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Title Effect of Ph Values on the Formation and Solubility Of
CORE Metadata, citation and similar papers at core.ac.uk Provided by Kyoto University Research Information Repository Effect of pH Values on the Formation and Solubility of Zinc Title Compounds Takada, Toshio; Kiyama, Masao; Torii, Hideo; Asai, Author(s) Toshihiro; Takano, Mikio; Nakanishi, Norihiko Bulletin of the Institute for Chemical Research, Kyoto Citation University (1978), 56(5): 242-246 Issue Date 1978-12-20 URL http://hdl.handle.net/2433/76795 Right Type Departmental Bulletin Paper Textversion publisher Kyoto University Bull.Inst. Chem.Res., Kyoto Univ., Vol. 56, No. 5, 1978 Effect of pH Values on the Formation and Solubility of Zinc Compounds Toshio TAKADA,Masao KIYAMA,Hideo TORII, Toshihiro AsAI* Mikio TAKANO**,and Norihiko NAKANISHI** ReceivedJuly 31, 1978 Aqueoussuspensions, prepared by mixingthe solution of NaOHand that ofzinc sulfate,chloride or nitrate,were subjected to agingat 25,50, and 70°C. Examinationof the productsby X-ray pow- der diffractionshowed that zinc oxide,basic zinc sulfate, chloride and nitrate are formeddepending mainlyon the pH. Their solubilitiesin the suspensionmedia with differentpH valueswere deter- mined at 25°C. INTRODUCTION In our laboratory, iron oxides and oxide hydroxides were prepared by wet methods such as the hydrolysis and slow oxidation of aqueous solutions of iron salts. The condi- tions for the formation of the oxides and oxide hydroxides') were reported together with their properties.2l The formation of a variety of products must be considered to be due to the difference in the nature -
Evolution and Understanding of the D-Block Elements in the Periodic Table Cite This: Dalton Trans., 2019, 48, 9408 Edwin C
Dalton Transactions View Article Online PERSPECTIVE View Journal | View Issue Evolution and understanding of the d-block elements in the periodic table Cite this: Dalton Trans., 2019, 48, 9408 Edwin C. Constable Received 20th February 2019, The d-block elements have played an essential role in the development of our present understanding of Accepted 6th March 2019 chemistry and in the evolution of the periodic table. On the occasion of the sesquicentenniel of the dis- DOI: 10.1039/c9dt00765b covery of the periodic table by Mendeleev, it is appropriate to look at how these metals have influenced rsc.li/dalton our understanding of periodicity and the relationships between elements. Introduction and periodic tables concerning objects as diverse as fruit, veg- etables, beer, cartoon characters, and superheroes abound in In the year 2019 we celebrate the sesquicentennial of the publi- our connected world.7 Creative Commons Attribution-NonCommercial 3.0 Unported Licence. cation of the first modern form of the periodic table by In the commonly encountered medium or long forms of Mendeleev (alternatively transliterated as Mendelejew, the periodic table, the central portion is occupied by the Mendelejeff, Mendeléeff, and Mendeléyev from the Cyrillic d-block elements, commonly known as the transition elements ).1 The periodic table lies at the core of our under- or transition metals. These elements have played a critical rôle standing of the properties of, and the relationships between, in our understanding of modern chemistry and have proved to the 118 elements currently known (Fig. 1).2 A chemist can look be the touchstones for many theories of valence and bonding. -
NBO Applications, 2020
