[go: up one dir, main page]

CN103601811A - Method for causticizing corn starch - Google Patents

Method for causticizing corn starch Download PDF

Info

Publication number
CN103601811A
CN103601811A CN201310569503.6A CN201310569503A CN103601811A CN 103601811 A CN103601811 A CN 103601811A CN 201310569503 A CN201310569503 A CN 201310569503A CN 103601811 A CN103601811 A CN 103601811A
Authority
CN
China
Prior art keywords
cornstarch
causticizing
gum
add
starch
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
CN201310569503.6A
Other languages
Chinese (zh)
Inventor
陈占金
郑洁
栾玲
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.)
Angang Group Mining Co Ltd
Original Assignee
Angang Group Mining 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 Angang Group Mining Co Ltd filed Critical Angang Group Mining Co Ltd
Priority to CN201310569503.6A priority Critical patent/CN103601811A/en
Publication of CN103601811A publication Critical patent/CN103601811A/en
Pending legal-status Critical Current

Links

Landscapes

  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

本发明提供了一种玉米淀粉的苛化方法,其特征在于,玉米淀粉下料水温度在40~50℃,边加料边搅拌,加料完成,充分搅拌均匀,形成悬浮液后,再加入重量与容量百分比为20%的氢氧化钠溶液,加入氢氧化钠固体质量与玉米淀粉质量比为4:100,之后,升温至65~75℃,苛化一小时,加水定容,得玉米淀粉溶液,保温备用。采用本发明的玉米淀粉苛化方法,制得的玉米淀粉溶液,性质均匀稳定,容易保存,不易变质。用作为铁矿物抑制剂,在配制过程不会出现“包团”的现象,淀粉利用率高。降低选矿药剂消耗5%以上,由于降低苛化温度,也降低了能耗。The invention provides a causticizing method of cornstarch, which is characterized in that the temperature of cornstarch feed water is 40-50°C, stirring while feeding, and after the feeding is completed, it is fully stirred evenly to form a suspension, and then the weight and Sodium hydroxide solution with a volume percentage of 20%, add sodium hydroxide solid mass to corn starch with a mass ratio of 4:100, then raise the temperature to 65-75°C, causticize for one hour, add water to constant volume, and obtain a corn starch solution. Keep warm. By adopting the cornstarch causticizing method of the present invention, the prepared cornstarch solution has uniform and stable properties, is easy to preserve, and is not easy to deteriorate. Used as an iron mineral inhibitor, there will be no "clustering" phenomenon during the preparation process, and the starch utilization rate is high. Reduce the consumption of beneficiation agents by more than 5%, and reduce the energy consumption due to the reduction of causticizing temperature.

Description

玉米淀粉的苛化方法Causticizing method of corn starch

技术领域 technical field

本发明涉及一种玉米淀粉的苛化方法。 The invention relates to a causticizing method of corn starch.

背景技术 Background technique

浮选是矿物选别的一种重要方法,一般需要将矿物磨细后加入选矿药剂进行分选。在赤铁矿的反浮选过程中,一般用玉米淀粉作为铁矿物的抑制剂。 Flotation is an important method of mineral separation. Generally, it is necessary to grind the minerals and add mineral dressing agents for separation. In the reverse flotation process of hematite, corn starch is generally used as an inhibitor of iron minerals.

淀粉是非极性矿物和赤铁矿反浮选的重要抑制剂。它能起抑制作用是由于变形淀粉分子上羟基、羧基等极性基的存在。所以淀粉可以通过氢键与水分子缔合,使受它作用的矿粒变为亲水性。玉米淀粉的苛化实际上就是一个改性过程,苛化可导致淀粉团粒发生了较大程度的膨胀和水合,使得淀粉分子基环间的氧桥断裂,降解程度加大,同时支链淀粉大分子发生氧化降解的几率增加 ,淀粉团粒的膨胀部分地破坏了淀粉分子内的羟基缔合,使羟基被氧化的几率增多,有利于提高淀粉分子间的作用力,生成的羧基相对较多,所以对铁矿物的抑制作用会明显提高。 Starch is an important depressant in reverse flotation of non-polar minerals and hematite. It can play an inhibitory role due to the existence of polar groups such as hydroxyl and carboxyl on the deformed starch molecule. Therefore, starch can associate with water molecules through hydrogen bonds, making the mineral particles affected by it become hydrophilic. The causticization of corn starch is actually a modification process. Causticization can lead to a large degree of swelling and hydration of starch aggregates, which makes the oxygen bridges between the starch molecular rings break and the degree of degradation increases. At the same time, the amylopectin is large The probability of oxidative degradation of molecules increases, and the swelling of starch aggregates partially destroys the association of hydroxyl groups in starch molecules, increasing the probability of hydroxyl groups being oxidized, which is conducive to improving the force between starch molecules and generating relatively more carboxyl groups. The inhibitory effect on iron minerals will be significantly improved.

