CN106595223A - 一种回收天然气中丙烷及碳三以上重烃的系统和方法 - Google Patents

一种回收天然气中丙烷及碳三以上重烃的系统和方法 Download PDF

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CN106595223A
CN106595223A CN201611026891.3A CN201611026891A CN106595223A CN 106595223 A CN106595223 A CN 106595223A CN 201611026891 A CN201611026891 A CN 201611026891A CN 106595223 A CN106595223 A CN 106595223A
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邱鹏
王登海
郑欣
刘子兵
薛岗
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Xian Changqing Technology Engineering Co Ltd
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Abstract

本发明提供了一种回收天然气中丙烷及碳三以上重烃的系统及方法,包括冷箱Ⅰ、丙烷蒸发器Ⅰ、脱乙烷塔、冷箱Ⅱ、低温分离器、重沸器以及压缩机、空冷器、水冷器、冷箱Ⅲ、丙烷蒸发器Ⅱ、分液罐。本发明其制冷剂获取自原料天然气中,制冷剂的组成以乙烷和丙烷为主,这种制冷剂不但能达到较低的制冷温度,而且还为脱乙烷塔提供了回流液,从而将C3 +组分的吸收分离过程整合到脱乙烷塔内,仅需要采用一具塔器就可以实现C3 +组分的回收。本发明具有工艺流程简单,设备数量少,系统压降小等优点。

