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Fluoride - Science topic

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For anion curve of 2, 4, 6 and 8 mg/L where the analytes are: fluoride, chloride, nitrate, phosphate, bromide, nitrite, sulfate. And for cations of 2, 4, 6 and 8 mg/L with the analytes: lithium, sodium, ammonium, potassium, calcium, magnesium
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To calculate the detection limit (LOD) and quantification limit (LOQ) in ion chromatography, use the formulas LOD = 3.3s/m and LOQ = 10s/m, where s is the standard deviation of the blank and m is the slope of the calibration curve. Construct a calibration curve with standards to ensure linearity and calculate s and m accurately.
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Let's say I am testing for fluoride in a water sample. I diluted the sample 10 times by making 10ml of sample into 100ml. I take absorbance of this diluted sample using UV-Vis. So, my doubt is, Should I multiply the absorbance value by 10 first and calculate the concentration or calculate the concentration first and then multiply it by 10? Where should I incorporate this dilution factor?
Thanks in advance!
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Did you simply measure the absorbance of the fluoride without any treatment? If so, when you introduce the dilution factor (DF) in your calculation does not matter, you should still get comparable result.
However, if your sample has been treated before measurement, say you added an indicator or you heated. When you introduce you DF depends on when the dilution was done. If dilution was done after treatment, then absorbance must be multiplied by DF before calculation of concentration; if dilution was done before treatment, then the concentration should be calculated first and afterwards multiplied by the DF.
Post-treatment dilution has a higher tendency of shifting the intercept of your calibration curve, while the pre-treatment dilution, theoretically, should not interfer with the intercept.
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lithium fluoride
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Üretilen lif kullanılan malzemeye zarar vermiyorsa her zaman kullanılabilir. Lifin uygulanacağı yüzeyin zarar görüp görmeyeceği malzeme yüzeyinin sahip olduğu özelliklere bağlı olur.
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I am trying to synthesize MXenes (Ti3C2Tx), using the MILD etching method (in-situ formation of HF by reaction of LiF + HCl). I am taking equal amounts of LiF powder (Sigma Aldrich, >99.99% trace metals basis) and Ti3C2Tx powder with 10ml of 9M HCl. LiF and HCl are stirred for around 30 minutes, followed by a slow addition of MAX precursor. The etching is done at 35 deg Celsius at 300 rpm for 24 hrs. The product is then centrifuged 10 times (10 minutes each). The supernatant after the last centrifugation is collected, and its SEM micrographs (also EDS mapping) show very high traces of fluoride particles (~1 um) and a much lesser trace of Titanium. Why did fluoride particles remain undissolved or not removed in the decant of the first few centrifuges? Also, is it possible that Titanium is also getting etched out?
Note: 1) Traces of Aluminium are also present, even more than Titanium.
2) The mixture of LiF and HCl remained fuzzy even after 30 minutes of stirring at 300 rpm.
3) All these are done in ambient environment
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LiF has poor solubility in water. Increase the number of washing cycles and try to use warm water to improve LiF solubility.
The presence of Al in EDS/SEM can indicate that the etching time was not sufficient. You can corroborate this with simple XRD analysis.
You do not specify the centrifugation parameters, but 3500-4500 rpm @ 5min should be sufficient to precipitate the impurities you have (Al, LiF, etc).
So:
  1. check you centrifugation parameters
  2. increase washing cycles and use warm water
  3. take XRD/EDS/Raman of sample to see if LiF and Ti3AlC2 peaks are still present
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The US Government Comparative Toxicogenomics database shows that Fluoride can inhibit Human immunity to viruses and pneumonia. Angiotensin I-Converting Enzyme (ACE), 2'-5'-Oligoadenylate Synthetase 1 (OAS1) and Intercellular Adhesion Molecule 1 (ICAM1) are included as susceptible epigenetic targets of the poison.
Wuhan is an area with high Fluoride exposure from atmospheric and groundwater pollution.
Are there more studies linking virus outbreaks or mutations with Fluoride?
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I've looked everywhere and can't find them in the literature
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Recently it has been shown that the spike glycoprotein of the new coronavirus SARS-CoV 2 contains a furin-like cleavage site, possibly a factor in its potency.
Coutard B, Valle C, de Lamballerie X, Canard B, Seidah NG, Decroly E. 2020. The spike glycoprotein of the new coronavirus 2019-nCoV contains a furin-like cleavage site absent in CoV of the same clade. Antiviral Research. 176: 104742. doi:10.1016/j.antiviral.2020.104742
It is also known that Fluoride interacts with Furin
Hasan MK, Alam S, Mirkovic J, Hossain MF. 2018. Screening of Human Proteins for Fluoride and Aluminum Binding. Bioinformation 14(2):68-74.
Is there evidence that Fluoride enhances the activity of Furin, also known as PACE Paired basic Amino acid Cleaving Enzyme?
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For the life time estimation of Corona virus on different metal surfaces and solvents, kindly read the recently published article: Theory for Nanoscale Curvature Induced Enhanced Inactivation Kinetics of SARS-CoV-2, Nanoscale 2022, 14, 5600-5611.
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Hello everyone,
I want to perform docking on a protein that has beryllium fluoride BeF3 as co-crystalized ligand connected to mg as cofactor. In schrodinger preperation wizard when i create zero-order metal bonds all beryllium and fluoride bonds break and further on in minmization process an error appears " restrained minmization procee failed". How can i keep the geometry and beryllium fluoride bonds during preparation? And why that error appears knowing that when i change the Be with zn atom or mg that error disappears!
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This is the error message
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Hello
I have demand for anhydrous Europium Fluoride . What is the best strategy from the oxide ?
Oxide- to hydrate chloride-oven dry -?? What is the best solvent system to go from chloride to fluoride (ionic solvent ?) ?
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Thank you, I need anhydrous material .( i.e. I manufacture simple hydrate salts, so the chemistry is pretty easy) . I was looking for a cheap available ionic solvent(s)
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I am updating my earlier review on the role of Fluoride doped Hydroxyapatite in Cancer and my current focus is on Psammoma Bodies which have been found, and identifed as high risk, in a very wide range of Cancers. These include Cancers of the Bone, Spine, Brain, Choroid Plexus, Dura Mater, Gliofibroma, Medulloblastoma, Meningioma, Cervix and Endometrium, Ovary, Kidney, Lung, Mesothelioma, Pancreas, Skin, Hemangioendothelioma, Olfactory Neuroblastoma, Duodenal Somatostatinoma, Stomach and Thyroid. Early studies did not have the benefit of advanced analytical techniques, or did not even consider the Fluoride content or composition of the mineralization. Can anyone help by supplying analytical data based on Raman spectroscopy, neutron activation, x-ray or wet analysis?
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Hello, Dear Geoff.
We continue to work on the subject you mentioned. There are methods that can analyze this.
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Apparently, one needs the solubility of fluoride. Which salt do we use as a reference?
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Dear Moses Egor sorry to see that your interesting technical question has not yet received any expert answers. As a synthetic inorganic chemist I'm clearly not a specialist in this field enough to provide you with a qualified answer. All I can do right now is suggest to you a potentially useful article which might perhaps help you in you analysis (I'm not sure if it does 😳):
Isotherm investigation for the sorption of fluoride onto Bio-F: comparison of linear and non-linear regression method
This paper is freely available as public full text (please see the attached pdf file).
Good luck with your work and best wishes!
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Dear colleagues, I would like to quantify Teflon (Polytetrafluoroethylene) degradation in a liquid media, it was recommended to me to use Ion-specific Electrode for Fluorine quantification. I wanted to know if there are other methods you would suggest.
Thank you for your help.
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Dear Nissem: P.S. For the second part of your question ("Or Fluorine release in aqueous solutions ?") please note that fluorine can only be released from any materials in the form of fluoride ions. You are absolutely right in that a specific fluoride ion electrode is useful to quantify the fluoride release. For a potentially useful protocol please have a look at the following article:
Quantitative Assessment of Fluoride Release and Recharge Ability of Different Restorative Materials in Different Media: An in Vitro Study
Fortunately this article has been posted by the authors as public full text on RG. Thus you can freely download it as pdf file and print it out if required.
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Human and animal studies have found increased serum Uric Acid levels are caused by Fluoride.
Uric Acid and its salts are known as a danger signal for activation of the NLRP3 gene (Nucleotide-Binding Oligomerization Domain, Leucine Rich Repeat And Pyrin Domain Containing 3) coding for the Inflammasone immune response leading to CASP1-catalyzed IL1B and IL18 maturation and secretion.