目前,选矿行业玉米淀粉的配制方法是先将需要配制的淀粉投入加有适量水的调浆桶搅拌均匀,升温配药桶至90℃,向配药桶加入适量的20%氢氧化钠溶液。然后在90℃条件下苛化一小时,加水定容,备用。从配制加料至苛化过程中均在90℃条件下,经常出现“包团”现象,即表面糊化的淀粉内部夹有生淀粉,并且“包团”很难充分破碎。这样在糊化结束后的料液中,仍然残留有生淀粉,而不能利用,不仅降低了淀粉的利用率,更重要的是会对选矿指标产生不良影响。因此,在选矿行业,使用玉米淀粉作为铁矿物的抑制剂时,玉米淀粉的苛化效果显得尤为重要。 At present, the preparation method of corn starch in the mineral processing industry is to first put the starch to be prepared into a mixing tank with an appropriate amount of water and stir evenly, then raise the temperature of the mixing tank to 90°C, and add an appropriate amount of 20% sodium hydroxide solution to the mixing tank. Then causticize at 90°C for one hour, add water to make up volume, and set aside. From the preparation and feeding to the causticization process, under the condition of 90°C, the phenomenon of "clustering" often occurs, that is, the gelatinized starch on the surface contains raw starch inside, and the "clustering" is difficult to fully break. In this way, raw starch still remains in the feed liquid after gelatinization, which cannot be used, which not only reduces the utilization rate of starch, but more importantly, it will have a negative impact on the beneficiation index. Therefore, in the mineral processing industry, when corn starch is used as an inhibitor of iron minerals, the causticizing effect of corn starch is particularly important.

发明内容 Contents of the invention

本发明的目的是提供一种玉米淀粉的苛化方法。 The purpose of this invention is to provide a kind of causticizing method of cornstarch.

按照本发明所述的玉米淀粉的苛化方法,其特征在于,玉米淀粉下料水温度在40~50℃,边加料边搅拌,加料完成,充分搅拌均匀,形成悬浮液后,再加入重量与容量百分比为20%的氢氧化钠溶液,加入氢氧化钠固体质量与玉米淀粉质量比为4:100 ,之后,升温至65~75℃,苛化一小时,加水定容,得玉米淀粉溶液,保温备用。 According to the causticizing method of cornstarch according to the present invention, it is characterized in that the temperature of cornstarch cutting water is 40-50°C, stirring while feeding, after the feeding is completed, fully stir evenly, and after forming a suspension, add the weight and Sodium hydroxide solution with a volume percentage of 20%, add sodium hydroxide solid mass to corn starch with a mass ratio of 4:100, then raise the temperature to 65-75°C, causticize for one hour, add water to constant volume, and obtain a corn starch solution. Keep warm.

按照本发明所述的玉米淀粉的苛化方法,其特征在于,在药剂配制桶中,加入玉米淀粉质量8~10倍的水,并加温,使水温度在40~50℃,加入玉米淀粉,边加料边搅拌,加料完成,充分搅拌均匀,形成悬浮液后,再加入重量百分比浓度为为20%的氢氧化钠溶液,加入氢氧化钠固体质量与玉米淀粉质量比为4:100 ,之后,升温至65~75℃,苛化一小时,加水定容,配制成重量百分比浓度为1.5~5%的玉米淀粉液,保温备用。 The method for causticizing cornstarch according to the present invention is characterized in that, in the medicament preparation tank, add water 8 to 10 times the weight of cornstarch, and heat it so that the water temperature is 40-50°C, then add cornstarch , stirring while feeding, the feeding is completed, fully stirred evenly, after forming a suspension, then add a sodium hydroxide solution with a concentration of 20% by weight, and add a solid mass of sodium hydroxide to a mass ratio of cornstarch of 4:100, and then , heat up to 65-75°C, causticize for one hour, add water to constant volume, prepare a cornstarch liquid with a concentration of 1.5-5% by weight, and keep it warm for later use.

