CN107268263A - 一种光学漂白剂bmc及其合成工艺 - Google Patents

一种光学漂白剂bmc及其合成工艺 Download PDF

Info

Publication number
CN107268263A
CN107268263A CN201710377842.2A CN201710377842A CN107268263A CN 107268263 A CN107268263 A CN 107268263A CN 201710377842 A CN201710377842 A CN 201710377842A CN 107268263 A CN107268263 A CN 107268263A
Authority
CN
China
Prior art keywords
water
acid
bleaching agent
temperature
bmc
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201710377842.2A
Other languages
English (en)
Inventor
任德生
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zhejiang Ming Sheng New Material Co Ltd
Original Assignee
Zhejiang Ming Sheng New Material Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zhejiang Ming Sheng New Material Co Ltd filed Critical Zhejiang Ming Sheng New Material Co Ltd
Priority to CN201710377842.2A priority Critical patent/CN107268263A/zh
Publication of CN107268263A publication Critical patent/CN107268263A/zh
Pending legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06LDRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L4/00Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/042Acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/044Hydroxides or bases
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/046Salts
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2068Ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2079Monocarboxylic acids-salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/28Heterocyclic compounds containing nitrogen in the ring
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/34Organic compounds containing sulfur
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395Bleaching agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Textile Engineering (AREA)
  • Detergent Compositions (AREA)

Abstract

本发明公开了一种光学漂白剂及其合成工艺,其技术要点是:本发明的配方包括组分A组分B和元明粉,在同E值的情况下,组分A组分B的质量之比为7:3,元明粉用于调节E值,最后配出的混合物E=218±5,所述组分A由邻苯二腈30g、Zn粉3.8g、钼酸铵0.3g、一缩二乙二醇240g、冰醋酸1g和氮气、磺酸150g、氢氧化钠130g、冰800g、水300g和30%‑‑32%盐酸合成;所述组分B由铝酞菁40g、氯磺酸150g、氢氧化钠130g、冰800g、水130g和30%‑‑32%盐酸合成。本发明相较于现有的TINOPAL BMC拥有更好的白度。

