Abstract:
A control scheme is set forth for conversion of variable composition synthesis gas to liquid fuels in a three-phase or slurry bubble column reactor (SBCR). The control scheme allows one to achieve constant or optimum liquid fuel production and constant or limited purge gas flow with highly variable synthesis gas feed condition. This is accomplished by adjusting one or more of the following independent variables: recycle ratio, water addition, and bypass flow.
Abstract:
There is provided a process control method for the production of acetic acid by the catalyzed carbonylation of methanol and a process for the manufacture of acetic acid using the process control method. The process control method comprises measuring various reactor component concentrations, specifically the active catalyst species, methyl iodide, water and methyl acetate by means of an infrared analyzer, and adjusting in response thereto the concentrations of at least the catalyst species, methyl iodide and water to optimize the acetic acid reaction.
Abstract:
Solid membranes comprising an intimate, gas-impervious, multi-phase mixture of an electronically-conductive material and an oxygen ion-conductive material and/or a mixed metal oxide of a perovskite structure are described. Electrochemical reactor components, such as reactor cells, and electrochemical reactors are also described. The reactor cells generally comprise first and second zones separated by an element having a first surface capable of reducing oxygen to oxygen ions, a second surface capable of reacting oxygen ions with an oxygen-consuming gas, an electron-conductive path between the first and second surfaces and an oxygen ion-conductive path between the first and second surfaces.
Abstract:
Apparatus and method for simultaneous recovery of hydrogen from water and from hydrocarbon feed material. The feed material is caused to flow over a heated catalyst which fosters the water-gas shift reaction (H.sub.2 O+COH.sub.2 +CO.sub.2) and the methane steam reforming reaction (CH.sub.4 +H.sub.2 O3 H.sub.2 +CO). Both of these reactions proceed only to partial completion. However, by use of a Pd/Ag membrane which is exclusively permeable to hydrogen isotopes in the vicinity of the above reactions and by maintaining a vacuum on the permeate side of the membrane, product hydrogen isotopes are removed and the reactions are caused to proceed further toward completion. A two-stage palladium membrane reactor was tested with a feed composition of 28% CQ.sub.4, 35% Q.sub.2 O (where Q=H, D, or T), and 31% Ar in 31 hours of continuous operation during which 4.5 g of tritium were processed. Decontamination factors were found to increase with decreasing inlet rate. The first stage was observed to have a decontamination factor of approximately 200, while the second stage had a decontamination factor of 2.9.times.10.sup.6. The overall decontamination factor was 5.8.times.10.sup.8. When a Pt/.alpha.-Al.sub.2 O.sub.3 catalyst is employed, decoking could be performed without catalyst degradation. However, by adjusting the carbon to oxygen ratio of the feed material with the addition of oxygen, coking could be altogether avoided.
Abstract translation:从水和烃进料同时回收氢的装置和方法。 使原料流过促进水煤气变换反应(H 2 O + CO + ZH 2 + CO 2)和甲烷蒸汽重整反应(CH 4 + H 2 O + Z 3 H 2 + CO)的加热催化剂。 这两个反应只进行部分完成。 然而,通过使用在上述反应附近仅对氢同位素可渗透的Pd / Ag膜,并且通过在膜的渗透侧保持真空,除去产物氢同位素并进一步进行反应 完成。 在连续操作的31小时内,用28%CQ4,35%Q2O(其中Q = H,D或T)和31%Ar的进料组成来测试两级钯膜反应器,其中4.5g氚 处理。 发现净化因子随进口速率的增加而增加。 观察到第一阶段的去污因子约为200,而第二阶段的去污因子为2.9×10 6。 整体去污因子为5.8×10 8。 当使用Pt /α-Al 2 O 3催化剂时,可以进行脱焦而没有催化剂降解。 然而,通过添加氧气调节进料的碳与氧比,可以完全避免焦化。
Abstract:
A reactor comprising: a hollow shell defining a hermetic enclosure; a plurality of tube sheets disposed within said hermetic enclosure, a first one of said plurality of tube sheets defining a first chamber; at least one reaction tube each having a first end and an opposing second end, said first end being fixedly attached and substantially hermetically sealed to one end of said plurality of tube sheets and opening into said first chamber, the second end being axially unrestrained; each of said reaction tubes is comprised of an oxygen selective ion transport membrane with an anode side wherein said oxygen selective ion transport membrane is formed from a mixed conductor metal oxide that is effective for the transport of elemental oxygen at elevated temperatures and at least a portion of said first and second heat transfer sections are formed of metal; each of said reaction tubes includes first and second heat transfer sections and a reaction section, said reaction section disposed between said first and second heat transfer sections; a reforming catalyst disposed about said anode side of said oxygen selective ion transport membrane; a first process gas inlet; a second process gas inlet; and, a plurality of outlets.
Abstract:
An electrochemical process for extracting oxygen from an oxygen-containing gas which uses an electrochemical cell having two zones separated by a multi-component membrane made from intimate, gas-impervious, multi-phase mixture of an electronically conductive phase and an oxygen ion-conducting phase. In one zone a gas containing oxygen is passed in contact with the membrane. In the other zone a gas capable of reacting with oxygen is passed in contact with the membrane.
Abstract:
Pyritic ores are heated with microwave energy in a fluidized bed to a temperature in the range of approximately 573 degrees Kelvin to 823 degrees Kelvin with a controlled amount of oxygen to promote the oxidation of the pyritic ores according to the reaction: 2FeS.sub.2 +3/2 O.sub.2 .fwdarw.Fe.sub.2 O.sub.3 +4S, thereby preventing the production of sulphur dioxide.
Abstract:
A method is described for maintaining constant chemical composition in solutions used for wet chemical processing. All chemical species that are deliberately included in the bath are kept at constant concentration primarily by a method of compensating for their depletion or generation with a set of feed solutions that are formulated and dosed into the bath in accordance with an overall material balance. Further, all chemical species not deliberately included in the bath are kept at constant concentration primarily by keeping the aggregate volume of replenishing stocks in strict proportion to the process service performed by the bath (e.g. the charge passed in an electroplating cell). Finally, a time-based scheme completes the control of the concentration of all bath species by controlling any species (whether deliberately included in the bath or not) that is depleted or generated as the result of chemical reactions which occur independently and/or spontaneously with time. Maintaining all bath chemical species at constant concentration prevents bath aging and permits production of more uniform work pieces from the bath.
Abstract:
A fluid bed reactor system and process employing a silyl chromate catalyst therein wherein the reactor system comprises a vertical reactor having a fluidizing medium permeable distribution plate towards the base thereof, a fluidizing medium supply line to supply fluidizing medium to the base of the reactor, a catalyst injection means to supply particulate catalyst to the side of the reactor, a polymer product recovery means to recover polymer product from the reactor and beneath the distribution plate, a fluidizing medium recycle line to recycle the fluidizing medium from and to the reactor, and a heat exchanger in the recycle line to remove heat of reaction from the recycled fluidizing medium.