Abstract:
Disclosed is a method of preparing isobutene in which high-purity isobutene is separated (prepared) from a C4 mixture by cracking glycol ether prepared from a C4 mixture (in particular, C4 raffinate-1) containing isobutene and a glycol. The method includes cracking glycol ether into isobutene and glycol at a temperature between 50° C. and 300° C. in the presence of a strongly acidic catalyst. The glycol ether may be prepared by reaction between a C4 mixture containing isobutene and glycol in the presence of an acid catalyst.
Abstract:
Disclosed is a method of preparing a glycol mono-tertiary-butyl ether compound using a C4 hydrocarbon mixture containing isobutene and a glycol compound as reactants, in which a glycol di-tertiary-butyl ether compound as a byproduct is decomposed into isobutene and a glycol compound and the obtained isobutene and glycol compound are recycled as reactants, whereby product yield per unit raw material may be maximized. The method includes a catalytic reaction step for preparing a glycol mono-tertiary-butyl ether compound and a glycol di-tertiary-butyl ether compound as a byproduct by reaction between a glycol compound and a C4 hydrocarbon mixture containing isobutene in the presence of an acidic catalyst, a byproduct extraction step for separating the glycol mono-tertiary-butyl ether compound and the glycol di-tertiary-butyl ether compound, prepared through the catalytic reaction step, using a hydrophilic extractant and a lipophilic extractant, and a byproduct decomposition and recycling step for decomposing the separated glycol di-tertiary-butyl ether compound into a glycol compound and isobutene and recycling the decomposed glycol compound and isobutene as the reactants to the catalytic reaction step.
Abstract:
A fuel oil detergent which efficiently constricts precipitate formation and octane number requirement increase in a carburetor, injector, and inlet system of an internal combustion engine, i.e., a hydropoly(oxyalkylene) oxyalkyl amine based compound, a process for preparing the compound, and a fuel oil composition including the compound.
Abstract:
A method for producing high reactive polybutene (HRPB), in which carbon-carbon double bond is positioned at an end of polybutene, is disclosed. The high reactive polybutene having 300˜5000 of number average molecular weight (Mn) can be produced from a raw material containing isobutene, wherein a polymerization reaction of the isobutene is carried out in the presence of a catalyst system including secondary alkylether, tertiary alcohol, and boron trifluoride, the amount of boron trifluoride is 0.05˜1.0 weight part per 100 weight part of isobutene, the mole ratio of a co-catalyst including secondary alkylether and tertiary alcohol:boron trifluoride is 1.0˜2.0:1, and the mole ratio of secondary alkylether:tertiary alcohol is 0.5˜1.2:1.
Abstract:
A method of separating glycol mono-tertiary-butyl ether and glycol di-tertiary-butyl ether by an extraction process using hydrophilic and lipophilic extracting agents is disclosed. The separation method includes the step of separating a mixture including glycol mono-tertiary-butyl ether of the following Chemical formula 1 and glycol di-tertiary-butyl ether of the following Chemical formula 2 with a hydrophilic extracting agent and a lipophilic extracting agent, wherein, R1 and R2 are independently, a hydrogen atom or an alkyl group of carbon number of 1 to 5, and n is an integer of 0 to 4.
Abstract translation:公开了通过使用亲水和亲脂性提取剂的提取方法分离二醇单叔丁基醚和二醇二叔丁基醚的方法。 分离方法包括用亲水性萃取剂和亲油性萃取剂分离包含以下化学式1的二醇单叔丁基醚和下列化学式2的二醇二叔丁基醚的混合物的步骤,其中 R 1和R 2独立地为氢原子或碳原子数为1〜5的烷基,n为0〜4的整数。
Abstract:
A method for producing high reactive polybutene (HRPB), in which carbon-carbon double bond is positioned at an end of polybutene, is disclosed. The high reactive polybutene having 300˜5000 of number average molecular weight (Mn) can be produced from a raw material containing isobutene, wherein a polymerization reaction of the isobutene is carried out in the presence of a catalyst system including secondary alkylether, tertiary alcohol, and boron trifluoride, the amount of boron trifluoride is 0.05˜1.0 weight part per 100 weight part of isobutene, the mole ratio of a co-catalyst including secondary alkylether and tertiary alcohol:boron trifluoride is 1.0˜2.0:1, and the mole ratio of secondary alkylether:tertiary alcohol is 0.5˜1.2:1.
Abstract:
Disclosed is a method of preparing isobutene in which high-purity isobutene is separated (prepared) from a C4 mixture by cracking glycol ether prepared from a C4 mixture (in particular, C4 raffinate-1) containing isobutene and a glycol. The method includes cracking glycol ether into isobutene and glycol at a temperature between 50° C. and 300° C. in the presence of a strongly acidic catalyst. The glycol ether may be prepared by reaction between a C4 mixture containing isobutene and glycol in the presence of an acid catalyst.
Abstract:
Disclosed is a method of preparing a glycol mono-tertiary-butyl ether compound using a C4 hydrocarbon mixture containing isobutene and a glycol compound as reactants, in which a glycol di-tertiary-butyl ether compound as a byproduct is decomposed into isobutene and a glycol compound and the obtained isobutene and glycol compound are recycled as reactants, whereby product yield per unit raw material may be maximized. The method includes a catalytic reaction step for preparing a glycol mono-tertiary-butyl ether compound and a glycol di-tertiary-butyl ether compound as a byproduct by reaction between a glycol compound and a C4 hydrocarbon mixture containing isobutene in the presence of an acidic catalyst, a byproduct extraction step for separating the glycol mono-tertiary-butyl ether compound and the glycol di-tertiary-butyl ether compound, prepared through the catalytic reaction step, using a hydrophilic extractant and a lipophilic extractant, and a byproduct decomposition and recycling step for decomposing the separated glycol di-tertiary-butyl ether compound into a glycol compound and isobutene and recycling the decomposed glycol compound and isobutene as the reactants to the catalytic reaction step.