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Featured researches published by Hiromitsu Matsuda.


Science of The Total Environment | 2000

Mercury emissions from a coal-fired power plant in Japan

Takahisa Yokoyama; Kazuo Asakura; Hiromitsu Matsuda; Shigeo Ito; Naoki Noda

The emissions study for mercury was conducted at a 700 MW coal-fired plant for the combustion of three types of coal with mercury concentrations of 0.0063, 0.0367 and 0.065 mg/kg. The power plant is equipped with a cold-side electrostatic precipitator and wet type flue gas desulfurization system. During full load operation of the boilers, samples of the input and output streams such as coal, coal ash, ESP ash and post-ESP particulates and flue gas were collected. The Hg concentrations in solid were measured by cold-vapor atomic absorption spectrometry (AAS) after appropriate preparation and acid digestion. Gaseous Hg was collected using a mixed solution of potassium permanganate and sulfuric acid and the Hg concentrations in the samples were measured using cold-vapor AAS. The results were used to examine: (1) overall mass balances; (2) relative distribution in the power plant; (3) equilibrium of Hg species using MALT-2 calculation program; and (4) Hg concentrations in stack emissions. The mass balances estimated in this study were 100, 138 and 89%, respectively, for the coals. Total Hg concentrations in stack gas were 1.113, 0.422 and 0.712 microg(m3N), respectively, for the coals. More than 99.5% of the Hg in the stack emissions were in gaseous form and the proportion in particulate form was extremely low. The relative distribution of Hg in ESP, FGD and Stack ranged from 8.3 to 55.2%, 13.3 to 69.2% and 12.2% to 44.4%, respectively. The results indicated that factors other than the Hg concentration of coals and efficiency of pollution control devices might affect Hg emissions from coal-fired plant. The calculated equilibrium of the distribution of Hg species using the MALT2 program suggest that it is necessary to consider condensation mechanism to interpret the affect of Hg species on the variations of the removal efficiencies of Hg in the ESP.


Advanced Powder Technology | 2003

Characteristics of particulate matter generated in pressurized coal combustion for high-efficiency power generation system

Ryoichi Kurose; Hiromitsu Matsuda; Hisao Makino; Akira Suzuki

Characteristics of particulate matter in pressurized coal combustion for high-efficiency power generation system are investigated by using the percolation model and the results are compared with experiments performed using drop tube furnace facilities (DTF). The results show that conversion for Plateau coal (high volatile matter and low ash contents) rises earlier than that for Newlands coal (low volatile matter and high ash content). For both coals, volatile consumption rate increases with increasing the gaseous temperature, whereas the char combustion rate increases with increasing both the gaseous temperature and the pressure. At the char-combustion-dominant stage after devolatilization, the characteristics of the particulate matter such as specific surface and porosity area are not affected by the gaseous temperature, but they are affected by the pressure and the coal properties. These results are of general agreement with the experiment by DTF and hence the present percolation model is valid for the prediction of the characteristics of the particulate matter in coal combustion.


Environmental Science & Technology | 2013

Elucidation of the mechanism of reaction between S2O8(2-), Selenite and Mn2+ in aqueous solution and limestone-gypsum FGD liquor.

Hiroyuki Akiho; Shigeo Ito; Hiromitsu Matsuda; Toshiaki Yoshioka

The mechanism of reaction between peroxodisulfate ion (S2O8(2-)), selenite (Se(IV)O3(2-)) and Mn(2+) as an inhibitor of selenite oxidation was studied using aqueous solutions composed of commercial reagents, as well as limestone-gypsum flue gas desulfurization (FGD) liquors sampled from coal fired power plants. The oxidation of selenite to selenate (Se(VI)O4(2-)) is promoted by the sulfate ion radical (SO4(-)) which results from decomposition of S2O8(2-). In the presence of Mn(2+), selenite oxidation was prevented due to the difference in rates of reaction with SO4(-). The ratio of the oxidation rate constants of selenite and Mn(2+) with SO4(-) was determined over a temperature range of 40-60 °C, and was found to be little influenced by the various coexisting components in FGD liquors.


Fuel | 2002

Gasification rate analysis of coal char with a pressurized drop tube furnace

Shiro Kajitani; Saburo Hara; Hiromitsu Matsuda


Environmental Science & Technology | 1991

Nitrous oxide emissions from fossil fuel fired power plants

Takahisa Yokoyama; Shaw Nishinomiya; Hiromitsu Matsuda


Fuel | 2011

Emission characteristics of NOx and unburned carbon in fly ash on high-ash coal combustion

Hirofumi Tsuji; Hiromi Shirai; Hiromitsu Matsuda; Priven Rajoo


Fuel | 2010

Effect of oxidizing agents on selenate formation in a wet FGD

Hiroyuki Akiho; Shigeo Ito; Hiromitsu Matsuda


Energy & Fuels | 2004

Application of Percolation Model to Ash Formation Process in Coal Combustion

Ryoichi Kurose; Hisao Makino; Hiromitsu Matsuda; Akira Suzuki


Archive | 2008

Process of treating selenium-containing liquid

Hiroyuki Akiho; Shigeo Ito; Hiromitsu Matsuda


Archive | 2013

SYSTEM FOR TREATING SELENIUM-CONTAINING LIQUID, WET FLUE GAS DESULFURIZATION DEVICE, AND METHOD FOR TREATING SELENIUM-CONTAINING LIQUID

Hiroyuki Akiho; Hiromitsu Matsuda; Shigeo Ito

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Shigeo Ito

Central Research Institute of Electric Power Industry

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Hiroyuki Akiho

Central Research Institute of Electric Power Industry

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Hisao Makino

Central Research Institute of Electric Power Industry

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Hiromi Shirai

Central Research Institute of Electric Power Industry

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Takahisa Yokoyama

Central Research Institute of Electric Power Industry

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Akimasa Yamaguchi

Central Research Institute of Electric Power Industry

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Hidehiro Kamiya

Tokyo University of Agriculture and Technology

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Hirofumi Tsuji

Central Research Institute of Electric Power Industry

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