TW200909572A - Process and apparatus for steam cracking hydrocarbon feedstocks - Google Patents

Process and apparatus for steam cracking hydrocarbon feedstocks Download PDF

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TW200909572A
TW200909572A TW097124712A TW97124712A TW200909572A TW 200909572 A TW200909572 A TW 200909572A TW 097124712 A TW097124712 A TW 097124712A TW 97124712 A TW97124712 A TW 97124712A TW 200909572 A TW200909572 A TW 200909572A
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vapor
liquid
heat exchange
exchange tubes
weight
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TW097124712A
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TWI500754B (en
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David B Spicer
Nicolantonio Arthur R Di
James M Frye
Richard C Stell
James N Mccoy
Robert D Strack
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Exxonmobil Chem Patents Inc
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/14Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils in pipes or coils with or without auxiliary means, e.g. digesters, soaking drums, expansion means
    • C10G9/18Apparatus
    • C10G9/20Tube furnaces

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

The present disclosure provides a process for treating a hydrocarbon feedstock comprising: (a) feeding the hydrocarbon feedstock at a linear velocity equal to or less than 0.9 m/s to a first preheating zone in the convection section of a steam cracking furnace; (b) preheating the hydrocarbon feedstock in the first preheating zone to vaporize less than 99 wt.% of the hydrocarbon feedstock to form a vapor-liquid mixture; (c) separating at least a portion of the vapor-liquid mixture to form a vapor fraction and a liquid fraction; and (d) feeding at least a portion of the vapor fraction to the steam cracking furnace.

Description

200909572 九、發明說明 與其他申請案的關係 本案請求2007年8月21日申請之國際專利申請案序 號PCT/US2007/018486的益處及優先權。 【發明所屬之技術領域】 本揭示內容有關在蒸汽裂解爐或熱解爐中製造輕質嫌 烴之方法,更特別的是蒸汽裂解含有至少0.01重量%低揮 發性化合物的烴類進料之方法。 【先前技術】 蒸汽裂解,亦稱爲熱解,長久以來用於將不同烴類進 料裂解爲烯烴,較佳爲如乙烯、丙烯及丁烯的輕質烯烴。 傳統蒸汽裂解利用具有兩個主要段的蒸汽裂解爐:對流段 及輻射段。該烴類進料經常以液體形式(除了以蒸氣形式 進入的輕質進料之外)進入該爐的對流段,其中典型以該 輻射段的熱煙道氣間接接觸且與蒸汽直接接觸而加熱且蒸 發該烴類進料。蒸發的進料及蒸汽混合物接著加入該裂解 發生的輻射段。所得的產物,包括烯烴,留在該蒸汽裂解 爐供進一步的下游處理。 傳統蒸汽裂解系統能有效裂解如天然氣液體(NGL ) 、製氣油及輕油的局品質進料。然而,蒸汽裂解經濟有時 候喜歡裂解如’以非限定例的方式,濃縮物之低成本重質 進料’該重質進料爲以小量與天然氣田的瓦斯、原油、常 -5- 200909572 壓重油(atmospheric resid),亦被稱爲常壓管式蒸餾爸 底部物(atmospheric pipestill bottom)及真空製氣油之生 產聯合產出的油,原油、真空製氣油及常壓重油含有高分 子量、具有超過590°C之沸點的低揮發性成分及/或有時候 具有超過760 °C之沸點的焦炭前驅物。當輕質成分蒸發時 這些進料的低揮發性成分及/或焦炭前驅物將以焦炭形式 舖在傳統蒸汽裂解爐的對流段。輕質成分完全被蒸發之處 的對流段下游僅可忍受非常小量的低揮發性成分及焦炭前 驅物,因爲該焦炭沈積正常將弄髒對流段的管子,降低熱 傳導效率且提高管子中的壓降。 此外’一些輕油受到含有低揮發性成分及焦炭前驅物 的重質原油污染。傳統蒸汽裂解爐沒有處理殘渣、原油或 許多被低揮發性成分及焦炭前驅物污染之受殘渣污染或原 油污染的製氣油或輕油的彈性。 爲了解決焦化問題,美國專利案號3,6 1 7,4 9 3,在此 以引用方式倂入本文’揭示應用原油的外部蒸發罐且揭示 應用第一閃蒸槽除去蒸氣形式的輕油及應用第二閃蒸槽除 去沸點介於2 3 0與5 9 0°C之間的蒸氣。蒸氣係在蒸汽裂解 爐中裂解爲烯烴’且來自第二閃蒸槽的分離液移出後,以 蒸汽洗滌,且作爲燃料。 美國專利案號3,718,709,在此以引用方式倂入本文 ,揭示將焦炭沈積減至最少的方法。其揭示利用超熱蒸汽 預熱熱解爐內側或外側的重質進料而蒸發50%重質進料預 熱,及移除殘餘物,(分離液)。對蒸發的烴類(其多半 -6- 200909572 含有輕質揮發烴類)進行裂解。 美國專利案號5,1 90,634,在此以引用方式倂入本文 ,揭示在小臨界量氫存在於對流段之下經由預熱該進料抑 制焦炭形成的方法。該對流段中存在的氫抑制該等烴類的 聚合反應,因而抑制焦炭形成。 美國專利案號5,580,443,在此以引用方式倂入本文 ,揭示先預熱進料然後自熱解爐對流段中的預熱器抽出之 方法。此預熱的進料接著與預定量的蒸汽(稀釋蒸汽)混 合然後加入蒸氣-液體分離器,以自該分離器分離且除去 所需比例之液體形式的低揮發性成分及焦炭前驅物。使來 自蒸氣-液體分離器的分離蒸氣返回該熱解爐以供加熱及 裂解。 美國專利案號6,632,351,在此以引用方式倂入本文 ’揭示熱解原油進料或含有瀝青進料的原油部分之方法及 熱解爐’其包含將含有瀝青進料的原油或原油部分供至對 流區內的第一段預熱器,其中含有瀝青進料的原油或原油 部分係於該第一段預熱器內加熱到至少3 7 5 °C的出口溫度 以製造熱蒸氣-液體混合物,自該第一段預熱器抽出該蒸 氣-液體混合物至蒸氣-液體分離器,分離且自該蒸氣-液體 分離器的液體除去氣體’且將除去的氣體供至該對流區中 所提供的第二預熱器’進一步加熱該氣體溫度至高於排出 該蒸氣-液體分離器的氣體溫度之溫度,將該預熱氣體加 入該熱解爐的輻射區’且熱解該氣體爲烯烴及相關副產物 200909572 美國專利案號7,097,75 8,在此以引用方式倂入本文 ,揭示提高蒸汽裂解系統的閃蒸罐的非揮發物除去效率之 方法。在進入該閃蒸罐以提高除去效率之前,將該對流段 的氣流自霧沫流動轉化爲環形流。將氣流自霧沫流動轉化 爲環形流係先使該氣流歷經至少一個膨脹器然後至不同程 度的彎曲部且強迫該流改變方向至少一次。氣流由霧沫變 爲環狀有助於聯合微細液滴且由此提高自蒸氣相除去彼等 的效率。 美國專利案號7,138,〇47,在此以引用方式併入本文 ,揭示供入或裂解含有非揮發性烴類的烴類進料之方法, 其包含:加熱該烴類進料,混合該烴類進料與流體及/或 主要稀釋蒸汽流以形成混合物,閃蒸該混合物以形成蒸氣 相及液相,且依據至少一個所選的程序操作參數(如進入 該閃蒸罐之前的閃蒸流溫度)改變與該烴類進料混合之流 體及/或主要稀釋蒸汽流的量。 2005年2月28日申請的美國專利案號11/068,615, 在此以引用方式倂入本文’描述裂解烴類進料的方法,其 混合烴類進料與流體(例如’烴類或水)形成被閃蒸形成 蒸氣相及液相的混合物流’接著裂解該蒸氣相以提供烯烴 ,在轉移管線父換器(transfer line exchanger)中冷卻產 物流出物,其中與該進料混合的流體量係依據所選的程序 操作參數(例如閃蒸該混合物流之即該混合物流的溫度) 改變。 2004年5月21日申請的美國專利案號1〇/851,434, -8- 200909572 在此以引用方式倂入本文,及2004年5月21日申請的美 國臨時申請案序號60/5 73,474,在此以引用方式倂入本文 ,描述提高用於蒸汽裂解系統的閃蒸罐之非揮發性除去效 率的方法,該閃蒸罐具有包含加入洗滌蒸汽的入口之下護 罩、用於再循環淬冷油的環分配器、防渦旋擋板及爐架。 因此具有小量焦炭形成的蒸汽裂解烴類進料需要新穎 且省能量的方法。發明人意外發現當進料在低於閾値的入 口線性速度下供入且該進料係預熱至低於閾値的溫度時可 忽略在第一預熱區的第一預熱段中之焦炭形成。再者,只 要至少1重量。/。的烴類進料排出液相的第一預熱區,該第 一預熱區的焦炭形成將降至最少。此揭示內容因此提供能 經由將進入該蒸汽裂解爐預熱段的進料線性速度最適化而 以該預熱區最少的焦炭形成及流經該對流段的進料低壓降 來處理烴類進料的蒸汽裂解法。 【發明內容】 在一些具體例中’本揭示內容提供一種用於處理烴類 進料的方法,其包含: (a ) 以等於或小於0 · 9 m/ s的線性速度將該烴類進 料供入蒸汽裂解爐之對流段的第一預熱區; (b)在該第—預熱區中預熱該烴類進料以蒸發低於 99重里。/。的烴類進料而形成蒸氣-液體混合物; (〇 分離該蒸氣-液體混合物之至少一部分而形成 蒸氣部分及液體部分;及 -9 - 200909572 (d) 將該蒸氣部分之至少一部分供至該蒸汽裂解爐 0 根據一個具體例,該對流段包含多個熱交換管組且該 烴類進料流入該等管內。 在—個較佳具體例中,該烴類進料係在0_05至0.85 m/s範圍,較佳爲0·1至〇·8 m/s’且更佳爲0.1至0.75 m/s,之線性速度下供至該第一預熱區。 在本揭示內容的一個較佳具體例中,該第一預熱區包 含第一預熱段及第二預熱段,其中該烴類進料係在7 9 0至 1 8 2 5 k P a - a (絕對千帕斯卡)範圍的壓力,較佳在7 9 0至 1450 kPa-a範圍,更佳在790至1400 kPa-a範圍,又更佳 在790至1200 kPa-a範圍,且最佳在790至1100 kPa-a 範圍,及25至250°C範圍的溫度下供應至該第一預熱段以 形成在約1〇〇至3 50 °C範圍的溫度下排出該第一預熱段 之預熱烴類產物,然後該預熱烴類產物之至少一部分係與 第一稀釋流一起被供應至該第二預熱段以形成在3 5 〇至 5 00 °C範圍的溫度下排出該第一預熱段之蒸氣-液體混合 物’且包含以該蒸氣-液體混合物中的烴類總重量計至少1 重量%的液相。 在一些方面中,該烴類進料包含蒸汽裂解製氣油和殘 餘物、製氣油、焦化汽油(coker naphtha )、蒸汽裂解粗 汽油(steam cracked naphtha)、催化裂解粗汽油、加氫 裂解產物、重組物、提餘液重組物、直餾輕油(virgin naphtha )、原油、常壓管式蒸餾釜底部物(atmospheric -10- 200909572 pipestill bottom)、包括底部物的真空管式蒸餾釜流、真 空製氣油、重氣油、受原油污染的輕油、常壓重油、重質 殘油' C"殘油混合物、輕油/殘油混合物、費托液( Fischer-Tropsch liquid)、費托氣、費托躐、蒸餾物及低 硫躐渣中之其一或更多。在一個具體例中,該烴類進料之 10至99_99重量%在低於根據ASTM D-2887測量的590 °C 時沸騰。在另一個具體例中,該烴類進料之10至95百分 比在低於根據ASTM D-2 8 87測量的5 90°C時沸騰。 在一個具體例中,本揭示內容也提供一種在具有輻射 段燃燒器及對流段的蒸汽裂解爐中將烴類進料裂解爲輕質 烯烴之方法,該對流段包含第一組、第二組及第三組熱交 換管,該方法包含: (a) 在790至1825 kP a-a範圍的壓力,較佳在790 至1450 kPa-a範圍,更佳在790至1400 kPa-a範圍,又 更佳在790至1 200 kPa-a範圍,且最佳在790至1100 kPa-a範圍,及25至2 5 0 °C範圍的溫度下供入呈至少99 重量%液相之該烴類進料至該對流段中所提供的第一組熱 交換管,且線性速度在〇 . 1至〇 · 9 m/ s的範圍; (b ) 預熱該烴類進料以形成具有低於35〇°C之溫度 的預熱烴類產物; (c) 以第一稀釋流供應該預熱烴類產物之至少一部 分至該第二組熱交換管以蒸發該烴類進料之至少一部分而 形成具有在350至500 °C範圍的溫度且包含以該蒸氣-液體 混合物中的烴類總重量計至少1重量%液體之蒸氣-液體混 -11 - 200909572 合物; (d ) 分離步驟(c )該蒸氣-液體混合物之至少一部 分以形成蒸氣部分及液體部分;及 (e ) 將步驟(d )該蒸氣部分之至少一部分供至該 第三組熱交換管且進一步至該蒸汽裂解爐的輻射段以形成 包含輕質烯烴的產物, 其中該烴類進料包含蒸汽裂解製氣油和殘餘物、製氣 油、焦化汽油、蒸汽裂解粗汽油、催化裂解粗汽油、加氫 裂解產物、重組物、提餘液重組物、蒸餾物、直餾輕油、 原油、常壓管式蒸餾釜底部物、包括底部物的真空管式蒸 餾釜流、真空製氣油、重氣油、受原油污染的輕油、常壓 重油、重質殘油、C4/殘油混合物、輕油殘油混合物及低 硫蠟渣中之其一或更多。 在一個具體例中,該蒸氣-液體混合物具有在400至 5 00 °C範圍的溫度且包含以該蒸氣-液體混合物中的烴類總 重量計至少2重量%液體且其中該烴類進料之50至99.99 重量%在低於根據ASTM D-2887測量的590 °C時沸騰。在 其他具體例中,該蒸氣-液體混合物具有在425至500°C範 圍的溫度且包含以該蒸氣-液體混合物中的烴類總重量計 至少3重量%液體且其中該烴類進料之4 0至9 9.9 9重量% 在低於根據ASTM D-2 8 8 7測量的5 90°C時沸騰。在又其他 具體例中,該蒸氣-液體混合物具有在4 3 5至5 0 (TC範圍的 溫度且包含以該蒸氣-液體混合物中的烴類總重量計至少4 重量%液體且其中該烴類進料之30至99.99重量%在低於 -12- 200909572 根據ASTM D-28 87測量的5 90°C時沸騰。在又其他具體例 中,該蒸氣-液體混合物具有在450至5〇(TC範圍的溫度且 包含以該蒸氣-液體混合物中的烴類總重量計至少5重量% 液體且其中該烴類進料之1〇至99.99重量%在低於根據 ASTM D-2 8 8 7測量的5 90 °C時沸騰。 現在提供一種適於將烴類進料蒸汽裂解爲輕質烯烴之 裝置,其中該烴類進料之10至99.99重量%在低於根據 ASTM D-28 87測量的590°C時沸騰,該裝置包含: (a ) 蒸汽裂解爐,其包含適於提供輻射熱的輻射段 燃燒器及具有第一組、第二組及第三組熱交換管的對流段 j (b ) 以在0.1至〇 · 9 m / s範圍的線性速度將該烴類 進料供入該第一組熱交換管的機構(means ); (c ) 維持該烴類進料在低於3 5 0 °C的溫度下排出該 第一組熱交換管的機構; (d ) 同時供應第一稀釋流與來自(c )的預熱烴類 產物至少一部分至適於蒸發低於9 9重量%的烴類進料之第 二組熱交換管而形成蒸氣-液體混合物的機構; (e) 維持該蒸氣-液體混合物在350至5〇(TC範圍的 溫度下排出該第二組熱交換管的機構; (f) 適於分離來自步驟(e )的蒸氣-液體混合物之 至少一部分而形成蒸氣部分及液體部分的容器;及 (g ) 將來自步驟(f )的蒸氣部分之至少〜部分供 M該第三組熱交換管的機構。 -13- 200909572 【實施方式】 本案揭示內容有關用於加熱且蒸汽裂解烴類進料以製 造輕質烯烴,例如,乙烯及/或丙烯的方法。蒸汽裂解爐 的典型產物包括’但不限於,乙烯、丙烯、丁烯、丁二烯 、苯、氫、甲烷及其他相關烯烴、烷烴及芳族產物。乙烯 爲主要產物’經常在15至30重量%的範圍,以蒸發的進 料之重量及組成爲底。此揭示內容的方法包含預熱烴類, 混合該預熱烴類與包含蒸汽、水、N2、H2及烴類中之至少 其一的稀釋流以形成混合物,進一步預熱該混合物以形成 蒸氣-液體混合物’在容器中分離該蒸氣-液體混合物之至 少一部分以形成蒸氣部分及液體部分,且將該蒸氣部分之 至少一部分供至該蒸汽裂解爐以供進一步加熱及裂解。 除非此揭示內容中另行指明,否則所有百分比、份數 、比例等等皆以重量計。化合物或成分的參照對象包括該 化合物或成分本身’及與其他化合物或成分的組合,如化 合物的混合物。再者,當用量、濃度或其他値或參數以較 佳上限値及較佳下限値列表的方式提供時,咸將此理解爲 明確揭不由任何一對較佳上限値及較佳下限値所形成的所 有範圍’而不管範圍是否單獨揭示。 用於此時,”低揮發性成分",有時候稱爲非揮發性成 分或殘餘物,爲具有根據ASTM D-28 87測量時高於59(TC 之標稱沸點的烴類進料部分。此揭示內容能以含有〇 . 〇 1 至9 0重量%低揮發性成分的烴類進料適切地進行。用於此 -14- 200909572 時,”焦炭前驅物",爲具有根據ASTM D-28 8 7測量時高於 7 60 °C之標稱沸點的烴類進料部分。此揭示內容能以含有 〇·〇1至90重量%焦炭前驅物的烴類進料適切地進行。該 烴類進料的沸點分佈係根據ASTM D-28 8 7經由氣體層析 蒸餾法(G C D )來測量。 用於此時該措辭”實質液相,,意指至少99重量%,較佳 地至少9 9.5重量%,又更佳地至少9 9 · 9重量%,且最佳地 至少99.99重量%液相。例如,呈實質液相的物流意指該 物流之至少9 9重量%,較佳地至少9 9.5重量%,又更佳地 至少9 9 _ 9重量% ’且最佳地至少9 9.9 9重量%係呈液相。 用於此時該措辭"蒸氣部分"意指主要地,較佳至少75 重重% ’更佳地至少9 〇重量%,又佳地至少9 5重量%呈蒸 氣相的部分。用於此時該措辭”液體部分"意指—個部分主 要’較佳至少7 5重量% ’更佳地至少9 0重量。/。,又佳地 至少9 5重量%呈液相。 用於此時該措辭”主要地,,或”主要,,意指多於5 〇重量% 。例如’稀釋流主要包含蒸汽意指該稀釋流包含多於5 〇 重量%蒸汽。 烴類進料 該經類進料可包含至少一部分,如在0.0 1至9 0重量 1至9 〇重里%,或5至9 0重量%的低揮發性成分及焦 炭前驅物。此進料可包含,以非限定例的方式,蒸汽裂解 製氣油和殘餘%、製氣油、加熱用油、噴射機燃料、柴油 -15- 200909572 '煤油、汽油、焦化汽油、蒸汽裂解粗汽油、催化裂解粗 汽油、加氫裂解產物、重組物、提餘液重組物、費托液( Fischei-Tropsch liquid)、費托製氣油、費托蠟、天然汽 油、蒸餾物、直餾輕油、常壓管式蒸餾釜底部物、包括底 部物的真空管式蒸餾釜流、寬沸點範圍輕油至製氣油濃縮 物、精煉廠的重質非直餾烴類流、真空製氣油、重氣油、 受原油污染的輕油、常壓重油、重質殘油、C4/殘油混合 物、輕油/殘油混合物、烴氣/殘油混合物、氫/殘油混合物 、製氣油/殘油混合物、原油及低硫蠟渣中之其一或更多 〇 該烴類進料可具有至少3 1 5 t的標稱沸騰終點,一般 大於510°C ’經常大於5 90°C,例如大於76(TC。經濟上較 佳的進料一般爲低硫蠟渣 '常壓重油、受原油污染的輕油 、不同殘餘物混合物及原油。 用於製造中等蒸餾物的氣體變液體(GTL )技術,如 SMDS、AGC-21及SSPD法顯示用於燃料替代物及較高價 値產物的巨大潛力。任何費托氣體變液體方法的產物可進 一步進行,視需要地加氫處理,分餾而成爲費托液(亦稱 之爲費托輕油)、費托製氣油(亦稱之爲費托氣)及費托 蠟。由這些GTL方法所製造的費托輕油、費托製氣油及 費托蠟由於其高濃度正鏈烷烴成分而對蒸汽裂解應用具有 吸引力。該費托液及費托氣的高烷烴含量使其能在傳統進 料不常見到的高嚴苛度下裂解。 在一些具體例中,發現本案揭示內容的方法有用於處 -16- 200909572 理包含至少1重量。/。之費托液、費托氣、費托蠟、原油、 原油餾分中之至少其一的進料。在其他具體例中,發現本 案揭示內容的方法有用於處理包含至少1重量%之費托液 殘餘物、費托氣殘餘物、費托液餾分及費托氣館分中之至 少其一的進料。 製程敘述 本案揭示內容係描述於下文同時參照第1圖,其爲本 案揭示內容許多具體例中之其一的例示。咸了解此揭示內 容範圍各個所述的處理步驟之間或一個處理步驟內所述的 起源與目的地之間可包括任何數目及類型的處理步驟。 蒸汽裂解爐可爲用於製造低分子量燒烴之任何類型的 傳統烯烴蒸汽裂解爐,尤其是包括管式蒸汽裂解爐。該蒸 汽裂解爐對流段內的管子可並排排成一組熱交換管,或該 等管子可排成經過該對流區的進料單一通道或多通道。在 入口處’該進料可分配至多個單通道管,或可供至一個單 通道管’所有進料經過該單通道管從管子入口流至出口, 且更佳經過整個對流區。較佳地,第一預熱區包含至少一 個配置在該蒸汽裂解爐對流區中之單一通道組熱交換管。 在較佳的具體例中,該對流區包含少於20個分成二或更 多組的通道管’該烴類進料經過彼等流動。在各組中,該 等管子可在一排內排成螺旋或彎曲型排列,且各組可具有 數排管子。 配置在有用於此揭示內容的蒸汽裂解爐對流區中之熱 -17 - 200909572 交換管的通道數目爲在1至20的範圍。在一些 ,配置在有用於此揭示內容的蒸汽裂解爐對流區 換管的通道數目爲2、4、6、8、10、12、14、1 20。在其他具體例中,配置在有用於此揭示內容 解爐對流區中之熱交換管的通道數目爲1、3、5 11、 13、 15、 17 或 19。 在一些具體例中,有用於此揭示內容的蒸汽 ,如第1圖所例不的,包含對流段3及輻射段1 3 段1 3包含提供輻射熱及熱煙道氣1 2的輻射燃燒 汽裂解爐1的對流段3包含第一預熱區5及第二 。該第一預熱區5包含第一預熱段7及第二預熱 第一預熱區及第二預熱區包含多組熱交換管。在 例中,該第一預熱段7包含第一組熱交換管1 5, 熱段9包含第二組熱交換管17,且該第二預熱區 第三組熱交換管19。該蒸汽裂解爐1也包含容:ξ 了解該蒸汽裂解爐1可包括任何數目的處理設備 、閥、注入點、計量器、計量錶及控制裝置。 將包含至少一部分,如〇 . 〇 1至9 0重量%,1 量%或5至90重量%低揮發性成分及焦炭前驅物 料3 1供應至蒸汽裂解爐1之對流段3中的第一 之第一預熱段7,且於其中預熱。該烴類進料的 熟悉此技藝者採取任何方式。無論如何,較佳爲 含以該爐輻射段1 3的熱煙道氣1 2間接接觸該第 7中的烴類進料。這可藉由,以非限定的方式, 具體例中 中之熱交 6、1 8 或 的蒸汽裂 、7、9、 裂解爐1 i。該輻射 器。該蒸 預熱區1 1 ;段9。該 一個具體 該第二預 [U包含 器53。咸 ,如,泵 .至90重 之烴類進 預熱區5 加熱可由 該加熱包 一預熱段 使該烴類 -18- 200909572 進料經過位在該第一預熱段7內的第一組熱交換管1 5而 完成。 維持該烴類進料供至該對流區之第一預熱段入口處的 壓力以確保壓力小於! 82 5 kPa-a’較佳爲小於1 480 kPa-a ,更佳爲小於1 400 kPa-a ’且最佳爲小於1 200 kPa-a。在 一些具體例中,維持該烴類進料供至該對流區之第一預熱 段入口處的壓力以確保壓力在790至1 825 kPa-a的範圍’ 更佳在790至1480 kPa-a,又更佳在790至1450 kPa-a’ 又更佳在790至140G kPa-a,又再更佳在790至1200 kPa-a,且最佳在790至Π00 kPa-a,及溫度在25至250 。(:的範圍,經常在5 0至2 0 〇 °C °控制該烴類進料供至該對 流區之第一預熱段入口處的供入速率以維持該烴類進料之 入口線性速度小於1 . 1 m/s ’較佳爲小於1 m/s ’更佳爲小 於0.9,又更佳爲0.05至〇·9 m/s ’又再更佳爲0·1至〇·9 m/s,且又更佳爲0.2至0.8 m/s。 在此揭示內容的較佳具體例中’該烴類進料之入口線 性速度係小於〇 _ 9 m / s。在其他具體例中’該烴類進料之 入口線性速度係在0.0 5至0.9 m/s的範圍。下列該烴類進 料之入口線性速度係有用的入口線性速度下限:〇 ·0 5、〇. 1 、0_2、0_3、0.4、0.5、〇.6、〇·7 及 〇.8。下列該烴類進料 之入口線性速度係有用的入口線性速度上限:0 ·9、0.8、 0.7、0.6、0.5、0.4、0.3、0·2 及 0·1。該煙類進料之入口 線性速度理想上落在任一個上述下限及任一個上述上限之 間的範圍,只要下限係小於或等於上限。該烴類進料之入 -19- 200909572 口線性速度在一個具體例中可以0 · 0 5至1範圍的量存在 ,或者〇.!至0_5,或者〇.4至〇 9,或者〇 5至〇 85 ,或 者〇_2至0.5,或者在另一個具體例中〇·5至〇.6。 我們意外發現該第一預熱區之第一預熱段中的焦炭形 成係可忽略的。再者’只要至少1重量%該烴類進料以液 相排出該第一預熱區’該第一預熱區的焦炭形成將降至最 少。因此可選擇該烴類進料之入口線性速度以維持最適熱 傳效率及低壓降。特定進料的適當線性速度將同時改善熱 傳效率且降低該第一預熱段下游的壓降。 該預熱烴類進料33排出該第一預熱段7且接著視需 要與流體3 5混合。此流體可爲液態烴類、水、蒸汽或其 混合物。較佳的流體爲水。該流體的溫度可爲低於、等於 或高於該預熱進料的溫度。該預熱烴類進料與該流體的混 合可在該蒸汽裂解爐1內側或外側進行,但是較佳爲在該 爐內側進行。該混合可使用此技藝中習知的任何混合裝置 完成。 該預熱進料在約100至3 50 t範圍的溫度下排出該 第一組熱交換管1 5,較佳地在丨5 〇至3 2 5 t的範圍,更 佳地在160至3〇〇 。〇的範圍,佳地在丨7〇至3〇〇 °C的範 圍。在一個較佳具體例中,該預熱烴類進料3 3以實質液 相排出該第一預熱段7。 在一個依據此揭示內容的較佳具體例中,第一稀釋流 37係與該預熱烴類進料混合。在一些具體例中’該第一稀 釋流包含蒸汽、水、氮、氫及烴類中之至少其一。較佳地 -20- 200909572 該第一稀釋流包含蒸汽及水之至少其一。該第一稀釋流較 佳可在所得的蒸汽混合物進入蒸汽裂解爐1對流段3的第 一預熱區5第二預熱段9以輻射段煙道氣額外加熱之前注 入該預熱烴類進料。 該第一稀釋流可具有高於、低於或同於預熱烴類進料 的溫度,但是較佳爲大於該預熱烴類進料的溫度且用於局 部蒸發該預熱烴類進料。或者,該第一稀釋流係於注入該 預熱烴類進料之前過度加熱。 該預熱烴類進料、第一稀釋流及視需要地流體的混合 物係在蒸汽裂解爐1對流段3之第二預熱區9中進一步加 熱以製造蒸氣-液體混合物。此加熱可,以非限定的方式 ,使該進料混合物通過位在該第二預熱區9內的第二組熱 交換管1 7且因此被該爐之輻射段的熱煙道氣加熱而完成 。如此受熱的混合物3 9以混合物流的形式離開該對流段 〇 該蒸氣-液體混合物流3 9溫度受到該進料中回收/蒸發 最多的揮發物限制同時避免該爐管中的焦化或從該容器運 輸混合物至該爐的管路及容器中的焦化。該蒸氣-液體流 3 9溫度的選擇亦係由該進料材料的組成決定。當該進料含 有較大量較輕質烴類時,該混合物流3 9的溫度可爲較低 。當該進料含有較大量低揮發性烴類時,該蒸氣-液體混 合物流3 9的溫度應該較高。藉由小心選擇混合物流溫度 ,此揭示內容可發現各種不同進料材料的應用。 經常地,該蒸氣-液體混合物流3 9的溫度係設定且控 -21 - 200909572 制在3 1 5與5 10°C之間,較佳爲3 70與490 °C之間,更佳 爲400與480 °C之間,且最佳爲430與475 °C之間。這些 値將隨沸騰曲線及該進料中的濃縮揮發物改變。 該蒸氣-液體混合物流3 9中的液相量係以該蒸氣-液體 混合物流39中的烴類總重量計算出來。該蒸氣-液體混合 物流39包含至少1重量%液體。該蒸氣-液體混合物流39 的液相量受到該進料中回收/蒸發最多的揮發物限制同時 避免該爐管中的焦化或從該容器運輸混合物至該爐的管路 及容器中的焦化。該蒸氣-液體流3 9溫度的選擇亦係由該 進料材料的組成決定。當該進料含有較大量較輕質烴類時 ,該混合物流3 9的液體含量可設得較低。當該進料含有 較大量低揮發性烴類時,該蒸氣-液體混合物流3 9的液體 含量應該設得較高。藉由小心選擇混合物流的液體含量, 此揭示內容可發現各種不同進料材料的應用。 在一些具體例中,該蒸氣-液體混合物流的液體含量 係在1重量%至99重量%的範圍。