308 results about "Iodide" patented technology

The invention discloses a cellulose paper-based diaphragm for a zinc-iodine battery as well as a preparation method and application of the cellulose paper-based diaphragm. The diaphragm is of a three-layer composite structure and comprises a matrix layer formed by paper pulp fibers such as softwood pulp, hardwood pulp, bamboo pulp or straw pulp through a wet papermaking technology, and compact functional layers which cover the two sides of the matrix layer and are formed by oxidized nanocellulose (TOCN). The preparation method mainly comprises the following steps: preparing the paper-based diaphragm matrix through wet papermaking, coating the two sides of the paper-based diaphragm matrix with TOCN aqueous dispersion, and finally carrying out hot-pressing drying treatment to enable the three layers to be tightly combined. According to the invention, the nano aperture and the surface negative electricity functional group of the TOCN layer are utilized, so that physical blocking and electrostatic repulsion of polyiodide ions can be realized at the same time, and the shuttle effect is effectively inhibited; and the uniform pore channels can guide zinc ions to uniformly deposit and inhibit dendritic crystal growth. The diaphragm is green in raw material, simple in process and low in cost, and the cycle life and coulombic efficiency of the battery can be remarkably improved when the diaphragm is applied to the zinc-iodine battery.

The invention discloses an electrolyte for improving the cycling stability of a zinc-sulfur battery and application of the electrolyte in a photoelectric storage integrated battery. The electrolyte comprises a solvent, an additive and zinc salt, the additive is iodide, and the iodide comprises iodine negative ions and positive ions or polar functional groups. The functional additive is added into the electrolyte, positive ions inhibit dendritic crystals and side reactions of zinc, and iodine negative ions accelerate reversible change between sulfur and zinc sulfide, so that the cycling stability of the zinc-sulfur battery is improved. A zinc-sulfur battery with high specific capacity and long cycle life is integrated with a solar battery, so that the photoelectric storage integrated battery with high overall conversion efficiency, high specific capacity and long cycle life is prepared.

The invention relates to an electrolyte for synergistically stabilizing positive electrode iodine multi-electron reaction through four-combination zinc salt and a high-surface-capacity zinc-iodine soft package battery. The electrolyte comprises the four-combination zinc salt and water, in the electrolyte, the total concentration of zinc ions in the four combinations of zinc salts is 2 + / -0.2 mol / L; the four-combination zinc salt is a four-combination zinc salt; the SO4 < 2-> in the electrolyte buffers the pH value of a system, so that side reaction of a negative electrode is reduced; cH3COO <-> can be cross-linked with I3 <->, so that shuttling of polyiodide is inhibited, and reversibility of a two-electron reaction is enhanced; bromide ions Br <-> in the electrolyte are chemically combined with I < + > through isohalogen to excite four-electron reaction; the trifluoromethanesulfonate OTf <-> with strong electronegativity surrounds the positive electricity I < + > by virtue of an ion atmosphere effect, so that active water molecule attack hydrolysis failure is avoided, a synergistic stable positive electrode iodine multi-electron reaction is realized, and the high-surface-capacity zinc-iodine soft package battery is beneficial to promoting the development of the zinc-iodine battery to practical application.

The invention discloses a battery electrolyte and a preparation method thereof, an aqueous zinc-iodine battery and terminal equipment. The battery electrolyte comprises an additive, an electrolyte and a solvent, the additive contains an amino functional group, and the concentration of the additive is 0.1 g / L-0. 5 g / L. In addition, the additive can also utilize a nitrogen-containing functional group to reduce the shuttle effect of polyiodide and prevent the loss of an iodine positive active material, so that the electrode of the zinc ion battery is protected, and the cycle life of the zinc ion battery is remarkably prolonged (the capacity is about 20mAh / g higher than that of an electrolyte without L-tyrosine).

