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Proceedings of the Chemical Society, Vol. 17, No. 231 |
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Proceedings of the Chemical Society, London,
Volume 17,
Issue 231,
1901,
Page 1-18
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摘要:
Jsssued 23/1/1901 PROCEEDINGS OF THE CHEMICAL SOCIETY. EDITED BY THE XECRETARIEX. ~~ Vol. 17. No.231. January 17th, 1901. Professor THORPE,C.B., F.R.S., President, in the Chair. Messrs. E. F. Hudson, H. A. Auden, and A. H. Mitchell were formally admitted Fellows of the Society. The following certificates were read for the first time :-Percival James Burgess, Singapore ; Raymond Dubois, Rutherglen, Victoria ; Oscar Loementhal, Mill Hill Park, London, W.; Walter Stevens Crocker, 25, Upper Parliament Street, Liverpool ;Herbert Ackernian Tozer, 113, Stepney Green, London, E. The following letter has been sent, at the direction of the Council, to Professor Markownikoff of the University of Moscow, a Foreign Member of the Society, on the occasion of the commemoration of the 40th year of his Doctorate.DEARSIR, At the last meeOing of the Council of the Chemical Society I had the pleasure of submitting your letter of December 8th, concerning the proposed celebration in honour of Prof. Dr. Wladimir Markowni- koff. I am instructed by the Council to inform you that it will not be possible for any of our Fellows to be present personally on February 25th, but I am to ask you to be so good as to convey to Prof. Markownikoff the hearty congratulations of our Society, and to express the wish that he may be spared to carry on his valuable and important investigations for many more years. We 2 rejoice that your distinguished countryman’s name appears in our list of Foreign Members, and I beg you to convey to him the assurance that his long devotion to that science which he has done SO much to advance by his researches is most highly appreciated by English chemists.Yours obedient1y, RAPHAEL ISIELDOLA, Fweig 1L Sewetary, DR. H. DECKER. Of the following papers, t,hose marked ++ were read :-*1. ‘‘ The preparation of iodic acid.” By A, Scott and W. Arbuckle. The usual method of preparing iodic acid by gently boiling iodine with nitric acid in a flask with a long neck, is tedious when any quantity is required and liable to great loss of iodine unless the source of heat is very carefully regulated. By using, first the ordinary form. and later a modified form, of Soxhlet’s fat extraction apparatus to contain the iodine, almost theoretical yields of iodic acid were obtained after a very short treatment with the boiling nitric acid.The liability, however, of the siphon tube to become chokecl with crys- mls of iodic acid led to the abandonment of this type of apparatus. After many trials with various forms of apparatus, the authors recom- mend the use of a round-bottomeJ flask having a ground-in neck carrying two tubes, to one of mliich is sealed a reflux condenser, and through the other is fitted LZ tube by means of which a current of oxygen is passed through the boiling liquid. With this apparatus finely powdered iodine boiied with ten times its weight of fuming nitric acid may be completely oxidised in 20-30 minutes. “2. Note on isomeric change and meta-substitution in benzenoid amines.” By A.Lapworth. The rules deduced from the two simplest change forms (Trms., 1898, 73. 45’7) depend on the assuinption made imp!icitly throughout the paper, that only one group can “migrate ” along any chain of atoms at any instant, that is, that exchange of groups is, as a rule, the result of the successive migration of t’lie two groups in revwse direc- tions. This view appears in general to be well founded, and it is easily demonstratecl that if it holds true, the rules deduced are necessaiily correct, the second being used where the valencp of an atom alters. It is of no consequence whatever how the migration is effected, so far as the applicability of the rules is concerned. 