NBO Bibliography 2020 2531 publications – Revised and compiled by Ariel Andrea on Aug. 9, 2021 Aarabi, M.; Gholami, S.; Grabowski, S. J. S-H ... O and O-H ... O Hydrogen Bonds-Comparison of Dimers of Thiocarboxylic and Carboxylic Acids Chemphyschem, (21): 1653-1664 2020. 10.1002/cphc.202000131 Aarthi, K. V.; Rajagopal, H.; Muthu, S.; Jayanthi, V.; Girija, R. Quantum chemical calculations, spectroscopic investigation and molecular docking analysis of 4-chloro- N-methylpyridine-2-carboxamide Journal of Molecular Structure, (1210) 2020. 10.1016/j.molstruc.2020.128053 Abad, N.; Lgaz, H.; Atioglu, Z.; Akkurt, M.; Mague, J. T.; Ali, I. H.; Chung, I. M.; Salghi, R.; Essassi, E.; Ramli, Y. Synthesis, crystal structure, hirshfeld surface analysis, DFT computations and molecular dynamics study of 2-(benzyloxy)-3-phenylquinoxaline Journal of Molecular Structure, (1221) 2020. 10.1016/j.molstruc.2020.128727 Abbenseth, J.; Wtjen, F.; Finger, M.; Schneider, S. The Metaphosphite (PO2-) Anion as a Ligand Angewandte Chemie-International Edition, (59): 23574-23578 2020. 10.1002/anie.202011750 Abbenseth, J.; Goicoechea, J. M. Recent developments in the chemistry of non-trigonal pnictogen pincer compounds: from bonding to catalysis Chemical Science, (11): 9728-9740 2020. 10.1039/d0sc03819a Abbenseth, J.; Schneider, S. A Terminal Chlorophosphinidene Complex Zeitschrift Fur Anorganische Und Allgemeine Chemie, (646): 565-569 2020. 10.1002/zaac.202000010 Abbiche, K.; Acharjee, N.; Salah, M.; Hilali, M.; Laknifli, A.; Komiha, N.; Marakchi, K. Unveiling the mechanism and selectivity of 3+2 cycloaddition reactions of benzonitrile oxide to ethyl trans-cinnamate, ethyl crotonate and trans-2-penten-1-ol through DFT analysis Journal of Molecular Modeling, (26) 2020. -
Synthesis and Characterization of Nano Zinc Peroxide Photocatalyst for the Removal of Brilliant Green Dye from Textile Waste Water
International Journal of ChemTech Research CODEN (USA): IJCRGG, ISSN: 0974-4290, ISSN(Online):2455-9555 Vol.10 No.9, pp 477-486, 2017 Synthesis and characterization of nano zinc peroxide photocatalyst for the removal of brilliant green dye from textile waste water. Prashant L. Chaudhari*, Pallavi C. Kale Department of Chemical Engineering, BharatiVidyapeeth University College of Engineering, Pune, India Abstract : The zinc peroxide nanoparticles were synthesized by using oxidation-hydrolysis- precipitation process.With zinc acetate as a predecessor, Hydrogen peroxide used as a oxidizing agent and polyethylene glycol 200 (PEG 200) was used as a surface modifier. Characterization of zinc peroxide nanoparticles was done by X-ray diffraction [XRD], Fourier transformer infra red [FTIR] and transmission electron microscope [TEM]. The parameters like pH, dye concentration, dosage of nanoparticle catalyst, temperature and contact time were studied for the application of Zinc peroxide nanopaticle as a catalyst for removal of a Brilliant green dye from synthetic sample. Excellent degradation efficiency of brilliant green dye was 86.68% achieved by zinc peroxide with PEG as a catalyst and 84.16% achieved by zinc peroxide without PEG as a catalyst at 120 min of photo catalytic reaction. The maximum degradation efficiency of brilliant green dye (86.68%) was achieved at the optimum operational conditions: initial concentration of dye 9mg/l, catalyst dosage of 200 mg, pH of solution will be in between 6-7. Keywords : Zinc peroxide nanoparticles, Brilliant green dye, Zinc oxide, Textile waste. Introduction The consumption of dyes was highly increased by textile industries in recent years and because of this scenario large amount of coloured wastewater from such industries create serious problems to the environment. -
