Mixture temperature prediction of waxy oil–water two-phase system flowing near wax appearance temperature

Temperature sensitivity of waxy crude oils makes it difficult to study their flow behaviour in the presence of water especially near their wax appearance temperature(WAT). In this study a method was proposed and implemented to mitigate such difficulties which was applied in predicting mixture temperatures(Tm) of a typical Malaysian waxy crude oil and water flow in a horizontal pipe. To this end, two analytical models were derived firstly from calorimetry equation which based on developed two correlations for defining crude oil heat capacity actualized from the existed specific heat capacities of crude oils. The models were then applied for a set of experiments to reach the defined three predetermined Tm(26 °C, 28 °C and 30 °C). The comparison between the predicted mixture temperatures(Tm,1and Tm,2) from the two models and the experimental results displayed acceptable absolute average errors(0.80%, 0.62%, 0.53% for model 1; 0.74%, 0.54%, 0.52% for model 2). Moreover,the average errors for both models are in the range of standard error limits(±0.75%) according to ASTM E230.Conclusively, the proposed model showed the ease of obtaining mixture temperatures close to WAT as predetermined with accuracy of ± 0.5 °C approximately for over 84% of the examined cases. The method is seen as a practical reference point to further study the flow behaviour of waxy crudes in oil–water two-phase flow system near sensitive temperatures.     

Note of the estimation of the Θ temperature and Ψ parameter from the critical temperature data

Summary Critical values of the polymer volume fraction _2,c and the interaction parameter _c have been computed for the case that the equation for the chemical potential of solvent contains terms _{c 2} ³ and _{c 2} ⁴ in addition to ₂ ² . For 0 _c 1/3, the limits for infinite chain length are _2,c = 0 and _c = 0.5. Quite different results are obtained for _c > 1/3, _2,c being finite and _c lower than 1/2. Conclusions for the estimation of the temperature and the entropy-of-dilution parameter are discussed.     

Resistivity–temperature characteristics of filler-dispersed polymer composites

Composites containing carbon nano tube (CNT) or carbon black (CB) conductive particle filler have the special characteristics of positive-temperature-coefficient (PTC) effects of resistivity. We quantitatively studied the relationship between poly(vinylidene fluoride) (PVDF) polymer's thermal volume expansion and the PTC effects of PVDF/CNT and PVDF/CB. The equation to revise filler content at each temperature due to the considerable thermal volume expansion rate of PVDF polymer indicates that filler content decreased with rising temperature. The graphs of filler content at room temperature plotted against apparent filler content with PTC effect were linear and their slopes were constant. From these graphs, we can determine the filler content necessary to occurring PTC effects. For example, the CNT content was 89% at room temperature, and the CB content was 93%. To our knowledge, this study is the first to report such phenomena.     

Adsorption of carbon dioxide at high temperature—a review

In this review, the adsorption of carbon dioxide on adsorbent materials at high temperature is examined critically. Adsorbent materials including carbon-based adsorbents, metal oxide sorbents, zeolites and hydrotalcite-like compounds (HTlcs) for carbon dioxide at high temperature are discussed. Research areas, which may make a significant impact in future are put forward.     

Co γ-irradiation-initiated RAFT polymerization of VAc at room temperature

In this work, the reversible addition-fragmentation chain transfer (RAFT) polymerization of vinyl acetate (VAc) was successfully performed at room temperature using ⁶⁰Co γ-irradiation as the initiation source. Under the dose rate of 10 Gy/min irradiation, the polymerization proceeded smoothly and converted approximately 90% of the monomer within 7 h. The molecular weight distribution (M_w/M_n) remained narrow (M_w/M_n < 1.35) up to 90% conversion. Compared to AIBN-initiated RAFT polymerization at 60 °C, ⁶⁰Co γ-irradiation-initiated RAFT polymerization is a technique that can better control the molecular weight, especially at high conversion. The ¹H NMR spectra and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry confirmed that most of the chain ends of poly(VAc) (PVAc) from γ-irradiated RAFT polymerization were living and can be reactivated for chain-extension reactions. The microstructures of PVAc from ⁶⁰Co γ-irradiated RAFT polymerization (almost head-to-tail addition) and AIBN-initiated RAFT polymerization (5% tail-to-tail addition) were different, as revealed by the ¹³C NMR spectra. For the first time, ⁶⁰Co γ-irradiation was used as an initiation source for RAFT polymerization of VAc at room temperature.     