Description

一种光学漂白剂BMC及其合成工艺
技术领域
本发明涉及一种光学漂白剂BMC及其合成工艺。
背景技术
组分B和组分A在光照条件下都可以起到漂白织物的作用,两者混合效果更佳,故BMC可用于处理织物产品,也可以作为添加剂添加到洗衣剂中,目前市场只有目前只有全世界只有原汽巴公司生产的TINOPAL BMC,但是TINOPAL BMC的漂白的白度不够。
发明内容
针对现有技术的不足,本发明提供了一种光学漂白剂BMC及其合成工艺。
附图说明
图1为本发明中锌酞菁溶解在DMF中的紫外吸收光谱图;
图2为本发明中组分A紫外吸收光谱图;
图3为本发明中组分B在氢氧化钠溶液中的菁紫外吸收光谱图;
图4为本发明中组分B在水溶液中的紫外吸收光谱图。
具体实施方式
通过图1至图4对本发明一种光学漂白剂BMC及其合成工艺作进一步的说明。
一种光学漂白剂BMC,本发明的配方包括组分A组分B和元明粉,在同E值的情况下,组分A组分B的质量之比为7:3,元明粉用于调节E值,最后配出的混合物E=218±5,所述组分A由邻苯二腈30g、Zn粉3.8g、钼酸铵0.3g、一缩二乙二醇240g、冰醋酸1g和氮气、磺酸150g、氢氧化钠130g、冰800g、水300g和30%--32%盐酸合成;所述组分B由铝酞菁40g、氯磺酸150g、氢氧化钠130g、冰800g、水130g和30%--32%盐酸合成。
将一缩二乙二醇投入到干燥的500ml四口瓶中,搅拌,通氮气以置换出瓶中的空气,再加入锌粉、钼酸铵和邻苯二腈,加热;当温度升到100-180℃时,滴加入冰醋酸,在100℃~160℃保温2-8h,降温,当温度降到100℃时,过滤;滤饼用水洗至滴下的滤液无色,再用甲醇洗涤,再水洗;烘箱中干燥;对烘干后的滤饼进行粉碎,进行E值、吸收值的检测。
1)将氯磺酸加入到500ml的洁净四口烧瓶中,搅拌,通氮气,把温度升到100-160℃,再用恒压滴液漏斗往里加锌酞菁,大约1-3小时加完,保温2-6小时;2)保温好后,将反应混合物倒入到溶有NaOH的冰水中,倒入时搅拌,测得PH=12.3,在30℃用30---32%的盐酸调节PH=0.5,搅拌30min,30℃过滤,滤时滤液为透明的浅蓝色液体;3)将滤饼溶于300ml水中,搅拌,用NaOH水溶液调节PH=6-10,蒸去水,烘干。
1)投料:做好一切准备后开始投料,取150g氯磺酸投入干净干燥以及装置好废气回收的4口反应瓶中;2)升温:投完后开始升温,开启氮气保护,升温至100-160℃;3)加铝酞青:将称量好的40g铝酞青倒入准备好的滴加漏斗中,匀速加入进行磺化反应,其温度控制在100-160℃,约1-3小时加完;4)保温:保温2-6小时;5)检测:保温结束后取样用氢氧化钠中和后进行吸收值检测是否反应完全;6)复配氢氧化钠溶液:氢氧化钠按照氯磺酸的投料量进行换算,总计为130g加130g水进行溶解;7)酸碱中和放热反应:将反应好的铝钛青溶剂慢慢倒入复配好的氢氧化钠溶液中,要求慢慢加入,并用小冰块不断进行冷却,确保反应过程中温度不能过高;8)PH值调整:放热完后,常温搅拌并用盐酸进行PH值调整,将其PH值调为6-10;9)浓缩:将调整好的溶液进行蒸馏浓缩,当物料开始发稠后进行转料到烘箱进行烘烤,温度在120-130度之间,直至烘干;10)检测:对烘干后的滤饼进行粉碎,进行E值、吸收值的检测。
计算组分A和组分B和元明粉的用量,在同E值的情况下,将组分A和组分B和元明粉按比例混合均匀。
对本发明中的光学漂白剂BMC与现在市场上的TINOPAL BMC做对比实验。
实施例一:
1、向装有温度计和冷凝管的100ml三口烧瓶中加入1.5g福建红茶和60ml去离子水,升温至100℃浸泡1h,过滤;将茶叶用40ml去离子水再浸泡1h,过滤,两次滤液合并定容至100ml,4g棉纤维在100℃茶水中搅拌2.5h,降至室温继续搅拌16h后向染液中加入5gNaCl,再升温至100℃搅拌2.5h;待染液冷却后,染色的棉纤维于60℃的水中浸洗两次,于100℃烘箱中烘干,将干燥后的棉纤维加入到含有5g/L标准洗涤剂的洗浴中于90℃洗涤20min,浴比为1:20 ;然后分别用温水和冷水洗涤后,置于100℃烘箱中干燥;取出,备用。
2、将重0.6g沾有茶渍的污布放入0.775ppm光学漂白剂的水溶液中进行洗涤,浴比为1:200 ;同时向该溶液中加入0.6g标准洗衣粉;升温至55℃,搅拌一小时;洗涤过程中用250瓦的红外灯进行照射,灯距液面距离为13厘米。
实施例二:
1、向装有温度计和冷凝管的100ml三口烧瓶中加入1.5g福建红茶和60ml去离子水,升温至100℃浸泡1h,过滤;将茶叶用40ml去离子水再浸泡1h,过滤,两次滤液合并定容至100ml,4g棉纤维在100℃茶水中搅拌2.5h,降至室温继续搅拌16h后向染液中加入5gNaCl,再升温至100℃搅拌2.5h;待染液冷却后,染色的棉纤维于60℃的水中浸洗两次,于100℃烘箱中烘干,将干燥后的棉纤维加入到含有5g/L标准洗涤剂的洗浴中于90℃洗涤20min,浴比为1:20 ;然后分别用温水和冷水洗涤后,置于100℃烘箱中干燥;取出,备用。
2、将重0.6g沾有茶渍的污布放入1.50ppm光学漂白剂的水溶液中进行洗涤,浴比为1:200 ;同时向该溶液中加入0.6g标准洗衣粉;升温至55℃,搅拌一小时;洗涤过程中用250瓦的红外灯进行照射,灯距液面距离为13厘米。
对比实验结果如下:
通过上述对比实验数据可知,本发明一种光学漂白剂BMC相较于现有的TINOPAL BMC相比有更好的白度。
以上所述仅是本发明的优选实施方式,本发明的保护范围并不仅局限于上述实施例,凡属于本发明思路下的技术方案均属于本发明的保护范围。应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理前提下的若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。