(12) Patent Application Publication (10) Pub. No.: US 2011/0027386 A1 Kurihara Et Al
US 20110027386A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2011/0027386 A1 Kurihara et al. (43) Pub. Date: Feb. 3, 2011 (54) ANTMICROBAL. ZEOLITE AND (30) Foreign Application Priority Data ANTMICROBAL COMPOSITION Feb. 22, 2006 (JP) ................................. 2006-045241 (75) Inventors: Yasuo Kurihara, Nagoya-shi (JP); Kumiko Miyake, Nagoya-shi (JP); Publication Classification Masashi Uchida, Nagoya-shi (JP) (51) Int. Cl. Correspondence Address: AOIN 59/6 (2006.01) NIXON & VANDERHYE, PC COB 39/02 (2006.01) 901 NORTH GLEBE ROAD, 11TH FLOOR AOIP I/00 (2006.01) ARLINGTON, VA 22203 (US) (52) U.S. Cl. .......................... 424/618; 423/701; 423/700 (73) Assignee: Sinanen Zeomic Co., Ltd., (57) ABSTRACT Nagoya-Shi (JP) The present invention relates to antimicrobial zeolite which comprises zeolite whereina hardly soluble zinc salt is formed (21) Appl. No.: 12/923,854 within fine pores present therein and an antimicrobial com position which comprises the foregoing antimicrobial Zeolite (22) Filed: Oct. 12, 2010 in an amount ranging from 0.05 to 80% by mass. The antimi crobial Zeolite according to the present invention can widely Related U.S. Application Data be applied, without causing any color change, even to the (63) Continuation of application No. 1 1/705,460, filed on goods which undergo color changes with the elapse of time Feb. 13, 2007. when the conventional antimicrobial zeolite is added. US 2011/002738.6 A1 Feb. 3, 2011 ANTMICROBAL. ZEOLITE AND 3. An antimicrobial composition comprising the foregoing ANTMICROBAL COMPOSITION antimicrobial zeolite as set forth in the foregoing item 1 or 2 in an amount ranging from 0.05 to 80% by mass. -
Ion in Fluorescence Tuning of Tridentate Pincers: a Review
molecules Review The Role of Zinc(II) Ion in Fluorescence Tuning of Tridentate Pincers: A Review Rosita Diana and Barbara Panunzi * Department of Agriculture, University of Napoli Federico II, via Università 100, 80055 Portici NA, Italy; [email protected] * Correspondence: [email protected] Academic Editors: Jorge Bañuelos Prieto and Ugo Caruso Received: 6 October 2020; Accepted: 25 October 2020; Published: 28 October 2020 Abstract: Tridentate ligands are simple low-cost pincers, easy to synthetize, and able to guarantee stability to the derived complexes. On the other hand, due to its unique mix of structural and optical properties, zinc(II) ion is an excellent candidate to modulate the emission pattern as desired. The present work is an overview of selected articles about zinc(II) complexes showing a tuned fluorescence response with respect to their tridentate ligands. A classification of the tridentate pincers was carried out according to the binding donor atom groups, specifically nitrogen, oxygen, and sulfur donor atoms, and depending on the structure obtained upon coordination. Fluorescence properties of the ligands and the related complexes were compared and discussed both in solution and in the solid state, keeping an eye on possible applications. Keywords: zinc ion; fluorescence; tridentate ligand 1. Introduction Over the past 20 years, fluorescence-responsive compounds are increasingly required for many technological applications, from lighting and switch devices to bio-imaging and analytical probes. Materials based on transition metal complexes were advantageously utilized. In this area, interest is growing in the abundant, less expensive, and environmentally “green” zinc(II) metal cation. Today, science is in great demand to address the challenge of sustainability. -