The invention relates to the technical field of chemistry, in particular to a synthesis process of 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride, which comprises the following steps: by taking 4-fluoro-3, 5-dimethylbromobenzene as a raw material and hydrazine hydrate as a hydrazine source, matching with alkali such as potassium hydroxide, sodium hydroxide or potassium phosphate and the like, reacting at the temperature of 60-80 DEG C to obtain the 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride. The preparation method comprises the following steps: by taking copper or nickel source catalysts such as cuprous bromide, cuprous iodide, nickel salicylate and the like, N, N-bis (2, 6-dimethylphenyl) oxamide as a ligand, hexadecyl trimethyl ammonium bromide as a stabilizer and a dioxane-water mixed system as a solvent, reacting at 80-110 DEG C under the protection of nitrogen, separating a reaction mixed solution after the reaction is finished, and separating the reaction liquid to obtain the target product. And purifying to obtain a finished product of the 4-fluoro-3, 5-dimethyl phenylhydrazine hydrochloride. Therefore, the problems that the synthesis of the 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride is poor in safety, low in production efficiency, poor in environmental friendliness, small in substrate application range and the like are solved.

The invention discloses cyclodextrin alkyl ether sulfonic acid as well as a preparation method and application thereof, and relates to the technical field of oil and gas field auxiliaries. The preparation method of the cyclodextrin alkyl ether sulfonic acid comprises the following steps: adding hydroxyl alkyl sulfonic acid into dichloromethane, adding alkali and a sulfonyl chloride reagent, and reacting for 3-5 hours to obtain sulfonate; the preparation method comprises the following steps: adding sulfonate into iodide, adding acetone, reacting for 5-8 hours, and removing excessive iodide after the reaction is finished, so as to obtain iodo-hydrocarbyl sulfonic acid; the preparation method comprises the following steps: dissolving cyclodextrin in tetrahydrofuran, cooling to 0 DEG C, adding alkali under the protection of nitrogen, reacting for 0.5-2 hours, then adding iodo-alkyl sulfonic acid, reacting for 30-60 hours at room temperature, cooling to 0 DEG C, and carrying out reduced pressure distillation to obtain cyclodextrin alkyl ether sulfonic acid; the cyclodextrin alkyl ether sulfonic acid prepared by the invention is used as a cosolvent of the powder resistance-reducing agent, can effectively prevent aggregation among molecules of the powder resistance-reducing agent, improves the dispersity, reduces agglomeration and precipitation phenomena, and meanwhile, can avoid pipeline blockage in a conveying process.

The invention relates to the technical field of zinc-iodine battery electrolyte, in particular to aqueous zinc-iodine electrolyte as well as a preparation method and application thereof. The aqueous zinc-iodine battery electrolyte contains an additive and a zinc salt, the molar concentration of the additive is 0.15 M to 0.8 M, and the additive is selected from one or more of triethylamine hydrochloride, 1-butyl-1-methylpyrrolidine chloride, 1, 3-dimethylimidazole chloride, pyridine hydrochloride, aniline hydrochloride, guanidine hydrochloride and 1-ethyl-3-methylimidazole chloride. The method can directionally regulate and control zinc negative electrode deposition and iodine positive electrode reaction kinetics, realizes four-electron reversible conversion, promotes uniform deposition of zinc ions and inhibits side reactions during charging, inhibits multi-iodide shuttle and I < + > hydrolysis during discharging, and has wide application prospects in the zinc-iodine battery electrolyte industry.

The invention relates to the technical field of iodide content detection, in particular to a method for determining radiochemical purity and iodine content of sodium iodide capsules for diagnosis by HPLC (High Performance Liquid Chromatography), which comprises the following steps: setting chromatographic conditions, and connecting a radioactive flow detector and an ultraviolet detector in series; preparing a disodium hydrogen phosphate solution, a glucose solution, a vitamin C solution, a first control solution, a potassium iodate solution, a second control solution, a carrier solution, a first sample solution, a second sample solution, a negative control solution and a test solution; and determining the radiochemical purity and iodide content of the first sample solution and the second sample solution in three batches based on the chromatographic conditions and the determination standard. According to the method, test parameters such as capsule sample analysis time, a pretreatment mode and a sample size are optimized, the radiochemical purity of the capsule is accurately determined, and the iodide content is controlled, so that the problem that main components cannot be accurately quantified and potential radioactive impurities cannot be detected by a traditional diagnosis sodium iodide [131I] capsule determination method is solved.

