Studies of propene conversion over H-ZSM-5 demonstrate the importance of propene as an intermediate in methanol-to-hydrocarbons chemistry

Funding Information: Johnson Matthey plc. is thanked for supplying the ZSM-5 zeolite and for financial support through the provision of industrial CASE studentships in partnership with the EPSRC (APH (EP/P510506/1), AZ (EP/N509176/1)). Experiments at the ISIS Neutron and Muon Source were made possible by a beam time allocation from the Science and Technologies Facilities Council. 53 The resources and support provided by the UK Catalysis Hubviamembership of the UK Catalysis Hub consortium and funded by EPSRC grants EP/R026815/1 and EP/R026939/1 are gratefully acknowledged. This research has been performed with the use of facilities and equipment at the Research Complex at Harwell; the authors are grateful to the Research Complex for this access and support.Peer reviewedPublisher PD

The Methyl Torsion in Unsaturated Compounds

The STFC Rutherford Appleton Laboratory is thanked for funding and access to neutron beam facilities. Computing resources (time on the SCARF compute cluster for the CASTEP calculations) was provided by STFC’s e-Science facility. Dr John Tomkinson (ISIS) is thanked for generously providing the INS spectra of the toluene isotopomers. A.Z. and A.P.H. would like to thank Johnson Matthey plc. For financial support through the provision of industrial CASE studentships in partnership with the EPSRC. The UK Catalysis Hub is kindly thanked for resources and support provided via our membership of the UK Catalysis Hub Consortium and funded by EPSRC grant: EP/R026939/1, EP/R026815/1, EP/R026645/1, EP/R027129/1 or EP/M013219/1(biocatalysis).Peer reviewedPublisher PD

Investigation of the dynamics of 1-octene adsorption at 293 K in a ZSM-5 catalyst by inelastic and quasielastic neutron scattering

The properties of 1-octene adsorbed in zeolite ZSM-5 at 293 K are studied by means of inelastic and quasielastic neutron scattering (INS and QENS) in order to investigate interactions relevant to the zeolite solid acid catalysis of fluidised catalytic cracking reactions. The INS spectrum is compared to that recorded for the solid alkene and reveals significant changes of bonding on adsorption at ambient temperatures; the changes are attributed to the oligomerization of the adsorbed 1-octene to form a medium chain n-alkane or n-alkane cation. QENS analysis shows that these oligomers are immobilised within the zeolite pore structure but a temperature-dependant fraction is able to rotate around their long axis within the pore channels

New Spectroscopic Insight into the Deactivation of a ZSM-5 Methanol-to-Hydrocarbons Catalyst

Funding Information: Johnson Matthey plc. is thanked for supplying the ZSM‐5 zeolite and for financial support through the provision of industrial CASE studentships in partnership with the EPSRC (APH (EP/P510506/1), AZ (EP/N509176/1)). Experiments at the ISIS Neutron and Muon Source were made possible by a beam time allocation from the Science and Technologies Facilities Council. The resources and support provided by the UK Catalysis Hub membership of the UK Catalysis Hub consortium and funded by EPSRC grants EP/R026815/1 and EP/R026939/1 are gratefully acknowledged. This research has been performed with the use of facilities and equipment at the Research Complex at Harwell; the authors are grateful to the Research Complex for this access and support. Dr Andrea Sauerwein and Dr Jonathan Bradley (Johnson Matthey) are thanked for their help in acquiring the Si and Al NMR spectra using the Bruker Avance Neo spectrometer.Peer reviewedPublisher PD

Onset of propene oligomerization reactivity in ZSM-5 studied by inelastic neutron scattering spectroscopy

The techniques of quasi-elastic and inelastic neutron scattering (QENS and INS) are applied to investigate the oligomerization of propene over a ZSM-5 zeolite. Investigations are performed at low temperatures, allowing identification of the onset of the oligomerization reaction and observation of the low-energy spectral changes due to intermediate formation that are difficult to observe by optical methods. Oligomerization proceeds via formation of a hydrogen-bonded precursor by an interaction of the propene with an internal acid site followed by protonation and chain growth with protonation being the rate-limiting step. The use of quasi-elastic neutron scattering to observe changes in system mobility with temperature via the elastic window scan technique allows identification of the active temperature range where catalyst activity commences and permits targeting of the more time-consuming INS investigations to conditions of interest. From examination of the product’s spectrum, the structure of the resulting oligomer is deduced to be primarily linear

sciCSR infers B cell state transition and predicts class-switch recombination dynamics using single-cell transcriptomic data

Class-switch recombination (CSR) is an integral part of B cell maturation. Here we present sciCSR (pronounced 'scissor', single-cell inference of class-switch recombination), a computational pipeline that analyzes CSR events and dynamics of B cells from single-cell RNA sequencing (scRNA-seq) experiments. Validated on both simulated and real data, sciCSR re-analyzes scRNA-seq alignments to differentiate productive heavy-chain immunoglobulin transcripts from germline 'sterile' transcripts. From a snapshot of B cell scRNA-seq data, a Markov state model is built to infer the dynamics and direction of CSR. Applying sciCSR on severe acute respiratory syndrome coronavirus 2 vaccination time-course scRNA-seq data, we observe that sciCSR predicts, using data from an earlier time point in the collected time-course, the isotype distribution of B cell receptor repertoires of subsequent time points with high accuracy (cosine similarity ~0.9). Using processes specific to B cells, sciCSR identifies transitions that are often missed by conventional RNA velocity analyses and can reveal insights into the dynamics of B cell CSR during immune response