压PB低于20巴。
4.根据权利要求1或2所述的方法,其特征在于,在所述步骤(vi),在液体膨胀涡轮(101)内,将出自所述第一热交换器(19)的过冷流(81)动力膨胀。
5.根据权利要求1或2所述的方法,其特征在于,在所述步骤(ii),在联接所述主涡轮(41)的辅助压缩机(39)内,至少部分地压缩初始的制冷流体流(73)。
6.根据权利要求1或2所述的方法,其特征在于,在所述步骤(i),将C2烃流(92)引入到所述压缩机(25)内,以形成初始的制冷流体流(73)的一部分。
7.根据权利要求1或2所述的方法,其特征在于,在所述步骤(iii),使被压缩的制冷流体流(75)与在所述第二热交换器(33)内流通的次级制冷流体(117)进行热交换,次级制冷流体(117)流通以实现第三制冷循环(105),在该第三制冷循环中,次级制冷流体在所述第二热交换器(33)的出口处被压缩,使次级制冷流体冷却并且至少部分地冷凝,然后使次级制冷流体在所述第二热交换器(33)内汽化之前进行膨胀。
8.根据权利要求7所述的方法,其特征在于,次级制冷流体(117)包含丙烷。
9.根据权利要求1或2所述的方法,其特征在于,在所述步骤(e)的膨胀之前,将出自所述中间涡轮(47)的流与天然气补给流(63)混合,所述天然气补给流在第四热交换器(51)内与顶部气体流(69)热交换而被冷却。
10.根据权利要求1或2所述的方法,其特征在于,顶部气体(69)的C2 +含量使得被所述第二热交换器(33)冷却的流为纯气态。
11.根据权利要求2所述的方法,其特征在于,所述高压PH在50巴至80巴之间。
12.根据权利要求2所述的方法,其特征在于,所述高压PH在60巴至75巴之间。
13.根据权利要求8所述的方法,其特征在于,所述次级制冷流体(117)还包含乙烷。
14.通过第一制冷循环(17)冷却得到的液化天然气流(11)的处理设备(9;99;104;125),该设备(9;99;104;125)包括:
-液化天然气流(11)过冷部件,其包括使液化天然气流与制冷流(83)进行热交换的第一热交换器(19);以及
-半开式的第二制冷循环(21),其独立于所述第一制冷循环(15),
其特征在于,所述设备包括:
-中间涡轮(47),其使出自所述第一热交换器(19)的过冷液化天然气流(57)动力膨胀;
-冷却和膨胀部件(53,61),其使出自所述中间涡轮(47)的流(59)冷却和膨胀;
-蒸馏塔(49),其与所述冷却和膨胀部件(53,61)连接;
-回收所述蒸馏塔(49)基部的除氮液化天然气流(67)的部件,和回收所述蒸馏塔(49)顶部的气体流(69)的部件;
-级式压缩机(25),其与回收所述蒸馏塔(49)顶部的气体流(69)的部件相连;以及
-为形成可燃气体而提取顶部气体流(69)的第一部分(16)的部件,其安插在所述压缩机(25)的中间压缩级(29D)处;
并且,其特征还在于,所述第二制冷循环(21)包括:
-由压缩至中间压力的顶部气体(69)的第二部分形成初始的制冷流体流(73)的部件;
-初始的制冷流体流(73)的压缩部件(39),其将初始的制冷流体流压缩到高于所述中间压力PI的高压PH,以形成被压缩的制冷流体流(75);
-第二热交换器(33),用以冷却被压缩的制冷流体流(75);
-分离部件,其将出自所述第二热交换器(33)的被压缩的制冷流体流(75)分离为主要的冷却流(79)和液化天然气的过冷流(77);
-第三热交换器(35),用以冷却所述过冷流(77);
-将出自所述第三热交换器(35)的过冷流(77)引入所述第一热交换器(19)的部件;
-出自所述第一热交换器(19)的过冷流(81)的膨胀部件(37;101),其使所述过冷流膨胀达到小于所述中间压力PI的低压PB,以形成基本液态的液化天然气过冷流(83);
-基本液态的液化天然气过冷流(83)的流通部件,其使基本液态的液化天然气过冷流(83)在所述第一热交换器内流通,以形成被加热的过冷流(85);
-主涡轮(41),其使主要的冷却流(79)基本膨胀到所述低压PB;
-混合部件,其使出自所述主涡轮(41)的冷却流与被加热的过冷流(85)进行混合以形成混合流(87);
-混合流(87)的流通部件,其使混合流先在所述第三热交换器(35)内、然后在所述第二热交换器(33)内相继地流通,以形成被加热的混合流(89);
-将被加热的混合流(89)引入到所述压缩机(25)内至位于所述中间压力级(29D)上游的低压级(29C)的部件。
15.根据权利要求14所述的设备(9;99;104;125),其特征在于,所述高压PH介于40巴至100巴之间。
16.根据权利要求14或15所述的设备(9;99;104;125),其特征在于,所述低压PB小于20巴。
17.根据权利要求14或15所述的设备(99;104;125),其特征在于,出自所述第一热交换器(19)的过冷流(81)的膨胀部件(37;101)包括液体膨胀涡轮(101)。
18.根据权利要求14或15所述的设备(9;99;104;125),其特征在于,所述的初始的制冷流体流(73)的压缩部件(39)包括辅助压缩机(39),该辅助压缩机与所述主涡轮(41)联接。
19.根据权利要求14或15所述的设备(99),其特征在于,所述第二制冷循环(21)包括将C2烃流(92)引入到所述压缩机(25)以形成初始的制冷流体流(73)的一部分的部件。
20.根据权利要求14或15所述的设备(104;125),其特征在于,所述第二热交换器(33)包括次级制冷流体(117)的流通部件,所述设备(104;125)包括第三制冷循环(105),该第三制冷循环包括:次级压缩部件(107),其压缩出自所述第三热交换器(33)的次级制冷流体(115);出自所述次级压缩部件(107)的次级制冷流体(117)的次级冷却和膨胀部件(109,111);以及,将出自所述次级膨胀部件(111)的次级制冷流体(119)引入所述第二热交换器(33)内的部件。
21.根据权利要求20所述的设备(104;125),其特征在于,次级制冷流体(117)包含丙烷。
22.根据权利要求14或15所述的设备(9;99;104;125),其特征在于,所述设备包括:将在所述中间涡轮中经过膨胀的过冷的液化天然气流(59)与天然气的补给流(63)混合的部件;以及第四热交换器(51),用以使补给流(63)与顶部气体流(69)进行热交换。
23.根据权利要求15所述的设备(9;99;104;125),其特征在于,所述高压PH在50巴至80巴之间。
24.根据权利要求15所述的设备(9;99;104;125),其特征在于,所述高压PH在60巴至75巴之间。
25.根据权利要求21所述的设备(104;125),其特征在于,所述次级制冷流体(117)还包含乙烷。