本发明的玉米淀粉的苛化方法,在玉米淀粉的苛化过程中,由于玉米淀粉的糊化温度点较低,因此,下料水的温度不应过高,一般不超过50℃。过高的下料水温会使玉米淀粉下料后,尚未充分的预糊化即进入糊化,从而引起淀粉结晶区的变化,而成为老化淀粉。经过我们大量的实验研究证明,玉米淀粉的糊化温度为65~75℃。由于玉米淀粉过细的粒度,能在较高的水温下形成“包团”现象,即表面糊化的淀粉内部夹有生淀粉,并且“包团”很难充分破碎。这样在苛化结束后的料液中仍然残留有生淀粉而不能利用,不仅降低了淀粉的利用率,更重要的是会对选矿指标产生不良影响。 In the causticizing method of cornstarch of the present invention, during the causticizing process of cornstarch, since the gelatinization temperature of cornstarch is relatively low, the temperature of the feed water should not be too high, generally not exceeding 50°C. Excessively high feed water temperature will cause corn starch to enter gelatinization without sufficient pre-gelatinization after feed, which will cause changes in the starch crystallization area and become aged starch. After a lot of experimental research, it has been proved that the gelatinization temperature of corn starch is 65-75°C. Due to the fine particle size of cornstarch, the phenomenon of "clustering" can be formed at a higher water temperature, that is, the gelatinized starch on the surface contains raw starch inside, and the "clustering" is difficult to fully break. In this way, raw starch still remains in the feed liquid after causticizing and cannot be used, which not only reduces the utilization rate of starch, but more importantly, it will have a negative impact on the beneficiation index.

采用本发明的玉米淀粉苛化方法,制得的玉米淀粉溶液,性质均匀稳定,容易保存,不易变质。用作为铁矿物抑制剂,在配制过程不会出现 “包团”的现象,淀粉利用率高。降低选矿药剂消耗5%以上,由于降低苛化温度,也降低了能耗。 By adopting the cornstarch causticizing method of the present invention, the prepared cornstarch solution has uniform and stable properties, is easy to preserve, and is not easy to deteriorate. Used as an iron mineral inhibitor, there will be no "clustering" phenomenon during the preparation process, and the starch utilization rate is high. Reduce the consumption of beneficiation agents by more than 5%, and reduce the energy consumption due to the reduction of causticizing temperature.

具体实施方式 Detailed ways

实施例:Example:

玉米淀粉的苛化方法:在药剂配制桶中,加入玉米淀粉质量8~10倍的水,并加温,使水温度在40~50℃,加入玉米淀粉,边加料边搅拌,加料完成,充分搅拌均匀,形成悬浮液后,再加入重量百分比浓度为20%的氢氧化钠溶液,加入氢氧化钠固体质量与玉米淀粉质量比为4:100 ,之后,升温至65~75℃,苛化一小时,加水定容,配制成重量百分比浓度为1.5~5%的玉米淀粉液,保温备用。 The causticizing method of corn starch: add water 8 to 10 times the mass of corn starch in the medicament preparation tank, and heat it so that the water temperature is 40 to 50°C, add corn starch, stir while adding, until the addition is complete, fully Stir evenly to form a suspension, then add a sodium hydroxide solution with a concentration of 20% by weight, and add a solid mass of sodium hydroxide to corn starch with a mass ratio of 4:100, and then heat up to 65-75°C and causticize for one hour, add water to make it volume, and prepare cornstarch liquid with a concentration of 1.5-5% by weight, and keep it warm for later use.

原方法从配制加料至苛化过程中均在90℃条件下,降低了淀粉的利用率,更重要的是会对选矿指标产生不良影响。玉米淀粉采用不同配置方法取得的试验数据及对同一批赤铁矿原矿样品进行浮选试验取得数据。实施例方法与原方法的对比数据如下: The original method is under the condition of 90°C from the process of preparation and feeding to causticization, which reduces the utilization rate of starch, and more importantly, it will have a bad influence on the beneficiation index. The test data obtained by using different configuration methods of corn starch and the data obtained by the flotation test of the same batch of hematite raw ore samples. The comparative data of embodiment method and former method are as follows:

例如:   玉米淀粉浓度   玉米淀粉的利用率   药剂消耗量      浮精品位    浮尾品位  For example: Concentration of cornstarch Utilization rate of cornstarch Chemical consumption Floating grade Floating tail grade

实施例1     1.5%        99%          600g/t          68.12%    11.28% Example 1 1.5% 99% 600g/t 68.12% 11.28%

原方法1     1.5%        98%          650g/t          68.06%    11.55%     Original method 1 1.5% 98% 650g/t 68.06% 11.55%

实施例2     2.5%        99%          710g/t          67.88%    10.51% Example 2 2.5% 99% 710g/t 67.88% 10.51%

原方法2     2.5%        98%          755g/t          67.86%    10.78% Original method 2 2.5% 98% 755g/t 67.86% 10.78%

实施例3     4%         99%          680g/t          67.28%    10.41% Example 3 4% 99% 680g/t 67.28% 10.41%

原方法3     4%         98%          730g/t          67.26%    10.68% Original method 3 4% 98% 730g/t 67.26% 10.68%

实施例4     6%         99%          685g/t          67.27%    10.50% Example 4 6% 99% 685g/t 67.27% 10.50%

原方法4     6%         98%          738g/t          67.23%    10.55% Original method 4 6% 98% 738g/t 67.23% 10.55%

实施例5     7.5%         99%        630g/t          67.68%    10.75% Example 5 7.5% 99% 630g/t 67.68% 10.75%

原方法5     7.5%         98%        680g/t          67.65%    10.78% Original method 5 7.5% 98% 680g/t 67.65% 10.78%

实施例6     9%          99%        685g/t          67.60%    10.48% Example 6 9% 99% 685g/t 67.60% 10.48%

原方法6     9%          98%        738g/t          67.58%    10.55% Original method 6 9% 98% 738g/t 67.58% 10.55%

实施例7     10%         99%        660g/t          67.52%    10.88% Example 7 10% 99% 660g/t 67.52% 10.88%

原方法7     10%         98%        670g/t          67.48%    10.92%。 The original method 7 10% 98% 670g/t 67.48% 10.92%.

Claims (2)

1. a causticization method for W-Gum, is characterized in that, W-Gum blanking water temp is at 40~50 ℃, while feeding in raw material, stir, fed in raw material, stirred, formed after suspension, adding sodium hydrate solid quality and W-Gum mass ratio is 4-5:100, afterwards, be warming up to 65~75 ℃, causticization one hour, add water constant volume, be mixed with weight percent and be 1.5~10% W-Gum liquid.
2. the causticization method of W-Gum according to claim 1, it is characterized in that, in medicament preparation bucket, add the water of 8~10 times of W-Gum quality, and heat, make water temp at 40~50 ℃, add W-Gum, while feeding in raw material, stir, fed in raw material, stir, form after suspension, adding sodium hydrate solid quality and W-Gum mass ratio is 4:100, afterwards, is warming up to 65~75 ℃, causticization one hour, add water constant volume, be mixed with weight and volume percent and be 1.5~5% W-Gum liquid, be incubated standby.
CN201310569503.6A 2013-11-13 2013-11-13 Method for causticizing corn starch Pending CN103601811A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310569503.6A CN103601811A (en) 2013-11-13 2013-11-13 Method for causticizing corn starch

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310569503.6A CN103601811A (en) 2013-11-13 2013-11-13 Method for causticizing corn starch

Publications (1)

Publication Number Publication Date
CN103601811A true CN103601811A (en) 2014-02-26

Family

ID=50120085

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310569503.6A Pending CN103601811A (en) 2013-11-13 2013-11-13 Method for causticizing corn starch

Country Status (1)

Country Link
CN (1) CN103601811A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104226488A (en) * 2014-07-29 2014-12-24 唐山学院 Preparation method of micro-fine particle hematite reverse flotation depressing agent
CN113477408A (en) * 2021-07-21 2021-10-08 东北大学 Application of curdlan serving as inhibitor in iron ore reverse flotation in mineral processing field and application method
CN114891128A (en) * 2022-03-18 2022-08-12 上海逢石科技有限公司 Preparation and use method of modified starch inhibitor for hematite reverse flotation