Description

一种回收天然气中丙烷及碳三以上重烃的系统和方法
技术领域
本发明属于天然气凝液回收技术领域,具体涉及一种回收天然气中丙烷及碳三以上重烃的系统和方法。
背景技术
天然气(含油田伴生气)中除含有甲烷以外,通常还含有一定量的丙烷及碳三以上重烃(简称C3 +混烃)。天然气凝液回收装置的主要功能是回收这部分C3 +混烃,从而获得高附加值的液烃产品。目前,常用的天然气凝液回收工艺包括冷油吸收法、冷凝分离法和直接换热法(Direct Heat Exchange,简称DHX)。其中,DHX工艺于20世纪80年代提出,该工艺是在冷凝分离法的基础之上,通过设置DHX塔增加了对C3 +混烃的吸收分离过程,从而大幅度提高C3 +混烃的回收率(可达到90%以上),该工艺在国内外得到广泛应用,是目前回收天然气中丙烷及碳三以上重烃的主要工艺技术。
但是,DHX工艺存在以下不足:① 工艺流程复杂,设备数量多,需要设置DHX塔和脱乙烷塔两具塔器(详见附图2);② 采用透平膨胀机制冷,通过对原料天然气进行膨胀制冷,造成原料天然气压降大,往往需要在下游设置压缩机对天然气进行增压,整个系统能耗高。
发明内容
本发明的目的是解决现有天然气回收C3 +混烃工艺技术存在的流程复杂,设备数量多,系统压降大等问题。
为此,本发明提供了一种回收天然气中丙烷及碳三以上重烃的系统,包括冷箱Ⅰ、丙烷蒸发器Ⅰ、脱乙烷塔、冷箱Ⅱ、低温分离器、重沸器、压缩机、空冷器、水冷器、冷箱Ⅲ、丙烷蒸发器Ⅱ、分液罐;
冷箱Ⅰ出口与丙烷蒸发器Ⅰ进口通过管线连接,丙烷蒸发器Ⅰ出口与脱乙烷塔中部通过管线连接,冷箱Ⅱ进口一端与脱乙烷塔顶部连接,出口一端与低温分离器通过管线连接,低温分离器顶部出口通过管线与冷箱Ⅰ相通,底部出口通过管线与压缩机进口端连接,压缩机出口与空冷器连接,空冷器、水冷器、冷箱Ⅲ、丙烷蒸发器Ⅱ、分液罐顶部进口依次串接,分液罐顶部出口与低温分离器中下部进口连通,分液罐底部出口与脱乙烷塔上部进口连通,脱乙烷塔底部出口与重沸器连通,重沸器上部出口与脱乙烷塔下部进口连通,重沸器底部出口连有排出管线。
所述低温分离器顶部出口与冷箱Ⅰ连通过管线和冷箱Ⅱ连通。
所述低温分离器底部出口与压缩机进口端之间还设有节流阀,节流阀的出口、冷箱Ⅱ、冷箱Ⅲ依次串接,冷箱Ⅲ出口与压缩机进口端连通。
本发明还提供了一种回收天然气中丙烷及碳三以上重烃的方法,包括以下步骤:
步骤1)将原料天然气依次经过冷箱Ⅰ和丙烷蒸发器Ⅰ预冷却,之后进入脱乙烷塔中部;
步骤2)脱乙烷塔顶的气相进入冷箱Ⅱ冷却至-50℃~-70℃,然后进入低温分离器分为气液两相;其中,气相返回冷箱Ⅱ进行热交换,液相经过节流阀降压后,返回冷箱Ⅱ进行热交换;
步骤3)将步骤2)热交换后的气相进入冷箱Ⅰ再与原料天然气换热;
步骤4)将步骤2)热交换后的液相进入冷箱Ⅲ再进行热交换,之后进入压缩机增压,增压后的气体依次经空冷器和水冷器进行冷却;
步骤5) 将步骤4)增压冷却后的气体依次进入冷箱Ⅲ和丙烷蒸发器Ⅱ冷却至-5℃~-40℃后,进入分液罐分为气液两相,其中,气相返回低温分离器,液相返回脱乙烷塔顶作为回流液;
步骤6) 脱乙烷塔底部的液体进入重沸器,产生的气相由重沸器顶部进入脱乙烷塔下部,重沸器底部产生丙烷及碳三以上重烃的混烃。
步骤(1)中经过冷箱Ⅰ预冷却后的天然气温度为-5℃~-40℃。
步骤2)中液相经节流阀节流后的压力为200kPa~500kPa。
步骤4)中压缩机增压压力比原料天然气压力高100kPa~500kPa。
本发明的有益效果是:
1、本发明提供的这种回收天然气中丙烷及碳三以上重烃的系统,将丙烷及碳三以上重烃的混烃(C3 +混烃)的吸收分离过程整合到脱乙烷塔内,仅需要采用一具塔器就可以实现C3 +混烃的回收,克服了现有设备数量多的缺陷。
2、本发明提供的这种回收天然气中丙烷及碳三以上重烃的方法,采用单塔回收,其制冷剂获取自原料天然气中,制冷剂的组成以乙烷和丙烷为主,这种制冷剂不但能达到较低的制冷温度,而且还为脱乙烷塔提供了回流液,实现C3 +混烃的回收。
下面将结合附图做进一步详细说明。
附图说明
图1是本发明的应用实例工艺流程示意图;
图2是现有DHX工艺流程示意图。
图中:1、冷箱Ⅰ;2、丙烷蒸发器Ⅰ;3、脱乙烷塔;4、冷箱Ⅱ;5、低温分离器;6、节流阀;7、冷箱Ⅲ;8、压缩机;9、空冷器;10、水冷器;11、丙烷蒸发器Ⅱ;12、分液罐;13、重沸器。
具体实施方式
实施例1:
本实施例提供了一种回收天然气中丙烷及碳三以上重烃的系统,包括冷箱Ⅰ1、丙烷蒸发器Ⅰ2、脱乙烷塔3、冷箱Ⅱ4、低温分离器5、重沸器13以及压缩机8、空冷器9、水冷器10、冷箱Ⅲ7、丙烷蒸发器11、分液罐12;