Uric acid also increases IL-1β, IL-2, IL-6, and TNF-α.
Monosodium Urate crystals induce Neutrophils to form Neutrophil Extracellular Traps (NETs), associated with severe COVID-19.
Uric Acid level could help to explain risk factors for severe COVID-19, such as Kidney disease and Diabetes.
African Americans are more at risk for Gout and Covid-19.
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Geoff Pain an interesting correlation and sophisticated question. Look, what I would like to present is a simplified iron (fe) perspective while trying to link with all of your proposals and observations. First, fluoride appears to cause iron overload:
Uric acid is suggested as a telltale signal of early iron overload
Finally, instead of a causative role, uric acid appears to be the way the body attempts to mitigate excess iron since it is a powerful heavy metal chelator
"Urate acts as a chelator for iron and, in turn, iron can modulate the activity of xanthine oxidase and the production of urate"
As we are aware covid-19 actively tries to increase the availability of serum iron levels to replicate faster
It would seem that high initial uric acid levels would signal the increase of iron or the fact that the patient has some form of iron overload in the first place. Then at the next stage, Covid19 would attack the areas that produce uric acid thus removing its chelating effects. Uric acid is synthesized mainly in the liver, intestines and vascular endothelium. So it is no surprise that
COVID-19-associated gastrointestinal and liver injury - Nature
Covid-19 is a vascular disease:
All of these mean that Hypouricemia would be the end game.
"studies have shown that serum uric acid concentrations were markedly lower in patients with severe COVID-19 disease"
Now I need a little help with why attacking the kidneys would be advantageous
but nobody is perfect;-)
Lancet: COVID-19 Virus Can Attack Kidneys, Speeding Death
Sincerely
Prof Christopher G YUKNA
PS Fernando Kemta Lekpa African Americans suffer from gout more often and have higher serum iron levels than the rest of the American population which in the context of this discussion may have been due to adapting to deal with the malaria parasite. Just an idea but the research supports the hypothesis.
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what is the exact role of urea and ammonium fluoride in hydrothermal synthesis
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Dear Bandi Hari addition of urea and ammonium fluoride has nothing to do with avoiding oxidation of ions. Especially vanadium with remain pentavalent throughout the reaction. As you can see from the attached reference, urea and ammonium fluoride as added as some kind of "surfactants" in order to influence the morphology of the resulting crystals (i.e. plate-like, rod-like etc.):
Surfactant assisted morphological transformation of rod-like ZnCo2O4 into
hexagonal-like structures for high-performance supercapacitors
(see attachment)
I hope this answers your original question. Good luck and best wishes, Frank Edelmann
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In the literature, different fluoride formulations have been documented for the formation of fluorapatite.
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Fluorapatite is not influenced by just one factor that is dentifrices, Its formation is a much dynamic process influenced by various factors ranging from
1. Systemic administration of fluoride at the time of enamel formation and early tooth eruption,
2. Daily dietary intake of fluoride,
3. Intake of fluoride from additional resources like Tea, fish vegetables, food cooked in Teflon coated utensils etc.
3. Loss of hydroxyapatite to gain of fluorapatite ratio,
4. Availability of free fluoride ions
5. Bare minimum concentration of 500 ppm for children and 800-1000 ppm and above the optimum level of fluoride for adult usage in dentifrices.
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Hello dear researchers, I need the Gutmann Donor Number of Fluoride in different solvents. I have checked in the literature, but there is no information regarding Fluoride. For example in the following paper, I could find the donor number of many ions such as chloride, Iodine, bromide.
Donor Numbers of Anions in Solution: the Use of Solvatochrornic Lewis Acid-Base Indicators
Thanks in advance for your help.
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We'r need a high purity lithium fluoride nanopowders.
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Dear Vladimir Paygin thank you for asking this interesting technical question. Please have a look at the following link:
This supplier promises worldwide shipping.
Please also see the following original research article in which the preparatiom of lithium fluoride nanoparticles is described:
THE EFFECT OF PRECIPITATION PARAMETERS ONPREPARATION OF LITHIUM FLUORIDE (LIF) NANO-POWDER
The article is freely available as public full text on RG.
Good luck with your research! 👍
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Hi, as stated. Can you still used an expired Fluoride-Oxalate tube for blood glucose and lactate examination?
I notice that there might be a problem in getting blood sample because the tube's vacuum might not work as well. But would the result of blood glucose and lactate examination be reliable if the tube had been expired for around 1 month?
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You must avoid using expired things.
You can use common blood tubes with anticiagulant (heparin and EDTA) for this. But to aboid glucose and lactate changes, you must immediately centrifuge the samples at 4 C and separate plasma and freeze or analyze it.
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Usually metallic fluorosilicates are reacted with Ca/Na/K etc metal or alloys to obtain fluoride salts and silicon. But These metals are not very easily produced other than electrolysis. Is it possible to reduce H2SiF6 chemically or with aid of electrolysis rather than their metallic salt? Can cheap reductants like Hydrogen/Carbon/Hydrocarbon do the job? (I do not know redox potential of hexafluorosilicate ion).
By the way, the reactant is from fertilizer industry, and Si is to be used in electronics.
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You can decompose H2SiF6 by heating into HF and SiF4 you can separate them by fractional distillation.
Then you can extract silicon by reducing SiF4 at high temperature into suitable reactors as:
SiF4 +2H2 = Si + 4 HF
Best wishes
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I need to do a research and I would like to measure the fluoride present in children's saliva at different times.
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Dear Flavio Salomao-Miranda thanks for the interesting question. Please see the following useful articles which are both freely available as public full texts on RG:
1. Salivary fluoride concentration after the use of a fluoridated dentifrice, preceded
2. Measuring fluoride in human saliva and water
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Is there a fluoride home application compliance test, that would tell the use of fluoride in past week or month? Something similar to the glycated hemoglobin test that tells you your average level of blood sugar over the past 2 to 3 months.
We are evaluating telephone interventions to increase fluoride compliance for post -radiation caries patients. We would like to use something more objective than just self reported yes or no.
There is an old and semi-invasive method, but has not been used much in recent research:
van der Merwe, E. H., Retief, D. H., Barbakow, F. H., & Friedman, M. (1974). An evaluation of an in vivo enamel acid etch biopsy technique for fluoride determination. The Journal of the Dental Association of South Africa = Die Tydskrif van Die Tandheelkundige Vereniging van Suid-Afrika, 29(2), 81–87.
Brudevold, F., Reda, A., Aasenden, R., & Bakhos, Y. (1975). Determination of trace elements in surface enamel of human teeth by a new biopsy procedure. Archives of Oral Biology, 20(10), 667–673. https://doi.org/10.1016/0003-9969(75)90135-1
Best regards,
Aleš
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Following
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regards
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You can use alumina crucible!
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Hi, I am currently writing my master thesis about fluoride removal with adsorption using different adsorbents. The problem is that the adsorbents I have used so far give very poor results, and almost do not remove any fluoride at all. Am I doing something wrong? How may I improve the results? What may be the reasons for the poor removal efficiency? Any shared thoughts on the matter is appreciated.
Details:
I have tested for Granulated Activated Carbon (GAC), Powdered Activated Carbon (PAC) and Activated Alumina(AA).
The experiment is batch operated with synthetic water composed of NaF and de-ionised water. Fluoride content is 10 mg/l and adsorbent dosage is ranged from 1-10 g/l. Agitation time on a mechanical shaker (250 rpm) is 2 hrs. GAC and PAC showed no valuable removal at all, while AA (which, according to literature, should show promising results) showed a bit higher removal efficiency(about 20%), but still not as high as expected.
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hi
is it possible that only some ppm level fluoride sorbent is activated by given methods you need to atjust the consentration of some suitable alums qty
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Beryllium is exceedingly toxic and known to interfere with Human enzymes.
Analysts have developed techniques to measure Beryllium in parts per Quadrillion.
Beryllium is present in Fluoride industrial waste dumped into drinking water supplies in Australia, measured by one supplier to be 95 gram per tonne (see attached analysis).
I wonder if anyone has studied the concentration of Beryllium in drinking water, its absorbed dose range and risk factors for various diseases, including cancers, as a result of this "Fluoridation" waste disposal? What are the effects on the Human foetus?
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Dear Prof.Geoff.,
It's a nice discussion. I have never heard that the effects of Berrylium at a certain dose can cause a lethal effect on human health and containing some carcinogenic effects upon the human cells.
Beryllium has some useful but undoubtedly harmful effects on health and well-being. Measures need to be taken to prevent hazardous exposure to this element, making its biological monitoring in the workplace essential.
