Catalytic dewaxing for low-sulfur or sulfur-containing environments configured in switching mode
A technology for catalytic dewaxing and dewaxing, which is used in the preparation of liquid hydrocarbon mixtures, hydrocarbon oil treatment products, and hydrocarbon oil treatment, and can solve problems such as sulfur content sensitivity
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[0094] In a first embodiment, a method of producing a lubricant base stock is provided. The method includes providing a processing train including a first catalyst being a hydrotreating catalyst and a second catalyst being a dewaxing catalyst. A first feedstock is processed in said processing train under first hydrotreating conditions and first catalytic dewaxing conditions to produce a total liquid product with a pour point of less than about -15°C and a yield of 700°F+ (371°C) For the low-sulfur dewaxing stage, the yields are similar or better than those produced by using conventional dewaxing catalysts, and for the sulfur-containing dewaxing stage, using the catalyst of the present invention, The yield is at least 10 wt % higher, or at least 15 wt % higher, or at least 17 wt % higher than that produced using conventional dewaxing catalysts. The first catalytic dewaxing conditions comprise a temperature of about 400°C or less, and the first hydrotreated feedstock has a Wppm...
Embodiment 1~5
[0151] Processing Example 1 ~ 5-catalyst, feed and processing conditions:
[0152] Table 1 provides a description of the various 130N raffinate hydroconversion (RHC) product feeds used. In some cases, the feed was spiked with Sulfrzol54 and octylamine to simulate no separation stage between the hydrotreating stage and the dewaxing stage (simulating a direct cascade) or to have at least one High-pressure separation stage (simulation of high-pressure separation).
[0153] Table 2 provides parameters for the various dewaxing catalysts used.
[0154] Table 3 provides a description of the various dewaxing catalysts used.
[0155] Table 4 provides preliminary lubricant base stock specifications.
[0156] Table 1
[0157]
[0158]
[0159] *130N raffinate hydroconversion (RHC) product spiked with Sulfrzol54 and octylamine
[0160] Table 2
[0161]
[0162] table 3
[0163]
[0164] Processing Experiment #1 Carried out under the following conditions: Simul...
Embodiment 1
[0187] Catalyst Example 1. In 65 / 35ZSM-48 (90 / 1SiO 2 :Al 2 O 3 ) / TiO 2 Up 0.6% by weight Pt(IW)
[0188] Will 65%ZSM-48 (90 / 1SiO 2 :Al 2 o 3 ) and 35% titanium dioxide were extruded to obtain 1 / 16" quadrulobe (quadrulobe). The extrudate was 2 Precalcination at 1000°F, ammonium exchange with 1 N ammonium nitrate, and subsequent drying at 250°F followed by calcination in air at 1000°F. The extrudates were then loaded with 0.6 wt% Pt by incipient wetness impregnation with platinum tetraammine nitrate, dried at 250°F, and calcined in air at 680°F for 3 hours. Table 5 provides via N 2 Surface area of extrudates obtained by porosimetry.
[0189] The activity of the above catalysts was determined using a batch micro-autoclave system. The catalyst was reduced under hydrogen followed by the addition of 2.5 g of 130N feed (cloud point 31). The reaction was run at 330°C for 12 hours at 400 psig. Cloud points were determined for two feed space velocities. The resu...
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Abstract
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