Fuji Silysia Chemical Ltd.

Kihara, Japan

Fuji Silysia Chemical Ltd.

Kihara, Japan
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In this report, the global Silica Gel market is valued at USD XX million in 2016 and is expected to reach USD XX million by the end of 2022, growing at a CAGR of XX% between 2016 and 2022. Geographically, this report is segmented into several key Regions, with production, consumption, revenue (million USD), market share and growth rate of Silica Gel in these regions, from 2012 to 2022 (forecast), covering North America Europe China Japan Southeast Asia India For more information or any query mail at sales@wiseguyreports.com Global Silica Gel market competition by top manufacturers, with production, price, revenue (value) and market share for each manufacturer; the top players including BASF Clariant Evonik Solvay W.R. Grace Merck Sorbead India Fuji Silysia Chemical On the basis of product, this report displays the production, revenue, price, market share and growth rate of each type, primarily split into Organic Silica Gel Inorganic Silica Gel On the basis on the end users/applications, this report focuses on the status and outlook for major applications/end users, consumption (sales), market share and growth rate of Silica Gel for each application, including Construction Industry Medicine Electronic Automobile Mechanical Other If you have any special requirements, please let us know and we will offer you the report as you want. Global Silica Gel Market Research Report 2017 1 Silica Gel Market Overview 1.1 Product Overview and Scope of Silica Gel 1.2 Silica Gel Segment by Type (Product Category) 1.2.1 Global Silica Gel Production and CAGR (%) Comparison by Type (Product Category) (2012-2022) 1.2.2 Global Silica Gel Production Market Share by Type (Product Category) in 2016 1.2.3 Organic Silica Gel 1.2.4 Inorganic Silica Gel 1.3 Global Silica Gel Segment by Application 1.3.1 Silica Gel Consumption (Sales) Comparison by Application (2012-2022) 1.3.2 Construction Industry 1.3.3 Medicine 1.3.4 Electronic 1.3.5 Automobile 1.3.6 Mechanical 1.3.7 Other 1.4 Global Silica Gel Market by Region (2012-2022) 1.4.1 Global Silica Gel Market Size (Value) and CAGR (%) Comparison by Region (2012-2022) 1.4.2 North America Status and Prospect (2012-2022) 1.4.3 Europe Status and Prospect (2012-2022) 1.4.4 China Status and Prospect (2012-2022) 1.4.5 Japan Status and Prospect (2012-2022) 1.4.6 Southeast Asia Status and Prospect (2012-2022) 1.4.7 India Status and Prospect (2012-2022) 1.5 Global Market Size (Value) of Silica Gel (2012-2022) 1.5.1 Global Silica Gel Revenue Status and Outlook (2012-2022) 1.5.2 Global Silica Gel Capacity, Production Status and Outlook (2012-2022) 2 Global Silica Gel Market Competition by Manufacturers 2.1 Global Silica Gel Capacity, Production and Share by Manufacturers (2012-2017) 2.1.1 Global Silica Gel Capacity and Share by Manufacturers (2012-2017) 2.1.2 Global Silica Gel Production and Share by Manufacturers (2012-2017) 2.2 Global Silica Gel Revenue and Share by Manufacturers (2012-2017) 2.3 Global Silica Gel Average Price by Manufacturers (2012-2017) 2.4 Manufacturers Silica Gel Manufacturing Base Distribution, Sales Area and Product Type 2.5 Silica Gel Market Competitive Situation and Trends 2.5.1 Silica Gel Market Concentration Rate 2.5.2 Silica Gel Market Share of Top 3 and Top 5 