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101007668A (en) * 2007-01-19 2007-08-01 盛力 Natural organic high-molecular flocculant and its preparation method
CN101704894A (en) * 2009-12-08 2010-05-12 湖南省铸万有实业有限公司 Corn starch pasting method
US20100298266A1 (en) * 2004-03-01 2010-11-25 Michael Boll Hydroxyethylstarch
CN102153664A (en) * 2011-01-17 2011-08-17 温州大学 Method for preparing nanometer lamellar sodium carboxymethyl starch
CN102274797A (en) * 2011-08-16 2011-12-14 鞍钢集团矿业公司 Sorting process capable of improving sorting indexes of siderite-containing ore
CN103193891A (en) * 2013-04-10 2013-07-10 郑桂富 Preparation method of starch acetoacetic ester

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100298266A1 (en) * 2004-03-01 2010-11-25 Michael Boll Hydroxyethylstarch
CN101007668A (en) * 2007-01-19 2007-08-01 盛力 Natural organic high-molecular flocculant and its preparation method
CN101704894A (en) * 2009-12-08 2010-05-12 湖南省铸万有实业有限公司 Corn starch pasting method
CN102153664A (en) * 2011-01-17 2011-08-17 温州大学 Method for preparing nanometer lamellar sodium carboxymethyl starch
CN102274797A (en) * 2011-08-16 2011-12-14 鞍钢集团矿业公司 Sorting process capable of improving sorting indexes of siderite-containing ore
CN103193891A (en) * 2013-04-10 2013-07-10 郑桂富 Preparation method of starch acetoacetic ester

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
张国庆: "不同淀粉对混合磁选精矿抑制效果的研究", 《金属矿山》 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104226488A (en) * 2014-07-29 2014-12-24 唐山学院 Preparation method of micro-fine particle hematite reverse flotation depressing agent
CN104226488B (en) * 2014-07-29 2016-08-03 唐山学院 The preparation method of microfine hematite reverse flotation inhibitor
CN113477408A (en) * 2021-07-21 2021-10-08 东北大学 Application of curdlan serving as inhibitor in iron ore reverse flotation in mineral processing field and application method
CN114891128A (en) * 2022-03-18 2022-08-12 上海逢石科技有限公司 Preparation and use method of modified starch inhibitor for hematite reverse flotation

Similar Documents

Publication Publication Date Title
CN102443071B (en) Composite modified starch as hematite reverse flotation inhibitor and preparation method thereof
CN105967266A (en) Efficient sewage treatment agent and preparation method thereof
CN101704895A (en) Preparation method of highly viscous feeding pregelatinized starch
CN103601811A (en) Method for causticizing corn starch
CN101525447A (en) Lignin-modified kaolin and application thereof as rubber reinforcing agent
CN103627055A (en) Method for preparing tire tread rubber by use of modified microcrystalline cellulose
CN109749168B (en) Nano zinc oxide/rubber composite material and preparation method thereof
CN104001627B (en) The inhibitor of calcic gangue mineral in a kind of Selective depression scheelite Ore
CN102234387A (en) Calcium sulfate whisker modified rubber and preparation process thereof
CN107176800B (en) A kind of liquid cement grinding additive and preparation method thereof
CN104437889A (en) Hematite anti-floatation depressor
CN104069952B (en) The inhibitor of gangue mineral and application thereof in a kind of graphite ore
CN105085947A (en) Multiwalled-carbon-nanotube-loaded polyimide high-dielectric-permittivity composite film doped with nano titanium carbide and used for capacitor and preparing method of composite film
CN103275404B (en) A kind of ethylene-propylene rubber(EPR)/agricultural waste gurry matrix material and its preparation method and application
CN103788263B (en) Method for preparing temperature-resistant and salt-resistant fluid loss reducer by using waste polystyrene foam
CN102585388A (en) Chlorinated polyethylene rubber material
CN107602953B (en) A kind of silica/natural rubber latex composite adhesive film and its preparation method and application
CN101525448A (en) Lignin-modified diatomite and application thereof as rubber reinforcing agent
CN107988838A (en) A kind of fluffy technology for making daily used paper
CN108285650B (en) A kind of barley grains-based composite packaging film and preparation method thereof
CN105597943A (en) Flotation depressing agent as well as preparation method and application thereof
CN106634688B (en) A kind of thermosetting property oxidation modification Cassava starch adhesive and preparation method thereof
CN110558477A (en) Low-digestibility rice flour and preparation method thereof
CN104624383B (en) Hematite reverse flotation inhibitor and preparation and use method thereof
CN107500800A (en) Porous ceramic film material containing copper tailing and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20140226