The invention belongs to the technical field of photoelectric materials and devices, and particularly relates to a perovskite thin film and a preparation method and application thereof. A fluorine-containing phosphazene compound is used as a ligand and is mixed with a perovskite precursor solution composed of lead iodide, formamidine iodine and cesium iodide, spin coating is performed, the fluorine-containing phosphazene compound and part of formamidine cations form hydrogen bonds, part of formamidine cations are anchored at the bottom of a perovskite film, Cs-formamidine cations are uniformly distributed, and the perovskite film is prepared. Meanwhile, the fluorine-containing phosphazene compound and Pb < 2 + > form a coordinate bond, Pb < 2 + > defects are passivated, and the perovskite thin film is obtained through anti-solvent treatment and annealing treatment. The fluorine-containing phosphazene compound interacts with the components in the perovskite precursor solution, so that the nucleation rate of perovskite can be increased, the crystallization rate can be slowed down, the tensile stress can be eliminated, the perovskite does not enter crystal lattices, and the stability and crystallinity of the film are guaranteed. The perovskite thin film can be used for an inverted perovskite solar cell, and the performance and the stability of a device are improved.

The invention discloses a method for preparing a perovskite solar cell based on a fused salt doped Spiro-OMeTAD hole transport layer, and the method comprises the steps: dissolving lead iodide and formamidine iodide in a mixed solvent of N, N-dimethylformamide and dimethyl sulfoxide according to a molar ratio of (0.8-1.5): 1 to prepare an FAPbI3 perovskite precursor solution; the method comprises the following steps: mixing cyclohexylamine trifluoroacetic acid and 4-tert-butylpyridine according to a molar ratio of 1: (8-14), dissolving the mixture in a 70-110 mg / mL Spiro-OMeTAD chlorobenzene solution, adding an acetonitrile solution of LiTFSi, and stirring at normal temperature to obtain a hole transport material Spiro-OMeTAD solution; spin-coating the FTO substrate with an electron transport layer material, spin-coating the electron transport layer with the FAPbI3 perovskite precursor solution, and annealing to form a perovskite thin film; the method comprises the following steps: spin-coating an ammonium butyrate iodide solution on a perovskite thin film to obtain an interface modification layer, spin-coating a hole transport material Spiro-OMeTAD solution on the interface modification layer to obtain a cyclohexylamine trifluoroacetic acid doped Spiro-OMeTAD hole transport layer, and evaporating an interface modification layer and a metal electrode on the Spiro-OMeTAD hole transport layer.

The invention discloses a preparation method of an efficient and stable wide-band-gap perovskite solar cell based on double-layer interface passivation, and relates to the technical field of solar photovoltaics. According to the method, on the basis of 9-octadecenyl amine iodide (OAmI) and phenethyl amine iodide (PEAI), the OAmI anchors a crystal boundary to inhibit ion migration, and cooperates with the PEAI to generate two-dimensional perovskite in situ to optimize energy band alignment, so that deep-shallow energy level defect synergistic passivation is realized. Under the optimal condition, the photoelectric conversion efficiency of the prepared solar cell reaches 22.54%, the initial efficiency of 86.4% is still kept after continuous irradiation of one sunlight for 500 hours, and the working stability of the wide-band-gap perovskite cell, especially the stability under the continuous illumination condition, is remarkably improved.

