Chelativorans petroleitrophicus sp. nov., a paraffin oil-degrading bacterium isolated from a mixture of oil-based drill cuttings and paddy soil.

We isolated a paraffin oil-degrading bacterial strain from a mixture of oil-based drill cutting and paddy soil, and characterized the strain using a polyphasic approach. The Gram-positive, aerobic, rod-shaped and non-spore-forming strain (SCAU 2101T) grew optimally at 50 °C, pH 7.0 and 0.5 % (w/v) NaCl. Phylogenetic analysis based on 16S rRNA gene sequence indicated that the strain represented a distinct clade in the genus Chelativorans, neighbouring Chelativorans intermedius LMG 28482T (97.1 %). The genome size and DNA G+C content of the strain were 3 969 430 bp and 63.1 mol%, respectively. Whole genome based phylogenomic analyses showed that the average nucleotide identity and digital DNA-DNA hybridization values between strain SCAU 2101T and C. intermedius LMG 28482T were 77.5 and 21.2 %, respectively. The major respiratory quinone was Q-10. The dominant fatty acids were C19 : 0 cyclo ω8c (50.6 %), summed feature 8 (C18 : 1 ω7c and/or C18 : 1 ω6c; 22.5 %) and C18 : 0 (13.8 %). The polar lipids of the strain included phosphatidylethanolamine, phosphatidylmonomethylethanolamine, phosphatidylglycerol, phosphatidylcholine and diphosphatidylglycerol. Based on the results, strain SCAU 2101T was considered to represent a novel species in the genus Chelativorans, for which the name Chelativorans petroleitrophicus sp. nov. is proposed. The type strain is SCAU 2101T (= CCTCC AB 2021125T=KCTC 92067T).

Hydration Kinetics of Portland Cement-Silica Fume Binary System at Low Temperature.

Portland cement-silica fume binary cementitious materials are widely used in engineering construction and have been investigated from micro- to macroscopic aspects. However, the theoretical background on the hydration kinetics of the binary system has not been sufficiently covered in the literature. In this study, the hydration dynamic characteristics of the Portland cement-silica fume binary system curing at low temperature were investigated. Hydration kinetics equations were optimized and a hydration model followed by a computer program was developed to calculate the reaction rate constant K and the reaction order n. This model presented that the hydration process of the binary system at low temperature could be divided into three stages, namely, nucleation and growth (NG), interactions at phase boundaries (I), and diffusion (D). The n values for the binary system varied in the range of 1.2 to 1.6, indicating that the hydration of the binary system at low temperature was a complex elementary reaction. Silica fume can reduce the total heat at the later stage of the hydration and the reaction order n, but increase the heat flow at the accelerating stage and the hydration rate constant K. Low temperature prolonged the hydration induction period, decreased and delayed the secondary exothermic peak, as well as reduced the n and K value.