Phosphoric Acid

Total Page:16

File Type:pdf, Size:1020Kb

Phosphoric Acid Common Name: PHOSPHORIC ACID CAS Number: 7664-38-2 RTK Substance number: 1516 DOT Number: UN 1805 Date: May 1997 Revision: April 2004 --------------------------------------------------------------------------- --------------------------------------------------------------------------- HAZARD SUMMARY WORKPLACE EXPOSURE LIMITS * Phosphoric Acid can affect you when breathed in. OSHA: The legal airborne permissible exposure limit * Phosphoric Acid is a CORROSIVE CHEMICAL and (PEL) is 1 mg/m3 averaged over an 8-hour contact can irritate and burn the eyes. workshift. * Breathing Phosphoric Acid can irritate the nose, throat and lungs causing coughing and wheezing. NIOSH: The recommended airborne exposure limit is * Long-term exposure to the liquid may cause drying and 1 mg/m3 averaged over a 10-hour workshift and cracking of the skin. 3 mg/m3, not to be exceeded during any 15 minute work period. IDENTIFICATION Phosphoric Acid is a colorless, odorless solid or a thick, clear ACGIH: The recommended airborne exposure limit is 1 mg/m3 averaged over an 8-hour workshift and liquid. It is used in rustproofing metals, fertilizers, detergents, 3 foods, beverages, and water treatment. 3 mg/m as a STEL (short term exposure limit). REASON FOR CITATION WAYS OF REDUCING EXPOSURE * Phosphoric Acid is on the Hazardous Substance List * Where possible, enclose operations and use local exhaust because it is regulated by OSHA and cited by ACGIH, ventilation at the site of chemical release. If local exhaust DOT, NIOSH, IRIS, NFPA and EPA. ventilation or enclosure is not used, respirators should be * This chemical is on the Special Health Hazard Substance worn. List because it is CORROSIVE. * Wear protective work clothing. * Definitions are provided on page 5. * Wash thoroughly immediately after exposure to Phosphoric Acid and at the end of the workshift. HOW TO DETERMINE IF YOU ARE BEING * Post hazard and warning information in the work area. In addition, as part of an ongoing education and training EXPOSED effort, communicate all information on the health and The New Jersey Right to Know Act requires most employers safety hazards of Phosphoric Acid to potentially exposed to label chemicals in the workplace and requires public workers. employers to provide their employees with information and training concerning chemical hazards and controls. The federal OSHA Hazard Communication Standard, 1910.1200, requires private employers to provide similar training and information to their employees. * Exposure to hazardous substances should be routinely evaluated. This may include collecting personal and area air samples. You can obtain copies of sampling results from your employer. You have a legal right to this information under OSHA 1910.1020. * If you think you are experiencing any work-related health problems, see a doctor trained to recognize occupational diseases. Take this Fact Sheet with you. PHOSPHORIC ACID page 2 of 6 This Fact Sheet is a summary source of information of all Mixed Exposures potential and most severe health hazards that may result from * Because smoking can cause heart disease, as well as lung exposure. Duration of exposure, concentration of the substance cancer, emphysema, and other respiratory problems, it may and other factors will affect your susceptibility to any of the worsen respiratory conditions caused by chemical exposure. potential effects described below. Even if you have smoked for a long time, stopping now will --------------------------------------------------------------------------- reduce your risk of developing health problems. HEALTH HAZARD INFORMATION WORKPLACE CONTROLS AND PRACTICES Acute Health Effects Unless a less toxic chemical can be substituted for a hazardous The following acute (short-term) health effects may occur substance, ENGINEERING CONTROLS are the most immediately or shortly after exposure to Phosphoric Acid: effective way of reducing exposure. The best protection is to enclose operations and/or provide local exhaust ventilation at * Contact can irritate and burn the eyes. the site of chemical release. Isolating operations can also * Breathing Phosphoric Acid can irritate the nose and throat reduce exposure. Using respirators or protective equipment is causing coughing and wheezing. less effective than the controls mentioned above, but is sometimes necessary. Chronic Health Effects The following chronic (long-term) health effects can occur at In evaluating the controls present in your workplace, consider: some time after exposure to Phosphoric Acid and can last for (1) how hazardous the substance is, (2) how much of the months or years: substance is released into the workplace and (3) whether harmful skin or eye contact could occur. Special controls Cancer Hazard should be in place for highly toxic chemicals or when * According to the information presently available to the New significant skin, eye, or breathing exposures are possible. Jersey Department of Health and Senior Services, Phosphoric Acid has not been tested for its ability to cause In addition, the following control is recommended: cancer in animals. * Where possible, automatically transfer solid Phosphoric Reproductive Hazard Acid or pump liquid Phosphoric Acid from drums or other * According to the information presently available to the New storage containers to process containers. Jersey Department of Health and Senior Services, Phosphoric Acid has not been tested for its ability to affect Good WORK PRACTICES can help to reduce hazardous reproduction. exposures. The following work practices are recommended: Other Long-Term Effects * Workers whose clothing has been contaminated by * Phosphoric Acid can irritate the lungs. Repeated exposure Phosphoric Acid should change into clean clothing may cause bronchitis to develop with cough, phlegm, promptly. and/or shortness of breath. * Do not take contaminated work clothes home. Family * Long-term exposure to the liquid may cause drying and members could be exposed. cracking of the skin. * Contaminated work clothes should be laundered by individuals who have been informed of the hazards of MEDICAL exposure to Phosphoric Acid. * Eye wash fountains should be provided in the immediate work area for emergency use. Medical Testing * If there is the possibility of skin exposure, emergency If symptoms develop or overexposure is suspected, the shower facilities should be provided. following are recommended: * On skin contact with Phosphoric Acid, immediately wash or shower to remove the chemical. At the end of the * Lung function tests. workshift, wash any areas of the body that may have contacted Phosphoric Acid, whether or not known skin Any evaluation should include a careful history of past and contact has occurred. present symptoms with an exam. Medical tests that look for * Do not eat, smoke, or drink where Phosphoric Acid is damage already done are not a substitute for controlling handled, processed, or stored, since the chemical can be exposure. swallowed. Wash hands carefully before eating, drinking, smoking, or using the toilet. Request copies of your medical testing. You have a legal right * For solid Phosphoric Acid, use a vacuum to reduce dust to this information under OSHA 1910.1020. during clean-up. DO NOT DRY SWEEP. PHOSPHORIC ACID page 3 of 6 PERSONAL PROTECTIVE EQUIPMENT QUESTIONS AND ANSWERS WORKPLACE CONTROLS ARE BETTER THAN PERSONAL PROTECTIVE EQUIPMENT. However, for Q: If I have acute health effects, will I later get chronic some jobs (such as outside work, confined space entry, jobs health effects? done only once in a while, or jobs done while workplace A: Not always. Most chronic (long-term) effects result from controls are being installed), personal protective equipment repeated exposures to a chemical. may be appropriate. Q: Can I get long-term effects without ever having short- OSHA 1910.132 requires employers to determine the term effects? appropriate personal protective equipment for each hazard and A: Yes, because long-term effects can occur from repeated to train employees on how and when to use protective exposures to a chemical at levels not high enough to make equipment. you immediately sick. The following recommendations are only guidelines and may Q: What are my chances of getting sick when I have been not apply to every situation. exposed to chemicals? A: The likelihood of becoming sick from chemicals is Clothing increased as the amount of exposure increases. This is * Avoid skin contact with Phosphoric Acid. Wear acid- determined by the length of time and the amount of resistant gloves and clothing. Safety equipment material to which someone is exposed. suppliers/manufacturers can provide recommendations on the most protective glove/clothing material for your Q: When are higher exposures more likely? operation. A: Conditions which increase risk of exposure include dust * All protective clothing (suits, gloves, footwear, headgear) releasing operations (grinding, mixing, blasting, dumping, should be clean, available each day, and put on before etc.), other physical and mechanical processes (heating, work. pouring, spraying, spills and evaporation from large * Safety equipment manufacturers recommend Natural Rubber, Nitrile Rubber, Polyvinyl Chloride, Viton or surface areas such as open containers), and "confined Neoprene as protective materials. space" exposures (working inside vats, reactors, boilers, small rooms, etc.). Eye Protection * For solid Phosphoric Acid wear impact resistant eye Q: Is the risk of getting sick higher for workers than for protection
Recommended publications
  • An Improved Process for the Production of Cumene
    Europaisches Patentamt European Patent Office © Publication number: 0 537 389 A1 Office europeen des brevets EUROPEAN PATENT APPLICATION © Application number: 91309531.1 int. Ci.5; C07C 2/66, C07C 2/86, C07C 6/12, C07C 15/085 (§) Date of filing: 16.10.91 ® Date of publication of application: @ Applicant: Council of Scientific and Industrial 21.04.93 Bulletin 93/16 Research Rafi Marg @ Designated Contracting States: New Delhi 110 001 (IN) BE DE FR GB IT NL @ Inventor: Pradhan, Ajit Ramchandra National Chemical Laboratory Pune-411008, Maharashtra(IN) Inventor: Rao, Bollapragad Seshagiri National Chemical Laboratory Pune-411008, Maharashtra(IN) 0 Representative: Collier, Jeremy Austin Grey et al J.A.Kemp & Co., 14 South Square, Gray's Inn London WC1R 5LX (GB) 0 An improved process for the production of cumene. © An improved process is disclosed for the preparation of cumene. Cumene is prepared by reacting benzene with a propylating agent in the presence of a catalyst containing metal loaded Zeolite EU-1 in a reactor in the range of a temperature of 150 to 250 °C and a pressure of 1 to 35 atmospheres, the propyl and diisopropylben- zene so formed are separated from the reactor effluent by conventional methods. The diisopropylbenzene is recycled back to the reactor. Simultaneous alkylation and transalkylation reactions occur in a single catalyst bed containing Zeolite EU-1 with a feed containing benzene, propylene and diisopropylbenzene. Cumenes are important chemical precursors in the production of detergents and polymers among others. Oi CO CO IV CO m Rank Xerox (UK) Business Services (3. 10/3.5x/3.0.
    [Show full text]
  • Not ACID, Not BASE, but SALT a Transaction Processing Perspective on Blockchains
    Not ACID, not BASE, but SALT A Transaction Processing Perspective on Blockchains Stefan Tai, Jacob Eberhardt and Markus Klems Information Systems Engineering, Technische Universitat¨ Berlin fst, je, [email protected] Keywords: SALT, blockchain, decentralized, ACID, BASE, transaction processing Abstract: Traditional ACID transactions, typically supported by relational database management systems, emphasize database consistency. BASE provides a model that trades some consistency for availability, and is typically favored by cloud systems and NoSQL data stores. With the increasing popularity of blockchain technology, another alternative to both ACID and BASE is introduced: SALT. In this keynote paper, we present SALT as a model to explain blockchains and their use in application architecture. We take both, a transaction and a transaction processing systems perspective on the SALT model. From a transactions perspective, SALT is about Sequential, Agreed-on, Ledgered, and Tamper-resistant transaction processing. From a systems perspec- tive, SALT is about decentralized transaction processing systems being Symmetric, Admin-free, Ledgered and Time-consensual. We discuss the importance of these dual perspectives, both, when comparing SALT with ACID and BASE, and when engineering blockchain-based applications. We expect the next-generation of decentralized transactional applications to leverage combinations of all three transaction models. 1 INTRODUCTION against. Using the admittedly contrived acronym of SALT, we characterize blockchain-based transactions There is a common belief that blockchains have the – from a transactions perspective – as Sequential, potential to fundamentally disrupt entire industries. Agreed, Ledgered, and Tamper-resistant, and – from Whether we are talking about financial services, the a systems perspective – as Symmetric, Admin-free, sharing economy, the Internet of Things, or future en- Ledgered, and Time-consensual.
