Future penetration and impacts of electric vehicles on transport energy consumption and CO_2 emissions in different Chinese tiered cities

This study focuses on the penetration of electric vehicles(EVs) within the private passenger vehicle market in selected Chinese cities categorized into different tiers. It presents an analysis of factors driving the market diffusion of EVs and the reasons for varying results across the investigated cities and provides estimates of related EV impacts on local energy consumption and CO_2 emissions. A nested multinomial model incorporating technological attributes of vehicles, energy prices, charging conditions,and incentive policies was developed for conducting a scenario analyses covering six cities. The results indicated that in a stagnation scenario in which policy support was absent, the market share of electric vehicles would be less than 7% in all six cities under investigation by 2030. In medium growth and rapid growth scenarios, the market share of EVs across the six cities was projected to be within the ranges of 29%–68% and 49%–80%, respectively. The impacts of EVs on gasoline demand depended not just on their cumulative sales but also on the share of electrified vehicle distance, and the CO_2 emission reduction effect was influenced by local EV stocks and the mix of local electricity sources. Battery costs, charging conditions, and energy prices were primary driving factors. Charging conditions and energy prices were key reasons for differences in the penetration curves among cities. These driving factors were further affected by differences in local income levels, housing and parking conditions, and availability of land resources. Subsidies were found to be effective in the short term, whereas in the medium term,tax breaks could serve as the main monetary incentive. In the long term, national policy should focus on technology-related RD, whereas local policies should focus on the operational phase and be tailored to specific local situations.     

Effect of Na<Subscript>2</Subscript>CO<Subscript>3</Subscript> and CaCO<Subscript>3</Subscript> on coreduction roasting of blast furnace dust and high-phosphorus oolitic hematite

Iron was recovered from blast furnace dust and high-phosphorus oolitic hematite in the presence of Na₂CO₃ and CaCO₃ additives. The functions of Na₂CO₃ and CaCO₃ during the coreduction roasting process were investigated by XRD and SEM-EDS analyses. Results indicate that these additives not only hinder the reduction of fluorapatite, CaCO₃ also decreases the P content of direct reduced iron (DRI) by increasing the reduction alkalinity. P remains as fluorapatite in the slag, which can be removed by grinding and magnetic separation under optimal conditions. The Na₂CO₃ promotes hematite reduction and improves the iron recovery (ε_Fe) by replacing the FeO from fayalite, which results in quick growth and aggregation of metallic iron and improvement of ε_Fe in DRI. A DRI with 91.88 mass% Fe, and 0.065 mass% P can be achieved at a recovery of 87.86 mass% under the optimal condition.     

Effects of CaO and Na<Subscript>2</Subscript>CO<Subscript>3</Subscript> on the reduction of high silicon iron ores

The effects of CaO and Na₂CO₃ on the reduction of high silicon iron ores at 1 250 °C were studied. The experimental results showed that the metallization rate was significantly hindered by the addition of CaO and Na₂CO₃, particularly at the early stage of roasting, compared to the rate without additives. In the absence of additives, iron oxides were quickly reduced to metallic iron, and fayalite was difficult to form. When CaO and Na₂CO₃ were added, the low reducible iron-containing silicate compounds formed and melted, subsequently retarding the metallization process. The inhibition of Na₂CO₃ was more noticeable than that of CaO, and higher Na₂CO₃ doses resulted in stronger inhibition of the increased metallization rate. However, when Na₂CO₃ was added prior to CaO, the liquid phase formed, which facilitated the growth of the metallic phase. To reinforce the separation of the metallic phase and slag, an appropriate amount of liquid phase generated during the reduction is necessary. It was shown that when 10% CaO and 10% Na₂CO₃ were added, a high metallization rate and larger metallic iron particles were obtained, thus further decreasing the required Na₂CO₃ dosage.     

Fundamental study of CO<Subscript>2</Subscript> control technologies and policies in China

The technical roadmap and policies for CO₂ mitigation suitable for China are a common center of attention in the fields of energy, environment, and management science in the country. Emphasizing interaction between technical research and policy research, this work discovers the potential breakthrough in the integrated field. The technical difficulties of recovering CO₂ are pointed out, the mechanism of combining CO₂ recovery with energy conversion is investigated, and the basic principle for integrating an environmental-friendly energy system is discussed. Moreover, the formulation of a new energy system that can recover CO₂ with very low or even zero energy penalty is proposed, while the assessment methodology and model system for the technical roadmap of CO₂ emission control are developed. Finally, a new technical roadmap constructing an energy network suitable for China is proposed, which may provide a new way for the development of sustainable energy and environment technologies. Supported by the major international cooperation projects of the National Natural Science Foundation of China (Grant No. 50520140517)     