Specified Chemical Substances List 4.0 Edition
Page: 1 /21 ES0101 TEAC Green Procurement Guideline Specified Chemical Substances List (4.0 edition) May/16/2019 TEAC CORPORATION ([email protected]) Page: 2 /21 Table of contents Table-1 List of Environment-related substance groups ………………………….. 3 (Substances to be prohibited)) Table-2 List of Environment-related substance groups ………………………….. 4 (Substances to be controlled) Table-3 List of example substances …………………..………………………….... 6 Document-1 Substances to be prohibited List of Exempted Items …………………… 19 Document-2 Standards for Chemical Content ………………………………………… 20 … Page: 3 /21 Table-1 List of Environment-related substance groups (Substances to be prohibited) Rank No Substance (Group) name Substances 1 Cadmium /Cadmium compunds to be 2 Hexavalent Chromium Compoumds prohibited 3 Lead /Lead compounds 4 Mercury /Mercury compounds 5 Polybrominated diphenylethers (PBBs) 6 Polybrominated Diphenylethers (PBDEs) 7 Phthalates (DEHP,BBP,DBP,DIBP) 8 Certain Azocolourants and Azodyes 9 Short Chain Chlorinated Paraffins 10 Form aldehyde 11 Pentachlorophenol (PCP) and its salts and esters 12 Monomethyl-dibromo-diphenyl methane (DBBT) 13 Monomethyltetrachlorodiphenylmethane (Trade Name:Ugilec 141) 14 Monomethyldichlorodiphenylmethane (Trade Name:Ugilec 121, Ugilec 21) 15 Perfluorooctane sulfonate and its salts (PFOS) 16 Cobalt chlorides 17 Dimethyl fumarate (DMF) 18 Arsenic /Arsenic compounds 19 Nickel and Nickel compounds 20 Chlorinated hydrocarbons 21 Polycyclic aromatic hydrocarbons (PAHs) 22 Perchlorates 23 Fluorinated greenhouse gases (PFC, -
The Relationship Between the Content of Zinc and Major Elements in Lake
OCHRONA ŚRODOWISKA I ZASOBÓW NATURALNYCH VOL. 25 NO 1(59): 17–23 ENVIRONMENTAL PROTECTION AND NATURAL RESOURCES 2014 DOI 10.2478/oszn-2014-0004 Izabela Bojakowska*, Tomasz Gliwicz*, Jarosław Kucharzyk* The relationship between the content of zinc and major elements in lake sediments in Poland Zależność między stężeniem cynku i pierwiastków głównych w osadach jezior w Polsce * Prof. dr hab. Izabela Bojakowska, dr Tomasz Gliwicz, mgr Jarosław Kucha- rzyk, Polish Geological Institute – National Research Institute, Rakowiecka 4 St., 00-975 Warsaw, Poland, phone: +48 22 45 92 296, e-mail: izabela. [email protected], [email protected], jaroslaw.kucharzyk@ pgi.gov.pl Keywords: lake sediments, zinc, major elements Słowa kluczowe: osady jeziorne, cynk, pierwiastki główne Abstract Streszczenie A total of 409 sediment samples were collected from lake deeps Z głęboczków jezior Pojezierzy: Wielkopolskiego, Pomorskiego of 260 lakes in the Greater Poland, Pomerania and Masuria Lake- i Mazurskiego pobrano 409 próbek osadów. We wszystkich prób- lands. All samples (fraction <0.2 mm) were analysed for the con- kach określono zawartość cynku oraz Ca, Mg, Fe, K, Mn, Na, P, S centration of zinc (Zn), Al, Ca, Mg, Fe, K, Mn, Na, P, S and TOC. i OWO. W osadach zawartość Zn zmieniała się w zakresie od <6 The Zn concentration in the lake sediments varied from <6 to 1006 do 1006 mg/kg, średnie stężenie wynosiło 93 mg/kg, a średnia geo- mg/kg, the average concentration was 93 mg/kg and the geometric metryczna – 74 mg/kg. W większości zbadanych próbek zawartość mean 74 mg/kg. In most of the samples, the Zn concentration was cynku była niższa od 200 mg/kg (za wyjątkiem 19 próbek). -
