CN1458243A - Process for hjydrogenation refining petroleum wax - Google Patents
Process for hjydrogenation refining petroleum wax Download PDFInfo
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- CN1458243A CN1458243A CN 02109666 CN02109666A CN1458243A CN 1458243 A CN1458243 A CN 1458243A CN 02109666 CN02109666 CN 02109666 CN 02109666 A CN02109666 A CN 02109666A CN 1458243 A CN1458243 A CN 1458243A
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Abstract
The petroleum wax hydrofining process is one process in single reactor with two kinds of graded and filled catalyst. Under hydrofining condition, the petroleum wax is first contacted with Mo-Ni catalyst, the refined product is then mixed with cold hydrogen and the mixture is finally contacted with W-Ni catalyst to obtain refined product with low S and N content and low fused ring arene content. The product has obviously improved stability. The said petroleum wax material includes paraffin and microcrystalline wax, and petroleum wax product of the present invention may be used in food product, medicine and cosmetics.
Description
1, technical field
The present invention relates to a kind of method of hydrorefining petroleum waxes, particularly adopt the hydrofinishing process of single reactor and two kinds of catalyzer grading loadings.The said petroleum wax of the present invention comprises paraffin and Microcrystalline Wax.
2, background technology
Petroleum wax is a kind of important chemical material, the petroleum wax of separating from petroleum fractions must be made with extra care, to remove wherein a spot of sulfur-nitrogen compound and condensed-nuclei aromatics, the petroleum wax that is used for food, medicine and makeup must carry out deep refining, and is harmless in the hope of accomplishing.
Hydrorefining petroleum waxes is a kind of under 2～16MPa hydrogen dividing potential drop, 230～360 ℃ of temperature, and petroleum wax mixes the fixed bed of back by single catalyst in the reactor with hydrogen, and petroleum wax obtains the purified process under catalyst action.With clay-filtered comparison, hydrorefining petroleum waxes has the product yield height, quality is good, characteristics such as no waste sludge discharge, and hydrofining has at present replaced the clay-filtered main method of petroleum wax purified that becomes.
The key distinction of hydrorefining petroleum waxes process and other petroleum products unifining process is petroleum wax hydrogenation process can only realize product under lower temperature of reaction a deep refining, high temperature will cause scission reaction that thereby the characteristic index of petroleum wax takes place to destroy, the oleaginousness and the penetration degree of petroleum wax are risen, therefore in the hydrorefining petroleum waxes process, require catalyzer to have higher hydrogenation activity and selectivity, at a lower temperature effective elimination sulfur-nitrogen compound and condensed-nuclei aromatics.
CN1176296A discloses a kind of hydrorefining paraffin wax method, adopt the two-stage catalytic agent, wherein first section catalyzer be second section 30～50%, different operational conditions is adopted in the two-stage catalytic agent, catalyzer there are not special requirement, by adjusting the hydrogenation degree of depth that operational condition reaches paraffin.But this technology still has further improved possibility.
CN1032408C announces a kind of Mo-Ni type catalyst for hydrorefining pertroleum wax and process for purification, and paraffin raw material is at hydrogen dividing potential drop 4.9MPa, 270 ℃ of temperature, volume space velocity 1.5h
-1, hydrogen wax is than contacting with described catalyzer under 100 the operational condition, can obtain qualified purified product.CN1044816C announces a kind of W-Ni type catalyst for hydrorefining pertroleum wax and process for purification, and paraffin raw material is at pressure 6.0MPa, 260 ℃ of temperature, volume space velocity 1.0h
-1, hydrogen wax is than contacting with described catalyzer under 300 the operational condition, can obtain qualified purified product.The hydrofinishing process of single reactor list catalyzer is all adopted in above-mentioned two inventions, and their common drawback is to obtain best desulfurization removing nitric and aromatic hydrocarbons saturation effect simultaneously, fails effectively to improve fully the stability of purified product.
3, summary of the invention
The objective of the invention is to overcome the deficiency of existing hydrorefining petroleum waxes technology, different characteristics according to various chemical reactions in the petroleum wax treating process, provide a kind of can the deep desulfuration denitrogenation and aromatic hydrocarbons saturated, effectively improve the hydrorefining petroleum waxes method of purified product stability.