在其他具體例中,該蒸 氣-液體混合物流的液體含量係在2重量%至60重量%的 範圍。在又其他具體例中,該蒸氣-液體混合物流的液體 含量係在5重量%至30重量%的範圍。下列該蒸氣-液體 混合物流的液體含量係有用的液體含量下限:1、2、3、4 、5、6、7、8、9、1 0、1 1、1 2及1 5。下列該蒸氣-液體 混合物流的液體含量係有用的液體含量上限:99、90、80 、70、60、50、40、30、25、20 及 15。該蒸氣-液體混合 物流的液體含量理想上落在任一個上述下限及任一個上述 -22- 200909572 上限之間的範圍,只要下限係小於或等於上限。 在較佳的具體例中’包含蒸汽、水、氮、_ Λ ^ ®及烴類中 之至少其一的稀釋流4 1,較佳主要爲蒸汽及/或水,係 在一組熱交換管43中加熱至想要的溫度,較佳爲過度加 熱。自該對流段3抽出所得的稀釋流45且視需要地,分 成第二稀釋流47,該第二稀釋流ο在該容器53之前與自 第二預熱段9抽出的蒸氣-液體混合物3 9混合, 7乂芳分稀 釋流49,該旁分稀釋流49繞過該容器且換成在該容器的 蒸氣部分在該爐的輻射段中裂解之前與該蒸氣部分混合。 在一個具體例中,此揭示內容可以作爲閃蒸第二稀釋流4 7 的所有稀釋流45 —起操作而沒有旁分流49。或者,此揭 示內容可以所有導向旁分流49的所有稀釋流45 一起操作 而沒有桌一稀釋流4 7。在依據此揭示內容的較佳具體例中 ,該第二稀釋流47對旁分流49的比例應該較佳爲1 : 2〇 至20. 1’且最佳爲1: 2至2: 1。該第二稀釋流47係與 該蒸氣-液體混合物流45在該容器53中閃蒸之前混合以 形成閃蒸流5 1。 較佳地’該第一稀釋流係在分開且該蒸氣-液體混合 物混合之前在該爐對流的過度加熱段4 3中過度加熱。該 閃蒸流4 7加至該蒸氣-液體混合物流3 9將確保該混合物 幾乎所有揮發性成分在進入該容器53之前蒸發。 該蒸氣-液體混合物及第二稀釋流的混合物5 1係接著 加入用於分離成下列兩部分的容器5 3 :主要包含揮發性烴 類的蒸氣部分及主要包含低揮發性烴類的液體部分。蒸氣 -23- 200909572 部分較佳以頭部蒸氣流5 5的方式自該容器5 3移除。^ / & 3的弟 氣流5 5,較佳地,供回至該蒸汽裂解爐1之對流& /ft 二預熱區1 1供選擇性加熱及進一步透過連通管59 1/' # > 自該 該蒸汽裂解爐的輻射段供裂解。以底部流5 7的方% 容器53移除分離的液體部分。 在至少一個容器中進行閃蒸。較佳地,該閃蒸1^ c 率 14〇〇 沒有迴流的一階段程序。該容器5 3正常在27 5 # -¾裙相間 kPa-a壓力下操作且在進入該容器53之前其溫度通吊 或稍微低於該混合物51的溫度。經常地,該容器5 3 力爲275至1400 kPa-a且溫度爲310至510 °C。較佳地’ 該容器53的壓力爲600至1100 kPa-a且溫度爲370至 490 °C。更佳地’該容器53的壓力爲700至1000 kPa-a且 溫度爲4〇〇至480 °C。最佳地,該容器53的壓力爲700至 760 kPa-a且溫度爲430至48〇〇c。根據該閃蒸流的溫度, 進入該容器53的50至95%混合物經常被蒸發爲該容器53 的上方部分’較佳爲60至95%,更佳爲65至95%,且最 佳爲7 0至9 5 %。 在該容器53中,該蒸氣部分55通常含有小於400 ppm的焦炭前驅物’較佳爲小於1〇〇 ppm,更佳爲小於8〇 ppm ’且最佳爲小於5 〇 ppm。該蒸氣部分富含揮發性烴類 (例如’ 5 5至7 0體積。/(> )及蒸汽(例如,3 〇至4 5體積。/。 )。該蒸氣相的沸騰終點正常低於7 6 〇 〇c。 持續自該容器5 3移除的蒸氣部分流5 5較佳爲藉由該 爐之對流段的煙道氣! 2在該蒸汽裂解爐下方對流段丨〗中 -24- 200909572 過度加熱至,例如,4 3 0至6 5 0 °C範圍的溫度。接著該蒸 氣部分係加入該蒸汽裂解爐的輻射段被裂解。 自該容器5 3移除的蒸氣部分流5 5可視需要在加入該 爐下方對流段1 1之前與旁分蒸汽流49混合。 裝置具體例 現在提供一種適於將烴類進料蒸汽裂解爲輕質烯烴之 裝置,其包含: (a) 蒸汽裂解爐,其包含適於提供輻射熱和熱煙道 氣的輻射段燃燒器及包含第一組、第二組及第三組熱交換 管的對流段; (b ) 以0. 1至0.9 m/s範圍的線性速度將該烴類進 料供入該第一組熱交換管的機構(m e an s ); (〇 ) 維持該烴類進料在低於3 5 0 °C的溫度下排出該 第一組熱交換管的機構; (d ) 同時供應第一稀釋流與來自(c )的預熱烴類 產物至少一部分至適於蒸發低於99重量%的烴類進料而形 成蒸氣-液體混合物的機構; (e ) 維持該蒸氣-液體混合物在350至500 °C範圍的 溫度下排出該第二組熱交換管的機構; (f) 適於分離來自步驟(e )的蒸氣-液體混合物之 至少一部分而形成蒸氣部分及液體部分的容器;及 (g ) 將來自步驟(f )的蒸氣部分之至少一部分供 至該第三組熱交換管且進一步至該蒸汽裂解爐的輻射段之 -25- 200909572 機構。 用於步驟(b )及(g )中供入的機構可爲任何 抽機制,或用於輸送材料的管路。用於步驟(c ) 2 中維持的機構可爲任何用於控制溫度、壓力、流速 控制及/或控制閥的傳統機制。一種用於維持該蒸J 混合物在3 5 0至5 0 0°C範圍的溫度下排出該第二組 管之機制爲在(d )之前將流體,如水,注入來自 預熱烴類產物。步驟(f )中的容器可爲能分離來 (e )的蒸氣-液體混合物而形成蒸氣部分及液體部 何類型的容器、槽或罐。在一個具體例中,步驟 的容器爲閃蒸罐。在此揭示內容的另一個具體例中 (f )中的容器爲柱、管、蒸餾塔、閃蒸塔及槽中 其一。 實施例 下列實施例例示本案揭示內容的一些具體例且 圖限制本案揭示內容的範圍。比較例1、2、3、4 例1、2、3及4爲預言性例子,彼等使用模型建 Simulated Sciences Provision 6_0 及 7.1 版來模擬 該p r 〇 V i s i ο η 7 · 1版係用於水力模擬。實施例2 A及 4A爲工廠設施所獲得的結果。 下列進料,A、B 1、C及D1係用於表1所示的 該等進料B2及D2係於實施例2A及4A中測試。 料的特徵爲使用1 )關於液體體積百分比沸點 傳統泵 泛(e ) 、反饋 R -液體 熱交換 (c )的 自步驟 分之任 (f)中 ,步驟 之至少 並非試 及實施 立程式 ,其中 實施例 模擬。 這些進 扭線的 -26- 200909572 ASTM 及/或2 層析法 ,該曲 定義的 線的圖 8 6 (在常壓下蒸餾石油產物的標準試驗方法); 關於重量百分比沸點曲線的A S T M D 2 8 8 7 (藉由 石油部分沸點範圍蒸分佈的標準試驗方法)方法 爲對應在1 5 / 5 ( 1 5個理論板,5 : 1迴流比)下 驗室技術或TBP之溫度對比於質量百分比蒸餾曲 。所有分子量値爲重量平均分子量。 -27- 200909572 表 1 進料: A B1 B2 C D1 D2 比重(g/ml) 0.8769 0.821 0.8302 0.8566 0.9082 0.8787 D86IBP(0.5 體積%),(。〇 63 62 122 236 309 277 D86 5 體積%,(°C) 143 315 D86 10 體積%,(。〇 131 99 172 290 362 346 D86 20 體積%,(。〇 219 377 D86 30 體積%,(°〇 225 159 257 319 403 398 D86 40 體積 288 413 D86 50 體積%,(°C) 307 240 318 342 434 431 D86 60 ffi*%,(°C) 347 455 D86 7〇 mm.%,CC) 400 316 375 364 466 490 D86 80 體積%,(°C) 405 553 D86 90 體積%,(。〇 535 472 456 394 508 711 D86 95 體積%,(。〇 515 815 D86EP(99_5 體積%),(。〇 662 626 643 440 546 871 分子量, 210 163 250 293 422 479 TBP(15/5)IBP(0_5 重量%),(°C) -1 -11 79 196 251 208 TBP(15/5)5 重量%,(°〇 79 35 119 232 335 307 TBP(15/5)10重量%,(°C) 119 73 154 287 360 346 TBP( 15/5)20 重量%,(。〇 186 118 219 316 396 388 TBP(15/5)30 重量%,(°C) 238 157 264 324 421 416 TBP(15/5)40 重量%,(°C) 285 221 301 333 442 437 TBP(15/5)50 重量%,(°〇 333 251 336 350 462 457 TBP( 15/5)60 重量%,(°C) 384 289 368 366 482 485 TBP( 15/5)70 重量0/〇,(°C) 438 350 401 378 503 534 TBP(15/5)80 重量%,(。〇 500 425 438 389 529 626 TBP( 15/5)90 重量%,(°〇 606 535 503 413 558 847 TBP( 15/5)95 重量%,(°C) 685 630 590 440 580 950 TBP(15/5)EP (99.5 重量%,(°C) 799 777 959 465 621 1032 黏度 @49°C,896kPa-a,(CP) 4.1564 1.708 3.21 5.0996 37.479 42.21 -28- 200909572 比較例1 進料A,原油進料,具有上述表1所列示的性質,係 作爲此實施例的烴類進料。在127 °C的溫度、2413 kPa-a 的壓力及111.8噸/hr的速率下將此具有比重0.8 769 ml/g 及平均分子量2 1 0的原油進料A供至該對流段3之第一組 熱交換管1 5的入口。該進料A,在此點時全爲液體,係 途經具有8排管子的第一組熱交換管1 5。該進料a係在 1 · 2 8 m / s的線性速度下供至該第一組對流段熱交換管1 5 的入口。該進料A係加熱至181°C的溫度且在2393 kPa-a 的壓力下以全液相排出。橫越該對流段之第一組熱交換管 1 5的壓降爲約2 1 k P a。 該受熱供料A以液相排出該第一組熱交換管1 5且與 流量3 0噸/ hr的蒸汽混合。與蒸汽混合之後,該烴類進 料之一部分係蒸發以形成具有以烴類進料及蒸汽合倂流的 總重量計7 1重量%液相的蒸氣-液體混合物。 後繼將該蒸氣-液體混合物供至具有比該第一組熱交 換管1 5的管直徑大約1 3 %之管直徑的第二組熱交換管1 7 。該蒸氣-液體混合物係在1 2 m/s的線性速度下供至該第 二組熱交換管17,其中該蒸氣-液體混合物係進一步加熱 至45 8 °C的溫度,且在該溫度及約952 kPa-a的壓力下排 出該弟一組熱交換管17。在該第二組熱交換管17的出口 處,排出該第二組熱交換管1 7的液體重量百分比當時係 下降至整個流的1 〇重量%。橫越該對流段之第二組熱交換 管1 7的壓降爲約1 448 kPa。橫越該對流段之第一組熱交 -29- 200909572 換管15及第二組熱交換管17的合倂壓降爲1 469 kPa。 該蒸氣-液體混合物在約3 5 m/s的線性速度下排出該 蒸汽裂解爐之對流段中的第二組熱交換管1 7且與流量約 2.7噸/hr在9 5 2 kPa-a的壓力下過度加熱至482°C的蒸汽 混合。所得的蒸氣-液體混合物在45 8 t的溫度及811.7 kPa-a的壓力下流至蒸氣-液體分離器53且由於添加過度 加熱流而具有佔整個流7重量%之液體重量百分比。 實施例1 進料A,原油進料,具有上述表1所列示的性質,係 作爲此實施例的烴類進料。在127°C的溫度、95 8 kPa-a的 壓力及111.8噸/hr的速率下將此具有比重0.8 7 6 9 ml/g及 平均分子量210的原油進料A供至該對流段3之第一組熱 交換管1 5的入口。該進料A,在此點時全爲液體’係途經 具有8個並行管子的第一組熱交換管15。該進料A係在 0.5 5 m/s的線性速度下供至該第一組對流段熱交換管1 5的 入口。該進料A係加熱至1 81 °C的溫度且在967 kPa-a的 壓力下以全液體排出。橫越該對流段之第一組熱交換管1 5 的壓降爲約-9 kP a (負壓降部分由於重力造成)。 該受熱供料A以液相排出該第一組熱交換管1 5且與 流量3 0.5噸/ h r在1 1 4 2 k P a - a及2 1 1。(:下的蒸汽混合。與 蒸汽混合之後,該烴類進料之一部分係蒸發以形成具有以 烴類進料及蒸汽合倂流的總重量計70.6重量%液相的蒸 氣-液體混合物。後繼將該蒸氣-液體混合物供至第二組熱 -30- 200909572 交換管1 7。該蒸氣-液體混合物係在1 1 _ 9 m/S的線性速度 下供至該第二組熱交換管1 7,其中該蒸氣-液體混合物係 進一步加熱至4 5 8 °c的溫度,且在該溫度及約8 1 9 kP a- a 的壓力下排出該第二組熱交換管1 7。在該第二組熱交換管 17的出口處,排出該第二組熱交換管17的液體重量百分 比當時係下降至整個流的1 0重量%。橫越該對流段之弟一 組熱交換管1 7的壓降爲約1 45 kPa。橫越該對流段之第一 組熱交換管1 5及第二組熱交換管1 7的合倂壓降爲1 3 6 kPa 〇 該蒸氣-液體混合物在約34.7 m/s的線性速度下排出 該蒸汽裂解爐之對流段中的第二組熱交換管1 7且與流量 約2.7 噸/hr在819 kPa-a的壓力下過度加熱至4821:的蒸 汽混合。所得的蒸氣-液體混合物在45 8 t的溫度及811.7 kPa-a的壓力下流至蒸氣-液體分離器53且由於添加過度 加熱流而具有佔整個流7重量%之液體重量百分比。 比較例2 進料B 1,輕質原油進料,具有上述表1所列示的性 質’係作爲此實施例的烴類進料。在8 8 °C的溫度、1 8 9 6 kPa-a的壓力及93.4噸/hr的速率下將此具有比重0.821 m 1 /g及平均分子量1 63的原油進料B 1供至該對流段3之 第一組熱交換管1 5的入口。該進料B 1,在此點時全爲液 體’係途經具有8個並行管子的第一組熱交換管1 5。該進 料B 1係在1 .2 3 m/s的線性速度下供至該第一組對流段熱 -31 - 200909572 交換管1 5的入口。該進料B 1係加熱至丨44 °C的溫度且在 1875 kPa-a的壓力下以全液體排出。橫越該對流段之第一 組熱交換管1 5的壓降爲約2 1 kPa。 該受熱供料B 1以液相排出該第一組熱交換管1 5且與 流量2 7噸/hr的蒸汽混合。與蒸汽混合之後,該烴類進 料之一部分係蒸發以形成具有以烴類進料及蒸汽合倂流的 總重量計6 3重量%液相的蒸氣-液體混合物。 後繼將該蒸氣-液體混合物供至具有比該第一組熱交 換管1 5的管直徑大約1 9 _ 4 %之管直徑的第二組熱交換管 1 7。該蒸氣-液體混合物係在1 〇 m / s的線性速度下供至該 第二組熱交換管1 7,其中該蒸氣-液體混合物係進一步加 熱至446°C的溫度,且在該溫度及約8 5 5 kPa-a的壓力下 排出該第二組熱交換管17。在該第二組熱交換管17的出 口處’排出該第二組熱交換管17的液體重量百分比當時 係下降至整個流的5重量%。橫越該對流段之第二組熱交 換管17的壓降爲約1027 kPa。橫越該對流段之第一組熱 交換管15及第二組熱交換管17的合倂壓降爲1 048 kP a。 該蒸氣-液體混合物在約2 6 m/ s的線性速度下排出該 蒸汽裂解爐之對流段中的第二組熱交換管1 7且與流量約 5 ·5噸/hr在8 5 5 kPa-a的壓力下過度加熱至473 °C的蒸汽 混合。所得的蒸氣-液體混合物在4 4 6。(:的溫度及8 8 9.5 kPa-a的壓力下流至蒸氣-液體分離器53且由於添加過度 加熱流而具有佔整個流4重量%之液體重量百分比。 -32- 200909572 實施例2 進料B 1 ’輕質原油進料,具有上述表1所列示的性 質,係作爲此實施例的烴類進料。在8 8 °C的溫度、9 7 9 kPa-a的壓力及93.4噸/hr的速率下將此具有比重〇.821 ml/g及平均分子量1 63的原油進料b 1供至該對流段3之 第一組熱交換管1 5的入口。該進料b 1,在此點時全爲液 體’係途經具有8個並行管子的第一組熱交換管15。該進 料B 1係在0.49 tn/s的線性速度下供至該第—組對流段熱 交換管15的入口。該進料B1係加熱至144。(:的溫度且在 989 kPa-a的壓力下以全液體排出。橫越該對流段之第— 組熱交換管15的壓降爲約-10 kPa(負壓降部分由於重力 造成)。 該受熱供料B 1以液相排出該第一組熱交換管1 5且與 流量26.6噸/hr在1142 kPa-a及211 °C下的蒸汽混合。與 蒸汽混合之後’該烴類進料之一部分係蒸發以形成具有以 烴類進料及蒸汽合倂流的總重量計6 3重量% '液相的蒸氣1 -液體混合物。 後繼將該蒸氣-液體混合物供至具有比該第一組熱交 換管1 5的管直徑大約44%之管直徑的第二組熱交換管1 7 。該蒸氣-液體混合物係在1 〇 · 5 m/ S的線性速度下供至該 第二組熱交換管17,其中該蒸氣-液體混合物係進一步加 熱至446C的溫度’且在該溫度及約896 kPa-a的壓力下 排出該第二組熱父換管17。在該第二組熱交換管17的出 口處,排出該第二組熱交換管1 7的液體重量百分比當時 -33- 200909572 係下降至整個流的5重量%。橫越該對流段之第二組熱交 換管1 7的壓降爲約1 1 7 kPa。橫越該對流段之第一組熱交 換管15及第二組熱交換管17的合倂壓降爲107 kP a。 該蒸氣-液體混合物在約26.4 m/s的線性速度下排出 該蒸汽裂解爐之對流段中的第二組熱交換管1 7且與流量 約5.5噸/hr在896 kPa-a的壓力下過度加熱至473 t的蒸 汽混合。所得的蒸氣-液體混合物在44 6 °C的溫度及8 8 9.5 kPa-a的壓力下流至蒸氣·液體分離器53且由於添加過度 加熱流而具有佔整個流4重量%之液體重量百分比。200909572 IX. RELATIONSHIP BETWEEN OTHER APPLICATIONS This application claims the benefit and priority of International Patent Application Serial No. PCT/US2007/018486, filed on August 21, 2007. TECHNICAL FIELD The present disclosure relates to a method for producing a light anaerobic hydrocarbon in a steam cracking furnace or a pyrolysis furnace, and more particularly, the steam cracking contains at least 0. A method of hydrocarbon feed of 01% by weight of a low volatility compound. [Prior Art] Steam cracking, also known as pyrolysis, has long been used to crack different hydrocarbon feedstocks into olefins, preferably light olefins such as ethylene, propylene and butene. Traditional steam cracking utilizes a steam cracking furnace with two main sections: the convection section and the radiant section. The hydrocarbon feed is often fed into the convection section of the furnace in liquid form (other than a light feed entering in the form of a vapor), wherein the hot flue gas of the radiant section is typically in indirect contact and heated in direct contact with the steam. And the hydrocarbon feed is evaporated. The evaporated feed and steam mixture is then added to the radiant section where the cracking takes place. The resulting product, including olefins, is retained in the steam cracker for further downstream processing. Conventional steam cracking systems are effective in cracking local quality feeds such as natural gas liquids (NGL), gas oils and light oils. However, the steam cracking economy sometimes prefers to crack as in a non-limiting way, the low-cost heavy feed of the concentrate. The heavy feed is a small amount of gas and gas in the natural gas field, often -5-200909572 Atmospheric resid, also known as the production of atmospheric pipestill bottom and vacuum gas oil, crude oil, vacuum gas oil and atmospheric heavy oil contain high molecular weight. A low volatility component having a boiling point in excess of 590 ° C and/or a coke precursor sometimes having a boiling point in excess of 760 ° C. The low volatility components and/or coke precursors of these feeds will be deposited as coke in the convection section of a conventional steam cracking furnace as the light components evaporate. Downstream of the convection section where the light components are completely evaporated can only tolerate very small amounts of low volatility components and coke precursors, as this coke deposit will normally foul the tubes in the convection section, reducing heat transfer efficiency and increasing the pressure in the tubes. drop. In addition, some light oils are contaminated by heavy crude oils containing low volatility components and coke precursors. Conventional steam crackers do not handle residues, crude oil or many of the gas or light oils that are contaminated with residue or oil contaminated with low volatility and coke precursors. In order to solve the problem of coking, U.S. Patent No. 3,6, 7, 4, 3, the disclosure of which is hereby incorporated by reference herein in A second flash tank is used to remove vapor having a boiling point between 203 and 590 °C. The vapor is cracked into olefins in a steam cracker and the separated liquid from the second flash tank is removed, washed with steam, and used as a fuel. U.S. Pat. It discloses the use of superheated steam to preheat the heavy feed inside or outside the pyrolysis furnace to evaporate 50% of the heavy feed preheat and remove the residue (separate). The vaporized hydrocarbons (mostly -6-200909572 containing light volatile hydrocarbons) are cracked. U.S. Patent No. 5,1,90, 634, the disclosure of which is incorporated herein by reference in its entirety in its entirety in the the the the the the the the the the The hydrogen present in the convection section inhibits the polymerization of the hydrocarbons, thereby inhibiting coke formation. U.S. Pat. This preheated feed is then mixed with a predetermined amount of steam (diluted steam) and then added to a vapor-liquid separator to separate from the separator and remove the low proportions of volatile components and coke precursors in liquid form in the desired proportions. The separated vapor from the vapor-liquid separator is returned to the pyrolysis furnace for heating and cracking. U.S. Patent No. 6,632, 351, the disclosure of which is incorporated herein by reference in its entirety in its entirety, the disclosure of the entire disclosure of the disclosure of the entire disclosure of a first stage preheater in the convection zone, wherein the crude oil or crude oil portion containing the bitumen feed is heated in the first stage preheater to an outlet temperature of at least 37.5 ° C to produce a hot vapor-liquid mixture, Extracting the vapor-liquid mixture from the first stage preheater to a vapor-liquid separator, separating and removing gas from the liquid of the vapor-liquid separator and supplying the removed gas to the first portion provided in the convection zone The second preheater 'further heats the temperature of the gas to a temperature