浸渍酸的英文翻译、例句

浸渍酸

词组短语: dipping acid

热门词汇: scarcity; skyrocket; hurrah; retort; sieve; submit; marshal; aim; outlandish; detrimental

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The present invention adopts the technical proposal of adopting ZSM-5 mesoporous molecular sieve raw powder with a silicon-aluminum mol ratio SiO2Al2O3 of 20 to 1000 and a weight percentage of 20 to 100 percent as well as at least one caking agent selected from SiO2, clay and Al2O3 to extrude, tablet or spray into shape; then treating for 1 to 8 hours by 0.1 to 3 mol/l of at least one ammonium liquor from ammonium nitrate, ammonium chloride or ammonium sulphate or 0.1 to 8.5 mol/l of at least one acid liquor from muriatic acid, nitric acid, vitriol or acetic acid under a temperature of 20 to 90 DEG C; then using steam to treat for 2 to 15 hours under the temperature condition of 400 to 700 DEG C; using a liquor of 0.1 to 3mol/l selected from at least one of oxalic acid, citric acid or maleic acid under a temperature condition of 20 to 90 DEG C to dip for 2 to 5 hours to obtain the modified molecular sieve catalyst, thus better solving the problems.

本发明通过采用硅铝比SiO2/Al2O3为20～1000重量百分比计20～100％的ZSM-5介孔分子筛原粉与余量的选自SiO2、粘土或Al2O3中至少一种粘结剂挤条、压片或喷球成型；再经过0.1～3摩尔/升选自硝酸铵、氯化铵或硫酸铵中的至少一种铵溶液或0.1～8.5摩尔/升选自盐酸、硝酸、硫酸或乙酸中的至少一种酸溶液在温度20～90℃下处理1～8小时；然后在温度为400～700℃条件下水蒸汽处理2～15小时；再用0.1～3摩尔/升选自草酸、柠檬酸或马来酸中至少一种在温度为20～90℃条件下浸渍2～5小时得所需改性分子筛催化剂的技术方案较好地解决了该问题，可用于甲醇转化制丙烯的工业生产中。

The Scandia doped tungsten powders were made by both liquid-solid doping method and liquid-liquid doping method on the basis of previous researches. The study shows that on the basis of improving pressing and sintering process, we can obtain sub-micron porous bodies with proper porosities.

研究表明在改进压制、烧结技术的基础上，可以获得具有适当孔度的亚微米结构多孔基体，氧化钪在基体中的分布得到进一步改善，在这种基体中铝酸盐的浸渍率可以达到常规浸渍阴极的要求。

The results show that the dissoluble tungstate can be impregnated into the pores of C/C composite materials....

研究结果表明，用浸渍法可将可溶性钨酸盐浸渍到炭/炭复合材料的孔隙中，将浸入炭/炭复合材料中的钨酸盐还原成金属钨可以在一定程度上改善炭/炭复合材料在X射线下的可视性。

The method comprises the steps of dipping and mixing the mipor asphaltic base globular active carbon prepared by the traditional method with an inorganic metal salt solution by a certain ration; heating under an inert atmosphere to 600 to 1200 DEG C at a temperature increasing rate of 1 to 20 DEG C/min for the secondary carbonization; using acid to wash off the remaining metal inside the carbonized material, so as to obtain the asphaltic base globular active carbon with a high mesoporous rate and narrow distribution of mesoporous spertures.

本发明提供了一种浸渍金属盐二次炭化制备中孔沥青基球形活性炭的方法，该方法是将传统方法制备得到的微孔沥青基球形活性炭按一定比例与无机金属盐溶液浸渍混合，然后在惰性气氛下以1～20℃/min的升温速率加热到600～1200℃下进行二次炭化，炭化料经酸洗除去内部残留的金属后，可制得中孔率较高、中孔孔径分布窄的沥青基球形活性炭。

The structural and photocatalytic properties of TiO〓 as well as surface acidity were greatly improved by sulfation. SO〓〓/TiO〓 solid superacid with Hammett constant Ho less than -12.14 was prepared by treating the TiO〓 with 1.0mol. L〓 sulfuric acid solution and then calcining at 450℃ for 3h. When compared to unmodified TiO〓, the SO〓〓/TiO〓 superacid catalyst exhibited higher anatase content, smaller crystal size, higher specific surface area, centralized pore size distribution, and the blue-shifted band edge of uv-vis adsorption spectra. Furthermore, the SO〓〓/TiO〓 superacid also showed excellent reaction activity and stability for CH〓Br photocatalytic decomposition even under the moist reaction conditions. The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明：SO〓〓与TiO〓表面的结合为螯合式双配位结构；TiO〓光催化剂表面经H〓SO〓浸渍处理后，提高了表面酸性，改善了催化剂结构和光催化性能，当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时，可制得SO〓〓/TiO〓超强酸催化剂(H〓＜-12.14)，其结构和光催化活性得到明显改善，与TiO〓相比，SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移，具有优异的光催化氧化活性、稳定性及抗湿性能，光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级，是一种有实际应用前景的高效光催化剂；由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型，认为在SO〓〓/TiO〓超强酸催化剂表面，由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心，其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移，具有可逆吸附水的性能，是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