Hydrorefining petroleum waxes method of the present invention is to adopt the fixed bed hydrogenation process for purification of single reactor, dual catalyst bed, comprises the method turpentole wax that adopts Mo-Ni catalyzer and two kinds of catalyzer grading loadings of W-Ni catalyzer.In the presence of hydrogen, the petroleum wax raw material at first contacts with the Mo-Ni catalyzer of first bed, under higher relatively temperature, realize desulfurization removing nitric and decolouring, the first bed refined products is mixed with the outer cold hydrogen that injects of device, under relatively low temperature, contact, reach the purpose that aromatic hydrocarbons is saturated, improve the purified product stability with the W-Ni catalyzer of second bed.
The first bed catalyst for refining of hydrorefining petroleum waxes method of the present invention is Mo-Ni type catalyst for refining MoO
315%～25%, NiO 2%～8%, specific surface area 〉=160m
2/ g, pore volume 〉=0.3ml/g are MoO preferably
317%～20%, NiO 4%～5%, specific surface area 220～280m
2/ g, pore volume 0.45～0.65ml/g.The second bed catalyst for refining is W-Ni type catalyst for refining WO
325%～35%, NiO 2%～8%, specific surface area 〉=160m
2/ g, pore volume 〉=0.3ml/g are WO preferably
329.5%～31.5%, NiO 4%～5%, specific surface area 200～240m
2/ g, pore volume 0.4～0.6ml/g.The admission space of two kinds of catalyzer is than being the Mo-Ni catalyzer: W-Ni catalyzer=40～80: 60～20.
The operational condition of the inventive method hydrorefining paraffin wax is the first bed hydrogen dividing potential drop, 4～10MPa, 270～330 ℃ of temperature of reaction, hydrogen wax volume ratio 100～1000; 230～270 ℃ of the second bed hydrogen dividing potential drop, 4～10MPa, temperature of reaction; Two bed cumulative volume air speeds, 0.5～3.0h
-1
The hydrorefined operational condition of Microcrystalline Wax is the first bed hydrogen dividing potential drop, 6～16MPa, 300～360 ℃ of temperature of reaction, hydrogen wax volume ratio 300～1000; 240～300 ℃ of the second bed hydrogen dividing potential drop, 6～16MPa, temperature of reaction; Two bed cumulative volume air speeds, 0.2～1.5h
-1
The temperature of reaction of second bed usually can be than low 10～100 ℃ of first bed, preferred 40～70 ℃.
Temperature head according to two beds regulation is injected a certain amount of cold hydrogen between two beds in device, realize that the first bed refined products is cooled to temperature required.The inventive method also can adopt two independently reactors, controls the temperature of second reactor with middle heat exchange or the method for injecting cold hydrogen.Concrete selection of catalysts, and two-stage catalytic agent consumption and operational condition can be determined by the requirement of the different and product property of processing feedstock property.
The second bed refined products obtains the deep desulfuration denitrogenation and takes off virtue and the obvious purpose product that improves of stability after gas-liquid separation, stripping drying.
Major impurity in the petroleum wax is sulfur-bearing, nitrogen, oxygen species and condensed-nuclei aromatics, under hydroconversion condition, sulfur-bearing simple in structure, nitrogen, oxygen compound are more easily removed, contain when mixing element and promptly contain condensed ring virtue nuclear in the structure, and condensed-nuclei aromatics then need comparatively just can remove under the exacting terms, and the best separately removes condition and inequality.Contain in the structure of condensed ring virtue nuclear and assorted element at some, it is saturated that reaction process is normally carried out aromatic ring earlier, be to take off assorted element then, therefore the catalysis system of function singleness generally can not satisfy and takes off assorted element and the saturated requirement of condensed-nuclei aromatics simultaneously, and both influence each other, cooperatively interact, not taking off the saturated function of assorted element interaction system can not give full play to, do not have the efficient of the assorted system of elements of taking off of saturated function also to be affected, both combinations have then produced 1+1 greater than 2 effect.The present invention is according to the characteristics of different impurities hydrogenation and removing reaction in the petroleum wax, adopt its different separately conditions that require that are fit to, the use different catalysts is also carried out under the different operating condition, can obtain the petroleum paraffin product of low-sulfur nitrogen, low condensed-nuclei aromatics content, and the stability of product obviously improves.The present invention be advantageous in that and to reach product depth purified purpose according to the filling ratio of paraffin sulphur nitrogen and two kinds of catalyzer of condensed-nuclei aromatics content adjustment.