Room temperature fatigue of ZrB2–SiC ceramic composites

Room temperature time dependent properties of ZrB₂–30 wt%SiC ceramic composite have been studied. Both static slow crack growth and cyclic fatigue deformation have been investigated. While static slow crack growth has been evaluated only in air, three different environments, water, air, and dry air, have been used to study the cyclic fatigue. It was established that under cyclic fatigue the environment plays an important role and humidity significantly facilitate crack growth in ZrB₂–30wt%SiC. The fractography of selected ZrB₂–30wt%SiC samples was performed and it was established that both defects introduced during machining as well as larger defects introduced during the processing served as fracture origins of ceramic composites.     

Hysteresis in the temperature dependence of the intensity of light scattering by boron oxide melt in the 300–450°C temperature range

It has been found that the temperature dependence of the intensity of the polarized V _v and depolarized H _v components of light scattering by a boron oxide melt in the range of 300–450°C is characterized by the existence of hysteresis: the specific feature of the change in the polarized V _v component is the formation of a minimum, while the specific feature in the behavior of the depolarized H _v component is associated with the appearance of a maximum in the sample heating mode; the cooling mode is accompanied by a monotonic change in the intensity of the light-scattering components. It has been found also that in the process of a low-temperature stabilization of the melt at 300°C, the polarized V _v component after reaching its minimum values increases up to the initial level, while the depolarized H _v component after passing its maximum decreases to the values smaller than the initial one. The characteristic time of the change in the intensity of the V _v component at 300°C is determined; its value was found to be ~100 min. It has been shown that an insignificant change in the melt synthesis conditions affects the detected features of the intensity change in the range of 300–450°C.     

Aqueous gelcasting of ZrB2–SiC ultra high temperature ceramics

ZrB₂–SiC ultra high temperature ceramics containing B₄C and C as sintering additives were successfully prepared by aqueous gelcasting and pressureless sintering. Polyacrylic acid (PAA) was used as the dispersant throughout this research. The various effects of zeta potential, pH value, dispersant concentration, solid loading and ball-milling time on the rheology and fluidity behavior of ZrB₂–SiC suspension were investigated in detail. A well-dispersed suspension with 50 vol.% solid loading was prepared at pH 10 with 0.4 wt.% PAA after ball milling at 240 rpm for 24 h. Then crack-free green ZrB₂–SiC ceramics were obtained by gelcasting process and then pressureless sintered at 2100 °C to about 98% relative density. The microstructure and mechanical properties were examined, and the flexural strength and fracture toughness were 405 ± 27 MPa and 4.3 ± 0.3 MPa m^1/2, respectively.     

New equation of ΔHbi for organic compound at different temperature

阐明Watson公式的不足和缺陷,应用分子热力学理论揭示出液体的汽化热取决于液体的分子间相互作用力,导出预测不同温度下有机纯质汽化热的新方程,其物理意义明确.经用39种结构类型的310个实验值检验,平均误差0.69%.Watson式为3.06%,本法的精度比Watson式高4.4倍以上.     

Low temperature firing of Co2Y–NiCuZn ferrite composites

Hexagonal structure magnetoplumbite ferrites have revealed a higher dispersion frequency than that of nickel ferrites because of the magnetoplumbite's magnetic anisotropy. The magnetoplumbite ferrite densification temperature always exceeds 1000 °C and the initial low temperature firing permeability of magnetoplumbite ferrites with added glass is too low (μ_i = 2–4). Therefore, it is desirable to develop a material that has a higher permeability at above 300 MHz and can be densified at temperatures below 900 °C. The Bi₂O₃–B₂O₃–ZnO–SiO₂ (BBSZ) glass addition effects on the densification and magnetic properties of Co₂Y–NiCuZn ferrite composites with various Co₂Y/NiCuZn ferrite ratios were investigated. The densification of Co₂Y–NiCuZn ferrite composites was enhanced by the addition of glass at low sintering temperatures (<900 °C) due to the liquid phase sintering. Co₂Y–NiCuZn ferrite composites with 4 wt% BBSZ glass sintered at 900 °C show a relative density above 90%, a high-initial-permeability of 5–6, a quality factor of above 30 in the 200–300 MHz frequency and a resonance frequency above 1 GHz, which can be used in high frequency multilayer chip inductors.     