A series of SiW_(12)/AC catalysts with different silicotungstic acid loadings supported on acti- vated carbon which was treated with 10% HNO_3 solution were prepared by an impregnation method and the catalytic performance of SiW_(12)/AC for the synthesis of trioxane were investigated.

以10%硝酸溶液处理过的活性炭为载体，采用不同质量分数的硅钨酸SiW_(12溶液为浸渍液，制备了不同负载量的SiW_(12)/AC催化剂，考察了催化剂在合成三聚甲醛中的催化性能，并用XRD、FT-IR、NH_3- TPD、BET、TG-DSC等手段对SiW_(12)/AC催化剂晶粒大小、催化剂表面的酸量及酸强度、比表面积及热稳定性等微观特性进行了表征。

The effects of technologic parameters, including concen- tration and temperature of ADP solution and galvanizing time on rising time of anodic oxide films are discussed. 2. After dipped in amino trimethylene phosphonic acid solution, anodic oxide films are annealed in pipe stove.

将化成箔在氨基三甲叉膦酸溶液中浸渍，取出烘干后再进行热处理，研究了 ATMP 溶液浓度、浸渍温度和热处理温度对氧化膜升压时间、比容、耐电压的影响，找到其最佳耐水合处理工艺；采用FT-IR对水合作用后的 ATMP 处理氧化膜和未经耐水合处理氧化膜进行了分析。

Using the method of macerating, ZrOCl_2 loading on D418 was produced. Influence including time of macerating, pH, and temperature on the amount of load was studied. The proper conditions show that, room temperature is appropriate, the suitable pH is equal to 5, and time of macerating is 16 hours.

采用浸渍法，以ZrOCl_2·2H_2O和氨基膦酸树脂D418为原料，制备大孔螯合树脂D418负载的氯氧化锆，考察了浸渍时间、pH、温度对负载量的影响，得出适宜的操作条件为：室温，pH=5，浸渍时间为16小(来源：ABC347b34论文网www.abclunwen.com)时。

The content of impregnated Ba, Ca aluminates in the bodies can meet the requirement of the conventional impregnated cathode.

在这种基体中铝酸盐的浸渍率可以达到常规浸渍阴极的要求。

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LAS：十二烷基苯磺酸钠

以CeCo3和TiO2为原料,采用浸渍法制备了CeO2-TiO2复合氧化物催化剂,并用SEM,BET,UV-vis,IR等手段对CeO2-TiO2进行了表征,以十二烷基苯磺酸钠(-)(LAS)的光降解为模型反应,考察了其光催化氧化活性,结果表明,

picklock wool：次优级绵羊毛(英国用语)

酸浸,浸渍 pickling | 次优级绵羊毛(英国用语) picklock wool | 拆痕,拆档(织疵) pick-out mark

Impregnated rag paper：浸渍毛纸

"Impregnated glass or acetate cloth 酸纤维布",,,,,,,1.2 | "Impregnated rag paper 浸渍毛纸",,,,,,,1.3 | "Polyester 玛拉胶带",,,,,,,2

ackey：硝硫混合酸浸渍液

acitrin 阿齐特林 | ackey 硝硫混合酸浸渍液 | aclantate 阿克兰酯

ackey：硝(酸)硫(酸)混合酸浸渍液

ackey：西非黄金海岸用银元, 电镀用的硝酸硫酸混合液

pickler：酸洗液

"手选台","picking table" | "酸洗液","pickler" | "浸渍酸洗","pickling"

dip pipe：洗涤管

dip pickling 浸渍酸洗 | dip pipe 洗涤管 | dip pole 地磁极

dipping acid：酸浸

dipping || 浸(人),泡,倾斜,偏斜,浸除 | dipping acid || 酸浸 | dipping coil || 浸渍线圈

acid dipping：酸浸

acid dip 酸浸渍 | acid dipping 酸浸 | acid dissoluble cement 酸溶性水泥

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