Research and application of CO<Subscript>2</Subscript> refrigeration and heat pump cycle

The environmental problem caused by refrigerant has become the focus all over the world. As the most typical natural refrigerant, CO₂, of course, becomes the research focus. This paper introduces the development and application status of CO₂ refrigeration and heat pump technology. The researches on CO₂ refrigeration and heat pump, carried out by Thermal Energy Research Institute, Tianjin University, also are presented in this paper. Supported by the National Natural Science Foundation of China (Grant Nos. 50676064, 50506019) and the National Hi-Tech Research and Development Program of China (“863” Project) (Grant No. 2007AA05Z262)     

Hydrothermally Synthesizing Nanospheres of Pd Loaded TiO<Subscript>2</Subscript> for Photocatalytically Reducing CO<Subscript>2</Subscript> in Isopropanol to Isopropyl Formate

Photocatalytic reduction of CO₂ was carried out on villiform spherical catalysts of Pd-TiO₂ in isopropanol solution. The catalysts were synthesized by hydrothermal method, their structures, morphologies and optical absorption properties were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM) and UV-vis absorption spectroscopy (UV-vis). The photocatalytic activities with different loading amounts and morphologies were evaluated for determining the dominant effect and optimizing the catalyst preparation. Based on a villiform spherical TiO₂ with the largest specific surface area in our experiments, we prepared a set of catalysts with various loading amounts of palladium and tested them by bubbling CO₂ through the slurry of catalyst and isopropanol. The highest formation rate of isopropyl formate was 276.6 μmol/g·cat/h. Eventually we proposed the reaction mechanism.     

Generation of electricity from CO<Subscript>2</Subscript> mineralization: Principle and realization

Current CO₂ reduction and utilization technologies suffer from high energy consuming. Thus, an energy favourable route is in urgent demanding. CO₂ mineralization is theoretically an energy releasing process for CO₂ reduction and utilization, but an approach to recovery this energy has so far remained elusive. For the first time, here we proposed the principle of harvesting electrical energy directly from CO₂ mineralization, and realized an energy output strategy for CO₂ utilization and reduction via a CO₂-mineralization fuel cell (CMFC) system. In this system CO₂ and industrial alkaline wastes were used as feedstock, and industrial valuable NaHCO₃ was produced concomitantly during the electricity generation. The highest power density of this system reached 5.5 W/m², higher than many microbial fuel cells. The maximum open circuit voltage reached 0.452 V. Moreover, this system was demonstrated viable to low concentration CO₂ (10%) and other carbonation process. Thus, the existing of an energy-generating and environmentally friendly strategy to utilize CO₂ as a supplement to the current scenario of CO₂ emission control has been demonstrated.     

Effect of ZnO-B<Subscript>2</Subscript>O<Subscript>3</Subscript> glass addition on the microwave dielectric properties of BaO-Nd<Subscript>2</Subscript>O<Subscript>3</Subscript>-TiO<Subscript>2</Subscript>-Bi<Subscript>2</Subscript>O<Subscript>3</Subscript> system

The effect of ZnO-B₂O₃(ZB) glass addition on the sintering behavior, microstructures and microwave dielectric properties of BaO-Nd₂O₃-TiO₂-Bi₂O₃ (BNTB) system was investigated with the aid of X-ray diffraction, scanning electron microscopy and capacitance meter. It is found that the ZB glass addition, acting as a sintering aid, can effectively lower the sintering temperature of BNTB system to 850 °C. The dielectric constant of BNTB-ZB ceramics increases with the increase of soaking time and the value of dielectric loss decreased with increasing soak time. The optical dielectric properties at 1 GHz of ɛ=74, tan δ=4×10⁻⁴, and TCC=25 ppm/°c were obtained for the BNTB system doped with 25 wt% ZB glass sintered at 850 °C for 2 h, representing that the BNTB-ZB ceramics could be promising for multilayer low temperature co-fired ceramics applications.     

Influences of heat treatments on crystallization in SiO<Subscript>2</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-MgO-K<Subscript>2</Subscript>O-F glass-ceramics

Five kinds of heating treatment processing were chosen according to the experiment result of differential scanning calorimeter to prepare SiO2-Al2O3-MgO-K2O-F glass ceramics samples.The effects of heat treatment processing on the crystallization of these samples were explored by X-ray diffraction and scanning electron microscopy techniques.The results indicate that phase separations can occur in the bulk regions of the glass sample when holding at 670 ℃ for 3 h.The phase separation can accelerate the precip...     