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FR0510329A FR2891900B1 (fr) | 2005-10-10 | 2005-10-10 | Procede de traitement d'un courant de gnl obtenu par refroidissement au moyen d'un premier cycle de refrigeration et installation associee. |
FR0510329 | 2005-10-10 | ||
PCT/FR2006/002273 WO2007042662A2 (fr) | 2005-10-10 | 2006-10-10 | Procede de traitement d'un courant de gnl obtenu par refroidissement au moyen d'un premier cycle de refrigeration et installation associee |
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CN101313188A CN101313188A (zh) | 2008-11-26 |
CN101313188B true CN101313188B (zh) | 2011-05-04 |
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CN2006800437214A Active CN101313188B (zh) | 2005-10-10 | 2006-10-10 | 液化天然气流的处理方法和相关装置 |
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US (1) | US7628035B2 (zh) |
EP (1) | EP1946026B1 (zh) |
JP (1) | JP4854743B2 (zh) |
KR (1) | KR101291220B1 (zh) |
CN (1) | CN101313188B (zh) |
CA (1) | CA2625577C (zh) |
EA (1) | EA011605B1 (zh) |
ES (1) | ES2665743T3 (zh) |
FR (1) | FR2891900B1 (zh) |
MY (1) | MY152657A (zh) |
NZ (1) | NZ567356A (zh) |
WO (1) | WO2007042662A2 (zh) |
Families Citing this family (17)
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FR2936864B1 (fr) * | 2008-10-07 | 2010-11-26 | Technip France | Procede de production de courants d'azote liquide et gazeux, d'un courant gazeux riche en helium et d'un courant d'hydrocarbures deazote et installation associee. |
DE102008056196A1 (de) * | 2008-11-06 | 2010-05-12 | Linde Ag | Verfahren zum Abtrennen von Stickstoff |
CN101508925B (zh) * | 2009-03-13 | 2012-10-10 | 北京永记鑫经贸有限公司 | 一种天然气液化工艺 |
FR2944523B1 (fr) | 2009-04-21 | 2011-08-26 | Technip France | Procede de production d'un courant riche en methane et d'une coupe riche en hydrocarbures en c2+ a partir d'un courant de gaz naturel de charge, et installation associee |
US10132561B2 (en) * | 2009-08-13 | 2018-11-20 | Air Products And Chemicals, Inc. | Refrigerant composition control |
US9441877B2 (en) | 2010-03-17 | 2016-09-13 | Chart Inc. | Integrated pre-cooled mixed refrigerant system and method |
EP2597406A1 (en) * | 2011-11-25 | 2013-05-29 | Shell Internationale Research Maatschappij B.V. | Method and apparatus for removing nitrogen from a cryogenic hydrocarbon composition |
US9097208B2 (en) | 2012-12-14 | 2015-08-04 | Electro-Motive Diesel, Inc. | Cryogenic pump system for converting fuel |
US11408673B2 (en) | 2013-03-15 | 2022-08-09 | Chart Energy & Chemicals, Inc. | Mixed refrigerant system and method |
US11428463B2 (en) | 2013-03-15 | 2022-08-30 | Chart Energy & Chemicals, Inc. | Mixed refrigerant system and method |
CA3140415A1 (en) | 2013-03-15 | 2014-09-18 | Chart Energy & Chemicals, Inc. | Mixed refrigerant system and method |
US20150276307A1 (en) * | 2014-03-26 | 2015-10-01 | Dresser-Rand Company | System and method for the production of liquefied natural gas |