Regards,
Md OSim,India
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 I know that we use IRM to seal cavity and sedation due to eugenol, but can eugenol be used as fluoride to seal dentinal tubule? or dentinal tubule is sealed by IRM due to zinc oxide?
I have a patient whose chief complaint is tooth biting sensitive after resin filling. She didn't feel sensitive with blowing, hot and cold.First I lowered the height of filling but in vain. Then I replaced the filling with IRM and she felt better. After 1 month I changed the restorative material with resin, she felt hurt again when biting. I used fluoride on her teeth and 1 month later, I recalled the patient today. She said it didn't hurt so much but still felt a little uncomfortable when biting. I tried to apply eugenol to her teeth and let her bite a cottonwool. She said she felt more comfortable.
I might keep using fluoride and eugenol with follow up. Is there any more effective treatment for biting sensitive due to dentin loss?
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The two materials, ZOE and topical Fluoride, are different with regard to their reactivity to dentin. Fluoride is incapable of sealing the exposed dentinal tubules. ZOE, on the other hand, plugs the open tubules with the formation of an insoluble CaZ-eugenolate complex.
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I contacted a US based company but they only supply to US licensed company. Plan to using it for in-vitro research 
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Have you tried VulcanChem or Zinc15?
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Could you identify references/publications for state-of-the-art technologies for cost effective treatment of brine generated from seawater to product of 99.6% content of Sodium Chloride? The main challenges are the removal oc calcium, magnesium, potassium, fluoride, boron, bromide and strontium - all of them have to be less than 5 mg/L in the brine.
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That's a good question
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I want to discuss the sulfuryl fluoride problem. We take rice samples from a rice storage warehouse that has never been fumigated, because the rice is sold quickly.
After laboratory testing, it turned out that the rice contained sulfuryl fluoride.
Where does the sulfuryl fluoride come from?
Does it come from fertilizer residues in the field? Or from the residue of rice sacks?
Please colleagues who have ideas?
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Dear Darwin H. Pangaribuan, another important aspect here is whether or not you exceeded the official threshold values for sulfuryl fluoride.
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The US Government Comparative Toxicogenomics Database associates Fluoride with Behçet's Disease, (closely matching Kawasaki Disease in symptoms), and specifically with APOA1, APOB, CAT, CXCL8 and ICAM1 genes. The database also associates Fluoride with Hemorrhagic Shock through ICAM1, IL6 and TNF genes, Cardiogenic Shock through SOD2, and Septic Shock through NOS2 and TNF genes. Many of these genes have been found to be involved in disease progression in Covid-19.
Previous research has linked Coronavirus with Kawasaki Disease, although this remains controversial. Esper F et al. 2005. The Journal of Infectious Diseases, Volume 191, Issue 4, 15 February Pages 499–502
Will the current surge in "Kawasaki-like" disease since the Covid-19 pandemic outbreak be seen through new light given advances in RNA detection?
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I understand that Roger Seheult, California, has been trying to understand the pathophysiology of Covid -19 based on his reading of the literature, including papers sent to him by others. There are a number of papers that address the value of NAC in treating respiratory illness and the effects of oxidative stress on von Willebrand factor. Roger came up with the idea of treating Covid19 with NAC but in MedCram 70 he notes that Alexey Polonikov, Kursk State Medical University has also reported a series of patients with Covid-19 and sees endogenous deficiency of glutathione as the most likely cause of serious manifestations and death. Polonikov sees oxidative stress as contributing to the hyperinflammation of the lung and poor antioxidant defences as being due to glutathione deficiency. He recommends treatment with N-acetylcysteine and reduced glutathione. Seheult notes that it appears that the impaired lung oxygenation is related in part to thromobosis of pulmonary arterioles because of the von Willibrand factor molecules from platelets adhering to one another. The clots consist of long strands bound to one another by disulphide bonds. The NAC or reduced glutathione break the linked chains apart by breaking up the SS bonds through reducing them by changing them to SH SH so that the chains are no longer linked together. When the clots are lysed with NAC the hypoxaemia may be relieved. Seheult notes that there are different VWF levels in Group O patients and some racial groups (higher in Americans of African heritage). SARSCoV2 can cause a550% increases in VWF levels and the NAC can reduce this. Polonikov measured the Reactive Oxygen Species/Glutathione ratio. Patients with ratios of 2.9 and 1.2 did better (recovered without treatment) than those with rations of 34.6 (unwell 13 days) and 6.9 (still unwell after 11 days). Clinical trials of NAC for prevention and treatment awaited.
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In 2002 a paper by Vickers et al reported that Fluoride and Chloride, but not Bromide enhanced the activity of the ACE2 enzyme, a Zinc metalloprotease.
Hydrolysis of Biological Peptides by Human Angiotensin-converting Enzyme-related Carboxypeptidase
What mechanism is behind this observation? Does Fluoride bind to the Zinc atom of the enzyme, or perhaps help to remove a proton from a water molecule bound to Zinc via formation of HF?
Would Chloride have a similar effect? Why does Bromide not behave in the same way?
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Very interesting question, I’m interested because dentists use/prescribe fluoride all the time.
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I need to sputter deposit lithium fluoride, is it possible to manipulate the target in open atmosphere to install it in the sputtering chamber, or are they meant only for use in vacuum or glovebox installed sputterings?
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Dear Efrain Ochoa, I think if you work quickly, you should be able to briefly handle your lithium fluoride sputtering targets in dry air. In the attached article it is atated that "LiF is an almost non-hygroscopic alkali halide with good stability and simple structure (few electrons). This should facilitate experimental and theoretical analysis." (marked in yellow).
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Silver Diamine Fluoride is a boon to the pediatric dentist as it arrests an active carious lesion.
SDF is a 38% Silver Diamine fluoride in a colorless liquid with a pH of 10.
The Functional indicator of effectiveness (ie caries arrest) is when staining of dentinal surfaces is visible.
My query is to know the time required for the arrest of an active carious lesion after the application of SDF.
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Any relevant studies (RCT) reporting the same ?
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How can I analyze flouride through HPLC ? is IC better over HPLC for fluoride analysis or ISE is evergreen? I am Curious to know any better analysis for ionic fluoride which is less time consuming. Implementation of IC over ISE is worth or not?
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You included little in the way of details. ISE is labor intensive and has problems with interferences. IC is easy enough to do but the sample should be clean. It is also very expensive to set up. HPLC is a non starter.
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During the analysis of urine samples in Ion Chromatography I found that the acetate peak is overshadowing my fluoride peak as their retention time is very close?One idea given was to alter the eluent composition?Currently i am using mobile phase 4 mM Sodium carbonate and 1.25 mM Sodium bicarbonate.Can anyone kindly suggest me optimal eluent concentration for separation of this two peaks?
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the issue with reducing the ionic strength of the eluent, as suggested in previous messages, is that stronger retained matrix anions will stick on the column. It is for this reason, that you should keep the need for either a column rinsing step with a higher ionic strength solution in mind (could be as simple as a step gradient) or that you consider a continuous linear gradient - usually using hydroxide based eluents. If you do not rinse the column regularly an increasing amount of ions will be concentrated on the column, and the retention times will shrink, and you will lose resolution.
Using a continuous hydroxide gradient, you'd be able to elute and analyze other inorganic and organic anions in the "salty" matrix as well. Having said "salty": Because of the high salt concentration of the urine sample, you should consider a high capacity ion-exchange column to prevent overloading. Modern ion exchangers provide high (loading) capacity and high chromatographic efficiency. This allows the analyst to separate close eluting peaks in high ionic strength matrices. Because of the high ion exchange capacity, the use of high ionic strength eluents is the consequence so that you please check the "suppression" capacity of the anion suppressor you use. In the case of continuously regenerated membrane-based suppressors, you have a high dynamic suppression capacity and in most cases, you are well equipped. In the case of discontinuously operated packed bed suppressors, you need to check the static capacity and see how long you can operate the pack bed suppressor column before you need to switch (hence, discontinuously operated).
I checked what is available on the Web, and found the following URL (see below). This is an older example of what was possible several years ago. Today, with the higher capacity column (see above) the separations will be much better and the peaks more efficient.
As I don't know the equipment you use, I would suggest checking the paper and getting in touch with your nearest customer support organization to see what is possible.
I hope this is of some help.
All the very best for your research,
Detlef.
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Titanium dioxide does not dissolve in ethanol, methanol, ethyl acetate etc. I'm aware it does dissolve well in hydrogen fluoride (HF). However, I need an alternative to HF.
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Thanks a lot Alessandro.