higher than the temperature of the gas exiting the vapor-liquid separator, adds the preheated gas to the radiation zone of the pyrolysis furnace' and pyrolyzes the gas into olefins and related by-products A method for increasing the non-volatiles removal efficiency of a flash tank of a steam cracking system is disclosed in U.S. Patent No. 7,097,75, incorporated herein by reference. The flow of the convection section is converted from a mist flow to an annular flow prior to entering the flash tank to increase removal efficiency. Converting the gas stream from the mist flow to the annular flow system first passes the gas stream through at least one expander and then to a different degree of curvature and forces the flow to change direction at least once. The flow of air from a mist to a ring helps to unite the fine droplets and thereby increase the efficiency of removing them from the vapor phase. U.S. Patent No. 7,138, the disclosure of which is incorporated herein by reference in its entirety, the disclosure the disclosure the disclosure the disclosure the disclosure the disclosure the disclosure the disclosure of The hydrocarbon feed is combined with a fluid and/or a main dilution vapor stream to form a mixture, flashing the mixture to form a vapor phase and a liquid phase, and operating parameters according to at least one selected program (eg, flash before entering the flash tank) The steaming temperature) changes the amount of fluid and/or primary dilution steam stream that is mixed with the hydrocarbon feed. U.S. Patent No. 11/068,615, filed on Jan. 28, 2005, the disclosure of which is incorporated herein by reference in its entirety, the disclosure of the entire disclosure of the disclosure of the disclosure of the disclosure of the disclosure of Forming a stream of the mixture that is flashed to form a vapor phase and a liquid phase, followed by cracking the vapor phase to provide an olefin, and cooling the product effluent in a transfer line exchanger, wherein the amount of fluid mixed with the feed is The operating parameters are varied depending on the selected program (e.g., flashing the mixture stream, i.e., the temperature of the mixture stream). U.S. Patent Application Serial No. 1/851,434, -8-2009, 095, filed on May 21, 2004, the disclosure of which is hereby incorporated by reference in its entirety in its entirety in its entirety in , 474, herein incorporated by reference, which is incorporated herein by reference, for the disclosure of the utility of the disclosure of the disclosure of the disclosure of the disclosure of the disclosure of the entire disclosure of the disclosure of the disclosure of the disclosure of the disclosure of A ring distributor for recirculating quenching oil, an anti-vortex baffle and a hob. Therefore, steam cracking hydrocarbon feeds with a small amount of coke formation require a novel and energy efficient process. The inventors have unexpectedly discovered that coke formation in the first preheating zone of the first preheating zone can be ignored when the feed is fed at an inlet linear velocity below the threshold enthalpy and the feedstock is preheated to a temperature below the threshold enthalpy. . Again, only at least 1 weight. /. The hydrocarbon feed exits the first preheating zone of the liquid phase, and coke formation in the first preheat zone is minimized. The disclosure thus provides for the treatment of hydrocarbon feedstocks by optimizing the linear velocity of the feed entering the preheating section of the steam cracking furnace with a minimum of coke formation in the preheating zone and a feed low pressure drop through the convection section. Steam cracking method. SUMMARY OF THE INVENTION In some embodiments, the present disclosure provides a method for treating a hydrocarbon feed comprising: (a) feeding the hydrocarbon at a linear velocity equal to or less than 0. 9 m/s. a first preheating zone fed to the convection section of the steam cracking furnace; (b) preheating the hydrocarbon feed in the first preheating zone to evaporate less than 99 mils. /. Hydrocarbon feed to form a vapor-liquid mixture; (〇 separating at least a portion of the vapor-liquid mixture to form a vapor portion and a liquid portion; and -9 - 200909572 (d) supplying at least a portion of the vapor portion to the steam Cracking Furnace 0 According to a specific example, the convection section comprises a plurality of heat exchange tubes and the hydrocarbon feed flows into the tubes. In a preferred embodiment, the hydrocarbon feed is between 0_05 and 0. The range of 85 m/s is preferably from 0·1 to 〇·8 m/s' and more preferably 0. 1 to 0. 75 m/s, supplied to the first preheating zone at linear velocity. In a preferred embodiment of the present disclosure, the first preheating zone includes a first preheating section and a second preheating section, wherein the hydrocarbon feed is between 790 and 1 8 2 5 k P a - a (absolute kilopascal) range of pressure, preferably in the range of 690 to 1450 kPa-a, more preferably in the range of 790 to 1400 kPa-a, more preferably in the range of 790 to 1200 kPa-a, and optimal Supplying to the first preheating zone at a temperature in the range of 790 to 1100 kPa-a and 25 to 250 °C to form the first preheating zone at a temperature ranging from about 1 Torr to 3 50 °C Preheating the hydrocarbon product, and then at least a portion of the preheated hydrocarbon product is supplied to the second preheating section along with the first dilution stream to form a discharge at a temperature ranging from 3 5 5 to 500 ° C The vapor-liquid mixture of the first preheating section and comprises at least 1% by weight of the liquid phase based on the total weight of the hydrocarbons in the vapor-liquid mixture. In some aspects, the hydrocarbon feed comprises steam cracked gas oil and residue, gas oil, coker naphtha, steam cracked naphtha, catalytically cracked naphtha, hydrocracked product Recombinant, raffinate recombination, virgin naphtha, crude oil, atmospheric pressure tube still bottom (atmospheric -10- 200909572 pipestill bottom), vacuum tube retort including bottom material, vacuum Gas oil, heavy gas oil, light oil contaminated with crude oil, atmospheric heavy oil, heavy residual oil 'C" residual oil mixture, light oil/residual oil mixture, Fischer-Tropsch liquid, Fischer-Tropsch gas One or more of Fischer-Tropsch, distillate and low-sulfur slag. In one embodiment, from 10 to 99_99% by weight of the hydrocarbon feed boils below 590 °C as measured according to ASTM D-2887. In another embodiment, the hydrocarbon feedstock is boiled at a ratio of from 10 to 95 percent below 5 90 ° C as measured according to ASTM D-2 8 87. In one embodiment, the present disclosure also provides a method of cracking a hydrocarbon feed to a light olefin in a steam cracking furnace having a radiant section combustor and a convection section, the convection section comprising the first set, the second set And a third set of heat exchange tubes, the method comprising: (a) a pressure in the range of 790 to 1825 kP aa, preferably in the range of 790 to 1450 kPa-a, more preferably in the range of 790 to 1400 kPa-a, and more preferably Feeding the hydrocarbon feed in a liquid phase of at least 99% by weight in the range of 790 to 1 200 kPa-a, and preferably in the range of 790 to 1100 kPa-a, and at a temperature in the range of 25 to 250 °C The first set of heat exchange tubes provided in the convection section, and the linear velocity is 〇.  a range of 1 to m·9 m/s; (b) preheating the hydrocarbon feed to form a preheated hydrocarbon product having a temperature below 35 °C; (c) supplying the pre-mixed stream At least a portion of the thermal hydrocarbon product to the second set of heat exchange tubes to evaporate at least a portion of the hydrocarbon feed to form a temperature having a temperature in the range of 350 to 500 ° C and comprising total hydrocarbons in the vapor-liquid mixture And at least a portion of the vapor-liquid mixture to form a vapor portion and a liquid portion; and (e) a step (() d) supplying at least a portion of the vapor portion to the third set of heat exchange tubes and further to the radiant section of the steam cracking furnace to form a product comprising light olefins, wherein the hydrocarbon feed comprises steam cracking gas and residual oil , gas oil, coking gasoline, steam cracking crude gasoline, catalytic cracking crude gasoline, hydrocracking products, recombination, raffinate recombination, distillate, straight-run light oil, crude oil, bottom of atmospheric pressure tube still The truth of the object, including the bottom Tube distillation tank flow, vacuum gas oil, heavy gas oil, crude oil contaminated light oil, atmospheric heavy oil, heavy residual oil, C4/residual oil mixture, light oil residual oil mixture and low sulfur wax residue One or more. In one embodiment, the vapor-liquid mixture has a temperature in the range of 400 to 500 ° C and comprises at least 2% by weight liquid based on the total weight of the hydrocarbons in the vapor-liquid mixture and wherein the hydrocarbon feed is 50 to 99. 99% by weight boiled below 590 °C as measured according to ASTM D-2887. In other embodiments, the vapor-liquid mixture has a temperature in the range of 425 to 500 ° C and comprises at least 3% by weight liquid based on the total weight of the hydrocarbons in the vapor-liquid mixture and wherein the hydrocarbon feedstock is 4 0 to 9 9. 9 9 wt% boils at a temperature lower than 5 90 ° C measured according to ASTM D-2 8 8 7 . In still other embodiments, the vapor-liquid mixture has a temperature in the range of 4 3 5 to 50 (TC range and comprises at least 4% by weight liquid based on the total weight of the hydrocarbons in the vapor-liquid mixture and wherein the hydrocarbon Feeding 30 to 99. 99% by weight is boiling at 5 90 ° C as measured according to ASTM D-28 87 below -12-200909572. In still other embodiments, the vapor-liquid mixture has a temperature in the range of 450 to 5 Torr (TC range and comprises at least 5% by weight liquid based on the total weight of the hydrocarbons in the vapor-liquid mixture and wherein the hydrocarbon feedstock 1〇 to 99. 99% by weight boils at a temperature lower than 5 90 °C measured according to ASTM D-2 8 8 7. There is now provided a device suitable for the steam cracking of a hydrocarbon feed to light olefins wherein the hydrocarbon feed is from 10 to 99. 99% by weight boiling below 590 ° C as measured according to ASTM D-28 87, the apparatus comprising: (a) a steam cracking furnace comprising a radiant section burner adapted to provide radiant heat and having a first set, a second The convection segment j (b ) of the group and the third group of heat exchange tubes is at 0. a linear velocity of 1 to 〇· 9 m / s to supply the hydrocarbon feed to the first set of heat exchange tubes (means); (c) maintaining the hydrocarbon feed below 305 °C a mechanism for discharging the first set of heat exchange tubes at a temperature; (d) simultaneously supplying a first dilution stream with at least a portion of the preheated hydrocarbon product from (c) to a hydrocarbon suitable for evaporation of less than 99% by weight a second set of heat exchange tubes to form a vapor-liquid mixture; (e) maintaining the vapor-liquid mixture at a temperature of 350 to 5 Torr (the temperature at which the second set of heat exchange tubes is discharged; (f a container adapted to separate at least a portion of the vapor-liquid mixture from step (e) to form a vapor portion and a liquid portion; and (g) to supply at least a portion of the vapor portion from step (f) to the third group Mechanism for heat exchange tubes. -13- 200909572 [Embodiment] The present disclosure relates to a method for heating and steam cracking a hydrocarbon feed to produce light olefins, such as ethylene and/or propylene. Typical products of steam cracking furnaces Including, but not limited to, ethylene, propylene, butylene, Diene, benzene, hydrogen, methane and other related olefins, alkanes and aromatic products. Ethylene as the main product 'often in the range of 15 to 30% by weight, based on the weight and composition of the evaporated feed. The method comprises preheating a hydrocarbon, mixing the preheated hydrocarbon with a dilute stream comprising at least one of steam, water, N2, H2, and a hydrocarbon to form a mixture, further preheating the mixture to form a vapor-liquid mixture Separating at least a portion of the vapor-liquid mixture in the vessel to form a vapor portion and a liquid portion, and supplying at least a portion of the vapor portion to the steam cracking furnace for further heating and cracking. Unless otherwise indicated in this disclosure, otherwise Percentages, parts, ratios, etc. are by weight. References to compounds or ingredients include the compound or ingredient itself' and combinations with other compounds or ingredients, such as mixtures of compounds. Further, when used, in concentration or in other amounts Or when the parameters are provided in the form of a preferred upper limit and a preferred lower limit, the salt is understood to be unambiguously disclosed. A preferred range of preferred upper limits 较佳 and preferred lower limits 而不 regardless of whether the ranges are disclosed separately. For this purpose, "low volatility components", sometimes referred to as non-volatile components or residues, are A hydrocarbon feed portion having a nominal boiling point above 59 (TC) as measured according to ASTM D-28 87. This disclosure can contain hydrazine.  