摘要:
The present invention concerns a mixture of inorganic nitrate salts, comprising LiNO3, NaNO3, KNO3 and CsNO3 wherein the LiNO3 content ranges from 17.5% by weight to 21.6% by weight, the NaNO3 content ranges from 10% by weight to 11% by weight, the KNO3 content ranges from 27.7% by weight to 32.6% by weight, the CsNO3 content ranges from 35.8% by weight to 43.8% by weight, including the interval bounds.
摘要:
The present invention concerns a mixture of inorganic nitrate salts, comprising LiNO3, NaNO3, KNO3 and CsNO3 wherein the LiNO3 content ranges from 17.5% by weight to 21.6% by weight, the NaNO3 content ranges from 10% by weight to 11% by weight, the KNO3 content ranges from 27.7% by weight to 32.6% by weight, the CsNO3 content ranges from 35.8% by weight to 43.8% by weight, including the interval bounds.
摘要:
A process for purifying an aqueous stream from a Fischer-Tropsch reaction that includes feeding the aqueous stream to a system that includes a distillation column equipped with a partial condenser and a total condenser, at least partially condensing the vaporized stream leaving the head of the distillation column and collecting a first distillate in which in heavier by-products, totally condensing the remaining portion of the vaporized stream leaving the partial condenser and collecting a liquid stream which is returned to the distillation column as a reflux and removing a purified aqueous stream from the bottom of the distillation column.
摘要:
The present invention relates to a process for the purification of an aqueous stream coming from the Fischer-Tropsch reaction which comprises:—feeding of the aqueous stream containing the organic by-products of the reaction to a system consisting of a distillation column equipped with a partial condenser and a total condenser;—partial condensation of the vaporized stream leaving the head of the column and collection of a first distillate enriched in the heavier by-products;—total condensation of the vaporized stream leaving the partial condenser and collection of a liquid stream which is partly sent back to the distillation column as reflux whereas the remaining part is collected as distillate;—extraction of the purified aqueous stream from the bottom of the distillation column.
摘要:
The invention relates to a continuous process for the preparation of phenol by means of the direct oxidation of benzene with hydrogen peroxide in the presence of a catalyst based on titanium silicalite TS-1 comprising: (a) running the process in a fixed bed reactor containing the catalyst based on TS-1 at a temperature ranging from 80-120° C. and at a pressure ranging from 3-15 atm; (b) feeding to the reactor a stream containing H2O2, benzene, sulfolane and water in a single or double phase, wherein the quantities of the single components are within the range of 0.2-6, 15-60, 30-80, 0.5-30 parts by weight, respectively, for every 100 units fed and whose total flow rate is calculated so that the residence time in the reactor (defined as the ratio between the quantity of catalyst by weight and the feeding flow rate) ranges from 0.3 to 2 min; (c) recovery of the products, by-products and solvent from the liquid stream leaving the reactor.
摘要翻译:本发明涉及一种通过在基于钛硅沸石TS-1的催化剂存在下用过氧化氢直接氧化苯的连续方法,其包括:(a)在含有 催化剂基于TS-1,温度范围为80-120℃,压力范围为3-15atm; (b)在单相或双相中向反应器中加入含有H 2 O 2,苯,环丁砜和水的流,其中单一组分的量在0.2-6,15-60,30-80,0.5- 对于每100个单位进料,分别计算30重量份,并且其总流速被计算为使得在反应器中的停留时间(定义为催化剂的重量比和进料流量之间的比率)为0.3-2 分钟 (c)从离开反应器的液体流中回收产物,副产物和溶剂。
摘要:
The invention relates to a continuous process for the preparation of phenol by means of the direct oxidation of benzene with hydrogen peroxide in the presence of a catalyst based on titanium silicalite TS-1 comprising: (a) running the process in a fixed bed reactor containing the catalyst based on TS-1 at a temperature ranging from 80-120° C. and at a pressure ranging from 3-15 atm; (b) feeding to the reactor a stream containing H2O2, benzene, sulfolane and water in a single or double phase, wherein the quantities of the single components are within the range of 0.2-6, 15-60, 30-80, 0.5-30 parts by weight, respectively, for every 100 units fed and whose total flow rate is calculated so that the residence time in the reactor (defined as the ratio between the quantity of catalyst by weight and the feeding flow rate) ranges from 0.3 to 2 min; (c) recovery of the products, by-products and solvent from the liquid stream leaving the reactor.
摘要翻译:本发明涉及一种通过在基于钛硅沸石TS-1的催化剂存在下用过氧化氢直接氧化苯的连续方法,其包括:(a)在含有 催化剂基于TS-1,温度范围为80-120℃,压力范围为3-15atm; (b)在单相或双相中向反应器中加入含有H 2 O 2 O 2,苯,环丁砜和水的流,其中单一组分的量在 对于每供给的100个单位,分别为0.2-6,15-60,30-80,0.5-30重量份的范围,并且计算其总流速使得在反应器中的停留时间(定义为 催化剂的重量和进料流量)为0.3〜2分钟; (c)从离开反应器的液体流中回收产物,副产物和溶剂。
摘要:
A process to activate a titanium silicalite catalyst for the oxidation of benzene to phenol is provided. The catalyst is activated in the reactor for the oxidation by feeding to a reactor containing the titanium silicalite catalyst, during a time of from 2 to 6 hours, at a temperature ranging from 20 to 120° C., an aqueous solution of ammonium acid fluoride in a concentration ranging from 0.1% to 1% by weight; and hydrogen peroxide in a concentration ranging from 3% to 10% by weight; feeding water to the reactor at the end of the reaction; and drying or calcining the catalyst contained in the reactor to obtain the activated catalyst. The catalyst is represented by the formula: xTiO2.(1−x)SiO2 wherein x is from 0.0001 to 0.04.
摘要:
A process to activate a titanium silicalite catalyst for the oxidation of benzene to phenol is provided. The catalyst is activated in the reactor for the oxidation by feeding to a reactor containing the titanium silicalite catalyst, during a time of from 2 to 6 hours, at a temperature ranging from 20 to 120° C., an aqueous solution of ammonium acid fluoride in a concentration ranging from 0.1% to 1% by weight; and hydrogen peroxide in a concentration ranging from 3% to 10% by weight; feeding water to the reactor at the end of the reaction; and drying or calcining the catalyst contained in the reactor to obtain the activated catalyst. The catalyst is represented by the formula: xTiO2.(1−x)SiO2 wherein x is from 0.0001 to 0.04.