To solve the problem of heavy oil demulsification difficulties in Liaohe Oilfield, phenolamine resin initiator was synthesized from p-trifluoromethyl phenol, and then FB series fluorinated polyether demulsifiers were synthesized by block polymerization using ethylene oxide (EO) and propylene oxide (PO) as raw materials. The demulsifiers were characterized by infrared spectroscopy, cloud point, hydrophilic–lipophilic balance (HLB) value, and surface tension. The demulsifying and dehydrating properties were tested by demulsifying and dehydrating experiments, the demulsification mechanism was analyzed by the microscopic demulsification process test, and the influence of demulsifier addition and demulsifying temperature on demulsifying performance was also studied. The results showed that under the condition of the optimum demulsification temperature of 60 °C and the optimum demulsifier dosage of 100 mg/L, the water removal (%) of fluorinated polyether demulsifier of FB 4 was the highest, and the overall water removal (%) of 50 mL crude oil emulsion in Liaohe Oilfield reached 90.33% within 2 h, which was better than the current demulsifier used in Liaohe crude oil.

Epoxy resin has become one of the most widely used polymers owing to their excellent comprehensive properties. However, the inherent inflammability of epoxy resin (EP) has seriously limited its application in a range of fields with high fire safety requirements. Herein, a novel shell–core hierarchy architecture (DAP@SiO₂) was prepared, composed of diammonium hydrogen phosphate (DAP) and in situ grown silica, and its structure and morphology were characterized by electron microscopy and infrared spectroscopy. The results indicated that silica particles were uniformly coated onto the surface of DAP. The modified DAP was used to reinforce the epoxy resin. The thermal stability of the EP blends was studied with the use of thermogravimetric analysis. The diammonium phosphate in DAP@SiO₂ flame retardant produces pyrolysis gases such as NH₃ and N₂ during decomposition, diluting the concentration of oxygen and flammable volatile products around the flame. Secondly, silica migrates to the surface of epoxy resin to form a shielding layer, forming compounds containing Si–O–Si and O–Si–C structures, which can be cross-linked with other condensed phase products, greatly improving the thermal stability of the carbon layer. Fire behavior was evaluated using the limiting oxygen index (LOI), vertical burning test, and the cone calorimetry, and the flame retardancy mode of action was explained. With 12% of DAP@SiO₂ involved, the EP blend passes UL-94 V-0 level, and its limiting oxygen index (LOI) reaches 33.2%. The incorporation of DAP@SiO₂ in an EP matrix showed a slight reduction in the heat release and smoke production. The flame retardant mode of the EP polymer shows that its flame retardant and smoke suppression characteristics are related to the interaction of flame retardants in the gas phase and condensed phase. The mechanical properties test results illustrated that the tensile strength, elastic modulus and impact strength of EP/3%DAP@SiO₂ are improved compared with pure EP. This is due to the crosslinking reaction between a large number of amino groups on the surface of DAP@SiO₂ and the epoxy group on the epoxy resin, which significantly enhances the interfacial compatibility between DAP@SiO₂ and epoxy resin, making the combination of DAP@SiO₂ and epoxy resin closer.

In this study, a novel spray drying-assisted self-assembly (SDAS) technology was proposed to prepare submicron elemental explosives with good morphology, uniform dispersion, and low sensitivity and spherical submicron RDX, HMX, and CL-20 particles without soft agglomeration were fabricated via such a method. Structural characterizations and thermal stability of the composites were systematically studied by scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimeter (DSC). Moreover, safety performance was analyzed by qualitative testing of impact sensitivity and friction sensitivity. The XRD analysis demonstrated that HMX and CL-20 refined by SDAS maintained the crystal structure of β-HMX and ε-CL-20 before and after refinement, whereas the HMX crystal structure after spray recrystallization refinement was transformed from β-HMX to α-HMX. The DSC results indicated that the thermal decomposition peak temperature of the three particles refined by the SDAS technology had a minimum advancement, and the thermal stability of the particles was relatively superior. More importantly, the H50 of the RDX, HMX, and CL-20 refined by this novel method was increased to 48.3 cm, 44.6 cm, and 31.1 cm, and the probability of friction explosion was decreased to 62%, 62%, and 80%, respectively, thus significantly improving the safety performance as compared with the sample refined by spray recrystallization.

This paper reported a new oily sludge compound cleaning agent formula, which used a combination of molecular simulation and experimental methods to study its interfacial formation energy (IFE), and exciting results were obtained. From a total of 24 surfactants in five categories, sodium silicate (Na₂SiO₃), sodium dodecylbenzene sulfonate, and fatty alcohol polyoxyethylene polyoxypropylene ether (JFC-SF) were screened out because of their excellent washing oil effect. Under a reasonable orthogonal system, when the mass ratio of the three surfactants was 3:1:1, the oil desorption effect was the best, the oil residual rate could reach 2.13%, and the oil removal efficiency could reach 93.53%. Verified by the molecular dynamics simulation module, the absolute value of the interface binding energy was the largest at this compound ratio, which was 465.71 kcal/mol. More importantly, we have discussed in depth the mechanism of adsorption and permeation of oily sludge by cleaning agents. Through single-factor influence experiments, the following optimized working condition parameters of the cleaning agent were determined: cleaning conditions with an agent content of 4%, a temperature of 70 °C, a stirring speed of 400 rpm, a cleaning time of 30 min, and a liquid–solid ratio (L/S) of 4:1. The research results laid the foundation for resource utilization, harmlessness, and reduction of oily sludge in the Liaohe oilfield.

In order to solve the problem of demulsification difficulties in Liaohe Oilfield, 24 kinds of demulsifiers were screened by using the interface generation energy (IFE) module in the molecular dynamics simulation software Materials Studio to determine the ability of demulsifier molecules to reduce the total energy of the oil–water interface after entering the oil–water interface. Neural network analysis (NNA) and genetic function approximation (GFA) were used as technical means to predict the demulsification effect of the Liaohe crude oil demulsifier. The simulation results show that the SDJ9927 demulsifier with ethylene oxide (EO) and propylene oxide (PO) values of 21 (EO) and 44 (PO) reduced the total energy and interfacial tension of the oil–water interface to the greatest extent, and the interfacial formation energy reached −640.48 Kcal/mol. NNA predicted that the water removal amount of the SDJ9927 demulsifier was 7.21 mL, with an overall error of less than 1.83. GFA predicted that the water removal amount of the SDJ9927 demulsifier was 7.41mL, with an overall error of less than 0.9. The predicted results are consistent with the experimental screening results. SDJ9927 had the highest water removal rate and the best demulsification effect. NNA and GFA had high correlation coefficients, and their R²s were 0.802 and 0.861, respectively. The higher R² was, the more accurate the prediction accuracy was. Finally, the demulsification mechanism of the interfacial film breaking due to the collision of fluorinated polyether demulsifiers was studied. It was found that the carbon–fluorine chain had high surface activity and high stability, which could protect the carbon–carbon bond in the demulsifier molecules to ensure that there was no re-emulsion due to the stirring external force.