Preparation and characterization of nanocomposite MgFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/SiO<Subscript>2</Subscript>

Nanocomposites MgFe₂O₄/SiO₂ were successfully synthesized by the sol-gel method in the presence of N, N-dimethylformamide (DMF). The formation of pure MgFe₂O₄ was confirmed by powder X-ray diffraction (XRD) and electron diffraction. The structural evolution of MgFe₂O₄ nanocrystals was followed by powder X-ray diffraction and IR absorption spectroscopy. The formation of spinel structure of MgFe₂O₄ started at 800 °C, and completed at 900 °C. The transmission electron microscopy (TEM) measurements suggest that the particle sizes increase with the increasing annealing temperature, and the mean particle sizes of the spherical samples annealed at 800 °C, 900 °C and 1 050 °C are ca. 3 nm, 8 nm and 11 nm, respectively. Magnetization measurements at room temperature and 78 K indicate superparamagnetic nature of these MgFe₂O₄ nanocrystals. Funded by the National Natural Science Foundation of China(No. 30771676), the Natural Science Foundation of Jiangsu Province (No. BK20081842), and the Foundation of Nanjing Bureau of Personal for the Returned Overseas Chinese Excellent Scholars     

A single-phase of supercritical CO<Subscript>2</Subscript>/ Polystyrene solution in foam extrusion

The high quality single-phase solution of CO2/ Polystyrene was achieved,by analyzing the influential factors for polymer microcellular foaming extrusion.The curve of pressure distribution along the barrel was determined.The axial position of gas-injecting port on the barrel was chosen form the results of stable foaming,and the number of gas-injecting ports in the circumference of the barrel was determined from the CO2 solubility in polymer.The effect of the screw rotation speed on CO2 solubility was studied,and the effects of pressure difference between the gas and the polymer melt on gas-injecting process and on the foaming stability were investigated.The influence of the gas temperature before injection on the single-phase of CO2/Polystyrene solution also was studied.     

Effect of temperature on polishing and flatting time of float-formed Li<Subscript>2</Subscript>O-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-SiO<Subscript>2</Subscript> glass

Li₂O-Al₂O₃-SiO₂ glass prepared from traditional melting and cooling process was investigated. The surface characteristic of LAS glass was studied by simulating tin bath with different temperature and time, and the effect of surface tension/viscosity ratio on flatting time was analyzed. The results demonstrated that LAS glass can polish effectively when polishing at 1 300 for 8 °C min, and the optimum flatting and polishing temperature was 1 250–1 300 °C.     

Effect of aluminum addition on microstructure and properties of SiO<Subscript>2</Subscript>-B<Subscript>2</Subscript>O<Subscript>3</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-CaO vitrified bond

Influence of aluminum addition on the structures and properties of SiO₂-B₂O₃-Al₂O₃-CaO vitrified bond at low sintering temperature and high strength was discussed. FTIR and XRD analyses were used to characterize the structures of the basic vitrified bond with different contents of aluminum. The bending strength and the thermal expansion coefficients were also tested. Meanwhile, the microstructures of composite specimens at sintering temperature of 660 °C were observed by scanning electron microscope (SEM). The experimental results showed that the properties of vitrified bond with 1wt% aluminum were improved significantly, where the bending strength, Rockwell hardness, and thermal expansion coefficient of the vitrified bond reached 132 MPa, 63 HRB, and 6.73×10^-6 °C^-1, respectively.     

Joining of 25CePO4／ZrO2 and ZrO2 on Green State Without Pressure

High-yielding low-cost vanadium oxide nanotubes were prepared by hydrothennal self-assembling process from vanadium pentoxide and organic molecules as structure-directing templates..Moreowr, a new method was discovered to determine the content of V (IV) in vanadium oxide nanotubes by thermograrimetric analysis ( TGA ). This method can be extended to determine the content of low oxidation state in other transition metal oxide nanomaterials.     

Optical and magnetic properties of Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>/SiO<Subscript>2</Subscript> nano-composite films

Fe₂O₃/SiO₂ nano-composite films were prepared by sol-gel technique combining heat treatment in the range of 100–900 °C. The particle size was observed by FE-SEM. Optical properties of the films were investigated by UV-visible spectra. Structural and magnetic characteristics were investigated through FT-IR and VSM. The transparency of the Fe₂O₃/SiO₂ nano-composite films decreased with the content of the Fe₂O₃. Water and organic solvent in the films were evaporated with heat treatment, so the transparency of the films was enhanced under high temperature. It is also found that the saturation magnetization (M _s) of the films increases with the temperature. As the content of the Fe₂O₃ increases, when the content of the Fe₂O₃ is around 30wt%, the M _s of the films has a maximum value.     

