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    • 1. 发明授权
    • Preparation of overbased magnesium sulfurized phenates
    • 高碱性镁硫化酚盐的制备
    • US4196089A
    • 1980-04-01
    • US917215
    • 1978-06-20
    • Charles L. PitzerNorman Jacobson
    • Charles L. PitzerNorman Jacobson
    • C07C319/10C07C67/00C07C313/00C07C321/26C10M159/22C10N10/04C10N30/04C10N40/25C10M1/40C07C37/00
    • C10M159/22C10M2219/02
    • Preparation of overbased magnesium sulfurized phenates having total base members in the range of about 200 to about 275 by a two-stage procedure, the first stage of which involves dissolving a sulfurized oil-soluble aliphatic hydrocarbyl-substituted phenol, particularly a C.sub.6 -C.sub.30 alkyl phenol, in certain types of high boiling organic polar solvents, exemplified particularly by methyl "Cellosolve," and admixing therewith magnesium oxide in an amount such that, upon refluxing the mixture, a fully neutralized sulfurized alkyl phenol results; and wherein, in the second stage of said procedure, the composition produced in the first stage of the procedure is overbased by admixing therewith a magnesium alkoxide carbonate complex in an amount such as to produce the final overbased magnesium sulfurized phenate compositions having the aforesaid total base number.
    • 通过两步法制备具有约200至约275范围内的总碱成分的高碱性硫化酚盐,其第一阶段包括将硫化油溶性脂族烃基取代的苯酚,特别是C 6 -C 30烷基 苯酚,在某些类型的高沸点有机极性溶剂中,特别是由“溶纤剂”表示,并与其混合氧化镁,其量使得在回流混合物时产生完全中和的硫化烷基酚; 并且其中在所述方法的第二阶段中,在该方法的第一阶段中制备的组合物通过与其混合使用的醇式烷氧基化碳酸酯络合物进行高碱性化,其量可以产生具有上述总碱的最终高碱性硫化镁的酚盐组合物 数。
    • 2. 发明授权
    • Method for the removal of chromium compounds from aqueous solutions
    • 从水溶液中去除铬化合物的方法
    • US5211853A
    • 1993-05-18
    • US923378
    • 1992-07-31
    • John R. JacksonCharles L. Pitzer
    • John R. JacksonCharles L. Pitzer
    • C02F1/70C02F9/00
    • C02F1/70C02F2101/22Y10S204/13Y10S210/913
    • A process for precipitating and removing chromium compounds in which chromium is in the hexavalent state from aqueous liquids, particularly, alkaline earth metal or alkali metal chlorate-rich solutions containing chloride, chlorate, and bichromate ions produced by the electrolysis of brine. In the process, hydroxylamine, hydroxylamine sulfate, hydroxylamine formate or hydroxylamine hydrochloride is used as a reducing agent to react and co-precipitate at a neutral or acid pH with hexavalent chromium ions present in the aqueous liquid, the reaction and precipitation taking place, generally, at a pH of about 4.0 to about 6.5 and, a temperature of about 50.degree. C. to about 100.degree. C. Precipitated oxides and hydroxides of divalent and trivalent chromium can be removed, for instance, by filtration. Reaction time to achieve a level of about 10 parts per million or less of chromium ions in the filtrate varies from less than about 5 hours to less than about 1 hour depending upon selection of reaction temperature and reaction pH. For instance, to achieve a level of 2 parts per million or less chromium ion after removal of the precipitate formed during the reaction at a pH of 5.0-5.5, a reaction time of 10 minutes at a temperature of 90.degree.-95.degree. C. is required. A reaction time of 30 minutes at a temperature of 70.degree. C. or 120 minutes at a temperature of 60.degree. C. provides a similar level of chromate ion removal.
    • 从含水液体,特别是含有通过电解盐水产生的氯化物,氯酸盐和重铬酸盐离子的碱土金属或富含碱金属的富含氯酸盐的溶液中析出并除去铬为六价态的铬化合物的方法。 在此过程中,使用羟胺,硫酸羟胺,羟胺盐酸盐或盐酸羟胺作为还原剂,在中性或酸性pH下与六水六价铬离子反应并共沉淀在水性液体中,发生反应和沉淀,一般 pH为约4.0至约6.5,温度为约50℃至约100℃。可以例如通过过滤除去二价和三价铬的沉淀氧化物和氢氧化物。 取决于反应温度和反应pH的选择,实现滤液中约10ppm或更少的铬离子水平的反应时间小于约5小时至小于约1小时。 例如,为了在去除反应中形成的沉淀物的pH为5.0-5.5之间达到每百万分之一或更少的铬离子的水平,在90-95℃的温度下反应10分钟。 是必须的。 在70℃或120分钟的温度下在60℃下反应30分钟,提供类似的铬酸根离子去除水平。