The hydrocarbon feed of from 1 to 90% by weight of the low volatility component is suitably carried out. For use in this-14-200909572, "Coke Precursor" is a hydrocarbon feed portion having a nominal boiling point above 7 60 ° C when measured according to ASTM D-28 8 7. This disclosure can contain The hydrocarbon feed of 1 to 90% by weight of the coke precursor is suitably carried out. The boiling point distribution of the hydrocarbon feed is measured by gas chromatography distillation (GCD) according to ASTM D-28 8 7. The phrase "substantially liquid phase" at this point means at least 99% by weight, preferably at least 9 9. 5重量%, more preferably at least 9 9 · 9 wt%, and most preferably at least 99. 99% by weight liquid phase. For example, a stream in a substantially liquid phase means at least 99% by weight of the stream, preferably at least 9 9. 5 wt%, more preferably at least 9 9 -9 wt% ' and optimally at least 9 9. 99% by weight is in the liquid phase. The phrase "vapor fraction" used herein at this time means primarily, preferably at least 75 wt%, more preferably at least 9 wt%, and more preferably at least 95 wt% of the vapor phase. The phrase "liquid portion" at this time means that the portion is mainly 'preferably at least 7.5 wt%', more preferably at least 90 wt%, and more preferably at least 95 wt% is in the liquid phase. At this point the phrase "mainly, or" primarily, means more than 5% by weight. For example, 'diluted stream mainly comprising steam means that the dilution stream contains more than 5% by weight of steam. Hydrocarbon feed. The feed may contain at least a portion, such as at 0. 0 1 to 90 0 weight 1 to 9 〇 by weight, or 5 to 90% by weight of low volatility components and coke precursors. This feed may include, by way of non-limiting example, steam cracking gas and residual %, gas, heating oil, jet fuel, diesel-15-200909572 'kerosene, gasoline, coking gasoline, steam cracking coarse Gasoline, catalytic cracking of crude gasoline, hydrocracking products, recombinants, raffinate recombination, Fischei-Tropsch liquid, Fischer-Tropsch gas, Fischer-Tropsch wax, natural gasoline, distillate, straight run light Oil, atmospheric tube distillation still bottom, vacuum tube distillation tank including bottoms, wide boiling range light oil to gas oil concentrate, heavy non-stratrocolt hydrocarbon stream in refinery, vacuum gas oil, Heavy gas oil, light oil contaminated by crude oil, heavy oil at atmospheric pressure, heavy residual oil, C4/residual oil mixture, light oil/residual oil mixture, hydrocarbon gas/residual oil mixture, hydrogen/residual oil mixture, gas oil/ One or more of the residual oil mixture, crude oil, and low sulfur wax residue. The hydrocarbon feed may have a nominal boiling endpoint of at least 3 15 t, typically greater than 510 ° C 'often greater than 5 90 ° C, for example Greater than 76 (TC. Economically preferred feed is generally low sulfur wax residue 'often Heavy-duty oil, light oil contaminated with crude oil, different residue mixtures, and crude oil. Gas-to-liquid (GTL) technologies used to make medium distillates, such as SMDS, AGC-21, and SSPD, are shown for fuel replacement and higher prices. The great potential of the hydrazine product. The product of any Fischer-Tropsch gas-to-liquid process can be further processed, optionally hydrotreated, fractionated to become a Fischer-Tropsch liquid (also known as Fischer-Tropsch light oil), Fischer-Tropsch gas oil (also It is called Fischer-Tropsch gas and Fischer-Tropsch wax. Fischer-Tropsch light oil, Fischer-Tropsch gas oil and Fischer-Tropsch wax produced by these GTL processes are attractive for steam cracking applications due to their high concentration of normal paraffin components. The high alkane content of the Fischer-Tropsch liquid and Fischer-Tropsch gas allows it to be cracked under the high severity that is not commonly found in conventional feeds. In some specific examples, the method disclosed in the present disclosure has been found to be useful for the use of -16-200909572 A feed comprising at least one weight of a charge liquid, a Fischer-Tropsch gas, a Fischer-Tropsch wax, a crude oil, a crude oil fraction, etc. In other specific examples, the method disclosed in the present disclosure is found to be useful for processing at least 1% by weight A feed of at least one of a Fischer-Tropsch liquid residue, a Fischer-Tropsch gas residue, a Fischer-Tropsch liquid fraction, and a Fischer-Tropsch gas column. Process Description The present disclosure is described below with reference to Figure 1, which is disclosed in the present disclosure. An illustration of one of many specific examples of content. Any number and type of processing steps may be included between the various processing steps described in this disclosure or between the origin and destination described within a processing step. The cracking furnace can be any type of conventional olefin steam cracking furnace for producing low molecular weight hydrocarbon burning, especially including a tubular steam cracking furnace. The tubes in the convection section of the steam cracking furnace can be arranged side by side into a group of heat exchange tubes, or The tubes may be arranged as a single or multiple channels of feed through the convection zone. At the inlet the feed can be dispensed to a plurality of single channel tubes or to a single channel tube. All feeds flow from the tube inlet to the outlet through the single channel tube, and preferably through the entire convection zone. Preferably, the first preheating zone comprises at least one single channel group heat exchange tube disposed in the convection zone of the steam cracking furnace. In a preferred embodiment, the convection zone comprises less than 20 channel tubes divided into two or more groups. The hydrocarbon feed flows through them. In each group, the tubes may be arranged in a spiral or curved arrangement in a row, and each group may have several rows of tubes. The number of channels disposed in the convection zone of the steam cracking furnace useful in this disclosure -17 - 200909572 is in the range of 1 to 20. In some, the number of channels that are configured to be exchanged in the convection zone of a steam cracker useful in this disclosure is 2, 4, 6, 8, 10, 12, 14, and 1 20 . In other embodiments, the number of channels disposed in the heat exchange tubes useful in the convection zone of the present invention is 1, 3, 5 11, 13, 15, 17, or 19. In some embodiments, the steam useful in this disclosure, as exemplified in FIG. 1, includes convection section 3 and radiant section 13 segment 13 including radiant combustion vapor cracking that provides radiant heat and hot flue gas 12 The convection section 3 of the furnace 1 comprises a first preheating zone 5 and a second. The first preheating zone 5 includes a first preheating section 7 and a second preheating first preheating zone and a second preheating zone comprising a plurality of sets of heat exchange tubes. In the example, the first preheating section 7 comprises a first set of heat exchange tubes 15 comprising a second set of heat exchange tubes 17, and a second set of heat exchange tubes 19 in the second preheating zone. The steam cracking furnace 1 also contains: ξ It is understood that the steam cracking furnace 1 can include any number of processing equipment, valves, injection points, meters, meters, and control devices. Will contain at least a part, such as 〇.  〇1 to 90% by weight, 1% by weight or 5 to 90% by weight of the low volatility component and the coke precursor material 31 are supplied to the first first preheating section 7 of the convection section 3 of the steam cracking furnace 1, and Preheat it in it. The hydrocarbon feed is familiar to those skilled in the art in any manner. In any event, it is preferred that the hot flue gas 12 containing the radiant section 13 of the furnace is in indirect contact with the hydrocarbon feed of the seventh. This can be done, in a non-limiting manner, in the specific example of the heat transfer 6, 18 or steam cracking, 7, 9, cracking furnace 1 i. The radiator. The steam preheating zone 1 1 ; segment 9. The one specific to the second pre-U is included. Salty, such as, pump. Up to 90 weights of hydrocarbons into the preheating zone 5 can be heated by the heating pack a preheating section to feed the hydrocarbons-18-200909572 through the first set of heat exchange tubes 1 located in the first preheating section 7 And finished. Maintain the pressure of the hydrocarbon feed to the inlet of the first preheat section of the convection zone to ensure that the pressure is less than! 82 5 kPa-a' is preferably less than 1 480 kPa-a, more preferably less than 1 400 kPa-a ' and most preferably less than 1 200 kPa-a. In some embodiments, maintaining the pressure of the hydrocarbon feed to the inlet of the first preheating section of the convection zone to ensure a pressure in the range of 790 to 1 825 kPa-a' more preferably at 790 to 1480 kPa-a More preferably at 790 to 1450 kPa-a' and more preferably at 790 to 140 G kPa-a, still more preferably at 790 to 1200 kPa-a, and optimally at 790 to 00 kPa-a, and at a temperature of 25 To 250. a range of (:), often controlling the feed rate of the hydrocarbon feed to the inlet of the first preheating section of the convection zone at 50 to 20 °C °C to maintain the inlet linear velocity of the hydrocarbon feedstock less than 1 .  1 m/s ' is preferably less than 1 m/s ‘ more preferably less than 0. 9, and more preferably 0. 05 to 〇·9 m/s ‘and even more preferably from 0·1 to 〇·9 m/s, and even more preferably 0. 2 to 0. 8 m/s. In a preferred embodiment of the disclosure, the inlet linear velocity of the hydrocarbon feed is less than _ _ 9 m / s. In other specific examples, the inlet linear velocity of the hydrocarbon feed is at 0. 0 5 to 0. A range of 9 m/s. The following inlet linear velocity of the hydrocarbon feed is a useful lower limit of the inlet linear velocity: 〇 · 0 5, 〇.  1, 0_2, 0_3, 0. 4, 0. 5, hehe. 6, 〇·7 and 〇. 8. The following inlet linear velocity of the hydrocarbon feed is a useful inlet linear velocity upper limit: 0 · 9, 0. 8, 0. 7, 0. 6, 0. 5, 0. 4, 0. 3, 0·2 and 0·1. The inlet linear velocity of the tobacco feed desirably falls within the range between any of the above lower limits and any of the above upper limits, as long as the lower limit is less than or equal to the upper limit. The hydrocarbon feed enters -19-200909572. The linear velocity of the mouth can exist in the range of 0 · 0 5 to 1 in a specific example, or 〇. ! to 0_5, or 〇. 4 to 〇 9, or 〇 5 to 〇 85, or 〇_2 to 0. 