(12) Patent Application Publication (10) Pub. No.: US 2015/0060952 A1 Takulapalli Et Al
US 20150.060952A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2015/0060952 A1 Takulapalli et al. (43) Pub. Date: Mar. 5, 2015 (54) FIELD EFFECT TRANSISTOR, DEVICE Publication Classification INCLUDING THE TRANSISTOR, AND METHODS OF FORMING AND USING SAME (51) Int. Cl. GOIN 27/214 (2006.01) (71) Applicants: Bharath Takulapalli, Chandler, AZ GOIN33/543 (2006.01) (US); INANOBIO LLC, Tempe, AZ (52) U.S. Cl. (US) CPC ........ G0IN 27/414 (2013.01); G0IN33/54366 72) Inventors: Bharath Takulapalli, Chandler, AZ USPC (2013.01); G0IN 27/4145257/253:438/49 (2001) (US); Abhinav Jain, Tempe, AZ (US) " ' " s (21) Appl. No.: 14/391,661 (57) ABSTRACT (22) PCT Filed: Apr. 9, 2013 (86). PCT No.: PCT/US2013/035852 The present disclosure provides an improved field effect tran S371 (c)(1), sistor and device that can be used to sense and characterize a (2) Date: Oct. 9, 2014 variety of materials. The field effect transistor and/or device including the transistor may be used for a variety of applica Related U.S. Application Data tions, including genome sequencing, protein sequencing, bio (60) Provisional application No. 61/621,966, filed on Apr. molecular sequencing, and detection of ions, molecules, 9, 2012, provisional application No. 61/802,235, filed chemicals, biomolecules, metal atoms, polymers, nanopar on Mar. 15, 2013. ticles and the like. - 33. 8 : Patent Application Publication Mar. 5, 2015 Sheet 1 of 10 US 2015/0060952 A1 s sa SSSS Patent Application Publication Mar. 5, 2015 Sheet 2 of 10 US 2015/0060952 A1 s Patent Application Publication Mar. -
Toxicological Profile for Zinc
TOXICOLOGICAL PROFILE FOR ZINC U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Agency for Toxic Substances and Disease Registry August 2005 ZINC ii DISCLAIMER The use of company or product name(s) is for identification only and does not imply endorsement by the Agency for Toxic Substances and Disease Registry. ZINC iii UPDATE STATEMENT A Toxicological Profile for Zinc, Draft for Public Comment was released in September 2003. This edition supersedes any previously released draft or final profile. Toxicological profiles are revised and republished as necessary. For information regarding the update status of previously released profiles, contact ATSDR at: Agency for Toxic Substances and Disease Registry Division of Toxicology/Toxicology Information Branch 1600 Clifton Road NE Mailstop F-32 Atlanta, Georgia 30333 ZINC vi *Legislative Background The toxicological profiles are developed in response to the Superfund Amendments and Reauthorization Act (SARA) of 1986 (Public law 99-499) which amended the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 (CERCLA or Superfund). This public law directed ATSDR to prepare toxicological profiles for hazardous substances most commonly found at facilities on the CERCLA National Priorities List and that pose the most significant potential threat to human health, as determined by ATSDR and the EPA. The availability of the revised priority list of 275 hazardous substances was announced in the Federal Register on November 17, 1997 (62 FR 61332). For prior versions of the list of substances, see Federal Register notices dated April 29, 1996 (61 FR 18744); April 17, 1987 (52 FR 12866); October 20, 1988 (53 FR 41280); October 26, 1989 (54 FR 43619); October 17, 1990 (55 FR 42067); October 17, 1991 (56 FR 52166); October 28, 1992 (57 FR 48801); and February 28, 1994 (59 FR 9486). -