3 Although in applying the rules it is sometimes convenient to assign successive positions of attachment of a labile group in its migration, it is not imagined that these are actually occupied, at least in the ordinary sense of the term.It may be supposed, for example, that the group is handed on in a still dissociated state from its initial to its final position, the others merely representing the possible places of attachment. The author hns advanced the view that naeta-substitution is the result of elimination of a hydrogen atom in the benzenoid nucleus (necessarily from the sneta-position) with a group in the complex formed by union of the side chain with the acting agent. Arm-strong has recently used a similar conception in explaining the formation of chloracetanilides from plienylacetylchloramines ;in the author's opinion, this would lead to the production of the metn-derivative, instead of, as is the case, the ortlio-and para-derivatives (compare Trcms., 1900, 77, 1051).In alluding to the formation of nzeta-sulphonic acids from benz-enoid amines (Zoc. cit., p. 457), the author suggested that it was the result of the migration of the -SO,H group in aniline sul-phates; this view must be rejected as impossible, as the necessary grouping is not present. The statement that metcc-derivatives are formed when the labile group 31 is separated from the benzene ring by two atoms only holds true when the grouping <->=X*Y*lI. is present or can be formed as an intermediate step.31: will migrate to the metmposition when separated by one atom on1-j-, from the nucleus if the intermediate compound is of the typo <>=X*M, and X is able to fall in valency by two units, for example, when X is a pentavalent nitrogen atom. Applying this to the case of the action of fuming sulphuric acid on dimethylaniline, the most probable explanation of the reaction is that dimethylaniline sulphate unites with sulphuric anhydride, and that from this compound sulphuric acid is then eliminated by loss of a hydrogen atom from the nucleus thus Me2 Me2 Me,.. ** N.SO,HiGSO,H Y<OSO,H Il H/\H H/\\H H H/"H // + H*OSO,H.= HI1IH''3 + = H(/ \/ '\ /H H H The latter substance must yield the meta-sulphonic acid if the sulpho-group then migrates, assuming, as usual, that the other atoms 4 retain their positions until this migration has ended.Or, expressing it in terms of the author’s rules, as the sulpho-group migrates the valency of the nitrogen must fall, since it cannot become attached to the nucleus by a treble binding ; $he nearest possible position of attachment for the labile group is, therefore, the P-position, hence, as the valencies of the carbon atoms remain cocstant, the next position must be imagined to be reached by an ay-change. This process can also be followed by using Thiele’s rule, but, in this case, it must be assumed that sulphuric acid is added in one way and eliminated in another, and as for this purpose it must he supposed that before addition it breaks up into HO and ‘SO,H instead of into H and OSO,H, the objection to this hypothesis is obvious.3. rL The preparation of esters from other esters of the same acid.” By T. S. Patterson and C. Dickinson. Experiments were described which had for their object the preparation of methyl ethyl tartrate. A substance was obtained having the observed rotation + 11-14’ at 18’ (I =200 mm.), which probably consisted chiefly of the compound sought. It showed no tendency to crystallise and as no method of purification, other than crystallisation, was likely to be suitable, these attempts to obtain a pure compound were abandoned. They had shown, however, that ethyl tartrate is largely converted into methyl tartrate by the action of methyl alcohol and hydrochloric acid.Experiments were then described showing that pure ethyl tartrate can be obtained from methyl tartrate and pure methyl tartrate from ethyl tartrate, by Fischer’s method, bence it is probable that any other ester may be prepared by an analogous process, under certain circumstances this might prove useful. Finally determinations of the rotation of methyl tartrate at temper-atures between 20’ and 100’ were given. 