5, or in another specific example 〇·5 to 〇. 6. We have unexpectedly found that the coke formation in the first preheating zone of the first preheating zone is negligible. Further, as long as at least 1% by weight of the hydrocarbon feed is discharged to the first preheating zone in a liquid phase, the coke formation of the first preheating zone will be minimized. The inlet linear velocity of the hydrocarbon feed can thus be selected to maintain optimum heat transfer efficiency and low pressure drop. The proper linear velocity of a particular feed will simultaneously improve heat transfer efficiency and reduce the pressure drop downstream of the first preheat section. The preheated hydrocarbon feed 33 exits the first preheat section 7 and is then mixed with the fluid 35 as needed. This fluid can be a liquid hydrocarbon, water, steam or a mixture thereof. A preferred fluid is water. The temperature of the fluid can be below, equal to, or above the temperature of the preheat feed. The mixing of the preheated hydrocarbon feed with the fluid can be carried out inside or outside the steam cracking furnace 1, but is preferably carried out inside the furnace. This mixing can be accomplished using any mixing device known in the art. The preheating feed exits the first set of heat exchange tubes 15 at a temperature in the range of about 100 to 35 volts, preferably in the range of 丨5 〇 to 3 2 5 t, more preferably 160 to 3 〇. Hey. The range of 〇 is in the range of 丨7〇 to 3〇〇 °C. In a preferred embodiment, the preheated hydrocarbon feed 3 3 exits the first preheat section 7 in a substantial liquid phase. In a preferred embodiment in accordance with the disclosure, a first dilution stream 37 is mixed with the preheated hydrocarbon feed. In some embodiments, the first diluent stream comprises at least one of steam, water, nitrogen, hydrogen, and hydrocarbons. Preferably -20- 200909572 the first dilution stream comprises at least one of steam and water. The first dilution stream is preferably injected into the preheated hydrocarbon before the resulting steam mixture enters the first preheating zone 5 of the convection section 3 of the steam cracking furnace 1 and the second preheating section 9 is additionally heated by the radiant section flue gas. material. The first dilution stream can have a temperature above, below, or the same as the preheated hydrocarbon feed, but is preferably greater than the temperature of the preheated hydrocarbon feed and is used to locally vaporize the preheated hydrocarbon feed. . Alternatively, the first dilution stream is overheated prior to injecting the preheated hydrocarbon feed. The preheated hydrocarbon feed, the first dilution stream, and optionally the mixture of fluids are further heated in a second preheating zone 9 of the convection section 3 of the steam cracking furnace 1 to produce a vapor-liquid mixture. This heating may, in a non-limiting manner, pass the feed mixture through a second set of heat exchange tubes 17 located in the second preheating zone 9 and thus be heated by the hot flue gas of the radiant section of the furnace. carry out. The thus heated mixture 39 exits the convection section as a stream of the mixture. The vapor-liquid mixture stream 39 is temperature-limited by the most recovered/evaporated volatiles in the feed while avoiding coking or the vessel from the vessel. Coking the mixture to the tubes and vessels of the furnace. The choice of temperature for the vapor-liquid stream 39 is also determined by the composition of the feed material. When the feed contains a relatively large amount of lighter hydrocarbons, the temperature of the mixture stream 39 can be lower. When the feed contains a relatively large amount of low volatility hydrocarbons, the temperature of the vapor-liquid mixed stream 39 should be relatively high. The application of various different feed materials can be found by careful selection of the mixture stream temperature. Frequently, the temperature of the vapor-liquid mixture stream 39 is set and controlled from -21 to 200909572 between 3 1 5 and 5 10 ° C, preferably between 3 70 and 490 ° C, more preferably 400. Between 480 ° C and preferably between 430 and 475 ° C. These enthalpies will vary with the boiling curve and the concentrated volatiles in the feed. The amount of liquid phase in the vapor-liquid mixture stream 39 is calculated as the total weight of hydrocarbons in the vapor-liquid mixture stream 39. The vapor-liquid mixture 39 comprises at least 1% by weight liquid. The amount of liquid phase of the vapor-liquid mixture stream 39 is limited by the most recovered/evaporated volatiles in the feed while avoiding coking in the furnace tubes or coking from the vessel to transport the mixture to the tubes and vessels of the furnace. The choice of temperature of the vapor-liquid stream 39 is also determined by the composition of the feed material. When the feed contains a relatively large amount of lighter hydrocarbons, the liquid content of the mixture stream 39 can be set lower. When the feed contains a relatively large amount of low volatility hydrocarbons, the liquid content of the vapor-liquid mixture stream 39 should be set higher. By carefully selecting the liquid content of the mixture stream, this disclosure can find application of a variety of different feed materials. In some embodiments, the vapor-liquid mixture stream has a liquid content ranging from 1% to 99% by weight. In other embodiments, the liquid content of the vapor-liquid mixture stream is in the range of from 2% by weight to 60% by weight. In still other embodiments, the liquid content of the vapor-liquid mixture stream is in the range of from 5% by weight to 30% by weight. The following liquid content of the vapor-liquid mixture stream is a useful lower liquid content: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1, 12 and 15. The liquid content of the following vapor-liquid mixture stream is the upper limit of useful liquid content: 99, 90, 80, 70, 60, 50, 40, 30, 25, 20 and 15. The liquid content of the vapor-liquid mixed stream desirably falls within the range between any of the above lower limits and any of the above upper limits of -22-200909572 as long as the lower limit is less than or equal to the upper limit. In a preferred embodiment, the dilution stream 41 comprising at least one of steam, water, nitrogen, _ Λ ^ ® and hydrocarbons is preferably primarily steam and/or water, in a group of heat exchange tubes. The heating in 43 is carried out to a desired temperature, preferably overheating. The resulting dilution stream 45 is withdrawn from the convection section 3 and, if necessary, divided into a second dilution stream 47, which is preceded by the vessel 53 and a vapor-liquid mixture withdrawn from the second preheating section 9 Mixing, a 7-minute dilution stream 49, the bypass dilution stream 49 bypasses the vessel and is exchanged for mixing with the vapor portion prior to cracking of the vapor portion of the vessel in the radiant section of the furnace. In one embodiment, the disclosure can operate as all of the dilution stream 45 of the flashed second dilution stream 47 without the bypass stream 49. Alternatively, this disclosure can operate with all of the dilution streams 45 leading to the side splits 49 without the table one dilution stream 47. In a preferred embodiment of the disclosure, the ratio of the second dilution stream 47 to the side stream 49 should preferably be 1: 2 〇 to 20.  1' and most preferably 1: 2 to 2: 1. The second dilution stream 47 is mixed with the vapor-liquid mixture stream 45 prior to flashing in the vessel 53 to form a flash stream 51. Preferably, the first dilution stream is overheated in the overheating section 43 of the furnace convection prior to separation and mixing of the vapor-liquid mixture. The addition of the flash stream 47 to the vapor-liquid mixture stream 39 will ensure that almost all of the volatile components of the mixture evaporate prior to entering the vessel 53. The vapor-liquid mixture and the second dilution stream mixture 5 1 are then added to a vessel 5 3 for separation into two parts: a vapor portion mainly comprising a volatile hydrocarbon and a liquid portion mainly comprising a low-volatile hydrocarbon. The vapor -23- 200909572 portion is preferably removed from the vessel 53 in a manner that the head vapor stream 5 5 . ^ / & 3, the gas stream 5 5 , preferably, is supplied back to the convection & / ft 2 preheating zone 1 of the steam cracking furnace 1 for selective heating and further transmission through the communication pipe 59 1 / ' # &gt From the radiant section of the steam cracking furnace for cracking. The separated liquid portion is removed with a square % container 53 of the bottom stream 57. Flashing is carried out in at least one container. Preferably, the flash 1^c rate is 14 〇〇 without a one-stage procedure for reflux. The container 53 is normally operated at a pressure of kPa-a between 27 5 # -3⁄4 skirts and its temperature is hoisted or slightly lower than the temperature of the mixture 51 before entering the container 53. Frequently, the container 53 has a force of 275 to 1400 kPa-a and a temperature of 310 to 510 °C. Preferably, the container 53 has a pressure of 600 to 1100 kPa-a and a temperature of 370 to 490 °C. More preferably, the container 53 has a pressure of 700 to 1000 kPa-a and a temperature of 4 to 480 °C. Most preferably, the container 53 has a pressure of 700 to 760 kPa-a and a temperature of 430 to 48 〇〇c. Depending on the temperature of the flash stream, 50 to 95% of the mixture entering the vessel 53 is often evaporated to the upper portion of the vessel 53' preferably from 60 to 95%, more preferably from 65 to 95%, and most preferably 7 0 to 9 5 %. In the vessel 53, the vapor portion 55 typically contains less than 400 ppm of coke precursor' preferably less than 1 〇〇 ppm, more preferably less than 8 〇 ppm ' and most preferably less than 5 〇 ppm. The vapor portion is enriched with volatile hydrocarbons (e.g., '5 5 to 70 vol. / (> ) and steam (e.g., 3 Torr to 45 vol.). The boiling end of the vapor phase is normally below 7 6 〇〇c. The vapor partial stream 5 5 that is continuously removed from the vessel 5 3 is preferably a flue gas by the convection section of the furnace! 2 in the convection section below the steam cracking furnace -24 -24- 200909572 Excessively heated to, for example, a temperature in the range of 4 30 to 65 ° C. The vapor portion is then lysed by the radiant section of the steam cracking furnace. The vapor partial stream removed from the vessel 53 can be optionally used. Mixing with the bypass steam stream 49 prior to the addition of the lower convection section 1 1 of the furnace. Apparatus specific examples now provide a apparatus suitable for steam cracking a hydrocarbon feed to light olefins comprising: (a) a steam cracking furnace, It comprises a radiant section burner adapted to provide radiant heat and hot flue gas and a convection section comprising the first, second and third sets of heat exchange tubes; (b) at 0.  1 to 0. a linear velocity in the range of 9 m/s to supply the hydrocarbon feed to the first set of heat exchange tubes (me an s); (〇) maintaining the hydrocarbon feed at a temperature below 305 °C a mechanism for discharging the first set of heat exchange tubes; (d) simultaneously supplying a first dilution stream with at least a portion of the preheated hydrocarbon product from (c) to a hydrocarbon feed suitable for evaporation of less than 99% by weight a mechanism for the vapor-liquid mixture; (e) a mechanism for maintaining the vapor-liquid mixture at a temperature ranging from 350 to 500 ° C for discharging the second group of heat exchange tubes; (f) for separating the vapor from step (e) a container forming at least a portion of the liquid mixture to form a vapor portion and a liquid portion; and (g) supplying at least a portion of the vapor portion from step (f) to the third group of heat exchange tubes and further to the radiation of the steam cracking furnace Duan Zhi-25- 200909572 Organization. The means for feeding in steps (b) and (g) may be any pumping mechanism or a conduit for conveying material. The mechanism used in step (c) 2 can be any conventional mechanism for controlling temperature, pressure, flow rate control, and/or control valves. A mechanism for maintaining the vaporized J mixture from exiting the second set of tubes at a temperature in the range of 350 to 500 °C is to inject a fluid, such as water, from the preheated hydrocarbon product prior to (d). The vessel in step (f) may be a vapor-liquid mixture capable of separating (e) to form a vapor portion and a liquid portion of a type of vessel, tank or tank. In one embodiment, the container of the step is a flash tank. In another embodiment of the disclosure, the vessel in (f) is one of a column, a tube, a distillation column, a flash column, and a tank. EXAMPLES The following examples illustrate some specific examples of the disclosure and are intended to limit the scope of the disclosure. Comparative Examples 1, 2, 3, and 4 Examples 1, 2, 3, and 4 are prophetic examples, and they use the model to build Simulated Sciences Provision 6_0 and 7. The 1st version is used to simulate the p r 〇 V i s i ο η 7 · 1 version for hydraulic simulation. Example 2 A and 4A are the results obtained for the factory facility. The following feeds, A, B 1, C and D1 were used for the feeds B2 and D2 shown in Table 1 and tested in Examples 2A and 4A. The material is characterized by the use of 1) the liquid volume percentage boiling point of the conventional pump (e), the feedback R-liquid heat exchange (c), the step (f), the step is at least not a trial and implementation program, wherein Example simulation. -26-200909572 ASTM and/or 2 Chromatography for these twist lines, Figure 86 of the line defined by the curve (Standard test method for distillation of petroleum products under normal pressure); ASTM D 2 8 for weight percent boiling point curves 8 7 (Standard test method for steam distribution by partial boiling point of petroleum) The method is to compare the temperature of the laboratory technology or TBP with the mass percentage distillation at 1 5 / 5 (15 theoretical plates, 5: 1 reflux ratio) song. All molecular weights 値 are weight average molecular weights. -27- 200909572 Table 1 Feed: A B1 B2 C D1 D2 Specific Gravity (g/ml) 0. 