Laura Robinson,
Toxicologist, Expert Witness

"Is as professional as she is knowledgeable and gets the job done." Ingvor Ohlsson, Solaster Production AB, (Sweden)

"I've know Laura for years as a colleague in the chemical industry - A very nice person, easy to talk to and a good listener, industrious and very, very keen on occupational safety in relation to chemicals. A good one to trust assessments of chemicals to!” Chris Braun, Senior toxicologist, AkzoNobel

"Laura is the consummate professional in her field, employing her substantial knowledge of chemical issues and global standards to assist companies with successfully managing their diverse regulatory issues." Michael S. Wenk M.Sc., MBA - Principal, m4 Consulting LLC

"With her easy going and approachable manner, Laura makes an invaluable contribution to any team working with occupational health issues. Her deep knowledge together with her broad experience is an asset in any toxicological or OSHA project." Anders Silfverstrand, Manager Chemical Health Risks, SCA

"As a Barrister, with extensive experience of expert witnesses in many fields, I can recommend Laura Robinson as accessible, personable, and able to explain extremely complex issues with ease and clarity. An excellent choice for toxicological advice or testimony.” James Kirby

Skype: laurarobinson23
Skype ID: laurarobinson23

 

 

 

 

 

Sodium thiosulfate

Industrial production and laboratory synthesis
On an industrial scale, sodium thiosulfate is produced chiefly from liquid waste products of sodium sulfide or sulfur dye manufacture. In the laboratory, this salt can be prepared by heating an aqueous solution of sodium sulfite with sulfur.
Principal reactions and applications
Sodium thiosulfate
Thiosulfate anion characteristically reacts with dilute acids to produce sulfur, sulfur dioxide and water:
Na2S2O3 + 2HCl 2NaCl + S + SO2 + H2O
This reaction is known as a clock reaction, because when the sulfur reaches a certain concentration the solution turns from colourless to a pale yellow. This reaction has been employed to generate colloidal sulfur. When the protonation is conducted at low temperatures, H2S2O3 (thiosulfuric acid) can be obtained. It is a strong acid pKa = 0.6, 1.7.
Iodometry
In analytical chemistry, the most important use comes from the fact that the thiosulfate anion reacts stoichiometrically with iodine, reducing it to iodide as it is oxidized to tetrathionate:
2 S2O32(aq) + I2(aq) S4O62(aq) + 2 I(aq)
Due to the quantitative nature of this reaction, as well as the fact that Na2S2O35H2O has an excellent shelf-life, it is used as a titrant in iodometry. Na2S2O35H2O is also a component of iodine clock experiments.
This particular use can be set up to measure the oxygen content of water through a long series of reactions. It is also used in estimating volumetrically, the concentrations of certain compounds in solution (hydrogen peroxide, for instance), and in estimating the chlorine content in commercial bleaching powder and water.
Photographic processing
The terminal sulfur atom in S2O32 binds to soft metals with high affinity. Thus, silver halides, e.g. AgBr, typical components of photographic emulsions, dissolve upon treatment with aqueous thiosulfate:
2 S2O32 + AgBr [Ag(S2O3)2]3 + Br-
In this application to photographic processing, discovered by John Herschel and used for both film and photographic paper processing, the sodium thiosulfate is known as a photographic fixer, and is often referred to as hypo, from the original chemical name, hyposulphite of soda.
Gold extraction
Sodium thiosulfate is one component of an alternative lixiviant to cyanide for extraction of gold. It forms a strong complex with gold(I) ions, [Au(S2O3)2]3-. The advantage of this approach is that thiosulfate is essentially non-toxic and that ore types that are refractory to gold cyanidation (e.g. carbonaceous or Carlin type ores) can be leached by thiosulfate. Some problems with this alternative process include the high consumption of thiosulfate, and the lack of a suitable recovery technique, since [Au(S2O3)2]3- does not adsorb to activated carbon, which is the standard technique used in gold cyanidation to separate the gold complex from the ore slurry.
Analytical chemistry
Sodium thiosulfate is also used in analytical chemistry. It can, when heated with a sample containing aluminum cation, produce a white precipitation:
2Al3+ + 3S2O32- + 3H2O 3SO2 + 3S + 2Al(OH)3
Medical
It is used as an antidote to cyanide poisoning. Thiosulfate acts as a sulfur donor for the conversion for cyanide to thiocyanate (which can then be safely excreted in the urine), catalyzed by the enzyme rhodanase.
It has also been used as treatment of calciphylaxis in hemodialysis patients with end-stage renal disease.