The petroleum wax of producing according to the method for the invention can be used for food, medicine and makeup.
4, embodiment
Specify the solution of the present invention and effect by the following examples.
The paraffin raw material that the embodiment of the invention and comparative example adopt is No. 58 dewaxed oils of Daqing crude oil and No. 66 dewaxed oils of Daqing crude oil, and the Microcrystalline Wax raw material of employing is No. 80 Microcrystalline Waxes of Nanyang crude oil.Paraffin character sees Table 1.
The character of the Mo-Ni catalyzer that the embodiment of the invention and comparative example adopt is MoO
318.9%, NiO4.2%, specific surface area 262m
2/ g, pore volume 0.56ml/g, the character of the W-Ni catalyzer of employing is WO
329.8%, NiO 4.5%, specific surface area 232m
2/ g, pore volume 0.48ml/g.
The embodiment of the invention adopts two kinds of catalyzer equal-volume fillings.
The embodiment of the invention 1, embodiment 2 and embodiment 3 adopt the outer method of injecting cold hydrogen of device to reduce the temperature of the first bed refined products.
The hydrorefined operational condition of the embodiment of the invention and comparative example and the results are shown in Table 2～4 wherein characterizes condensed-nuclei aromatics content with the simplified method ultraviolet absorptivity.
Table 1 petroleum wax character
| Project | No. 58 paraffin | No. 66 paraffin | No. 80 Microcrystalline Waxes |
| Fusing point, ℃ | ????58.35 | ????66.80 | |
| Melt drop temperature, ℃ | ??81.2 | ||
| Oleaginousness, % | ????0.43 | ????0.41 | ??2.25 |
| Light stability, number | ????9 | ????＞9 | ??＞9 |
| Sulphur, μ g/g | ????67 | ????86 | ??565 |
| Nitrogen, μ g/g | ????35 | ????53 | ??298 |
| Ultraviolet absorptivity (simplified method) 280nm 290nm | ????0.608 ????0.485 | ????0.794 ????0.623 | ??4.671 ??4.105 |
Table 2 58 wax hydrofining operational condition and results
Table 3 66 wax hydrofining operational condition and results
Table 4 No. 80 Microcrystalline Wax hydroprocessings condition and result
| Project | Embodiment 1 | Comparative example 1 | Comparative example 2 |
| Operational condition | |||
| Catalyzer | ?Mo-Ni+W-Ni | ????Mo-Ni | ??W-Ni |
| The hydrogen dividing potential drop, MPa | ?6.0 | ????6.0 | ??6.0 |
| One bed temperature, ℃ | ?280 | ????280 | ??280 |
| Two bed temperatures, ℃ | ?240 | The same | The same |
| The cumulative volume air speed, h -1 | ?1.5 | ????1.5 | ??1.5 |
| Hydrogen wax volume ratio | 300 (beds) | ????300 | ??300 |
| Quality product | |||
| Fusing point, ℃ | ?58.35 | ????58.35 | ??58.35 |
| Oleaginousness, % | ?0.43 | ????0.43 | ??0.44 |
| Light stability, number | ?2-3 | ????3-4 | ??3-4 |
| Sulphur, μ g/g | ?22.5 | ????22.4 | ??26.3 |
| Nitrogen, μ g/g | ?15.6 | ????15.5 | ??19.0 |
| Ultraviolet absorptivity (simplified method) 280nm 290nm | ?0.034 ?0.020 | ????0.062 ????0.045 | ??0.044 ??0.029 |