4. ‘‘ Tecomin. A colouring matter derived from ‘Bignonia tecoma’.” By T. H. Lee. The new colouring matter is a yellow, crystalline, substance soluble in alcohol with an orange colour, insoluble or very slightly soluble in water ;the solution becomes rose-red with alkalis and clear yellow with acids ; 2 C.C.N/100 alkali or acid causes the colour change ; it is not affected by any but the strong mineral acids, but the presence of organic acids renders the end reaction indistinct.The wood contains a reddish-brown resin soluble in alcohol from which it is difficult to free the tecomin; also a deep brown colouring matter which dissolves in aqueous alkalis and is precipitated by acids. It is used locally as a dye for cotton and as a stain for mood. 5. (‘Anew method for the measurement of ionic velocities in aqueous solution.” By B. D. Steele, B.Sc. The author described a new method for the direct measurement of ionic velocities in aqueous solution. Masson (Phil. Trans., 1899, 192, A, 331) has succeeded in obtaining satisfactory measurements in gelatine, and for a fern ions; Whetham (Phil.Tyans., 1893, 184,A, 337) has made measurements in water. The method now described should be a perfectly general one, as the use of coloured indicator solutions is no longer necessary, and hence the range of ions which may be used as indicators is largely increased. The method consists in enclosing the liquid to be measured between two partitions of gelatine, which contains the indicator ion in solution; on the passage of the current the cation of the solution is followed by the cation of the indicator, and the anion of the solution by the corresponding anion of the indicator. It is necessary in all cases that these indicator ions should move more slowly than the measured ion. The position of the boundary between the two solutions is easily seen, on account of the difference in refraction, and the motion is measured by means of a cathetometer.If the above-mentioned con- dition is fulfilled the relative velocity of the boundary is not influenced by changing the indicators, thus (CuSO, and K,CrO,), (CuSO, and NaC2H,0,), and (CdSO, and NaC,H,O,) all gave the same value for the transport number of MgSO,. The absolute velocity of a few ions has also been calculated and compared with the velocities found by Kohlrausch, and a very fair agreement is shown to exist between the two sets of measurements, 6. ‘‘Metal-ammonia compounds in aqueous solution. Part 11. The absorptive powers of dilute solutions of salts of the alkali metals.” By H.M. Dawson and J. McCrae. The influence exerted by the addition of salts of the alkali metals on the distribution of ammonia between water and chloroform at 20” has been investigated. It has been found that so long as the ammonia concentration in the aqueous phase is less than 0.5 normal, the altera- tion of the distribution coefficient is proportional to the salt concen- ~tration, that is, the expression k-k‘ is constant, where k is the n distribution coefficient with pure water (26*28), and k’ is the observed. distribution coefficient with salt solution of normality n. This constant it is proposed to call the ‘‘equivalent alteration of the distribution coefficient.” The alteration for each salt is composed sdditively of two vitlues, one dependent upon the cation, the other upon the anion.Since, according to the views of Abegg and Bodlander, “ammonia-complex ” formation tlakes place only with the cation, the differences in the values of the alteration for salts of one metal express the differences in the physical actions of t,he anions ; but differences in the values for salts containing the same anion do not measure the differences in the physical actions of the cations because of the complicating influence of complex formation. The lithium salts show the greatest t’endency to form ammonia addition compouncls, ammonium salts show it to a less degree, whilst for sodium salts it is probably very SIKLII, ilut greater than for potassium salts.When the ammonia concentration is greater than 0.5 normal, irregu- larities occur, and it has beeii found that foy increasing salt concen-i% -k’tration and constant ammonia concentration the value of -1L decreases, whilst for constant salt concentration and increasing aui- monia concentration it increases. Non-electrolytes (urea and cane sugar) also considerably affect the distribution coefficient, so that Dalton’s law is not obeyed. These results indicate that the solvent power of water is changed to a varying extent by the different ions. The intrinsic property of the ion which is the cause of this difference is not deducible from the ionic theory as it stands at present. 