A high-temperature plastic pyrolysis process that can produce high yields of ethylene, propylene and other light olefins from waste plastics is disclosed. The plastic feed is pyrolyzed at a high temperature of about 600 to about 900° C. directly to monomers, such as ethylene and propylene. During pyrolysis, the plastic feed is contacted with a diluent gas stream at a mole ratio of carbon feed to diluent gas of 0.6 to 20.

A plastic pyrolysis process produces light olefin product and heavier products. The light olefin products are separated in a recovery process while the heavier product can be sent to a cracking unit to be further cracked to desired products. The cracked effluent stream may be subjected to the recovery process along with the light olefin product.

The present disclosure relates to methods for processing plastic waste pyrolysis gas, such as methods wherein clogging of the systems used in the method is avoided or at least alleviated.

The present disclosure relates to methods for processing plastic waste pyrolysis gas, such as methods wherein clogging of the systems used in the method is avoided or at least alleviated.

A method and apparatus for continuously treating acid gases including recovering absorbent chemicals by introducing streams leaving a regenerator and/or leaving an absorber into a static mixing zone wherein supplemental washing water is added to recover absorbent chemicals. Improvements to the prior art methods are provided where one or more absorbent chemical recovery units are included to increase the amount of recovered absorbent chemicals exiting the regenerator and/or exiting the absorber are increased and/or maximized. Absorbent chemical recovery units can include mixing units where liquid is added to the stream of sour gas and absorbent chemical to mix with and absorb the absorbent chemical from the stream.

A method and apparatus for continuously treating acid gases including recovering absorbent chemicals by introducing streams leaving a regenerator and/or leaving an absorber into a static mixing zone wherein supplemental washing water is added to recover absorbent chemicals. Improvements to the prior art methods are provided where one or more absorbent chemical recovery units are included to increase the amount of recovered absorbent chemicals exiting the regenerator and/or exiting the absorber are increased and/or maximized. Absorbent chemical recovery units can include mixing units where liquid is added to the stream of sour gas and absorbent chemical to mix with and absorb the absorbent chemical from the stream.

A halides removal washing system for absorbing halides from a process gas within a process gas duct comprising a wash water injection nozzle and anti-precipitation means arranged around the nozzle, injection pipe and within the process gas duct.

A halides removal washing system for absorbing halides from a process gas within a process gas duct comprising a wash water injection nozzle and anti-precipitation means arranged around the nozzle, injection pipe and within the process gas duct.

The present invention is directed to metallocene catalyzed oligomerization of olefin feed stock without fractionation of alkane and olefin.

Methods and systems for recovering naphtha blend stock from hydrocarbons produced in a fluid catalytic cracking (FCC) process. In particular, the disclosure concerns gas plants for an FCC process, wherein the gas plant uses a dividing wall column. The dividing wall column essentially performs the functions that are performed in a traditional FCC gas plant by three different columns, namely, a primary absorber, a stripper, and a debutanizer.