Accuracy of intraoral scanners versus traditional impressions: a rapid umbrella review

PURPOSE This study aimed to (1) report the trueness and precision of intraoral scanning (IOS) in dentistry based on recent secondary sources and to (2) appraise the reporting quality of the titles and abstracts of the included literature. MATERIALS AND METHODS This rapid overview searched the PubMed/Medline and Cochrane Database of Systematic Reviews in March 2021 to identify reviews reporting on the accuracy of IOS. The reference list from the eligible studies was also screened for identification of other potentially eligible studies. The inclusion criteria consisted of English language systematic reviews or meta-analyses published between 2019 and 2021. The exclusion criteria were primary studies, narrative review, and extraoral scanners. The assessment of reporting quality of abstracts of systematic reviews was performed using the reporting checklist PRISMA extension for Abstracts (PRISMA-A). This was a self-funded research project. RESULTS Out of the full text screened 25 records, 11 reviews were included. Most studies supported the IOS approach being as precise and accurate as the conventional one. Only one study significantly favored the conventional approach over the IOS, and two studies abstained from making a recommendation. The IOS was significantly superior to the traditional technique in terms of patient preference and time efficiency. After applying PRISMA-A, recommendations for improvements on titles and abstracts of future reviews of IOS and conventional impressions are provided. CONCLUSION Laboratory data indicated similar accuracy between IOS and conventional impressions, whereas clinical data found the same in less than 4-unit fixed dental prostheses. For more extensive definitive fixed solutions or removable prostheses, the conventional approach is recommended. IOS was superior in terms of patient preference and time reduction. More clinical trials are required to determine the clinical effectiveness of incorporating IOS in broader scenarios. Better quality of reporting secondary sources abstract is advised

The variation in composition of ultramafic rocks and the effect on their suitability for carbon dioxide sequestration by mineralization following acid leaching

Carbon dioxide capture and storage by mineralization has been proposed as a possible technology to contribute to the reduction of global CO2 levels. A main candidate as a feed material, to supply Mg cations for combination with CO2 to form carbonate, is the family of ultramafi c rocks, Mgrich silicate rocks with a range of naturally occurring mineralogical compositions. A classifi cation scheme is described and a diagram is proposed to display the full range of both fresh and altered ultramafi c rock compositions. This is particularly for the benefi t of technologists to raise the awareness of the variation in possible feedstock materials. A systematic set of acid leaching experiments, in the presence of recyclable ammonium bisulphate, has been carried out covering the range of ultramafi c rock compositions. The results show that lizardite serpentinite releases the most Mg with 78% removed after 1 h, while an olivine rock (dunite) gave 55% and serpentinized peridotites intermediate values. Antigorite serpentinite only released 40% and pyroxene- and amphibole-rich rocks only 25%, showing they are unsuitable for the acid leaching method used. This wide variation in rock compositions highlights the necessity for accurate mineralogical characterization of potential resources and for technologists to be aware of the impact of feed material variations on process effi ciency and development

Influence of electrode processing and electrolyte composition on multiwall carbon nanotube negative electrodes for sodium ion batteries

Dr. A. Fuente Cuesta would like to thank Agency for Green Technology (AGT), Dr. S. A. M. Dickson would like to thank the Faraday Institution NEXGENNA project (FIRG018), and C. Lonsdale would like to thank the Faraday Institution FUSE Internship Programme for funding. The authors also acknowledge the EPSRC (grant codes EP/L017008/1, EP/T019298/1, and EP/R023751/1).Nanostructured one-dimensional multiwall-carbon nanotubes have a variety of advantageous properties including good electrical conductivity and mechanical strength, and thus have been widely investigated for use in lithium-ion battery electrodes as conductive and microstructural additives, though also possess some electrochemical activity. Their application to sodium-ion batteries has been less extensively researched, and therefore a greater understanding of the electrochemical reaction with sodium, and effects of slurry composition and electrolyte formulation is warranted. Here, we report the fabrication of aqueous and organic multi-wall carbon nanotube negative electrodes processed by ball milling. The binder of choice is noted to greatly affect the electrochemical performance, both in terms of capacity retention and rate capability over a range of current densities from 25 to 500 mA g-1. Switching from a carbonate- to diglyme-based electrolyte considerably improves initial coulombic efficiencies (~10 to 60%), attributed to less extensive formation of solid electrolyte interphase, and enables a reversible mechanism with capacities up to 150 mAh g-1 over 100 cycles depending upon the binder used.Publisher PDFPeer reviewe

Manganese catalysed synthesis of polyketones using hydrogen borrowing approach.

We report here a new method to make polyketones from the coupling of diketones and diols using a manganese pincer complex. The methodology allows us to access a new type of polyketone (polyarylalkylketone) containing aryl, alkyl, and ether functionalities bridging the gap between the two classes of commercially available polyketones – aliphatic polyketones and polyaryletherketones. Using this methodology, twelve new polyketones have been synthesized and characterised using various analytical techniques to understand their chemical, physical, morphological, and mechanical properties. Based on previous reports and our studies, we suggest that the polymerization occurs via a hydrogen-borrowing mechanism that involves the dehydrogenation of diols to dialdehyde followed by aldol condensation of dialdehyde with diketones to form chalcone derivatives and their subsequent hydrogenation to form polyarylalkylketones

How the Neoproterozoic S-isotope record illuminates the genesis of vein gold systems: an example from the Dalradian Supergroup in Scotland

The genesis of quartz vein-hosted gold mineralization in the Neoproterozoic–early Palaeozoic Dalradian Supergroup of Scotland remains controversial. An extensive new dataset of S-isotope analyses from the Tyndrum area, together with correlation of the global Neoproterozoic sedimentary S-isotope dataset to the Dalradian stratigraphy, demonstrates a mixed sedimentary and magmatic sulphur source for the mineralization. d34S values for early molybdenite- and later gold-bearing mineralization range from 22 to +12‰, but show distinct populations related to mineralization type. Modelling of the relative input of magmatic and sedimentary sulphur into gold-bearing quartz veins with d34S values of +12‰ indicates a maximum of 68% magmatic sulphur, and that S-rich, SEDEX-bearing, Easdale Subgroup metasedimentary rocks lying stratigraphically above the host rocks represent the only viable source of sedimentary sulphur in the Dalradian Supergroup. Consequently, the immediate host rocks were not a major source of sulphur to the mineralization, consistent with their low bulk sulphur and lack of metal enrichment. Recent structural models of the Tyndrum area suggest that Easdale Subgroup metasedimentary rocks, enriched in 34S, sulphur and metals, are repeated at depth owing to folding, and it is suggested that these are the most likely source of sedimentary sulphur, and possibly metals, for the ore fluids