The invention is applicable to the technical field of metal organic framework materials, and provides a pillararene-based metal organic framework material and a preparation method thereof.The pillararene-based metal organic framework material takes a compound PY2-P5 as a ligand, and the material is one of PMOF1, PMOF2 and PMOF3; the PMOF1 is of a Cu4I4 cubic tetramer structure; the PMOF2 is of a Cu4I4 ladder tetramer structure, and the Cu4I4 ladder tetramer structure is a And the PMOF3 has a CuI one-dimensional chain structure. By introducing the pillararene ligand and regulating and controlling the coordination mode of the pillararene ligand and cuprous iodide, the metal organic framework material with stable structure and functional characteristics is constructed, the metal organic framework material has the dual advantages of host recognition site and fluorescence signal response, and can selectively distinguish 1-bromoalkane and 2-bromoalkane; a remarkable fluorescent blue shift signal is shown in the adsorption process, so that the visualization of molecular recognition and sensing is realized; the excellent molecular recognition capability of pillararene is maintained, the stability and reusability of the material are improved through framing, and a new way is provided for selective detection and separation of volatile organic compounds.

The application discloses a perovskite solar cell passivated by a sulfur-containing passivation agent, and a passivation layer is formed on an APbX3 peroviskite film by using the sulfur-containing passivation agent. 2+ S in the sulfur-containing passivation agent interacts with the weakly acidic Pb as a Lewis base, and H in the passivation molecule can form a hydrogen bond with the nearby iodide to further strengthen the interaction, reduce the surface defect density of the APbX3 peroviskite film, improve the interface energy level matching between the peroviskite and the charge transport layer, reduce the environmental resistance of the peroviskite solar cell, and greatly improve the photoelectric conversion efficiency and stability of the APbX3 peroviskite solar cell.

The application belongs to the field of organic synthesis, and particularly relates to a synthesis method of 2-(3,3-dimethylbutyl)pyridine. 2-vinylpyridine, brominated tertiary butane, a mixed solution of dimethyl ether and isopropyl ether as a reaction system solvent, nickel iodide as a nickel salt, bipyridine as a ligand, dicyclohexylmethylamine as a base in the system, 2,6-dimethyl-3,5-diethyl-1,4-dihydropyridine as a reducing agent, a photocatalyst 2,4,5,6-tetrakis(9 ‑ Carbazole) - m-phenylenedinitrile, under the condition of room temperature and nitrogen atmosphere, a reduction cross-coupling reaction is used to synthesize 2-(3,3-dimethylbutyl)pyridine. The application uses inexpensive nickel metal as a catalyst, constructs a cross-coupling reaction of carbon-carbon bond, and has the advantages of mild reaction condition, high economy and the like.

The invention provides a series of polybenzyl bromide or polybenzyl iodide-based monomolecular resin photoresists as well as a preparation method and application thereof. The monomolecular resin can be used as a main body material of the photoresists. The raw materials are cheap and easily available, and the synthesis process is simple. According to the compound disclosed by the invention, adamantane is taken as a core unit, a plurality of benzyl bromide or benzyl iodine groups, adamantane and a benzene ring are externally connected, and bromine atoms or iodine atoms are additionally introduced, so that the sensitivity and the etching resistance of the photoresist can be improved to the maximum extent.

This invention discloses an in-situ removal process for total inorganic iodide in water based on oxidation-adsorption, belonging to the field of water treatment technology. The process includes: first, taking raw water containing inorganic iodide, adding bicarbonate and adjusting the pH of the solution to 7-7.5; then, adding ferrous salt to the raw water; finally, adding KMnO4 to the raw water with added ferrous salt under stirring conditions, reacting to prepare a MnO2-nascent iron particle complex; on the one hand, promoting the removal of total inorganic iodide from water through mild oxidation-adsorption. ‑ Oxidation transformation occurs to generate HOI / I2; on the other hand, the in-situ products HOI / I2 are adsorbed and fixed through adsorption / co-precipitation methods, and nascent iron is captured through surface coordination or electrostatic adsorption. This invention achieves the capture of I2 under neutral / weakly alkaline drinking water conditions through a mild and controllable oxidation-adsorption synergistic mechanism. ‑ Simultaneous adsorption and removal of its conversion products are achieved to ensure that total iodine is removed to the required standard.

