Provided is a method of preparing a diester-based material, more particularly, a method of preparing a diester-based material, which is carried out by a continuous preparation process of a diester-based material including a reaction part in which a total of n reaction units from a first reaction unit to an nth reaction unit are connected in series, the reaction unit including a reactor which esterifies dicarboxylic acid and alcohol, including: esterifying dicarboxylic acid and alcohol in a reactor of the first reaction unit to produce a reaction product, and supplying a lower discharge stream including the reaction product to a reaction unit at a rear end through a lower discharge line; and supplying a liquid material through a liquid supply line connected to a lower discharge line of the reactor of the first reaction unit.

The present invention relates to a method of manufacturing a diester-based compound, and, more particularly, to a method of manufacturing a diester-based compound, which is performed using a continuous process including a reaction part in which a total of n reaction units spanning from a first reaction unit to an nth reaction unit are connected in series, wherein each of the reaction units includes a reactor, and the method includes: supplying a feed stream including a dicarboxylic acid and an alcohol into the first reactor; esterifying the feed stream to prepare a reaction product; and supplying a lower discharge stream including the reaction product into the reactor of the rear reaction unit. In this case, a conversion rate of the esterification reaction in the first reactor is controlled in a range of 50 to 80%.

The present disclosure relates to a volume tailorable manufacturing system for quality assured manufacturing of biosafety level classified biopharmaceutical products and a method for tailoring a production volume capability of a manufacturing system. The volume tailorable manufacturing system comprises one or more multi-product suites and a control facility configured to control a unidirectional flow in a circulation system of the one or more multi-product suites. The circulation system is configured to interconnect the one or more multi-product suites and comprises separated supply and return systems. The supply system comprising at least one inlet, the return system comprising at least one outlet that is paired with the inlet and provided at a spatially predetermined position from the inlet, and each inlet/outlet pair comprises a seal when not connected to an adjacent multi-product suite.

Disclosed is a method for the producingtiona target compoundby oxidative coupling of methane. A starting gas mixture is provided which contains an olefin, carbon monoxide, carbon dioxide and optionally hydrogen, wherein the olefin is subjected to hydroformylation with the carbon monoxide and the hydrogen of the starting mixture to obtain an aldehyde, wherein the paraffin and the olefin have a carbon chain with a first carbon number and the aldehyde has a carbon chain with a second carbon number which is greater by one than the first carbon number. The carbon dioxide present in the starting mixture is removed upstream and/or downstream of the hydroformylation. The carbon dioxide is subjected to dry reforming with methane to obtain carbon monoxide, and that the carbon monoxide subjected to hydroformylation comprises at least part of the carbon monoxide obtained in the dry reforming .

The invention relates to C.sub.5+ hydrocarbon conversion. More particularly, the invention relates to separating a vapor phase product and a liquid phase product from a heated mixture that includes steam and C.sub.5+ hydrocarbons, catalytically cracking the liquid phase product and steam cracking the vapor phase product.

Removal of solids accumulations that are attached to an inlet tube sheet of a heat exchanger in a hydrogenation reactor system by injecting a flush liquid through an injection port on the heat exchanger. Injecting the flush liquid removes portions of the solids accumulations.

Aldehyde generation includes providing a first input stream, a second input, and an alkene substrate to a reactor system. The first input stream includes a catalyst, a ligand, and an organic solvent. The second input stream includes a mixture of carbon monoxide (CO) and hydrogen gas (H.sub.2). The alkene substrate is in either gaseous form or liquid form, the liquid form of the alkene substrate being provided with the first input stream, the gaseous form of the alkene substrate being provided with the second input stream. The reactor system includes a first reactor and a second reactor, where the second reactor is gas permeable and positioned within the first reactor.

Embodiments of the present disclosure are directed to a diesel reformer system comprising: a diesel autothermal reforming unit; a post-reforming unit disposed downstream of the autothermal reforming unit; a heat exchanger disposed downstream of the post-reforming unit; and a desulfurization unit disposed downstream of the heat exchanger.

The present disclosure relates a system of preparing a phthalonitrile-based compound using a continuous process, the preparation system including: a first reaction unit filled with a mixture including a phthalic acid-based compound and a nitrile-based compound; a second reaction unit connected to the first reaction unit; and a discharge unit connected to the second reaction unit, and in the second reaction unit, there is a fluid flow from the first reaction unit direction to the discharge unit direction, wherein the length of the second reaction unit in the fluid flow direction is 10 fold or more the mean square root of the cross-sectional area perpendicular to the fluid flow direction; and a method of preparing a phthalonitrile-based compound using the same.

Methods and apparatus for introducing a gas into the reaction zone of a reactor. Such methods and apparatus can more evenly distribute the gas throughout the reaction zone. Spargers for introducing a gas into the reaction zone of a reactor can be employed in systems and methods for carrying out the liquid-phase oxidation of an oxidizable compound, such as para-xylene.