Effect of calcination temperature on the oxidation of benzene with ozone at low temperature over mesoporous α-Mn2O3

Highly ordered mesoporous α-Mn₂O₃ was synthesized from cubic mesoporous silica (KIT-6) via nano-casting method. The mesoporous α-Mn₂O₃ thus obtained was calcined at 200-500 °C, and characterized using XRD, N₂ sorption and temperature-programmed reduction (TPR). The calcination temperature did not significantly affect the BET surface areas, mesopore sizes, pore structures and crystallinities of the mesoporous α-Mn₂O₃ materials. The mesoporous α-Mn₂O₃ calcined at 300 °C showed the highest catalytic activity due to its high reduction ability revealed from the TPR analysis. However, the catalytic activity was negligible without ozone. In addition, the selectivity to CO₂ was about 90% and this seems to be an advantage of mesoporous α-Mn₂O₃ for removing benzene using ozone.     

Non-fluorinated,room temperature curable hydrophobic coatings by sol–gel process

Non-fluorinated hydrophobic silica surfaces were generated on soda lime glass (SLG) substrates using hexamethyldisilazane (HMDS) as a surface modifying agent. Silica coatings were fabricated by dip coating of a sol derived from base catalyzed hydrolysis and condensation of tetraethoxysilane (TEOS). Two methodologies were adopted to generate the hydrophobic surface; one where the hydrophilic silica coated surface was treated by immersion into different concentrations of alcoholic solutions of HMDS varying from 2.5 wt% to 15 wt%. In the other method, HMDS was directly added to a mixture of TEOS, water, ethanol, and ammonium hydroxide and coatings were deposited using this sol by dip coating and spray coating. Water contact angles (WCA) were measured to study the effect of HMDS treatment times and concentrations on hydrophobicity in the first case, and in the second case, WCA were measured for dip and spray coated samples. UV–visible transmission, scratch resistance, and thermal stability of the coatings were determined. The WCA increased from 66 ± 2° to 125 ± 4° after the treatment of the silica coatings with HMDS. In case of coatings generated from direct addition of HMDS to silica sol, WCA varied from 145 ± 2° to 166 ± 4° for dip and spray coated surfaces respectively. Surface morphology was studied to explain the difference in hydrophobicity of coatings generated using the two methods.     

Polymerization temperature effects on the properties of l-lactide and ε-caprolactone copolymers

Summary The large difference in reactivity of L-lactide and -caprolactone in ring opening polymerization with stannous octoate, leads to the formation of copolymers with blocky structures. By varying the polymerization temperature, copolymers with different average sequence lengths and molecular weights can be synthesized. It is shown that the average monomer sequence length has a large effect on the thermal and mechanical properties of these copolymers.     

High temperature mechanical properties of laminated ZrB2–SiC based ceramics

Two laminated ZrB₂-SiC based ceramics were prepared by tape casting and subsequent hot pressing, with BN (LZB) and graphite (LZG ) as interface layers. The LZB specimen presents flexural strength of 381 MPa at room temperature and 111 MPa at 1500 °C; while the LZG specimen shows flexural strength of 414 MPa at room temperature and 377 MPa at 1500 °C. In addition, the flexural strength of LZG specimen is always higher than that of the LZB specimen in the temperature range from room temperature to 1500 °C. Such higher strength is attributed to the healing of surface microcracks and pores by the SiO₂ glass phase, producing less glass phase in graphite interface layers at high temperature.     

Room temperature ionic liquids as replacements for conventional solvents – A review

Room temperature ionic liquids are salts that are liquids at ambient temperature. They are excellent solvents for a broad range of polar organic compounds and they show partial miscibility with aromatic hydrocarbons. Typical room temperature ionic liquids have a stable liquid range of over 300 K and have a very low vapor pressure at room temperature. Ionic liquids that are not hydrolyzed show a wide range of solubility in water. These unique properties have suggested that they might be useful as environmentally benign solvents that could replace volatile organic compounds (VOC). By varying the length and branching of the alkane chains of the cationic core and the anionic precursor, the solvent properties of ionic liquids should be able to be tailored to meet the requirements of specific applications to create an almost infinitely set of “designer solvents”. A review of recent applications of ionic liquids is presented along with some results of measurements of liquid-liquid equilibria and partition coefficients with alcohols. The results are compared with predictions based on quantum mechanic calculations.     