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Kombucha, a fermented Tea with low pH, contains substantial Fluoride in the form of Hydrogen Fluoride as well as the ion. Kombucha has been associated with many adverse effects, including acute pulmonary edema, metabolic acidosis, elevated levels of lactic acid, with uncompensated respiratory acidosis, and death.
The US Government Comparative Toxicogenomics Database lists the PDHA1 gene as a target of Fluoride leading to Lactic Acidosis. Fluoride is a known inhibitor of Pyruvate Dehyrogenase Phosphatases.
I wonder if anyone has analyzed the fermented liquid or floating bacterial yeast colonies for organoFluorine compounds? Most Kombucha brews contain ethanol.
Tea is known to contain neurotoxic Fluoroacetate and is likely to contain Fluorocitrate. What other Fluorine compounds might be expected due to fermentation?
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Quite an interesting query..Will follow up the discussion for my better understanding..
Thanks for the Sharing..
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The demonstration of the existence of Silicon TetraFluoride in volcanic emissions and the importance of monitoring it, and its ratio to Hydrogen Fluoride gas, in prediction of eruptions is relatively recent.
This leads me to ask if perhaps Sulfur Fluoride compounds might also be present, especially where high levels of Hydrogen Sulfide and elemental Sulfur are observed.
I will be most grateful for any literature references.
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It is possible that sulfur hexafluoride, SF6, is present in volcanic emissions (see reference below). Among all sulfur fluorides, SF6 ist by far the most stable. The compound is rather inert and also a very potent greenhouse gas.
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I was previously told by my dentist that tea contains high fluoride, therefore drinking more of it (without sugar) can help protect teeth from caries.
On the other hand, as many people prefer to drink tea with sugar, that may enhance the bacteria causing the dental problems.
Any scientific evidence if tea is good or not for the dental hygiene?
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Dear Hani,
this is an interesting question. Of the many benefits of tea, idid not know that this was one of them. I do not know if fluoridated water is necessary, but it would be an enhancement. I am sending 2 links. Green and oolong teas fight cavities.
brigid
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Can someone please suggest the best method for measurement of fluoride? How reliable is Ion Selective electrode (ISE)? Which is better - using ISE or SPADNS method in UV Spectrophotometer?
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Fluoride can be determined by potentiometric (ISE), colorimetric (SPADNS) and Gas chromatographic(GC) methods. However colorimetric method is time consuming and not used in biological media such as blood and urine. ISE method is most frequently used method for fluoride measurement in biological media. It utilizes a membrane consisting of a slice of single crystal of lanthanum fluoride doped with europium(II). SPADNS method is used in UV Spectrophotometer.
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The tragic loss of life and injury resulting from the December 2019 eruption of the Whakaari White Island volcano, located to the east of New Zealand, is trending in global media.
There was an earlier eruption there in 1914 that killed 10 people.
I am interested that reporters are not discussing Hydrogen Fluoride gas emissions from this volcano that is known to emit 1500 to 2000 kilogram of HF gas each day, when it is in its "quiet" mode. HF inhalation has caused death in numerous industrial accidents, usually within 24 hours and burns to the skin from this gas have claimed victims some days later.
Students were used on White Island as human Guinea pigs who were not wearing gas masks and it was estimated that some breathed in up to 8 ppm HF during their island visit.
Please let me know if you find media reports mentioning Hydrogen Fluoride as the most lethal gas associated with the deaths and casualties.
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I was interested to learn that Hydrogen Fluoride gas was measured using FTIR spectrometry from a boat as well as on the crater at Whakaari White Island, New Zealand. Reference: Love SP et al. 2000. Passive Infrared Spectroscopic Remote Sensing of Volcanic Gases: Ground-Based Studies at White Island and Ruapehu, New Zealand, and Popocatepetl, Mexico. in Remote Sensing of Active Volcanism. Volume 16. Wiley
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I need to know how to cal culate the entalphy of Fluoride adsorption on Ion oxide nano particles is speontaneous. further how can I decide the Gibbs free energy of MgF+ ion par. is it stable in natural conditions?
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Adsorption is a spontaneous process. Otherwise, without your help, fluorine molecules will be adsorbed on metal oxide nanoparticles. You need to determine the equilibrium constant of adsorption at two temperatures, and from these data you can determine the change in enthalpy during adsorption. With the help of the equilibrium constant, you can determine the change in Gibbs energy in the process of adsorption. There are a lot of mistakes in your question. You have to clarify your question.
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I am working with mica contaminated soil; mica being the source of fluorine, I would like to check the fluoride content of the soil. Can anyone please help me out to find the protocol of this.
Thanks in advance
Sandip Mondal
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Conclusions: NTP concludes that Fluoride is presumed to be a cognitive neurodevelopmental hazard to humans. This conclusion is based on a consistent pattern of findings in human studies across several different populations showing that higher Fluoride exposure is associated with decreased IQ or other cognitive impairments in children.
Please will you share this dramatic news in your networks?
The draft NTP report, written and reviewed by a team of 51 scientists is here:
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The draft report is horrendous. The information on the thyroid issue is so wrong, it is mind-boggling. Not surprised though.
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Can anyone help with literature on reactions of Glyphosate, N-(phosphonomethyl)glycine), or its degradation products such as (Aminomethyl)phosphonic acid with Fluoride, HF or Fluorine? Material safety data sheets simply state that they are incompatible with Fluorine. Of interest are reports of complexes of Uranium and Europium where Glyphosate and Fluoride are brought into close proximity. This brings into question the wider subject of Fluoride attack on Phosphorus in biological systems and the basis of observed epigenetic interference with human genes.
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Dear Geof,
I had a look at material safety data sheet of Glyphosate and it states that this compound is sensitive to fluorine due to high oxidation potential of F2.
This seems reasonable as C-P bond in Glyphosate looks like something that can get oxidised quite easily. I have found a couple of articles supporting this hypothesis:
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Copper (I) fluoride or copper (I) Iodide?
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Can easily be determined with thermodynamic calculations.
2CuI + H2(g) = 2Cu + 2HI(g)
deltaG - temp.
kcal - oC
36.896 - 0
33.206 - 100
29.696 - 200
26.361 - 300
23.372 - 400
21.107 - 500
2CuF + H2(g) = 2Cu + 2HF(g)
deltaG - temp.
kcal - oC
-16.351 - 0
-19.961 - 100
-23.382 - 200
-26.635 - 300
-29.741 - 400
-32.716 - 500
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Can someone please explain me the difference between protonation and ionization? Am studying about the adsorptive mechanism of fluoride ions and came across the following sentance in a literature.
The effect of pH on the surface charge of HAp particles can
be attributed to the protonation and ionization of the OH
functional groups present at the HAp−water interface. The OH
group would be protonated below pH 8 and ionized above pH
8.
Can anyone explain me this
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Thank you Sabarija for your important question.
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Researchers in hydrogeology, hydrogeochemistry, environmental geology
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Dear Dr. Nwanosike
Bone char is a good option, there are several studies of groundwater fluorine removal using this material:
Best Regards.
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Hello, in our lab we've been using anion chromatography with conductimetric detection for the determination of 6 anions in tap and natural waters, namely Fluoride, Chloride, Nitrite, Nitrate, Sulphate and Phosphate. The main disadvantage we encounter is that we need 50 minutes per sample to resolve and quantify properly these 6 anions.
I've read some articles about indirect UV photometry with C18 ODS coated colums describing conditions really faster than our current method. Does anybody perform regularly any alternative chromatography under these conditions? Any other suggested approach will be really appreciated, specially if tested in "real world" conditions.
Thank you very much,
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I should add, the ICS5000 instrument also has an anion suppressor which will greatly influence the analysis. Some for purchasing the columns please be aware that may not speed up the analysis in your system.
regards,
B
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I have to coat Sapphire windows with reflective dielectric multilayers for Hydrogen fluoride environment. HF pressure inside vacuum chamber is 10 mbar. I have coating material : HfO2, ZrO2, SiO2, Ta2O5, TiO2, Gd2O3 and some other oxide and fluorides.
Please recommend some anti-corrosion coating material from above listed or any other which can work in HF gaseous environment.
Thanks
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Thanks Goyal Ji
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I wonder if anyone can help with references to the health status of professional Tea tasters, given that Fluoride is absorbed directly through the oral cavity?
I am looking for data on the quality of their teeth, any oral cancer, plus wider potential impacts on the rest of the tasters bodies.
Is the development of electronic "tongues" related to health issues as well as seeking objectivity?