The invention discloses a sulfaguanidine modified inorganic tin-based perovskite light-emitting diode and a preparation method thereof, and belongs to the field of luminescent material preparation, the preparation method comprises the following steps: preparing a perovskite precursor solution which comprises cesium iodide, stannous iodide, sulfaguanidine and an organic solvent; applying the perovskite precursor solution to a substrate to form a wet film; carrying out annealing treatment on the wet film so as to form a perovskite light-emitting layer containing CsSnI3 perovskite and sulfaguanidine; a hole transport layer is formed on an anode conductive substrate, and a perovskite light-emitting layer is adopted on the hole transport layer; and sequentially forming an electron transport layer, an electron injection layer and a cathode electrode on the perovskite light-emitting layer. The process is simple and suitable for popularization and application.

The invention relates to a catalytic quasi-solid ionic conductor, a preparation method and application thereof, and an aqueous zinc ion battery, and belongs to the field of aqueous zinc ion battery electrolyte preparation. The preparation method of the catalytic quasi-solid ionic conductor comprises the following steps: mixing ZSM-5 molecular sieve powder with a metal nitrate solution, carrying out a hydrothermal reaction, centrifuging, washing and drying after the reaction is completed to obtain a monatomic-loaded molecular sieve, then preparing the monatomic-loaded molecular sieve into a sheet, dropwise adding a trace amount of electrolyte for infiltration, and drying to obtain the catalytic quasi-solid ionic conductor. The catalytic quasi-solid ionic conductor is obtained. The catalytic quasi-solid ionic conductor has the following advantages: (1) rich monatomic catalytic sites can accelerate iodine conversion, reduce accumulation of polyiodide, and inhibit the shuttle effect through strong adsorption, thereby avoiding capacity fading and cathode corrosion; (2) molecular sieve pore channels can limit the activity of water molecules and inhibit side reactions; (3) zinc ions can be guided to be uniformly deposited, and dendritic crystal growth is inhibited; and (4) the cathode material has good adaptability.

This invention discloses a method for preparing high-purity hydroiodic acid based on an electrodialysis system, belonging to the fields of chemical engineering and new energy technology. The method includes: introducing a first iodide solution into the material chamber of a three-compartment bipolar membrane electrodialysis system; after acid-base preparation, a second iodide solution is obtained; the obtained second iodide solution is then introduced into the desalination and concentration chambers of a two-compartment homogeneous membrane electrodialysis system for electrodialysis concentration, yielding a third and fourth iodide solution; the products from each stage can be reused or sold after processing. This invention avoids the generation of the byproduct iodate, directly generating a high-purity, high-concentration hydroiodic acid solution, eliminating cumbersome and expensive purification steps, and completely achieving product separation. The process is simple, safe, and environmentally friendly. The acid produced by the three-compartment bipolar membrane electrodialysis system becomes a qualified hydroiodic acid product after passing through an MVR evaporation system, and the produced alkali, as a byproduct, can be sold or utilized, turning waste into treasure.

This invention relates to a 1,1,2,2-tetrahydroperfluoroalkyl-substituted allyl quaternary ammonium salt, its preparation method, and its application, belonging to the field of flocculation treatment technology for high-salt industrial wastewater from natural gas purification. To address the problem that the synthesis of cationic polymer flocculants in existing technologies requires large amounts of surfactants and involves complex operations, this application employs a substitution reaction between 1,1,2,2-tetrahydroperfluoroalkyl iodide and N-methylallylamine; iodomethane is then reacted with the substitution reaction product to undergo quaternization, yielding a 1,1,2,2-tetrahydroperfluoroalkyl-substituted allyl quaternary ammonium salt; the 1,1,2,2-tetrahydroperfluoroalkyl-substituted allyl quaternary ammonium salt is polymerized with acrylamide to obtain a novel cationic polyacrylamide flocculant. The synthesis of cationic fluorocarbon-modified hydrophobic associative polyacrylamide flocculants using an aqueous solution polymerization method is simple, requires no surfactants, and experiments show that the prepared flocculant exhibits excellent flocculation performance.

