Rare-earth-based catalytic material and alcohol fuel thereof

Abstract

The invention relates to the technical field of rare earth-based catalytic materials, in particular to a rare earth compound catalytic material and an alcohol fuel additive thereof. The invention provides a rare earth compound catalytic material used in fuel, the catalytic material comprises a hydroxyl group, a phenyl group, a C5-C25 group, a carboxyl group, an amido group or a metal element, and the alcohol fuel comprises C1-C7 alcohol and hydrocarbon. The catalyst can promote sufficient combustion of fuel, improve the combustion efficiency and reduce pollutant emission, and has great significance in solving the environmental protection problem of fossil fuel and accelerating the fuel.

Description

Technical Field

[0001] This invention relates to the field of rare earth-based catalytic materials technology, and in particular to a rare earth-based catalytic material and its alcohol fuel additive. Background Technology

[0002] Alcohol-based fuels are fuels primarily composed of alcohols. They exist in liquid or solid form. As a form of biomass energy, like nuclear, solar, hydro, and wind power, it is an environmentally friendly and clean energy source. Faced with the depletion of fossil fuels, alcohol-based fuels are the most promising new alternative energy source.

[0003] However, alcohol-based fuels are unstable in combustion, their combustion efficiency needs improvement, and they lack relevant catalysts, resulting in significant pollutant emissions. This leads to low combustion efficiency and large variations in combustion emissions, especially for fuels used in internal combustion engines of power systems. They are not well adapted to the linear acceleration or motion of internal combustion engines. In addition, existing alcohol fuel catalysts have limited performance, require large quantities, or have poor temperature resistance. Furthermore, there is a lack of methods for preparing relevant catalyst additives. All of these problems seriously restrict the healthy and rapid development of alcohol-based fuels. Summary of the Invention

[0004] To address one of the aforementioned problems, this application provides a rare earth compound catalyst material for use in fuels, wherein the rare earth compound comprises hydroxyl groups, phenyl groups, and C5-C6 groups. 25 Groups, carboxyl groups, amine groups, and metal elements, wherein the rare earth compound contains the chemical formula (C 28 H 42 Substances containing MN2O3)n have the following molecular structural formula I; where M is a metal.

[0005]

[0006] Preferably, C5 to C 25 The group includes oleic acid, and the metal includes one or more of cerium, samarium, neodymium, terbium, dysprosium, zinc, copper, aluminum, platinum, palladium, rhodium, and ruthenium.

[0007] Preferably, containing (C) 28 H 42 The preparation method of substance MN2O3)n, wherein M is a metal, is to dissolve N-(3-cyanophenyl)prop-2-ene amide and oleate in an organic solvent at a molar ratio of 1:1, add an initiator, heat to a certain temperature and then react at a constant temperature. During the reaction, the solution is controlled to not exceed a certain viscosity. After the reaction, the solvent is evaporated, dried and pulverized to form the target substance.

[0008] This application has at least one of the following beneficial effects:

[0009] 1. Contains (C)28 H 42 CuN2O3)n or substances containing molecular structure formula II have a certain adsorption and chelation effect on metal ions.

[0010] 2. Substances containing molecular structure formula II have certain temperature resistance or adaptability to high temperatures, and can be used as catalysts for long-lasting and stable fuel catalytic combustion or as stable new material catalysts.

[0011] 3. Contains (C) 28 H 42 The novel material CuN2O3)n can be used as a catalyst. This catalyst can catalyze fuel combustion, and in particular, a small amount of the catalyst can promote the complete combustion of fuel, improve combustion efficiency, and reduce pollutant emissions. Attached Figure Description

[0012] Figure 1 : for containing (C 28 H 42 Infrared spectrum of CuN2O3)n. Detailed Implementation

[0013] A rare earth compound catalyst for fuel, wherein the rare earth compound comprises hydroxyl groups, phenyl groups, and C5-C6 groups. 25 Groups, carboxyl groups, amine groups, and metal elements, wherein the rare earth compound contains the chemical formula (C 28 H 42 Substances containing MN2O3)n have the following molecular structural formula I; where M is a metal.

[0014]

[0015] The C5~C 25 The group includes oleic acid, and the metal includes one or more of cerium, samarium, neodymium, terbium, dysprosium, zinc, copper, aluminum, platinum, palladium, rhodium, and ruthenium.