Manufacturers 2.5.3 Mergers & Acquisitions, Expansion 7 Global Silica Gel Manufacturers Profiles/Analysis 7.1 BASF 7.1.1 Company Basic Information, Manufacturing Base, Sales Area and Its Competitors 7.1.2 Silica Gel Product Category, Application and Specification 7.1.2.1 Product A 7.1.2.2 Product B 7.1.3 BASF Silica Gel Capacity, Production, Revenue, Price and Gross Margin (2012-2017) 7.1.4 Main Business/Business Overview 7.2 Clariant 7.2.1 Company Basic Information, Manufacturing Base, Sales Area and Its Competitors 7.2.2 Silica Gel Product Category, Application and Specification 7.2.2.1 Product A 7.2.2.2 Product B 7.2.3 Clariant Silica Gel Capacity, Production, Revenue, Price and Gross Margin (2012-2017) 7.2.4 Main Business/Business Overview 7.3 Evonik 7.3.1 Company Basic Information, Manufacturing Base, Sales Area and Its Competitors 7.3.2 Silica Gel Product Category, Application and Specification 7.3.2.1 Product A 7.3.2.2 Product B 7.3.3 Evonik Silica Gel Capacity, Production, Revenue, Price and Gross Margin (2012-2017) 7.3.4 Main Business/Business Overview 7.4 Solvay 7.4.1 Company Basic Information, Manufacturing Base, Sales Area and Its Competitors 7.4.2 Silica Gel Product Category, Application and Specification 7.4.2.1 Product A 7.4.2.2 Product B 7.4.3 Solvay Silica Gel Capacity, Production, Revenue, Price and Gross Margin (2012-2017) 7.4.4 Main Business/Business Overview 7.5 W.R. Grace 7.5.1 Company Basic Information, Manufacturing Base, Sales Area and Its Competitors 7.5.2 Silica Gel Product Category, Application and Specification 7.5.2.1 Product A 7.5.2.2 Product B 7.5.3 W.R. Grace Silica Gel Capacity, Production, Revenue, Price and Gross Margin (2012-2017) 7.5.4 Main Business/Business Overview 7.6 Merck 7.6.1 Company Basic Information, Manufacturing Base, Sales Area and Its Competitors 7.6.2 Silica Gel Product Category, Application and Specification 7.6.2.1 Product A 7.6.2.2 Product B 7.6.3 Merck Silica Gel Capacity, Production, Revenue, Price and Gross Margin (2012-2017) 7.6.4 Main Business/Business Overview 7.7 Sorbead India 7.7.1 Company Basic Information, Manufacturing Base, Sales Area and Its Competitors 7.7.2 Silica Gel Product Category, Application and Specification 7.7.2.1 Product A 7.7.2.2 Product B 7.7.3 Sorbead India Silica Gel Capacity, Production, Revenue, Price and Gross Margin (2012-2017) 7.7.4 Main Business/Business Overview 7.8 Fuji Silysia Chemical 7.8.1 Company Basic Information, Manufacturing Base, Sales Area and Its Competitors 7.8.2 Silica Gel Product Category, Application and Specification 7.8.2.1 Product A 7.8.2.2 Product B 7.8.3 Fuji Silysia Chemical Silica Gel Capacity, Production, Revenue, Price and Gross Margin (2012-2017) 7.8.4 Main Business/Business Overview For more information or any query mail at sales@wiseguyreports.com ABOUT US: Wise Guy Reports is part of the Wise Guy Consultants Pvt. Ltd. and offers premium progressive statistical surveying, market research reports, analysis & forecast data for industries and governments around the globe. Wise Guy Reports features an exhaustive list of market research reports from hundreds of publishers worldwide. We boast a database spanning virtually every market category and an even more comprehensive collection of rmaket research reports under these categories and sub-categories. For more information, please visit https://www.wiseguyreports.com