    [Show full text]
  • 5. POTENTIAL for HUMAN EXPOSURE 5.1 OVERVIEW White
    WHITE PHOSPHORUS 157 5. POTENTIAL FOR HUMAN EXPOSURE 5.1 OVERVIEW White phosphorus can enter the environment from its production, use, accidental spills during loading and unloading for shipment, and accidental spills during transport. Hazardous wastes sites containing white phosphorus can also be a source of phosphorus in the environment. White phosphorus has been found in at least 77 of the 1,430 current or former EPA National Priorities List (NPL) hazardous waste sites (HazDat 1996). However, the number of sites evaluated for white phosphorus is not known. The frequency of these sites within the United States can be seen in Figure 5-l. The persistence of elemental phosphorus in the air is very short due to oxidation to phosphorus oxides and ultimately to phosphorus acids. However, the particulate phosphorus aerosol may be coated with a protective oxide layer that may prevent further oxidation and extend the lifetime of particulate phosphorus in air. Both wet and dry deposition remove unreacted elemental phosphorus and the degradation products from the air. Similarly, elemental phosphorus oxidizes and hydrolyzes in water and in soil. A small amount of elemental phosphorus is lost from soil and water by volatilization. Phosphorus is used as a fumigant in the storage of grain. Because of ease of application, pellets of aluminum or magnesium phosphide are commonly used (Garry et al. 1993). Phosphine, a highly toxic gas, is generated from phosphide. The rate of formation of phosphine (permissible exposure limit [PEL], 0.4 mg/m3) is dependent on the ambient temperature and humidity. Its release is rapid, and it is extremely fatal to the unprotected person (Garry et al.
    [Show full text]
  • Failures in DBMS
    Chapter 11 Database Recovery 1 Failures in DBMS Two common kinds of failures StSystem filfailure (t)(e.g. power outage) ‒ affects all transactions currently in progress but does not physically damage the data (soft crash) Media failures (e.g. Head crash on the disk) ‒ damagg()e to the database (hard crash) ‒ need backup data Recoveryyp scheme responsible for handling failures and restoring database to consistent state 2 Recovery Recovering the database itself Recovery algorithm has two parts ‒ Actions taken during normal operation to ensure system can recover from failure (e.g., backup, log file) ‒ Actions taken after a failure to restore database to consistent state We will discuss (briefly) ‒ Transactions/Transaction recovery ‒ System Recovery 3 Transactions A database is updated by processing transactions that result in changes to one or more records. A user’s program may carry out many operations on the data retrieved from the database, but the DBMS is only concerned with data read/written from/to the database. The DBMS’s abstract view of a user program is a sequence of transactions (reads and writes). To understand database recovery, we must first understand the concept of transaction integrity. 4 Transactions A transaction is considered a logical unit of work ‒ START Statement: BEGIN TRANSACTION ‒ END Statement: COMMIT ‒ Execution errors: ROLLBACK Assume we want to transfer $100 from one bank (A) account to another (B): UPDATE Account_A SET Balance= Balance -100; UPDATE Account_B SET Balance= Balance +100; We want these two operations to appear as a single atomic action 5 Transactions We want these two operations to appear as a single atomic action ‒ To avoid inconsistent states of the database in-between the two updates ‒ And obviously we cannot allow the first UPDATE to be executed and the second not or vice versa.
