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高温煤焦油加氢制取轻质燃料油工艺的运行实践 总被引:3,自引:1,他引:2
文章介绍了黑龙江省七台河宝泰隆煤化工有限责任公司以地产煤焦油为原料,采用加氢精制和加氢裂化等相结合的工艺,将高温煤焦油的馏份油逐步加工,逐步分离,生产出优质燃料油调和组份。在高温煤焦油加氢生产燃料油的过程中,为得到高燃料油收率,必须采用加氢精制和加氢裂化相结合的工艺,为高温煤焦油的加工开辟了新的路线。 相似文献
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介绍了煤焦油加氢反应机理,结合目前国内煤焦油加氢技术和酒钢自产煤焦油性质,对焦油加氢制燃料油的工艺路线、工艺条件、催化剂类型等进行研究,并对酒钢煤焦油加氢制燃料油可行性进行了分析。 相似文献
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本文简单介绍煤焦油及其加工工艺,以介绍煤焦油在高温下加氢制取轻质燃料油的加工过程为重点。在高温下以煤焦油为原料加氢制备轻质燃料油可以增加煤炭副产品的产品价值和使用价值,这也符合开发新能源、原料废物循环使用、环保的政策。显而易见,煤焦油的加工工艺有非常广阔的前景。 相似文献
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高温煤焦油加氢生产燃料油的条件苛刻,工艺复杂,操作难度大。文章介绍了黑龙江省七台河宝泰隆煤化工有限责任公司通过调整生产工艺路线,增加部分未转化油入加氢精制,降低加氢精制的操作难度,提高加氢裂化的稳定性,达到降低加氢精制和加氢裂化在生产工程中相互制约和相互影响的目的,使整套装置的安全性和稳定性得到提高。 相似文献
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Three inputs were necessary to make catalytic hydrogenation of coal possible. One was the ammonia synthesis which, in 1910, introduced high pressure and temperature into the chemical industry. The second was the experimentation by F. Bergius who showed, in 1913, that coal can be liquefied by adding hydrogen at high pressure and temperature. The liquid products were similar to coal tar. They were not of the quality required for gasoline or diesel fuel production. The use of catalysts to refine the coal oil appeared then to be hopeless since coals contained sulfur, a poison for all then known hydrogenation catalysts. The third input was methanol synthesis in 1923. M. Pier found selective, oxidic catalysts that were less sensitive to sulfur than e.g. the metallic catalyst for the ammonia synthesis.In 1924 M. Pier, in the laboratories of the BASF, prepared sulfur resistant coal hydrogenation catalysts: sulfides and oxides of molybdenum, tungsten, and the iron group metals. With these catalysts it became possible to add hydrogen; split carbon-carbon bonds; and eliminate such heteroelements as sulfur, oxygen and nitrogen from coals and oils. Thus fuels were produced that met petroleum fuel specifications.Optimum catalyst action was achieved by subdividing coal hydrogenation into two stages. The coal was converted, with a dispersed catalyst in the “liquid phase”, into middle oil. This was then hydrogenated over fixed bed catalyst, in the “vapor phase”, to gasoline. On this basis a large scale demonstration plant for the liquefaction of central German brown coal was erected in 1927.The development of catalysts for these two stages proceeded on different routes. Liquid phase catalysts were discarded after one pass through the reactor. They were cheap, or used in very small amounts. It was found soon that coal of different rank required different catalysts, and that the mineral matter of the coal played an important role.The first commercially used vapor phase catalysts were of the hydrorefining type. Hydrocracking activity was achieved by using high temperatures. A great step forward was made in 1930 when a special preparation of tungsten disulfide permitted hydrocracking activity at low temperatures. Thus the first essentially dual function catalyst was found. Its hydrocracking activitity was further increased, and gasolines with a higher octane number were obtained by using it on acidic supports such as materials containing alumina-silica.Such supported catalysts were poisoned by the nitrogen compounds present in coal oils. Therefore a refining step for these oils was needed. The vapor phase was subdivided into the “prehydrogenation” (hydrorefining) and “splitting hydrogenation” (hydrocracking) steps. Further development of catalysts with specific functions for these two steps proceeded rapidly. In addition, separate catalysts were developed for the production of gasolines with a high content of aromatics.The various catalysts developed primarily for the hydrogenation of coal derived oils introduced hydrogen processing into the petroleum refining industry. There they were further modified and improved for the processing of petroleum. These improved catalysts, in turn, will be of help to a future coal liquefaction industry. 相似文献
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对鲁奇炉气化炉生产煤气过程副产的煤焦油,利用现有的加氢工艺技术,进行加氢精制,脱除油中的硫、氮、氧等杂原子及对烯烃、芳烃、不饱和烃等加氢饱和过程,生产出优质的石脑油和燃料油,提高了煤焦油的附加值,并保护了环境。 相似文献
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利用小型固定床加氢实验装置,将煤焦油和其加氢后的尾油混合,在温度(360~420)℃、压力(13~15)MPa、氢油体积比(1 500~1 700)∶1和液体体积空速0.25 h-1条件下进行加氢处理,所得产品切割得到的汽油馏分、柴油馏分和尾油馏分,分别占产物质量的16.12%、78.83%和5.05%,且产品中硫、氮含量很低,汽油中硫含量16.7μg·g~(-1),氮含量36μg·g~(-1),柴油中硫含量102.6μg·g~(-1),氮含量97μg·g~(-1),可用作清洁燃料。结果表明,尾油循环在煤焦油加氢过程中对煤焦油具有稀释作用,不仅减轻了设备负荷,同时也可以提高汽油和柴油收率。因此,以煤焦油加氢尾油循环加氢是一种高效、绿色环保制备燃料油的方法。 相似文献