冷箱Ⅰ1出口与丙烷蒸发器Ⅰ2进口通过管线连接,丙烷蒸发器Ⅰ2出口与脱乙烷塔3中部通过管线连接,冷箱Ⅱ4进口一端与脱乙烷塔3顶部连接,出口一端与低温分离器5通过管线连接,低温分离器5顶部出口通过管线与冷箱Ⅰ1相通,底部出口通过管线与压缩机8进口端连接,压缩机8出口与空冷器9连接,空冷器9、水冷器10、冷箱Ⅲ7、丙烷蒸发器11、分液罐12顶部进口依次串接,分液罐12顶部出口与低温分离器5中下部进口连通,分液罐12底部出口与脱乙烷塔3上部进口连通,脱乙烷塔3底部出口与重沸器13连通,重沸器13上部出口与脱乙烷塔3下部进口连通,重沸器13底部出口连有排出管线。
这种回收天然气中丙烷及碳三以上重烃的系统,与现有的DHX工艺中的设备(如图2所示)相比,将C3 +混烃的吸收分离过程整合到脱乙烷塔3内,仅需要采用一具塔器就可以实现C3 +混烃的回收。
实施例2:
在实施例1的基础上,本实施例提供了一种回收天然气中丙烷及碳三以上重烃的系统,所述低温分离器5顶部出口与冷箱Ⅰ1连通过管线和冷箱Ⅱ4连通。
低温分离器5顶部排出的气相为冷箱Ⅱ4提供冷量,之后气相进入冷箱Ⅰ1与原料天然气换交热。
所述低温分离器5底部出口与压缩机8进口端之间还设有节流阀6,节流阀6的出口、冷箱Ⅱ4、冷箱Ⅲ7依次串接,冷箱Ⅲ7出口与压缩机8进口端连通。
低温分离器5底部出口排出的液相经过节流阀6降压后,温度降低,返回冷箱Ⅱ4提供冷量后复热,复热后的液相进入冷箱Ⅲ7再换热升温,之后进入压缩机8增压,增压后依次经空冷器9和水冷器10冷却。
本实施例提供了的这种回收天然气中丙烷及碳三以上重烃的系统,冷箱Ⅱ4、冷箱Ⅲ7的制冷剂获取自原料天然气中。
实施例3:
在实施例2的基础上,本实施例提供了一种回收天然气中丙烷及碳三以上重烃的方法,包括以下步骤:
步骤1)将原料天然气依次经过冷箱Ⅰ1和丙烷蒸发器Ⅰ2预冷却,之后进入脱乙烷塔3中部;
步骤2)脱乙烷塔3顶的气相进入冷箱Ⅱ4冷却至-50℃~-70℃,然后进入低温分离器5分为气液两相;其中,气相返回冷箱Ⅱ4进行热交换,液相经过节流阀6降压后,返回冷箱Ⅱ4进行热交换;
步骤3)将步骤2)热交换后的气相进入冷箱Ⅰ1再与原料天然气换热;
步骤4)将步骤2)热交换后的液相进入冷箱Ⅲ7再进行热交换,之后进入压缩机8增压,增压后的气体依次经空冷器9和水冷器10进行冷却;
步骤5) 将步骤4)增压冷却后的气体依次进入冷箱Ⅲ7和丙烷蒸发器11冷却至-5℃~-40℃后,进入分液罐12分为气液两相,其中,气相返回低温分离器5,液相返回脱乙烷塔3顶作为回流液;
步骤6) 脱乙烷塔3底部的液体进入重沸器13,产生的气相由重沸器13顶部进入脱乙烷塔3下部,重沸器13底部产生丙烷及碳三以上重烃的混烃(即C3 +混烃)。
其中,步骤2)中脱乙烷塔3顶的气相进入冷箱Ⅱ4冷却至-50℃~-70℃,以确保低温分离器5分出的液相主要由乙烷和丙烷构成。
本实施例提供的这种回收天然气中丙烷及碳三以上重烃的方法,采用单塔回收,其制冷剂获取自原料天然气中,制冷剂的组成以乙烷和丙烷为主,这种制冷剂不但能达到较低的制冷温度,而且还为脱乙烷塔3提供了回流液,实现C3 +混烃的回收。
实施例4:
在实施例3的基础上,本实施例提供了一种如图1所示的回收天然气中丙烷及碳三以上重烃的方法,包括以下步骤:
步骤1)将原料天然气依次经过冷箱Ⅰ1和丙烷蒸发器Ⅰ2预冷却,天然气的温度由40℃降低至-5℃~-40℃之后进入脱乙烷塔3中部;
步骤2)脱乙烷塔3顶的气相进入冷箱Ⅱ4冷却至-60℃,然后进入低温分离器5分为气液两相;其中,气相返回冷箱Ⅱ4热交换升温至-39℃,液相经过节流阀6降压后温度降低至-78℃,返回冷箱Ⅱ4热交换升温至-33℃;
步骤3)将步骤2)热交换后的气相进入冷箱Ⅰ1再与原料天然气换热升温至35℃;
步骤4)将步骤2)热交换后的液相再进入冷箱Ⅲ7热交换升温至35℃,之后进入压缩机8增压,增压后的气体依次经空冷器9和水冷器10进行冷却至40℃;
步骤5) 将步骤4)增压冷却后的气体依次进入冷箱Ⅲ7和丙烷蒸发器11冷却至-5℃~-40℃后,进入分液罐12分为气液两相,其中,气相返回低温分离器5,液相返回脱乙烷塔3顶作为回流液;
步骤6) 脱乙烷塔3底部的液体进入重沸器13,产生的气相由重沸器13顶部进入脱乙烷塔3下部,重沸器13底部产生丙烷及碳三以上重烃的混烃。
其中,步骤2)中液相经节流阀6节流后的压力为200kPa~500kPa。节流后压力越高,后续增压功率越低,但是节流后压力过高,会导致冷箱冷量供给不足,应综合平衡考虑。
步骤4)中压缩机8增压压力应比原料天然气压力高100kPa~500kPa,以确保分液罐12分出的气、液两相物流能分别返回低温分离器5和脱乙烷塔3。
本发明中冷箱Ⅰ、冷箱Ⅱ、冷箱Ⅲ、丙烷蒸发器Ⅰ、丙烷蒸发器Ⅱ、脱乙烷塔3、低温分离器5、节流阀6、压缩机8、空冷器9、水冷器10、分液罐12、重沸器13均为现有装置。
以上各实施例没有详细叙述的方法和结构属本行业的公知常识,这里不一一叙述。
以上例举仅仅是对本发明的举例说明,并不构成对本发明的保护范围的限制,凡是与本发明相同或相似的设计均属于本发明的保护范围之内。