    [Show full text]
  • Phosphoric Acid 706-798-4346 Section 1.0 Product and Company Information
    MATERIAL SAFETY DATA SHEET PRAYON INC. P.O. Box 1473 1610 Marvin Griffin Road Augusta, GA 30903-1473 PHOSPHORIC ACID 706-798-4346 SECTION 1.0 PRODUCT AND COMPANY INFORMATION PRODUCT NAME: PHOSPHORIC ACID (36-85%) MSDS Number: P007664382 Chemical Name: Phosphoric acid MSDS Origination Date: 10/01/2000 Synonyms: Phos acid, orthophosphoric acid MSDS Revision Date: 01/05/2006 IN THE EVENT OF A CHEMICAL EMERGENCY, SPILL, LEAK, FIRE, EXPOSURE, OR ACCIDENT Call CHEMTREC: 1-800-424-9300. Toll free in the continental U.S., Hawaii, Puerto Rico, Canada, Alaska, or U.S. Virgin Islands. For calls originating elsewhere dial 703-527-3887 (collect calls accepted). For additional non-emergency information call: 706-798-4346 SECTION 2.0 COMPOSITION / INGREDIENTS INFORMATION Component CAS No. % By Weight OSHA PEL* ACGIH TLV* Phosphoric acid 7664-38-2 36-85 1 mg/m3 1 mg/ m3 Water 7732-18-5 15-64 N/A N/A *Based on 8-hour time weighted averages SECTION 3.0 HAZARD IDENTIFICATION WARNING STATEMENTS: DANGER: CAUSES EYE AND SKIN BURNS MAY BE HARMFUL IF SWALLOWED CORROSIVE TO MILD STEEL EMERGENCY OVERVIEW: APPEARANCE AND ODOR: Slightly viscous, clear liquid with no odor POTENTIAL HEALTH EFFECTS: Likely Routes of Entry: Skin & Eye contact EYE CONTACT: This product can cause serious eye burns. Damage may be permanent. SKIN CONTACT: Corrosive to the skin. Causes burns. Burning may be delayed. INHALATION: Breathing of vapor or mist may be irritating to the respiratory tract. Serious cases of inhalation may cause respiratory problems and late pulmonary edema. INGESTION: May be harmful if swallowed.
    [Show full text]
  • United States Patent 0 "Ice Patented Mar
    3,504,046 United States Patent 0 "Ice Patented Mar. 31, 1970 1 2 higher temperature would make such a difference in the 3 504,046 ALKYLATION OF NAPHTHALENE WITH PRO isomer product ratio. PYLENE IN THE PRESENCE OF PHOSPHORIC In accordance with the present invention the solid ACID CATALYST phosphoric acid catalyst and the naphthalene are charged Edward Jonathan Scharf, Somerville, and Herbert Ru into a suitable reaction vessel, such as an autoclave. The ‘dolph Kemme, Piscataway, N.J., assignors to American system is purged with nitrogen and then with propylene. Cyanamid Company, Stamford, Conn., a corporation of The mixture is then heated to the desired temperature, Maine agitation started and the reaction allowed to proceed un No Drawing. Filed Apr. 26, 1968, Ser. No. 724,626 der autogenous pressure. Upon completion of the reac Int. Cl. C07c 3/54 10 tion, the reactor is cooled, the product mixture with US. Cl. 260-671 2 Claims drawn and the catalyst separated. Any of the solid phosphoric acid catalysts disclosed ABSTRACT OF THE DISCLOSURE in US. Patent Nos. 2,575,457, 2,584,102, 3,183,233 and 3201,486 may be used in the invention. In general, The alkylation of naphthalene with propylene in the 15 they are comprised of phosphoric acid on an inert presence of solid phosphoric acid catalysts is conducted support, such as kieselguhr. They are used in the alkyla at temperatures above about 300° 0., whereby the ratio tion reaction in an amount, based on the total weight of beta- to alpha-isopropyl naphthalene in the product of naphthalene and proylene used, of at least about 1% is substantially increased.