[0016] The following describes a substance containing (C) 28 H 42The preparation method of substance MN2O3)n, where M represents a metal, is illustrated in the following examples using copper as the metal of M. 100g of N-(3-cyanophenyl)prop-2-enamide and copper oleate in a 1:1 molar ratio are dissolved in 2000g of xylene, an organic solvent. 0.5g of azodimethoxyisoheptanenitrile initiator is added. The solution temperature is raised to 50℃ or the solution becomes viscous to 3mPa·s, and then the reaction is carried out at a constant temperature of 50-70℃. During the reaction, the viscosity of the reaction solution is measured and maintained below 6mPa·s. After 8-12 hours of reaction, the solvent is evaporated, the solution is dried, and the solute is pulverized to form a target substance of approximately 100 mesh. A sample of this target substance is added to xylene at room temperature and tested for dissolution time; it dissolves within 30 seconds. Then, the KBr pellet coating method is used to pass the solution of the target substance in xylene through the coated film to obtain the infrared spectrum of the target substance (see [link to KBr pellet coating method]). Figure 1 ),Depend on Figure 1 It can be seen that the stretching vibration of the terminal olefin C=C bond in the reactant N-(3-cyanophenyl)prop-2-enamide occurs at 1640 cm⁻¹. - The significant weakening or disappearance of the peak near ¹ indicates that polymerization has occurred. After the carboxylate ion coordinates with the metal, its C=O stretching vibration peak changes, manifesting as a change in the peak value between 1590-1650 cm⁻¹. - ¹(Asymmetric stretching) and 1400-1450cm - ¹A broadened or split absorption band appears near (symmetric stretching), confirming the participation of copper oleate in the reaction, and at 1430 cm⁻¹ - ¹and 1550cm - The paired appearance of peaks indicates the symmetric stretching vibration of copper carboxylate, further suggesting a weakly cross-linked or complexly associated molecular structure at the carboxyl group position of the divalent copper ion, at 2200 cm⁻¹. - ¹ A clear cyano peak and 1670 cm⁻¹ - The strong amide carbonyl peak at 1870 cm⁻¹ is a key indicator of the successful incorporation of the N-(3-cyanophenyl)prop-2-enamide structural unit into the polymer. - ¹The strong aliphatic CH (-CH3,-CH2-) stretching vibrations in the vicinity primarily originate from the long alkyl chain and polymer backbone of copper oleate. 3000-3100cm - ¹The =CH stretching vibration on the nearby weak aromatic ring is a marker of the presence of the aromatic ring. Based on the above analysis, this preparation method produces at least one aromatic ring containing (C). 28 H 42 CuN2O3)n or a substance containing the following molecular structural formula II was generated.

[0017]

[0018] This application prepares a product containing (C) 28 H 42CuN2O3)n or the generation of substances containing molecular structural formula II is a simple and convenient method.

[0019] Furthermore, including (C) 28 H 42 CuN2O3)n or substances containing molecular structural formula II are placed in a solution containing one or more metal ions selected from at least cerium, samarium, neodymium, terbium, dysprosium, zinc, aluminum, platinum, palladium, rhodium, and ruthenium. After adjusting the pH of the solution to 6-9 and adsorbing and chelating for 48 hours, substances containing (C) 28 H 42 CuN2O3)n or substances containing molecular structural formula II were generated by calcination, ashing, and acid dissolution. Atomic absorption spectrometry was then used to analyze the acid solution, revealing the presence of corresponding metal ions, indicating the presence of (C) 28 H 42 CuN2O3)n or substances containing molecular structure formula II have an adsorption and chelation effect on the above metal ions.

[0020] For those containing (C) 28 H 42 Temperature resistance test of CuN2O3)n or substances containing molecular structural formula II:

[0021] Take (C) 28 H 42 10g of a dry powder containing molecular structure II (CuN2O3)n was dissolved in 200g of xylene solution at room temperature. After stirring for 1 minute, the viscosity of the solution was measured to be 5.8 mPa·s using a six-speed rotational viscometer.

[0022] Temperature resistance performance comparison test, taking (C) 28 H 42 10g of a dry powder containing molecular structure II (CuN2O3)n was added to dimethyl silicone oil and stirred and heated to 200℃ for 5 minutes. Then, 10g of the dry powder was filtered out and dissolved in 200g of xylene solution at room temperature. After stirring for 1 minute, the viscosity of the solution was measured to be 5.8 mPa·s using a six-speed rotational viscometer. Therefore, it can be concluded that the dry powder contains (C... 28 H 42 CuN2O3)n or substances containing molecular structure formula II have certain temperature resistance or adaptability to high temperatures. The above-mentioned substances containing benzene and cyano multi-branched structures are beneficial to the temperature resistance of the substances and can be used as catalysts or stable catalysts for the catalytic combustion of fuels.

[0023] The following describes an embodiment of an alcohol fuel, comprising, by weight, 0.01 to 85 parts of C1 to C7 alcohols and 5 to 50 parts of aromatics. Preferably, the composition further includes C3 to C7 alcohols. 12The composition includes 3-30 parts alkane, 0.0001-5 parts catalyst, 0.5-10 parts stabilizer, 0.1-3 parts preservative; 0.1-25 parts lubricant, 0.1-5 parts antioxidant, and 0.1-4 parts dispersant; the C1-C7 alcohol is one or more of methanol, ethanol, propanol, butanol, pentanol, and heptanol; the aromatic hydrocarbon is one or more of benzene, toluene, xylene, and trimethylbenzene; and the C3-C7 alcohol... 12 Alkanes are C3 to C4. 12 One or more of the hydrocarbons, wherein the catalyst is a (C)-containing hydrocarbon. 28 H 42 The active ingredient is one or more of CuN2O3, peroxide, and nitrate ester; the stabilizer is one or more of methyl tert-butyl ether, ethylene glycol methyl ether, ethylene glycol ethyl ether, petroleum ether, acetone, butanone, and n-propanol; the preservative is benzotriazole or imidazoline oleate; the lubricant is liquid paraffin or white oil; the antioxidant is one or more of di-tert-butyl-p-cresol, phenol, and butylated hydroxyanisole; and the dispersant is one or more of polyetheramine and polyisobutyleneamine.