Matsumoto T.,University of Miyazaki | Fukuda K.,University of Miyazaki | Sugano K.,University of Miyazaki | Matsumoto J.,University of Miyazaki | And 3 more authors.
Kagaku Kogaku Ronbunshu | Year: 2017

A cobalt-free humidity indicator (HDI) for silica gel was developed using tetraphenylporphyrin (Tpp), which showed a distinguishable color change depending on pH. The HDI was prepared by mixing dichloro (tetraphenylporphyrinato)- phosphorus chloride (PTpp) and MgCl2 with SiO2 and drying at 130°C for 24 h. During the preparation, the PTpp was decomposed into the protonated Tpp (H2Tpp2+). The pH change arose from proton release by the reaction of MgCl2 with silanol of the SiO2 under dry conditions and neutralization under humid conditions. The HDI showed green color due to H2Tpp2+ under dry conditions and orange color due to Tpp under humid conditions. However, the HDI underwent partial decoloration on extended exposure to sunlight. Here, to prevent this decoloration, UV-absorbents coumarin and dibenzosuberenone were loaded onto the HDI. The HDIs with coumarin and without coumarin were irradiated at 352 nm and their microscopic absorption spectra were measured on a confocal laser scanning microscope. The absorbance at 650 nm and 515 nm of the HDI were monitored under dry and wet conditions, respectively. The light-protecting ability of UV-absorbent was analyzed by assuming that the decomposition process obeyed first-order kinetics. It was concluded that the additions of 0.125 wt% of coumarin and 0.050 wt% of dibenzosuberenone were effective to prevent decoloration of green color of H2Tpp2+ as well as orange color of Tpp. © 2017 The Society of Chemical Engineers, Japan.


Kish W.S.,North Carolina State University | Kish W.S.,Pfizer | Sachi H.,Fuji Silysia Chemical Ltd. | Naik A.D.,North Carolina State University | And 7 more authors.
Journal of Chromatography A | Year: 2017

This work presents the selection and characterization of erythropoietin (EPO)-binding cyclic peptide ligands. The sequences were selected by screening a focused library of cyclic depsipeptides cyclo[(Nα-Ac)Dap(A)-X1-X6-AE], whose structure and amino acid compositions were tailored to mimic the EPO receptor. The sequences identified through library screening were synthesized on chromatographic resin and characterized via binding-and-elution studies against EPO to select a pool of candidate ligands. Sequences with higher hydrophobicity consistently showed stronger binding to EPO, with the exception of FSLLSH, which was noted for its lower hydrophobicity and high EPO binding. Mutagenesis studies performed on FSLLSH with natural and non-natural amino acid substitutions led to the identification of critical EPO-binding determinants, and the discovery of new peptide ligands. In particular, histidine-scanning mutagenesis performed on three lead sequences yielded the discovery of variants whose EPO-binding is more pH-sensitive, which facilitates EPO recovery. Selected ligands were studied to correlate the elution yield to the salinity of the binding buffer and the elution pH. Elution yields were consistently higher when EPO binding was performed at low ionic strength. The crystal structures of lead cyclic peptides were docked in silico against EPO to estimate the binding affinity in solution. Isotherm adsorption studies performed on FSLLSH indicated that the cyclic version of the ligand (KD = 0.46 μM) has a higher affinity for EPO than its corresponding linear variant (KD = 1.44 μM). Collectively, these studies set the stage for use of the cyclic peptide ligands as EPO purification and detection tools. © 2017 Elsevier B.V.


Weihs D.,Technion - Israel Institute of Technology | Kesselman E.,Technion - Israel Institute of Technology | Schmidt J.,Technion - Israel Institute of Technology | Talmon Y.,Technion - Israel Institute of Technology | And 5 more authors.
Journal of Physical Chemistry B | Year: 2017

For extremely asymmetric n-hexyl(n-decyl)phosphate (HDeP), n-hexyl(n-dodecyl)phosphate (HDoP), and n-hexyl(n-cetyl)phosphate (HCeP), the effect of the long-chains on the dynamic behavior of their aggregate structures in water was examined by cryo-TEM imaging, SANS, and X-ray diffraction techniques. The cryo-TEM images demonstrated the complex and dynamic behavior of the aggregates, and its dependence on the length of the long-chain. Application of the one-dimensional aggregate theory to the SANS results led to the conclusion that the existence of a limiting size also depended on the length of the main long-hydrocarbon chain and affected strongly the dynamic behavior of the aggregates, causing breakage of thread-like micelles or ribbon-like aggregates. The X-ray diffraction patterns of the lyotropic liquid crystalline samples of HDeP and HCeP were used to estimate the aggregate structures of this limited size. © 2017 American Chemical Society.