Claims (5)

1.一种光学漂白剂BMC,其特征在于:本发明的配方包括组分A组分B和元明粉,在同E值的情况下,组分A组分B的质量之比为7:3,元明粉用于调节E值,最后配出的混合物E=218±5,所述组分A由邻苯二腈30g、Zn粉3.8g、钼酸铵0.3g、一缩二乙二醇240g、冰醋酸1g和氮气、磺酸150g、氢氧化钠130g、冰800g、水300g和30%--32%盐酸合成;所述组分B由铝酞菁40g、氯磺酸150g、氢氧化钠130g、冰800g、水130g和30%--32%盐酸合成。
2.根据权利要求1所述的一种光学漂白剂BMC的合成方法,其特征在于:将一缩二乙二醇投入到干燥的500ml四口瓶中,搅拌,通氮气以置换出瓶中的空气,再加入锌粉、钼酸铵和邻苯二腈,加热;当温度升到100-180℃时,滴加入冰醋酸,在100℃~160℃保温2-8h,降温,当温度降到100℃时,过滤;滤饼用水洗至滴下的滤液无色,再用甲醇洗涤,再水洗;烘箱中干燥;对烘干后的滤饼进行粉碎,进行E值、吸收值的检测。
3.根据权利要求2所述的一种光学漂白剂BMC的合成方法,其特征在于: 1)将氯磺酸加入到500ml的洁净四口烧瓶中,搅拌,通氮气,把温度升到100-160℃,再用恒压滴液漏斗往里加锌酞菁,大约1-3小时加完,保温2-6小时;2)保温好后,将反应混合物倒入到溶有NaOH的冰水中,倒入时搅拌,测得PH=12.3,在30℃用30---32%的盐酸调节PH=0.5,搅拌30min,30℃过滤,滤时滤液为透明的浅蓝色液体;3)将滤饼溶于300ml水中,搅拌,用NaOH水溶液调节PH=6-10,蒸去水,烘干。
4.根据权利要求3所述的一种光学漂白剂BMC的合成方法,其特征在于:1)投料:做好一切准备后开始投料,取150g氯磺酸投入干净干燥以及装置好废气回收的4口反应瓶中;2)升温:投完后开始升温,开启氮气保护,升温至100-160℃;3)加铝酞青:将称量好的40g铝酞青倒入准备好的滴加漏斗中,匀速加入进行磺化反应,其温度控制在100-160℃,约1-3小时加完;4)保温:保温2-6小时;5)检测:保温结束后取样用氢氧化钠中和后进行吸收值检测是否反应完全;6)复配氢氧化钠溶液:氢氧化钠按照氯磺酸的投料量进行换算,总计为130g加130g水进行溶解;7)酸碱中和放热反应:将反应好的铝钛青溶剂慢慢倒入复配好的氢氧化钠溶液中,要求慢慢加入,并用小冰块不断进行冷却,确保反应过程中温度不能过高;8)PH值调整:放热完后,常温搅拌并用盐酸进行PH值调整,将其PH值调为6-10;9)浓缩:将调整好的溶液进行蒸馏浓缩,当物料开始发稠后进行转料到烘箱进行烘烤,温度在120-130度之间,直至烘干;10)检测:对烘干后的滤饼进行粉碎,进行E值、吸收值的检测。
5.根据权利要求4所述的一种光学漂白剂BMC的合成方法,其特征在于:计算组分A和组分B和元明粉的用量,在同E值的情况下,将组分A和组分B和元明粉按比例混合均匀。
CN201710377842.2A 2017-05-25 2017-05-25 一种光学漂白剂bmc及其合成工艺 Pending CN107268263A (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710377842.2A CN107268263A (zh) 2017-05-25 2017-05-25 一种光学漂白剂bmc及其合成工艺

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710377842.2A CN107268263A (zh) 2017-05-25 2017-05-25 一种光学漂白剂bmc及其合成工艺