8769 0. 821 0. 8302 0. 8566 0. 9082 0. 8787 D86IBP (0. 5 vol%), (.〇63 62 122 236 309 277 D86 5 vol%, (°C) 143 315 D86 10 vol%, (.〇131 99 172 290 362 346 D86 20 vol%, (.〇219 377 D86 30 vol%, (°〇225 159 257 319 403 398 D86 40 volume 288 413 D86 50 vol%, (°C) 307 240 318 342 434 431 D86 60 ffi*%, (°C) 347 455 D86 7〇mm. %,CC) 400 316 375 364 466 490 D86 80 vol%, (°C) 405 553 D86 90 vol%, (.〇535 472 456 394 508 711 D86 95 vol%, (.〇515 815 D86EP (99_5 vol% ), (.〇662 626 643 440 546 871 Molecular weight, 210 163 250 293 422 479 TBP(15/5) IBP (0_5 wt%), (°C) -1 -11 79 196 251 208 TBP(15/5) 5 wt%, (°〇79 35 119 232 335 307 TBP(15/5) 10% by weight, (°C) 119 73 154 287 360 346 TBP( 15/5) 20% by weight, (.〇186 118 219 316 396 388 TBP(15/5)30% by weight, (°C) 238 157 264 324 421 416 TBP(15/5)40% by weight, (°C) 285 221 301 333 442 437 TBP(15/5)50 Weight %,(°〇333 251 336 350 462 457 TBP( 15/5) 60% by weight, (°C) 384 289 368 366 482 485 TBP( 15/5)70 Weight 0/〇, (°C) 438 350 401 378 503 534 TBP(15/5) 80% by weight, (.〇500 425 438 389 529 626 TBP( 15/5) 90% by weight, (°〇606 535 503 413 558 847 TBP( 15/5) 95% by weight , (°C) 685 630 590 440 580 950 TBP(15/5)EP (99. 5 wt%, (°C) 799 777 959 465 621 1032 Viscosity @49°C, 896kPa-a, (CP) 4. 1564 1. 708 3. 21 5. 0996 37. 479 42. 21 -28- 200909572 Comparative Example 1 Feed A, crude oil feed, having the properties listed in Table 1 above, was used as the hydrocarbon feed of this example. At a temperature of 127 ° C, a pressure of 2413 kPa-a and 111. At a rate of 8 tons / hr, this has a specific gravity of 0. A crude oil feed A of 8 769 ml/g and an average molecular weight of 210 is supplied to the inlet of the first set of heat exchange tubes 15 of the convection section 3. The feed A, at this point, is all liquid and passes through a first set of heat exchange tubes 15 having eight rows of tubes. The feed a is supplied to the inlet of the first set of convection heat exchange tubes 15 at a linear velocity of 1 · 28 m / s. The feed A was heated to a temperature of 181 ° C and discharged in a total liquid phase at a pressure of 2393 kPa-a. The pressure drop across the first set of heat exchange tubes 15 of the convection section is about 2 1 k P a. The heated feed A exits the first set of heat exchange tubes 15 in a liquid phase and is mixed with steam having a flow rate of 30 tons/hr. After mixing with the steam, a portion of the hydrocarbon feed is vaporized to form a vapor-liquid mixture having a liquid phase of 71% by weight based on the total weight of the hydrocarbon feed and the vapor turbulent stream. The vapor-liquid mixture is subsequently supplied to a second set of heat exchange tubes 17 having a tube diameter of about 13% larger than the tube diameter of the first set of heat exchange tubes 15. The vapor-liquid mixture is supplied to the second set of heat exchange tubes 17 at a linear velocity of 12 m/s, wherein the vapor-liquid mixture is further heated to a temperature of 45 8 ° C, and at the temperature and about The set of heat exchange tubes 17 is discharged at a pressure of 952 kPa-a. At the outlet of the second set of heat exchange tubes 17, the weight percentage of liquid exiting the second set of heat exchange tubes 17 was then reduced to 1% by weight of the entire stream. The pressure drop across the second set of heat exchange tubes 17 of the convection section is about 1 448 kPa. The combined pressure drop across the first set of heat exchangers -29-200909572 and the second set of heat exchange tubes 17 across the convection section is 1 469 kPa. The vapor-liquid mixture exits the second set of heat exchange tubes 17 in the convection section of the steam cracking furnace at a linear velocity of about 35 m/s and is about 2. 7 tons/hr of steam was overheated to 482 °C at a pressure of 9.5 2 kPa-a. The resulting vapor-liquid mixture is at a temperature of 45 8 t and 811. The pressure of 7 kPa-a flows to the vapor-liquid separator 53 and has a liquid weight percentage of 7% by weight of the entire stream due to the addition of the excessive heating stream. Example 1 Feed A, crude oil feed, having the properties listed in Table 1 above, was used as the hydrocarbon feed of this example. At a temperature of 127 ° C, a pressure of 95 8 kPa-a and 111. At a rate of 8 tons / hr, this has a specific gravity of 0. A crude oil feed A of 8 7 6 9 ml/g and an average molecular weight of 210 is supplied to the inlet of the first set of heat exchange tubes 15 of the convection section 3. The feed A, at this point, is all liquid' passing through a first set of heat exchange tubes 15 having eight parallel tubes. The feed A is at 0. The inlet to the first set of convection heat exchange tubes 15 is supplied at a linear velocity of 5 5 m/s. The feed A was heated to a temperature of 1 81 ° C and discharged as a whole liquid at a pressure of 967 kPa-a. The pressure drop across the first set of heat exchange tubes 15 of the convection section is about -9 kP a (the negative pressure drop is partially due to gravity). The heated feed A discharges the first set of heat exchange tubes 15 in a liquid phase and has a flow rate of 3 0. 5 tons / h r at 1 1 4 2 k P a - a and 2 1 1 . (: under steam mixing. After mixing with steam, one portion of the hydrocarbon feed is vaporized to form having a total weight of hydrocarbon feed and vapor combined turbulence. A vapor-liquid mixture of 6 wt% liquid phase. This vapor-liquid mixture is subsequently supplied to a second set of heat -30-200909572 exchange tubes 17 . The vapor-liquid mixture is supplied to the second set of heat exchange tubes 17 at a linear velocity of 1 1 _ 9 m/s, wherein the vapor-liquid mixture is further heated to a temperature of 4 58 ° C, and The second set of heat exchange tubes 17 is discharged at a temperature of about 8 1 9 kP a- a. At the outlet of the second group of heat exchange tubes 17, the weight percentage of liquid discharged from the second group of heat exchange tubes 17 was then reduced to 10% by weight of the entire stream. The pressure drop across a group of heat exchange tubes 17 of the convection section is about 1 45 kPa. The combined pressure drop across the first set of heat exchange tubes 15 and the second set of heat exchange tubes 17 of the convection section is 136 kPa. The vapor-liquid mixture is about 34. At a linear velocity of 7 m/s, the second set of heat exchange tubes in the convection section of the steam cracking furnace is discharged and the flow rate is about 2. 7 tons/hr was overheated to 4,821: steam mixing at a pressure of 819 kPa-a. The resulting vapor-liquid mixture is at a temperature of 45 8 t and 811. The pressure of 7 kPa-a flows to the vapor-liquid separator 53 and has a liquid weight percentage of 7% by weight of the entire stream due to the addition of the excessive heating stream. Comparative Example 2 Feed B 1, a light crude oil feed having the properties listed in Table 1 above was used as the hydrocarbon feed of this example. At a temperature of 8 8 ° C, a pressure of 1 8 9 6 kPa-a and 93. At a rate of 4 tons / hr, this has a specific gravity of 0. A crude feed B 1 of 821 m 1 /g and an average molecular weight of 1 63 is supplied to the inlet of the first set of heat exchange tubes 15 of the convection section 3. The feed B1, at this point, is all liquid' passing through a first set of heat exchange tubes 15 having eight parallel tubes. The feed B 1 is at 1 . At the linear velocity of 2 3 m/s, the inlet to the first set of convection section heat -31 - 200909572 exchange tube 15 is supplied. The feed B 1 was heated to a temperature of 丨 44 ° C and discharged as a full liquid at a pressure of 1875 kPa-a. The pressure drop across the first set of heat exchange tubes 15 of the convection section is about 21 kPa. The heated feed B1 was discharged in the liquid phase from the first set of heat exchange tubes 15 and mixed with steam having a flow rate of 27 tons/hr. After mixing with the steam, a portion of the hydrocarbon feed is vaporized to form a vapor-liquid mixture having a liquid phase of 6.3 wt% based on the total weight of the hydrocarbon feed and vapor turbulent stream. The vapor-liquid mixture is subsequently supplied to a second set of heat exchange tubes 17 having a tube diameter of about 1 9 _ 4 % of the tube diameter of the first set of heat exchange tubes 15 . The vapor-liquid mixture is supplied to the second set of heat exchange tubes 17 at a linear velocity of 1 〇m / s, wherein the vapor-liquid mixture is further heated to a temperature of 446 ° C, and at the temperature and about The second set of heat exchange tubes 17 are discharged under a pressure of 8 5 5 kPa-a. The percentage by weight of the liquid exiting the second set of heat exchange tubes 17 at the outlet of the second set of heat exchange tubes 17 was then reduced to 5% by weight of the entire stream. The pressure drop across the second set of heat exchange tubes 17 of the convection section is about 1027 kPa. The combined pressure drop across the first set of heat exchange tubes 15 and the second set of heat exchange tubes 17 of the convection section is 1 048 kP a. The vapor-liquid mixture exits the second set of heat exchange tubes 17 in the convection section of the steam cracking furnace at a linear velocity of about 26 m/s and at a flow rate of about 5 · 5 tons / hr at 8 5 5 kPa - Under a pressure of a, the steam was overheated to 473 °C. The resulting vapor-liquid mixture was at 4 4 6 . (: temperature and 8 8 9. The pressure of 5 kPa-a flows to the vapor-liquid separator 53 and has a liquid weight percentage of 4% by weight of the entire stream due to the addition of the excessive heating stream. -32- 200909572 Example 2 Feed B 1 'Light crude oil feed having the properties listed in Table 1 above was used as the hydrocarbon feed of this example. At a temperature of 8 8 ° C, a pressure of 9 7 9 kPa-a and 93. This has a specific gravity at a rate of 4 tons / hr. A crude oil feed b 1 of 821 ml/g and an average molecular weight of 1 63 is supplied to the inlet of the first group of heat exchange tubes 15 of the convection section 3. The feed b1, at this point, is all liquid' passing through a first set of heat exchange tubes 15 having eight parallel tubes. The feed B 1 is at 0. The inlet to the first-stage convection section heat exchange tube 15 is supplied at a linear velocity of 49 tn/s. The feed B1 is heated to 144. The temperature of (: is discharged as a whole liquid at a pressure of 989 kPa-a. The pressure drop across the first heat exchange tubes 15 of the convection section is about -10 kPa (the negative pressure drop is partly due to gravity). The heated feed B 1 discharges the first set of heat exchange tubes 15 in a liquid phase and with a flow rate of 26. 6 tons / hr of steam at 1142 kPa-a and 211 °C. After mixing with the steam, one portion of the hydrocarbon feed is vaporized to form a vapor 1-liquid mixture having a liquid phase of 6.3 wt% of the total weight of the hydrocarbon feed and vapor turbulent stream. The vapor-liquid mixture is subsequently supplied to a second set of heat exchange tubes 17 having a tube diameter of about 44% greater than the tube diameter of the first set of heat exchange tubes 15. The vapor-liquid mixture is supplied to the second set of heat exchange tubes 17 at a linear velocity of 1 〇·5 m/s, wherein the vapor-liquid mixture is further heated to a temperature of 446 C and at the temperature and at about 896 The second set of hot parent exchange tubes 17 is discharged under the pressure of kPa-a. At the outlet of the second set of heat exchange tubes 17, the weight percentage of liquid exiting the second set of heat exchange tubes 17 is then reduced from -33 to 200909572 to 5% by weight of the entire stream. The pressure drop across the second set of heat exchange tubes 17 of the convection section is about 1 17 kPa. The combined pressure drop across the first set of heat exchange tubes 15 and the second set of heat exchange tubes 17 of the convection section is 107 kP a. The vapor-liquid mixture is at about 26. At a linear velocity of 4 m/s, the second set of heat exchange tubes in the convection section of the steam cracking furnace is discharged and the flow rate is about 5. 5 tons/hr was overheated to 473 t of steam mixing at a pressure of 896 kPa-a. The resulting vapor-liquid mixture is at a temperature of 44 6 ° C and 8 8 9. The pressure of 5 kPa-a flows to the vapor/liquid separator 53 and has a liquid weight percentage of 4% by weight of the entire flow due to the addition of the excessive heating flow.