| Project | Embodiment 2 | Comparative example 3 | Comparative example 4 |
| Operational condition | |||
| Catalyzer | ?Mo-Ni+W-Ni | ????Mo-Ni | ??W-Ni |
| The hydrogen dividing potential drop, MPa | ?6.0 | ????6.0 | ??6.0 |
| One bed temperature, ℃ | ?290 | ????270 | ??270 |
| Two bed temperatures, ℃ | ?240 | The same | The same |
| The cumulative volume air speed, h -1 | ?1.5 | ????1.5 | ??1.5 |
| Hydrogen wax volume ratio | 300 (beds) | ????300 | ??300 |
| Quality product | |||
| Fusing point, ℃ | ?66.80 | ????66.80 | ??66.70 |
| Oleaginousness, % | ?0.42 | ????0.42 | ??0.42 |
| Light stability, number | ?3 | ????4 | ??4 |
| Sulphur, μ g/g | ?26.7 | ????26.6 | ??32.4 |
| Nitrogen, μ g/g | ?18.1 | ????17.9 | ??20.8 |
| Ultraviolet absorptivity (simplified method) 280nm 290nm | ? ?0.043 ?0.033 | ? ????0.072 ????0.060 | ? ??0.052 ??0.040 |
| Project | Embodiment 3 | Comparative example 5 | Comparative example 6 | Comparative example 7 |
| Operational condition | ||||
| Catalyzer | ??Mo-Ni ??+W-Ni | ??Mo-Ni | ??W-Ni | ??Mo-Ni ??+Mo-Ni |
| The hydrogen dividing potential drop, MPa | ??13.0 | ??13.0 | ??13.0 | ??13.0 |
| One bed temperature, ℃ | ??320 | ??300 | ??300 | ??320 |
| Two bed temperatures, ℃ | ??260 | The same | The same | ??260 |
| The cumulative volume air speed, h -1 | ??0.8 | ??0.8 | ??0.8 | ??0.8 |
| Hydrogen wax volume ratio | 500 (beds) | ??500 | ??500 | 500 (beds) |
| Quality product | ||||
| Melt drop temperature, ℃ | ??80.9 | ??81.0 | ??80.8 | ??80.9 |
| Oleaginousness, % | ??2.28 | ??2.25 | ??2.27 | ??2.27 |
| Color (match), number | ??+22 | ??+4 | ??+3 | ??+16 |
| Sulphur, μ g/g | ??33.4 | ??33.1 | ??54.3 | ??43.6 |
| Nitrogen, μ g/g | ??23.2 | ??23.1 | ??42.5 | ??31.8 |
| Ultraviolet absorptivity (simplified method) 280nm 290nm | ? ??0.622 ??0.378 | ? ??2.655 ??2.043 | ? ??1.984 ??1.680 | ? ??1.873 ??1.506 |
Claims (10)
1, a kind of method of hydrorefining petroleum waxes, adopt two bed series systems, the service temperature of second bed is lower than the service temperature of first bed, it is characterized in that first bed uses Mo-Ni type Hydrobon catalyst, second bed uses W-Ni type Hydrobon catalyst, and the volume ratio of first bed and the second bed catalyzer is 40～80: 60～20.
2,, it is characterized in that described Mo-Ni type Hydrobon catalyst contains MoO by weight according to the described hydrorefining petroleum waxes method of claim 1
315%～25%, NiO 2%～8%, specific surface area 〉=160m
2/ g, pore volume 〉=0.3ml/g.
3,, it is characterized in that described middle Mo-Ni type Hydrobon catalyst contains MoO by weight according to claim 1 or 2 described hydrorefining petroleum waxes methods
317%～20%, NiO 4%～5%, specific surface area 220～280m
2/ g, pore volume 0.45～0.65ml/g.
4,, it is characterized in that described W-Ni type Hydrobon catalyst contains WO by weight according to the described hydrorefining petroleum waxes method of claim 1
325%～35%, NiO 2%～8%, specific surface area 〉=160m
2/ g, pore volume 〉=0.3ml/g.
