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Dehydration reactor processes, product

Description A heated mixture of ethanol vapor and steam is fed to an adiabatic dehydration reactor (1). The steam provides heat for the endothermic reaction and pushes the reaction to 99-"% conversion of ethanol with 99-"% selectivity to ethylene. Recovered H O is stripped of light ends (2) and recycled as process steam. Product ethylene is compressed and put through a water wash (3) before passing to the ethylene oxide reactor section. [Pg.111]

The polymerization process by azeotropic dehydrative condensation of LA seems promising for obtaining a high molecular weight PLA with improved cost performance. However, the use of solvents such as diphenyl ether results in multiple reactors and complex facilities of the process control, leaving the price of PLA expensive. Also, it is hard to remove solvent completely from the end product. Meanwhile, the azeotropic dehydrative condensation process inherits the... [Pg.22]

The production of ethylene by dehydration of ethanol is a proven technology and was demonstrated and implanented on large scale (Winter, 1976). Braskem started a full-scale plant in Brazil in 2010 (Braskem, 2012). The process consists of a dehydration reactor and several subsequent purification steps in order to obtain polymer-grade ethylene (composition 99.95 wt% ethylene, 0.05 wt% ethane, 5ppm CO and lOppm CO (Kochar et al., 1981)). Figure 4.6 iUustrates the ethanol dehydration process investigated in this study and lists the input data used for process simulation. [Pg.88]

Figure 2 illustrates the three-step MIBK process employed by Hibernia Scholven (83). This process is designed to permit the intermediate recovery of refined diacetone alcohol and mesityl oxide. In the first step acetone and dilute sodium hydroxide are fed continuously to a reactor at low temperature and with a reactor residence time of approximately one hour. The product is then stabilized with phosphoric acid and stripped of unreacted acetone to yield a cmde diacetone alcohol stream. More phosphoric acid is then added, and the diacetone alcohol dehydrated to mesityl oxide in a distillation column. Mesityl oxide is recovered overhead in this column and fed to a further distillation column where residual acetone is removed and recycled to yield a tails stream containing 98—99% mesityl oxide. The mesityl oxide is then hydrogenated to MIBK in a reactive distillation conducted at atmospheric pressure and 110°C. Simultaneous hydrogenation and rectification are achieved in a column fitted with a palladium catalyst bed, and yields of mesityl oxide to MIBK exceeding 96% are obtained. [Pg.491]

Water formed in the reaction as well as some undesirable by-products must be removed from the acetic acid solvent. Therefore, mother Hquor from the filter is purified in a residue still to remove heavies, and in a dehydration tower to remove water. The purified acetic acid from the bottom of the dehydration tower is recycled to the reactor. The water overhead is sent to waste treatment, and the residue still bottoms can be processed for catalyst recovery. Alternatively, some mother Hquor from the filter can be recycled directiy to the reactor. [Pg.488]

Manufacture. Much of the diethyl ether manufactured is obtained as a by-product when ethanol (qv) is produced by the vapor-phase hydration of ethylene (qv) over a supported phosphoric acid catalyst. Such a process has the flexibiHty to adjust to some extent the relative amounts of ethanol and diethyl ether produced in order to meet existing market demands. Diethyl ether can be prepared directly to greater than 95% yield by the vapor-phase dehydration of ethanol in a fixed-bed reactor using an alumina catalyst (21). [Pg.427]

The advance of sulfur trioxide as sulfating agent largely depended on advances in sulfonation/sulfation reactor development and changes in raw material quality. Undiluted sulfur trioxide cannot be used as a sulfating agent except in special cases where suitable equipment is used because of its violent nature. Sulfur trioxide diluted in an inert gas, usually air, when used in batch processes can cause excessive dehydration and dark-colored products. However, batch processes were used years ago and inert liquid solvents were often suggested or used to moderate the reaction. Inadequate reaction conditions lead to a finished product that can contain dialkyl sulfate, dialkyl ether, isomeric alcohols, and olefins whereas inadequate neutralization conditions can increase the content of the parent alcohol due to hydrolysis of the unstable acid sulfate accompanied by an increase of mineral sulfate. [Pg.231]

Aluminum fluoride is produced when partially dehydrated alumina hydrate reacts with hydrofluoric acids gas. The solid aluminum fluoride produced is cooled with noncontact cooling water prior to further processing, while the gases from the reactor are scrubbed with water to remove unreacted hydrofluoric acid from the gas stream. Aluminum fluoride is mainly used in the production of... [Pg.920]

C 0 and H O, unavoidable by-products of alcohols synthesis. Considering chemical reactions of table H, water and carbon dioxide appear as equiva-lentby-products due to shift conversion equilibrium, equation (1). Most other low temperature alcohol synthesis catalysts have a rather high shift activity as well. CO removal fhom reacted syngas of synthesis loop, before recycling to reactor, leads to a significant decrease of water formation which, in turn, results in a lower water content in the raw alcohols, leading to simplified fhactionation-dehydration processes. [Pg.46]

NH1CONH2 + H2O. The processing is complicated because of the severe corrosiveness of the reactants, usually requiring reaction vessels that are lined with lead, titanium, zirconium, silver, or stainless steel. The second step of the process requires a temperature of about 200 C to effect the dehydration of the ammonium carbamate. The processing pressure ranges from 160 to 250 atmospheres. Only about one-half of the ammonium carbamate is dehydrated in the first pass. Thus, the excess carbamate, after separation from the urea, must be recycled to the urea reactor or used for other products, such as the production of ammonium sulfate. [Pg.1651]


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