    [Show full text]
  • Preparation of Diammonium Hydrogenphosphate Student Worksheet
    Preparation of diammonium hydrogenphosphate Student worksheet Diammonium hydrogenphosphate (DAP) is a simple salt, but a complex fertiliser, as it is a source of two nutrients – nitrogen and phosphorous. It can be made by partially neutralising dilute phosphoric acid with dilute ammonia solution. Ammonia is titrated with phosphoric acid using methyl orange indicator to find the volume of acid that reacts with 10 cm3 of ammonia to form ammonium dihydrogenphosphate: H3PO4(aq) + NH3(aq) NH4H2PO4(aq) Then you add this volume of acid to 20 cm3 of ammonia to form diammonium hydrogen phosphate. H3PO4(aq) + 2NH3(aq) (NH4)2HPO4(aq) Equipment and materials • Evaporating basin • Filter funnel, filter paper and conical flask (to stand funnel on) • Tripod and gauze • Glass rod. • Bunsen burner • 1 mol dm−3 phosphoric acid • 10 cm3 pipette • 1 mol dm−3 ammonia solution • Burette and stand • Methyl orange indicator solution • 100 cm3 conical flask Method Care: Wear eye protection. 1 mol dm−3 ammonia solution and 1 mol dm−3 phosphoric acid are irritants to the eyes, lungs and the respiratory system. Work in a well-ventilated lab. 1. Use a pipette to transfer 10 cm3 of 1 mol dm−3 ammonia solution to a conical flask. Add a few drops of methyl orange indicator to the conical flask, and stand it on a white background. 2. Note the initial burette reading before adding 1 mol dm–3 phosphoric acid to the flask from a burette until the indicator changes colour. Make a note of the volume of acid added. 3. Use a pipette to transfer 20 cm3 of 1 mol dm−3 ammonia solution to an evaporating basin.
    [Show full text]
  • Influence of Ph-Control in Phosphoric Acid Treatment of Zinc Oxide
    Cerâmica 63 (2017) 197-202 http://dx.doi.org/10.1590/0366-69132017633662149 197 Influence of pH-control in phosphoric acid treatment of zinc oxide (Influência do controle do pH no tratamento de óxido de zinco com ácido fosfórico) H. Onoda1, M. Chemel2 1Department of Informatics and Environmental Sciences, Kyoto Prefectural University, 1-5, Shimogamo Nakaragi-cyo, Sakyo-ku, Kyoto 606-8522, Japan 2Ecol de Biologie Industrielle, 32 Boulevard du Port, 95094 CERGY Cedex, France [email protected] Abstract Zinc oxide is often used as a white pigment for cosmetics; however, it shows photocatalytic activity that causes decomposition of sebum on the skin when exposed to the ultraviolet radiation in sunlight. In this work, zinc oxide was reacted with phosphoric acid at various pH values to synthesize a novel white pigment for cosmetics. The chemical composition, powder properties, photocatalytic activities, colors, and smoothness of these pigments were studied. The obtained materials exhibited X-ray diffraction peaks relating to zinc oxide and phosphate after phosphoric acid treatment. The ratio of zinc phosphate to zinc oxide was estimated from inductively coupled plasma - atomic emission spectroscopy results. Samples treated at pH 4-7 yielded small particles with sub-micrometer sizes. The photocatalytic activity of zinc oxide became lower after phosphoric acid treatment. Samples treated at pH 4-7 showed the same reflectance as zinc oxide in both the ultraviolet and visible ranges. Adjustment of the pH was found to be important in the phosphoric acid treatment of zinc oxide. Keywords: zinc oxide, phosphoric acid treatment, photocatalytic activity, particle size. Resumo O óxido de zinco é comumente usado como um pigmento branco para cosméticos; entretanto, apresenta atividade fotocatalítica que provoca a decomposição do sebo na pele quando exposto à radiação ultravioleta na luz solar.
