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loser木虫 (小有名气)
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[求助]
请帮助润色一段话
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| Figure 1 and 2 show that 0.6wt‰ amount of iron existed on the fresh catalyst, which is from the raw materials for preparation of catalyst. The Fe component on the fresh catalyst has no negative effect on the hydroisomerization reaction, since Fe locates in the catalyst support bulk with an inert state. The Fe content after reaction increases remarkably to more than 1.2 wt‰, e.g., 2Kh and 8Kh in Figure 1 and 2. All the Fe species adsorbed during reactions locates on the catalyst surface with reduced or oxidized states. These Fe components on the surface will have a series of complicated negative effects on the surface acidic sites and metallic sites, or even plug the pores of catalysts after long time enrichment of Fe from reagent oils. Further more, the solid Fe deposits on the catalyst can hardly be removed no matter by reductive or oxidative treating method. So Fe species in the reagent oils must be removed before reaction. |
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mac194
铁虫 (职业作家)
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【答案】应助回帖
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RXMCDM: 金币+1, 多谢应 2014-04-01 14:56:51
RXMCDM: 翻译EPI+1 2014-04-02 10:37:29
RXMCDM: 金币+30 2014-04-02 10:37:54
RXMCDM: 金币+1, 多谢应 2014-04-01 14:56:51
RXMCDM: 翻译EPI+1 2014-04-02 10:37:29
RXMCDM: 金币+30 2014-04-02 10:37:54
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[ 感谢奖赏 ] Because of the way it's prepared, fresh catalyst is held intact and protected especially on the outside by inert steel. That outside layer (0.6wt‰ as shown in Fig's 1 and 2) keeps acidic and metallic sites, especially those on the surface available for reaction. Access to those sites can be reduced, sometimes completely if reactive iron were allowed to accumulate or even plug surface pores of the catalyst. The catalyst can become useless once hydroisomerization or unchecked long-term contact with iron-rich reagent oils more than doubles superficial iron to 1.2 wt‰, or to 2Kh and 8Kh in Figures 1 and 2, respectively Since solid iron deposits are nearly impossible to remove, reagent oils must be rid of its iron content as much as possible [prior to reaction] in order to preserve the catalyst. 附注: - 润色目的是要比原文更易读,更能吸引读者, LZ 原意我已由外入内,更故事化的表达了 - 不要突换动词时态,除非谈及实验当时,否则一贯现在式最好 - 并非 "Figure 1, Figure 2" 不可, "Fig's 1 and 2" 缩写也行 - "with reduced or oxidized states" 表示带电,易产生反应(即 "reactive"  - "can hardly be removed no matter by ..." = "nearly impossible to remove" - 预计"support bulk" 原意是 "保持完整" = "keep intact" - 翻译假设活性点越难进,催化剂就越不中用 |
4楼2014-04-01 09:47:48
★ ★ ★ ★ ★
RXMCDM: 金币+1, 多谢应助！ 2014-03-31 22:20:30
loser: 金币+34, 翻译EPI+1, ★有帮助, 3 2014-04-02 08:37:59
RXMCDM: 翻译EPI-1 2014-04-02 10:37:20
RXMCDM: 金币-30 2014-04-02 10:37:42
RXMCDM: 金币+1, 多谢应助！ 2014-03-31 22:20:30
loser: 金币+34, 翻译EPI+1, ★有帮助, 3 2014-04-02 08:37:59
RXMCDM: 翻译EPI-1 2014-04-02 10:37:20
RXMCDM: 金币-30 2014-04-02 10:37:42
| Fig1 and Fig2 show that on the fresh catalyst there is a mixture of 0.6wt‰ iron , which is from the raw materials ,The catalyst prepared by the raw materials. |
2楼2014-03-31 22:09:54
RXMCDM
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| Figure 1 and 2 showed that 0.6wt‰ amount of iron existed on the fresh catalyst, which is from the raw materials for catalyst preparation and has no negative effect on the hydroisomerization reaction, since it is located in the catalyst support bulk with an inert state. The Fe content after reaction increases remarkably to more than 1.2 wt‰ as the 2Kh and 8Kh shown in Figure 1 and 2. At same time , all the Fe species adsorbed during reactions and located on the catalyst surface are either reduced or oxidized . These Fe components on the surface have a series of complicated negative effects on the acidic and metallic sites of the surface , or even plug the catalysts pores under long time Fe enrichment of reagent oil. Further more, the solid Fe deposits on the catalyst can hardly be removed either by reductive or oxidative treating method. For this reason, Fe species in the reagent oil must be removed before reaction. |
3楼2014-03-31 22:18:28
RXMCDM
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5楼2014-04-01 15:03:59