The invention belongs to the field of organic synthesis, and particularly relates to a synthetic method of a diaryl methane compound. A toluene derivative as shown in a formula 1, an aryl iodide as shown in a formula 2 and a styrene derivative as shown in a formula 3 are subjected to a reaction in the presence of a catalytic amount of PdCl2 (dppf) and 4, 6-di (diphenylphosphine) phenazine and an equivalent amount of LiN (SiMe3) 2 and CsF to synthesize the diaryl methane compound as shown in a formula 4. The coupling reaction of the toluene derivative, the aryl iodide and the styrene derivative is realized by adopting a catalytic amount of PdCl2 (dppf), and the palladium catalyst shows obvious catalytic performance.

The invention belongs to the technical field of luminescent materials, and discloses a heavily-doped Eu (II) hybrid metal iodide scintillator and a preparation method and application thereof. The chemical composition formula of the hybrid metal iodide is OrSr (1-v) Eu (II) vI. According to the invention, a glass tube is sintered at a low temperature by using a flame spray gun under the vacuum degree of 10 <-3 >-10 <-5 > Pa through a vacuum sintering process, wherein the raw materials which are ground and mixed uniformly are ground and mixed uniformly. The heavily doped Eu (II) hybrid metal iodide is obtained, the material shows the characteristics of high luminous intensity, good scintillation performance, good concentration quenching characteristic, wide excitation range and the like, and a ceramic wafer prepared through cold pressing sintering can be used in the field of X-ray imaging.

The invention provides an electroplating solution containing a novel additive and application of the electroplating solution in copper electroplating. The pyridine-2-acetaldehyde oxime methyl iodide is used as a novel copper electroplating additive (leveling agent) for the copper electroplating process, the cost is low, safety and no pollution are achieved, and the novel additive stably exists in the electroplating liquid. The novel additive is applied to the electrocoppering process, compact filling from bottom to top can be achieved, the surface of a plating layer is bright and flat, different adsorption behaviors of the additive can be regulated and controlled by regulating and controlling distribution of current density at interfaces of the inner surface and the outer surface of a micropore, and therefore the additive can be widely applied to high-density interconnection of electronic devices and can be applied to electrocoppering. And high-quality and high-stability signal transmission is satisfied.

The invention discloses a difunctional alcohol dehydrogenase derived from Geobacillus thermodenitrifis, the difunctional alcohol dehydrogenase takes NAD < + > as a cofactor, can specifically catalyze a continuous oxidation reaction of omega-hydroxy fatty acid, and catalyzes the omega-hydroxy fatty acid to synthesize alpha, omega-binary fatty acid through single enzyme catalysis without an aldehyde intermediate. The alcohol dehydrogenase has dual catalytic functions of alcohol oxidation and aldehyde oxidation, the oxidation process from hydroxymethylene to carboxyl can be completed in one step, the reaction steps are simplified, accumulation and separation of intermediate aldehyde are avoided, the conversion efficiency is improved, and the alcohol dehydrogenase is alpha, omega-dibasic fatty acid and is a novel alcohol dehydrogenase. The invention provides a simple and efficient biocatalysis way for biosynthesis of dodecanedioic acid, especially dodecanedioic acid, and has important industrial application value.

The application discloses a method for preparing chiral amino alcohol compounds by using water as a hydrogen source and nickel metal as a catalyst. The method comprises the following steps: dissolving a nickel metal catalyst, zinc powder, an additive and a ligand in a dry organic solvent under an inert gas atmosphere; then adding an o-phthalimido ketone compound and water; and reacting at 40-70 DEG C to obtain a target product. The additive is one or more of silver iodide, cuprous bromide, cuprous iodide and cuprous chloride. The ligand is ( S, S p )- t‑ Bu-Phosferrox, S, S p )-Bn-Phosferrox, R, R p )-Ph-Phosferrox or R, R p )- i‑ Pr-Phosferrox. The application uses water as a hydrogen source and nickel metal as a catalyst to catalyze amino ketone compounds to obtain a series of chiral amino alcohol compounds. The method is simple, clean and environmentally friendly, and is suitable for the conventional preparation of chiral amino alcohol compounds.