in foot baths for prophylaxis of ringworm, and as a topical antifungal agent for tinea versicolor.
in measuring the volume of extracellular body fluid and the renal glomerular filtration rate.
Other uses
Sodium thiosulfate is also used:
As a component in hand warmers and other chemical heating pads that produce heat by exothermic crystallization of a supercooled solution.
In Bleach
In pH testing of bleach substances. The universal indicator and any other liquid pH indicator are destroyed by bleach, rendering them useless for testing the pH. If one first adds sodium thiosulfate to such solutions, it will neutralize the color-removing effects of bleach and allow one to test the pH of bleach solutions with liquid indicators. The relevant reaction is akin to the iodine reaction: thiosulfate reduces the hypochlorite (active ingredient in bleach) and in so doing becomes oxidized to sulfate. The complete reaction is:
4 NaClO + Na2S2O3 + 2 NaOH 4 NaCl + 2 Na2SO4 + H2O
To dechlorinate tap water for aquariums or treat effluent from waste water treatments prior to release into rivers. The reduction reaction is analogous to the iodine reduction reaction. Treatment of tap water requires between 0.1 grams and 0.3 grams of pentahydrated (crystalline) sodium thiosulfate per 10 liters of water.
To lower chlorine levels in swimming pools and spas following super chlorination.
To remove iodine stains, e.g. after the explosion of nitrogen triiodide.
In bacteriological water assessment.
In the tanning of leather.
To demonstrate the concept of reaction rate in chemistry classes. The thiosulfate ion can decompose into the sulfite ion and a colloidal suspension of sulfur, which is opaque. The equation for this acid-catalysed reaction is as follows:
S2O32(aq) SO32(aq) + S(s)
To demonstrate the concept of supercooling in physics classes. Melted sodium thiosulfate is very easy to overcool to room temperature and when crystallization is forced, the sudden temperature jump to 48.3C can be experienced by touch.
As part of patina recipes for copper alloys.
Often used in pharmaceutical preparations as an anionic surfactant to aid in dispersion.
It can also be used as a very interesting solute in supersaturation experiments.
References
^ a b Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5
^ Charles Robert Gibson (1908). The Romance of Modern Photography, Its Discovery & Its Achievements. Seeley & Co. p. 37. http://books.google.com/books?id=whYaAAAAMAAJ&pg=PA37&dq=hyposulphite-of-soda+herschel+fixer+hypo&lr=&as_brr=1&as_pt=ALLTYPES&ei=czVdSaipAYWekwSc_vW5Dg. 
^ Aylmore, M. G.; Muir, D. M. "Thiosulfate Leaching of Gold - a Review", Minerals Engineering, 2001, 14, 135-174
^ "Toxicity, Cyanide: Overview - eMedicine". http://emedicine.medscape.com/article/814287-overview. Retrieved 2009-01-01. 
^ Hall AH, Dart R, Bogdan G (June 2007). "Sodium thiosulfate or hydroxocobalamin for the empiric treatment of cyanide poisoning?". Ann Emerg Med 49 (6): 80613. doi:10.1016/j.annemergmed.2006.09.021. PMID 17098327. 
^ Cicone JS, Petronis JB, Embert CD, Spector DA (June 2004). "Successful treatment of calciphylaxis with intravenous sodium thiosulfate". Am. J. Kidney Dis. 43 (6): 11048. doi:10.1053/j.ajkd.2004.03.018. PMID 15168392. 
^ Sodium thiosulfate at Dorland's Medical Dictionary
v  d  e
  Sodium compounds
NaAlO2  NaBH3(CN)  NaBH4  NaBr  NaBrO4  NaCH3COO  NaCN  NaC6H5CO2  NaC6H4(OH)CO2  NaCl  NaClO  NaClO2  NaClO3  NaClO4  NaF  NaH  NaHCO3  NaHSO3  NaHSO4  NaI  NaIO3  NaIO4  NaMnO4  NaNH2  NaNO2  NaNO3  NaN3  NaOH  NaO2  NaPO2H2  NaReO4  NaSCN  NaSH  NaTcO4  NaVO3  Na2CO3  Na2C2O4  Na2CrO4  Na2Cr2O7  Na2MnO4  Na2MoO4  Na2O  Na2O2  Na2O(UO3)2  Na2S  Na2SO3  Na2SO4  Na2S2O3  Na2S2O4  Na2S2O5  Na2S2O6  Na2S2O7  Na2S2O8  Na2SeO3  Na2SeO4  Na2SiO3  Na2Te  Na2TeO3  Na2Ti3O7  Na2U2O7  NaWO4  Na2Zn(OH)4  Na3N  Na3P  Na3VO4  Na4Fe(CN)6   Na5P3O10
v  d  e
Antifungals (D01 and J02)
Wall/
membrane
Ergosterol
inhibitors
Azoles
(lanosterol 14
alpha-demethylase inhibitors)
Imidazoles
topical: Bifonazole, Clomidazole, Clotrimazole#, Croconazole, Econazole, Fenticonazole, Ketoconazole, Isoconazole, Miconazole#, Neticonazole, Oxiconazole, Sertaconazole, Sulconazole, Tioconazole
Triazoles
topical: (Fluconazole#, Fosfluconazole)
systemic: (Fluconazole, Itraconazole, Posaconazole, Voriconazole)
Benzimidazoles
topical: Thiabendazole
Polyene antimycotics
(ergosterol binding)
topical: (Natamycin, Nystatin#)
systemic: (Amphotericin B#)
Allylamines
(squalene monooxygenase
inhibitors)
topical: (Amorolfine, Butenafine, Naftifine, Terbinafine)
systemic: (Terbinafine)
-glucan synthase
inhibitors
echinocandins (Anidulafungin, Caspofungin, Micafungin)
Intracellular
Pyrimidine analogues/
Thymidylate synthase inhibitors
Flucytosine#
Mitotic inhibitors
Griseofulvin#