Okabayashi H.-F.,Nagoya Institute of Technology | Izawa K.-I.,Fuji Silysia Chemical Ltd. | Sumiya A.,Nagoya Institute of Technology | Eastoe J.,University of Bristol | O'Connor C.J.,University of Auckland
Bulletin of the Chemical Society of Japan | Year: 2010

The IR spectra in the 13001450 cm-1 region, which reflect the CH and CH2 deformation vibrational modes of the succinate skeleton, have been investigated in detail for sodium dialkylsulfonates (alkyl groups: Ethyl, n-propyl, n-butyl, n-hexyl, n-heptyl, n-octyl, n-decyl, and n-dodecyl) and sodium 1,2-bis(2-ethylhexyl)sulfosuccinate (sodium 1,2-bis(2- ethylhexyloxycarbonyl)ethanesulfonate) (AOT). The results have provided clear evidence that two configurations, arising from the difference in the torsion angles of the succinate skeleton, are preferentially stabilized in aqueous solution as well as in the solid state, depending upon the concentration. Thus, the IR spectra of this region can be used as a powerful tool for elucidation of the mechanism of the disorderorder transition in aggregate systems of AOT or its homologs at the molecular level. © 2010 The Chemical Society of Japan.


Suciu C.V.,Fukuoka Institute of Technology | Tani S.,Fukuoka Institute of Technology | Yaguchi K.,Fuji Silysia Chemical Ltd
Acta Mechanica | Year: 2010

In this work, fatigue fracture tests on liquid-repellent nanoporous silica micro-particles dispersed in water are reported; then, models of the grain cracking and fragmentation are proposed. Such tests can be regarded, from an external standpoint, as conducted under temporally variable but spatially uniform pressure distribution in the liquid surrounding the silica grains, or from an internal standpoint, as surface fatigue that occurs at the cyclical adsorption/desorption of water in/from the nanoporous particles. The test rig represents a compression-decompression cylinder divided into two chambers, one of constant volume and the other of variable volume. Silica is introduced inside the cavity of fixed volume, and a micro-filter is used to separate it from the chamber of variable volume, in which only water is supplied. Experimental results suggest that the fatigue fracture of silica particles occurs from the inside, explosion-like, oppositely to the previously reported implosion-like collapse of silica under wet pressurization. This is accompanied by enhancement of the hydrophilic silanol groups on the silica surface and by redistribution of the size of particles and pores. Critical numbers of cycles to achieve fracture of the silica particles obtained experimentally, and from the models of grain cracking and fragmentation, under cyclical pressurization, are in good agreement. © 2010 Springer-Verlag.


Trademark
Fuji Silysia Chemical Ltd. | Date: 2016-06-13

Chemicals; industrial chemicals; chemicals for industrial purposes; chemicals for industrial use; humidity agents; humidity controlling agents; humidity conditioning agents.


Trademark
Fuji Silysia Chemical Ltd. | Date: 2011-07-19

Chromatography columns for industrial purposes; thin layer plates for chromatography for industrial purposes; chromatography columns for laboratory use; thin layer plates for chromatography for laboratory use.


Patent
Fuji Silysia Chemical Ltd. | Date: 2014-07-16

Porous silica-carbon composites are obtained by mixing fine particulate carbon dispersed in water by a surfactant, alkali metal silicate aqueous solution, and mineral acid so as to produce co-dispersion in which silica hydrosol, produced by reaction of the alkali metal silicate and the mineral acid, and the fine particulate carbon are uniformly dispersed, and gelling silica hydrosol, contained in the co-dispersion, and making the co-dispersion into porous bodies. The porous silica-carbon composites are prepared so as to have specific surface area from 20 to 1000 m^(2)/g, pore volume from 0.3 to 2.0 ml/g, and average pore diameter from 2 to 100 nm.


Patent
Fuji Silysia Chemical Ltd. | Date: 2012-09-06

Porous silica-carbon composites are obtained by mixing fine particulate carbon dispersed in water by a surfactant, alkali metal silicate aqueous solution, and mineral acid so as to produce co-dispersion in which silica hydrosol, produced by reaction of the alkali metal silicate and the mineral acid, and the fine particulate carbon are uniformly dispersed, and gelling silica hydrosol, contained in the co-dispersion, and making the co-dispersion into porous bodies. The porous silica-carbon composites are prepared so as to have specific surface area from 20 to 1000 m^(2)/g, pore volume from 0.3 to 2.0 ml/g, and average pore diameter from 2 to 100 nm.

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