實施例2A 進料B2 ’輕質原油進料,具有上述表1所列示的性 質,係作爲此實施例的烴類進料。在1 1 5 °C的溫度、約 1 3 5 5 kPa-a的壓力及61.5噸/hr的速率下將此具有比重 〇.83〇2 ml/g的輕質原油進料B2供至該對流段3之第一組 熱交換管1 5的入口。該進料B2,在此點時全爲液體,係 途經具有8個並行管子的第—組熱交換管15。該進料B2 係在0·36 m/s的線性速度下供至該第一組對流段熱交換管 1 5的入口。該進料B 2係在該對流段3之第一組熱交換管 1 5中加熱且在估評96重量。液相下排出。 排出該弟一組熱交換管15之受熱供料B2與流量11.6 噸/hr在2999 kPa-a及138。(:下的水及流量2.4噸/ hr在 1138 kPa-a及19PC下的蒸汽混合。與水及蒸汽混合之後 ,該烴類進料之一部分係蒸發以形成具有以烴類進料及蒸 -34- 200909572 汽合倂流的總重量計估計77重量%液相的蒸氣-液體混合 物。 後繼將該蒸氣-液體混合物供至第二組熱交換管1 7。 該蒸氣-液體混合物係在約1.0 7 m / s的估#線性速度下供 至該第二組熱交換管17,其中該蒸氣-液體混合物係進一 步加熱至421°C的溫度,且在該溫度及約834 kPa-a的壓 力下排出該第二組熱交換管17。在該第二組熱交換管17 的出口處,排出該第二組熱交換管17的液體重量百分比 當時係下降至整個流的估計8重量%。橫越該對流段之第 一組熱交換管15及第二組熱交換管17的壓降爲約521 kPa 〇 比較例3 進料C,重質常壓製氣油(HAGO )進料’具有上述 表1所列示的性質,係作爲此實施例的烴類進料。在99 °C 的溫度' 910 kPa-a的壓力及95噸/hr的速率下將此具有 比重0.8566 ml/g及平均分子量293的進料C供至該對流 段3之第一組熱交換管15的入口。該進料C’在此點時 全爲液體,係途經具有8個並行管子的第一組熱交換管1 5 。該進料C係在1 · 3 3 m/s的線性速度下供至該第一組對流 段熱交換管1 5的入口。該進料C係加熱至256 °C的溫度 且在862 kPa-a的壓力下以全液體排出。橫越該對流段之 第—組熟交換管1 5的壓降爲約4 8 k P a。 該受熱供料C以液相排出該第一組熱交換管1 5且具 -35- 200909572 有32 m/s的線性速度。 實施例3 進料C,重質常壓製氣油(HAGO)進料,具有上述 表1所列示的性質,係作爲此實施例的烴類進料。在9 9 °C 的溫度、876 kPa-a的壓力及95噸/hr的速率下將此具有 比重0.8 5 66 ml/g及平均分子量293的進料C供至該對流 段3之第一組熱交換管1 5的入口。該進料C,在此點時 全爲液體’係途經具有8個並行管子的第一組熱交換管1 5 。該進料C係在〇 . 8 2 m/s的線性速度下供至該第一組對流 段熱交換管1 5的入口。該進料C係加熱至256 °C的溫度 且在8 62 kPa-a的壓力下以全液體排出。橫越該對流段之 第一組熱交換管1 5的壓降爲約1 4 kPa。 該受熱供料C以液相排出該第一組熱交換管1 5且具 有3 1 .7 m/s的線性速度。 比較例4 進料D1,低硫真空製氣油(LSVGO )進料,具有上 述表1所列示的性質,係作爲此實施例的烴類進料。在 110°C的溫度、724 kPa-a的壓力及68噸/hr的速率下將 此具有比重0.9〇82 ml/g及平均分子量422的進料D1供至 該對流段3之第一組熱交換管15的入口。該進料D1,在 此點時全爲液體,係途經具有8個並行管子的第一組熱交 換管1 5。該進料D 1係在1 .3 1 m/s的線性速度下供至該第 -36- 200909572 一組對流段熱交換管1 5的入口。該進料d 1係加熱至2 9 2 °C的溫度且在6 83 kPa-a的壓力下以全液相排出。橫越該 對流段之第一組熱交換管1 5的壓降爲約2 1 7 kPa。 該受熱供料D1以液相排出該第一組熱交換管1 5且具 有1 7 m / s的線性速度。 實施例4 進料D1,低硫真空製氣油(LSVGO),具有上述表1 所列示的性質,係作爲此實施例的烴類進料。在Π 〇 r的 溫度、730 kPa-a的壓力及68噸/hr的速率下將此具有比 重0.90 82 ml/g及平均分子量422的進料D1供至該對流段 3之第一組熱交換管15的入口。該進料D1,在此點時全 爲液體,係途經具有8個並行管子的第一組熱交換管1 5。 該進料D 1係在0 · 3 m/s的線性速度下供至該第一組對流段 熱交換管15的入口。該進料D1係加熱至292 °C的溫度且 在75 8 kPa-a的壓力下以全液體排出。橫越該對流段之第 一組熱交換管15的壓降爲約_28 kPa (負壓降部分由於重 力造成)。 該受熱供料D1以液相排出該第一組熱交換管15且具 有17.4 m/s的線性速度。Example 2A Feed B2' Light crude oil feed having the properties listed in Table 1 above was used as the hydrocarbon feed of this example. The light crude oil feed B2 having a specific gravity of 〇.83〇2 ml/g is supplied to the convection at a temperature of 1 15 ° C, a pressure of about 135 kPa-a, and a rate of 61.5 ton / hr. The inlet of the first set of heat exchange tubes 15 of section 3. The feed B2, at this point, is all liquid and passes through a first set of heat exchange tubes 15 having eight parallel tubes. The feed B2 is supplied to the inlet of the first set of convection heat exchange tubes 15 at a linear velocity of 0·36 m/s. The feed B 2 was heated in the first set of heat exchange tubes 15 of the convection section 3 and was evaluated at 96 weights. Discharged in the liquid phase. The heated feed B2 of the set of heat exchange tubes 15 is discharged at a flow rate of 11.6 ton / hr at 2999 kPa-a and 138. (: water and flow 2.4 tons / hr steam mixing at 1138 kPa-a and 19 PC. After mixing with water and steam, one part of the hydrocarbon feed is evaporated to form a hydrocarbon feed and steam - 34- 200909572 The total weight of the steam turbulent flow is estimated to be 77% by weight of the vapor-liquid mixture of the liquid phase. The vapor-liquid mixture is subsequently supplied to the second group of heat exchange tubes 17. The vapor-liquid mixture is at about 1.0. 7 m / s estimated # linear speed to the second set of heat exchange tubes 17, wherein the vapor-liquid mixture is further heated to a temperature of 421 ° C, and at this temperature and a pressure of about 834 kPa-a The second set of heat exchange tubes 17 is discharged. At the outlet of the second set of heat exchange tubes 17, the weight percentage of liquid exiting the second set of heat exchange tubes 17 is then reduced to an estimated 8% by weight of the entire stream. The pressure drop of the first set of heat exchange tubes 15 and the second set of heat exchange tubes 17 of the convection section is about 521 kPa. 〇Comparative Example 3 Feed C, Heavy Normal Pressed Gas Oil (HAGO) Feed' has the above Table 1. The properties listed are for the hydrocarbon feed of this example. At a temperature of 99 °C' The feed C having a specific gravity of 0.8566 ml/g and an average molecular weight of 293 was supplied to the inlet of the first group of heat exchange tubes 15 of the convection section 3 at a pressure of 910 kPa-a and a rate of 95 ton / hr. C' is completely liquid at this point, passing through a first set of heat exchange tubes 15 having 8 parallel tubes. The feed C is supplied to the first group at a linear velocity of 1 · 3 3 m/s. The inlet of the convection section heat exchange tube 15. The feed C is heated to a temperature of 256 ° C and discharged as a whole liquid at a pressure of 862 kPa-a. The first group of cooked exchange tubes 156 across the convection section The pressure drop is about 4 8 k P a. The heated feed C exits the first set of heat exchange tubes 15 in a liquid phase and has a linear velocity of -35-200909572 of 32 m/s. Example 3 Feed C Heavy heavy gas oil (HAGO) feed having the properties listed in Table 1 above as the hydrocarbon feed of this example at a temperature of 9 9 ° C, a pressure of 876 kPa-a and 95 Feed C having a specific gravity of 0.8 5 66 ml/g and an average molecular weight of 293 is fed to the inlet of the first set of heat exchange tubes 15 of the convection section 3 at a rate of ton/hr. Time is all liquid Passing through a first set of heat exchange tubes 15 having 8 parallel tubes. The feed C is supplied to the inlet of the first set of convection heat exchange tubes 15 at a linear velocity of 0.82 m/s. Feed C was heated to a temperature of 256 ° C and discharged as a full liquid at a pressure of 8 62 kPa-a. The pressure drop across the first set of heat exchange tubes 15 of the convection section was about 14 kPa. The heated feed C exits the first set of heat exchange tubes 15 in a liquid phase and has a linear velocity of 3 1 .7 m/s. Comparative Example 4 Feed D1, a low sulfur vacuum gas oil (LSVGO) feed having the properties listed in Table 1 above, was used as the hydrocarbon feed of this example. The feed D1 having a specific gravity of 0.9 〇 82 ml/g and an average molecular weight 422 was supplied to the first set of heat of the convection section 3 at a temperature of 110 ° C, a pressure of 724 kPa-a, and a rate of 68 ton / hr. The inlet of the exchange tube 15. The feed D1, at this point, is all liquid and passes through a first set of heat exchange tubes 15 having eight parallel tubes. The feed D 1 is supplied to the inlet of the 364-200909572 set of convection section heat exchange tubes 15 at a linear velocity of 1.31 m/s. The feed d 1 was heated to a temperature of 2 9 2 ° C and discharged at full pressure in a pressure of 6 83 kPa-a. The pressure drop across the first set of heat exchange tubes 15 of the convection section is about 2 17 kPa. The heated feed D1 exits the first set of heat exchange tubes 15 in a liquid phase and has a linear velocity of 17 m / s. Example 4 Feed D1, a low sulfur vacuum gas oil (LSVGO) having the properties listed in Table 1 above, was used as the hydrocarbon feed of this example. The feed D1 having a specific gravity of 0.90 82 ml/g and an average molecular weight 422 was supplied to the first group of heat exchanges of the convection section 3 at a temperature of Π 〇r, a pressure of 730 kPa-a, and a rate of 68 ton / hr. The inlet of the tube 15. The feed D1, at this point, is all liquid and passes through a first set of heat exchange tubes 15 having eight parallel tubes. The feed D 1 is supplied to the inlet of the first set of convection heat exchange tubes 15 at a linear velocity of 0 · 3 m/s. The feed D1 was heated to a temperature of 292 ° C and discharged as a whole liquid at a pressure of 75 8 kPa-a. The pressure drop across the first set of heat exchange tubes 15 across the convection section is about _28 kPa (the negative pressure drop is partially due to gravity). The heated feed D1 exits the first set of heat exchange tubes 15 in a liquid phase and has a linear velocity of 17.4 m/s.

實施例4A 進料D2,低硫蠟渣(LSWR)進料,具有上述表1所 列示的性質,係作爲此實施例的烴類進料。在93 °C的溫度 -37- 200909572 、約925 kPa-a的壓力及65噸/hr的速率下將此具有比重 0.8787 ml/g的輕質原油進料D2供至該對流段3之第—組 熱交換管1 5的入口。該進料D2,在此點時全爲液體,係 途經具有8個並行管子的第一組熱交換管1 5。該進料d 2 係在0 · 4 4 m/ s的線性速度下供至該第一組對流段熱交換管 15的入口。該進料D2係在該對流段之第一組熱交換管15 中加熱且在估計1⑽重量%液相下排出。 排出該第一組熱交換管15之受熱供料D2與流量2.6 噸/hr在1100 kPa-a及120°C下的水及流量15_6噸/hr在 92 5 kPa-a及2 1 0°C下的蒸汽混合。與水及蒸汽混合之後, 該烴類進料之一部分係蒸發以形成具有以烴類進料及蒸汽 合倂流的總重量計估計94.6重量%液相的蒸氣-液體混合 物。 後繼將該蒸氣-液體混合物供至第二組熱交換管1 7。 該蒸氣-液體混合物係在約23.75 m/s的估計線性速度下供 至該第二組熱交換管1 7,其中該蒸氣-液體混合物係進一 步加熱至45 5 °C的溫度,且在該溫度及約827 kPa-a的壓 力下排出該第二組熱交換管1 7。在該第二組熱交換管1 7 的出口處,排出該第二組熱交換管1 7的液體重量百分比 當時係下降至以整個流的烴類總重量計估計3 2重量% (以 整個流的總重量計估計25重量% )。橫越該對流段之第一 組熱交換管1 5及第二組熱交換管1 7的壓降爲約9 8 kP a。 下表(表2 )列示比較例1至4及實施例1至4的所 有壓降。槪括地,在小於1 . 1 m/s的線性速度下供應進料 -38- 200909572 至該第一組熱交換管,可達成橫越該第一組及尤其是第二 組熱交換器之較低的壓降。實施例1及2之第二組熱交換 管的壓降小於比較例1及2之第二組熱交換管的壓降約9 倍。由於低壓降,此揭示內容的方法具有在較低入口壓力 下供應烴類進料的優點,其省下蒸汽裂解法所需的能量。 再者,較低的入口壓力造成第一組及第二組熱交換管出口 處較低的出口壓力,其具有應用較低壓力之第一及第二稀 釋流的優點。經由降低第一及第二稀釋流所需的壓力,此 揭示內容的方法提供節能且有蒸汽裂解效率的優點。 表2 第一組熱交 換管的壓降 (kPa) 第二組熱交 換管的壓降 (kPa) 第一及第二組熱交 換管的合倂壓降 (kPa) 比較例1 21 1448 1469 實施例1 -9 145 136 比較例2 21 1027 1048 實施例2 -10 117 107 實施例2A 521 比較例3 48 ΝΑ ΝΑ 實施例3 14 ΝΑ ΝΑ 比較例4 41 ΝΑ ΝΑ 實施例4 -28 ΝΑ ΝΑ 實施例4A 98 由前述敘述,熟悉此技藝者可輕易確定此揭示內容的 基本特徵,且不悖離其精神及範圍,可完成此揭示內容的 不同變化及修飾使其適於不同的用法及條件。 -39- 200909572 儘管本發明已經對照特定具體例予以描述且例示,但 是普通熟悉此技藝者將明白此揭示內容本身能做許多變化 而不一定要例示於此。爲此理由,於是,爲了判定本發明 真實範圍的目的應該僅能參照後附的申請專利範圍。 【圖式簡單說明】 第1圖爲此揭示內容的蒸汽裂解爐之槪略流程圖。 【主要元件符號說明】 1 :蒸汽裂解爐 3 :對流段 5 :第一預熱區 7 :第一預熱段 9 :第二預熱段 1 1 :第二預熱區 12 :熱煙道氣 1 3 :輻射段 1 5 :第一組熱交換管 1 7 :第二組熱交換管 1 9 :第三組熱交換管 3 1 :烴類進料 3 3 :預熱烴類進料 3 5 :流體 3 7 :第一稀釋流 -40- 200909572 39 :蒸氣-液體混合物流 4 1 :稀釋流 43 :熱交換管 4 5 :稀釋流 4 7 :第二稀釋流 4 9 ‘·芳分稀釋流 5 1 :閃蒸流 53 :容器 5 5 :頭部蒸氣流 5 7 :底部流 59 :連通管 % -41 -Example 4A Feed D2, low sulfur wax residue (LSWR) feed, having the properties listed in Table 1 above, was used as the hydrocarbon feed for this example. The light crude oil feed D2 having a specific gravity of 0.8787 ml/g is supplied to the convection section 3 at a temperature of 93 ° C -37 - 200909572, a pressure of about 925 kPa-a and a rate of 65 tons / hr - The inlet of the heat exchange tube 15 is grouped. The feed D2, at this point, is all liquid, passing through a first set of heat exchange tubes 15 having eight parallel tubes. The feed d 2 is supplied to the inlet of the first set of convection heat exchange tubes 15 at a linear velocity of 0 · 4 4 m / s. The feed D2 is heated in the first set of heat exchange tubes 15 of the convection section and is discharged at an estimated 1 (10) weight percent liquid phase. The heated feed D2 discharged from the first group of heat exchange tubes 15 and the flow rate of 2.6 tons/hr at 1100 kPa-a and 120 ° C in water and flow rate 15-6 ton / hr at 92 5 kPa-a and 2 1 0 ° C The steam is mixed underneath. After mixing with water and steam, a portion of the hydrocarbon feed is vaporized to form a vapor-liquid mixture having an estimated 94.6 wt% liquid phase based on the total weight of the hydrocarbon feed and the vapor turbulent stream. This vapor-liquid mixture is subsequently supplied to the second set of heat exchange tubes 17. The vapor-liquid mixture is supplied to the second set of heat exchange tubes 17 at an estimated linear velocity of about 23.75 m/s, wherein the vapor-liquid mixture is further heated to a temperature of 45 5 ° C and at this temperature The second set of heat exchange tubes 17 is discharged at a pressure of about 827 kPa-a. At the outlet of the second set of heat exchange tubes 17, the percentage by weight of the liquid exiting the second set of heat exchange tubes 17 is then reduced to an estimated 32% by weight based on the total weight of the hydrocarbons of the entire stream (to the entire stream) The total weight is estimated to be 25% by weight). The pressure drop across the first set of heat exchange tubes 15 and the second set of heat exchange tubes 17 across the convection section is about 9 8 kP a. The following table (Table 2) lists all of the pressure drops of Comparative Examples 1 to 4 and Examples 1 to 4. In addition, feeding the feed -38-200909572 to the first set of heat exchange tubes at a linear velocity of less than 1.1 m/s, achievable across the first set and especially the second set of heat exchangers Lower pressure drop. The pressure drop of the second group of heat exchange tubes of Examples 1 and 2 was less than about 9 times the pressure drop of the second group of heat exchange tubes of Comparative Examples 1 and 2. Due to the low pressure drop, the method of this disclosure has the advantage of supplying a hydrocarbon feed at a lower inlet pressure, which saves the energy required for steam cracking. Moreover, the lower inlet pressure results in a lower outlet pressure at the outlets of the first and second sets of heat exchange tubes, which has the advantage of applying a lower pressure first and second dilution streams. The method of the disclosure provides the advantage of being energy efficient and having steam cracking efficiency by reducing the pressure required for the first and second dilution streams. Table 2 Pressure drop of the first set of heat exchange tubes (kPa) Pressure drop of the second set of heat exchange tubes (kPa) Combined pressure drop of the first and second sets of heat exchange tubes (kPa) Comparative Example 1 21 1448 1469 Implementation Example 1 -9 145 136 Comparative Example 2 21 1027 1048 Example 2 - 10 117 107 Example 2A 521 Comparative Example 3 48 ΝΑ 实施 Example 3 14 ΝΑ ΝΑ Comparative Example 4 41 ΝΑ 实施 Example 4 -28 ΝΑ 实施 Example 4A 98 From the foregoing description, those skilled in the art can readily determine the basic features of the disclosure, and the various changes and modifications of the disclosure can be adapted to different usages and conditions without departing from the spirit and scope thereof. Although the present invention has been described and illustrated with respect to the specific embodiments thereof, it will be apparent to those skilled in the art that For this reason, therefore, for the purpose of determining the true scope of the present invention, reference should be made only to the scope of the appended claims. [Simple description of the drawing] Fig. 1 is a schematic flow chart of the steam cracking furnace for the disclosure. [Main component symbol description] 1 : Steam cracking furnace 3 : Convection section 5 : First preheating zone 7 : First preheating section 9 : Second preheating section 1 1 : Second preheating zone 12 : Hot flue gas 1 3 : radiant section 15: first group of heat exchange tubes 1 7 : second group of heat exchange tubes 1 9 : third group of heat exchange tubes 3 1 : hydrocarbon feed 3 3 : preheating hydrocarbon feed 3 5 : Fluid 3 7 : First Dilution Stream - 40 - 200909572 39 : Vapor - Liquid Mixture Stream 4 1 : Dilution Stream 43 : Heat Exchange Tube 4 5 : Dilution Stream 4 7 : Second Dilution Stream 4 9 '· Fractional Diluted Flow 5 1 : flash stream 53 : container 5 5 : head vapor stream 5 7 : bottom stream 59 : connecting tube % -41 -

