A multi-bed catalytic converter comprising: a plurality of catalytic beds which are traversed in series by a process gas, sequentially from a first catalytic bed to a last catalytic bed of said plurality, and at least one inter-bed heat exchanger (7) positioned between a first catalytic bed and a second catalytic bed of said plurality, wherein at least the last catalytic bed of said plurality is adiabatic and is made of fine catalyst with a particle size not greater than 2 mm.

The invention relates to an integrated process for assessing one or more properties of a catalyst. In the method, a standard chemical reactor or reactors is/are provided, and a bypass means is also provided, to transport a sample of whatever is added to the industrial reactor, to the test reactor. Both gases and liquids are transferred to the test reactor.

The invention concerns particles which may include a catalytically active component, in the form of a three-dimensional ellipsoidal shape having three major axes at least two of which axes are of different lengths. Beds of such particles are useful for forming particle beds through which a fluid may flow.

A continuous flow catalytic reactor, an assembling method therefor and an application thereof includes a reaction vessel, a filler packaged in the reaction vessel and a charged catalytic component; the charged catalytic component is fixed to the filler under an action of a direct-current electric field. The continuous flow catalytic reactor may be applied to continuous flow reactions such as a monosaccharide epimerization reaction. A monosaccharide epimerization reaction method includes: providing the continuous flow catalytic reactor; electrically connecting the continuous flow catalytic reactor with a direct-current power supply, thereby to forming the direct-current electric field by electrically connecting the continuous flow catalytic reactor with the direct-current power supply; and heating a reactor container to a target temperature, and inputting a monosaccharide solution from a liquid flow inlet of the reaction vessel and then collecting a solution containing a target product from a liquid flow outlet of the reaction vessel.

Processes for dehydrogenation of a hydrocarbon feedstock are described. The process can be run at lower H.sub.2/HC ratios and lower RITs while maintaining coke production at the same level as operation at higher H.sub.2/HC ratios and higher RITs without decreasing the yield per pass. Acceptable levels of coke were achieved when operating the process at low hydrogen to hydrocarbon molar ratio in the range of 0.01 to 0.40 and reactor inlet temperatures in the range of 500-645 C.

Some embodiments relate to an apparatus for holding a workpiece under tension while one or more operations are performed on the workpiece, the apparatus comprising: a frame; a first spindle rotatably coupled to the frame; a first coupler configured to couple the first spindle to a first end of the workpiece; a second spindle rotatably coupled to the frame; and a second coupler configured to couple the second spindle to a second end of the workpiece; wherein a distance between the first and second couplers is adjustable to hold the workpiece under tension between the couplers while the one or more operations are performed, and wherein the workpiece can be rotated with the couplers relative to the frame about a common axis of rotation extending between the couplers. Some embodiments relate to a system comprising a controller for controlling rotation of the workpiece. Embodiments also relate to processes comprising holding a workpiece under tension while performing one or more operations on the workpiece. Some of the processes, systems and apparatuses described may be particularly useful for cold spraying delicate workpieces such as 3D printed static mixers.

The present application relates to a process for producing normally gaseous, normally liquid, and optionally normally solid hydrocarbons from synthesis gas in a three-phase reactor, said reactor comprising a top middle and bottom part wherein the bottom and top part are fluidly connected via one or more reactor tubes, wherein one or more reactor tubes comprise randomly stacked catalyst bodies held stationary in the reactor tube and the reactor is at least partially filled with a liquid medium, said process comprising the steps of: (i) introducing the synthesis gas into the reactor via the bottom part; and (ii) contacting the synthesis gas with a stationary catalyst to catalytically convert the synthesis gas at an elevated temperature to obtain the normally gaseous, normally liquid, and optionally normally solid hydrocarbons from synthesis gas; (iii) withdrawing the normally gaseous, normally liquid, and optionally normally solid hydrocarbons; wherein the catalyst bodies have an open celled foam structure.

Processes for dehydrogenation of a hydrocarbon feedstock are described. The process can be run at lower H.sub.2/HC ratios and lower RITs while maintaining coke production at the same level as operation at higher H.sub.2/HC ratios and higher RITs without decreasing the yield per pass. Acceptable levels of coke were achieved when operating the process at low hydrogen to hydrocarbon molar ratio in the range of 0.01 to 0.40 and reactor inlet temperatures in the range of 500-645 C. The process uses a low coke catalyst.

Large pill dehydrogenation catalysts and large screens slot width are combined in dehydrogenation units to reduce the pressure drop across the catalyst bed and reactor screens compared to conventional screen and catalyst size combinations. The catalyst has an average pill diameter in the range of 1.6 mm to 3.0 mm, and the slot width of the screen is in the range of about 30% to about 60% of the pill diameter.

Disclosed are ruthenium-based catalyst systems, hafnium-based catalyst systems, and yttrium-based catalyst systems for use in ammonia decomposition. Catalyst systems include ruthenium, hafnium, and/or yttrium optionally in combination with one or more additional metals that can be catalytic or catalyst promoters. Hafnium-based and yttrium-based catalyst systems can be free of ruthenium. The catalyst systems also include a support material. Disclosed catalyst systems can decompose ammonia at relatively low temperatures and can provide an efficient and cost-effective route to utilization of ammonia as a carbon-free hydrogen storage and generation material.