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Tea tasting is the process in which a trained taster determines the quality of a particular tea. Due to climatic conditions, topography, manufacturing process, and different clones of the Camellia sinensis plant (tea), the final product may have vastly differing flavours and appearance
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For example,I have a sample of TaO2F (Tantalum dioxyfluoride, but I doubt about Oxygen and Fluorine ratio). I want to solve the crystal structure. PXRD and Single crystal do not give any indication which atom is oxygen and which one is Fluorine. From SEM-EDS I can get some quantitative information but that is not that much reliable. In this case, how should I approach to solve it?
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to use neutron scattering method
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Hey all
It is well known that Fluoride is a main ingredient in toothpaste of great debate and potentials, according to its ionic nature it can be mainly measured by ion selective electrodes
Are there other easier methods like kits or facile instrumental techniques for this purpose ?
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There is a paper that goes into detail about the methods to determine fluoride in toothpastes:
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Most basically, does the test for fluoride include the fluoride of calcium fluoride, which is insoluble?
What amount of sodium fluosilicate, fluosilicic acid, and sodium fluoride, individually, must be added to 100 g (or liter, or whatever) of water at ~20 C to achieve a 1 ppm concentration of fluoride ions (as determined by ASTM D1179)?
Do these compounds dissociate completely? What amount of insoluble (from pubchem) calcium fluoride must be added? The test for fluoride measures only monatomic F- ions, correct?
How about a soluble but undissociating (like ethanol) fluoride salt, if one exists?
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To convert fluoride compound into fluoride ion for sodium fluoride (NaF) divide by 2.21. For sodium silicofluoride (Na2SIF6) divide by 1.65. For fluorosilicic acid (H2SiF6) divide by 1.26. Thus, 1 mg of NaF contain 0.45 mg F ion, Na2SIF6 contain 0.61 mg F ion, and H2SiF6 contain 0.79 mg F ion. Collectively, the sum of F ions in one mg of these compounds is 1.85 mg. If all these compounds are used to fluoridate water at one mg F ion per liter, then the 1.85 mg should added to 1,850 ml of water OR 0.1 mg per 100 ml. If individually then turn to the conversion ratio as above. Good luck.
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I need it for determination of iodide and fluoride in urine and blood samples using ION SELECTIVE ELECTRODE AND ION CHROMATOGRAPHY.
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For the measurent of iodine in urine and serum please refer J Rendi 1998.
for Fluoride refer K ItaI 2001
detailed information on line available
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I use Spadans method. Because of sample turbidity and high TSS, even with filtration or dilution, i cant measure the F concentration.
Does any one have any suggestion fort his problem?
Thank u.
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Effectively the potentiometric method is the most appropriate you have to opt for a combined F electrode
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I am doing work on fluoride containing semiconductor wastewater and discovered that at pH lower than 5, the particles were stable and did not aggregate. The zeta potential values at pH 2 to pH5 were ~ +6.93 mV and particle size remained ~ 1586.6 d.nm. The agglomeration took place between pH7.1 (zeta potential = 0. Point of zero charge and at pH 7.5 , zeta potential -5.23mV). Floc size at peak was ~5000 d.nm, which then dropped at pH 8 to 2000d.nm.
As the pH increased from pH 8 to pH 12, the zeta potential was -4mV (pH 8) to +20mV (pH12) with concomitant increase in particle size from 2000d.nm to 5000d.nm. Would appreciate some clarifications on my data .
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Dear Alan,
We published a paper in Journal of "Desalination and Water Treatment" in 2014. I have attached the paper to the answer. In Figure 7 a, b, c, d there are 1 to 3 peaks. What do you think of the results? I measured particle size and size distribution of pure water and get 1 or two peaks. The results are repeatable. Please measure at least 6 times of each sample then give your invaluable explanation and insightful conclusion.
Thank you very much in advance.
Kind regards,
Li Shu
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I am having issues with pH test strips. I have two different pH probes and bromethyl blue indicator that tell me my solution is neutral (7.1) but every time the pH strips read closer to 6.
Does anyone know what could cause the strips to read more acidic than the solution actually is? The strips are not expired and I trust the bromethyl blue indicator along with the two pH probes are trustworthy (they all agree). My solution contains fluoride ions if that matters?
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It could be that the solution is too dilute to overwhelm the buffering capacity of the indicator itself.
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Interleukin 17 (IL-17) is a class of closely related molecules known to be increased in the human body by exposure to Fluoride by ingestion from water and food, or metabolism of Fluorocarbon anaesthetics and propellants. IL-17 causes Autoimmune Diseases including Psoriasis, Rheumatoid Arthritis, Asthma, Lupus, Multiple Sclerosis, Inflammatory Bowel Disease, Transplant rejection, and destruction of Liver and Heart Cells. IL-17 is also implicated in Skin Cancer.
Other Interleukins are known to be elevated by Fluoride, leading to attacks on other critical cellular and organ systems. Australia's National Health and Medical Research Council actively suppresses this Interleukin science while promoting Water Fluoridation using industrial waste. Can the science community influence this behaviour?
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Dear Michael after reading your answer i did look up to the internet and started reaading bout flouride in water.
I am now able to get some insight about the big problem the humans are facing.
Lets hope that the council for water management will take up the issue in a more seroius manner.
It also has made a difference to my understnading of the disease patterns of autoimmunity.
Thank you for the insights.
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Bifluoride ion has a very stable F-H-F structure that can bend in the solid state. It forms Hydrogen bonds readily. I am looking for any evidence, e.g. 19F or 1H NMR , infrared spectroscopy, protein crystallography, that it might exist in vivo. Its presence in whole blood, serum, plasma, muscle or other cells could help to explain examples of surprisingly low F- measured with an ion selective electrode after dosing an organism with a known amount of Fluoride.
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Dear Geoff,
That is an interesting hypothesis regarding the low |F-| concentrations measured with an ion-selective electrode. I don't know if there are any experimental measurements, but from my point of view, as a theoretical chemist, I'd say an assessment of the stability of FHF in aqueous solution is paramount as a first step to understand speciation of F- in biological media. Quite often, stable structures formed either in gas-phase or in solids are highly unstable in aqueous solution. Furthermore, I believe experimental data regarding the stability of FHF in aqueous solution is much easier to come by in the literature than in biological samples.
I hope this helps.
All the best.
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some times , there is more than 150 ppm Si and much more Al in solution !
can i use Standard addition method for this sample???
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The Si-F bond is quite strong, so you might have to drive precipitation of insoluble polysilicates before attempting to measure the F- liberated.
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We treat wastewater containing HF via precipitation flocculation filtration and are looking for a quick method to confirm the treated wastewater, typically 2-3 small batches per day, is below 180 mg/l Fl as fluoride salts. It is typically at 5 - 20 mg/l.
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Ion selective electrode method is best for Fluoride analysis. Thirmo Orion ion meters are very good for Fluoride.
SPADNS method (APHA) is also good if the F conc is low (0-1.4mg/L). Refere APHA for detailed protocol.
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Australia's National Health and Medical Research Council (NHMRC) produced a sham review of Water Fluoridation in 2017 by deliberately ignoring over 3000 peer-reviewed scientific papers on Fluoride Toxicology. One important paper the NHMRC suppressed dealt with the mechanism by which Fluoride damages your teeth, with or without metal ions like Aluminium. Fluoride causes increased SATB1, a factor associated with Malignant Cancers and their Metastasis, with many relevant publications relating to Leukemia, Melanoma, Laryngeal and Nasopharyngeal squamous cell carcinoma, cancers of the Bladder, Breast, Cervix, Colon, Kidney, Lung, Ovary, Prostate, Uterus, and Liver.
A couple of papers: Zhang Y, Kim JY, Horst O, Nakano Y, Zhu L, Radlanski RJ, Ho S, Den Besten PK - "Fluorosed mouse ameloblasts have increased SATB1 retention and Gαq activity" PLoS One 9(8):e103994
Fluoride interferes with FoxP3
Zhang G, Zhou B, Han T, Wang M, Du X, Li Q, Wang J. 2012. Decreased percentages of CD4+CD25+ regulatory t cells and foxp3 expression in the spleen of female mice exposed to fluoride. Fluoride 45(4)357-364.
Observed increases in cancer incidence over four decades follow the roll out of Fluoridation and increased Dental Fluorosis. Surely it is time to ban Fluoridation worldwide?
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I agree, none of the articles talks about fluorosis, but the original question is: why if it has been shown that fluoride is toxic, it has not been banned, my answer is yes, Fluoride is toxic, but for produce the effects that are mentioned in the articles on which Dr. Pain is based, the doses are much higher than those used to prevent the caries process.