7. ‘(The amide, anilide, and toluidides (ortho- and para-) of glyceric acid.” By P.F. Frankland, F. M. Wharton, and H. Aston. These compounds have been prepared by the authors with the object of investigating the influence on the rotation produced by replacing the alkoxyl group by the amido-group and its substituted derivatives. Alter a review of the limited number of cases at present available for ascertaining these relations, the authors pointed out that so far it was observable that if in an homologous series of ethereal salts the rota- tion is raised by successive additions of CH,, then the amide has a similar but still higher rotation than the ethereal salts, but that if the successive additions of CH, lead to diminished rotation, then the corresponding amide has a lower rotation than the ethereal salts.The first of these relations is exhibited by the derivatives of tartaric, malic, and glyceric acids, whilst the only hitherto known example of the second is furnished by the corresponding derivatives of mandelie acid. The result of substituting in the amido-group appears in all cases to be an increase in the rotatory effect of the latter. In the case of malic acid, the anilide has a greater molecular rotation than the amide, the o-toluidide greater still, and the p-toluidide the greatest of all. In the case of glyceric acid, on the other hand, although the anilide has a greater molecular rotation than the amide, the rotation of the p-toluidide is less than that of the anilide, and the rotation of the o-toluidide is about the same as that of the amide.The amido-compounds prepared by the authors appear to be the only ones which have hitherto had their rotation determined in the liquid state ; in the case of the o-toluidide, however, this could unfortunately not be effected, as this, on fusion, at once acquired a strong colour. In consequence of this, the rotation of a11 the compounds in question was determined also in methyl alcohol solution. The corresponding compoiinds of inactive glyceric acid were also prepared, and their melting points compnred with those of the active substances. ANNIVERSARY DINNER. It has been decided by the Council to arrange for a Dinner of the Fellows of the Society and their friends on Wednesday, March 27th, 1901, the day preceding that fixed €or the Annual General Meeting.Further particulars will shortly be announced. At the next meeting, on February 7th, there will be a ballot for the election of Fellows, and the following papers will be communicated :-‘‘ The action of hydrogen bromide on carbohydrates.” By H. J. H. Eent,on and Mildred Gostling. ‘‘Note on a method of comparing the affinity-values of acids.” By H. J. H Fenton and H. 0. Jones. S CERTIFICATES OF CANDIDATES FOR ELECTION AT THE NEXT BALLOT. The following Candidates have been proposed for election. A ballot will be held on Thursday, February 7th, 1901. N.B.-The names of those who sign from ‘L General Knowledge ” are printed in italics. Aitken, Andrew Charles, Rio Marina, Isola d’Elba, Italy.Analytical Chemist. Six years assistant to Rlessrs. Tatlock and Thomson, Analytical Chemists, Glasgow. Two years sole Chemist with the White Lead Company, Limited, Glasgow. For the last two years representative in Elba for Messrs. H. Borner and Co., Limited, London. R. R. Tatlock. Horatio Ballantyne. R. T. Thomson. Robt. D. Connell. Jccmes E. $‘erguson. Barrie, Thomas Stewart, 77, Sinclair Drive, Langside. Principal of the West of Scotland College of Pharmacy, 157, St. Vincent Street, Glasgow. Student of Chemistry at Grove Street Public School 1891-1893, Technical College 1893-1894, both in Glasgow ; also in Crumphill Public School, Paisley, 1894-1895 ; gained the Minor Qualification (Oct., 1896) and the Major Diploma (Jan., 1898) of the Pharmaceutical Society of Great Britain ; elected a Member of that body, 1900.Teacher of Chemistry at the West of Scotland College of Pharmacy, Glasgow, and Consulting Chemist there. Author of a book on “Volumetric Analysis ” adapted for pharma-ceutical students, and contributor of various articles dealing with the analysis of arsenates, lactophosphates, calamine, iodides, &c., to the Phawrmceuticul Journal and the Chemist and Druggist during the years 1899 and 1900. G, G. Henderson. Thoa. Maben. James Robson. Thomcts Grap. Matthew A. Parker. Bedwell, John Cardew, B.Sc. (London), 65, High St., Colchester. Private Tutor and Science Teacher. For 3 years Assistant Leoturer on Chemistry at Colchester Technical College.Student at Technical Laboratory, Chelmsford 1 