南堡35-2CEP平台净化水缓冲罐存在问题及改造措施

南堡35-2油田属于高粘重质油油田,油田CEP平台处理B平台热采井采出液的难度大。含油污水进入净化水缓冲罐后,造成顶部浮油聚集、底部沉积污泥。目前净化水缓冲罐内没有底部排污管线,只有固定式单管收油装置,且操作复杂,排油效率低。由于收油及排污不彻底,净化水缓冲罐净化水含油基本上比核桃壳滤器出口含油高4~7ppm。因此,需要对净化水缓冲罐内增加浮动式收油装置和底部排污管线,来达到提高注水水质的目的。     

Evaluation of Oxygen-Limitation on Lipid Oxidation and Moisture Content in Corn Oil at Elevated Temperature

The role of oxygen-limitation on lipid oxidation and moisture content were tested in corn oil heated to 60, 100, and 140 °C. The degree of oxidation was determined by analyzing headspace oxygen content, conjugated dienoic acids (CDA), and p-anisidine value (p-AV). The moisture content in bulk oil was analyzed by the Karl Fischer method. Oxygen-limited samples heated to 100 and 140 °C had significantly more lipid oxidation than oxygen-unlimited samples at early timepoints (p < 0.05). After this period, the oxygen-unlimited samples had more lipid oxidation based on CDA and p-AV assays. During those initial periods, oxygen-limited samples had significantly higher moisture content than oxygen-unlimited samples (p < 0.05), which implies that moisture content in oils plays an important role in the rate of lipid oxidation. The increased moisture content in bulk oil under oxygen-limited conditions is due to headspace moisture rather than moisture inside the oil. However, the effects of oxygen-limitation on lipid oxidation were less clear at 60 °C than at 100 or 140 °C.     

Higher Oxidation State Responsible for Ozone Decomposition at Room Temperature over Manganese and Cobalt Oxides: Effect of Calcination Temperature

The heterogeneous catalytic decomposition of ozone was investigated over unsupported manganese and cobalt oxide at room temperature. All catalysts were characterized by X-ray diffraction (XRD), N₂ adsorption–desorption (Brunauer–Emmet–Teller method), H₂-temperature programmed reduction (H₂-TPR) and X-ray photoelectron spectroscopy (XPS). The catalytic activity test indicated that these oxides had a good activity on ozone conversion meanwhile the catalysts remained highly active over time under reaction conditions. The treated temperature of the catalyst had a significant impact on the performance of ozone abatement and the samples treated at lower temperature showed higher activity. The surface area decreased obviously when developing the calcination temperature and H₂-TPR results demonstrated that much higher oxidation state of metal ions and active oxygen species were maintained on the surface under low treated temperature. XPS analysis showed that there were higher oxidation states of metal ions (Mn⁴⁺ and Co³⁺) and adsorbed oxygen species on the surface of catalysts treated at lower temperature, both of which play a significant role in ozone decomposition. However, the activity of manganese oxide was higher than that of cobalt oxide and the possible reason for this phenomenon was discussed.     

Effect of nanocarbon sources on microstructure and mechanical properties of MgO–C refractories

A study of microstructural evolution, mechanical and thermo-mechanical properties of MgO–C refractories, based on graphite oxide nanosheets (GONs), carbon nanotubes (CNTs) and carbon black (CB), was carried out by means of X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDS), three-point bending and thermal shock tests. Meanwhile, these results were compared to the conventional MgO–C refractory containing 10 wt% flaky graphite prepared under the same conditions. The results showed that higher cold modulus of rupture was obtained for the composition containing GONs, and the composition containing CNTs exhibited larger displacement after coking at 1000 °C and 1400 °C. Also, the addition of nanocarbons led to an improvement of the thermal shock resistance; in particular, both compositions containing CNTs and CB had higher residual strength ratio, approaching the thermal shock resistance of the reference composition containing 10 wt% flaky graphite, as it was associated with the presence of nanocarbons and in-situ formation of ceramic phases in the matrix.     

Spark plasma sintering of oxides and carbide dispersed zirconia inert matrix fuels

Zirconia-based inert matrix fuels reinforced by ZrC were synthesized via spark plasma sintering (SPS). Composites with full density were obtained. In order to prevent the oxidation introduced by dispersed ZrC in the bulk composite, SiC and ZrB₂ were later added into the composite and their capability to improve oxidation resistance was examined. SiC was found to form an oxidation layer which could enhance the oxidation resistance. In addition, micro hardness was improved attributing to effective sintering facilitated by silica flow and distribution of ZrC. With an optimum sintering condition and the addition of SiC, thermal conductivity was improved at higher temperature with the help of unoxidized ZrC reinforcement in the bulk composite.     