Chemical Names and CAS Numbers Final
Chemical Abstract Chemical Formula Chemical Name Service (CAS) Number C3H8O 1‐propanol C4H7BrO2 2‐bromobutyric acid 80‐58‐0 GeH3COOH 2‐germaacetic acid C4H10 2‐methylpropane 75‐28‐5 C3H8O 2‐propanol 67‐63‐0 C6H10O3 4‐acetylbutyric acid 448671 C4H7BrO2 4‐bromobutyric acid 2623‐87‐2 CH3CHO acetaldehyde CH3CONH2 acetamide C8H9NO2 acetaminophen 103‐90‐2 − C2H3O2 acetate ion − CH3COO acetate ion C2H4O2 acetic acid 64‐19‐7 CH3COOH acetic acid (CH3)2CO acetone CH3COCl acetyl chloride C2H2 acetylene 74‐86‐2 HCCH acetylene C9H8O4 acetylsalicylic acid 50‐78‐2 H2C(CH)CN acrylonitrile C3H7NO2 Ala C3H7NO2 alanine 56‐41‐7 NaAlSi3O3 albite AlSb aluminium antimonide 25152‐52‐7 AlAs aluminium arsenide 22831‐42‐1 AlBO2 aluminium borate 61279‐70‐7 AlBO aluminium boron oxide 12041‐48‐4 AlBr3 aluminium bromide 7727‐15‐3 AlBr3•6H2O aluminium bromide hexahydrate 2149397 AlCl4Cs aluminium caesium tetrachloride 17992‐03‐9 AlCl3 aluminium chloride (anhydrous) 7446‐70‐0 AlCl3•6H2O aluminium chloride hexahydrate 7784‐13‐6 AlClO aluminium chloride oxide 13596‐11‐7 AlB2 aluminium diboride 12041‐50‐8 AlF2 aluminium difluoride 13569‐23‐8 AlF2O aluminium difluoride oxide 38344‐66‐0 AlB12 aluminium dodecaboride 12041‐54‐2 Al2F6 aluminium fluoride 17949‐86‐9 AlF3 aluminium fluoride 7784‐18‐1 Al(CHO2)3 aluminium formate 7360‐53‐4 1 of 75 Chemical Abstract Chemical Formula Chemical Name Service (CAS) Number Al(OH)3 aluminium hydroxide 21645‐51‐2 Al2I6 aluminium iodide 18898‐35‐6 AlI3 aluminium iodide 7784‐23‐8 AlBr aluminium monobromide 22359‐97‐3 AlCl aluminium monochloride -
Zinc Oxide—From Synthesis to Application: a Review
Materials 2014, 7, 2833-2881; doi:10.3390/ma7042833 OPEN ACCESS materials ISSN 1996-1944 www.mdpi.com/journal/materials Review Zinc Oxide—From Synthesis to Application: A Review Agnieszka Kołodziejczak-Radzimska * and Teofil Jesionowski Institute of Chemical Technology and Engineering, Faculty of Chemical Technology, Poznan University of Technology, M. Sklodowskiej-Curie 2, PL-60965 Poznan, Poland; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +48-61-665-3626; Fax: +48-61-665-3649. Received: 17 December 2013; in revised form; 25 March 2014 / Accepted: 27 March 2014 / Published: 9 April 2014 Abstract: Zinc oxide can be called a multifunctional material thanks to its unique physical and chemical properties. The first part of this paper presents the most important methods of preparation of ZnO divided into metallurgical and chemical methods. The mechanochemical process, controlled precipitation, sol-gel method, solvothermal and hydrothermal method, method using emulsion and microemulsion enviroment and other methods of obtaining zinc oxide were classified as chemical methods. In the next part of this review, the modification methods of ZnO were characterized. The modification with organic (carboxylic acid, silanes) and inroganic (metal oxides) compounds, and polymer matrices were mainly described. Finally, we present possible applications in various branches of industry: rubber, pharmaceutical, cosmetics, textile, electronic and electrotechnology, photocatalysis were introduced. This review provides useful information for specialist dealings with zinc oxide. Keywords: zinc oxide; synthesis; modification; application 1. Introduction Zinc oxide, with its unique physical and chemical properties, such as high chemical stability, high electrochemical coupling coefficient, broad range of radiation absorption and high photostability, is a multifunctional material [1,2].