year, and at Colchester Technical College 3 years. Desirous to obtain Society’s Journal for assistance in research. Thos. S. Dymond. William Briggs. Frank Hughes. W. A. #henstone. J. FP.Shephei*cl. Bult, Herbert John, 165, Brixton Hill, S.W. Chemist. Three years student at Finsbury Technical College. Two years in laboratory at St. George’s Hospital, last 18 months as Chief Assistant. For some time in charge of laboratory of Messrs. Thomas Farmer and Co., Silvertown. Two years Chief Assistant to Dr. P. Dvorkovitz, Petroleum expert. One year Head Chemist and Assistant Engineer at European Petroleum Co.’s Thames H:tven Refinery. Some time chemist to Rlr. A. Adiassewich, Petroleum expert. Three years private practice.R. Meldola. Lawrence Briant. Boverton Redwood, F. Southerden. A1.tln-w J.Stayey. Burrows, Merrick William, Dunkirk, Devizes ; 4, St. George’s Terrace, Wilton, Taunton. Science Master (Huish School, Taunton). For three years, 189 1-1894, student in Owens College Chemical Department. B.Sc. Vict., Hons. Chemistry, 1894. M.Sc. 1898. Assisted Prof. Dixon in research on the action of carbonic acid on heated carbon 1894-1895. H. B. Dixon. G. H. Bailey. W. H. Perkin, jun. William A. Bone. U. L.Chapan. Cohen, Robert Waley, 11, I3yde Park Terrace, London, W. B.A. Cambridge. Has long been interested in Chemistry, and proposes to devote himself to some branch of Industrial Chemistry. Made Chemistry an important subject at Cambridge, and desires to join the Society in order to continue and extend his knowledge of the subject by means of its meetings and publications. W.A. Shenstone. H. J. H. Fenton. H. E. Roscoe. W. T. N. Spivey. C. T. Heycock. 10 Cousins, Herbert Henry, Government Laboratories, I<i ngst on, J:tinnica. Government Analyst and Sgricultural Chemist. First Class Hon. Chemistry, Oxford. Xh. Eighteen months in 1abor.itory of V. Meyer, Heidelberg. Assistant Demonstrator to Wayuflete Pro- fessor, , Oxford. Lecturer on Chemistry, University Extension. Lecturer on Chemistry at S.E. Agricultural College, Wye. Now Chemist for Jamaicn. Pitper with J. E. iXar*h in I’mns., 1S91. ‘‘Farm Foods,” 1S95. “ Chem. of Garden,’’ 1S9S.l:e..;earches on hop analysis, insecticides, mnnurinq of crops, &c. John Percivd. W. W.Fisher. A. D. Hall. V. H. Veley. J. E. Xarsh. Daniel, Gilbert Howard, 21, Church Walk, Ulverston. Head Naster, Higher Grade and Technical Schools, Ulverston. B.Sc. (Lond.), 1890. Registered Teacher (South Kensington) in Prac. and Theor. Org. Chon]. and in Yrac. and Theor. Inorg. Chem. Head Master of JInryport Higher Grade School and Chemistry Lec- turer in the Evening Classes also, 1891-97. Head Master of Bristol North Street Higher Grade School and Evening Class Lecturer, 1897-1 900. J. H. Hnynes. R.X. Cahill. It. L. Taylor. E’. IT,JPornieZl. James Foulds. Dodd, Robert, 28, Sibella Road, Clapharn, S.W. Student at King’s College. Now Chemist in Borscic Acid Works, One year at the “ Allan Glen’s School,” Glasgom.Three years St. Clement Danes Schools. Stiident in the Chemical Department King’s College, London, during 1896-1897, 1837-1898. John 11,Thomson. 0s.car Guttnzccm. Herbert Jackson. B. E. R.,\ew~ads. Patrick H. Kirkaldy. Arhw R.Ling. Thos. A. Cheethatn. Eudolpl~Xessel. Donnan, Frederick George, M.A., Ph.D., Chemical Laboratory, University College, Gower Street, W. Assistant, Chemical Department, University College, Gower Street, W. Author of following papers : “An Attempt to give a simple Theoretical Explanation of Raoult’s Law,” Phil. Mug., Nov., 1892, 411; ‘‘Electrolytic Dissociation and Light-Absorption in Solutions,” Zeitschr. Phgs. Ch., 19, 465 ; “ The Saturation-Pressures of the 11 System, T\Ig*K*Cl*SO,,”Sitx.Bey. Aknd., 52, 1S97;“Theory of the Thomson-Effect in a Binary Electrolyte,” Phil. Mag., June, 1898, 529 ; “Theory of the Hall-Effect in a Binary Electrolyte,” Phil. Mag., Nov., 1S98, 465 ; 6‘ The Isothermal Pressure-Surface for one Double and two Single Salts,” Joum. Yhys. Ch., 2,417 ;‘LThe Nature of Soap ‘6Emulsions,” Zeitschr. Phys. Ch., 31,42 ; Relative Rates of Effusion Qf Helium, Argon, and some other Gases,” Pld. iWag., May, 1900,433. William Ramsay. Edtvnrd C. Cyril Baly. Morris W.Travers. Alex. &I. Kellas. Vaughan Harley. J. Nevi11 Huntly. Emery, John Alfred, Cinderford, Gloucestershire. Head Master. Higher Grade Bd. Schools, Cinderford, Glos. Super-intendent