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Gas field C is an unconventional tight gas reservoir located in the central of China which has prominent characteristics, including thin formation, low permeability and poor reservoir connectivity which significantly impact on the field development. Horizontal wells multistage hydraulic fracturing has been proven to be an effective technique to recover the hydrocarbons from this gas field. However, with continuous production overtime, reservoir pressure declines which results in a decrease in gas production rate below the critical gas velocity, leading to accumulation of liquid in the wellbore (liquid loading), which further results in back pressure and damage to the formation. Currently, gas field C loses up to 1500 mmscf/year in gas production and associated revenue due to liquid loading. Some other factors which hinders effective deliquification of the gas wells include remote well pad locations, poor road conditions during harsh weather conditions, friction with local communities, limited manpower to daily effectively analyze over 200 wells for liquid loading diagnostics and operational risks during well intervention. To tackle these challenges, a new versatile intelligent dosing technology has been piloted to reduce liquid loading. This remote-control dosing unit is located at the well pad and is equipped with automatic valves that can dispense two different chemicals (soap and methanol) in one unit. A key new feature of this system is the ability to receive and implement instructions that optimizes the dosing rate and frequency. This remote-control functionality eliminates on-site operator intervention and HSE risks especially in winter when the well pads could be inaccessible with poor road conditions.

Subulura chinensis Schwartz, 1926 is a hitherto poorly known nematode species. The morphology of S. chinensis has not been sufficiently well described. In addition, the molecular data from species of the Subuluroidea are extremely limited. The detailed morphology of S. chinensis was studied using light microscopy and, for the first time, scanning electron microscopy, based on newly collected specimens from the little owl Athene noctua (Scopoli) (Strigiformes: Strigidae) in China. The internal transcribed spacer (ITS) of ribosomal DNA and mitochondrial cytochrome c oxidase subunit 1 (cox1) target regions of S. chinensis were first amplified by polymerase chain reaction (PCR), then sequenced and analysed for the molecular identification of this species. Our SEM observations showed for the fist time the detailed morphology of the cephalic extremity, precloacal pseudo-sucker, caudal papillae, gubernaculum, phasmids and vulva of S. chinensis, and also determined the presence of a small, single medio-ventral precloacal papilla in the male. Moreover, we detected the presence of 0.08–0.40% and 0–1.30% nucleotide divergence among different individuals of S. chinensis in the ITS and cox1 regions, respectively. The supplementary morphological characters and genetic data will be very useful for the diagnosis of this poorly known species.

Aiming at the defects of repeating searching the path, low efficiency and the slow speed of the traditional topology algorithm, proposes a network topology algorithm based on Breadth-First-Search in this paper.Introduces the topology modeling method,and the electric equipment is abstracted into nodes and branches,making the topology process not constrained by the network connection and structure,enhancing universal property of the algorithm.Then introduces the traditional method, and analysises the disadvantages. At the same time,puts forward a new method. Uses node-branch adjacency list in the new method,which improves the topology speed.When the local switch information is changed, can modify the node-branch adjacency list to conduct the local re-topology,so it improves the topology flexibility. Finally, through the example, proves the superiority and practicability of this algorithm.

The quaternary TixZr1-xMnFe gettering alloys (x =0, 0.1, 0.2, 0.3 and 0.4) were synthesized successfully by arc melting and their phase structures along with microstructures had been investigated by optical microscopy (OM), scanning electron microscopy (SEM), X-ray diffraction (XRD) and transmission electron microscopy (TEM). It showed that the addition of Ti did not change the phase structure of ZrMnFe of C14 laves phase. XRD results showed that Ti successfully replaced part of the Zr and the decrease of interplanar spacing had a linear relationship with the increase of Ti content. The success of this trial preparation provides reference for nuclear industry gettering materials.

A new copper(II) complex, [Cu(naph-leu)phen]CH3OH·0.5H2O, in which naph-leu is the tridentate Schiff base ligand derived from the condensation of 2-hydroxy-1-naphthaldehyde and L-leucine, phen is phenanthroline, has been synthesized and characterized by elemental analyses, IR spectra and single crystal X-ray diffraction. The DNA-binding properties of this complex have been investigated by absorption spectra, fluorescence spectra and circular dichroism (CD) spectra, as well as viscosity measurement. Results show that this copper(II) complex binds to calf thymus DNA (CT-DNA) in an intercalative mode and its intrinsic binding constant Kb is 4.87×103 L·mol−1. Furthermore, the DNA cleavage activity of this copper(II) complex has also been investigated by submarine gel electrophoresis. Interestingly, it was found that this complex can cleave the supercoiled plasmid pBR322 DNA to both nicked and linear forms.