Publications (1)

Publication Number Publication Date
CN107268263A true CN107268263A (zh) 2017-10-20

Family

ID=60064244

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710377842.2A Pending CN107268263A (zh) 2017-05-25 2017-05-25 一种光学漂白剂bmc及其合成工艺

Country Status (1)

Country Link
CN (1) CN107268263A (zh)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030022179A (ko) * 2003-01-27 2003-03-15 권종호 마이크로파 에너지를 이용한 금속 및 무금속 프탈로시아닌의 합성법
CN1833019A (zh) * 2003-08-06 2006-09-13 宝洁公司 包含光漂白组分和荧光增白组分的用于处理纺织品的组合物
CN101153458A (zh) * 2006-09-29 2008-04-02 沈阳新纪化学有限公司 一种酞菁类光学漂白剂及其制备和应用
CN103740126A (zh) * 2007-11-26 2014-04-23 宝洁公司 洗涤剂组合物
CN105131001A (zh) * 2015-08-25 2015-12-09 辽宁大学 一种无取代锌酞菁的合成方法
CN106496238A (zh) * 2016-10-19 2017-03-15 东北大学 一种溶剂热法制备金属酞菁化合物的方法

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030022179A (ko) * 2003-01-27 2003-03-15 권종호 마이크로파 에너지를 이용한 금속 및 무금속 프탈로시아닌의 합성법
CN1833019A (zh) * 2003-08-06 2006-09-13 宝洁公司 包含光漂白组分和荧光增白组分的用于处理纺织品的组合物
CN101153458A (zh) * 2006-09-29 2008-04-02 沈阳新纪化学有限公司 一种酞菁类光学漂白剂及其制备和应用
CN103740126A (zh) * 2007-11-26 2014-04-23 宝洁公司 洗涤剂组合物
CN105131001A (zh) * 2015-08-25 2015-12-09 辽宁大学 一种无取代锌酞菁的合成方法
CN106496238A (zh) * 2016-10-19 2017-03-15 东北大学 一种溶剂热法制备金属酞菁化合物的方法

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
刘延春等: "新型光漂剂的漂白剂性能研究", 《日用化学工业》 *
周春隆等: "《有机颜料化学及工艺学》", 30 June 2014, 中国石化出版社 *

Similar Documents

Publication Publication Date Title
CN100543012C (zh) 制备1,4-二氨基-2,3-二氰基蒽醌的方法
CN111943922B (zh) 一种从吸附活性炭中回收3,3′,4,4′-二苯醚四甲酸二酐和活性炭再利用的方法
CN107268263A (zh) 一种光学漂白剂bmc及其合成工艺
CN106635571A (zh) 一种带吸色功能的洗衣片及其制备方法
CN105061244B (zh) 甘氨酸铁锌配合物的制备方法
CN110256238A (zh) 一种长链混合二元酸的精制方法
CN106831588A (zh) 一种食品添加剂柠檬黄的合成方法
CN103306134A (zh) 一种类能改性蛋白质纤维的表面处理剂及其制备方法和用途
CN105524485B (zh) 一种活性红染料的制备方法
CN106496068B (zh) 丙二酸二甲酯的制备方法
CN102660131A (zh) 还原黄3rt的生产方法
CN104195820B (zh) 一种棉用抗皱剂及其制备方法和应用
CN106543101B (zh) 一种苯达松脱色和提纯方法
CN106543098A (zh) 一种多功能型紫外线吸收剂的制备方法及其应用
CN102344420B (zh) 一种三(三溴苯氧基)三嗪的制备方法
CN103420935B (zh) 一种处理糖精钠结晶母液的方法
CN106008239A (zh) 一种溶剂蓝35的生产方法
CN1286920C (zh) 活性红sbe及其合成方法
CN208717203U (zh) 一种新型磺化对位酯生产系统
CN109971203A (zh) 一种色素柠檬黄的制备方法
CN110066230A (zh) 一种新型磺化对位酯生产系统和工艺
CN104447308B (zh) 尼泊金甲酯的合成方法
CN205216527U (zh) 醋酸锰生产尾气的处理装置
CN117089222A (zh) 一种阳离子黄色染料及其制备方法
CN215901729U (zh) 一种高纯度甲醇镁的间歇反应装置

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20171020