CA2855383C (en) * | 2014-06-27 | 2015-06-23 | Rtj Technologies Inc. | Method and arrangement for producing liquefied methane gas (lmg) from various gas sources |
AR105277A1 (es) | 2015-07-08 | 2017-09-20 | Chart Energy & Chemicals Inc | Sistema y método de refrigeración mixta |
FR3038964B1 (fr) | 2015-07-13 | 2017-08-18 | Technip France | Procede de detente et de stockage d'un courant de gaz naturel liquefie issu d'une installation de liquefaction de gaz naturel, et installation associee |
CA2903679C (en) | 2015-09-11 | 2016-08-16 | Charles Tremblay | Method and system to control the methane mass flow rate for the production of liquefied methane gas (lmg) |
WO2017171171A1 (ko) * | 2016-03-31 | 2017-10-05 | 대우조선해양 주식회사 | 선박 |
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2005
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2006
- 2006-10-09 US US11/539,828 patent/US7628035B2/en active Active
- 2006-10-10 JP JP2008534049A patent/JP4854743B2/ja active Active
- 2006-10-10 CN CN2006800437214A patent/CN101313188B/zh active Active
- 2006-10-10 CA CA2625577A patent/CA2625577C/fr active Active
- 2006-10-10 EP EP06820179.7A patent/EP1946026B1/fr active Active
- 2006-10-10 KR KR1020087008586A patent/KR101291220B1/ko active IP Right Grant
- 2006-10-10 ES ES06820179.7T patent/ES2665743T3/es active Active
- 2006-10-10 EA EA200801047A patent/EA011605B1/ru not_active IP Right Cessation
- 2006-10-10 MY MYPI20081035 patent/MY152657A/en unknown
- 2006-10-10 WO PCT/FR2006/002273 patent/WO2007042662A2/fr active Application Filing
- 2006-10-11 NZ NZ567356A patent/NZ567356A/en not_active IP Right Cessation
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US5421165A (en) * | 1991-10-23 | 1995-06-06 | Elf Aquitaine Production | Process for denitrogenation of a feedstock of a liquefied mixture of hydrocarbons consisting chiefly of methane and containing at least 2 mol % of nitrogen |
US6308531B1 (en) * | 1999-10-12 | 2001-10-30 | Air Products And Chemicals, Inc. | Hybrid cycle for the production of liquefied natural gas |
Also Published As
Publication number | Publication date |
---|---|
EA011605B1 (ru) | 2009-04-28 |
KR101291220B1 (ko) | 2013-07-31 |
ES2665743T3 (es) | 2018-04-27 |
EA200801047A1 (ru) | 2008-08-29 |
US20070095099A1 (en) | 2007-05-03 |
NZ567356A (en) | 2011-04-29 |
CA2625577C (fr) | 2014-08-19 |
EP1946026A2 (fr) | 2008-07-23 |
FR2891900B1 (fr) | 2008-01-04 |
WO2007042662A2 (fr) | 2007-04-19 |
FR2891900A1 (fr) | 2007-04-13 |
EP1946026B1 (fr) | 2018-01-17 |
JP4854743B2 (ja) | 2012-01-18 |
JP2009512831A (ja) | 2009-03-26 |
US7628035B2 (en) | 2009-12-08 |
WO2007042662A3 (fr) | 2007-06-28 |
MY152657A (en) | 2014-10-31 |
CN101313188A (zh) | 2008-11-26 |
CA2625577A1 (fr) | 2007-04-19 |
KR20080063470A (ko) | 2008-07-04 |
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