Teacher of Physics and Chemistry in above schools.Holder Qf Certificates in above subjects under Science and Art Dept., South Kensington. Teacher of Pupil Teachers’ Classes in Chemistry, &c. J. Jackson. Sydney Young. Thomas Edwards. F, TVcdlis Stoddart. Thos. W. Berry. Austin Keen. Ferguson,Reginald Williams, A.R.C.S., S, Havelock Terrace, Paisley Road, Glasgow. Senior Assistant in the Chemical Department of the Leeds Institute of Science, Art and Literature. National Scholar in Chemistry and Physics ;Associate (in Chemistry) of the RoTal College of Science, London. “Stenhouse Scholar ” and Associate of the Glasgow Technical College. For 6 years a Student of Chemistry under, successively, Prof. Dittmar, Prof. Thorpe, and Prof.Tilden. Since 1895 engaged in lecturing on Chemistry in the schools of the Leeds Institute, and in the management of a large Chemical Laboratory. T. E. Thorpe. W. Palmer Wynne. William A. Tilden. George Ward. Thomas Pairley. Houlderahaw, Arthur, 71, Lavender Gardens, West Jesmond, Newcastle-on-Tyne. Science Instructor in Chemistry, Physiology, and Hygiene in Elementary School. Studied Inorganic and Organic Chemistry for many years, and secured several Certificates in same at South Ken- sington Exams. 1st Class Certificates in advanced Physiology (Queen’s Prize, 1892, one of five), and Hygiene, and Teacher of these subjects for some years under Science and Art Department. Reasons : To become better acquainted with recent researches in Chemistry 12 by means of the Journal of the Society, and to participate in the privileges granted to Fellows. T.W. Lockwood. Joseph Browiz. I. Pa,tchett. R.S. Ccclt,ilZ. Prank R. Dudderidge. Oliver Kirk. W.Goddard. Howard,Bernard Farmborough, Devon House, Buckhurst Hill, Essex. Chemical Student at the City and Guilds of London Institute, Technical College, Finsbury. Educated at Marlborough College, 1894-1898. Since then Chemical Student under Professor Meldola, F.R.S., F.I.C., F.C.S., at Technical College, Finsbiiry. R. Meldola. F. Southerden. David Howard. D. Lloyd Howard. Alfred G. Howard. Hughes, Edward, Rectory, Barmou th. Clerk in Holy Orders. I am much interested in Chemistry, prac- tical and theoretical, and desire to avail myself of the publications of the Society.I was a pupil of Prof. Vacher, Editor of Fresenius Quant. and Qual. Analyses. Watson Smith. Thomas Wardle. R. Le Neve Foster. TK F. Kentiicg Stock. Alex. K. iVil2er. Hutton, Robert Salmon,M.Sc., Owens College, Manchester. Demonstrator in Electrochemistry. Student for 4 years in Chemical Laboratories, Owens College. B.Sc. Hons. Chem., 1897. Has in-vestigated the " Compound Line Spectrum of Hydrogen '' given by specially purified hydrogen (Phil. Mug., Sept., 1898). Has studied physical chemistry for 2 years in Leipzig under Prof. Ostwald, and in Paris under Prof. Moissan. H. B. Dixon. G. H. Bailey. W. H. Perkin, jum E. J. Russell. William A. Bone. D. L. Chapman. Ionides, Stephen Archigenes, Balliol College, Oxforll.Student of Chemistry at Balliol College, Oxford. D. H. Nagel. A. F. Walden. H. €3. Hartley. P. Elford. H. T,. Bowman. 13 Jones,John Lloyd Thomas Major, I.M.S., United Service Club, Calcutt,a. Deputy Assay Master, Calcutta, and lately for 18 years Acting Assay Master, Calcutta. Bachelor of Medicine, University of Dur-ham. Nember of the Royal College of Surgeons, England. Diplo-mate of Public Health, Cambridge University. Passed the Course of Instruction in Assaying at the Royal College of Science, South Kensington, and Royal Mint, London. W. C. Roberts-Austen. Chapman Jones. F. W. Bayly. T. E. Thorpe. T. K. Rose. W. J. Russell. Jones, Robert Henry, Glen A!byn, Coity Road, Bridgend, Glam.Science Master, County School, Bridgend, Glam. B.Sc. (Vic.). 1st Class Hon. in Chem. 1896. Research St,udent with Prof. Dixon 1896-8. Dalton Chemical Scholar of Owens College, 1897. Original work : “Instantaneous pressure produced on Collision of two Explosion Waves,” Manch. Lit. and Phil. SOC. 3f.S~. (Vic.), 1899. 1898-9 Science Master, Wellington Coll., Salop ;1899, Science Master, County Sch., Bridgend. H. B. Dixon. W. K. Perkin, jun. W. A. Bone. E. J. Russell. H. C.H. Carpentev. van der Linde, Harold Theodor Granville, 101, Tyndall Avenue, Toronto, Canada. Chief Chemist, Gutta Percha and Rubber Manufacturing Co. of Toronto. Above position (with average of four assistants) for past seven years, previous to which I mas Manager (with charge of chemical laboratory) to the Edison General Electric Co.