Claims (7)

1.一种回收天然气中丙烷及碳三以上重烃的系统,其特征在于:包括冷箱Ⅰ(1)、丙烷蒸发器Ⅰ(2)、脱乙烷塔(3)、冷箱Ⅱ(4)、低温分离器(5)、重沸器(13)、压缩机(8)、空冷器(9)、水冷器(10)、冷箱Ⅲ(7)、丙烷蒸发器Ⅱ(11)、分液罐(12);
冷箱Ⅰ(1)出口与丙烷蒸发器Ⅰ(2)进口通过管线连接,丙烷蒸发器Ⅰ(2)出口与脱乙烷塔(3)中部通过管线连接,冷箱Ⅱ(4)进口一端与脱乙烷塔(3)顶部连接,出口一端与低温分离器(5)通过管线连接,低温分离器(5)顶部出口通过管线与冷箱Ⅰ(1)相通,底部出口通过管线与压缩机(8)进口端连接,压缩机(8)出口与空冷器(9)连接,空冷器(9)、水冷器(10)、冷箱Ⅲ(7)、丙烷蒸发器Ⅱ(11)、分液罐(12)顶部进口依次串接,分液罐(12)顶部出口与低温分离器(5)中下部进口连通,分液罐(12)底部出口与脱乙烷塔(3)上部进口连通,脱乙烷塔(3)底部出口与重沸器(13)连通,重沸器(13)上部出口与脱乙烷塔(3)下部进口连通,重沸器(13)底部出口连有排出管线。
2.根据权利要求1所述的一种回收天然气中丙烷及碳三以上重烃的系统,其特征在于:所述低温分离器(5)顶部出口与冷箱Ⅰ(1)连通过管线和冷箱Ⅱ(4)连通。
3.根据权利要求1所述的一种回收天然气中丙烷及碳三以上重烃的系统,其特征在于:所述低温分离器(5)底部出口与压缩机(8)进口端之间还设有节流阀(6),节流阀(6)的出口、冷箱Ⅱ(4)、冷箱Ⅲ(7)依次串接,冷箱Ⅲ(7)出口与压缩机(8)进口端连通。
4.一种回收天然气中丙烷及碳三以上重烃的方法,其特征在于,包括以下步骤:
步骤1)将原料天然气(1)依次经过冷箱Ⅰ(1)和丙烷蒸发器Ⅰ(2)预冷却,之后进入脱乙烷塔(3)中部;
步骤2)脱乙烷塔(3)顶的气相进入冷箱Ⅱ(4)冷却至-50℃~-70℃,然后进入低温分离器(5)分为气液两相;其中,气相返回冷箱Ⅱ(4)进行热交换,液相经过节流阀(6)降压后,返回冷箱Ⅱ(4)进行热交换;
步骤3)将步骤2)热交换后的气相进入冷箱Ⅰ(1)再与原料天然气(1)换热;
步骤4)将步骤2)热交换后的液相进入冷箱Ⅲ(7)再进行热交换,之后进入压缩机(8)增压,增压后的气体依次经空冷器(9)和水冷器(10)进行冷却;
步骤5) 将步骤4)增压冷却后的气体依次进入冷箱Ⅲ(7)和丙烷蒸发器Ⅱ(11)冷却至-5℃~-40℃后,进入分液罐(12)分为气液两相,其中,气相返回低温分离器(5),液相返回脱乙烷塔(3)顶作为回流液;
步骤6) 脱乙烷塔(3)底部的液体进入重沸器(13),产生的气相由重沸器(13)顶部进入脱乙烷塔(3)下部,重沸器(13)底部产生丙烷及碳三以上重烃的混烃(15)。
5.根据权利要求4所述的一种回收天然气中丙烷及碳三以上重烃的方法,其特征在于:步骤(1)中经过冷箱Ⅰ(1)预冷却后的天然气温度为-5℃~-40℃。
6.根据权利要求4所述的一种回收天然气中丙烷及碳三以上重烃的方法,其特征在于:步骤2)中液相经节流阀(6)节流后的压力为200kPa~500kPa。
7.根据权利要求4所述的一种回收天然气中丙烷及碳三以上重烃的方法,其特征在于:步骤4)中压缩机(8)增压压力比原料天然气(1)压力高100kPa~500kPa。
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