5,, it is characterized in that described W-Ni type Hydrobon catalyst contains WO by weight according to claim 1 or 4 described hydrorefining petroleum waxes methods
329.5%～31.5%, NiO 4%～5%, specific surface area 200～240m
2/ g, pore volume 0.4～0.6ml/g.
6, according to the described hydrorefining petroleum waxes method of claim 1, it is characterized in that described petroleum wax is a paraffin, its hydrofining condition is: the first bed hydrogen dividing potential drop, 4～10MPa, 270～330 ℃ of temperature of reaction, hydrogen wax volume ratio 100～1000; 230～270 ℃ of the second bed hydrogen dividing potential drop, 4～10MPa, temperature of reaction; Two bed cumulative volume air speeds, 0.5～3.0h
-1
7, according to the described hydrorefining petroleum waxes method of claim 1, it is characterized in that described petroleum wax is a Microcrystalline Wax, its hydrofining condition is: the first bed hydrogen dividing potential drop, 6～16MPa, 300～360 ℃ of temperature of reaction, hydrogen wax volume ratio 300～1000; 240～300 ℃ of the second bed hydrogen dividing potential drop, 6～16MPa, temperature of reaction; Two bed cumulative volume air speeds, 0.2～1.5h
-1
8,, it is characterized in that adopting the method for injecting cold hydrogen by the export-oriented first bed reaction product of reactor to reduce the temperature of reaction of second bed according to claim 6 or 7 described hydrorefining petroleum waxes methods.
9,, it is characterized in that the described second bed temperature of reaction is than low 10～100 ℃ of the first bed temperature of reaction according to claim 1,6 or 7 described hydrorefining petroleum waxes methods.
10,, it is characterized in that the described second bed temperature of reaction is than low 40～70 ℃ of the first bed temperature of reaction according to the described hydrorefining petroleum waxes method of claim 9.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB02109666XA CN1183232C (en) | 2002-05-15 | 2002-05-15 | Process for hjydrogenation refining petroleum wax |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB02109666XA CN1183232C (en) | 2002-05-15 | 2002-05-15 | Process for hjydrogenation refining petroleum wax |
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| CN1458243A true CN1458243A (en) | 2003-11-26 |
| CN1183232C CN1183232C (en) | 2005-01-05 |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101942341A (en) * | 2009-07-09 | 2011-01-12 | 中国石油化工股份有限公司抚顺石油化工研究院 | Hydrogenated modification method for petroleum wax substance |
| CN101619241B (en) * | 2008-07-04 | 2013-04-10 | 中国石油化工股份有限公司 | Method for hydrofining paraffin wax |
| CN102021034B (en) * | 2009-09-15 | 2013-12-04 | 中国石油天然气股份有限公司 | Preparation method of white microcrystalline wax |
| RU2549558C1 (en) * | 2014-02-04 | 2015-04-27 | Общество с ограниченной ответственностью "ЛУКОЙЛ-Нижегороднефтеоргсинтез" (ООО "ЛУКОЙЛ-Нижегороднефтеоргсинтез") | Method of production of highly purified solid petroleum paraffins |
-
2002
- 2002-05-15 CN CNB02109666XA patent/CN1183232C/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101619241B (en) * | 2008-07-04 | 2013-04-10 | 中国石油化工股份有限公司 | Method for hydrofining paraffin wax |
| CN101942341A (en) * | 2009-07-09 | 2011-01-12 | 中国石油化工股份有限公司抚顺石油化工研究院 | Hydrogenated modification method for petroleum wax substance |
| CN102021034B (en) * | 2009-09-15 | 2013-12-04 | 中国石油天然气股份有限公司 | Preparation method of white microcrystalline wax |
| RU2549558C1 (en) * | 2014-02-04 | 2015-04-27 | Общество с ограниченной ответственностью "ЛУКОЙЛ-Нижегороднефтеоргсинтез" (ООО "ЛУКОЙЛ-Нижегороднефтеоргсинтез") | Method of production of highly purified solid petroleum paraffins |
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| Publication number | Publication date |
|---|---|
| CN1183232C (en) | 2005-01-05 |
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