Progress in the catalyst for ethylene/α-olefin copolymerization at high temperature

Ethylene/α-olefin copolymers are one of the most widely-used polyolefin materials. With the continuous improvement of polyolefin catalysts, high-performance polyolefin materials were synthesized by adjusting the chain microstructure, changing the comonomer type and comonomer insertion amount, among which the ethylene/α-olefin random copolymer elastomer (POE) and olefin block copolymer elastomer (OBC) are the most famous and well accepted by the market. The excellent properties of POE and OBC first depend on their polymer chain microstructure. The chain microstructure of polyolefins is fundamentally determined by the catalysts, polymerization conditions, comonomer feed policies, and reaction engineering. High-performance ethylene/α-olefin copolymer elastomers are currently prepared by high-temperature solution polymerization process, which needs to be carried out at a temperature above the melting point of the polymer and is beneficial to speed up the polymerization reaction rate and control the polyolefin chain microstructure. However, the high-temperature solution polymerization process launched more stringent requirements for the olefin coordination polymerization catalyst. Systematic reports on catalysts for high-temperature solution copolymerization of ethylene and α-olefins are lacking. In this review, we screened some catalysts suitable for the controllable copolymerization and high-temperature solution copolymerization of ethylene/α-olefin based on the catalyst's heat resistance, copolymerization activity, comonomer insertion ability, molecular weight, and distribution of the copolymer, including traditional Z–N catalysts, metallocene catalysts, and post-metallocene catalysts. And the future development of catalysts for high-temperature solution copolymerization of olefins, catalysts for precise control of polyolefin chain microstructures, and catalysts for olefin copolymerization with polar monomers at high temperature are envisaged.     

Exploring temperature dependence of the toughening behavior of β-nucleated impact polypropylene copolymer

In this study, the effects of α- and β-nucleating agents (α-NA and β-NA) on the toughening behavior of impact polypropylene copolymer were ascertained with respect to three test temperatures (23, 0 and ?15 °C). The addition of α-NA impacted the toughness slightly for all test temperatures. However, the tendency of impact strength vs. β-NA content at 0 °C significantly differs from that of the other two temperatures. Importantly, a close correlation between toughness at 0 °C and chain mobility of the amorphous portion has been well revealed for the first time by achieving a linearly fitting between impact strength at 0 °C and β-relaxation peak intensity in DMA spectrum. A comparative investigation between the situations containing α-NA or β-NA offers new insights into the physical origin of the toughening behavior for a multiphase multicomponent polyolefin system. The chain mobility of matrix amorphous portion plays a dominant role on toughening.     

SnO2‐supported palladium catalysts: activity in deNOx at low temperature

High surface area tin dioxide (174 m²/g) has been synthetised and characterised by XRD, TEM and UV‐visible DRS. DRS gives evidence for the formation of oxygen vacancies (donor levels) under reducing conditions. CO adsorption gives rise to terminal carbonyl species linked to Sn⁴⁺ and Sn²⁺. Palladium–tin oxide catalysts have been prepared from various precursors (Pd(acac)₂ and Pd(NO₃)₂) and by different preparation methods (grafting, photodeposition); they are active in deNOx reactions at low temperature (180 °C) in the presence of stoichiometric CO–NO–O₂ mixtures. A mechanism involving palladium and oxygen vacancies is proposed. This revised version was published online in July 2006 with corrections to the Cover Date.     

Size and temperature dependence of nanodiamond–nanographite transition related with surface stress

A model for the equilibrium transition size and temperature between nanodiamond and nanographite was established in terms of the effect of surface stress on the internal pressure of nanocrystals. It was found that as size and temperature decreased, the relative stability of diamond in comparison with graphite increased. The obtained result is consistent with other theoretical and experimental results.     

Microstructural and Mössbauer properties of low temperature synthesized Ni-Cd-Al ferrite nanoparticles

We report the influence of Al³⁺ doping on the microstructural and Mössbauer properties of ferrite nanoparticles of basic composition Ni_0.2Cd_0.3Fe_{2.5 - x}Al_xO₄ (0.0 ≤ x ≤ 0.5) prepared through simple sol-gel method. X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray, transmission electron microscopy (TEM), Fourier transformation infrared (FTIR), and Mössbauer spectroscopy techniques were used to investigate the structural, chemical, and Mössbauer properties of the grown nanoparticles. XRD results confirm that all the samples are single-phase cubic spinel in structure excluding the presence of any secondary phase corresponding to any structure. SEM micrographs show the synthesized nanoparticles are agglomerated but spherical in shape. The average crystallite size of the grown nanoparticles was calculated through Scherrer formula and confirmed by TEM and was found between 2 and 8 nm (± 1). FTIR results show the presence of two vibrational bands corresponding to tetrahedral and octahedral sites. Mössbauer spectroscopy shows that all the samples exhibit superparamagnetism, and the quadrupole interaction increases with the substitution of Al³⁺ ions.