(manufacturing every description of electric appliance and insulated conductor) in Canada, for four years. At Edinburgh University passed in first B.Sc. and first and second M.B., C.M. Exams. Alex, Crum Brown. Charles G. Cresswell. W. H. Ellis. G. G. Henderson. Duvid Howard. Martin, Nicholas Henry, Ravenswood, Low Fell, Gateshead, and Royal Societies Club, London. Pharmaceutical Chemist. Manufacturer of pure chemicals. Chair-man of the Newcastle Section of the Society of Chemical Industry. P. Phillips Bedson. Wyndham R. Dunstan. Alexander Scott. F. C. Garrett. 8. Hoare Collins. 14 Meneies, James, 39, Winterbrook Road, Heme Hill, London, S.E. Chemical Engineer.Studied chemistry and passed examinations at Clausthal Mining College, Germany, afterwards in the Berlin “ Poly-technik.” Was 24 years with D. A. Sutherland, Erq., F.C.S., F.I.C., as Assistant. At present with J. C. Butterfield, Esq., F.I.C., F.C.S., 3LI.M.M., M.R.I. Sutherland. Robert N. Lennox.D. 9. James ItIactear. J. C. Butterfield. Y’honms Fuidey. Moir, James, M.A., B.Sc., The Ash, 62, Hamilton Place, Aberdeen, Scotland. 1551 Exhibition Scholar, Aberdeen University. Joint author with Dr. Japp of paper on ‘‘ Constitution of Amarine, its so-called Dialkyl- and Diacyl-derivatives, and of Isoainarine ” (J. C. S.,May, 1900). Lately Junior Assistant, Chemical Department, Aberdeen University. At present Research Student at Central Technical Inst., South Kensington.Henry E. Armstrong. Gerald T. Moody. F. R.Japp. W. A. Davis. T. Martin Lowry. Meredith, William, 63, Albion Place, Ulverston. Lecturer for 15 years in Chemistry and Physics. Superintendent of‘ Evening Continuation School. At Ulverston I have no means of access to the Society’s Journal, and I should find it of real interest and benefit to me in my work. Wm. Cranfield. G. S. Turpin. A. E. Tutton. Clqmnn Jones. James C. Philip. Nunn, Arthur W., 313, Sydenham Road, Sydenham, S.E. Analytical Chemist. Has been for IS years and is now engaged in analytical work, chiefly foods and drugs. Has contributed several papers on Pharmaceutical Chemistry, e.g. ‘‘ On a supposed change in Calomel when kept in contact with Sugar for a long time.” Has passed the Major Examination of the Pharmaceutical Society.Has delivered public lectures in his parish. John Attfield. C. A. Hill. W, Watscn Will. W. Chas. Sayers. 15.A. D.Jowett. 15 Page, Theodore Henry, 40, Wilson Road, Camberwell, S.E. At present employed in Research Laboratories of London Essence Co., George Street, Camherwell. Associate of City and Guilds of London Institute (Chem. Dept.). Henry E. Armstrong. T. 31. Lowry. William J. Pope. Edwin C. Jee. Gerald T. 3Ioody. William A. Lethbridge. Price, Thomas Slater, University College, Sheffield. Demonstrator in Chemistry. “The Amy1 (Secondary Eutyl Methyl) derivatives of Glyceric, Diacetylglyceric and Di benzoylglyceric acids, active and inactive ” (Journ.Che7n. Soc., 1897, p. 253) (in conjunction with Prof. Frankland.). ‘‘Die Reaktion zmischen Kdium-persulphat und Iodkalium, und Katalyse bei derselben,” Zeit.f.Phys. Chemie, 27, 474 ; ‘‘On the Temperature Coefficient of Ester saponification,” SwedislL Acndeiny, 1900 ; ‘(The Reaction between Ethyl Alcohol and Hydrochloric Acid,” Pyoceedings Chem. Soc., Nov., 1900. 1851 Exhi-bition Scholar in Chemistry, lS06 -1599. Ph.D. (Leipzig), 1895. D.Sc. (Lond.), 1900. A.I.C., Jan., 1900. W. Carleton Williams. Henry J. S. Sand. Percy F. Frankland. George Young. W. R. Innes. Radcliffe, Lionel Guy, 6, Alma Terrace, Old Trafford, Ilanchester. Lecturer in Chemistry. Lectures on Organic and Inorganic Chemistry, at the Municipal Technical School, Manchester ; also had experience in Technical Chemistry in Colour Works.Has also published original work on the following subjects : On ‘‘Curcumine ” (Journal of 8ocietg of Byere cmcl Colozwists) ; on “ Carthamine ” (ibid.); ‘‘ The Oximes of Indigotin and Indirubin, &c.” (ibicl.) ; together with Dr. L. Xarchlewski, ‘‘ Zur Kenntniss des Indigotins ” (Joui-ncclfiir pruktische Chenzie) and in (Ber. cl. deutsclten Chem. Ges.) “Note on the constitution of Indicsn, R.C.” (Journal SOC.of Chenz. Idustry), &c. W. H. Perkin, jun. John hllan. Edw. Schunck. Jas. Grant. Jul. Hiibner. Ramsden, William