A kind of method that adamantyl ionic liquid promotes the catalytic production of alkylated gasoline
A technology for alkylating gasoline and ionic liquids, applied in chemical instruments and methods, liquid hydrocarbon mixture production, physical/chemical process catalysts, etc., can solve inconspicuous problems, improve selectivity, suppress side reactions, and recycle The effect of the number of times up
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[0028] The method for preparing alkylated oil provided by the present invention is to contact and react isoparaffins and olefins in the presence of a catalyst under alkylation conditions to produce polyalkylene oil with isooctane (especially trimethylpentane) as the main component. branched chain hydrocarbons. A small amount of adamantyl ionic liquid with the functions of increasing the transfer speed of hydride ions, improving the performance of the acid / hydrocarbon two-phase interface, and maintaining the acidity of the system is added to the main catalyst.
[0029] In the present invention, unless otherwise specified, all percentages are in weight units, and all equipment and raw materials can be purchased from the market or commonly used in this industry. The methods in the following examples, unless otherwise specified, are conventional methods in the art.
Embodiment 1
[0032] Preparation of N,N,N-Dimethylbutylammonium Bistrifluoromethanesulfonimide Ionic Liquid (ADM-IL 01)
[0033] The preparation of N,N,N-dimethylbutylammonium bistrifluoromethanesulfonimide ionic liquid is completed through the following three steps.
[0034] 1) Synthesis of N,N-dimethylamantadine: Take 0.1 mol of amantadine in a three-necked flask, add 100 mL of isopropanol, stir and heat to 35°C. Then, 0.5 mol formic acid was slowly added dropwise with a constant pressure dropping funnel (the dropwise addition was completed in 40 minutes), and the mixture was heated to 50°C. Take 0.2mol formaldehyde and add it under strong stirring with a constant pressure dropping funnel (4.5h dropwise). The mixture was heated to 80 °C and maintained at reflux for 21 h. After cooling, alkalinize with NaOH solution until pH = 13, the solution is separated, the upper layer is extracted with n-hexane, and the solvent is evaporated using a rotary evaporator with a maximum rotary evaporatio...
Embodiment 2
[0038] Preparation of N,N,N-Dimethyldodecyladamantanium Bistrifluoromethanesulfonimide Ionic Liquid (ADM-IL 02)
[0039] The operation steps are as in Example 1. First, N,N-dimethylamantadine is synthesized by reacting amantadine with formic acid and formaldehyde, and then N,N-dimethylamantadine is reacted with the same molar amount of dodecane bromide to synthesize N,N,N-Dimethyldodecyladamantanium bromide, lastly N,N,N-Dimethyloctyladamantanium bromide and LiNTf 2 The ion exchange reaction completes the preparation of N,N,N-dimethyl dodecyl adamantyl ammonium bistrifluoromethanesulfonimide ionic liquid.
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