In some parts of my country, drinking water contains cyanide, but the doses are lower than those that produce toxic effects.
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Discoloration of demineralized or cavitated surface of tooth is a major drawback of SDF (Silver Diamine Fluoride). This agent permanently blackens carious enamel and dentinal lesions.
Since, it is not mandatory to excavate the infected dentin before SDF application,and there is no tooth preparation also how would the longevity and aesthetics of such restorations be?
Any studies reporting the same?
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I have started using SDF recently. I use GIC to mask the Black colour in Primary teeth. The far reaching benefits of SDF do not compel us to excavate discoloured dentin. A sandwich restoration of GIC+ Light cured composite helps for sure.
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The author of literature (Prog. Polym. Sci. 26 (2001) 3-65) said:' poly(tetrafluoroethylene) and some of its derivatives exhibit the lowest known dielectric constants with values of e between 1.9 and 2.1. It is well known that the incorporation of fluorinated substituents into polymers decreases the dielectric constant due to the small dipole and the low polarizability of the C-F bond as well as the increase in free volume.' Similar descriptions had been emerged in many literatures. However, the bond moment of C-F is 1.83 Debye, much higher than that of C-H (0.2). On the other hand, the dielectric constant of polyvinyl fluoride (PVF) is 8.5, much higher than that of polyethylene (2.3). So, I wonder to know, is fluorine atom increase or decrease the dielectric constant of polymer?
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It could be a better hypothesis. By the way, I am not a specialist either. I just came across the following chapter, which should be useful:
Engineering » Electrical and Electronic Engineering » "Dielectric Material", book edited by Marius Alexandru Silaghi, ISBN 978-953-51-0764-4, Published: October 3, 2012 under CC BY 3.0 license. © The Author(s).
Chapter 1
Polymer Dielectric Materials
By Zulkifli Ahmad DOI: 10.5772/50638
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The stock of underground water is reducing everyday at a great speed. According to many scientists, the next world war may be started for capturing of water resources. Many diseases are created for mixing of arsenic, fluoride etc. poison with underground water due to this reason. In such a condition, nobody is even thinking seriously about the importance of unnecessary wastage of underground water. The attached articles may speak some other related important points also.
At that condition, do you think there should be some rationing in use of underground water? There shuld be some provision of fine for wastage?
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The major environmental impacts associated to groundwater over-drafting are decline of water level, water scarcity, damage to connected wetlands, and sometimes salt-water intrusion.
So. there should be some national policy on the groundwater extraction - a regulatory authority need to be established to ensure the sustainable use of this natural resource. Tax based on the quantity of withdrawal can be imposed to minimize the wastage of water.
Regards
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Fluoride is one important contaminant released by geogenic process.
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Dear Sunil,
The removal of fluoride from an aquifer itself is not possible. But, its concentration can be reduced through dilution by injecting water into the aquifer (artificial recharge). Some have already mentioned this.
Various researchers have applied this method and was found to be effective in insitu dilution of fluoride content.
However, several investigations have been carried out on defluoridation of groundwater (pumping out groundwater) - Prof. Achour has given some indications.
I have provided a brief review on defluoridation of groundwater on reply of a question. You may read the same (link given below).
In this context, I like to mention that we have developed a method for defluoridation of water and filed for patent (The technology already transferred).
Best wishes
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esthetics, fluoride release, tooth bonding, strength
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Due to the different natures of both materials (glass ionomer and composites) a few rules should be observed: glass ionomer adheres better to the root surface, while composites adhere better to enamel. Therefore it is crucial not to remove any healthy enamel at the CEJ and preserve even small amounts that would help to bond the composite to. To combine the advantages of both materials, the sandwich technique is being used. https://www.slideshare.net/mobile/ruhi_kashmiri/sandwich-technique-61386414
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The sample is dissolved in hexane. I think, that the concentration of TBu-F is in the range of µg/ml. I need to measure the concentration of fluoride in the sample. Should I carry out some derivatisation reaction?
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TBA fluoride is thermally unstable.  It decomoses into butene and tributylamine.  This process is spontaneous in either the gas phase or in liquid solution starting around 30-35C.  If I remember correctly, this reaction is called a Hoffman elimination.  The fluoride is less stable than the hydroxide or other salts of TBA.
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I want to utilize it for some florid sensitive reactions,
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immunocytology investigation
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I want to reduce the COBB value of Coated While Line Chip Board. Any suggestions are welcome!
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labricarion may be?
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I'm looking to replace hydrofluoric acid, which is highly dangerous to handle, in a factory making aluminium products.
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Often, hydrofluoric acid ― when used as etchant ― can be substituted by Buffered Hydrofluoric Acid (BHF) or Buffered Oxide Etch (BOE) (*), which often contains NH4F and HF aq.; by NH4HF2 (or KHF2) + HCl conc. aq.; or by hexafluorosilicic acid (fluosilic acid). 
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Fluoride is major contaminant in groundwater.
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You need to synthesize selective binders such as calixpyrroles or other pyrrole derivatives for fluoride ion binding and load them on to solid nanomaterials for example magnetic nanoparticles etc. If you search on google you may get many such articles. 
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chemical exchange takes place with the oxides of metals, Al, Si, and Fe during the adsorption process. so, after adsorption the fluoride present in the red mud is in stable or unstable form?.
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after fluoride adsorption with red mud, the leaching tests with the residue showed appreciable leaching of the fluoride back into the water. 
Is there any method to stop the leaching of fluoride back into the water, by adding some chemical or so?.
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There are a lot papers about the expose of TiO2 (001) surface by using fluoride based chemicals. What kinds of mechinism is there. And what is the advantage by exposing 001 surface 
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I think it has to be something like glass etching by HF! it is like making some scratches on a surface and making a coarse surface.
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Do Fluoride have any correlation with trace elements other than B and As. Any suggestions will be highly appreciated. 
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hi see this attach can help  you 
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What could be the source of fluoride in groundwater when there are no fluoride bearing minerals in the catchment or anywhere along the river course and also anthropocentric influence is also minimum.
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Deep groundwater and/or geothermal waters is generally high in Flouride cocentration. In the a river stream that is recharged by groundwater it is neccesary to check such possibilities...
Good luck!
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I am doing substitution reaction between fluoro substitutes pyridine with tert butlyl amine in ACN solvent. We use 8 eq of amine and heat to 60-70 C. My concern is about the byproduct HF forms during reaction, whether this reaction could be possible to do in GLR or SSR without any effect of fluorides on reactor. If not how to conduct these type of reaction on large scale
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i think no as there will be no free HF
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What are the minimum parameters we have to maintain in the drinking water, and what is the limit ??
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Dear Saravanan,
Here is an interesting document concerning health risks from drinking demineralised water. You will also find the quality standards required. This document is from WHO.
With my best regards
Prof. Bachir ACHOUR
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I have prepared until now all my pollen samples using hydrofluoric acid to dissolve silica, but this product is really dangerous and I wanna know if it is possible, using for example dense liquor, have good pollen sample preparation without using hydrofluoric acid.
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David:
You may like to have a look at this helpful link:
Best
Syed
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Phenyl Methyl Sulphonyl Fluoride
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What do you mean with your question "PMSF equivalents"? Do you want to use a different inhibitor with similar functionality?
AEBSF (sometimes referred to as Pefabloc) is also a sulfonyl fluoride that inhibits a range of serine proteases. Although one of the above comments mentioned that these are specific for active site serines, AEBSF and related compounds can also react with tyrosine residues. See: https://www.ncbi.nlm.nih.gov/pubmed/23601632 and https://www.ncbi.nlm.nih.gov/pubmed/23601643
An alternative may be DFP (diisopropylfluorophosphate), which is a general serine hydrolase inhibitor that also reacts with active site serines.
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Dumoulin, E describes the usefulness of using granulised fluoride and citrate for stabilizing of plasma homocysteine levels. Are fluoride citrate granule containing vacutainers still available for use like the Greiner product, or is there an alternative?
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Biosorption / Adsorption studies / Fluoride
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Pl. refer the paperof Emmanual et al 2008  which gives answer to your doubt.
Prepare a standard graph and post the OD of treated solution. You will get the concentration. Now calculate percentage 
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I am trying to synthesize InF3 salt in bulk amount but I couldn't found any information about it.
I tried to react In2O3 with HF acid at room temperature, but I got around  83% of InOHF2 and only 17 % InF3. InOHF2 is not suitable for my application, so I need to remove this phase from my powder.
I would highly appreciate if someone can help me in this matter or if someone can provide me with related literature.
Thanks! 