Claims (1)

200909572 十、申請專利範圍 1 . 一種用於處理烴類進料之方法,其包含: a. 以等於或小於0 · 9 m/s的線性速度將該烴類進料供 入蒸汽裂解爐之對流段的第一預熱區; b. 在該第一預熱區中預熱該烴類進料以蒸發低於99 重量%的烴類進料而形成蒸氣-液體混合物; c_分離該蒸氣-液體混合物之至少一部分而形成蒸氣部 分及液體部分;及 d.將該蒸氣部分之至少一部分供至該蒸汽裂解爐。 2 如申請專利範圍第1項之方法,其中該烴類進料以 實質液相供入。 3 .如申請專利範圍第1項之方法,其中該第一對流段 包含多個熱交換管組且該烴類進料流入該等管內。 該線性速度f系 該線性速度f系 該第一預熱區 進料係在7 9 0 圍的溫度下供 °C範圍的溫度 該預熱烴類產 二預熱段以形 一預熱段之蒸 4.如申請專利範圍第1項之方法,其中 在0.05至0.85 m/s的範圍。 5 .如申請專利範圍第1項之方法,其ψ 在0. 1至0.80 m/s的範圍。 6 _如申請專利範圍第1項之方法,其中 包含第一預熱段及第二預熱段,其中該煙類 至1 480 kPa-a範圍的壓力及25至25 0。(:範 應至該第一預熱段以形成在約1〇〇至35〇 下排出該第一預熱段之預熱烴類產物,然後 物之至少一部分係以第一稀釋流供應至該第 成在35〇至500 °C範圍的溫度下排出該第 -42. 200909572 氣-液體混合物’以該蒸氣-液體混合物中的烴類總重量計 至少1重量%該蒸氣-液體混合物係呈液相,且以該蒸氣-液體混合物中的烴類總重量計至少60重量%該蒸氣-液體 混合物係呈蒸氣相。 7.如申請專利範圍第1項之方法,其中該烴類進料之 1 〇至9 9.9 9重量%在低於根據A S T M D - 2 8 8 7測量的5 9 0 °C 時沸騰。 8 ·如申請專利範圍第1項之方法,其中該預熱烴類產 物係實質液相。 9 ·如申請專利範圍第1項之方法,其中該蒸氣-液體混 合物具有在400至50(TC範圍的溫度且包含以該蒸氣-液體 混合物中的烴類總重量計至少2重量%液體且其中該烴類 進料之50至99.99重量%在低於根據ASTM D-28 87測量 的5 90 °C時沸騰。 1 0 .如申請專利範圍第1項之方法,其中該蒸氣-液體 混合物具有在4 5 0至5 0 0 t範圍的溫度且包含以該蒸氣液 體混合物中的烴類總重量計至少5重量%液體且其中該烴 類進料之10至99.99重量%在低於根據ASTM D-28 87測 量的5 9 0 °C時沸騰。 1 1 .如申請專利範圍第1項之方法,其進一步包含在 該步驟(c )之前混合第二稀釋流與該蒸氣-液體混合物。 1 2 ·如申請專利範圍第n項之方法,其中第二稀釋流 包含蒸汽。 1 3 _ —種在具有對流段的蒸汽裂解爐中裂解烴類進料 -43- 200909572 之方法’該對流段包含第一組、第二組及第三組熱 ,該方法包含: a_供入具有至少1重量%低揮發性成分及至少 量%焦炭前驅物的烴類進料至該對流段中所提供的 熱交換管’且入口線性速度等於或小於〇_9 m/s ; b.預熱該烴類進料以形成具有低於35(rc之溫 熱烴類產物; c ·以第一稀釋流供應該預熱烴類產物之至少一 該第二組熱交換管以蒸發該烴類進料之至少一部分 具有在350至500 °C範圍的溫度且包含以該蒸氣-液 物中的烴類總重量計至少1重量%液體之蒸氣-液體 d.分離步驟(c)該蒸氣-液體混合物之至少一 形成蒸氣部分及液體部分;及 e ·將步驟(d )該蒸氣部分之至少一部分供至 組熱交換管。 1 4 .如申請專利範圍第1 3項之方法,其進一步 步驟(d )之前混合第二稀釋流至該蒸氣-液體混合$ i 5 _如申請專利範圍第1 3項之方法,其進一步 步驟(e)之前混合該蒸氣部分與包含蒸汽的第三 〇 1 6 .如申請專利範圍第1 3項之方法,其中該烴 之10至95百分比在低於根據ASTM D-2 8 8 7測量的 時沸騰。 交換管 〇_1重 第一組 度的預 部分至 而形成 體混合 混合物 部分以 該第三 包含在 勿。 包含在 稀釋流 類進料 5 90〇C -44- 200909572 1 7 ·如申請專利範圍第1 3項之方法,其中該烴類進料 包含蒸汽裂解製氣油和殘餘物、製氣油、加熱用油、噴射 機燃料、柴油、煤油、汽油、焦化汽油(coker naphtha) 、蒸汽裂解粗汽油、催化裂解粗汽油、加氫裂解產物、重 組物、提餘液重組物、費托液(Fischer-Tropsch liquid) 、費托氣、費托蠟、蒸餾物、原油、常壓管式蒸餾釜底部 物(atmospheric pipestill bottom)、包括底部物的真空管 式蒸餾釜流、真空製氣油、重氣油、受原油污染的輕油、 常壓重油、重質殘油、C4/殘油混合物、輕油殘油混合物 及低硫蠟渣中之其一或更多。 1 8 · —種在具有輻射段燃燒器及對流段的蒸汽裂解爐 中將烴類進料裂解爲輕質烯烴之方法,該對流段包含第一 組、第二組及第三組熱交換管,該方法包含: a.在790至1480 kPa-a範圍的壓力及25至250 °C範圍 的溫度下供入該烴類進料至該對流段中所提供的第一組熱 交換管,且線性速度等於或小於0.9 m/s ; b _熱該烴類進料以形成具有低於3 5 0。(:之溫度的預熱 烴類產物; c .以第一稀釋流供應該預熱烴類產物之至少一部分至 該第二組熱交換管以蒸發該烴類進料之至少一部分而形成 具有在350至5〇(TC範圍的溫度且包含以該蒸氣_液體混合 物中的烴類總重量計至少1重量%液體之蒸氣-液體混合物 * d.分離步驟(C )該蒸氣-液體混合物之至少一部分以 -45- 200909572 形成蒸氣部分及液體部分;及 e.將步驟(d)該蒸氣部分之至少一部分供3 組熱交換管。 19.如申請專利範圍第18項之方法,其中該蒸 混合物具有在400至500。〇範圍的溫度且包含以該 體混合物中的烴類總重量計至少2重量%液體且ί 類進料之50至99·99重量%在低於根據ASTM D-量的5 90°C時沸騰。 2 〇.如申請專利範圍第1 8項之方法,其中該蒸 混合物具有在425至500 °C範圍的溫度且包含以該 體混合物中的烴類總重量計至少3重量%液體且姜 類進料之40至99.99重量%在低於根據AS TM D-量的5 9 0 °C時沸騰。 2 1 .如申請專利範圍第1 8項之方法,其中該蒸 混合物具有在4 5 0至500 °C範圍的溫度且包含以該 體混合物中的烴類總重量計至少5重量%液體,5 烴類進料之1〇至99.99重量%在低於根據ASTM 測量的5 9 0 °C時沸騰。 22 .如申請專利範圍第1 8項之方法,其中該澤 交換管的總壓降由該第一組熱交換管引入點的壓丈 第一組熱交換管排出點算出來係小於1 〇〇 kPa。 2 3.如申請專利範圍第18項之方法,其中該穿 交換管的總壓降由該第二組熱交換管引入點的壓丈 第二組熱交換管排出點算出來係小於5 00 kPa。 .該第二 氣-液體 蒸氣-液 ;中該烴 2 8 8 7 測 氣-液體 蒸氣-液 ;中該烴 28 87 測 氣-液體 蒸氣-液 .其中該 D-2887 丨一組熱 ^減去該 ;二組熱 4咸去該 -46- 200909572 24. —種適於將烴類進料蒸汽裂解爲輕質烯烴之 ,其包含: a·蒸汽裂解爐,其包含適於提供輻射熱和熱煙道 輻射段燃燒器及具有第一組、第二組及第三組熱交換 對流段; b _以等於或小於0 · 9 m / s的線性速度將該烴類進 入該第一組熱交換管的機構; c_維持該烴類進料在低於35〇°C的溫度下排出該 組熱交換管的機構; d. 同時供應第一稀釋流與來自(c )的預熱烴類 至少一部分至適於蒸發低於99重量%的烴類進料之第 熱交換管而形成蒸氣-液體混合物的機構; e. 維持該蒸氣-液體混合物在3 50至5 00°C範圍的 下排出該第二組熱交換管的機構: f·適於分離來自步驟(e )的蒸氣-液體混合物之 一部分而形成蒸氣部分及液體部分的容器;及 g.將來自步驟(f)的蒸氣部分之至少一部分供至 三組熱交換管的機構。 25.如申請專利範圍第24項之裝置’其進一步包 (f)之前混合第二稀釋流至該蒸氣-液體混合物的機1 裝置 氣的 管的 料供 第一 產物 二組 溫度 至少 該第 含在 -47-200909572 X. Patent application scope 1. A method for treating a hydrocarbon feed comprising: a. feeding the hydrocarbon feed to a steam cracking furnace at a linear velocity equal to or less than 0. 9 m/s. a first preheating zone of the section; b. preheating the hydrocarbon feed in the first preheating zone to vaporize less than 99% by weight of the hydrocarbon feed to form a vapor-liquid mixture; c_ separating the vapor - Forming at least a portion of the liquid mixture to form a vapor portion and a liquid portion; and d. supplying at least a portion of the vapor portion to the steam cracking furnace. 2 The method of claim 1, wherein the hydrocarbon feed is supplied in a substantial liquid phase. 3. The method of claim 1, wherein the first convection section comprises a plurality of heat exchange tubes and the hydrocarbon feed flows into the tubes. The linear velocity f is the linear velocity f, and the first preheating zone feed system is at a temperature of 690° for a temperature in the range of °C. The preheating hydrocarbon is produced in a preheating section to form a preheating section. Steaming 4. The method of claim 1, wherein the range is from 0.05 to 0.85 m/s. 5. The method of claim 1, wherein the range is from 0.1 to 0.80 m/s. 6 _ The method of claim 1, wherein the first preheating section and the second preheating section comprise a pressure in the range of 1 480 kPa-a and 25 to 25 0. (: Fan should go to the first preheating section to form a preheated hydrocarbon product that exits the first preheating section at about 1 to 35 Torr, and then at least a portion of the product is supplied to the first dilution stream The first step is to discharge the -42.200909572 gas-liquid mixture at a temperature ranging from 35 Torr to 500 ° C. The vapor-liquid mixture is at least 1% by weight based on the total weight of the hydrocarbons in the vapor-liquid mixture. And the vapor-liquid mixture is at a vapor phase of at least 60% by weight based on the total weight of the hydrocarbons in the vapor-liquid mixture. 7. The method of claim 1, wherein the hydrocarbon feed is 1 〇 to 9 9.9 9 wt% boiling at a temperature lower than 590 ° C measured according to ASTM D 2 8 8 7. 8 The method of claim 1, wherein the preheated hydrocarbon product is a substantially liquid phase 9. The method of claim 1, wherein the vapor-liquid mixture has a temperature in the range of 400 to 50 (TC range and comprises at least 2% by weight liquid based on the total weight of the hydrocarbons in the vapor-liquid mixture and Wherein 50 to 99.99% by weight of the hydrocarbon feed is below The method of claim 5, wherein the vapor-liquid mixture has a temperature in the range of 4500 to 500 t and comprises The total weight of hydrocarbons in the vapor liquid mixture is at least 5% by weight liquid and wherein 10 to 99.99% by weight of the hydrocarbon feed boils below 590 ° C as measured according to ASTM D-28 87. 1 1 The method of claim 1, further comprising mixing the second dilution stream with the vapor-liquid mixture prior to the step (c). 1 2 · The method of claim n, wherein the second dilution The stream comprises steam. 1 3 _ - a method of cracking a hydrocarbon feed in a steam cracking furnace having a convection section - 43 - 200909572 'The convection section comprises a first set, a second set and a third set of heat, the method comprising : a_ feeding a hydrocarbon feed having at least 1% by weight of low volatility components and at least a quantity of coke precursor to the heat exchange tubes provided in the convection section and having an inlet linear velocity equal to or less than 〇_9 m/ b; preheating the hydrocarbon feed to form less than 35 (rc a warm hydrocarbon product; c. supplying at least one of the second set of heat exchange tubes of the preheated hydrocarbon product in a first dilution stream to evaporate at least a portion of the hydrocarbon feed having a range of from 350 to 500 °C a temperature and comprising at least 1% by weight of a vapor-liquid of the liquid in the vapor-liquid. d. separation step (c) at least one of the vapor-liquid mixture forms a vapor portion and a liquid portion; and e At least a portion of the vapor portion of step (d) is supplied to the set of heat exchange tubes. 1 4 . The method of claim 13 , wherein the further step (d ) is followed by mixing the second dilution stream to the vapor-liquid mixture $ i 5 — as in the method of claim 13 of the patent scope, further steps (e) a method of previously mixing the vapor portion with a third gas containing steam. The method of claim 13 wherein the hydrocarbon is 10 to 95 percent lower than measured according to ASTM D-2 8 8 7 It is boiling. The exchange tube 〇_1 is heavier than the first part of the first group to form the body mixture mixture portion and the third portion is included. The method of claim 1, wherein the hydrocarbon feed comprises steam cracking gas and oil, gas, oil, and heating. Oil, jet fuel, diesel, kerosene, gasoline, coker naphtha, steam cracking of crude gasoline, catalytic cracking of crude gasoline, hydrocracking products, recombinants, raffinate recombination, Fischer-liquid (Fischer- Tropsch liquid), Fischer-Tropsch gas, Fischer-Tropsch wax, distillate, crude oil, atmospheric pipestill bottom, vacuum tube stillter flow including bottoms, vacuum gas oil, heavy gas oil, One or more of light oil, atmospheric heavy oil, heavy residual oil, C4/residual oil mixture, light oil residual oil mixture and low sulfur wax residue contaminated by crude oil. 1 8 a method for cracking a hydrocarbon feed into a light olefin in a steam cracking furnace having a radiant section burner and a convection section, the convection section comprising the first, second and third sets of heat exchange tubes The method comprises: a. feeding the hydrocarbon feed to a first set of heat exchange tubes provided in the convection section at a pressure in the range of 790 to 1480 kPa-a and a temperature in the range of 25 to 250 °C, and The linear velocity is equal to or less than 0.9 m/s; b _ heat the hydrocarbon feed to form having less than 350. (preheating the hydrocarbon product at a temperature; c. supplying at least a portion of the preheated hydrocarbon product to the second set of heat exchange tubes in a first dilution stream to evaporate at least a portion of the hydrocarbon feed to form 350 to 5 Torr (temperature in the range of TC and comprising at least 1% by weight of liquid vapor-liquid mixture based on the total weight of hydrocarbons in the vapor-liquid mixture* d. Separation step (C) at least a portion of the vapor-liquid mixture Forming a vapor portion and a liquid portion at -45-200909572; and e. supplying at least a portion of the vapor portion of step (d) to three sets of heat exchange tubes. 19. The method of claim 18, wherein the steamed mixture has At a temperature in the range of from 400 to 500. Torr and comprising at least 2% by weight of liquid based on the total weight of the hydrocarbons in the bulk mixture and from 50 to 99.99% by weight of the feed in an amount less than 5 according to ASTM D-amount The method of claim 18, wherein the steamed mixture has a temperature in the range of 425 to 500 ° C and comprises at least 3 weights based on the total weight of the hydrocarbons in the bulk mixture. % liquid and ginger feed 40 to 99.99% by weight is boiling at a temperature lower than 590 ° C according to the AS TM D- quantity. The method of claim 18, wherein the steamed mixture has a temperature of 4500 to 500 ° The temperature in the range of C comprises at least 5% by weight liquid based on the total weight of the hydrocarbons in the bulk mixture, and from 1 Torr to 99.99% by weight of the 5 hydrocarbon feed boiling below 590 °C as measured according to ASTM. 22. The method of claim 18, wherein the total pressure drop of the exchange tube is less than 1 算出 from the discharge point of the first set of heat exchange tubes of the first set of heat exchange tubes. The method of claim 18, wherein the total pressure drop of the through-exchange tube is calculated by the second group of heat exchange tubes at the point of introduction of the second group of heat exchange tubes, and is less than 5 00 kPa. The second gas-liquid vapor-liquid; the hydrocarbon 2 8 8 7 gas-liquid vapor-liquid; the hydrocarbon 28 87 gas-liquid vapor-liquid. wherein the D-2887 丨 group Heat ^ minus this; two groups of heat 4 salt to the -46- 200909572 24. a suitable for steam cracking of hydrocarbon feedstock into light olefins, its package Included: a. a steam cracking furnace comprising a burner adapted to provide radiant heat and hot flue radiant sections and having a first, second and third set of heat exchange convection sections; b _ to be equal to or less than 0 · 9 m a linear velocity of the s into the first set of heat exchange tubes; c_ maintaining the hydrocarbon feed at a temperature below 35 ° C to discharge the set of heat exchange tubes; d. Supplying a first dilution stream with at least a portion of the preheated hydrocarbon from (c) to a first heat exchange tube suitable for vaporizing less than 99% by weight of the hydrocarbon feed to form a vapor-liquid mixture; e. maintaining the vapor a means for discharging the second set of heat exchange tubes at a temperature in the range of from 3 50 to 500 ° C: f. adapted to separate a portion of the vapor-liquid mixture from step (e) to form a vapor portion and a liquid portion a container; and g. a mechanism for supplying at least a portion of the vapor portion from step (f) to the three sets of heat exchange tubes. 25. The apparatus of claim 24, wherein the further dilution (f) of the second dilution stream is mixed with the vapor-liquid mixture of the apparatus 1 device gas for the first product two sets of temperatures at least the first At -47-
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