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RMMB0W0H–A bottle of one molar 1M sodium thiosulphate liquid to be used for bromine spillage, as used in a UK secondary school, London, UK.
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. Journal. i dh, ii duced ; tr. a I men I with potassium bii Inornate(2 mols.) and sodium thiosulphate (1 mol.); ti atmenfchromic acid and sodium nitrite; treatmnth potassium chromate (1 mol.) and a basicchromic salt (1 mol.). Instead of using excess of hydro-i ic acid in the dyeing process, nitric or sulphuric acidsmay be used, and a part of thi mineral acid may beadvantageously replaced by an organic acid (particularlyformic or oxalic acid). The dyeing] may be carried out ,by immersing the mordanted fibre in the acid solutionof aniline for a short time, ami then removing it, andallowing the Stock Photohttps://www.alamy.com/licenses-and-pricing/?v=1https://www.alamy.com/journal-i-dh-ii-duced-tr-a-i-men-i-with-potassium-bii-inornate2-mols-and-sodium-thiosulphate-1-mol-ti-atmenfchromic-acid-and-sodium-nitrite-treatmnth-potassium-chromate-1-mol-and-a-basicchromic-salt-1-mol-instead-of-using-excess-of-hydro-i-ic-acid-in-the-dyeing-process-nitric-or-sulphuric-acidsmay-be-used-and-a-part-of-thi-mineral-acid-may-beadvantageously-replaced-by-an-organic-acid-particularlyformic-or-oxalic-acid-the-dyeing-may-be-carried-out-by-immersing-the-mordanted-fibre-in-the-acid-solutionof-aniline-for-a-short-time-ami-then-removing-it-andallowing-the-image337026021.html
RM2AG8T3H–. Journal. i dh, ii duced ; tr. a I men I with potassium bii Inornate(2 mols.) and sodium thiosulphate (1 mol.); ti atmenfchromic acid and sodium nitrite; treatmnth potassium chromate (1 mol.) and a basicchromic salt (1 mol.). Instead of using excess of hydro-i ic acid in the dyeing process, nitric or sulphuric acidsmay be used, and a part of thi mineral acid may beadvantageously replaced by an organic acid (particularlyformic or oxalic acid). The dyeing] may be carried out ,by immersing the mordanted fibre in the acid solutionof aniline for a short time, ami then removing it, andallowing the
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. Hydroxylamine : its quantitative determination and some double salts . ne solu-tion and titrate back with sodium thiosulphate. If the amounts ofhydroxylamine and used iodine are figured from atomic weights, onemolecule of hydroxylamine salt requires two atoms of iodine. It fol-lows that one molecule of hydroxylamine is oxidized by two atoms ofiodine if the hydriodic acid formed is neutralized at once,2NH^0H+SIg=Np0+Hg0+4HI and proves accurately this formula by eudio-metric analysis of gases formed by the oxidation.The results obtained by this method were unsatisfactory.Iodine solution of whi Stock Photohttps://www.alamy.com/licenses-and-pricing/?v=1https://www.alamy.com/hydroxylamine-its-quantitative-determination-and-some-double-salts-ne-solu-tion-and-titrate-back-with-sodium-thiosulphate-if-the-amounts-ofhydroxylamine-and-used-iodine-are-figured-from-atomic-weights-onemolecule-of-hydroxylamine-salt-requires-two-atoms-of-iodine-it-fol-lows-that-one-molecule-of-hydroxylamine-is-oxidized-by-two-atoms-ofiodine-if-the-hydriodic-acid-formed-is-neutralized-at-once2nh0hsig=np0hg04hi-and-proves-accurately-this-formula-by-eudio-metric-analysis-of-gases-formed-by-the-oxidationthe-results-obtained-by-this-method-were-unsatisfactoryiodine-solution-of-whi-image372159268.html
RM2CHD8XC–. Hydroxylamine : its quantitative determination and some double salts . ne solu-tion and titrate back with sodium thiosulphate. If the amounts ofhydroxylamine and used iodine are figured from atomic weights, onemolecule of hydroxylamine salt requires two atoms of iodine. It fol-lows that one molecule of hydroxylamine is oxidized by two atoms ofiodine if the hydriodic acid formed is neutralized at once,2NH^0H+SIg=Np0+Hg0+4HI and proves accurately this formula by eudio-metric analysis of gases formed by the oxidation.The results obtained by this method were unsatisfactory.Iodine solution of whi
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RFWGK6PY–Sodium thiosulfate, chemical structure. 3D rendering. Atoms are represented as spheres with conventional color coding: sulfur (yellow), oxygen (red),
. A treatise on pharmacy for students and pharmacists. Six-sided prism. Axes of the monoclinic system. Monoclinic double pyramid. Crystals of this system have three unequal axes, two being obliquelyinclined to each other, the other axis forming right angles with thesetwo. See Fig. 189. The fundamental forms of this system are the monoclinic doublepyramid or octohedron, Fig. 190, and the monoclinic prism, Fig. 191. Ferrous sulphate, borax, lead acetate, cupric acetate, tartaric acid,potassium chlorate and sodium acetate, sulphate, thiosulphate, phos-phate and carbonate, crystallize in this syst Stock Photohttps://www.alamy.com/licenses-and-pricing/?v=1https://www.alamy.com/a-treatise-on-pharmacy-for-students-and-pharmacists-six-sided-prism-axes-of-the-monoclinic-system-monoclinic-double-pyramid-crystals-of-this-system-have-three-unequal-axes-two-being-obliquelyinclined-to-each-other-the-other-axis-forming-right-angles-with-thesetwo-see-fig-189-the-fundamental-forms-of-this-system-are-the-monoclinic-doublepyramid-or-octohedron-fig-190-and-the-monoclinic-prism-fig-191-ferrous-sulphate-borax-lead-acetate-cupric-acetate-tartaric-acidpotassium-chlorate-and-sodium-acetate-sulphate-thiosulphate-phos-phate-and-carbonate-crystallize-in-this-syst-image370780627.html
RM2CF6ED7–. A treatise on pharmacy for students and pharmacists. Six-sided prism. Axes of the monoclinic system. Monoclinic double pyramid. Crystals of this system have three unequal axes, two being obliquelyinclined to each other, the other axis forming right angles with thesetwo. See Fig. 189. The fundamental forms of this system are the monoclinic doublepyramid or octohedron, Fig. 190, and the monoclinic prism, Fig. 191. Ferrous sulphate, borax, lead acetate, cupric acetate, tartaric acid,potassium chlorate and sodium acetate, sulphate, thiosulphate, phos-phate and carbonate, crystallize in this syst
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