Study of high-pressure air jet controlled compression ignition with compound thermodynamic cycle for combustion and emission formation process

2020 ◽  
pp. 146808742096933
Author(s):  
Xiangyu Meng ◽  
Sicheng Liu ◽  
Jingchen Cui ◽  
Jiangping Tian ◽  
Wuqiang Long ◽  
...  
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Low Temperature ◽  
Formation Process ◽  
Combustion Process ◽  
Thermodynamic Cycle ◽  
Compression Ignition ◽  
Temperature Reaction ◽  
Air Jet ◽  
High Temperature Reaction

A novel method called high-pressure air (HPA) jet controlled compression ignition (JCCI) based on the compound thermodynamic cycle was investigated in this work. The combustion process of premixed mixture can be controlled flexibly by the high-pressure air jet compression, and it characterizes the intensified low-temperature reaction and two-stage high-temperature reaction. The three-dimensional (3D) computational fluid dynamics (CFD) numerical simulation was employed to study the emission formation process and mechanism, and the effects of high-pressure air jet temperature and duration on emissions were also investigated. The simulation results showed that the NOx formation is mainly affected by the first-stage high-temperature reaction due to the higher reaction temperature. Overall, this combustion mode can obtain ultra-low NOx emission. The second-stage high-temperature reaction plays an important role in the CO and THC formation caused by the mixing effect of the high-pressure air and original in-cylinder mixture. The increasing air jet temperature leads to a larger high-temperature in-cylinder region and more fuel in the first-stage reaction, and therefore resulting in higher NOx emission. However, the increasing air jet temperature can significantly reduce the CO and THC emissions. For the air jet duration comparisons, both too short and too long air jet durations could induce higher NOx emission. A higher air jet duration would result in higher CO emission due to the more high-pressure air jet with relatively low temperature.

Ni6B22O39·H2O – extending the field of nickel borates

2017 ◽  
Vol 72 (12) ◽  
pp. 967-975 ◽  
Author(s):  
Martin K. Schmitt ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
High Temperature ◽  
Temperature Reaction ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
High Temperature Reaction ◽  
High Pressure High Temperature ◽  
Related Phase

AbstractNi6B22O39·H2O was synthesized in a high-pressure/high-temperature reaction at 5 GPa/900°C. It crystallizes in the orthorhombic space group Pmn21 (no. 31) with the lattice parameters a=7.664(2), b=8.121(2) and c=17.402(2) Å. The crystal structure is discussed with regard to the isotypic compounds M6B22O39·H2O (M=Fe, Co) and the structurally related phase Cd6B22O39·H2O. Furthermore, the characterization of Ni6B22O39·H2O via X-ray powder diffraction and vibrational spectroscopy is reported.

The mechanism of the Pinacol-Pinacone rearragement. VI. Low temperature kinetics

1957 ◽  
Vol 10 (2) ◽  
pp. 160 ◽  
Author(s):  
JF Duncan ◽  
KR Lynn
Keyword(s):  
Activation Energy ◽  
High Temperature ◽  
Low Temperature ◽  
Hydrogen Ion ◽  
Ion Concentration ◽  
Temperature Reaction ◽  
Hydrogen Ion Concentration ◽  
High Temperature Reaction ◽  
Stage Process ◽  
Low Temperature Kinetics

The low temperature rearrangement of pinacol to pinacone appears to be second order with respect to the hydrogen ion concentration. The activation energy is, however, similar to that of the high temperature reaction. This is interpreted as indicating that in the low temperature reaction the synartetic step is formed by a two stage process, through a stable intermediate, and each stage requires the participation of a hydrogen ion.

Mastication of Rubber a Study of Some of the Oxidation Rocesses Involved

1939 ◽  
Vol 12 (2) ◽  
pp. 163-175 ◽  
Author(s):  
W. F. Busse ◽  
E. N. Cunningham
Keyword(s):  
High Temperature ◽  
Low Temperature ◽  
Thermal Oxidation ◽  
Oxygen Concentration ◽  
High Temperatures ◽  
Nitroso Compounds ◽  
Temperature Reaction ◽  
Vulcanized Rubber ◽  
High Temperature Reaction ◽  
Internal Mixer

Abstract The rate of breakdown of smoked sheet, pale crepe, and sprayed-latex rubber in a laboratory internal mixer is a minimum at temperatures around 240° F., and the rate may be increased as much as four- or five-fold by either raising or lowering the temperature 80° F. The high-temperature reaction (above 240° F.) probably is similar to the thermal oxidation which occurs when rubber is heated in air, since the rates of both reactions are increased by increasing the oxygen concentration, and they are reduced by adding antioxidants. The low-temperature reaction (below 240° F.) may involve a mechanical acti-vation of the rubber, as in milling. The rate of this reaction first increases and then remains constant or decreases slightly as the oxygen concentration in the temperature during mastication is increased from about 0.5% to 20% to 100%. Some nitroso compounds are powerful stiffeners of rubber, and they change the softness-retentivity relation, making it more like that of reclaim or semi-vulcanized rubber. The effect of most commonly used “softeners” on the plasticity of rubber is small compared with the effect of changing the mastication temperature ±40° F. Exceptions to this are certain vulcanization accelerators (at high temperatures), hydrazine compounds and thiophenols, which appear to be true mastication acelerators or oxidation catalysts.

scholarly journals High-pressure Synthesis of New layered Oxyhalide Perovskites

2014 ◽  
Vol 70 (a1) ◽  
pp. C762-C762
Author(s):  
Yoshihiro Tsujimoto ◽  
Yoshitaka Matsushita ◽  
Kazunari Yamaura ◽  
Tetsuo Uchikoshi
Keyword(s):  
High Pressure ◽  
Magnetic Properties ◽  
High Temperature ◽  
Transition Metal Oxides ◽  
Temperature Reaction ◽  
High Temperature Reaction ◽  
Square Planar ◽  
Pressure Synthesis ◽  
Structural And Magnetic Properties ◽  
High Valent

The development of transition metal oxides with perovskite-based structure has stimulated the search for mixed anion systems such as oxynitrides, oxyhalides and oxysulfides because incorporation of two different anions in one structure offers further opportunity to effectively induce chemical and physical properties that the pure oxides cannot possess. Such mixed anion phases, however, are difficult to be synthesized by a conventional high-temperature reaction. In this study, we have employed a high pressure technique to overcome this issue, and succeessfully synthesized a series of new layered oxhalide compounds. We present structural and magnetic properties of high-valent nickel oxyhalides Sr2NiO3X (X = F, Cl), and square-planar coordinated oxychlorides Sr2MO2Cl2 (Mn, Ni) and Ba2PdO2Cl2, isostructural with superconducting parent compund Ca2CuO2Cl2.

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