    [Show full text]
  • SQL Vs Nosql: a Performance Comparison
    SQL vs NoSQL: A Performance Comparison Ruihan Wang Zongyan Yang University of Rochester University of Rochester [email protected] [email protected] Abstract 2. ACID Properties and CAP Theorem We always hear some statements like ‘SQL is outdated’, 2.1. ACID Properties ‘This is the world of NoSQL’, ‘SQL is still used a lot by We need to refer the ACID properties[12]: most of companies.’ Which one is accurate? Has NoSQL completely replace SQL? Or is NoSQL just a hype? SQL Atomicity (Structured Query Language) is a standard query language A transaction is an atomic unit of processing; it should for relational database management system. The most popu- either be performed in its entirety or not performed at lar types of RDBMS(Relational Database Management Sys- all. tems) like Oracle, MySQL, SQL Server, uses SQL as their Consistency preservation standard database query language.[3] NoSQL means Not A transaction should be consistency preserving, meaning Only SQL, which is a collection of non-relational data stor- that if it is completely executed from beginning to end age systems. The important character of NoSQL is that it re- without interference from other transactions, it should laxes one or more of the ACID properties for a better perfor- take the database from one consistent state to another. mance in desired fields. Some of the NOSQL databases most Isolation companies using are Cassandra, CouchDB, Hadoop Hbase, A transaction should appear as though it is being exe- MongoDB. In this paper, we’ll outline the general differences cuted in iso- lation from other transactions, even though between the SQL and NoSQL, discuss if Relational Database many transactions are execut- ing concurrently.
    [Show full text]
  • Aluminum Phosphates
    Dr. Ralf Giskow, The Variety of Phosphates Jörg Lind, Erwin Schmidt Chemische Fabrik Budenheim KG, for Refractory and Technical D-55257 Buden- heim www.budenheim- Applications by the Example cfb.com of Aluminium Phosphates In 1669 the chemical element phos- Phase-I-content influences, for phorus was discovered by H. Brandt, example, the dissolution property of an alchemist. In 1694 Boyle made STPP in water. The choice of the the first phosphoric acid by dissolv- right phosphate can already be the ing phosphorus pentoxide (P2O5) in crucial point even with such a “sim- water. This was the start of the phos- ple“ phosphate like sodium tripoly- phorus chemistry. Since this time phosphate. phosphoric acid and its salts have a The next step into the direction firm place in chemistry and technical of complexity is a phosphate called applications. Phosphates are part of sodium hexametaphosphate (SHMP) our life and are used in a variety of in colloquial language. In fact, the ways also in industrial fields like chemical name is a mistake. The refractories, glass, ceramics, con- name sodium hexametaphosphate struction industry and for a lot of would stand for a sodium phosphate other technical purposes. with a ring structure (“meta”). But SHMP has a chaintype structure as can be proved. These melted glassy polyphosphates (SHMP) with pH-val- Fig. 1 Phosphates in Refractory phosphates are polyphosphates with ues between three and nine, most of FABUTIT 734, a modified STPP and Technical Industries different chain lengths. The average the products also in an instantised against a standard The most common and well known chain length and thus the properties quality (Fig.