[0024] Example 1

[0025] An alcohol fuel, comprising, by weight, 85 parts methanol and 15 parts toluene.

[0026] A method for preparing an alcohol fuel involves first adding 15 parts of toluene, then adding 85 parts of methanol and mixing thoroughly.

[0027] Example 2

[0028] The only difference between this embodiment and Embodiment 1 is that, by weight, the components include 85 parts methanol, 15 parts toluene, and (C) 28 H 42 0.001 parts of the catalyst of CuN2O3)n substance.

[0029] Example 3

[0030] The only difference between this embodiment and Example 1 is that, by weight, methanol 45 parts, ethanol 10 parts, propanol 10 parts, toluene 15 parts, 2-methylbutane 3 parts, containing (C 28 H 42 The catalyst of CuN2O3)n is 0.001 parts, methyl tert-butyl ether is 2 parts, oleic acid imidazoline is 0.1 parts, white oil is 15 parts, and di-tert-butyl-p-cresol is 1 part.

[0031] A method for preparing an alcohol fuel involves first adding 15 parts toluene and 3 parts 2-methylbutane, mixing thoroughly, then adding 45 parts methanol, 10 parts ethanol, and 10 parts propanol, mixing thoroughly again, then adding 2 parts methyl tert-butyl ether, 1 part di-tert-butyl-p-cresol, and 15 parts white oil, mixing thoroughly, and finally adding (C...28 H 42 The catalyst of CuN2O3)n was 0.001 parts and the oleic acid imidazoline was 0.1 parts. The mixture was stirred and reacted evenly.

[0032] Example Effect Test: Take the alcohol fuel samples prepared in Examples 1-3 and test them according to national standards, including calorific value. Use an engine to test CO emissions and acceleration performance. Acceleration performance test is conducted by adjusting the throttle of the internal combustion engine or engine from small to large (speed range 1500-2500 r / min) to see if the engine speed increases linearly.

[0033] The test results are shown in Table 1 below.

[0034] Table 1 Test Project Example 1 Example 2 Example 3 Calorific value (MJ / kg) 17 21 31.3 CO emissions (%) 0.7 0.04 0.3 Acceleration performance (linearity) no yes yes

[0035] The test results in the table show that the calorific value of Example 2 increased by approximately 23% compared to Example 1, and the CO emissions of Example 2 decreased by approximately 95% compared to Example 1. The difference between Example 1 and Example 2 is that Example 2 added an ingredient containing (C) 28 H 42 A catalyst containing CuN2O3)n was used, and in Example 3, a catalyst containing (C)n was also used. 28 H 42 The test data for the CuN2O3)n substance were also superior to those of Example 1, indicating that its effect was stable in fuel. This further confirms the principle or function of the above-mentioned copper-based or cyano-based catalysts in catalytically producing hydrocarbons or catalytically reforming alcohols. The stable acceleration performance of Examples 1 and 2 indicates the presence of (C)n. 28 H 42 CuN2O3)n substances or their structures give them stable catalytic properties, thus it can be known that substances containing (C) 28 H 42 The catalyst of CuN2O3)n has the effect of catalyzing fuel combustion, especially a small amount of catalyst promotes complete combustion, improves combustion efficiency, and reduces pollutant emissions; in addition, the calorific value of the alcohol fuel of this application is adjustable and high, which is well adapted to the internal combustion engine or engine tested with it.

Claims

1. A rare earth compound catalytic material for fuel, characterized in that, Rare earth compounds contain hydroxyl groups, phenyl groups, and C5-C6 groups. 25 Groups, carboxyl groups, amine groups, and metal elements, wherein the rare earth compound contains the chemical formula (C 28 H 42 Substances containing MN2O3)n have the following molecular structural formula I; where M is a metal. 。 2. The rare earth compound catalyst material for fuel as described in claim 1, characterized in that, The C5~C 25 The group includes oleic acid, and the metal includes one or more of cerium, samarium, neodymium, terbium, dysprosium, zinc, copper, aluminum, platinum, palladium, rhodium, and ruthenium.

3. A rare earth compound catalyst material for fuel as described in claims 1-2, characterized in that, Contains (C) 28 H 42 The preparation method of MN2O3)n, wherein M is a metal, is as follows: N-(3-cyanophenyl)prop-2-ene amide and oleate are dissolved in an organic solvent in a molar ratio of 1:1, an initiator is added, the mixture is heated to a certain temperature and then reacted at a constant temperature. During the reaction, the solution is controlled to not exceed a certain viscosity. After the reaction, the solvent is evaporated, the mixture is dried and pulverized to form the target substance.

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