The enthalpies of dilution of matrine (MAT) in pure water and aqueous sodium chloride solutions were determined by isothermal titration microcalorimetry at 298.15 K, and the corresponding homogeneous enthalpic interaction coefficients were calculated according to the modified McMillan–Mayer model. The values of enthalpic pair-wise interaction coefficients, h 2, are all positive and become more positive with increasing concentration of sodium chloride.

The low-temperature heat capacities of berberine hydrochloride were measured over the temperature range from 78 to 350 K by an adiabatic calorimeter. The thermodynamic functions H T − H 298.15 and S T − S 298.15 were derived from the heat capacity data. The results showed that the structure of berberine hydrochloride was stable over the temperature range from 78 to 350 K. The thermal stability of the compound was further tested by DSC and TG measurements. The results were in agreement with those obtained from adiabatic calorimetry experiment. The standard molar enthalpy of formation in the crystalline state of berberine hydrochloride was obtained from the standard molar energies of combustion in oxygen at T = 298.15 K, measured by a rotating-bomb combustion calorimeter.

The dilution enthalpies of D-mannitol and D-sorbitol in aqueous sodium chloride solution at various concentrations have been determined by isothermal microcalorimetry at 298.15 K. The homogeneous enthalpic interaction coefficients over a quite large range of concentration of aqueous sodium chloride solutions have been calculated according to the excess enthalpy concept. The results show that enthalpic pairwise interaction coefficients (h 2) of D-mannitol and D-sorbitol are positive in aqueous sodium chloride solution and become more positive with increase of the concentration of sodium chloride. The results are interpreted in terms of the different conformations of the two polyols, solute-solute and solute-solvent interactions involved by solvent effects.

A series of organotin (IV) compounds of the type [R3SnL]2, R is Me (1), Bu (2), [R2SnL]2, R is Ph (3), Me (4), Bu (5), L is pyruvic acid thiophene-2-carboxylic hydrazone, and R2SnL, R is Me (6), Bu (7), Ph (8), L is salicylaldehyde thiophene-2-carboxylic hydrazone have been synthesized in 1:1 molar ratio. All compounds were characterized by elemental analysis, IR, 1H NMR, 13C NMR and 119Sn NMR spectra. The crystal structure of compounds 1, 3, 4, 8 have been determined by X-ray single crystal diffraction analyses, study found that the compounds 1 and 3 are rendered one-dimensional chain structure and the tin atoms are five-coordinated in a distorted trigonal-bipyramidal geometry. The compound 4 has a dimeric structure and the central tin atom is rendered seven-coordinate in a distorted pentagonal-bipyramid configuration. While the compound 8 is a monomer in which the tin atom adopts five-coordinated in distorted trigonal-bipyramidal geometry.

A series of diorganotin(IV) and triorganotin(IV) compounds of the type [R2Sn(pca)2ClSnR3]2 (R PhCH2 1, 2-ClC6H4CH2 2, 2-FC6H4CH2 3, 4-FC6H4CH2 4, 4-CNC6H4CH2 5, 4-ClC6H4CH2 6, 2,4-Cl2C6H3CH2 7; Hpca 2-methylpyrazine-5-acid), [(nBu)3Sn(pca)]∞ 8, [(CH3)2Cl2Sn(pca)Sn(CH3)2(pca)]∞ 9, {[(nBu)2Sn(pca)]2O}2 10 and {[Ph2Sn(pca)]3O2[Ph2Sn(OCH3)]} 11 have been obtained by reactions of 2-methylpyrazine-5-acid with triorganotin(IV) chloride, diorganotin(IV) dichloride, and diorganotin(IV) oxide. All compounds were characterized by elemental, IR, and NMR spectra analyses. The crystal structure of compounds 1, 8–11 were determined by X-ray single crystal diffraction, which revealed that compound 1 was tetranuclear macrocyclic structures with seven-coordinate and five-coordinate tin atoms, compounds 8 and 9 were polymeric chain structures with five-coordinate and seven-coordinate tin atoms, compounds 10 and 11 were monomeric structures with six-coordinate and five-coordinate tin atoms.