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Since aqueous solutions are needed you probably are going to form the hydrated form in most cases.. here's a procedure that i found to work up to 5g.
In2(SO4)3xH2O (3.3 g, 6.4 mmol) was dissolved in hot freshly distilled water (50 mL). A concentrated solution of NaOH (5 mL of 10 M) was added until a white solid precipitated. The solid was filtered off and washed with water. The solid was then suspended again in water (10 mL) in a Teflon beaker (important to use teflon container at this stage) and HF 40% (5 mL, 115 mmol) were added, giving a clear solution. After several minutes a white solid started to precipitate and the mixture was allowed to stand overnight. The solvent was decanted off and the solid dried in vacuo. Yield: 0.89 g, 62%.
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I have prepared the nanocomposite of metal oxide with graphene oxide. It was used for the removal of fluoride ions from water by fixed bed column studies. I want to determine the porous properties of the fixed bed column.
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Shweta,
This is simple!
Make a column: say with radius r, height h, calculate volume: [(pie)r2.h] (V ml), then fill column with water up to  level of stuff, then collect water in a measuring cylinder. Say volume of water is 'x' ml.  This x represents volume of voids in column of your material. The ratio "x/V' gives you porosity of the material stuffed in the column.
I could understand that you are interested in porosity of the material in column.  If you are interested in determination of porosity of material, you can do so by determining the parameter by 'mercury posorosimeter' or porosity can also be determined while determining BET surface area of the material.
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In my study, the fluoride (F) shows a significant negative relation with total hardness (TH) (r= -0.635). F also exhibits significant negative correlations with Ca and Mg.
TH is positively correlated with Ca, Mg and HCO3.
1)      In this case what salts are responsible for hardness of groundwater? Are these bicarbonate salts, Ca (HCO3)2 and Mg (HCO3)2 ?
2)      Can we say that the negative relation of F with TH is due to the precipitation of Ca and Mg ions in the TH as carbonates and/or ion exchange of Ca with Na?
But Ca/Na exchange will not change bicarbonate, and also is not true for precipitation.
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Ca binds to F as CaF2. That's why you find a negative correlation between these two ions. If you plot logaritmic concentrations of these two you could find a linear relation. Check with a good textbook on water chemistry; my favorite is Stumm- Morgan Aquatic Chemistry (a bit old now, but still good).
Agrees with Andrew Butler.
Anders Wilander
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Some  researchers mentioned that high pH resulted in elevated fluoride concentration in groundwater.
It is found true; it is also seen that in the same area at some other locations though the pH is high but fluoride concentration is low.  What's the explanation?
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Dear Dr. Bhojraj Nandlal - The pH has a significant role in F solubility; at a pH range of 5 - 6.5, F solubility is low and the F is adsorbed on the surface of the clay . The higher pH values (>7) of groundwaters are found to be greater than the point of zero charge (PZC) of most minerals (>7–8); in such system, the surface charge of the solids is neutral or slightly negative, which depresses the adsorption of negatively charged F . Conversely, as OH and F ions have similar ionic radius (0.136 nm), the OH in groundwater can replace the exchangeable F of clay minerals (biotite/muscovite, illite, chlorite, and amphiboles) resulting in increase of F concentration in groundwater.
Thanks for your query.
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How the speciation and genesis of fluoride, nitrogen, phosphorus, iron etc .can be explained from the Eh-pH Stability diagrams?
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This book can help you, also you can used and modify other experimental condition with a program name Medusa, for pourbaix diagrams.
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The analyses of stable isotopes δ2H and δ18O have great significance in the groundwater studies, particularly to understand the mixing of surface and groundwater. How the stable isotope studies help in comprehending the mechanism of fluoride mobilization in groundwater?
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All waters have "fingerprints" of naturally occurring isotopes that provide information about their origin. Among the most powerful and cost-effective fingerprinting tools are the ratios of stable isotopes of hydrogen--deuterium to hydrogen (D/H)--and of oxygen-18 to oxygen-16 (18O/16O). For example, the D/H and 18O/16O ratios in precipitation vary according to elevation and distance from the ocean. An altitude difference of 250 meters produces a clear and measurable change in the two ratios, which is preserved once the precipitation infiltrates to the aquifer.
The stable (2H, 18O) isotopes in integration with radioactive (3H, 14C) can provide detailed insight into and assess the mean groundwater recharge in river basins, regional groundwater flow velocity and residence time, contamination characteristics, flow-paths of intermixing, and identification and delineation of recharging zones and protection zones in the aquifer system. The D/H and 18O/16O ratios can be used also to discriminate among multiple water sources within an aquifer.
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Some earlier studies demonstrated that the pH has a significant role in fluoride solubility. Anion exchange hypothesis has been proposed to explain the phenomenon. That is at alkaline conditions (pH>7), the OH− in groundwater replace the exchangeable F− of clay minerals (biotite/muscovite etc.) and thus increase the fluoride concentration in groundwater. Can somebody explain this process in detail?
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Thanks to Dr Arvind Singh and Dr Virendra Kumar Saxena for providing information.
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I am working on hydrothermal fluorite geochemistry.
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Dear Dr. Censi,
Thanks for your helpful questions.
Best wishes
Mansour
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Fluorine is a common element that does not occur in the elemental state in nature
because of its high reactivity. It accounts for about 0.3 g/kg of the Earth’s crust and
exists in the form of fluorides in a number of minerals, of which fluorspar, cryolite
and fluorapatite are the most common.
Exposure to excessive consumption of fluoride over a lifetime may lead to increased likelihood of bone fractures in adults, and may result in effects on bone leading to pain and tenderness. Children aged 8 years and younger exposed to excessive amounts of fluoride have an increased chance of developing pits in the tooth enamel, along with a range of cosmetic effects to teeth.
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Dear Dr. Prakash,
I have shared the following write-up to some researchers. You can go through the same.
 A brief account on fluoride removal (based on literatures):  
Various techniques and materials were explored throughout the world for defluoridation of groundwater. The techniques can broadly be classified into four categories:
Adsorption technique, Ion-exchange technique, Precipitation technique, and Other techniques, which include electro chemical defluoridation and reverse osmosis.
Materials used as defluoridation agents in these four techniques are:
Adsorption: Carbon materials, Activated Alumina, Magnesia, Tricalcium phosphate, Calcite, Hydroxy apatite, Wood, Lignite, Activated char coal, Fish bone char, Processed bone, Nut shells, Avaram bark, Paddy husk, Coffee husk, Tea waste, Jute waste, Coir pitch, Fly ash, Bauxite, Serpentine
Ion-exchange : a) Anion exchange resins-  NCL poly anion resin, Tulsion A27, Lewatit-MIH-59, Amberlite IRA-400, Deacedodite FF-IP, Waso resin-14, Polystyrene. b) Cation exchange resins: Defluoron-1, Defluoron-2, Carbion.
Precipitation: Lime, Alum, Lime & Alum (Nalgonda technique), Alum flock blanket method, Poly Aluminium Chloride (PAC), Poly Aluminium Hydroxy Sulphate (PAHS), Brushite.
Others:  Electrochemical method (Aluminium electrode), Electro dialysis, Electrolysis, Reverse Osmosis.
The basic characteristics of an ideal defluoridation process are the following:
o   Cost-effective
o   Independent of input fluoride concentration, alkalinity, pH, temperature
o   Easy to handle/operate by rural population - the major sufferer
o   Not affect the taste of water
o   Not add other undesirable substances (eg. Aluminum) to treated water
Defluoridation can be introduced at two organizational levels; as household defluoridation for consumption of single household members and as community defluoridation  for the public use in a village.
The defluoridation processes available today are not totally successful. Nalgonda and  Krass processes for defluoridation have some merits.
This is for your kind information that at CSIR-CMERI, Durgapur we are working on the defluoridation of groundwater. We have already developed a process (adsorption technique) for defluoridation and filed a patent in April, 2016.
We have also designed and developed a 'Domestic Defluoridation Unit' for reducing the fluoride content in water. In addition to the removal of fluoride, the unit also arrests other common contaminants found in the groundwater. This unit is suitable for domestic purposes in the fluoride affected rural areas.
Specifications
·         No electricity
·         No chlorine, no bromine, no iodine used
·         No running water required
·         Flow rate: 5 L / hour
·         Adsorbent life (proposed): ~2000 L
·         Storage capacity: 18 L
 Techno- Socio-Economic analysis
·         Adsorbent replacement cost: Rs. 600/-
·         Maintenance cost/month: 150/- (~500 L p.m.)
·         The commercial filtration unit addressing the defluoridation of water for domestic purposes is not  available in the market. The developed filtration unit could be promising for commercialization.
