Two-laboratory collaborative study on identification of mycobacteria: molecular versus phenotypic methods

Previous studies have indicated that the conventional tests used for the identification of mycobacteria may (i) frequently result in erroneous identification and (ii) underestimate the diversity within the genus Mycobacterium. To address this issue in a more systematic fashion, a study comparing phenotypic and molecular methods for the identification of mycobacteria was initiated. Focus was given to isolates which were difficult to identify to species level and which yielded inconclusive results by conventional tests performed under day-to-day routine laboratory conditions. Traditional methods included growth rate, colonial morphology, pigmentation, biochemical profiles, and gas-liquid chromatography of short-chain fatty acids. Molecular identification was done by PCR-mediated partial sequence analysis of the gene encoding the 16S rRNA. A total of 34 isolates was included in this study; 13 of the isolates corresponded to established species, and 21 isolates corresponded to previously uncharacterized taxa. For five isolates, phenotypic and molecular analyses gave identical results. For five isolates, minor discrepancies were present; four isolates remained unidentified after biochemical testing. For 20 isolates, major discrepancies between traditional and molecular typing methods were observed. Retrospective analysis of the data revealed that the discrepant results were without exception due to erroneous biochemical test results or interpretations. In particular, phenotypic identification schemes were compromised with regard to the recognition of previously undescribed taxa. We conclude that molecular typing by 16S rRNA sequence determination is not only more rapid (12 to 36 h versus 4 to 8 weeks) but also more accurate than traditional typing.     

Electrochemical pre-treatment of effluents containing chlorinated compounds using an adsorbent

Electrochemical pre-treatment of industrial wastewater to remove refractory and/or toxic organic components, making them more amenable to biological treatment, is likely to be more cost-effective than using a physical or chemical process for complete organic removal. This paper demonstrates the use of a carbon-based adsorbent material that preferentially removes chlorinated organic compounds. Electrochemical regeneration of the adsorbent is shown to be a quick, easy and cheap process, because the adsorbent is both highly electrically conducting and non-porous. High regeneration rates over a number of cycles were obtained by passing a charge of 25 C g⁻¹ through a bed of adsorbent particles, at a current density of 20 mA cm⁻² for 10 min. The energy required to remove a kg of COD from an industrial wastewater was calculated to be 27 kWh.     

Comparison of the Effect of a Hydrocarbon Oil and a Terpene Tackifier on the Autohesion of Styrene-Butadiene Rubber

Blends of uncrosslinked styrene-butadiene rubber (SBR) with a terpene tackifier resin or a naphthenic oil have been characterized, and their autohesion and cohesion determined using a T-peel geometry. SBR/oil blends are homogeneous at all proportions, while SBR/resin blends, based on DSC and DMA analysis, undergo bulk phase separation at about 50% resin. However, migration of tackifier to the surface region is proposed at much lower resin contents. Compositions diluted with oil have autohesion similar to the neat SBR. This is attributed to compensating effects; although oil hastens self-bond formation by increasing chain mobility, this is nearly equally balanced by more facile chain separation during bond rupture. In short, oil-diluted compositions are soft and weak. On the other hand, SBR compositions containing small amounts of resin have high autohesion. Resin-diluted specimens deform easily at low strain, just as those containing oil, but intertwined chains of the former have greater resistance to separation, due at least in part to higher glass transition temperatures. It is proposed that autohesion is further enhanced by migration of tackifier to the surface. This causes SBR/resin compositions to be both soft and strong-a necessary condition for high autohesion.     

Al2O3/SiC复合陶瓷的反应烧结

在空气中于1600℃对Al2O3/0.78%SiC纳米复合体进行2h的反应烧结,制得Al2O3/5%莫来石复合陶瓷,其中的莫来石分为两类,即3Al2O3·2SiC和Al5.65Si0.35O9.175。采用SEM和TEM研究Al2O3/莫来石复全陶瓷的微观结构。对Al2O3/莫来石复合陶瓷的密度和力学性能如杨氏模量、泊松比、硬度、韧性和强度进行了研究。     

SOLUBILITY OF CO2 AND H2S IN A HINDERED AMINE SOLUTION

The solubility of H₂S and CO₂ in aqueous solutions of the sterically hindered amine, 2-amino-2-methyl-1-propanol (AMP), was determined at 40 and 100°C. Partial pressures of C)₂ ranged from approximately 2 to 6000 kPa and of H₂S from 2 to 2200 kPa. The solubility results were compared with previously reported acid gas solubilities in aqueous monoethanolamine (MEA) solutions.