The application belongs to the technical field of photovoltaic devices, and relates to preparation and application of a multifunctional organic additive doped CsSnI3 perovskite film; during preparation, a perovskite spin coating liquid is spin coated on an ITO glass substrate to form a precursor film, and the precursor film is subjected to annealing treatment to obtain a CsSnI3 perovskite film; the perovskite spin coating liquid is formed by adding stannous fluoride and 3-amino-pyrazine-2-carboxamide (3-APCA) to a perovskite precursor solution and stirring; the perovskite precursor solution is formed by dissolving cesium iodide and stannous iodide in an organic solvent; and the application is applied to solar cells, light-emitting diodes, photoelectric detectors, photoelectric catalysis and energy storage. The method introduces the multifunctional organic additive 3-APCA, realizes Sn 2+ oxidation inhibition, optimizes film crystallinity and passivates defects, and significantly improves the quality of the CsSnI3 perovskite film; and the application range is wide.

The application provides a synthesis method of 1-substituted phenanthrene compounds, which comprises the following steps: mixing ortho-substituted aryl diazonium salt with KI, adding a palladium acetate catalyst, adding norbornadiene, adding a base, adding an organic phosphine ligand, adding 2-halobenzoic acid, heating to 80-150 DEG C in an aprotic solvent under a nitrogen atmosphere, and reacting for 2-10 hours to obtain the 1-substituted phenanthrene compounds. The method uses cheap and easily obtained ortho-substituted aryl diazonium salt instead of expensive aryl iodide to prepare 1-substituted phenanthrene compounds, and has the characteristics of easy raw material, mild conditions and simple operation, and is a simple synthesis method of 1-substituted phenanthrene compounds.

The application discloses an improved plant liquid culture medium, which comprises inorganic nutrients required by plant basic growth and does not comprise compounds containing an EDTA ligand skeleton and iodide. The application also discloses application of the improved plant liquid culture medium in mercury compound metabolism research. The application is based on the technical problem of finding that a culture medium substrate mediates abiotic transformation and causes error defects, and by eliminating the compounds containing the EDTA ligand skeleton and the iodide which induce abiotic transformation of mercury compounds, the application is applied to block the abiotic transformation path of methyl mercury in the mercury compound metabolism research, and eliminate the 'false positive' error in the metabolism research.

The invention belongs to the technical field of medicine preparation, and particularly relates to a fenoprofen calcium preparation method which comprises the following steps: 1) m-hydroxyacetophenone and bromobenzene generate an intermediate 1, namely m-phenoxyacetophenone under the action of alkali and cuprous iodide; 2) reacting the intermediate 1 with ethyl chloroacetate under the action of strong base, and then performing hydrolysis and decarboxylation reaction to generate an intermediate 2, namely 2-(3-phenoxy phenyl) propionaldehyde; the invention discloses a preparation method of fenoprofen calcium, which comprises the following steps: (1) preparing fenoprofen, (2) preparing fenoprofen, (3) carrying out oxidation reaction on an intermediate 2 to obtain fenoprofen, (4) reacting fenoprofen with a sodium hydroxide solution to obtain fenoprofen sodium, and (5) salifying fenoprofen sodium with a calcium chloride solution to obtain fenoprofen calcium.

The invention relates to the technical field of drug detection and analysis, in particular to a diiodide detection method, dichloromethane-acetone-methanol-ammonia water (7: 1: 1: 1) is used as a developing solvent, the concentration of diiodide in reaction liquid during nitration reaction of diiodide in the lobaplatin production process is detected, the method can accurately judge whether nitration reaction is complete or not, and the detection result is accurate. And the diiodide is ensured to be completely reacted in the nitration reaction process. The obtained method is suitable for detecting and judging the lobaplatin nitration reaction endpoint, the result is accurate and reliable, good specificity, durability and solution stability are achieved, and the detection time is short.