·         Unit can be deployed in the fluoride rich regions of India through Govt./ NGO support 
We are conducting a research project entitled “Geochemical modelling of fluoride contamination in groundwater of the Birbhum District, West Bengal” which primarily aims to explore the origin and enrichment mechanism of fluoride in groundwater. This study has encouraged us to undertake the work on defluoridation of groundwater.
We have a plan to deploy some working models of the ‘Defluoridation Unit’ in the fluoride affected villages of Birbhum district, West Bengal.
Please give your feedback.
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how to calculate percentage removal of fluoride?
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Madam Deepmoni,
I have seen your question in the last week.
From the given data, it seems that 90% of fluoride has been reduced in the treated water.
But, the data provided are insufficient to say anything about efficiency. To measure the efficiency, three parameters are to be considered:
Quality: The quality of treated water – the targeted parameter including the other important water quality parameters should be within the desirable limit as per the drinking water standard (BIS/WHO). For e.g. groundwater of an area is fluoride contaminated (F>1.50 mg/L); if  the treated water contains Fe or say Al above the the enviable limit, then the treatment process is not effective.
Quantity: The rate of flow that is the production of treated water (litre per hour).
Cost: The quantity of filter media/adsorbent, adsorbent life - say after 2000 litre  the change of adsorbent is required, electricity required or not for operation and ultimately the cost of one litre of treated  water say 40 paise /litre.
From the above information, a relative measurement of efficiency of the treatment process can be done.
Please give your feedback.
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Has anyone coupled the Integrion HPIC with the MSQ mass spec? I had a go at by using an AXP pump to run water into the suppressor and an AXP-MS pump to run acetonitrile into the MSQ. The sample goes pass through the a guard column (Ionpac AG18) and separation column (Ionpac AS18) respectively into the conductivity detector before mixing with acetonitrile into the MSQ. I tested the system with 10 ppm fluoride solution in SIM mode at 39.10 m/z. This was detected by the conductivity detector but not the MSQ. I also noticed that at the end of the run, the sequence cannot be terminated and it keeps saying the injection is running even though it had finished a long time ago. Any suggestion?
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Why are you looking for fluoride in SIM at m/z 39.10 amu; isn't that for potassium in positive ion mode? Fluoride should be @ m/z 19.00 amu in negative ion mode. Fluoride might be too volatile to give a good signal. I have seen Cl, Br, and I on other mass spectrometers in negative ion mode by direct infusion.
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Removal of fluoride from Drinking water sources...
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Depending on the scale that you want to carry out defluoridation, the technique employed will differ, but studies have shown that sub-urban and rural communities in most sub-saharan  and Asian countries that dont have access to clean municipal rely heavily on groundwater for their domestic use and often has high concentration of fluoride beyond recommended limits by WHO, these communities require to defluoridate their water at low cost and with very simple technology to operate. Adsorption has been observed by many researchers to be the best option but the challenge is availability of low cost, high capacity adsorbents based on locally available and abundant materials. My research group at University of Venda South Africa is experimenting with smectite clay rich soils found locally in Limpopo province either in their raw form or modified with metal oxides in an attempt to develop high capacity fluoride adsorbents. 
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For groundwater numerical modeling studies, I like to procure the Argus ONE software. I need the contact details of the developer/manufacturer and/or distributor (India).
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Hello,
I am looking to do TOF-SIMS and XPS experiments on TiO2 and MgF2 crystal surfaces. These experiments require ultra-cleaning methods that will create extremely clean surfaces. My colleague recommends RCA, but I would like to hear other ideas as well.
People in optics recommend cleaning MgF2 with some solvents, but that method definitely won't be clean enough.
TiO2 can be cleaned with Ar+ ion bombardment, but I don't have the equipment for that.
Thank you for your answers, and I would especially appreciate it if you could also provide a reference.
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The first cleaning steps depend on the nature of the contaminats and they are straight forward and you have various options: solvent treatment, (nonionic!) detergent solution eventually combined with ultrasound, piranha solution...
For the last flush use a solvent grade with a low content of nonvolatile substances e.g. isopropanol. Let the solvent run off rather than drying it on the surface.
Finally, you will have to remove the layer of adsorbed substances from the high surface free energy surfaces of TiO2 and MgF2. Since the adsorbate layer forms quickly upon exposure to atmosphere you will have to do this in the high vacuum of your analytical instrument immediately before your measurements. I am pretty sure that there is an ion gun at your XPS instrument.   
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For correlate the water and soil parameter in same study area.
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Today, water is one of several sources of fluoride. Fluoride is a mineral that occurs naturally and is released from rocks into the soil, water, and air. Almost all water contains some fluoride. Fluoride can also be added to drinking water supplies as a public health measure for reducing cavities. Decisions about adding fluoride to drinking water are made at the state or local level. Nearly all water contains some fluoride,Fluoride is known to contaminate groundwater reserves globally.Fluoride, which exists naturally in water sources, is derived from fluorine, a common element in the Earth's crust. It is well known that fluoride helps prevent and even reverse the early stages of tooth decay. Natural contamination of groundwater by fluoride causes irrepairable damage to plant and human health. High oral intake of fluoride results in physiological disorders, skeletal and dental fluorosis, thyroxine changes and kidney damage in humans.
Organic matter (%) = Total organic carbon (%) x 1.72
Soil carbon is present in two forms: inorganic and organic. Soil inorganic carbon consists of mineral forms of C, either from weathering of parent material, or from reaction of soil minerals with atmospheric CO2. Carbonate minerals are the dominant form of soil carbon in desert climates. Soil organic carbon is present as soil organic matter. It includes relatively available C as fresh plant remains and relatively inert C in materials derived from plant remains: humus and charcoal.
The carbon cycle is a fundamental part of life on earth. ‘Soil organic carbon’ (SOC) – the amount of carbon stored in the soil is a component of soil organic matter – plant and animal materials in the soil that are in various stages of decay. Soil organic carbon is the basis of soil fertility. It releases nutrients for plant growth, promotes the structure, biological and physical health of soil, and is a buffer against harmful substances. Soil organic carbon, the major component of soil organic matter, is extremely important in all soil processes. Organic material in the soil is essentially derived from residual plant and animal material, synthesised by microbes and decomposed under the influence of temperature, moisture and ambient soil conditions. Organic matter makes up just 2-10% of the soils mass but has a critical role in the physical, chemical and biological function of agricultural soils. Carbon is a measureable component of soil organic matter.
Organic matter contributes to nutrient turnover and cation exchange capacity, soil structure, moisture retention and availability, degradation of pollutants, greenhouse gas emissions and soil buffering.
Total organic carbon (TOC) is the carbon (C) stored in soil organic matter (SOM). Organic carbon (OC) enters the soil through the decomposition of plant and animal residues, root exudates, living and dead microorganisms, and soil biota. SOM is the organic fraction of soil exclusive of nondecomposed plant and animal residues.
Fluorocarbons, sometimes referred to as perfluorocarbons or PFCs, are, strictly speaking, organofluorine compounds with the formula CxFy, i.e. they contain only carbon and fluorine,though the terminology is not strictly followed.] Compounds with the prefix perfluoro- are hydrocarbons, including those with heteroatoms, wherein all C-H bonds have been replaced by C-F bonds Fluorocarbons and their derivatives are useful fluoropolymers, refrigerants, solvents, and anesthetics.
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PVDF: Polyvinylidene fluoride
PVC: poly vinyl chloride 
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Simply find a solvent for PVC such as ethane-1.2-chloride, which is not soluble PVDF !?
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methyl 3-bromopropionate is my substrate. I'm attempting nucleophilic fluorination using KF as a fluoride source with tetraethylene glycol as the solvent, but so far its not working.
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I would rather oxidize 3-fluoropropanol and make esterification, you can get it rather cheap, look at www.molbase.com. The beta-elimination will occur whatever you take, with tosylate it is hardly better. If there is no direct conversion of beta-halopropionic esters to the fluoride in literature, most probably it just too tedious to make.
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Hi all,
I need to make a PVA based thin film, however I need to reduce its refractive index from ~1.50 (typical RI for PVA) to around 1.44. Is there anyway, such as adding other chemicals to the PVA aqueous solution to reduce the refractive index after drying?
From the help of Kai and Alan (it was my fault that I did not explain the problem clearly to them), I tried adding KF (potassium fluoride) or PEG, but they does not "mix" with PVA, you can see distinct layers after mixing them together (PVA floating on top).
Please advice if you have any idea! Thanks very much!
Paul
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Alan, you are so helpful!!