Others
Bromochlorosalicylanilide  Methylrosaniline  Tribromometacresol  Undecylenic acid  Polynoxylin  Chlorophetanol  Chlorphenesin  Ticlatone  Sulbentine  Ethyl hydroxybenzoate  Haloprogin  Salicylic acid  Selenium sulfide#  Ciclopirox  Amorolfine  Dimazole  Tolnaftate  Tolciclate  Sodium thiosulfate#  Whitfield's ointment#  Potassium iodide#
Tea tree oil citronella oil lemon grass orange oil patchouli lemon myrtle
PCP: Pentamidine Dapsone Atovaquone
#WHO-EM. Withdrawn from market. CLINICAL TRIALS: hase III. Never to phase III
see also diseases
v  d  e
Antidotes (V03AB)
Nervous system
Nerve agent / Organophosphate poisoning
Atropine#  Biperiden  Diazepam#  Oximes (Pralidoxime, Obidoxime)  see also Cholinesterase
Opioid overdose
Diprenorphine  Doxapram  Nalorphine  Naloxone#  Naltrexone  Nalmefene
Barbiturate overdose
Bemegride  Ethamivan
Benzodiazepine overdose
Cyprodenate  Flumazenil
GHB overdose
Physostigmine  SCH-50911
Reversal of neuromuscular blockade
Sugammadex
Cardiovascular
Heparin
Protamine#
Digoxin toxicity
Digoxin Immune Fab
Beta blocker
Glucagon
Other
Methanol / Ethylene glycol poisoning
Ethanol  Fomepizole
Paracetamol toxicity (Acetaminophen)
Acetylcysteine#   Glutathione  Methionine#
Arsenic poisoning
Dimercaprol#  Succimer
Cyanide poisoning
nitrite (Amyl nitrite, Sodium nitrite#)  Sodium thiosulfate#  4-Dimethylaminophenol  Hydroxocobalamin
Toxic metals (cadmium, mercury, lead, thallium)
Edetates  Dimercaprol#  Prussian blue
Hydrofluoric acid
Calcium gluconate#
Other
Prednisolone and promethazine  oxidizing agent (potassium permanganate)  iodine-131 (Potassium iodide)  Methylthioninium chloride#
Emetic
Ipecacuanha (Syrup of ipecac)  Copper sulfate
#WHO-EM. Withdrawn from market. CLINICAL TRIALS: hase III. Never to phase III
Categories: Thiosulfates | Sodium compounds | Photographic chemicals | Antidotes | World Health Organization essential medicinesHidden categories: Chemboxes which contain changes to watched fields

 

(ArticlesBase SC #2800746)

aoao - About the Author:I am China Manufacturers writer, reports some information about body shape lotion , alpha lipoic acid lotion.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


 

Science Home Tutoring | Toxicology Talks | NLP Training | YouTube | Twitter | LinkedIn | Photos | Twitter Pictures
Toxicology Consulting Ltd, UK Reg: 6891619
West Sussex, UK
Toxicological Consulting, Toxicology Training, Forensic Toxicologist, Toxicological Writing and Toxicologist Expert Witness Services, Toxicology Poisoning Advice
Expert Witness, REACH Legislation, Training Manuals, Policy and Procedures, Data Safety Sheets, Manual Handling, Health and Safety
Copyright 2009 www.occupationaltoxicology.co.uk All Rights Reserved
Tel: 07985 923707 Email: toxicologyconsulting@gmail.com