Cecil, 13, Effra Road, Rathmines, Dublin. Junior Assistant and Demonstrator.I was a student in the Chem. Dept. of Univ. Coll. Nottingham, for over 3 year.;, then acted 16 as Lecture Assist. to Prof. Snape, U.C.W., Aberystwyth, for 3 years, and am now Junior Assistant and Demonstrator to Prof. J.E. Reynolds, T.C., Dublin, with whom I was associated in some work on the electrolytic estimation of bismuth. This work has been published in a short article. J. Emerson Reynolds. Frank Clowes. Emil A. Werner. J. Bernard Coleman. Edward T. Shelbouim. Scott, Herbert Kilburn, P.O.B. 634, Rio de Janeiro, Brazil. Mining Engineer, Metallurgist, and Analytical Chemist (consulting). Was with Dr. E. Riley, City Road, London, in 1892. Later Chemist Elba Iron Mines, afterwards, 1895, Chief Engineer and Manager. Manager, Manganese Mines, Brazil, 1895 -1900.Now established in Rio de Janeiro as above. Author of “ Iron Mines of Elba,” 1895, “Nanganese Ores of Brazil,” 1900 (Proc. Iyon and Steel Insiitute). Edwd. Riley. B. A. Burrell. Archie H. Strong. Robt. D. Connell. James E. Ferguson. Smith, Harry Metcalfe, 79, Helix Road, Brixton, London, S.W. Analytical Chemist. Fellow of the Institute of Chemistry. Mem-ber of the Society of Public Analysts. Now, and for 10 years past, Assistant to Dr. Thos. Stevenson, Guy’s Hospital. Joint author with Norman Leonard, B.Sc., of a number of papers on analytical subjects contributed to The Analyst. Thos. Steven son. Charles E. Groves. William Ramsay. J. Norman Collie. Norman Leonard. Talbot, John, Tunstall House, Harrow.Assistant Science Master at Harrow School. Late Scholar of Trinity College, Cambridge. B.A. (Camb.), 1st Class, parts I and 11, Nat. Science Tripos. B.Sc. (Lond.), Exhibitioner in Chemistry and Physics, and Medal in Physics at Intermed. B.Sc. First Class Honours Physics, Final B,Sc. M. M. Pattison Muir. T. B. Wood. S. Ruhemann. W. T. N. Spivey. R. S. Morrell. B. P. Lascelles. 17 Thomas,IAlbert Edward, B.Sc. (Lond.), A.I.G., 34, South Road, Kingswood, Bristol. Assistant Lecturer on Chemistry and Physics, Merchant Ven- turers’ Tech. Coli., Bristol. B.Sc. (Lond.), with Honours in Chem- istry and Physics. A.I.C. by examination. First Class Honours in Theor. and Pract. Inorganic Chemistry, &c. (South Kensington).5; years’ teaching experience as above. J. Wertheimer. Arnold Philip. G. P. Darnell-Smith. Ernest H. Cook. Sydney Young. Waterhouse, James, Oak Lodge, Court Road, Eltham, Kent. Major-General, Indian Staff Corps. Late Assistant Surveyor-General of India, in charge Photographic and Lithographic Office, S.I.D., Calcutta. Has published original researches on the action of eosin and other dyes on photographic plates ; on the action of thio-carbamides in reversing the photographic image on gelatine dry plates ; and on the sensitiveness of silver to light. R. Meldola. John Spiller. Chapman Jones. Charles H. Bothamley. J. W. Swan. Wayland, William A., 4,Harefield Road, Brockley, S.E. Manufacturing and Analytical Chemist. A manufacturer of chemicals, also analyst, specialising water, malt, hops, &c. Interested in chemistry in its relation to the brewing and sugar industries. William J.Pope. Herbert F. Fermor. Stanley J. Peachey. Alfred W. Harvey. Arthur H. Coot,e. Wilson, James Scott, Brad ford St., Waleall. Medical Officer of Health. M.D., C.M. Glas. Univ. D.P.H. Camb. For twelve months a student in the Laby. of Dr. B. Hill, Birmingham, and at present engaged in chemical work in connection with Public Health. Alfred Hill. James Robt. Kaye. Chas. A. MacMunn. Fi.ank CEowes. J,B. Cobman. 18 The following Certificate mas authorised by Council under Eye-Law I (3) :-Haddon, Henry Edward, Pnmplernousses, 3fauritius. Chemist of the “ Beau Plan ” Sugar Estates Company, Limited.Analytical Chemist of the Faculte‘ de Medicine et Pliarmncie de Lyon. Ex-Chemist of the ‘(Sucrei-ie Centrale ” de Rlenux, Seine et Marne, France. Ex-Chemist of the (( Las Angustias ” factory, Granada, Spain. Member of the Chemical Society of Paris. Member of the Association des Chimistes de Sucreries, France. Author of several papers 011 cafetannic acid and milk. Ex-Ag. Assistant Director of the “Statioc Agronomique ” of Mauritius. Vivian E. Lemes.
ISSN:0369-8718
DOI:10.1039/PL9011700001
出版商:RSC
年代:1901
数据来源: RSC
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