    [Show full text]
  • Low Temperature Phosphoric Acid Treatment of Zinc Oxide for Nobel White Pigments
    Ceramics-Silikáty 63 (3), 291-296 (2019) www.ceramics-silikaty.cz doi: 10.13168/cs.2019.0023 LOW TEMPERATURE PHOSPHORIC ACID TREATMENT OF ZINC OXIDE FOR NOBEL WHITE PIGMENTS #HIROAKI ONODA, DAIKI HIGASHIDE Department of Informatics and Environmental Sciences, Kyoto Prefectural University, 1-5, Shimogamo Nakaragi-cyo, Sakyo-ku, Kyoto 606-8522, Japan #E-mail: [email protected] Submitted March 15, 2019; accepted accepted April 27, 2019 Keywords: Zinc oxide, Photocatalytic activity, Powder processing Zinc oxide that has the photocatalytic activity is used as white pigment for cosmetics. A certain degree of sebum on the skin is decomposed by the ultraviolet radiation in sunlight. In this work, zinc oxide was shaken with phosphoric acid to synthesize a white pigment for cosmetics. Zinc oxide was set with 0.1 mol∙l-1 of phosphoric acid at P/Zn = 1/1 and 1/2, and then shaking in water at 30, 40, 50 °C for 1, 3, 6 hours. The chemical composition, powder properties, photocatalytic activity, color phase, and smoothness of the obtained powder were studied. The P/Zn ratio in preparation had influence on the reaction between phosphoric acid and zinc oxide. The photocatalytic activity of zinc oxide was inhibited by phosphoric acid treatment. The treated samples at 50 °C had enough high reflectance at the visible light region. INTRODUCTION difficult to determine because the pore sizes of the skin are affected by such factors as age, gender, and climate As a white pigment, zinc oxide is used for cosmetic [9]. Furthermore, overly large particles are inappropriate applications [1].
    [Show full text]
  • APPENDIX G Acid Dissociation Constants
    harxxxxx_App-G.qxd 3/8/10 1:34 PM Page AP11 APPENDIX G Acid Dissociation Constants §␮ ϭ 0.1 M 0 ؍ (Ionic strength (␮ † ‡ † Name Structure* pKa Ka pKa ϫ Ϫ5 Acetic acid CH3CO2H 4.756 1.75 10 4.56 (ethanoic acid) N ϩ H3 ϫ Ϫ3 Alanine CHCH3 2.344 (CO2H) 4.53 10 2.33 ϫ Ϫ10 9.868 (NH3) 1.36 10 9.71 CO2H ϩ Ϫ5 Aminobenzene NH3 4.601 2.51 ϫ 10 4.64 (aniline) ϪO SNϩ Ϫ4 4-Aminobenzenesulfonic acid 3 H3 3.232 5.86 ϫ 10 3.01 (sulfanilic acid) ϩ NH3 ϫ Ϫ3 2-Aminobenzoic acid 2.08 (CO2H) 8.3 10 2.01 ϫ Ϫ5 (anthranilic acid) 4.96 (NH3) 1.10 10 4.78 CO2H ϩ 2-Aminoethanethiol HSCH2CH2NH3 —— 8.21 (SH) (2-mercaptoethylamine) —— 10.73 (NH3) ϩ ϫ Ϫ10 2-Aminoethanol HOCH2CH2NH3 9.498 3.18 10 9.52 (ethanolamine) O H ϫ Ϫ5 4.70 (NH3) (20°) 2.0 10 4.74 2-Aminophenol Ϫ 9.97 (OH) (20°) 1.05 ϫ 10 10 9.87 ϩ NH3 ϩ ϫ Ϫ10 Ammonia NH4 9.245 5.69 10 9.26 N ϩ H3 N ϩ H2 ϫ Ϫ2 1.823 (CO2H) 1.50 10 2.03 CHCH CH CH NHC ϫ Ϫ9 Arginine 2 2 2 8.991 (NH3) 1.02 10 9.00 NH —— (NH2) —— (12.1) CO2H 2 O Ϫ 2.24 5.8 ϫ 10 3 2.15 Ϫ Arsenic acid HO As OH 6.96 1.10 ϫ 10 7 6.65 Ϫ (hydrogen arsenate) (11.50) 3.2 ϫ 10 12 (11.18) OH ϫ Ϫ10 Arsenious acid As(OH)3 9.29 5.1 10 9.14 (hydrogen arsenite) N ϩ O H3 Asparagine CHCH2CNH2 —— —— 2.16 (CO2H) —— —— 8.73 (NH3) CO2H *Each acid is written in its protonated form.
    [Show full text]