By this invention processes are provided for the conversion of carbohydrate to ethylene glycol by retro-aldol catalysis and sequential hydrogenation using control methods having at least one of acetol (hydroxyacetone) and a tracer as inputs.

A method and system for renewing spent fluid catalytic cracking (SFCC) catalysts are disclosed which comprises: treating SFCC catalysts using a static reactor designed to uniformly distribute with an oxalic acid solution and its reflux to obtain leached SFCC catalysts; washing with aqueous solution and filtering to collect cleaned and treated SFCC catalyst; and c) executing the cleaned and treated SFCC catalyst with thermal treatment to obtain renewed FCC catalysts.

The present disclosure relates to processes for production of polyolefins from olefin monomer(s) in a gas phase reactor using condensing agent(s) (CAs), and in particular relates to controlling condensed phase cooling in a gas phase reactor used to polymerize olefin monomer(s). The method may include introducing first and second condensing agent(s) into the reactor at ratio(s) determined by ascertaining a stick limit for the first condensing agent, calculating an equivalence factor relating the first and second condensing agents, ascertaining total allowable condensing agent, and calculating amount of the first condensing agent removed and replaced by the second condensing agent. The method may further include calculating the dew point limit of a gas phase composition including olefin monomer(s) as well as the first and second condensing agents; and determining if introducing a mixture comprising the olefin monomer(s) and the condensing agent composition would exceed the calculated dew point limit.

A methanol synthesis plant comprising: a feed pretreating section operable to pretreat a feed stream; a synthesis gas (syngas) generation section comprising one or more reactors operable to produce a syngas synthesis product stream comprising synthesis gas from the feed stream; a methanol synthesis section comprising one or more methanol synthesis reactors operable to produce a synthesis product comprising methanol; and/or a methanol purification section operable to remove at least one component from the synthesis product to provide a purified methanol product; wherein the methanol synthesis plant is configured such that, relative to a conventional methanol synthesis plant, more of the net energy required by the methanol synthesis plant, the feed pretreating section, the syngas generation section, the methanol synthesis section, the methanol purification section, or a combination thereof, is provided by a non-carbon based energy source, a renewable energy source, and/or electricity.

A variable 3D CD nozzle includes: a flexible body defining a flow path having an inlet extending through a narrowed throat to an expanded outlet, wherein the flexible body comprises a plurality of flexible members movably interconnected together; and at least one means for changing a shape of the flexible body to change a dimension or location of the throat plane relative to at least one of the inlet plane or outlet plane. A method of changing airflow in a nozzle includes operating at least one means for changing the shape of the flexible nozzle body to change the dimension or the location of the throat plane. A method of testing an object includes placing a test object in the test region of the test cell and passing a test gas from the outlet opening of the nozzle onto the test object.

A method for controlling temperature of a chemical reaction without measuring a temperature of the chemical reaction. Changes in mass of a chemical reaction are monitored and are used to calculate the temperature of the system. The reaction can be maintained at a desired temperature (T) without measuring the temperature. The disclosed method is useful for reactions that occur at non-equilibrium conditions where any measured temperature would presume steady-state conditions.

A method for continuously producing a product (A1) by way of at least two coupled-together chemical reactions (C1, C2), wherein at least two input substances (E1, E2) are fed to a first chemical reaction (C1), wherein a plurality of intermediate substances (Z1, Z2) are produced from the input substances (E1, E2) by the first chemical reaction (C1), wherein at least one of the intermediate substances (Z2) is fed to a second chemical reaction (C2), wherein the at least one fed intermediate substance (Z2) is further processed by the second chemical reaction (C2), in particular using at least one further substance (W1, W2) in a second chemical reaction (C2) to form a plurality of output substances (A1, A2), that is to say to form the chemical product (A1) and at least one further output substance (A2), wherein the flow rates (F.sub.i) of the fed substances (E1, E2, Z1, W1, W2, A2) that are fed to one of the reactions (C1, C2) are set by a respective actuating element (V.sub.E1, V.sub.E2, V.sub.W1, V.sub.W 2, V.sub.Z 2, V.sub.A1), wherein each of the fed substances is assigned a separate actuating element, wherein a manipulated variable (S.sub.E2,R, S.sub.i,R) that is stipulated by a controller (R.sub.E2, R.sub.i) is respectively applied to at least one of the actuating elements, wherein, for changing the production rate of the chemical product (A1), a temporary manipulated variable (S.sub.E2,temp, S.sub.i,temp) is respectively applied during a transient phase (II, III) to at least one of these actuating elements (V.sub.E2, V.sub.i) instead of the manipulated variables (S.sub.E2, R, S.sub.i,R) stipulated by the respective controllers (R.sub.E2, R.sub.i), wherein the temporary manipulated variable (S.sub.E2,temp, S.sub.i,temp) or the temporary manipulated variables is/are generated by at least one control unit (SE) in dependence on a default value (NV).

A method of simultaneously modifying degradation rates of at least two compounds including a first compound having a first unmodified degradation rate constant k.sub.1 and a second compound having a second unmodified degradation rate k.sub.2 is provided. The method includes combining a first composition including the first compound with a second composition including the second compound, degrading the first compound and forming a first degradation product; and degrading the second compound and forming a second degradation product. The second degradation product modifies the first unmodified degradation rate constant k.sub.1 of the first compound to a first modified degradation rate k.sub.1′ and the first degradation product modifies the second unmodified degradation rate k.sub.2 of the second compound to a second modified degradation rate k.sub.2′. Compositions resulting from the method are also provided.

The invention relates to a reactor (1) for a chemical reaction, comprising a housing (10) and a reaction chamber (3), a nozzle member (30) with an inlet (32) for letting at least one reactant flow into the reaction chamber (3), wherein the nozzle member (30) is mounted in a movable manner relative to the housing (10), a sensor device (80) by means of which at least one measuring quantity can be detected during the chemical reaction, and an adjusting device (50) by means of which at least one mounting parameter influencing the movement of the nozzle member (30) can be adjusted, a control unit (70) configured for receiving from the sensor device (80) a measurement signal of the sensor device (80) based on the measuring quantity and generating a control signal for the adjusting device (50) depending on the measurement signal. The invention further relates to a method for controlling the chemical reaction.

The present disclosure is generally directed to a new and innovative system, process and method that utilize a new “non-oxygen type of oxidizers” process for methane (CH.sub.4) upgrading to value-added products such as olefins and aromatics (i.e., benzene, toluene and xylene (BTX)) etc. and further removing toxic impurities such as sulphur-containing compounds (i.e. H.sub.2S) by using the sulphur as a source of radical.