An initial study on feasible treatment of Serbian lignite through utilization of low-rank coal upgrading technologies

Despite benefiting from vast fuel reserves, combustion of low-rank coals is commonly characterized by low thermal efficiency and high pollutant emissions, partly due to high moisture content of the coals in question. Thus, removal of moisture from low-rank coals is deemed an important quality upgrading method. The paper provides an overview of the current status of low-rank coal upgrading technologies, particularly with respect to utilization of drying and dewatering procedures. In order to examine the influence of relevant parameters on the moisture removal process, a model of convective coal drying in a packed, as well as in a fluid bed combustion arrangement, is developed and presented. Product-specific data (intraparticle mass transfer, gas–solid moisture equilibrium) related to the coal variety addressed herein (lignite) are obtained through preliminary investigations. Effective thermal conductivity of the packed bed as defined by Zehner/Bauer/Schlünder is used to define heat transfer mechanisms occurring in the packed bed. Similar two-phase fluidization model has been validated for different types of biomaterials.     

Nanocrystalline Nd2O3: Preparation,phase evolution,and kinetics of thermal decomposition of precursor

Nd₂O₃ was synthesized by calcining Nd₂(C₂O₄)₃·10H₂O in air. The precursor and its calcined products were characterized by thermogravimetry and differential scanning calorimetry, Fourier transform infrared spectroscopy, X-ray powder diffraction, and scanning electron microscopy. The results showed that high-crystallized Nd₂O₃ with hexagonal structure was obtained when the precursor was calcined at 1223 K in air for 2 h. The crystallite size of Nd₂O₃ synthesized at 1223 K for 2 h was about 48 nm. The thermal decomposition of the precursor in air experienced three steps, which are first, the dehydration of 10 crystal water molecules; then, the decomposition of Nd₂(C₂O₄)₃ into Nd₂O₂CO₃; and last, the decomposition of Nd₂O₂CO₃ into hexagonal Nd₂O₃. Based on the KAS equation, the values of the activation energies associated with the thermal decomposition of Nd₂(C₂O₄)₃?10H₂O were determined.     

Synthesis and characteristics of fly ash and bottom ash based geopolymers–A comparative study

The research was carried out to develop geopolymers mortars and concrete from fly ash and bottom ash and compare the characteristics deriving from either of these products. The mortars were produced by mixing the ashes with sodium silicate and sodium hydroxide as activator solution. After curing and drying, the bulk density, apparent density and porosity, of geopolymer samples were evaluated. The microstructure, phase composition and thermal behavior of geopolymer samples were characterized by scanning electron microscopy, XRD and TGA-DTA analysis respectively. FTIR analysis revealed higher degree of reaction in bottom ash based geopolymer. Mechanical characterization shows, geopolymer processed from fly ash having a compressive strength 61.4 MPa and Young's modulus of 2.9 GPa, whereas bottom ash geopolymer shows a compressive strength up to 55.2 MPa and Young's modulus of 2.8 GPa. The mechanical characterization depicts that bottom ash geopolymers are almost equally viable as fly ash geopolymer. Thermal conductivity analysis reveals that fly ash geopolymer shows lower thermal conductivity of 0.58 W/mK compared to bottom ash geopolymer 0.85 W/mK.     

Evaluation of hot corrosion behavior of CSZ,CSZ/micro Al2O3 and CSZ/nano Al2O3 plasma sprayed thermal barrier coatings

Hot corrosion is one of the main destructive factors in thermal barrier coatings (TBCs) which come as a result of molten salt effect on the coating–gas interface. Hot corrosion behavior of three types of plasma sprayed TBCs was evaluated: usual CSZ, layer composite of CSZ/Micro Al₂O₃ and layer composite of CSZ/Nano Al₂O₃ in which Al₂O₃ was as a topcoat on CSZ layer. Hot corrosion studies of plasma sprayed thermal barrier coatings (TBCs) were conducted in 45 wt% Na₂SO₄+55 wt% V₂O₅ molten salt at 1050 °C for 40 h. The graded microstructure of the coatings was examined using scanning electron microscope (SEM) and X-ray diffractometer (XRD) before and after hot corrosion test. The results showed that no damage and hot corrosion products was found on the surface of CSZ/Nano Al₂O₃ coating and monoclinic ZrO₂ fraction was lower in CSZ/Micro Al₂O₃ coating in comparison with usual CSZ. reaction of molten salts with stabilizers of zirconia (Y₂O₃ and CeO₂) that accompanied by formation of monoclinic zirconia, irregular shape crystals of YVO₄, CeVO₄ and semi-cubic crystals of CeO₂ as hot corrosion products, caused the degradation of CSZ coating in usual CSZ and CSZ/Micro Al₂O₃ coating.