Preparation,structure and dielectric properties of tungsten bronze ferroelectrics in SrO-Eu<Subscript>2</Subscript>O<Subscript>3</Subscript>-TiO<Subscript>2</Subscript>-Nb<Subscript>2</Subscript>O<Subscript>5</Subscript> system

Compounds Sr4Eu2Ti4Nb6O30 and Sr5EuTi3Nb7O30 with filled tetragonal tungsten bronze structure were prepared,and the dielectric characteristics and ferroelectric transition were investigated.Both ceramics displayed weak frequency dependence in room temperature dielectric constant,which decreased from 125 to 118 for Sr4Eu2Ti4Nb6O30,from 206 to 195 for Sr5EuTi3Nb7O30 in the frequency range of 10 kHz to 1 MHz.The present ceramics showed a diffuse ferroelectric phase transition.The frequency independent transition temperature (Tm) indicated the above compounds had no relaxor property.The diffuseness (γ) was 1.45 and 1.64 for Sr4Eu2Ti4Nb6O30 and Sr5EuTi3Nb7O30 respectively.The weak ferroelectric of the present materials are indicated from the P-E hysteresis loops,and a small 2Pr of 0.596 μC/cm2 and 0.068 μC/cm2 were observed for Sr4Eu2Ti4Nb6O30 and Sr5EuTi3Nb7O30 respectively.     

Effect of Grain Size of CaCO3 and SiO2 on the Formation of C3S Under Different Conditions

The effect of grain size of CaCO3 and SiO2 on the formation of C3S under various conditions, such as rapid heating rate（800 ℃/min）, normal heating rate（30 ℃/min） and in the presence or absence of ZnO, was studied. The results show that the decomposition temperature of CaCO3, the temperature of appearance of liquid phase and the f-CaO content descend when the grain size of CaCO3 and SiO2 becomes smaller, which attributes to the reactive activity enhancement of powders due to the decrease of the particle size. When the grain size of CaCO3 and SiO2 is below 1 μm, the rate of the formation of C3S is greatly raised. A rapid sintering rate and the presence of ZnO have an important effect on the formation of C3S and can lower the temperature of the formation of C3S by about 50 ℃.     

Conformation of Organic Chain in Phase Transition of Hybrid （Cl2H25NH3）2MnCl4

The structural change in phase transition of hybrid （Cl2H25NH3）2MnCl4 was investigated. The temperature and the structures of the phase transition is investigated by thermal gravimetry （TG） and differential scanning calorimetry （DSC）, infrared spectrum （IR） and X-ray diffraction （XRD）. The results suggest that the phase transition is reversible and the structural change arises from the conformation change of the organic chain. The interlayer distance increases when the hybrid transforms from low temperature phase to high temperature phase. This is explained by the diffusion of gauche-bond along the organic chains and they move away from each other when the phase transition occurs. Combining the experimental data with theoretical calculation, we propose that organic chain of the hybrid in high temperature phase is the conformation of gauche-bond alternating with trans bond （noted as GTG＇TGTG＇TGTG＇T）.     

Syntheses and evaluations of CdS with various morphologies for photocatalytically reducing CO<Subscript>2</Subscript>

A series of CdS with various shapes of microsphere, flower-like and leaf-like were templatefreely synthesized by a hydrothermal method. Powder X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM) and UV-vis absorption spectroscopy (UV-vis) were applied to characterize the morphology, optical and other physical properties of the as-prepared CdS. An optical spectrum analyzer was used to measure the wavelength of the illuminant on the slurry in the activity evaluations of photocatalytic reduction of CO₂ over CdS. Both sources of cadmium and sulfur had great impact on the CdS morphology as can be seen in the SEM images. By means of a series of activity evaluations, the microspheric CdS made from cadmium nitrate and thioacetamide showed better photocatalytic activity for the reduction of CO₂ to methyl formate (MF) in methanol than the flower-like and leaf-like CdS catalysts.     

Microstructure and mechanical properties of TiB<Subscript>2</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> composites

Effects of Al2O3 and Ni as the additives on the sinterability, microstructure and mechanical properties were systematic studied. The experimental results show that only a relative density about 96.2% of hot-pressing TiB2-30%Al2O3 can be attained due to the plate-like TiB2 particle and its random orientation and excessive Al2O3 grain growth. When sintering temperature is higher than 1 700 ℃, TiB2 grain growth can be found, which obvious improves flexural strength of TiB2 matrix but decreases toughness. It seems that mechanical properties of TiB2-Al2O3 composites are mainly depended on relative density besides grain growth. otherwise, they will be determined by relative density and TiB2 matrix strength together. Anyway, Al2O3 addition can weaken the grain boundary and thus improve the toughness of the materials. A flexural strength of 529 MPa, Vickers hardness of 24.8 GPa and indentation toughness of 4.56 MPa·m1/2 can be achieved inTiB2-30vol% Al2O3.